Variant report

Variant	rs529800586
Chromosome Location	chr17:17108236-17108237
allele	C/T
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:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:17106584..17108304-chr17:17112310..17114870,2	K562	blood:
2	chr17:17107449..17110459-chr17:17138885..17140924,4	K562	blood:
3	chr17:17107445..17110008-chr17:17138195..17140495,3	K562	blood:
4	chr17:17083452..17086510-chr17:17107054..17109094,3	K562	blood:
5	chr17:17099063..17102775-chr17:17103264..17109484,6	K562	blood:
6	chr17:17107449..17109941-chr17:17138935..17142587,4	MCF-7	breast:
7	chr17:16890452..16892957-chr17:17108135..17110227,2	MCF-7	breast:
8	chr17:17043821..17046160-chr17:17108071..17109890,2	MCF-7	breast:
9	chr17:17108079..17111792-chr17:17180254..17184300,4	K562	blood:
10	chr17:17107370..17109135-chr17:17133343..17134970,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000133030	Chromatin interaction
ENSG00000264187	Chromatin interaction
ENSG00000266498	Chromatin interaction
ENSG00000154803	Chromatin interaction
ENSG00000230969	Chromatin interaction
ENSG00000141030	Chromatin interaction

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833380	chr17:17088416-17241206	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv1065811	chr17:17104760-17225204	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	esv3324366	chr17:17107227-17112025	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17093600-17108400	Weak transcription	Thymus	Thymus
2	chr17:17095200-17108400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr17:17104200-17108800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr17:17104200-17110400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr17:17104400-17114000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr17:17104600-17108800	Enhancers	Left Ventricle	heart
7	chr17:17104800-17114000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr17:17105000-17116200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr17:17106000-17108600	Enhancers	Right Ventricle	heart
10	chr17:17106200-17108400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr17:17106200-17109200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr17:17106400-17108800	Enhancers	Right Atrium	heart
13	chr17:17106400-17110400	Enhancers	Fetal Brain Male	brain
14	chr17:17106600-17108400	Enhancers	Fetal Muscle Leg	muscle
15	chr17:17106600-17108600	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr17:17106600-17108600	Enhancers	Spleen	Spleen
17	chr17:17106800-17108400	Enhancers	Brain Hippocampus Middle	brain
18	chr17:17106800-17109000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr17:17107000-17108600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr17:17107000-17108600	Flanking Active TSS	Hela-S3	cervix
21	chr17:17107200-17108400	Enhancers	Brain Angular Gyrus	brain
22	chr17:17107200-17108400	Flanking Active TSS	GM12878-XiMat	blood
23	chr17:17107200-17108600	Flanking Active TSS	Colon Smooth Muscle	Colon
24	chr17:17107200-17108600	Enhancers	Placenta	Placenta
25	chr17:17107200-17108600	Enhancers	Lung	lung
26	chr17:17107200-17108600	Flanking Active TSS	Rectal Smooth Muscle	rectum
27	chr17:17107200-17109000	Enhancers	Aorta	Aorta
28	chr17:17107200-17109200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr17:17107200-17109400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
30	chr17:17107200-17110000	Flanking Active TSS	Adipose Nuclei	Adipose
31	chr17:17107400-17108400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr17:17107400-17108400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
33	chr17:17107400-17108400	Enhancers	Fetal Heart	heart
34	chr17:17107400-17108400	Enhancers	Fetal Intestine Large	intestine
35	chr17:17107400-17108400	Enhancers	Stomach Mucosa	stomach
36	chr17:17107400-17108400	Enhancers	HMEC	breast
37	chr17:17107400-17108600	Enhancers	Primary hematopoietic stem cells	blood
38	chr17:17107400-17108600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
39	chr17:17107400-17108600	Enhancers	Psoas Muscle	Psoas
40	chr17:17107400-17108600	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr17:17107400-17108600	Enhancers	Small Intestine	intestine
42	chr17:17107400-17108800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
43	chr17:17107400-17108800	Flanking Active TSS	K562	blood
44	chr17:17107400-17109400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
45	chr17:17107400-17109400	Flanking Active TSS	Brain Anterior Caudate	brain
46	chr17:17107600-17108400	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr17:17107600-17108400	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
48	chr17:17107600-17108400	Flanking Active TSS	Brain Substantia Nigra	brain
49	chr17:17107600-17108400	Genic enhancers	Fetal Intestine Small	intestine
50	chr17:17107600-17108400	Enhancers	Fetal Kidney	kidney

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