Variant report

Variant	rs16886411
Chromosome Location	chr6:75992857-75992858
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:75951699..75955124-chr6:75992599..75996025,9	K562	blood:
2	chr6:74180943..74183846-chr6:75992415..75994208,2	K562	blood:
3	chr6:75992636..75994360-chr6:75994591..75996094,2	K562	blood:
4	chr6:75951366..75953542-chr6:75992434..75995845,4	K562	blood:
5	chr6:75951485..75954328-chr6:75992401..75995008,3	MCF-7	breast:
6	chr6:75982220..75984333-chr6:75991304..75993082,2	MCF-7	breast:
7	chr6:75959944..75962259-chr6:75992382..75994540,2	K562	blood:

Variant related genes	Relation type
ENSG00000112697	Chromatin interaction
ENSG00000135297	Chromatin interaction
ENSG00000225793	Chromatin interaction
ENSG00000112695	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs15616	0.81[ASN][1000 genomes]
rs16886197	1.00[CEU][hapmap]
rs16886390	1.00[CEU][hapmap];0.84[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs16886391	1.00[CEU][hapmap];0.84[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs1831689	1.00[EUR][1000 genomes]
rs2300791	1.00[CEU][hapmap]
rs2300794	1.00[CEU][hapmap]
rs240374	0.90[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs240388	0.82[CHB][hapmap];0.92[JPT][hapmap];0.81[ASN][1000 genomes]
rs240390	0.82[CHB][hapmap];0.92[JPT][hapmap];0.81[ASN][1000 genomes]
rs240392	0.81[ASN][1000 genomes]
rs240423	0.82[CHB][hapmap];0.84[JPT][hapmap]
rs240432	0.82[CHB][hapmap];0.92[JPT][hapmap];1.00[MEX][hapmap];0.81[ASN][1000 genomes]
rs2703710	0.82[JPT][hapmap]
rs2808191	0.82[JPT][hapmap]
rs2808196	0.82[JPT][hapmap]
rs2842457	0.82[JPT][hapmap];1.00[MEX][hapmap]
rs2951933	0.82[JPT][hapmap];1.00[MEX][hapmap]
rs2951935	0.81[JPT][hapmap]
rs2951948	0.81[JPT][hapmap]
rs2951953	0.82[JPT][hapmap];1.00[MEX][hapmap]
rs2998376	0.82[JPT][hapmap]
rs3756794	0.94[ASN][1000 genomes]
rs3777512	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3822870	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs414624	0.82[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs545588	1.00[CEU][hapmap]
rs560250	1.00[CEU][hapmap]
rs581649	1.00[CEU][hapmap]
rs658592	1.00[CEU][hapmap]
rs6927227	1.00[CEU][hapmap]
rs7741596	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016804	chr6:75775846-76188585	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv538310	chr6:75775846-76188585	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv1024079	chr6:75848556-76238519	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	nsv1027915	chr6:75893542-76510113	Active TSS Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
5	nsv538311	chr6:75893542-76510113	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
6	nsv603763	chr6:75923605-76009426	Genic enhancers Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
7	nsv603764	chr6:75963751-76025603	Weak transcription Active TSS Genic enhancers Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
8	nsv830698	chr6:75968810-76115592	Strong transcription Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:75974200-75993000	Weak transcription	Placenta	Placenta
2	chr6:75978600-75993600	Weak transcription	Esophagus	oesophagus
3	chr6:75982600-75993600	Weak transcription	Spleen	Spleen
4	chr6:75983000-75993200	Weak transcription	Fetal Muscle Trunk	muscle
5	chr6:75983000-75993400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr6:75987400-75993600	Weak transcription	Lung	lung
7	chr6:75987800-75996200	Active TSS	GM12878-XiMat	blood
8	chr6:75988000-75993000	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr6:75988000-75993000	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr6:75988000-75993200	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr6:75988000-75993200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
12	chr6:75988200-75993000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr6:75988800-75993400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr6:75988800-75993400	Weak transcription	Pancreas	Pancrea
15	chr6:75988800-75993600	Weak transcription	Gastric	stomach
16	chr6:75989200-75995800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr6:75989400-75993400	Flanking Active TSS	HUVEC	blood vessel
18	chr6:75989400-75993800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr6:75990000-75995400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr6:75990200-75993000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chr6:75990200-75993200	Enhancers	Brain Cingulate Gyrus	brain
22	chr6:75990200-75996400	Active TSS	ES-I3 Cell Line	embryonic stem cell
23	chr6:75990600-75993200	Weak transcription	Stomach Mucosa	stomach
24	chr6:75991000-75993000	Enhancers	Primary B cells from cord blood	blood
25	chr6:75991000-75996000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr6:75991000-75996000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr6:75991200-75995400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr6:75991200-75995400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr6:75991400-75993000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr6:75991400-75993600	Flanking Active TSS	Dnd41	blood
31	chr6:75991400-75993800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr6:75991400-75995200	Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr6:75991400-75995600	Active TSS	H1 Cell Line	embryonic stem cell
34	chr6:75991400-75995600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr6:75991400-75995600	Active TSS	HMEC	breast
36	chr6:75991400-75995600	Active TSS	NHLF	lung
37	chr6:75991600-75993000	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr6:75991600-75993000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
39	chr6:75991600-75993000	Flanking Active TSS	NHEK	skin
40	chr6:75991600-75996000	Active TSS	Pancreatic Islets	Pancreatic Islet
41	chr6:75991600-75997000	Active TSS	A549	lung
42	chr6:75991800-75993000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr6:75991800-75993200	Enhancers	Fetal Heart	heart
44	chr6:75991800-75993400	Enhancers	Primary B cells from peripheral blood	blood
45	chr6:75991800-75993400	Active TSS	HepG2	liver
46	chr6:75991800-75994200	Active TSS	Right Atrium	heart
47	chr6:75991800-75995400	Active TSS	Aorta	Aorta
48	chr6:75991800-75995600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
49	chr6:75991800-75995600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr6:75991800-75995800	Active TSS	NHDF-Ad	bronchial

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links