Variant report

Variant	rs10986118
Chromosome Location	chr9:101164772-101164773
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10986112	0.85[ASN][1000 genomes]
rs16915579	0.83[AMR][1000 genomes]
rs16915623	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs60358936	0.85[EUR][1000 genomes]
rs7034300	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7048744	1.00[CHB][hapmap];1.00[JPT][hapmap];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	nsv430085	chr9:100928245-101339645	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv831664	chr9:101024862-101205637	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:101144000-101172000	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr9:101156600-101172000	Weak transcription	Fetal Brain Female	brain
3	chr9:101159000-101172800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr9:101160800-101166600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr9:101163600-101164800	Enhancers	H9 Cell Line	embryonic stem cell
6	chr9:101163800-101164800	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr9:101163800-101164800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr9:101163800-101164800	Enhancers	Brain Cingulate Gyrus	brain
9	chr9:101164000-101164800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr9:101164200-101164800	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr9:101164200-101165800	Enhancers	Fetal Stomach	stomach
12	chr9:101164200-101168600	Weak transcription	Fetal Muscle Leg	muscle
13	chr9:101164400-101169000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr9:101164400-101169400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr9:101164600-101165000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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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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