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

TagContent
EnhancerAtlas ID
HS145-08935 
Organism
Homo sapiens 
Tissue/cell
NHBE 
Coordinate
chr16:11733990-11734970 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12444261chr1611734642hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr16:11734679-11734697GGAAAGAAGGAAGCCAAG+6.44
GFI1MA0038.2chr16:11734361-11734373CAAATCACTGCC+6.04
NFE2L1MA0089.2chr16:11734506-11734521ATTGCTGAGTCACAG-6.85
Nfe2l2MA0150.2chr16:11734508-11734523TGCTGAGTCACAGCT-6.27
Number of super-enhancer constituents: 9             
IDCoordinateTissue/cell
SE_10082chr16:11732751-11735626CD14
SE_27070chr16:11733498-11735486Esophagus
SE_31920chr16:11733571-11735481Gastric
SE_42648chr16:11733494-11735628Lung
SE_48190chr16:11733483-11735670Psoas_Muscle
SE_50207chr16:11733587-11735573Sigmoid_Colon
SE_52871chr16:11733490-11735455Small_Intestine
SE_53430chr16:11733432-11735522Spleen
SE_61608chr16:11668804-11735966Toledo
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr161173409111734770
Number: 1             
IDChromosomeStartEnd
GH16I011639chr161173287411736153
Enhancer Sequence
CACTCTGCCA GGGCTGGGTC CTTATTAGGC ATTCACGGCT GGATCCGCAG GGCTGAGCAC 60
TGCATCCAGC ACATAGTAGC TGCTCAGCAC ATGTTCGTGG AGCGACTGAG TGTGTAAGTC 120
AGTGAATGAA CAAACGAATG AAGGGGTTCT CGCTCTGATA CTTGTTCTGC AGCCTGGGAA 180
ACTGAAGCTC AGAGATGAAG TGACTTCACC GAGGTCACAC GGACAGTGGG CGGCAGAACT 240
GGAGCTACCT ACGCAATTGG GATTATGAAA TATTTCACAA GTGCCAAGAA GTGCACATGA 300
TGCAGGGCTC TAGAAGGCTT CCTCTTTGAT TTGTCACAGT CCCTGCAGCA GAGAGGCAGC 360
CCAAGGCTCT GCAAATCACT GCCACTTCAT CACGGCTGCA GCCACCCTTG TGCAGGCCCC 420
AGCTCGAGGT CTTCTCACTC GATGCTGGTA TGGGGGTGAT GATCATCCAT CTGGCAGGTC 480
ACAAGGACAA CCCTCGGGAT GGGAAATCTG ATCCTAATTG CTGAGTCACA GCTAAAGGGC 540
AGAATGACGT CGTCTGTAAC CATGGCATGC ATTCCAAACT CAGCCCCAGC TTGGCTTCTC 600
CTCAAGTTTG AGTGAGCCCC TGTCAGTCTA CACCACCCCT CCTCATGTTC GGCTGTTTTC 660
AAGCCGGCAC ACTGGCAAAG ATGCTGCCAG GAAAGAAGGA AGCCAAGCCC AGGGAGAGGA 720
GAGAGCTGGT TTGCTGTGGG TGGCCAGGAA CAAGGTCCCG TGTGTGGAGG AGACAGAACA 780
CAGTCATGAT ATCAGGCCGG GAGCAGTGGC TGACTCCTGT AATCTCAGAA TTTGGGGAGG 840
CTGAGGTGGG AGGACGGCTC GAGCCCAGGA GTTCAAGACC AGCCTGGGAA ACATAAGGAA 900
ACCCATCTCT ATTTAAAAAA AAAAATCAGC CAAGCATGGT GGTGCATACC TGTAGTATCT 960
GCCACATGGG AGGCTGGGGC 980