Tag | Content |
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EnhancerAtlas ID | HS101-05896 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr10:99523930-99525340 |
Target genes | Number: 12 | Name | Ensembl ID |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_47588 | chr10:99524102-99525638 | Pancreas |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr10 | 99524322 | 99524624 | chr10 | 99524857 | 99524970 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I097762 | chr10 | 99521938 | 99525775 |
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Enhancer Sequence | TCAATTAGGA ATTTTACTGA GCACCTATTA TGGACAGGCA CTGCTAGGTC ATGGCTTTTG 60 GTTAATAAAA ATAGTCATTA CCATTTAATG GACATCTACA TGCTGTGCGT TGTACTTTTC 120 ATGCATTTTC CCACTTAACC CTCAGCAACC CTGTGAAATA GACATTTTTA CTCCATTTTA 180 CAGCTGGGCA CTATTCCCGA TGTCACGCAG TCACTAAGTC ACAGGATTAG AAGCCAGGAC 240 TGGACTGTAT CTGCCTCTTC TCACCCCAAC ACGGAGTGTT CAGCTGCCTC CTCCCCTGTC 300 TGTCCTGTTC TTTATTAGAA CTCTGATTTT GTCCCCAGCT GAAAAAGCTT GACTTCCTTT 360 GCTGTCTTGC ACCTAGGGGT GGCCATGTGA CTTAGTTTTG GCCAGTGAGC TAGAAGTGGA 420 AATCTACTAG GTGGGATTGC TGGGGAAATT TCTGTTTTCC TGATCAAAGG GGCCAGAGGC 480 AGCTGACAAG CTGTGCTCCT CGCCCTTCCC CGCCTTGCTG TCTGGAATGT GGTGGAGAAG 540 TTGGAAGGAG GCATTGTCTA TAACCACGAG AGCAAACGTC ACCCCATGGC AGAGCAGGAA 600 GGCAGTTGGA CATAGACCTC CCACCTGTCC ACCTCCACCC CTCTTGTGTG GAGAAGCTGG 660 GGTTTCGGTT CCTGGGGTTT CTGTTATGTG TGGTTGGGGG CCGCATCGTT CACTGCACCC 720 AGGTGCTCTT GGGGCAGCAC AGCTGCTGGG TCTCCAGCCA GCGGGAGGGA GTCTTGTGTG 780 ACTGAAGGGA ATGAAGGGTG GGGCTCAAGC CTGGAAGGAC CTCCCTGGTC TTTGGGAAGA 840 TTCTTCTTGG TCCCAGAAAA GAGATTCTTG GCGAGTCTGA CAGCAGATGT TGGGGGACAG 900 CAGATGTTTC AAGCTGGGCC CTGACCCCTT GTGGGGGTAG AGGAGTGCCT TCCTGGGCTT 960 CACGGGATGG GCTAAGGGAG TCCTCCCCTC GCCCTGCTGC CCCACAGCTG CCAGCATCTG 1020 GCAGAAGTCA GTGTAGTACT TCAGCCAGGG CAGACCCAGT CCTGTGTGTG CCATGGAAAA 1080 TCATCCCTGG TCCTGGTTGA CCACAGAAGT GTCCGTAAAC ATTTGGTCAG GGTAGGAGGC 1140 TGGGAGACAA GGCGCAGATT CAGGGAGCCA GGTGCACTGG GCAGGGTTTG GGCGCGGATG 1200 GGTGAGGGAG GAGCAAGGCG GCCTGTGCAG CTGTTGACCT GCGGCGAGGC CACCTGCCTG 1260 CCCGGGGTGA TTTATGGGCG CGCTGTCGGA CCACCTGCTA GCCAGACCTC AGGCGAATGT 1320 GCGCTCATGG CCCACAGAAG AACTCAGCCC CTGGCCCCTC TGGAGTCATT TCCCTGAGGT 1380 GACGTTCACC TCTGGGAGCG GAAGCCAAGG 1410
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