Variant report

Variant	rs16897105
Chromosome Location	chr8:99817178-99817179
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs16897124	0.89[MKK][hapmap]
rs2028974	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891218	chr8:99507313-99906221	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1027025	chr8:99672977-100115315	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	nsv539690	chr8:99672977-100115315	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
4	nsv891220	chr8:99681858-99867419	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
5	nsv1025685	chr8:99706280-99826236	Strong transcription ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv539691	chr8:99706280-99826236	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
7	nsv1031089	chr8:99715785-100399935	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:99809600-99820000	Weak transcription	Ovary	ovary
2	chr8:99809600-99820600	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr8:99809800-99819800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr8:99809800-99819800	Weak transcription	A549	lung
5	chr8:99809800-99820400	Weak transcription	Osteobl	bone
6	chr8:99809800-99823000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr8:99809800-99823000	Weak transcription	HMEC	breast
8	chr8:99811800-99820200	Weak transcription	Fetal Lung	lung
9	chr8:99812600-99819600	Weak transcription	Colon Smooth Muscle	Colon
10	chr8:99813000-99818600	Weak transcription	Adipose Nuclei	Adipose
11	chr8:99813200-99819200	Weak transcription	Fetal Muscle Trunk	muscle
12	chr8:99813200-99821000	Weak transcription	Left Ventricle	heart
13	chr8:99813400-99820000	Weak transcription	Fetal Intestine Large	intestine
14	chr8:99813400-99828200	Weak transcription	Fetal Muscle Leg	muscle
15	chr8:99813600-99819800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr8:99813800-99836400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr8:99813800-99836400	Weak transcription	Fetal Stomach	stomach
18	chr8:99814000-99818800	Weak transcription	Pancreas	Pancrea
19	chr8:99814000-99819800	Weak transcription	Liver	Liver
20	chr8:99814000-99820000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr8:99814200-99817400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr8:99814200-99820000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr8:99814200-99826600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr8:99814400-99819800	Weak transcription	Fetal Intestine Small	intestine
25	chr8:99814400-99820800	Weak transcription	NHEK	skin
26	chr8:99814400-99821200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr8:99814400-99823000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr8:99814600-99821000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr8:99814800-99820000	Weak transcription	Small Intestine	intestine
30	chr8:99815600-99820400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr8:99816000-99817200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr8:99816600-99817800	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