Variant report

Variant	rs17075482
Chromosome Location	chr13:51826044-51826045
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:51820571..51823207-chr13:51824938..51826606,2	MCF-7	breast:
2	chr13:51825741..51827924-chr13:51832786..51834447,2	MCF-7	breast:

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1022854	1.00[CHB][hapmap];0.87[YRI][hapmap];0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4942982	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6561627	0.86[YRI][hapmap]
rs7995246	1.00[CHB][hapmap];0.91[YRI][hapmap];0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9535627	0.82[CEU][hapmap];0.83[YRI][hapmap];0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs9568572	1.00[CHB][hapmap]
rs9591400	1.00[CHB][hapmap]
rs9596486	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs9596491	0.86[YRI][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832611	chr13:51766472-51938314	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription 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	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:51816200-51836600	Weak transcription	Adipose Nuclei	Adipose
2	chr13:51816800-51836000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr13:51817400-51827200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr13:51817600-51827200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr13:51817800-51827600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr13:51818800-51832800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr13:51820800-51833000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr13:51821200-51829600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr13:51821400-51827200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr13:51821400-51829600	Weak transcription	Right Atrium	heart
11	chr13:51821400-51833200	Weak transcription	Fetal Muscle Trunk	muscle
12	chr13:51821400-51833800	Weak transcription	Gastric	stomach
13	chr13:51821600-51836200	Weak transcription	Fetal Muscle Leg	muscle
14	chr13:51821600-51839000	Weak transcription	Esophagus	oesophagus
15	chr13:51821600-51845000	Weak transcription	Fetal Brain Male	brain
16	chr13:51821800-51831400	Weak transcription	Fetal Lung	lung
17	chr13:51822200-51833200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr13:51822600-51831000	Enhancers	Fetal Heart	heart
19	chr13:51823400-51827800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
20	chr13:51824200-51828200	Strong transcription	HUES6 Cell Line	embryonic stem cell
21	chr13:51824200-51844000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr13:51824400-51827800	Strong transcription	HUES48 Cell Line	embryonic stem cell
23	chr13:51824400-51836600	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr13:51824600-51827200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr13:51824800-51827000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
26	chr13:51824800-51827200	Strong transcription	Fetal Brain Female	brain
27	chr13:51824800-51828000	Strong transcription	H9 Cell Line	embryonic stem cell
28	chr13:51825000-51826600	Strong transcription	Fetal Stomach	stomach
29	chr13:51825000-51828000	Strong transcription	HUES64 Cell Line	embryonic stem cell
30	chr13:51825000-51829000	Strong transcription	H1 Cell Line	embryonic stem cell
31	chr13:51825000-51833000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr13:51825200-51828000	Weak transcription	Right Ventricle	heart
33	chr13:51825200-51832800	Weak transcription	Fetal Thymus	thymus
34	chr13:51825200-51833200	Weak transcription	Rectal Smooth Muscle	rectum
35	chr13:51825400-51826200	Strong transcription	Brain Inferior Temporal Lobe	brain
36	chr13:51825400-51826600	Strong transcription	Brain Germinal Matrix	brain
37	chr13:51825400-51828200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
38	chr13:51825400-51840600	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr13:51825600-51826400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr13:51825600-51826400	Strong transcription	Aorta	Aorta
41	chr13:51825600-51826600	Strong transcription	Spleen	Spleen
42	chr13:51825600-51827000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr13:51825600-51827000	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr13:51825600-51827000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr13:51825600-51827200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr13:51825600-51827600	Weak transcription	Colon Smooth Muscle	Colon
47	chr13:51825600-51828000	Genic enhancers	Brain Hippocampus Middle	brain
48	chr13:51825600-51829400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr13:51825800-51826200	Strong transcription	Lung	lung
50	chr13:51825800-51826400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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