Variant report

Variant	rs4888430
Chromosome Location	chr16:75494424-75494425
allele	C/T
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	MAX	chr16:75494382-75494768	H1-hESC	embryonic stem cell:	n/a	n/a
2	MAX	chr16:75494362-75494753	H1-hESC	embryonic stem cell:	n/a	n/a
3	SIN3A	chr16:75494422-75494719	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:75492483..75495341-chr16:75495841..75499470,4	K562	blood:
2	chr16:75465942..75469515-chr16:75494275..75497182,4	K562	blood:

Variant related genes	Relation type
ENSG00000261476	TF binding region
ENSG00000166822	Chromatin interaction
ENSG00000153774	Chromatin interaction
ENSG00000261717	Chromatin interaction

Extended variants
information (count: 195 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:186)

rs_ID	r²[population]
rs100912	0.89[CHB][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs1011121	0.81[CEU][hapmap];0.90[CHB][hapmap];0.82[JPT][hapmap]
rs1030261	0.97[ASN][1000 genomes]
rs1030262	0.98[ASN][1000 genomes]
rs10514393	0.85[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap]
rs10514396	0.82[CEU][hapmap];0.90[CHB][hapmap];0.91[JPT][hapmap];0.84[YRI][hapmap];0.82[AFR][1000 genomes]
rs10781976	0.84[CEU][hapmap];0.89[CHB][hapmap];0.81[JPT][hapmap]
rs10781977	0.80[CHB][hapmap]
rs10871308	0.80[CHB][hapmap]
rs10871311	0.80[ASN][1000 genomes]
rs10871312	0.97[ASN][1000 genomes]
rs10871313	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1109342	0.89[CHB][hapmap];0.91[JPT][hapmap]
rs11149812	0.85[CHB][hapmap]
rs11149813	0.83[CHB][hapmap]
rs11149815	0.89[CHB][hapmap];0.88[JPT][hapmap]
rs11149820	0.81[AFR][1000 genomes]
rs11149831	0.90[CHB][hapmap];0.91[JPT][hapmap];0.80[ASN][1000 genomes]
rs11640018	0.89[CHB][hapmap];0.86[JPT][hapmap]
rs11641249	0.96[ASN][1000 genomes]
rs11641430	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11641532	0.85[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap];0.84[YRI][hapmap]
rs11641801	0.80[ASN][1000 genomes]
rs11643207	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11644306	0.97[ASN][1000 genomes]
rs11644639	0.80[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs11645691	0.86[CHB][hapmap]
rs11646677	0.82[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap]
rs11648176	0.80[ASN][1000 genomes]
rs11649638	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11865296	0.83[ASN][1000 genomes]
rs12051137	0.95[ASN][1000 genomes]
rs12149063	0.90[CHB][hapmap];0.91[JPT][hapmap];0.80[ASN][1000 genomes]
rs12443904	0.84[AFR][1000 genomes]
rs12444589	0.89[CHB][hapmap];0.91[JPT][hapmap];0.80[ASN][1000 genomes]
rs12446877	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12448829	0.87[ASN][1000 genomes]
rs12918797	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12924333	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12927562	0.96[ASN][1000 genomes]
rs12928036	0.90[JPT][hapmap];0.96[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs12929673	0.81[ASN][1000 genomes]
rs12932606	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12933281	0.95[CHB][hapmap];0.95[JPT][hapmap];0.96[ASN][1000 genomes]
rs1364078	0.95[CHB][hapmap];0.90[JPT][hapmap];0.84[YRI][hapmap]
rs1424013	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1542864	0.95[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs1549306	0.89[CHB][hapmap];0.91[JPT][hapmap]
rs1559339	0.84[CEU][hapmap];0.89[CHB][hapmap];0.81[JPT][hapmap]
rs166013	0.84[CHB][hapmap]
rs17696696	0.89[CHB][hapmap];0.91[JPT][hapmap]
rs17696749	0.82[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap]
rs17696831	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1834013	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1834014	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1862705	0.81[CHB][hapmap]
rs1862706	0.90[CHB][hapmap];0.91[JPT][hapmap]
rs1895490	0.90[CHB][hapmap];0.91[JPT][hapmap]
rs2059256	0.81[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];0.84[YRI][hapmap]
rs2059257	0.85[CHB][hapmap]
rs2161648	0.80[CEU][hapmap];0.90[CHB][hapmap];0.82[JPT][hapmap]
rs2161684	0.95[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs2242405	0.80[CHB][hapmap]
rs247427	0.85[CHB][hapmap]
rs247438	0.85[CHB][hapmap]
rs247454	0.88[ASN][1000 genomes]
rs2738809	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2738812	0.82[ASN][1000 genomes]
rs2738813	0.82[ASN][1000 genomes]
rs2738814	0.83[ASN][1000 genomes]
rs28558946	0.97[ASN][1000 genomes]
rs2865528	0.84[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs2865530	0.90[CHB][hapmap];0.91[JPT][hapmap]
rs2865531	0.84[CHB][hapmap];0.91[JPT][hapmap]
rs28655617	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2903033	0.95[CHB][hapmap];0.91[JPT][hapmap]
rs3115960	0.88[CEU][hapmap];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34021527	0.85[ASN][1000 genomes]
rs34539062	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34918083	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34996006	0.93[ASN][1000 genomes]
rs35209155	0.81[ASN][1000 genomes]
rs35214308	0.93[ASN][1000 genomes]
rs35263058	0.84[CHB][hapmap];0.91[JPT][hapmap]
rs35683383	0.94[ASN][1000 genomes]
rs35737321	0.83[AFR][1000 genomes]
rs3743607	0.86[JPT][hapmap]
rs3743609	0.86[AFR][1000 genomes]
rs37592	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs37593	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs37594	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs37595	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs37597	0.92[ASN][1000 genomes]
rs37599	0.82[ASN][1000 genomes]
rs37602	0.85[CHB][hapmap];0.82[JPT][hapmap];0.82[ASN][1000 genomes]
rs37605	0.81[ASN][1000 genomes]
rs37606	0.96[ASN][1000 genomes]
rs3784936	0.86[CHB][hapmap]
rs3851733	0.85[CEU][hapmap];0.91[JPT][hapmap]
rs3851734	0.84[CEU][hapmap]
rs3863445	0.85[CEU][hapmap];0.85[CHB][hapmap];0.91[JPT][hapmap]
rs40446	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4146809	0.89[CHB][hapmap];0.91[JPT][hapmap]
rs4146810	0.82[CEU][hapmap];0.90[CHB][hapmap];0.91[JPT][hapmap]
rs4243111	0.84[CEU][hapmap];0.89[CHB][hapmap];0.80[JPT][hapmap]
rs4536500	0.80[CHB][hapmap]
rs4638613	0.84[CEU][hapmap];0.89[CHB][hapmap];0.91[JPT][hapmap]
rs468079	0.80[CHB][hapmap]
rs4887823	0.84[CEU][hapmap];0.90[CHB][hapmap];0.91[JPT][hapmap]
rs4887824	0.90[CHB][hapmap];0.91[JPT][hapmap]
rs4887825	0.81[ASN][1000 genomes]
rs4887828	0.84[CHB][hapmap]
rs4887829	0.81[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4888376	0.81[CEU][hapmap];0.90[CHB][hapmap];0.82[JPT][hapmap]
rs4888377	0.94[CHB][hapmap]
rs4888378	0.89[CHB][hapmap];0.86[JPT][hapmap]
rs4888379	0.85[CEU][hapmap];0.90[CHB][hapmap];0.91[JPT][hapmap];0.90[YRI][hapmap]
rs4888380	0.91[JPT][hapmap];0.83[YRI][hapmap]
rs4888383	0.90[CHB][hapmap];0.91[JPT][hapmap]
rs4888386	0.85[CHB][hapmap];0.91[JPT][hapmap]
rs4888387	0.84[CHB][hapmap];0.91[JPT][hapmap]
rs4888388	0.90[CHB][hapmap];0.91[JPT][hapmap]
rs4888389	0.85[CHB][hapmap];0.91[JPT][hapmap]
rs4888393	0.89[CHB][hapmap]
rs4888396	0.86[CHB][hapmap]
rs4888405	0.89[CHB][hapmap];0.91[JPT][hapmap]
rs4888406	0.80[AFR][1000 genomes]
rs4888415	0.82[CEU][hapmap];0.87[CHB][hapmap];0.91[JPT][hapmap];0.80[ASN][1000 genomes]
rs4888416	0.90[CHB][hapmap];0.91[JPT][hapmap]
rs4888425	0.95[CHB][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs4888426	0.93[ASN][1000 genomes]
rs4888427	0.96[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs4888431	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4888432	0.90[CHB][hapmap];0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs4993969	0.89[CHB][hapmap];0.85[JPT][hapmap]
rs4993971	0.85[CHB][hapmap]
rs56004344	0.86[ASN][1000 genomes]
rs56116092	0.96[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs59155720	0.94[ASN][1000 genomes]
rs59347518	0.92[ASN][1000 genomes]
rs59465235	0.96[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs60730309	0.80[AFR][1000 genomes]
rs62060550	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62060551	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62062567	0.83[AFR][1000 genomes]
rs62062568	0.84[AFR][1000 genomes]
rs6564261	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67409275	0.84[AFR][1000 genomes]
rs7188231	0.82[AFR][1000 genomes]
rs7188604	0.90[CHB][hapmap];0.91[JPT][hapmap];0.80[ASN][1000 genomes]
rs7189407	0.85[CHB][hapmap]
rs7191890	0.83[ASN][1000 genomes]
rs7193828	0.89[ASN][1000 genomes]
rs7194035	0.89[ASN][1000 genomes]
rs7195161	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7198873	0.92[ASN][1000 genomes]
rs7199062	0.96[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs7199132	0.89[CHB][hapmap];0.95[JPT][hapmap];0.80[ASN][1000 genomes]
rs7200053	0.93[ASN][1000 genomes]
rs7202596	0.97[ASN][1000 genomes]
rs7203157	0.90[CHB][hapmap];0.91[JPT][hapmap]
rs7204984	0.95[CHB][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs7206665	0.90[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs7499872	0.80[AFR][1000 genomes]
rs766521	0.89[CHB][hapmap];0.91[JPT][hapmap]
rs766522	0.85[CHB][hapmap]
rs8046109	0.84[CEU][hapmap];0.91[JPT][hapmap]
rs8046416	0.85[CHB][hapmap]
rs8048677	0.86[CHB][hapmap]
rs8048816	0.85[CHB][hapmap]
rs8050059	0.89[CHB][hapmap];0.91[JPT][hapmap]
rs8054586	0.86[CHB][hapmap]
rs8055490	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8055609	0.86[CHB][hapmap]
rs8055974	0.80[CHB][hapmap];0.81[ASN][1000 genomes]
rs8056141	0.83[ASN][1000 genomes]
rs8057084	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8063068	0.96[ASN][1000 genomes]
rs889446	0.85[CHB][hapmap]
rs977985	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs977986	0.81[ASN][1000 genomes]
rs977987	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9922008	0.88[CHB][hapmap]
rs9923834	0.81[ASN][1000 genomes]
rs9933255	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9934007	0.80[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916502	chr16:74845880-75732365	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	131 gene(s)	inside rSNPs	diseases
2	nsv931939	chr16:75261354-75765025	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
3	nsv1065995	chr16:75373756-75626027	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
4	nsv1063718	chr16:75395969-75608071	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	64 gene(s)	inside rSNPs	diseases
5	esv2758432	chr16:75419614-75576971	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
6	esv2758657	chr16:75419614-75576971	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
7	nsv525955	chr16:75473332-75628345	Strong transcription Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
8	nsv457521	chr16:75487758-75603925	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
9	nsv572979	chr16:75487758-75603925	Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs4888430	RP11-252K23.2	cis	lung	GTEx
rs4888430	CFDP1	Cis_1M	lymphoblastoid	RTeQTL
rs4888430	RP11-252K23.2	cis	Esophagus Mucosa	GTEx
rs4888430	RP11-252K23.2	cis	Thyroid	GTEx
rs4888430	RP11-252K23.2	cis	Artery Tibial	GTEx

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:75468800-75497000	Weak transcription	NHLF	lung
2	chr16:75469400-75497000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr16:75469400-75497400	Weak transcription	Psoas Muscle	Psoas
4	chr16:75473600-75496000	Weak transcription	HMEC	breast
5	chr16:75477800-75497000	Weak transcription	NHDF-Ad	bronchial
6	chr16:75481800-75497600	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr16:75483200-75495800	Weak transcription	Fetal Brain Male	brain
8	chr16:75483800-75496000	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr16:75484000-75496600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr16:75484000-75496800	Weak transcription	Primary hematopoietic stem cells	blood
11	chr16:75485400-75496800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr16:75485600-75495800	Weak transcription	Stomach Smooth Muscle	stomach
13	chr16:75485600-75496400	Weak transcription	Primary B cells from peripheral blood	blood
14	chr16:75485600-75497200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr16:75485800-75494600	Weak transcription	Brain Substantia Nigra	brain
16	chr16:75485800-75494600	Weak transcription	Hela-S3	cervix
17	chr16:75485800-75495200	Weak transcription	Dnd41	blood
18	chr16:75485800-75496000	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr16:75485800-75496400	Weak transcription	Primary B cells from cord blood	blood
20	chr16:75485800-75496400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr16:75485800-75496800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr16:75485800-75496800	Weak transcription	Fetal Kidney	kidney
23	chr16:75485800-75496800	Weak transcription	Rectal Smooth Muscle	rectum
24	chr16:75485800-75497000	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr16:75485800-75497000	Weak transcription	Fetal Thymus	thymus
26	chr16:75485800-75497000	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr16:75485800-75497200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr16:75485800-75497400	Weak transcription	Fetal Brain Female	brain
29	chr16:75485800-75497600	Weak transcription	Aorta	Aorta
30	chr16:75486000-75496800	Weak transcription	Thymus	Thymus
31	chr16:75486400-75496800	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr16:75487000-75495600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr16:75487200-75494800	Weak transcription	Brain Hippocampus Middle	brain
34	chr16:75487200-75496600	Weak transcription	HUVEC	blood vessel
35	chr16:75488200-75495400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr16:75489000-75496800	Weak transcription	K562	blood
37	chr16:75489400-75495400	Enhancers	Small Intestine	intestine
38	chr16:75489800-75497400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr16:75490400-75496400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr16:75491000-75496800	Enhancers	Fetal Intestine Large	intestine
41	chr16:75491600-75494600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr16:75491800-75497200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr16:75491800-75497200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr16:75491800-75497400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr16:75492000-75496000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr16:75492000-75496800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr16:75492400-75495000	Weak transcription	Stomach Mucosa	stomach
48	chr16:75492400-75495200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr16:75492400-75496200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr16:75492600-75495000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links