Variant report

Variant	rs73242829
Chromosome Location	chr8:59212254-59212255
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10504250	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11778230	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12678008	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12678010	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16923289	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1840795	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4475466	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55663455	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55733713	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56321097	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58339852	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs59723829	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61239649	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7007933	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7825749	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7826459	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[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	esv2761427	chr8:59204373-59242564	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:59210400-59212800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr8:59210400-59212800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr8:59210600-59212400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr8:59210600-59212600	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr8:59210600-59212600	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr8:59210600-59212800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr8:59210800-59212800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr8:59210800-59213000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr8:59211000-59212400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr8:59211000-59212600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr8:59211200-59212400	Weak transcription	Fetal Heart	heart
12	chr8:59211200-59212600	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr8:59211600-59213200	Enhancers	Left Ventricle	heart
14	chr8:59211800-59212800	Weak transcription	Right Atrium	heart
15	chr8:59212200-59213200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr8:59212200-59213600	Enhancers	Placenta	Placenta

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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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