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

TagContent
EnhancerAtlas ID
HS098-47797 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr6:15753960-15755500 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1887604chr615754758hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr6:15755056-15755074GGAAGAAATGAAGGTTGG+6.15
EWSR1-FLI1MA0149.1chr6:15755052-15755070GGAAGGAAGAAATGAAGG+7.71
Stat6MA0520.1chr6:15754817-15754832ACTTCTCAGGAAGTG-7.63
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr61575454915754910
Enhancer Sequence
GAGTTTGGTA AAATCATGTT CCTCTCCCTC CTCACTTATG GGATAGGGTG GGTAGGGCCT 60
CTTTCCTCGG TTGTTATCTG AGCAGAGGAT AGTAATTCCA TCTTCCTTCA GTGCCAGGTG 120
GGCTGTGAAT GTGAACTTGT CCTCAAAATG CAGTTTCACC TTCCTGTTGT TGATGTCCAA 180
GTCTGAGGTA AAGCAGCGGA GCAGAGGGTT GGCACTGTGT GTGTTCTCTG TGAAGCCCAA 240
GGTGTACCAG TACCCTGACA TAAACTGGGG AAGGGGCACA CAATGAGTGT ATCATTCCGG 300
GTCCAAGCAG AGAAGAAGAT GGATATGTAT ATATAATTCA TTTGAAACAC AATTATAGGA 360
GCTGGCTAAG CAGCCTCCCC AAGGCTGTTT CCTTGACTAA TGTTTGAGCC TGAAGTCCAT 420
GAGCAGGCAG GCAAGGAGAG CTGATGAGAG CAACCTAGAA CCCCACGGGT TCTAGGCCAG 480
ACTGAAACTC ATCCTTTTTT TTCCCTCTCA CCTTGATGAT GAGGGTATCC TGCAGAAGTT 540
GAGGCCCTGT GTCATGTTGC TGAACAAGTC ATCACCCACC CCAGGGGTCA GAGAAGCTGT 600
AGGAAGGTCC AGAGGGAAGG GAGGGCAGCG ACAGGCCCAA CCACAGCTTC ATGTCAACGA 660
GGTGAGTCAG CAGATCAGCA AAGCCTGTCC ATGTGCTGCA AAATGGCTGT CCCTGCCATG 720
CCTCCCTCCA TCTCTCATGA GAGAATAGCC CTCTAGCTCT TCCTAACTGG AAACACAGGA 780
GAAAGAATTC TGGGAAATGT AGTCTAGCCT AGCCAAGTTA GCATATTCCA AAGCTCACTA 840
AGGCTGTGGC TCTGCCCACT TCTCAGGAAG TGAGTTTGGT CTTTAAACCA ATACCATGTG 900
GCCTCCCGTT TCCCCAGCTG TTTTCTGCCT CTGCTGGCAG AGCCGCTTGT GTTAGTCCAG 960
GCCAAGGAGC AGACACCAAG CTAGATTACA TGTGCAAGAT ATTTACTAGG GGAAACACCT 1020
ATGAAAGAAA ACAGGGAGGA AGCCGAGAAA AACTTGGAGA GCTTTCATAC CATGATGCGA 1080
GTCCAACCTG GGGGAAGGAA GAAATGAAGG TTGGATAGAA ACGACAGACT TCGATGCAAT 1140
TCTAAGGAAG GTTGGGCAAT GCTGCCTGTC AGAGCAGCCC TGCTTTTCCC TGAGGCAGGT 1200
CTGTTTTAGC ATCCCGATGT GCTTAGGAGC AGCATTTGGG AAGTGTGGCC TGCAGGAAAA 1260
CGCAGAGTTG CATTTCAGAG CACAGCGTTG GGGGCTCCTC GATCAATTGC TCTCCCGGCA 1320
ATAGGAGGTC CAAAGGTGCC TTGTCCTGGC CATGCTGCCT CGTTCTCATT TCTTGCTTTG 1380
GTCAAAACTC AATCAGCCCA CCTTCCTCTT TTGGAGCATG AGAAGTAACT AACTAGGGCC 1440
AGGAGTCTTG CTGGCGCCTC TTTTGCCCAA TGCCTGATTT CTGTTCAATC AGGATAAGCT 1500
GTCAGGAGGA GATGGTGGCC ATACTTGGAG GTGAAGGGAA 1540