Variant report

Variant	rs7986020
Chromosome Location	chr13:93802012-93802013
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12874252	1.00[YRI][hapmap]
rs16948658	1.00[YRI][hapmap]
rs60253448	1.00[AMR][1000 genomes]
rs73540341	1.00[AMR][1000 genomes]
rs73540354	1.00[AMR][1000 genomes]
rs73554228	1.00[AMR][1000 genomes]
rs73628654	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73628694	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73628695	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73633698	1.00[AMR][1000 genomes]
rs8001040	1.00[YRI][hapmap];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 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	nsv832682	chr13:93700861-93874801	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv900912	chr13:93800114-93853929	Enhancers Weak transcription	Chromatin interactive region	1 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	chr13:93799000-93802400	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr13:93800000-93802400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr13:93800000-93802800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr13:93800000-93802800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr13:93800000-93803000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr13:93800000-93803000	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr13:93800000-93803200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr13:93800000-93803400	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr13:93800200-93803400	Weak transcription	HSMM	muscle
10	chr13:93800400-93802200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr13:93800400-93802400	Weak transcription	HMEC	breast
12	chr13:93800400-93803000	Weak transcription	Osteobl	bone
13	chr13:93800400-93803200	Weak transcription	NH-A	brain

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Input of quick search could be:

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

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