Tag | Content |
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EnhancerAtlas ID | HS180-30151 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr20:44747030-44748520 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr20:44748038-44748059 | CACAGCTTTCACTTTCACCTG | + | 6.14 | PRDM1 | MA0508.2 | chr20:44748046-44748056 | TCACTTTCAC | + | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_10442 | chr20:44745998-44751095 | CD19_Primary | SE_11466 | chr20:44745633-44753083 | CD20 | SE_59007 | chr20:44727732-44759865 | Ly3 |
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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 | GCTGTGAGTT GTTTTTGCCC CGACCAGACG GGAGTTGGGA GTGGGGAATG AGAAGGAAAG 60 GGAAGGAAGA CTTCGGGGAA GAGGCCTTCC TGGCTGATTT TTGTGGGGGC AGGAGGGTGG 120 GTGGGAGCTG GGCAAGGTGC CCCCGCTCCT GGCTGAATGG GGTGGGCTGC CTCTCTCTTC 180 TCCCGGGCTG GGGTCCCGGG AGCGGCCTAC AGGGGCCGCT CAGGGAAGGC ACTGGCTGCC 240 CAAGCGTGCC TAGACGGCCT GGACGGGTTT AGGGAGCCTC AGAGGCTGGC CACACAGAGA 300 CTGGTAGGGG GTTCAGAGGG CGGGAAGTGA GGCGGACCAA GGGAAGGGGC GGGTCTGGCC 360 CGTTTCCTGT CCCCTTCTTA TTGTGGACAG ATGCCAGCCT CTGTAAGTAG TTATCATCTC 420 CTTGCCAGCT GGGGCTGCCT TCTTCCAGGG CATCTTGTGG GAACAAGAGA TGGGTGCAGA 480 GGCCCAGGTA CTTTTGTGAG AAGGCAAGGA GCTTTTAACA TCGCCTTCCA CCCCGAACCG 540 TATCTTGGGT GTTCCAACCT AGGAGGAATC CCCAGGGCTT TGCCTTTTTC TCCTGAATTT 600 AAGATGACAT AGGAGACCCC TGGGGAGATG AACAGTTTAT GGGACACAAT AAAGGGTTAG 660 GAGACCAGAG TTCTGGTTGG CTCTGACAGG GCTGGTGATC AGAGGGCTGG AGAAACCAGG 720 GGTTTCTCCA GGCACCAGAG GGGCTCAGAG CCAACCAAGC ATATCTCCGG GATTTTCAGA 780 AGCCTACACT TGACTCACTT TTTGTTTAAA TGTATTTTTG TAGTTCCTCA TTCTGGAGGC 840 TGGGAATCCC CCAAGTACCT GGCTCCTTCA TCCCAGCCCC TCTGGCCTCC CCCTACTTTA 900 GAGGGCTGTA GATTCCTGCC TGAAGCCTGG GCAGGAATGA CCCATGGTAT CAAGGAAAGC 960 AAGGGAAGCA GCAAGGGAAG AGAGGGAGTG GGGAGGCTGC TTTGGTCCCA CAGCTTTCAC 1020 TTTCACCTGA AGCAATGGCT CTTAGGGAAC AGGGAGGCAG GGGGAGGGCG GAGCTGGAAA 1080 GAGGTAAAGG GGGGCCCTTG TGGTAGGAGT GGAGAAAGAG CCAGAGGAGG TGGGGTGAAG 1140 GGTGTGATCC AGGCTTCTCA AGAGCAGAGT TTGCCCTCAT AACTCCCAAC TTTGGCTCCA 1200 GGTAGAGGCT GGGCTGTGAC AACAATGTCA GAAGCTATCT ATTGAGGGCT TCTTGTGTGT 1260 CAGGCTCTGA GCCAAACACT GCCTGTTTTC TTTGTCTGAT TTCTCACAAC TCCCCCATTA 1320 TACAGATGGG CAAATTGAGG CTCAGAAAGG GGGATTGTCT TGCCAAAGGT CTCATAGCTA 1380 GCTAATGGAA GAACCTGGTT GTGAATCTAC ATCTGCATGA TTCCCGAGCC TGCCTCTCAG 1440 ATAGTGAGAG TCTCCAAGCT CTGGTCCTGA GCTGTTTTGT GGCAGAAGGA 1490
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