Variant report

Variant	rs7783610
Chromosome Location	chr7:33211924-33211925
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1008582	0.81[CHB][hapmap]
rs1009355	0.95[CHB][hapmap];0.83[JPT][hapmap]
rs10250045	0.90[CHB][hapmap]
rs10257361	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs10268074	0.90[CHB][hapmap]
rs10279081	0.86[CEU][hapmap];0.90[CHB][hapmap]
rs1030029	0.93[CEU][hapmap];1.00[CHB][hapmap]
rs10951383	0.90[CHB][hapmap]
rs12155105	0.87[CHB][hapmap]
rs12537278	0.90[CHB][hapmap]
rs12537836	0.86[ASN][1000 genomes]
rs12671191	0.90[CHB][hapmap]
rs1345308	0.95[CHB][hapmap]
rs1362371	0.95[CHB][hapmap]
rs1420147	0.92[CEU][hapmap];0.81[EUR][1000 genomes]
rs1420148	0.95[CHB][hapmap];0.83[JPT][hapmap]
rs1420158	0.95[CHB][hapmap]
rs1420159	0.85[CEU][hapmap];0.94[CHB][hapmap]
rs1548880	0.95[CHB][hapmap];0.84[JPT][hapmap]
rs1592465	0.84[CHB][hapmap]
rs1894873	0.95[CHB][hapmap]
rs1969575	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2024430	0.90[CHB][hapmap]
rs4720109	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4720115	0.95[CHB][hapmap]
rs4723261	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4723272	0.95[CHB][hapmap];0.83[JPT][hapmap]
rs6462463	0.81[EUR][1000 genomes]
rs6462467	0.90[CHB][hapmap]
rs6950434	0.93[CEU][hapmap];1.00[CHB][hapmap];0.81[EUR][1000 genomes]
rs6960483	0.95[CHB][hapmap];0.83[JPT][hapmap]
rs6976311	0.81[CHB][hapmap]
rs721533	0.93[CEU][hapmap];1.00[CHB][hapmap];0.81[EUR][1000 genomes]
rs759396	0.95[CHB][hapmap];0.84[JPT][hapmap]
rs764041	0.88[CHB][hapmap]
rs7778657	0.90[CHB][hapmap]
rs7779367	0.85[CEU][hapmap];0.90[CHB][hapmap]
rs7780194	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7791710	0.93[CEU][hapmap];1.00[CHB][hapmap];0.81[EUR][1000 genomes]
rs7806637	0.87[ASN][1000 genomes]
rs964707	0.93[CEU][hapmap];1.00[CHB][hapmap];0.81[EUR][1000 genomes]
rs986553	0.93[CEU][hapmap];1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029220	chr7:32921484-33262190	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
2	nsv830942	chr7:33048075-33246735	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv830943	chr7:33167106-33352759	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
4	nsv933792	chr7:33169693-33216984	ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:33184800-33217200	Weak transcription	Brain Hippocampus Middle	brain
2	chr7:33185400-33218000	Weak transcription	Brain Angular Gyrus	brain
3	chr7:33185600-33224000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr7:33190000-33217600	Weak transcription	Left Ventricle	heart
5	chr7:33190200-33230400	Weak transcription	Gastric	stomach
6	chr7:33195200-33220200	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr7:33196800-33217200	Weak transcription	Brain Substantia Nigra	brain
8	chr7:33197000-33222200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr7:33197200-33220400	Weak transcription	Brain Anterior Caudate	brain
10	chr7:33198000-33213800	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr7:33198400-33217600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr7:33200200-33217600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr7:33202400-33219800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr7:33203800-33221200	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr7:33204400-33217600	Weak transcription	Brain Cingulate Gyrus	brain
16	chr7:33205200-33213800	Weak transcription	Psoas Muscle	Psoas
17	chr7:33206200-33225400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr7:33206400-33213800	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr7:33206400-33217600	Weak transcription	Thymus	Thymus
20	chr7:33206400-33220200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr7:33206400-33221200	Weak transcription	Colonic Mucosa	Colon
22	chr7:33206400-33230400	Weak transcription	Right Ventricle	heart
23	chr7:33206600-33215000	Weak transcription	Aorta	Aorta
24	chr7:33206600-33217200	Weak transcription	Adipose Nuclei	Adipose
25	chr7:33206600-33217400	Weak transcription	Colon Smooth Muscle	Colon
26	chr7:33206600-33217600	Weak transcription	Esophagus	oesophagus
27	chr7:33206600-33217600	Weak transcription	Ovary	ovary
28	chr7:33206600-33217600	Weak transcription	Spleen	Spleen
29	chr7:33206600-33217800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr7:33206600-33222600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr7:33206600-33230400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr7:33206600-33232600	Weak transcription	Pancreas	Pancrea
33	chr7:33206600-33234800	Weak transcription	Rectal Smooth Muscle	rectum
34	chr7:33206800-33212000	Weak transcription	Primary T cells from cord blood	blood
35	chr7:33206800-33213400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr7:33206800-33213400	Weak transcription	Liver	Liver
37	chr7:33206800-33222400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr7:33206800-33230400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr7:33210800-33230200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr7:33211400-33212400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr7:33211800-33217600	Weak transcription	Right Atrium	heart

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