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

TagContent
EnhancerAtlas ID
HS110-00298 
Organism
Homo sapiens 
Tissue/cell
KATO3 
Coordinate
chr1:201986440-201988760 
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
ATTTGGAAAA AGGCTTTTAC TTACATTTCC CTTCTGAAGT GTGAGCCAGT TAGACAAAGG 60
GGATGCGGGC CAGGGCGTAG GTCTAGCCTC AGAAGCTGGG GAAGCTTTCA CAGCTACTTA 120
GTCTAAAAAT GACCCCATTT CTTGGAAATT ATGCATTAGA CTCTGGTCTA GTTTCCCTAG 180
CCACAATATC TCGGGGTCCT TGCACCCTTA AAAGAGGTGA CCCAGCTGGG CGCGGTAGTT 240
CACGCCTGTA ATCCTCGTAC TTTGGGAAGC CAAGGCGGGA GGATCACGAG GTCAGAAGAT 300
CGAGGCCATC ATGGCCAACA CGGTGAAACC CCGTCTCTAC TAAACATACA AAAATTAGCT 360
GGGCATGCTG GCACGCGCCT GTAGTCCGAG CTACTCAGGA GGCTGAGGCA GGAGAATCAC 420
TTGAACCCAG GAGGCGGAGG TTGCAGTGAG CTAAGATCAT GCCACTGCAC TCCAGCCTGG 480
TGACACAGGG AGACTCTGTC TCAAAAAAAA GAAGAGAGGT GACCCAGTGT GGCCTGAAGT 540
CACCTAGCCA AGAAGTGGGG GAGGGGCCTC TAGAGCCCGG GACATGCTTG TTCAGCCTCC 600
CTTGACTCCC AGCCTCTTCA GCTTCTAAAG GAGATCCTAG CAGGGAGGAG GGCTGGGAAT 660
ATGGCGCTCA GCCCCTTCAC CCTCTTCTGG AGGGCTGGGG GCAGGTGCTG CCCGCTGCGT 720
GCTGACCTTT GCCCTGCCAT TTGCAGTTTA TGAGGCGCTT TCCTCATCCC ATTATCTCAT 780
TTGATCCGCC CCACAGCTCG CTGAGGAGAC CAGGTGTCCC CATTTTACTG ACAAGGCTAG 840
TGGTGGGCTG AAGTCACTGA CTGGGTGAGA GCGGGGCCAG CTCACAGCAT GCCTGCCTCC 900
ACGCTGCAGC TCAGTGAGAC CACCTGGGCA GGTGGCCTCT GCAGGGCAGC GCCTGGGACA 960
GCCTGGAAGA CGGCAGCTCT GGGAGGGACG CCTTTCTCCC CAACAGTTCT CTGCCCTCTC 1020
ACCCCTCAGG ATGCTGCAGA GTCCTGGCAC GGGCCCCTGG GCTGGCCTCC GTGCTGCCCT 1080
CTCTGTCGGG CACCAGTCAC CCTTACCCCG ACTCTCACCA GCCCAGGGGC CTCCTAGCAG 1140
GAGACGGCCC GGTCTCTCGC CCACCAGAGT CTGCATCCCC TCAGGTGTGT CCTGGGCTGG 1200
GGAGTGGGGG TGGGGAGGAA GCCACAGGGC CGGGCTGTTT ATATCCCGCC CTGCCGGAGC 1260
TGCTGGTCAC CTCTTATCTG CTTCTGTGGG ATTGGGTGTG TCGCTGAGCA GGTCAGAGGG 1320
AGGTCACCCC TCCCGTCGTG TTTGGGTGTG CCTGAGGAGG GGCTGGGGTT GGCCCCCTGG 1380
GACAGTTCCT GGCTTATCCC ACAGCCCCAC CTGTCCCACC AATTCTGGGG AAGTCTGGCT 1440
TCTCCTGGGG GAAGTGGGTG AAGGGGTTGC ATTTCTGAGG AGTCTGGTTT CAATCTGCTC 1500
TCTCTCTCTG CTGTTGTCTG TTTACACATC TCTCTCTCTC GCCGGGCTGT GAGCACCTCT 1560
GGGCAAGTGC TGGGGCTTAC TCACCTCAGC ACCTTGCACA GCGCCTGGCA CAGAGGAGGT 1620
GCTCGATAAA TATTTGCTAA ATGGCCCCGT GACTCTCCCT GCCCTGGCCA CTACCTCCCC 1680
CACACACCAC ACACATTCAT ACACACTCAT GGGAACCAAA GTCACACACA CTCACACTCA 1740
CAAAGATAAA TATTCACAAG CCCTCACTCA CATGCCCCTG CACGCACTGC AGACGCTGCC 1800
TGCTCTCACA CACTCGCATG GACCGTATTC ACAACCTCAC ACACTTGCAC ACACCAGCGC 1860
ACGCAACACA CTCCCACCTC ACAGTCTCAC ATAGCCACAC CCAGGCCTGC CTGCACGACT 1920
CACCTCCTCC CTCGGGGTCC TTCTATGAAG CATTTCCTGA CCTCCTCTTT GGCCCTTTTC 1980
CCCCACCAGA TGGGTTCAGC CCTTGCCTCC AGTCAGGACA GGCCTGGTAA TTTGCAGAGC 2040
CCAGTGCAAA GTGAAAGCCT GGGCCCTTGT TAAAGAATTA TTAGGCTGGG CGCAGTGGCT 2100
CATGCCAGTA ATCCCACACT TTGGGAGGCC GAGGCGGGTG GATCGCCTGA GGTCAGGAGT 2160
TTGAGACCAG CCTGACCAAC ATGGCGAAAC CCCATCTCTA CTAAAAATAC AAAATTAGCT 2220
GGGCGTGGTG GTGTGCGCCT GTAATCCTAG CTACTCTGGA GGTTGAGGCA GAAGAATCGC 2280
TTGAACCTGG GAGGCGGAGG TTGCCGTGAA CCAAGATCAT 2320