Variant report

Variant	rs13333997
Chromosome Location	chr16:31181111-31181112
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:31170386..31172385-chr16:31178863..31181752,2	MCF-7	breast:
2	chr16:31180680..31182749-chr16:31185450..31188484,3	K562	blood:
3	chr16:31180952..31183135-chr16:31190313..31192972,3	MCF-7	breast:
4	chr16:31181056..31182579-chr16:31469550..31472018,2	MCF-7	breast:
5	chr16:31180374..31184503-chr16:31189156..31192914,6	K562	blood:
6	chr16:31180661..31184658-chr16:31189568..31192705,8	MCF-7	breast:

Variant related genes	Relation type
ENSG00000260267	Chromatin interaction
ENSG00000089280	Chromatin interaction
ENSG00000140691	Chromatin interaction
ENSG00000262366	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs1052352	0.89[ASN][1000 genomes]
rs11864632	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12926743	0.90[EUR][1000 genomes]
rs12929077	0.83[EUR][1000 genomes]
rs12935054	0.92[EUR][1000 genomes]
rs13336592	0.83[EUR][1000 genomes]
rs17708638	0.84[EUR][1000 genomes]
rs2288005	0.87[ASN][1000 genomes]
rs2735393	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3764323	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4496161	0.83[ASN][1000 genomes]
rs4889537	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4889538	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4889633	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs57348955	0.85[ASN][1000 genomes]
rs7184910	0.84[ASN][1000 genomes]
rs7186832	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7187143	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs741810	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8056505	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062456	chr16:30442166-31253997	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
2	nsv542898	chr16:30442166-31253997	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
3	nsv905729	chr16:30642867-31247924	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	387 gene(s)	inside rSNPs	diseases
4	nsv431451	chr16:30682399-31340999	Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	350 gene(s)	inside rSNPs	diseases
5	nsv905734	chr16:30877544-31191482	Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
6	nsv905735	chr16:30890538-31247924	Strong transcription Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	264 gene(s)	inside rSNPs	diseases
7	nsv457483	chr16:30903679-31191482	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
8	nsv571820	chr16:30903679-31191482	Enhancers Genic enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
9	esv1797877	chr16:30948643-31188432	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
10	nsv905740	chr16:31066249-31232437	Flanking Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	202 gene(s)	inside rSNPs	diseases
11	nsv905741	chr16:31066249-31247924	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	202 gene(s)	inside rSNPs	diseases
12	nsv905742	chr16:31102321-31247924	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	188 gene(s)	inside rSNPs	diseases
13	nsv542900	chr16:31137352-31197027	Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	165 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs13333997	PYDC1	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31154400-31190400	Weak transcription	Right Atrium	heart
2	chr16:31177200-31188400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr16:31180400-31181400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr16:31180400-31181600	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr16:31180400-31181600	Weak transcription	Placenta	Placenta
6	chr16:31180600-31181600	Weak transcription	Fetal Intestine Large	intestine
7	chr16:31180600-31181600	Weak transcription	Spleen	Spleen
8	chr16:31180600-31181800	Weak transcription	Fetal Intestine Small	intestine
9	chr16:31180600-31187600	Weak transcription	Thymus	Thymus
10	chr16:31180800-31181200	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr16:31180800-31181200	Weak transcription	Hela-S3	cervix
12	chr16:31180800-31181200	Weak transcription	HepG2	liver

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