| Tag | Content |
|---|
EnhancerAtlas ID | HS091-21399 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:77705160-77707300 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr17:77707047-77707068 | AAACTGAAAGTGGAAGTGCGA | - | 6.85 | | ZNF263 | MA0528.1 | chr17:77705473-77705494 | TCCCTCTCCCTTCCATCCTTT | - | 6.1 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_27903 | chr17:77703646-77707943 | Fetal_Intestine | | SE_28807 | chr17:77703752-77705877 | Fetal_Intestine_Large | | SE_28807 | chr17:77705942-77708143 | Fetal_Intestine_Large |
|
Enhancer Sequence | ACTGCCCTGT GACGGGGCCT GGGGGTGGGA GGGCCTGAGA AACCAGATGG CACAGAGCCG 60
TGTCGTGCAG GATAAAGGGG AGAGGTCCTT GCTCCAGGCA CAGGACAGAG CCAAGGGGAC 120
CATTAGGAAT CCTCACCGTT GGTAGCAACA GATCCGGGAC AAAGAAAAAT GACCAGGGGG 180
GTCCTTAAAC CCGTGGCCAC AGCCAGGGCA GCAACCCCAG AAGGCTTCAG GAGGAGGGGA 240
GTGTGGCGGG CTCCCCGCTG GCTCCCATGG CTCCCCTCCC CTGCCCGCCC CTCCAGCTGG 300
CTGTGTCAGC CTCTCCCTCT CCCTTCCATC CTTTCCATTT TCCACCCAAC ACCTCCCTGA 360
CAGATCTGCC CAGGCTGTAG AAAATACAGA CATAGGTTTT TAAAAAGCCA AATATGGGGC 420
CAGGCTCAGT GGCCCACGCC TGTAATCCCA GCACTTTGAG AGGCTGAGGC GGGCGGATCA 480
CTGGAGGTCA GGAGTTCGAG ACCTGCCTGG CCAACATGGC GAAACCCCAT CTCTACTAAA 540
AATACAAACA TTAGCCAGGC ATGATGGTGC ATGCTTGTAA TCCCAGCTAC TTGGGAGGCT 600
GAGACAGGAG AATTGCATGA ACCCAGGAGG TGGAAGTTGC AGTGAGCTGA GATCGCACCA 660
CTGCACTCCA GCCTGGGTGA CAAAGCAAGA CTGCATATAA TATATATATA CATATATATA 720
TACATATATA TATATATACA TATATACACA TATATATATA TATATATATA TATATATATA 780
TATATATACA CACATATATA TATATATATG AGGCCAAGGC AGGAGGATTG CTGGAGTCCA 840
GGAGGTAGAG GCTGCAGTGA GCTGCAATCA CACCACTGCA CTCCAGCCTG GGTGACAGAG 900
CAAGACCCTG TGTCAAAAAA ACAAACAATA ATAAAATAAT AAAAAGCCAA GTACCACAAA 960
AAAGGTGTTA GAGAATTGAA AAGCAATTGG CCCTCCCTAG GGGCTCAGCC ACCTCCCAAA 1020
CCTGCGTCAT CCTCCAAAGA CCCTGCGTGG GTGTCCCAGG GCGCCTGCAA CAAAGATCTG 1080
CAGACTGGCT TAAACCCACA GAAACGGATC CGCATGCTTC TGGAGGCCAG AAGGCCAAAC 1140
CCAGGGCATT GCAGGGCTGC ACCCACCCGG AAGGTTCCAG CAGAGGCTCC CTCCTCACCT 1200
CTTCTGGCTC CTGGGGCCTC GGCAATCCTT GGCATTCCTG GGCTGACGGC AGCATCACTC 1260
CGACCTCTCC CCACGTCTCC CCAGGGCCTT TCCCCTGTGT GTGTGTGTCT GTATTCAAAC 1320
TTTCCTCTTC TCACTAGTAC ACCAGTCGCT GAATTTCGGG TCCACACTTC TCTGGTATAC 1380
ATCTCCTTAC CCTAGCTAAT CACATCTGCA AAGACCCTAT TTCTAAATAA GGCCACGTTC 1440
TAAGGTTCCA AGTGAGCATG AATGTGGTGG GACACCATCC ACCCCAACAC AGGCAGCTCA 1500
TCCCCACACC AGCCTTTCTG CCCCTTCTAA CCGCAAATGG AGGTGTGCGG GTCTCCCGTC 1560
TGCGCAGCGC CTCTTTTGCT CTCTGTATCG CAGATGAGGA CGGGAGGGAC CTTCTCCACA 1620
TCATCTCTCC TTTTGCACCT TTTGGACTTA GTACCATGTG CACGTGTTTC CTGTACAAAA 1680
ATAAATTCAA AAAATCTCCT GGAGCTCCAC GTAGTTCACT GAAATTCCTG CCTGGGATCT 1740
CGTCTGATGG CTGGGCCATC ATTTATTTAA TGAGTTCCTT CCTGACGGCC GTGGAGGTCA 1800
CCCGCAATCT TTTGCTAAAG CAAACAAGGC TGCCACCAGG ATCCCTGCAC ACGCATTCGT 1860
GCCTGTGTGC CCGTCCAGCT GTGGGACAAA CTGAAAGTGG AAGTGCGATT GCTAAAACAG 1920
GTCAAAGAAC ACGTGTCTAT TTGTCTCAGA CATGACCTCA AACCTTGGCT CCCACGGGGC 1980
AGTGCAGGAG GAAGTCTGCT CCCCCCAGCC CTGCCCCAGG CCCACTCCCC ACCCAGCACA 2040
CAGGGAAACC TGGGCTGTTT TGACTTCGCC TCTTCCAGCC CTGGGTCCGG CCTTCGCTGT 2100
GACCCCGGTC CATCCCGCCG CCCTCTGCAC CTCTTCCTCC 2140
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