Tag | Content |
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EnhancerAtlas ID | HS105-48292 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:233981890-233983400 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_09311 | chr2:233981155-233985071 | CD14 | SE_10919 | chr2:233975132-233986167 | CD20 | SE_13493 | chr2:233983214-233985075 | CD34_Primary_RO01536 |
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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 |
GH02I233118 | chr2 | 233983041 | 233983798 |
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Enhancer Sequence | CTGTGGAATG GGGAACGAAG TGTGGCAGCC TGGGCCATTA GGAACCAAGG GCAGTCCCCT 60 CCTTGGTCAG AAGTGTGGCT GGTGCTAACC TCCCGATTCG AACCTGGACG CTTCATCGGG 120 GGACGCAGGC ATTTGTTTTC CCTCTGTCTC CTTGGGCGCC TTTTCACCAT GGCCTTCACG 180 TGCTGAGCAT CTTCCATTTG CTCCCCAGTT CATTCGCTTC CCTGCCCCCT GCTTTCTCAT 240 TGGGTTTGGC CAATGGGAGC CGCAGCCAGA TGAGAGGAAA GTTTTTTGGC GGGGGAGGGG 300 ATCTACTGCC CTGCTCGCAT CCTGTAAGGT CTCCATGGTA GCTCCACGGG AGGCCACAGC 360 GCCTGCTGGG CGGCCCCCTC TGGGTTCCAG CACCTGCTTC TTGCCTGTGA TCTTCCCAGG 420 GTGGTAACTA CTATGAGTTC GGGGGGGCTG TACTGCCTGT TATTGGTATC CCTATGCCCT 480 GTCCCTACAT GTTCTCCCCA AGTTCCCCCG TTTAATGAGA CATCTGCCTC CTGCCGGGAC 540 TCTGGATCGT GCACATGAAA AACGCACATG ACACCTTGTT CACATTTTGC CTTTTACAGT 600 TGCTGAAAAG GCACCACCTT TAGCAACGTG CTGGGGGATG TGAGTGAGGG CAGCTCCCCT 660 GCTTGCCACT GTTTCTCTGC ATCCCCAGTC CCAGATGCAT GGAAGACCCT CCCTGACCAT 720 CCCTCCTCCT GGCTCCAACT CTTGTCTGTC ATCCTGACCC AAGGCGGCAA ATCCATGGAA 780 CCACTAAATG CTGCTCCAAT TGCCAGGCCC TGCTGCACAG TCTGGGGATG GCACAGCCAT 840 GAGCAGACCT GTCCTGACTG TGGGCACACA GCTGGGTGGA TATGGACCTG GCCTGCTGTG 900 GGTGGGAACC CCCAGGCCTG TCCCAGCAGG ACCCACCTAC TCCTGCTGGC CTGTGGATGT 960 CAATACACTG TCCACCTGGA AGCCCCTCCT GGCTTTGACT GGGTGGGGAT TGTTAGGTCA 1020 CACCCAGGCA CGGTTGCCCT TCAAACAGAC TCCTCCCCCT ACCGGCCACT CTGCCCTGTC 1080 CCCTCGGCCA TCGTACCCTG ATGCAGGACC TTTCTGGGCC CAGGTTCAGA ATGCAACACC 1140 ATGTGTGGGC TGCTCCTCTC TGCACTGCAC ACACTGAGGC CAGACCATGC TCCTCACCAC 1200 CCACCCGTCT AGACCACGCT CCCCACCCCT CCGCTGTCTG GGCCGGCTCT GTAGCTTCTA 1260 TGATCCCCTT CTTGGGCTCT GACTCTTTCT CTTCCTGTTC TAGAATGTGC TTTGAACGTA 1320 AGTTCTCTGT TTTCCTTGTC AAAGCTTAGG GCCAAGAGCA AAGCCTTATG AAGACACCTT 1380 CCTGGACATT TTCTCCGGGG ACACCTGCCT TTGCCTGGTT GGTGCCCCGC CTTTGCCATC 1440 TCCTGTCTGC ACTGCCTGCA GGCACAGGGT GCTTCCTGCG GGCCCACTGC ACACAGCAGG 1500 TTTTCCCTCA 1510
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