Variant report

Variant	rs6714903
Chromosome Location	chr2:10919957-10919958
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:10919808..10922131-chr2:10929132..10931329,2	K562	blood:
2	chr2:10919855..10921861-chr2:10927232..10928745,2	K562	blood:

Extended variants
information (count: 30 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10182400	0.90[EUR][1000 genomes]
rs10192112	0.89[EUR][1000 genomes]
rs10197595	0.89[EUR][1000 genomes]
rs10200007	0.89[EUR][1000 genomes]
rs10520049	0.99[EUR][1000 genomes]
rs11489	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11885932	0.81[EUR][1000 genomes]
rs12617247	0.92[EUR][1000 genomes]
rs12617440	0.96[EUR][1000 genomes]
rs13404780	0.90[EUR][1000 genomes]
rs1387568	0.92[EUR][1000 genomes]
rs17364770	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17364812	0.96[EUR][1000 genomes]
rs17365015	0.99[EUR][1000 genomes]
rs17365299	0.93[EUR][1000 genomes]
rs17455729	0.94[EUR][1000 genomes]
rs17455876	0.99[EUR][1000 genomes]
rs2357816	0.88[EUR][1000 genomes]
rs3856467	0.94[EUR][1000 genomes]
rs6718547	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6722515	0.99[EUR][1000 genomes]
rs6733037	0.85[EUR][1000 genomes]
rs6756520	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6756672	0.84[EUR][1000 genomes]
rs73174526	0.89[EUR][1000 genomes]
rs7561135	0.90[EUR][1000 genomes]
rs7570179	0.90[EUR][1000 genomes]

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	nsv1000953	chr2:10717304-10921805	Strong transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv535584	chr2:10717304-10921805	Bivalent Enhancer Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv1000731	chr2:10758657-10943882	Strong transcription Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6714903	PDIA6	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:10908600-10924400	Weak transcription	Psoas Muscle	Psoas
2	chr2:10913200-10920200	Weak transcription	NH-A	brain
3	chr2:10913400-10920200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr2:10914200-10920000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr2:10914600-10920200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr2:10914600-10922400	Weak transcription	Fetal Kidney	kidney
7	chr2:10914600-10931600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr2:10915000-10920000	Weak transcription	Primary hematopoietic stem cells	blood
9	chr2:10915000-10920000	Weak transcription	Brain Angular Gyrus	brain
10	chr2:10915000-10921600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr2:10915200-10920200	Weak transcription	HSMMtube	muscle
12	chr2:10915200-10923000	Weak transcription	Fetal Brain Male	brain
13	chr2:10915600-10920000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr2:10915600-10920200	Weak transcription	HMEC	breast
15	chr2:10915600-10920400	Weak transcription	Stomach Mucosa	stomach
16	chr2:10915600-10921800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr2:10915600-10939800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr2:10915600-10950400	Weak transcription	Right Atrium	heart
19	chr2:10915800-10920000	Weak transcription	Fetal Lung	lung
20	chr2:10915800-10929000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr2:10916000-10920400	Weak transcription	Hela-S3	cervix
22	chr2:10916000-10921800	Weak transcription	Small Intestine	intestine
23	chr2:10916200-10920000	Weak transcription	HUVEC	blood vessel
24	chr2:10916200-10920400	Weak transcription	Colon Smooth Muscle	Colon
25	chr2:10916200-10939200	Strong transcription	Fetal Stomach	stomach
26	chr2:10916400-10921400	Strong transcription	Fetal Brain Female	brain
27	chr2:10916400-10922200	Weak transcription	Fetal Heart	heart
28	chr2:10916400-10923200	Weak transcription	NHDF-Ad	bronchial
29	chr2:10916400-10923600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr2:10916400-10923600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr2:10916400-10928600	Strong transcription	Fetal Intestine Small	intestine
32	chr2:10916400-10931200	Strong transcription	Cortex derived primary cultured neurospheres	brain
33	chr2:10916400-10931600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr2:10916400-10938600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr2:10916600-10943800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
36	chr2:10916800-10920000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr2:10916800-10933800	Strong transcription	Spleen	Spleen
38	chr2:10916800-10937400	Strong transcription	Lung	lung
39	chr2:10916800-10942400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr2:10917000-10920600	Strong transcription	Placenta	Placenta
41	chr2:10917000-10926600	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr2:10917000-10930400	Strong transcription	GM12878-XiMat	blood
43	chr2:10917000-10930600	Strong transcription	NHEK	skin
44	chr2:10917000-10933600	Strong transcription	Primary T cells from cord blood	blood
45	chr2:10917000-10939400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr2:10917200-10925800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr2:10917200-10929000	Strong transcription	Duodenum Mucosa	Duodenum
48	chr2:10917200-10931000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr2:10917200-10931000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr2:10917200-10933400	Strong transcription	Duodenum Smooth Muscle	Duodenum

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