Variant report

Variant	esv3312326
Chromosome Location	chr15:75203067-75210644
allele	n/a
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	CTCF	chr15:75208714-75208761	GM10248	blood:	n/a	n/a
2	E2F6	chr15:75203968-75204219	K562	blood:	n/a	n/a
3	MAX	chr15:75204148-75204155	K562	blood:	n/a	n/a
4	MAX	chr15:75203943-75204153	K562	blood:	n/a	chr15:75204047-75204056 chr15:75204046-75204056 chr15:75204047-75204056 chr15:75204046-75204056 chr15:75204045-75204058 chr15:75204047-75204056 chr15:75204046-75204057 chr15:75204046-75204057 chr15:75204046-75204057
5	MAX	chr15:75203959-75204289	K562	blood:	n/a	chr15:75204047-75204056 chr15:75204046-75204056 chr15:75204047-75204056 chr15:75204046-75204056 chr15:75204045-75204058 chr15:75204047-75204056 chr15:75204046-75204057 chr15:75204046-75204057 chr15:75204046-75204057
6	MTA3	chr15:75205783-75206115	GM12878	blood:	n/a	n/a
7	MTA3	chr15:75205367-75205871	GM12878	blood:	n/a	n/a
8	MYC	chr15:75204000-75204200	K562	blood:	n/a	chr15:75204047-75204056 chr15:75204046-75204056 chr15:75204047-75204056 chr15:75204046-75204056 chr15:75204045-75204058 chr15:75204047-75204056 chr15:75204046-75204057 chr15:75204046-75204057 chr15:75204046-75204057
9	MYC	chr15:75203982-75204134	K562	blood:	n/a	chr15:75204047-75204056 chr15:75204046-75204056 chr15:75204047-75204056 chr15:75204046-75204056 chr15:75204045-75204058 chr15:75204047-75204056 chr15:75204046-75204057 chr15:75204046-75204057 chr15:75204046-75204057
10	NFATC1	chr15:75203987-75204324	GM12878	blood:	n/a	n/a
11	NFATC1	chr15:75205389-75205977	GM12878	blood:	n/a	n/a
12	POLR2A	chr15:75207979-75208021	HepG2	liver:	n/a	n/a
13	POLR2A	chr15:75204480-75204486	HepG2	liver:	n/a	n/a
14	POLR2A	chr15:75204092-75204126	GM12878	blood:	n/a	n/a
15	POLR2A	chr15:75204682-75206388	PFSK-1	brain:	n/a	n/a
16	POLR2A	chr15:75205464-75206140	K562	blood:	n/a	n/a
17	POLR2A	chr15:75204443-75204453	GM12878	blood:	n/a	n/a
18	POLR2A	chr15:75207098-75207256	K562	blood:	n/a	n/a
19	POLR2A	chr15:75207918-75208107	GM12878	blood:	n/a	n/a
20	POLR2A	chr15:75204559-75205234	K562	blood:	n/a	n/a
21	POLR2A	chr15:75208017-75208373	K562	blood:	n/a	n/a
22	POLR2A	chr15:75206928-75207456	K562	blood:	n/a	n/a
23	POLR2A	chr15:75205367-75206041	HepG2	liver:	n/a	n/a
24	POLR2A	chr15:75206802-75207953	GM12892	blood:	n/a	n/a
25	POLR2A	chr15:75205331-75206037	GM12891	blood:	n/a	n/a
26	POLR2A	chr15:75204136-75204163	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr15:75205796-75206042	HCT-116	colon:	n/a	n/a
28	POLR2A	chr15:75204455-75204540	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr15:75207274-75207426	K562	blood:	n/a	n/a
30	POLR2A	chr15:75207707-75208088	K562	blood:	n/a	n/a
31	POLR2A	chr15:75203858-75205058	K562	blood:	n/a	n/a
32	POLR2A	chr15:75204042-75204702	K562	blood:	n/a	n/a
33	POLR2A	chr15:75205289-75206638	GM12892	blood:	n/a	n/a
34	POLR2A	chr15:75206112-75206616	PFSK-1	brain:	n/a	n/a
35	POLR2A	chr15:75210463-75210749	PFSK-1	brain:	n/a	n/a
36	POLR2A	chr15:75206914-75207369	GM12891	blood:	n/a	n/a
37	POLR2A	chr15:75210492-75210693	K562	blood:	n/a	n/a
38	POLR2A	chr15:75204531-75204784	HepG2	liver:	n/a	n/a
39	POLR2A	chr15:75203246-75203335	HepG2	liver:	n/a	n/a
40	POLR2A	chr15:75204854-75205046	Hela-S3	cervix:	n/a	n/a
41	POLR2A	chr15:75209969-75210623	GM12878	blood:	n/a	n/a
42	POLR2A	chr15:75205616-75206092	Hela-S3	cervix:	n/a	n/a
43	POLR2A	chr15:75206900-75207333	K562	blood:	n/a	n/a
44	POLR2A	chr15:75206265-75206658	GM12891	blood:	n/a	n/a
45	POLR2A	chr15:75204324-75204325	HUVEC	blood vessel:	n/a	n/a
46	POLR2A	chr15:75209923-75210125	HepG2	liver:	n/a	n/a
47	POLR2A	chr15:75210019-75210306	K562	blood:	n/a	n/a
48	POLR2A	chr15:75205026-75205032	A549	lung:	n/a	n/a
49	POLR2A	chr15:75208710-75208978	PFSK-1	brain:	n/a	n/a
50	POLR2A	chr15:75204082-75204116	MCF-7	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:75135584..75137401-chr15:75203123..75205783,2	K562	blood:
2	chr12:120729160..120731044-chr15:75203299..75205954,2	MCF-7	breast:
3	chr15:75196237..75205947-chr15:75227299..75233104,18	K562	blood:
4	chr15:75182811..75184655-chr15:75210487..75213459,2	K562	blood:
5	chr12:17463250..17464018-chr15:75207507..75208367,2	MCF-7	breast:
6	chr15:75205785..75208557-chr15:75213491..75215641,2	MCF-7	breast:
7	chr15:75202900..75206033-chr15:75227299..75230499,5	K562	blood:
8	chr15:75167340..75169926-chr15:75209940..75212819,2	K562	blood:
9	chr15:75197065..75200816-chr15:75202380..75207504,10	K562	blood:
10	chr15:75210535..75212443-chr15:75223416..75224933,2	MCF-7	breast:
11	chr15:75210612..75213940-chr15:75219994..75223601,6	K562	blood:
12	chr15:75197394..75200411-chr15:75201554..75203474,3	MCF-7	breast:
13	chr15:75202516..75204204-chr15:75228807..75231774,3	MCF-7	breast:
14	chr15:75194057..75196372-chr15:75204591..75207418,2	MCF-7	breast:
15	chr15:75210105..75212833-chr15:75214992..75217105,2	K562	blood:
16	chr15:75210426..75213159-chr15:75229718..75232065,4	K562	blood:
17	chr15:75198819..75200407-chr15:75202109..75204144,2	MCF-7	breast:
18	chr15:75204201..75207198-chr15:75248620..75251894,3	MCF-7	breast:
19	chr15:75204307..75205904-chr15:75218795..75220535,2	MCF-7	breast:

Variant related genes	Relation type
FAM219B	TF binding region
ENSG00000198794	chromatin interactions
ENSG00000178741	chromatin interactions
ENSG00000178718	chromatin interactions
ENSG00000140474	chromatin interactions
ENSG00000178802	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000178761	chromatin interactions

Extended variants
information (count: 293 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188083581	chr15:75203179-75203180	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs202185622	chr15:75203182-75203183	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs68036747	chr15:75203200-75203201	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs142834127	chr15:75203223-75203224	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs540916723	chr15:75203255-75203256	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs552647719	chr15:75203290-75203291	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs574395332	chr15:75203298-75203299	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs369448171	chr15:75203310-75203311	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs183603850	chr15:75203313-75203314	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs542507781	chr15:75203327-75203328	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs188316747	chr15:75203329-75203330	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs564006879	chr15:75203355-75203356	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs370933911	chr15:75203486-75203487	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs531107596	chr15:75203499-75203500	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs28715665	chr15:75203521-75203522	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs546468403	chr15:75203525-75203526	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs180937896	chr15:75203544-75203545	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs187266958	chr15:75203545-75203546	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs566645066	chr15:75203577-75203578	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs568326044	chr15:75203581-75203582	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs535769212	chr15:75203603-75203604	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs373545854	chr15:75203638-75203639	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs376176751	chr15:75203714-75203715	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs374215168	chr15:75203715-75203716	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs548056310	chr15:75203735-75203736	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs569660747	chr15:75203758-75203759	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs536837550	chr15:75203798-75203799	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs552046309	chr15:75203799-75203800	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs369774178	chr15:75203804-75203805	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs564550502	chr15:75203805-75203806	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs528681282	chr15:75203808-75203809	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs547215666	chr15:75203812-75203813	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs201897443	chr15:75203835-75203836	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs570628990	chr15:75203836-75203837	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs370883722	chr15:75203891-75203892	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs150103601	chr15:75204006-75204007	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs11072512	chr15:75204026-75204027	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs568837363	chr15:75204061-75204062	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs117379467	chr15:75204168-75204169	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs74708455	chr15:75204182-75204183	Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs557840967	chr15:75204208-75204209	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs535472630	chr15:75204283-75204284	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs572100229	chr15:75204358-75204359	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs151051712	chr15:75204374-75204375	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs576050154	chr15:75204415-75204416	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs546488048	chr15:75204439-75204440	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs564478261	chr15:75204469-75204470	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs573397741	chr15:75204525-75204526	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs74612574	chr15:75204565-75204566	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs367621039	chr15:75204580-75204581	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Epilepsy	22083797	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	16616336	CNVD

Chromatin state (count:359 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75199600-75229400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr15:75199800-75204000	Weak transcription	Lung	lung
3	chr15:75199800-75209400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr15:75199800-75219600	Weak transcription	Aorta	Aorta
5	chr15:75200000-75203800	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr15:75200000-75203800	Weak transcription	Osteobl	bone
7	chr15:75200000-75204000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr15:75200000-75204000	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr15:75200000-75204000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr15:75200000-75204000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr15:75200000-75204000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr15:75200000-75204000	Weak transcription	Primary hematopoietic stem cells	blood
13	chr15:75200000-75204000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr15:75200000-75204000	Weak transcription	NHLF	lung
15	chr15:75200000-75204200	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr15:75200000-75205400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr15:75200000-75205400	Weak transcription	Rectal Smooth Muscle	rectum
18	chr15:75200000-75205400	Weak transcription	HSMMtube	muscle
19	chr15:75200000-75205600	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr15:75200000-75205600	Weak transcription	Primary B cells from cord blood	blood
21	chr15:75200000-75206400	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr15:75200000-75207000	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr15:75200000-75207000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr15:75200000-75207000	Weak transcription	Esophagus	oesophagus
25	chr15:75200000-75207200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr15:75200000-75207200	Weak transcription	Gastric	stomach
27	chr15:75200000-75209600	Weak transcription	Psoas Muscle	Psoas
28	chr15:75200000-75209800	Weak transcription	Ovary	ovary
29	chr15:75200000-75209800	Weak transcription	Small Intestine	intestine
30	chr15:75200000-75211000	Weak transcription	Fetal Kidney	kidney
31	chr15:75200000-75211600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr15:75200000-75221000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr15:75200000-75224000	Weak transcription	Stomach Mucosa	stomach
34	chr15:75200200-75203200	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr15:75200200-75203200	Weak transcription	Left Ventricle	heart
36	chr15:75200200-75203800	Weak transcription	Adipose Nuclei	Adipose
37	chr15:75200200-75203800	Weak transcription	Brain Hippocampus Middle	brain
38	chr15:75200200-75203800	Weak transcription	Duodenum Mucosa	Duodenum
39	chr15:75200200-75203800	Weak transcription	Fetal Intestine Large	intestine
40	chr15:75200200-75203800	Weak transcription	Stomach Smooth Muscle	stomach
41	chr15:75200200-75203800	Weak transcription	Hela-S3	cervix
42	chr15:75200200-75204000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr15:75200200-75204000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr15:75200200-75204000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr15:75200200-75204000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr15:75200200-75204000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr15:75200200-75204000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr15:75200200-75204000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr15:75200200-75204000	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr15:75200200-75204000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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