Variant report

Variant	rs2602036
Chromosome Location	chr15:99759831-99759832
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10152912	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs1223950	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs1223951	0.81[CHB][hapmap];0.81[JPT][hapmap]
rs1238348	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12907394	0.91[CHB][hapmap];0.82[JPT][hapmap];0.81[MEX][hapmap]
rs12911768	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs12915090	1.00[ASW][hapmap]
rs1567416	0.81[JPT][hapmap]
rs1976589	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs2048301	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs260114	1.00[ASW][hapmap]
rs2602018	1.00[ASW][hapmap];0.82[CHB][hapmap]
rs2602021	1.00[ASW][hapmap]
rs2602026	1.00[ASW][hapmap];0.82[CHB][hapmap]
rs2602030	0.82[CHB][hapmap];0.81[GIH][hapmap];0.82[JPT][hapmap]
rs2623184	0.87[ASW][hapmap];1.00[YRI][hapmap]
rs2623190	1.00[ASW][hapmap]
rs2623191	1.00[ASW][hapmap]
rs2623199	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2862139	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs4965217	0.86[ASW][hapmap]
rs4965221	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4965224	0.82[CHB][hapmap];0.82[JPT][hapmap];0.81[MEX][hapmap]
rs7164003	0.82[CHB][hapmap];0.82[JPT][hapmap]
rs7183226	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.92[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8042021	0.89[CHB][hapmap];0.81[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531079	chr15:98907913-99878547	Strong transcription Weak transcription Genic enhancers Active TSS Enhancers ZNF genes & repeats Flanking 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 miRNA target site	97 gene(s)	inside rSNPs	diseases
2	nsv1039575	chr15:98982045-99924685	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
3	nsv869529	chr15:99416774-99903351	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
4	nsv1055008	chr15:99477144-100019861	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
5	nsv1045124	chr15:99504843-99847210	Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
6	nsv1038870	chr15:99510479-99768374	Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
7	nsv904543	chr15:99513231-99991506	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
8	nsv533926	chr15:99519820-99997114	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
9	nsv915926	chr15:99519820-100138705	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
10	nsv1051782	chr15:99621061-99792967	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
11	nsv916822	chr15:99621061-99878564	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
12	nsv949203	chr15:99621061-99932797	Strong transcription Weak transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
13	nsv817289	chr15:99621061-100138705	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
14	nsv431411	chr15:99621061-100143999	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer 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
15	nsv570716	chr15:99629901-99916332	Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
16	nsv904546	chr15:99696046-100166300	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
17	nsv1052528	chr15:99736977-99874210	Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
18	nsv1036346	chr15:99752391-100365458	Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
19	nsv542520	chr15:99752391-100365458	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:99673200-99789400	Weak transcription	Small Intestine	intestine
2	chr15:99717400-99761000	Weak transcription	Gastric	stomach
3	chr15:99724400-99769600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr15:99728400-99760000	Weak transcription	NHDF-Ad	bronchial
5	chr15:99732800-99761000	Weak transcription	Lung	lung
6	chr15:99733000-99760400	Weak transcription	Esophagus	oesophagus
7	chr15:99733400-99787400	Weak transcription	NHEK	skin
8	chr15:99740200-99760800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr15:99740200-99761000	Weak transcription	Fetal Kidney	kidney
10	chr15:99740200-99763800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr15:99749800-99789400	Weak transcription	Brain Cingulate Gyrus	brain
12	chr15:99750000-99789400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr15:99750200-99761000	Weak transcription	HUVEC	blood vessel
14	chr15:99751800-99768600	Strong transcription	Fetal Muscle Leg	muscle
15	chr15:99752800-99766800	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr15:99753000-99761000	Weak transcription	Fetal Intestine Small	intestine
17	chr15:99753000-99763800	Weak transcription	Fetal Heart	heart
18	chr15:99753200-99766800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr15:99753400-99767000	Weak transcription	NHLF	lung
20	chr15:99754400-99768000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr15:99754400-99768600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr15:99754400-99768800	Strong transcription	Fetal Intestine Large	intestine
23	chr15:99754800-99769000	Strong transcription	Adipose Nuclei	Adipose
24	chr15:99755200-99762400	Strong transcription	Osteobl	bone
25	chr15:99755200-99762600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr15:99755400-99768800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr15:99755600-99767800	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr15:99755600-99768000	Strong transcription	Liver	Liver
29	chr15:99756200-99765000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr15:99756400-99765200	Strong transcription	Fetal Lung	lung
31	chr15:99756600-99768800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr15:99756600-99769000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr15:99756600-99789400	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr15:99756800-99761600	Strong transcription	Left Ventricle	heart
35	chr15:99756800-99768800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr15:99756800-99768800	Strong transcription	Fetal Muscle Trunk	muscle
37	chr15:99756800-99769000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr15:99757000-99768200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr15:99757200-99760000	Weak transcription	Brain Germinal Matrix	brain
40	chr15:99757400-99761400	Strong transcription	A549	lung
41	chr15:99757600-99762000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
42	chr15:99757600-99762400	Strong transcription	Placenta	Placenta
43	chr15:99757600-99763400	Strong transcription	Dnd41	blood
44	chr15:99757600-99764400	Strong transcription	Ovary	ovary
45	chr15:99757600-99765800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr15:99757600-99768800	Strong transcription	Duodenum Smooth Muscle	Duodenum
47	chr15:99757800-99762600	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr15:99757800-99763000	Strong transcription	HepG2	liver
49	chr15:99757800-99764200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr15:99757800-99768600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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