Variant report

Variant	nsv1021753
Chromosome Location	chr7:50671350-50694457
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:323)
CpG islands
(count:0)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:323 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:50682508-50683119	HepG2	liver:	n/a	n/a
2	CEBPB	chr7:50678399-50678617	IMR90	lung:	n/a	n/a
3	CTCF	chr7:50682560-50682710	AG09309	skin:	n/a	n/a
4	CTCF	chr7:50682600-50682750	NHEK	skin:	n/a	n/a
5	CTCF	chr7:50682557-50682690	GM19240	blood:	n/a	n/a
6	CTCF	chr7:50678034-50678105	MCF-7	breast:	n/a	n/a
7	CTCF	chr7:50678180-50678330	HCPEpiC	choroid plexus:	n/a	n/a
8	CTCF	chr7:50682580-50682730	Caco-2	colon:	n/a	n/a
9	CTCF	chr7:50682579-50682732	LNCaP	prostate:	n/a	n/a
10	CTCF	chr7:50682540-50682690	GM12874	blood:	n/a	n/a
11	CTCF	chr7:50682507-50682904	MCF-7	breast:	n/a	n/a
12	CTCF	chr7:50681966-50682049	MCF-7	breast:	n/a	n/a
13	CTCF	chr7:50682580-50682730	HRPEpiC	eye:	n/a	n/a
14	CTCF	chr7:50678760-50678910	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr7:50682560-50682710	GM06990	blood:	n/a	n/a
16	CTCF	chr7:50682568-50682729	LNCaP	prostate:	n/a	n/a
17	CTCF	chr7:50682491-50682754	T-47D	breast:	n/a	n/a
18	CTCF	chr7:50682580-50682730	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr7:50682548-50682666	GM12891	blood:	n/a	n/a
20	CTCF	chr7:50682579-50682679	Lung_OC	lung:	n/a	n/a
21	CTCF	chr7:50682580-50682730	SK-N-SH_RA	brain:	n/a	n/a
22	CTCF	chr7:50682600-50682644	GM13977	blood:	n/a	n/a
23	CTCF	chr7:50688940-50689090	Caco-2	colon:	n/a	n/a
24	CTCF	chr7:50682640-50682790	HFF-Myc	foreskin:	n/a	n/a
25	CTCF	chr7:50682500-50682650	BE2_C	brain:	n/a	n/a
26	CTCF	chr7:50682540-50682690	HMEC	breast:	n/a	n/a
27	CTCF	chr7:50682480-50682630	GM12869	blood:	n/a	n/a
28	CTCF	chr7:50682204-50683004	SK-N-SH	brain:	n/a	n/a
29	CTCF	chr7:50682600-50682750	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr7:50682520-50682670	HAc	cerebellar:	n/a	n/a
31	CTCF	chr7:50682640-50682790	HMEC	breast:	n/a	n/a
32	CTCF	chr7:50682480-50682630	GM12864	blood:	n/a	n/a
33	CTCF	chr7:50682483-50682708	MCF-7	breast:	n/a	n/a
34	CTCF	chr7:50682563-50682705	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr7:50682600-50682750	HepG2	liver:	n/a	n/a
36	CTCF	chr7:50682540-50682690	GM12864	blood:	n/a	n/a
37	CTCF	chr7:50682740-50682890	A549	lung:	n/a	n/a
38	CTCF	chr7:50682491-50682773	MCF-7	breast:	n/a	n/a
39	CTCF	chr7:50678100-50678250	HCFaa	heart:	n/a	n/a
40	CTCF	chr7:50682472-50682823	GM12878	blood:	n/a	n/a
41	CTCF	chr7:50682540-50682690	GM12866	blood:	n/a	n/a
42	CTCF	chr7:50682480-50682630	NHLF	lung:	n/a	n/a
43	CTCF	chr7:50682560-50682702	Fibrobl	skin:	n/a	n/a
44	CTCF	chr7:50682800-50682950	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr7:50682538-50682736	HepG2	liver:	n/a	n/a
46	CTCF	chr7:50682520-50682670	GM12865	blood:	n/a	n/a
47	CTCF	chr7:50689027-50689128	MCF-7	breast:	n/a	chr7:50689083-50689099
48	CTCF	chr7:50682460-50682610	GM12868	blood:	n/a	n/a
49	CTCF	chr7:50682600-50682750	HMF	breast:	n/a	n/a
50	CTCF	chr7:50682540-50682690	HVMF	connective:	n/a	n/a

No data

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:50535593..50536314-chr7:50677309..50677832,2	MCF-7	breast:
2	chr7:50674486..50677439-chr7:50677838..50679790,2	K562	blood:
3	chr19:13263530..13264171-chr7:50686207..50686991,2	NB4	blood:
4	chr7:50691904..50693711-chr7:51130670..51132568,2	MCF-7	breast:
5	chr7:50687199..50689206-chr7:50691884..50694076,2	K562	blood:
6	chr7:50671344..50672957-chr7:50675090..50677359,2	K562	blood:
7	chr7:50677711..50679445-chr7:50681048..50682933,2	K562	blood:
8	chr7:50681994..50683696-chr7:50848659..50850969,2	MCF-7	breast:
9	chr7:50682338..50683151-chr7:50746616..50747511,5	MCF-7	breast:
10	chr7:50687199..50689206-chr7:50691884..50694076,2	K562	blood:
11	chr4:25161558..25162216-chr7:50680800..50681655,2	HCT-116	colon:
12	chr7:50685540..50687929-chr7:50689189..50691157,2	MCF-7	breast:
13	chr7:50685467..50688142-chr7:50689785..50691543,2	K562	blood:
14	chr7:50672342..50675062-chr7:50858858..50861329,2	K562	blood:
15	chr7:50671344..50672957-chr7:50675090..50677359,2	K562	blood:
16	chr7:50685540..50687929-chr7:50689189..50691157,2	MCF-7	breast:
17	chr7:50677711..50679445-chr7:50681048..50682933,2	K562	blood:
18	chr7:50685467..50688142-chr7:50689785..50691543,2	K562	blood:
19	chr7:50680803..50682728-chr7:50861117..50864019,2	K562	blood:

No data

Variant related genes	Relation type
GRB10	TF binding region
ENSG00000109618	chromatin interactions
ENSG00000106070	chromatin interactions

Extended variants
information (count: 943 )
Associated
traits (count: 127 )

Variant overlapped rSNPs/rCNVs (count:943 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12718729	chr7:50671350-50671351	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs532453701	chr7:50671373-50671374	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs77778873	chr7:50671383-50671384	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs111840874	chr7:50671445-50671446	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7456867	chr7:50671481-50671482	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs186124303	chr7:50671482-50671483	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs137884948	chr7:50671513-50671514	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs149016453	chr7:50671524-50671525	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs552165611	chr7:50671538-50671539	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs565792822	chr7:50671551-50671552	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535169161	chr7:50671553-50671554	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs144638444	chr7:50671554-50671555	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs568670092	chr7:50671563-50671564	Strong transcription Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116820375	chr7:50671601-50671602	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552314555	chr7:50671616-50671617	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs374110985	chr7:50671703-50671704	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs201369855	chr7:50671714-50671715	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs61756585	chr7:50671754-50671755	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs79207373	chr7:50671792-50671793	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376974161	chr7:50671793-50671794	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148145615	chr7:50671797-50671798	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368448396	chr7:50671838-50671839	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541947747	chr7:50671844-50671845	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs530488063	chr7:50671914-50671915	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs142905810	chr7:50671920-50671921	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs575369214	chr7:50671921-50671922	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs544018533	chr7:50671927-50671928	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs373021745	chr7:50671938-50671939	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564000133	chr7:50671939-50671940	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs373747219	chr7:50671994-50671995	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs200886440	chr7:50672017-50672018	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs148015359	chr7:50672022-50672023	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs371726545	chr7:50672025-50672026	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs374282211	chr7:50672048-50672049	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs1800602	chr7:50672088-50672089	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs1800603	chr7:50672092-50672093	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs545792860	chr7:50672093-50672094	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191779854	chr7:50672101-50672102	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs183633035	chr7:50672102-50672103	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs372644163	chr7:50672130-50672131	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs186497238	chr7:50672131-50672132	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs41298764	chr7:50672134-50672135	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs114852605	chr7:50672136-50672137	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs115437394	chr7:50672149-50672150	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs191336491	chr7:50672155-50672156	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs571110828	chr7:50672179-50672180	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs564599314	chr7:50672182-50672183	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs570505659	chr7:50672202-50672203	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552993576	chr7:50672215-50672216	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369690771	chr7:50672229-50672230	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:127)

Disease	PMID	Source
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Biliary cancer	19435499	CNVD
Wilms tumour	21544195	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	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
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	17237825	CNVD
Gastric cancer	24379144	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal cancer	21851588	CNVD
Non-small cell lung cancer	17643093	CNVD
Ovarian cancer	18182111	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17369134	CNVD
Barrett''s esophagus	18559552	CNVD
head and neck squamous cell carcinoma	16943533	CNVD
Anaplastic thyroid cancer	17079354	CNVD
Basal-like breast cancer	17875215	CNVD
Colorectal cancer	16882699	CNVD
Colorectal cancer	18794099	CNVD
Gastrointestinal stromal cancer	17643098	CNVD
Lung cancer	18381415	CNVD
Metastatic colorectal cancer	17664472	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	17673923	CNVD
Non-small cell lung cancer	17975165	CNVD
Non-small cell lung cancer	19622585	CNVD
Ovarian cancer	16607561	CNVD
Squamous cell cancer	19670535	CNVD
head and neck squamous cell carcinoma	16818711	CNVD
small cell lung cancer	18829487	CNVD
Breast cancer	17661082	CNVD
Adenocarcinoma	19260752	CNVD
Esophageal cancer	16575012	CNVD
Lung adenocarcinoma	19138956	CNVD
Lung adenocarcinoma	18379350	CNVD
Lung adenocarcinoma	18258923	CNVD
Lung cancer	19138956	CNVD
Lung cancer	18379350	CNVD
Lung cancer	18258923	CNVD
Non-small cell lung cancer	18304967	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	19260752	CNVD
Non-small cell lung cancer	17079354	CNVD
Non-small cell lung cancer	18559607	CNVD
Rectal cancer	19506820	CNVD
Triple-negative breast cancer	18950515	CNVD
head and neck squamous cell carcinoma	18813952	CNVD
Non-small cell lung cancer	17504988	CNVD
Non-small cell lung cancer	16943533	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	17538160	CNVD
Colorectal cancer	19712476	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19671679	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
small cell lung cancer	20016488	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Cancer	20164919	CNVD
Colorectal cancer	21645411	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:806 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:50652000-50671800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr7:50652400-50687400	Weak transcription	Right Atrium	heart
3	chr7:50653200-50672400	Weak transcription	NHEK	skin
4	chr7:50654000-50680000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr7:50657200-50678000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr7:50658200-50675800	Strong transcription	HSMMtube	muscle
7	chr7:50658200-50682000	Weak transcription	Colonic Mucosa	Colon
8	chr7:50658200-50690400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr7:50658800-50673200	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr7:50658800-50686800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr7:50658800-50690000	Weak transcription	Fetal Kidney	kidney
12	chr7:50659000-50678600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr7:50659200-50672200	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr7:50659200-50677000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr7:50659200-50680000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr7:50659200-50683600	Weak transcription	Small Intestine	intestine
17	chr7:50659400-50675800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr7:50659600-50675600	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr7:50659800-50679000	Weak transcription	NHDF-Ad	bronchial
20	chr7:50659800-50687800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr7:50659800-50697200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr7:50660000-50675600	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr7:50660400-50673400	Weak transcription	Fetal Brain Female	brain
24	chr7:50660600-50688000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr7:50660800-50673400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr7:50661000-50673600	Weak transcription	Esophagus	oesophagus
27	chr7:50662800-50671400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr7:50663800-50674400	Strong transcription	Left Ventricle	heart
29	chr7:50663800-50675800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr7:50664600-50675800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
31	chr7:50664800-50674400	Strong transcription	Skeletal Muscle Male	skeletal muscle
32	chr7:50664800-50675800	Strong transcription	Adipose Nuclei	Adipose
33	chr7:50665000-50688000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
34	chr7:50666000-50675600	Strong transcription	Stomach Smooth Muscle	stomach
35	chr7:50666600-50671600	Weak transcription	Colon Smooth Muscle	Colon
36	chr7:50666600-50672600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr7:50666600-50677600	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr7:50666600-50680400	Weak transcription	Brain Angular Gyrus	brain
39	chr7:50666800-50671800	Weak transcription	Placenta	Placenta
40	chr7:50666800-50673800	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr7:50667000-50671400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr7:50667000-50686200	Strong transcription	Primary neutrophils fromperipheralblood	blood
43	chr7:50667200-50682000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr7:50667600-50681600	Weak transcription	HepG2	liver
45	chr7:50668000-50689000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr7:50668600-50675800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
47	chr7:50668600-50676200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr7:50668800-50671600	Strong transcription	HUVEC	blood vessel
49	chr7:50669000-50677200	Weak transcription	Stomach Mucosa	stomach
50	chr7:50669600-50672400	Strong transcription	HSMM	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links