Tag | Content |
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EnhancerAtlas ID | HS180-00122 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:3335310-3336440 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr1:3335514-3335527 | GAACCTTCTGGAA | - | 6.15 | KLF16 | MA0741.1 | chr1:3335332-3335343 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr1:3335333-3335343 | GGGGCGGGGC | - | 6.02 |
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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 |
GH01I003415 | chr1 | 3332483 | 3336699 |
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Enhancer Sequence | AGGTGCTGCG TGGGCTGGGT GTGGGGGCGG GGCCGCCTGC CTCCGTGCAC CGCTGACCCA 60 CTCCTAGGAG TAAGTATGCC ATTCCCAGGG CTCCCTGCTG GAGTGAGCAG GCAGTGGGCA 120 GGGCCGGGTG CTGAATTCTG GTCACTCTGG CCCTCCCCTC CTGGCCTCAG CAGGATGTTT 180 GAGGATGAGG CAGGAGGTGC CCAGGAACCT TCTGGAAGGC ATCTGCCTGG CTCTCAAAGA 240 TGTGAGGGAG CAGCTCTCCA CCCACCCTAG GGTGTTCACT GGGGCAGGGG ATCCTCATCA 300 GAGCAGGGCT GACCAGAGCC AGGGCCCAGA GGGTCCACAT GGGAGAAAAC CTCAGCTTCC 360 CCACACCCAG CCCAACTCCG TTCATCTCAC GACGGCCATA GCTGCCCCCA CACCCCCACT 420 TCTGGTGGGC CAGGGAGTGG GCCAAAGGCA GAGTGAGACT CCGTGCAAAT GCGGGTCCCC 480 ACCCCCCACT TGGAGCCCAC TGAGGGATTC CACGGGGTCC CGGGGACAGC CTGGATGGGA 540 AGCGGTGCGT CTGCTTCCAG GATCCCCCCG TGCTCCTCTC ATCTGAGGAG CCGGCTGGCA 600 CCTGCAGTGA AGCAGTCACA CAGCTCATCG GGATGGGGGA GGCATTGAAT TTGGGGCTCA 660 CAACAGCCTC CCAACAGGCT TGTCATCCCA TTTCAAAGAT GAGGGGCCCG AGGCTCAGAG 720 ATGCCCCATG AATCACCGGG GTCAGTGCCT GGGAGTGGGC ATTTTAAGCG AGAGCCCCAG 780 ACAATGGTAA CTGGGAGGCG AATGGGGAAA CGCTGGTTTT CTGCCAAGGC TGGTTTAGTG 840 ACACATGCAG GGTGTGTCTG TTCACAGAGG CCATTGGGGA TAAAGAGTGC TTCACACGGC 900 TTAAGTTGAC AGCATAAGAT TTCTGTCCTC TGGCCACACA GAGCTAGAGG GGCCACATGA 960 TAGTGCAGGC ACTGGGGACT CAGTCTGTGT CTCCATCCCT GGGGAAGGAG ACCAGCTGAG 1020 GCACCTGTGC ATGTCGTGGT CACTGACCCC CACTCTGAGA CAGAGCAAGC ATCCCCGGCT 1080 GCCCCAGGGC TGTGTCCCAA CTCGCAGGGT AAATGACAGC TTATACCACT 1130
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