Variant report

Variant	rs1634265
Chromosome Location	chr17:45237204-45237205
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr17:45236609-45237392	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:45235479..45238611-chr17:45239349..45243601,4	K562	blood:

Variant related genes	Relation type
CDC27	TF binding region
ENSG00000262265	Chromatin interaction

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1106950	0.95[CEU][hapmap]
rs11653589	0.85[JPT][hapmap]
rs1476498	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1713493	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs3851792	0.83[JPT][hapmap]
rs8068715	0.85[JPT][hapmap]
rs8071243	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs858670	0.95[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.90[YRI][hapmap];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs858677	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs858678	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs867859	0.94[CEU][hapmap]
rs908359	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062983	chr17:45030095-45789543	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
2	nsv833467	chr17:45063935-45252624	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	esv1796833	chr17:45212898-45244822	Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	esv3408242	chr17:45235345-45237851	Strong transcription Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
5	esv3325368	chr17:45235562-45247410	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	esv3393378	chr17:45235569-45249387	Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	esv5729	chr17:45235587-45249403	Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	esv3384942	chr17:45235611-45244927	ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	esv3431533	chr17:45235611-45247332	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	esv3364168	chr17:45235631-45247302	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
11	esv3422702	chr17:45235632-45247304	Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45234600-45249200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr17:45234600-45249400	Strong transcription	A549	lung
3	chr17:45235200-45247200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr17:45235400-45240000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr17:45235800-45237400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr17:45235800-45237400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr17:45235800-45237400	Strong transcription	Gastric	stomach
8	chr17:45235800-45237400	Strong transcription	Spleen	Spleen
9	chr17:45235800-45237800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr17:45235800-45237800	Weak transcription	K562	blood
11	chr17:45235800-45238000	Strong transcription	ES-I3 Cell Line	embryonic stem cell
12	chr17:45235800-45238000	Strong transcription	Left Ventricle	heart
13	chr17:45235800-45238000	Strong transcription	Sigmoid Colon	Sigmoid Colon
14	chr17:45235800-45238000	Strong transcription	Thymus	Thymus
15	chr17:45235800-45238000	Weak transcription	HSMM	muscle
16	chr17:45235800-45238200	Strong transcription	Primary neutrophils fromperipheralblood	blood
17	chr17:45235800-45238200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr17:45235800-45238200	Strong transcription	Stomach Smooth Muscle	stomach
19	chr17:45235800-45238400	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr17:45235800-45238400	Strong transcription	Brain Hippocampus Middle	brain
21	chr17:45235800-45238800	Strong transcription	Primary B cells from peripheral blood	blood
22	chr17:45235800-45238800	Strong transcription	Primary T helper cells fromperipheralblood	blood
23	chr17:45235800-45238800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr17:45235800-45238800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr17:45235800-45238800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr17:45235800-45238800	Strong transcription	Adipose Nuclei	Adipose
27	chr17:45235800-45238800	Strong transcription	NHLF	lung
28	chr17:45235800-45239000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr17:45235800-45239000	Weak transcription	Primary B cells from cord blood	blood
30	chr17:45235800-45239000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr17:45235800-45239000	Strong transcription	Fetal Stomach	stomach
32	chr17:45235800-45239000	Strong transcription	Lung	lung
33	chr17:45235800-45239200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr17:45235800-45239200	Strong transcription	Primary monocytes fromperipheralblood	blood
35	chr17:45235800-45239200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr17:45235800-45239200	Strong transcription	Duodenum Smooth Muscle	Duodenum
37	chr17:45235800-45239200	Strong transcription	Fetal Intestine Small	intestine
38	chr17:45235800-45239200	Strong transcription	Fetal Muscle Leg	muscle
39	chr17:45235800-45239400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
40	chr17:45235800-45239400	Strong transcription	Cortex derived primary cultured neurospheres	brain
41	chr17:45235800-45239400	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr17:45235800-45239400	Strong transcription	Rectal Mucosa Donor 29	rectum
43	chr17:45235800-45239400	Strong transcription	GM12878-XiMat	blood
44	chr17:45235800-45239400	Strong transcription	HUVEC	blood vessel
45	chr17:45235800-45239400	Strong transcription	Monocytes-CD14+_RO01746	blood
46	chr17:45235800-45239600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr17:45235800-45239600	Strong transcription	Duodenum Mucosa	Duodenum
48	chr17:45235800-45239800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr17:45235800-45239800	Strong transcription	Fetal Brain Female	brain
50	chr17:45235800-45239800	Strong transcription	Rectal Mucosa Donor 31	rectum

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