Variant report

Variant	rs61923612
Chromosome Location	chr12:12565101-12565102
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs16907998	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17312055	1.00[ASN][1000 genomes]
rs2013675	1.00[ASN][1000 genomes]
rs4570678	1.00[ASN][1000 genomes]
rs55946646	1.00[ASN][1000 genomes]
rs56188411	1.00[ASN][1000 genomes]
rs56325045	1.00[ASN][1000 genomes]
rs56340010	1.00[ASN][1000 genomes]
rs58809132	1.00[ASN][1000 genomes]
rs61913515	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61913534	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	nsv949003	chr12:11938229-12618690	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	esv1812889	chr12:12510842-12593406	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	11 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	chr12:12537200-12576000	Weak transcription	Primary B cells from cord blood	blood
2	chr12:12552000-12569000	Weak transcription	Hela-S3	cervix
3	chr12:12557200-12572400	Weak transcription	Primary T cells from cord blood	blood
4	chr12:12558000-12586000	Weak transcription	Pancreas	Pancrea
5	chr12:12562000-12565600	Weak transcription	GM12878-XiMat	blood
6	chr12:12562400-12576200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr12:12564600-12565400	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr12:12564800-12565200	Enhancers	Rectal Mucosa Donor 29	rectum
9	chr12:12564800-12565400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr12:12564800-12565600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr12:12564800-12565800	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr12:12564800-12565800	Enhancers	HepG2	liver
13	chr12:12565000-12565800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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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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