EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS154-10657 
Organism
Homo sapiens 
Tissue/cell
Osteoblast 
Coordinate
chr19:2587440-2589010 
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
CTGCAAGGGG CTGGGAAAGT TCCTGGGACC CAAAGGAGCT GTGAGATCTA GCGCCTGGGA 60
TGGCAGAGGC TCTGGCCGGT GAGGACAACA GCCGGCGTCA GCTCGGGGGT CGGTACGCAG 120
GCGGCCACCT TGTAACGGCC ACAAACGGGC TTCAAAGGGG AGGCAGGCCT GGGCTGCTGA 180
GTCACCCGGG CCTCATGCAG TTCACAAAAA GCTGTAACTC GAGGCAGCAT CACACCGACC 240
GTGGAAGCAT GGAAGGGAGG GGGACGCTGT CTCAGCCTCC AGGAGCTACC TGGCAGGCTG 300
AGGCAGGAGA ATCACTTGAA CCTGGGAGGC AGAGGTTGCG GTGAGCCAAG ATCGTGCCAC 360
TGCACTCCAG CCTGGGCGAC ACAGCAAGAC TCTCATCTCA AGAAAAGAGA GAGAAAGAGA 420
GAAGGAAGGA AGGAAGGAAG GAAGGAAGGA AAGAAAAGAA AAGAAGGAGA GAGAGAGAGA 480
AGGAAGGAAG GAAAGAAAAG AAAAAGAAAG AAAGAACAGG AACAAGATAA GGGTGGCCAC 540
TCTCACTGTT TCTATTCAGT ATTGTTATTG CAAATTCAAG CCAGGGCAAC TGGGCATGAA 600
AAGGAAATGA AAAGCATCCA GATTGGAGCA AGAGAAGAAA AACCATCTCT CTATTTGCAA 660
ACGGCCTGTT GTGGTGTAAA AGGTCCCCGG GTACAATTTG TGCAGCAGAA ATACGGCACT 720
TCACAGGCTG CTTAGAAACC TAGCAAGTCC CTTGAGCACA AACTATTTTC CTAAGCTTGG 780
TGGGGGCGTG AGAGGGTGGC CGGGGACTGG TGACAATGTT GTTTGTGCAC TGGGAGAGTC 840
CGGCTGAATT GCAACTGGCC TTTACATCCT AATCAGCTCC CTGAGGACAA CCCGAAAGAC 900
ATCAGATTAA AAAGTCACAA TGAGATAAAC CAGCACGACG CGGCTCTCTG CAAAGCGACA 960
GGTAGTAAAC AGACCTTAAC GCACGTCATG AGGTTTGTTT TTCTTTTAAA AGTCAACAGC 1020
TGGTGAATCG CACAGGGCCG GGCAGGGCGG TCAAAGGGCC CGTTCCCCCG GCTGGGAAAA 1080
AAGCAGGAGC CCAGGGCGGC GGCAGCTGGA CGCGGGCCCC GTGGAACTTT CTCCCGTCAG 1140
TCAGGGGCCG TATTTCTTAG CCATCCTCCT CTGACCTTCA TTTCAAACCG CCTGCTGACG 1200
CATCTAACCT TGGCCCGTTC CGTGGGAACT CCAGACTCAG GGTGACCAAC CCCAGCTGGG 1260
TTACCCAGGG TTGTCCTGGT TGGAGTGGCT CCAAGTCCTC AGACCCAGCA AACCCAGGCT 1320
TGCTGATCAC ACCGCAGACC CCACCAGGTG GTCATCTTTC TGGGGAAACT GGCTTCTTTT 1380
CCTCCCCGAC TCCCTTGCTT TGTCTTCGTG GTGGCACCTC TCTTCCCAGG TGCTCAGGTG 1440
TGACATCAGC CGTCCCTTGC TGGCCCTGGT GCCAGCTGAC TCCCAGGTCT CCTTTCTCTT 1500
CTTTAAGATG GAGTCTCCCT CTGTGACCCA GGCTGGAGTG TAATGGCGCG ATCTTGGCTC 1560
ACCACAACCT 1570