Tag | Content |
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EnhancerAtlas ID | HS191-12567 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr14:102089620-102091520 |
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 | chr14:102090607-102090628 | CTCTCTTCTCTCTCTTCCCCC | - | 6.4 |
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| Number: 2 | ID | Chromosome | Start | End |
GH14I101623 | chr14 | 102089844 | 102089938 | GH14I101624 | chr14 | 102091101 | 102091130 |
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Enhancer Sequence | GGGTGGGAGA CTAGGAGAGG TGAGAGCAGG AGCTACGGGA GGGCAGAGCC CTGGGGTCTA 60 GTCCGCCTAC CAGGGCCACA GGGAGCCATG GATGGTGCTA GGCAGGGAGG AACCTGGTCA 120 GATGGGTGGG TTAGGAAGAC GGTTCTGGAT CTAAGAGGGA AATAGCTCAG GAGGCAGGGG 180 AGAAGGTGTG AGGGAAAATG CAAGGGCCAG TGCAGGCCTG AGAGGCGCTT GTCTGGAGTC 240 CAGGGGTCAC TCCTGGCTCT CAGAGCAACG ACAGTGGGGT GAGCAGCTTC CTGTGTTCCC 300 AGCTCTGGGA AAAGCTTCTG CTTTCCGTCT CTAGGTCAGT GTCTTCTCCC AGCTCCAGAT 360 TCACATGGCC ACCTGCCCGG CAGCCACCCC ACCCATAAAC AGTGAATGGG TGGTTAGCTC 420 CTAACCTGGC CCCTCAAGCT CCTCATCTCC CCAGCCTGCT CCACCACCAT CCTCCCCATC 480 TCAGCACCTC CCTCCCTCCA GGGCTTAGGC ACCTCCCTCC CTCCAGGGCT CAGACCCAGA 540 CCCTGGAGTC ACCTTAGCTC CTGTCTGTCA CCCCAGCACC TGGCCCACCA TGCAGCTCTG 600 CTGTCTCCTC CTATCCAGGT TTATCCCAAA TCCAGCCGGT CCCCTCCATA GCCACAGCTC 660 TGGTCTGAGC CACCACCCTG CTCTCCTGTG GATCACAGTA GGGGCCTCTC GGCAGGCAGC 720 CCCAGCCCTC ACCCCACATC CTGGTTCTCA TGCAGCCAGA AGCACCCCGA AATCCTGCAC 780 TGAATCACCA CCCTGCTCTG CTCCAAACCC ACCAGGAAGG TCCAGCTCAC TCTCAGTCCT 840 CACCCACTGC CACACCTGGC CTGGCCCCAA CCCTGCCCTG GCCTCATCTC CCACTGTCCA 900 CTTTCCCCTC CGCTGGCCTG AGCACTCCTC AAACTCACCA GGCAACTCCT GCCTCAGGGC 960 CTGTGCGCTT GCTGTTCCTG GAATGTCCTC TCTTCTCTCT CTTCCCCCTC CCATCCCCAG 1020 GCACATTGTA TGGTCCCTGT ATTCATTCCA TTTAAATATC TCCTCTCCAG CCTGGCTCCT 1080 GTGGGACCCC CCTTCCCGTT AGTCTCCATC CCGTCACCCA GATTTTCTCC GCAGCACTGC 1140 ACCTTCACCC TGCATTCGGT CATGATCGCA CTGCTCACTG TCTGCCTCCC TCTCTAGATT 1200 GTCAGCGCCC TGAGATCAGG ATTCTGACCT TCTTGTTCAC AACTGGAACC CCAGTGCCGA 1260 GAAGGGGCCT GCTGTGAGCA GGGCAGAGCA TGTGCACCCA CTGAGTGAGC GAGTGACCAT 1320 TGCAGCCTCA CTCCTGCGCT GCATTCCGCA GCATTCTTTC ACATCCATGG TTTCCCCCGA 1380 GGCCCCTCAG GAACAAAGGC TCAGAGAGGG TGGGAGAAGT GTGCAGGGTC ACACGTGCTT 1440 CCCCTCCTCC CTTTATGGGG TCCTGTGGAG GAAGGGGAGG CCTGACTGCA CACTGCAGAG 1500 GCCAGGGCAG GGCAGAGAGA CTCCCACGCA TGCTACTCCA GGGATGGGGC CTGGAGGGAG 1560 GCTCCCGTGC GTGCTAGTCC AGGGCCTGTG GAGGAAGGAG ACGCCTGACC TCACACTGCA 1620 GAGGCCGGGG CAGGGCAGGG AGATTCCTGT GCATGCTACT CTAGGGATGG GGCCTGGATT 1680 CTTCAGTGGG TCCCTGGGCA AGTCAGGCTC CCTAAATGCC CCACTGTAGG TGCCTGCAGT 1740 AACAAGAACA AGAAGGGCAG GGCATGCAGC AAAGCCACAA GGCACAGGCT GCGCACACCT 1800 ACTGGCTGTG ACCCTGAGCA AGTTACATAA CTACTCTGTG CCTCAATGCT CTCATCTGTA 1860 AAGTGAGAGT AACAATTTCT GCCTACCTGA CAGGGCTAAG 1900
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