Variant report

Variant	rs62482239
Chromosome Location	chr7:100217810-100217811
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:100214867..100218269-chr7:100226903..100230336,3	MCF-7	breast:
2	chr7:100216968..100219531-chr7:100237387..100239485,2	K562	blood:
3	chr7:100206101..100213131-chr7:100214394..100226559,23	K562	blood:
4	chr7:100217471..100219602-chr7:100221708..100224435,2	MCF-7	breast:
5	chr19:56225201..56225701-chr7:100217318..100218312,2	MCF-7	breast:
6	chr7:100209889..100213905-chr7:100214080..100218119,4	MCF-7	breast:
7	chr7:100214319..100217158-chr7:100217696..100220266,2	MCF-7	breast:
8	chr7:100209281..100214029-chr7:100217234..100224358,8	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000106330	Chromatin interaction
ENSG00000106327	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10487157	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10953298	1.00[ASN][1000 genomes]
rs11764045	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11766643	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11767547	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11770389	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11983745	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12532878	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13227444	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2075674	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28584500	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41303510	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62482237	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62482238	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62482242	0.82[AMR][1000 genomes]
rs6958696	0.80[AMR][1000 genomes]
rs6969584	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6969697	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73156234	0.80[AMR][1000 genomes]
rs73407376	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7457024	1.00[ASN][1000 genomes]
rs7786877	0.98[ASN][1000 genomes]
rs7812123	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7812235	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[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	esv1829095	chr7:99814675-100494084	Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	393 gene(s)	inside rSNPs	diseases
2	nsv888777	chr7:100014711-100221867	Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	304 gene(s)	inside rSNPs	diseases
3	nsv888778	chr7:100014711-100236593	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	310 gene(s)	inside rSNPs	diseases
4	nsv888779	chr7:100014711-100313420	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	321 gene(s)	inside rSNPs	diseases
5	nsv888782	chr7:100064719-100236593	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
6	nsv888785	chr7:100141861-100313420	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
7	nsv888786	chr7:100159567-100313420	Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
8	nsv831072	chr7:100162503-100362835	Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
9	nsv888790	chr7:100200674-100232387	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	37 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs62482239	MOSPD3	cis	Whole Blood	GTEx

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100210600-100224400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr7:100211000-100223800	Weak transcription	Fetal Kidney	kidney
3	chr7:100211000-100224600	Weak transcription	Small Intestine	intestine
4	chr7:100211200-100218600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr7:100211200-100221600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr7:100211200-100221800	Weak transcription	HSMMtube	muscle
7	chr7:100211200-100223800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr7:100211200-100224000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr7:100211200-100224000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr7:100211200-100224000	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr7:100211200-100224000	Weak transcription	Brain Angular Gyrus	brain
12	chr7:100211200-100224000	Weak transcription	Lung	lung
13	chr7:100211200-100224000	Weak transcription	Psoas Muscle	Psoas
14	chr7:100211200-100224000	Weak transcription	Right Ventricle	heart
15	chr7:100211200-100224400	Weak transcription	Left Ventricle	heart
16	chr7:100211400-100218000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr7:100211400-100218000	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr7:100211400-100218000	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr7:100211400-100218200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr7:100211400-100220800	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr7:100211400-100221800	Weak transcription	Esophagus	oesophagus
22	chr7:100211400-100223400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr7:100211400-100223800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr7:100211400-100224000	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr7:100211400-100224000	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr7:100211400-100224000	Weak transcription	Brain Substantia Nigra	brain
27	chr7:100211400-100224000	Weak transcription	Colonic Mucosa	Colon
28	chr7:100211400-100224000	Weak transcription	HSMM	muscle
29	chr7:100211400-100224000	Weak transcription	HUVEC	blood vessel
30	chr7:100211400-100224600	Weak transcription	Spleen	Spleen
31	chr7:100211400-100230400	Weak transcription	Pancreas	Pancrea
32	chr7:100211600-100219200	Weak transcription	Brain Cingulate Gyrus	brain
33	chr7:100211600-100220200	Strong transcription	Fetal Muscle Trunk	muscle
34	chr7:100211800-100218000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr7:100211800-100223800	Weak transcription	Primary B cells from peripheral blood	blood
36	chr7:100211800-100223800	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr7:100211800-100224000	Weak transcription	Brain Hippocampus Middle	brain
38	chr7:100212000-100223600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr7:100212000-100223600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr7:100212000-100223600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr7:100212000-100223800	Weak transcription	Fetal Brain Male	brain
42	chr7:100212200-100220000	Strong transcription	Brain Germinal Matrix	brain
43	chr7:100212200-100221800	Weak transcription	Primary T helper cells fromperipheralblood	blood
44	chr7:100212200-100223800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr7:100212200-100223800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr7:100212200-100223800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr7:100212200-100224000	Weak transcription	Primary hematopoietic stem cells	blood
48	chr7:100212600-100223400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr7:100212600-100224400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr7:100212800-100218000	Weak transcription	Ovary	ovary

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