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

TagContent
EnhancerAtlas ID
HS045-03375 
Organism
Homo sapiens 
Tissue/cell
Fetal_lung 
Coordinate
chr1:110470440-110471470 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs333947chr1110470764hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:110471340-110471358GGAAGGGAGGAAAGGAAG+6.05
RELAMA0107.1chr1:110470914-110470924GGGAATTTCC+6.02
ZNF263MA0528.1chr1:110471247-110471268GGAGGAGGTAGGAGGTGAGGC+6.07
Number of super-enhancer constituents: 8             
IDCoordinateTissue/cell
SE_00603chr1:110467604-110475254Adipose_Nuclei
SE_04393chr1:110469347-110472853Brain_Anterior_Caudate
SE_06043chr1:110464238-110474855Brain_Hippocampus_Middle
SE_32320chr1:110469375-110474485Gastric
SE_47194chr1:110462831-110479044Panc1
SE_50838chr1:110468044-110473482Sigmoid_Colon
SE_53269chr1:110469281-110473349Small_Intestine
SE_53713chr1:110465215-110474535Spleen
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1110470445110471000
Number: 1             
IDChromosomeStartEnd
GH01I109925chr1110467674110475106
Enhancer Sequence
CCACAGAAAA TGCAGACACC AGCACCTCAG CCCTAAGCAG CTAGAAGATG GGGCAGCAGG 60
CTGGAACTCG CTCACTGGGT CCTTCTCCCC TCCTGGGCCC TAGCTGGGCC TGTGGCCTGG 120
CTGTACCCAG CATGGCTCAT GTCCAGTTTA TGGTTCCCCT TCTTTCCCTC TAGAGCATGG 180
GAATGGGCAG GGAGCCAGAG GCTGTGGTTC CATCTTCCCT CCTTACCCAG TAGGGCCTAT 240
GGATGTTAGG GAGGGAGGCT CCACACAAGG TCCAAAGTCA AACTGTTGGA TGGGGTCCAG 300
GGGATTTCTG CTCTGGGAAC AAAGCGTCCT GAGGATGCTG GGCAAGAGGA CAAGGATGGG 360
GGTGGAAGGC GAGAGGACAA GGCCCTGACT CCCATGGATG ATGCGGGAGG CAAGGCCCTC 420
GGCCCATCCA GGAGGGGCTG GGTTGCTTAG GGGTCGCGTG CCAAATGACA GTGTGGGAAT 480
TTCCTTGTCC TGGCACTGCC TCTAGACTTT TCCTCTCTGG CCCAAGTTGT TCCTCTTCAG 540
CTAGCTCTGC CCTACTGTCT TGAACATCAT ATGTGATGCC CCTCTGATGA AATGAAAGAT 600
TCTTCTTTGC TAGTGTTAGC AGGAATCACC CTTTGTTCAC TGGACCAAGG CCAATGAGAT 660
GACCTCGCCT GAGGAGGGGT CCAAAGACAT TCAAGTGCCC GCTTCGCTCC TTGTCAGAGC 720
CCTCTGCTTG AGCAGTAACC CCTCTTCCCA GCCCTGCCCA GACCTCTCCC GGGCCCCGTT 780
ATCTTCCACT GAGGCCCTGA TTCCCCAGGA GGAGGTAGGA GGTGAGGCCA GTTGGGCCAG 840
AGGCCTGGGC TGGTGCCAGA GAAAGCTGCC TGGTCTCTCT GTGGTGTCTG GAAAGGCCAG 900
GGAAGGGAGG AAAGGAAGTC CTGCCTGCAG CACCGCCAGC AGCCCACAGG AATGCCACAC 960
CTCCCAATCC ATGTCCTCAA CGACCCTCCC CGCATTCCCA CTCTGCTGAC TAGCCTTTCC 1020
TTCTCTCCCA 1030