Variant report

Variant	rs8051349
Chromosome Location	chr16:12105523-12105524
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:12104065..12105673-chr16:12116123..12118604,2	MCF-7	breast:

Extended variants
information (count: 16 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11641950	0.83[AMR][1000 genomes]
rs11648404	1.00[CEU][hapmap];0.84[CHB][hapmap];0.94[JPT][hapmap];0.97[YRI][hapmap]
rs11648938	1.00[CEU][hapmap];0.83[CHB][hapmap];0.82[JPT][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11862467	0.80[AMR][1000 genomes]
rs2869492	0.92[CEU][hapmap]
rs6498262	0.81[AMR][1000 genomes]
rs8044943	0.84[AMR][1000 genomes]
rs8045634	0.96[CEU][hapmap];0.92[CHB][hapmap];0.94[JPT][hapmap];0.81[EUR][1000 genomes]
rs8050827	0.96[CEU][hapmap];0.84[CHB][hapmap];0.94[JPT][hapmap];0.86[YRI][hapmap];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs8051012	0.85[AMR][1000 genomes]
rs8062691	1.00[CEU][hapmap];0.83[CHB][hapmap];0.82[JPT][hapmap];0.85[YRI][hapmap];0.92[AMR][1000 genomes];0.95[EUR][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	nsv1042660	chr16:11846873-12110435	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv905347	chr16:12010444-12243329	Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
3	nsv1043096	chr16:12013915-12840769	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
4	nsv482458	chr16:12014925-12145977	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
5	nsv1043959	chr16:12039346-12285269	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs8051349	RP11-166B2.1	cis	Esophagus Muscularis	GTEx
rs8051349	RP11-166B2.1	cis	Skin Sun Exposed Lower leg	GTEx
rs8051349	RP11-166B2.1	cis	Artery Tibial	GTEx
rs8051349	RP11-166B2.1	cis	Thyroid	GTEx
rs8051349	RP11-166B2.1	cis	Heart Left Ventricle	GTEx
rs8051349	RP11-166B2.1	cis	Adipose Subcutaneous	GTEx
rs8051349	RP11-166B2.1	cis	Nerve Tibial	GTEx

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12071400-12130800	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr16:12071800-12140200	Weak transcription	Fetal Intestine Small	intestine
3	chr16:12079600-12109600	Weak transcription	Gastric	stomach
4	chr16:12085400-12118200	Weak transcription	Esophagus	oesophagus
5	chr16:12088600-12109200	Weak transcription	Fetal Kidney	kidney
6	chr16:12088600-12110000	Weak transcription	NH-A	brain
7	chr16:12088800-12106600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr16:12088800-12108200	Weak transcription	Fetal Muscle Trunk	muscle
9	chr16:12088800-12115400	Weak transcription	Placenta	Placenta
10	chr16:12092400-12105600	Weak transcription	Rectal Smooth Muscle	rectum
11	chr16:12092400-12110200	Weak transcription	NHEK	skin
12	chr16:12092600-12107800	Weak transcription	Liver	Liver
13	chr16:12094200-12105600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr16:12094200-12110000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr16:12096800-12110000	Weak transcription	Osteobl	bone
16	chr16:12096800-12111800	Weak transcription	Ovary	ovary
17	chr16:12097000-12107800	Weak transcription	Fetal Lung	lung
18	chr16:12097000-12109400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr16:12097200-12107800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr16:12097600-12110200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr16:12098400-12136000	Weak transcription	Fetal Stomach	stomach
22	chr16:12098600-12109400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr16:12098600-12118200	Weak transcription	Pancreas	Pancrea
24	chr16:12099000-12109400	Weak transcription	Brain Germinal Matrix	brain
25	chr16:12099400-12108200	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr16:12099400-12118400	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr16:12099600-12111800	Weak transcription	Fetal Muscle Leg	muscle
28	chr16:12099600-12112600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr16:12099600-12135200	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr16:12099600-12141200	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr16:12101400-12110200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr16:12101800-12110000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr16:12101800-12111600	Weak transcription	HSMMtube	muscle
34	chr16:12101800-12121400	Weak transcription	Stomach Smooth Muscle	stomach
35	chr16:12101800-12123600	Weak transcription	Lung	lung
36	chr16:12101800-12129800	Weak transcription	Aorta	Aorta
37	chr16:12102000-12124200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr16:12102800-12106000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr16:12103000-12105800	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr16:12103600-12106200	Enhancers	Primary hematopoietic stem cells	blood
41	chr16:12104200-12107400	Enhancers	Primary B cells from peripheral blood	blood
42	chr16:12104200-12111600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr16:12104400-12105800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr16:12104400-12109800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr16:12104600-12105600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr16:12104600-12105600	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr16:12104600-12109400	Weak transcription	Left Ventricle	heart
48	chr16:12104600-12110600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr16:12104600-12116400	Weak transcription	Brain Hippocampus Middle	brain
50	chr16:12104800-12105800	Enhancers	Primary T cells from cord blood	blood

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