| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:98995790-98996130 | Common:3; Rare:166 | ||||
| chr4:99088639-99088978 | Common:22; Rare:346 | ||||
| chr4:99563560-99563890 | Common:6; Rare:260 | ||||
| chr4:99563910-99564240 | Common:4; Rare:205; Clinvar:6; Clinvar (benign):4 | ||||
| chr4:99816703-99816855 | Common:1; Rare:15 | ||||
| chr4:99894334-99894671 | Common:8; Rare:301 | ||||
| chr4:99946484-99946881 | Rare:330 | ||||
| chr4:99949661-99950037 | Common:7; Rare:200 | ||||
| chr4:99950151-99950665 | Common:1; Rare:309 | ||||
| chr4:100190310-100190720 | Common:7; Rare:76 | ||||
| chr4:101346350-101346780 | Common:6; Rare:180 | ||||
| chr4:101346817-101347232 | Common:7; Rare:181 | ||||
| chr4:101347234-101347897 | Common:16; Rare:435 | ||||
| chr4:101347910-101348252 | Rare:233 | ||||
| chr4:101411698-101411829 | Common:1; Rare:27 |