Variant report

Variant	rs7187802
Chromosome Location	chr16:30639710-30639711
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:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:30617317..30620136-chr16:30639446..30642000,2	K562	blood:
2	chr16:30535774..30538341-chr16:30638616..30641301,3	MCF-7	breast:
3	chr16:30639009..30641962-chr16:30644620..30646873,2	MCF-7	breast:
4	chr16:30441082..30442394-chr16:30639571..30640733,5	K562	blood:
5	chr16:30595303..30597100-chr16:30638655..30641608,2	MCF-7	breast:
6	chr16:30429607..30431783-chr16:30638612..30641034,2	MCF-7	breast:
7	chr16:30454893..30456842-chr16:30638548..30640357,2	K562	blood:
8	chr16:30631964..30634523-chr16:30638900..30640577,2	MCF-7	breast:
9	chr16:30638840..30641606-chr16:30661205..30662742,2	MCF-7	breast:
10	chr16:30555913..30558805-chr16:30639399..30642318,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000169957	Chromatin interaction
ENSG00000156858	Chromatin interaction
ENSG00000199787	Chromatin interaction
ENSG00000197162	Chromatin interaction
ENSG00000179958	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs12918327	0.87[ASN][1000 genomes]
rs28728333	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28841118	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34699226	0.80[ASN][1000 genomes]
rs35661204	0.82[ASN][1000 genomes]
rs36064568	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4485386	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs55875685	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6565195	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6565196	0.85[EUR][1000 genomes]
rs67693285	0.89[ASN][1000 genomes]
rs7184055	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7185620	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7186852	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7187071	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7188789	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7191389	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7191761	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7194347	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7197475	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7204632	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7499339	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9925025	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9927137	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062456	chr16:30442166-31253997	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
2	nsv542898	chr16:30442166-31253997	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
3	nsv905727	chr16:30564526-30689696	Active TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
4	nsv469724	chr16:30632445-30840263	Strong transcription Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	143 gene(s)	inside rSNPs	diseases
5	nsv482704	chr16:30632445-30840263	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	143 gene(s)	inside rSNPs	diseases
6	nsv833188	chr16:30632446-30840263	Active TSS Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	143 gene(s)	inside rSNPs	diseases
7	nsv978132	chr16:30635969-30640484	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:30631400-30640000	Weak transcription	Fetal Brain Male	brain
2	chr16:30631800-30640000	Weak transcription	Fetal Intestine Large	intestine
3	chr16:30634200-30640000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr16:30634400-30640000	Weak transcription	Fetal Kidney	kidney
5	chr16:30634600-30640000	Weak transcription	Fetal Intestine Small	intestine
6	chr16:30634600-30640000	Weak transcription	Hela-S3	cervix
7	chr16:30635200-30640000	Weak transcription	Liver	Liver
8	chr16:30636000-30639800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr16:30636000-30639800	Weak transcription	Duodenum Mucosa	Duodenum
10	chr16:30636000-30640000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr16:30636000-30640000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr16:30636000-30640000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr16:30636000-30640000	Weak transcription	NHEK	skin
14	chr16:30636200-30640000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr16:30638000-30640000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr16:30638200-30640000	Weak transcription	Brain Hippocampus Middle	brain
17	chr16:30638200-30642000	Enhancers	HepG2	liver
18	chr16:30638200-30645000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr16:30638600-30640000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr16:30638600-30640000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr16:30639400-30640000	Active TSS	Skeletal Muscle Male	skeletal muscle
22	chr16:30639400-30640000	Enhancers	K562	blood
23	chr16:30639400-30640600	Enhancers	Dnd41	blood
24	chr16:30639600-30640200	Active TSS	Colonic Mucosa	Colon
25	chr16:30639600-30640200	Active TSS	Placenta	Placenta

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