Tag | Content |
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EnhancerAtlas ID | HS138-00895 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:44265160-44266640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:44265972-44265993 | TTTTCCTTTTAGTTTCTCTTT | + | 6.96 | Stat6 | MA0520.1 | chr1:44266580-44266595 | CATTTCTTAAGAAAT | + | 6.13 | Stat6 | MA0520.1 | chr1:44266581-44266596 | ATTTCTTAAGAAATG | - | 6.13 | Tcf12 | MA0521.1 | chr1:44265478-44265489 | CAGCAGCTGTT | - | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr1 | 44265434 | 44265559 | chr1 | 44265188 | 44265345 | chr1 | 44265795 | 44266290 | chr1 | 44265644 | 44265843 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I043799 | chr1 | 44265188 | 44267077 |
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Enhancer Sequence | CCATTCCTCA TAGATGGAAC CTTCTGTGTG TGTCCTAACA AGACAGAAGA GGCAAATAGG 60 CTCCCTCAGC CCTCCCTGAT AAAAATATCA ATCCCATCCT AGGGGTGGAG CCCTCATGAC 120 CTAATTACCT TCTAAAGGCC CTACCTCTTA ATACTATCAC ATTGGATATC AGGTTCCAGC 180 ACATGAATTC ACAGGGGACA CCCAACATTC AGACCATTTC AGTGAGTATT TATGCCCTAT 240 CTATCCCATG AGGTGGTAAG CTCCATGAAG TTTAAGATAC AAACTGCAGA GTGAGCCATT 300 TTTTCCCATT TCCTGTACCA GCAGCTGTTT TGACATGCTG TCCCTCCTAA TCCTCCTGCA 360 GCTTAGTGCA AGATGCCCTG GGATGGCCCG GACACAGTTG ATGCTGTGAA TAGGATTAAA 420 TTCACTGCAG TACTCAGCCC TAGATATCTG CTATTTTCCC AAGACAGAAG AGAGATAGAT 480 GGGTGCAGTG ACATTTTTGG CTGCTGTGGG AGGGGGCTTC CAGGGCTCCT TCTGTAGCCT 540 GTGATTCTCT TACCTGGGGC CAAGGACATG TCATGCTCCC TTGGCCCCCA GTATGCCACG 600 TTGGAGAAGA GCTGTGCTGT GCTCAGATGG AGGCCTGATA GTCACAGGGG ACTCTGTTAC 660 CAGAAGCTTC CTACTAGGCC TCTCACCTCC CCCACACCAA CATACACCCA TTTGAGATTG 720 GATCTTAGTT TGTAAACTTC TAAGTTATTT TACTGAATCA GTTAATTTAG TCTAGGTCAG 780 TGGGCTTTTC TGTGTTTATT TTAGAAAAAT GCTTTTCCTT TTAGTTTCTC TTTGATTAAT 840 TGATCCCATG TTGTGGTTTA TTTCCCTGAC TTGAGATGAT GTGGGAGCTA TTTGCACTTT 900 GGCCAGACCT TCTCAGGCCT CTTTTGACTC CCATGATTCA TGTGTGGTAT GGCCAGGGCC 960 TTCTGACATC ACCCTGGGGC AGGAGATGGG AGGTAATAGT ACATCATTGC TGTCATGGAA 1020 ACTGTGCTGC TAATGTGAGG GTCTGCTTTT CTTGTTTCCT CTGAGAGTCA TTGTGGGCAT 1080 AACGTAAAGG AAAGAATCAG CCCTGGGTTG GTTCCACGGC ATCCCTGCTA GCCTACTTCA 1140 TGATTGGGGG ATCTTGAACA TATCTCCCCT GTCTAAACCT CTCTTTCCTC ATCTGTAAAA 1200 TATAGTACCT GCCTCATGGG GCTGTATAGG TGACAGTACT GAGAACAGCA TGAATACAAA 1260 GGAAGATGCT CAATAAATAG TAGTTCCTCT CAGTCCCTTC ATTCTGCAAG CCTGACAGCC 1320 CATTTGGAAC TATTGCCAAC TTCTTCCTCC ACCCAAGCCA TGGCATATAT TACATATGTT 1380 TAATATACCC CATGACTTTT TTTTAGAGAT TGTACAGTGA CATTTCTTAA GAAATGATAG 1440 AGCTGTTTTG GCTAGGGTAG GTCCTCATTC CATTTACTGC 1480
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