Variant report

Variant	rs10986044
Chromosome Location	chr9:101135387-101135388
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type
1	chr9:101106377..101108690-chr9:101133845..101135932,2	K562	blood:
2	chr9:101131416..101134090-chr9:101135125..101136966,2	MCF-7	breast:
3	chr9:101127682..101131370-chr9:101135028..101139404,5	K562	blood:
4	chr9:101135309..101136944-chr9:101137021..101138773,2	K562	blood:
5	chr9:101132158..101134151-chr9:101134451..101136659,2	MCF-7	breast:
6	chr9:101125471..101127480-chr9:101134828..101138522,3	K562	blood:
7	chr9:101134634..101137375-chr9:101146278..101148960,2	K562	blood:
8	chr9:101135309..101137051-chr9:101137273..101139774,2	K562	blood:

No data

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10818828	0.86[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10818832	1.00[JPT][hapmap];0.94[YRI][hapmap];0.88[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs10818833	1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs10986017	0.82[JPT][hapmap]
rs10986039	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10986041	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10986060	1.00[JPT][hapmap];0.86[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs10986071	0.85[CHB][hapmap]
rs12340940	0.86[ASN][1000 genomes]
rs16915236	0.89[EUR][1000 genomes]
rs3780430	0.82[JPT][hapmap]
rs3780432	0.82[JPT][hapmap]
rs552989	0.86[CHB][hapmap];0.86[ASN][1000 genomes]
rs565349	0.86[CHB][hapmap]
rs661105	0.86[CHB][hapmap];0.94[YRI][hapmap];0.90[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs661532	0.86[CHB][hapmap];0.94[YRI][hapmap];0.93[AFR][1000 genomes];0.87[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:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:101126600-101142600	Weak transcription	Brain Angular Gyrus	brain
2	chr9:101128200-101164200	Weak transcription	Brain Germinal Matrix	brain
3	chr9:101129000-101156000	Weak transcription	Fetal Brain Female	brain
4	chr9:101130800-101135600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr9:101131200-101135600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr9:101131400-101135400	Weak transcription	NH-A	brain
7	chr9:101132800-101142800	Weak transcription	Right Atrium	heart
8	chr9:101133400-101138000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr9:101133400-101139400	Enhancers	Pancreas	Pancrea
10	chr9:101133400-101142400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr9:101133600-101135800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr9:101134000-101136000	Enhancers	Fetal Brain Male	brain
13	chr9:101134000-101136600	Enhancers	K562	blood
14	chr9:101134200-101142600	Enhancers	Fetal Intestine Large	intestine
15	chr9:101134400-101142400	Enhancers	Fetal Intestine Small	intestine
16	chr9:101134600-101135800	Enhancers	Fetal Muscle Leg	muscle
17	chr9:101134600-101136800	Enhancers	NHDF-Ad	bronchial
18	chr9:101134600-101139400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr9:101134800-101140000	Weak transcription	Spleen	Spleen
20	chr9:101134800-101142400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr9:101134800-101143000	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr9:101135200-101135400	Weak transcription	Fetal Muscle Trunk	muscle
23	chr9:101135200-101136800	Enhancers	Osteobl	bone
24	chr9:101135200-101138400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links