Variant report

Variant	rs10949383
Chromosome Location	chr6:16831939-16831940
allele	A/G
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]
rs10949382	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10949386	0.80[AMR][1000 genomes]
rs11963177	0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12526558	0.85[ASN][1000 genomes]
rs12528183	0.84[ASN][1000 genomes]
rs12529016	0.84[ASN][1000 genomes]
rs16869947	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16879271	0.84[ASN][1000 genomes]
rs16879276	0.82[ASN][1000 genomes]
rs16879284	0.84[ASN][1000 genomes]
rs16879290	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57355941	0.84[ASN][1000 genomes]
rs59333382	0.84[ASN][1000 genomes]
rs59690250	0.85[ASN][1000 genomes]
rs685355	0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6942123	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs770940	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[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	nsv1015992	chr6:16469059-16846847	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv538148	chr6:16469059-16846847	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 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	chr6:16825400-16832200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr6:16826400-16832600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr6:16828400-16836200	Weak transcription	GM12878-XiMat	blood
4	chr6:16829200-16832000	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr6:16829400-16836600	Weak transcription	Right Atrium	heart
6	chr6:16831000-16832200	Weak transcription	Fetal Heart	heart
7	chr6:16831000-16836200	Weak transcription	Fetal Thymus	thymus
8	chr6:16831200-16832200	Weak transcription	Hela-S3	cervix
9	chr6:16831400-16832800	Enhancers	Adipose Nuclei	Adipose
10	chr6:16831400-16833400	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr6:16831400-16836600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr6:16831600-16836200	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr6:16831800-16833400	Enhancers	Liver	Liver

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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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