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

TagContent
EnhancerAtlas ID
HS095-01684 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr1:110469670-110471470 
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
GGCTGGGTGA ATGACTAACC AACCAACTAT CTTGGTAACT GCCTAACTGA CCAGCTGTTG 60
CTTGGGGAGC CCATTGAGCA ACTGACTAGC TGATTGCCTG ACTAATTGGC TGGTTGGCTG 120
ACTAGCTGGG GTGACCCAGT CAAGTTTCCA GTCACATCCT TTACCAAGTG CAAGCCAGTG 180
CCGCAGGGCT CTCCCATGTG TGGAGTGACA GGTCTGGGCC CCTTCTAGAG AGATAGGGAA 240
TTTGGCAAAT GCTCAAAACC AGGGGAACCT ATTTAGACAA GAACCAGCAG TAACAACATA 300
TCTGGAATCC TGGGGTCTAC CTTGTCAGTG GGGTGGGCTA AGATGGGTGA GTGGGTCAGC 360
TGGGGCACTG GCAAGACTGT GAAATGACCC AGGCCTCCTC AGAACTGGTT GCTGGTGGCT 420
CAGTGCCACA ACACCCTTCC CACGGGTCGT CTGTCCCCAA ACCCCTCGCC GTGGTCTTGG 480
CCCTCTGTCC CACCCCTCTA CACGCCCACC CTCCTTTCCC CACTTGCTTA TTCTCAGGCC 540
CGTCCCAAGC TTTCCTCTTC CCCCTCAAGA TTTCACTTGG AGAGGGAATC CAGGGCAGGG 600
GCTACATCCA GATCCCACTT GGCCCGGCAG GTCCAGCCCT AAGGTGGTCT CCAGGCCAGG 660
CACCAGTGGC CTTGGAGAGA TTGAGTGCCA GCCCCTAGAG TGACTGCTGC TGTGATTTGA 720
GAAGTGAGAG AGAGAAACAT AGAGGCAGAG ACTGAGATAG GGACTCAGAG CCACAGAAAA 780
TGCAGACACC AGCACCTCAG CCCTAAGCAG CTAGAAGATG GGGCAGCAGG CTGGAACTCG 840
CTCACTGGGT CCTTCTCCCC TCCTGGGCCC TAGCTGGGCC TGTGGCCTGG CTGTACCCAG 900
CATGGCTCAT GTCCAGTTTA TGGTTCCCCT TCTTTCCCTC TAGAGCATGG GAATGGGCAG 960
GGAGCCAGAG GCTGTGGTTC CATCTTCCCT CCTTACCCAG TAGGGCCTAT GGATGTTAGG 1020
GAGGGAGGCT CCACACAAGG TCCAAAGTCA AACTGTTGGA TGGGGTCCAG GGGATTTCTG 1080
CTCTGGGAAC AAAGCGTCCT GAGGATGCTG GGCAAGAGGA CAAGGATGGG GGTGGAAGGC 1140
GAGAGGACAA GGCCCTGACT CCCATGGATG ATGCGGGAGG CAAGGCCCTC GGCCCATCCA 1200
GGAGGGGCTG GGTTGCTTAG GGGTCGCGTG CCAAATGACA GTGTGGGAAT TTCCTTGTCC 1260
TGGCACTGCC TCTAGACTTT TCCTCTCTGG CCCAAGTTGT TCCTCTTCAG CTAGCTCTGC 1320
CCTACTGTCT TGAACATCAT ATGTGATGCC CCTCTGATGA AATGAAAGAT TCTTCTTTGC 1380
TAGTGTTAGC AGGAATCACC CTTTGTTCAC TGGACCAAGG CCAATGAGAT GACCTCGCCT 1440
GAGGAGGGGT CCAAAGACAT TCAAGTGCCC GCTTCGCTCC TTGTCAGAGC CCTCTGCTTG 1500
AGCAGTAACC CCTCTTCCCA GCCCTGCCCA GACCTCTCCC GGGCCCCGTT ATCTTCCACT 1560
GAGGCCCTGA TTCCCCAGGA GGAGGTAGGA GGTGAGGCCA GTTGGGCCAG AGGCCTGGGC 1620
TGGTGCCAGA GAAAGCTGCC TGGTCTCTCT GTGGTGTCTG GAAAGGCCAG GGAAGGGAGG 1680
AAAGGAAGTC CTGCCTGCAG CACCGCCAGC AGCCCACAGG AATGCCACAC CTCCCAATCC 1740
ATGTCCTCAA CGACCCTCCC CGCATTCCCA CTCTGCTGAC TAGCCTTTCC TTCTCTCCCA 1800