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

TagContent
EnhancerAtlas ID
HS116-16932 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr19:13170780-13172340 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1382358chr1913171424hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
SP1MA0079.4chr19:13171209-13171224GAGGGGCGTGGTCAG-6.19
SP4MA0685.1chr19:13171207-13171224GGGAGGGGCGTGGTCAG-6.01
USF2MA0526.2chr19:13171876-13171892GGGAGTCACGTGGCCT+6.38
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_00024chr19:13160708-13176960Adipose_Nuclei
SE_01540chr19:13160665-13178618Aorta
SE_02418chr19:13171180-13172515Astrocytes
SE_03137chr19:13170783-13178623Brain_Angular_Gyrus
SE_03859chr19:13170623-13178764Brain_Anterior_Caudate
SE_04986chr19:13170672-13191599Brain_Cingulate_Gyrus
SE_05848chr19:13160560-13191529Brain_Hippocampus_Middle
SE_06678chr19:13160758-13191322Brain_Hippocampus_Middle_150
SE_07717chr19:13170719-13191634Brain_Inferior_Temporal_Lobe
SE_08780chr19:13171120-13171533Brain_Mid_Frontal_Lobe
SE_08780chr19:13172144-13172306Brain_Mid_Frontal_Lobe
SE_26520chr19:13170726-13172925Esophagus
SE_29770chr19:13170653-13173122Fetal_Muscle
SE_31390chr19:13170808-13172511Gastric
SE_33451chr19:13170810-13173012H2171
SE_35947chr19:13170773-13172690HMEC
SE_40665chr19:13170765-13182230Left_Ventricle
SE_41557chr19:13170783-13171698LNCaP
SE_41557chr19:13171785-13172566LNCaP
SE_42481chr19:13160839-13178550Lung
SE_44148chr19:13169444-13174963NHDF-Ad
SE_44758chr19:13170742-13172615NHLF
SE_45899chr19:13170746-13173452Osteoblasts
SE_46667chr19:13170877-13171728Ovary
SE_46667chr19:13171802-13172399Ovary
SE_47172chr19:13160769-13173616Panc1
SE_47634chr19:13170755-13172452Pancreas
SE_48143chr19:13169567-13183512Psoas_Muscle
SE_48559chr19:13170693-13178599Right_Atrium
SE_51076chr19:13169565-13183749Skeletal_Muscle
SE_54519chr19:13170666-13172644Stomach_Smooth_Muscle
SE_57153chr19:13171180-13172733VACO_400
SE_67980chr19:13100968-13183275TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr191317136913172271
Number: 1             
IDChromosomeStartEnd
GH19I013050chr191316104913173134
Enhancer Sequence
AGTAGAGACG GGGTTTCACC ATTGTTGCCC TGGGTGGTCT CGAACTCCTG AGCTCAGGCG 60
ATCCACTCGC CTCAGCCTCT CAAAGTGCTG AGATTACAGG CATGAGCCAC CGCACCCGGC 120
CAAGAGGAAC GCTTTTGGCC TCCATTTCTT CCCTCCACTT CAGCCTCTGC TTTGGCAGGC 180
TCTGGGGTGG GAGTAAGCCT GTTCTCAGCT CCCCTTTACT AGGGACAGGT AATTCCACTC 240
TGGCTGCTCC TTGGAGAACA GAGTGGATGA ACTCAGTCCC CACCTCTCAG AGGGACCTAG 300
TACAGAGCCC AGCCCCCACT CTGAGGAAGC CTTGGATGGG CCATTCCTGG CCCAGAGCCT 360
GAGGCCATTG GAAAGGGCCT ATATCTGGAA CGGGTGAAGG AGAGAGCCCG GGAGCCTCAC 420
TGTGGGTGGG AGGGGCGTGG TCAGCCAGCC TTGCCTCCTG GGGCATCAGC TCCCAGCTTG 480
TGCTGCACCC TCTGACCACA ACTTTGTGGG GCGCCTGCTG TGTGCAGAAT CTACCCCGAA 540
ACCTATAGCT TAGGAGAAGC CTGGGTAAGC TGCTAATGGC TGGTAGTATG GGTGTCCAAG 600
GACCTGTTGG AGGAGCCCAG TCCAGCCCTA CATGTGTGAC CCTTGGTGCC TGGCAAGGCG 660
GGGGGGTAGG GAGCAGCCCT CGCACAGCCA GCTAGACTGT TTTGCTCTGG GGCCTGAGGA 720
TTGCGGGGCC AGGGAAGCAA CCAGGCCCAG TCTGGGGCCC TGTGAAGCGA TCTGCACTGC 780
CCAGGGTCAG GGGGATGGGG GGGTCGGCCT CACCTCGGCT AACCTCCCAG CGGAACAAAG 840
GGGCCTTTCT CCACGCCCGC CCGGGAGGGT GTGCCCGCCC GGCTGCTGCC GCCACTGCAG 900
AGGGCGCTGA TTTTTTTTTT CTTCCTGACT TTTCTCCATT TCTGTCTCTG GTTCCTGATC 960
TCTGACTTTT ATTCTCCATT TTTTCACTTT TTATGGGGAT GGGGTAGAGA TCTTCCTTTT 1020
CAAGTGTTTA CCAATTGCAG AGACAAGTCT GCACTGCCAA AAGGTGAGGG CATCCTGGGT 1080
GCGTTAGGAA TACTCCGGGA GTCACGTGGC CTTAGACCCC CCCCTCCCCC CCAAATCGAG 1140
GGCAGCTCCG TTCTGAAAGA AGCAGGCAGG ATTCAGAGCG GCAGCCACAC AGGGTGGGAC 1200
CGGGCTCACT GGATAACCCC CAGTCAAGCT ATGCACCTGG CAGGTCCCCC GCCTTCTATT 1260
CGCCCACCCA TTTCGCAGTC CCCTTTCCAT CCGGCCCATG CACCGCAAGC TGTTCCTAAT 1320
CAATGCGAAC GGGAAACTCG GCCCTCATAT CACGGGATGT GTTTGGCAGC GACAGCAACA 1380
GGAGCCGCTG CCACGGGCAG CTCCTTCCTT GGTGCATAAA CCAGGGTCCC AGTGGCCTGG 1440
GCCTGAGTGG GTTCTTCTCC TTCCTCTTGG GACCCCCTGG GTATGCAGAG GGAACCACAT 1500
CCCCTGGAGC TCTGGGCCGG TCGCTGGCCG CGCCCCGCCG CAGCCCTCGG AGGGCAGCTA 1560