EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS118-09003 
Organism
Homo sapiens 
Tissue/cell
Liver 
Coordinate
chr19:2586970-2589240 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11672460chr192588423hg19
TF binding sites/motifs
Number: 26             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr19:2587875-2587893GGAAGGAAGGAAGGAAAG+10.53
EWSR1-FLI1MA0149.1chr19:2587863-2587881GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr19:2587867-2587885GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr19:2587871-2587889GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr19:2587682-2587700GGAAGCATGGAAGGGAGG+6.54
EWSR1-FLI1MA0149.1chr19:2587855-2587873AGAGAGAAGGAAGGAAGG+6.71
EWSR1-FLI1MA0149.1chr19:2587913-2587931AGAGAGAAGGAAGGAAGG+6.71
EWSR1-FLI1MA0149.1chr19:2587879-2587897GGAAGGAAGGAAAGAAAA+7.52
EWSR1-FLI1MA0149.1chr19:2587921-2587939GGAAGGAAGGAAAGAAAA+7.52
EWSR1-FLI1MA0149.1chr19:2587917-2587935AGAAGGAAGGAAGGAAAG+8.46
EWSR1-FLI1MA0149.1chr19:2587859-2587877AGAAGGAAGGAAGGAAGG+9.09
FOSL2MA0478.1chr19:2587616-2587627CTGAGTCACCC-6.02
IRF1MA0050.2chr19:2587934-2587955GAAAAGAAAAAGAAAGAAAGA-6.48
JUNBMA0490.1chr19:2587616-2587627CTGAGTCACCC-6.02
NFE2L1MA0089.2chr19:2587612-2587627GCTGCTGAGTCACCC-6.1
Nfe2l2MA0150.2chr19:2587614-2587629TGCTGAGTCACCCGG-6.46
ZNF263MA0528.1chr19:2587876-2587897GAAGGAAGGAAGGAAAGAAAA+6.11
ZNF263MA0528.1chr19:2587918-2587939GAAGGAAGGAAGGAAAGAAAA+6.11
ZNF263MA0528.1chr19:2587857-2587878AGAGAAGGAAGGAAGGAAGGA+6.14
ZNF263MA0528.1chr19:2587872-2587893GAAGGAAGGAAGGAAGGAAAG+6.48
ZNF263MA0528.1chr19:2587683-2587704GAAGCATGGAAGGGAGGGGGA+6.52
ZNF263MA0528.1chr19:2587902-2587923GAAGGAGAGAGAGAGAGAAGG+6.74
ZNF263MA0528.1chr19:2587860-2587881GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr19:2587864-2587885GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr19:2587868-2587889GAAGGAAGGAAGGAAGGAAGG+6.94
ZfxMA0146.2chr19:2587603-2587617CAGGCCTGGGCTGC-6.2
Number of super-enhancer constituents: 10             
IDCoordinateTissue/cell
SE_01272chr19:2588004-2589020Adrenal_Gland
SE_31670chr19:2586921-2590048Gastric
SE_40931chr19:2586993-2589097Left_Ventricle
SE_42475chr19:2587037-2589100Lung
SE_47688chr19:2587195-2587775Pancreas
SE_47688chr19:2588055-2589023Pancreas
SE_49019chr19:2586964-2589052Right_Atrium
SE_53390chr19:2587822-2589101Spleen
SE_61224chr19:2586887-2637887HBL1
SE_65339chr19:2585603-2590108Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1925880022588286
Number: 1             
IDChromosomeStartEnd
GH19I002586chr1925866292589279
Enhancer Sequence
GGACTCCATC TCAAAAAAAA AAAAAAAAAA AAAAAAAGAA TGTCACCTTG AAATCATAAT 60
GACAGTGGAG AATCCTGGCA TCCACTACCA CGCAACACCA CATCCGGCTA ATTTTTGGCC 120
CCAGACGTCA CCCGATGTCC CCCAGGGGCT AGGATCAGCC GCAGGTTAGG ACCCCTGGGT 180
TGGAGGTTTC ACCACGGAGA GTTGCGGCGG CAAGAAGACA CCAGGAGGAA GTGACCTGCA 240
CACAATCACC AGATCGTCCC TGAGCATCTG GCTCTAGGGT CTCTGCCTGG ACCGAAGCAT 300
TCCCAGGTGC AGACCCAGGG GTCTCTCCTG TCCCTCCGAC CTCACCTGCG TACCCTGCGT 360
TGCTTCCTCT GCCGGGGAAG CTCACCCACG TTCTCAGGTC CTGGGCGGAA GGGCAGAGGG 420
CTCCCCGGGC ACAATGTCTT CTGATGAGAA TCACAGCTGC TGAGATGCAA CTGCAAGGGG 480
CTGGGAAAGT TCCTGGGACC CAAAGGAGCT GTGAGATCTA GCGCCTGGGA TGGCAGAGGC 540
TCTGGCCGGT GAGGACAACA GCCGGCGTCA GCTCGGGGGT CGGTACGCAG GCGGCCACCT 600
TGTAACGGCC ACAAACGGGC TTCAAAGGGG AGGCAGGCCT GGGCTGCTGA GTCACCCGGG 660
CCTCATGCAG TTCACAAAAA GCTGTAACTC GAGGCAGCAT CACACCGACC GTGGAAGCAT 720
GGAAGGGAGG GGGACGCTGT CTCAGCCTCC AGGAGCTACC TGGCAGGCTG AGGCAGGAGA 780
ATCACTTGAA CCTGGGAGGC AGAGGTTGCG GTGAGCCAAG ATCGTGCCAC TGCACTCCAG 840
CCTGGGCGAC ACAGCAAGAC TCTCATCTCA AGAAAAGAGA GAGAAAGAGA GAAGGAAGGA 900
AGGAAGGAAG GAAGGAAGGA AAGAAAAGAA AAGAAGGAGA GAGAGAGAGA AGGAAGGAAG 960
GAAAGAAAAG AAAAAGAAAG AAAGAACAGG AACAAGATAA GGGTGGCCAC TCTCACTGTT 1020
TCTATTCAGT ATTGTTATTG CAAATTCAAG CCAGGGCAAC TGGGCATGAA AAGGAAATGA 1080
AAAGCATCCA GATTGGAGCA AGAGAAGAAA AACCATCTCT CTATTTGCAA ACGGCCTGTT 1140
GTGGTGTAAA AGGTCCCCGG GTACAATTTG TGCAGCAGAA ATACGGCACT TCACAGGCTG 1200
CTTAGAAACC TAGCAAGTCC CTTGAGCACA AACTATTTTC CTAAGCTTGG TGGGGGCGTG 1260
AGAGGGTGGC CGGGGACTGG TGACAATGTT GTTTGTGCAC TGGGAGAGTC CGGCTGAATT 1320
GCAACTGGCC TTTACATCCT AATCAGCTCC CTGAGGACAA CCCGAAAGAC ATCAGATTAA 1380
AAAGTCACAA TGAGATAAAC CAGCACGACG CGGCTCTCTG CAAAGCGACA GGTAGTAAAC 1440
AGACCTTAAC GCACGTCATG AGGTTTGTTT TTCTTTTAAA AGTCAACAGC TGGTGAATCG 1500
CACAGGGCCG GGCAGGGCGG TCAAAGGGCC CGTTCCCCCG GCTGGGAAAA AAGCAGGAGC 1560
CCAGGGCGGC GGCAGCTGGA CGCGGGCCCC GTGGAACTTT CTCCCGTCAG TCAGGGGCCG 1620
TATTTCTTAG CCATCCTCCT CTGACCTTCA TTTCAAACCG CCTGCTGACG CATCTAACCT 1680
TGGCCCGTTC CGTGGGAACT CCAGACTCAG GGTGACCAAC CCCAGCTGGG TTACCCAGGG 1740
TTGTCCTGGT TGGAGTGGCT CCAAGTCCTC AGACCCAGCA AACCCAGGCT TGCTGATCAC 1800
ACCGCAGACC CCACCAGGTG GTCATCTTTC TGGGGAAACT GGCTTCTTTT CCTCCCCGAC 1860
TCCCTTGCTT TGTCTTCGTG GTGGCACCTC TCTTCCCAGG TGCTCAGGTG TGACATCAGC 1920
CGTCCCTTGC TGGCCCTGGT GCCAGCTGAC TCCCAGGTCT CCTTTCTCTT CTTTAAGATG 1980
GAGTCTCCCT CTGTGACCCA GGCTGGAGTG TAATGGCGCG ATCTTGGCTC ACCACAACCT 2040
CCCCCTTCCA GGTTCAAGCG ATTCTCCTGC CTCAGCCTCC CAAGTAGCTG GGATTACAGG 2100
CATGAGCCAC CACACCTGGC TAATTTTGTA TTTTTAGTAG AGATGGGGTT TCTCCACCTT 2160
GGTCAGGCTG GTCTCGAACT CCCAACCTCA GGTGATCCGC CTGCCTCAGC CTCCCAAAGT 2220
GCTGGGATTC CAGGCATGAG CCACCACGCC CGGCCGTCTC TTTCTTCTAA 2270