Variant report

Variant	rs11768912
Chromosome Location	chr7:104294485-104294486
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1072699	0.93[CEU][hapmap]
rs10953443	0.93[CEU][hapmap];0.82[EUR][1000 genomes]
rs12705266	0.93[CEU][hapmap];0.82[EUR][1000 genomes]
rs1547977	1.00[CHB][hapmap];0.82[ASN][1000 genomes]
rs1547978	0.82[ASN][1000 genomes]
rs6951477	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6974634	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73181859	0.83[EUR][1000 genomes]
rs759532	1.00[CHB][hapmap]
rs7812002	0.86[CEU][hapmap];0.82[EUR][1000 genomes]
rs9692289	1.00[CHB][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024532	chr7:104281393-104299847	Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS	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	chr7:104290400-104295000	Enhancers	Colon Smooth Muscle	Colon
2	chr7:104290400-104295600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr7:104291000-104295600	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr7:104292000-104295000	Weak transcription	Brain Germinal Matrix	brain
5	chr7:104292000-104296000	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr7:104294200-104294600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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