| No. |
Chromosome Location |
Chromatin state |
Cell line |
Tissue |
| 1 |
chr6:30135600-30141200 |
Strong transcription |
HepG2 |
liver
|
| 2 |
chr6:30139000-30152000 |
Weak transcription |
Liver |
Liver
|
| 3 |
chr6:30139400-30140600 |
Bivalent Enhancer |
Primary B cells from peripheral blood |
blood
|
| 4 |
chr6:30139400-30140800 |
Bivalent Enhancer |
Primary T helper cells PMA-I stimulated |
--
|
| 5 |
chr6:30139600-30140600 |
Flanking Bivalent TSS/Enh |
Foreskin Fibroblast Primary Cells skin01 |
Skin
|
| 6 |
chr6:30139600-30140600 |
Weak transcription |
Duodenum Mucosa |
Duodenum
|
| 7 |
chr6:30140000-30140600 |
Bivalent Enhancer |
Primary T helper memory cells from peripheral blood 2 |
blood
|
| 8 |
chr6:30140000-30140800 |
Bivalent Enhancer |
Fetal Thymus |
thymus
|
| 9 |
chr6:30140200-30140600 |
Bivalent Enhancer |
Foreskin Fibroblast Primary Cells skin02 |
Skin
|
| 10 |
chr6:30140200-30140800 |
Bivalent Enhancer |
H9 Cell Line |
embryonic stem cell
|
| 11 |
chr6:30140400-30140600 |
Flanking Bivalent TSS/Enh |
HUES48 Cell Line |
embryonic stem cell
|
| 12 |
chr6:30140400-30140800 |
Bivalent Enhancer |
HUES64 Cell Line |
embryonic stem cell
|
| 13 |
chr6:30140400-30140800 |
Bivalent Enhancer |
iPS-15b Cell Line |
embryonic stem cell
|
| 14 |
chr6:30140400-30141200 |
Bivalent Enhancer |
iPS DF 19.11 Cell Line |
embryonic stem cell
|
| 15 |
chr6:30140400-30141200 |
Bivalent Enhancer |
Fetal Intestine Small |
intestine
|
