EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS176-19180 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr19:46791920-46793320 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11671710chr1946791934hg19
TF binding sites/motifs
Number: 23             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr19:46792155-46792173GGAGGGAGGGAGGGAGGG+6.03
EWSR1-FLI1MA0149.1chr19:46792159-46792177GGAGGGAGGGAGGGAGGG+6.03
EWSR1-FLI1MA0149.1chr19:46792081-46792099GAAATGAAGGAAGGAGGA+6.21
EWSR1-FLI1MA0149.1chr19:46792150-46792168GGAAGGGAGGGAGGGAGG+7.08
EWSR1-FLI1MA0149.1chr19:46792092-46792110AGGAGGAAGGAAGGAAGG+7.85
EWSR1-FLI1MA0149.1chr19:46792096-46792114GGAAGGAAGGAAGGGAAG+8.57
MITFMA0620.2chr19:46792767-46792785GTTGGTCATGTGACTTCC+6.18
MITFMA0620.2chr19:46792767-46792785GTTGGTCATGTGACTTCC-6.18
STAT1MA0137.3chr19:46793185-46793196TTTCCTGGAAA-6.62
Stat4MA0518.1chr19:46793182-46793196ACATTTCCTGGAAA-6.41
ZNF263MA0528.1chr19:46792094-46792115GAGGAAGGAAGGAAGGGAAGG+6.1
ZNF263MA0528.1chr19:46792142-46792163GAAGGAGAGGAAGGGAGGGAG+6.39
ZNF263MA0528.1chr19:46792139-46792160AGAGAAGGAGAGGAAGGGAGG+6.49
ZNF263MA0528.1chr19:46792148-46792169GAGGAAGGGAGGGAGGGAGGG+6.54
ZNF263MA0528.1chr19:46792086-46792107GAAGGAAGGAGGAAGGAAGGA+6.55
ZNF263MA0528.1chr19:46792093-46792114GGAGGAAGGAAGGAAGGGAAG+6.74
ZNF263MA0528.1chr19:46792101-46792122GAAGGAAGGGAAGGGGAAGGG+6.86
ZNF263MA0528.1chr19:46792147-46792168AGAGGAAGGGAGGGAGGGAGG+6.99
ZNF263MA0528.1chr19:46792160-46792181GAGGGAGGGAGGGAGGGACGG+6
ZNF263MA0528.1chr19:46792152-46792173AAGGGAGGGAGGGAGGGAGGG+7.05
ZNF263MA0528.1chr19:46792097-46792118GAAGGAAGGAAGGGAAGGGGA+7.07
ZNF263MA0528.1chr19:46792090-46792111GAAGGAGGAAGGAAGGAAGGG+7.79
ZNF263MA0528.1chr19:46792156-46792177GAGGGAGGGAGGGAGGGAGGG+7.97
Number of super-enhancer constituents: 9             
IDCoordinateTissue/cell
SE_27946chr19:46792069-46793558Fetal_Intestine
SE_28936chr19:46791917-46793672Fetal_Intestine_Large
SE_30198chr19:46791978-46793929Fetal_Muscle
SE_40980chr19:46791479-46793912Left_Ventricle
SE_42682chr19:46791903-46793939Lung
SE_49076chr19:46792088-46793432Right_Atrium
SE_49717chr19:46792161-46792660Right_Ventricle
SE_54344chr19:46791375-46794680Spleen
SE_54901chr19:46792014-46793795Stomach_Smooth_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr194679212146793106
Number: 1             
IDChromosomeStartEnd
GH19I046287chr194679079846793790
Enhancer Sequence
CCGGACATAG TGGCGCACAC CTGTAATCCC GGCTACTCGG GAGGCTGAGG CACGAGAATT 60
ACTTGAATAT GGGAGGCAGA GGTTGTAGTG AGCTGAGATT GCCATTGCAC TCCAGACTGG 120
GCAACAGAGT GAGACTCCAT CTCAAAAAAA AAAAAAAAAA AGAAATGAAG GAAGGAGGAA 180
GGAAGGAAGG GAAGGGGAAG GGAAGGAAGA GAGACAGAGA GAGAAGGAGA GGAAGGGAGG 240
GAGGGAGGGA GGGAGGGACG GACAGACGGA CGGACGGAAC TAACTCTATG AGTCACAGAG 300
AGGTTAAGTA ATTTGTTCAA GGTTCTGCAG CTGGTAAATG ATGGGATTAG AATGCAGGCA 360
GCCTGGCTCC AGAGTCCACT ATAGGAAAAC ATTGGAGCCC ACTTAATGGG GCTGCTGTGA 420
CATTCCAATG TGAACAGGAA TGCCAAGGGC TCAGGACAGC GCTTGGCACA GGATCTGTGC 480
ATCATGCTTG GAACTGGTGC TGTTTATTTC CATCACCTGA TTCTGGGTTG GCCTTGGCTT 540
GGGTTTGGAG GGATTTTCTG CCCCTGGCAG TGTTCCAGGG GTGGCAGCTG GACTTTTTAA 600
ATCCAAGGAC CTTGTTAGGA GTCAGAGTTG GGCAAGGGGA GACTGGAGAT AAAATCCGAT 660
CACAAGAGGT AGCTATGAAT AGGTCAGGAG CAATTCTCCC CAGCCTTGAG CAGTAGGGAG 720
GATGAGTCAA CAGAAGTGAA CTCACCCTTC CTACTTGTTA TAGAATTATA CATCCATGAC 780
TGTACCATGT GACTTTACAT GTCTTCTTGA GTATGTCAAA TACATTCCCT GACCCACTGA 840
GGTCAGGGTT GGTCATGTGA CTTCCTGTGG CCAATAGGAT GTGAGTCATA CCCAATAAAG 900
ATAACCAGAC CTGATGGTAA GTAGAATATC CATGAAGATG TGCAGGAGAC CATGGCCAGC 960
AACACTGGCT TATCAGAACT GGGTTCATGC ACAGGTCTGA GTTTTTGTTG CTGAACCCTC 1020
TTTCCCTGTC AATAAGACAA GCATTTATTC CCCAGTATCC CAAGGCCTAT GACTCCACCT 1080
CCAGGCTGCC ACTCATAGGT GGAGCTCACC TGGCACCTGC GGCTGGAACA TCTACTTATC 1140
ACCTTTCCAT GTGGCTCCTT GGGCTTCCTC ACATCATGGC AGCTAGGTCC CAGGGGCTAT 1200
GGGACCTAGC TAGATATTGT GCTTCATAGC TAGATACGGT GCTATGAAGA GTGTGGCAGT 1260
TGACATTTCC TGGAAATGGT CACAGTAATA TTTTGAGTCT CACATGCTCT CCCTTGTGGT 1320
AGCTTGCCCC TCCCATCAAA AGGCAGAGTA TTTTCCTTTT CTTGAAGCTG GGCAGAACTT 1380
TGTGATTGCC TTGACAGAGG 1400