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

TagContent
EnhancerAtlas ID
HS081-01624 
Organism
Homo sapiens 
Tissue/cell
HACAT 
Coordinate
chr1:201986510-201988730 
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Klf1MA0493.1chr1:201988332-201988343AGCCACACCCA+6.14
NR2C2MA0504.1chr1:201987451-201987466TGCCCTCTCACCCCT-6.45
NR2C2MA0504.1chr1:201987162-201987177TGACCTTTGCCCTGC-6.4
Nr2f6MA0677.1chr1:201987162-201987176TGACCTTTGCCCTG-6.45
RARA(var.2)MA0730.1chr1:201987749-201987766AGGTCAGAGGGAGGTCA+6.41
RESTMA0138.2chr1:201988024-201988045CTCAGCACCTTGCACAGCGCC+7.87
RxraMA0512.2chr1:201987162-201987176TGACCTTTGCCCTG-6.09
Stat4MA0518.1chr1:201986574-201986588CCATTTCTTGGAAA-6.27
ZfxMA0146.2chr1:201988564-201988578GAGGCCGAGGCGGG-6.01
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_23058chr1:201983954-201986869Colon_Crypt_1
SE_23058chr1:201986872-201988608Colon_Crypt_1
SE_23723chr1:201986197-201986763Colon_Crypt_2
SE_23723chr1:201986912-201988613Colon_Crypt_2
SE_24689chr1:201983940-201986805Colon_Crypt_3
SE_24689chr1:201986888-201988638Colon_Crypt_3
SE_25977chr1:201976074-201988947Duodenum_Smooth_Muscle
SE_26730chr1:201985712-201988797Esophagus
SE_27624chr1:201975812-201989193Fetal_Intestine
SE_28545chr1:201974530-201989440Fetal_Intestine_Large
SE_31432chr1:201983938-201989177Gastric
SE_33417chr1:201986876-201989229H2171
SE_33792chr1:201978127-201990221HCC1954
SE_34304chr1:201974676-201989923HCT-116
SE_34741chr1:201985668-201989981HeLa
SE_41626chr1:201986352-201986765LNCaP
SE_41626chr1:201986861-201988608LNCaP
SE_43434chr1:201986069-201986790MCF-7
SE_43434chr1:201986862-201988630MCF-7
SE_47796chr1:201986464-201986785Pancreas
SE_47796chr1:201986886-201988593Pancreas
SE_50066chr1:201978058-201988672Sigmoid_Colon
SE_52354chr1:201976011-201988714Small_Intestine
SE_56834chr1:201983957-201986837VACO_400
SE_56834chr1:201986879-201988600VACO_400
SE_57376chr1:201986910-201988595VACO_503
SE_57945chr1:201986912-201988581VACO_9m
SE_65333chr1:201986253-201989108Pancreatic_islets
SE_67013chr1:201986876-201989229H2171
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr1201987200201988600
chr1201987611201988279
chr1201986905201988549
Enhancer Sequence
CAGGGCGTAG GTCTAGCCTC AGAAGCTGGG GAAGCTTTCA CAGCTACTTA GTCTAAAAAT 60
GACCCCATTT CTTGGAAATT ATGCATTAGA CTCTGGTCTA GTTTCCCTAG CCACAATATC 120
TCGGGGTCCT TGCACCCTTA AAAGAGGTGA CCCAGCTGGG CGCGGTAGTT CACGCCTGTA 180
ATCCTCGTAC TTTGGGAAGC CAAGGCGGGA GGATCACGAG GTCAGAAGAT CGAGGCCATC 240
ATGGCCAACA CGGTGAAACC CCGTCTCTAC TAAACATACA AAAATTAGCT GGGCATGCTG 300
GCACGCGCCT GTAGTCCGAG CTACTCAGGA GGCTGAGGCA GGAGAATCAC TTGAACCCAG 360
GAGGCGGAGG TTGCAGTGAG CTAAGATCAT GCCACTGCAC TCCAGCCTGG TGACACAGGG 420
AGACTCTGTC TCAAAAAAAA GAAGAGAGGT GACCCAGTGT GGCCTGAAGT CACCTAGCCA 480
AGAAGTGGGG GAGGGGCCTC TAGAGCCCGG GACATGCTTG TTCAGCCTCC CTTGACTCCC 540
AGCCTCTTCA GCTTCTAAAG GAGATCCTAG CAGGGAGGAG GGCTGGGAAT ATGGCGCTCA 600
GCCCCTTCAC CCTCTTCTGG AGGGCTGGGG GCAGGTGCTG CCCGCTGCGT GCTGACCTTT 660
GCCCTGCCAT TTGCAGTTTA TGAGGCGCTT TCCTCATCCC ATTATCTCAT TTGATCCGCC 720
CCACAGCTCG CTGAGGAGAC CAGGTGTCCC CATTTTACTG ACAAGGCTAG TGGTGGGCTG 780
AAGTCACTGA CTGGGTGAGA GCGGGGCCAG CTCACAGCAT GCCTGCCTCC ACGCTGCAGC 840
TCAGTGAGAC CACCTGGGCA GGTGGCCTCT GCAGGGCAGC GCCTGGGACA GCCTGGAAGA 900
CGGCAGCTCT GGGAGGGACG CCTTTCTCCC CAACAGTTCT CTGCCCTCTC ACCCCTCAGG 960
ATGCTGCAGA GTCCTGGCAC GGGCCCCTGG GCTGGCCTCC GTGCTGCCCT CTCTGTCGGG 1020
CACCAGTCAC CCTTACCCCG ACTCTCACCA GCCCAGGGGC CTCCTAGCAG GAGACGGCCC 1080
GGTCTCTCGC CCACCAGAGT CTGCATCCCC TCAGGTGTGT CCTGGGCTGG GGAGTGGGGG 1140
TGGGGAGGAA GCCACAGGGC CGGGCTGTTT ATATCCCGCC CTGCCGGAGC TGCTGGTCAC 1200
CTCTTATCTG CTTCTGTGGG ATTGGGTGTG TCGCTGAGCA GGTCAGAGGG AGGTCACCCC 1260
TCCCGTCGTG TTTGGGTGTG CCTGAGGAGG GGCTGGGGTT GGCCCCCTGG GACAGTTCCT 1320
GGCTTATCCC ACAGCCCCAC CTGTCCCACC AATTCTGGGG AAGTCTGGCT TCTCCTGGGG 1380
GAAGTGGGTG AAGGGGTTGC ATTTCTGAGG AGTCTGGTTT CAATCTGCTC TCTCTCTCTG 1440
CTGTTGTCTG TTTACACATC TCTCTCTCTC GCCGGGCTGT GAGCACCTCT GGGCAAGTGC 1500
TGGGGCTTAC TCACCTCAGC ACCTTGCACA GCGCCTGGCA CAGAGGAGGT GCTCGATAAA 1560
TATTTGCTAA ATGGCCCCGT GACTCTCCCT GCCCTGGCCA CTACCTCCCC CACACACCAC 1620
ACACATTCAT ACACACTCAT GGGAACCAAA GTCACACACA CTCACACTCA CAAAGATAAA 1680
TATTCACAAG CCCTCACTCA CATGCCCCTG CACGCACTGC AGACGCTGCC TGCTCTCACA 1740
CACTCGCATG GACCGTATTC ACAACCTCAC ACACTTGCAC ACACCAGCGC ACGCAACACA 1800
CTCCCACCTC ACAGTCTCAC ATAGCCACAC CCAGGCCTGC CTGCACGACT CACCTCCTCC 1860
CTCGGGGTCC TTCTATGAAG CATTTCCTGA CCTCCTCTTT GGCCCTTTTC CCCCACCAGA 1920
TGGGTTCAGC CCTTGCCTCC AGTCAGGACA GGCCTGGTAA TTTGCAGAGC CCAGTGCAAA 1980
GTGAAAGCCT GGGCCCTTGT TAAAGAATTA TTAGGCTGGG CGCAGTGGCT CATGCCAGTA 2040
ATCCCACACT TTGGGAGGCC GAGGCGGGTG GATCGCCTGA GGTCAGGAGT TTGAGACCAG 2100
CCTGACCAAC ATGGCGAAAC CCCATCTCTA CTAAAAATAC AAAATTAGCT GGGCGTGGTG 2160
GTGTGCGCCT GTAATCCTAG CTACTCTGGA GGTTGAGGCA GAAGAATCGC TTGAACCTGG 2220