Tag | Content |
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EnhancerAtlas ID | HS048-37580 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr9:100554630-100556000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr9:100555579-100555597 | GGAGGCAAGGGAGGCAGG | + | 6.09 | JUN | MA0488.1 | chr9:100555496-100555509 | GAGATGAGGTCAT | + | 6.11 | JUND(var.2) | MA0492.1 | chr9:100555495-100555510 | TGAGATGAGGTCATC | + | 6.6 | Klf12 | MA0742.1 | chr9:100554887-100554902 | AAGAAGGGTGTGGCC | - | 6.25 | Klf1 | MA0493.1 | chr9:100554891-100554902 | AGGGTGTGGCC | - | 6.32 |
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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 |
GH09I097792 | chr9 | 100555074 | 100556088 |
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Enhancer Sequence | TGGATATATA TGAGTGTGAG CTAGACAGAG CTGTATGTAG TTTTGGGAGG CACTGCAGCA 60 TATTCAAAGC CTTGGGCCAG AGGAGCTCAG GAGCTCACCA GGGAGAAGAT GGATCTAAAG 120 AAGGAGATCT ATGGCCAAGA CTTGCAGCAC TATGACATTT AGAAATCAAG CAGCAAATGT 180 GCAGGGCTGC TAAGGAGACT ACAAAGGGAC AACTAAAAAG ATATGATATT CTAGAAGCCA 240 AGAGAAGAAA GCAGTTCAAG AAGGGTGTGG CCAACTCTAT CAACCATATA ATACGCTGCT 300 GAGAGATCAA ATAAGGACAG AGAAGTGACC ACTGGAGGTC ATCAGCAGCC TCGTGAAAAA 360 CAGTCTCAGT GGGGTGGAAG AAAGAGAGGA CCCATAGCAC AGGGCTGAGC AGAGAATCAA 420 AGGTGAGGAA GTAGACACAG GAGACAACTC CCTGAAAAGG GCTTCTGTGA GGGACAGCAG 480 AGAACTAGAT CAGCTACAGG AAAAGGTAGG GTAAGGAAAA GGCTCTGCAA ACCCTGGAGA 540 TACTGGAACA GGTCTGCATT TTGGGGGAAT GATCTGAGTG GAAAGAAAGA ACCTAGAGAT 600 GCAGCAGAGA TAGGAGAATT GCAGAAGCAA AGTCCTCTAA AAAACCAAGA GGCCAGAGGA 660 TTAAGCTTAC AAGCGAAGAG GGTTTCTCTT GGTAAAAGCA AAGATACTTT ATCCACAGCA 720 ATATGAAGAC ACGAAGGAAA TATTAACACA AATTCAGATG AATTGGGAGG TATGCTGGGA 780 AGATAAAGGT CCTCCTTTAT CAAGGACACA GCCAAACCAT ATCAAGGAGG ACCTATATAA 840 CTGCTTCTAT TTTTTCAGTG AAATATGAGA TGAGGTCATC AGGTAAGAAT GAGGGAAGAT 900 AACAAGGTGG ATGGCCCTTC CTGACAGATA AGAGGCCCCA GTAAGTGAGG GAGGCAAGGG 960 AGGCAGGAGG TAAAAATGTG AAATAGTTGT TTTGAAGACT GGGAAGTGGA ACACATAGTG 1020 AAGGGTAGGA TTGCTGAGCA GGGCTGAGTG CTCATTTGAG ATCTGTGGTC ATGAATTTAA 1080 AGCAAGACCA GTTGGTCTAG ATATATGTTT TTCTCTCATG ACGTTTACCG GCTTGAGTTC 1140 AGGTATGTAG TAGTCAGATG TGTAGGCTTA AGCTGAGAGC AAATATGAAG GAAGAAGAGT 1200 GGAATACAGG AATTAGAATA CTTGAAATAG AGTAGTTATG ATGATGAACC ACAGAAATTT 1260 AGCTGGTTAA GGAAGGAAGT GAGAACCTGA GGGAAATGAC AGATAGTGGG AAAAGTGGAA 1320 GGGCCAGTGT ATTGGAAGTC TTGATGAGGT GGATTGGAAA TACTGCCCCA 1370
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