Tag | Content |
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EnhancerAtlas ID | HS091-48670 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr9:130265920-130267200 |
Target genes | Number: 24 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr9:130266421-130266440 | TGGCCTCCAGGGGGCGCTG | + | 8.05 | HINFP | MA0131.2 | chr9:130266457-130266469 | CAGCGTCCGCAG | + | 6.02 | JUN(var.2) | MA0489.1 | chr9:130266590-130266604 | GTGAGTCATTTCCC | - | 6 | Myog | MA0500.1 | chr9:130267026-130267037 | AACAGCTGCAG | + | 6.02 | Tcf12 | MA0521.1 | chr9:130267026-130267037 | AACAGCTGCAG | + | 6.62 | ZNF263 | MA0528.1 | chr9:130266641-130266662 | CCCCTCAGTTCCCCCTCCTCC | - | 6.86 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_00872 | chr9:130266016-130272828 | Adrenal_Gland | SE_01693 | chr9:130265211-130267528 | Aorta | SE_26528 | chr9:130265976-130269416 | Esophagus | SE_31422 | chr9:130266250-130267751 | Gastric | SE_46654 | chr9:130266483-130266807 | Ovary | SE_52507 | chr9:130266416-130267306 | Small_Intestine | SE_65259 | chr9:130266014-130269978 | Pancreatic_islets | SE_68760 | chr9:130265824-130267688 | H9 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I127502 | chr9 | 130265015 | 130272722 |
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Enhancer Sequence | CAGGTAGGGC CATCTCGAAT GTCGTGTTAT CCCAGCGCCC CCTTCACAGG TGGAGAGACC 60 AGGGCCCAGA GGCAGCCAGG GCCGGTGATG GCTGCGGCCT GTGCCTCCAT GAGCGGAGGA 120 GCCCTGTGTG TTCCGTCCAT TATCCCAGTG AGGCAGCTGA GGCTGATGGG GGTAAATGCT 180 CAGGGCCTTG CAACTGGGAC ATGGTGATGC GGGGTTTGAG GCCCAGAAGC ATCCTCACCT 240 TCAAGCCCGT GCGGTTGTGC AGGTTGGTCA CTGCACAATT CTTGGAGCCA TATACACTTG 300 CACTCGCTGC AGAGGTGCAC GTTGATTATG CATTTTCCGG CAGACGGCGT TGAGCCAGGT 360 GCAGCCTCTT CCTTGGGCTC GTGGCAGGCC TGCTTGGAGC ACCTGGGCTC TGCCTCCAGC 420 TCATTCAGTG ATCGTGGCCA GTGTTTGGGC TCCTTTCCCT GTGCATTCAA CACAGGACGT 480 GATGCAGCCC TGACCGGCTG GTGGCCTCCA GGGGGCGCTG AGTGCTTGCC CCAAGTACAG 540 CGTCCGCAGA AGCAGGCAGG AGAGTTCAGG TCCTGGGGTG GCAGAACAGC CCTACGCCTG 600 GGCCTGTTTC CCTCTCACTG AGACCATCAG TCCTGTGCAC TGAACAGGGC AGGCGAATAC 660 CCTTTGTCGT GTGAGTCATT TCCCAGGCAG GAGCTGGGTG GCCTTTTCCC ACCCACAGTT 720 CCCCCTCAGT TCCCCCTCCT CCCAACACCC TCCTGGGCTC AACTTGGCCA AGAGGGGAGA 780 GACTGAGGCA GGTGGGGCTA CCTCCTGGAG CGCAGTGCTT TGCAGATCTC CTTACGCTCT 840 CACTAGGGCC CAGGGAGGCC TCATGGAGGA TCTCGAGGCT CAGTGACCTG CCAAGGACAA 900 CAGCAAGGGA CAGCCGCATC CCTGGTCTCC GGCCACACAG CCCCGTGTTC TGCACCTCAG 960 CCCTTGTTGA CCGAGGGAGG CCCAGGCCCA AGCCCTAGGC CACCATGGAC AGGCTGGCAC 1020 CAGGGAAGCC AACATCCCCA AGGTGACTGG CTGCCACCCC ACCAGTAGGG ACATGTTTTT 1080 ACCCATAGAT GGGGCAACCC ACCCCCAACA GCTGCAGGGG CTCGAGGGCT GTTCCTGTAC 1140 CACATAGGCT CAGCCCAGGT CCCCACCTTC CAAGGCCTCA GTGTACACAT CGGTGAAATG 1200 GTGGTGACGA CTGTGTCCAC TTTCTAGAGC TCTCTCGAGG CTGCTGTTCC TGCACACAAG 1260 GCGCTTGGCC CACAGTGAGC 1280
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