Human Assembly | Chr | Position (strand) | Source |
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GRCh37 | 6 | 169,997,898 - 169,998,059 | UniSTS | GRCh37 | 6 | 169,997,844 - 169,998,052 | UniSTS | GRCh37 | 6 | 169,997,957 - 169,998,059 | UniSTS | Build 36 | 6 | 169,739,882 - 169,739,984 | RGD | Celera | 6 | 170,708,141 - 170,708,300 | UniSTS | Celera | 6 | 170,708,200 - 170,708,300 | RGD | Celera | 6 | 170,708,087 - 170,708,293 | UniSTS | Cytogenetic Map | 6 | q27 | UniSTS | HuRef | 6 | 167,419,922 - 167,420,022 | UniSTS | HuRef | 6 | 167,419,863 - 167,420,022 | UniSTS | HuRef | 6 | 167,419,809 - 167,420,015 | UniSTS | Marshfield Genetic Map | 6 | 190.14 | RGD | Genethon Genetic Map | 6 | 201.1 | UniSTS | TNG Radiation Hybrid Map | 6 | 85013.0 | UniSTS | deCODE Assembly Map | 6 | 188.38 | UniSTS | Stanford-G3 RH Map | 6 | 6741.0 | UniSTS | GeneMap99-GB4 RH Map | 6 | 648.15 | UniSTS | Whitehead-RH Map | 6 | 851.7 | UniSTS | Whitehead-YAC Contig Map | 6 | | UniSTS | NCBI RH Map | 6 | 1674.5 | UniSTS | GeneMap99-G3 RH Map | 6 | 7044.0 | UniSTS |