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

TagContent
EnhancerAtlas ID
HS050-40676 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr2:239412570-239413920 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs72993073chr2239412925hg19
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr2239412892239412967
chr2239413457239413602
Enhancer Sequence
TCTGTCCTTT TACTACCTTT ACAAAAACCA CTTTTGCAAA ACAGTAGAGA GAGTTCAAAT 60
TCTAAAGTGA GGGAGGGGTG GATTGAGGAG CAGATTGCCC AGTTTGTCCA CAGATCTTCA 120
TGCTATTCTG CATCTGCTGG GAGTGGGAAA AGCTTGGGGG CTGCCACCCC TGAGGATCAG 180
ATATTTATGT GACAGATGAA CCCTCCTGCT AACGCTGCTG TATTGAAAAG TCCCAAGAAA 240
GAGCAGTCCC AAAGGGAGTC CAGCTGGGCC CTGGGACCTG CACTGATCCC AAAGCTGCCT 300
AAAAGAAAAC GCCTGGGGCG CACCTATAGC TCCAGGAGGA AAATGGCCAA GGGCGCGCAG 360
CAGACTGCCG ATGGGAAACA CCTGTTCTCC GGGCTCGTGG GGGCTGGCCA GGCATTGTTC 420
TCTATTTGCG TGTTTTGCTT TCAGCTCATT CAAACTCAAT ATAGTGGTGA AATTAAGTAC 480
ATCATCAACC TAAAGCTACC AAACCAAATA CATAAATGGA AGGATTTGAA AAATCTGTAA 540
TAGCTGGGGT GAGGCTGGCC TCGGGCCAGC TGGGCTGCCC GGACAATGGA GGCAGTATGA 600
GTGCTTGGGC CACAGCGGGA GGGCGAGTTT CCACCCCGGG GTGGCCTGGG GATCTGATCC 660
AGCCTGAGGA AGGGCTTGGG TGGAGCCCCG AGGGGGCTGG AGGGCTGCCG GGGTGGGGGG 720
GCTCTAACCT GCAGACGTGA GCCCCCAAAG CCGGCTGTCA TCATGCGGGC CGCGGGGGGA 780
GCCATGCTGT GTGGGAAGCA GGGGCGGTGG GATCCGGAGG GGGAAGGTGT GGAAATTTGA 840
CACAAACGCA AATGTTTTAC CTTCTAAATC ACCTTGGTCT TGCAGTTGAA AATTCTCCCT 900
GAACTTCCCA CCCCAAATGT CTCAGGGAGG GGGAATCTGG GCAGCTTCTC GCTTTCCAAA 960
GTCACAAGTC ATAATTCTTT CTTCCTGCTG CAACCGGCGC AGGCTGAGTT CTGAATGTGG 1020
TGCTGAGATG GTGTGAAAAT CTCCGAGAAT ATCTGGGGAC CTTGCACCTC CACCCCCACC 1080
CAGACCCCGC AGTGACTGGG TGGACTTTCC AAGGCGGTTC CGTTTGGGGT TCTGCGCTCC 1140
TAAGGAACTC TGTTAGCCAG GAGGGCCAAG GCCCCTGCGC CCTCAGATGT GATTCACTGA 1200
CCACCTTCAG CCTAAAATGG CTTTGGAGAG CTGGAGGCCA GGTAGTGTGT TGACCGAGGC 1260
CACACTGAGC ACCCCTCACA TCTGCCCTCT GTGCAATGCC TGTGCACACT GGTCACTGTG 1320
GCTTCCAAGG AGCCGGCCTC CTTTCACTGC 1350