Tag | Content |
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EnhancerAtlas ID | HS048-07188 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr11:74281660-74283110 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr11:74282006-74282027 | GGAGAAGGACGAGAGGAGAGG | + | 6.16 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH11I074570 | chr11 | 74281641 | 74282808 |
| Enhancer Sequence | GAGGTCCTAT CTTTATTGTT ATTCTTCATG GAGGAAGGAG CGGCAATAAC TCCTAATGGG 60 AGATAGCAAA AGGAGAGGTG ACTCTGCCAT CTGCTGCTCA CTGATGGTAT GTACCTACAG 120 GCCTTCAGTA GGATTTAGGT GCCACCCTTA TAAAGGGTCA GCTCTGAAAG TCTTTGCTGG 180 GGACATCTCC AATATCCTAA TTTGATGGTT GGGGTGTCAG GCACATGGAG GCCTTATATC 240 CCAATACCTG GAAACCATGA AGCCGGCTCC AAGGTAAAGC CCACAAGCTG AATCTGACCT 300 CTGGTAGGCA TCAGGCATGT GTTGCCACAG AGCTAAAAGT GTGGCTGGAG AAGGACGAGA 360 GGAGAGGAAA GAGGATTGCG GTGGGAGTCG CCAAGAAAGC TGGAAGCCAT TGCACAGCTC 420 CAGGAACAGG GGCAAGGGCT GAGGTAAAAA AAAAAAAAAA AGAGAGAGAA ATGAGTGGAT 480 TTGAGAAACA GTACAAGAAA ATCCGACTTG ATAAGACATT GGATTCAGAG AATGAAGGGC 540 TGGAACTGCC AGTGCCTGCC AGTGAGTTGT ACTTTGTGCT ACCAACTAAT CTTCGTAGAA 600 CTTCAGTTTG ATTATTCATT ACCTCCAGCC TATTTTGGCT TCCTACTGAA ATCAGGACAC 660 AAGGAAATTT GTCACCAGGT AGACAATAAA TGTCCCTCCC CACCCCCTGC CAGTCACCCC 720 ACTAGTCTTA TTAGGAATCC TACACTTGGT AGGAATTAAG AAGTCTTGAC TGTGAGTCCC 780 AAGTTCAGTC ATTTTCTGGC TGACTGACCT TGGGGAAAGT GACCAAACAC CTGGGAGTTT 840 AGTTTTCTCA TCTTCAGTTT ACTCATCTGA ACAATGGAGC AATGGCAACA ACAGCTCCCT 900 TTAGGCTGAG CCAAGCTTCA TACAAGCTAA TGTCAGACAT CTATCATCTT ATTGAATTCT 960 TGCAACCCCA GGAAATGGGC ACTACCATTA CCCCCATTAT TCAAATGAGG ACACTGAAGC 1020 TCTGAGAAAT TGAGTGGCTT GCCCAAGGCC ATATAGCTAG AAAGTGGGAG AAGCTGTCTT 1080 TCCAACTCAG ACTGCTTAGC TCCAAAGCTT TACTGCTCTG GATCTCTGTC TCAGTGAGCT 1140 TTTGCTATAA AATGACCCAC CCTGAAACAC AGTGGCTTAA AACAACAATC ATTTTGTTTA 1200 GTTCACAGTT CTAAGGTACA GTATATTTAT ACAGGTCACA GTTTTGATCT TGGCCAATTT 1260 AGCTGATCTA TGCTGGATTC CCACATGCAT GGGTCTGTGG ATAGCTGGTA AGTTGGCTCA 1320 ATCACATATT TGGTGACTGG CAGTTGGCTG GAGCACCCTG ATGCTCCTCC ATATAGCCTC 1380 TCATCTTCCA GCAGGCTAGC TTAGGCTCAT TGACTTGGCG GGCTAAAGAT TCCAAGTTTA 1440 ACAAGAGAAG 1450
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