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

TagContent
EnhancerAtlas ID
HS182-22077 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr9:130307220-130309600 
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
GACAGATGGG GAAACTGAGG CTGGGGAAAT GGGGAAAAGC TGCCCAGGGT CCCATTGCCC 60
TGTTAGTGTC CCAGCTCCTC TGAGACCATC TTGGGGAGAA ACAGGTGAAT GGGGCTTTCA 120
CACCCAGCGA ACCCAAGCGA ACCGCAACCT CAGCCCCTCA GCTTCCTCCT CAGCGGAGGA 180
AATCTGGCCT CTGGCCTTGG GGTCCCACGT CTACAGTGCC CTCCTAGCGT CCACCCCTTG 240
TGCCTGGCCA ACTCCTCTTT CTCCTCCCCA GGCTCAAGTG CCACCTCCTC GGAACCCTCC 300
CTCCAGACAA GTCCCGGCCT CCCAGGTCTC CACAGCCTCC CTGGCCTCCA CTCCCACAGC 360
CCCTGGCCTG CTCCCCGGCA CTCCCCTCAA CCACAGTTAA TGCCTCATCT GAGACGCTCC 420
CCGGACTGAG ACTGCTCTCC GCTGTCTCCC CAGCACCCAG CTCCCGCCAG GCCCAGGGGG 480
GTGCTTGATA AACAAGTGCC GAACAAGTGT TAGGTCACCC AGCCTCAGGC GCCAAACAGG 540
TCACCAGGGA GGCCATGGTG GGCAGGGACT CAGTCTGAGG GCACAGGCCG TCTGGGTCTC 600
ATCACAGAGG CAGGTCAGGC CCAACAGAGC CAGGAGTCAG CTGGGGTTTT TCACAAGGCT 660
GCCTTGAAAA CTCTTCTCGG TTGGCAAATA TTTAACCAGG GCTGGGCCAC AACAGGTCTG 720
GTGGGGAAGG GTGAGCTTTG AGGCAGGAGG GCTGGGAGGA GAGGGCGGGG CTGAGGCGGG 780
AGCCCAGAGA AATGCACCCA AAAAAACGGG TGACCCAAAA CCCGCCCACT GGGGCTGCCC 840
TTTCCTTTAC ACCTCGAGGC CGCCTGGTGG GAGGAAGTCC ATTCCCATCT TGACACAAAC 900
AGAAGGAAAC AAAAGCCCTC TCATCCCCTC CTGCCCCCCA CCCCGCCTGC CTGGCAGCGG 960
CCCCAGCCCA CAGCCCACAG TGGCAGCTTG TTCTGGGAGC CCAGGATGAG GCATGCCTGC 1020
CGTCTGGGAA CACAGATCCT CGCTGGGAGG GCAGCCCAGG GGGTGCCGAG GCCCCCAGCA 1080
GCGTCACCAC CCAGAGCAGG ACCCACACTC CAGGGGGTGG GCACCCAAGG CTGCCATCCT 1140
GCGGCCCCCT GGCCAAGGCC ACGCCCAAGG AGGAGGCTGA TCTATGACAG TGATTGTGTA 1200
GACACGACCC TCCTTTCCTC TCACATGGAG TCACCCTTTC CTGTTGACTT TTTCTCCACA 1260
ATGTCTCTGG CCTTCATTCC TTTCTTGTCA TCCTCACCAC CCCCACAGGA GCCTGAGCCT 1320
TAGCCAGCCA CCTGTCAAAA CTGCCCAGGC CCCAGAGGAG CATCCCCACG CCTGTCCACA 1380
GGTGCTCCTC ATACCCCTTC TCTCAGTCAC GTCCAGGGCC GAGGCTGGAC TGGGAACCCA 1440
GGGTGCTCTG CTGTGGCTCG TGCACATTGG CAGGTGCCCC CCACGGGCCT GGACACCTGC 1500
CCTGGGCCTG AGAACCCACC ACCAATGTTC CCCTCAGCGT CCAGCCTGGT GTTGGACCTT 1560
GAGATATGCA GGAAGAGCCT GTGGTCAAGC CCTTCCCCCA AGATGTCCGC AGTGTCAACC 1620
ACTCAGCCCC GCCCCATCAG ACAGGTCACA ACCACTGGGG CAGGGCTGAG GACAGGACCC 1680
AGCCCAGATC CCATGTCCTC CATCAGCCAG CGCGGGCCAA GCCAAAATGG CAGATGTCAG 1740
GCGAGTCACC AAGTTCAGGC GAGGCTCTGA GGCTTCATCA CGATGGCCAA GAAAGGGTTT 1800
ATGTTGCTCT CACTCATTCA TTCAGCAATC CTGGCCACTG GGTACTCAGG AGAGAGTACC 1860
CTAATGAGGG AGGCAGATTG TCAACAAAAA CTACAATTAC TAGGAGCCCC AACTGGGAGA 1920
AGCACAGGAG GTCACAGGAG CCCAGGAAGG TGACTGACCA AGCCTGCAGG GTCACGGAAG 1980
CCTCCCAGAG GGAGGTAGCA GCTGAGACAC AAAGAGTCCC TGCTAGGGGA GGGAGGACAC 2040
CGGGAAGGGA GTGTGTGCCA AGCAGAAGAC CCGAGAAAGG CCAAGATTCG GACAGGCATG 2100
AAAGAGTTAA TCCATTCCAC AAAGATTTAT CAGCACGTCC TAGGTCAAGA AGGACCCTTC 2160
AACAGTGCAG TGTCAAGGTC CTGGAACCAG ATCTCAGTTC AAATCCTAAC TCCACCCTTT 2220
GCTGGCTATA GGACTTTCAG CAACACATGG CTCAATTCTC TCTGAACCTC TGTTTCCTCA 2280
GCTGTAACAT GGGAGTAACA GCAACCTGGC CAGGTGCGGT GGCTCACGCC TATAATCCCA 2340
GCACTTTGGG AGGTCACCTA AGGTCAGGAG TTTGAGACCA 2380