Variant report

Variant	rs2505198
Chromosome Location	chr10:38393183-38393184
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 125 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:116)

rs_ID	r²[population]
rs11011452	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11011461	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1138252	0.94[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs1329786	0.90[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs1548255	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs176876	0.97[ASN][1000 genomes]
rs176877	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs176879	0.94[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs176880	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs176881	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs176882	0.94[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs176885	0.94[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs176886	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs176887	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs176889	0.94[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs1813028	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1854563	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1985707	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1998062	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2008449	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2021649	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2021650	0.94[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2023299	0.92[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2023351	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2144859	0.87[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs2178962	0.94[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2180412	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2263162	0.92[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2263163	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2263164	0.92[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2384730	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2384731	0.89[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs2472173	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2472174	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2472175	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2472176	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2472177	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2472178	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2472179	0.85[ASN][1000 genomes]
rs2472180	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2472181	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2472183	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2474554	0.84[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs2474563	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2474564	0.92[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs2474565	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2474566	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2474567	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2474568	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2474569	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2474570	0.87[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs2474571	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2474572	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2474573	0.94[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2474574	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2474575	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2474579	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2474580	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2474581	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2474584	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2474586	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2474587	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2474588	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2474590	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2474591	0.93[ASN][1000 genomes]
rs2474594	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2474595	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2474596	0.90[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2474597	0.93[ASN][1000 genomes]
rs2474598	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2474599	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2474610	0.87[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs2504120	0.94[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2504121	0.92[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2504127	0.94[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2504139	0.94[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2504140	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2504141	0.94[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2504142	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2504143	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2504148	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2504149	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2505179	0.92[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2505185	0.92[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs2505186	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2505187	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2505188	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2505189	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2505190	0.89[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs2505191	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2505193	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2505194	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2505195	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2505196	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2505197	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2505235	0.89[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2505236	0.86[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2505237	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2505241	0.82[EUR][1000 genomes]
rs2505244	0.92[ASN][1000 genomes]
rs2505248	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2505249	0.87[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs2505250	0.84[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs2505251	0.86[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs2505252	0.86[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs2505258	0.89[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2505259	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2505260	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2983343	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6482060	0.85[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs71491246	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7915062	0.92[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs9299760	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs932538	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9417297	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9418322	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895030	chr10:37715737-38674609	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv1045684	chr10:37765361-38426204	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	nsv540564	chr10:37765361-38426204	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv1040704	chr10:37940024-38451917	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
5	nsv1051121	chr10:38155991-38426204	Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
6	nsv540565	chr10:38155991-38426204	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
7	nsv540566	chr10:38301001-38680127	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
8	nsv550419	chr10:38311777-38501654	Enhancers Strong transcription Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
9	nsv6465	chr10:38377662-38422125	Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs2505198	ZNF37A	Cis_1M	lymphoblastoid	RTeQTL
rs2505198	HSD17B7///HSD17B7P2///LOC730412	Cis_1M	lymphoblastoid	RTeQTL
rs2505198	HSD17B7P2	cis	Whole Blood	GTEx
rs2505198	ZNF37A///ZNF37B	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:38384400-38396400	Weak transcription	HUVEC	blood vessel
2	chr10:38385400-38394400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr10:38385600-38396200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr10:38386000-38395200	Weak transcription	Hela-S3	cervix
5	chr10:38386200-38396000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
6	chr10:38386800-38395800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr10:38386800-38396200	ZNF genes & repeats	Fetal Brain Female	brain
8	chr10:38386800-38396200	ZNF genes & repeats	Fetal Lung	lung
9	chr10:38387600-38398800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr10:38387800-38396800	ZNF genes & repeats	Liver	Liver
11	chr10:38388200-38396200	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr10:38388200-38399200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
13	chr10:38388600-38394800	Weak transcription	NHDF-Ad	bronchial
14	chr10:38388600-38397600	Weak transcription	NH-A	brain
15	chr10:38389200-38395800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
16	chr10:38389200-38396000	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
17	chr10:38389600-38393200	Weak transcription	Fetal Thymus	thymus
18	chr10:38389600-38395800	ZNF genes & repeats	Dnd41	blood
19	chr10:38389800-38393800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
20	chr10:38390000-38395800	ZNF genes & repeats	Adipose Nuclei	Adipose
21	chr10:38390400-38393800	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
22	chr10:38390600-38394000	ZNF genes & repeats	Fetal Intestine Large	intestine
23	chr10:38390600-38395600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
24	chr10:38390600-38396000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
25	chr10:38390800-38393200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr10:38390800-38393800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr10:38390800-38395600	ZNF genes & repeats	Colon Smooth Muscle	Colon
28	chr10:38391000-38393800	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
29	chr10:38391000-38393800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr10:38391000-38395600	ZNF genes & repeats	A549	lung
31	chr10:38391000-38396000	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr10:38391000-38396200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr10:38391200-38393400	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
34	chr10:38391200-38393600	ZNF genes & repeats	Brain Anterior Caudate	brain
35	chr10:38391200-38393600	ZNF genes & repeats	Brain Substantia Nigra	brain
36	chr10:38391200-38393800	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
37	chr10:38391200-38393800	ZNF genes & repeats	Stomach Smooth Muscle	stomach
38	chr10:38391200-38395000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr10:38391200-38395600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
40	chr10:38391200-38395600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
41	chr10:38391200-38396000	ZNF genes & repeats	Fetal Kidney	kidney
42	chr10:38391200-38396400	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
43	chr10:38391400-38393200	ZNF genes & repeats	Primary B cells from peripheral blood	blood
44	chr10:38391400-38393200	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
45	chr10:38391400-38393400	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
46	chr10:38391600-38393600	ZNF genes & repeats	GM12878-XiMat	blood
47	chr10:38391600-38395600	ZNF genes & repeats	Fetal Brain Male	brain
48	chr10:38391600-38395800	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr10:38391600-38396000	ZNF genes & repeats	Primary B cells from cord blood	blood
50	chr10:38391800-38393400	ZNF genes & repeats	Psoas Muscle	Psoas

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