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

TagContent
EnhancerAtlas ID
HS104-15664 
Organism
Homo sapiens 
Tissue/cell
HUVEC 
Coordinate
chr12:112841640-112842860 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11066284chr12112842275hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr12:112842447-112842458GCAGGGTGTGG-6.62
NFAT5MA0606.1chr12:112842308-112842318ATTTTCCATT+6.02
NFATC1MA0624.1chr12:112842308-112842318ATTTTCCATT+6.02
NFATC3MA0625.1chr12:112842308-112842318ATTTTCCATT+6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12112842120112842353
Enhancer Sequence
AGCCATCCTC CCATCTCAGC CTCTCAAGTA GCTGGAACCA CAGGTACACG CAGGCTGGGC 60
TTATTTATTT TTTGAGACAG AGTTTTGCTC TTGTTGCCCA GGCTGGAGTG CACACATTAC 120
AGGTGTGAGC CACTGTGCCT GGCTCAAGTT TTTTTTTTTA ATAAAAATGT TACTTATATA 180
AACATGACAT GTCATTTTAA AATATTCTAG CAACTTTTTT TTTTTGAGAC AGTCTTGCTC 240
TGTCGCCCAG GCTGGAGTGC AGTGGTGTGA TGTCACTTAC TGCAACCTCT GCCTCCCGTC 300
CAAATTCTCC TGCCTCAGCC TCCCGAGTAG CTGGGATTAT AGATACCTGC CACCATGTCC 360
AGCTAATTTT TTTTTGTATT TTTAGTGGAG ATGGGGTTTC ACCATGTTCG CCAGGCTGGT 420
TTCAAAATCC TGACCTCAGC TGATCAGCCC ACTTCGGCCT CCCAAAGGGC TGGGATTACA 480
GGTTGAGCCA TGGCACCCAG CCTTTTTTCA CCTTTTTTGG ACACAGGGTC TGTCATCCAG 540
GATGGTGTGC AGTGGTGAAA TCACAGGTCA CCACAGCCTG GACCTCCTAG GCTCAAGTGA 600
GCCTCCTGGC CCCACCTCCC AAAATGTGGG GGTTTCAGGT GGAAGCCAGC ACACACAGCC 660
CATTTTTCAT TTTCCATTGG CAAAAATCCA AGTTTGATAA CCTACCTATA AGAAGATGGG 720
TACTCTGTAC ATTTCCAGAA CAAATAAAGT GGTCTAACAC TTGGGAGTGT TTGGAAGAAT 780
CTGCCAAAAT TAAAATGCAC AAATCTGGCA GGGTGTGGTG GCTTATGCCT ATAATCCCAA 840
TACCTTGAGG TCTAGGCAGG AGGATAGCTA GAGCCCAGGA GTTGAACCAG CCCAGGCAAT 900
AGGAACTGGG GCCATATGTG ATAAACGTGC CCATGAACAG CCACTGCACT GGCCTGGGAA 960
ACAAGAGCAC GGCCTCATAA TTATTGGGGA GGAGTTGAGA ATTGAGCACA GCGGGGAGAA 1020
ATGGGAGTTT GTTGTCTGAG TAGTCAGCAG TTATTCTCTT CTCTCATCCA TGTACAGTTT 1080
AGCACTGACT TCTTCAGGGA CGAGTGAGAA AATGCCACCA CTTCACAATG GTAGAGGGTG 1140
GGTGAAAAAG TTATTAGCCA GGCACCAAGA ACCAATCTGA AGCCAAGAAC AGCAATGCAA 1200
AGCCAACAAA CTAGCTCTCT 1220