Tag | Content |
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EnhancerAtlas ID | HS105-23146 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr13:109807390-109810110 |
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) |
ZNF263 | MA0528.1 | chr13:109809780-109809801 | TCCCTTCCTTTTCCCTCCCCC | - | 6.47 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_36306 | chr13:109806480-109811018 | HMEC | SE_64525 | chr13:109806086-109811668 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I109153 | chr13 | 109805787 | 109815118 |
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Enhancer Sequence | GGAAATTGGC ACAACTTAAT TTTCTGTGCA TTTTTGGGTA CTGAAAACCT TATTTATACT 60 GACAGTCATT TTTTAGCTTT ACTATCAATG CATTCTTCCC TTGCTCAGCA CATATGTTGT 120 TGAAGACATC GCTCTGTTTC CTACTTCAGT TGGTGTTTTC TAGCACAAAC CATCTCCTTC 180 GACTTGGCGG GGGGGTGGGT GACAAGAGTT AGGAGTGAAG GAGGAGCAGA CATTTCCATT 240 CCTCCCCGCT TAACCTGGAG GATAAGTATC TGCGGCACTC GCTACCAGAG AAGAATGCTT 300 AAAACATAAG TTCAAGAGGA ATTTCGATCT ACTCCAGGGT GGTGATTTCA TAAGGGGTTA 360 TTAACAAGTA GGAAGGAATG TCGGGAGCCC AGCCCGAGAC ATTTAAAGTC AGTAGAGGGC 420 CGGGCAAATC CAGTTTCTCA GCACACGCAA CCTTTCCAAG GTCTGCAGTG ATGTATTTTT 480 CTGTTTCTTA AGTAATCAAT GCTTATAGAA ATATGACCTG TCCACATAGT GTGGGTAACA 540 GCTGTGTCAC AAGAGTAACT GCCTGGGAAC CCAGTTCTCT TCCCAGATCT CCATCACCAC 600 TAGACTCAGA CGCCCTCTCT TGATATATTT CTGCAAGCAT TCACAAAGGG ATGATAAAAT 660 CTGTTGCACG TTTTCAAAAG GCAATTAGAA TTGTGCTGTT CAAAACATGC ATAATTGCAG 720 TGTGTCACCT CCATGAGTTT AACACATTTC CCCTGTAGCA GTCTCCACTC TCCTCACATC 780 CACCCATCTC CACTGAACTC TCTCTTCTTG AGTTTCAGAT TAGCCTCTGT GGTTCTTTAC 840 ATCTGAAATT CGTCTTTCTG AGAGGCAATA ACACAAATAT TTGGATTATG CTATCATGGA 900 AAGGAAAGAA AATTCTATCA TGTAAAAGAA AAAACATATT ATGTAAAAGA AAACAAATCA 960 CTTCCTAGAA GCTTATAAAG TAGGATGCAG GTCGACTTGA GAGGGGTGTC AAAGCCCTGT 1020 TTGCATTTCT TCCTCATGTG CAGTAATACA GGGTTTCAGA GAAATCTATA TTTTAGAGAT 1080 TTAAAAGGAG TTGCCCTGTG TAACACAAAC TAGATTTGGT TTAACACAAG CTAGACGCCA 1140 ATTTCAGGTC GAAGTGCTTG TATCCAAATT TAATTACGCA CCATCTATGT GTATCTGCAA 1200 GCGCTGTCGA GCTGCGACTT CTAAATTTTA CAAACGAGAA CTTGAGAAGT GGTGGGAGCC 1260 TGCCAGGCAC CTCTCTCTGC ATTTGTACTT TTCCTTAATG CCAAGTAGGA AAAAACAAGC 1320 ACATTCCCTT CATGCAATAG CCTTTCTGAA GAGGAATTTT CCTATAGAGT TTCAGAATGA 1380 GTTATAGCCA GTATGAGTAA TGAGTTTAAA ATGTATTTTC ACATTTTTTA TGCCTTACAT 1440 AGCACTCTCA GTATTAAGTC AGCCAAACAG CTATAGTTTG TTTTTCTCCT GCGTTACTGA 1500 AACCCGGATC CCATCTCATA GGATTCTAAA ATACACTCTA ATCTGATCTC TAGCGCAGGT 1560 ACCTAAGAGA AAAGTGGTGT TTTCAGCATC TTGTTGGGGA AACATTCCAT GGCTCCTTTC 1620 TCTCCCCTGC TTCCTGGCCT TTCCCCAGCA CTGACGCTGT CAGCCGCCCT GCGTGCCACA 1680 CAGTCCTGCC CTCTGCCAAG GCTCCTGGCC TGCAGCCCCT CCTGCAAGCC CACATCTGCC 1740 CTCCTGCACG CCCACATCTG CCCTCCTGCA CGGCAGTCAC CTGGGCGTCC CCTCCTGCTA 1800 CCTCCTCACA CTCGAGAGTG TCTCTTCCTT GAAAATTTCT CCTTCCTGAG AGATTTTTAA 1860 GTCTCTCCTA GCTGTTTCCT TTCCAGTCCT AATAAATTCT CTTCTTCAAA AAATTGCCAC 1920 TCAATTTAAT CCTCAGGCCT GCGGCTGTCA CTTCAAAGTC AACAAGTACA ACCCCAGATG 1980 CACCCTGCTC TTCAGGTGGG AGCTGCTGCT CTGAACCACG CCCCAGCTGT GGTCCCCATC 2040 AGGTCCCAGT TCTCCCGCTC AGTGGGATTG AACTCAGCTT CCTCCTGCCT TTCCACTCCT 2100 CCTTCTGCTT CCCCAGCCTC TCCCCTGACT CTCTTTCTAC TTCTAATCTC TCCTCAAGGT 2160 CCATTCAGCT GTATACTTTC TTTGCTAGAT TAGTATTTAC AAAAAAAAAA AAAAAAAAAA 2220 AAAAAAACCT TATTCTTCAC AGCATGCCCT TGCTCAAAAT ACTTGCTGGA ACCCAGTCCT 2280 GTGATGCTCA TAGACTCCAA AGCTCTCTGC TCCCACTTCC CGGTGCGGAG GTGTGGGCAG 2340 AGCCAGCCTC CCCTCCCTCA CGAGTGCAGT CAGCTCTGCC TCTGCGGCAT TCCCTTCCTT 2400 TTCCCTCCCC CTCTCCACAT TCCGTCCTCA ACTCAAAATC CACTGCTTCT TCCTCCTGCC 2460 TACACAACAA AGGCTCACCT GGCTGCTCCA GCCCACTCTG ACCTCTCCTA AGAATTCCTA 2520 GAGCATTTTG CAGAGCTCCC ATCCCAGCCC CCTGGCCCTT TGCAACCTTA ACACATGCCT 2580 TGAAGGCACC TTGAAGACAG TCCCCCTTAG AGCTGAGTCA CCACAGAGAA GCCTGGGGAA 2640 AAGCACCCCT TAGAATGCAC CCTGGATGTC CCTGTCACAT GGGTTGGCAT TATAAGTGTC 2700 AAAGGCTTTA ACAAGTGAAT 2720
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