Tag | Content |
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EnhancerAtlas ID | HS105-15213 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr11:75099450-75100670 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr11:75100030-75100051 | GAAAAAAAAATGAAAATAAAA | - | 6.36 | Myod1 | MA0499.1 | chr11:75100217-75100230 | TGCAGCTGCTCCT | + | 6.15 | STAT1 | MA0137.3 | chr11:75099885-75099896 | TTTCTGGGAAA | + | 6.02 | STAT3 | MA0144.2 | chr11:75099885-75099896 | TTTCTGGGAAA | + | 6.32 | Zfx | MA0146.2 | chr11:75100642-75100656 | GAGGCCGAGGCGGG | - | 6.01 |
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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: 2 | ID | Chromosome | Start | End |
GH11I075385 | chr11 | 75096397 | 75100243 | GH11I075389 | chr11 | 75100381 | 75100445 |
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Enhancer Sequence | AAGTTAAAGC TCTCTCTTCC CTGTCATACC TGGTTCCTGT CCCTCCCTGG TCAGCTTGGC 60 TGCATGCCAG TCCTTGGCTC TTCCCCTCCC CACTTGCCTC CAAGCTAACC AGCTGCCTGT 120 TCACACAGCC TTATTCTGGG TAGGAAGCTG GGAAGTTGGT AGCATTGGCT TGTTAGCCTC 180 TTGTTCCTGT CCTCCAGCTA CTTAAGTGGA GTCACACAGT ATATTCAGAC CCATATGTGT 240 GGATTTCACT AGTCAAATCC TGGGAAGCCA GTCTCCTGCC TGTTGTTTCT GTGGGGCATG 300 CCCACCCCCC GCTATGTATT GTTCTCCATG CTCAGGCCTT TGAATGGAGT TTGAATGGGG 360 TTACCAATGG TGTCCACTTG GCTGGGGGCC AGGTTTGTAA TGGCGGTAGG ATGCGGAGAG 420 CAGCAGCCCC AACCCTTTCT GGGAAACAAA TTGACCACGT TGCTGTAGTT GGTTGTTATG 480 ACCACCAGAG TGCGCAGTAT GCACAGTTTT GGGAGAGCCA GTTAAGAAGG GTGGCATTTT 540 AAACCTAAAA TTAAGTGATA GCAAAGACGG AACTTATGAT GAAAAAAAAA TGAAAATAAA 600 ATTAAACTAG ATAAACCTAC TGCCTCTGGG TATTCCAGCT GTGTTCCCTG TCTTCAACCT 660 GGGCTCAGTA ACAGCGCTTC AAGAAGGGTC CAGCTGGTCT TTCTTACCTG GCTGACCACT 720 GAAACTGCCC TCCCGCTCCT GGCCCTTTTT GGCCCTGGGA AGGCCCTTGC AGCTGCTCCT 780 GGGCCCCATC TCTCTAGAAC AGATGCTGGT CCCATGCCCC TGCATGACGC CTGATGGGGC 840 TGGGACATCC TTGGCCTTTC TGTTCCAGCA GTCTGATCTG TGGCCGACTT CTTCCCACAT 900 TTTTCCTTTG AAGGAGCTTT CTCTGTCCTC TACGTTGTGG TAGTGTGGTC CTTTTGCCTG 960 TAACGAAATA GTGCCTGCTC TGTGTAAGAA TGAAAGGCAC TGGTGTCTTG TGGTCTTCCC 1020 CTAAGAGCAG AGATATGAGC CACGTGTTCG TGTTGGGTAG GACTTGTTGA AACTGACTCA 1080 CTAAACAAAA ACACTGAAGA TTAATGTAAA CCTAAATGCC AAATTGTTTG TCTGCATTAA 1140 AAGCAATGAC GGCCGGGCGC GGTGGCTCAC GCCTATAATC CCAGCACTTT GGGAGGCCGA 1200 GGCGGGTGGA TCATGAGGTC 1220
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