| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4867624-4867895 | Common:4; Rare:77 | ||||
| chr19:5293222-5293433 | Common:1; Rare:93 | ||||
| chr19:5622742-5623181 | Common:5; Rare:168 | ||||
| chr19:5680904-5681169 | Rare:82 | ||||
| chr19:5978078-5978415 | Common:3; Rare:130 | ||||
| chr19:6684790-6685081 | Rare:82; Clinvar (benign):1 | ||||
| chr19:7395022-7395185 | Common:4; Rare:50 | ||||
| chr19:7488997-7489175 | Common:2; Rare:80 | ||||
| chr19:7629532-7629844 | Common:5; Rare:111; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636969-7637143 | Common:2; Rare:57; Clinvar (benign):1 | ||||
| chr19:8308308-8308638 | Common:2; Rare:102 | ||||
| chr19:8321316-8321568 | Common:2; Rare:115 | ||||
| chr19:8390068-8390412 | Common:1; Rare:97 | ||||
| chr19:8444814-8444996 | Common:2; Rare:79 | ||||
| chr19:8514154-8514227 | Common:1; Rare:19 |