| Tag | Content |
|---|
EnhancerAtlas ID | HS007-17617 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr9:130319300-130320970 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
| | Number of super-enhancer constituents: 40 | ID | Coordinate | Tissue/cell |
| SE_00872 | chr9:130317420-130325981 | Adrenal_Gland | | SE_01693 | chr9:130317394-130321858 | Aorta | | SE_02373 | chr9:130319279-130321682 | Astrocytes | | SE_02928 | chr9:130319219-130319761 | Bladder | | SE_02928 | chr9:130319765-130321498 | Bladder | | SE_06387 | chr9:130317152-130326181 | Brain_Hippocampus_Middle | | SE_09759 | chr9:130317143-130321943 | CD14 | | SE_23282 | chr9:130319231-130321813 | Colon_Crypt_1 | | SE_23944 | chr9:130319366-130320321 | Colon_Crypt_2 | | SE_23944 | chr9:130320324-130320747 | Colon_Crypt_2 | | SE_25019 | chr9:130319352-130320112 | Colon_Crypt_3 | | SE_26215 | chr9:130316993-130319507 | Duodenum_Smooth_Muscle | | SE_26215 | chr9:130319724-130321507 | Duodenum_Smooth_Muscle | | SE_26528 | chr9:130315417-130326976 | Esophagus | | SE_30306 | chr9:130319232-130321677 | Fetal_Muscle | | SE_31422 | chr9:130317318-130326302 | Gastric | | SE_34381 | chr9:130317259-130332904 | HCT-116 | | SE_34621 | chr9:130315344-130339309 | HeLa | | SE_38118 | chr9:130316747-130321656 | HUVEC | | SE_38969 | chr9:130317305-130326011 | IMR90 | | SE_42140 | chr9:130317363-130326177 | Lung | | SE_44201 | chr9:130317110-130326096 | NHDF-Ad | | SE_44773 | chr9:130317296-130326154 | NHLF | | SE_45705 | chr9:130315396-130327025 | Osteoblasts | | SE_46654 | chr9:130319347-130321513 | Ovary | | SE_47421 | chr9:130319048-130326186 | Panc1 | | SE_47474 | chr9:130319348-130319651 | Pancreas | | SE_47474 | chr9:130320050-130320751 | Pancreas | | SE_48868 | chr9:130319239-130325845 | Right_Atrium | | SE_50184 | chr9:130317343-130325919 | Sigmoid_Colon | | SE_52507 | chr9:130317294-130325898 | Small_Intestine | | SE_53712 | chr9:130317359-130322847 | Spleen | | SE_54748 | chr9:130318900-130321223 | Stomach_Smooth_Muscle | | SE_55718 | chr9:130319316-130326160 | u87 | | SE_57980 | chr9:130319252-130320789 | VACO_9m | | SE_63440 | chr9:130298563-130342452 | NCI-H69 | | SE_63712 | chr9:130320459-130321895 | HSMM | | SE_65259 | chr9:130317505-130323112 | Pancreatic_islets | | SE_67516 | chr9:130319316-130326160 | u87 | | SE_68760 | chr9:130319056-130321854 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGCTATAATT GCAATACTGC ACTCCAGCCT GGGCAACAGT GCAAGACCCT GTCTCAAAAA 60
CAAAAATGAA TCACAACCAT GTGAGAAGGG CTACAGGTAC ACACGGGTGG CCAAGGGGCT 120
GTGGGAGCTC AGAGGAAGAG CCTGATCCAG CCTACCAGGA GTGGGGCTAC TGGCTGCAGG 180
GCTTGGTCTG TGAGGGCATT TCAGGGTCTG GGCTTGACCT CGAGGGCACA GGACAGCCTG 240
GAAGGGTCAG TCTGAAGGAG GGTGACACAT GGTTAGTAGC AAGGTCACTC TACTACCAGA 300
GGCTCTTATC CAACCCCTCC ATTGAACCAT GGGGGAAACT GAGGCTTGGA GGAGAGGCAG 360
GAGTTCACCC AAGGCCACAG AGGTCTGAAG CAGGACCGGC CTCCCATCTA CAGAGCTGGA 420
CTCCCAGAAG CCACACAGGG GACTGCAGGA AGAGGGGAGG GAGGGCGGGG GCTCAGCCCC 480
AATTGCACAG GAAGTCTGCC AGGCTCCACC CGGGGGCCTC CAGGCAGGGC AAGCTGCCCA 540
GCCCCCAGCC TGCAGGGCAG GCACCAGAAA CAGCTCCTCT CGGATTCTGC CACAATCTCA 600
GCAGGAAGAC AGGAAAGCTG AGCTGGGCAG CCTGCTAAAG TCAGGCCAGG ATTGGAGGTT 660
TGGCCTCCCA GGACCAGGCC GGCTCTCAGG TCACTGAGAA AGTCACTCCT CTGCTCCAAG 720
AGGGGCCCCT GCCTCTGGCC AGAGAGAAAT GAAGAGTTTC TGAGATCCCA GTTGGCCTCG 780
GGTCAGGGTG AGTGAAAGGG CTCAGTGTAT TCAACCAGTT GGCTCAAATC TTTCCCCATC 840
CTGCCACCCT CCTTGAGAGA TGGGGTGACC TCCACTCTAG AGATGGGGAA CTGAGGCCCA 900
GAGGAGAGAC GCCCCTTGAC CAAGGTCACA CAGTGAGCTG TGACTGTCCC AAGCTGGGCC 960
AGGAGGGCTG ACCCCAGGAG AGTCCTAGGG GGTCAGCCCC TACCTCCTTG GAAGAAAGGG 1020
CTGCCCCTTC CCCCTCCTCT TTTCCTGGCA GCCTGAAATA TAGGAGTGGG GGTGGGAGGG 1080
GAGTGTGGCT TTGGCTTTTT AAGTCCAACA CAGCCCCTCA CTGTCTGCGC ATAGACGGGC 1140
CTGGGCTGTC TCCTCGGACA CAGGCCCATC TGTGAGGCCC GCACAGGGCT TGCTTCTCTC 1200
CCAGAGAGCT TGTTTGTTTA CCCAGTTTTC ATAATTATAA GTTCTGCAGC CCCACCCGGC 1260
CCAATCATTC CTTCCCTCAC CATCCCTTGC CGTCTGGGGC CCTGCACGGG TGCGGGGGGT 1320
GGGAGTACGA AGTCGGAGAG GGAAAAGCTT CATGCTGGGG TCAAGGCCCT GGGTTCCAGC 1380
CAAGCTCTGG TGCCCCTGAG AGCATAGGCA TGTCCCATCA TCTTCCTGGG CCTCAGTTTA 1440
CTGGGGCATG AGAAAAAGGA GGGGATTGGT TAGAGGAGCT CATGGGGTCC TCCAGAACTA 1500
GGACGAGGAA GGGTCTGGGC CTGAAAAAGA AAAGCAGACA CTTCTCATCA GCACCTCAAA 1560
AATCAAGGCA GGGCTAGGGG AGGTGTGGTA GGGTGAGAGG CACACACCTT CCCCAGCCCA 1620
TCAGGCCTGC CCACCCCAAA GCTCAAACTC AGCTCTCTTT TCTACCCTTC 1670
|
