Variant report

Variant	rs67984036
Chromosome Location	chr15:82312711-82312712
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs12902481	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12902907	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13379788	0.89[ASN][1000 genomes]
rs34082296	0.93[AFR][1000 genomes]
rs34593711	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs34913882	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs35573193	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4325512	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs56407036	0.89[ASN][1000 genomes]
rs58069813	0.89[ASN][1000 genomes]
rs60636752	0.89[ASN][1000 genomes]
rs67548148	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs67817019	0.83[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs67824562	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7162970	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74028455	0.89[ASN][1000 genomes]
rs74028456	0.89[ASN][1000 genomes]
rs74028457	0.89[ASN][1000 genomes]
rs8031443	0.86[AFR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833067	chr15:82234980-82450485	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	esv2422504	chr15:82293064-82426400	Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:82308200-82331600	Weak transcription	Fetal Brain Female	brain
2	chr15:82308600-82315000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr15:82308800-82313600	Enhancers	Primary hematopoietic stem cells	blood
4	chr15:82310000-82315400	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr15:82310600-82315200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr15:82311000-82313200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr15:82311200-82315200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr15:82311400-82315000	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr15:82312400-82315000	Enhancers	K562	blood

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links