EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS195-00541 
Organism
Homo sapiens 
Tissue/cell
VCaP 
Coordinate
chr1:223920250-223922940 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs140084787chr1223920445hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ArMA0007.3chr1:223922394-223922411TGGCACACCATGTACCA-6.01
Gata4MA0482.1chr1:223920574-223920585TCTTATCTCCC+6.62
Nr5a2MA0505.1chr1:223921780-223921795GACCTCAAGGCCAGC+6.22
USF2MA0526.2chr1:223921349-223921365CCAGGTCACGTGAGTC+6.03
Number of super-enhancer constituents: 28             
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_24051chr1:223922112-223922463Colon_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: 3             
ChromosomeStartEnd
chr1223921475223921876
chr1223922041223922091
chr1223922066223922385
Number: 1             
IDChromosomeStartEnd
GH01I223730chr1223917704223922480
Enhancer Sequence
TGGTTTTGGT AGGTTTTGGC CGGCTTCTTT ACTGCAACTG TTTTATCAGC AAGGTCTTTA 60
TGACCTGTAT CTTGTGCCGA CTTCCTATCT CATCCTGTGA CTTAGAATGC CTTAACTGTC 120
TGGGAATGCA GCCCAGTAGG TCTCAGCCTC ATTTTACTCA GCTCTTATTC AAGATGGAGT 180
TGCTCTAGTT CACACGCCTC TGACACATGT TCAGAAATAA TGGTGATTTT CTTCTACAGG 240
TGGGGACGTT AGCATTATAA TGACATGGTA AAGTTCTGAA GGTAACAAGG GGTTGCCTGT 300
TCCAGTTTCT GCCAGTTTTG GGGGTCTTAT CTCCCTCTGG TATCTGGGCA GAGGTCAAGA 360
AGCTCTGGCA CCATCAGGGG CCAGCTTGTT TCTTTAAGCA GCTGTGCCTA CAAATAAAGG 420
GACTAAAGAA AACAATAAGA AAACCCAGTT ATTTCCTGGG GGTTGCTCTG GTATCCAGCG 480
TGTTTTACTT CACCAAGCGC AATTCTTCCC AGTGCAGGCA CTGGGTGTAA CTGTGACAGC 540
CAGCACCAAC CTGCCCACAC ACCTCCTGTC CTGCAGGACT GTCAGCAGCC TCTGCACTAT 600
AGTGTGACAG AGCCACAGGT AGCTCAGGTG TGCCTCAGCC CAGCCTCTCC TGCACTCCCC 660
CTCCCCTGGC TCCCCAACTC TGCCTCACTT CTGTTTGTGA AGGAAAGACA GCAGTAGCGG 720
AAGGGAAAGA AGGAGAAAAT GCAGAGCAAA TATTATGCTT TCCTCTTGGA AAACCTCCAG 780
GAGCTGCAAA TATTAGTAAT CCAGCTGCAT CCCACCCCCC AGGATGGGCT GGGCCTGTCA 840
CACAGCCAAC CTTCAGGATG CAGACACCCA GGCTGGGGAG CACAGCTCTG GAAATTTACT 900
GACATGGCCC TGAATGAATT TATCTTTTCA GTAGAAGGCC CTGGAGTTTA AAGGAGTCAT 960
TCATAAGGTC TGTCTGGGAG TGCCTTGTCC TCAGAGGAGG GTCTGGGTGG GTTGGAGTGG 1020
AAGGAAGGGC TGGCTACCTG GTGTGCTCTC CGTGGGTCCC CAAGAAAGGC AGCCCTGCTG 1080
GGGGCAGTGA AGCCCTTATC CAGGTCACGT GAGTCTTGGA AGGGGAAGGC TGCTGTGCTT 1140
AACGATTCAA AAACACAAAT CAAACCTCCT TTCCCAAACA AATTAGAAGG TGTGGAGGAA 1200
GCTTGAATTC AGAGAGGATT TCCCAGAGAC CCATAGGCAA AAGTGGCTTA ACTGAGCCCA 1260
GTGGGTGTCC CAGAATGGGC CAGAGAGAAT GACACTAAAA AGTCTTTGAA CAAATGAGCA 1320
AATGAATACA GGAATGCTCA TCTGCCATAG GCACAAACGT GGTAAACGTT CCCTGAGAGA 1380
ACTGACAGCC CAGGGGTGCA GGGAGAGAAA CGGTCCCAAC TGCAGACTGG GTCCCAACTG 1440
CAGACTCGGT CCCAACTGCA GACTCAGGAG GAGGGAGGCT GTTAAGGGGC CGTCTTTCCT 1500
TCTGTTATGT GAGGAGAAAA GCAGGGAAGG GACCTCAAGG CCAGCCTCTC CCAGGAGCTG 1560
CTGTTCTCAG CCCCGGGATC CAGCGCTACA GGGAAGTGCA GGGGAGGCTC CACAGTCCCG 1620
GCTGGAGACC CGGTCAGGCC TGGGTGGCCA CTCTTCTTTG TAGTGGCCAC CCTCGTGTCA 1680
CCAGCAAATG CTTTTGTATC TACACCCTTC TCAGTGCTCC CCCTCTTTTA AAAAATGTAC 1740
TTTCTTTTTT TAAAAAGAGT TGGGTCTTGC CTTGTCACCT ATGCTGGAGT GCAGTGTTGC 1800
TGTCACAGCT CACTGCAAAC TCCACCTCCT GGGCTCAACC CATCCTCCCA CCTCAGCCTC 1860
CCAGGTAGCT GGGACCACAG GCACACACCA GGACACCTCG CCCAGTGCTC ACTATTTACC 1920
TTTATTTCTT CCTTATTCGG ACACCCCTTG CTTCCAAAGA AGAGTTTCGG AAGGCTCAAG 1980
ACGGTGAGAC AGACACCTTA TGCACTGCTT CACTCTCCCC CGCAGCTCCC CTCCCTCCTC 2040
ACTGACCCCC GGCCACAACC CTCTCTCCTT GCCCCTCACC AGCCGGCACC CTTGGCAACC 2100
CTGGCACCCT TTCGAGGACA AGACTGCCAA ATGTGGCCAA GGTCTGGCAC ACCATGTACC 2160
AATCGAAACT CCACTTCCCT TGAGTTTCAG TTTCCACGCC TATAAAATTA GCAAATGAAA 2220
AGAGCAAACA CTTGGAGACA CTGTTCTCAA TGCTTTGCAT ATTTTTTTCA TTTAATTCTC 2280
AGTGCCATGA GACAGTCTAT TATTATTAAA CCTATGTTAT ATATGAGGAA ACTGAGGCAC 2340
AGAGGGAGTA GTTTCCCCAG GTCACAGTCA GGATTTGAAC TCCATGGTCT GGCTCTAGTG 2400
TTTCCCAACC ATTCGGGGTG GGAGTGGGAG AGAAACCAGA CTGCTCTCCC TAGAAAACAG 2460
CATGTGTTTG CATGTGTGCC AAATTTGCAC AAAACATTTG GGGTTCCAGG TCTCTAAAGC 2520
CCATCCATGG AACCCCGGTT TCCCTTCTCT CACGTGATCC TAACAACCTG CCGAGGATAC 2580
ACCTCATCAT GATCCTCCTT TCACAGCTGA GAACACACCA GCTTAGAGAA ATTAAGAAGT 2640
GTATCCAAGC TCACACAATC TTAAGTGGCC AGATCAGGAC CAAAATCCAG 2690