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

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EnhancerAtlas ID
HS060-13890 
Organism
Homo sapiens 
Tissue/cell
GM12891 
Coordinate
chr17:1939390-1939820 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3752962chr171939543hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RFX1MA0509.2chr17:1939558-1939574GGTTGCCTTGGCAACG+6.08
RFX1MA0509.2chr17:1939558-1939574GGTTGCCTTGGCAACG-6.15
RFX2MA0600.2chr17:1939558-1939574GGTTGCCTTGGCAACG-6.75
RFX2MA0600.2chr17:1939558-1939574GGTTGCCTTGGCAACG+6.85
RFX5MA0510.2chr17:1939558-1939574GGTTGCCTTGGCAACG-7.43
RFX5MA0510.2chr17:1939558-1939574GGTTGCCTTGGCAACG+7.51
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1719393941939620
Enhancer Sequence
GTGGGGCCAG GACACCTGGA CGGTGGCGGG GCTGGCAGGG AGGCAGGCTG CACATTCATC 60
TTCCCCATGG CAGTGCCTTC TTGTCCTGCT TGGAGACACA AGGTCCCTCC TGGTTTCTGG 120
GGTGGCCTCT GCCTTCCCGC TCTGCAGGTA GATCTTTCCT TTGGATTTGG TTGCCTTGGC 180
AACGGTGCTC TGTCCCAGAT GCAGGTGTTT GAAAGGCTGT TGGTTGTAGA GCAGGCTGGG 240
CCCCGGCCGG GTGACAGAGA AGTCTGATTG AGAAGGAGCT TCTAGGGGAT CTGTGACCCC 300
CCTCTTCTCC TACCCTGTCC TTTTACCCCC AGGCTGAAGC CACTGCGCCT GGCTGCTCAG 360
AGACCTGAGC CTGGCCGGGC CCTCTGCTGC TCCTGCCTTC CCAAACAGCC CCTGAACTCC 420
TCCCTCCCAC 430