| Tag | Content |
|---|
EnhancerAtlas ID | HS091-47067 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr8:144804630-144806100 |
Target genes | | Number: 40 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr8:144804768-144804787 | TGCCGCCCCCTAGAGGCCC | - | 6.67 | | TCF7L2 | MA0523.1 | chr8:144805180-144805194 | AAAGATCAAAGGGG | + | 6.58 | | ZNF263 | MA0528.1 | chr8:144804964-144804985 | AGAGGAGAGAAGGGGAGAGAG | + | 6.08 | | ZNF263 | MA0528.1 | chr8:144805485-144805506 | GGGGGAGGGCGGGGAAGGACA | + | 6.11 | | ZNF263 | MA0528.1 | chr8:144804969-144804990 | AGAGAAGGGGAGAGAGAAGGG | + | 6.12 | | ZNF263 | MA0528.1 | chr8:144805614-144805635 | GGAGGAGGCGGAGGAGGGATC | + | 6.15 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_23703 | chr8:144804264-144806300 | Colon_Crypt_1 | | SE_23962 | chr8:144804578-144806376 | Colon_Crypt_2 | | SE_24801 | chr8:144802592-144806500 | Colon_Crypt_3 | | SE_27089 | chr8:144804859-144805937 | Esophagus | | SE_34308 | chr8:144804486-144806610 | HCT-116 | | SE_41660 | chr8:144804797-144805575 | LNCaP |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I143722 | chr8 | 144804721 | 144805854 |
|
Enhancer Sequence | TAAGCAGCCA TCGTTCCTCC CCTCCCCTCT GAGGTCACAG CATCCACTAG CTGGGGGCCC 60
CGGCCCCTTT CCTGAAGCCT CCACTCCTCT GAGGACCCCA CCCCACCCCC GTCCTGAAAC 120
CTCCACCCCA GAGCCCAGTG CCGCCCCCTA GAGGCCCTGC CCACTGCACA TCCAGCACTG 180
GGCTTTTCCC TCCAGGTTTG CCTGGGGCAG CTTCTTGTTC TTTGTCCATC ATTTCCTTAC 240
CTGCTGTGGC TTCAGGGTCC AGGCTGCCCC CCAGGGTGGT CCTGTGGGGT AGGGATGTAG 300
GGTCACCCCC TGGCCATGTT TGTGACTCTG AGCCAGAGGA GAGAAGGGGA GAGAGAAGGG 360
GGACACCCCT CCCCCTGCTG TCAGGGACTG CAGCCTGCGC CCCCTAGTAT GGCCACTGCA 420
CCTGATCTGT CTTCAGGTCT CCGTAGGTGA GGGTGGGAGA CAGACATCTC GCGAGGTCAG 480
GGTTACCTCC TCTTGTCACC CCCAGGCAAG GTCCCTGGTG TGAGTTCAGG CCAGGGCTGT 540
GCAGGGCTGC AAAGATCAAA GGGGCCCTGT GGGCACAGAC CTGTGTCCTA GGGTGCCAGG 600
TGTCCTCAGC TGCACCTGCC CATGGGTTGG GGTTGGAACA CAAGGAGGCA GCTGGAAAGC 660
TCACAGGCTG GAGGAGCTCA CAGTCTAAAG GGCGCGGCCT GTGCTGTCGG TGGCGGAGTT 720
GGGCTGCCAG GCTCACAGTC TGGGAAGCTC ATAGGCCGGA GGAGCTCACA GTTTGAAGGG 780
TGCGGCCTGT GCTGTGGTCG GTGTTGGGCT GCCAGGAGAG GGGCGCTGCT GGGTTGTGGA 840
AGCCATTGCC ACCATGGGGG AGGGCGGGGA AGGACAAGAT GTGGGTGGGG GAGCTGAGCA 900
GAAGGTGAGA GCTGGCGCTG CCCTGGTGCT GGACCAGGCA CCTGCAAGAG ACTCAGAAAG 960
GGAGGCTGGG TTTGGGAGAA GGTTGGAGGA GGCGGAGGAG GGATCGGGAG GGCCCGAGGA 1020
AGCGGTGAGC CAGTCAGAGA CCCAGCCCAG GGGCTGTTTC CTGAGGGGGC TGCCGAGGGA 1080
GGTGCTTGTT GAGCTTCAAA AGCCCAAGGC GCAGGCCCAG GGTGCTGAAC AAGCAGGACA 1140
GAGAGGCTGT GGGAGAGGAA GCTGCAGAGA GGCCACGGGG CTGCAGGGTT GGAGGCTTGG 1200
CCTCAGGCTG GGCAGTGTGT GGTGGGGCTG CTGAGTGGGG AATCGCAGGT GGGCACCCAG 1260
GAGTGTGCCT GCACAGGGGG CATCGGGGAC AGGGACAGGA GAGCAGCGTG AAGTTGGGGA 1320
GGCCAAGGTG GGCCTTGGAA GTGGAGCTGG GGGGTCTTTA GTGCCCCCCA CAGGGGTGGG 1380
TGGTGGGTCC ACAGGGGAAA TCTGGGAGGC CACGTGGTTA AAGGCTGCAG GATGTAACTG 1440
GGCGATTATA CACACTGGGG AACATGCTAG 1470
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