Tag | Content |
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EnhancerAtlas ID | HS187-10481 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr17:40693220-40694660 |
Target genes | Number: 26 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_24066 | chr17:40692725-40693505 | Colon_Crypt_2 | SE_24066 | chr17:40693510-40694022 | Colon_Crypt_2 | SE_25138 | chr17:40692712-40694055 | Colon_Crypt_3 | SE_28881 | chr17:40692606-40694128 | Fetal_Intestine_Large | SE_35596 | chr17:40692565-40694399 | HepG2 | SE_57057 | chr17:40692969-40693927 | VACO_400 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 40693346 | 40693790 | chr17 | 40694063 | 40694180 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I042540 | chr17 | 40692702 | 40698177 |
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Enhancer Sequence | GCAGGTACAG TGCCTGGGTG GGGTGGGAGA GCCCCCCAGA CCCTCAAAAA GAAGGGAGTA 60 GCAGATGTCA GTAGGGGTAG GCAGAGGGAC TGGAATAATG CCTCGCCATA ACACACAGTA 120 CTTCATAGTT TACCAAGCAC GTGTACACAT GCGTTGTCTC AGTGAATCCC ACTGTGGTTG 180 AGAGGTGAGC TCTGGAAGCC AACAACCTGG GTCACACCTC GCGCTCCTAT TTCCTGGCCG 240 TGTGACTTAT GACTCATGAC CTCCTTCCCA GTGTCTCGTT TGCTTTTCCT GTAAACTGGG 300 ACTACCTCAT AGGTAGAATA ACGCCTGGCC CAGAGCAAAG GCCACTAAGA GCTAGCTATG 360 AACAAGGATT TTGTTTCATC TCTGCGTGGT TGCTGAAGTA GGCACTGCAG GCAGGAGGTG 420 AGTGGATGTG CCTAAAGGCA CTAAGTGCGC ATCCTGCTAC AAAACTGTGA AGCCAGGGCT 480 CCTTCCTGCC ACTTAAAGGA GGAGTGGAGC AGAGGGCGCC CAAGTCAGGA ATGACTTAGT 540 GGAGAGGCGT CTGTGTTGGC CAGGAAGGGA ACAGATCAGC TCAGCCTTTC TTGAGCAGTA 600 CTGCTCCAAG TGTGACCCAA AACCAGCAGC AGCAGCAGCA GCAGCCCGAG CTGTGAGATG 660 GCAAATTCTC AGGCCCTACC CAAGACCTGA AGGAGAAGCT ACATTTTTTT TTTTTTTGAG 720 ACAGATTTCA CTCTGTTGCT GAGGCTGGAG CACAGTGGCA CAATCTCATC TCACTGCAAC 780 CTTCGTCTCC TAGGTTCAAG CGATTCTCCT GCCTCAGCCT CCCGAGTAGC TGGGACTATA 840 GGCACCCGCC ACCACGCCCG GCAATTTTTG TTTGTTTTGA GATAGAGTCT CGCTCTGTCA 900 CCCAGGCTGG AGTGCAGTGG CACGATCTCA GTTCACTGCA ACCTCTGCTT CCTGAGTTCA 960 AGCGATTCTC CTGCCTCAGC CTCCTGAGTA GCTGGGATTA CAGGCGCCCC CCAACCACAC 1020 TCGGCTAATT TTTGTATTTT TAGTAGAGAC GGGGTTTCGC TATGTAGGTC AAGCTGGTTT 1080 CAAACTCCTG ACCTCAAATG ATTCGCCCAC TTCAGCCTCC CAAAGTGCTG GGATTACAGG 1140 TGTGAGCCAC CTTGCCTGGC CAATTTTTGT ATTTTTAGTA GAAACAGGTT TCACCATGGT 1200 GGCCAGACTG GTCTCAAACT CCTGACCTCA GGTGAACTGC CCACCTCAGC CTCCCAAAGT 1260 ACTGGTATTA CAGGCGTGAT CCACTGCGAC TGGCCTTGAT TTTGTTTTTG AGACAGAATC 1320 TTACTCTGTC GCCCAGACTG GAGTGCAGTG GCACAATCTC AGCTCACTGC AACTTCTGCC 1380 TCATGGGTTC AAGTGATTCT TGTGCCTCTA CCTCCCGAGT AGCCGGGATT ACAGGCACCT 1440
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