Variant report

Variant	rs9328272
Chromosome Location	chr6:4732607-4732608
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:4730542..4732664-chr6:4733935..4736268,2	K562	blood:
2	chr6:4731639..4734329-chr6:4773986..4778095,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPP40-7	chr6:4732329-4733160	NONHSAT107486

Variant related genes	Relation type
ENSG00000236336	Chromatin interaction
ENSG00000153046	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10458178	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11242974	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11242977	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11242978	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11755832	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11759784	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12196896	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12208133	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12211355	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12214737	0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1933225	0.81[ASN][1000 genomes]
rs35640627	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35836829	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4960042	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6597094	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6597095	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6915353	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6917691	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6931290	0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6931832	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6932591	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6937790	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6938514	0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6941511	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6941562	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7745237	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7748184	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7748335	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7748862	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7762773	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7762927	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7767658	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7767968	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs907841	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9328271	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9328273	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9328274	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9378409	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9378410	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9378411	0.85[CHB][hapmap];0.84[JPT][hapmap];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9378906	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9378907	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9378908	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9378909	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9378910	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9392062	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9392064	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9392626	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9392628	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9392629	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9392630	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9392631	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9392632	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9392634	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9392635	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9405764	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9405765	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9405766	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9405767	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9405768	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9405769	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9405770	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9405771	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9405772	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9405773	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9405774	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9405776	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9504222	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3366530	chr6:4471528-4865322	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	esv3429586	chr6:4719363-4792438	Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1017938	chr6:4729592-4774914	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1023527	chr6:4729592-5387176	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4724200-4733000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr6:4724600-4733000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr6:4728000-4734400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:4728200-4733000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr6:4728400-4733200	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr6:4728600-4734400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr6:4728800-4732800	Weak transcription	Placenta	Placenta
8	chr6:4728800-4733000	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr6:4728800-4733000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr6:4728800-4733000	Weak transcription	Colonic Mucosa	Colon
11	chr6:4728800-4733200	Weak transcription	Stomach Mucosa	stomach
12	chr6:4729000-4733000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr6:4729000-4733000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr6:4729400-4732800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr6:4729400-4733000	Weak transcription	Duodenum Mucosa	Duodenum
16	chr6:4729400-4733000	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr6:4729600-4733000	Weak transcription	Fetal Intestine Large	intestine
18	chr6:4729800-4733000	Weak transcription	Fetal Intestine Small	intestine
19	chr6:4731400-4733000	Weak transcription	K562	blood
20	chr6:4732000-4733200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr6:4732400-4735400	Enhancers	Placenta Amnion	Placenta Amnion
22	chr6:4732600-4732800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr6:4732600-4732800	Enhancers	HMEC	breast

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