Variant report

Variant	rs11045273
Chromosome Location	chr12:20629112-20629113
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:8)

rs_ID	r²[population]
rs11613220	1.00[CHB][hapmap]
rs4762759	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4762764	1.00[CHB][hapmap]
rs6487099	1.00[CHB][hapmap]
rs7134968	1.00[CHB][hapmap]
rs7484304	1.00[CHB][hapmap]
rs7487227	1.00[CHB][hapmap]
rs7977362	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048067	chr12:20363755-20874845	Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv541408	chr12:20363755-20874845	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv1046870	chr12:20509914-20711535	Active TSS Genic enhancers Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
4	nsv541409	chr12:20509914-20711535	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
5	nsv1042315	chr12:20531641-20629866	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv557701	chr12:20614024-20643574	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:20607800-20645000	Weak transcription	Right Ventricle	heart
2	chr12:20619200-20654200	Weak transcription	Fetal Stomach	stomach
3	chr12:20623200-20635200	Weak transcription	Fetal Intestine Large	intestine
4	chr12:20626400-20630000	Weak transcription	Colon Smooth Muscle	Colon
5	chr12:20627800-20630000	Weak transcription	Rectal Smooth Muscle	rectum
6	chr12:20627800-20635600	Weak transcription	Hela-S3	cervix
7	chr12:20628600-20644400	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr12:20628800-20629200	Enhancers	Muscle Satellite Cultured Cells	--
9	chr12:20628800-20630400	Weak transcription	Right Atrium	heart
10	chr12:20628800-20631400	Enhancers	NHDF-Ad	bronchial
11	chr12:20628800-20633000	Weak transcription	Left Ventricle	heart
12	chr12:20628800-20636800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr12:20629000-20629200	Enhancers	NHLF	lung
14	chr12:20629000-20629600	Weak transcription	Aorta	Aorta
15	chr12:20629000-20630200	Enhancers	Osteobl	bone
16	chr12:20629000-20630800	Weak transcription	Ovary	ovary
17	chr12:20629000-20635200	Weak transcription	Fetal Intestine Small	intestine

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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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