Variant report

Variant	rs774342
Chromosome Location	chr9:101134328-101134329
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:101106377..101108690-chr9:101133845..101135932,2	K562	blood:
2	chr9:101121184..101122748-chr9:101132251..101134952,2	K562	blood:
3	chr9:101122486..101124143-chr9:101132735..101134592,2	MCF-7	breast:

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10985425	1.00[CHB][hapmap]
rs497371	1.00[JPT][hapmap]
rs514993	1.00[JPT][hapmap]
rs518655	1.00[JPT][hapmap]
rs553139	1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs583115	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs583641	1.00[JPT][hapmap]
rs625500	1.00[JPT][hapmap]
rs644842	1.00[JPT][hapmap];1.00[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:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:101120600-101134400	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr9:101126600-101142600	Weak transcription	Brain Angular Gyrus	brain
3	chr9:101128200-101164200	Weak transcription	Brain Germinal Matrix	brain
4	chr9:101129000-101156000	Weak transcription	Fetal Brain Female	brain
5	chr9:101130400-101134800	Weak transcription	Brain Cingulate Gyrus	brain
6	chr9:101130800-101135600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr9:101131200-101135600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr9:101131400-101135200	Weak transcription	Osteobl	bone
9	chr9:101131400-101135400	Weak transcription	NH-A	brain
10	chr9:101132600-101134600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr9:101132800-101142800	Weak transcription	Right Atrium	heart
12	chr9:101133400-101138000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr9:101133400-101139400	Enhancers	Pancreas	Pancrea
14	chr9:101133400-101142400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr9:101133600-101135800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr9:101134000-101136000	Enhancers	Fetal Brain Male	brain
17	chr9:101134000-101136600	Enhancers	K562	blood
18	chr9:101134200-101134800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
19	chr9:101134200-101134800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
20	chr9:101134200-101134800	Bivalent Enhancer	Fetal Stomach	stomach
21	chr9:101134200-101142600	Enhancers	Fetal Intestine Large	intestine

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