Variant report

Variant	rs73287426
Chromosome Location	chr17:16175675-16175676
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:16175415..16178833-chr17:16340980..16343676,3	K562	blood:
2	chr17:16165701..16168526-chr17:16175025..16177234,2	K562	blood:
3	chr17:16174439..16177068-chr17:16182949..16184575,2	MCF-7	breast:
4	chr17:16175613..16177526-chr17:16233253..16235585,2	K562	blood:

Variant related genes	Relation type
ENSG00000175061	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs1006958	1.00[EUR][1000 genomes]
rs57100283	1.00[EUR][1000 genomes]
rs57540884	1.00[EUR][1000 genomes]
rs57939654	1.00[EUR][1000 genomes]
rs57958152	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58069228	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58203269	1.00[EUR][1000 genomes]
rs58213352	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58937503	1.00[EUR][1000 genomes]
rs59191673	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59414015	1.00[EUR][1000 genomes]
rs59837344	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60277322	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60436356	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs61360753	1.00[EUR][1000 genomes]
rs61479315	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs61529373	1.00[EUR][1000 genomes]
rs7212903	1.00[EUR][1000 genomes]
rs7217230	1.00[EUR][1000 genomes]
rs7219038	1.00[EUR][1000 genomes]
rs7225649	1.00[EUR][1000 genomes]
rs73281934	1.00[EUR][1000 genomes]
rs73281961	1.00[EUR][1000 genomes]
rs73281967	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73281977	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73281979	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73281980	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73281981	1.00[EUR][1000 genomes]
rs73287023	1.00[EUR][1000 genomes]
rs73287032	1.00[EUR][1000 genomes]
rs73287067	1.00[EUR][1000 genomes]
rs73287076	1.00[EUR][1000 genomes]
rs73287082	1.00[EUR][1000 genomes]
rs73287088	1.00[EUR][1000 genomes]
rs73287090	1.00[EUR][1000 genomes]
rs73287414	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73287419	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73287423	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73287425	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73287441	1.00[EUR][1000 genomes]
rs73288903	1.00[EUR][1000 genomes]
rs73288904	1.00[EUR][1000 genomes]
rs8066726	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8067000	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8068254	1.00[EUR][1000 genomes]
rs8069679	1.00[EUR][1000 genomes]
rs8071289	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8075170	1.00[EUR][1000 genomes]
rs8079037	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv934185	chr17:15552960-16551197	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	190 gene(s)	inside rSNPs	diseases
2	esv3330182	chr17:15652014-16569534	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
3	esv3446844	chr17:15654843-16572246	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
4	nsv1063459	chr17:15804228-16543593	Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
5	nsv907715	chr17:16019978-16206540	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	44 gene(s)	inside rSNPs	diseases
6	nsv907717	chr17:16076898-16239832	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	44 gene(s)	inside rSNPs	diseases
7	nsv528263	chr17:16097430-16196996	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	41 gene(s)	inside rSNPs	diseases
8	esv3326983	chr17:16138963-16210147	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	21 gene(s)	inside rSNPs	diseases
9	nsv907719	chr17:16161036-16185122	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv1063764	chr17:16171649-16662914	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	120 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:16133800-16176200	Weak transcription	NHEK	skin
2	chr17:16154400-16176600	Weak transcription	Hela-S3	cervix
3	chr17:16157400-16185200	Weak transcription	Gastric	stomach
4	chr17:16159200-16178400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr17:16159400-16189200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr17:16159600-16188800	Weak transcription	Stomach Smooth Muscle	stomach
7	chr17:16159600-16189000	Weak transcription	Brain Anterior Caudate	brain
8	chr17:16160000-16183000	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr17:16160400-16188400	Weak transcription	Liver	Liver
10	chr17:16163400-16189200	Weak transcription	Left Ventricle	heart
11	chr17:16163600-16189200	Weak transcription	Pancreas	Pancrea
12	chr17:16164000-16176400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr17:16164000-16176400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr17:16164000-16180800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr17:16164000-16182400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr17:16164000-16182400	Weak transcription	Fetal Muscle Leg	muscle
17	chr17:16164000-16185000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr17:16164000-16189000	Weak transcription	Fetal Brain Female	brain
19	chr17:16164000-16189000	Weak transcription	Rectal Smooth Muscle	rectum
20	chr17:16164200-16182200	Weak transcription	Fetal Stomach	stomach
21	chr17:16164600-16176000	Weak transcription	Fetal Intestine Small	intestine
22	chr17:16164600-16182200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr17:16166200-16205400	Weak transcription	Brain Hippocampus Middle	brain
24	chr17:16168600-16188800	Weak transcription	Fetal Intestine Large	intestine
25	chr17:16169200-16176400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr17:16171000-16181600	Weak transcription	HepG2	liver
27	chr17:16171400-16188200	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr17:16171400-16189000	Weak transcription	Spleen	Spleen
29	chr17:16171600-16175800	Weak transcription	Small Intestine	intestine
30	chr17:16171600-16176400	Weak transcription	K562	blood
31	chr17:16171600-16178000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr17:16171600-16182200	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr17:16171600-16188200	Weak transcription	Duodenum Mucosa	Duodenum
34	chr17:16171800-16177800	Weak transcription	Primary hematopoietic stem cells	blood
35	chr17:16172000-16180400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr17:16172000-16185200	Weak transcription	Lung	lung
37	chr17:16172600-16188200	Weak transcription	GM12878-XiMat	blood
38	chr17:16173000-16187800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr17:16173000-16188200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr17:16173200-16177000	Weak transcription	Primary B cells from peripheral blood	blood
41	chr17:16173200-16180400	Weak transcription	Primary T helper cells fromperipheralblood	blood
42	chr17:16173200-16183200	Weak transcription	Primary T cells from cord blood	blood
43	chr17:16173200-16185400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr17:16173200-16186800	Weak transcription	Fetal Lung	lung
45	chr17:16173200-16187800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr17:16173200-16188000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
47	chr17:16173400-16176000	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr17:16173400-16176200	Weak transcription	NHLF	lung
49	chr17:16173400-16176400	Weak transcription	Osteobl	bone
50	chr17:16173400-16176600	Weak transcription	HSMM	muscle

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