Variant report

Variant	rs34100116
Chromosome Location	chr1:197892551-197892552
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10922333	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10922334	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11577674	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12024850	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12046958	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12727777	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12729300	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12750987	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1909507	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2358777	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4147202	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999662	chr1:197821769-197892803	Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
2	esv2762214	chr1:197821769-197897496	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
3	esv3436153	chr1:197892029-197896227	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:197889400-197893000	Weak transcription	Right Atrium	heart
2	chr1:197891800-197893600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr1:197892000-197892800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr1:197892000-197895600	Weak transcription	Ovary	ovary
5	chr1:197892200-197892600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
6	chr1:197892400-197892600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
7	chr1:197892400-197892600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
8	chr1:197892400-197892600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell

Quick Search:

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

what's new

Quick links