Tag | Content |
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EnhancerAtlas ID | HS092-16967 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr14:101543120-101544600 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr14:101544521-101544532 | CCACACCCTGT | + | 6.14 | Myod1 | MA0499.1 | chr14:101544127-101544140 | AGGGGCAGCTGCT | - | 6.18 | Rxra | MA0512.2 | chr14:101543128-101543142 | TGAACTATGACCCC | - | 6 | ZNF263 | MA0528.1 | chr14:101544068-101544089 | GGAGGAGGGAGGGGCGGATGG | + | 7.42 | ZNF740 | MA0753.2 | chr14:101544478-101544491 | GGGGGGGGGGGGG | - | 6.03 | ZNF740 | MA0753.2 | chr14:101544479-101544492 | GGGGGGGGGGGGG | - | 6.03 | ZNF740 | MA0753.2 | chr14:101544480-101544493 | GGGGGGGGGGGGG | - | 6.03 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I101076 | chr14 | 101543309 | 101544539 |
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Enhancer Sequence | GCGTGCTCTG AACTATGACC CCACAGAGAG ACCACCACCT CCCCGCAACT GCCTGGCAGG 60 GCGCACCAGG CTGCAGAGAC AAAGGAATGG GACCTTTAGA AGCCTGGACC AGTTACTGGC 120 ACTGGGCGCC CACCTCTGGG TTGGGGAAAA TGCCGTGTGC CCAGTGCAGC CCCAAGATGC 180 TTCCTGGCCA AGAGGACCCC GTTCGTCAAG GCCTTTACAC CCCTTATCTC CCCCAATGCC 240 CTTTCCTGGC AGCCAGCCAG TGGTTCCACC TTTCCCCTTT TCAGCCAAAA AAAAGTAAAC 300 GCAGGCCAGA GAAGCCACCT GCCTGCGGTC CCACAGCCCG AGGTGGAGGC GGAGGGGGTG 360 CTGCCACTCC AAATCTGGGC GCCCCCACCC CAGTGCCCCC CTCCCGAGAA TAGAGCCCAG 420 AGCCAGAAGA AATCCGCCCT TGGGGCCAGG CTGGGTGGAC ATGGAGAGGG GGTAGAGGAA 480 TGCCGGCGGG AGGTACTGAA GGCTGCGGGG GTGAGGGGGG TTGAGGGGTC CCCAGGGGTC 540 CCTGCCCTGC AGTTCTTTGG GGTTCACAGA TTGGAAAAGC TGGTGCCCTT CTGAGGGTGG 600 GTGGGGGTGG CGGCAGAGGC AGAATAAAAC CCCCTCCCCT AGAGCCGGGG TGGCTCAGCG 660 GAATCATCGA GAATGAGACC GCTGGTTGCT AATGGGCTTG GGGAAAATGG GATGCAATTT 720 CCCCGGTGTT TTTCAGGCCC AGAGCTATTG AATAAATGAA GTGCGCGCCG GCGGAGTCAG 780 TAACTCACTG CGCGGCTCCC GGCAGGCGGG GGCGGAGTGG GGGCCGCAGA ACCGGACGTG 840 CCTGGCGAGG TTCAGAGGCG CTAGCGGTGT GGTGGGTGGG CAGCGCCGGG ATGGCTGGAG 900 GGAGGGGCTA CGGGGGGAGG CGCTGCCGAT CCCACACTGA TCTGGCGGGG AGGAGGGAGG 960 GGCGGATGGG GTTTGCTGGA GAACTTGACC TTGCTTCGCT CCCCTCAAGG GGCAGCTGCT 1020 GGGAGACCAA GTGTCACCGG CTGGCAATCA GGGCCCCAAG CCTGGAGACT TCTGGACAAG 1080 CGGAGGCAAG CCGACCATGA CGGCTTGGGT GCAGGGAGCA GGTGTCTGAG CCTTTGACGT 1140 AGACTTCCCG AGCCCCCACT GCACGGTGCA GGGGAGGGGC GGCGCAGGGA GGAGAGCGGG 1200 TTTCCGAGAG CCGCACATTT ACCAGACATC ACAGCCACCC CTCCGCTGAG CTGGGGGCTG 1260 CTCTGGGTTC GGGATCTGCA GCTCACAGAG CCCCTGCAAC GCTGTCCCAC CCCCAGCCTC 1320 CAGAAGAGGA TGGAGGACTG CCAGACCGGC TCAGGCCTGG GGGGGGGGGG GGGTGAGGGG 1380 CTGCCGTGGG CTTCAGGGCC CCCACACCCT GTTGGAGCAC CCTAGGGGGA CGGCAGACCG 1440 CCTCGCTCTC TGCCTGGTTC CTCTGGGTAT TTGCTGGGTG 1480
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