Variant report

Variant	rs2708393
Chromosome Location	chr1:103313743-103313744
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs2249139	1.00[YRI][hapmap]
rs2252081	1.00[YRI][hapmap]
rs2615974	1.00[YRI][hapmap]
rs2615979	1.00[AFR][1000 genomes]
rs2615995	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs2616004	1.00[AFR][1000 genomes]
rs2616017	1.00[YRI][hapmap]
rs2616019	1.00[YRI][hapmap]
rs2622852	1.00[YRI][hapmap]
rs2622856	1.00[YRI][hapmap]
rs2622859	1.00[YRI][hapmap]
rs2708394	1.00[AFR][1000 genomes]
rs2783563	0.83[AFR][1000 genomes]
rs2783568	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs2783571	0.83[AFR][1000 genomes]
rs3102054	1.00[YRI][hapmap]
rs566963	1.00[AFR][1000 genomes]
rs582739	1.00[AFR][1000 genomes]
rs584056	1.00[AFR][1000 genomes]
rs6674525	0.86[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830882	chr1:103192683-103355802	Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv522922	chr1:103305021-103764640	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:103311200-103319200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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