Variant report

Variant	rs13096323
Chromosome Location	chr3:101461177-101461178
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs1031710	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1138818	0.83[ASN][1000 genomes]
rs11706986	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11710805	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11711079	0.82[ASN][1000 genomes]
rs11712748	0.82[ASN][1000 genomes]
rs11714278	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11717046	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11720745	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11914318	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11919389	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11925001	0.82[ASN][1000 genomes]
rs12636557	0.82[ASN][1000 genomes]
rs13059470	0.85[ASN][1000 genomes]
rs13060963	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13061565	0.82[ASN][1000 genomes]
rs13065944	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13066768	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13068350	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13069443	0.81[ASN][1000 genomes]
rs13077703	0.82[ASN][1000 genomes]
rs13077925	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13081846	0.82[ASN][1000 genomes]
rs13084432	0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13099674	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13100262	0.80[ASN][1000 genomes]
rs17411983	0.83[ASN][1000 genomes]
rs1963961	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1963962	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2288272	0.82[ASN][1000 genomes]
rs2303474	0.82[ASN][1000 genomes]
rs2318090	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3094295	0.82[ASN][1000 genomes]
rs3094296	0.82[ASN][1000 genomes]
rs3094297	0.83[ASN][1000 genomes]
rs3109756	0.83[ASN][1000 genomes]
rs34181125	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34301719	0.81[ASN][1000 genomes]
rs34376498	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34624546	0.82[ASN][1000 genomes]
rs34883763	0.84[ASN][1000 genomes]
rs35117343	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35315807	0.81[ASN][1000 genomes]
rs35850993	0.80[AFR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs36002990	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3806653	0.83[ASN][1000 genomes]
rs3806654	0.83[ASN][1000 genomes]
rs55654108	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55859364	0.84[ASN][1000 genomes]
rs56291106	0.82[ASN][1000 genomes]
rs59596156	0.82[ASN][1000 genomes]
rs62282218	0.82[ASN][1000 genomes]
rs62284198	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62284199	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6768327	0.99[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7629753	0.82[ASN][1000 genomes]
rs7651721	0.82[ASN][1000 genomes]
rs9830943	0.84[ASN][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	nsv497784	chr3:101315009-102092989	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv997407	chr3:101384031-101611391	Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
3	nsv536675	chr3:101384031-101611391	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	76 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs13096323	RP11-49I4.3	cis	Esophagus Muscularis	GTEx
rs13096323	NXPE3	cis	Esophagus Muscularis	GTEx

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:101445600-101497400	Weak transcription	Fetal Heart	heart
2	chr3:101451600-101463400	Weak transcription	HepG2	liver
3	chr3:101451800-101476600	Weak transcription	Psoas Muscle	Psoas
4	chr3:101453400-101478400	Weak transcription	Small Intestine	intestine
5	chr3:101453800-101473600	Weak transcription	HSMMtube	muscle
6	chr3:101453800-101474200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr3:101453800-101487000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr3:101454000-101474000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr3:101454200-101473000	Weak transcription	HSMM	muscle
10	chr3:101454200-101474200	Weak transcription	HMEC	breast
11	chr3:101454400-101464400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr3:101454600-101463800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr3:101454600-101473400	Weak transcription	Hela-S3	cervix
14	chr3:101454600-101476400	Weak transcription	NHEK	skin
15	chr3:101454600-101476600	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr3:101454800-101474200	Weak transcription	Rectal Smooth Muscle	rectum
17	chr3:101454800-101476600	Weak transcription	A549	lung
18	chr3:101455000-101463600	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr3:101455200-101476600	Weak transcription	Pancreas	Pancrea
20	chr3:101455400-101463800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr3:101455400-101473000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr3:101455400-101473000	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr3:101455400-101473400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr3:101455400-101473400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr3:101455400-101474200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr3:101455400-101474200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr3:101455400-101474200	Weak transcription	Aorta	Aorta
28	chr3:101455400-101474200	Weak transcription	Brain Angular Gyrus	brain
29	chr3:101455400-101474200	Weak transcription	Brain Substantia Nigra	brain
30	chr3:101455400-101474200	Weak transcription	Colonic Mucosa	Colon
31	chr3:101455400-101474200	Weak transcription	Esophagus	oesophagus
32	chr3:101455400-101474200	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr3:101455400-101474400	Weak transcription	Ovary	ovary
34	chr3:101455400-101474400	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr3:101455400-101474600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr3:101455400-101476200	Weak transcription	NHLF	lung
37	chr3:101455400-101476600	Weak transcription	Right Ventricle	heart
38	chr3:101455400-101476600	Weak transcription	K562	blood
39	chr3:101455400-101477800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr3:101455600-101463400	Weak transcription	Brain Anterior Caudate	brain
41	chr3:101455600-101463600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr3:101455600-101463600	Weak transcription	Dnd41	blood
43	chr3:101455600-101463800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr3:101455600-101464200	Weak transcription	HUVEC	blood vessel
45	chr3:101455600-101473400	Weak transcription	Brain Hippocampus Middle	brain
46	chr3:101455600-101474000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr3:101455600-101474000	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr3:101455600-101474000	Weak transcription	Thymus	Thymus
49	chr3:101455600-101474200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr3:101455600-101474200	Weak transcription	Primary neutrophils fromperipheralblood	blood

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