Variant report

Variant	rs73294361
Chromosome Location	chr17:17427986-17427987
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs57531156	0.90[AFR][1000 genomes]
rs61544091	0.88[AFR][1000 genomes]
rs67953560	0.87[AFR][1000 genomes]
rs73296530	0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv482648	chr17:17315268-17455442	Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv907731	chr17:17358004-17504856	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv907735	chr17:17381764-17448589	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	nsv907736	chr17:17381764-17465458	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	nsv907741	chr17:17404586-17429927	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv907742	chr17:17404586-17432744	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
7	nsv907743	chr17:17404586-17448589	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
8	nsv907744	chr17:17404586-17504856	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
9	nsv907745	chr17:17411211-17429927	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv907746	chr17:17412032-17478917	Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv907747	chr17:17412032-17504856	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
12	nsv907748	chr17:17412032-17782404	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
13	nsv523094	chr17:17415217-17430649	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
14	nsv907749	chr17:17417169-17448589	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
15	nsv524158	chr17:17420199-17430649	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
16	nsv574526	chr17:17422608-17444369	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
17	nsv470579	chr17:17424332-17493810	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17411000-17428600	Weak transcription	Brain Hippocampus Middle	brain
2	chr17:17411000-17428600	Weak transcription	Right Atrium	heart
3	chr17:17411000-17428800	Weak transcription	Brain Anterior Caudate	brain
4	chr17:17411400-17428600	Weak transcription	Brain Cingulate Gyrus	brain
5	chr17:17413200-17437400	Weak transcription	Aorta	Aorta
6	chr17:17417600-17429400	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr17:17418200-17478000	Weak transcription	Primary T cells from cord blood	blood
8	chr17:17419400-17430800	Weak transcription	Placenta	Placenta
9	chr17:17419600-17447000	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr17:17420000-17428600	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr17:17420000-17429600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr17:17420000-17429800	Weak transcription	Right Ventricle	heart
13	chr17:17420600-17434400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr17:17421000-17439200	Weak transcription	HSMM	muscle
15	chr17:17424600-17460000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr17:17424800-17428600	Weak transcription	Esophagus	oesophagus
17	chr17:17424800-17428800	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr17:17424800-17429600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr17:17425000-17430800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr17:17425000-17431200	Weak transcription	Spleen	Spleen
21	chr17:17425400-17429800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr17:17425600-17429400	Weak transcription	Stomach Smooth Muscle	stomach
23	chr17:17425800-17428600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr17:17425800-17428600	Weak transcription	Brain Germinal Matrix	brain
25	chr17:17425800-17429200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr17:17426200-17428600	Enhancers	Thymus	Thymus
27	chr17:17426800-17428600	Weak transcription	Fetal Intestine Small	intestine
28	chr17:17426800-17428800	Weak transcription	Lung	lung
29	chr17:17426800-17429200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr17:17427000-17428000	Weak transcription	Fetal Thymus	thymus
31	chr17:17427000-17428400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr17:17427000-17428400	Weak transcription	Adipose Nuclei	Adipose
33	chr17:17427000-17428600	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr17:17427000-17428600	Weak transcription	Ovary	ovary
35	chr17:17427000-17428600	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr17:17427000-17429400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr17:17427000-17436200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr17:17427200-17428400	Weak transcription	Fetal Muscle Trunk	muscle
39	chr17:17427200-17428600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr17:17427200-17440600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr17:17427400-17428600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr17:17427400-17428600	Weak transcription	Primary hematopoietic stem cells	blood
43	chr17:17427400-17428600	Weak transcription	Gastric	stomach
44	chr17:17427400-17428800	Weak transcription	Duodenum Mucosa	Duodenum
45	chr17:17427400-17429400	Weak transcription	Fetal Heart	heart
46	chr17:17427400-17432400	Weak transcription	HepG2	liver
47	chr17:17427600-17428600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr17:17427600-17428600	Weak transcription	Liver	Liver
49	chr17:17427600-17428600	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr17:17427600-17428600	Weak transcription	Stomach Mucosa	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links