Variant report

Variant	rs1465429
Chromosome Location	chr19:21052944-21052945
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	chr19:21051172..21052986-chr19:21053944..21056414,2	MCF-7	breast:

Extended variants
information (count: 115 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:95)

rs_ID	r²[population]
rs10405074	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10412338	0.97[ASN][1000 genomes]
rs10412523	0.97[ASN][1000 genomes]
rs10414014	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10416206	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10418943	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10419167	0.97[ASN][1000 genomes]
rs10420060	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10420272	0.90[ASN][1000 genomes]
rs10420474	0.91[ASN][1000 genomes]
rs10422272	0.97[ASN][1000 genomes]
rs10422308	0.96[ASN][1000 genomes]
rs10426078	0.96[ASN][1000 genomes]
rs10426307	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11085403	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11879744	0.81[ASN][1000 genomes]
rs11879840	0.81[ASN][1000 genomes]
rs11880895	0.81[ASN][1000 genomes]
rs11882347	0.81[ASN][1000 genomes]
rs12150898	0.80[ASN][1000 genomes]
rs13343465	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13345292	0.96[ASN][1000 genomes]
rs13345335	0.96[ASN][1000 genomes]
rs1465427	0.81[ASN][1000 genomes]
rs1465428	0.81[ASN][1000 genomes]
rs1465430	0.81[ASN][1000 genomes]
rs16997414	0.97[ASN][1000 genomes]
rs16997443	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16997445	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17618044	0.81[ASN][1000 genomes]
rs17618080	0.81[ASN][1000 genomes]
rs1985456	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2042265	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2545228	0.81[ASN][1000 genomes]
rs28699298	0.80[ASN][1000 genomes]
rs28720017	0.81[ASN][1000 genomes]
rs3867193	0.84[ASN][1000 genomes]
rs55965424	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56089621	0.81[ASN][1000 genomes]
rs56099007	0.81[ASN][1000 genomes]
rs56119047	0.81[ASN][1000 genomes]
rs56142010	0.84[ASN][1000 genomes]
rs56205787	0.81[ASN][1000 genomes]
rs56892523	0.81[ASN][1000 genomes]
rs58752759	0.81[ASN][1000 genomes]
rs58780581	0.84[ASN][1000 genomes]
rs59677924	0.81[ASN][1000 genomes]
rs59841381	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59954926	0.81[ASN][1000 genomes]
rs59964227	0.96[ASN][1000 genomes]
rs59977060	0.86[ASN][1000 genomes]
rs60548145	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs60969663	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs61002752	0.81[ASN][1000 genomes]
rs61385453	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62123184	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62123185	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62123192	0.81[ASN][1000 genomes]
rs62123194	0.80[ASN][1000 genomes]
rs62123195	0.81[ASN][1000 genomes]
rs62123196	0.81[ASN][1000 genomes]
rs62123197	0.81[ASN][1000 genomes]
rs62123198	0.81[ASN][1000 genomes]
rs62123199	0.81[ASN][1000 genomes]
rs62123200	0.81[ASN][1000 genomes]
rs62123201	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62123207	0.81[ASN][1000 genomes]
rs62123208	0.81[ASN][1000 genomes]
rs62123209	0.81[ASN][1000 genomes]
rs62123213	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62123216	0.81[ASN][1000 genomes]
rs62123217	0.81[ASN][1000 genomes]
rs62123220	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62123226	0.81[ASN][1000 genomes]
rs62123227	0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62123229	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62123230	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62123239	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62123244	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62123245	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62123246	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62123247	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62124024	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62124028	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62124029	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62124030	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62124032	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62125465	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62125651	0.81[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs67268757	0.81[ASN][1000 genomes]
rs73007009	0.81[ASN][1000 genomes]
rs73530516	0.88[ASN][1000 genomes]
rs73535110	0.81[ASN][1000 genomes]
rs73927842	0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8182471	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv911325	chr19:20151257-21071548	ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	49 gene(s)	inside rSNPs	diseases
2	esv2752729	chr19:20818886-21169554	ZNF genes & repeats Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv1062776	chr19:20818886-21273361	Weak transcription Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv932110	chr19:20818886-21278952	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	esv2763043	chr19:20818886-21290543	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv1064103	chr19:20845947-21062996	ZNF genes & repeats Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	nsv1063954	chr19:21000562-21177577	Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
8	nsv578946	chr19:21014403-21151796	ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
9	esv3385528	chr19:21030777-21495566	Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
10	nsv960809	chr19:21031718-21121801	Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	esv3380168	chr19:21032661-21103629	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	nsv1055738	chr19:21040181-21109969	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	esv3348077	chr19:21041161-21103393	ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
14	nsv522090	chr19:21041350-21109784	ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv578947	chr19:21041350-21109784	Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv817536	chr19:21041855-21348237	Strong transcription Enhancers Genic enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
17	esv1848134	chr19:21049520-21084070	ZNF genes & repeats Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
18	esv3361385	chr19:21052081-21060609	ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
19	nsv578948	chr19:21052924-21094854	ZNF genes & repeats Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
20	nsv515576	chr19:21052924-21101749	Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1465429	ZNF85	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21049400-21071800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
2	chr19:21052200-21063600	ZNF genes & repeats	Adipose Nuclei	Adipose
3	chr19:21052600-21053200	Active TSS	Fetal Heart	heart
4	chr19:21052600-21053200	ZNF genes & repeats	Spleen	Spleen

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