| Tag | Content |
|---|
EnhancerAtlas ID | HS118-19398 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr9:102117880-102119640 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr9:102117919-102117930 | CAGCAGCTGTC | - | 6.14 | | Tcf12 | MA0521.1 | chr9:102117919-102117930 | CAGCAGCTGTC | - | 6.02 | | ZNF263 | MA0528.1 | chr9:102119187-102119208 | AGAGGAGAGGGAGGTGGGAGG | + | 6.69 | | ZNF263 | MA0528.1 | chr9:102119196-102119217 | GGAGGTGGGAGGGAAGAGGGA | + | 6.97 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_51391 | chr9:102117539-102123394 | Skeletal_Muscle |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I099356 | chr9 | 102118606 | 102119483 |
|
Enhancer Sequence | CAGTCTGGTG GGAGAGACAG ATACACAAGT CAGCCATCCC AGCAGCTGTC TTGTGTGATG 60
TTCTATGAAA GAGAGGCTGT GTGCTACCCC AGGAACAAGG AAGATGCAGG ATAGCAATGA 120
AAGAAGGCTT CTCAAATATG CCACAGCTGG ATGCAGAACA GGGAATGGGG AGTGAGTATC 180
TGTCAGACAG AAGTGGAAGG AGAGCATTCC AGACAGGGTA TGGAATCTCC TTCCTCAAGG 240
GCAAGGACTT TGGAGTATCT GGGATGTTGA TGGTCTGGTG TGACCAAAAC TCAGTGGGAG 300
ATGAGGCTGA AGGGTAAGCC AGGGCTTGAT CATGGAAGGA AGTCTTAGTG TGTGTGCCGA 360
AGGGTATGGG CTCAAATTTG AGGGCACTAA ACAGGCACGG AAGGTTCCAA GCCTGGAACT 420
CACAGCTGCA GCTCACTCTG GTGGGTTTAT TCATGGGGCC CTGCTCAAAT CTTCCCTAGC 480
AAAGCTGCTT TCTCTCTAGA TCGGGGTTTC TCAACAGCAA CACTATCATT TGAGGCTGGA 540
TTATTCTTTG TTGGGGGTGG GGGCTGTTCT GTGCATCAGA GGCTGTTCAG CAACAGCATC 600
CTTAGCCTCT ATTCACTAGA TTCTGGTAGC ACTTCCCCAG TTTCCACAAC CAACAACGTC 660
TTCAAACATT ACCAGAAGTC CCCTGGGTGG CAAAATAGCT CCTGATTGAG AATCCCTGAT 720
TTGTTTTTCT TTTTTGTGAA TATGTACACA GATGACTCCT CCTGTATTTG TCCTCTTCCC 780
TCTCCCCAAG GCCTGGCAAT GTCCTGCTTC CAGCCTTTCC ATGAGGGACA CTGGATGCTG 840
CCATTGGCTC CCTGCATTGC CTTATTTCAG CACCTGTGGC TCATGCTCGT GGAGCTGGGG 900
CTGGTTGTGG GGAAGCAGCT GCCAATAGCT CTGTCTACCT CTGGATCGGG TCAGTAAGGC 960
ACCTCATCTC CTGCAGGGCA CACCATGTAG TGTCCAGGAG CTTCCCGGTT GGATTCCCAC 1020
CCCAAGGTCA GCTGGGAACA GAACTGTCCA AGCCTGTTGG CCCTGTACCC TCTGTCCGTC 1080
AGTCTCACTG TCTGCTACGC TGCAGTCTGG AGGGAAGCAT CAGCTCAGGA AGCCTGCCAG 1140
GGAGAGGGCA GCAGGCCGGG GACAGAGGGC AGGTGGTGGT AGCTGGAGAC CATGTGACTC 1200
CTGGAGGCTG TGTGTGTCAC AGGGCAGAGC TGGCCACTGG CTCTTCCCTT GGCTCAGCCT 1260
GAGAAGCCTT CACATGACAT CTCTGTGGGA GCCTTCATGT TGTGGGCAGA GGAGAGGGAG 1320
GTGGGAGGGA AGAGGGAAGT GTTTTTAGGA TCCAAGCTAG AAATACAAAA TACATTTGTG 1380
AATCACAAGC TGATCCTCAT CACATGACCA CAATAGCTTT GCCAATGCAG AAATCAGGCT 1440
TCGGACACAC ATACGAAAAA ATCTATCCTG CCCCTGCTAT GTCTGGGCTG TGGTGGCCAA 1500
GAGAGTAAGA GAGTAAGAAA GTGGGGCACT GGAATTGGAG CAGGAGGCCA GGGAGCCAGC 1560
TATGCAGCCG GTCTCCATGT CCCAAAGCGT CACCAAAACC AGAACACAAA ACCAGCCCCC 1620
ATTCCAGCAT TTTCTACATG CTTATTCATA TGGTAATCTC ATAACAGCCA CATTTCCCAG 1680
TGGAAAACCG AGGCCCAGAG TGATTCCTCC ATGTTCCATT TTCTTCCTTC CTTAGAGTTT 1740
CCAGGGTTCA ATCTATATAT 1760
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