Variant report

Variant	rs8061189
Chromosome Location	chr16:11951749-11951750
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:11950150..11954789-chr16:11962017..11966243,4	MCF-7	breast:
2	chr16:11495775..11497476-chr16:11950228..11952643,2	K562	blood:
3	chr16:11944931..11948457-chr16:11949497..11952956,3	K562	blood:
4	chr16:11944103..11947078-chr16:11947331..11952478,7	MCF-7	breast:

Variant related genes	Relation type
ENSG00000263307	Chromatin interaction
ENSG00000171490	Chromatin interaction
ENSG00000188897	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10744977	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11075022	0.89[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs11570136	0.81[CEU][hapmap]
rs11646545	0.92[CEU][hapmap];0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11647818	0.90[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11649405	0.89[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs12925740	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs153025	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs154148	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs171656	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2018199	0.88[CEU][hapmap]
rs2075158	0.88[CEU][hapmap]
rs2075159	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs251723	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28279	0.84[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs33619	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs33620	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs33623	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs33631	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs33635	0.88[CEU][hapmap];0.80[EUR][1000 genomes]
rs33637	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs33640	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs33643	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs33645	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs33647	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs33648	0.82[EUR][1000 genomes]
rs33649	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs33651	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs33652	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs33653	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs33654	0.84[EUR][1000 genomes]
rs33655	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs33660	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35153773	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs40311	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs42424	0.80[EUR][1000 genomes]
rs4429311	0.81[CEU][hapmap]
rs4493057	0.80[CEU][hapmap]
rs4511557	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap];0.80[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs456325	0.85[CEU][hapmap]
rs718081	0.89[CEU][hapmap];0.83[JPT][hapmap];0.89[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs7185589	0.87[ASN][1000 genomes]
rs7193470	0.83[ASN][1000 genomes]
rs7196913	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7197111	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7198817	0.92[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7202234	0.92[CEU][hapmap];0.81[CHB][hapmap];0.83[JPT][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8046617	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8047726	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8059891	0.85[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043909	chr16:11839910-12007435	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS 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	35 gene(s)	inside rSNPs	diseases
2	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
3	nsv571458	chr16:11925008-12087282	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs8061189	GSPT1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:11946200-11975600	Weak transcription	Aorta	Aorta
2	chr16:11946400-11969400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr16:11946400-11969400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr16:11946400-11969400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr16:11946400-11975600	Weak transcription	Esophagus	oesophagus
6	chr16:11946600-11958400	Weak transcription	Psoas Muscle	Psoas
7	chr16:11946600-11959600	Weak transcription	NHLF	lung
8	chr16:11946600-11961200	Weak transcription	Stomach Mucosa	stomach
9	chr16:11946600-11961400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr16:11946600-11961400	Weak transcription	Fetal Kidney	kidney
11	chr16:11946600-11961400	Weak transcription	HSMM	muscle
12	chr16:11946600-11961800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr16:11946600-11961800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr16:11946600-11961800	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr16:11946600-11962000	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr16:11946600-11962200	Weak transcription	Primary hematopoietic stem cells	blood
17	chr16:11946600-11962400	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr16:11946600-11962400	Weak transcription	HSMMtube	muscle
19	chr16:11946600-11966800	Weak transcription	Lung	lung
20	chr16:11946600-11969000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr16:11946600-11970400	Weak transcription	Right Atrium	heart
22	chr16:11946800-11956600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr16:11946800-11962000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr16:11946800-11962200	Weak transcription	Thymus	Thymus
25	chr16:11947000-11954600	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr16:11947000-11961800	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr16:11947000-11962000	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr16:11947000-11962000	Weak transcription	Fetal Muscle Leg	muscle
29	chr16:11947000-11962400	Weak transcription	Fetal Intestine Large	intestine
30	chr16:11947000-11969400	Weak transcription	Right Ventricle	heart
31	chr16:11947200-11960000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr16:11947200-11966800	Weak transcription	Small Intestine	intestine
33	chr16:11947200-11967200	Weak transcription	Fetal Intestine Small	intestine
34	chr16:11947200-11967200	Weak transcription	Fetal Stomach	stomach
35	chr16:11947200-11968800	Weak transcription	Ovary	ovary
36	chr16:11948000-11961600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr16:11948000-11962600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr16:11948000-11963400	Weak transcription	Spleen	Spleen
39	chr16:11948200-11959400	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr16:11948200-11960600	Weak transcription	Pancreas	Pancrea
41	chr16:11948200-11961200	Weak transcription	NHEK	skin
42	chr16:11948200-11962200	Weak transcription	Fetal Muscle Trunk	muscle
43	chr16:11948200-11962400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr16:11948400-11962400	Weak transcription	Primary B cells from peripheral blood	blood
45	chr16:11948400-11962400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr16:11948400-11963200	Weak transcription	Fetal Lung	lung
47	chr16:11948400-11969000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr16:11948600-11959400	Weak transcription	Duodenum Mucosa	Duodenum
49	chr16:11948600-11961400	Weak transcription	Primary T cells from cord blood	blood
50	chr16:11948600-11962000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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