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

TagContent
EnhancerAtlas ID
HS028-00291 
Organism
Homo sapiens 
Tissue/cell
Colo829 
Coordinate
chr1:206654130-206655000 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs17022427chr1206654497hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr1:206654792-206654813GGAGCAGGGAGGAGGAAGAGG+6.39
ZNF263MA0528.1chr1:206654786-206654807GGTGGAGGAGCAGGGAGGAGG+6.59
ZNF263MA0528.1chr1:206654789-206654810GGAGGAGCAGGGAGGAGGAAG+6.91
ZNF263MA0528.1chr1:206654783-206654804GGAGGTGGAGGAGCAGGGAGG+7.17
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr1206654677206654826
chr1206654444206654508
chr1206654628206654823
Number: 1             
IDChromosomeStartEnd
GH01I206480chr1206654141206655107
Enhancer Sequence
TGGCCTCCCT ATCCCAAGAA GGGGCTTGTG TCCTGCCAAG TCCTTCTCTG AATGATTTAG 60
AGTGCTCACC CTATGCCAAG TGCCAGCAGA ACTCTAGGGG GAGGACACAC ACCCACGCAC 120
AGTTCCTGGA TGTGACCAGG GATGGAGATC CAGGTGGTCT CGTTCTCCAT GCCTCATCTC 180
CTGCTTTCTC TGAGTCTTCA ACTTATCCTT GCCTTCCTTG GGTTCCCTGC CCCAATCTTT 240
GGAACCCCAC TCCCTCCACT CCCTTGTCTT GGGCTAATAA GGGGGGATGG GTTGGAAAAA 300
GAGAGAGACC GGGCAGGAGG AAGCCAAGTG GAAGGGTCTG GAGATGGGGA ATGTGGGAAG 360
ACTTCATTGG CCAGAGCACG ATTGAGAAGT AGGCACAGCA CCCCAAATCC TGGAAGGCAC 420
GAGGCCATGG TACGGGTGAG GGTGGGAGCT CTGCAGCCTA GGGATGCCAC TGGTGACAGG 480
AGTCTTTGGG AACAGAAGAT CAGAGACTGC CCATATGCCT GAAGGCCCCC TCCTCCCGCC 540
ACCCCCAGCC CTTGTCCTCA GGGAGCTCCA GGGAGTTTCC CAGCTGTGGG CTGACTCATG 600
CAGCCCCGCG TGCCTCCTGC TTCGCAGCAG CAACTCAGTT GATGGGGCAG CTGGGAGGTG 660
GAGGAGCAGG GAGGAGGAAG AGGAGCATCT CCAGATAACA GGGATGGAGT CTCCATCCAG 720
ACTGAGCCCC TCTCAAATGG TGACAGAGAG TAGGGTTCAG TCAGCAGAAC TGCAAGTGAA 780
TCTCCTTTGA GCAGAGCTCT GTCCAGGGCA CAGAGGGGGC TCCAGGGGTA GATGTGGCAT 840
CCTGTCATTC AGAGAGGCCC ATGCTTCCTC 870