Variant report

Variant	rs10121203
Chromosome Location	chr9:8833227-8833228
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10116689	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10118318	0.87[CHB][hapmap]
rs10119815	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10120450	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10120478	0.87[CHB][hapmap]
rs10120501	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10124428	0.80[CHB][hapmap]
rs10739173	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10758996	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10758997	0.87[CHB][hapmap]
rs10759007	0.80[CHB][hapmap]
rs10815961	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10815964	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs10977314	0.87[CHB][hapmap]
rs1434253	0.89[CEU][hapmap];0.87[CHB][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1434254	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1434256	0.87[CHB][hapmap]
rs1434258	0.87[CHB][hapmap]
rs1434273	0.89[CEU][hapmap];0.80[CHB][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1836227	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1836229	0.89[CEU][hapmap];0.80[CHB][hapmap];0.88[EUR][1000 genomes]
rs1836230	0.85[CEU][hapmap];0.82[EUR][1000 genomes]
rs1836231	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2053125	1.00[CEU][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4372066	0.87[CHB][hapmap]
rs6477358	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7048621	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7048788	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7864437	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7864663	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7864670	0.87[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022796	chr9:8360729-9110046	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv892235	chr9:8700396-8865925	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1025800	chr9:8712487-9030627	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv539980	chr9:8712487-9030627	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv892236	chr9:8745520-8870553	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv1015898	chr9:8753534-9011443	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv892240	chr9:8796449-8834108	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8821400-8835000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:8822200-8838600	Weak transcription	Osteobl	bone
3	chr9:8823000-8835000	Weak transcription	Fetal Muscle Leg	muscle
4	chr9:8823400-8845000	Weak transcription	Fetal Brain Female	brain
5	chr9:8823800-8835000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr9:8826000-8835000	Weak transcription	Aorta	Aorta
7	chr9:8826000-8837400	Weak transcription	Primary hematopoietic stem cells	blood
8	chr9:8826000-8842600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr9:8826200-8834600	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr9:8826200-8834800	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr9:8826200-8834800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr9:8826600-8834400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr9:8826600-8834600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr9:8830000-8833400	Enhancers	Brain Substantia Nigra	brain
15	chr9:8830400-8833400	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr9:8831000-8834600	Weak transcription	Fetal Kidney	kidney
17	chr9:8831200-8833600	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr9:8831400-8833400	Enhancers	Brain Cingulate Gyrus	brain
19	chr9:8831800-8833400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr9:8831800-8833400	Enhancers	Fetal Lung	lung
21	chr9:8832000-8833400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr9:8832000-8834600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr9:8832200-8834600	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr9:8832400-8833400	Enhancers	Brain Angular Gyrus	brain
25	chr9:8832400-8834600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr9:8832800-8842800	Weak transcription	Fetal Brain Male	brain
27	chr9:8833000-8833400	Enhancers	Ovary	ovary
28	chr9:8833000-8833600	Enhancers	Fetal Heart	heart
29	chr9:8833000-8837400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr9:8833200-8834000	Weak transcription	Brain Hippocampus Middle	brain
31	chr9:8833200-8834600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr9:8833200-8834600	Weak transcription	Brain Anterior Caudate	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links