Variant report

Variant	rs854779
Chromosome Location	chr17:18044270-18044271
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:18044115..18044841-chr17:18120469..18121362,2	K562	blood:
2	chr17:18044182..18045939-chr17:18050102..18052001,2	MCF-7	breast:
3	chr17:18042232..18044800-chr17:18055136..18057841,3	K562	blood:
4	chr17:18042805..18044736-chr17:18086569..18089339,2	K562	blood:
5	chr17:18039043..18041825-chr17:18043264..18046470,4	K562	blood:
6	chr17:18042115..18044970-chr17:18226720..18228381,2	MCF-7	breast:
7	chr17:18039531..18041825-chr17:18044151..18046470,2	K562	blood:
8	chr17:18044150..18045078-chr17:18059256..18060265,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000091542	Chromatin interaction
ENSG00000266677	Chromatin interaction
ENSG00000267350	Chromatin interaction
ENSG00000091536	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 12 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs11870766	0.86[JPT][hapmap]
rs12150618	0.86[JPT][hapmap]
rs12936694	1.00[CHD][hapmap];0.86[JPT][hapmap]
rs12937300	0.90[CHD][hapmap]
rs12939469	1.00[CHD][hapmap];0.86[JPT][hapmap]
rs12939757	0.90[CHD][hapmap]
rs12945597	0.90[CHD][hapmap]
rs12952556	0.90[CHD][hapmap]
rs1378601	0.84[CEU][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];0.86[JPT][hapmap];0.92[MEX][hapmap];0.84[TSI][hapmap];0.88[EUR][1000 genomes]
rs1378602	0.84[CEU][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];0.86[JPT][hapmap];0.88[MEX][hapmap];0.84[EUR][1000 genomes]
rs1563631	0.90[CHD][hapmap]
rs1979276	0.90[CHD][hapmap]
rs2245737	0.86[GIH][hapmap];0.81[TSI][hapmap]
rs2273028	0.90[CHD][hapmap]
rs2360234	1.00[CHD][hapmap];0.86[JPT][hapmap]
rs2605135	0.93[GIH][hapmap];0.86[TSI][hapmap]
rs2605136	0.81[CHD][hapmap]
rs2605142	0.90[CHD][hapmap]
rs2746025	0.90[CHD][hapmap]
rs2746027	0.90[CHD][hapmap]
rs2746028	0.86[GIH][hapmap];0.84[TSI][hapmap]
rs2746029	0.91[GIH][hapmap];0.89[TSI][hapmap]
rs3794782	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4603612	0.91[CHD][hapmap];0.86[JPT][hapmap]
rs4924839	0.84[CEU][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];0.86[JPT][hapmap];0.88[MEX][hapmap];0.85[EUR][1000 genomes]
rs4924840	0.86[JPT][hapmap]
rs4924841	1.00[CHD][hapmap];0.86[JPT][hapmap]
rs4925171	0.90[CHD][hapmap]
rs712270	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs712273	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7207123	0.81[CHD][hapmap]
rs7215839	0.90[CHD][hapmap]
rs8069321	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8071834	0.84[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];0.86[JPT][hapmap];0.88[MEX][hapmap];0.85[EUR][1000 genomes]
rs854771	0.91[CHD][hapmap];1.00[JPT][hapmap]
rs854772	0.96[CEU][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.98[TSI][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs854775	0.96[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs854776	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs854781	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs854795	0.92[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];0.86[JPT][hapmap];0.88[MEX][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs854804	0.88[CEU][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];0.86[JPT][hapmap];0.83[MEX][hapmap];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs860567	1.00[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs860568	1.00[CHD][hapmap];0.86[JPT][hapmap]
rs865923	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs921986	0.90[CHD][hapmap]

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	nsv531183	chr17:17571035-18205309	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
2	nsv916653	chr17:17651916-18454952	Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Weak transcription ZNF genes & repeats 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 miRNA target site	144 gene(s)	inside rSNPs	diseases
3	nsv533142	chr17:17691726-18236686	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
4	nsv482491	chr17:17959577-18153920	Enhancers Genic enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
5	nsv1061162	chr17:17978838-18259234	Flanking Active TSS Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
6	nsv492305	chr17:17980441-18424702	Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
7	nsv907769	chr17:18000321-18064195	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	nsv457697	chr17:18003845-18046290	Strong transcription Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
9	nsv574527	chr17:18003845-18046290	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
10	nsv907770	chr17:18003845-18098018	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
11	nsv907771	chr17:18013560-18098018	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
12	nsv470580	chr17:18029857-18060192	Active TSS Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases
13	nsv907772	chr17:18030524-18098018	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
14	nsv510702	chr17:18037676-18116801	Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases

mRNA abundance (count:12)

SNP	Gene	Cis/trans	Tissue	Source
rs854779	FLJ36492	cis	multi-tissue	Pritchard
rs854779	LOC162632	cis	parietal	SCAN
rs854779	SHMT1	cis	parietal	SCAN
rs854779	TOP3A	cis	cerebellum	SCAN
rs854779	SHMT1	cis	cerebellum	SCAN
rs854779	USP32P2	cis	lung	GTEx
rs854779	LOC162632	cis	cerebellum	SCAN
rs854779	LRRC48	cis	parietal	SCAN
rs854779	TOM1L2	cis	cerebellum	SCAN
rs854779	MYO15A	cis	cerebellum	SCAN
rs854779	SHMT1	Cis_1M	lymphoblastoid	RTeQTL
rs854779	FLII	cis	cerebellum	SCAN

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:18039600-18046800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr17:18039800-18046200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr17:18040200-18044800	Enhancers	Liver	Liver
4	chr17:18040600-18056000	Weak transcription	Gastric	stomach
5	chr17:18040800-18056400	Weak transcription	Right Atrium	heart
6	chr17:18041600-18045000	Enhancers	Placenta	Placenta
7	chr17:18041800-18044400	Weak transcription	Fetal Intestine Small	intestine
8	chr17:18041800-18044600	Enhancers	HepG2	liver
9	chr17:18041800-18044800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr17:18042800-18044600	Enhancers	Placenta Amnion	Placenta Amnion
11	chr17:18043000-18045000	Enhancers	Fetal Muscle Trunk	muscle
12	chr17:18043200-18044600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr17:18043400-18045200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr17:18043400-18046200	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr17:18043600-18046800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr17:18044000-18044600	Enhancers	Fetal Thymus	thymus
17	chr17:18044000-18045000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr17:18044000-18046000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr17:18044200-18044400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr17:18044200-18044600	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr17:18044200-18044600	Enhancers	Brain Anterior Caudate	brain
22	chr17:18044200-18044600	Enhancers	Esophagus	oesophagus
23	chr17:18044200-18044600	Enhancers	Pancreas	Pancrea
24	chr17:18044200-18044600	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr17:18044200-18045000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
26	chr17:18044200-18045400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle

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