Variant report

Variant	rs62427621
Chromosome Location	chr6:163570573-163570574
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs12197662	0.83[ASN][1000 genomes]
rs13209731	0.90[ASN][1000 genomes]
rs16894545	0.95[ASN][1000 genomes]
rs16894549	0.93[ASN][1000 genomes]
rs34774992	0.86[ASN][1000 genomes]
rs35399057	0.93[ASN][1000 genomes]
rs55733913	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs66502444	0.90[ASN][1000 genomes]
rs73010724	0.93[ASN][1000 genomes]
rs73010727	0.93[ASN][1000 genomes]
rs7742985	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7758571	1.00[ASN][1000 genomes]

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	nsv917926	chr6:162646457-163609259	Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv932127	chr6:163000261-163950870	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1026490	chr6:163133433-163705708	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv869286	chr6:163146342-163697445	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv916587	chr6:163337791-163606120	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv886917	chr6:163507051-163573962	Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163568600-163574000	Enhancers	Fetal Brain Male	brain
2	chr6:163568800-163572200	Enhancers	Brain Germinal Matrix	brain
3	chr6:163569400-163571800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
4	chr6:163569800-163570600	Enhancers	Primary hematopoietic stem cells	blood
5	chr6:163569800-163570600	Active TSS	Brain Hippocampus Middle	brain
6	chr6:163570000-163571800	Enhancers	Brain Substantia Nigra	brain
7	chr6:163570000-163572200	Enhancers	Brain Anterior Caudate	brain
8	chr6:163570200-163570800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
9	chr6:163570200-163571000	Active TSS	iPS-15b Cell Line	embryonic stem cell
10	chr6:163570400-163570600	Flanking Active TSS	Brain Cingulate Gyrus	brain
11	chr6:163570400-163570600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
12	chr6:163570400-163571000	Weak transcription	Fetal Brain Female	brain
13	chr6:163570400-163571800	Enhancers	Brain Angular Gyrus	brain
14	chr6:163570400-163590400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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

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