Variant report

Variant	rs2623185
Chromosome Location	chr15:99733343-99733344
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10902539	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1670213	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1670216	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1670224	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1670230	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1703762	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs1703763	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1703766	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1703771	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs187755	0.86[EUR][1000 genomes]
rs260114	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2602016	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2602018	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2602020	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2602022	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2602025	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2602026	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2602031	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2602035	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2602038	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2623188	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2623189	0.91[AMR][1000 genomes]
rs2623190	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2623191	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2924346	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3210942	0.85[AMR][1000 genomes]
rs4602019	0.88[ASN][1000 genomes]
rs4965217	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6598224	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6598225	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7163625	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 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

No data

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:99673200-99789400	Weak transcription	Small Intestine	intestine
2	chr15:99697000-99756400	Weak transcription	Stomach Mucosa	stomach
3	chr15:99711600-99738600	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr15:99715600-99738600	Weak transcription	Hela-S3	cervix
5	chr15:99717400-99761000	Weak transcription	Gastric	stomach
6	chr15:99717800-99758000	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr15:99718200-99749200	Weak transcription	HUVEC	blood vessel
8	chr15:99721200-99738600	Weak transcription	HSMMtube	muscle
9	chr15:99721200-99758400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr15:99721600-99735600	Weak transcription	Dnd41	blood
11	chr15:99721800-99742400	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr15:99722000-99758400	Weak transcription	Right Ventricle	heart
13	chr15:99722200-99739800	Weak transcription	NHLF	lung
14	chr15:99722400-99752200	Weak transcription	Osteobl	bone
15	chr15:99722600-99757600	Weak transcription	Psoas Muscle	Psoas
16	chr15:99722800-99738200	Weak transcription	HSMM	muscle
17	chr15:99723000-99749000	Weak transcription	Colon Smooth Muscle	Colon
18	chr15:99723200-99738400	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr15:99724400-99769600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr15:99726000-99736400	Weak transcription	NH-A	brain
21	chr15:99726000-99749400	Weak transcription	Brain Cingulate Gyrus	brain
22	chr15:99726400-99742600	Weak transcription	Brain Anterior Caudate	brain
23	chr15:99726600-99735400	Weak transcription	Stomach Smooth Muscle	stomach
24	chr15:99726600-99758200	Weak transcription	HMEC	breast
25	chr15:99728400-99760000	Weak transcription	NHDF-Ad	bronchial
26	chr15:99730400-99739000	Weak transcription	Left Ventricle	heart
27	chr15:99730800-99733600	Strong transcription	Duodenum Mucosa	Duodenum
28	chr15:99730800-99733800	Strong transcription	Adipose Nuclei	Adipose
29	chr15:99730800-99734000	Strong transcription	Liver	Liver
30	chr15:99730800-99734200	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr15:99731000-99733800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr15:99731000-99740200	Strong transcription	Fetal Lung	lung
33	chr15:99731200-99734000	Strong transcription	Primary hematopoietic stem cells	blood
34	chr15:99731200-99734000	Strong transcription	Fetal Muscle Leg	muscle
35	chr15:99731200-99734200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
36	chr15:99731200-99734400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr15:99731400-99733600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr15:99731400-99733800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr15:99731400-99733800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr15:99731400-99733800	Strong transcription	Rectal Mucosa Donor 31	rectum
41	chr15:99731400-99734200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
42	chr15:99731400-99735000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr15:99731600-99733400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr15:99731600-99733800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr15:99731600-99734200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr15:99731600-99734200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr15:99731800-99739800	Weak transcription	HepG2	liver
48	chr15:99732000-99736000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr15:99732200-99733800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr15:99732200-99733800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links