| Tag | Content |
|---|
EnhancerAtlas ID | HS091-25110 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:11925200-11926420 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ALX3 | MA0634.1 | chr2:11925491-11925501 | TCTAATTAAA | + | 6.02 | | CTCF | MA0139.1 | chr2:11925220-11925239 | GGGCGCCCTCTGGTGGCCG | - | 8.46 | | Myog | MA0500.1 | chr2:11926255-11926266 | CTGCAGCTGTC | - | 6.62 | | PHOX2A | MA0713.1 | chr2:11925493-11925504 | TAATTAAATTA | - | 6.62 | | PROP1 | MA0715.1 | chr2:11925493-11925504 | TAATTAAATTA | + | 6.32 | | PROP1 | MA0715.1 | chr2:11925493-11925504 | TAATTAAATTA | - | 6.62 | | Phox2b | MA0681.1 | chr2:11925493-11925504 | TAATTAAATTA | - | 6.62 | | Tcf12 | MA0521.1 | chr2:11926255-11926266 | CTGCAGCTGTC | - | 6.14 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65880 | chr2:11925248-11926182 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I011784 | chr2 | 11924789 | 11925454 |
|
Enhancer Sequence | AGGTACCGCG GGCCTCGCGC GGGCGCCCTC TGGTGGCCGC CGGTCAGAAG GCGCAGAGGC 60
TTAGGCTTCT CCAAGGAGTG CGTGTCAAGG CAGCTTTTCC CTTGGTTGCG GTTAATGATA 120
GCACAGATGA TAGCACCGAA CTCATAATCC CGATGTTTCT GGCTTGCAGT TAGTCGGCCT 180
CAGAGTTCTG TGGGTCACCC ATGGCTCGGG CCATCGTTGT GTGTCTCCTG TGCCCCAGGC 240
TAGCACTGCA GAGATGGCCT CCAGAGGCCT GCAGGCTAGA GGGGGTGTCA GTCTAATTAA 300
ATTAGAGGGT GTCGGCAGCG AGAGAGAAGT GCGCCGGCGC CTTGGAACAG GGAGGTCTGA 360
GTTTGTCGGA GGAGGGCTGG GAACTTTTCC CAGCTGGATT CAAAGGGCGT TAATCGGGTG 420
GGCTTAGGTG ATTCATTCAC AGCACCTGCC ACATTCGTAG CAATGCACTC CCAGGGCCTC 480
CTGACAGTTC CATGGCAGGG TGTGCCCACG CCCCCCAGTG GGTGCAGTCA GCAGTTATCA 540
GCTGGGGACT AGACACAGTG GCCCTGCACC CCTCCCGCCC CCTCTCTCAC CACTGCCTCT 600
TTTCCATCCC CTCGTGGTAT TTCTAGCAGG GAAGGGGCCG AGGCTGTGTA CTTCTTCCCT 660
CTACCTCTCA GGAGCCACCC CCATCTCCCC TTCCAACCAG GGCTGCCATG TGAGACTCCT 720
GCCTCCACCC TGGTCCCTTC AAGGCTTTGG GAATTTTTTC TTCCGCAAAG ATTGAGACCT 780
TTTTGTTCTC ACGCCCGTGC CAGCCAGTCC CTTGAGAGCG GAAACAAGAT TGTGTGCTGG 840
GTCCCGCCGG CTCCATTCAT TCACTCAGTT TTCCTAGGGC CACACATTAA TACCCAGCCT 900
CACTGTGTTT CTGAAGTCAT GGGGGCTCTC TGGACACTGG CGTGAGGAGT CCCCTGGGCG 960
TTCCCTCCCT GATATACATG AGCTGGTGGG GGTGGGGTGG CAGCACTGAC AAGGCTGGGC 1020
ACCGTTATCT GAGTGTTATC TCATGGGGCC AGGATCTGCA GCTGTCCAGT CCTTACAGGT 1080
GAGGCCAGAT CGTCACAGTC AGGAGACCCC AGGAGAGTCC CCGGAGGTCC TGATTAGGGC 1140
TCTGAGGGTG CATGTTGAAG CCAGTCAGGC TGGCATCAAG ACCCAGGGAC TCTTTTCCTG 1200
GACGGAGGAG ATTCTCAGTG 1220
|
