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

TagContent
EnhancerAtlas ID
HS050-31179 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr18:24337080-24338120 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs527616chr1824337424hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HNF1AMA0046.2chr18:24337538-24337553AGTTAATCATTAGCA-6.2
HNF1AMA0046.2chr18:24337538-24337553AGTTAATCATTAGCA+6.4
HNF1BMA0153.2chr18:24337539-24337552GTTAATCATTAGC+6.17
HNF1BMA0153.2chr18:24337539-24337552GTTAATCATTAGC-6.32
ZNF263MA0528.1chr18:24337896-24337917TCCCCATTTTCCTTCTCCTTT-6.01
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr182433709924337764
Number: 1             
IDChromosomeStartEnd
GH18I026757chr182433728824338050
Enhancer Sequence
TGTCACACTG AAAAGAGAAG ACTGCATTGA GGTGATGCTC CAAAAGGAGC AGCTTTGATG 60
CAAAAGAAGC AAAACCCTTT TGTTTCTTGG GCTTATACGA AGGTACTTCC TTTAGATCAG 120
AGTCGGGATG CATACACACT ACAAAAACTG GAATGAAAAA GGCAAACCAT TTTTACTCAA 180
CAGAATTCTC TGTACAGGTC AAGGAAATGC CAAACTTAAC AGATGTCTTA GACTGTGCCC 240
TGCAGGTCAA TAAATTAGAG TTTTGTTGAA CCAGGAAGAG GAAGGAATTC CAGGACTTCA 300
GGTCCCCAAA TGGAAATGCC CCTTAGGACA AGTCTAAACT AGGCAAATAG CACTGGAGCT 360
CCTCCAAGTC AGTTGGCTCA GTCTCGTGTA ACTCATTTCT GGCCCCCCTG AAGCTGTTTG 420
TTCAACTGTG CCTTCTACAA CGCTACAGTG TCAAAGAGAG TTAATCATTA GCAAGTGTGA 480
ATAATGTCAG TGTAACGCAG CATGATTGCA GTTCAGTCTG TTTTGACAAA ATTCTAAGCA 540
TTTGTCAGAG TTTACCAAAA AACAAAAAAC AACATGACCA CAGAATGTTA AAATAGCATG 600
AAGTTTGGGG AGCAGTTAAT TCACTTTCTA GCATTTTACA TCACCATTCT CATCGTTTTC 660
CCAGAGGAGA GTGTTGGGTG AGGCCCTCCA GGTGATGCAG TATTACTGAC TGGCCTGGTA 720
TGGTCTGATT CAGTTCAAGT CAGCTTAATG CAGCTCACCT CCAGAGATCC AGGCTTTGGA 780
GAATGATCTA AAGGTTTAGG TGTAGGGTCC TTAACCTCCC CATTTTCCTT CTCCTTTGTC 840
AGAGCCACCT ACTGCCATAG AATTAATATG GACCCATCTG TGATGCAGAG CCTGTTAGGC 900
CTCCTGCTTG TCCCCTGGGC TGGGGATCAT AATGAGTCCA AGCCCTCCCT TTTGACTGGA 960
ACTGCAGGGG CCCTGGTCCT GGAACTCTGA GGTTGAGAAT GGGATGTAAA GCTATATTCC 1020
AGCAAGCACT GAAGGATGAG 1040