EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-83439 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr9:130307070-130309720 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1891730chr9130309028hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF5MA0599.1chr9:130308845-130308855GCCCCGCCCC+6.02
SP2MA0516.2chr9:130308841-130308858CTCAGCCCCGCCCCATC+6.18
SP2MA0516.2chr9:130307978-130307995GAGAGGGCGGGGCTGAG-6.34
Number of super-enhancer constituents: 42             
IDCoordinateTissue/cell
SE_00872chr9:130307100-130309530Adrenal_Gland
SE_01693chr9:130306961-130309439Aorta
SE_02373chr9:130307115-130309071Astrocytes
SE_02928chr9:130307014-130307921Bladder
SE_02928chr9:130307931-130309075Bladder
SE_06387chr9:130306787-130309382Brain_Hippocampus_Middle
SE_09759chr9:130307399-130308808CD14
SE_23282chr9:130307005-130309400Colon_Crypt_1
SE_23944chr9:130307025-130309323Colon_Crypt_2
SE_25019chr9:130306996-130309121Colon_Crypt_3
SE_26215chr9:130306862-130308979Duodenum_Smooth_Muscle
SE_26528chr9:130306979-130309763Esophagus
SE_30306chr9:130307079-130308183Fetal_Muscle
SE_30306chr9:130308225-130308976Fetal_Muscle
SE_31422chr9:130306988-130309744Gastric
SE_34381chr9:130307293-130309172HCT-116
SE_34621chr9:130307025-130309715HeLa
SE_36116chr9:130306964-130309134HMEC
SE_37370chr9:130303549-130309613HSMMtube
SE_38118chr9:130307095-130309348HUVEC
SE_41594chr9:130306994-130309597LNCaP
SE_42140chr9:130306957-130309660Lung
SE_44201chr9:130306954-130309354NHDF-Ad
SE_44773chr9:130307002-130309462NHLF
SE_45705chr9:130295920-130309670Osteoblasts
SE_46654chr9:130307439-130308653Ovary
SE_46654chr9:130308770-130309105Ovary
SE_47421chr9:130307032-130309038Panc1
SE_47474chr9:130307029-130307910Pancreas
SE_47474chr9:130307913-130309626Pancreas
SE_50184chr9:130306967-130309642Sigmoid_Colon
SE_52096chr9:130306944-130309175Skeletal_Muscle_Myoblast
SE_52507chr9:130306965-130309353Small_Intestine
SE_53712chr9:130307483-130308862Spleen
SE_54748chr9:130301339-130309339Stomach_Smooth_Muscle
SE_55718chr9:130307336-130308761u87
SE_63440chr9:130298563-130342452NCI-H69
SE_63712chr9:130306930-130309344HSMM
SE_64980chr9:130307148-130308824NHEK
SE_65259chr9:130301019-130309850Pancreatic_islets
SE_67516chr9:130307336-130308761u87
SE_68760chr9:130306962-130308837H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr9130307843130308200
chr9130307429130308679
chr9130308703130309290
chr9130308124130309455
Number: 1             
IDChromosomeStartEnd
GH09I127533chr9130295863130309594
Enhancer Sequence
CCGCACCCGG CCATGGCTGT TATCTTGGCC TTTGGTGCTG GTAGAATCCC TGCCATGGCA 60
CATTCCCTCA TTCATGGGCC AGCCACATAC TCCTAAGAGG CCACTGGACC TGGGAAGGGA 120
CCTCCAAGAT CAAGTCCAAA CTATCTTTTG GACAGATGGG GAAACTGAGG CTGGGGAAAT 180
GGGGAAAAGC TGCCCAGGGT CCCATTGCCC TGTTAGTGTC CCAGCTCCTC TGAGACCATC 240
TTGGGGAGAA ACAGGTGAAT GGGGCTTTCA CACCCAGCGA ACCCAAGCGA ACCGCAACCT 300
CAGCCCCTCA GCTTCCTCCT CAGCGGAGGA AATCTGGCCT CTGGCCTTGG GGTCCCACGT 360
CTACAGTGCC CTCCTAGCGT CCACCCCTTG TGCCTGGCCA ACTCCTCTTT CTCCTCCCCA 420
GGCTCAAGTG CCACCTCCTC GGAACCCTCC CTCCAGACAA GTCCCGGCCT CCCAGGTCTC 480
CACAGCCTCC CTGGCCTCCA CTCCCACAGC CCCTGGCCTG CTCCCCGGCA CTCCCCTCAA 540
CCACAGTTAA TGCCTCATCT GAGACGCTCC CCGGACTGAG ACTGCTCTCC GCTGTCTCCC 600
CAGCACCCAG CTCCCGCCAG GCCCAGGGGG GTGCTTGATA AACAAGTGCC GAACAAGTGT 660
TAGGTCACCC AGCCTCAGGC GCCAAACAGG TCACCAGGGA GGCCATGGTG GGCAGGGACT 720
CAGTCTGAGG GCACAGGCCG TCTGGGTCTC ATCACAGAGG CAGGTCAGGC CCAACAGAGC 780
CAGGAGTCAG CTGGGGTTTT TCACAAGGCT GCCTTGAAAA CTCTTCTCGG TTGGCAAATA 840
TTTAACCAGG GCTGGGCCAC AACAGGTCTG GTGGGGAAGG GTGAGCTTTG AGGCAGGAGG 900
GCTGGGAGGA GAGGGCGGGG CTGAGGCGGG AGCCCAGAGA AATGCACCCA AAAAAACGGG 960
TGACCCAAAA CCCGCCCACT GGGGCTGCCC TTTCCTTTAC ACCTCGAGGC CGCCTGGTGG 1020
GAGGAAGTCC ATTCCCATCT TGACACAAAC AGAAGGAAAC AAAAGCCCTC TCATCCCCTC 1080
CTGCCCCCCA CCCCGCCTGC CTGGCAGCGG CCCCAGCCCA CAGCCCACAG TGGCAGCTTG 1140
TTCTGGGAGC CCAGGATGAG GCATGCCTGC CGTCTGGGAA CACAGATCCT CGCTGGGAGG 1200
GCAGCCCAGG GGGTGCCGAG GCCCCCAGCA GCGTCACCAC CCAGAGCAGG ACCCACACTC 1260
CAGGGGGTGG GCACCCAAGG CTGCCATCCT GCGGCCCCCT GGCCAAGGCC ACGCCCAAGG 1320
AGGAGGCTGA TCTATGACAG TGATTGTGTA GACACGACCC TCCTTTCCTC TCACATGGAG 1380
TCACCCTTTC CTGTTGACTT TTTCTCCACA ATGTCTCTGG CCTTCATTCC TTTCTTGTCA 1440
TCCTCACCAC CCCCACAGGA GCCTGAGCCT TAGCCAGCCA CCTGTCAAAA CTGCCCAGGC 1500
CCCAGAGGAG CATCCCCACG CCTGTCCACA GGTGCTCCTC ATACCCCTTC TCTCAGTCAC 1560
GTCCAGGGCC GAGGCTGGAC TGGGAACCCA GGGTGCTCTG CTGTGGCTCG TGCACATTGG 1620
CAGGTGCCCC CCACGGGCCT GGACACCTGC CCTGGGCCTG AGAACCCACC ACCAATGTTC 1680
CCCTCAGCGT CCAGCCTGGT GTTGGACCTT GAGATATGCA GGAAGAGCCT GTGGTCAAGC 1740
CCTTCCCCCA AGATGTCCGC AGTGTCAACC ACTCAGCCCC GCCCCATCAG ACAGGTCACA 1800
ACCACTGGGG CAGGGCTGAG GACAGGACCC AGCCCAGATC CCATGTCCTC CATCAGCCAG 1860
CGCGGGCCAA GCCAAAATGG CAGATGTCAG GCGAGTCACC AAGTTCAGGC GAGGCTCTGA 1920
GGCTTCATCA CGATGGCCAA GAAAGGGTTT ATGTTGCTCT CACTCATTCA TTCAGCAATC 1980
CTGGCCACTG GGTACTCAGG AGAGAGTACC CTAATGAGGG AGGCAGATTG TCAACAAAAA 2040
CTACAATTAC TAGGAGCCCC AACTGGGAGA AGCACAGGAG GTCACAGGAG CCCAGGAAGG 2100
TGACTGACCA AGCCTGCAGG GTCACGGAAG CCTCCCAGAG GGAGGTAGCA GCTGAGACAC 2160
AAAGAGTCCC TGCTAGGGGA GGGAGGACAC CGGGAAGGGA GTGTGTGCCA AGCAGAAGAC 2220
CCGAGAAAGG CCAAGATTCG GACAGGCATG AAAGAGTTAA TCCATTCCAC AAAGATTTAT 2280
CAGCACGTCC TAGGTCAAGA AGGACCCTTC AACAGTGCAG TGTCAAGGTC CTGGAACCAG 2340
ATCTCAGTTC AAATCCTAAC TCCACCCTTT GCTGGCTATA GGACTTTCAG CAACACATGG 2400
CTCAATTCTC TCTGAACCTC TGTTTCCTCA GCTGTAACAT GGGAGTAACA GCAACCTGGC 2460
CAGGTGCGGT GGCTCACGCC TATAATCCCA GCACTTTGGG AGGTCACCTA AGGTCAGGAG 2520
TTTGAGACCA GCCTGGCCAA CATGGTGAAA CACCGTCTCT ACTAAAAATA CAAAAATTAG 2580
CTAGGCATGG TGGCGCATGC CTATAATCCC AACTGCTCGG AAGGTTGAGG CAGGAGAATC 2640
GCTTGAACCT 2650