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

TagContent
EnhancerAtlas ID
HS187-21033 
Organism
Homo sapiens 
Tissue/cell
Th1 
Coordinate
chr6:32577200-32578270 
SNPs
Number: 3             
IDChromosomePositionGenome Version
rs660895chr632577380hg19
rs674313chr632578082hg19
rs9271176chr632578127hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr6:32577820-32577838GGGAGGAGGCAGGGAAGG+6.02
FOSL2MA0478.1chr6:32577842-32577853GGATGACTCAT+6.62
JUNBMA0490.1chr6:32577842-32577853GGATGACTCAT+6.62
RELMA0101.1chr6:32577700-32577710GGAAATCCCC-6.02
ZNF263MA0528.1chr6:32577821-32577842GGAGGAGGCAGGGAAGGAGCA+7.06
Number of super-enhancer constituents: 7             
IDCoordinateTissue/cell
SE_09772chr6:32575020-32579267CD14
SE_10156chr6:32569301-32580242CD19_Primary
SE_10892chr6:32567429-32580604CD20
SE_13242chr6:32576704-32578573CD34_Primary_RO01480
SE_20126chr6:32575078-32579405CD56
SE_32552chr6:32571514-32580098GM12878
SE_62290chr6:32551894-32608897Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr63257729732577935
Number: 1             
IDChromosomeStartEnd
GH06I032602chr63256980132580098
Enhancer Sequence
TGGTTAATTA AGACAGTAGG AGGCGTAGAG AAAATATAAT GAAACGATAT GTAAGGGAAA 60
CGAAGGATGA AAGATGCAGG CAGGGAGAGG AGTACTGTCT GATGGGAGTG AAGATTCTTC 120
CTTCAGGAAT GGAAGGGGAT GCACAGAGTG AAGCCACCCA ACAAAAACAA GACTTGTATA 180
GCTATAGATG GAAGGGAAAT CAACCAGGAA ATTATTTTGG AAATCCCAGT GTAGTTACAA 240
GTCTAGGAAG TAATAGTTAG AATGAAGAGT TTGTATTTAC TGAGCACTAA TATTCTCATA 300
ATCATGCTAG GAAATATCAC TTGATAAAGA TAGAAAGATG AGTCGTTTAA GAAGGAATAC 360
ATGTCTCTTT TCAGAGGCAG TACCCGCAGG CAGTTCTCAA ACCCAGAATC TGCCTCATCA 420
GTCTCAGTTC AGGTTACTTC GTTTCAGGGA AGGCATTCCA GCTTCTTGCA CTAGGCATTT 480
CAAGAAAGAA AAGCATTCCT GGAAATCCCC AATCGGTCAC AGGCATGTTT CTCCAACCAA 540
TAGGAATAGA GAATGAGGCA GCATCACTTG TCTCCAGCAG ATACATCTGC TAAGAAGGTC 600
TGATCTGATC CCAGGTCTTG GGGAGGAGGC AGGGAAGGAG CAGGATGACT CATGAGTGGT 660
GAGAAGAATG GCTGACGATG TAGTTTCATG GAAAGAAATA AGATACCCCA TGTGGAGAGA 720
CAAGATACCA TATTTTGTAG TTGTGAAGCA GAGTAAAGAC TGAGACTCTT AGTACTTAGT 780
ATTGGTGGGG GAGAAGAGGT TACCTGATAT TTTTCATGCC TCTGTGGGAA GTCCCTGGTC 840
AGTTTTAAAA GGGAAGGGCA TGACTATGAC GCTGGATTCT CCCTGCTAGT GATGCATGAG 900
CACCTGTGGT GAACGAGATG GAAATGATGA AGAAGCCCAT GATCCCACCT GCTGATTGTC 960
ATAGGACAAT TTGAGGGAAA GTCACATTAT CATGTGCTGA TTATTTTGCT CTAGCAAAGT 1020
AGTACTTCCA GGTGTATTAT CTCAATTAAT CATTATTTTT GTTAACTGCT 1070