Variant report

Variant	rs1668567
Chromosome Location	chr15:42304115-42304116
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:42302667..42304179-chr15:42329977..42332936,2	MCF-7	breast:
2	chr15:42302877..42304522-chr15:42314324..42316672,2	MCF-7	breast:

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs11857594	0.89[AFR][1000 genomes]
rs1668555	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1668556	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1668560	0.90[ASN][1000 genomes]
rs1668561	0.92[ASN][1000 genomes]
rs1668580	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1668581	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1668582	0.95[ASN][1000 genomes]
rs1668583	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1668584	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1704353	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1704359	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1704362	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1704366	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1704367	0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1704373	0.92[ASN][1000 genomes]
rs1704376	0.92[ASN][1000 genomes]
rs1823552	0.80[ASN][1000 genomes]
rs2598465	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2598466	0.80[ASN][1000 genomes]
rs2598467	0.80[ASN][1000 genomes]
rs2665200	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2665202	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2665203	0.87[ASN][1000 genomes]
rs2665207	0.80[ASN][1000 genomes]
rs2665210	0.80[ASN][1000 genomes]
rs2665211	0.80[ASN][1000 genomes]
rs2724935	0.90[ASN][1000 genomes]
rs2724937	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2724939	0.87[ASN][1000 genomes]
rs2724940	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2724944	0.80[ASN][1000 genomes]
rs2724945	0.80[ASN][1000 genomes]
rs34595238	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs35435358	0.89[AFR][1000 genomes]
rs35670495	0.87[ASN][1000 genomes]
rs62004270	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62004283	0.82[AMR][1000 genomes]
rs937991	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs937992	0.90[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs937993	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[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	nsv931223	chr15:41989960-42781757	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
2	nsv1035998	chr15:42098896-42434254	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
3	nsv1038933	chr15:42138456-42309087	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	30 gene(s)	inside rSNPs	diseases
4	nsv529687	chr15:42157320-42621682	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
5	nsv1054728	chr15:42177772-42310009	Enhancers Genic enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
6	nsv1049445	chr15:42239738-42830484	Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
7	nsv542366	chr15:42239738-42830484	Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42290400-42310400	Weak transcription	Right Atrium	heart
2	chr15:42301800-42306000	Enhancers	Fetal Intestine Small	intestine
3	chr15:42302000-42304600	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr15:42302000-42305400	Enhancers	Placenta	Placenta
5	chr15:42302000-42306000	Enhancers	Fetal Intestine Large	intestine
6	chr15:42302200-42304200	Weak transcription	Esophagus	oesophagus
7	chr15:42302200-42304200	Enhancers	HMEC	breast
8	chr15:42302200-42304600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr15:42302600-42304600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr15:42303600-42304200	Enhancers	NHEK	skin
11	chr15:42303600-42304600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr15:42303600-42304800	Enhancers	GM12878-XiMat	blood
13	chr15:42303600-42305000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr15:42303600-42309000	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr15:42303800-42304200	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr15:42303800-42305400	Weak transcription	Lung	lung
17	chr15:42304000-42305000	Enhancers	Duodenum Mucosa	Duodenum
18	chr15:42304000-42305000	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr15:42304000-42305400	Enhancers	Pancreas	Pancrea
20	chr15:42304000-42305600	Enhancers	Stomach Mucosa	stomach

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