Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:959054-959511 | Common:5; Rare:337 | ||||
chr1:960313-960698 | Common:5; Rare:146 | ||||
chr1:960700-960960 | Common:3; Rare:154 | ||||
chr1:966394-966526 | Common:2; Rare:53 | ||||
chr1:1000005-1000524 | Common:16; Rare:320 | ||||
chr1:1000580-1001120 | Common:11; Rare:239 | ||||
chr1:1013325-1013557 | Common:7; Rare:132 | ||||
chr1:1019729-1020173 | Common:2; Rare:138 | ||||
chr1:1116035-1116290 | Rare:73 | ||||
chr1:1231883-1232299 | Rare:278; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr1:1273782-1274083 | Common:4; Rare:223 | ||||
chr1:1307811-1308160 | Rare:167 | ||||
chr1:1308411-1308665 | Common:16; Rare:209 | ||||
chr1:1324576-1324979 | Common:6; Rare:344 | ||||
chr1:1349315-1349616 | Common:4; Rare:196 |