Variant report

Variant	rs10817703
Chromosome Location	chr9:117802985-117802986
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr9:117802187-117803589	U87	brain:	n/a	n/a

Variant related genes	Relation type
TNC	TF binding region

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10122770	1.00[CEU][hapmap];0.95[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10817704	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10817707	0.98[AFR][1000 genomes]
rs10982495	0.91[EUR][1000 genomes]
rs10982498	0.82[CEU][hapmap];1.00[GIH][hapmap];0.91[EUR][1000 genomes]
rs10982499	0.82[CEU][hapmap];1.00[GIH][hapmap];0.91[EUR][1000 genomes]
rs10982505	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10982514	1.00[YRI][hapmap];0.96[AFR][1000 genomes]
rs10982515	0.81[EUR][1000 genomes]
rs12156603	0.82[CEU][hapmap]
rs12156617	0.82[CEU][hapmap]
rs12380780	0.81[EUR][1000 genomes]
rs1757095	0.81[EUR][1000 genomes]
rs73551065	0.91[EUR][1000 genomes]
rs73553151	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73553161	0.98[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs7864743	0.85[CEU][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831696	chr9:117701582-117874150	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv615250	chr9:117768021-118012841	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv916912	chr9:117770039-118014140	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv1840787	chr9:117787173-117803882	Weak transcription Genic enhancers Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
5	esv1826575	chr9:117787173-117805719	Genic enhancers Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
6	nsv519131	chr9:117796986-117804667	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117773400-117803200	Weak transcription	Esophagus	oesophagus
2	chr9:117781800-117808600	Weak transcription	Fetal Intestine Small	intestine
3	chr9:117782400-117848200	Weak transcription	Brain Substantia Nigra	brain
4	chr9:117789000-117808600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:117791600-117833200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr9:117792800-117815000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr9:117795200-117803400	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr9:117797400-117807400	Genic enhancers	Cortex derived primary cultured neurospheres	brain
9	chr9:117797800-117803400	Enhancers	Rectal Smooth Muscle	rectum
10	chr9:117798200-117805000	Weak transcription	HSMM	muscle
11	chr9:117798600-117804200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr9:117798800-117803600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr9:117798800-117804800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr9:117799200-117805000	Weak transcription	HSMMtube	muscle
15	chr9:117799200-117819800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr9:117799400-117817000	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr9:117799800-117804600	Strong transcription	NHEK	skin
18	chr9:117800000-117806600	Strong transcription	NH-A	brain
19	chr9:117800200-117803400	Strong transcription	HUES6 Cell Line	embryonic stem cell
20	chr9:117800200-117803400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr9:117800400-117803200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr9:117800400-117803400	Strong transcription	NHLF	lung
23	chr9:117800400-117803600	Strong transcription	NHDF-Ad	bronchial
24	chr9:117800600-117803000	Genic enhancers	Duodenum Smooth Muscle	Duodenum
25	chr9:117800600-117803200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr9:117800600-117808600	Weak transcription	Fetal Intestine Large	intestine
27	chr9:117800800-117803400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr9:117800800-117804200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr9:117800800-117804600	Strong transcription	Osteobl	bone
30	chr9:117800800-117805200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr9:117800800-117805600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr9:117800800-117825000	Weak transcription	Fetal Muscle Leg	muscle
33	chr9:117800800-117825200	Weak transcription	Fetal Muscle Trunk	muscle
34	chr9:117801000-117803200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr9:117801000-117804400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr9:117801000-117812400	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr9:117801000-117819200	Weak transcription	HMEC	breast
38	chr9:117801200-117803600	Genic enhancers	Stomach Smooth Muscle	stomach
39	chr9:117801400-117803600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr9:117801600-117803400	Strong transcription	Fetal Stomach	stomach
41	chr9:117801800-117820200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr9:117802000-117803200	Weak transcription	Aorta	Aorta
43	chr9:117802000-117803400	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr9:117802200-117803600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr9:117802200-117848200	Weak transcription	Spleen	Spleen
46	chr9:117802400-117806000	Genic enhancers	Colon Smooth Muscle	Colon
47	chr9:117802600-117803400	Strong transcription	HUES64 Cell Line	embryonic stem cell
48	chr9:117802600-117803400	Strong transcription	Fetal Lung	lung
49	chr9:117802600-117803600	Strong transcription	Fetal Kidney	kidney
50	chr9:117802600-117812400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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