EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS116-35308 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr9:127043980-127046370 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs7861040chr9127044135hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr9:127045265-127045283GGCAGGAAGGAGGGAATC+6.02
KLF4MA0039.3chr9:127046130-127046141CCACACCCTGC+6.62
PLAG1MA0163.1chr9:127044893-127044907GGGGCCACAGGGGG+6.18
SP8MA0747.1chr9:127044914-127044926GACACGCCCACT+6.37
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_01861chr9:127043953-127046452Aorta
SE_02294chr9:127043937-127045792Astrocytes
SE_03002chr9:127044065-127045325Bladder
SE_03002chr9:127045330-127046413Bladder
SE_04593chr9:127044035-127046338Brain_Anterior_Caudate
SE_06625chr9:127043834-127049648Brain_Hippocampus_Middle
SE_09789chr9:127043706-127046156CD14
SE_23712chr9:127043999-127046004Colon_Crypt_1
SE_24006chr9:127044045-127046083Colon_Crypt_2
SE_26169chr9:127043599-127046347Duodenum_Smooth_Muscle
SE_27460chr9:127044035-127046123Esophagus
SE_29975chr9:127043997-127046387Fetal_Muscle
SE_31765chr9:127044041-127046389Gastric
SE_36996chr9:127041377-127050527HSMMtube
SE_38009chr9:127039597-127046184HUVEC
SE_38868chr9:127043970-127046447IMR90
SE_42506chr9:127043941-127049998Lung
SE_44293chr9:127044212-127046445NHDF-Ad
SE_44809chr9:127043918-127049996NHLF
SE_45648chr9:127040018-127051411Osteoblasts
SE_47283chr9:127041647-127050279Panc1
SE_47557chr9:127044376-127046209Pancreas
SE_49326chr9:127043970-127046367Right_Atrium
SE_50283chr9:127041756-127046427Sigmoid_Colon
SE_52726chr9:127043913-127046460Small_Intestine
SE_54297chr9:127043843-127046283Spleen
SE_60448chr9:127019058-127056389DHL6
SE_65907chr9:127043647-127046632Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr9127044810127045891
chr9127045133127045416
chr9127045925127046114
chr9127044082127044798
Enhancer Sequence
CTAGCCAGGC TGATCTCGAA CTCCCGACCT CAGGTGATCT GCCTACCTCG GCCTCCCAAA 60
GTGCTGGGAT TACAGGCGTA AGCCACCACA CCCGGCCTGT CCTTTCTTTT ATGAAAGATG 120
GTGATACTAG GTGGACGTTT TATTTTAGAT GCCAGAAAAC TCTGGCAACC TATGTCTATC 180
TTCAAAATGT GGGAGAGGCT GTCCAGGCCT GTGACACCTC CAGGCCCGGA AGCCATTGAT 240
GTACTTCTGT ACCCCAGACA CAGAAGTGGA GCCCGGGGCA GACTTTGATG CCTCAAGAAC 300
CTCTGAGTCA TGGCCACACG TGAGCCCCCG GCTCTGCCCT GGTGTGCGGT GGGGCGTATT 360
GGTTTCCTAG GGATATTATA ACAAATTACT GCAAACTGGG TGCTTGAAAA CAATAGAAAT 420
TCATTCTCTC TTGGAGAATC CTGGAGGCGT GATGCCTGAA ATCAGGCTGG TGGTAGGCTC 480
AGTTCCCGTG GAGGCTCTGA CAAAGCACCT GCCGTGCCTT TTTCTGGCTT CTGGCAGGCG 540
CTAGCCACCC TCCTTGTTCC TTGTTCCGTG TTCCGTGGCT CGTCTACACA TCCCTCCAGT 600
GCTCGCCTCT GTCGCCACAT GGCCTTCTTC CTTGTGCGTC TGTCTCTGTG TCCATCCCTC 660
ATAGAAAGAC ACCCGTCATT GAATTTGGGC CACCCTAATC CCATGTGACC CCAGCTTAAC 720
TTGATTAGTA TCTCCAAGTA AGGGCCTATG CCCCAGTTCC AGATAGACAA GGGTTTGGGG 780
GGAACATTAC TCTGGGGGCG TAAGGGATGA GGAGGGCAGG TCCAGGGAGC CTGCCCTCAT 840
TCCCAGGAGG AGACAGGAGA CCAAGGAGCA GAGTCTGGCG GGGGAACGCT GTCACCACAG 900
CAAGGGCCAG GCTGGGGCCA CAGGGGGTGG GTCAGACACG CCCACTGAAT ACTCAGGGGC 960
ACGGGAGGGC CGGGATCCCC CTGACTCTCT GCATCCCAGA TTCATTCCTA CGCTTTCATA 1020
CAGGCCCCAA AGACAAGTGC TGAGTAGATC TGGGTCTTCA GCACGATGTT TTTTAAAAAC 1080
AGGCTTGCAG CGTTTGGTCC TTTGGTGGCA CCAGCCAGGA CCACTGAGGG CTGAGAACGT 1140
CTCAGCGCCC AGCATAGGCC GCCAGCCCTG GCTCTGCTCT TTTGGGTTAG AGAGCGGCCC 1200
CTCCCAGTAA TGACAGGGCC CGCCATTCCC GGCAGCGCCC ACCAGCACAG CCTCCCCCGC 1260
TTTGTGGACA AAGGGCAGCC TGTGGGGCAG GAAGGAGGGA ATCCAGCCTC CCCTGTTCCC 1320
CCAGAGGCCT TTATCTATTT TGGCAAAGGC CCTGTGATCA GACGTTTCCG CCCTGACAAC 1380
TCCCTGCCAA GTGATCTCAA GCAAGGGAGT CCCAGAGCCC TGCTGAGCCC CACTTCTCTC 1440
CTGTGAAGTA GGAGGCACAG TTCCAGCCCT GACCCTCTCA GGAAGGCTGG GGATGACAAG 1500
GCAAACCCTT CCCGTGCCTA GCCCAGGGCC TGGCACATAG TAGGTGCTCA GTCAATACTG 1560
AATGAGAGAG AGCATCTTGG AGCCCAGAAC GTAAATTTCA TGCCACTCCT GCGACGGAGC 1620
CTCAGTGGGG CCTCTTGGGA AGGAGAATCT ATAGGCATTT CCTTCCCCAC GTCCTAGGAC 1680
ACAGTTAGCT GAGACGACCG GGCAGGGGTG GGGAAGTTGA GTGCACGGGT GTAGCACTGG 1740
ACGGAGGACA GAGGCTGCTA AGCTGCATCT CAGGCATTGA TTGGCATTGA GGAAAACCCA 1800
CCTAGACTTG GTATCGCGGG AGGGAGGGTC ATGTGCAGGG AGCCCTGGAA GGGAGCCTGG 1860
AGAGCTGGGT GCCAGCCCTG GCTCTGCACC CCTTACCAGC CATGTGCAGG TCATGGCAGT 1920
GCCCTGTGGA TCCTACTTCC TGAACCTCCC CTCTGCAGGC TTGATGCCAC TGCTGTCATT 1980
TCGGCCTCTA TCCCACAACT CGCACAGGGC TTGCCTCACC TTTAGGCCTT TGCACGTGCC 2040
ATGCCCTCTG CCTGGAGTGC CCTGCCCCTA TTCCTCCACT CAGAGCTGCT TCCCGTTCCG 2100
AGGAAAAATC CCATGCCCCA GGTAGACTGC ACGCACATTT TCTTGTGTTT CCACACCCTG 2160
CTTTGCAGAG CAGCGGGCAC CCTGGTTGTA GTTTAAGGGA CGCCTGAGAG CCCCATTGAG 2220
GATGGAGATT GGTCCCCCTT GCCTGGCACA CGCTTGGTGC CCAGCACTTG TGTGTCCATT 2280
GAGTGAGCAA ATAATGGAAT GTCTGGAGGC ATGTGACGCC TCTGCTGTGT GGCTTGGTTT 2340
CCCCATCTTT AAAATACCAG ATGTGGGCCA GGCGCAGTGG CTCTCGCCTA 2390