EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS116-03075 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr1:223920120-223922240 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs140084787chr1223920445hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gata4MA0482.1chr1:223920574-223920585TCTTATCTCCC+6.62
Nr5a2MA0505.1chr1:223921780-223921795GACCTCAAGGCCAGC+6.22
USF2MA0526.2chr1:223921349-223921365CCAGGTCACGTGAGTC+6.03
Number of super-enhancer constituents: 27             
IDCoordinateTissue/cell
SE_00224chr1:223917623-223923297Adipose_Nuclei
SE_01908chr1:223920427-223922082Aorta
SE_02306chr1:223920308-223921944Astrocytes
SE_04026chr1:223920429-223923012Brain_Anterior_Caudate
SE_05036chr1:223920530-223922321Brain_Cingulate_Gyrus
SE_05972chr1:223920132-223922577Brain_Hippocampus_Middle
SE_07159chr1:223920244-223923166Brain_Hippocampus_Middle_150
SE_07996chr1:223920284-223922259Brain_Inferior_Temporal_Lobe
SE_09681chr1:223920277-223921825CD14
SE_19702chr1:223921073-223922029CD4p_CD25-_Il17p_PMAstim_Th17
SE_23408chr1:223920555-223922971Colon_Crypt_1
SE_24051chr1:223920713-223921438Colon_Crypt_2
SE_24051chr1:223921499-223922031Colon_Crypt_2
SE_25230chr1:223920636-223922879Colon_Crypt_3
SE_26209chr1:223920732-223921934Duodenum_Smooth_Muscle
SE_26925chr1:223921184-223922005Esophagus
SE_31491chr1:223920239-223923646Gastric
SE_33950chr1:223920559-223921591HCC1954
SE_38254chr1:223917692-223922239HUVEC
SE_41495chr1:223920316-223922995Left_Ventricle
SE_42269chr1:223920225-223923100Lung
SE_45872chr1:223920277-223921720Osteoblasts
SE_49408chr1:223920327-223922010Right_Atrium
SE_50365chr1:223920440-223922961Sigmoid_Colon
SE_53249chr1:223920551-223922027Small_Intestine
SE_65644chr1:223920306-223922506Pancreatic_islets
SE_68376chr1:223892363-223922876TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1223921475223921876
chr1223922041223922091
Number: 1             
IDChromosomeStartEnd
GH01I223730chr1223917704223922480
Enhancer Sequence
ATTATTCATG CCTCCTCTTT TTAGATCACG TAGGGTAACT TCCTGATGTT GCCATGGCAT 60
CTGTAAACTG TCATGGCTCT GGTGGGAGTG TAGCAGTGAG GACGAGCAGA GGTCACTCTT 120
GTCACCATCT TGGTTTTGGT AGGTTTTGGC CGGCTTCTTT ACTGCAACTG TTTTATCAGC 180
AAGGTCTTTA TGACCTGTAT CTTGTGCCGA CTTCCTATCT CATCCTGTGA CTTAGAATGC 240
CTTAACTGTC TGGGAATGCA GCCCAGTAGG TCTCAGCCTC ATTTTACTCA GCTCTTATTC 300
AAGATGGAGT TGCTCTAGTT CACACGCCTC TGACACATGT TCAGAAATAA TGGTGATTTT 360
CTTCTACAGG TGGGGACGTT AGCATTATAA TGACATGGTA AAGTTCTGAA GGTAACAAGG 420
GGTTGCCTGT TCCAGTTTCT GCCAGTTTTG GGGGTCTTAT CTCCCTCTGG TATCTGGGCA 480
GAGGTCAAGA AGCTCTGGCA CCATCAGGGG CCAGCTTGTT TCTTTAAGCA GCTGTGCCTA 540
CAAATAAAGG GACTAAAGAA AACAATAAGA AAACCCAGTT ATTTCCTGGG GGTTGCTCTG 600
GTATCCAGCG TGTTTTACTT CACCAAGCGC AATTCTTCCC AGTGCAGGCA CTGGGTGTAA 660
CTGTGACAGC CAGCACCAAC CTGCCCACAC ACCTCCTGTC CTGCAGGACT GTCAGCAGCC 720
TCTGCACTAT AGTGTGACAG AGCCACAGGT AGCTCAGGTG TGCCTCAGCC CAGCCTCTCC 780
TGCACTCCCC CTCCCCTGGC TCCCCAACTC TGCCTCACTT CTGTTTGTGA AGGAAAGACA 840
GCAGTAGCGG AAGGGAAAGA AGGAGAAAAT GCAGAGCAAA TATTATGCTT TCCTCTTGGA 900
AAACCTCCAG GAGCTGCAAA TATTAGTAAT CCAGCTGCAT CCCACCCCCC AGGATGGGCT 960
GGGCCTGTCA CACAGCCAAC CTTCAGGATG CAGACACCCA GGCTGGGGAG CACAGCTCTG 1020
GAAATTTACT GACATGGCCC TGAATGAATT TATCTTTTCA GTAGAAGGCC CTGGAGTTTA 1080
AAGGAGTCAT TCATAAGGTC TGTCTGGGAG TGCCTTGTCC TCAGAGGAGG GTCTGGGTGG 1140
GTTGGAGTGG AAGGAAGGGC TGGCTACCTG GTGTGCTCTC CGTGGGTCCC CAAGAAAGGC 1200
AGCCCTGCTG GGGGCAGTGA AGCCCTTATC CAGGTCACGT GAGTCTTGGA AGGGGAAGGC 1260
TGCTGTGCTT AACGATTCAA AAACACAAAT CAAACCTCCT TTCCCAAACA AATTAGAAGG 1320
TGTGGAGGAA GCTTGAATTC AGAGAGGATT TCCCAGAGAC CCATAGGCAA AAGTGGCTTA 1380
ACTGAGCCCA GTGGGTGTCC CAGAATGGGC CAGAGAGAAT GACACTAAAA AGTCTTTGAA 1440
CAAATGAGCA AATGAATACA GGAATGCTCA TCTGCCATAG GCACAAACGT GGTAAACGTT 1500
CCCTGAGAGA ACTGACAGCC CAGGGGTGCA GGGAGAGAAA CGGTCCCAAC TGCAGACTGG 1560
GTCCCAACTG CAGACTCGGT CCCAACTGCA GACTCAGGAG GAGGGAGGCT GTTAAGGGGC 1620
CGTCTTTCCT TCTGTTATGT GAGGAGAAAA GCAGGGAAGG GACCTCAAGG CCAGCCTCTC 1680
CCAGGAGCTG CTGTTCTCAG CCCCGGGATC CAGCGCTACA GGGAAGTGCA GGGGAGGCTC 1740
CACAGTCCCG GCTGGAGACC CGGTCAGGCC TGGGTGGCCA CTCTTCTTTG TAGTGGCCAC 1800
CCTCGTGTCA CCAGCAAATG CTTTTGTATC TACACCCTTC TCAGTGCTCC CCCTCTTTTA 1860
AAAAATGTAC TTTCTTTTTT TAAAAAGAGT TGGGTCTTGC CTTGTCACCT ATGCTGGAGT 1920
GCAGTGTTGC TGTCACAGCT CACTGCAAAC TCCACCTCCT GGGCTCAACC CATCCTCCCA 1980
CCTCAGCCTC CCAGGTAGCT GGGACCACAG GCACACACCA GGACACCTCG CCCAGTGCTC 2040
ACTATTTACC TTTATTTCTT CCTTATTCGG ACACCCCTTG CTTCCAAAGA AGAGTTTCGG 2100
AAGGCTCAAG ACGGTGAGAC 2120