Tag | Content |
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EnhancerAtlas ID | HS091-03053 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:156035900-156038060 |
Target genes | Number: 20 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
INSM1 | MA0155.1 | chr1:156037122-156037134 | TGCCAGGGGGCA | + | 6.62 | IRF1 | MA0050.2 | chr1:156037033-156037054 | AAAAAGAAAAAGAAAGTGTCT | - | 6.49 | ZNF263 | MA0528.1 | chr1:156035960-156035981 | GGAGGAGAAGTGGGGGAGGAG | + | 6.51 | ZNF263 | MA0528.1 | chr1:156035971-156035992 | GGGGGAGGAGGAGGCAAGGGG | + | 6.89 | Zfx | MA0146.2 | chr1:156036786-156036800 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I156066 | chr1 | 156035792 | 156036591 |
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Enhancer Sequence | AGCCCGGGCC TGGGGGGCTG CTGGGTGGTG GGAGTTCTGG GGAAGTCGAG GAACACTTCT 60 GGAGGAGAAG TGGGGGAGGA GGAGGCAAGG GGGCTCAGCA GTGGGCTCTG GGGGGTGGGG 120 ATGGAGATCA CAGAAGATAA AAGGTACTGT AAACAGAAAC AGCACAAGCC AGGATATAGT 180 AACACTGACT AGTACTACTA AAAGCAGGAA TCATTGCCAC TTACTAAGCC TTTGCTATGT 240 GCCCAGGAAG GGACAAGTTA CTTTACATTT GGCATTTTAT GTAACCCTTA AAGTACCACA 300 GGAGTAAAGT GCTATAATTA GTTAATTTCT GTATAAATAC AAACAAGGTG AAATCAGGGT 360 GGAGCTAGGA TGGGGGCGAG CTGCACGGAT CGAGAGCGCC CCCTCACTTC CGCACAATGC 420 TCTGCACTTG GCAACTTTCA TCTAACCACA GAGGACCAAA AGCTGAACCC AGCATCTGCA 480 TTTTATGAAG ACTCAGAGGA CACACAGGAG GTTAGGCCTC CTGACACCAC ATCCGAAGTG 540 TCTCTTAGGC CGGGTGTGTT GGCTCACACC TGTAATCCCA GCACTTTGGG AGGCCAAGGT 600 GGGTGGATCG CTTGAGCTCA TGAATTCGAG ACCAGCCTGG GCAACATGGC AAAATCCTGT 660 CTCTACCAAA AATATAAAAA ATTGGCCGGG CTTGGTGGTG CGTACCTGTA GTCCCAGATA 720 CTTGAGAAGC TAAGGTGGGA GGATGGCTTG AACCCGGGAG GCGGAAGTTG CAGTGAGCCG 780 AAATCGCCCC ACTGCACTCC AGCCTGGGTG ACAAAGCGAT ACTGTGTCTC AAGAAAAAAG 840 TGTCAGCTGG GCGCGGTAGC TCACACCTGT AATCCCAGCA CTTTGGGAGG CCGAGGCGGG 900 CAGATCACAA GGTCAGGAGT TCGAGACCAG CCTGGCCAAC AGTGAAACCC CCGTCTCTAC 960 TAAAAATACA AAAATTAGCC AGGCATGGTG GTGGGTGCCT GTAATCCCAA CTACTCGGGA 1020 GGCTGAGACA GGAGAATCAC TCGAACCTGG GAGGTGGAGG TTGCAGTGAG CCAAGATCAT 1080 GCCACTGCAC TCCAGCCTAG CGACAGAGCA AGACTCTGTC TCAAAAAAAA AAAAAAAAGA 1140 AAAAGAAAGT GTCTTCCAGT CAGTGTGAGG CCTAAGCATG TGAAATGGGG TCTGTTTGTG 1200 TGTATATGGG GTGGATAGCA CTTGCCAGGG GGCAGGAAGC AAGAGTCAGG GGCTTTGGTT 1260 ACACATGCTC CTCGTTACCT GATCTCTTAT GAGCCTCAGT TGACTCATCA ATGAATTGGG 1320 AGTTAGACAT CACTAGTCTG AAGACATCCC ATCCAACTCC AAGAGGGAGA CTGGATGCTT 1380 TCAGTGATGC CTTGAATGGT CAGGCCAGGG ACTGCTGCAA GAGGTAGGCA TTCAGCTAAT 1440 CCTAGAAAGA AGGCCACGGG AGAGAACAGG CCACTGTTAA GGAGCCATGT GAGGAAGATC 1500 TTGAAGGTGG CAGAGTTGGC TAAAGCCCAG ATGTGCACTG GTGGAGAGTA GGGGCTAAAA 1560 TCAGGACGAG AACCTGAGAA AGTAGAGGGG CTGGCTGTGA GGAAGCCAAT AGAGATTTTA 1620 GAGCAGGGAG GTGAAACTTT ATTTATTTAG TTAGTTAGTT GAGACAAATT TTCACTCTTG 1680 TTGCCGAGGC TGGAGTGCAA TGGAGCGATC TCAGATCACT GCAACTTCCG CTTCCCGAGT 1740 TCAAGCAATT CTCCTGCCTC AGCCTTCCGA GTAGCTGGGA TTACAAGCAT GCGCCATCAT 1800 GCCCGGCTAA TTTTTGTATT TTTAGTAGAG ATGGGGTTTC TCCATATTGG TTAGGCTAGT 1860 CTTGAACTCC TCACCTCAGG TGATCCACCC GCCTTGGCCT CCCAAAGTGC TGGGATTACA 1920 GGCGTGAGCC ACCGCGCCTG GCCGAGGGAG GTGAAACTTT ACAGGCTCCA AGACTAGTGT 1980 CCCTGGAAGG CAGAGGAGCC TTGGGCTGCT CTGTTGGGTT CTGGGCCCCT GGCCGCAAGT 2040 TTCTGTATTT CCTGATCTCT AGTACTCTGA TCCCGGGTGT TCCAGCTTGA CGGCTCTGCT 2100 CTGATGCTGG GTCCAATGCC TCTGATCGTA TCTCTGTCCA TCCTTCTCAT TCCCACCCAG 2160
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