Tag | Content |
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EnhancerAtlas ID | HS118-05938 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr14:70470810-70473360 |
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) |
GSC | MA0648.1 | chr14:70471973-70471983 | GGGGATTAGC | - | 6.02 | HNF4G | MA0484.1 | chr14:70472205-70472220 | TGGACTTTGGTCCTT | - | 6.73 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34800 | chr14:70458321-70472832 | HeLa |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I070004 | chr14 | 70471439 | 70472899 |
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Enhancer Sequence | GGCACCTTGG TTACCAAACG AGCCTCCACT GGGAGAGCTT CTGATTCTTT CTCCAGGAAG 60 ACTGCATCAT TCATCAAGGC ATCTTCCCAG TCCATGTTTT CATGGCTTGT GGCTCTTCTT 120 CAGTTCTTCC GCGTATGGTT CTCTGTAAGA TTAGCCTTTT TTCTTGCACT TATTTTTCAG 180 ATGGACTTTA CGATGCTTCA TATTATAGGT CAATTTGGCT AGGCCATCCT GCCCAGTTGT 240 TTGGCCAAAC ACTCATCTAG ATATTGGTGT GAAGGTATTT TGTGGATGTG GTCAACATTT 300 ACAGTCAATT GACTTCAGAT AAAACAGGTT GCCCTTCATA ATGTGGGTGG GTCCCATCCA 360 ATCAGTGGAA GGGCTTAAGA GCAAAGACTG AGGTTTCCCC AAAAAGAAGG AATTCCCTCT 420 CCAGACTGTA ACATGGAAAT CCTTCTTGAG TTTCCAGTCT GCTGACCTGA CCTATTGATA 480 TTGGACTCAA GACTGCCCCA TCACTCTTAC CTGAATTTCT AGCCTATTGG CCTGCCCAAC 540 ATATTTTAGA TTTGCCAGCC CCTATAATTA CATAGCCAAT TCCTTAAAAT ATCACTCTCT 600 CTCTCTCTCT TTATGTATAT GTGTGTGTAT CTATAATCTG TAGATATCTA GCACTTGTCC 660 CTGTGCTAGC CCTTCCAAAA CAAATAGATA TAAAGATACA TACACACATA CATATACGCC 720 TGTCTCTGTC TTCTGTTGGT TCTCTTTCTC TGCAGAACCC TGAGTGACAC AGACCTTCTC 780 TGTCTACTGT CTGCTCTCTC CACCCGTCTC CCCCTTTGAC CTCCACTTCC TCCATCACCA 840 TGAGGTTCCC ATGTTCTTTC TCCAAAAAGC TTACAGCATA GCTGGTCTAC CAATAACTGC 900 TGACTGCATG TGCAGAAGGT GCTTTGGTGT TGGGTTACCC AGGATCTCAG CTTTTCTGTC 960 TGCTCCTTTC TTCAGCAGTT CCTCCTCTGG AAGGCAGTGT CTAGAAAGAA AGGCCAGCCC 1020 AAAGATCTGA AACTCAAATC TTGTAATGTT TATGTTTTTT GGCCATTTTT GCTTTAAACA 1080 AAAAAAGAAG AGAAAGGAAA AAGATGATGA AGAAGAAAAG GTTTCTGGGA TAAAAGACTA 1140 AACTCTGGGC TAAAATCAAG TCTGGGGATT AGCTGAGGAT TTAGGTTATC CATGCTTTCC 1200 TTTGTTCCTA ATCACCATGA GTAATTGAGA GGCACAGAGG CCTGGGCTAG TCCTAGCCGA 1260 CAGAGCTGTG CTCCAGGCTT ATCCTCTCTT GGTGGGATGT GAAAGAACCC GTGCCCTGGG 1320 CCTGGAGACA GGGTTCATGT TTGTCTGGTC CAACCTCTTT TTTCCTCTCC TGTCTCCTGC 1380 CCTGCCCACT CCTGCTGGAC TTTGGTCCTT CTTTGCTATG TGCAATTAGT GGTGGACAGG 1440 GTTGTGTGCC TTCTGGTGAC AAGGGGTGGA CATGGTTTCA CTTCTATCTG AGTATTTACC 1500 ATGTGCCAGA CTAGGTACTG GACAGTTTGC TTGGATGTTT TTTCTATTGT GTTTCTTCTC 1560 TTAGGCAGTC AGAGGTTTGT CAGTGAAACT TTAACCACTC ATTGCCAAGT GCGGAATGAC 1620 CTGACTCTCA CTTCTTCTCT GCACCATCTG AGGGACAGGA TTATAGGGGC GGGCGTGTGA 1680 GTGTGTATGT GTGGCCATGC ATTTCCATGC CCCCCTGGAC AGCCCTGATT GTTCCCTCTC 1740 CCCTTCCGTT TATGGCTTCC AGGTGTTTAC AGATGGTCCT GGCCCATTCT CATAGATACC 1800 TGGCCAGACC TTCTAATCTT GTCATCTTTC CCTGAGTGTT CCTGAGCACA GATTATTTTA 1860 GAATAGTGTG TGTTCACTTC TGGGGAGCTC CCTCTCTGAA CCCATGATCA TGAAGAGACC 1920 CACAAAATAG GCCCCCTGTC TTGCATTCTG GAAGGGGACT TCTTGGTACC TAAGAAAACT 1980 GATAGATGTG AATTTTAAGA CCCATTTGGG ATTTAGGTAA CTGAGAAGGA AAGAGGATGA 2040 TAGTGGCCCC ATGGGTGGTC TGGCTTTTTG GGTCCGCCAC TTCCTAGTTC TGTGATCTTG 2100 ATCCAATGAC TCTGCCAGTC TGTGTTTCTG CACCTTCTTC TATTCAGTGA GGATAAGAAG 2160 AACACTATTT TAGAGGCTTG TTTGAGTTTG AAGTGAGTTA ATACAAGCAA ACTGCCCAGT 2220 ACCAAGTCTG GCACATGGTA AATACTCAAA TAAATGTTAG CTATTGTTAT TCATTTTAGA 2280 GTTCTGCAAT GGTGGATGAG TTACAAATTT GGGTCCTCAG ATATGGAATA AGCTTATGCC 2340 CTGTGGTACT TACTGATTAG CATATGCATG ACCCATAACC TCTAGAGAAG CCCTTCAAGA 2400 ATAATTGATT GGTTGACTGA AGGGCTTACA GGGCTACAAA AATACGTACA GGGTAAATTG 2460 ATGAATAGTT AAGGAGGTCT AGATGTTTCA GTTATCTGCT GCTGTGTAAC AGACTGCTCC 2520 GAAATGTACT GGCTTACCAT AAAAATAATT 2550
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