Variant report

Variant	rs17758463
Chromosome Location	chr4:7396858-7396859
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:7385620..7387196-chr4:7395929..7398822,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10000132	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs10000236	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10005361	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10005455	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10008226	0.88[YRI][hapmap]
rs12500803	0.87[EUR][1000 genomes]
rs12500834	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12511951	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12512241	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12512986	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13103153	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13146595	1.00[JPT][hapmap]
rs28760558	0.86[AFR][1000 genomes]
rs7356467	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9995355	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9997600	0.86[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916610	chr4:7238883-7731946	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv593569	chr4:7291363-7626136	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1011547	chr4:7318232-7637410	Active TSS ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	nsv537017	chr4:7318232-7637410	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1003679	chr4:7319111-7449262	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv469758	chr4:7370083-7546250	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7384200-7399600	Weak transcription	Right Atrium	heart
2	chr4:7389800-7399800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:7390800-7397400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr4:7391800-7402000	Enhancers	Brain Germinal Matrix	brain
5	chr4:7393600-7400800	Bivalent Enhancer	Fetal Muscle Leg	muscle
6	chr4:7393800-7398200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
7	chr4:7394000-7397600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr4:7394400-7397000	Enhancers	Fetal Lung	lung
9	chr4:7394400-7400000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr4:7395000-7397000	Weak transcription	Brain Hippocampus Middle	brain
11	chr4:7395000-7397000	Weak transcription	Fetal Thymus	thymus
12	chr4:7395600-7397400	Weak transcription	HSMMtube	muscle
13	chr4:7395800-7399400	Weak transcription	Brain Anterior Caudate	brain
14	chr4:7395800-7399400	Weak transcription	Brain Substantia Nigra	brain
15	chr4:7396200-7397000	Bivalent Enhancer	Stomach Mucosa	stomach
16	chr4:7396200-7397000	Enhancers	A549	lung
17	chr4:7396200-7397200	Enhancers	Fetal Brain Female	brain
18	chr4:7396200-7397200	Enhancers	Fetal Intestine Small	intestine
19	chr4:7396200-7398400	Bivalent Enhancer	Fetal Stomach	stomach
20	chr4:7396400-7397000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr4:7396400-7397800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr4:7396400-7398200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr4:7396400-7398400	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr4:7396600-7399400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr4:7396800-7397200	Enhancers	Fetal Intestine Large	intestine
26	chr4:7396800-7397200	Bivalent Enhancer	HSMM	muscle
27	chr4:7396800-7401400	Enhancers	Brain Cingulate Gyrus	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links