Tag | Content |
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EnhancerAtlas ID | HS068-05678 |
Organism | Homo sapiens |
Tissue/cell | GM18526 |
Coordinate | chr9:127042760-127044510 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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| Number of super-enhancer constituents: 43 | ID | Coordinate | Tissue/cell |
SE_01861 | chr9:127041756-127043926 | Aorta | SE_01861 | chr9:127043953-127046452 | Aorta | SE_02294 | chr9:127041734-127043104 | Astrocytes | SE_02294 | chr9:127043937-127045792 | Astrocytes | SE_03002 | chr9:127041823-127043169 | Bladder | SE_03002 | chr9:127044065-127045325 | Bladder | SE_04593 | chr9:127044035-127046338 | Brain_Anterior_Caudate | SE_06625 | chr9:127041509-127043638 | Brain_Hippocampus_Middle | SE_06625 | chr9:127043834-127049648 | Brain_Hippocampus_Middle | SE_09789 | chr9:127043706-127046156 | CD14 | SE_23712 | chr9:127043999-127046004 | Colon_Crypt_1 | SE_24006 | chr9:127044045-127046083 | Colon_Crypt_2 | SE_26169 | chr9:127040868-127043262 | Duodenum_Smooth_Muscle | SE_26169 | chr9:127043599-127046347 | Duodenum_Smooth_Muscle | SE_27460 | chr9:127041771-127043821 | Esophagus | SE_27460 | chr9:127044035-127046123 | Esophagus | SE_29975 | chr9:127041731-127043291 | Fetal_Muscle | SE_29975 | chr9:127043997-127046387 | Fetal_Muscle | SE_31765 | chr9:127041848-127043061 | Gastric | SE_31765 | chr9:127044041-127046389 | Gastric | SE_36996 | chr9:127041377-127050527 | HSMMtube | SE_38009 | chr9:127039597-127046184 | HUVEC | SE_38868 | chr9:127041773-127043793 | IMR90 | SE_38868 | chr9:127043970-127046447 | IMR90 | SE_42506 | chr9:127041753-127043788 | Lung | SE_42506 | chr9:127043941-127049998 | Lung | SE_44293 | chr9:127041757-127043818 | NHDF-Ad | SE_44293 | chr9:127044212-127046445 | NHDF-Ad | SE_44809 | chr9:127041738-127043771 | NHLF | SE_44809 | chr9:127043918-127049996 | NHLF | SE_45648 | chr9:127040018-127051411 | Osteoblasts | SE_47283 | chr9:127041647-127050279 | Panc1 | SE_49326 | chr9:127041787-127043648 | Right_Atrium | SE_49326 | chr9:127043970-127046367 | Right_Atrium | SE_50283 | chr9:127041756-127046427 | Sigmoid_Colon | SE_52726 | chr9:127041767-127043867 | Small_Intestine | SE_52726 | chr9:127043913-127046460 | Small_Intestine | SE_54297 | chr9:127041784-127043103 | Spleen | SE_54297 | chr9:127043303-127043836 | Spleen | SE_54297 | chr9:127043843-127046283 | Spleen | SE_60448 | chr9:127019058-127056389 | DHL6 | SE_65907 | chr9:127041740-127043255 | Pancreatic_islets | SE_65907 | chr9:127043647-127046632 | Pancreatic_islets |
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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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Enhancer Sequence | CCTGGAGTTG CTGGAGAAGA AACATTCCTC ACGCTCATGC GAATGTTTCC CTGGGCTGCT 60 GTCCCAGCAC TGGGTACCGT GGGGCAGACA TGGGTGTGAC GTTTTCCAAG CACGAGGTGA 120 CCAGTGTCCA TTGGGTCATC AGGCCTCCAG GGCCACATGT TTGGAAAGCT ATTCCTGGAG 180 CACCAGGCAT CTGGCACCTC GCTCTGTGGC TAGGCACGGG TTTATGAGGG GACCCTGCAG 240 AGAGCTGGGG TCCTCAGCCT TGACATTTGC ACATTGTGTA TAATTTCACG CTTTGCTTTG 300 CTTTTTTCTC TTCATTTTTT TCTTTTTTTG AGACAGGGTC TTGCTCTGTT GCCCAGGCTG 360 GAGGGTAGTG TCGTGATCTC GGCTCACTGC AGCCTTGACT TCCTGGGCTC AAGGGATCCT 420 CCCACCTCAG CCTCCCAAGC AGCTGGTGCT ACAGGTGCAT GCCACCACAG CTAATTTTTG 480 TATTTTTTGT GGAGATGGGG TTTCTCCACA TGTTGGCCAG GCTGGTCTCG AACTCCTGAC 540 CTCAGGTGAT CCACCCACCT CAGCCTCACA AAGCGCTTTT GTTTTTCTTG AGAAAGATCA 600 GAGCTTCCCT GCTGCATCTC CCGCTTTTCG CTTGTGTTTT CTTTTCTTCC TCACCAGCAG 660 GCTGCCTGGT GACTGGCCTG GGGGCCTCTT CCCTCAGACC AGGAAATCAC CCAGTACTCC 720 GAGAGTGTTC ACTAGAATTA CCCTCATGTT CACTGGAATA TACTGGTCAG ATTTCTGAGA 780 GGGAGACCCC CTTTTTGTAC TCATAGGAGA ATGGAGGAGG CCGGCCATGC TTCTCCTCAG 840 CCACGATTGA AAAAGTCACC TAGCACAGTG GCCTGAGTCC ACTGGTTCCC AAATCCCAGA 900 CCCAGGCCAG GCCTAGGGCC GTGTGAAGTC TTCCGCGGAC CCACGGTGAA ATAAGAAAAG 960 GAAGGCCTGG CTTGGCATAG CTACTTTCCA TGTCAGCTGT TTTTTCTTTT TTTTTTTTTT 1020 TTTTTTTTTT TTTTTTGGAG GCAGAATCTC ACTCTGTCGC CCAGACTGGA GTGCAGTGGT 1080 GCGATCCCAG CTCACTGCAA GCTCCACCTC CAGGGTTGAA GTGATTCTCC TGCTTCAGCC 1140 TCCTGAGTAG CTGGGATTAC AGGTGCCTGC CACCACACCC AGCTAATTTT GTATTTTAGT 1200 AGAGACAGGG TTTTACCATG CTAGCCAGGC TGATCTCGAA CTCCCGACCT CAGGTGATCT 1260 GCCTACCTCG GCCTCCCAAA GTGCTGGGAT TACAGGCGTA AGCCACCACA CCCGGCCTGT 1320 CCTTTCTTTT ATGAAAGATG GTGATACTAG GTGGACGTTT TATTTTAGAT GCCAGAAAAC 1380 TCTGGCAACC TATGTCTATC TTCAAAATGT GGGAGAGGCT GTCCAGGCCT GTGACACCTC 1440 CAGGCCCGGA AGCCATTGAT GTACTTCTGT ACCCCAGACA CAGAAGTGGA GCCCGGGGCA 1500 GACTTTGATG CCTCAAGAAC CTCTGAGTCA TGGCCACACG TGAGCCCCCG GCTCTGCCCT 1560 GGTGTGCGGT GGGGCGTATT GGTTTCCTAG GGATATTATA ACAAATTACT GCAAACTGGG 1620 TGCTTGAAAA CAATAGAAAT TCATTCTCTC TTGGAGAATC CTGGAGGCGT GATGCCTGAA 1680 ATCAGGCTGG TGGTAGGCTC AGTTCCCGTG GAGGCTCTGA CAAAGCACCT GCCGTGCCTT 1740 TTTCTGGCTT 1750
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