Variant report

Variant	nsv441808
Chromosome Location	chr7:6854110-6864083
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:51)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:51 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr7:6861480-6861661	IMR90	lung:	n/a	chr7:6861544-6861553 chr7:6861542-6861553
2	CTCF	chr7:6855541-6855596	LNCaP	prostate:	n/a	n/a
3	EBF1	chr7:6855414-6855674	GM12878	blood:	n/a	chr7:6855538-6855551 chr7:6855539-6855549 chr7:6855540-6855549
4	GATA2	chr7:6861636-6861653	SH-SY5Y	brain:	n/a	n/a
5	MYC	chr7:6854857-6854901	MCF-7	breast:	n/a	n/a
6	MYC	chr7:6854803-6854908	MCF-7	breast:	n/a	n/a
7	POLR2A	chr7:6854812-6854938	MCF-7	breast:	n/a	n/a
8	POLR2A	chr7:6855088-6855265	GM12878	blood:	n/a	n/a
9	POLR2A	chr7:6854788-6854932	MCF-7	breast:	n/a	n/a
10	POLR2A	chr7:6854788-6855080	GM12878	blood:	n/a	n/a
11	POLR2A	chr7:6854781-6856056	GM12878	blood:	n/a	n/a
12	POLR2A	chr7:6855436-6855495	H1-hESC	embryonic stem cell:	n/a	n/a
13	POLR2A	chr7:6857130-6857171	MCF-7	breast:	n/a	n/a
14	POLR2A	chr7:6856859-6856912	HUVEC	blood vessel:	n/a	n/a
15	POLR2A	chr7:6855541-6855578	HUVEC	blood vessel:	n/a	n/a
16	POLR2A	chr7:6856185-6857415	GM12892	blood:	n/a	n/a
17	POLR2A	chr7:6855194-6855736	K562	blood:	n/a	n/a
18	POLR2A	chr7:6856312-6857008	GM12892	blood:	n/a	n/a
19	POLR2A	chr7:6854794-6854985	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr7:6854817-6855251	GM12878	blood:	n/a	n/a
21	POLR2A	chr7:6856162-6857412	GM12878	blood:	n/a	n/a
22	POLR2A	chr7:6854735-6855229	GM12892	blood:	n/a	n/a
23	POLR2A	chr7:6856703-6856970	GM12878	blood:	n/a	n/a
24	POLR2A	chr7:6855472-6855521	GM12878	blood:	n/a	n/a
25	POLR2A	chr7:6862398-6862490	MCF-7	breast:	n/a	n/a
26	POLR2A	chr7:6855009-6855073	K562	blood:	n/a	n/a
27	POLR2A	chr7:6854714-6855681	GM12892	blood:	n/a	n/a
28	POLR2A	chr7:6855404-6855452	GM12878	blood:	n/a	n/a
29	POLR2A	chr7:6856266-6856282	K562	blood:	n/a	n/a
30	POLR2A	chr7:6855965-6856297	HepG2	liver:	n/a	n/a
31	POLR2A	chr7:6856650-6856912	K562	blood:	n/a	n/a
32	POLR2A	chr7:6855077-6855084	K562	blood:	n/a	n/a
33	POLR2A	chr7:6857020-6857253	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr7:6859375-6859510	HUVEC	blood vessel:	n/a	n/a
35	POLR2A	chr7:6856852-6857219	GM12878	blood:	n/a	n/a
36	POLR2A	chr7:6854778-6855618	GM12892	blood:	n/a	n/a
37	POLR2A	chr7:6856875-6857093	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr7:6856941-6856956	K562	blood:	n/a	n/a
39	POLR2A	chr7:6856806-6856844	HUVEC	blood vessel:	n/a	n/a
40	POLR2A	chr7:6856514-6857118	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr7:6856356-6857354	GM12892	blood:	n/a	n/a
42	POLR2A	chr7:6857089-6857193	K562	blood:	n/a	n/a
43	POLR2A	chr7:6856884-6857111	HepG2	liver:	n/a	n/a
44	POLR2A	chr7:6854062-6854577	GM12878	blood:	n/a	n/a
45	POLR2A	chr7:6863192-6863296	MCF-7	breast:	n/a	n/a
46	POLR2A	chr7:6854796-6855156	HepG2	liver:	n/a	n/a
47	POLR2A	chr7:6854991-6855381	PANC-1	pancreas:	n/a	n/a
48	POLR2A	chr7:6856681-6857174	GM12878	blood:	n/a	n/a
49	POLR2A	chr7:6854749-6855100	GM12892	blood:	n/a	n/a
50	POLR2A	chr7:6856862-6856873	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6861742-6861792	NB4	blood:	n/a
2	chr7:6861742-6861792	HMEC	breast:	n/a
3	chr7:6861742-6861792	GM19239	blood:	n/a
4	chr7:6861742-6861792	HAEpiC	amniotic membrane:	n/a
5	chr7:6861742-6861792	ECC-1	luminal epithelium:	n/a
6	chr7:6861742-6861792	Hepatocyte	liver:	n/a
7	chr7:6861742-6861792	HIPEpiC	eye:	n/a
8	chr7:6861742-6861792	CMK	blood:	n/a
9	chr7:6861742-6861792	AG10803	skin:	n/a
10	chr7:6861742-6861792	HEK293	kidney:	embryo
11	chr7:6861742-6861792	SK-N-SH_RA	brain:	n/a
12	chr7:6861742-6861792	GM12891	blood:	n/a
13	chr7:6861742-6861792	ProgFib	skin:	n/a
14	chr7:6861742-6861792	SKMC	muscle:	n/a
15	chr7:6861742-6861792	SK-N-SH	brain:	n/a
16	chr7:6861742-6861792	NT2-D1	testis:	n/a
17	chr7:6861742-6861792	PANC-1	pancreas:	n/a
18	chr7:6861742-6861792	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:6861742-6861792	H1-hESC	embryonic stem cell:	embryo
20	chr7:6861742-6861792	GM12878	blood:	n/a
21	chr7:6861742-6861792	HNPCEpiC	eye:	n/a
22	chr7:6861742-6861792	ovcar-3	ovarian:	n/a
23	chr7:6861742-6861792	U87	brain:	n/a
24	chr7:6861742-6861792	NHDF-neo	bronchial:	n/a
25	chr7:6861742-6861792	AG04449	skin:	fetal
26	chr7:6861742-6861792	RPTEC	kidney:	n/a
27	chr7:6861742-6861792	HL-60	blood:	n/a
28	chr7:6861742-6861792	NHBE	bronchial:	n/a
29	chr7:6861742-6861792	LNCaP	prostate:	n/a
30	chr7:6861742-6861792	MCF10A-Er-Src	breast:	n/a
31	chr7:6861742-6861792	HRE	kidney:	n/a
32	chr7:6861742-6861792	BJ	skin:	n/a
33	chr7:6861742-6861792	GM12892	blood:	n/a
34	chr7:6861742-6861792	HUVEC	blood vessel:	n/a
35	chr7:6861742-6861792	HCPEpiC	choroid plexus:	n/a
36	chr7:6861742-6861792	SAEC	small airway:	n/a
37	chr7:6861742-6861792	PrEC	prostate:	n/a
38	chr7:6861742-6861792	HepG2	liver:	n/a
39	chr7:6861742-6861792	GM06990	blood:	n/a
40	chr7:6861742-6861792	AG09319	gingival:	n/a
41	chr7:6861742-6861792	MCF-7	breast:	n/a
42	chr7:6861742-6861792	A549	lung:	n/a
43	chr7:6861742-6861792	HEEpiC	esophagus:	n/a
44	chr7:6861742-6861792	AoSMC	blood vessel:	n/a
45	chr7:6861742-6861792	NH-A	brain:	n/a
46	chr7:6861742-6861792	SK-N-MC	brain:	n/a
47	chr7:6861742-6861792	Caco-2	colon:	n/a
48	chr7:6861742-6861792	HCF	heart:	n/a
49	chr7:6861742-6861792	T-47D	breast:	n/a
50	chr7:6861742-6861792	Hela-S3	cervix:	n/a

No data

Variant related genes	Relation type
CCZ1B	TF binding region
CCZ1B	CpG island

Extended variants
information (count: 582 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:582 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145260041	chr7:6854122-6854123	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs113037857	chr7:6854142-6854143	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs552005434	chr7:6854146-6854147	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs182312487	chr7:6854225-6854226	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs572217717	chr7:6854234-6854235	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs546079817	chr7:6854236-6854237	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs147610105	chr7:6854250-6854251	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs57389608	chr7:6854266-6854267	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs11769113	chr7:6854272-6854273	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs61406768	chr7:6854277-6854278	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs140135954	chr7:6854282-6854283	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs561792632	chr7:6854296-6854297	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs374226938	chr7:6854302-6854303	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs60726007	chr7:6854312-6854313	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs546071014	chr7:6854340-6854341	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs187418851	chr7:6854354-6854355	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs137998747	chr7:6854367-6854368	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs60908776	chr7:6854372-6854373	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs372190290	chr7:6854373-6854374	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs565674948	chr7:6854378-6854379	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs189822152	chr7:6854385-6854386	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs369856072	chr7:6854387-6854388	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs201773082	chr7:6854423-6854424	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs376254803	chr7:6854440-6854441	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs569912315	chr7:6854457-6854458	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs377404953	chr7:6854479-6854480	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs370149338	chr7:6854486-6854487	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs138393587	chr7:6854506-6854507	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs143064541	chr7:6854511-6854512	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs58851147	chr7:6854512-6854513	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs373962454	chr7:6854524-6854525	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs534811722	chr7:6854572-6854573	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs62441814	chr7:6854616-6854617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200834010	chr7:6854651-6854652	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182336326	chr7:6854721-6854722	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs545768036	chr7:6854722-6854723	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs74296214	chr7:6854750-6854751	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs186998940	chr7:6854771-6854772	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs201412009	chr7:6854782-6854783	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs116997173	chr7:6854785-6854786	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs190336162	chr7:6854794-6854795	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs200922002	chr7:6854803-6854804	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs554919545	chr7:6854807-6854808	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs533191535	chr7:6854840-6854841	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs576280166	chr7:6854843-6854844	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs183303499	chr7:6854857-6854858	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs561889775	chr7:6854859-6854860	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs202054778	chr7:6854890-6854891	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs551267846	chr7:6854920-6854921	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs200941590	chr7:6854921-6854922	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:325 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6831400-6856600	Weak transcription	Thymus	Thymus
2	chr7:6832000-6855000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr7:6832000-6856000	Weak transcription	Fetal Brain Female	brain
4	chr7:6832000-6856400	Weak transcription	Fetal Intestine Large	intestine
5	chr7:6832000-6864600	Weak transcription	Primary T cells from cord blood	blood
6	chr7:6832000-6864800	Weak transcription	Fetal Thymus	thymus
7	chr7:6832200-6860800	Weak transcription	Brain Anterior Caudate	brain
8	chr7:6832400-6856600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr7:6832400-6864600	Weak transcription	Fetal Lung	lung
10	chr7:6832600-6858000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr7:6832600-6861000	Weak transcription	HUVEC	blood vessel
12	chr7:6832600-6864600	Weak transcription	NHLF	lung
13	chr7:6833000-6865200	Weak transcription	Left Ventricle	heart
14	chr7:6833000-6865200	Weak transcription	Ovary	ovary
15	chr7:6833200-6865200	Weak transcription	Pancreas	Pancrea
16	chr7:6833600-6864600	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr7:6833600-6865200	Weak transcription	Duodenum Mucosa	Duodenum
18	chr7:6834000-6866000	Weak transcription	Gastric	stomach
19	chr7:6840000-6865200	Weak transcription	Colonic Mucosa	Colon
20	chr7:6846600-6864600	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr7:6847400-6864600	Weak transcription	Stomach Smooth Muscle	stomach
22	chr7:6847600-6857200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr7:6847800-6864800	Weak transcription	NH-A	brain
24	chr7:6848200-6860600	Weak transcription	Aorta	Aorta
25	chr7:6848200-6864600	Weak transcription	Colon Smooth Muscle	Colon
26	chr7:6848400-6864800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr7:6848800-6863400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr7:6849000-6855200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr7:6849000-6856600	Weak transcription	Brain Hippocampus Middle	brain
30	chr7:6849000-6858200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr7:6849000-6863200	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr7:6849000-6863200	Strong transcription	Monocytes-CD14+_RO01746	blood
33	chr7:6849000-6864600	Weak transcription	Brain Angular Gyrus	brain
34	chr7:6849200-6856600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr7:6849400-6856600	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr7:6849400-6858600	Strong transcription	Primary T helper cells fromperipheralblood	blood
37	chr7:6849400-6862800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr7:6849400-6863000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr7:6849600-6863400	Strong transcription	Fetal Stomach	stomach
40	chr7:6849800-6864600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr7:6850000-6861800	Strong transcription	Adipose Nuclei	Adipose
42	chr7:6850000-6863200	Strong transcription	Primary monocytes fromperipheralblood	blood
43	chr7:6850200-6855800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr7:6850400-6860400	Weak transcription	Brain Substantia Nigra	brain
45	chr7:6850400-6865200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr7:6850400-6866000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr7:6850600-6854400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr7:6850600-6854600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr7:6850600-6855600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr7:6850600-6863400	Strong transcription	Fetal Intestine Small	intestine

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