Tag | Content |
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EnhancerAtlas ID | HS180-47686 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr8:98830010-98831360 |
Target genes | |
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_41359 | chr8:98830348-98831212 | Left_Ventricle |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH08I097818 | chr8 | 98830441 | 98831093 |
|
Enhancer Sequence | TTTTGCCATG TTGACCAGGC TGGTCTCGAA CTCCTGACCT CAGGTGATCC GCCCACCTTG 60 GCCTCCCAAA GTGCTGAGAT TACAGGCGTG AGCCACCATG CCCAGCCTGC AACCTCAATC 120 TTCTGGGCTC AAGTGATCCT TCCACCTTAG CCTCCCAAGT AGTTTGGACT ACAGACATGC 180 ACCACCATGC CCGGCTAAAT TTGTATTTTT AGTAGAGATG GGGTTTGACT ATGTTGTCCA 240 GGCTGGTCTC AAACACCTGC ACTCAAGCAA TCTGCCTGCC TCAGCCTCCC AAAGTGCTGA 300 AATTACAGGC ATGAGCCACT GTGCTTGGCC AAGTTATTTT ATTAATAAAA GAGTAAAGTT 360 GCATGATCTG ATCACAAAGA ATGACGATTT TATTTCTTAG ATATTTTGTC CCAAGTGAAA 420 GGAGACTGAA AACCATTAGG TGGTGTTCAC CCTGGTGAGC AGGAGCCAAG CCCATGAGTC 480 ATGGGCCTTC TCCATGTTCT TCCTCAACAT TGGAAACAAC TTTGTTTTGG AATATTGCTC 540 GTGAGGAATC CAAACACATA GTGTTGAATG GTGAAGGGAG ATAAAAGATG AGATAGCACA 600 GTAGGCTGCC TTCCCATTCA CTTGCCTAGG CCAGTGATGT AGGCGTTGAT CAATGCTGTG 660 TGAGTGTTCT GTGGGGAAAG TCCGGCAACT CCCTCTAACC ATAGTAGCAG ACTTTGATCC 720 TCCTGAAAAG GTTCCCTTTG ACCTGGTTGT TAAGCATTGT GGATGGTAGT GCTTGATTAT 780 TTCCCCCCAC CCTGGAAGTA CTTGCTAGTA TAAGAGAATA TGCTGTCTTG GGAGAAGTAC 840 CATCAACAAA AATGCTCTTT GCAAAGAAGA CCTCATTTTA GTAGGTTTCT GTCCCTTGCC 900 CTGCATATGC CCTTTAGAAT GGTTCAGAAC TTTTGAGACA TGGTCTGGCT CTGTCGCCCG 960 GGCGGCTGGA GTGCAGTGGC ATGATCTCGC TCACTGCAAC CTCCACCACC AGGGCTCAAG 1020 TGATTTGCTC ACCCCAGCCT CCCAAGTAGC TGAGCTGGGC GACAGAGAGA AACTCCATCT 1080 CAAAAAAGAA AAAAAAAAAA AAAAGGAATG GTTCAGAACT TGCAGAGAAT ACAAATTTCA 1140 GAGATCCCTG GATATACAAA ATGTCCCTGG ATACCGATCA CTGACGTCTT TTATATGGTA 1200 AGAGGGCAGA GTCAGGCTAG AAATTTTGTA TTGGTTCTAA ATAATAGCTG TCTGCTTTAA 1260 TCAGTTGCTT TCTGATAAGC ATGTCTGAAT TGGTGCCCAA GGAATACTGT CTGGAATGAT 1320 TAATGAGATT TGCTAATGAG GCCCTTTTCT 1350
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