| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:47960804-47960941 | Common:1; Rare:50; Clinvar:3 | ||||
| chr8:55773331-55773492 | Common:3; Rare:51 | ||||
| chr8:60516793-60517009 | Common:3; Rare:80 | ||||
| chr8:63038766-63038919 | Common:2; Rare:58 | ||||
| chr8:70608254-70608553 | Common:3; Rare:83 | ||||
| chr8:86514350-86514478 | Common:1; Rare:31 | ||||
| chr8:91070023-91070346 | Common:1; Rare:114 | ||||
| chr8:96235502-96235650 | Common:1; Rare:77; Clinvar (benign):2 | ||||
| chr8:96261586-96261946 | Common:5; Rare:113 | ||||
| chr8:98117144-98117317 | Common:2; Rare:58 | ||||
| chr8:103415071-103415461 | Common:6; Rare:203 | ||||
| chr8:108443463-108443658 | Common:3; Rare:83 | ||||
| chr8:109334067-109334396 | Common:1; Rare:85 | ||||
| chr8:120445120-120445425 | Common:1; Rare:68 | ||||
| chr8:124539042-124539190 | Common:2; Rare:82; Clinvar (benign):5; Clinvar (pathogenic):1 |