EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS002-10004 
Organism
Homo sapiens 
Tissue/cell
A375 
Coordinate
chr9:130307080-130309270 
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: 2             
ChromosomeStartEnd
chr9130307843130308200
chr9130307429130308679
Number: 1             
IDChromosomeStartEnd
GH09I127533chr9130295863130309594
Enhancer Sequence
CCATGGCTGT TATCTTGGCC TTTGGTGCTG GTAGAATCCC TGCCATGGCA CATTCCCTCA 60
TTCATGGGCC AGCCACATAC TCCTAAGAGG CCACTGGACC TGGGAAGGGA CCTCCAAGAT 120
CAAGTCCAAA CTATCTTTTG GACAGATGGG GAAACTGAGG CTGGGGAAAT GGGGAAAAGC 180
TGCCCAGGGT CCCATTGCCC TGTTAGTGTC CCAGCTCCTC TGAGACCATC TTGGGGAGAA 240
ACAGGTGAAT GGGGCTTTCA CACCCAGCGA ACCCAAGCGA ACCGCAACCT CAGCCCCTCA 300
GCTTCCTCCT CAGCGGAGGA AATCTGGCCT CTGGCCTTGG GGTCCCACGT CTACAGTGCC 360
CTCCTAGCGT CCACCCCTTG TGCCTGGCCA ACTCCTCTTT CTCCTCCCCA GGCTCAAGTG 420
CCACCTCCTC GGAACCCTCC CTCCAGACAA GTCCCGGCCT CCCAGGTCTC CACAGCCTCC 480
CTGGCCTCCA CTCCCACAGC CCCTGGCCTG CTCCCCGGCA CTCCCCTCAA CCACAGTTAA 540
TGCCTCATCT GAGACGCTCC CCGGACTGAG ACTGCTCTCC GCTGTCTCCC CAGCACCCAG 600
CTCCCGCCAG GCCCAGGGGG GTGCTTGATA AACAAGTGCC GAACAAGTGT TAGGTCACCC 660
AGCCTCAGGC GCCAAACAGG TCACCAGGGA GGCCATGGTG GGCAGGGACT CAGTCTGAGG 720
GCACAGGCCG TCTGGGTCTC ATCACAGAGG CAGGTCAGGC CCAACAGAGC CAGGAGTCAG 780
CTGGGGTTTT TCACAAGGCT GCCTTGAAAA CTCTTCTCGG TTGGCAAATA TTTAACCAGG 840
GCTGGGCCAC AACAGGTCTG GTGGGGAAGG GTGAGCTTTG AGGCAGGAGG GCTGGGAGGA 900
GAGGGCGGGG CTGAGGCGGG AGCCCAGAGA AATGCACCCA AAAAAACGGG TGACCCAAAA 960
CCCGCCCACT GGGGCTGCCC TTTCCTTTAC ACCTCGAGGC CGCCTGGTGG GAGGAAGTCC 1020
ATTCCCATCT TGACACAAAC AGAAGGAAAC AAAAGCCCTC TCATCCCCTC CTGCCCCCCA 1080
CCCCGCCTGC CTGGCAGCGG CCCCAGCCCA CAGCCCACAG TGGCAGCTTG TTCTGGGAGC 1140
CCAGGATGAG GCATGCCTGC CGTCTGGGAA CACAGATCCT CGCTGGGAGG GCAGCCCAGG 1200
GGGTGCCGAG GCCCCCAGCA GCGTCACCAC CCAGAGCAGG ACCCACACTC CAGGGGGTGG 1260
GCACCCAAGG CTGCCATCCT GCGGCCCCCT GGCCAAGGCC ACGCCCAAGG AGGAGGCTGA 1320
TCTATGACAG TGATTGTGTA GACACGACCC TCCTTTCCTC TCACATGGAG TCACCCTTTC 1380
CTGTTGACTT TTTCTCCACA ATGTCTCTGG CCTTCATTCC TTTCTTGTCA TCCTCACCAC 1440
CCCCACAGGA GCCTGAGCCT TAGCCAGCCA CCTGTCAAAA CTGCCCAGGC CCCAGAGGAG 1500
CATCCCCACG CCTGTCCACA GGTGCTCCTC ATACCCCTTC TCTCAGTCAC GTCCAGGGCC 1560
GAGGCTGGAC TGGGAACCCA GGGTGCTCTG CTGTGGCTCG TGCACATTGG CAGGTGCCCC 1620
CCACGGGCCT GGACACCTGC CCTGGGCCTG AGAACCCACC ACCAATGTTC CCCTCAGCGT 1680
CCAGCCTGGT GTTGGACCTT GAGATATGCA GGAAGAGCCT GTGGTCAAGC CCTTCCCCCA 1740
AGATGTCCGC AGTGTCAACC ACTCAGCCCC GCCCCATCAG ACAGGTCACA ACCACTGGGG 1800
CAGGGCTGAG GACAGGACCC AGCCCAGATC CCATGTCCTC CATCAGCCAG CGCGGGCCAA 1860
GCCAAAATGG CAGATGTCAG GCGAGTCACC AAGTTCAGGC GAGGCTCTGA GGCTTCATCA 1920
CGATGGCCAA GAAAGGGTTT ATGTTGCTCT CACTCATTCA TTCAGCAATC CTGGCCACTG 1980
GGTACTCAGG AGAGAGTACC CTAATGAGGG AGGCAGATTG TCAACAAAAA CTACAATTAC 2040
TAGGAGCCCC AACTGGGAGA AGCACAGGAG GTCACAGGAG CCCAGGAAGG TGACTGACCA 2100
AGCCTGCAGG GTCACGGAAG CCTCCCAGAG GGAGGTAGCA GCTGAGACAC AAAGAGTCCC 2160
TGCTAGGGGA GGGAGGACAC CGGGAAGGGA 2190