EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS176-42818 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr9:130307470-130309180 
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: 1             
ChromosomeStartEnd
chr9130307843130308200
Number: 1             
IDChromosomeStartEnd
GH09I127533chr9130295863130309594
Enhancer Sequence
ACTCCTCTTT CTCCTCCCCA GGCTCAAGTG CCACCTCCTC GGAACCCTCC CTCCAGACAA 60
GTCCCGGCCT CCCAGGTCTC CACAGCCTCC CTGGCCTCCA CTCCCACAGC CCCTGGCCTG 120
CTCCCCGGCA CTCCCCTCAA CCACAGTTAA TGCCTCATCT GAGACGCTCC CCGGACTGAG 180
ACTGCTCTCC GCTGTCTCCC CAGCACCCAG CTCCCGCCAG GCCCAGGGGG GTGCTTGATA 240
AACAAGTGCC GAACAAGTGT TAGGTCACCC AGCCTCAGGC GCCAAACAGG TCACCAGGGA 300
GGCCATGGTG GGCAGGGACT CAGTCTGAGG GCACAGGCCG TCTGGGTCTC ATCACAGAGG 360
CAGGTCAGGC CCAACAGAGC CAGGAGTCAG CTGGGGTTTT TCACAAGGCT GCCTTGAAAA 420
CTCTTCTCGG TTGGCAAATA TTTAACCAGG GCTGGGCCAC AACAGGTCTG GTGGGGAAGG 480
GTGAGCTTTG AGGCAGGAGG GCTGGGAGGA GAGGGCGGGG CTGAGGCGGG AGCCCAGAGA 540
AATGCACCCA AAAAAACGGG TGACCCAAAA CCCGCCCACT GGGGCTGCCC TTTCCTTTAC 600
ACCTCGAGGC CGCCTGGTGG GAGGAAGTCC ATTCCCATCT TGACACAAAC AGAAGGAAAC 660
AAAAGCCCTC TCATCCCCTC CTGCCCCCCA CCCCGCCTGC CTGGCAGCGG CCCCAGCCCA 720
CAGCCCACAG TGGCAGCTTG TTCTGGGAGC CCAGGATGAG GCATGCCTGC CGTCTGGGAA 780
CACAGATCCT CGCTGGGAGG GCAGCCCAGG GGGTGCCGAG GCCCCCAGCA GCGTCACCAC 840
CCAGAGCAGG ACCCACACTC CAGGGGGTGG GCACCCAAGG CTGCCATCCT GCGGCCCCCT 900
GGCCAAGGCC ACGCCCAAGG AGGAGGCTGA TCTATGACAG TGATTGTGTA GACACGACCC 960
TCCTTTCCTC TCACATGGAG TCACCCTTTC CTGTTGACTT TTTCTCCACA ATGTCTCTGG 1020
CCTTCATTCC TTTCTTGTCA TCCTCACCAC CCCCACAGGA GCCTGAGCCT TAGCCAGCCA 1080
CCTGTCAAAA CTGCCCAGGC CCCAGAGGAG CATCCCCACG CCTGTCCACA GGTGCTCCTC 1140
ATACCCCTTC TCTCAGTCAC GTCCAGGGCC GAGGCTGGAC TGGGAACCCA GGGTGCTCTG 1200
CTGTGGCTCG TGCACATTGG CAGGTGCCCC CCACGGGCCT GGACACCTGC CCTGGGCCTG 1260
AGAACCCACC ACCAATGTTC CCCTCAGCGT CCAGCCTGGT GTTGGACCTT GAGATATGCA 1320
GGAAGAGCCT GTGGTCAAGC CCTTCCCCCA AGATGTCCGC AGTGTCAACC ACTCAGCCCC 1380
GCCCCATCAG ACAGGTCACA ACCACTGGGG CAGGGCTGAG GACAGGACCC AGCCCAGATC 1440
CCATGTCCTC CATCAGCCAG CGCGGGCCAA GCCAAAATGG CAGATGTCAG GCGAGTCACC 1500
AAGTTCAGGC GAGGCTCTGA GGCTTCATCA CGATGGCCAA GAAAGGGTTT ATGTTGCTCT 1560
CACTCATTCA TTCAGCAATC CTGGCCACTG GGTACTCAGG AGAGAGTACC CTAATGAGGG 1620
AGGCAGATTG TCAACAAAAA CTACAATTAC TAGGAGCCCC AACTGGGAGA AGCACAGGAG 1680
GTCACAGGAG CCCAGGAAGG TGACTGACCA 1710