| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:139404056-139404281 | Rare:70 | ||||
| chr5:139482230-139482565 | Common:3; Rare:54 | ||||
| chr5:139482608-139482899 | Rare:43 | ||||
| chr5:139561122-139561415 | Common:1; Rare:119 | ||||
| chr5:139561727-139561815 | Rare:33 | ||||
| chr5:140107625-140107846 | Rare:81 | ||||
| chr5:140174878-140175280 | Common:1; Rare:115 | ||||
| chr5:140303065-140303227 | Common:1; Rare:50 | ||||
| chr5:140346573-140346721 | Common:1; Rare:43 | ||||
| chr5:140547383-140547719 | Common:3; Rare:69 | ||||
| chr5:140557404-140557557 | Common:2; Rare:97 | ||||
| chr5:140564273-140564568 | Common:2; Rare:72 | ||||
| chr5:140564573-140564843 | Rare:75 | ||||
| chr5:140633529-140633808 | Common:5; Rare:59 | ||||
| chr5:140647579-140647924 | Common:5; Rare:141; Clinvar:4; Clinvar (benign):3 |