Tag | Content |
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EnhancerAtlas ID | HS139-00777 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr1:23157840-23159690 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr1:23159451-23159464 | GAATGTTCTGGAA | - | 6.62 | IRF1 | MA0050.2 | chr1:23159603-23159624 | TTTTTCTTTTTCTTTTTCTTT | + | 6.17 | IRF1 | MA0050.2 | chr1:23157853-23157874 | TAGCAGAAAGTGAAAGCATTT | - | 6.19 | IRF2 | MA0051.1 | chr1:23157857-23157875 | AGAAAGTGAAAGCATTTT | + | 6.29 | TBX21 | MA0690.1 | chr1:23158262-23158272 | AAGGTGTGAA | + | 6.02 | TBX2 | MA0688.1 | chr1:23158262-23158273 | AAGGTGTGAAA | + | 6.62 |
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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 |
GH01I022824 | chr1 | 23151232 | 23159621 |
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Enhancer Sequence | CTACCTCCCC CCTTAGCAGA AAGTGAAAGC ATTTTGCACA AAAACTCAGC TGTAGGCATT 60 GTGTAATAGC ATTGATCTAT CCAAAAATAT TGAGTGCCTA CTGTGTGCCA GGCAGCCTGT 120 GAAGCCTTTT GCGTGAATCC TCTCATTTCA ACCCAGGAAC CCTTACAAGT CAGTCTACTA 180 TTATTTCCAT TTTATGGATG AAGAAACTGA GGCTCAAGGA GCCTGAGTGG TTTGCCTAAG 240 GTCAAGCAGA GCAGGGCAGG AATCCAGGGC TTTCCAAATT CAGAGCCTTA ACACCATGCC 300 ACACTGTGCT GGCAGAGATA GCAAGAGTTG TTGGAGATGA TTATAAGGGG AGGGCCAAAA 360 TGATCGTGGG AATCCAATCC CCGTGGCAGT AGGTGGGAGA TGCTGACCTG GGCTTCCTCA 420 GAAAGGTGTG AAATGTTGAC ACCCTCCCCT TGGGCTCTTC AAGGGCTCAA GAGGGGCTGT 480 GTTAGGCTGG GCTGGAAACA GAGGGCTGAC CATCATGGGT TCCAGAGGGA GCTATCCACC 540 CCCCTACCTA GCCAGAGGCA GCCAGGATTC CATTAACCTG ATTCTCTGCC CCACATAAAC 600 CTGCAAAGGG AGCCCCTGGA GGGAGGGGTA CTGGGGAGAG GAAGAATTGG GCTTCCCCAG 660 GCCCCAAATG GAGCAGCCAG TGGTGCTAGT TTCCTCTCTT GCAGTCCAGG AGGACCTTCG 720 AGGCCCCTGG CTGTTTGAGC GGGGAATAGG GAGAGCGATG GAGAGCCAGA AAGTAGGGAC 780 AAGAGACTCC AGGCTGGGGT GCAACAGCAG GAATAGCAGG AACAGGGTGC ACGTCATCAG 840 AACAATGGGT CCTGAGTCAC TCTGTGCCTG CCCAGCCCTG CATGGCCCTG GGTGAGTCAT 900 GTCACTTCTC TGAGCTGTGG GTTCTTCCTC AATAGTAAGG GCAAACCAAT GCCACCTCTC 960 AGTGTTGCTG GGCTGATTCA CAATACCGGG CCTCAAGAAA TGGTGGCTGT TGCCAATGCT 1020 ATAATTTTAC AATCTTGACC CCATGTATCC CTTCTCAGCT TGCAAGCCAC ATTCATCCTT 1080 TTTCTCCTTG GAGCCTCACA ATACTTCTGC AAGGTGTCCA GGATTCTTAC CAGAGAGGTT 1140 AAGGGACTTG TTCAGAATCA CACAGCTTCT AACCCTTGGC CTGGGATGCA CCCCTAGTGA 1200 TTGTCATGGA GTGGGCCATC CCAGCCAGGC TACGCCACTC TTCTTCAGTC TGGGTGGTTG 1260 CTATTCCTCT GCCATGATTC ACGTCAGATG CCTCTTCCTC CAGGAATCCC TCCCTGACCA 1320 CACAAGAGCC TGGTTAGTAC AACTCTCTGC TTTCCCACAA CCTTTGAGAC ATTTATCAGA 1380 GTGTTTATCA GCAGTCATCA CAACCGTTAG GTGCTCCCAC CTAAGACTTT GAGGGTTCAG 1440 CCAATACTTT ATAATAGAAG AAGAGGGGGT ACAATAAATA TTTTGTTAAT GACTACAGCA 1500 CCTGTACAAA GGGACAGATA GGTGTCCACA GACTCACATG TATAAGTAAC AGTCATGCAT 1560 GCACAGCCAT GCACATGTGG CTTAGTGAAT ACACATGTAT ACAGACAGGG AGAATGTTCT 1620 GGAACATGAA TTGTGCTCAT GTGGATGCCC CATCCCCCCA CCCCCATATA AACACATAAA 1680 AATACTAGAG ATGATATTGA TACAACCTGG TAAGAGAGAA AGGAAAATCC TTGGGTGACT 1740 TGGTTTTTCA TTTAAGGGAT TTTTTTTTCT TTTTCTTTTT CTTTTTTTGA GACAGAGTCT 1800 CGCTCTTTTG CCCAGGCTGG AGTTCAGTGG CGCAGTCTCG GCTCGCTGCA 1850
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