Variant report

Variant	nsv1020791
Chromosome Location	chr7:50673666-50694457
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:318)
CpG islands
(count:0)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:318 , 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	chr7:50682608-50682693	Medullo	brain:	n/a	n/a
4	CTCF	chr7:50682560-50682710	GM12878	blood:	n/a	n/a
5	CTCF	chr7:50682492-50682723	MCF-7	breast:	n/a	n/a
6	CTCF	chr7:50682568-50682729	LNCaP	prostate:	n/a	n/a
7	CTCF	chr7:50682563-50682694	SK-N-SH_RA	brain:	n/a	n/a
8	CTCF	chr7:50682600-50682750	SK-N-SH_RA	brain:	n/a	n/a
9	CTCF	chr7:50682700-50682850	HCM	heart:	n/a	n/a
10	CTCF	chr7:50682520-50682670	SAEC	small airway:	n/a	n/a
11	CTCF	chr7:50682620-50682770	HPF	lung:	n/a	n/a
12	CTCF	chr7:50682580-50682730	GM12865	blood:	n/a	n/a
13	CTCF	chr7:50682620-50682770	A549	lung:	n/a	n/a
14	CTCF	chr7:50682600-50682750	HPF	lung:	n/a	n/a
15	CTCF	chr7:50682580-50682730	NB4	blood:	n/a	n/a
16	CTCF	chr7:50682480-50682630	GM12864	blood:	n/a	n/a
17	CTCF	chr7:50682580-50682730	NHDF-neo	bronchial:	n/a	n/a
18	CTCF	chr7:50688913-50689023	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr7:50688940-50689090	Caco-2	colon:	n/a	n/a
20	CTCF	chr7:50682560-50682702	Fibrobl	skin:	n/a	n/a
21	CTCF	chr7:50682580-50682730	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr7:50682540-50682690	HCFaa	heart:	n/a	n/a
23	CTCF	chr7:50682540-50682690	HFF	foreskin:	n/a	n/a
24	CTCF	chr7:50689063-50689142	MCF-7	breast:	n/a	chr7:50689083-50689099
25	CTCF	chr7:50682563-50682705	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr7:50682562-50682690	GM19238	blood:	n/a	n/a
27	CTCF	chr7:50681966-50682049	MCF-7	breast:	n/a	n/a
28	CTCF	chr7:50682580-50682730	HAc	cerebellar:	n/a	n/a
29	CTCF	chr7:50682560-50682710	GM12871	blood:	n/a	n/a
30	CTCF	chr7:50682580-50682730	GM12867	blood:	n/a	n/a
31	CTCF	chr7:50682497-50682768	MCF-7	breast:	n/a	n/a
32	CTCF	chr7:50682571-50682696	A549	lung:	n/a	n/a
33	CTCF	chr7:50682600-50682750	NHEK	skin:	n/a	n/a
34	CTCF	chr7:50682560-50682710	AG09309	skin:	n/a	n/a
35	CTCF	chr7:50682520-50682670	K562	blood:	n/a	n/a
36	CTCF	chr7:50682540-50682690	GM12866	blood:	n/a	n/a
37	CTCF	chr7:50678180-50678330	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr7:50682460-50682610	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr7:50682740-50682890	A549	lung:	n/a	n/a
40	CTCF	chr7:50682600-50682750	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr7:50682580-50682730	HCT-116	colon:	n/a	n/a
42	CTCF	chr7:50682483-50682708	MCF-7	breast:	n/a	n/a
43	CTCF	chr7:50682660-50682810	BJ	skin:	n/a	n/a
44	CTCF	chr7:50682472-50682823	GM12878	blood:	n/a	n/a
45	CTCF	chr7:50682600-50682644	GM13977	blood:	n/a	n/a
46	CTCF	chr7:50682560-50682710	HMF	breast:	n/a	n/a
47	CTCF	chr7:50682611-50682702	GM10266	blood:	n/a	n/a
48	CTCF	chr7:50682540-50682690	AG09319	gingival:	n/a	n/a
49	CTCF	chr7:50682540-50682690	HRE	kidney:	n/a	n/a
50	CTCF	chr7:50682525-50682762	Spleen_OC	spleen:	n/a	n/a

No data

(count:18 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 813 )
Associated
traits (count: 127 )

Variant overlapped rSNPs/rCNVs (count:813 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3807549	chr7:50673666-50673667	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs550967974	chr7:50673672-50673673	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs536468402	chr7:50673673-50673674	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs7780697	chr7:50673681-50673682	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs547559163	chr7:50673689-50673690	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs567382875	chr7:50673694-50673695	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs536524549	chr7:50673714-50673715	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs548490431	chr7:50673748-50673749	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs556150071	chr7:50673801-50673802	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs34787183	chr7:50673810-50673811	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs117896224	chr7:50673816-50673817	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs369632086	chr7:50673823-50673824	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs538197347	chr7:50673856-50673857	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs28458270	chr7:50673857-50673858	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs77532435	chr7:50673918-50673919	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs201160497	chr7:50674004-50674005	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs189686355	chr7:50674008-50674009	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs574126424	chr7:50674012-50674013	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs373904659	chr7:50674023-50674024	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs368078458	chr7:50674040-50674041	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs61734187	chr7:50674043-50674044	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs374360989	chr7:50674083-50674084	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs562798543	chr7:50674103-50674104	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs76258614	chr7:50674113-50674114	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs368801380	chr7:50674125-50674126	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs372429316	chr7:50674154-50674155	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375849950	chr7:50674155-50674156	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs144455752	chr7:50674160-50674161	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs41315249	chr7:50674162-50674163	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs56380597	chr7:50674174-50674175	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs564578011	chr7:50674196-50674197	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs527362888	chr7:50674198-50674199	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs564027309	chr7:50674237-50674238	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs569882241	chr7:50674238-50674239	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs528102377	chr7:50674284-50674285	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs547203335	chr7:50674305-50674306	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs567376822	chr7:50674310-50674311	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs370293765	chr7:50674311-50674312	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs550004115	chr7:50674364-50674365	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs4947411	chr7:50674409-50674410	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs538976210	chr7:50674411-50674412	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs558170294	chr7:50674421-50674422	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs559049383	chr7:50674455-50674456	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs571698400	chr7:50674475-50674476	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs568169835	chr7:50674510-50674511	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs534223748	chr7:50674531-50674532	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs537047909	chr7:50674537-50674538	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs553943780	chr7:50674593-50674594	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs574086783	chr7:50674621-50674622	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs370922308	chr7:50674626-50674627	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	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:760 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:50652400-50687400	Weak transcription	Right Atrium	heart
2	chr7:50654000-50680000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr7:50657200-50678000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr7:50658200-50675800	Strong transcription	HSMMtube	muscle
5	chr7:50658200-50682000	Weak transcription	Colonic Mucosa	Colon
6	chr7:50658200-50690400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr7:50658800-50686800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr7:50658800-50690000	Weak transcription	Fetal Kidney	kidney
9	chr7:50659000-50678600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr7:50659200-50677000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr7:50659200-50680000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr7:50659200-50683600	Weak transcription	Small Intestine	intestine
13	chr7:50659400-50675800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr7:50659600-50675600	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr7:50659800-50679000	Weak transcription	NHDF-Ad	bronchial
16	chr7:50659800-50687800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr7:50659800-50697200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr7:50660000-50675600	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr7:50660600-50688000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr7:50663800-50674400	Strong transcription	Left Ventricle	heart
21	chr7:50663800-50675800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr7:50664600-50675800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr7:50664800-50674400	Strong transcription	Skeletal Muscle Male	skeletal muscle
24	chr7:50664800-50675800	Strong transcription	Adipose Nuclei	Adipose
25	chr7:50665000-50688000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
26	chr7:50666000-50675600	Strong transcription	Stomach Smooth Muscle	stomach
27	chr7:50666600-50677600	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr7:50666600-50680400	Weak transcription	Brain Angular Gyrus	brain
29	chr7:50666800-50673800	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr7:50667000-50686200	Strong transcription	Primary neutrophils fromperipheralblood	blood
31	chr7:50667200-50682000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr7:50667600-50681600	Weak transcription	HepG2	liver
33	chr7:50668000-50689000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr7:50668600-50675800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
35	chr7:50668600-50676200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr7:50669000-50677200	Weak transcription	Stomach Mucosa	stomach
37	chr7:50669600-50674400	Strong transcription	Psoas Muscle	Psoas
38	chr7:50669600-50676000	Strong transcription	Osteobl	bone
39	chr7:50670000-50674200	Strong transcription	Aorta	Aorta
40	chr7:50670000-50674400	Strong transcription	Right Ventricle	heart
41	chr7:50670000-50674400	Strong transcription	Spleen	Spleen
42	chr7:50670000-50675200	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr7:50670000-50676200	Strong transcription	Cortex derived primary cultured neurospheres	brain
44	chr7:50670200-50674800	Strong transcription	Hela-S3	cervix
45	chr7:50670200-50675600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr7:50670600-50674000	Strong transcription	Sigmoid Colon	Sigmoid Colon
47	chr7:50670600-50674200	Strong transcription	Gastric	stomach
48	chr7:50670600-50674200	Strong transcription	Rectal Smooth Muscle	rectum
49	chr7:50670600-50674400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr7:50670600-50674400	Strong transcription	Fetal Intestine Small	intestine

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