Variant report

Variant	rs4463206
Chromosome Location	chr5:115453671-115453672
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:115431884..115434416-chr5:115451435..115454225,2	K562	blood:
2	chr5:115419680..115422174-chr5:115452572..115455057,2	MCF-7	breast:
3	chr5:115445954..115448911-chr5:115452951..115455275,2	K562	blood:

Variant related genes	Relation type
ENSG00000145781	Chromatin interaction
ENSG00000271918	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10042163	1.00[CEU][hapmap];0.83[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10055039	1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs1113805	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs11957456	1.00[CEU][hapmap];0.94[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12653124	0.91[CEU][hapmap];0.83[CHB][hapmap];0.80[JPT][hapmap];0.83[YRI][hapmap];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1396480	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1508874	1.00[CEU][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1508884	1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs153614	0.91[CEU][hapmap];0.94[CHB][hapmap];1.00[YRI][hapmap];0.84[EUR][1000 genomes]
rs168833	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[YRI][hapmap]
rs194182	1.00[CEU][hapmap];0.89[CHB][hapmap];0.85[JPT][hapmap];0.83[YRI][hapmap];0.84[EUR][1000 genomes]
rs2063252	0.89[AFR][1000 genomes]
rs2136206	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2136212	1.00[CEU][hapmap];0.83[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs253960	1.00[CEU][hapmap];0.93[CHB][hapmap];0.83[YRI][hapmap]
rs254149	0.89[CHB][hapmap]
rs28125	1.00[CEU][hapmap];0.94[CHB][hapmap];0.83[YRI][hapmap]
rs37182	1.00[CEU][hapmap];0.94[CHB][hapmap];0.83[YRI][hapmap]
rs4084413	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4441909	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4920906	1.00[YRI][hapmap];0.89[AFR][1000 genomes]
rs4921061	0.97[AFR][1000 genomes]
rs6594941	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6594955	1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs6860795	1.00[CEU][hapmap];0.83[CHB][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6878279	1.00[YRI][hapmap]
rs6896229	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72804879	0.82[EUR][1000 genomes]
rs7701512	0.91[CEU][hapmap];0.82[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7726112	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7726721	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7733750	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7733992	1.00[CEU][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs784482	1.00[CEU][hapmap];0.94[CHB][hapmap];0.82[YRI][hapmap]
rs785368	0.91[CEU][hapmap]
rs804141	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs9285884	1.00[CEU][hapmap];0.83[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9326985	1.00[CEU][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9326992	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9687859	1.00[CEU][hapmap];0.82[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949677	chr5:115104829-115496168	Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv882736	chr5:115254723-115552945	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	nsv882737	chr5:115263853-115552945	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
4	esv34146	chr5:115315944-115729919	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
5	nsv527320	chr5:115382097-115573543	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
6	nsv1027266	chr5:115382704-115501792	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
7	esv2755349	chr5:115384101-115733101	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
8	nsv1032199	chr5:115384131-115525738	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
9	esv2830404	chr5:115386661-115490546	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
10	nsv1019972	chr5:115386860-115563533	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
11	nsv537869	chr5:115386860-115563533	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
12	nsv1018861	chr5:115397834-115563533	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
13	nsv537870	chr5:115397834-115563533	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
14	esv2762538	chr5:115436508-115455707	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115433600-115457200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr5:115444400-115456800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr5:115448400-115456600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr5:115449000-115466000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr5:115449200-115457600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr5:115449400-115465600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr5:115450000-115454800	Weak transcription	Dnd41	blood
8	chr5:115450000-115455800	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr5:115450000-115455800	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr5:115450000-115473400	Weak transcription	Fetal Lung	lung
11	chr5:115450200-115455200	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr5:115450200-115469600	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr5:115450400-115454600	Weak transcription	Primary hematopoietic stem cells	blood
14	chr5:115450400-115455600	Weak transcription	Fetal Stomach	stomach
15	chr5:115450600-115454600	Weak transcription	Primary T cells from cord blood	blood
16	chr5:115450600-115455200	Weak transcription	Fetal Intestine Large	intestine
17	chr5:115450600-115457800	Weak transcription	Aorta	Aorta
18	chr5:115450600-115458800	Weak transcription	Primary B cells from peripheral blood	blood
19	chr5:115450800-115455400	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr5:115451000-115455600	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr5:115451000-115473200	Weak transcription	Ovary	ovary
22	chr5:115451000-115481200	Weak transcription	Left Ventricle	heart
23	chr5:115451200-115454800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr5:115451200-115457000	Weak transcription	Gastric	stomach
25	chr5:115451200-115470800	Weak transcription	Primary B cells from cord blood	blood
26	chr5:115453400-115455200	Weak transcription	Fetal Intestine Small	intestine
27	chr5:115453600-115458600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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