Variant report

Variant	rs2974490
Chromosome Location	chr5:113405876-113405877
allele	C/T
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:9)

rs_ID	r²[population]
rs1158117	0.80[ASN][1000 genomes]
rs1586429	0.80[ASN][1000 genomes]
rs17136230	0.87[ASN][1000 genomes]
rs2416364	0.80[ASN][1000 genomes]
rs2954377	0.89[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs2954379	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2974487	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2974491	0.89[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs874734	0.88[ASN][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	nsv471042	chr5:113160490-113440892	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv882726	chr5:113404933-113555626	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:113399000-113406200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:113404400-113408800	Weak transcription	Fetal Heart	heart
3	chr5:113405600-113406000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr5:113405600-113406600	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr5:113405800-113406200	Enhancers	H9 Cell Line	embryonic stem cell
6	chr5:113405800-113406200	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr5:113405800-113406400	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr5:113405800-113406400	Enhancers	H1 Cell Line	embryonic stem cell
9	chr5:113405800-113406400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr5:113405800-113406600	Enhancers	HUES6 Cell Line	embryonic stem cell

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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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