Variant report

Variant	rs73034495
Chromosome Location	chr1:180027229-180027230
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:180009514..180012969-chr1:180025548..180028168,4	MCF-7	breast:
2	chr1:179850606..179853026-chr1:180024273..180027735,3	K562	blood:
3	chr1:180023147..180025587-chr1:180027128..180029217,2	K562	blood:

Variant related genes	Relation type
ENSG00000143337	Chromatin interaction
ENSG00000272906	Chromatin interaction
ENSG00000135837	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs3842887	0.88[AFR][1000 genomes]
rs57875912	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58605404	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59265893	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59508309	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60065834	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60495007	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60594364	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61371401	0.84[AFR][1000 genomes]
rs61554984	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73032356	0.84[AFR][1000 genomes]
rs73032361	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73032364	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73032365	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73032367	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73032369	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73032376	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73032384	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73032387	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73032389	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73032395	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73032399	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73034469	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73034472	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73034474	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73034477	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73034478	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73034489	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73036405	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73036409	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73036413	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73036425	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73036432	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73036436	1.00[AFR][1000 genomes]
rs73036437	1.00[AFR][1000 genomes]
rs73036439	0.96[AFR][1000 genomes]
rs73036466	0.88[AFR][1000 genomes]
rs73039980	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73039985	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73039997	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73041713	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429936	chr1:179790343-180214343	Active TSS Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	esv1815608	chr1:179813499-180067988	Strong transcription Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
3	nsv872573	chr1:179929388-180093066	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
4	nsv466228	chr1:179944901-180067988	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv548340	chr1:179944901-180067988	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv520322	chr1:179944901-180071987	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv548341	chr1:179945390-180067914	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv520278	chr1:179945390-180093066	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
9	nsv548342	chr1:179958809-180067988	Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv548343	chr1:179958809-180071987	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
11	nsv548344	chr1:179960787-180071987	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
12	nsv3755	chr1:179998860-180043554	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
13	nsv1000698	chr1:179999669-180042521	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179941400-180031800	Weak transcription	Spleen	Spleen
2	chr1:179970800-180076800	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr1:179976200-180063600	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr1:179980400-180027400	Strong transcription	Dnd41	blood
5	chr1:179981000-180059000	Strong transcription	HUES64 Cell Line	embryonic stem cell
6	chr1:179983600-180083400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr1:179989800-180034200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr1:179992400-180031400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr1:179992400-180032200	Weak transcription	Esophagus	oesophagus
10	chr1:180000200-180029200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr1:180000600-180039800	Strong transcription	Primary T cells fromperipheralblood	blood
12	chr1:180000800-180083400	Strong transcription	Primary T helper cells fromperipheralblood	blood
13	chr1:180002400-180085000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr1:180008800-180028200	Strong transcription	Fetal Intestine Large	intestine
15	chr1:180009000-180027800	Strong transcription	Fetal Muscle Trunk	muscle
16	chr1:180009000-180041200	Strong transcription	Duodenum Mucosa	Duodenum
17	chr1:180009000-180069600	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr1:180009200-180051800	Strong transcription	Fetal Thymus	thymus
19	chr1:180009200-180070000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr1:180010200-180029000	Strong transcription	Primary B cells from cord blood	blood
21	chr1:180010200-180040400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr1:180010200-180052000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr1:180010600-180051800	Strong transcription	Liver	Liver
24	chr1:180010800-180028600	Strong transcription	Adipose Nuclei	Adipose
25	chr1:180012400-180031600	Weak transcription	Gastric	stomach
26	chr1:180012800-180050400	Weak transcription	Stomach Mucosa	stomach
27	chr1:180013000-180031800	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr1:180013000-180080000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr1:180013600-180027600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr1:180014600-180031600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr1:180016000-180031600	Weak transcription	Right Ventricle	heart
32	chr1:180016400-180049600	Weak transcription	NHEK	skin
33	chr1:180017400-180027600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
34	chr1:180017400-180028400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr1:180020000-180036400	Weak transcription	Fetal Brain Male	brain
36	chr1:180020800-180031600	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr1:180021200-180031400	Weak transcription	NHLF	lung
38	chr1:180021400-180031600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr1:180021400-180062200	Weak transcription	Fetal Heart	heart
40	chr1:180023000-180031000	Weak transcription	Colonic Mucosa	Colon
41	chr1:180023400-180031200	Weak transcription	NH-A	brain
42	chr1:180023600-180031400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr1:180023600-180031600	Weak transcription	HepG2	liver
44	chr1:180023800-180030600	Weak transcription	HMEC	breast
45	chr1:180023800-180031400	Weak transcription	Fetal Kidney	kidney
46	chr1:180023800-180031400	Weak transcription	HSMMtube	muscle
47	chr1:180023800-180031600	Weak transcription	Brain Cingulate Gyrus	brain
48	chr1:180023800-180031600	Weak transcription	Rectal Smooth Muscle	rectum
49	chr1:180023800-180031800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr1:180024000-180028400	Strong transcription	Primary neutrophils fromperipheralblood	blood

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