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EnhancerAtlas ID | HS176-18784 | Organism | Homo sapiens | Tissue/cell | SK-N-SH | Coordinate | chr19:17199940-17201160 | | Number of super-enhancer constituents: 16 | ID | Coordinate | Tissue/cell |
SE_01695 | chr19:17198741-17202174 | Aorta | SE_07171 | chr19:17199604-17200787 | Brain_Hippocampus_Middle_150 | SE_07171 | chr19:17200970-17202230 | Brain_Hippocampus_Middle_150 | SE_09204 | chr19:17198739-17204010 | CD14 | SE_11414 | chr19:17199340-17203397 | CD20 | SE_19835 | chr19:17200842-17202819 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_32165 | chr19:17199462-17201891 | Gastric | SE_32675 | chr19:17200275-17202398 | GM12878 | SE_42559 | chr19:17199714-17202163 | Lung | SE_44945 | chr19:17199363-17202117 | NHLF | SE_45910 | chr19:17198739-17202233 | Osteoblasts | SE_50282 | chr19:17198861-17203978 | Sigmoid_Colon | SE_52769 | chr19:17198898-17203282 | Small_Intestine | SE_53370 | chr19:17198927-17203538 | Spleen | SE_59337 | chr19:17188995-17222500 | Ly3 | SE_62772 | chr19:17177847-17247718 | Tonsil |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTGCAGGTGT AGAAAAATGA GGACAAAGGT CTCTAAGTCG TCCTCCCACT CTGAGCCACC 60 CTGACCAATA GGCTGACTTT GTGGTCATTC CTTCGTGTGT GTGTGTCCAT CTTTCCCATA 120 CTGCCCATGA GCGTTTCTTC TAAAAAAAAA AAAAATCCTC AACAGGATCA GGGAAATGTA 180 CACAAAATGT GAAATGCACT GAATGCTGCA CGATGCATCC TAAATGAGTC TGCTGTAATG 240 CTAGTTAGCC TTCCCTTAGC TTGAGAATGA TTTCATCCTA TAAACATGTG GCTTCAAATT 300 ATGGCCTTAT ATAAACGAAA CGGCTACGCC ACACTTTCTG GAGGCCCCGT CCGGAGGCCT 360 TTATTCTCCA GTAAATTCCG AATCCTCCGC CAAACTGGTA GGCAGAACCC TACTTTCTGT 420 GCAGCCGGCC TTGAGAGCGG CTAATTCACA TCCGGCCACT GACCCCCACC CCCAGGGCCT 480 GTTTTTTTTC GTTGTCATGC CTTTCCTTGC ACCTCCTTTC TATGAGAACA CAAGGAAAAG 540 GCCCTGAATT GAGATTGGCA TTTTTTCAGA GTGCAGAAAG CATATACTGG CCTGGTTTTA 600 CATAGCCATT TCTTTTTGCA CCGCTCCGTT TTTTTAAAAG GAGTGATCAT TTTTATTGTA 660 GTGAAATGCA CATAACGTGT AATTTATCAT GAGTAACATT CAGTGCATTC ACAGTGTTGT 720 GCCAACACCA GCTCTATCTG ATTCCAGAAC ACTTTCATTC CCCAAAAGGA AACCCCGTCC 780 CCATTAGCCA TCACTCCCCA CTCCTCATCC CCTAGCTCCT GACAACGACT CATCACTTTC 840 TGTGTCTGTG GATTTGTCTG TTCTGGCATT CTGGACATTT CTATAAATGG AGTCACACCC 900 CATATGGTCT TTCGTGTCTG ACTTCTCTCA CTCAGCATCA TGTTTTTTAG TTTCATCCAC 960 GTTATAGCAT GAATCGGTGC TTCCTTCCTT TTTTTTTTTT TTTTTTTTTT TTTTTTTTTT 1020 TTTTTTTTTT TGAGATAAGG TCTGGCCCTG TTGGCCAAGT TGGAGTGCAG TGGCACAATC 1080 TTGGTTCACT GCAGCCTCTG CCTCCCAGGC CCAAGCCATC TTCCCACCTC AGCCTCCTGA 1140 GTAGCTGGGA TTACAGGCAC ACACCACCAC ACCTGGCTAA TTTTTGTGTT GTTTTTTTTC 1200 TGTAGAGACG AGGTTTCGCC 1220
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