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

TagContent
EnhancerAtlas ID
HS158-00420 
Organism
Homo sapiens 
Tissue/cell
Pancreas 
Coordinate
chr1:10735170-10738350 
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MEOX2MA0706.1chr1:10735240-10735250AGTAATTAAC+6.02
RREB1MA0073.1chr1:10735850-10735870CCCCCCCCCACCCCCAACAA+6.91
TFAP2AMA0003.3chr1:10735568-10735579AGCCTCAGGCA+6.32
ZBTB7AMA0750.2chr1:10735575-10735588GGCACTTCCGGGA-6.32
ZIC1MA0696.1chr1:10737869-10737883GGCCCCCTGCTGCG+7.01
ZIC3MA0697.1chr1:10737869-10737884GGCCCCCTGCTGCGG+6.25
ZIC4MA0751.1chr1:10737869-10737884GGCCCCCTGCTGCGG+6.14
ZNF143MA0088.2chr1:10735773-10735789CAGGGCACTATGGGAA-6.24
ZNF263MA0528.1chr1:10737332-10737353GGAGCAGGAGGGGGCAGGGGA+7.4
ZNF740MA0753.2chr1:10735848-10735861ACCCCCCCCCCAC+6.32
Number of super-enhancer constituents: 21             
IDCoordinateTissue/cell
SE_23439chr1:10734421-10736602Colon_Crypt_1
SE_23439chr1:10736646-10738355Colon_Crypt_1
SE_24212chr1:10734337-10736492Colon_Crypt_2
SE_24212chr1:10737206-10737677Colon_Crypt_2
SE_24212chr1:10737778-10738142Colon_Crypt_2
SE_25175chr1:10734217-10738863Colon_Crypt_3
SE_26713chr1:10734646-10736359Esophagus
SE_26713chr1:10736607-10738272Esophagus
SE_28494chr1:10735553-10738837Fetal_Intestine
SE_30102chr1:10736768-10740350Fetal_Muscle
SE_31374chr1:10732699-10751186Gastric
SE_33519chr1:10736191-10741085H2171
SE_37889chr1:10737466-10743900HSMMtube
SE_40607chr1:10733336-10741092Left_Ventricle
SE_41555chr1:10735242-10738779LNCaP
SE_42099chr1:10732695-10754653Lung
SE_47486chr1:10735220-10735816Pancreas
SE_48591chr1:10736516-10740326Right_Atrium
SE_54510chr1:10711383-10754578Stomach_Smooth_Muscle
SE_63296chr1:10733447-10756197NCI-H82
SE_65281chr1:10730535-10740589Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11073668210738250
Number: 1             
IDChromosomeStartEnd
GH01I010662chr11072254410750567
Enhancer Sequence
GCCCATGTTT GCACAGAAAA GCTCACGGCA GGTCCCCCCT CCTGACGAAG TGACTTATTA 60
AAGTTTAAAC AGTAATTAAC AGAACAATAA AAATAAAGGG ATGTTTGGGG AGTCGTAGCG 120
CACACAGGGT TTTTGGCAGT GCCAGCAGTT TTTCAGTGCC CTGCGCTGGC AGCAAAATGT 180
GACTGTGAAG CCAGTGGGGA CAGAGGACGG GGCCAGGGTC GAGCCAGGGA GTCCTGAGGC 240
CTAAAGGGCC AGAAACCCCG AGGCAAGGCT GGCGGGAAGG AATGGGGGTC CTGGGGTGGC 300
AGGGTGGGCA CAGTGCGAGC AGGCGGGGTG GTCTGGCATG GGCAGGGAAC AGGCCTGGGT 360
GGGGAGGCTT CAAGAGGGGT GAGGCCAGTG CCCAGCTCAG CCTCAGGCAC TTCCGGGAGC 420
CCAGTGCCTC GGTCACATCC GGCCAACTCC GCACGGACCT GGCTGGGGGA GGTGCCAGGT 480
CCCCCGACAC TGCGGGCATT AGGAGACCCT GCAGTTAATG ATTCCTGGGG CTGGACCCCA 540
GCCACTCTGG GCTCCTCTCC CAGTTGGGCA GGTACCCCTA CCCCTGCCTC TGGATCCTGT 600
GGCCAGGGCA CTATGGGAAC TCTCCTGGCC CCTATTAAGC ATGGGTAAGG ACTCGGGGGC 660
CAGCCAGCCT AGCACATGAC CCCCCCCCCA CCCCCAACAA AGGGAGAAAG TGGCCAGCTT 720
CCTGGGCCAG GTGGGTCCCC AGCGGCAAAG TCCTCTTTCC CCAAGGTTTG CAGGGAGCTG 780
GCCTGGCAGG CCGGTCCGGG CCAGAGCTGC CTGGGATGGG CAGGGCTAGG CCTGTTACCC 840
TCAGCCTTGC CTCTTCTCCC TCAAGTTCCA TCCCAGGGGC TCAGACACCT GCCTGCCAGG 900
GATGGCAGAG ACAGTCAGGA TGAACCAGGC GCCCAACCCC AGCAGCCAGG GAGGGGCCCC 960
AGGAAGAGGG CGGGGCTCCC CCTGGACCTA GGCCTGCTCA GAGGCTTGGG GGCCAAGGAA 1020
GGAGGGACAG CAGGAACCCC TGAGGGTCAC ACAGAATGTG TGATCTCAGG GTGGTGACAA 1080
ACCCATGCCA ACCAAGTGAC AGACACCAAG GCCCTGCTGG ACTGGCCCGG ACCCCCGTCC 1140
CCCATGCTGC TTCTCATTCC CTCTCCCGGA AGCCCTGGGC TCCCGCTATT GTCGGCCACG 1200
TTGAGGGAGG GCCCCTGCCT GTCCCATGCT CACCCCTGTC CTTCCTCTCC AAGGAGAGCC 1260
ACCACAGAAG CAAAGCTCTC ACTCCATCAC ACAGCGTTAG CCCCAAAAGG TGACCTTTCA 1320
ACAGAACATC CCCAATGCAG GCTCTTCCCA CCAGGACAAA GAAGACACCA AGAGCCCCCG 1380
GGGAGGCCTC TCCACCATCC TCTGAACAAA GGGGCTCTCC TCCTGGGCTC CTCCATCTCT 1440
CTCTGTGCCT CTCCATCTCT CTCTGTGCCT CGGTGGACCA ACCTGCCTAG GGGTGCCCTG 1500
GGATCCTATT TCCACAGCAG GCCTCCCTCC ACCTTGGTGC CTGCCCTCGA CCAGCCTACA 1560
GCTCAGAAAC GAGCCCCTGG CCCGGGGCGA GCAGCCCCAC AGTTTCCTGA CGTGGACGCC 1620
TTTGCTGGTT CCTCCACGTC CCAGCCACAC AGGCCAGCAG GAGCCTCTGT GAAGCCTGCA 1680
TGGAGAAGAG ATGCTGGGCT GGGCCAGAGA CTCTCTCTAA CATCCTGTCT CCCGGGATCT 1740
AGGTCCTGGC AGCTGGCGGG TATCAAGGGC ATGCACTCTG TCCGGGCTGA ACCCCATACT 1800
GCCTGGCTCT GCCACTGCCT CTCGCTGAGG CCCCTGTGGG CACAGCCAGT CAGGGGGTGC 1860
AGGGCCCCAC AGACTTCAGT GCTGCCTGGG CTCTGGCACG TAGGACGTGA AGGAAAGCCA 1920
GCAGCTTTTC TCCCCCTCTT TCCTGGGCAG AGCCCCCTGG GGCTCCATCG CCCCCCGCCT 1980
CCAAGATGAG TGAGTCACGG TGAGGGCAGA GTGGAGGGTC GAGACAGAGA GAGCTCAGGA 2040
GGGGGCAGGT GATGCCTCCC AAGCCTCCAG CCGCTCTGCT CAGGCTGGAA GGAACGCCAG 2100
GAGCTCACAC TCCCTCGCTG CTGGAGGAGG CAGACGGAGT CACCCAGCGC CAAAGCCTCG 2160
CTGGAGCAGG AGGGGGCAGG GGAAGGCACC TTCAGGGTCA GGGGAAGGAT TGACAGAGGG 2220
CAAGGCAGAG GGTGTCTGGG TGGCACCGAG GAGGGCAGGA GGGGACAGGG GCCTTCTCAT 2280
GGGTACGTCT AAAGTGGGCA AACAGGGAAG CAGCTGCTCG TCCTGACCCA CTGTTTCTAG 2340
AACCTGTGTG TGGGGCATGG CAGGGGTGTG GCAAGTGGCT CTGGCTGGAC ACGGAGCTAA 2400
GGAGGGCAGC CTGCACTTAG GTCCAACGCA CCTTGGGACA GGGGACAGCT ATCAGGGTGG 2460
AGGCTGTCCT AGGTGCACAG AACTTTAGAC CTGGAAAGGG ACCGAGGTCC AAGAGGCTGA 2520
GAAACTTGGC AAAAGCCCAG GCCACTCACT CGTGAGGACT AGGCAGATCC AGGGGCCCAG 2580
TTCCCAGTCT GAGCCCTCTC CGGCCCAGCA AATCCAATGC TACACATTTC TGTTTCAAAG 2640
CAGAGCTTTC CGCAGCCTTG GAGATTGCAC CAGGCCCCTC GGGCCCCAAA TACCACAAAG 2700
GCCCCCTGCT GCGGAGGATT TGAGCCACAC ATGGCCCAGT GGGCAAGGAC CCCAAATGGC 2760
TCTGAACCAG CACCTGCGGT GTGCGAGGCC TGGAAGCCAG GCTCCCCCGT TCTCCAGGGG 2820
AAGCAAAGTG GAGGCTGGCT GCGTGGCCTG GCTGACCCAC CGGAAATGGG TAGGACGTGT 2880
GTGGCAGGAG GGGACCTTTC TCTTGCAGGG ACTGAGACCC TGAGACCTTC CAATGTGTGT 2940
TGATGGGGAG ACAGGGCAGG CGCTCTCTGG GGATGAGAGG GAAAGCCTGG ACTAGAGAGG 3000
CCCCGGACAG CAGGCCCAGC CCAGGAGAGG CGGCGGCGTG GGCAGCAGGT GGCAGAGGAA 3060
CACGGGGTGG CACACCACCC GCCCTCCCTG CAGCCCGTCT CCACAATCCC CTTGCTGAGG 3120
CCAGCGACGG CGACCATGAC GAGGACATGA GGGGACTAAT TTAGGAGTAT TTTTAAAACG 3180