Variant report

Variant	rs2447215
Chromosome Location	chr15:43941722-43941723
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	POU2F2	chr15:43941593-43942157	GM12878	blood:	n/a	n/a
2	POLR2A	chr15:43941576-43941779	GM12878	blood:	n/a	n/a
3	EBF1	chr15:43941664-43942043	GM12878	blood:	n/a	chr15:43941896-43941909 chr15:43941898-43941907
4	SPI1	chr15:43941665-43941774	GM12878	blood:	n/a	n/a
5	TAF1	chr15:43940574-43941889	H1-hESC	embryonic stem cell:	n/a	n/a
6	EBF1	chr15:43941590-43942053	GM12878	blood:	n/a	chr15:43941896-43941909 chr15:43941898-43941907
7	POLR2A	chr15:43940716-43942212	H1-hESC	embryonic stem cell:	n/a	n/a
8	TAF1	chr15:43941614-43942044	Hela-S3	cervix:	n/a	n/a
9	POLR2A	chr15:43941656-43941958	HUVEC	blood vessel:	n/a	n/a
10	POLR2A	chr15:43941542-43942083	Hela-S3	cervix:	n/a	n/a
11	POLR2A	chr15:43940710-43942109	Hela-S3	cervix:	n/a	n/a
12	POLR2A	chr15:43941526-43942103	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr15:43940739-43942035	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr15:43940921-43942115	GM12892	blood:	n/a	n/a
15	POLR2A	chr15:43941540-43942091	H1-hESC	embryonic stem cell:	n/a	n/a
16	SPI1	chr15:43941647-43942007	K562	blood:	n/a	chr15:43941879-43941892
17	SPI1	chr15:43941609-43942027	GM12878	blood:	n/a	chr15:43941879-43941892
18	POLR2A	chr15:43941587-43942154	GM12892	blood:	n/a	n/a
19	POLR2A	chr15:43940696-43942095	HepG2	liver:	n/a	n/a
20	POLR2A	chr15:43941621-43941786	GM12878	blood:	n/a	n/a
21	POLR2A	chr15:43941566-43942151	GM12878	blood:	n/a	n/a
22	SPI1	chr15:43941604-43942005	K562	blood:	n/a	chr15:43941879-43941892
23	POLR2A	chr15:43940977-43942045	K562	blood:	n/a	n/a
24	POLR2A	chr15:43941562-43942129	GM12878	blood:	n/a	n/a
25	POLR2A	chr15:43941511-43941890	GM12878	blood:	n/a	n/a
26	HEY1	chr15:43941600-43941863	K562	blood:	n/a	chr15:43941691-43941706
27	SPI1	chr15:43941609-43942004	GM12891	blood:	n/a	chr15:43941879-43941892
28	HEY1	chr15:43941561-43942136	K562	blood:	n/a	chr15:43941691-43941706
29	POLR2A	chr15:43941588-43942121	GM12891	blood:	n/a	n/a
30	SPI1	chr15:43941607-43942079	GM12891	blood:	n/a	chr15:43941879-43941892

Variant related genes	Relation type
CATSPER2	TF binding region

Extended variants
information (count: 123 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs11856184	0.98[ASN][1000 genomes]
rs11857661	1.00[ASN][1000 genomes]
rs12443102	1.00[ASN][1000 genomes]
rs2259174	0.88[ASN][1000 genomes]
rs2411284	0.80[AFR][1000 genomes]
rs2439	0.88[ASN][1000 genomes]
rs2447193	1.00[ASN][1000 genomes]
rs2447195	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2447196	0.90[ASN][1000 genomes]
rs2447197	0.89[ASN][1000 genomes]
rs2447198	0.81[ASN][1000 genomes]
rs2447208	1.00[ASN][1000 genomes]
rs2447210	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2447211	1.00[ASN][1000 genomes]
rs2447212	1.00[ASN][1000 genomes]
rs2447213	0.98[ASN][1000 genomes]
rs2447216	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2470120	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2470121	1.00[ASN][1000 genomes]
rs2470124	0.84[ASN][1000 genomes]
rs2470135	0.85[EUR][1000 genomes]
rs2614819	0.91[ASN][1000 genomes]
rs2614822	0.91[ASN][1000 genomes]
rs28366727	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28606452	0.97[ASN][1000 genomes]
rs28704825	0.84[ASN][1000 genomes]
rs28758851	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2915776	0.98[ASN][1000 genomes]
rs2915779	0.96[ASN][1000 genomes]
rs2915792	0.92[ASN][1000 genomes]
rs2920780	0.90[ASN][1000 genomes]
rs2920781	0.93[ASN][1000 genomes]
rs2920782	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2927070	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2927071	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2927072	0.98[ASN][1000 genomes]
rs2927075	0.96[ASN][1000 genomes]
rs2957636	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2957637	0.98[ASN][1000 genomes]
rs2957639	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3099045	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3099047	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35654783	0.83[EUR][1000 genomes]
rs4332723	0.82[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs4924720	0.83[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs57865312	0.98[ASN][1000 genomes]
rs7175129	0.83[EUR][1000 genomes]
rs8042868	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:75 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1846172	chr15:43632138-44116986	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
2	esv1846701	chr15:43759774-44116986	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
3	nsv437799	chr15:43784000-43989518	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Active TSS Enhancers Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv832988	chr15:43804641-43976862	Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
5	nsv428304	chr15:43823158-44008580	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	esv2758379	chr15:43823158-44148641	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
7	esv2760028	chr15:43823158-44148641	Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
8	nsv427960	chr15:43823158-44148641	Flanking Active TSS Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
9	nsv428633	chr15:43823160-44008580	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
10	nsv1039949	chr15:43831879-43992646	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
11	esv2757598	chr15:43831923-44058634	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription 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	31 gene(s)	inside rSNPs	diseases
12	esv2761766	chr15:43834318-44014255	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
13	nsv904148	chr15:43836478-43961204	Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
14	nsv904149	chr15:43836478-44011113	Weak transcription Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
15	nsv904150	chr15:43836478-44040965	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
16	nsv1039818	chr15:43845410-43988541	Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
17	nsv1048041	chr15:43845410-43991014	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
18	esv2760393	chr15:43845422-44024490	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
19	nsv870240	chr15:43851142-43988761	Strong transcription Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
20	nsv534652	chr15:43851548-43948346	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
21	nsv994950	chr15:43851548-43951301	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
22	nsv904153	chr15:43852043-43951118	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
23	nsv904154	chr15:43852043-43961204	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
24	nsv904155	chr15:43852043-43988573	Weak transcription Strong transcription Bivalent Enhancer Active TSS Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
25	nsv904156	chr15:43852043-44011113	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
26	nsv904157	chr15:43852043-44019592	Bivalent Enhancer Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
27	nsv904158	chr15:43852043-44053617	Strong transcription Flanking Active TSS Active TSS Enhancers Weak transcription 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	31 gene(s)	inside rSNPs	diseases
28	esv3413623	chr15:43852060-43973058	Weak transcription Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
29	esv13634	chr15:43852144-43988641	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
30	esv3506095	chr15:43853954-43953553	Weak transcription Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
31	esv3506097	chr15:43853954-43953553	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
32	nsv1514	chr15:43859260-43996580	Weak transcription Strong transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
33	nsv904161	chr15:43873489-43961204	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
34	nsv904162	chr15:43873489-44011113	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
35	nsv904163	chr15:43873489-44023963	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
36	esv2421427	chr15:43885118-43988553	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
37	nsv1037786	chr15:43888926-44318587	Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
38	nsv542370	chr15:43888926-44318587	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription 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 miRNA target site	90 gene(s)	inside rSNPs	diseases
39	nsv868983	chr15:43888927-43951301	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
40	nsv915702	chr15:43888952-43951317	ZNF genes & repeats Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
41	esv33424	chr15:43888955-43995223	Strong transcription Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
42	esv3443586	chr15:43889625-43973121	Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
43	nsv569245	chr15:43891512-43980509	Weak transcription Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
44	nsv569246	chr15:43891512-43980721	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
45	nsv1035221	chr15:43893072-43976406	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
46	nsv1036941	chr15:43893072-43988312	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
47	nsv1047829	chr15:43893072-43988541	Strong transcription Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
48	nsv1037061	chr15:43893072-43990416	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
49	nsv1040028	chr15:43893072-43992646	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
50	nsv1049269	chr15:43893072-43995876	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs2447215	CKMT1A	cis	Esophagus Mucosa	GTEx
rs2447215	STRCP1	cis	Thyroid	GTEx
rs2447215	ZSCAN29	cis	Thyroid	GTEx
rs2447215	AC011330.5	cis	Artery Tibial	GTEx
rs2447215	AC011330.5	cis	Thyroid	GTEx

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43921400-43950400	Weak transcription	Aorta	Aorta
2	chr15:43921800-43952600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr15:43923200-43951800	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr15:43931200-43943600	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr15:43931200-43952000	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr15:43931200-43952600	Weak transcription	Left Ventricle	heart
7	chr15:43931400-43942400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr15:43932800-43943600	Weak transcription	NHEK	skin
9	chr15:43935200-43942200	Weak transcription	Esophagus	oesophagus
10	chr15:43935400-43943200	Weak transcription	Ovary	ovary
11	chr15:43936000-43951800	Weak transcription	Primary T cells from cord blood	blood
12	chr15:43936000-43956000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr15:43936400-43943800	Weak transcription	Fetal Brain Male	brain
14	chr15:43937200-43943200	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr15:43937400-43942000	Strong transcription	Fetal Intestine Small	intestine
16	chr15:43937600-43942000	Weak transcription	Liver	Liver
17	chr15:43937600-43943400	Weak transcription	Adipose Nuclei	Adipose
18	chr15:43937600-43943400	Weak transcription	Brain Germinal Matrix	brain
19	chr15:43937800-43942000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr15:43937800-43943200	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr15:43938200-43943600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr15:43938400-43942200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr15:43939000-43942400	Strong transcription	Duodenum Mucosa	Duodenum
24	chr15:43939200-43942200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr15:43939200-43942200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr15:43939200-43942400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr15:43939200-43951000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr15:43939400-43943600	Weak transcription	Primary B cells from peripheral blood	blood
29	chr15:43939600-43941800	Strong transcription	Lung	lung
30	chr15:43939800-43942400	Weak transcription	Placenta	Placenta
31	chr15:43940200-43941800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr15:43940200-43942200	Strong transcription	Right Ventricle	heart
33	chr15:43940200-43942400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
34	chr15:43940400-43942200	Weak transcription	Pancreas	Pancrea
35	chr15:43940600-43942200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr15:43940600-43942400	Strong transcription	Gastric	stomach
37	chr15:43940600-43943600	Weak transcription	Brain Angular Gyrus	brain
38	chr15:43940800-43941800	Strong transcription	Sigmoid Colon	Sigmoid Colon
39	chr15:43940800-43942200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
40	chr15:43940800-43943000	Weak transcription	Colonic Mucosa	Colon
41	chr15:43940800-43943200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr15:43940800-43943600	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr15:43941000-43941800	Weak transcription	Primary T cells fromperipheralblood	blood
44	chr15:43941000-43941800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr15:43941000-43941800	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
46	chr15:43941000-43942000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr15:43941000-43942200	Strong transcription	Spleen	Spleen
48	chr15:43941000-43942400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr15:43941000-43942400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr15:43941000-43942400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood

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