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

TagContent
EnhancerAtlas ID
HS008-00632 
Organism
Homo sapiens 
Tissue/cell
BJ 
Coordinate
chr11:64682280-64684430 
Target genes
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs188954228chr1164682925hg19
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr11:64683973-64683988GGGGTCAAGAGGTCA+8.07
Nr2f6MA0677.1chr11:64683329-64683343AAGGTTAGAGGTCA+6.06
RARAMA0729.1chr11:64683973-64683991GGGGTCAAGAGGTCAGGG+6.56
RREB1MA0073.1chr11:64682613-64682633CCCACCACCAACCCCAAACA+6.16
RREB1MA0073.1chr11:64682610-64682630CCCCCCACCACCAACCCCAA+6.93
RREB1MA0073.1chr11:64682607-64682627CCCCCCCCCACCACCAACCC+7.34
TCF7L2MA0523.1chr11:64682551-64682565AGAGTTCAAAGGGA+6.28
ZNF740MA0753.2chr11:64682605-64682618CCCCCCCCCCCAC+6.92
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr116468287064682981
chr116468286364683400
chr116468340064683600
Enhancer Sequence
TCATTCCCCA GCCAAGCTAG GCTCCAGCCA GGGACTCAGA GCAACTAGGA TGAAACTCAA 60
GAGGTGAGCA GGTGCTTGGG GGTGGTGAGG GGGCTGGTGG GGGGGCCGTG GGGAAGACGC 120
CTAACCCAGC CTGGGCCGTC AGAGGAGGGG CAAGCTGAAG AATAAAGGGA GGGGGGATAG 180
GCGCTGGTAG AAGGTGGTGT GTTGCAGGCA CAGGACAACA TGGGCACATG TATGGCAGAG 240
TCCAGAATAC CCATGTTCAC CCTGGATGAG CAGAGTTCAA AGGGACAGTG TCCAAGAGAG 300
GGGCTGACCT AATGCCAGAT GGGACCCCCC CCCCCCACCA CCAACCCCAA ACACCTAGTG 360
TAGCTGTGCC TCTCTGTGAG GCACAAGGCT GAGCCCCTGG CTAAAATGTC CATGCTGGAG 420
TTGTACCCCT GCCAACCTGG AAGCTCCTGG AGGGCTGTAC CCCACCTGCC TCCCCCGTCA 480
CCCCAGGTGC CACCCAGAAA GGGCCTCAGT AAACTGGTTG GATCCAAGAA TAAAAAAGCA 540
CATGGCAGAG CAGATGGGAG TCCAAATTCC TCACCCAGAG ACCCACAGCT CGGGAAACTG 600
AGGCCTAGAG ACAGGACTAA TCTAGTCACC CAGTATACAA CAGGGACTGA GACTGGGATG 660
CGGGCCTCTT TCTTTTCATG CCACTTCAGA GGCCCCAGAT ACTCAGTTTC TTTGGGGGCC 720
TTCAAGGCGG GGCCTGCAGG CTGAGCTGGG AGGGAGGAGG GGCTGGTTAT CAAGAAAGCG 780
CCTGCATTCC ACCAGGGCCC TAGAGAAGCC AATTCAATCC CCAACAAGAG GGCAGGGAAC 840
AGGAGTAGGG GCGTTTTCTG GAGCTGAAAG TAAAAAGGGG AAGCCTAGGG CTGGGTATGG 900
TGGTTCATGC CTATAATCTC AGCACTTTGG GAGGCTGAGG TGGGAGGATC CCTTCAGGGG 960
TTCAAGGCTA GCCTGGGCAA CATAGCGAAA TCCTGTCTCT ATAAAAATAA AAAAGGGGCA 1020
GCCTAGAGAC GGCCTTAGAG GCTGAGGCTA AGGTTAGAGG TCAGAGAGGG CTTCCTACAC 1080
CAGAATTCAC AGACAGCAGG CCACTGGGGG GTGCCCCCAG TTCAGGGCCC ACGATTATCC 1140
TACCCCACAT TTGCTCACCA GGGCCTGGCC TACCCCCAAA GCCTAGCTCT TCTGCCCAGA 1200
TTAGCAGCCC CCTGAGTCCA GCCACAAAAC TGAGAAGTCC CTGCCTCCAT GCCCACCCCT 1260
GCTGCTCTGG ACCTGGTGGA TCGACCAGGA CGCGCCTCTA ATTGGTGGCT CCTTCAAAGC 1320
TCCCCAGGTC AGCTGAGCTG TGAGTCAGGG CTCCTCACCG TTCCCAGCCT CAAGCCTCTG 1380
ACCTTACACC TCTTGGCCTC CCTAGCATCT CCCTTGGCCT CCTCCCGGCT TGAAGCCAGA 1440
TCTCCCCACC TTTCCTCCAG GGCCTCCCTC CAGGCAGGGA CACTGAGCCG GGGGGGTCGG 1500
TGGGAGATGT AGGTGGGGGC CATCCAGTCC CTCCCTAGAC ACCCACTTGG CCCATCCCAC 1560
TCTCCCAAAA GCAGGAAGTA GGCAGCGACC CAGGCACACG AGGTGTTGAT CAACACTGGT 1620
ACTGACGTAC TGACGCGGTT GTTGACATAC ACATCCGGTG GTTTGTTGAT CCCACCTACG 1680
GGCTCAGGAC CGTGGGGTCA AGAGGTCAGG GCACATGATC CACAGGTGTC CTCGCCAGGG 1740
CTCCGGACCC CTACCAGCTT CCCCCACCAG CTGCGCAGGC CCAAGTCTGT CACTGCCCTG 1800
GCCCAGCTCA GTTCCTACGC TCCCTCCCCA GCCCCTCCTC AGCCCGAGAG CCAACCTCCT 1860
TAACTCAGCC CCCAAACTCG ACGAGTTTGT CTTGCATTCT CCAGACAGGT GATCTTGCCC 1920
TCTCCAGCCT CAGTTTCTCC TCCCGTGGAG ACAGAAACCC CTTCCCGCTC AGTTTCTGGC 1980
TCTGGTAAGG AACTGAAGAG GCCAGCCGGG GTGCCTCTGA CGCCTGGAGA GGGCAAGATT 2040
CCCCTGGCCT CTCTACGCCC GGTGCCTGAT CCCCCAGCCC GATCCTGCCG CAGGGAGCCT 2100
CAGGTCGCTG CGCTCCCACC CTCCGCACCT TCCTGGACTC GGGCCTGGCT 2150