Variant report

Variant	rs221743
Chromosome Location	chr6:165871819-165871820
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs1033671	0.93[CHB][hapmap];0.86[JPT][hapmap];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs221739	1.00[CHB][hapmap];0.87[JPT][hapmap];0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs221741	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs221745	0.87[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs221749	0.81[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.81[YRI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][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	esv3417270	chr6:165682773-166023032	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
2	nsv886928	chr6:165722345-166197889	Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv830863	chr6:165803464-165970091	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:165836000-165873200	Weak transcription	Fetal Brain Male	brain
2	chr6:165854800-165881800	Weak transcription	Hela-S3	cervix
3	chr6:165857400-165873600	Weak transcription	Brain Germinal Matrix	brain
4	chr6:165857400-165886200	Weak transcription	Left Ventricle	heart
5	chr6:165857400-165919400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr6:165859000-165873400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr6:165863200-165882000	Weak transcription	HSMM	muscle
8	chr6:165870000-165872400	Weak transcription	Fetal Kidney	kidney
9	chr6:165870000-165874800	Weak transcription	Right Atrium	heart
10	chr6:165870000-165876800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr6:165870200-165873200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr6:165870600-165873400	Enhancers	Fetal Lung	lung
13	chr6:165870800-165872800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr6:165871800-165872000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
15	chr6:165871800-165872000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr6:165871800-165872000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
17	chr6:165871800-165872200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr6:165871800-165872200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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

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