Variant report

Variant	rs27632
Chromosome Location	chr5:14187991-14187992
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:14172374..14175679-chr5:14185951..14189494,3	MCF-7	breast:
2	chr5:14186990..14191289-chr5:14196188..14199111,4	MCF-7	breast:
3	chr5:14143292..14145490-chr5:14185700..14188808,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000038382	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs152781	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs164109	0.84[YRI][hapmap]
rs245513	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2463803	0.82[CEU][hapmap]
rs26290	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs26292	1.00[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs27367	1.00[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs27666	1.00[CEU][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs32977	1.00[CEU][hapmap]
rs32978	1.00[CEU][hapmap]
rs32979	1.00[CEU][hapmap]
rs33028	1.00[CEU][hapmap];1.00[YRI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs33029	1.00[CEU][hapmap];0.92[YRI][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs33030	1.00[CEU][hapmap];0.84[YRI][hapmap];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs348113	1.00[CEU][hapmap]
rs348116	1.00[CEU][hapmap]
rs40298	1.00[CEU][hapmap]
rs42289	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62344640	0.97[EUR][1000 genomes]
rs62346562	0.94[EUR][1000 genomes]
rs696289	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs696290	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv516415	chr5:13788886-14210897	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
2	nsv534466	chr5:13847044-14246208	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
3	esv1830112	chr5:14147376-14222601	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv1825924	chr5:14147376-14270450	Flanking Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv830209	chr5:14154989-14301758	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv948355	chr5:14160447-14395478	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
7	esv1792551	chr5:14180257-14202590	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:14175000-14191600	Weak transcription	Primary hematopoietic stem cells	blood
2	chr5:14177200-14189400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr5:14177400-14191800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr5:14179200-14189800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr5:14181200-14189200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr5:14181400-14188600	Enhancers	Sigmoid Colon	Sigmoid Colon
7	chr5:14181400-14189800	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr5:14181400-14191800	Enhancers	Fetal Heart	heart
9	chr5:14181600-14189000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr5:14182000-14190200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr5:14182800-14188600	Enhancers	Adipose Nuclei	Adipose
12	chr5:14183000-14189200	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr5:14183600-14193000	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr5:14184000-14191400	Weak transcription	Fetal Intestine Large	intestine
15	chr5:14184400-14190000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr5:14184400-14197200	Weak transcription	Duodenum Mucosa	Duodenum
17	chr5:14184600-14202600	Weak transcription	Fetal Intestine Small	intestine
18	chr5:14184800-14188400	Enhancers	Colon Smooth Muscle	Colon
19	chr5:14185000-14190000	Enhancers	Rectal Smooth Muscle	rectum
20	chr5:14185400-14188400	Flanking Active TSS	NHEK	skin
21	chr5:14185600-14194200	Enhancers	NHDF-Ad	bronchial
22	chr5:14185800-14188400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr5:14185800-14189600	Weak transcription	Aorta	Aorta
24	chr5:14185800-14189800	Weak transcription	Fetal Muscle Trunk	muscle
25	chr5:14185800-14189800	Weak transcription	Lung	lung
26	chr5:14185800-14190000	Weak transcription	Pancreas	Pancrea
27	chr5:14185800-14190800	Enhancers	HSMMtube	muscle
28	chr5:14186000-14188400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr5:14186000-14189800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr5:14186000-14189800	Weak transcription	Gastric	stomach
31	chr5:14186000-14190600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr5:14186000-14199800	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr5:14186000-14200000	Weak transcription	Esophagus	oesophagus
34	chr5:14186200-14189600	Weak transcription	HepG2	liver
35	chr5:14186200-14190000	Weak transcription	Fetal Brain Male	brain
36	chr5:14186200-14190200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr5:14186400-14188800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr5:14186400-14189800	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr5:14186400-14189800	Weak transcription	Stomach Mucosa	stomach
40	chr5:14186400-14190800	Enhancers	NH-A	brain
41	chr5:14186400-14190800	Enhancers	NHLF	lung
42	chr5:14186600-14188400	Weak transcription	Fetal Brain Female	brain
43	chr5:14186600-14188800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr5:14186600-14189400	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr5:14186600-14189600	Enhancers	HMEC	breast
46	chr5:14186600-14190000	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr5:14186600-14190200	Weak transcription	Fetal Stomach	stomach
48	chr5:14186600-14190400	Weak transcription	Fetal Lung	lung
49	chr5:14186600-14190800	Enhancers	Osteobl	bone
50	chr5:14186600-14191200	Weak transcription	Placenta	Placenta

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