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

TagContent
EnhancerAtlas ID
HS049-03152 
Organism
Homo sapiens 
Tissue/cell
Fetal_spinal_cord 
Coordinate
chr17:5568230-5569560 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs8077015chr175569266hg19
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1755684925568883
chr1755689345569003
Enhancer Sequence
CGGTATTTTA AAATCATTAG ATTTCACATA TAAATCCGAT GTTCTGAATT TTATCTTAAA 60
ATATAGGGTG ATCCGGCAAC AATTGGACCT ATACTCCTGC CTGTTTCAGA GCCTCCTAGG 120
CAATTCCAGC TGGAGGTGGA ACGTTCCCAG GTGAGGTAGG CCCTGCAGAC GTGGGAGTGG 180
GGTCACTGTC ACCCAAAAGG AGGAGCATCG GCTTTTTAGA CCGGGGCCTG AGGAGCCCCC 240
AAGGGAAGTG TCTGAACCAC GCAGGTTCCT TACAGTCTTG AGCTCAGATT TAACTTGACA 300
AGTGCTGAGT GCAGCGGGAC TCTTAGCCAC ATTGATCCGG ACACTAAACT CCTATTAATG 360
TAGTCAGAGA AAGCAATTGC TTTCTTGGCA GCCACATGCG GCTGGCGGCT CGCACAGACC 420
TTGCAGTCAG ATGGAGACAC CAGGACCGCC CCGTGGGAGC AGCTGTGAGC TAAGACTTCC 480
GCGCCTGGGT ATCCAGCCTC AGTGCAGGCT TCACGCTCTG GCTCTGTCAG TGTGGACTGT 540
CACTTTAGCT GCCAGCCTTT CCTGTGAGTG GCATCCTCAG CTGTCCCCTG CACTGGCCCC 600
TTGGCATTTT CCTAACCCCT ACACAAAAGG GCAGCGGGAT CTTGGCTAGG GGGCTCAGAG 660
CAATGCTCCC TGCTCCCCAA TTTGGCCTTC CCTGCTAACA TCCCCTTCCC TGGTGTTCTG 720
ACCCTTTTTG GCTTCCTCCC TCAGCACATG CAGGCCCCCC CCCCATGCTC TGTTTTGGAT 780
GTGTCTTCCT GGTGCTCCCT CCTCAGGCTC ACTCCAGTGG ACATGATTTT GCTTCTGACC 840
TCTGGACTTA TGCACCTTTG CCAGGCCCAA CAGCTTCTCC CTTTTTCGTG CTATGTGGGG 900
ACTGTGACGG CCAGGACCCC TTCCCAGCCC CCGCAGCGCC CCCCTCAGTC ACCAAAGTCT 960
GTCTTTTTTA CTCTCTGATA TCTTCGAAGT TGTCCATTTC TTTCACCCCC AGTGCCATGC 1020
GTGTCCAGCC CAATCTCTCA CCTGGCTGCT CCCAGAGCCT CTGACCTGTA CTCCCTGCCT 1080
CCAGGCTTTT CGCCTCCAGC CCACTTTCCA ACAGCAGCCG GAGAGCTCTC TTCAGAGGAC 1140
AAACCTGACC ATGGCAACTC TGTCCAGAAT CCTTCAATGC ATCGTTCCGG ATTTCAAGAT 1200
GAAGCCTGAG TTCCAGGCAG TTCCAGACTT GGCCCCGGTT CTCTCCTCCA GCCTCATGGC 1260
TCCCCGCATC CATCCCCCAG TCCATGTTCT GGCCATACTG GTCCATTTGC AGCACGCTTG 1320
CTTCCTCTGA 1330