Tag | Content |
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EnhancerAtlas ID | HS092-14815 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr13:74511560-74513370 |
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 | chr13:74512489-74512505 | CGTTAAGTAAACATTC | + | 6.86 | FOXC1 | MA0032.2 | chr13:74512492-74512503 | TAAGTAAACAT | + | 6.02 | IRF1 | MA0050.2 | chr13:74511763-74511784 | AAGTTGAAAGAGAAAGTACAT | - | 7 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I073937 | chr13 | 74512126 | 74513280 |
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Enhancer Sequence | CTCAGAGTAT TTAATTTCCT TAAGAAATAT TCCTTTTTAC AAAGCACTGA CCCTATAAAA 60 ATGCAAATAA CTCTAGGAAA GGGCACTTTA CATTCTCTTC AACTAATGAG ACTGTGGTTA 120 GAACTGGTCA TCTGTTGGTA CCTTGAACCA TTACAGCACC ATCAGAGCGC AGGGACATCT 180 GGATTGTGGG TGGCAGGAGA ATTAAGTTGA AAGAGAAAGT ACATTGCTAA AGGGAAGAAG 240 GGCAGAATTC TCAACTTCAT AGCTTTGCCC AGGGCAGGCC CTGAGGGAAA GGATTTGTCT 300 GCCTGCTATA TTTCCCTTGG GTACTATCTG TAATTACTAT CACAGCTCAT TGATTTTCAA 360 TTCCTTGTAT TAATATATTT ATTGGCCATT CTGACATTAT TAAAATCAGT CTAACTCTGC 420 ATCTTTAGTG GAGGATACCT CTTCTTAAAA TAGGAGTTTT GCAAGAGCAG ATATTTCTTT 480 CCGCTTAAAA AAAAAAATGG TCTTCTCACA TTAGCCATAA CACAGCAACT GCAAATGTTT 540 TTCTTTGAAG CCAGGTAGTG ACATGCAAAG ATTTCACTAC AGATCAAAAG ATCTCAAGCA 600 GCAGGTCATC AGAGAATATT AAATGATAAG CAAACTCGTA TTTCCAAGAT AATTCTACCA 660 ATTTAGTCAA ACGCTGGCCC CTGTTCCACA GCAGGAGAGG GAATAATGAG CCCCTGGTTA 720 AAGGGTAATG CAAGTGGCAT TTTTAATAAT GCCCTTTTTT CACTTCTGAT AAAGTCATTA 780 AAGTAACACT GTCTTACTAC GCCTTTACGC ACAGATGTAC ACTAGATCGT TAGTGTAAAA 840 TTAAATAGGT TTACTGAGGA AAAAAGTTAG GCTAATTGTT GGGTTTTTTC CCCCTAATGC 900 TACTGAATTT TAATGTAATT TATTTCCTGC GTTAAGTAAA CATTCCATAG CACATTTCCA 960 GGTTCAGCTA CAATACCTGC ACCCGTCTAT ATTTCTTTAT TAAGCCTAAC GACTGGAGTC 1020 TTTTTCAAAA AAGCACCCGT CTCCAAATCC TCTCAATTCC AGTGTGGCAA ACAGCCTCTC 1080 ACTTACAACA AATAGCACAT GAATGAATCA CCACTTATTG AGCCCTGCCG ATTCATAAGC 1140 TCCTGTGCTG AGATGATGAG GAATAACAAG AAACATAAAG CATAAGCTCT GCTCTTAAGG 1200 AAGTTACATT ACAGCTGACT TCATGATGCT AGTCAGCTCT TGGTGATATA GGAATAGCTT 1260 CAACACCTTG TTATTAATGT CCTGCAGAAT GGTTTCTAAG AGTTACTGCA AGCTGCCTCT 1320 AGGGAAAAGA CTGAGTCTCC CTTATCCTCT TTTGTTCTGC CTCTAAAATG AGGGAGTGCA 1380 TAGGAATCTC TGGTCTGGCC AAGGTGGATA TTTCCTGGTA GTTAAGGCAT GGAGTATTGA 1440 CGTGATTCTA TACTTGTCTG CGGCAATGCC TGCACCCTTT CTAGCTACAT GGCTATGGCA 1500 AAGAGGCATC AGGCTCGCTT CCCCAAGGGT AACAGAAAGG AATCTGTCTT CCACTCAATT 1560 ACTGACTGCT TAGAGCACTT AAAATGAGCA AAACACCCAA TCTCTTTCCC TGTTTCTGCC 1620 GCACTATTGC CGCTCTTCTC TGCCGGCCCA CGGATCAGAA CTGTACCTGG TTCTACAGGA 1680 GAGAAGAGAG GCAGGATAAC CAATGGCTTC AACACCCTTG CAGTTAGTGT AGACACTCAG 1740 GTCAGCTCCT TCCCCGCGGC AGATTCCTCA GACTTAGGAA ATAAACAGTG AGGGTGACTA 1800 AGAAATGTTG 1810
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