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

TagContent
EnhancerAtlas ID
HS024-00874 
Organism
Homo sapiens 
Tissue/cell
Cerebellum 
Coordinate
chr1:110469980-110471470 
Target genes
Number: 4             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs333947chr1110470764hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:110471340-110471358GGAAGGGAGGAAAGGAAG+6.05
GFI1MA0038.2chr1:110470377-110470389TGCTGTGATTTG-6.52
Gfi1bMA0483.1chr1:110470377-110470388TGCTGTGATTT-6.62
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
TGGGGTCTAC CTTGTCAGTG GGGTGGGCTA AGATGGGTGA GTGGGTCAGC TGGGGCACTG 60
GCAAGACTGT GAAATGACCC AGGCCTCCTC AGAACTGGTT GCTGGTGGCT CAGTGCCACA 120
ACACCCTTCC CACGGGTCGT CTGTCCCCAA ACCCCTCGCC GTGGTCTTGG CCCTCTGTCC 180
CACCCCTCTA CACGCCCACC CTCCTTTCCC CACTTGCTTA TTCTCAGGCC CGTCCCAAGC 240
TTTCCTCTTC CCCCTCAAGA TTTCACTTGG AGAGGGAATC CAGGGCAGGG GCTACATCCA 300
GATCCCACTT GGCCCGGCAG GTCCAGCCCT AAGGTGGTCT CCAGGCCAGG CACCAGTGGC 360
CTTGGAGAGA TTGAGTGCCA GCCCCTAGAG TGACTGCTGC TGTGATTTGA GAAGTGAGAG 420
AGAGAAACAT AGAGGCAGAG ACTGAGATAG GGACTCAGAG CCACAGAAAA TGCAGACACC 480
AGCACCTCAG CCCTAAGCAG CTAGAAGATG GGGCAGCAGG CTGGAACTCG CTCACTGGGT 540
CCTTCTCCCC TCCTGGGCCC TAGCTGGGCC TGTGGCCTGG CTGTACCCAG CATGGCTCAT 600
GTCCAGTTTA TGGTTCCCCT TCTTTCCCTC TAGAGCATGG GAATGGGCAG GGAGCCAGAG 660
GCTGTGGTTC CATCTTCCCT CCTTACCCAG TAGGGCCTAT GGATGTTAGG GAGGGAGGCT 720
CCACACAAGG TCCAAAGTCA AACTGTTGGA TGGGGTCCAG GGGATTTCTG CTCTGGGAAC 780
AAAGCGTCCT GAGGATGCTG GGCAAGAGGA CAAGGATGGG GGTGGAAGGC GAGAGGACAA 840
GGCCCTGACT CCCATGGATG ATGCGGGAGG CAAGGCCCTC GGCCCATCCA GGAGGGGCTG 900
GGTTGCTTAG GGGTCGCGTG CCAAATGACA GTGTGGGAAT TTCCTTGTCC TGGCACTGCC 960
TCTAGACTTT TCCTCTCTGG CCCAAGTTGT TCCTCTTCAG CTAGCTCTGC CCTACTGTCT 1020
TGAACATCAT ATGTGATGCC CCTCTGATGA AATGAAAGAT TCTTCTTTGC TAGTGTTAGC 1080
AGGAATCACC CTTTGTTCAC TGGACCAAGG CCAATGAGAT GACCTCGCCT GAGGAGGGGT 1140
CCAAAGACAT TCAAGTGCCC GCTTCGCTCC TTGTCAGAGC CCTCTGCTTG AGCAGTAACC 1200
CCTCTTCCCA GCCCTGCCCA GACCTCTCCC GGGCCCCGTT ATCTTCCACT GAGGCCCTGA 1260
TTCCCCAGGA GGAGGTAGGA GGTGAGGCCA GTTGGGCCAG AGGCCTGGGC TGGTGCCAGA 1320
GAAAGCTGCC TGGTCTCTCT GTGGTGTCTG GAAAGGCCAG GGAAGGGAGG AAAGGAAGTC 1380
CTGCCTGCAG CACCGCCAGC AGCCCACAGG AATGCCACAC CTCCCAATCC ATGTCCTCAA 1440
CGACCCTCCC CGCATTCCCA CTCTGCTGAC TAGCCTTTCC TTCTCTCCCA 1490