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

TagContent
EnhancerAtlas ID
HS047-28750 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr6:30058890-30060470 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3132681chr630060041hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr6:30059675-30059693TCTCCCTCCCTCCCTTCC-6.25
EWSR1-FLI1MA0149.1chr6:30059683-30059701CCTCCCTTCCTTCCTCTC-6.88
EWSR1-FLI1MA0149.1chr6:30059679-30059697CCTCCCTCCCTTCCTTCC-8.13
ZNF263MA0528.1chr6:30059684-30059705CTCCCTTCCTTCCTCTCCTCT-6.3
ZNF263MA0528.1chr6:30059678-30059699CCCTCCCTCCCTTCCTTCCTC-6.74
ZNF263MA0528.1chr6:30059679-30059700CCTCCCTCCCTTCCTTCCTCT-6.81
ZNF263MA0528.1chr6:30059675-30059696TCTCCCTCCCTCCCTTCCTTC-7.48
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr63005935130060199
Number: 1             
IDChromosomeStartEnd
GH06I030090chr63005857330060526
Enhancer Sequence
ACTGGCCGAC TGTGCAGGGC TTTGTCATTG TCAGGACTTC ATTCAGTACT GGGTGAGGTG 60
AGCCTACCAG GGGTTGGAGT TGGTGGGAAG GGGCTGACTT CTGGACGTGA GTTACTGCAT 120
TGGTTGTGGA GTGTGAGAGC AAAGGAGGAG GCAGGAAGCT CTAACGAATT TGGCCCCACC 180
ATGGGGAGGA TGGAGCTGCC AGTGACTGCA GTGGGAAGAA CTGTGAGGAG CTGGCCTGGG 240
CAGGAATATC AGGGGTGGCA TGTTGGACAT GTGAAGCCAG GAGGCCTGTG GGCCATCCAA 300
CAGTGCTGTG AACTGTGCAG CCCGATGTAA GCATATCTGA CATTAGGAGT GGTGGAGAAA 360
CAAAAAGAAC AAGGATAGTT CATTTTAACA CAGTAATAAT TTTATAATTT TATAATTTTC 420
AAATCATTAA AGATTTTACT ACTTTCTTAA CTACTCCAGG AGCCTGTGTC ACATTCCAGT 480
CACAGGGAGG AAACTGGGGG CCATGCAGGA TAAAGGTCAA AGCCTGCATG CTGGGACTCA 540
AGTGCTTCCT CCCCAACAGT ATTAGAACAC CAACTCCCAG GAGCACAGAG ACTTGAAGAG 600
AGTGTCCGGG TCGTGGACTA TGAGTCAGAG AAACCAAGCC AGGGGCATGC AAGGCAGCAC 660
GAGGCAGAGC AGGGAAACCC AGCAAGGGAG GTGGCAACGC ACAGTGACCT AGAAAAGCCT 720
GATGAGCTGA GAGCCAGCCG ACAACAGGCC CCATGTGCCT CTGTGTCTTG GTCCACATGA 780
TAGACTCTCC CTCCCTCCCT TCCTTCCTCT CCTCTGGTGA CCAGTAGCTA AAACATCACT 840
GGCACGCTGC TGGCATCCAG CCTGCCAATT AGTTCAGGAG CCACTCCCTC TGACTGCCTC 900
CTGAGCCTCA GATGTTACCT CCCCTGTCTC CCAAACACAC CCCTCCAGCT CTGTCCTGCC 960
TGCCCTGAAT CTCTGGAAGG AAAACTTGCC CTGGGACCTG CCTTGGACTC TCTGGTTCCC 1020
CTCATCCAGC CCCTCCCTGC GCAGAACATG GCATCTCGTG CCCTTTTATC TGCCATTTCT 1080
GGCCACCTTT GCAAGCGTCC TTGAAACCAG CGCTTGGTAG AGTTATCCAC GCCCATGTGA 1140
GGCTCCCCTG CCCCCTGGGT GGTGTATGTG GCAGGAGGAG CAGGGAGGAG CTTCAAGGAA 1200
GCAGAGGGAA AGGAACCTAT AAGAGTTCTT GGGATGGCTT CCAGGAAGCT GTGAGGACAG 1260
AGCTATGCTG AAAGGAGAAA GGCAAAGGCT ACAGAAAAGT GAACACTGAA GAGGAATTAG 1320
GCAAGAACAA AGCCTACCAA GTTAGAAGAA GGGAATGAGA GGGCGAAACA ACAGCACCAG 1380
AAAGGAATGA GGTTGCCGGG CACGGTGGCT CATACCTGTA ATCCCAGCAC TTTGGGAGGC 1440
CGAGGCAGGC GAACCACCTG AGGTCGGGAG TTCGAGACCA GCCTGACCAA CATGGAGAAA 1500
CCCTGTCTCT ACTAAAAATA CAAAATTAGC TGGGTATGGT GGTGCATGTC TGTAATCCCA 1560
GCTACTCAGT GAGGCTGAGG 1580