Variant report

Variant	rs10260637
Chromosome Location	chr7:137516329-137516330
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10230788	1.00[CEU][hapmap];0.84[CHB][hapmap];0.84[JPT][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10254224	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10256707	1.00[CEU][hapmap];0.84[CHB][hapmap];0.85[JPT][hapmap];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10257218	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10277821	0.82[CHB][hapmap];0.92[ASN][1000 genomes]
rs1109272	0.80[EUR][1000 genomes]
rs11980215	0.90[ASN][1000 genomes]
rs1871213	0.92[EUR][1000 genomes]
rs28408194	0.87[EUR][1000 genomes]
rs28491578	0.85[EUR][1000 genomes]
rs28634434	0.90[EUR][1000 genomes]
rs28892326	0.95[ASN][1000 genomes]
rs34309725	0.92[EUR][1000 genomes]
rs3800672	0.85[CHB][hapmap];0.88[JPT][hapmap];0.86[ASN][1000 genomes]
rs3823554	1.00[CEU][hapmap];0.83[CHB][hapmap];0.85[JPT][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6974718	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6978230	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs7796821	1.00[CEU][hapmap];0.84[CHB][hapmap];0.85[JPT][hapmap];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022793	chr7:137187383-137619359	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv831150	chr7:137500559-137652808	Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137506000-137516600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr7:137506200-137516600	Weak transcription	Fetal Brain Female	brain
3	chr7:137506200-137516800	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr7:137506200-137517000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr7:137506200-137517000	Weak transcription	HSMMtube	muscle
6	chr7:137506800-137526400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr7:137514600-137519800	Weak transcription	Brain Angular Gyrus	brain
8	chr7:137515000-137517200	Weak transcription	Osteobl	bone
9	chr7:137515200-137523600	Weak transcription	Aorta	Aorta
10	chr7:137515400-137517000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr7:137516000-137517400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr7:137516000-137518600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr7:137516200-137516600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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