Variant report

Variant	rs9991015
Chromosome Location	chr4:92520419-92520420
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10014070	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10516896	1.00[CHB][hapmap]
rs1112026	0.88[ASN][1000 genomes]
rs1112027	0.88[ASN][1000 genomes]
rs12644168	0.88[ASN][1000 genomes]
rs12645064	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs12646476	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12646530	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12646638	1.00[CHB][hapmap]
rs12646710	1.00[CHB][hapmap]
rs12647856	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12649845	1.00[CHB][hapmap]
rs12650644	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16996271	1.00[CHB][hapmap]
rs17018502	1.00[CHB][hapmap]
rs17018506	1.00[CHB][hapmap]
rs17018547	1.00[CHB][hapmap]
rs17018549	1.00[CHB][hapmap]
rs55650022	0.88[ASN][1000 genomes]
rs55696065	0.88[ASN][1000 genomes]
rs57113538	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs57495859	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58459157	0.88[ASN][1000 genomes]
rs59578018	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6835588	1.00[CHB][hapmap]
rs73836227	0.88[ASN][1000 genomes]
rs73836230	0.88[ASN][1000 genomes]
rs73836231	0.88[ASN][1000 genomes]
rs73836234	0.94[ASN][1000 genomes]
rs73836235	0.94[ASN][1000 genomes]
rs73836237	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73836286	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73836287	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73836288	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73836289	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73836290	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73836291	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73836293	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73836294	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73836295	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73836296	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73836297	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73836299	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73836301	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73837936	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73838026	0.88[ASN][1000 genomes]
rs73838045	0.88[ASN][1000 genomes]
rs73838050	0.88[ASN][1000 genomes]
rs7654717	0.88[ASN][1000 genomes]
rs7659358	1.00[CHB][hapmap]
rs7697141	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs7699803	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869023	chr4:91940838-92935383	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv879573	chr4:92281419-92520419	Weak transcription ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv879575	chr4:92322333-92520419	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv879576	chr4:92356118-92651110	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv879579	chr4:92373327-92520419	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv879580	chr4:92373327-92551065	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv879583	chr4:92379081-92539867	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv594861	chr4:92379081-92898309	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv948428	chr4:92382683-93161851	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	nsv594862	chr4:92392152-93222515	Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
11	nsv461585	chr4:92395356-92761582	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv594863	chr4:92395356-92761582	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv999961	chr4:92396538-93213898	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
14	nsv537178	chr4:92396538-93213898	Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
15	nsv533406	chr4:92396539-93184304	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
16	nsv530154	chr4:92396539-93359983	Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
17	nsv879585	chr4:92415529-92520419	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
18	nsv879586	chr4:92432161-92520419	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	n/a	n/a	inside rSNPs	diseases
19	nsv879587	chr4:92432161-92539867	Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
20	nsv1006366	chr4:92481747-92755677	Enhancers Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
21	nsv1003269	chr4:92488825-92758977	Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
22	nsv869490	chr4:92506402-93219336	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
23	nsv999701	chr4:92518040-93233556	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
24	nsv537180	chr4:92518040-93233556	Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:92518600-92522400	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr4:92518800-92521200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr4:92519000-92522600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr4:92519000-92522600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr4:92519000-92522600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:92519200-92522600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr4:92520200-92522400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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