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

TagContent
EnhancerAtlas ID
HS044-13458 
Organism
Homo sapiens 
Tissue/cell
Fetal_kidney 
Coordinate
chr9:90872680-90874270 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs10746837chr990873653hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MAFGMA0659.1chr9:90873036-90873057TTAATGCTGATTCTGCATTTC+6.56
MAFGMA0659.1chr9:90873036-90873057TTAATGCTGATTCTGCATTTC-6.68
MAFKMA0496.2chr9:90873037-90873056TAATGCTGATTCTGCATTT+6.44
MAFKMA0496.2chr9:90873037-90873056TAATGCTGATTCTGCATTT-6.63
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr99087340790873950
Number: 1             
IDChromosomeStartEnd
GH09I088257chr99087195190874154
Enhancer Sequence
TCCACCTGCC TCGGCCTCCC AAAGTGCTGG GATTACAGGC GTGAGCCACT GCGCCTGGCC 60
TACATGTTTT TTAGCCTCAA GTGTCTGGAT AACACAATGA AAGCATGCTT GCCTGCTGGA 120
TTGTACAGAC CAAGCCCCTC AGCATGCACA AATGGTTATC TTCAGTCACT TATACTTCCT 180
AAGTTACCAG AATAACCTTG CACTCTCTCT CCCTTTGGCA ACACAAACCT CATAGATTGG 240
AAAATAGTCT TTTCTGCTGT CTTAATGCTT GCTTGCTTTC TATTCAAAAA CTACTGCATG 300
ACTATACAGC ATTTGAAACT CACTGTCTGA TTGGAATTTG GGAAACATTG GCTTTCTTAA 360
TGCTGATTCT GCATTTCCTG CTGAAATTGA GCTCTCAGCT TTGAGCAGTC CCACTGAAAC 420
CAGGGGCAGC CAGCCGGATT CTCTGCAAGT CAGGAAATGA GAGCCAGACT CCCTTGCTTG 480
TCTCTATGGA CACTGGAGTC GGTTTCCCTT CCTGGGCAGA TGAAAGGGTG AGGTCATTGC 540
ACATGATTGA GTGGTGGAGA AACTCAGCCT TCTAGAAACT AAGACCAAGC AATCATCTCA 600
CAAGAAAACA TTTTGGAAGC TAGGTTTTCA TCAACAACAT TAAATAAATC ACTGGTTTTT 660
AAAGACCGGT AAACCCCAAT GGCAGTCTGT CTGGATTTGT TCTAAAACTT AAAGCATGAG 720
TTTTGCTTGT AAATGAGAGT TCCCTGAAAT GCCAGCAAAA AAAAAAAAAA AAAAAAGCAA 780
ACCCAATCCT TTGGGTAATA GGAACCACAA CAAGGAAAAA TAGGAACCGC AACAAGGAAA 840
AACATTTTTT TAAATAAATA AAACATTTCA TGTTTATCCT CAGCAATTTC GTGTTTAAAA 900
GAAACAAACT CTACAACTGC TCAGCATTCT TCACAAGGAA GGTGTGCCTT CAGCCTCCCG 960
GAAAAGTCTC TCGGCTGGTA TGACCTGGCC TGTTGCCGGG AAAAAGTGAG ATTTGGCAGA 1020
CACGGGCGTC GGGACAGCCT GCATGGTTAC TGGACTGCAA GGTCTGGCCC CGTCAAAGCA 1080
GACAGCTCTA TTATCCCCAC AGCCTGCAGA ACTGGGGTCA GGCGTGTCCT GATGCTGGAT 1140
CTCTGCCCTC CTTCTCCCGG TTCTCACCCT GTAGGTGTCG GATTTGACCA TTTGCACAAC 1200
AACCCTCACG TTGTCATTCC CAGATCCTCA TTGGTGCATT GTTCTTTTTG TTTATAGTAA 1260
ACTTTATTTT TTTAGAGCAG TTTCAGGTTC ACAGCAAAAA GGAGCAGAAA ATACAGAGCA 1320
TTCCCATATC TCCCCTGCCC TATAGACACA CAGCCTCTCC CATTGTCAAC ATCCCCCACA 1380
GAGTGGTCCA TCTGTTACCA TTGATGAACC TACACTGACA CATCATCACC CAAATCCGTG 1440
GTTGACACCG GGGTTCACTC TTGGCATTGT ACATTCTGTG GGCTTGGACA AATGTATAAT 1500
GATGTGTCCA CCACTGCGGT ATCCCACAGA CTAGCTTCAC TGTCTTAAAA ATCCTCTATG 1560
CTTGACTGAT TCATCTCTAA TCTTTTTTTT 1590