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EnhancerAtlas ID | HS184-08942 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr13:28534300-28535440 | | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_23065 | chr13:28533714-28538330 | Colon_Crypt_1 | SE_23742 | chr13:28534343-28536294 | Colon_Crypt_2 | SE_24684 | chr13:28534085-28536347 | Colon_Crypt_3 | SE_27619 | chr13:28525608-28557466 | Fetal_Intestine | SE_28541 | chr13:28532710-28556725 | Fetal_Intestine_Large | SE_47978 | chr13:28534333-28535661 | Pancreas | SE_50220 | chr13:28534107-28538004 | Sigmoid_Colon | SE_52415 | chr13:28534087-28538099 | Small_Intestine | SE_56837 | chr13:28534098-28536240 | VACO_400 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAACATCGTG TGCAAAATGA CCCTTTTAGA ATGGTATAGT CCCTCTCCCC CAATTTTGTT 60 TTTCTTAAAC ATTCAACAAA CCCAAGAATC TCTCCTGCCT GACTTAGTTT TAACTTAGTT 120 TCAACAGGCC CACGACCAAC GTAGAAAAAT CTTGCAGCGC CCGGGTTTGG GCTCAGCCGG 180 AGTCGGCAGA GGCGCTTGCA CCTCCCAACT GGGTGAAAAC TGGAACCTTT CCGGGTTCAC 240 GAGCCCAAGC CCCATCTCTT CCCAGAGCGC GCGCGCCCTC TGGCGCCTGA ACCGGCGACT 300 GGACGCGGTG GAGGCGTGGG ATTCGGAGGC CGGGACCCCA AGCTCTGCGC TGGAGGCGTC 360 AGGAGCCGCG AGGTCATCCG GTCTCAACCT CAGGCGCCCC TGTGCAGGCC TCCCTACACT 420 CCTCAAGCTG CGCTCCCTAC TCGTGCCACA TCCCTTGTTC CGTAGGTATT GCTTCGGGGG 480 TGACACAGTT GGCGTTAGAA GCGCGGTGGC CTCACTTGCC GGAGAGGGTC TTGGTTTTGC 540 GCCTTTTTCC GTGGCCCGGG AGGCTTGCCA GGCGCTCGCA GCAGCGAGCC GGGTGCTTGC 600 ATCTCAGAGA GCAGCCGAGC TCCCTTCCCT GGCCCCGTAC CCGCGTGCAA GGGGACCGAG 660 CCCCGGGAAG GGGAAGAACT TGTAATCGCT TGCAGCGGGA CAATGTCGAC TTTTGAACCT 720 CTAACCACTA AGCAAACAAC CCATGTGCTC TTGCTCCACT GTCCAAACAG GGTTTATTGA 780 CAGGCGTTTC ACGGCAACGC ATAGCAACCC CGGCGGCTAG GGGGCGGGCC TGTGGGCGCG 840 GCCGGGGCGC GGGGAGACCT GCGGGGCACC GGGGCTCAGA CCGGCCCTGA CCCAGGACCC 900 CTGACCCAGG ACCCCTCGCC CAGCGGACCC GGACACGGCT TCCTCCTCTG CCCGGCACCC 960 CCCGACCCCA CGCCCCGCAC TCCTCCCTCT GGCTTCGAGG CCAGGCGCCC GCGGGCCGGG 1020 CCACCGGAGC CCCTTTCCCA ATCCTGGAGC TGTATACGCC ACCCGGAAGG GCCGCGGAAT 1080 TGGAGAGGTG CTGCAGAGGG TCTATACCTC TTGCTGTTTC CCGGCTCTGC TCATCTTCCC 1140
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