Variant report

Variant	rs6604883
Chromosome Location	chr1:224241262-224241263
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11808698	1.00[EUR][1000 genomes]
rs4653495	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4653900	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs57413443	1.00[EUR][1000 genomes]
rs61110106	1.00[EUR][1000 genomes]
rs6689279	1.00[EUR][1000 genomes]
rs73116483	1.00[EUR][1000 genomes]
rs73118461	1.00[EUR][1000 genomes]
rs7522421	1.00[EUR][1000 genomes]
rs7551343	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757772	chr1:223935220-224363163	Genic enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	esv2759000	chr1:223935220-224363163	Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv427941	chr1:224085052-224363163	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers 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 target site	27 gene(s)	inside rSNPs	diseases
4	esv16231	chr1:224204343-224241314	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv832692	chr1:224206536-224407717	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:224238400-224241400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr1:224238800-224242400	Weak transcription	Right Atrium	heart
3	chr1:224238800-224244400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:224239000-224241800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr1:224239600-224241400	Enhancers	Muscle Satellite Cultured Cells	--
6	chr1:224240000-224241800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr1:224240600-224241400	Enhancers	NHLF	lung
8	chr1:224240600-224242000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr1:224241000-224242600	Enhancers	HUVEC	blood vessel
10	chr1:224241000-224245000	Weak transcription	NHEK	skin
11	chr1:224241000-224245200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr1:224241000-224245400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr1:224241000-224245400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr1:224241000-224245400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr1:224241200-224241600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr1:224241200-224245000	Weak transcription	HMEC	breast
17	chr1:224241200-224245400	Weak transcription	HSMM	muscle
18	chr1:224241200-224245400	Weak transcription	NH-A	brain
19	chr1:224241200-224245600	Weak transcription	NHDF-Ad	bronchial

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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