Tag | Content |
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EnhancerAtlas ID | HS176-19152 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr19:45601260-45602460 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_01185 | chr19:45598986-45606662 | Adrenal_Gland | SE_24339 | chr19:45601036-45601709 | Colon_Crypt_2 | SE_27949 | chr19:45600329-45609568 | Fetal_Intestine | SE_28778 | chr19:45600193-45609635 | Fetal_Intestine_Large | SE_31565 | chr19:45593912-45609498 | Gastric | SE_53046 | chr19:45600935-45605560 | Small_Intestine | SE_65319 | chr19:45593945-45609978 | Pancreatic_islets | SE_68798 | chr19:45601034-45602079 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 45601584 | 45601804 | chr19 | 45601389 | 45602402 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I045096 | chr19 | 45599815 | 45609495 |
|
Enhancer Sequence | TTTCCTCACC TGTGAAACAG GGCCAGTGAT CCCTGCCCTG CAGACCACCA GGATGTCAGA 60 GGATAGGGTG AACCTGCTGG GGGCAGGTCT CCTCAGCAAG CCACAGCCAG GTGTGTGTAG 120 ATGGGCAGGG AAGCTCGGGG AGGAGGCAGG CTGGGAATCG TGAGTGAAAG AGGCCGCTTC 180 AGCACTGCCA GGCTGGGCAC GTGGGTGCCC GTGGGGAGCG AGCTAGCCGG CTGCACTGCA 240 CCCCATCATG TTGTGGCAGA CCCTTCAGCT CTTCTGAAGG CCAAGGCCAG ACTTACACAA 300 GGAACCCATC AGGCCAAACT GCAGGAATGA CCTGAGGCTC GGCTGGTCTC CTCAGTCCCA 360 GCTGAACTCT GTGGGGTTGG AAAGATAGGC ATGTGAGAGG GACTTGTGAT GAGAGCACAT 420 GACACCAGCC ACAGTCCGGG AGACTCATCT CCCCTCCTCC AGTCCTGCCG GTGACTCACT 480 CCCTGCTCCC TGACCATCAG TCCTCCAGTG TGTGTGCGTT GGGGGTTTGC CCACTAGGAA 540 GCTACTTGCA TGAAGTCAAG GTGTCTGCAG GGCAGGGTGA GGGGGCCCAA GCATGCTACC 600 ATCTCTGGCC ACCTGAGCTT TGGAAGGCAG CGGGAGGGGT GGGGGCAGGG TGTTCTTAAA 660 TGCGGATCTT AGGGCATGGA AATGCCATAC TGTTGGCTAT TGAAACCCGT GCTGCAGATT 720 CAGTCCTAAA AGCAGGCTGG ACAGGTAGAC ATGCATCTGT CAGTGGTGGA AAGAGGCCCC 780 AGGTTAGAGA ATCGGCTTGC TTCAGCATTC GTGGTGGAGC TGCTGGGGAG TAGGGAACAG 840 GGTCGAGGCG GGTGCTTTGA TGCATCTGCT CAGATTTCCG TCTGGGCCCA GCTCCACCTC 900 CTGCTGCTGG AGTTGGCAAG TAGACCCTGC CACTGAGCAG CCACGTGACT TTGGCGATTG 960 TTCTCTCTGC CTCGATTTTT CTGTGTCTAA AATGCAGCAG TATGTCCTCA TAGGGTGATT 1020 GGGAGGATTA AGTGAGATAA CACAGTGCCT GATCCATAGT AAATGCCCAG CAAATGCCTC 1080 CCTTGTTATT CCTGTCATCA CCACTCCTCT GCCCCCACCT ATAGCCCTAA CATTTTGTTT 1140 CTGTTTCCTG CCCGTGTTGT GTATTTGTAC TCCTCTTTCC CCTATAGTGT CCCACGTCAG 1200
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