Variant report

Variant	rs6448177
Chromosome Location	chr4:10666272-10666273
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:10658968..10660496-chr4:10663948..10666416,2	MCF-7	breast:
2	chr4:10662152..10664444-chr4:10666207..10668655,2	K562	blood:

Extended variants
information (count: 46 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10516208	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];0.82[GIH][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10938919	0.81[YRI][hapmap];0.84[EUR][1000 genomes]
rs10938921	0.91[ASN][1000 genomes]
rs11723092	1.00[ASW][hapmap];0.96[CEU][hapmap];0.80[GIH][hapmap];0.82[LWK][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes]
rs11723949	0.95[EUR][1000 genomes]
rs11725559	0.96[CEU][hapmap];0.81[YRI][hapmap];0.97[EUR][1000 genomes]
rs11726388	0.83[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs11734917	0.92[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs11737643	0.95[EUR][1000 genomes]
rs11933682	0.80[MEX][hapmap];0.87[TSI][hapmap]
rs12233843	0.93[ASW][hapmap];0.87[TSI][hapmap];0.83[EUR][1000 genomes]
rs12499294	0.97[EUR][1000 genomes]
rs12501252	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.85[GIH][hapmap];0.81[JPT][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12509884	0.92[CEU][hapmap];0.81[YRI][hapmap];0.93[EUR][1000 genomes]
rs13107947	0.84[EUR][1000 genomes]
rs13111831	0.84[EUR][1000 genomes]
rs13119277	1.00[ASW][hapmap];0.85[CEU][hapmap];0.82[GIH][hapmap];1.00[TSI][hapmap];0.95[EUR][1000 genomes]
rs13128842	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13136927	0.86[ASW][hapmap];0.84[MEX][hapmap];0.92[MKK][hapmap];0.87[TSI][hapmap];0.85[YRI][hapmap]
rs13139842	0.84[EUR][1000 genomes]
rs13143538	0.95[EUR][1000 genomes]
rs17267821	0.92[CEU][hapmap];0.81[YRI][hapmap];0.97[EUR][1000 genomes]
rs3935222	0.87[ASW][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.91[JPT][hapmap];0.94[MKK][hapmap];0.83[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs4235336	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.87[GIH][hapmap];0.91[JPT][hapmap];0.88[LWK][hapmap];0.96[MEX][hapmap];0.91[MKK][hapmap];0.98[TSI][hapmap];0.89[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4296670	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes]
rs4309833	0.82[CEU][hapmap];0.83[MEX][hapmap];0.85[TSI][hapmap];0.80[EUR][1000 genomes]
rs4339204	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61796835	0.95[EUR][1000 genomes]
rs6850317	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7677121	0.91[CEU][hapmap];0.97[EUR][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	nsv1003454	chr4:9805223-10710990	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
2	nsv537023	chr4:9805223-10710990	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
3	nsv1004801	chr4:9814720-10674528	Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
4	nsv537024	chr4:9814720-10674528	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
5	nsv931483	chr4:9814721-10716463	Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
6	nsv1009972	chr4:9903566-10710990	Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
7	nsv537027	chr4:9903566-10710990	Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases
8	nsv1010620	chr4:9937123-10686682	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
9	nsv530280	chr4:9947818-10940041	Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
10	nsv869057	chr4:10013411-10875454	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	65 gene(s)	inside rSNPs	diseases
11	nsv997936	chr4:10040713-11009045	Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription 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	65 gene(s)	inside rSNPs	diseases
12	nsv593727	chr4:10397327-10694991	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
13	nsv517971	chr4:10399068-10893253	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
14	nsv878694	chr4:10407572-10783606	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
15	nsv878697	chr4:10501373-10831866	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
16	nsv829860	chr4:10598743-10764854	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs6448177	HS3ST1	cis	parietal	SCAN
rs6448177	ACOX3	cis	parietal	SCAN

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10664600-10667000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr4:10665400-10666800	Enhancers	Muscle Satellite Cultured Cells	--
3	chr4:10665400-10666800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr4:10665400-10666800	Enhancers	HUVEC	blood vessel
5	chr4:10665600-10666800	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr4:10665600-10666800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr4:10665600-10666800	Enhancers	NH-A	brain
8	chr4:10665600-10667000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr4:10665800-10666400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr4:10665800-10666400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:10665800-10666600	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr4:10665800-10666800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr4:10665800-10666800	Enhancers	Rectal Smooth Muscle	rectum
14	chr4:10665800-10666800	Enhancers	Osteobl	bone
15	chr4:10666000-10666400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr4:10666000-10666400	Enhancers	Esophagus	oesophagus
17	chr4:10666000-10666600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr4:10666000-10666600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr4:10666000-10666600	Enhancers	NHEK	skin
20	chr4:10666000-10666600	Enhancers	NHLF	lung
21	chr4:10666000-10666800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr4:10666000-10666800	Enhancers	Fetal Thymus	thymus
23	chr4:10666000-10666800	Enhancers	Lung	lung
24	chr4:10666000-10666800	Enhancers	HMEC	breast
25	chr4:10666000-10667000	Enhancers	GM12878-XiMat	blood
26	chr4:10666200-10666400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr4:10666200-10666400	Enhancers	Fetal Muscle Trunk	muscle
28	chr4:10666200-10666600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr4:10666200-10666600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr4:10666200-10666600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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