Variant report

Variant	rs71563176
Chromosome Location	chr7:66626718-66626719
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs71563149	1.00[AFR][1000 genomes]
rs71563152	1.00[AFR][1000 genomes]
rs71563179	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 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	nsv831019	chr7:66516808-66720485	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	9 gene(s)	inside rSNPs	diseases
5	esv1802655	chr7:66576034-66634666	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
6	esv1816643	chr7:66576034-66634666	Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
7	esv1840497	chr7:66576034-66634666	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
8	esv1851064	chr7:66576034-66634666	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
9	esv1850306	chr7:66601324-66632583	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
10	esv1832033	chr7:66601324-66637001	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
11	esv1822512	chr7:66613751-66637001	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases
12	esv1826252	chr7:66613751-66637001	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
13	esv1810114	chr7:66621964-66636410	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	n/a	n/a	inside rSNPs	diseases
14	esv2422035	chr7:66621964-66676630	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:66585200-66627200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr7:66594800-66626800	Weak transcription	Dnd41	blood
3	chr7:66595000-66627400	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr7:66608800-66628200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr7:66608800-66632600	Weak transcription	Ovary	ovary
6	chr7:66612400-66627600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr7:66614200-66628000	Weak transcription	K562	blood
8	chr7:66616000-66626800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr7:66617200-66628200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr7:66617200-66628400	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr7:66617400-66627400	Weak transcription	Primary T cells from cord blood	blood
12	chr7:66619400-66627600	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr7:66619600-66626800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr7:66619600-66628000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr7:66620600-66631000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr7:66620800-66628400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr7:66621000-66628200	Weak transcription	Thymus	Thymus
18	chr7:66621400-66628200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr7:66621400-66631400	Weak transcription	Adipose Nuclei	Adipose
20	chr7:66621600-66628400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr7:66621600-66672000	Weak transcription	Fetal Intestine Large	intestine
22	chr7:66621800-66627200	Weak transcription	Fetal Stomach	stomach
23	chr7:66621800-66628200	Weak transcription	Primary B cells from peripheral blood	blood
24	chr7:66623400-66627600	Weak transcription	Fetal Intestine Small	intestine
25	chr7:66625200-66627800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr7:66626200-66626800	Enhancers	HMEC	breast
27	chr7:66626200-66627000	Enhancers	NHEK	skin
28	chr7:66626200-66627400	Enhancers	Hela-S3	cervix
29	chr7:66626400-66627000	Enhancers	Muscle Satellite Cultured Cells	--
30	chr7:66626600-66626800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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