EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-13781 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr19:13171330-13172980 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1382358chr1913171424hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
USF2MA0526.2chr19:13171876-13171892GGGAGTCACGTGGCCT+6.38
Number of super-enhancer constituents: 34             
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_08780chr19:13172464-13173193Brain_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_41557chr19:13172631-13174288LNCaP
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: 2             
ChromosomeStartEnd
chr191317136913172271
chr191317240013172610
Number: 1             
IDChromosomeStartEnd
GH19I013050chr191316104913173134
Enhancer Sequence
TAGGAGAAGC CTGGGTAAGC TGCTAATGGC TGGTAGTATG GGTGTCCAAG GACCTGTTGG 60
AGGAGCCCAG TCCAGCCCTA CATGTGTGAC CCTTGGTGCC TGGCAAGGCG GGGGGGTAGG 120
GAGCAGCCCT CGCACAGCCA GCTAGACTGT TTTGCTCTGG GGCCTGAGGA TTGCGGGGCC 180
AGGGAAGCAA CCAGGCCCAG TCTGGGGCCC TGTGAAGCGA TCTGCACTGC CCAGGGTCAG 240
GGGGATGGGG GGGTCGGCCT CACCTCGGCT AACCTCCCAG CGGAACAAAG GGGCCTTTCT 300
CCACGCCCGC CCGGGAGGGT GTGCCCGCCC GGCTGCTGCC GCCACTGCAG AGGGCGCTGA 360
TTTTTTTTTT CTTCCTGACT TTTCTCCATT TCTGTCTCTG GTTCCTGATC TCTGACTTTT 420
ATTCTCCATT TTTTCACTTT TTATGGGGAT GGGGTAGAGA TCTTCCTTTT CAAGTGTTTA 480
CCAATTGCAG AGACAAGTCT GCACTGCCAA AAGGTGAGGG CATCCTGGGT GCGTTAGGAA 540
TACTCCGGGA GTCACGTGGC CTTAGACCCC CCCCTCCCCC CCAAATCGAG GGCAGCTCCG 600
TTCTGAAAGA AGCAGGCAGG ATTCAGAGCG GCAGCCACAC AGGGTGGGAC CGGGCTCACT 660
GGATAACCCC CAGTCAAGCT ATGCACCTGG CAGGTCCCCC GCCTTCTATT CGCCCACCCA 720
TTTCGCAGTC CCCTTTCCAT CCGGCCCATG CACCGCAAGC TGTTCCTAAT CAATGCGAAC 780
GGGAAACTCG GCCCTCATAT CACGGGATGT GTTTGGCAGC GACAGCAACA GGAGCCGCTG 840
CCACGGGCAG CTCCTTCCTT GGTGCATAAA CCAGGGTCCC AGTGGCCTGG GCCTGAGTGG 900
GTTCTTCTCC TTCCTCTTGG GACCCCCTGG GTATGCAGAG GGAACCACAT CCCCTGGAGC 960
TCTGGGCCGG TCGCTGGCCG CGCCCCGCCG CAGCCCTCGG AGGGCAGCTA GTGTTAACTC 1020
GCTGCGCCAC CTAGCTATGG CGTCCAGGAG TGCAGCGCTT CGCTCCCTGA ACCGCGTCGC 1080
TTCCTGAGCC GCGCCGCTCC CTGAGCCGTG CTGCTCGGCA GCCTGGGGAA AACCTCTTTT 1140
TGGTCCTTCA GGGAGCTATG AATGAGGAAT TTGGCAGCTG TCAGTCGGAG GATCAGTGTC 1200
ACTTTGTTCC TTCAGCAGCC TTTGCTGTCC TTATGCAAGC TTGGTACTTT ATAGTATATA 1260
AAACTCAAAG TTAAAATATG TTAAAAAAAA ATCTGTAAAA ATCCCCACTC ACATCTCATG 1320
TTGCTGAGCA GGTCTTGGTT GTGTTGCACC AAGAAGCAGG AGAGACACAC TGGAGGTCTA 1380
ACAGCAGCAA GTCTAGGATT TGGAGCCTAG GCTTCTGATT CCAGGCCCAG GGCTCTATGC 1440
AGCACTCGGT GCCGTCCTAT TCAACCCATC CCTGCCCAGG CTCTTAGGGC TCCAAGCTGG 1500
AAATTTGCAG TCAAAGGCCC AGATTCCTCG TATTTCCTCT GGACAGCTCT GGACAGTGGC 1560
TGCCTTCGGG TCTCCAGGGC AAGGAGAAGA GCAGGCCTGC GAGAGAGTGC TCTGCCTTCC 1620
CCTGCTGTGC TGTTCTCAGT GAGGCTCCAG 1650