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

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EnhancerAtlas ID
HS056-15698 
Organism
Homo sapiens 
Tissue/cell
GC_B_cell 
Coordinate
chr9:107730040-107731190 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NRF1MA0506.1chr9:107730827-107730838GCGCATGCGCG+6.02
NRF1MA0506.1chr9:107730826-107730837CGCGCATGCGC-6.02
Nr2f6(var.2)MA0728.1chr9:107730052-107730067GAGGTCAGGAGTTCA+6.22
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9107730510107730878
Number: 1             
IDChromosomeStartEnd
GH09I104967chr9107730021107731977
Enhancer Sequence
GGTGGATCAC CTGAGGTCAG GAGTTCAAGA CCAGCCTTGC TGACATGGTG AAACCCAGTC 60
TCTACTAAAA ATACAAAAAT TAGCTGGGTG GTAGTGGCAC GCGCCTGTAA TACCAGCTAC 120
TTGGGAGGCT GAAGCAGGAG ACTCTCTTGA GCCTGGGAGG CAGAGGTTGC GGTGAGCCGA 180
GATCGCGCCA CTGCACTCCA GCCTGGGCAA CAGGGTGAGA CTACGTCTCA AAAAAAAAAA 240
AAAAAAAAAA AAAAAAGAAG AAGAAATTTA ACATACAGGC GATTTTTCAG GTTCTCATTT 300
GCTAAACCAA CAATGCAGAA TTTGTGAAGT AGGGGCAACA AGTTGCTGAA CCTGAGAGAC 360
GCCTCTAAAT GCGCTCAGAG GTTATTTCAA CTGTGCTGTT TGCTAGTTCA GGTACAACAG 420
GCAAGACAGA AAGATGCCAC CGCTCTCTCC ACCCTCCCAG CGCCGGATCA CAGAGCGCAG 480
ACCATGCACC CAGCCTTCCA CACACGTCGC GATCTCGCCG CTTTAAGCTG CTGGGTACCC 540
TCGGCCCGCC CACAAGAAGG CGGGGCGGCG CGGGGTCTGC TGGGAGTTGT AGTTTCGGGC 600
CGGGCCCGAG AGCTTCTTGA CTCGTTTCCT TCTACCCCCA CCGCCGCACA GCTGCCTATG 660
GACTCTGGAG TTGCTGTGTA TTGAGCATGG GGCACAGCCG GGGGTAAAAG GGGAGAAGGC 720
TCCTTTAATC TGCGGATCGG GGCGCCGTTG ATGAGTGTTA GAGGTGTTGG AACGCAGAGT 780
AAGCGGCGCG CATGCGCGGC TGCCGGAGGT GGGGGCCGCT CCTCCCGTGC CACTCAGGGG 840
CTGGCTGCTG CCTTAGGGCT GACTGGGCTC ATAGGTAGGG CCTGCGGTGC AAGTTTGTGA 900
TAACACTGCC TGTAGGCTGC GGTTGTTAAG GCAGAGATTT GAAGGGGGTC GGTTGGGGGT 960
GCTGGGTAGT GTCAGTAATC AAGGGTTTTA ATCGCTACTC CATCCTGGCT TTCGGGAACC 1020
TCCCACCTCC TACCCTTTCC CAGTTTGCAG AATTGCAGCT TTCCCCATCC CCCACCCCGA 1080
TCGCTTCGTG GGAAGCCTTT CCATACTGTG TTGTGAAATC CGTTAGACCT CAGCCAAGGC 1140
CTTTTAGCCC 1150