EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS048-38102 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr9:130318860-130321750 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs2491105chr9130320283hg19
rs72767980chr9130320557hg19
Number of super-enhancer constituents: 45             
IDCoordinateTissue/cell
SE_00872chr9:130317420-130325981Adrenal_Gland
SE_01693chr9:130317394-130321858Aorta
SE_02373chr9:130319279-130321682Astrocytes
SE_02928chr9:130319219-130319761Bladder
SE_02928chr9:130319765-130321498Bladder
SE_06387chr9:130317152-130326181Brain_Hippocampus_Middle
SE_09759chr9:130317143-130321943CD14
SE_23282chr9:130317392-130319209Colon_Crypt_1
SE_23282chr9:130319231-130321813Colon_Crypt_1
SE_23944chr9:130319366-130320321Colon_Crypt_2
SE_23944chr9:130320324-130320747Colon_Crypt_2
SE_25019chr9:130319352-130320112Colon_Crypt_3
SE_26215chr9:130316993-130319507Duodenum_Smooth_Muscle
SE_26215chr9:130319724-130321507Duodenum_Smooth_Muscle
SE_26528chr9:130315417-130326976Esophagus
SE_30306chr9:130319232-130321677Fetal_Muscle
SE_31422chr9:130317318-130326302Gastric
SE_34381chr9:130317259-130332904HCT-116
SE_34621chr9:130315344-130339309HeLa
SE_36116chr9:130317008-130319218HMEC
SE_38118chr9:130316747-130321656HUVEC
SE_38969chr9:130317305-130326011IMR90
SE_41594chr9:130321067-130321767LNCaP
SE_42140chr9:130317363-130326177Lung
SE_44201chr9:130317110-130326096NHDF-Ad
SE_44773chr9:130317296-130326154NHLF
SE_45705chr9:130315396-130327025Osteoblasts
SE_46654chr9:130319347-130321513Ovary
SE_47421chr9:130319048-130326186Panc1
SE_47474chr9:130319348-130319651Pancreas
SE_47474chr9:130320050-130320751Pancreas
SE_47474chr9:130321444-130321790Pancreas
SE_48868chr9:130319239-130325845Right_Atrium
SE_50184chr9:130317343-130325919Sigmoid_Colon
SE_52507chr9:130317294-130325898Small_Intestine
SE_53712chr9:130317359-130322847Spleen
SE_54748chr9:130318900-130321223Stomach_Smooth_Muscle
SE_55718chr9:130319316-130326160u87
SE_57980chr9:130319252-130320789VACO_9m
SE_63440chr9:130298563-130342452NCI-H69
SE_63712chr9:130320459-130321895HSMM
SE_64980chr9:130317080-130319154NHEK
SE_65259chr9:130317505-130323112Pancreatic_islets
SE_67516chr9:130319316-130326160u87
SE_68760chr9:130319056-130321854H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9130319753130319894
Enhancer Sequence
TAATAACCTT TACAATCCAG TGGAGTAGAA GCATCATCAT GCCCATTTTA CAGCCAATGA 60
AACTAAGGCA TAAAGCCTGA CCTAGGGTAC TTGTTCAGCT GCTGGTGGAG CAAGTCTGAG 120
CTGTGAGGCC ACCTGTCCAC CTCAGGGGAG CCCATGGTGA GTTAGCCCGC AGGTACTCAT 180
ATCACAGATG GGAATTAGAA TCACAACCAC GGGCTGGGCG TGGTGGCTCA AACACCTGTA 240
ATCCCAGCAC TTTGGGAGGC CAGGCAGGAG GATGGCTTAG CTCAGGAGTT TGAGACCAGC 300
CTGGGTAACA CAGGGAGACT CTGCCTATAC AAAATATAAA AATAAATTAG CCCCATGTGG 360
TGGTGCACAC CTGGGGTCCC AGCTACTGGG GAGACTGAGG CAGAAGGATT GCCGGAGCCC 420
GGGAGGTTGA GGCTGCAGTA AGCTATAATT GCAATACTGC ACTCCAGCCT GGGCAACAGT 480
GCAAGACCCT GTCTCAAAAA CAAAAATGAA TCACAACCAT GTGAGAAGGG CTACAGGTAC 540
ACACGGGTGG CCAAGGGGCT GTGGGAGCTC AGAGGAAGAG CCTGATCCAG CCTACCAGGA 600
GTGGGGCTAC TGGCTGCAGG GCTTGGTCTG TGAGGGCATT TCAGGGTCTG GGCTTGACCT 660
CGAGGGCACA GGACAGCCTG GAAGGGTCAG TCTGAAGGAG GGTGACACAT GGTTAGTAGC 720
AAGGTCACTC TACTACCAGA GGCTCTTATC CAACCCCTCC ATTGAACCAT GGGGGAAACT 780
GAGGCTTGGA GGAGAGGCAG GAGTTCACCC AAGGCCACAG AGGTCTGAAG CAGGACCGGC 840
CTCCCATCTA CAGAGCTGGA CTCCCAGAAG CCACACAGGG GACTGCAGGA AGAGGGGAGG 900
GAGGGCGGGG GCTCAGCCCC AATTGCACAG GAAGTCTGCC AGGCTCCACC CGGGGGCCTC 960
CAGGCAGGGC AAGCTGCCCA GCCCCCAGCC TGCAGGGCAG GCACCAGAAA CAGCTCCTCT 1020
CGGATTCTGC CACAATCTCA GCAGGAAGAC AGGAAAGCTG AGCTGGGCAG CCTGCTAAAG 1080
TCAGGCCAGG ATTGGAGGTT TGGCCTCCCA GGACCAGGCC GGCTCTCAGG TCACTGAGAA 1140
AGTCACTCCT CTGCTCCAAG AGGGGCCCCT GCCTCTGGCC AGAGAGAAAT GAAGAGTTTC 1200
TGAGATCCCA GTTGGCCTCG GGTCAGGGTG AGTGAAAGGG CTCAGTGTAT TCAACCAGTT 1260
GGCTCAAATC TTTCCCCATC CTGCCACCCT CCTTGAGAGA TGGGGTGACC TCCACTCTAG 1320
AGATGGGGAA CTGAGGCCCA GAGGAGAGAC GCCCCTTGAC CAAGGTCACA CAGTGAGCTG 1380
TGACTGTCCC AAGCTGGGCC AGGAGGGCTG ACCCCAGGAG AGTCCTAGGG GGTCAGCCCC 1440
TACCTCCTTG GAAGAAAGGG CTGCCCCTTC CCCCTCCTCT TTTCCTGGCA GCCTGAAATA 1500
TAGGAGTGGG GGTGGGAGGG GAGTGTGGCT TTGGCTTTTT AAGTCCAACA CAGCCCCTCA 1560
CTGTCTGCGC ATAGACGGGC CTGGGCTGTC TCCTCGGACA CAGGCCCATC TGTGAGGCCC 1620
GCACAGGGCT TGCTTCTCTC CCAGAGAGCT TGTTTGTTTA CCCAGTTTTC ATAATTATAA 1680
GTTCTGCAGC CCCACCCGGC CCAATCATTC CTTCCCTCAC CATCCCTTGC CGTCTGGGGC 1740
CCTGCACGGG TGCGGGGGGT GGGAGTACGA AGTCGGAGAG GGAAAAGCTT CATGCTGGGG 1800
TCAAGGCCCT GGGTTCCAGC CAAGCTCTGG TGCCCCTGAG AGCATAGGCA TGTCCCATCA 1860
TCTTCCTGGG CCTCAGTTTA CTGGGGCATG AGAAAAAGGA GGGGATTGGT TAGAGGAGCT 1920
CATGGGGTCC TCCAGAACTA GGACGAGGAA GGGTCTGGGC CTGAAAAAGA AAAGCAGACA 1980
CTTCTCATCA GCACCTCAAA AATCAAGGCA GGGCTAGGGG AGGTGTGGTA GGGTGAGAGG 2040
CACACACCTT CCCCAGCCCA TCAGGCCTGC CCACCCCAAA GCTCAAACTC AGCTCTCTTT 2100
TCTACCCTTC GCCTCCCAGA GAATACTGCT CTCAAAAAAA GCAAAAACAA AAAGCAAAAC 2160
AGAAGTGCAA TTGTCAGCTC CCTCCTCCTC TAGATGCCTG AATCACCCCT TAAATCTCTG 2220
ACAGGCCGGG CAAAGGACAC ACAGCTTCCC TAAGAATTCA GCTAAAACGC AATTGCCATT 2280
TACTGAGCAC CCTGCACAGG CCAGGAACTG CGCAGTGCAC CTCCCAGAAC CTTCACCCAG 2340
CCCAAAGGCA GGGAGCACCA ATCCCATCTT AGCGACAACT GGACCTCCAA GGAGGAGAGC 2400
TGTGTGCCGA AGGCCACACA GCTTTCAGTG ACAGAAGCAT ACTGCCACCA GGTCAAAGCC 2460
AGACACGCTG CCTCTTGAGA TGGGCCGACT GAGTGCTGAA ACCAACATAC ACTCTGGGAA 2520
ACAAAGATCC ACGGGCTTTG TAACATGAGC CACAGCACAT CCAGCTTGAT GGAACCTTCT 2580
TGGCTGGCAT GAGTTCCATG AGATCAGGGC TCATGTCACT GCTTTGTCCC CAGTTCCCAG 2640
CTCAGGCCAG GAACAGGACA GCTTTCAGAG CAAGCTCTTC CTTCAACGGC AAGATGGCCT 2700
CCTGCAATGT GGAGGTGCTG CACCTGCTCT GTGCCTTCAG TGCAGCCTAA GGCCCACAGG 2760
TTCCTAAGGG GTCACAGCTG GAAGTGCATG CCCGTTGCAC AGATAGGCAA AGTGAGGAGG 2820
AGGCACAGAG AAAAGGAAGG GCTTGTCAGA GGCCTCCAGG CACCCATCCT GGGGAGCCTG 2880
CCTCCTAGCC 2890