Tag | Content |
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EnhancerAtlas ID | HS180-42238 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr6:52976660-52978190 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr6:52977628-52977649 | ACCATGACCCAGGACAGCGCC | + | 6.33 | ZNF263 | MA0528.1 | chr6:52977315-52977336 | CCTTCCCCACCCTCCAGCTCC | - | 6.07 | ZNF263 | MA0528.1 | chr6:52977318-52977339 | TCCCCACCCTCCAGCTCCTCC | - | 6.41 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 52977099 | 52978012 | chr6 | 52977017 | 52978121 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I053111 | chr6 | 52976675 | 52978470 |
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Enhancer Sequence | TTTCCTATCA GATATTCTTC CTGTACTCTC GCCCCTTCCC AATCAAAACG CTGGCATCAG 60 GTTAGTCTGA GGCACAACCT TCCTCTGTTA TCCACAAGTT GTGACCTTCT AAACTTTCTA 120 CAGCCTGCTG TCTCTGGCAA GGGTGATGAA CTCAAACACC TGTGAAGGTC CAGAGGACAC 180 CACAAGTGAG TGAGGTGGAC CAGGTGTGCA GGCAGTGGCA AGCCAGACCC TGTGTCTCTT 240 GCCTGAAAGG GAAGCGGCTA CTCAGCTTCC GTTCGAAGAT TCTCTATAAG GCCTGACCTT 300 CCTATTTTTA AAGAGAAGCT GGAAATCCAT GTTGTTTGTG AAATGTTGTA TGCTTAACCA 360 AACTCAAGTT TAAAAGGAAA AAAATAAAAA CACGATACAG GTCAAACAAA AGCCATCTGC 420 AGGATGAGTG GAATCGGCCA ATTTTTGACC CTTGGTATGC AGGTTAAAGC CCAAATAATA 480 AACTTTGCAT TCTAGGTCTG TACAGGTTTG ACACTAACCT ACCTTTCCAG CTCGCCTCCT 540 GCTCCTCCTC CAGGTCTGCT CCTAGCCAAG AATAGTTCTG GTTCCCAGGA CACCCAAAGC 600 CCCTCCCTAC CCCTGCCCCT TTGCTCTGCT GGCATCTGGA ATGCTCTTTC TCTCACCTTC 660 CCCACCCTCC AGCTCCTCCT GGAAGTTCTA CTATTCCTCC TGGAGGCTTT CCACAGTTTA 720 ACTCCAGCCA ATGAATGATT AAATAATTAC ACACAATCTA CTCCCCCTGG GCCTCCAGGG 780 CACTCTCAAA GAGCTCTGTT TCACCTGTGT TTACTTTCTA CCACATCCTG GCCAGTGCCA 840 CACCTCAGAA GGCTTCAGAG AAAAATTGTG ACTAACTGAC TTGTGTCACT TCTCTCCTAC 900 TAAATCATAA GCAAGTTGTC TGCAGAGCCC CCCACTGCCA GCTCCTTGCC CCAGCTCCTC 960 CCACCACCAC CATGACCCAG GACAGCGCCT TATAGGTCCC AGATGACTGT CAAGGCTTCT 1020 TGAAAGCTTT GGCTCTAAGG GATTAAACTG GAAGACTGCA GCTGATTAAC TCACTAGGTT 1080 TAAATTAAGT TCTTGGGCTT GCTGCAAGCA GAGCAAAACT CTCCCGTCTC TCTGCAGCCC 1140 CTTCTCAGGC CTCTGCTCTC TTTGTGGGCA TGGCCAGTGT CTCTTAGCTG CATCCTGGGT 1200 CACTCAAGGT CTCAGGGTAG GAGAGCTGGA TGTACAAATC ACACCCTCAT CCTCCTGGGG 1260 GAGTGGATCC AGGTGCTGGT GGAGGGATGC CAGCATCACC TGGAAGCAGA AAGTTATGCC 1320 CTGAGGGAGC TGTCCCTTGT TTGACTAATC CAAATTAATA CCACTATTAT TGTCTTACAG 1380 TGTTAGGGCC ATGAGAGGCC ATATAGCCAT TTAGACTGAA GGAGGAAACC GAGACCCAGA 1440 GAAGCATGAT TTGCCCAAAG ACAGGGTAAG GGTGAACTCT AGATAGGATC CAGGACATCT 1500 AACTCCAACT CTGGAGACTT TTTTCCACTA 1530
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