Variant report

Variant	rs17706174
Chromosome Location	chr2:173708855-173708856
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:173706643..173709122-chr2:173725202..173727159,2	MCF-7	breast:

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10514633	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1104635	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17704262	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17704332	0.90[EUR][1000 genomes]
rs17704976	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17705358	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17705390	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17705429	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17705626	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17705739	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17705834	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17705852	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17706349	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17706854	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17706880	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17755063	0.90[EUR][1000 genomes]
rs17755348	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17756405	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17756703	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17756739	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17756834	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17756942	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17757877	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72900203	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72900214	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72900223	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72900226	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72900228	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72900229	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72900230	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72900235	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72900240	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72900243	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72900248	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72902287	0.90[EUR][1000 genomes]
rs72902296	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72906101	0.83[AMR][1000 genomes]
rs72906193	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72906194	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72906196	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72908114	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72908118	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72908120	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72908147	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72908174	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72908191	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72908195	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72908196	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72908198	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72908199	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72908213	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72908214	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72908215	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72908218	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72908222	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72908226	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72908230	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72908233	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72908246	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72908248	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72908250	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72908256	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72908260	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72908274	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72908277	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72908283	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72908285	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7420491	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs951314	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs951315	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533927	chr2:173161637-173796894	Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	esv2760591	chr2:173396905-173719520	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:173689200-173723200	Weak transcription	Esophagus	oesophagus
2	chr2:173700000-173710000	Weak transcription	Psoas Muscle	Psoas
3	chr2:173701600-173709800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr2:173705800-173714400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr2:173707200-173710800	Enhancers	Fetal Thymus	thymus
6	chr2:173707400-173709000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr2:173707400-173709200	Enhancers	NHEK	skin
8	chr2:173707400-173709800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr2:173707400-173714800	Enhancers	Fetal Heart	heart
10	chr2:173707600-173711400	Weak transcription	Aorta	Aorta
11	chr2:173707800-173711400	Weak transcription	Lung	lung
12	chr2:173707800-173712000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr2:173708200-173713400	Weak transcription	Thymus	Thymus
14	chr2:173708400-173709200	Enhancers	Brain Anterior Caudate	brain
15	chr2:173708400-173709200	Enhancers	Stomach Mucosa	stomach
16	chr2:173708400-173713600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr2:173708600-173712400	Enhancers	Right Ventricle	heart
18	chr2:173708800-173709000	Enhancers	Small Intestine	intestine
19	chr2:173708800-173709200	Enhancers	Gastric	stomach
20	chr2:173708800-173709400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr2:173708800-173709400	Enhancers	Brain Angular Gyrus	brain
22	chr2:173708800-173709400	Enhancers	Pancreas	Pancrea
23	chr2:173708800-173709800	Weak transcription	Fetal Brain Female	brain
24	chr2:173708800-173710200	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr2:173708800-173710200	Enhancers	Adipose Nuclei	Adipose
26	chr2:173708800-173710400	Enhancers	Left Ventricle	heart
27	chr2:173708800-173712400	Enhancers	Right Atrium	heart
28	chr2:173708800-173713200	Weak transcription	Fetal Intestine Large	intestine

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