EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS040-03353 
Organism
Homo sapiens 
Tissue/cell
Esophagus 
Coordinate
chr1:223920390-223921880 
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: 1             
ChromosomeStartEnd
chr1223921475223921876
Number: 1             
IDChromosomeStartEnd
GH01I223730chr1223917704223922480
Enhancer Sequence
TCTCAGCCTC ATTTTACTCA GCTCTTATTC AAGATGGAGT TGCTCTAGTT CACACGCCTC 60
TGACACATGT TCAGAAATAA TGGTGATTTT CTTCTACAGG TGGGGACGTT AGCATTATAA 120
TGACATGGTA AAGTTCTGAA GGTAACAAGG GGTTGCCTGT TCCAGTTTCT GCCAGTTTTG 180
GGGGTCTTAT CTCCCTCTGG TATCTGGGCA GAGGTCAAGA AGCTCTGGCA CCATCAGGGG 240
CCAGCTTGTT TCTTTAAGCA GCTGTGCCTA CAAATAAAGG GACTAAAGAA AACAATAAGA 300
AAACCCAGTT ATTTCCTGGG GGTTGCTCTG GTATCCAGCG TGTTTTACTT CACCAAGCGC 360
AATTCTTCCC AGTGCAGGCA CTGGGTGTAA CTGTGACAGC CAGCACCAAC CTGCCCACAC 420
ACCTCCTGTC CTGCAGGACT GTCAGCAGCC TCTGCACTAT AGTGTGACAG AGCCACAGGT 480
AGCTCAGGTG TGCCTCAGCC CAGCCTCTCC TGCACTCCCC CTCCCCTGGC TCCCCAACTC 540
TGCCTCACTT CTGTTTGTGA AGGAAAGACA GCAGTAGCGG AAGGGAAAGA AGGAGAAAAT 600
GCAGAGCAAA TATTATGCTT TCCTCTTGGA AAACCTCCAG GAGCTGCAAA TATTAGTAAT 660
CCAGCTGCAT CCCACCCCCC AGGATGGGCT GGGCCTGTCA CACAGCCAAC CTTCAGGATG 720
CAGACACCCA GGCTGGGGAG CACAGCTCTG GAAATTTACT GACATGGCCC TGAATGAATT 780
TATCTTTTCA GTAGAAGGCC CTGGAGTTTA AAGGAGTCAT TCATAAGGTC TGTCTGGGAG 840
TGCCTTGTCC TCAGAGGAGG GTCTGGGTGG GTTGGAGTGG AAGGAAGGGC TGGCTACCTG 900
GTGTGCTCTC CGTGGGTCCC CAAGAAAGGC AGCCCTGCTG GGGGCAGTGA AGCCCTTATC 960
CAGGTCACGT GAGTCTTGGA AGGGGAAGGC TGCTGTGCTT AACGATTCAA AAACACAAAT 1020
CAAACCTCCT TTCCCAAACA AATTAGAAGG TGTGGAGGAA GCTTGAATTC AGAGAGGATT 1080
TCCCAGAGAC CCATAGGCAA AAGTGGCTTA ACTGAGCCCA GTGGGTGTCC CAGAATGGGC 1140
CAGAGAGAAT GACACTAAAA AGTCTTTGAA CAAATGAGCA AATGAATACA GGAATGCTCA 1200
TCTGCCATAG GCACAAACGT GGTAAACGTT CCCTGAGAGA ACTGACAGCC CAGGGGTGCA 1260
GGGAGAGAAA CGGTCCCAAC TGCAGACTGG GTCCCAACTG CAGACTCGGT CCCAACTGCA 1320
GACTCAGGAG GAGGGAGGCT GTTAAGGGGC CGTCTTTCCT TCTGTTATGT GAGGAGAAAA 1380
GCAGGGAAGG GACCTCAAGG CCAGCCTCTC CCAGGAGCTG CTGTTCTCAG CCCCGGGATC 1440
CAGCGCTACA GGGAAGTGCA GGGGAGGCTC CACAGTCCCG GCTGGAGACC 1490