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

TagContent
EnhancerAtlas ID
HS118-01557 
Organism
Homo sapiens 
Tissue/cell
Liver 
Coordinate
chr1:204445820-204449200 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1980050chr1204446688hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr1:204448382-204448403TCCTCCCCTCTTCCCTCACCC-6.43
ZNF263MA0528.1chr1:204448378-204448399TTCCTCCTCCCCTCTTCCCTC-6
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_00064chr1:204447165-204449222Adipose_Nuclei
SE_01898chr1:204446732-204449955Aorta
SE_03188chr1:204445701-204449764Brain_Angular_Gyrus
SE_03975chr1:204443311-204451730Brain_Anterior_Caudate
SE_04850chr1:204441602-204452008Brain_Cingulate_Gyrus
SE_05834chr1:204441572-204454041Brain_Hippocampus_Middle
SE_06778chr1:204441694-204452486Brain_Hippocampus_Middle_150
SE_07775chr1:204441566-204452208Brain_Inferior_Temporal_Lobe
SE_10905chr1:204440571-204455347CD20
SE_24481chr1:204446396-204446926Colon_Crypt_2
SE_24481chr1:204447117-204447620Colon_Crypt_2
SE_24481chr1:204447850-204448210Colon_Crypt_2
SE_24481chr1:204448283-204449367Colon_Crypt_2
SE_25125chr1:204446211-204447705Colon_Crypt_3
SE_25125chr1:204447777-204450200Colon_Crypt_3
SE_25573chr1:204447782-204451557DND41
SE_26688chr1:204446142-204447580Esophagus
SE_26688chr1:204447747-204450316Esophagus
SE_31610chr1:204446257-204447742Gastric
SE_31610chr1:204447799-204450438Gastric
SE_37407chr1:204442628-204450806HSMMtube
SE_42225chr1:204446187-204447730Lung
SE_42225chr1:204447736-204452375Lung
SE_49909chr1:204444472-204450053RPMI-8402
SE_50149chr1:204447708-204450485Sigmoid_Colon
SE_52421chr1:204446127-204447357Small_Intestine
SE_52421chr1:204447689-204449720Small_Intestine
SE_58430chr1:204415099-204506026Ly1
SE_59794chr1:204415680-204491493Ly4
SE_61475chr1:204430067-204500813Toledo
SE_62377chr1:204415291-204492168Tonsil
SE_65868chr1:204446405-204446982Pancreatic_islets
SE_65868chr1:204448014-204448665Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1204446278204447400
Number: 3             
IDChromosomeStartEnd
GH01I204477chr1204446360204447003
GH01I204478chr1204447118204447620
GH01I204479chr1204447921204451603
Enhancer Sequence
CAGCCCATCC AGGGAGAGAT GGCTGGGGCC AATGCCACTA TGTCACACAA CTCTAGGGGG 60
CACCCCACAC ATTGTATTCT ATGTGAATGA TACCCCCGAC CACAAAAATG AAAACCATGT 120
GAATGGTGCC TCCTGGAGTT ATACACCTTG GTGGTTCAGG CTGCGTTCTC TCCTAATGTC 180
CACCTCTTAG AAAACAGATG GAAATCGTCC AGAAGGTCTG TTACAGCCAG TTTTCTTTCA 240
CCACCTGCCT GCAATAATTG TTAACATTTC TCCACATTTG CTCTCTTTCT TGCTCTGCTT 300
TACCATTTAA AAGTAAGATG CCCTTTGCAA AGTGTTTGTA AGAAACACTT TGCCTCTAAA 360
AACTTCAGCC TGAATCTCTA AGAGCAAGGG CATTCTCCTA TGTAAAACAC AATGCCATGA 420
GCACACCCAC AAAACTTAAC ATTGACAACA ATAATATTAT CTAATGCACA CTCCACATTT 480
GAGTGACCGC AATTGTCATC TGCGAAGCTT TAAAAATATA CACATTCCCG ACCTCTCCTC 540
TGGAAGTTCT GACTCAGTAG GGTGAGTCCC TGGATGCTGG ATGCTTCAGT AGCCCCTAAA 600
GTGATTCAAA TGTGCAGCCA GGTTTGACCC CACAGAAGAG GGTTTCAGAA CTCTCAGGAA 660
GACAAGAAGA CCTGGGTAGA GGCACCCCAA AAAGCACCAG TCAGCTGAAG AAACAAGAGG 720
ACATGCCTAT GGCCAAGCAG GTCGGTGCCA GGGTCTGAGC TGCACCAGGC ACCAAACTCA 780
GTCTCACAGC TGCCCACAGA TGGCTGAGGG CTAGCCGGGG AGGAAATGGG GTCAGGACAG 840
AGTGACACAA TGGTTCAGAG TCAAAGGATG GAAAGAAAGG AGAGGGCACT CCCTCCAGTG 900
GAGCTGGCTC TGTTTAGTCC CTGTGCCAGA GAGGGAGGAG CCCAGGGGCC ACCACTGGAG 960
CCAGTGGGTG GTGAGGGTTC CTGCTGTCTT GCTGGAAGGC ACCCTAACAG AATTGTTCTC 1020
CTTGGGACTG GGAGAATCTA GAGGGGTCTG GGTCATCTCT TCCCCATACC CTGAGCCACA 1080
GATTGGATCC CAAAGGGTGT TGAGTACCAG CTACATGCCA GGCCAGGCAC ATACATATCT 1140
AAAGACTACA AGTATTCAGA TGACTATGGC ACAATTCCAG GGAGCTTACA ATCTAGCAAA 1200
GGTGGCAGAC ACATACATAA AGAATTCAAT CCCCTCTTGG GGTGTAAAGC AGGAAGCAAG 1260
AAGGTACTGC ATGTCTTGGA CCATCTTCAG TGGGCAGGGA AAATGGAAAG CTCTCAAGCA 1320
AGGCGGTGAA GAATATGCAG GGTTTCAAGC CCCCAGTCTT GGGCATCCTG ATTTTCAGTA 1380
GATTTTACTA AGGGAAGAGA CTCAGCTCTA GGACTTCCCC AGGAAGGGAC CCTCAGCACT 1440
TCCCCTAAGG ACAGGCAGGG TCAGGGAGTC AGAGGCCATT AGGACTTAAA CCCTTTGGTG 1500
TCCAGGTTTT TCTCTTCAGA GAGGACCTCC ACTTCTGTCC ATCCCCCAGC ACCCACACTC 1560
ACCCATACCC CCAATCCCAC CTCCTTTGCA GCCAGGGACC CTGCCTCGCA TCTCACTCCA 1620
CACACATGCC GCTGGCTCCA ACTGCCCCTC CCACAGCCCG GCTCTAACAG GGAACATCAA 1680
CACACTGCCA GGAATCCGAC TCCTACAGCA GGGAGGTGTA TTAAGGTCAA GCAAGCCGGC 1740
TCCCCCAGCC TCCAACAGAT GTGCATCTGA TCCCTGCTTC CTTATGGAAA ACCCACAGGT 1800
TGTATACAGC TCTATAAGCT TTTTTGATGG CAGGTCTATT ACAGAATCAC ATGCATCCAT 1860
AAGGTCTTTC TCTTCTCTAG TGTGCGTGCC CTCTGGGTGC CTCTCATCTA GTTCCAAATG 1920
TGAGAAGACA AAATAACAGC TTGTGTTTTC TTCCCACTTA TACATCCCCT CTCTAGTGAC 1980
CTCTATAGCT AAACTAAAGC AGCCGCACAT GGTCTGGCAT TTCCTACCAG GACTTACTCT 2040
CCATTATTCT ACTCTCTGGG CATACCATAC CCTGGACTCT CCATTAATTT GAAGCCAAAG 2100
TGCACACAAG AGTTTAGTGG AAGTCTTTCT GGGTCCTAGA CAATCAGAGG GACAGAAGCT 2160
TGGAGCCTGT GGGACACAGC TACATAAAGT CAGGTCTGCA TGCACTGCTG ACTCCAACTC 2220
AGAGACCCCG ATTCTAGCTC AGAAACCATT TGGTCTCATG CACACACATA GAATCCTTGG 2280
AGATCATAGC TCCTGCTACA TACCCTGTAG ACTGTGGGCT CTGTGTTATG AGGAGACCAG 2340
GATGGAAGAG GTGAGGCAGC TTGTGGCTCC TCTAAAAACT TTCCTTCCTC TAGAGCTGGC 2400
AATTTTGATT GCAGGGTCAG GAACCAGAAG CTGGCAATCA ACTGAATGGA ACATTTGGCA 2460
AAGAAGGAAG AAAAGCTTTG GCAGTACGTG TATTTCTAAC CCAGGAATCA TCCCAGGAGC 2520
CAGAGCAGCC ACATCTCTGT CTGGTTCCTA CTTCCTGCTT CCTCCTCCCC TCTTCCCTCA 2580
CCCAAGAACC AATCCTTCTC ATCCAGTTCA CCCCAGGTTC CAAGGGCATG GTAGTTATGA 2640
GGGACTCCTC CAGCTTTCTT GGCCTTCCAG AGAAAGGTAG GGGGACAGGG AAGGTCCCAG 2700
GATGACCTCC CCTGACCAAC CTTGGCCTCC AGCTGAGGAG ACCACCGAGG GAACTTCTTT 2760
ACACACAACT TTCACACCAG CCCATCCTGT ATCAGAAAAA CAACCACAGA ATTTCCAAAA 2820
AGCAACACCT AGGAAACCCT AAACGCTCTG AAAATACTGT AGATGCTGTG AAGTATAAAC 2880
AAAGGTCCTC TGAAAGAGGA CACAGAAAAT GGGTGGAGTT AGAGACGAAG ACACAGTAGC 2940
TCTCTTTAGG CCTGGCCTCC CCCATCTACC ATCCTCCTCA GCTTTGCCTC GATACAGCAT 3000
TTGCTTCCTA TAAACTGAGG TCTTCTGCAA GGCCCAGATT GTCACCACTG TCACCTCCAG 3060
CCTCAGTTCA GCTTCCTTAG CTCATGCCCT TGGGAATCCA GTTCTGCAGG ATTCATTCCT 3120
GTGTGGGTGG GGAAAACTCC CTGGAGGATG CCAGCCTGTT CAGCAGAGTC CATAAAGCAA 3180
GTCCCAGCTG TTCCCATCCA GCCAGGGCAC CAAAGTGAGG AAACAACATA ACAACAAGGC 3240
TCTGCTCTGC CTGGAGGGCT CATCAGAGAG AGGACAGGAG AGGCCACGGC AGAGGAGCTG 3300
CCTCCGCAGG TCTTCTGCAC TGGGCTCGGC GGGGCCGGGC TAACCCATCC AGGTCTGCAA 3360
GGAGCAAGGA GGCAGTGTGG 3380