Variant report

Variant	rs12591751
Chromosome Location	chr15:50972497-50972498
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:50967277..50972737-chr15:50976604..50980349,6	K562	blood:
2	chr15:50970140..50972080-chr15:50972168..50973694,2	MCF-7	breast:
3	chr15:50966292..50969121-chr15:50972031..50974489,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000092439	Chromatin interaction

Extended variants
information (count: 135 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:108)

rs_ID	r²[population]
rs11070798	0.87[EUR][1000 genomes]
rs11070799	0.88[EUR][1000 genomes]
rs11070800	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs11070801	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11070802	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11070805	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11070807	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11634746	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11636964	0.93[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs11637228	0.89[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs12437770	0.88[ASN][1000 genomes]
rs12437783	0.88[ASN][1000 genomes]
rs12437803	0.88[ASN][1000 genomes]
rs12438305	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12439744	0.93[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs12440712	0.83[ASN][1000 genomes]
rs12440864	0.81[ASN][1000 genomes]
rs12441679	0.88[EUR][1000 genomes]
rs12442197	0.89[ASN][1000 genomes]
rs12442721	0.90[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs12442787	0.93[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs12443147	0.99[ASN][1000 genomes]
rs12591188	1.00[ASN][1000 genomes]
rs12592778	0.82[ASN][1000 genomes]
rs12593556	0.83[ASN][1000 genomes]
rs12595082	0.81[ASN][1000 genomes]
rs12595151	0.86[EUR][1000 genomes]
rs12595562	1.00[ASN][1000 genomes]
rs1395297	0.80[EUR][1000 genomes]
rs17645523	0.87[EUR][1000 genomes]
rs17645649	0.88[EUR][1000 genomes]
rs17645826	0.89[EUR][1000 genomes]
rs17645935	0.89[ASN][1000 genomes]
rs1986074	0.83[EUR][1000 genomes]
rs2011064	0.93[AFR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2063010	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2115671	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2292174	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2414060	0.86[EUR][1000 genomes]
rs2414064	0.81[ASN][1000 genomes]
rs2630	0.84[EUR][1000 genomes]
rs28494067	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs28718130	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs28817917	0.80[AFR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2899462	0.88[EUR][1000 genomes]
rs3101852	0.84[EUR][1000 genomes]
rs3101853	0.83[EUR][1000 genomes]
rs3101854	0.83[EUR][1000 genomes]
rs3101855	0.86[EUR][1000 genomes]
rs3101856	0.80[EUR][1000 genomes]
rs3105590	0.86[EUR][1000 genomes]
rs3105591	0.86[EUR][1000 genomes]
rs3109879	0.82[EUR][1000 genomes]
rs3109880	0.81[EUR][1000 genomes]
rs3109881	0.82[EUR][1000 genomes]
rs3109884	0.82[EUR][1000 genomes]
rs3109888	0.86[EUR][1000 genomes]
rs3109891	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs3109892	0.85[EUR][1000 genomes]
rs3109894	0.86[EUR][1000 genomes]
rs3109895	0.86[EUR][1000 genomes]
rs3131573	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs3131577	0.86[EUR][1000 genomes]
rs3131578	0.86[EUR][1000 genomes]
rs3131580	0.84[EUR][1000 genomes]
rs3131581	0.83[EUR][1000 genomes]
rs3131582	0.93[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs3131585	0.84[EUR][1000 genomes]
rs3131586	0.80[EUR][1000 genomes]
rs3131587	0.84[EUR][1000 genomes]
rs3131589	0.83[EUR][1000 genomes]
rs3131590	0.83[EUR][1000 genomes]
rs3131596	0.86[EUR][1000 genomes]
rs34386878	0.90[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs35701852	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3848129	0.88[EUR][1000 genomes]
rs3848130	0.93[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs4509958	0.90[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs4775893	0.88[EUR][1000 genomes]
rs4775897	0.93[AFR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs55916605	0.83[ASN][1000 genomes]
rs56015123	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56015830	0.87[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs56069965	0.93[AFR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56080544	0.93[AFR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs56118429	0.92[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs56944208	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs57002197	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs59685680	0.88[ASN][1000 genomes]
rs60155540	0.88[ASN][1000 genomes]
rs62017189	0.93[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs62017197	0.93[AFR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs62017203	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62017204	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62017206	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62017210	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62017243	0.96[AFR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7167138	0.93[AFR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72740456	0.80[ASN][1000 genomes]
rs72740476	0.83[ASN][1000 genomes]
rs72740493	0.88[ASN][1000 genomes]
rs8023644	0.90[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs8027316	0.82[EUR][1000 genomes]
rs8029073	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs8033256	0.91[AFR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8036588	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs934624	0.93[AFR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs934625	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045456	chr15:50592472-51019873	Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
2	nsv948579	chr15:50645530-51045564	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
3	nsv1053966	chr15:50715572-51133186	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
4	nsv542383	chr15:50715572-51133186	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
5	nsv1043805	chr15:50715572-51208891	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
6	nsv542384	chr15:50715572-51208891	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
7	nsv1047443	chr15:50744781-51647023	Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
8	nsv1051990	chr15:50745814-51133186	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
9	nsv1054970	chr15:50761410-51036625	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
10	nsv457134	chr15:50770868-51184583	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
11	nsv471242	chr15:50770868-51184583	Genic enhancers ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
12	nsv569396	chr15:50770868-51184583	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
13	nsv457135	chr15:50770868-51189707	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
14	nsv569397	chr15:50770868-51189707	Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
15	nsv1048621	chr15:50775451-51115535	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
16	nsv1047039	chr15:50782070-51187804	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
17	nsv542385	chr15:50782070-51187804	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
18	nsv457136	chr15:50789125-51294995	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
19	nsv569398	chr15:50789125-51294995	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
20	nsv431389	chr15:50795835-50979738	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
21	nsv1036081	chr15:50818569-51097229	Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
22	nsv1055112	chr15:50822035-51133186	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
23	nsv1042372	chr15:50846461-51208891	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
24	nsv542386	chr15:50846461-51208891	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
25	nsv569399	chr15:50874964-51562198	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
26	nsv569400	chr15:50874964-51767265	ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
27	nsv1051400	chr15:50890333-51046283	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12591751	SPPL2A	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:50906400-50977400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:50923400-50977600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr15:50923600-50977600	Weak transcription	Brain Substantia Nigra	brain
4	chr15:50935000-50975800	Weak transcription	Pancreas	Pancrea
5	chr15:50938800-50976200	Weak transcription	Gastric	stomach
6	chr15:50939400-50975400	Weak transcription	Brain Angular Gyrus	brain
7	chr15:50943400-50973600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr15:50943400-50975200	Weak transcription	Spleen	Spleen
9	chr15:50946200-50977200	Weak transcription	Rectal Smooth Muscle	rectum
10	chr15:50946800-50977600	Weak transcription	Brain Cingulate Gyrus	brain
11	chr15:50948800-50975600	Weak transcription	Thymus	Thymus
12	chr15:50948800-50977200	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr15:50949000-50977800	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr15:50949200-50977000	Weak transcription	Brain Anterior Caudate	brain
15	chr15:50949200-50977200	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr15:50950000-50976200	Weak transcription	Fetal Brain Female	brain
17	chr15:50950000-50976800	Weak transcription	Brain Hippocampus Middle	brain
18	chr15:50950000-50976800	Weak transcription	Stomach Smooth Muscle	stomach
19	chr15:50950000-50977000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr15:50950000-50977000	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr15:50950200-50977400	Weak transcription	Fetal Lung	lung
22	chr15:50950800-50977400	Weak transcription	Ovary	ovary
23	chr15:50951000-50976800	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr15:50954400-50977200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr15:50954600-50975600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr15:50955000-50975600	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr15:50955000-50975800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr15:50955600-50976600	Weak transcription	HUVEC	blood vessel
29	chr15:50956200-50975000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr15:50956200-50976800	Weak transcription	Primary hematopoietic stem cells	blood
31	chr15:50956200-50977000	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr15:50956200-50977400	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr15:50957400-50977600	Weak transcription	Fetal Intestine Large	intestine
34	chr15:50959200-50976800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr15:50959400-50972600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr15:50959400-50975600	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr15:50959600-50973800	Weak transcription	Fetal Muscle Trunk	muscle
38	chr15:50959800-50978000	Weak transcription	Esophagus	oesophagus
39	chr15:50960600-50976000	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr15:50961200-50977000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr15:50961600-50975400	Weak transcription	Duodenum Mucosa	Duodenum
42	chr15:50961800-50973400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr15:50961800-50973600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr15:50965200-50976000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr15:50966200-50976800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr15:50966400-50975200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr15:50966400-50976600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr15:50966600-50975200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr15:50966600-50976400	Weak transcription	Fetal Thymus	thymus
50	chr15:50967200-50976000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links