Variant report

Variant	rs7669896
Chromosome Location	chr4:119510402-119510403
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:119503145..119504877-chr4:119508741..119511511,2	K562	blood:
2	chr4:119508532..119510926-chr4:119602289..119604089,2	MCF-7	breast:
3	chr4:119505891..119507633-chr4:119509359..119512309,2	MCF-7	breast:

Extended variants
information (count: 39 )
Associated
traits (count: 11 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10004322	1.00[ASN][1000 genomes]
rs10022024	1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.87[TSI][hapmap];1.00[ASN][1000 genomes]
rs10031029	0.87[ASN][1000 genomes]
rs10857060	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11734153	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11945703	0.94[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap]
rs12331454	0.97[ASN][1000 genomes]
rs12648682	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs12648778	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs13115157	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs13124091	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs13137401	1.00[ASN][1000 genomes]
rs13146440	0.94[CHB][hapmap];0.93[CHD][hapmap];0.93[JPT][hapmap]
rs13146816	0.94[CHB][hapmap];0.93[CHD][hapmap];0.93[JPT][hapmap]
rs2029399	0.94[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap]
rs2046779	0.94[CHB][hapmap];0.90[CHD][hapmap];0.93[JPT][hapmap]
rs2389780	1.00[ASN][1000 genomes]
rs3087958	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs35890030	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3733517	0.89[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap]
rs4001330	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6813357	0.94[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap]
rs6821350	0.94[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap]
rs6836005	0.84[CHB][hapmap];0.92[JPT][hapmap]
rs6847706	0.94[CHB][hapmap];0.93[CHD][hapmap];0.93[JPT][hapmap]
rs6857285	0.94[CHB][hapmap];0.93[CHD][hapmap];0.93[JPT][hapmap]
rs71610209	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs71610221	0.82[EUR][1000 genomes]
rs72676188	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7653962	0.94[CHB][hapmap];0.93[JPT][hapmap]
rs7656990	1.00[CHB][hapmap];0.96[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.87[TSI][hapmap];1.00[ASN][1000 genomes]
rs7689541	1.00[ASN][1000 genomes]
rs7692721	0.94[CHB][hapmap];0.93[CHD][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap]
rs7695602	0.94[CHB][hapmap];0.93[CHD][hapmap];0.93[JPT][hapmap]

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	nsv519017	chr4:118828807-119771481	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv1002771	chr4:119125361-119571237	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	esv3355840	chr4:119296640-119774737	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv427693	chr4:119493919-119674742	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv980150	chr4:119499004-119514502	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:11)

SNP	Gene	Cis/trans	Tissue	Source
rs7669896	PRSS12	cis	parietal	SCAN
rs7669896	RP11-384K6.2	cis	Skin Sun Exposed Lower leg	GTEx
rs7669896	RP11-384K6.2	cis	Thyroid	GTEx
rs7669896	RP11-384K6.6	cis	Adipose Subcutaneous	GTEx
rs7669896	RP11-384K6.6	cis	Artery Tibial	GTEx
rs7669896	RP11-384K6.2	cis	Whole Blood	GTEx
rs7669896	RP11-384K6.6	cis	Esophagus Mucosa	GTEx
rs7669896	RP11-384K6.6	cis	Nerve Tibial	GTEx
rs7669896	RP11-384K6.6	cis	Thyroid	GTEx
rs7669896	RP11-384K6.2	cis	Artery Tibial	GTEx
rs7669896	RP11-384K6.2	cis	Nerve Tibial	GTEx

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:119506600-119512800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:119507200-119512400	Weak transcription	Hela-S3	cervix
3	chr4:119507200-119512600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:119507400-119512200	Weak transcription	Stomach Mucosa	stomach
5	chr4:119507400-119512400	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr4:119507800-119512000	Weak transcription	Left Ventricle	heart
7	chr4:119507800-119513200	Weak transcription	Spleen	Spleen
8	chr4:119508000-119512000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr4:119508000-119512000	Weak transcription	Pancreas	Pancrea
10	chr4:119508000-119512000	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr4:119508000-119512200	Weak transcription	K562	blood
12	chr4:119508000-119512400	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr4:119508000-119512400	Weak transcription	Fetal Muscle Trunk	muscle
14	chr4:119508000-119512400	Weak transcription	Ovary	ovary
15	chr4:119508000-119512600	Weak transcription	HSMM	muscle
16	chr4:119508200-119512400	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr4:119508600-119512000	Weak transcription	Adipose Nuclei	Adipose
18	chr4:119508800-119511800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr4:119508800-119512400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:119509000-119512400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr4:119509400-119512200	Weak transcription	Liver	Liver
22	chr4:119510400-119510800	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr4:119510400-119512400	Enhancers	Primary monocytes fromperipheralblood	blood

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