| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:100088840-100089170 | Rare:131; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr13:100588348-100588429 | Rare:25 | ||||
| chr13:100588556-100588912 | Common:6; Rare:112 | ||||
| chr13:100673978-100674474 | Common:3; Rare:149 | ||||
| chr13:100674509-100674590 | Rare:22 | ||||
| chr13:100674651-100675396 | Common:8; Rare:284 | ||||
| chr13:101415679-101415864 | Common:2; Rare:46 | ||||
| chr13:101416204-101416544 | Common:3; Rare:74 | ||||
| chr13:101416688-101416734 | Common:1; Rare:11 | ||||
| chr13:101416849-101416931 | Rare:14 | ||||
| chr13:101416951-101417242 | Common:1; Rare:48 | ||||
| chr13:102596124-102596590 | Common:3; Rare:78 | ||||
| chr13:102596660-102597087 | Common:1; Rare:164; Clinvar (benign):1 | ||||
| chr13:102773342-102773978 | Common:3; Rare:196 | ||||
| chr13:102798510-102798537 | Rare:9 |