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

TagContent
EnhancerAtlas ID
HS042-48692 
Organism
Homo sapiens 
Tissue/cell
Fetal_brain 
Coordinate
chr9:130307030-130309110 
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
CCTCGGCCTC CCGAAGTGCT AGGATTACAG GCATGAGCCA CCGCACCCGG CCATGGCTGT 60
TATCTTGGCC TTTGGTGCTG GTAGAATCCC TGCCATGGCA CATTCCCTCA TTCATGGGCC 120
AGCCACATAC TCCTAAGAGG CCACTGGACC TGGGAAGGGA CCTCCAAGAT CAAGTCCAAA 180
CTATCTTTTG GACAGATGGG GAAACTGAGG CTGGGGAAAT GGGGAAAAGC TGCCCAGGGT 240
CCCATTGCCC TGTTAGTGTC CCAGCTCCTC TGAGACCATC TTGGGGAGAA ACAGGTGAAT 300
GGGGCTTTCA CACCCAGCGA ACCCAAGCGA ACCGCAACCT CAGCCCCTCA GCTTCCTCCT 360
CAGCGGAGGA AATCTGGCCT CTGGCCTTGG GGTCCCACGT CTACAGTGCC CTCCTAGCGT 420
CCACCCCTTG TGCCTGGCCA ACTCCTCTTT CTCCTCCCCA GGCTCAAGTG CCACCTCCTC 480
GGAACCCTCC CTCCAGACAA GTCCCGGCCT CCCAGGTCTC CACAGCCTCC CTGGCCTCCA 540
CTCCCACAGC CCCTGGCCTG CTCCCCGGCA CTCCCCTCAA CCACAGTTAA TGCCTCATCT 600
GAGACGCTCC CCGGACTGAG ACTGCTCTCC GCTGTCTCCC CAGCACCCAG CTCCCGCCAG 660
GCCCAGGGGG GTGCTTGATA AACAAGTGCC GAACAAGTGT TAGGTCACCC AGCCTCAGGC 720
GCCAAACAGG TCACCAGGGA GGCCATGGTG GGCAGGGACT CAGTCTGAGG GCACAGGCCG 780
TCTGGGTCTC ATCACAGAGG CAGGTCAGGC CCAACAGAGC CAGGAGTCAG CTGGGGTTTT 840
TCACAAGGCT GCCTTGAAAA CTCTTCTCGG TTGGCAAATA TTTAACCAGG GCTGGGCCAC 900
AACAGGTCTG GTGGGGAAGG GTGAGCTTTG AGGCAGGAGG GCTGGGAGGA GAGGGCGGGG 960
CTGAGGCGGG AGCCCAGAGA AATGCACCCA AAAAAACGGG TGACCCAAAA CCCGCCCACT 1020
GGGGCTGCCC TTTCCTTTAC ACCTCGAGGC CGCCTGGTGG GAGGAAGTCC ATTCCCATCT 1080
TGACACAAAC AGAAGGAAAC AAAAGCCCTC TCATCCCCTC CTGCCCCCCA CCCCGCCTGC 1140
CTGGCAGCGG CCCCAGCCCA CAGCCCACAG TGGCAGCTTG TTCTGGGAGC CCAGGATGAG 1200
GCATGCCTGC CGTCTGGGAA CACAGATCCT CGCTGGGAGG GCAGCCCAGG GGGTGCCGAG 1260
GCCCCCAGCA GCGTCACCAC CCAGAGCAGG ACCCACACTC CAGGGGGTGG GCACCCAAGG 1320
CTGCCATCCT GCGGCCCCCT GGCCAAGGCC ACGCCCAAGG AGGAGGCTGA TCTATGACAG 1380
TGATTGTGTA GACACGACCC TCCTTTCCTC TCACATGGAG TCACCCTTTC CTGTTGACTT 1440
TTTCTCCACA ATGTCTCTGG CCTTCATTCC TTTCTTGTCA TCCTCACCAC CCCCACAGGA 1500
GCCTGAGCCT TAGCCAGCCA CCTGTCAAAA CTGCCCAGGC CCCAGAGGAG CATCCCCACG 1560
CCTGTCCACA GGTGCTCCTC ATACCCCTTC TCTCAGTCAC GTCCAGGGCC GAGGCTGGAC 1620
TGGGAACCCA GGGTGCTCTG CTGTGGCTCG TGCACATTGG CAGGTGCCCC CCACGGGCCT 1680
GGACACCTGC CCTGGGCCTG AGAACCCACC ACCAATGTTC CCCTCAGCGT CCAGCCTGGT 1740
GTTGGACCTT GAGATATGCA GGAAGAGCCT GTGGTCAAGC CCTTCCCCCA AGATGTCCGC 1800
AGTGTCAACC ACTCAGCCCC GCCCCATCAG ACAGGTCACA ACCACTGGGG CAGGGCTGAG 1860
GACAGGACCC AGCCCAGATC CCATGTCCTC CATCAGCCAG CGCGGGCCAA GCCAAAATGG 1920
CAGATGTCAG GCGAGTCACC AAGTTCAGGC GAGGCTCTGA GGCTTCATCA CGATGGCCAA 1980
GAAAGGGTTT ATGTTGCTCT CACTCATTCA TTCAGCAATC CTGGCCACTG GGTACTCAGG 2040
AGAGAGTACC CTAATGAGGG AGGCAGATTG TCAACAAAAA 2080