Variant report

Variant	rs17741591
Chromosome Location	chr14:47816119-47816120
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	SPI1	chr14:47815896-47816655	GM12878	blood:	n/a	chr14:47816245-47816254 chr14:47816204-47816217
2	PAX5	chr14:47816101-47816349	GM12878	blood:	n/a	chr14:47816245-47816254
3	REST	chr14:47816108-47816320	Hela-S3	cervix:	n/a	n/a
4	SPI1	chr14:47816006-47816381	GM12891	blood:	n/a	chr14:47816245-47816254 chr14:47816204-47816217
5	SPI1	chr14:47815993-47816393	GM12891	blood:	n/a	chr14:47816245-47816254 chr14:47816204-47816217
6	SPI1	chr14:47816080-47816429	GM12878	blood:	n/a	chr14:47816245-47816254 chr14:47816204-47816217
7	SPI1	chr14:47816090-47816412	HL-60	blood:	n/a	chr14:47816245-47816254 chr14:47816204-47816217

Variant related genes	Relation type
MDGA2	TF binding region

Extended variants
information (count: 30 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10130426	0.86[ASN][1000 genomes]
rs10134522	0.81[ASN][1000 genomes]
rs10148539	0.86[ASN][1000 genomes]
rs10149191	0.86[ASN][1000 genomes]
rs10150578	1.00[CHB][hapmap];0.92[JPT][hapmap];0.83[ASN][1000 genomes]
rs11157553	0.81[ASN][1000 genomes]
rs11620638	0.82[EUR][1000 genomes]
rs11850343	1.00[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs12436849	0.81[ASN][1000 genomes]
rs12436870	0.81[ASN][1000 genomes]
rs17673119	0.81[ASN][1000 genomes]
rs28535248	0.84[ASN][1000 genomes]
rs28882510	0.86[ASN][1000 genomes]
rs4898565	0.86[ASN][1000 genomes]
rs7141653	0.81[ASN][1000 genomes]
rs7152013	1.00[CHB][hapmap];0.92[JPT][hapmap];0.84[ASN][1000 genomes]
rs8004035	1.00[CHB][hapmap];0.92[JPT][hapmap];0.81[ASN][1000 genomes]
rs8010964	0.81[ASN][1000 genomes]
rs8012719	1.00[CHB][hapmap];0.95[CHD][hapmap];0.92[JPT][hapmap];0.84[ASN][1000 genomes]
rs8013050	1.00[CHB][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs8015000	0.85[EUR][1000 genomes]
rs8017252	0.82[EUR][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	nsv1040847	chr14:46905206-47869359	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv542085	chr14:46905206-47869359	ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1049865	chr14:46905406-47869220	Enhancers Bivalent/Poised TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv542087	chr14:46905406-47869220	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1048316	chr14:47297113-47885723	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1046326	chr14:47629646-47845903	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv530661	chr14:47754197-47937396	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv498118	chr14:47754197-48274409	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:47812600-47819000	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr14:47813000-47816600	Enhancers	Brain Cingulate Gyrus	brain
3	chr14:47813400-47816200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr14:47813800-47819000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr14:47813800-47822200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr14:47814200-47816200	Enhancers	Brain Substantia Nigra	brain
7	chr14:47814200-47816400	Enhancers	Brain Hippocampus Middle	brain
8	chr14:47815000-47816200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr14:47815800-47816800	Enhancers	Brain Angular Gyrus	brain
10	chr14:47816000-47816200	Enhancers	Brain Inferior Temporal Lobe	brain

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