Variant report

Variant	nsv970789
Chromosome Location	chr7:5958445-6027048
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:629)
CpG islands
(count:489)
Chromatin interactive
region (count:0)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:629 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr7:6023679-6023828	GM12878	blood:	n/a	n/a
2	BHLHE40	chr7:5971591-5971870	HepG2	liver:	n/a	n/a
3	CEBPB	chr7:5996596-5996886	K562	blood:	n/a	n/a
4	CEBPB	chr7:5994775-5995059	K562	blood:	n/a	n/a
5	CEBPB	chr7:5994679-5995123	K562	blood:	n/a	n/a
6	CEBPD	chr7:5994811-5995057	K562	blood:	n/a	n/a
7	CTCF	chr7:6011709-6011764	GM12891	blood:	n/a	n/a
8	CTCF	chr7:6023940-6024090	GM12870	blood:	n/a	n/a
9	CTCF	chr7:6010848-6011022	MCF-7	breast:	n/a	n/a
10	CTCF	chr7:6024020-6024170	AG09319	gingival:	n/a	n/a
11	CTCF	chr7:6023640-6023790	NHEK	skin:	n/a	n/a
12	CTCF	chr7:6010897-6010968	GM19239	blood:	n/a	n/a
13	CTCF	chr7:6023680-6023830	BE2_C	brain:	n/a	n/a
14	CTCF	chr7:6023660-6023810	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr7:6000629-6000686	GM13976	blood:	n/a	n/a
16	CTCF	chr7:6023640-6023790	SAEC	small airway:	n/a	n/a
17	CTCF	chr7:6023632-6023892	Gliobla	brain:	n/a	n/a
18	CTCF	chr7:5965247-5965339	GM20000	blood:	n/a	n/a
19	CTCF	chr7:6023657-6023822	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr7:6023540-6023690	HAc	cerebellar:	n/a	n/a
21	CTCF	chr7:6023640-6023790	HEK293	kidney:	n/a	n/a
22	CTCF	chr7:6023620-6023770	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr7:6023660-6023810	GM12874	blood:	n/a	n/a
24	CTCF	chr7:6023640-6023790	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr7:6023660-6023810	HPAF	blood vessel:	n/a	n/a
26	CTCF	chr7:6010845-6010990	NHEK	skin:	n/a	n/a
27	CTCF	chr7:6010905-6010978	Gliobla	brain:	n/a	n/a
28	CTCF	chr7:6010868-6011012	MCF-7	breast:	n/a	n/a
29	CTCF	chr7:6023632-6023914	A549	lung:	n/a	n/a
30	CTCF	chr7:6023660-6023810	NHEK	skin:	n/a	n/a
31	CTCF	chr7:6023631-6023865	GM13976	blood:	n/a	n/a
32	CTCF	chr7:6023900-6024050	AG04450	lung:	n/a	n/a
33	CTCF	chr7:6023660-6023810	NHLF	lung:	n/a	n/a
34	CTCF	chr7:6023619-6023907	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr7:6023640-6023790	HRE	kidney:	n/a	n/a
36	CTCF	chr7:6023628-6023900	K562	blood:	n/a	n/a
37	CTCF	chr7:6000840-6000990	K562	blood:	n/a	n/a
38	CTCF	chr7:6023585-6023891	IMR90	lung:	n/a	n/a
39	CTCF	chr7:6009399-6009405	GM12891	blood:	n/a	n/a
40	CTCF	chr7:6010878-6011009	GM12892	blood:	n/a	n/a
41	CTCF	chr7:6023675-6023848	Fibrobl	skin:	n/a	n/a
42	CTCF	chr7:6023689-6023841	GM13977	blood:	n/a	n/a
43	CTCF	chr7:6023640-6023790	GM12873	blood:	n/a	n/a
44	CTCF	chr7:6023660-6023810	AG09309	skin:	n/a	n/a
45	CTCF	chr7:6023640-6023790	GM12870	blood:	n/a	n/a
46	CTCF	chr7:6023660-6023810	GM12872	blood:	n/a	n/a
47	CTCF	chr7:6023660-6023810	HEK293	kidney:	n/a	n/a
48	CTCF	chr7:6023640-6023790	HMF	breast:	n/a	n/a
49	CTCF	chr7:6023540-6023690	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr7:6023673-6023867	GM20000	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6026863-6026913	NHBE	bronchial:	n/a
2	chr7:6026863-6026913	NHBE	bronchial:	n/a
3	chr7:6014034-6014084	HCF	heart:	n/a
4	chr7:6003569-6003619	GM12892	blood:	n/a
5	chr7:5963438-5963488	HEK293	kidney:	embryo
6	chr7:6010084-6010134	GM19239	blood:	n/a
7	chr7:6026932-6026982	NH-A	brain:	n/a
8	chr7:6014034-6014084	U87	brain:	n/a
9	chr7:6006566-6006616	U87	brain:	n/a
10	chr7:6014034-6014084	GM12891	blood:	n/a
11	chr7:6010084-6010134	BJ	skin:	n/a
12	chr7:6026932-6026982	CMK	blood:	n/a
13	chr7:6014034-6014084	HRE	kidney:	n/a
14	chr7:6026932-6026982	IMR90	lung:	fetal
15	chr7:6026809-6026859	GM12892	blood:	n/a
16	chr7:6026863-6026913	HMEC	breast:	n/a
17	chr7:6026863-6026913	PFSK-1	brain:	n/a
18	chr7:6006566-6006616	HL-60	blood:	n/a
19	chr7:6010084-6010134	A549	lung:	n/a
20	chr7:6003569-6003619	HIPEpiC	eye:	n/a
21	chr7:6026863-6026913	HCPEpiC	choroid plexus:	n/a
22	chr7:6026863-6026913	GM06990	blood:	n/a
23	chr7:5963438-5963488	SK-N-MC	brain:	n/a
24	chr7:5963438-5963488	HCT-116	colon:	n/a
25	chr7:6010084-6010134	HCM	heart:	n/a
26	chr7:6026863-6026913	ProgFib	skin:	n/a
27	chr7:6003569-6003619	GM19239	blood:	n/a
28	chr7:6026863-6026913	AG04449	skin:	fetal
29	chr7:6026863-6026913	SAEC	small airway:	n/a
30	chr7:6006566-6006616	MCF10A-Er-Src	breast:	n/a
31	chr7:6026932-6026982	HRE	kidney:	n/a
32	chr7:6014034-6014084	SK-N-MC	brain:	n/a
33	chr7:5963438-5963488	SK-N-SH_RA	brain:	n/a
34	chr7:6014034-6014084	CMK	blood:	n/a
35	chr7:6006566-6006616	NHBE	bronchial:	n/a
36	chr7:6026932-6026982	HPAEpiC	pulmonary alveolar:	n/a
37	chr7:5963438-5963488	BE2_C	brain:	n/a
38	chr7:6026809-6026859	AoSMC	blood vessel:	n/a
39	chr7:6003569-6003619	AG10803	skin:	n/a
40	chr7:6014034-6014084	SKMC	muscle:	n/a
41	chr7:6026932-6026982	NB4	blood:	n/a
42	chr7:6006566-6006616	GM12892	blood:	n/a
43	chr7:6014034-6014084	SK-N-SH_RA	brain:	n/a
44	chr7:6010084-6010134	BE2_C	brain:	n/a
45	chr7:6010084-6010134	HRPEpiC	eye:	n/a
46	chr7:6003569-6003619	Caco-2	colon:	n/a
47	chr7:6026809-6026859	SAEC	small airway:	n/a
48	chr7:6010084-6010134	NT2-D1	testis:	n/a
49	chr7:6010084-6010134	AG09309	skin:	n/a
50	chr7:6026932-6026982	ProgFib	skin:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OCM-2	chr7:5964372-5964445	NONHSAT118958
2	lnc-OCM-2	chr7:5965263-5965571	NONHSAT118958

No data

Variant related genes	Relation type
RSPH10B	TF binding region
CCZ1	TF binding region
RSPH10B	CpG island
CCZ1	CpG island

Extended variants
information (count: 1249 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1249 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200137255	chr7:5958464-5958465	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs201292887	chr7:5958495-5958496	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576473925	chr7:5958540-5958541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543472233	chr7:5958542-5958543	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375103243	chr7:5958633-5958634	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs138701366	chr7:5958650-5958651	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574057807	chr7:5958664-5958665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554111646	chr7:5958691-5958692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541553485	chr7:5958757-5958758	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372487579	chr7:5958760-5958761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576238351	chr7:5958787-5958788	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200172018	chr7:5958788-5958789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200845756	chr7:5958792-5958793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559910947	chr7:5958811-5958812	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527510748	chr7:5958819-5958820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371464524	chr7:5958821-5958822	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs111749505	chr7:5958831-5958832	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552037266	chr7:5958857-5958858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564055448	chr7:5958868-5958869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531290667	chr7:5958908-5958909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549520881	chr7:5958909-5958910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568088553	chr7:5959072-5959073	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535197323	chr7:5959088-5959089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547545154	chr7:5959202-5959203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs62453623	chr7:5959264-5959265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566264363	chr7:5959278-5959279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs199876580	chr7:5959297-5959298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540056884	chr7:5959309-5959310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558463885	chr7:5959408-5959409	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373055774	chr7:5959430-5959431	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs116538166	chr7:5959433-5959434	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs200812052	chr7:5959485-5959486	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs537409463	chr7:5959492-5959493	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs555465955	chr7:5959494-5959495	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs377419270	chr7:5959495-5959496	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs574023745	chr7:5959496-5959497	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs145821480	chr7:5959497-5959498	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs139249929	chr7:5959526-5959527	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs143251519	chr7:5959528-5959529	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs563998540	chr7:5959545-5959546	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs192141490	chr7:5959592-5959593	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs148556585	chr7:5959595-5959596	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs560971904	chr7:5959622-5959623	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs531499051	chr7:5959637-5959638	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs375526683	chr7:5959644-5959645	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs543747905	chr7:5959653-5959654	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs199977794	chr7:5959661-5959662	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs561506810	chr7:5959673-5959674	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs528915945	chr7:5959680-5959681	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs547477936	chr7:5959681-5959682	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Developmental delay	21147756	CNVD
Prostate cancer	18632612	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
Urothelial carcinoma	21177765	CNVD
Bladder cancer	21909424	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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ovarian cancer	21781307	CNVD
small cell lung cancer	17426248	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Gastric cancer	22014070	CNVD

Chromatin state (count:423 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5938200-5962800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr7:5938200-5963400	Weak transcription	Colon Smooth Muscle	Colon
3	chr7:5938200-5969400	Weak transcription	Brain Cingulate Gyrus	brain
4	chr7:5938400-5963600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:5938400-5966600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr7:5938400-5966800	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr7:5938400-5966800	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr7:5938400-5967800	Weak transcription	HSMMtube	muscle
9	chr7:5938400-5971000	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr7:5938400-5971400	Weak transcription	Fetal Muscle Trunk	muscle
11	chr7:5938400-5972600	Weak transcription	Fetal Brain Female	brain
12	chr7:5938600-5962400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr7:5939600-5964200	Weak transcription	Brain Angular Gyrus	brain
14	chr7:5939800-5963200	Weak transcription	A549	lung
15	chr7:5939800-5966400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr7:5943400-5971000	Weak transcription	Pancreas	Pancrea
17	chr7:5944400-5962600	Weak transcription	Fetal Intestine Large	intestine
18	chr7:5944600-5963200	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr7:5945400-5972600	Weak transcription	Gastric	stomach
20	chr7:5946400-5972400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr7:5947000-5969200	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr7:5947400-5962200	Weak transcription	Brain Hippocampus Middle	brain
23	chr7:5947600-5963400	Weak transcription	Stomach Smooth Muscle	stomach
24	chr7:5950000-5961800	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr7:5950000-5966800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr7:5950000-5971600	Weak transcription	Esophagus	oesophagus
27	chr7:5950000-5972000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr7:5951000-5962400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr7:5951000-5966000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr7:5951200-5960000	Weak transcription	Primary B cells from peripheral blood	blood
31	chr7:5951200-5962200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr7:5951200-5963000	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr7:5951200-5963400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr7:5951200-5963800	Weak transcription	Placenta	Placenta
35	chr7:5951200-5964000	Weak transcription	Brain Anterior Caudate	brain
36	chr7:5951200-5966600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr7:5951200-5966600	Weak transcription	Osteobl	bone
38	chr7:5951200-5966800	Weak transcription	Dnd41	blood
39	chr7:5951200-5967000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr7:5951200-5967200	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr7:5951200-5967600	Weak transcription	Thymus	Thymus
42	chr7:5951200-5969000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr7:5951200-5971000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr7:5951400-5967000	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr7:5951400-5968800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr7:5951400-5969000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr7:5951400-5971000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr7:5951400-5971600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr7:5951800-5962200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr7:5951800-5964800	Weak transcription	Ovary	ovary

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