Variant report

Variant	rs60690617
Chromosome Location	chr11:101939709-101939710
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11824945	1.00[ASN][1000 genomes]
rs12417666	1.00[ASN][1000 genomes]
rs17097406	1.00[ASN][1000 genomes]
rs17688499	1.00[ASN][1000 genomes]
rs17761725	1.00[ASN][1000 genomes]
rs4754036	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4754037	1.00[ASN][1000 genomes]
rs58795913	1.00[ASN][1000 genomes]
rs59695661	1.00[ASN][1000 genomes]
rs60312944	1.00[ASN][1000 genomes]
rs73593082	1.00[ASN][1000 genomes]
rs73593084	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73593085	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73593091	1.00[ASN][1000 genomes]
rs73593096	1.00[ASN][1000 genomes]
rs73593099	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7936815	1.00[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	esv3362945	chr11:101736547-102114246	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv898333	chr11:101832670-102079986	Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:101919400-101939800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr11:101919400-101944000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr11:101919400-101956800	Weak transcription	Osteobl	bone
4	chr11:101922400-101958000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr11:101935600-101940800	Weak transcription	NHEK	skin
6	chr11:101935800-101940800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr11:101935800-101940800	Weak transcription	HMEC	breast
8	chr11:101936000-101940400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr11:101936200-101940800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:101938000-101952200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr11:101939200-101939800	Enhancers	Placenta	Placenta

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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