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

TagContent
EnhancerAtlas ID
HS155-14482 
Organism
Homo sapiens 
Tissue/cell
Ovary 
Coordinate
chr9:130307060-130309270 
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
GCATGAGCCA CCGCACCCGG CCATGGCTGT TATCTTGGCC TTTGGTGCTG GTAGAATCCC 60
TGCCATGGCA CATTCCCTCA TTCATGGGCC AGCCACATAC TCCTAAGAGG CCACTGGACC 120
TGGGAAGGGA CCTCCAAGAT CAAGTCCAAA CTATCTTTTG GACAGATGGG GAAACTGAGG 180
CTGGGGAAAT GGGGAAAAGC TGCCCAGGGT CCCATTGCCC TGTTAGTGTC CCAGCTCCTC 240
TGAGACCATC TTGGGGAGAA ACAGGTGAAT GGGGCTTTCA CACCCAGCGA ACCCAAGCGA 300
ACCGCAACCT CAGCCCCTCA GCTTCCTCCT CAGCGGAGGA AATCTGGCCT CTGGCCTTGG 360
GGTCCCACGT CTACAGTGCC CTCCTAGCGT CCACCCCTTG TGCCTGGCCA ACTCCTCTTT 420
CTCCTCCCCA GGCTCAAGTG CCACCTCCTC GGAACCCTCC CTCCAGACAA GTCCCGGCCT 480
CCCAGGTCTC CACAGCCTCC CTGGCCTCCA CTCCCACAGC CCCTGGCCTG CTCCCCGGCA 540
CTCCCCTCAA CCACAGTTAA TGCCTCATCT GAGACGCTCC CCGGACTGAG ACTGCTCTCC 600
GCTGTCTCCC CAGCACCCAG CTCCCGCCAG GCCCAGGGGG GTGCTTGATA AACAAGTGCC 660
GAACAAGTGT TAGGTCACCC AGCCTCAGGC GCCAAACAGG TCACCAGGGA GGCCATGGTG 720
GGCAGGGACT CAGTCTGAGG GCACAGGCCG TCTGGGTCTC ATCACAGAGG CAGGTCAGGC 780
CCAACAGAGC CAGGAGTCAG CTGGGGTTTT TCACAAGGCT GCCTTGAAAA CTCTTCTCGG 840
TTGGCAAATA TTTAACCAGG GCTGGGCCAC AACAGGTCTG GTGGGGAAGG GTGAGCTTTG 900
AGGCAGGAGG GCTGGGAGGA GAGGGCGGGG CTGAGGCGGG AGCCCAGAGA AATGCACCCA 960
AAAAAACGGG TGACCCAAAA CCCGCCCACT GGGGCTGCCC TTTCCTTTAC ACCTCGAGGC 1020
CGCCTGGTGG GAGGAAGTCC ATTCCCATCT TGACACAAAC AGAAGGAAAC AAAAGCCCTC 1080
TCATCCCCTC CTGCCCCCCA CCCCGCCTGC CTGGCAGCGG CCCCAGCCCA CAGCCCACAG 1140
TGGCAGCTTG TTCTGGGAGC CCAGGATGAG GCATGCCTGC CGTCTGGGAA CACAGATCCT 1200
CGCTGGGAGG GCAGCCCAGG GGGTGCCGAG GCCCCCAGCA GCGTCACCAC CCAGAGCAGG 1260
ACCCACACTC CAGGGGGTGG GCACCCAAGG CTGCCATCCT GCGGCCCCCT GGCCAAGGCC 1320
ACGCCCAAGG AGGAGGCTGA TCTATGACAG TGATTGTGTA GACACGACCC TCCTTTCCTC 1380
TCACATGGAG TCACCCTTTC CTGTTGACTT TTTCTCCACA ATGTCTCTGG CCTTCATTCC 1440
TTTCTTGTCA TCCTCACCAC CCCCACAGGA GCCTGAGCCT TAGCCAGCCA CCTGTCAAAA 1500
CTGCCCAGGC CCCAGAGGAG CATCCCCACG CCTGTCCACA GGTGCTCCTC ATACCCCTTC 1560
TCTCAGTCAC GTCCAGGGCC GAGGCTGGAC TGGGAACCCA GGGTGCTCTG CTGTGGCTCG 1620
TGCACATTGG CAGGTGCCCC CCACGGGCCT GGACACCTGC CCTGGGCCTG AGAACCCACC 1680
ACCAATGTTC CCCTCAGCGT CCAGCCTGGT GTTGGACCTT GAGATATGCA GGAAGAGCCT 1740
GTGGTCAAGC CCTTCCCCCA AGATGTCCGC AGTGTCAACC ACTCAGCCCC GCCCCATCAG 1800
ACAGGTCACA ACCACTGGGG CAGGGCTGAG GACAGGACCC AGCCCAGATC CCATGTCCTC 1860
CATCAGCCAG CGCGGGCCAA GCCAAAATGG CAGATGTCAG GCGAGTCACC AAGTTCAGGC 1920
GAGGCTCTGA GGCTTCATCA CGATGGCCAA GAAAGGGTTT ATGTTGCTCT CACTCATTCA 1980
TTCAGCAATC CTGGCCACTG GGTACTCAGG AGAGAGTACC CTAATGAGGG AGGCAGATTG 2040
TCAACAAAAA CTACAATTAC TAGGAGCCCC AACTGGGAGA AGCACAGGAG GTCACAGGAG 2100
CCCAGGAAGG TGACTGACCA AGCCTGCAGG GTCACGGAAG CCTCCCAGAG GGAGGTAGCA 2160
GCTGAGACAC AAAGAGTCCC TGCTAGGGGA GGGAGGACAC CGGGAAGGGA 2210