Variant report

Variant	nsv1022759
Chromosome Location	chr7:70236919-70292317
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:830)
CpG islands
(count:1222)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:830 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:70246580-70246894	HepG2	liver:	n/a	n/a
2	ATF2	chr7:70258518-70258992	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr7:70264860-70265281	GM12878	blood:	n/a	n/a
4	BACH1	chr7:70277553-70277731	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr7:70264853-70265265	GM12878	blood:	n/a	n/a
6	BATF	chr7:70264945-70265249	GM12878	blood:	n/a	n/a
7	BATF	chr7:70241538-70241996	GM12878	blood:	n/a	n/a
8	BATF	chr7:70241512-70241829	GM12878	blood:	n/a	n/a
9	BCL11A	chr7:70264860-70265214	GM12878	blood:	n/a	n/a
10	BCL11A	chr7:70241509-70241830	GM12878	blood:	n/a	n/a
11	BCL11A	chr7:70264916-70265214	GM12878	blood:	n/a	n/a
12	BHLHE40	chr7:70243687-70244081	GM12878	blood:	n/a	n/a
13	BHLHE40	chr7:70241598-70242216	GM12878	blood:	n/a	n/a
14	BHLHE40	chr7:70246523-70246847	HepG2	liver:	n/a	n/a
15	BHLHE40	chr7:70244421-70244574	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:70250727-70250742	A549	lung:	n/a	n/a
17	BRCA1	chr7:70277589-70277745	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr7:70259112-70259395	HepG2	liver:	n/a	chr7:70259259-70259270 chr7:70259258-70259271
19	CEBPB	chr7:70258165-70258365	HepG2	liver:	n/a	n/a
20	CEBPB	chr7:70254214-70254423	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:70246417-70246750	HepG2	liver:	n/a	n/a
22	CEBPB	chr7:70275643-70275871	HepG2	liver:	n/a	chr7:70275762-70275779
23	CEBPB	chr7:70275646-70275979	HepG2	liver:	n/a	chr7:70275762-70275779
24	CEBPB	chr7:70254236-70254480	K562	blood:	n/a	n/a
25	CEBPB	chr7:70250396-70250674	HepG2	liver:	n/a	chr7:70250526-70250537
26	CEBPB	chr7:70275675-70275878	K562	blood:	n/a	chr7:70275762-70275779
27	CEBPB	chr7:70277650-70277842	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr7:70259127-70259380	IMR90	lung:	n/a	chr7:70259259-70259270 chr7:70259258-70259271
29	CEBPB	chr7:70275577-70275965	HepG2	liver:	n/a	chr7:70275762-70275779
30	CEBPB	chr7:70259112-70259411	A549	lung:	n/a	chr7:70259259-70259270 chr7:70259258-70259271
31	CEBPB	chr7:70250424-70250609	Hela-S3	cervix:	n/a	chr7:70250526-70250537
32	CEBPB	chr7:70250444-70250691	MCF-7	breast:	n/a	chr7:70250526-70250537
33	CEBPB	chr7:70259155-70259386	K562	blood:	n/a	chr7:70259259-70259270 chr7:70259258-70259271
34	CEBPB	chr7:70257703-70257833	HepG2	liver:	n/a	n/a
35	CEBPB	chr7:70275639-70275877	A549	lung:	n/a	chr7:70275762-70275779
36	CEBPB	chr7:70250452-70250691	A549	lung:	n/a	chr7:70250526-70250537
37	CHD1	chr7:70240706-70241046	GM12878	blood:	n/a	n/a
38	CHD2	chr7:70244473-70244530	GM12878	blood:	n/a	n/a
39	CHD2	chr7:70241529-70241934	GM12878	blood:	n/a	n/a
40	CHD2	chr7:70246524-70246836	HepG2	liver:	n/a	n/a
41	CHD2	chr7:70254011-70254064	GM12878	blood:	n/a	n/a
42	CTCF	chr7:70272699-70272995	K562	blood:	n/a	n/a
43	CTCF	chr7:70240680-70240830	NHLF	lung:	n/a	n/a
44	CTCF	chr7:70240620-70240770	GM12872	blood:	n/a	n/a
45	CTCF	chr7:70277680-70277830	GM12871	blood:	n/a	n/a
46	CTCF	chr7:70277580-70277730	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr7:70277600-70277750	GM12864	blood:	n/a	n/a
48	CTCF	chr7:70272713-70272906	T-47D	breast:	n/a	n/a
49	CTCF	chr7:70272750-70272924	MCF-7	breast:	n/a	n/a
50	CTCF	chr7:70240700-70240850	HEEpiC	esophagus:	n/a	n/a

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70254810-70254860	GM12878	blood:	n/a
2	chr7:70258010-70258060	AG09309	skin:	n/a
3	chr7:70254810-70254860	GM12878	blood:	n/a
4	chr7:70258010-70258060	AG09309	skin:	n/a
5	chr7:70255210-70255260	HIPEpiC	eye:	n/a
6	chr7:70252571-70252621	SK-N-SH	brain:	n/a
7	chr7:70254810-70254860	HNPCEpiC	eye:	n/a
8	chr7:70258753-70258803	AG09309	skin:	n/a
9	chr7:70252282-70252332	GM12892	blood:	n/a
10	chr7:70258726-70258776	NHDF-neo	bronchial:	n/a
11	chr7:70252335-70252385	NHBE	bronchial:	n/a
12	chr7:70255985-70256035	SK-N-SH	brain:	n/a
13	chr7:70258649-70258699	HNPCEpiC	eye:	n/a
14	chr7:70254810-70254860	BJ	skin:	n/a
15	chr7:70258649-70258699	AG04450	lung:	fetal
16	chr7:70258649-70258699	HEEpiC	esophagus:	n/a
17	chr7:70252953-70253003	HCF	heart:	n/a
18	chr7:70255985-70256035	HCPEpiC	choroid plexus:	n/a
19	chr7:70258726-70258776	HRPEpiC	eye:	n/a
20	chr7:70255332-70255382	MCF-7	breast:	n/a
21	chr7:70255804-70255854	IMR90	lung:	fetal
22	chr7:70258753-70258803	GM19239	blood:	n/a
23	chr7:70255210-70255260	HEEpiC	esophagus:	n/a
24	chr7:70252448-70252498	SKMC	muscle:	n/a
25	chr7:70254810-70254860	A549	lung:	n/a
26	chr7:70252953-70253003	Hela-S3	cervix:	n/a
27	chr7:70257926-70257976	K562	blood:	n/a
28	chr7:70255985-70256035	ProgFib	skin:	n/a
29	chr7:70258753-70258803	PFSK-1	brain:	n/a
30	chr7:70255804-70255854	ovcar-3	ovarian:	n/a
31	chr7:70238460-70238510	LNCaP	prostate:	n/a
32	chr7:70252953-70253003	GM12892	blood:	n/a
33	chr7:70252282-70252332	NHBE	bronchial:	n/a
34	chr7:70257960-70258010	U87	brain:	n/a
35	chr7:70258649-70258699	GM06990	blood:	n/a
36	chr7:70258649-70258699	HIPEpiC	eye:	n/a
37	chr7:70255210-70255260	Hela-S3	cervix:	n/a
38	chr7:70254810-70254860	SK-N-SH_RA	brain:	n/a
39	chr7:70255416-70255466	HRE	kidney:	n/a
40	chr7:70255332-70255382	GM12878	blood:	n/a
41	chr7:70252953-70253003	PFSK-1	brain:	n/a
42	chr7:70255332-70255382	CMK	blood:	n/a
43	chr7:70258753-70258803	PANC-1	pancreas:	n/a
44	chr7:70255416-70255466	HRCEpiC	kidney:	n/a
45	chr7:70252953-70253003	HEK293	kidney:	embryo
46	chr7:70257960-70258010	PrEC	prostate:	n/a
47	chr7:70252335-70252385	GM12891	blood:	n/a
48	chr7:70252448-70252498	NB4	blood:	n/a
49	chr7:70252662-70252712	H1-hESC	embryonic stem cell:	embryo
50	chr7:70255416-70255466	SAEC	small airway:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:70243263..70245358-chr7:70247619..70249234,2	K562	blood:
2	chr7:70266587..70269315-chr7:70270383..70272758,2	K562	blood:
3	chr7:70255328..70258832-chr7:70260648..70264116,3	K562	blood:
4	chr7:70266587..70269315-chr7:70270383..70272758,2	K562	blood:
5	chr7:70255328..70258832-chr7:70260648..70264116,3	K562	blood:
6	chr7:70244569..70247076-chr7:70250539..70253250,4	K562	blood:
7	chr7:69997760..70000305-chr7:70252452..70255075,2	MCF-7	breast:
8	chr7:70243263..70245358-chr7:70247619..70249234,2	K562	blood:

No data

Variant related genes	Relation type
AUTS2	TF binding region
AUTS2	CpG island
ENSG00000158321	chromatin interactions

Extended variants
information (count: 2120 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2120 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141163033	chr7:70236925-70236926	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs150304913	chr7:70236937-70236938	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191216830	chr7:70236957-70236958	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115382631	chr7:70236962-70236963	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555258380	chr7:70236970-70236971	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs543638091	chr7:70236971-70236972	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs527684614	chr7:70236984-70236985	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549441223	chr7:70236987-70236988	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs116675335	chr7:70237057-70237058	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs114646276	chr7:70237072-70237073	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs556602686	chr7:70237076-70237077	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs183504320	chr7:70237077-70237078	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs61687916	chr7:70237096-70237097	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs573748345	chr7:70237110-70237111	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs544202280	chr7:70237117-70237118	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs369192804	chr7:70237137-70237138	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs572640215	chr7:70237138-70237139	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs539823557	chr7:70237148-70237149	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs374668597	chr7:70237154-70237155	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs137890900	chr7:70237177-70237178	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs111927681	chr7:70237214-70237215	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs377547505	chr7:70237219-70237220	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs376976614	chr7:70237222-70237223	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs146152256	chr7:70237243-70237244	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs533103846	chr7:70237262-70237263	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs75990240	chr7:70237299-70237300	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs560559376	chr7:70237307-70237308	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs527821525	chr7:70237311-70237312	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs549379633	chr7:70237328-70237329	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs561240645	chr7:70237335-70237336	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs6950762	chr7:70237337-70237338	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs113209511	chr7:70237343-70237344	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs189861884	chr7:70237345-70237346	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs539210953	chr7:70237353-70237354	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs181132267	chr7:70237381-70237382	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs371355023	chr7:70237399-70237400	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs187135911	chr7:70237402-70237403	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs2069284	chr7:70237415-70237416	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs533614690	chr7:70237437-70237438	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs189976667	chr7:70237447-70237448	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs528468858	chr7:70237505-70237506	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs182018714	chr7:70237509-70237510	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs186396342	chr7:70237553-70237554	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs190904187	chr7:70237579-70237580	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs556421267	chr7:70237584-70237585	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs6947003	chr7:70237585-70237586	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs9986982	chr7:70237605-70237606	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs545172810	chr7:70237647-70237648	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs182376411	chr7:70237648-70237649	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs370725421	chr7:70237675-70237676	Enhancers Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16461572	CNVD
Acute monocytic leukemia	16498392	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
Williams Syndrome	20824207	CNVD
Dyslexia	22102821	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:846 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70214800-70250000	Weak transcription	Psoas Muscle	Psoas
2	chr7:70218600-70241600	Weak transcription	Fetal Heart	heart
3	chr7:70222000-70258000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr7:70223200-70238000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:70223400-70237400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr7:70226400-70254800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:70227400-70237400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
8	chr7:70227400-70253000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr7:70227600-70237400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
10	chr7:70227600-70241400	Strong transcription	Dnd41	blood
11	chr7:70228000-70249400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr7:70228400-70250000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr7:70228400-70257400	Weak transcription	Right Atrium	heart
14	chr7:70228600-70238400	Strong transcription	Primary T cells from cord blood	blood
15	chr7:70228600-70238600	Weak transcription	Brain Angular Gyrus	brain
16	chr7:70228800-70238000	Weak transcription	Brain Substantia Nigra	brain
17	chr7:70228800-70241600	Weak transcription	NHDF-Ad	bronchial
18	chr7:70229000-70239200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr7:70229400-70240200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr7:70229400-70259600	Strong transcription	Fetal Muscle Trunk	muscle
21	chr7:70229400-70259600	Strong transcription	Rectal Mucosa Donor 29	rectum
22	chr7:70229600-70240200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr7:70229600-70241600	Strong transcription	Fetal Muscle Leg	muscle
24	chr7:70229600-70242200	Weak transcription	Small Intestine	intestine
25	chr7:70229800-70241200	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr7:70230000-70239400	Strong transcription	Fetal Thymus	thymus
27	chr7:70230000-70241200	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr7:70230200-70254000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr7:70230200-70257400	Strong transcription	Rectal Mucosa Donor 31	rectum
30	chr7:70230400-70242400	Weak transcription	Primary B cells from peripheral blood	blood
31	chr7:70230600-70241800	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr7:70230600-70250000	Weak transcription	Right Ventricle	heart
33	chr7:70231000-70239000	Strong transcription	Liver	Liver
34	chr7:70231000-70250000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr7:70231200-70237400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr7:70231400-70246400	Strong transcription	Fetal Intestine Large	intestine
37	chr7:70231600-70250000	Weak transcription	NHLF	lung
38	chr7:70231800-70241200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr7:70231800-70241200	Weak transcription	Brain Cingulate Gyrus	brain
40	chr7:70231800-70241600	Weak transcription	Spleen	Spleen
41	chr7:70231800-70244000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr7:70232000-70237800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr7:70232000-70239000	Weak transcription	Lung	lung
44	chr7:70232000-70239400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr7:70232000-70241400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr7:70232000-70241800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr7:70232000-70241800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr7:70232000-70244200	Weak transcription	Gastric	stomach
49	chr7:70232000-70246400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr7:70232000-70250000	Weak transcription	Pancreas	Pancrea

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