Variant report

Variant	rs10229944
Chromosome Location	chr7:66731726-66731727
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11770046	1.00[ASN][1000 genomes]
rs2003206	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56081654	0.96[EUR][1000 genomes]
rs56376467	0.96[EUR][1000 genomes]
rs66701377	0.96[EUR][1000 genomes]
rs67934921	0.96[EUR][1000 genomes]
rs73144570	0.96[EUR][1000 genomes]

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	esv2758118	chr7:66401430-66859253	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	esv2759535	chr7:66401430-66859253	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv888330	chr7:66502171-66877880	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
4	nsv1032237	chr7:66644492-66785029	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv970518	chr7:66647675-66742783	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1027702	chr7:66722103-66841913	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
7	nsv1031048	chr7:66722103-66844039	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10229944	TYW1	cis	Heart Left Ventricle	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:66667800-66738400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr7:66694800-66766600	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr7:66701600-66766600	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr7:66717400-66766200	Weak transcription	Fetal Muscle Leg	muscle
5	chr7:66717400-66766400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr7:66717600-66732800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr7:66717600-66735400	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr7:66717600-66756200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr7:66717800-66766400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr7:66718800-66735200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr7:66719000-66732800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr7:66719000-66766400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr7:66719800-66766200	Weak transcription	Spleen	Spleen
14	chr7:66721800-66756000	Weak transcription	Fetal Intestine Small	intestine
15	chr7:66722400-66740600	Weak transcription	Primary T cells from cord blood	blood
16	chr7:66722800-66732800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr7:66723000-66733000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr7:66723000-66734000	Weak transcription	Ovary	ovary
19	chr7:66723000-66739000	Weak transcription	Fetal Brain Female	brain
20	chr7:66723800-66766400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr7:66725800-66766200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr7:66725800-66766400	Weak transcription	Adipose Nuclei	Adipose
23	chr7:66727200-66732800	Weak transcription	Brain Hippocampus Middle	brain
24	chr7:66727600-66749600	Weak transcription	Aorta	Aorta
25	chr7:66727600-66766200	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr7:66728600-66732800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr7:66728600-66733000	Weak transcription	Thymus	Thymus
28	chr7:66728600-66766600	Weak transcription	Brain Angular Gyrus	brain
29	chr7:66729000-66767000	Weak transcription	Gastric	stomach
30	chr7:66729200-66735000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr7:66730800-66732400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr7:66731000-66733000	Weak transcription	Fetal Stomach	stomach

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