| Tag | Content |
|---|
EnhancerAtlas ID | HS091-16143 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:4700480-4701960 |
Target genes | | Number: 28 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr16:4700666-4700685 | TGCTGCCCCCTAGAGGCCA | - | 7.48 | | HES2 | MA0616.2 | chr16:4700635-4700645 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr16:4700975-4700985 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr16:4700635-4700645 | GGCACGTGCC | - | 6.02 | | HES2 | MA0616.2 | chr16:4700975-4700985 | GGCACGTGCC | - | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28424 | chr16:4701793-4706763 | Fetal_Intestine | | SE_31575 | chr16:4701105-4706699 | Gastric |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH16I004649 | chr16 | 4699975 | 4701230 | | GH16I004651 | chr16 | 4701886 | 4706629 |
|
Enhancer Sequence | CCAGGTGGGT CTGGACAGGG CTGTCTCATG GGGCTGTGGG GGTGGGAGGC CCCTGTCCCC 60
AGCAGTCCGC ATCCCAGCCA TGAGGGCAAG CAGGCACCAA ATCACCCCTA AAGGGGGCAG 120
AGCTCCTGGC AGGATTCCAG TTGAGCTTGG GTGTGGGCAC GTGCCCTGGA ATGGGTTGTG 180
TCCTGGTGCT GCCCCCTAGA GGCCAGATGG CCAGGGGCAG GTCACTGAGA AACAGAGCAG 240
CCATACTGAA TGGGTGCGTC TGGGCTGCAA CGGCTGCGGA ACATGGTGGA TTTGATTCCA 300
GCCTTCTTGG ATGACTTTCT TTACAAGGCA AAAATAGTAT TTACAGACTG GGCATTGTGG 360
CTCACGCCTG TAATCCCAGC ACTTGGGGAG GCTGAGGCGG GCAGATCACC TGAGGTCAGG 420
AGTTTGAGAC AAGCCTGGCC AAAATGGTGA AACCCCGTCT CTACTGAAAA AAAAGAAAAA 480
TTAGCCGGGT GTGGTGGCAC GTGCCTGTAA TCCCAACTAC TCGGGAGGCT GAGGCAGGAG 540
AATCACTTGA ATCTGAGAGG CGGAGGTGGC AGTGAGCCGA GATTGCACCA CTACACTCCA 600
GACTGGGCAA CAAAGGGAGA CTGTCTCAAA GAAAAAAAAA AAAAAGAATA TTTACTTTCC 660
CTAGAACAGT GGGCAAGAGA CATGGTCCAA AGGAGAGATG CAGACAGCTG GCTAACATCT 720
TCCCCTCGTT GCCAGAGAAG GGCACATTCG AGTACTGTCA TAGTACTCGA GTACTGTGAG 780
CTGTCTGTTC AGCACACATG TGGCACCTGC TGCGTGCCTA GTGCTCTTCC AGGGCTTGGG 840
GTGAAAGCAG ACCCTGCCTC TGCTACCTGG TGGGGGCGTA GACAATTAAT ACGGGACAAA 900
TGGGTAGAAG AGAGAAGGGG CAGAAAGGGA GGCTCTACTG GAGAGGCCAT GGCTGAACCA 960
AGCCATGATA GGTGGGAAGG GGGCCCCTCC AGAAGAAGCT AGAAGGCAGG GGGCCTGGGA 1020
ACAGAGGAAG AGGTGAGAGG GTGCAGGCCT CAGGGGACAG GAGGCCGGAA GAGCCAGTAA 1080
ACTTTGGGGG CCCTGGGGCG GGTTGCTGAG CTGTGCTCGT AGGAAGCTTT GGGGATGGAA 1140
AGGGTGGGGA CTGAGGAAGG GGCTGAGGGT GCTCGGGGCA GTGATGGATA TGGGAAGCCT 1200
GGGAGAGCAG GTTGGGGATG GGCAGCCCCA GCGTGCAGGG GTCTGGCGTT GAGGCTGCCT 1260
GGCTGGATTT GCTCAGGGTG ATTTGGTCCT GGCCGTTGCG TGTGCTGGCT GCGTGGCCTG 1320
CAGCTTCTAC CTGTAAATGA GAACAGTGCA CCCAGTATAG CCCCTCCCAT GGGACTAGAT 1380
CCCAGGGATA CCCTCTGGGG CTGTGGCTGC TGCACCCTGA CCCGTTTTCT GTTGTTGGCT 1440
GCTCCTGAGG GAGTCACCTG GGGCCCTGTG GTTTTTCTCC 1480
|
