Variant report

Variant	rs10890403
Chromosome Location	chr1:47009343-47009344
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:47008125..47011332-chr1:47013107..47016538,3	K562	blood:
2	chr1:47009141..47012032-chr1:47183376..47185595,2	K562	blood:
3	chr1:47005992..47007886-chr1:47008521..47010850,2	MCF-7	breast:
4	chr1:46992147..46995347-chr1:47008706..47012363,4	K562	blood:
5	chr1:46920354..46923380-chr1:47007793..47010498,3	K562	blood:
6	chr1:47008373..47012047-chr1:47032869..47035437,3	K562	blood:

Variant related genes	Relation type
ENSG00000159658	Chromatin interaction
ENSG00000225667	Chromatin interaction
ENSG00000079277	Chromatin interaction
ENSG00000162456	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10890404	0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs11801320	0.88[ASN][1000 genomes]
rs12131300	0.86[EUR][1000 genomes]
rs1258043	0.93[ASN][1000 genomes]
rs1258044	0.94[ASN][1000 genomes]
rs1258049	0.91[ASN][1000 genomes]
rs2146562	0.86[EUR][1000 genomes]
rs36045414	0.86[EUR][1000 genomes]
rs4442318	0.89[EUR][1000 genomes]
rs61395024	0.92[ASN][1000 genomes]
rs7523809	0.98[ASN][1000 genomes]
rs8602	0.84[ASN][1000 genomes]
rs885127	0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2761743	chr1:46339858-47026743	Active TSS Weak transcription Bivalent Enhancer Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
2	nsv1001455	chr1:46828004-47326539	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv534950	chr1:46828004-47326539	Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv1000562	chr1:46832451-47027044	Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv1015045	chr1:46910546-47067492	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
6	nsv534952	chr1:46910546-47067492	Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
7	nsv1009193	chr1:46939999-47085667	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
8	nsv998422	chr1:46969626-47023671	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
9	nsv534953	chr1:46969626-47023671	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
10	nsv1010578	chr1:46977818-47010579	Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	nsv1009899	chr1:47007765-47062737	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
12	nsv534954	chr1:47007765-47062737	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
13	nsv1008246	chr1:47007844-47069845	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:46999600-47035000	Weak transcription	Right Atrium	heart
2	chr1:47007400-47009800	Bivalent Enhancer	Fetal Brain Male	brain
3	chr1:47008400-47009600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
4	chr1:47008400-47009800	Weak transcription	Pancreas	Pancrea
5	chr1:47008600-47009400	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
6	chr1:47008800-47009400	Bivalent Enhancer	Brain Hippocampus Middle	brain
7	chr1:47008800-47009600	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
8	chr1:47009000-47010200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
9	chr1:47009000-47010400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
10	chr1:47009200-47009400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
11	chr1:47009200-47009400	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
12	chr1:47009200-47009400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
13	chr1:47009200-47009400	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr1:47009200-47009400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr1:47009200-47009600	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:47009200-47009600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
17	chr1:47009200-47009600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr1:47009200-47009600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr1:47009200-47009600	Enhancers	Right Ventricle	heart
20	chr1:47009200-47010000	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
21	chr1:47009200-47010000	Bivalent Enhancer	Fetal Muscle Leg	muscle
22	chr1:47009200-47010200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
23	chr1:47009200-47010200	Bivalent Enhancer	Fetal Stomach	stomach
24	chr1:47009200-47010200	Enhancers	K562	blood
25	chr1:47009200-47010400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
26	chr1:47009200-47010400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell

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