Variant report

Variant	rs7921382
Chromosome Location	chr10:19169862-19169863
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1028925	0.90[ASN][1000 genomes]
rs10826577	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1329221	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1329222	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1556113	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2104699	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4443968	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4465267	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4607963	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6481555	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6481556	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7071978	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7082839	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7086992	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7908741	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7916006	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7917968	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894915	chr10:18984571-19257664	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv550123	chr10:19090812-19228730	Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv894916	chr10:19095467-19429415	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv518006	chr10:19160029-19170218	Active TSS Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
5	nsv5999	chr10:19163832-19199133	Enhancers Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:19169000-19170200	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr10:19169200-19170200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
3	chr10:19169200-19170200	Active TSS	HUES6 Cell Line	embryonic stem cell
4	chr10:19169200-19170200	Active TSS	HUES64 Cell Line	embryonic stem cell
5	chr10:19169400-19170000	Active TSS	H1 Cell Line	embryonic stem cell
6	chr10:19169400-19170000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr10:19169400-19170000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr10:19169400-19170000	Active TSS	H9 Cell Line	embryonic stem cell
9	chr10:19169400-19170000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr10:19169400-19170200	Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr10:19169400-19170200	Active TSS	iPS-15b Cell Line	embryonic stem cell
12	chr10:19169600-19170000	Active TSS	iPS-18 Cell Line	embryonic stem cell
13	chr10:19169800-19170200	Active TSS	A549	lung

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

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