Variant report

Variant	rs10224676
Chromosome Location	chr7:33547541-33547542
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10232000	0.91[YRI][hapmap]
rs10235827	1.00[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10238097	1.00[CEU][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10245585	1.00[CEU][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10251071	0.82[YRI][hapmap];1.00[AFR][1000 genomes]
rs10267018	1.00[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10272151	1.00[CEU][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10275218	1.00[CEU][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10279696	1.00[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11981868	1.00[CEU][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016416	chr7:33241443-33559477	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv830944	chr7:33389892-33549882	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv933237	chr7:33470390-33574046	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv933018	chr7:33506325-33707270	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv830945	chr7:33526648-33670592	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:33534200-33552400	Weak transcription	Pancreas	Pancrea
2	chr7:33537000-33552200	Weak transcription	Aorta	Aorta
3	chr7:33540800-33568600	Weak transcription	Left Ventricle	heart
4	chr7:33541200-33554600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr7:33541400-33567200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr7:33542400-33547800	Weak transcription	HSMM	muscle
7	chr7:33542400-33574200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr7:33543000-33557000	Weak transcription	Gastric	stomach
9	chr7:33543200-33548000	Weak transcription	Primary T cells from cord blood	blood
10	chr7:33543400-33550600	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr7:33543400-33555000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr7:33543600-33549600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr7:33543600-33552800	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr7:33543600-33574200	Weak transcription	Ovary	ovary
15	chr7:33543800-33551600	Weak transcription	Brain Substantia Nigra	brain
16	chr7:33543800-33555800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr7:33544000-33552000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr7:33544000-33552000	Weak transcription	Primary hematopoietic stem cells	blood
19	chr7:33544200-33551200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:33544200-33552400	Weak transcription	Psoas Muscle	Psoas
21	chr7:33544800-33548200	Weak transcription	Adipose Nuclei	Adipose
22	chr7:33545800-33551000	Weak transcription	Liver	Liver
23	chr7:33545800-33554800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr7:33546600-33549000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr7:33547000-33579400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr7:33547200-33547600	Strong transcription	HUES6 Cell Line	embryonic stem cell
27	chr7:33547200-33547600	Enhancers	Fetal Lung	lung
28	chr7:33547400-33551200	Weak transcription	Fetal Kidney	kidney
29	chr7:33547400-33557000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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