Tag | Content |
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EnhancerAtlas ID | HS138-00487 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:25968180-25969720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr1:25969548-25969558 | TTTAATTAGA | - | 6.02 | JUN(var.2) | MA0489.1 | chr1:25969475-25969489 | TGGAAATGACTCAT | + | 6.5 | PPARG | MA0066.1 | chr1:25968204-25968224 | GTAGTTCCCTTTGACCCACT | + | 6.31 | RORA(var.2) | MA0072.1 | chr1:25968214-25968228 | TTGACCCACTTATG | - | 6.07 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 25969200 | 25969622 | chr1 | 25969249 | 25969578 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I025640 | chr1 | 25967182 | 25970575 |
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Enhancer Sequence | CCTCGACTTA TCTCTTTTCT GGCTGTAGTT CCCTTTGACC CACTTATGGA AGAGGTTGGA 60 AATTTTCTGT ATTTATTAAG ACCTGCACCG AAATTGAGTG AGAAAAAAGC TGGAGACAAG 120 AGTCAAAACT GAGTTTTCCA GAGTTAAGAG CAGACACTGT TTACATGATA CGGATAAGCC 180 ATGAATTTAT TAAAACTTTA AGAGAAATAT TGAAAACACC TACCATCTAT TGAGTCTCAG 240 TTGCAAGAGC TGAAGGAAAG ACAAAGACGA GTCTCTGGCT TTAAGGAATT TTATTGTGTA 300 ATCTTGGCAT GTACTGGAAT CACTTCTAAC CACATACAGA TGCATGGATG TAGGGAAATA 360 TTACTTGGCT GCATCAATAT TTGCCTGTCC CACCTAAATC TTTTTTGAGG AAGTAGCCAG 420 GACATAAACA GCTGAAATGA AAATATTTGC TTGTCCCGAA GTCGATTTCC CCACAGGCCA 480 TCGCCCTCCC TCCTGTGGCT GCCTCTGCTA TTCTCATTAG CTAAGCAGCC TTGCCCTTAC 540 AGAGATCCTG AGGGCCTTAC AGAGATCCTG AGGGCAACAA AGCCGGTGGT CATCTGTAAA 600 ATCCAGTAAC TGATTGATGC TCAGGAAATA GGAGATACTG AAGAAGTGAA AGAGCCTAAC 660 CCAGTCCCAG GTGGTTCCGA CTCTGCAGCC GTGCTCTGCT GTTTCATCTC AGCCATGCCA 720 GGTGCTAGAC GTGACTTCAC CTGAGAATTG CTGACCTGGG TTGATCAGAT CAAATCTATC 780 CAGGCCACCT CTGGCAGAGC AGCAGAAAGT GAGAATATGC TGTAGATTAG TGTGAGAATC 840 CTCCCCAGGG CTTAATGATG GTCCCTTGGA GAGCTCTGTT TCTATGCAAG AAACCTGTGA 900 ATTCTCAACC TTTGCCAACT TGCAATCGTT CTTCAATCTG CCCCAACTAT TTCTAGCAAA 960 TTCTTTGGCT AATACAGCAT AGAAAACACA TCCTATTTGT CCCAGACTTA TTTCATTCCA 1020 GCTTCAAGGG GTGGACATTT AGCCTAAGAG CATTCATAGA GAGTCAGACT TCAGAGAATA 1080 TATTTCCCTC TGTTAAATCG TATATGAAAC CAAGCTTGCT CCGAGGCCGC TGGCTGCAGG 1140 AAGCAGTGAC GAGGATGGAG CTTGGCAGAT GGTTGTAGCT GTGGTTTCCT GGAGGCCTGT 1200 GTGGGGAGAT GATTGTTTGT ATATTGGTTT TCATTTATGT ATTGGTCTTA TTTTCATCTT 1260 CCTGAGGTAC CCAGATGCTA TGGTGATAGA TTGATTGGAA ATGACTCATT TGTCAGGGTT 1320 CTGTGGGGGA CGTAGGTTCC CTTCTCATGC GCAGCAGAGT CTAAGATGTT TAATTAGACG 1380 CTGAGACATT TCTGCATGGG TCCATTTCTG CCCATTCTCC CAGGTGGACG CCATTTCTTA 1440 GATTGCAGAG GGACGGGGTT GGGGAGGGAC CTTCTAGTTC TCCATCCTCT CCCTCTATCC 1500 TCTTATTTTG TCTGGCTGCA GTCCTTAGTC CTACCTCCCT 1540
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