Variant report

Variant	rs8063728
Chromosome Location	chr16:81960263-81960264
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr16:81957443-81962184	GM12892	blood:	n/a	n/a
2	POLR2A	chr16:81959785-81961424	GM12891	blood:	n/a	n/a
3	POLR2A	chr16:81960151-81961824	GM12891	blood:	n/a	n/a
4	POLR2A	chr16:81959468-81960416	GM12892	blood:	n/a	n/a
5	POLR2A	chr16:81957433-81960989	GM12878	blood:	n/a	n/a
6	POLR2A	chr16:81957417-81960296	GM12892	blood:	n/a	n/a
7	POLR2A	chr16:81959450-81961683	GM12891	blood:	n/a	n/a
8	POLR2A	chr16:81959346-81961769	GM12891	blood:	n/a	n/a
9	POLR2A	chr16:81959425-81961193	GM12892	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:81958643..81960384-chr16:81960629..81962269,2	K562	blood:
2	chr16:81959648..81962343-chr16:82020413..82022447,2	K562	blood:
3	chr16:81959537..81963642-chr16:81965973..81970581,4	K562	blood:

Variant related genes	Relation type
PLCG2	TF binding region

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11646679	0.81[ASN][1000 genomes]
rs12444459	1.00[CHB][hapmap]
rs12445489	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12446596	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12448089	0.87[EUR][1000 genomes]
rs12596249	0.93[CHB][hapmap];0.81[ASN][1000 genomes]
rs12716924	0.89[CEU][hapmap];0.93[CHB][hapmap];0.92[JPT][hapmap]
rs12716925	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12716926	0.93[CEU][hapmap];0.92[CHB][hapmap];0.85[JPT][hapmap];0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12716927	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13333420	0.88[CHB][hapmap];0.81[ASN][1000 genomes]
rs16955980	0.82[ASN][1000 genomes]
rs17202296	0.85[CEU][hapmap];1.00[CHB][hapmap];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3813010	0.94[CEU][hapmap];0.93[CHB][hapmap];0.93[JPT][hapmap];0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3922849	0.93[CHB][hapmap];0.81[ASN][1000 genomes]
rs4243222	0.93[CHB][hapmap]
rs4243223	0.93[CHB][hapmap]
rs4243224	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4306504	0.93[CHB][hapmap]
rs4313806	0.92[CHB][hapmap]
rs4366702	1.00[CEU][hapmap];0.93[CHB][hapmap];0.93[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4426346	0.81[ASN][1000 genomes]
rs4888189	0.90[CEU][hapmap];0.93[CHB][hapmap];0.93[JPT][hapmap];0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4888190	0.89[CEU][hapmap];0.91[EUR][1000 genomes]
rs4889441	0.92[CHB][hapmap]
rs4889442	0.94[CEU][hapmap];0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6564938	0.89[CEU][hapmap];0.92[CHB][hapmap];0.93[JPT][hapmap];0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6564940	0.86[JPT][hapmap]
rs7192724	1.00[CHB][hapmap];0.85[ASN][1000 genomes]
rs7193086	0.93[CHB][hapmap]
rs7201045	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs7203619	0.81[CHB][hapmap]
rs8063604	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9929503	0.90[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs9931137	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9938623	0.93[CHB][hapmap];0.82[JPT][hapmap];0.82[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv573365	chr16:81804972-81975892	Strong transcription Bivalent/Poised TSS Weak transcription ZNF genes & repeats Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:81909400-81961800	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr16:81920400-81982000	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr16:81924400-81961600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr16:81924400-81970000	Weak transcription	Fetal Intestine Large	intestine
5	chr16:81925800-81992600	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr16:81933000-81983600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr16:81934600-81961200	Weak transcription	Colonic Mucosa	Colon
8	chr16:81934800-81971600	Weak transcription	Right Atrium	heart
9	chr16:81936000-81982000	Weak transcription	Gastric	stomach
10	chr16:81936000-81984600	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr16:81937000-81969800	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr16:81941600-81966000	Weak transcription	Placenta	Placenta
13	chr16:81945000-81984600	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr16:81946200-81985200	Weak transcription	Rectal Smooth Muscle	rectum
15	chr16:81947000-81969200	Weak transcription	Pancreas	Pancrea
16	chr16:81950600-81982000	Strong transcription	GM12878-XiMat	blood
17	chr16:81951200-81962200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr16:81951400-81971400	Weak transcription	Left Ventricle	heart
19	chr16:81952000-81982800	Strong transcription	Primary B cells from peripheral blood	blood
20	chr16:81952400-81983000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr16:81952600-81970600	Strong transcription	Spleen	Spleen
22	chr16:81952600-81981800	Strong transcription	Primary B cells from cord blood	blood
23	chr16:81952800-81973000	Strong transcription	Duodenum Mucosa	Duodenum
24	chr16:81952800-81984600	Strong transcription	Liver	Liver
25	chr16:81953000-81977400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr16:81953400-81962200	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr16:81954800-81962200	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr16:81954800-81991800	Weak transcription	Fetal Thymus	thymus
29	chr16:81955400-81970200	Weak transcription	Brain Substantia Nigra	brain
30	chr16:81956400-81971400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr16:81956400-81971600	Weak transcription	Fetal Kidney	kidney
32	chr16:81956800-81962000	Weak transcription	HMEC	breast
33	chr16:81957000-81971200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr16:81957400-81961200	Weak transcription	Lung	lung
35	chr16:81957600-81960600	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr16:81958200-81962800	Strong transcription	Fetal Intestine Small	intestine
37	chr16:81958600-81960400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr16:81958800-81960600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr16:81959200-81960800	Weak transcription	Adipose Nuclei	Adipose
40	chr16:81959600-81983800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
41	chr16:81960000-81966000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr16:81960000-81969800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr16:81960200-81962200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr16:81960200-81966600	Strong transcription	Primary hematopoietic stem cells	blood

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