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

TagContent
EnhancerAtlas ID
HS136-04769 
Organism
Homo sapiens 
Tissue/cell
Monocyte 
Coordinate
chr12:69432900-69434680 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1908671chr1269433404hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr12:69434574-69434595TTTTTCTTTTTCTTTTTTTTT+6.09
IRF1MA0050.2chr12:69434568-69434589TTTTTCTTTTTCTTTTTCTTT+6.17
Nr2f6(var.2)MA0728.1chr12:69434240-69434255GAGGTCAGGAGTTCA+6.22
Nr2f6(var.2)MA0728.1chr12:69433436-69433451CGATCTCTTGACCTC-6
SOX10MA0442.2chr12:69434094-69434105AAAACAAAGAC+6.14
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr126943370469434066
chr126943372169434090
Number: 1             
IDChromosomeStartEnd
GH12I069039chr126943358069434090
Enhancer Sequence
AGTTATTAGT CCAACATAAC TGTGATTTTG AACACTTATT TATTGGGCAC CTCTTCTGTG 60
CTAGGTGCAA GGGTTATCTC CTGTAATCTT TATAACAATG AAATCAATAC TATTATTATC 120
CAATTATGTA ACCAAGGAAA CTGATGCTTA GCAAGGTTAA GTAGCTTTCT CAAGGTCAAG 180
GTGAGTGGTG GAGCAAGCAG GTAAACCCAT GTGTGTCTAA GGCCACAGCC TATGCTCTAG 240
TCACCAGGTA ATCATTGATC TCTCTGGAAT ATCCACAGTT GGAAAGCAAG GACTTTGCAA 300
CTTGCTGCTG AATGTATTTC TTTTCTTTTC TTTTTTTAGA CCGAGTCTCG TTCTGTCACC 360
AGGCTGGAGT GCAGTGGCGC AATCTCGGCT CATTGCAACC TCCACCTCCC AGGTTCAAGT 420
GAGTCTCCTG CCTCAGCCTC CCCAGTAGCT GGGACTACAG GCGCACACCA ACACACCCAG 480
CTAATTTTTG TATTTTTAGT AAAGACGGGG TTTCACCATG TTGGCCAGGA TGGTCTCGAT 540
CTCTTGACCT CGTGACCCAC CCACCTTGGC CTCCCAAAGT GCAGGGATTA TAGGTGTGAG 600
CCGCTGTGCC CAGCCGCCGC TGAATGTATT TCTTACCACC AATCTGTTCA GTCATTACTA 660
TTCCTTCCCC CTTTCCTAAG TACCATGGGA AATGAAGCAT AAAGCACTCA AAGTCCAAGG 720
AAAAGGCAAC ATTCAGGATT CAGTTCCAGA ATGTCTGCCT CTTCCAGACC CATGCTCCCA 780
CCAGTTGGCC ATGCATTCTC AACTTGCATG CCTATGTCAT CTGTCTCTTC TGACCCTGAA 840
GAAAGCTTCT ATTCACTCCA TGAGCACCTG CACCTTCACT GAGTCAATAG TGAGTGGCTG 900
CTATCTGCAC CAAAATCCAT TGCTCAATAT TCTTTCTTCT CCATTCCAAA TGGTTCCTCA 960
TTTCTGTGAA AGCCCACATG GTCTTACCAT ATGTCTCGTT GTCTTGGTAG TAAACGCATT 1020
TTTAAAAACA AATATGTCAG CATCATTTTG TTTTTTTTCA TTAGTGGTCT CATGTTACAG 1080
TCATAACAGG TTGCATAATG GTTACATCTA GTACAAAATA ATGCTATTGT GTTTTCTCTT 1140
GGAGGCTGTT ATCTAGTTAC ATTGCTTGTG ACTAGCTAAG GAGGATATTG TAGAAAAACA 1200
AAGACCTTCA AGGTAGACAG ACCTGACTCT GAATTCTGAC TTTATCATCC ATTCATTTAA 1260
AAATATTTAT TCAAGGCCAG GCGCGGAGGC TCATAGCTGT AGTCCCAGCA CTTTGGGAAG 1320
CCGAGGCGGA TGGATCACCT GAGGTCAGGA GTTCAAGACC AGCCATGGTC TTGAAATCCC 1380
ATCTCTACTA AAAAATACAA AAAATTCGTT AGGTGTGGTG GCACACGCCT GTAATCTCAG 1440
CTACTTGGGA GGCTGAGGCA GGAGAATTGC TATATATATA TATTCCTGGT ACGTAGTAGG 1500
TCCTGAATAA ATATGTATAT ATACTCCAAT TTTAACATTT CCTATGCCCC TTCCCTGCTT 1560
TATTTTTCTC CTCAGCATAT CATTGGCTAA TATAGCTTTT TCTCCTCATT TGTCTTGATT 1620
AATGTCTATC TCACTCCACT TGAACATAAG CTCCATGAAG ACAGTGTTTT TTTCTTTTTC 1680
TTTTTCTTTT TTTTTTTAAT ACAGTCTTGC TCTGTTGCCC AGGCTGGAGT GCAGTGGCTC 1740
AATCACAGCT CACTGCAGCC TCGAACTTCT GGGCTCGAGC 1780