Variant report

Variant	rs3848058
Chromosome Location	chr13:94185960-94185961
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs1445245	0.84[CEU][hapmap]
rs1445276	1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs17234663	1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs17300373	1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs1900047	0.84[CEU][hapmap]
rs3814275	0.90[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs3910918	0.90[ASN][1000 genomes]
rs72640595	0.86[ASN][1000 genomes]
rs72641606	0.93[ASN][1000 genomes]
rs72641623	0.93[ASN][1000 genomes]
rs7317039	0.95[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs7326571	0.95[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs7987709	0.93[ASN][1000 genomes]
rs7987887	0.95[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs9301890	0.84[CEU][hapmap]
rs9301891	0.84[CEU][hapmap]
rs9516244	0.90[CHD][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs9516250	0.93[ASN][1000 genomes]
rs9516251	0.95[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs9516253	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs9516255	0.90[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs9524111	0.92[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs9524112	0.93[ASN][1000 genomes]
rs9524114	0.92[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs9524115	0.84[ASN][1000 genomes]
rs9524116	0.92[ASN][1000 genomes]
rs9524117	0.84[ASN][1000 genomes]
rs9524121	0.95[CHD][hapmap];0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs9524122	0.92[CHD][hapmap];0.93[JPT][hapmap];0.93[ASN][1000 genomes]
rs9524123	0.93[ASN][1000 genomes]
rs9524124	0.84[ASN][1000 genomes]
rs9524125	0.91[ASN][1000 genomes]
rs9524126	0.95[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs9524127	0.92[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs9556306	1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs9561383	1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs9561388	0.93[ASN][1000 genomes]
rs9645881	0.94[JPT][hapmap];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869070	chr13:93347616-94286933	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1053035	chr13:93842576-94229732	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv541880	chr13:93842576-94229732	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv530636	chr13:93997311-94281707	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv916039	chr13:94035909-94191105	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv562749	chr13:94083352-94263206	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv948714	chr13:94100104-94699435	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv900922	chr13:94105666-94281492	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	esv2758340	chr13:94174654-94348179	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	esv2759958	chr13:94174654-94348179	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:94177600-94188000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr13:94182800-94186000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr13:94182800-94186200	Weak transcription	Psoas Muscle	Psoas
4	chr13:94185000-94186000	Weak transcription	Ovary	ovary
5	chr13:94185000-94186600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr13:94185000-94190400	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr13:94185200-94186200	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr13:94185400-94186800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr13:94185600-94186000	Enhancers	Colon Smooth Muscle	Colon
10	chr13:94185800-94186600	Enhancers	Small Intestine	intestine

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