Tag | Content |
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EnhancerAtlas ID | HS101-42231 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr8:33390460-33391660 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr8:33391304-33391319 | CAAGTCAAAAGGTCA | + | 6.49 | ZNF263 | MA0528.1 | chr8:33391377-33391398 | CCCTCCTTTTATTCCTGCTCT | - | 6.33 |
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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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Enhancer Sequence | GTCTTGCTGT GTTGCCCAGG CTGATCTTGA ATTCCTGGTC TCAAGTGATC CTCCTGCCTC 60 AGCCTCCTAA AGTGCTGGGA TTACAGGCAT GAGCCAGTGT ATCCTGCTCA TTCACTGTTC 120 AACACACTCA ATTTTTCCTT CACCCCATGA ATCCAGCAAA ACTGCTTTTG CTCAGGCCCC 180 CAGTAGCCTC CTCATTGCCA AATTCAATGG AGTGAAGTGG TATGCCCTCG ACTCACTGCA 240 ACCTCCGCCT CCTGGGTTCA AGCACTTCTC GTGCCTCAGC CTCCCAAGTA GCTGGGATTA 300 CAGGTGTGCA CCACACACCT GGCTAATTTT TGTATTTTTA GTAGACATGG GGTTTCACCG 360 TGTTGGCCAG GCTGGTTTTG AACTCCTGAC CTGAGGTGAT TGGCCTACCG GGGCCTTCCA 420 AAGGGCTGGG ATTACAAGCA TGAGATAATG CGCCCGCCCT GCCCGGCTCA TTCTTTTTTT 480 TTTTTTTTTT TTTTTTTTTG AAACAAAGTC TTACTTTGTT ACAGTAGGTA GCTGGTCAGG 540 CATGAGCAGG GCAGGAGAGG GCTCCGCCCA ACACACACAA ATATCAGGAA TATCAGGCAA 600 CCATCAGGTG ATGATCAGGC AGTTGTTAAC TGTCTTTCTA AAATAGTAAT TGGTCACAGC 660 CAGTGCCAGG GAAAGGCAGT GTCCTAATAC ATGGAAAACA CATGAAATGT GATCAGTGGC 720 TTCTTGAGAA GACCTCAGGG GTTGGGCAAG TGGGCTCAGG AATGTGCCTG CAGACAGCCC 780 ACCCCAAGGG ATGAATCAGG GGAGAAGTAA CAAGACCGCA GAAGCATGCC AGCGTATAAA 840 ACCCCAAGTC AAAAGGTCAA ACCGCACACT TGTCTTTCAA GTCACACACT TGGTCCTCGT 900 CCAAGTGTAG GTTCTTTCCC TCCTTTTATT CCTGCTCTAA AGCTTTTCAA TAAACTTTCA 960 CTCCTGCTCT AAAACTTGCC TTGGTTTCTC CTTTTGCCTT AGGTCCCTCG GTTGAATTCT 1020 TTCTTCTGAG GAAGCAAGAT TTGAGGTTGC TGCAGACCCC TACAAATTGG CCTTGTCTAA 1080 CATATTTTGG TGCCATGTGA CTCGGATACC TTCCACCAGT AACAACTCTG TTGTCCAAAC 1140 TAGGGTGCAG TGGCGCAACC ATGGCTCACT GCAGCCTTGA CCTCCCAGGT TCAAGGGAGC 1200
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