Variant report

Variant	rs58384262
Chromosome Location	chr8:107955401-107955402
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	chr8:107948303..107950286-chr8:107953514..107955561,2	K562	blood:

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs16875389	0.93[ASN][1000 genomes]
rs16875405	0.93[ASN][1000 genomes]
rs16875425	0.93[ASN][1000 genomes]
rs16875432	0.93[ASN][1000 genomes]
rs16875434	0.93[ASN][1000 genomes]
rs16875435	0.93[ASN][1000 genomes]
rs16875446	0.93[ASN][1000 genomes]
rs16875449	0.93[ASN][1000 genomes]
rs55650515	0.93[ASN][1000 genomes]
rs55864521	0.93[ASN][1000 genomes]
rs55898208	0.93[ASN][1000 genomes]
rs55934744	0.93[ASN][1000 genomes]
rs55985213	0.93[ASN][1000 genomes]
rs56224374	0.90[AFR][1000 genomes]
rs56370064	0.93[ASN][1000 genomes]
rs56373658	0.90[AFR][1000 genomes]
rs57066864	0.93[ASN][1000 genomes]
rs57124302	0.93[ASN][1000 genomes]
rs57226667	0.93[ASN][1000 genomes]
rs57686955	0.93[ASN][1000 genomes]
rs57904969	0.93[ASN][1000 genomes]
rs58180593	0.86[ASN][1000 genomes]
rs58449156	0.86[ASN][1000 genomes]
rs58519081	0.93[ASN][1000 genomes]
rs58538201	0.93[ASN][1000 genomes]
rs59141056	0.93[ASN][1000 genomes]
rs59178284	1.00[AFR][1000 genomes]
rs59297130	0.93[ASN][1000 genomes]
rs59392221	1.00[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs59747457	0.93[ASN][1000 genomes]
rs60105649	0.93[ASN][1000 genomes]
rs60602031	0.93[ASN][1000 genomes]
rs60683190	0.93[ASN][1000 genomes]
rs60857656	0.87[AFR][1000 genomes]
rs61080146	0.93[ASN][1000 genomes]
rs61170285	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61218099	0.92[AFR][1000 genomes]
rs61467464	0.93[ASN][1000 genomes]
rs73699628	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73699630	0.93[ASN][1000 genomes]
rs73699631	0.93[ASN][1000 genomes]
rs73699635	0.93[ASN][1000 genomes]
rs73699636	0.93[ASN][1000 genomes]
rs73699639	0.93[ASN][1000 genomes]
rs73699641	0.93[ASN][1000 genomes]
rs73699642	0.93[ASN][1000 genomes]
rs73699644	0.93[ASN][1000 genomes]
rs73699645	0.93[ASN][1000 genomes]
rs73699647	0.93[ASN][1000 genomes]
rs73699648	0.93[ASN][1000 genomes]
rs73699649	0.93[ASN][1000 genomes]
rs73699664	0.90[AFR][1000 genomes]
rs73699668	0.93[ASN][1000 genomes]
rs73699674	0.93[ASN][1000 genomes]
rs73699680	0.92[AFR][1000 genomes]
rs73699699	0.87[ASN][1000 genomes]

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	nsv1029202	chr8:107796289-108384241	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv539712	chr8:107796289-108384241	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1034210	chr8:107796489-108384102	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv539713	chr8:107796489-108384102	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv529383	chr8:107796490-108368465	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv915821	chr8:107796490-108393008	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv916496	chr8:107813722-108338822	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1028726	chr8:107816841-108392547	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv497805	chr8:107852509-108368371	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv1028916	chr8:107925350-107974654	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv516674	chr8:107944671-107955559	Enhancers Weak transcription Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv2761458	chr8:107947610-107958891	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv465759	chr8:107948846-107993651	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv611850	chr8:107948846-107993651	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:107952400-107955800	Weak transcription	Osteobl	bone
2	chr8:107952400-107957400	Weak transcription	Aorta	Aorta
3	chr8:107952600-107958800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr8:107954000-107959000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr8:107954400-107959200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr8:107955200-107956400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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