EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS050-70538 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr9:130323030-130325920 
Number of super-enhancer constituents: 46             
IDCoordinateTissue/cell
SE_00872chr9:130317420-130325981Adrenal_Gland
SE_01693chr9:130322009-130325913Aorta
SE_02373chr9:130323282-130325892Astrocytes
SE_02928chr9:130322679-130324302Bladder
SE_02928chr9:130324345-130325856Bladder
SE_06387chr9:130317152-130326181Brain_Hippocampus_Middle
SE_09759chr9:130322806-130326072CD14
SE_23282chr9:130323163-130325043Colon_Crypt_1
SE_23282chr9:130325132-130325833Colon_Crypt_1
SE_23944chr9:130323262-130324921Colon_Crypt_2
SE_25019chr9:130324113-130324796Colon_Crypt_3
SE_25019chr9:130325377-130325797Colon_Crypt_3
SE_26215chr9:130322499-130326139Duodenum_Smooth_Muscle
SE_26528chr9:130315417-130326976Esophagus
SE_30306chr9:130323737-130325879Fetal_Muscle
SE_31422chr9:130317318-130326302Gastric
SE_34381chr9:130317259-130332904HCT-116
SE_34621chr9:130315344-130339309HeLa
SE_36116chr9:130322946-130325607HMEC
SE_38118chr9:130322586-130326189HUVEC
SE_38969chr9:130317305-130326011IMR90
SE_41594chr9:130323077-130324112LNCaP
SE_41594chr9:130324151-130325102LNCaP
SE_41594chr9:130325172-130325835LNCaP
SE_42140chr9:130317363-130326177Lung
SE_44201chr9:130317110-130326096NHDF-Ad
SE_44773chr9:130317296-130326154NHLF
SE_45705chr9:130315396-130327025Osteoblasts
SE_46654chr9:130323088-130325840Ovary
SE_47421chr9:130319048-130326186Panc1
SE_47474chr9:130322751-130325126Pancreas
SE_47474chr9:130325216-130325839Pancreas
SE_48868chr9:130319239-130325845Right_Atrium
SE_50184chr9:130317343-130325919Sigmoid_Colon
SE_52507chr9:130317294-130325898Small_Intestine
SE_53712chr9:130323006-130326083Spleen
SE_54748chr9:130323218-130326182Stomach_Smooth_Muscle
SE_55718chr9:130319316-130326160u87
SE_57405chr9:130322420-130323990VACO_503
SE_57405chr9:130324273-130325080VACO_503
SE_63440chr9:130298563-130342452NCI-H69
SE_63712chr9:130323123-130324217HSMM
SE_63712chr9:130324355-130325919HSMM
SE_64980chr9:130323149-130325587NHEK
SE_65259chr9:130323187-130326122Pancreatic_islets
SE_67516chr9:130319316-130326160u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr9130323600130325600
chr9130323554130325675
chr9130323277130323553
Enhancer Sequence
AAGAAATAAG GACTACGTGT GTTGGGGGCC AGAGCTCATC ACACCCCTTG ATGGTCTCAC 60
AGGCATGCAC CTCTATTTCT ACATAGAAGC CACCAGCCCT GCCTTTGGAA GGCATCTTGA 120
GACCCCTACA AAAGGGTTTT CAGAGGCAGA GAATTCCCAA GAGTAGATAC TGGCCTTGAG 180
GTCACAGACA GGGAGAAAAG GCACAGAGAG GCATGGCCAT TGGGTCCAGA GTCACACAGC 240
AAGTGGTCAA TGGGACCAGG CTTAAGGCTT ACAAGTCTAG TTCTTGACAC ATGGGTGGGC 300
AAGGAGGGAG CATGTTCCCA TCCATCTTCT AACCCTTTTC CTCTGTGCAC TGCCAAATGC 360
CAGGCACAGA GTGGATGCTG CTGCGGAGTG ACTGACCTTG CTGGAACCAC AGCCCCATCC 420
CACCGTCCTC CAGGAACTCG CTGAATACCC CAGGGGTCCA GGGCCATAGG CTGGTGCTCC 480
TCTGACCTTG GAAGGGAAGA AGATTCTCAT ATTTAGGGCT GCTTAGGAAA GGAGTGGGTC 540
ATGTCAACTT CCTGGAGCAC ATGGCAGGGA GCAGGGGATG CACGAGGCCA CAGACAGACC 600
AGACACATCT CCCTGGGTGT CAAGTTAGCT CAATAAAGTC ACAATCATAA CAGCTACCAC 660
TCACATATTG TCACCTCCCA CCAACACTGT TCTGCGCTGA CCAGGGGACT TGACCTTCAT 720
ACCTTGAGAT GCCAGAACTC TCATCCTCAT GTAAGGAGGG CTCTAAGACT CAGACAGGTT 780
GACTAACTTG CCCCCGAACA CCAGTCCATC CAGTGGCAGA GCCAGGACTC AAACCCAGTC 840
TGACTGCAAA GCCTTACCCC AAAACCTCTG GGCTCCCTGC TTCTTCAGGC TTACCATCCA 900
CCACGTCACC AGGCAGGCCC CTTCACCTTC GTGGGCCAGA AGCAGCCCAG CTCCAAAAAA 960
ATGGGACCAG TCCCAGGGGG TGGACACTTC CTGTTCTTCC AGTTTTAAAA TTTTTGAGAT 1020
CAAAAGATTG TACCCTTCCA TGACTCAGGC CCTAAGATTC TACCAGGAGA AGAGAATGGC 1080
TTTGCTCCAC CCTCACGGGT TTTAAACCTA GGCATCTGCC CGGACTCCTT CCTTAAACCT 1140
CTGCCCAGCA GCGTCTACAG AATACCCTTC TTCCTCCAGC ACAGAAGTGG ATGGGGTGGG 1200
GCAGGGGAAG GAAAAAGCAG TGCAGGAATT TCTGCAACCG CAGGATGATG CTTGCAGGAG 1260
CCCGGGGTGC AGTGAGTCAT GAGCTCTGCC CGCGGGGAAG GAGGAGGGGG GCGCAGGGAC 1320
GGAGAATGGG GCTGGTCAGA GGCTGTGAGT CTCAGACTGA GTAATGACGG GTGGGATAGA 1380
TTTGTGCAAC CTATGGGAGG GAGACTGACA CAAGCTGCTC TATTCCCACT CGGCTCCTCC 1440
TCCCACTTCC TCTCCCCGCC TCCGAAAGCT TACCTCTCTT GGAGGCCTTT TTCAGTGTCC 1500
CCCTGCCCAG TCTGGGCACC ACGGATGACA TACTAATAGC AGAACGTGGT TTAAATAGCT 1560
AAGGCCTTGG ACTATCCGAT CCAGGCCTGC CACTGAGGTG GGAATTCAAT AAGATGATAC 1620
AGACAAAGGA AGGCTTGGCA CATAGCAAGT GCTCAGTTAA ACCGTTGCTA ATGTTTACAG 1680
TTATCACTCC GAGCCTGATT ACTGCCCCTC CCTGCTCTAT CAACCATGTC TTCAGACAGA 1740
AAATATATAT CCATTCCTAC ACACCGCAGG CTAGACTCTA TGGCCACACA CCCAGAGGCC 1800
ATGGTCATCA GTCCCCGTCC CCAGTACACA GGCAGCCCCT TCAAGCCCAC TAGCCCCGAA 1860
CGATGCTCAG AGATGGCAGG AAGGAGCCTC CCTCTAAATG CCCAGGTTGG CGGAAGCAGA 1920
GCACGGGAAG AGTTGGGCTG GGAGATGAAT CGGTCTTCGA CAGGGAAGTT GACTGGAGCC 1980
AGAAAAGAAA CACACACAGT GGCTCTGTTT GCCCCTACAA ACCAACATGT GAGAAACAAC 2040
CTCATGTCCA GCATTAGGGA AAAAGCTGGG AAAGTGACCC TCTGTCCTCA AATGGAATAA 2100
AATGCAGCCT TTGGGGATGC TTCCAGGGAG GTTTTAATGA CCTGGGAGAG ATGTTTACTA 2160
TAGATCATGT AGTGAAAGAA GCAAGACACA AACTTGAGTC ATGGTCCCGG TAAAGTGTAA 2220
TGATCGACAC AGATGGGAAG TACTCCCAGA GGATGAAGTG GTTATCGCAG GACGGCGGGT 2280
GAGTGGTTCC TAGTCCTGTT TTTCCGCTTC ACTCCTTGGA CAGCAGGGAG GGCAGCCATG 2340
GCCCCGCGTG GGTTTAGAAA GGTCCCTTTG GCAGCGTGTG TGGGAAGGAC TAGAGGCTCC 2400
GAGGAGGCTG GAGCAGCTCT GAGTAGGCGA GGCCGGCACT CAGGCCCCAG CAGTGGAAAA 2460
GGAACAGAGT CAGGGGGACT AGAGGAGGCT GGATGGAGGG GAAGGCAGGG TCAAAGCCAA 2520
CAAAAGCATG TTATATAAGA CCCAACAGAG AGACAGCATC ATCCCCAGAC ACTTCGCCCC 2580
CAGGGGCTGA CCCGGACCTT GGCTAAGGGC AGCGGCCCAG GCCCAGGCAC TGCTTCCGGC 2640
CAGCCTGGTC TCTCTGCAAA GTCCAGGGGA GCAAAGAGGA AGCCACACAG CAGGGTGAGG 2700
GGTGGCAGAA GGTGGAACCC CTCCATCCCT TCACTCTTGG CATCTACAGC CACTTCCCAA 2760
ATGTTGAGAG GTAGATTTTT TTTTTTTTTG AGACAGAGTC TCACTCTGTC ACCCAGGCTG 2820
GAGTGCAATG GTGCGATCTC GTCTCACTGC AACCTCCACC TCCCGGGTTC AAGCGATTCT 2880
TGTGCCGCAG 2890