Variant report

Variant	rs17170145
Chromosome Location	chr7:33297897-33297898
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10486525	0.84[AFR][1000 genomes]
rs1117311	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13235723	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17170138	0.84[AFR][1000 genomes]
rs17170140	0.84[AFR][1000 genomes]
rs17170143	0.84[AFR][1000 genomes]
rs17170155	0.84[AFR][1000 genomes]
rs34950347	0.84[AFR][1000 genomes]
rs55865959	0.82[AFR][1000 genomes]
rs60268357	0.84[AFR][1000 genomes]
rs6944559	0.82[AFR][1000 genomes]
rs6952244	0.84[AFR][1000 genomes]
rs6969284	0.84[AFR][1000 genomes]
rs6973552	0.84[AFR][1000 genomes]
rs73307398	0.84[AFR][1000 genomes]
rs73307399	0.84[AFR][1000 genomes]
rs73307400	0.84[AFR][1000 genomes]
rs73309308	0.84[AFR][1000 genomes]
rs73309310	0.84[AFR][1000 genomes]
rs73309312	0.84[AFR][1000 genomes]
rs73309316	0.84[AFR][1000 genomes]
rs73309318	0.84[AFR][1000 genomes]
rs73309324	0.82[AFR][1000 genomes]
rs73688093	0.84[AFR][1000 genomes]
rs7793667	0.82[AFR][1000 genomes]
rs7793862	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7798118	0.84[AFR][1000 genomes]
rs7808472	0.82[AFR][1000 genomes]

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	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
2	nsv606610	chr7:33218763-33486316	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1016416	chr7:33241443-33559477	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv916660	chr7:33272493-33506384	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:33283800-33316000	Weak transcription	Ovary	ovary
2	chr7:33288800-33317600	Weak transcription	Gastric	stomach
3	chr7:33289400-33309000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr7:33289600-33310800	Weak transcription	Psoas Muscle	Psoas
5	chr7:33290000-33316200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr7:33290800-33309000	Weak transcription	Fetal Stomach	stomach
7	chr7:33290800-33316400	Weak transcription	Aorta	Aorta
8	chr7:33291200-33298000	Weak transcription	NHDF-Ad	bronchial
9	chr7:33291200-33316000	Weak transcription	Primary T cells from cord blood	blood
10	chr7:33291600-33305200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr7:33291800-33307600	Weak transcription	Left Ventricle	heart
12	chr7:33293400-33302200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr7:33295400-33299800	Weak transcription	HepG2	liver
14	chr7:33295800-33298000	Weak transcription	Stomach Mucosa	stomach
15	chr7:33295800-33298400	Enhancers	Fetal Lung	lung
16	chr7:33297400-33310800	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr7:33297600-33298600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr7:33297600-33298600	Enhancers	Osteobl	bone
19	chr7:33297800-33298200	Enhancers	Muscle Satellite Cultured Cells	--
20	chr7:33297800-33298200	Enhancers	Colon Smooth Muscle	Colon
21	chr7:33297800-33298400	Enhancers	Adipose Nuclei	Adipose
22	chr7:33297800-33298600	Enhancers	Liver	Liver
23	chr7:33297800-33298800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr7:33297800-33298800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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