Variant report

Variant	rs7707525
Chromosome Location	chr5:108021162-108021163
allele	C/T
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:12)

rs_ID	r²[population]
rs10040128	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12719098	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13169679	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13169987	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1355079	0.86[EUR][1000 genomes]
rs2940517	0.87[EUR][1000 genomes]
rs2940518	0.86[EUR][1000 genomes]
rs34251389	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34825344	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35710353	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs869287	0.87[EUR][1000 genomes]
rs9326743	0.87[EUR][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	nsv882689	chr5:107595383-108299744	Enhancers ZNF genes & repeats Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv1024076	chr5:107991426-108028223	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:108007000-108034800	Weak transcription	Right Atrium	heart
2	chr5:108017400-108021200	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr5:108017400-108022000	Weak transcription	Brain Angular Gyrus	brain
4	chr5:108017600-108021200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:108017600-108021200	Weak transcription	HepG2	liver
6	chr5:108017600-108021600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr5:108017600-108023600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr5:108017600-108023600	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr5:108018200-108023000	Weak transcription	GM12878-XiMat	blood
10	chr5:108020800-108021200	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr5:108020800-108021200	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr5:108020800-108022200	Enhancers	H9 Cell Line	embryonic stem cell
13	chr5:108021000-108021200	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr5:108021000-108021200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
15	chr5:108021000-108021200	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr5:108021000-108021400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr5:108021000-108022000	Enhancers	Primary B cells from peripheral blood	blood
18	chr5:108021000-108022000	Enhancers	Stomach Mucosa	stomach
19	chr5:108021000-108024000	Enhancers	H1 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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