Tag | Content |
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EnhancerAtlas ID | HS138-01730 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:92074020-92076330 |
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) |
IRF1 | MA0050.2 | chr1:92075197-92075218 | AGGATGAAAGTGAAAGCTGGG | - | 6.13 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 92074449 | 92074838 | chr1 | 92075181 | 92075471 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I091608 | chr1 | 92074061 | 92078134 |
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Enhancer Sequence | CATTTGCTTT TGGGTTCTTG GTCATGAAAT CTTTGCCTAG GCCAATGTCT AGAAGGGTTT 60 GTCCAATGTT ATCTTAGAGA ATTTTTATAA TTTCAGGCTT TAGATTTAAG TCCTTGATCC 120 ATCTTGAGTT GATTTTTGTA TAAGGTGAGA GATGAGGATC CAGTTTCATT ATCCTGTATG 180 TGGCTAGCCA ATTATCCCAG CACCATTTGT TGAACAGGCA GTCTTTTCCG CACTTTATGT 240 TTTTGTTTGC CAAGCCTGAT TTTTAATGAC TACAGATTAT TCCATTTATG GGTACACCAC 300 AATTTATCTA ATCATTCTCT TGTGGGTAGA CATTTAGGTT ACTTATGATT TATTAATATA 360 ATAAAAATAT ACATGTATTG TGTATCAAAG TTAGACACAT ATATATGAAA GATGAGCAGC 420 TTCTCAAAAG CTGTGTATTT GTTTCCAAAG GCTGGTGCCC TGCAGTGGCC ACACGAGGAC 480 CTTCAGAATG TACACATAGT GACTAATGGT AACACTGGAA ATCATCAAAC TGCCAGGGTC 540 CTGCCAGCAC TCAGCATTTG CTCTTCCACA TGAGAAAGTC CCTACAGGGA ATGGGAGTTA 600 ATGTCAGCAT GTCAGTACAT ACAGTCTGTT CTCAGTGAAT CTGGAAGCTT GTCTTCCTAG 660 ATGCCTATGG CTGAGTCGCT GAAAAGATTT TTGACTCAGG GCTTCAGAAG ATACCTCAGT 720 GCTAAATCAC CCAGAGCAGC GTTTCAGATT CAGAAGCTGC GTCACCTGTG GGCAGAACAG 780 AACTCAGCTA CGGACTTAAA GTTCCAGAGC TCAGTAGCAT CAAAGCACAA GGGACAGAGA 840 CCCAAAGGAT CCATGAATGG GGACTGAGAC CCGAAGGATC CATGAATGAG GGCTGAGCCA 900 TGTGGTGTGT ACACACCCAC AACATGTGAG TGAGAGCTGC GCCCACAATC TCCTGTAGGT 960 CAGCCTCCAG GCCATGCAGA CAGCCCCATA CCCTAAATCC CATGTACGCC ATCTACGTTT 1020 CTTCTCTCTA CTTTGTTTAA TAAATCAAAA ATTGGCTAAA GGGAGGAGGT GGTCAAGGAT 1080 GCCATGACCC ACTAAACAGT CTAAACAGAA CGCAGCAATG TCACTACACT AGAGCTGGAA 1140 ATGGGGTAGC AGAATGCCAG CTCCCATAGC AAACCCCAGG ATGAAAGTGA AAGCTGGGGT 1200 GAAAAGGCCT AGAACTTGCT TCCAGAGCAC AGGTGACAGA ATCCCTGAAC GTGAAACATT 1260 CTTCTCTCGG GGATGATGAC TTAGCACTGA GGTATCTTCT GGAGCCCTGA GTCACTCAGC 1320 TCCAGGAATG ATGGGTGTGG ACCAGACTGG AAATTCACTG GACCGTTTTC AGTGTAACTT 1380 GGACCCAACC TAAGCATCTG GGGGACCTGG AAGAGACCCA TGTCATCTGG TCTAGGCCCC 1440 AGTTCCAGGC AAATGGTAGA AAAGCTTTTC GTTATGGGAT GACTCTGATC CTGAGCTGAC 1500 AGGAGAATCC CATAGAATTG AGACGCTCCA GCACCACCTT GGATTTTGCC CCACTGTCTG 1560 GTTCTGTGAA AGAGCGAAAA AAGTCAGGAT GAATGAACCA GTGCATGAAC AAATACATCA 1620 TAGCCTTCCT TCCTCCGCAA AGGTAGAATC TTGGCAGTAG CCATCTGCCA GGGCAAGGAA 1680 TGGCCTGAGA GGGTTAGGGG AGAGGCAGAG ATGTCTAGGA AGTCATGAGG CTGCCACACA 1740 GTAGGAAGAG GAAGGCCTTC CATCTGCGGC TCCAGCCACA ATTCAGGAGA TCCCTGAGCT 1800 CCACCCATGG AAGCTTGGAC AAGCCACATC TCTGTTCCTA ATATGTTCCT ACATATGTTC 1860 TCTAATCTCT AATATGGGAA GAATAGTCAC AGCTTCCCTG CTTCCTCTGT GAGATAACAC 1920 AGTCTTAACT GTTTTCACTG AAAAGTTGTC AGTGCACCCA CAACTCCACC CTCCCTACTG 1980 ACTCTGGGGC TGGCGAGCAG CCTTTCCCAA TGTAATTATG GTTTCAGAAC TTGATTTGAT 2040 CCGTGTAATA AGCAAAACCA TGTAATGAAA AGCCATGTTA AATGGAAATC CCATCCGAGT 2100 ATTTTTGTGC TGGATCTTAG GAAGAACTCA AAGTGGGACA CGTGAGGAGA GGACTGTGCT 2160 GATGAGAGCA AAGGAGAGAG CTGGGGTCTT GGAATAGGAA AAGGCCCATA GGTACTAGGA 2220 AGCTAATGAG TAACTAGCCA TGGGCTACTG TGGTAAGAAG GGCAAGTATT TTGGATAAAA 2280 CATGGAAGGG CTTCTTAACA GAAAAGGTTT 2310
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