| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:71895902-71896044 | Common:2; Rare:47 | ||||
| chr16:72008452-72008987 | Common:7; Rare:200; Clinvar (benign):2 | ||||
| chr16:72093520-72093979 | Common:1; Rare:117 | ||||
| chr16:72094340-72094664 | Common:2; Rare:61 | ||||
| chr16:73047737-73047965 | Rare:53 | ||||
| chr16:73047986-73048436 | Common:3; Rare:121 | ||||
| chr16:73048544-73048709 | Common:1; Rare:41 | ||||
| chr16:73059123-73059412 | Common:7; Rare:57 | ||||
| chr16:74296176-74296352 | Common:1; Rare:41 | ||||
| chr16:74296400-74297130 | Common:4; Rare:237 | ||||
| chr16:74606634-74606895 | Common:1; Rare:114 | ||||
| chr16:74606996-74607419 | Common:2; Rare:182 | ||||
| chr16:74666783-74667078 | Common:5; Rare:115 | ||||
| chr16:74700211-74700356 | Common:1; Rare:28 | ||||
| chr16:74700465-74701247 | Common:5; Rare:160 |