Variant report

Variant	rs67763506
Chromosome Location	chr17:59557892-59557893
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs2270150	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3744435	0.82[AMR][1000 genomes]
rs3785822	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3785823	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3785825	0.95[ASN][1000 genomes]
rs62071332	0.95[ASN][1000 genomes]
rs7213643	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7214133	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73334581	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8070051	0.95[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833506	chr17:59362377-59562984	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	334 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:59543200-59564800	Genic enhancers	NHLF	lung
2	chr17:59545600-59563000	Weak transcription	Lung	lung
3	chr17:59548200-59563400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr17:59553000-59563800	Weak transcription	Fetal Intestine Large	intestine
5	chr17:59554400-59559600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr17:59554400-59564000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr17:59554800-59560800	Weak transcription	Fetal Brain Male	brain
8	chr17:59555000-59563200	Strong transcription	Fetal Muscle Leg	muscle
9	chr17:59555800-59563200	Genic enhancers	Fetal Lung	lung
10	chr17:59556800-59560400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr17:59557000-59558200	Strong transcription	Fetal Intestine Small	intestine
12	chr17:59557600-59559000	Strong transcription	Placenta	Placenta
13	chr17:59557800-59559800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr17:59557800-59562400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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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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