EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS045-05657 
Organism
Homo sapiens 
Tissue/cell
Fetal_lung 
Coordinate
chr1:223920320-223922500 
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
CTTGTGCCGA CTTCCTATCT CATCCTGTGA CTTAGAATGC CTTAACTGTC TGGGAATGCA 60
GCCCAGTAGG TCTCAGCCTC ATTTTACTCA GCTCTTATTC AAGATGGAGT TGCTCTAGTT 120
CACACGCCTC TGACACATGT TCAGAAATAA TGGTGATTTT CTTCTACAGG TGGGGACGTT 180
AGCATTATAA TGACATGGTA AAGTTCTGAA GGTAACAAGG GGTTGCCTGT TCCAGTTTCT 240
GCCAGTTTTG GGGGTCTTAT CTCCCTCTGG TATCTGGGCA GAGGTCAAGA AGCTCTGGCA 300
CCATCAGGGG CCAGCTTGTT TCTTTAAGCA GCTGTGCCTA CAAATAAAGG GACTAAAGAA 360
AACAATAAGA AAACCCAGTT ATTTCCTGGG GGTTGCTCTG GTATCCAGCG TGTTTTACTT 420
CACCAAGCGC AATTCTTCCC AGTGCAGGCA CTGGGTGTAA CTGTGACAGC CAGCACCAAC 480
CTGCCCACAC ACCTCCTGTC CTGCAGGACT GTCAGCAGCC TCTGCACTAT AGTGTGACAG 540
AGCCACAGGT AGCTCAGGTG TGCCTCAGCC CAGCCTCTCC TGCACTCCCC CTCCCCTGGC 600
TCCCCAACTC TGCCTCACTT CTGTTTGTGA AGGAAAGACA GCAGTAGCGG AAGGGAAAGA 660
AGGAGAAAAT GCAGAGCAAA TATTATGCTT TCCTCTTGGA AAACCTCCAG GAGCTGCAAA 720
TATTAGTAAT CCAGCTGCAT CCCACCCCCC AGGATGGGCT GGGCCTGTCA CACAGCCAAC 780
CTTCAGGATG CAGACACCCA GGCTGGGGAG CACAGCTCTG GAAATTTACT GACATGGCCC 840
TGAATGAATT TATCTTTTCA GTAGAAGGCC CTGGAGTTTA AAGGAGTCAT TCATAAGGTC 900
TGTCTGGGAG TGCCTTGTCC TCAGAGGAGG GTCTGGGTGG GTTGGAGTGG AAGGAAGGGC 960
TGGCTACCTG GTGTGCTCTC CGTGGGTCCC CAAGAAAGGC AGCCCTGCTG GGGGCAGTGA 1020
AGCCCTTATC CAGGTCACGT GAGTCTTGGA AGGGGAAGGC TGCTGTGCTT AACGATTCAA 1080
AAACACAAAT CAAACCTCCT TTCCCAAACA AATTAGAAGG TGTGGAGGAA GCTTGAATTC 1140
AGAGAGGATT TCCCAGAGAC CCATAGGCAA AAGTGGCTTA ACTGAGCCCA GTGGGTGTCC 1200
CAGAATGGGC CAGAGAGAAT GACACTAAAA AGTCTTTGAA CAAATGAGCA AATGAATACA 1260
GGAATGCTCA TCTGCCATAG GCACAAACGT GGTAAACGTT CCCTGAGAGA ACTGACAGCC 1320
CAGGGGTGCA GGGAGAGAAA CGGTCCCAAC TGCAGACTGG GTCCCAACTG CAGACTCGGT 1380
CCCAACTGCA GACTCAGGAG GAGGGAGGCT GTTAAGGGGC CGTCTTTCCT TCTGTTATGT 1440
GAGGAGAAAA GCAGGGAAGG GACCTCAAGG CCAGCCTCTC CCAGGAGCTG CTGTTCTCAG 1500
CCCCGGGATC CAGCGCTACA GGGAAGTGCA GGGGAGGCTC CACAGTCCCG GCTGGAGACC 1560
CGGTCAGGCC TGGGTGGCCA CTCTTCTTTG TAGTGGCCAC CCTCGTGTCA CCAGCAAATG 1620
CTTTTGTATC TACACCCTTC TCAGTGCTCC CCCTCTTTTA AAAAATGTAC TTTCTTTTTT 1680
TAAAAAGAGT TGGGTCTTGC CTTGTCACCT ATGCTGGAGT GCAGTGTTGC TGTCACAGCT 1740
CACTGCAAAC TCCACCTCCT GGGCTCAACC CATCCTCCCA CCTCAGCCTC CCAGGTAGCT 1800
GGGACCACAG GCACACACCA GGACACCTCG CCCAGTGCTC ACTATTTACC TTTATTTCTT 1860
CCTTATTCGG ACACCCCTTG CTTCCAAAGA AGAGTTTCGG AAGGCTCAAG ACGGTGAGAC 1920
AGACACCTTA TGCACTGCTT CACTCTCCCC CGCAGCTCCC CTCCCTCCTC ACTGACCCCC 1980
GGCCACAACC CTCTCTCCTT GCCCCTCACC AGCCGGCACC CTTGGCAACC CTGGCACCCT 2040
TTCGAGGACA AGACTGCCAA ATGTGGCCAA GGTCTGGCAC ACCATGTACC AATCGAAACT 2100
CCACTTCCCT TGAGTTTCAG TTTCCACGCC TATAAAATTA GCAAATGAAA AGAGCAAACA 2160
CTTGGAGACA CTGTTCTCAA 2180