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

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EnhancerAtlas ID
HS050-54230 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr5:65738710-65739950 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10514995chr565739439hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gata1MA0035.3chr5:65738995-65739006ACAGATAAGGA-6.14
Sox6MA0515.1chr5:65739565-65739575CCATTGTTTT+6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr56573873165739365
Number: 2             
IDChromosomeStartEnd
GH05I066444chr56573896165739110
GH05I066443chr56573942165739570
Enhancer Sequence
AGTACATTTT TGGTAATCTG CTACTAGAAA CAGTAGAGGG AACTTCAGAT GCACCGCCAA 60
AAAGAAGATT TAAAGGGGAC ATGACAGCTG TTTTCGATCA TGTGAAGAGG GAGAAGGCTT 120
ATCTGTGTTT TTCCAGAGGG CACAATTAGG GAAAGTGAGT AGTGATAAGA GGAGTCAGAC 180
TTGGGCATAA ATTACAGAAG AATCTTTGCT TTTGTGAGCT GACCAACAAT GGAATCCACT 240
GCATTGCAAA ACCGTCTTCT GGCAGGTCAA GAAAACTGCC AAAGCACAGA TAAGGAAGAT 300
GGGGCCCAGA AAGATTTAGT GACCTGGACA AGGGCACATG GCCAGTGAAT GGAGGGCCTG 360
GCTTGGAACC CAGAGTGCAA GGCAGTCTGG GTCATTCAAC CCTTGGCCAG TAATGATTTT 420
AACGTTTGCT TTTTCAACCA CAAAGCTTCA TGATGGATTG TAATTTTGAT GAAGTACATG 480
CTCCAAGGCG AATGTGTGGG AGTGAGTCTC TGAGCTAGCA AGTAAATACC CACATCTCAA 540
ACAGACTTTG AAGTTCCATG CGTGTGGAAT ACACAACAAT TCTTGTGATG TATAATAATT 600
TCCTTTTGCT TCATTATGAA AAGCAGTTAA TGCTTATGGT GATGAACAAA AAGTAAAGAA 660
AACTAAGAAA GTGAAGGTTC CTATCAGAAA TATGAAGGTT TGCATTAATT AGAGTGGCAT 720
GTTAAATTTG ATGATGATAA GCATCTGTGA TGTGCAATTG TTTCATTGAA TGTTCCATAG 780
TTTTGGCTGT CTGCCACAGG AACATTTGAA ATGTTCAAGG AAATGATCAA GAAGAACAAC 840
TATTCTGTAC TCATTCCATT GTTTTCCATA AGTTCCCTTG TTCTTTTGCT CTAAATAATT 900
TGAATACTAG TTGTGGGGAA AAAGAAAAGA TCCCTAATCA ATTCTTACGA AGTGTGGGGA 960
GGTATTGCAC ACAGGCGTCT CATGATATGT GGCTTCTCTG CAGGTCCACA CAGCCTGTGA 1020
AAGTCCCTGG CTCCTCTGAC TTGTCAGATG TTCCGGGTTG GTGTGACTCC AAATACAGTC 1080
TCAAGGACAG ACACCAAGTC CGAGATGTTT CTGCCTTTCC CTTTAAGAAA TAGGCCTATT 1140
CTTGTCAGCT CTAGGCCTGA AGGCATTGTT TCAGAGTCAA TCACTTTAAA CATTTCCCCC 1200
AGGACAGCAG AGGCAATTCA AGCTTAAATA GTGAAGCCAT 1240