Tag | Content |
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EnhancerAtlas ID | HS092-01134 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:33982170-33984040 |
Target genes | Number: 14 | 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) |
FOSL1 | MA0477.1 | chr1:33982290-33982301 | GATGAGTCACC | - | 6.32 | Foxd3 | MA0041.1 | chr1:33983280-33983292 | AAATGTTTGTTT | + | 6.27 | JUN(var.2) | MA0489.1 | chr1:33982286-33982300 | AAGAGATGAGTCAC | + | 6.17 | JUND | MA0491.1 | chr1:33982290-33982301 | GATGAGTCACC | - | 6.62 |
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Enhancer Sequence | CTGGGAACAA ACAGATCACA CCTGAGTTTG CAAAGAAAAA AGAGGCAGTG GGAGGGGAGG 60 GGCCGGGAGC AGAGGAGGAA AAGCAAAGCG GCAAAGAAAA GAAGGCACAA GCGGGAAAGA 120 GATGAGTCAC CTCAATCTTC ACTTTGATTT TTAATCTTCC CAGGTTGGGG ATGGGGGTAG 180 GTAGGGAATA CGTGCAGCAG AACATGTATT TTTCTGTCTT TTTCCCTTGC AGGGCCAACT 240 TCGCCATTAG ACCTGGAGGC CCAGTGCTTG GGGGCCACCA TACTTTTAGG AACCCAGGAA 300 AACATTCTAA TTTTAGTTTC TTTCAAAATC AGATGAAAAA AAAAAAATGA CTAGGATAAT 360 AATGGCTCTG TAATAAAGAA TCCAGGCTGG ATTATATTCA TTTTTGTAGT GACACAGTTG 420 TGAAATCTCA TTTTTGATAC TTTTTTTTAA TGGAGGAAGG GTTGGCAAAC ATCATCACAC 480 AGCCCTGTTC CCCCGCCCTG TTACTCACTG ACCGCACAGG CCTCGTTGCT TCCTTAGTAG 540 GGTGTTTATT TTAATTTCAG CTTTTCTCCT TGGCATTATT TAAAAAAAAA TTACCATCTA 600 GTCACTCATT TGCAATGTGT GTGTGTCTGT TCAGGGTGGC TCTTGCTTTC TTTATGCTCC 660 AGCTGTGGGC AGAAGTGGTC AGAGGGGCCC TGCTGGAGAC CTGTGGGCTG GGCAGTGGGT 720 TCAGAGCCTG CTGGCAAGGG GCCAATGCTG AGGGCTGGCC AGATGTGGAG CCACCAACCC 780 CAGCCGACCC GGAGGTGACA GCATGGCGCA CACCAGCACC TGGAACCCAG CAGAACCCAG 840 GTGTGGAGCA AGAGTGACTG TGTGGAGGTC AGCGGCATTC TTGTTTCTTT CTTACACTGT 900 TCAATAATTC ATGCAGTGAA TCAGATTCAT CACTGATCAT CTCCAAGCCC CGATTTACAT 960 CATCAGAGGG GATTTTTCTT TTTCTCTTTT GCCTTCTATT GATAAGAGTT CTGAGAAGGA 1020 AAAAATAAAG ATTGGGCATA CAGATGAAAC TTGAGGAGTA ATTTTGGCAT GCTAAAACAA 1080 TCCCACTGGA ATAAGGGGGA ACCCTTATTT AAATGTTTGT TTTGGAGAGA CGTAAAAAGA 1140 TGGGGAAAAG CTCTTTCCAT AAATTGTTTG TATTCAGGAG CTGCATCTGC TGAGTCCCTG 1200 ACTCACTCAC CATCTGGGAC TCAGGCTGAA ACTGTGAAAT CCTCCAGGAG TTGTGAGGCA 1260 GAAAGGGAGT AAAGCACGTC AGGGGCTGGG CAGTGATAAT GACATTTGCT GCTCTTGTAA 1320 CCCCCTCCGC AGGAACTGTC CCCACCATCT CTGTTGGTGG CCTTTGCAGG CACCCTCATA 1380 AAAGCCTGTT TCCTCGCTGC ACTGCCATTT GTGTGTGGCT GGGAGAATCT GCCACGTGAG 1440 CGGCCATGCA CAGGAGCGTG GGGAGGGAGC GCAACACTAG CCCTGGGTTT GGCTGGTGGC 1500 CCACTTGGCG GATTTTCCAC CGCCCTCACT GGGAATCCCT ACCTGGCTGG CTCTGTGACT 1560 CTTCTCCCCA GAGTCCTTCA GCACAGGACC TGAGAGGGGG CACCTGCCTA TCCCCAGAAA 1620 GCGGGATGTG TGGGAGAAGA CAGTTCTCAG AGGGGTGCAG CTTGGACATC GTGTTGGGGC 1680 AACTCCTGAA GGGTCATAGG TCCCAGAGGT GAGGGTGTCA TCGAAGGAGG ACACAGTGAG 1740 GAAGAGGCAG TGCCTTTTAG ATTCATCAGT TCCTTCCCAG TGGGCCTGTC AGATGCATGC 1800 CTGTGTGCAT GTATGCGTAT GTGTGTGTGT GTGTGTGCAT GACCGTGTAC ACGTGTGGGT 1860 GTGTCTGCCC 1870
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