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

TagContent
EnhancerAtlas ID
HS105-30577 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr16:31129210-31130640 
Target genes
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs9925964chr1631129895hg19
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EsrraMA0592.2chr16:31129399-31129410TTGACCTTGAA-6.14
Foxd3MA0041.1chr16:31130477-31130489GTTTGTTTGTTT+6.32
KLF16MA0741.1chr16:31129234-31129245GGGGGCGGGGC-6.02
KLF5MA0599.1chr16:31129235-31129245GGGGCGGGGC-6.02
KLF5MA0599.1chr16:31129265-31129275GGGGCGGGGC-6.02
KLF5MA0599.1chr16:31129331-31129341GGGGCGGGGC-6.02
SP1MA0079.4chr16:31129329-31129344GAGGGGCGGGGCTTG-6.34
SP2MA0516.2chr16:31129328-31129345GGAGGGGCGGGGCTTGA-6.29
SP4MA0685.1chr16:31129327-31129344AGGAGGGGCGGGGCTTG-6.49
Number of super-enhancer constituents: 3             
IDCoordinateTissue/cell
SE_09570chr16:31122347-31132628CD14
SE_26229chr16:31128868-31132413Duodenum_Smooth_Muscle
SE_26836chr16:31128082-31131019Esophagus
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr163112961631130225
Enhancer Sequence
GGCGTGAGGG CGGGGCCCAG GGCTGGGGGC GGGGCGGAGC TCAGGGCCAG GGGGTGGGGC 60
GGGGCCTGAG GACAGGCTGT CAGTGAGGCC AAGATCCGGG GGCTGGGAGT GGAGAGGAGG 120
AGGGGCGGGG CTTGAGGAAA GAACGCCGCG TTCCGGGCGC TGAGAAACCA GCCGGGTTGT 180
GGGAGGCTGT TGACCTTGAA TTATGCCGAG CGACGCCTAC AAACCCACCG CTCAGGCCTT 240
CACCAGGATT GTTCCCATTC CACTTCCTTG CCCAGTCTTA GGCTTCATTC CTTTTTCTTG 300
CTAACGCTGC TTCCTCACCC TCTCTTGTCT CTGCGTCTTC TTTTTCCATT TGTCCCTGGC 360
AGCCATCCGC AGAGAGAAGA CCTTCCAGAA ACAACAGGCT TCCCTTTCCT AAAGTTCTGC 420
TGCCTTCTCT CATTTTCAAA ATTAACCCCA AACTCCTTAG GGTGGCATTC ATTTTTGTGA 480
CCTCTCCAGT TTCTAGCCAA CACTAGGAAA GGGCATTGCC AGGCCAGAAC ACACTGTGCC 540
CTCTGAAGAC CACACGCCCT TTACCACCTG TGCCCTTTGC TTGGAATGCT TTTTCTTCCC 600
TTTCTCCTTG TTTGCCTGCC TAGCTCCTAC TCATCCTCTT AGCTTCATAT CCTTTGTGAT 660
GTCATCCTTG ATTCCCCTTC AGGCAAAGTG AGTGGTTCCC TTCTCTATGT TCCTGCAACA 720
TTTTTTTCCT ACCTCAGTCA TAGTTTTTGT AACATTATGT TGTAATTTTC TCTCTCTGTC 780
TTCCTCCATC ATACTGGGAA CTTCTGGAGG GCAGCACTTC TTGTGATTCA TCACTGTGTC 840
CTCTGTACCC GGCAACAACA CAGCATAGGG CCAGACACGT AGTGGTTGCC TTACTCATTT 900
ATTGAATGCT CTGCTAATTG TCAGGTGCGC TGCTAAAAAT TTTGGAGGCA TTAATTCACC 960
TTCTAAGGTT GGTACTATTA TCCCTTTTGT CTTTTTTTTT TTTTTTTTTT TTGAGACAGG 1020
ATCTCGCTCT GTCACCCAGG TGGGATTGCC GTGGCACGAT GACAGCTCAC TGAAGCCTAG 1080
ACCTTCTAGG CTCAAGTGAT CCTCCCACCT CACCCTCTCA GAGTGTTGGG ATTACTGGCA 1140
TGAGCCACTG TGCCCAGCTG TTATCCCTTT TCACAGATGA AGAGACTGAG GCTCAGAAAG 1200
ATGGAATAAC TTGCTCAGTT ACACATAGCT AGGAAGTAGG GAGCTGGAAT TTTGTGTATT 1260
TTTTTTTGTT TGTTTGTTTG AGATGGAATC GCTCTCTGTT GCCAGGCTGG AGTGCAGTGG 1320
CGCCATCTTG GCTCACTGCG ATCTCTGCCT CCCGGATTCA AGCGATTCTC CTGCCTCAAC 1380
CTCCTGAGTA GCTGGGACTA CAGTTGTGCG CCACCACACC CAGCTAATTT 1430