Variant report

Variant	rs10402322
Chromosome Location	chr19:18626732-18626733
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:18620896..18622979-chr19:18626184..18627867,2	K562	blood:
2	chr19:18624925..18627602-chr19:18688802..18692839,3	K562	blood:
3	chr19:18611587..18620542-chr19:18622883..18629236,13	MCF-7	breast:
4	chr19:18625885..18628372-chr19:18639821..18642383,2	MCF-7	breast:
5	chr19:18624462..18627368-chr19:18641564..18644052,2	K562	blood:
6	chr19:18625178..18627279-chr19:18954295..18956518,2	K562	blood:
7	chr19:18624024..18629348-chr19:18653543..18656506,5	K562	blood:
8	chr19:18625937..18627483-chr19:18684789..18686553,2	K562	blood:
9	chr19:18620364..18629414-chr19:18629622..18635316,18	MCF-7	breast:
10	chr19:18625528..18629549-chr19:18629615..18633672,9	K562	blood:
11	chr19:18618174..18621109-chr19:18623910..18627140,6	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000268938	Chromatin interaction
ENSG00000105656	Chromatin interaction
ENSG00000269191	Chromatin interaction
ENSG00000105701	Chromatin interaction

Extended variants
information (count: 82 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10409346	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10409408	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10410797	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10413922	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10416993	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10418331	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10418554	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10420384	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10423802	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10426768	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1045631	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11668704	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11670392	0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11672385	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11879757	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12980726	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12982295	0.82[ASN][1000 genomes]
rs12983263	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1469412	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1469413	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1971093	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2013069	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2162797	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2303692	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28534973	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2891676	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34213500	0.81[ASN][1000 genomes]
rs35004712	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35742476	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4006662	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4303657	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4580317	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4808135	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4808802	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4808803	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4808805	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4808806	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4808807	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4808808	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4808811	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4808812	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4808813	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55715336	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs57923655	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6512268	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6512269	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6512270	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6512271	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7246788	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7247540	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7249760	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7251232	0.84[EUR][1000 genomes]
rs7252130	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7252185	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7255936	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7256530	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7258891	0.81[ASN][1000 genomes]
rs7259135	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7507218	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8100343	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8102717	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8104247	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8106068	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8106332	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8111397	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8111582	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8111824	0.81[ASN][1000 genomes]
rs8112372	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8112859	0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs888668	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs888669	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv911274	chr19:18440942-18691942	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
2	nsv1057795	chr19:18453362-18883844	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
3	nsv543925	chr19:18453362-18883844	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
4	nsv428018	chr19:18454891-18663981	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
5	nsv1060687	chr19:18522527-18643218	Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
6	nsv532615	chr19:18534867-18796031	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
7	nsv1061733	chr19:18574940-18679155	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
8	nsv1055794	chr19:18611545-18676933	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
9	nsv911281	chr19:18613917-18758255	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
10	nsv911282	chr19:18624964-18928480	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
11	nsv911283	chr19:18626732-18689830	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs10402322	SSBP4	Cis_1M	lymphoblastoid	RTeQTL
rs10402322	LOC646044///SSBP4	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18600400-18630600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr19:18613800-18631000	Weak transcription	Fetal Brain Female	brain
3	chr19:18618800-18630000	Weak transcription	Primary hematopoietic stem cells	blood
4	chr19:18618800-18630800	Weak transcription	Thymus	Thymus
5	chr19:18618800-18631000	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr19:18620200-18630600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr19:18621600-18630200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr19:18623200-18627400	Enhancers	Primary T cells fromperipheralblood	blood
9	chr19:18623400-18628000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr19:18623600-18627800	Enhancers	Left Ventricle	heart
11	chr19:18623600-18627800	Enhancers	Right Atrium	heart
12	chr19:18623600-18628000	Enhancers	Fetal Heart	heart
13	chr19:18623600-18631000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr19:18623800-18626800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr19:18623800-18628200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr19:18623800-18628200	Enhancers	Liver	Liver
17	chr19:18623800-18631000	Enhancers	Fetal Intestine Large	intestine
18	chr19:18624000-18626800	Enhancers	NHDF-Ad	bronchial
19	chr19:18624000-18627800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr19:18624200-18627000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr19:18624200-18627000	Enhancers	NHLF	lung
22	chr19:18624200-18628000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr19:18624200-18630800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr19:18624400-18630200	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr19:18624600-18628000	Genic enhancers	Fetal Intestine Small	intestine
26	chr19:18624800-18626800	Enhancers	Fetal Lung	lung
27	chr19:18624800-18626800	Enhancers	NH-A	brain
28	chr19:18624800-18627400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr19:18624800-18627400	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr19:18624800-18628000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
31	chr19:18624800-18628000	Enhancers	Esophagus	oesophagus
32	chr19:18624800-18628000	Enhancers	Lung	lung
33	chr19:18624800-18628000	Enhancers	Small Intestine	intestine
34	chr19:18624800-18628200	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr19:18625000-18630200	Weak transcription	Rectal Smooth Muscle	rectum
36	chr19:18625400-18626800	Enhancers	Brain Angular Gyrus	brain
37	chr19:18625400-18626800	Enhancers	Brain Substantia Nigra	brain
38	chr19:18625400-18626800	Enhancers	Fetal Kidney	kidney
39	chr19:18625400-18626800	Enhancers	HUVEC	blood vessel
40	chr19:18625400-18627200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr19:18625400-18627200	Enhancers	Stomach Mucosa	stomach
42	chr19:18625400-18627800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr19:18625400-18627800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr19:18625400-18627800	Enhancers	Brain Hippocampus Middle	brain
45	chr19:18625400-18627800	Enhancers	Psoas Muscle	Psoas
46	chr19:18625400-18627800	Enhancers	Sigmoid Colon	Sigmoid Colon
47	chr19:18625400-18628000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr19:18625400-18628000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr19:18625400-18628000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr19:18625400-18628000	Enhancers	Pancreas	Pancrea

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