Variant report

Variant	rs1738233
Chromosome Location	chr6:38766488-38766489
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs1615441	0.94[JPT][hapmap]
rs1616105	0.94[JPT][hapmap]
rs1618774	0.94[JPT][hapmap]
rs1618834	0.93[ASN][1000 genomes]
rs1622275	0.81[CHB][hapmap];0.82[ASN][1000 genomes]
rs1678664	0.81[CHB][hapmap]
rs1678666	0.90[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs1678674	0.85[CHB][hapmap];0.88[JPT][hapmap];0.84[ASN][1000 genomes]
rs1678676	0.92[ASN][1000 genomes]
rs1678686	0.81[CHB][hapmap];0.82[ASN][1000 genomes]
rs1678710	0.94[JPT][hapmap]
rs1678711	0.94[JPT][hapmap]
rs1678716	0.94[JPT][hapmap]
rs1678719	0.94[JPT][hapmap]
rs1678720	0.94[JPT][hapmap]
rs1678721	0.94[JPT][hapmap]
rs1678722	0.94[JPT][hapmap]
rs1678724	0.94[JPT][hapmap]
rs1678728	0.94[JPT][hapmap]
rs1678729	0.94[JPT][hapmap]
rs1678731	0.94[JPT][hapmap]
rs1678732	0.89[JPT][hapmap]
rs1678733	0.94[JPT][hapmap]
rs1678734	0.94[JPT][hapmap]
rs1678735	0.94[JPT][hapmap]
rs1678737	0.94[JPT][hapmap]
rs1678738	0.87[JPT][hapmap]
rs1678741	0.94[JPT][hapmap]
rs1678743	0.83[JPT][hapmap]
rs16891139	0.83[JPT][hapmap]
rs1738188	0.82[JPT][hapmap]
rs1738189	0.94[JPT][hapmap]
rs1738190	0.94[JPT][hapmap]
rs1738191	1.00[JPT][hapmap]
rs1738193	0.94[JPT][hapmap]
rs1738194	0.94[JPT][hapmap]
rs1738198	0.94[JPT][hapmap]
rs1738200	0.94[JPT][hapmap]
rs1738206	0.94[JPT][hapmap]
rs1738207	0.94[JPT][hapmap]
rs1738209	0.94[JPT][hapmap]
rs1738210	0.93[JPT][hapmap]
rs1738224	0.91[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs1738226	0.80[CHB][hapmap];0.82[ASN][1000 genomes]
rs1738234	0.91[ASN][1000 genomes]
rs1738237	0.95[ASN][1000 genomes]
rs1738242	0.91[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs1738246	0.90[ASN][1000 genomes]
rs1738249	0.81[CHB][hapmap];0.84[ASN][1000 genomes]
rs6912563	0.80[CHB][hapmap];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv885817	chr6:38036420-39019503	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers 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	26 gene(s)	inside rSNPs	diseases
2	nsv830642	chr6:38645056-38800657	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv830643	chr6:38726675-38905589	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv462915	chr6:38728142-38773293	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv602959	chr6:38728142-38786528	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv470814	chr6:38728142-38790149	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv462916	chr6:38747770-38782401	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv602960	chr6:38747770-38782401	Flanking Active TSS Enhancers Genic enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:38763400-38768600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr6:38763600-38766800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:38764600-38766800	Enhancers	K562	blood
4	chr6:38764800-38768400	Enhancers	NHEK	skin
5	chr6:38765000-38766600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:38765400-38766600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:38766000-38767000	Weak transcription	HUVEC	blood vessel
8	chr6:38766200-38766600	Enhancers	Pancreas	Pancrea
9	chr6:38766400-38766600	Enhancers	Esophagus	oesophagus
10	chr6:38766400-38767200	Bivalent Enhancer	Fetal Muscle Leg	muscle
11	chr6:38766400-38768400	Enhancers	HMEC	breast

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