Variant report

Variant	rs4646401
Chromosome Location	chr17:17422420-17422421
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs9909800	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:23 , 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	nsv907729	chr17:17338536-17425279	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	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
4	nsv907733	chr17:17381764-17422608	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	nsv907734	chr17:17381764-17425858	Enhancers Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
6	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
7	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
8	nsv907738	chr17:17404586-17422608	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
9	nsv907739	chr17:17404586-17424333	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Genic enhancers 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
10	nsv907740	chr17:17404586-17425858	Strong transcription Enhancers Bivalent Enhancer Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Active 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
11	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
12	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
13	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
14	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
15	esv1803680	chr17:17408484-17426009	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
16	nsv574525	chr17:17411030-17422608	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
17	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
18	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
19	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
20	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
21	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
22	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
23	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

No data

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17401000-17425400	Weak transcription	Thymus	Thymus
2	chr17:17407400-17425400	Weak transcription	Stomach Smooth Muscle	stomach
3	chr17:17407800-17422600	Weak transcription	Brain Germinal Matrix	brain
4	chr17:17410200-17426400	Weak transcription	Fetal Intestine Large	intestine
5	chr17:17411000-17428600	Weak transcription	Brain Hippocampus Middle	brain
6	chr17:17411000-17428600	Weak transcription	Right Atrium	heart
7	chr17:17411000-17428800	Weak transcription	Brain Anterior Caudate	brain
8	chr17:17411400-17423000	Weak transcription	Lung	lung
9	chr17:17411400-17428600	Weak transcription	Brain Cingulate Gyrus	brain
10	chr17:17411600-17425600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr17:17413200-17437400	Weak transcription	Aorta	Aorta
12	chr17:17414000-17424000	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr17:17415000-17425800	Weak transcription	Dnd41	blood
14	chr17:17415000-17426000	Strong transcription	Liver	Liver
15	chr17:17415400-17425600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr17:17415600-17423400	Weak transcription	Ovary	ovary
17	chr17:17415600-17424000	Weak transcription	Gastric	stomach
18	chr17:17416200-17425600	Weak transcription	Primary hematopoietic stem cells	blood
19	chr17:17416200-17425600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr17:17416200-17425600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr17:17416600-17423800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr17:17417600-17429400	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr17:17418200-17478000	Weak transcription	Primary T cells from cord blood	blood
24	chr17:17418600-17423200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr17:17418800-17424200	Weak transcription	Fetal Brain Female	brain
26	chr17:17419200-17424400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr17:17419200-17425800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr17:17419200-17426200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr17:17419400-17423400	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr17:17419400-17426400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr17:17419400-17430800	Weak transcription	Placenta	Placenta
32	chr17:17419600-17425800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr17:17419600-17447000	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr17:17419800-17426800	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr17:17420000-17424400	Weak transcription	HSMMtube	muscle
36	chr17:17420000-17425600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr17:17420000-17425800	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr17:17420000-17426400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr17:17420000-17426400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr17:17420000-17426400	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr17:17420000-17426600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr17:17420000-17427000	Weak transcription	HepG2	liver
43	chr17:17420000-17428600	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr17:17420000-17429600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr17:17420000-17429800	Weak transcription	Right Ventricle	heart
46	chr17:17420200-17422800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr17:17420200-17423400	Weak transcription	Adipose Nuclei	Adipose
48	chr17:17420200-17425600	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr17:17420400-17424000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr17:17420400-17425000	Weak transcription	Osteobl	bone

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