Tag | Content |
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EnhancerAtlas ID | HS092-02703 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:98551040-98553790 |
Target genes | |
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) |
FOXA1 | MA0148.4 | chr1:98552201-98552217 | TATTATGTAAACATAT | + | 6.17 | FOXC1 | MA0032.2 | chr1:98552204-98552215 | TATGTAAACAT | + | 6.32 | TFAP4 | MA0691.1 | chr1:98551178-98551188 | AACAGCTGAT | + | 6.02 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I098085 | chr1 | 98550630 | 98554094 |
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Enhancer Sequence | TTAGAGTCTA GTATTTCCTT GTCTTAAGAC TGATCACACT TAATTGTGGT TATATAGTGT 60 CTGTCTTTTT TGTTGGAATG AAGACTGTGA GGAGTTGAGA ACTATCAGTT CCCTGAGCCT 120 AACATTTAGA TACTGAATAA CAGCTGATTA CATGAATGAA TGAAGAATAT TTGTTAGAAG 180 ACAGAATTTT TTTAGAATTT TAAATTGCAG AGATCAAGTG AGAAGGTTCC AGTTGTATTA 240 GATCTGAGAA ATGTGATTAA AGCAGTGTTT TTGCAAGATT AATTTGACAT TTTTCTGTTG 300 AAACAGATTA GGGACAGATT AGATGGAGGT TTGTAGTGAT GAGAACATAG ACAAGTGGCT 360 TCATATTAGA GTCACCTGGT GATATTAAAA AAAATACCTG TTTCCCAAGC TGCCCCAGAC 420 TGATTAAATT CACTGATTGC AAGAAAACCT AGGATTTGTA CTTTTTTAAG TCAAACGCTC 480 ACACCCATCC AGGATTTTCT GAAGTTAAAA TGGTAACAGT ATAATTGGTA TGGGCAAAAT 540 ATATTTTTCC TAAGAATGAT AGAATGTGAA TGTGGGCTTT TCAAGTCTAG TGGACCAGAG 600 AGCCCCATTG CAGTGTTAAA GAAATGGCGA AGTAGAAGAG GGGAGTTGTT TTAAAGAAAG 660 AGAGAGTGAC CAGGCCAAAA GTGGCTCAGT ACTTTGGGAG GCTGGGGGGA CAGATCACCT 720 GAGCCCAGGA GTTTGAGACC AGCCTGGGCA ACATGGCAAA ACCCTGTCTC TACCAAAAAT 780 TCAAAAAATT AGCCAGGCAT GGTGGCATGC ATCTGTGGTC ACAGCTACTC AGGAGTTTGA 840 GGCGTGAGAA TCTCTTGAGC CCAGGAGGTG GAGGTTGCAG TGAGTCAGGA TCATGCACTC 900 CAGACTGGGT GACAGAGGGA AACCCCATCT CACTATCTCC AAAAAAAAAA AAAAAAAAAA 960 AAAGGAGGAG TAAGTTTTAG GCATGTGGGA CACATATGTG TATATATACA CATATATACA 1020 CATACAATAT ATACACATAT ATGTGTGTAT ATATACACAT ACAATATATA CACATATATG 1080 TGTGTATATA TACACACATT TACACATACA ATATATACAC ATATATACAT ATATAATATA 1140 TAATATTATG TGTATATATA ATATTATGTA AACATATATC ACATATTAAA TATGTATATA 1200 GGTATATATG TATATATATG TTTAAATACC TGACCATCTT CTACTAAGTT ATGATTCAAA 1260 TGTTCCGTTA TCTAGGAGGC TTCCTCTCCT CTGCAGGGCC CATTGTCCTA GCTACACCTC 1320 AATAACTGCT TTCTTTTCTT TTTTTTTTTT GTCTTTTCCT CAACTCAATT CTAAGCTCTC 1380 TAAGGACAAG TATGTTGCCT TACTCATACT TGTGAACTCA GTGCTCAGGA CACTGGCATG 1440 CATAGAATAA ACACCCTCTG AATGTTTGCA GAATGAGTCA GTGATTAGAT ATGAGACTGG 1500 ATGAATTCTC CTGAAGAGTA AATGCTAAGG AGAAAAGAGT GTCTTGTAGG AGGCATTTGC 1560 AGACAGACGA AGCTATAGAG AGGGACAATG CAAGTAACCT CAAATGAGAG TGTGGAAAGG 1620 CGGGAAAGCA GCCAGAGCTT CATTGTTATG AAAAAAGAGT GAAATGTGCT CTGTTGAAGA 1680 GTTGAAGAAT GAACAAAGGA TATTTAGTTT GAATGGAAGC TCAGTAATGA GAAATGAGAA 1740 TGGTTGAGTT CTTAAAAGAA GCAAGTAAAG AAGAGGATTT GTGGGCTACT AATCTCATTC 1800 AGTGAATCTC ATACGACCCT TGCCTAGTGT TAAATATGTT AATGAATTCA TGTCATGCTG 1860 CTCAGTCTTA CTAGCCTTCA TCATCCAGAG TAAAATGCAT ATGATTCCTA TGAAAATTTG 1920 TGGAAAGGAA TATATTAATA GGTTAGAAGA ATTAGAAGAA TGAAAAGAAA TAATTTTTGC 1980 TTTTTAAATG GAGAATCATG CATATTTGGA GACACAAGGG AAGAAGCCCA TGGAGAAGGA 2040 GAGATGAAGC TGTAAAAGAA AGATGCTATG AATGTGCTCT CGACAGGTGA GAAGATGCCT 2100 CGACAGGTGA GGAGAGAGTA TTGTGAGCCC AAGTAGAGGA GATGGCTTTG AGATGCAGAA 2160 AAATATCTCT TTCTCAAGAC CCCATTTATT TTAGACGGTT CGCGGAGCAA TGGTGCTCAA 2220 TCAATCTTTA CCATAGTTAT TACATAAACC CTTTATACAT TTCATCATTA ATATTCTTTT 2280 CTACTATGGT TTGAGATGCA GAATAAGGAA GATAAACCTA TTTGTCAGTA TTTGACCATA 2340 ATCAAAATCA ATTTTTATCT GGAGTCTTTA TGTTTGTTGC ATGTGTATAT GTGTTTAAAA 2400 ACTAAGTTCT GGGAAGATAG CATTACACTT AATTCCGTTG GATTACTTTT GGATCATGTA 2460 AGCATACTGA TTTCTAACTT GTTTAAATAT TTGAATTATT TGATTCTCTA CCAGAGATTA 2520 ATAACTCTAA AAAAATTTAC TGGTTGGATT AAAAGTGCCT GTAGTTTATC CCTATATTTC 2580 ATAGAGTACA GAGCGAGATA GCACATTTGT CTGACAAATT TATATTTATG TCAGATAATA 2640 TCAGTTTTGT TATCACCATC TGCATTCTGC TATATTTTAA CAACAATGTG AACAGTATAC 2700 ATATAAAATT GTGGATTTAC ATGAGATATC ATCATTAATT TTCAAATAAC 2750
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