Tag | Content |
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EnhancerAtlas ID | HS101-07567 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr11:47976580-47977640 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr11:47977173-47977194 | ATAAAGAAACTGAAACTCAAA | - | 7.4 | IRF8 | MA0652.1 | chr11:47977176-47977190 | AAGAAACTGAAACT | + | 6.03 | IRF9 | MA0653.1 | chr11:47977175-47977190 | AAAGAAACTGAAACT | + | 7.05 |
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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 |
GH11I047954 | chr11 | 47976226 | 47977519 |
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Enhancer Sequence | TGCCTGGGCC TCCCAAAGTG CTGAGATTAC AGGTGTGAGC TACCGCGCCC TGCAGGTTTT 60 CCTTTTTAGT AGTGACTTCA TCTGTCACAT TGAACTTTAT GTTGGTTAAA GCAATTCTAA 120 CTGCTGTAAC AGCTAAAACC TCATCAGTTA ATGCTATAAA GGTTTGTTTC TTGCTCATGT 180 AGAGTCCAAA TCAGATGTCT CTTATTGACA ACAAGAGCTG TACTCCACGT TGCCGTTCAG 240 GGATCCAGAC ACAGAGATTC TGTCAGTTTC ACCAGGTCAT TTGAAGGGTT GCCCTGGGCC 300 CATAAGCATA AAAGGTTTTA TGGGCTAAGC CTGGAAATAG CTTGCAAAGC ACACTTTTGC 360 TCACATTTCA CTGCTAGAGC TTGAGCACAG GGCAGCATCT ATCTGCAAGG GAGTCTGGGA 420 AATGTAGTCT AGCTGGGTCA CCAGGAAGAA AAGGAAATGG ATTTGGTAAT CAGGTAGCAA 480 TATCTGCTCT AAGCTTTATA GAGAATTAAA GGACTGTGAT GGGCATTCTG TATAAATTAA 540 TTCATTTTGC CCTCACAATA ACACTTCAAG TGGGCATTGT CCTCACTTTA CAGATAAAGA 600 AACTGAAACT CAAAGAGGTG AAAGACTTGC CCAAGGTCAT ATAGCTTTAC AGTCATGGAG 660 CTAGAGTTAA AGTCTTATCT GCCTATGTTC TTCTCATTAC ACCCATTTGC CTCTTTGAAT 720 TATACAAGAA AGATGGAGGG AGAGAGAAAC TACATATCTA TAGTCCTTTT CCTATGAGGC 780 TGATCCACAT ATAGGGTTTC CTTTGGTTTT CTCCAAGGTC ATGGATTTTA CCCATAATCA 840 GTCGTCTCTT ACCAGTGGAT AGGGGAGGAC CAAACTACAG CATTTGGTAC CCACAAATAG 900 CCTGGGTTTC ACTTGAGTGG GTCTGGCTAG GATGTGTCCT TTTTCTGGGT ACATGACATT 960 TGGGAACAGT CATTTGAACA ATGGACTTAT ATCTATAGAT ATACATGTAG ATATAGATGT 1020 AGATGAGATA TAGATAAAAA ATACTTAGAA GTAAAAACAA 1060
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