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

TagContent
EnhancerAtlas ID
HS146-07490 
Organism
Homo sapiens 
Tissue/cell
NHDF 
Coordinate
chr19:13171780-13173350 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
USF2MA0526.2chr19:13171876-13171892GGGAGTCACGTGGCCT+6.38
Number of super-enhancer constituents: 32             
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_08780chr19:13172144-13172306Brain_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_41557chr19:13171785-13172566LNCaP
SE_41557chr19:13172631-13174288LNCaP
SE_42481chr19:13160839-13178550Lung
SE_44148chr19:13169444-13174963NHDF-Ad
SE_44758chr19:13170742-13172615NHLF
SE_45899chr19:13170746-13173452Osteoblasts
SE_46667chr19:13171802-13172399Ovary
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
chr191317240013172610
Number: 2             
IDChromosomeStartEnd
GH19I013062chr191317329213176213
GH19I013050chr191316104913173134
Enhancer Sequence
GGGGTAGAGA TCTTCCTTTT CAAGTGTTTA CCAATTGCAG AGACAAGTCT GCACTGCCAA 60
AAGGTGAGGG CATCCTGGGT GCGTTAGGAA TACTCCGGGA GTCACGTGGC CTTAGACCCC 120
CCCCTCCCCC CCAAATCGAG GGCAGCTCCG TTCTGAAAGA AGCAGGCAGG ATTCAGAGCG 180
GCAGCCACAC AGGGTGGGAC CGGGCTCACT GGATAACCCC CAGTCAAGCT ATGCACCTGG 240
CAGGTCCCCC GCCTTCTATT CGCCCACCCA TTTCGCAGTC CCCTTTCCAT CCGGCCCATG 300
CACCGCAAGC TGTTCCTAAT CAATGCGAAC GGGAAACTCG GCCCTCATAT CACGGGATGT 360
GTTTGGCAGC GACAGCAACA GGAGCCGCTG CCACGGGCAG CTCCTTCCTT GGTGCATAAA 420
CCAGGGTCCC AGTGGCCTGG GCCTGAGTGG GTTCTTCTCC TTCCTCTTGG GACCCCCTGG 480
GTATGCAGAG GGAACCACAT CCCCTGGAGC TCTGGGCCGG TCGCTGGCCG CGCCCCGCCG 540
CAGCCCTCGG AGGGCAGCTA GTGTTAACTC GCTGCGCCAC CTAGCTATGG CGTCCAGGAG 600
TGCAGCGCTT CGCTCCCTGA ACCGCGTCGC TTCCTGAGCC GCGCCGCTCC CTGAGCCGTG 660
CTGCTCGGCA GCCTGGGGAA AACCTCTTTT TGGTCCTTCA GGGAGCTATG AATGAGGAAT 720
TTGGCAGCTG TCAGTCGGAG GATCAGTGTC ACTTTGTTCC TTCAGCAGCC TTTGCTGTCC 780
TTATGCAAGC TTGGTACTTT ATAGTATATA AAACTCAAAG TTAAAATATG TTAAAAAAAA 840
ATCTGTAAAA ATCCCCACTC ACATCTCATG TTGCTGAGCA GGTCTTGGTT GTGTTGCACC 900
AAGAAGCAGG AGAGACACAC TGGAGGTCTA ACAGCAGCAA GTCTAGGATT TGGAGCCTAG 960
GCTTCTGATT CCAGGCCCAG GGCTCTATGC AGCACTCGGT GCCGTCCTAT TCAACCCATC 1020
CCTGCCCAGG CTCTTAGGGC TCCAAGCTGG AAATTTGCAG TCAAAGGCCC AGATTCCTCG 1080
TATTTCCTCT GGACAGCTCT GGACAGTGGC TGCCTTCGGG TCTCCAGGGC AAGGAGAAGA 1140
GCAGGCCTGC GAGAGAGTGC TCTGCCTTCC CCTGCTGTGC TGTTCTCAGT GAGGCTCCAG 1200
TTCCTTCCTC TGGTCATTCC AGCCCTTGAG TATGGTGCAA GTATGTTCAG TCCTGTGTCT 1260
GGAACCAGCT CGGCTTTGCA GGAAGATTAG CAGCATCAGG GTTTCCACAT TAATTCACTG 1320
GACATGAGTG TCGGTGGTTG GGCTGCAAGA AAGCTATTCT TTCTTCAGGA GGGGGAAGAT 1380
GTCAGCTAGC TGGTGCCTCT GTTCCCTGGG TGGTCAGTGT AGCCATGGTT TGAAGAAGGA 1440
TCTAGAAGGG TCTCTTTGGA GTCTTATCAT CCACTGCAGC TGTGCTTTGA GATGTGGGGG 1500
ATGTAGCAGC AAACAAAACC AACAGAGAGG GCTTGTCCTC AAGGGGCTGA TGGTCTAGTG 1560
GGGTGTTCCT 1570