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

TagContent
EnhancerAtlas ID
HS182-05643 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr12:132662650-132663950 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs75407077chr12132663167hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EBF1MA0154.3chr12:132663148-132663162TGTCCCTTGGGATT-6.24
KLF16MA0741.1chr12:132663670-132663681GCCCCGCCCCC+6.02
KLF5MA0599.1chr12:132663670-132663680GCCCCGCCCC+6.02
Myod1MA0499.1chr12:132663005-132663018TCCAGCTGTCCCT+6.16
SP4MA0685.1chr12:132663667-132663684CGAGCCCCGCCCCCTCC+6.16
ZNF740MA0753.2chr12:132662876-132662889CCGCCCCCCCCAC+7.82
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr12132662941132663228
chr12132663524132663727
chr12132662936132663290
chr12132663332132663875
Number: 1             
IDChromosomeStartEnd
GH12I132178chr12132662746132663750
Enhancer Sequence
TCTGCCGGGC ACAGTGGCTC GCGCCTGTAA TCCCAGCTCT TTGGGAGGCC AAAGTGGGAG 60
GAGTGTTTGA GGCTGGGAGC TCGAGACCAG GCTGGGCAAC ATGGCAACAA AAAAAATTAA 120
AAACTTAGCT GGGTATGGCG GTGTGCACCT GTAGTCCCAG TGACCGGGGA GGGTGTGACG 180
GGAGGGTGGG GAGCCCGGGA GTTTGAGGCT GTACTGAGCT CAGAACCCGC CCCCCCCACC 240
CCCTGCACTC CAGCCTGGGC GACAGAATGA GACCCCTGAA AAGTGTTGGT TTCTGACTTT 300
TTTCGTTTTT GAAATCGTTT CCGGCTGGCC CAAGTCGAAA AATAATGCAG ATGTCTCCAG 360
CTGTCCCTGA GAACACTTCC TGTTCCTTGA TCTGTGGCTT GTGATTCTCC CCCCGCCCCC 420
ACTCCCCTTA CATGGGGCTG TGGCTGCCCC CAGCCTTTCC CTTTCGTGAC CTCAGGATTG 480
TATGACTGCA GGTTGGGCTG TCCCTTGGGA TTCAGGGCCT CAAATGTACC TGCTGACCAG 540
TTGAAGAGTG CTGACCAGCT GTCCTGCTGA ACACCTCTCA ATCTGGATTT TTGACATTTC 600
CCTGTGATTA AATTCAGGGA ATCCAGCTTT GGTGACAGAG CCACTGAAGC AAGGCTGTTC 660
CCTGCTTGGA GACGCACCCA CTTTACACGT GTAGGGTGGC GAGTCTGACA AACGCAGCCA 720
CAGGCAGCCC CCACCGGGGG AGCCGGACGT TTCCATCCAC CCAGACAGCA GCGTTCACGC 780
CCAGGACCAT GTGGGCCTGC GCCCCGGGCC GCACCTGCCT CTCCTGCATT CCGTGTCTGG 840
CATCTTGTGT CGTTGCCACC CTGCGTGCCA TGTCTGGCTT CTCTCTCTCA GCGAGTGTCC 900
TCCGTGTCTC CGAGTCGCGC CCGTTCTGTT GTGCGTAAAT GCCGTTCTCA GAGCTGTTGT 960
TTGTTTAGGG ATGTATCATG TTTTCAGCTT AACATTTGTG CCATTCGTGT GCCCTGGCGA 1020
GCCCCGCCCC CTCCAAGTTA CTGGCGTGCT GTGGGCGTTC TCGGGTTTCT ACTCTTCCTG 1080
CTGTCGCCAG CGCAGCCGAA GCACCAAGCA GGAAGCTCTG CCGAGTTCTT GGCTTCAGGT 1140
AACGTGTCAG ACCCAGGGCA TGAGCTCCAG TCCCTCTTGC CTCCACAAAG GACAGCACAT 1200
TTCCAGTTCA GGGTGCTGTG GCCGACACCG TGCGTGTGGC TGGGGCCAGT GTCACCGCGA 1260
ATCTCGGCTG CTCCACGCCC TTGCTGTGGG CTTGGGGCCA 1300