Tag | Content |
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EnhancerAtlas ID | HS073-03846 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr13:113228220-113229630 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr13:113229255-113229273 | GGGAGGGAGGGAGGAAGC | + | 6.36 | FOXH1 | MA0479.1 | chr13:113228361-113228372 | CCCAATCCACA | + | 6.14 | FOXH1 | MA0479.1 | chr13:113228417-113228428 | CCCAATCCACA | + | 6.14 | FOXH1 | MA0479.1 | chr13:113228476-113228487 | CCCAATCCACA | + | 6.14 | FOXH1 | MA0479.1 | chr13:113228535-113228546 | CCCAATCCACA | + | 6.14 | FOXH1 | MA0479.1 | chr13:113228593-113228604 | CCCAATCCACA | + | 6.14 | FOXH1 | MA0479.1 | chr13:113228650-113228661 | CCCAATCCACA | + | 6.14 | FOXH1 | MA0479.1 | chr13:113228706-113228717 | CCCAATCCACA | + | 6.14 | RUNX1 | MA0002.2 | chr13:113229186-113229197 | AAACCACAAAC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr13 | 113228854 | 113229333 | chr13 | 113229418 | 113229542 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I112573 | chr13 | 113227900 | 113230513 |
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Enhancer Sequence | TCTCCATCCT AGGAAGGAAG TGGAACTATG AGTGGCACCT GGAAATTCAA GTGGGCACTC 60 TGAGCTCAGT ATGGCTTCCT CTGCCCAATC CGCAGAGAAT CTTTAAGTGA GCACTCTGAG 120 CTCACAGTGT GGCTTCCCCT GCCCAATCCA CAGAGAATCT TCAAGTGGGC ACTCTGAGCT 180 CAGTGTGGCT TCCCCTGCCC AATCCACAGA GAATCTTCAA GTGGGCACTC TGAGCTCACA 240 GTGTGGCTTC CCCCTGCCCA ATCCACAGAG AATCTTCAAG TGGGCACTCT GAGCTCACAG 300 TGTGGCTTCC CCCTGCCCAA TCCACAAAGA ATCTTCAAGT GGGCACTCCA CGCTCACAGT 360 GTGGCTTCCC CTGCCCAATC CACAGAGAAT CTTCAAGTGA GCACTCTGAG CTCAGTGTGG 420 CTTCCCCCTG CCCAATCCAC AGAGAATCTT CAAGTGGGCA CTCTGAGCTC AGTGTGGCTT 480 CCCCTGCCCA ATCCACAGAG AATCTTCAAG TGGGCACTCT GAGCTCACAG TGTGACTTCC 540 CCTGCCCAAT CCATAGACAA TCCAAAATCC CCAGAAATGT AACAAAGGAT TTAAGGAAGA 600 TATAAACAAA ACCAGAAAAG TGGATCTAAG AAGAGCACTC TTGGTGAAAC AGAAACTGAA 660 GAATCCCTGA AAGATGTAAA GAAAACAAAC AGGATTGACT TGAAAGAAGA AACTAGAGAC 720 AGAAGTCATC TCCGTCAAGA CAGAGTAAGC ACACTCCACT ACTGATGACA ATGTAAAACT 780 CTGGCAAAAA TACATAAAAC ACCTCCAATC AGACTCTGAA CAATGGGTAA GAGAAGCAGA 840 CTGGGTATGA AACTGATGAA TCAAAGGAAA TCCTGGAATG ACTTCCCCCA TTTTTGCTTT 900 TTGATATTTT CTTTATCTGT TTGCTGTTTA CTGCACCAGC TGGGGCTGGG TAACACTCCA 960 AAACCCAAAC CACAAACAGG CAAAGACAGA AAAACCTCCG AGCCAGGCCC AGTCTCCCCA 1020 GCCAGGGCCC AGGTGGGGAG GGAGGGAGGA AGCACCACAG CTCTCCCAGC CCTGCGCCAG 1080 GCTACCAGCC CCTTCTACCT TCAGGGGCAC CCCCGCAGTG GGCTGCCCCA TTCCACACTT 1140 GACAAGAACC AATAATGGCC CCAAAACTCC ATCACAAGGC TGGCAGGCTG GGGGTTCGGA 1200 TTTTAGCCAG AACATGAGGA AATGTGTTGG GAACCAGAGT GAGGGCAGCA GCACAGAAGA 1260 GGAAGCTGGA AAAAGTCACC CCTTAAAGCT GTGTACTATC GAGAAGGAGC CCAACTGAGA 1320 CATGATGAAA GATATCCTTA AAAATGAAAG GAAGAAGAAA GATATTCCAT GAAAACACTA 1380 TTCAAAGAAC GTGAACTGGC TACATTTCTA 1410
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