Variant report

Variant	rs17081346
Chromosome Location	chr5:177895383-177895384
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:177885956..177889656-chr5:177894667..177897889,3	MCF-7	breast:
2	chr5:177894292..177896063-chr5:177897258..177899224,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10062593	1.00[CEU][hapmap]
rs1546222	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs17052428	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17081216	1.00[MEX][hapmap]
rs2133280	0.91[CHB][hapmap];0.98[CHD][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs2546631	0.80[ASN][1000 genomes]
rs2546632	0.87[ASN][1000 genomes]
rs2546633	0.99[ASN][1000 genomes]
rs2546634	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2546635	0.98[ASN][1000 genomes]
rs2546636	1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2546637	0.87[ASN][1000 genomes]
rs2546638	0.87[ASN][1000 genomes]
rs2546639	0.97[ASN][1000 genomes]
rs2647697	1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2647698	0.90[ASN][1000 genomes]
rs2672823	0.87[CHB][hapmap];0.88[CHD][hapmap];0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs2672824	0.83[CHB][hapmap];0.88[CHD][hapmap];0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs2672831	0.95[ASN][1000 genomes]
rs2672832	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2672834	0.97[ASN][1000 genomes]
rs2672835	0.86[ASN][1000 genomes]
rs2672837	0.85[ASN][1000 genomes]
rs533024	1.00[CEU][hapmap]
rs535011	1.00[CEU][hapmap]
rs59608037	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61562605	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs61693781	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66934098	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs67085711	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6868472	1.00[CEU][hapmap];0.82[CHB][hapmap];0.91[JPT][hapmap];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6868772	1.00[CEU][hapmap]
rs6868991	1.00[CEU][hapmap];0.81[CHB][hapmap];0.88[CHD][hapmap];0.91[JPT][hapmap];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6877016	1.00[CEU][hapmap]
rs6896228	0.81[JPT][hapmap]
rs72648838	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72648839	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7706759	0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs7728076	0.81[JPT][hapmap]
rs869405	1.00[CEU][hapmap];0.82[YRI][hapmap]

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	nsv948342	chr5:177384542-178168737	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Weak transcription 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	141 gene(s)	inside rSNPs	diseases
2	nsv1029398	chr5:177502106-178070654	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	136 gene(s)	inside rSNPs	diseases
3	nsv1024689	chr5:177638936-177926244	Enhancers Bivalent Enhancer Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv537968	chr5:177638936-177926244	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
5	nsv427739	chr5:177766033-177966666	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv883210	chr5:177771925-177980792	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv883213	chr5:177811754-177947771	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv462570	chr5:177860454-178010145	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv600423	chr5:177860454-178010145	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv1029822	chr5:177872333-177931889	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv1033039	chr5:177873974-177926244	Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv537971	chr5:177873974-177926244	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	nsv883214	chr5:177876309-178047217	Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
14	nsv1030915	chr5:177880081-177934927	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177877800-177895400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:177887200-177896600	Enhancers	Fetal Stomach	stomach
3	chr5:177887800-177897600	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr5:177890400-177895400	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr5:177890600-177901600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr5:177891000-177897600	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr5:177892600-177895400	Enhancers	Placenta	Placenta
8	chr5:177892800-177896800	Weak transcription	Fetal Heart	heart
9	chr5:177893400-177897600	Enhancers	Lung	lung
10	chr5:177893600-177895400	Enhancers	Fetal Thymus	thymus
11	chr5:177893600-177895600	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr5:177893600-177895800	Enhancers	Esophagus	oesophagus
13	chr5:177893600-177896000	Enhancers	Fetal Muscle Leg	muscle
14	chr5:177893600-177896200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr5:177893600-177896200	Enhancers	Pancreas	Pancrea
16	chr5:177893600-177896400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
17	chr5:177893600-177898000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr5:177894000-177895600	Enhancers	Primary hematopoietic stem cells	blood
19	chr5:177894000-177895600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr5:177894000-177895600	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr5:177894000-177896000	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr5:177894000-177896200	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr5:177894000-177897200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr5:177894200-177895400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr5:177894200-177895600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr5:177894200-177895600	Enhancers	Colon Smooth Muscle	Colon
27	chr5:177894200-177895600	Enhancers	Fetal Kidney	kidney
28	chr5:177894200-177895600	Enhancers	Right Atrium	heart
29	chr5:177894200-177895600	Enhancers	HUVEC	blood vessel
30	chr5:177894200-177895600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
31	chr5:177894200-177895800	Enhancers	Colonic Mucosa	Colon
32	chr5:177894200-177895800	Enhancers	Left Ventricle	heart
33	chr5:177894200-177895800	Enhancers	Ovary	ovary
34	chr5:177894200-177896000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr5:177894200-177896200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr5:177894200-177896200	Enhancers	Right Ventricle	heart
37	chr5:177894200-177896200	Enhancers	Spleen	Spleen
38	chr5:177894200-177896600	Enhancers	Primary B cells from cord blood	blood
39	chr5:177894400-177895600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr5:177894400-177895600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr5:177894400-177895600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
42	chr5:177894400-177895600	Flanking Active TSS	Adipose Nuclei	Adipose
43	chr5:177894400-177896400	Enhancers	Skeletal Muscle Male	skeletal muscle
44	chr5:177894400-177899400	Weak transcription	Fetal Intestine Small	intestine
45	chr5:177894600-177895400	Weak transcription	Gastric	stomach
46	chr5:177894600-177897000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr5:177894600-177902000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr5:177894800-177895400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr5:177894800-177895600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr5:177894800-177895600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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