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

TagContent
EnhancerAtlas ID
HS043-03618 
Organism
Homo sapiens 
Tissue/cell
Fetal_heart 
Coordinate
chr1:204445720-204448470 
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: 32             
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_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
AGTCTTCAAG GGCTACTAGG GATTCTGTAT AAAAACAAAT AGCCATGTCG GTCCCTTGAA 60
AGAGGAAGGG TAGATCAGGG CCTGCGTCTC TGCTACTCTG CAGCCCATCC AGGGAGAGAT 120
GGCTGGGGCC AATGCCACTA TGTCACACAA CTCTAGGGGG CACCCCACAC ATTGTATTCT 180
ATGTGAATGA TACCCCCGAC CACAAAAATG AAAACCATGT GAATGGTGCC TCCTGGAGTT 240
ATACACCTTG GTGGTTCAGG CTGCGTTCTC TCCTAATGTC CACCTCTTAG AAAACAGATG 300
GAAATCGTCC AGAAGGTCTG TTACAGCCAG TTTTCTTTCA CCACCTGCCT GCAATAATTG 360
TTAACATTTC TCCACATTTG CTCTCTTTCT TGCTCTGCTT TACCATTTAA AAGTAAGATG 420
CCCTTTGCAA AGTGTTTGTA AGAAACACTT TGCCTCTAAA AACTTCAGCC TGAATCTCTA 480
AGAGCAAGGG CATTCTCCTA TGTAAAACAC AATGCCATGA GCACACCCAC AAAACTTAAC 540
ATTGACAACA ATAATATTAT CTAATGCACA CTCCACATTT GAGTGACCGC AATTGTCATC 600
TGCGAAGCTT TAAAAATATA CACATTCCCG ACCTCTCCTC TGGAAGTTCT GACTCAGTAG 660
GGTGAGTCCC TGGATGCTGG ATGCTTCAGT AGCCCCTAAA GTGATTCAAA TGTGCAGCCA 720
GGTTTGACCC CACAGAAGAG GGTTTCAGAA CTCTCAGGAA GACAAGAAGA CCTGGGTAGA 780
GGCACCCCAA AAAGCACCAG TCAGCTGAAG AAACAAGAGG ACATGCCTAT GGCCAAGCAG 840
GTCGGTGCCA GGGTCTGAGC TGCACCAGGC ACCAAACTCA GTCTCACAGC TGCCCACAGA 900
TGGCTGAGGG CTAGCCGGGG AGGAAATGGG GTCAGGACAG AGTGACACAA TGGTTCAGAG 960
TCAAAGGATG GAAAGAAAGG AGAGGGCACT CCCTCCAGTG GAGCTGGCTC TGTTTAGTCC 1020
CTGTGCCAGA GAGGGAGGAG CCCAGGGGCC ACCACTGGAG CCAGTGGGTG GTGAGGGTTC 1080
CTGCTGTCTT GCTGGAAGGC ACCCTAACAG AATTGTTCTC CTTGGGACTG GGAGAATCTA 1140
GAGGGGTCTG GGTCATCTCT TCCCCATACC CTGAGCCACA GATTGGATCC CAAAGGGTGT 1200
TGAGTACCAG CTACATGCCA GGCCAGGCAC ATACATATCT AAAGACTACA AGTATTCAGA 1260
TGACTATGGC ACAATTCCAG GGAGCTTACA ATCTAGCAAA GGTGGCAGAC ACATACATAA 1320
AGAATTCAAT CCCCTCTTGG GGTGTAAAGC AGGAAGCAAG AAGGTACTGC ATGTCTTGGA 1380
CCATCTTCAG TGGGCAGGGA AAATGGAAAG CTCTCAAGCA AGGCGGTGAA GAATATGCAG 1440
GGTTTCAAGC CCCCAGTCTT GGGCATCCTG ATTTTCAGTA GATTTTACTA AGGGAAGAGA 1500
CTCAGCTCTA GGACTTCCCC AGGAAGGGAC CCTCAGCACT TCCCCTAAGG ACAGGCAGGG 1560
TCAGGGAGTC AGAGGCCATT AGGACTTAAA CCCTTTGGTG TCCAGGTTTT TCTCTTCAGA 1620
GAGGACCTCC ACTTCTGTCC ATCCCCCAGC ACCCACACTC ACCCATACCC CCAATCCCAC 1680
CTCCTTTGCA GCCAGGGACC CTGCCTCGCA TCTCACTCCA CACACATGCC GCTGGCTCCA 1740
ACTGCCCCTC CCACAGCCCG GCTCTAACAG GGAACATCAA CACACTGCCA GGAATCCGAC 1800
TCCTACAGCA GGGAGGTGTA TTAAGGTCAA GCAAGCCGGC TCCCCCAGCC TCCAACAGAT 1860
GTGCATCTGA TCCCTGCTTC CTTATGGAAA ACCCACAGGT TGTATACAGC TCTATAAGCT 1920
TTTTTGATGG CAGGTCTATT ACAGAATCAC ATGCATCCAT AAGGTCTTTC TCTTCTCTAG 1980
TGTGCGTGCC CTCTGGGTGC CTCTCATCTA GTTCCAAATG TGAGAAGACA AAATAACAGC 2040
TTGTGTTTTC TTCCCACTTA TACATCCCCT CTCTAGTGAC CTCTATAGCT AAACTAAAGC 2100
AGCCGCACAT GGTCTGGCAT TTCCTACCAG GACTTACTCT CCATTATTCT ACTCTCTGGG 2160
CATACCATAC CCTGGACTCT CCATTAATTT GAAGCCAAAG TGCACACAAG AGTTTAGTGG 2220
AAGTCTTTCT GGGTCCTAGA CAATCAGAGG GACAGAAGCT TGGAGCCTGT GGGACACAGC 2280
TACATAAAGT CAGGTCTGCA TGCACTGCTG ACTCCAACTC AGAGACCCCG ATTCTAGCTC 2340
AGAAACCATT TGGTCTCATG CACACACATA GAATCCTTGG AGATCATAGC TCCTGCTACA 2400
TACCCTGTAG ACTGTGGGCT CTGTGTTATG AGGAGACCAG GATGGAAGAG GTGAGGCAGC 2460
TTGTGGCTCC TCTAAAAACT TTCCTTCCTC TAGAGCTGGC AATTTTGATT GCAGGGTCAG 2520
GAACCAGAAG CTGGCAATCA ACTGAATGGA ACATTTGGCA AAGAAGGAAG AAAAGCTTTG 2580
GCAGTACGTG TATTTCTAAC CCAGGAATCA TCCCAGGAGC CAGAGCAGCC ACATCTCTGT 2640
CTGGTTCCTA CTTCCTGCTT CCTCCTCCCC TCTTCCCTCA CCCAAGAACC AATCCTTCTC 2700
ATCCAGTTCA CCCCAGGTTC CAAGGGCATG GTAGTTATGA GGGACTCCTC 2750