Tag | Content |
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EnhancerAtlas ID | HS091-47100 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr8:145647280-145648980 |
Target genes | Number: 34 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr8:145648908-145648929 | GGGGGAGGGTAGGCGAGAGGG | + | 6.14 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28686 | chr8:145647674-145649096 | Fetal_Intestine_Large | SE_32083 | chr8:145647861-145649027 | Gastric |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I144422 | chr8 | 145647738 | 145650169 |
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Enhancer Sequence | CCAGCTACTC AGGAAGGTAA GGCAGGAGAA TTGCTTGAAC CCTGGAGGCA GAGGTTGCAG 60 TGAGCCGAGA TCACACCATT GCACTCTAGC CTAGGTGACA GAGCGAGAGT CCGTCTCAAA 120 AAAAAAAAAA CAAAAATTAA ATTTAAAAAA ATACATGCCT GGCACCCAGT GGCTCACACC 180 TGTAATCCCA GTACTTTGGG AGGCCAAGGC AGGCGGATCA CCTGAGGTTG GGAGTTGGAG 240 ACCAGCCTGA CCAAACATGG AGAAACCCGA TCTCTACTAA AAATACAAAA TTAGCCGGGA 300 ATGGTGGCGT GCCCCTGTAG TCCCAGCTAC TCAGGAGGCT GAGACAGGAG AATCACTTGA 360 ACCCGGGAGG TGGAGGTCGC AGTGAGCCGA GATCGCGCCA TTGCACTTCA CCCTGGGCGA 420 GAGAGAGCGA CTCCTCAAAA AAAAAAAAAA AGATCAAAAT GACCCTTCCT GGCCACCTGC 480 CCCCCTTGAC ACACACACGT TTCTGGGTGC TGGTCCTCCC TCGAAGCACC CCGTACCCAC 540 ATGTGCCTGT CAAGGACATC GAGCCCCAGG GCCCGACCCG ACAGTGCCCT TCCTCAACTC 600 CCTTGGGTGT CCTGGATCCT GCTGTCCTGG GGGCTCTTCT CTGGCTCCTT GGTCAGTCTC 660 TTCCCACTTC CCATGGCAGT GCCCCTGGCC AGTCCTCCGG CTTCTTGGCG GGACTCAGCC 720 TCCCTCTCCA GCCACTGACA TCGTCATCCT GCTTGACGGC CCCCCTTGGC CGTCTGAGAG 780 GCAGTCCCCA CTCAGCCTGT GCACAGAGCC CACCTGCCTC CATGATGTCC CAAGCCCCCA 840 CGGAAATCCA AGCGACTTGA TTTTCACTAT CTGCCTTTCT CTACACACCT CATTCCACCG 900 GCTCTAGATG CCACAGATGT CAAGAGGTTC TGGCATTCTC AGTCGCTAAG AGAGAAAAAT 960 TCTACAATGA CACCCTGGCA CGTCCCTTAT CCTGAGGGCA TAGTTGCTAA GATGTGAAGC 1020 ACGCGGCTCT TGGAACCCAG AGGTGTGGTG TGTGGTCTGC TGCTTTTCCC TGGGGGCAGC 1080 AGCAGGTGTG CAGCACACGC TGTGGAATGG ACGGCGTCCA CCACCCGCTG CCTCCCCACC 1140 AGGCCCAGCC TTGACTCTTG GGCTTTGCCC AGGGGCTTGG GGAGAGGCCC TGGTGGTGGG 1200 CATGACAAAC TCCCACCCAA TGAGTAATTG GCTGGAGCTG CAGATAAGTC AGGAGTCCTG 1260 GGCCAGGGTG CAGTCATCCG AGTGGAGAGG TGGGTGTGGA GCAGCTGACA GCATGAAGTG 1320 CACCCCGCCT CTGAGCCCAG CCTGGCCTGG TGTGCTGGGA CCTGACTGCA CTCAGAAGAC 1380 CTGGTGCTGC CCTGGGCTTC AGTGAGGCGT GGGGAGGGGT GGCAGGCAGC CTCCCCTGTG 1440 GCCAGAGTCA AGCCACGCCT GGCCCAGGTG GTAGACCTGT TCTCCAGGCC TCGGGGCTAT 1500 GGAAACGCCC CTGCCTCCTA TTATGTGCCC AGGCAGAGCC CACCAGGGAA GCAGCCGTCA 1560 CTGAGTGATG CAGGCCATGA GGAATGCAGT GGCAGGGACA GAGCCAGGGC CGGGCCACCA 1620 CACAGGTCGG GGGAGGGTAG GCGAGAGGGG CTCTATGCTG AGAGTCCCAG GAGGGTGGAG 1680 AGAATACACA GGGCAGGCCT 1700
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