Tag | Content |
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EnhancerAtlas ID | HS047-09585 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr13:99649850-99651060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr13:99649863-99649881 | ACTTCCTTCCCTCACTCC | - | 6.07 | FOS | MA0476.1 | chr13:99650366-99650377 | AATGAGTCACA | - | 6.62 | RUNX1 | MA0002.2 | chr13:99650268-99650279 | AAACCACAGAA | - | 6.32 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_64474 | chr13:99649031-99651971 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I098996 | chr13 | 99649140 | 99651890 |
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Enhancer Sequence | TTGGTCTCTC AACACTTCCT TCCCTCACTC CATCCACATC AGACTATTTC CAGGGATTGC 60 CATGGGCAGC CTTCACTGTT CTTTGTGGGA ATTATTTTCC TGTCTCTGTG CATTGCTGGC 120 TTGCAATTCC AGCCCTGGCT GGTCAGGAAT ACTCCAGTCA CCCCCTGACT TTGTGCATCT 180 TTGTTATACA ATAGAAAACA TTTCCATGTG GGGATTCTGG GAGAATAACT GAGAAGCATG 240 CTGCTTTCCA GCCCCGTAGC TAACGAGAGG TCTGTTCTGC CAAAGTGTGG CACTGGCCCA 300 GCCCCACCCT TGACCAACAC AGCAGATTCT CCTAAGTCCC CAGGATCATC TCTGTAAAAG 360 CCCTGAGGAT TTTCTCAGAC TAGGGCTGAG GCCATTCTGC TCTTCCAAGA TTTGCTGCAA 420 ACCACAGAAA CATCTCCAGG GTGATGGTGA GGGTGTCATG CATGTGACAC CTGCCATTCT 480 CCTCAGCTTT TCCTCTGTAC TTGGTGGACC TCTGTGAATG AGTCACAGAT GAGAACAGCT 540 GAGGTGGGGC CGGGATAGAC AGTGGAGCCT TGGGGCAAGG GTGATGGCAG CTGGCAGGCA 600 TGCATCATCA GAGAAGCCAG ACAGGGCAGC AAGGTCCGGG CACCCAGACA CCCACAGCGC 660 ACATGTCTCA ATTCACTAAA TGAAGTGGAA GCCCCTGAAG GTAGGACCCA CCCTACCCTC 720 AAGATGCAAA CTCTGCTCAC CCTCTGGGTA TCCACTAAGA CTGATTATTT GTCTAGGCAT 780 AGAGACAAAT GGGAAACACC TGGCACCAAT TATGTGTGGA GCACTCGAAA ATCCTTTTTA 840 ACCTCGGATG CACTTACAGC ACTCATGGCC TTGGTTTCCA TCTGAATGAT CCGGGCAGAG 900 TCTCACACCA AGCTTCCAAA ACCCTTTTAA GAATTTCCGA ACCAAGAGAC TTGGTGAAAT 960 CCATGAATGA GGAAGTCTTG TGGTACAGGA AGCATGGTCC AGGTCAGCCC CTACCCTACC 1020 CACCTGGCCT CTTCCAATCC ATCACCCACC CAGGCACAGA GGAGCAACAT TCTCAAATGG 1080 GGCTGAGATT AGGCTGCATG GCCCCTAATC GTCCAACTGC TAAAGTCTAG GCACAGACTC 1140 GTTGGGACCC CTCATCTCAC CCTCCAATGA TTACCATATA GTCATGGAGA GAGGCGAAGG 1200 CACAGACAAT 1210
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