Tag | Content |
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EnhancerAtlas ID | HS092-25066 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr2:176719080-176721130 |
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) |
FOSL2 | MA0478.1 | chr2:176720623-176720634 | GGGTGACTCAG | + | 6.02 | JUNB | MA0490.1 | chr2:176720623-176720634 | GGGTGACTCAG | + | 6.02 | PBX1 | MA0070.1 | chr2:176720223-176720235 | TCATCAATCATA | + | 6.11 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I175852 | chr2 | 176717585 | 176721888 |
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Enhancer Sequence | TCGTTGCCTT TGTTGCAGAG ACTAAGCTAA TTGAACATGA TACAGTATGA AGATAATTAA 60 CACCCATGAG TTTGTTAATT GCCTGTTAGC ATTACAACAC AGTCTCTTGG TTTCTTTTTA 120 ACTGTCTCCT TTGTAGCCTC TTACTTCCCT TAAAATGGTG CAGGACCTGT TTAACTGGCA 180 ATGATATCTT GGAGTTTATT AACCCTTTTA AAATTTTTTT TTTTTTTAAA AAAAGCCATC 240 TTAATGAAGC ATATTGCATG TGCTTGTTAA ATGCAAGCTC CCACTTTGTC GCTCTATTTT 300 CCCAAGATTG GAAATTTGTT TTACAGATAC TGTACAAACT ATGTTTATTT TTCGTGCTAA 360 TTTATTTCAA GCAATTTAGC CATTATAAAT GCTCTTGAAA AAAAAACAGC TTTAGTGGTT 420 CCCTTTATTA CTCAGCTGCT CTGCTTTCGA GAGTAAGCGA TAAATGTCTT TGAGGGTTGG 480 AATATTAATT GAAGGCAGCA TCTGGTCAGC AGCTGACCGG CTCCAGTTGT CCTGCTCCAA 540 CCGAGCAGGC GAGAAAGAAG CTTTGCTGGC TCTCTTTGCC AGGCTCTCAC TTTTCCTTGG 600 AGCCATGGAC TAAATGAACC CCCATTTTAT CTCTGCTGGA TCACTGCATG GATGCCAGAA 660 AATCAATTGG GCAGGAAAAT CTGTTAATCT AAAGTGAATT CAATCTAAGG AATCATTTAA 720 AATAAAAATT TCAATCATTA CTTTTTCAGA AAAGCACTTT TTTCCCTCAA GTCTGTGTGT 780 ACATGTCATG ACGATACTTC GAAAGGACCT ATAGCAAGAG TAATTTGAAG TCAATAGAAT 840 TGTCTTGCAA AGAACAATTT GCTTTTTGGA AAAAAAAAAA AATAGGGTGG CTGATTACAA 900 ACTTAAGAGG AAATGGAAAA CCCAAACACT GTGTGGCCAG AAACCATTAA CACACTCTAG 960 CCCAGAATAC ACATCAGGAC AGATTTTTCT CCTGTTGAGA AGGAATACCT TGGCTGTGTT 1020 ACAATTGTTT AACTTGGATT TTCCTGCACG ATCCTCTGTG TTTGTCGTTA CCATGTCGCG 1080 GTTAATACTT GCTGGTAAGC CAGTCCCAGG GGAGCCATTT CTAGTGCCCA ATTACAAGTT 1140 CTATCATCAA TCATAAGTAT TATTTATTCA ACAAAATGAA TTGCTAATTA ATAACTGATG 1200 AGCATTATGG CCTTGAAGAC TATAACACTA TTAATTATGG TTGGCATGAA AGGGGTCTAC 1260 CTGGCACATT TTCACCACAA TTAGCCCTGG AAGCTTTCAT GGACTATGTC TATTAAGATA 1320 ATATAAGAAA AGGCTGACCT TCCTTCCCCT CCTGCATAAG GACTAATACA TTATCTCAGG 1380 TTAGAACTTC ACCAAATCAA CCCCGGTATT CCAACATTGT TTTTCCTGTG CACCATGACT 1440 TGTATGAGAA GCATGGCATG GAGAAAAGAA CTCCCCATAG AGGTTGGCAG GTACAAAATG 1500 CAGCCACACA TGCCCAGCCG TGCTCCTGCT GAAATGCTGC AAGGGGTGAC TCAGCCATAG 1560 CCTAGCACTT GGAATGTGGC TGCCAGCTTA TTTTTAGACT CAGTTGTTGC CCAGCTCCTG 1620 TTCTGAGCTC TGGGTCCAGG CACACAGCAG CTAAATCACT TCAGCAGGCA GCTGGCAGAC 1680 GAAGACTGTT CACATTTACT GGCAGGCTGG TGGGAGTACA TCGTTCACCT TAAGGACTTC 1740 CTGATCAGAC ACTTAAAGAA GGGAAGCTAA GAAATGCCCT CTTGCCCACT ACTGGGGAAG 1800 GAGAAAACAG TAGGTTTGAA GAATGAACAC ACACAAAAAT ATAATACTGC TGTGAACCTC 1860 TTTGAAAGCA GAACAAATCT ACTACCTCTG TGCTCTGTGT AGCTAAGTCT CTATGCCCAA 1920 AGCTCTGTGG GTGACCAAAT ATGGGTGGAT GATAAAGCAC TGCAAAGACT TTTTAAAGTT 1980 ATACGAATAA TATAAGGGAA AAACTTTTTT CCTCCTGCAT ATGTGTAAGC TCTAGAAGGA 2040 AAGAGCTTGT 2050
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