Variant report

Variant	rs9899922
Chromosome Location	chr17:15393586-15393587
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:15393209..15396185-chr17:15400258..15402130,2	MCF-7	breast:
2	chr17:15392637..15397367-chr17:15398758..15404412,8	K562	blood:
3	chr17:15392701..15397152-chr17:15398701..15402500,5	K562	blood:

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

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

rs_ID	r²[population]
rs11651787	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11653403	0.87[CEU][hapmap];0.83[JPT][hapmap];0.83[EUR][1000 genomes]
rs1465251	0.87[CEU][hapmap];0.83[JPT][hapmap];0.83[EUR][1000 genomes]
rs1465252	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2052022	0.85[ASN][1000 genomes]
rs236810	0.83[LWK][hapmap];0.92[MKK][hapmap]
rs28411195	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs28733269	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2938158	0.80[LWK][hapmap];0.90[MKK][hapmap]
rs4572441	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55749051	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62069953	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62072569	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62072571	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs716389	0.88[ASW][hapmap];0.91[CEU][hapmap];0.93[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];0.99[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7211982	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7215138	1.00[JPT][hapmap]
rs8076852	0.91[CEU][hapmap];0.87[CHB][hapmap];0.92[JPT][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9901383	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9903674	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9908651	0.91[CEU][hapmap];0.93[CHB][hapmap];0.89[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9911005	0.91[CEU][hapmap];0.87[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];0.92[JPT][hapmap];0.85[MKK][hapmap];0.95[TSI][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9911822	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9913509	0.91[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv492304	chr17:15043353-15611753	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv916652	chr17:15093600-15856310	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
3	nsv427990	chr17:15154329-15434020	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv949172	chr17:15206970-15416808	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
5	nsv1055677	chr17:15294011-15561130	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
6	nsv1059056	chr17:15294011-15856861	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
7	nsv1058286	chr17:15315763-15561130	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
8	nsv543213	chr17:15315763-15561130	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15340600-15399600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr17:15359200-15404600	Weak transcription	Primary T cells from cord blood	blood
3	chr17:15367400-15394200	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr17:15368000-15393600	Weak transcription	Aorta	Aorta
5	chr17:15368400-15405400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr17:15368800-15394000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr17:15369000-15393600	Weak transcription	Brain Cingulate Gyrus	brain
8	chr17:15369000-15401600	Weak transcription	Brain Germinal Matrix	brain
9	chr17:15369200-15405000	Weak transcription	Esophagus	oesophagus
10	chr17:15373200-15393600	Weak transcription	Brain Hippocampus Middle	brain
11	chr17:15373200-15393600	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr17:15377200-15394200	Weak transcription	Stomach Mucosa	stomach
13	chr17:15377400-15406400	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr17:15377600-15393800	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr17:15379400-15393600	Weak transcription	HSMMtube	muscle
16	chr17:15379400-15393600	Weak transcription	Osteobl	bone
17	chr17:15379600-15393800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr17:15382800-15394400	Weak transcription	Spleen	Spleen
19	chr17:15383200-15419600	Weak transcription	Thymus	Thymus
20	chr17:15383400-15394000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr17:15383400-15402200	Weak transcription	A549	lung
22	chr17:15383400-15455000	Weak transcription	Gastric	stomach
23	chr17:15383600-15393600	Weak transcription	Brain Anterior Caudate	brain
24	chr17:15383600-15393600	Weak transcription	NH-A	brain
25	chr17:15383600-15393800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr17:15383600-15393800	Weak transcription	NHLF	lung
27	chr17:15383600-15395800	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr17:15383800-15393600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr17:15383800-15393600	Weak transcription	HSMM	muscle
30	chr17:15383800-15393800	Weak transcription	Colon Smooth Muscle	Colon
31	chr17:15383800-15394200	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr17:15383800-15398400	Weak transcription	Fetal Kidney	kidney
33	chr17:15383800-15401400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr17:15383800-15405200	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr17:15383800-15406000	Weak transcription	NHEK	skin
36	chr17:15384000-15393600	Weak transcription	Hela-S3	cervix
37	chr17:15384200-15393600	Weak transcription	Brain Substantia Nigra	brain
38	chr17:15384400-15394000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr17:15384600-15406200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr17:15385400-15395800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr17:15385600-15418000	Weak transcription	Pancreas	Pancrea
42	chr17:15385800-15393600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr17:15387200-15394200	Weak transcription	Psoas Muscle	Psoas
44	chr17:15387200-15400000	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr17:15387200-15403800	Weak transcription	Liver	Liver
46	chr17:15387200-15417000	Weak transcription	Small Intestine	intestine
47	chr17:15387400-15393600	Weak transcription	Fetal Intestine Large	intestine
48	chr17:15387400-15399400	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr17:15387400-15405000	Weak transcription	Lung	lung
50	chr17:15387600-15393600	Weak transcription	Brain Angular Gyrus	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links