Variant report

Variant	rs9481897
Chromosome Location	chr6:119601583-119601584
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:119590898..119593723-chr6:119598543..119602207,4	K562	blood:
2	chr6:119590898..119592984-chr6:119600707..119602898,2	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs17442478	0.86[AFR][1000 genomes]
rs17442505	0.86[AFR][1000 genomes]
rs17526989	0.86[AFR][1000 genomes]
rs17527003	0.86[AFR][1000 genomes]
rs28635805	0.86[AFR][1000 genomes]
rs6569064	0.86[AFR][1000 genomes]
rs6917219	1.00[AFR][1000 genomes]
rs6926266	1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs6941142	1.00[YRI][hapmap]
rs73767443	0.91[AFR][1000 genomes]
rs73769020	0.94[AFR][1000 genomes]
rs73769050	0.94[AFR][1000 genomes]
rs7740969	1.00[AFR][1000 genomes]
rs7743309	0.86[AFR][1000 genomes]
rs7748940	0.86[AFR][1000 genomes]
rs7757386	0.94[AFR][1000 genomes]
rs7763451	0.86[AFR][1000 genomes]
rs7763610	0.86[AFR][1000 genomes]
rs7767940	0.86[AFR][1000 genomes]
rs7769071	1.00[AFR][1000 genomes]
rs7769133	1.00[AFR][1000 genomes]
rs9481896	1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs9481899	1.00[AFR][1000 genomes]
rs9481905	0.94[AFR][1000 genomes]
rs9481906	1.00[AFR][1000 genomes]
rs9489646	0.86[AFR][1000 genomes]
rs9489647	1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs9489648	0.86[AFR][1000 genomes]
rs9489649	0.86[AFR][1000 genomes]
rs9489655	0.92[AFR][1000 genomes]
rs9489656	1.00[AFR][1000 genomes]
rs9489657	0.92[AFR][1000 genomes]
rs9489658	0.92[AFR][1000 genomes]
rs9489659	0.92[AFR][1000 genomes]
rs9489660	1.00[AFR][1000 genomes]
rs9489666	1.00[AFR][1000 genomes]
rs9489684	0.88[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025995	chr6:119407742-119709548	Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv1017507	chr6:119465981-119664949	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	esv3447598	chr6:119558591-120119384	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	esv3389526	chr6:119558598-120190087	ZNF genes & repeats Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119558800-119602000	Weak transcription	Gastric	stomach
2	chr6:119589200-119611000	Weak transcription	Rectal Smooth Muscle	rectum
3	chr6:119590600-119621800	Weak transcription	Placenta	Placenta
4	chr6:119590800-119617400	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr6:119590800-119626600	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr6:119591000-119624200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr6:119591200-119602000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr6:119591200-119604600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr6:119592000-119602200	Weak transcription	Left Ventricle	heart
10	chr6:119592000-119604200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr6:119592200-119622200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr6:119592400-119604800	Weak transcription	Fetal Intestine Large	intestine
13	chr6:119592400-119610600	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr6:119592400-119620800	Weak transcription	Duodenum Mucosa	Duodenum
15	chr6:119592400-119633600	Weak transcription	Primary T cells from cord blood	blood
16	chr6:119592600-119622200	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr6:119592600-119627200	Weak transcription	Dnd41	blood
18	chr6:119593000-119622200	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr6:119593000-119624800	Weak transcription	Fetal Thymus	thymus
20	chr6:119593000-119626800	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr6:119593200-119604600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr6:119594200-119605000	Strong transcription	HepG2	liver
23	chr6:119595400-119601600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr6:119597200-119627400	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr6:119597600-119604800	Weak transcription	GM12878-XiMat	blood
26	chr6:119597600-119610800	Weak transcription	Fetal Kidney	kidney
27	chr6:119597800-119602000	Weak transcription	NHLF	lung
28	chr6:119597800-119604400	Weak transcription	Primary B cells from cord blood	blood
29	chr6:119598600-119602800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr6:119598600-119603000	Strong transcription	Liver	Liver
31	chr6:119599200-119619400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr6:119599600-119603400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr6:119599800-119611400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
34	chr6:119599800-119632600	Weak transcription	Spleen	Spleen
35	chr6:119600000-119602000	Weak transcription	Fetal Intestine Small	intestine
36	chr6:119600000-119604400	Weak transcription	Fetal Lung	lung
37	chr6:119600000-119608800	Strong transcription	Primary hematopoietic stem cells	blood
38	chr6:119600000-119629000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr6:119600200-119604200	Weak transcription	Aorta	Aorta
40	chr6:119600200-119604600	Weak transcription	Pancreas	Pancrea
41	chr6:119600200-119605000	Weak transcription	Lung	lung
42	chr6:119600400-119624000	Weak transcription	Fetal Stomach	stomach
43	chr6:119600600-119602000	Strong transcription	Adipose Nuclei	Adipose
44	chr6:119600600-119602400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr6:119601000-119601600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr6:119601000-119602000	Enhancers	Muscle Satellite Cultured Cells	--
47	chr6:119601000-119602800	Enhancers	Hela-S3	cervix
48	chr6:119601000-119606400	Weak transcription	NHEK	skin
49	chr6:119601200-119601600	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr6:119601200-119602400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links