Tag | Content |
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EnhancerAtlas ID | HS092-02915 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:113117300-113119600 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxq1 | MA0040.1 | chr1:113118314-113118325 | AATTGTTTATT | + | 6.02 | HSF1 | MA0486.2 | chr1:113118324-113118337 | TTCTGGAATTTTC | + | 6.17 | JUN(var.2) | MA0489.1 | chr1:113118224-113118238 | AGGGGATGAGTCAT | + | 6.91 | RELA | MA0107.1 | chr1:113119150-113119160 | GGGAATTTCC | + | 6.02 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I112575 | chr1 | 113117644 | 113118760 |
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Enhancer Sequence | CCATAAATAA AAAGTACAGA TAAAAAACAT AAAGGGAGGA AATAAACATA ATTAATAAAT 60 AAGAATACAA ATGAATAAGA ATAGTGGTTA CCTTTAGGTA GGAAGGGAGG TTGTAATGGG 120 AAAGGGCAGT CAGGTAGGCG TCTGTGGGTT GATAATGTTC TGTTTCTTGA TCTCGATAGT 180 TTTCAAGCAT TTACTTTGTA ATAAATCATT AAGATGCACA TTTTTGTCTC ATACACTTTG 240 CTGCATGTGT AGTAGAACTC ATAATAAAAA GTTTACAAGG CTGGGCGCGG TGGCTTATGC 300 CTGTAATCCC AGCACTTTGG GAGGCTGAGG CGGGCGGATC ACAAGGTCAG GAGATCGAGA 360 CCATACTAGC TAACATGGTG AAACCTCGTC TCTACTAAAA ATACAAAATA ATTAGCTGGG 420 CGTGGTGGCG CGCACCTGTA GTCCCAGCTA CTTGGGAGGC TGAGGCAGAA GAATCGCTTG 480 AACTCTGGAG GCGGAGGTTG CAGTGAGCCA AGATTCTGCC ACTGTACTCC AGCTTGGGCG 540 AAAGCAAAAC TCTGTCTAAA GAAAAATAAA AGTTTACAGT ACTCACTCCT TATCCTCAGT 600 ACATATGTTT TAAGACTCCC AGTGGATATC TGAAACCACA AATAGTACCA AACCCTACGT 660 ACACCATGTT TTTTCCTCTA AATATATGCC CATGATAGAA TTTAATTTAT AATTTAGGCA 720 CAGTAAGAGA CTAATAACAA TAACTAATGA TAAAATAGAA CAGTTATAAC AATATGTCAA 780 TCTTGCATTT GGGGTCACTA TTAAGTAAGA TAAAGGTTAC CTGAACACAA GCACTATGAT 840 ACCATGACAG TCGATCTGAT AACCGAGTTG GCTACTAAGT GACTAATGGG CGGGTAGCAT 900 AGACAGTGTT GGATATGCTG GACAAGGGGA TGAGTCATGT ACTAGCCTGG ATGGAGGGGG 960 ATGGTGTAAG ATTTCATCAA GCTACTCAGA ACGGCATGCA ACTTAAAACT TATGAATTGT 1020 TTATTTCTGG AATTTTCCAT GTAATATTTT CAGACAGAGG CTGACTGTGG TAACTGAAAC 1080 CATGGAATGC AAAACCATAG ATATGGGTGA ACCGCTGTCT TTAAATTTAT GGAACCAGTG 1140 TCACTTAATG AGAGAATGGT ATAAATATTT GTTGACTCTC TTTCTTGGAT TTAAGTACTT 1200 TTCTTAACCA TATCTTTACT TACTCTAACA GGCTTACAAC ATCCTTTTCT TGGAAATTAT 1260 CTTTTAGCAA TTAATCTCTT TACTGTAGCT CTTTAGCTTC CAAGCTCTAT TAACACCCTT 1320 TCACTGGAAT CAATAGCTAT AATTACTTTC CGTAGTAAGG GCATCTATTC TTGAATTGTC 1380 TATACTTCCT AACATGGGGC ATTGTTTGTA GAACCCCAAT TTTTTTTTTG AGATGGGGTT 1440 TCACTCTGTC ACCCAAGGCT TCAGTGCAGT GGCGTGATTG CAGCTCACTA CAGTCTCGAC 1500 CTCCTGGACT CAAGCAATCT TCTCCCCTTG GTCTCCCAAG TAGCTGAGAC AACAGGAAGC 1560 ATCACCACAC TCAGATAATT TTTATATTTT TTGCAGAGAT GAGGTCTCAC CACATTGCCC 1620 AGCCGCTAGT CCCAAACTCC TGGGCTCAAG TAATCCTCCC ACCTCGGCCT CCCAAAGTGT 1680 TGAGATTATA GGCATGAGCC ACTGTGCCCA GCCCAAACCC CAAAATTTAA TTTTGTGTTG 1740 TAACACACAA AGATTAAGCA ATAATTTGTA TAACTGCAAG GTGTACAATA TAAAGACAAA 1800 GCAAGTATAT AGACTCATTG GGGACGAAAT AAGCATCAGC CAGTTTTTCT GGGAATTTCC 1860 ACATCTGCCT CCTATCATTG ATTATTTTAA TCTGTTTGTC TTCAGTTTTT GTCTACCCAA 1920 CCCTAGTTCA AAACCCAGGC ATCTGTCTAG AAAAAGCTTT CACAGTAACA GGAAATTTGA 1980 TTTAGTGATA AGAAATATGA ATAATCTTTT ATTAAGACCA ACCCATTATT TATTTTCTAC 2040 AACTATACTA AAAGAACAGC TAAGTGAACA CAGTTCAAAT TATATTTTGA TAGTAATTAC 2100 AAAGCATATA GCTAACTATT GCTCCTATCT ACCTTTCTAA ATGCCTAAAT GTTTCAACGT 2160 CCCCTGTAAG GTGAATAATA AGCATCAAAA TATAGCAGAT TAAAACAATT CTGCACCAAA 2220 TTATGGTGAC CCAGACTCTG GTCTACGAAC TGTCATCAAT TTGATAAACT TAAATAAAGG 2280 TAGTATTTTT ATCATAAAAT 2300
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