Variant report

Variant	rs184577355
Chromosome Location	chr17:17599474-17599475
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:17597833..17600762-chr17:17692593..17694977,2	MCF-7	breast:
2	chr17:17593686..17602682-chr17:17684488..17692992,14	MCF-7	breast:
3	chr17:17597308..17599805-chr17:17722220..17725065,2	MCF-7	breast:
4	chr17:17566041..17569411-chr17:17596920..17599764,3	MCF-7	breast:
5	chr17:17597397..17599561-chr17:17661548..17663067,2	MCF-7	breast:
6	chr17:17597749..17599526-chr17:17663082..17665675,2	MCF-7	breast:
7	chr17:17597823..17600507-chr17:17743270..17745727,2	K562	blood:
8	chr17:17591306..17603641-chr17:17622226..17637880,43	MCF-7	breast:
9	chr17:17597990..17601613-chr17:17723911..17725744,3	MCF-7	breast:
10	chr17:17594258..17600676-chr17:17738917..17745175,15	MCF-7	breast:
11	chr17:17594932..17600890-chr17:17651321..17655426,6	MCF-7	breast:
12	chr17:17596829..17599707-chr17:17608179..17611084,3	K562	blood:
13	chr17:17598092..17600072-chr17:17758359..17760671,2	MCF-7	breast:
14	chr17:17596829..17599707-chr17:17608593..17611084,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000108557	Chromatin interaction
ENSG00000072310	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	nsv1065270	chr17:17430116-17823086	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
3	nsv543236	chr17:17430116-17823086	Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
4	nsv833384	chr17:17491483-17645648	Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
5	nsv869118	chr17:17509896-17599850	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv907752	chr17:17569012-17750907	Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
7	nsv531183	chr17:17571035-18205309	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
8	nsv907753	chr17:17573539-17747289	Genic enhancers Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
9	nsv907754	chr17:17573539-17782404	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
10	nsv1061126	chr17:17578826-17803194	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
11	nsv543238	chr17:17578826-17803194	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
12	nsv543239	chr17:17580295-17599851	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
13	nsv907755	chr17:17581184-17610587	Enhancers Genic enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
14	nsv833385	chr17:17594037-17765578	Enhancers Genic enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
15	nsv1058884	chr17:17594370-17803194	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
16	nsv543240	chr17:17594370-17803194	Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
17	nsv543241	chr17:17596222-17703059	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
18	nsv1064176	chr17:17596222-17803194	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
19	nsv543242	chr17:17596222-17803194	Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
20	nsv1062361	chr17:17598407-17746899	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
21	nsv543243	chr17:17598407-17746899	Genic enhancers Enhancers Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
22	nsv827911	chr17:17598715-17599975	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17594200-17599600	Enhancers	Fetal Brain Male	brain
2	chr17:17596600-17599600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
3	chr17:17597400-17607000	Enhancers	Fetal Heart	heart
4	chr17:17598600-17607000	Enhancers	Fetal Lung	lung
5	chr17:17598800-17599600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr17:17598800-17599600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr17:17598800-17599600	Enhancers	Placenta	Placenta
8	chr17:17598800-17599600	Enhancers	Fetal Thymus	thymus
9	chr17:17598800-17599600	Enhancers	NH-A	brain
10	chr17:17598800-17600000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr17:17598800-17600800	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr17:17598800-17600800	Enhancers	NHDF-Ad	bronchial
13	chr17:17598800-17601000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr17:17598800-17601200	Enhancers	Brain Substantia Nigra	brain
15	chr17:17598800-17601400	Enhancers	Fetal Intestine Small	intestine
16	chr17:17598800-17602200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr17:17598800-17602400	Enhancers	Gastric	stomach
18	chr17:17598800-17602800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr17:17598800-17603400	Enhancers	Spleen	Spleen
20	chr17:17598800-17603600	Enhancers	Esophagus	oesophagus
21	chr17:17598800-17603600	Enhancers	Right Atrium	heart
22	chr17:17598800-17604400	Enhancers	Fetal Muscle Trunk	muscle
23	chr17:17598800-17604800	Enhancers	Placenta Amnion	Placenta Amnion
24	chr17:17598800-17606800	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr17:17598800-17608000	Enhancers	Lung	lung
26	chr17:17598800-17608000	Enhancers	Pancreas	Pancrea
27	chr17:17598800-17608200	Enhancers	Left Ventricle	heart
28	chr17:17599000-17600200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr17:17599000-17600400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr17:17599000-17600600	Enhancers	Brain Angular Gyrus	brain
31	chr17:17599000-17600800	Enhancers	HSMMtube	muscle
32	chr17:17599000-17601000	Enhancers	HSMM	muscle
33	chr17:17599000-17601400	Enhancers	Fetal Intestine Large	intestine
34	chr17:17599000-17602000	Enhancers	Primary T cells fromperipheralblood	blood
35	chr17:17599000-17602200	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr17:17599000-17602400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr17:17599000-17602600	Enhancers	Colon Smooth Muscle	Colon
38	chr17:17599000-17602800	Enhancers	Liver	Liver
39	chr17:17599000-17603200	Enhancers	Brain Anterior Caudate	brain
40	chr17:17599000-17603400	Enhancers	Brain Hippocampus Middle	brain
41	chr17:17599000-17603400	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr17:17599000-17603400	Enhancers	Rectal Mucosa Donor 29	rectum
43	chr17:17599000-17603600	Enhancers	Brain Cingulate Gyrus	brain
44	chr17:17599000-17603600	Enhancers	Right Ventricle	heart
45	chr17:17599000-17603800	Enhancers	Adipose Nuclei	Adipose
46	chr17:17599000-17604400	Enhancers	Fetal Muscle Leg	muscle
47	chr17:17599000-17605800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr17:17599000-17606000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr17:17599200-17599600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr17:17599200-17599600	Enhancers	Duodenum Mucosa	Duodenum

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