Tag | Content |
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EnhancerAtlas ID | HS092-10816 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr11:126416750-126418850 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr11:126416806-126416817 | TCAAGGTCAAA | + | 6.14 | RORA | MA0071.1 | chr11:126416805-126416815 | ATCAAGGTCA | + | 6.02 | ZBTB18 | MA0698.1 | chr11:126418779-126418792 | CCACATCTGGAAG | - | 6.11 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I126547 | chr11 | 126417121 | 126417710 |
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Enhancer Sequence | GGCTAGCATC ATGAGTATAC CCATTTCGCA GATGAGAACA TAGAGGTCAA GAGAGATCAA 60 GGTCAAAGTC ATATACTGAG ACAGGAACAG AACTAATTTT TAAAAAACAT TATTATTGTT 120 ATTTGTTTGT TTGACCTCCA AGGAAAGGTT CTCTGGGACA CTGAGTGTGT TTGCTTCACA 180 CAAATAAATA ATCTGTATAG TATTTTACAA GTTTATAAAG AGTGTTCACC CATGTTACTT 240 GGTGGGTCCC CACAAGGCAG GTATGATTTA CTCTTGTTTG ACAAAGCTCA CACAACCAGT 300 TAGTGGCAGA TCTGGGCTCT AAAACATTAT TTCCCAAAGT GGATTTCAGG GACCACTAGT 360 CCTGACACAT GCTGCAGGAA AAATGTTTTG TGGTCAAATG AGTTTGGGAA CTCTGTGAGT 420 CATATCCCCT TTGGGTGGCT TACCATGGCC TTTGGTGTAT TAGTGTCTCT GAGAAGTTCT 480 GCAGGAAAGA CTCTCATTTT GTTAGGTCTC ATGTAGCTTC TCCCCACCGT GTCTAATCAC 540 GAAGGCTGCA TCTGACGGAA AACCTATTAA CATGCTACAG AAATGCTGCC TGTGTGTACG 600 CGTGATCCCT CCTCCCCCGT GTGTTTGGAG GCAGTGAGGA TTAGAGCGTG GCTGGGAGAG 660 GAGCGTGCAG GGGTAAGGAC GGGGTAGGGG ACCCACTGCT GGGGACTACT AGAGCTGAAG 720 CTCCCCTCCT CAGGCTGTGT CCTCTCTTTC CCTCTGGGCA GTGCAGAAAA TTCACTCAAT 780 ATTAGGCACA GTCAGCCCAG CCCATATCTG GGGCAGGATC AGAGGGGCCG CCTGAGTGGC 840 GGAGTGGGGG GTCTGTGGTC AGTGAATGGT GGGAGATTTG GGGACGGCAG TCCTTGGCCA 900 TGGGGAAAAA TCAACAGGGA CCCACAATAG GGGCTTAGTC AAGTCTGCCC TGGACGATGG 960 TGGGGAAGTC ACCCTATCCT CGTCGCCCAG ACACAAAGCT CCCGAGGCAG GGTGGAAGTA 1020 AGAAGGCCAG GCTTTGGCGT TCAGCTGGCT TACTCTAACA TCTGTGTGCC TTTAGGTGAT 1080 GATCTAATCT GTCTGAGCCT CTGTTTCTTC CTCCTCAGAA TGTGGATAAC ACTACCCACT 1140 TTGTGACGTG GTGAGGATTA GATGGTGCAA GTGTGCAAAA GTACCCTCCT TGGCCCTCGT 1200 CTTTGTGTGT CAGCTCCATC TCTCTTCCCC TGCTTTTTTG GAGCCCCTCA GTCAGAACAA 1260 ATAGCTTCCC ACCTCCAGTC CTCCACGAGC CTGTCATCTG TACCTCTCTT TAGTTCTCCC 1320 ATCGCCCTGC CTTCTGCCAT TTTATTATAT GCCCATCTCC CCAATGGACC TGAAGTTCTC 1380 TGCAGGCTGC TGCTGACTCT CTCAGTGCCC ACTTGTATCT GCAGGCCCGA CCATCCCGCG 1440 TCTTCAGGCC AACCTCCCAT TGCCGGTGTC TGGACCCCTT CTCTTGAGGG CTTTCTCTTT 1500 AGTTGCGGAG GCCACTGTGC CCTCACACAG AGCAGGCCAG ACCTGCTGGG AGACAACACC 1560 CTCACCCAGC AGCACTCCAC CCATGCCCTA CAGGAGCTGG TGCAGAAATA CCCCACCGCT 1620 TGGGTGCCCT AGCTGTGAGG TGGTGTTCAA TAGCACTTCT CAGAGTTTCT TACTGGGACT 1680 GGGCTCTGGC TGCCCATAGT GGTAGCAGGT TTGGGGTCCC CCCATGCCGA TGCCTCCTTT 1740 CCCATGTCAA TTTCCAACCC TCCCGCTGGC ACCTCTGCAC CTTCATGAGG AATGACTACA 1800 CTAGCGCTCT TGCTTAGGGC CTGCTTCCAG GGGAACCTGA GGTAAGATAA GGGCATCCTC 1860 CAGGTGTCAT TCATCTCTGC GTACACAGTG GGTGCTGATG AATCTCTGAA TCCAGCAGAA 1920 ATGAGCCATA GGAACAGCGC AGGGGTGACT GTCAATCAAG GCAATGACGT CAGTGGGCTC 1980 ACCACGTGGG TGGGTCCTGG GAGCAACGAG ATAGAATACC TGCTCCCTTC CACATCTGGA 2040 AGCATCCACA GCCACACTCA CACCTCTGTA CCTTCCCCAC CTAATGTTTA GTCAAACCTT 2100
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