Variant report

Variant	nsv887493
Chromosome Location	chr7:8202132-8230591
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:513)
CpG islands
(count:122)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:513 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:8216966-8217395	K562	blood:	n/a	n/a
2	ARID3A	chr7:8230147-8230157	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:8230029-8230312	K562	blood:	n/a	n/a
4	ATF1	chr7:8216885-8217196	K562	blood:	n/a	n/a
5	ATF2	chr7:8215532-8217304	GM12878	blood:	n/a	n/a
6	ATF2	chr7:8217670-8218413	GM12878	blood:	n/a	n/a
7	ATF2	chr7:8229834-8230375	GM12878	blood:	n/a	n/a
8	ATF2	chr7:8215686-8217327	GM12878	blood:	n/a	n/a
9	ATF2	chr7:8217852-8218398	GM12878	blood:	n/a	n/a
10	ATF2	chr7:8229876-8230448	GM12878	blood:	n/a	n/a
11	BACH1	chr7:8214770-8214772	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:8215611-8215628	K562	blood:	n/a	n/a
13	BATF	chr7:8215801-8216654	GM12878	blood:	n/a	chr7:8216248-8216259
14	BCL11A	chr7:8215921-8216655	GM12878	blood:	n/a	n/a
15	BCL11A	chr7:8216863-8217119	GM12878	blood:	n/a	n/a
16	BCL11A	chr7:8216833-8217128	GM12878	blood:	n/a	n/a
17	BCL11A	chr7:8215849-8216693	GM12878	blood:	n/a	n/a
18	BCL3	chr7:8215788-8217164	GM12878	blood:	n/a	n/a
19	BCL3	chr7:8215871-8216586	GM12878	blood:	n/a	n/a
20	BCLAF1	chr7:8215513-8217294	GM12878	blood:	n/a	n/a
21	BCLAF1	chr7:8215658-8216668	GM12878	blood:	n/a	n/a
22	BCLAF1	chr7:8229877-8230402	GM12878	blood:	n/a	chr7:8230069-8230078
23	BHLHE40	chr7:8226004-8226016	K562	blood:	n/a	n/a
24	BHLHE40	chr7:8215676-8217394	GM12878	blood:	n/a	n/a
25	BHLHE40	chr7:8216890-8217167	K562	blood:	n/a	n/a
26	BHLHE40	chr7:8212665-8212736	GM12878	blood:	n/a	n/a
27	BHLHE40	chr7:8219292-8219381	GM12878	blood:	n/a	n/a
28	BHLHE40	chr7:8207938-8207942	K562	blood:	n/a	n/a
29	BHLHE40	chr7:8230040-8230581	K562	blood:	n/a	n/a
30	BRCA1	chr7:8208937-8209105	GM12878	blood:	n/a	n/a
31	BRCA1	chr7:8222513-8222686	GM12878	blood:	n/a	n/a
32	CEBPB	chr7:8212240-8212609	IMR90	lung:	n/a	chr7:8212417-8212428
33	CEBPB	chr7:8212217-8212640	MCF-7	breast:	n/a	chr7:8212417-8212428
34	CEBPB	chr7:8212247-8212599	H1-hESC	embryonic stem cell:	n/a	chr7:8212417-8212428
35	CEBPB	chr7:8212278-8212610	A549	lung:	n/a	chr7:8212417-8212428
36	CEBPB	chr7:8212224-8212616	K562	blood:	n/a	chr7:8212417-8212428
37	CEBPB	chr7:8212284-8212652	A549	lung:	n/a	chr7:8212417-8212428
38	CEBPB	chr7:8212270-8212601	HepG2	liver:	n/a	chr7:8212417-8212428
39	CEBPB	chr7:8212250-8212610	Hela-S3	cervix:	n/a	chr7:8212417-8212428
40	CEBPB	chr7:8227793-8228058	A549	lung:	n/a	chr7:8227888-8227901 chr7:8227890-8227901
41	CEBPB	chr7:8212287-8212633	MCF-7	breast:	n/a	chr7:8212417-8212428
42	CEBPB	chr7:8212263-8212563	K562	blood:	n/a	chr7:8212417-8212428
43	CEBPB	chr7:8215629-8217349	GM12878	blood:	n/a	n/a
44	CEBPB	chr7:8215564-8215929	HepG2	liver:	n/a	n/a
45	CHD1	chr7:8214489-8214988	GM12878	blood:	n/a	n/a
46	CHD1	chr7:8215197-8218247	GM12878	blood:	n/a	n/a
47	CHD2	chr7:8214458-8214925	GM12878	blood:	n/a	n/a
48	CHD2	chr7:8229864-8230417	GM12878	blood:	n/a	n/a
49	CHD2	chr7:8215325-8217197	GM12878	blood:	n/a	n/a
50	CREB1	chr7:8216826-8217299	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:8215896-8215946	SAEC	small airway:	n/a
2	chr7:8215896-8215946	HepG2	liver:	n/a
3	chr7:8215896-8215946	H1-hESC	embryonic stem cell:	embryo
4	chr7:8229083-8229133	HRPEpiC	eye:	n/a
5	chr7:8215896-8215946	ovcar-3	ovarian:	n/a
6	chr7:8229083-8229133	T-47D	breast:	n/a
7	chr7:8215896-8215946	GM12892	blood:	n/a
8	chr7:8229083-8229133	PANC-1	pancreas:	n/a
9	chr7:8229083-8229133	MCF-7	breast:	n/a
10	chr7:8215896-8215946	HCT-116	colon:	n/a
11	chr7:8215896-8215946	AG09319	gingival:	n/a
12	chr7:8215896-8215946	HCF	heart:	n/a
13	chr7:8229083-8229133	HPAEpiC	pulmonary alveolar:	n/a
14	chr7:8229083-8229133	PrEC	prostate:	n/a
15	chr7:8215896-8215946	A549	lung:	n/a
16	chr7:8229083-8229133	HL-60	blood:	n/a
17	chr7:8215896-8215946	Caco-2	colon:	n/a
18	chr7:8215896-8215946	PFSK-1	brain:	n/a
19	chr7:8215896-8215946	CMK	blood:	n/a
20	chr7:8215896-8215946	HPAEpiC	pulmonary alveolar:	n/a
21	chr7:8229083-8229133	HCM	heart:	n/a
22	chr7:8215896-8215946	HCM	heart:	n/a
23	chr7:8215896-8215946	PANC-1	pancreas:	n/a
24	chr7:8215896-8215946	GM12878	blood:	n/a
25	chr7:8229083-8229133	GM12892	blood:	n/a
26	chr7:8215896-8215946	AG04449	skin:	fetal
27	chr7:8229083-8229133	HMEC	breast:	n/a
28	chr7:8215896-8215946	Hela-S3	cervix:	n/a
29	chr7:8215896-8215946	RPTEC	kidney:	n/a
30	chr7:8215896-8215946	MCF-7	breast:	n/a
31	chr7:8215896-8215946	BE2_C	brain:	n/a
32	chr7:8229083-8229133	CMK	blood:	n/a
33	chr7:8215896-8215946	NT2-D1	testis:	n/a
34	chr7:8229083-8229133	AG04450	lung:	fetal
35	chr7:8215896-8215946	GM19239	blood:	n/a
36	chr7:8229083-8229133	LNCaP	prostate:	n/a
37	chr7:8215896-8215946	AoSMC	blood vessel:	n/a
38	chr7:8215896-8215946	HMEC	breast:	n/a
39	chr7:8229083-8229133	HCF	heart:	n/a
40	chr7:8215896-8215946	SKMC	muscle:	n/a
41	chr7:8229083-8229133	RPTEC	kidney:	n/a
42	chr7:8229083-8229133	GM06990	blood:	n/a
43	chr7:8215896-8215946	MCF10A-Er-Src	breast:	n/a
44	chr7:8229083-8229133	ovcar-3	ovarian:	n/a
45	chr7:8215896-8215946	NH-A	brain:	n/a
46	chr7:8229083-8229133	HepG2	liver:	n/a
47	chr7:8215896-8215946	HL-60	blood:	n/a
48	chr7:8229083-8229133	SK-N-SH	brain:	n/a
49	chr7:8215896-8215946	HEK293	kidney:	embryo
50	chr7:8215896-8215946	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr7:8227315..8228126-chr7:8240839..8241708,2	K562	blood:
2	chr7:8008227..8010223-chr7:8228966..8231576,2	MCF-7	breast:
3	chr7:8227287..8229114-chr7:8244454..8246101,2	K562	blood:
4	chr7:8007571..8010439-chr7:8221411..8223196,2	MCF-7	breast:
5	chr7:8202112..8204427-chr7:8208191..8210317,2	MCF-7	breast:
6	chr7:8175278..8177805-chr7:8220931..8222819,2	K562	blood:
7	chr7:8215446..8219264-chr7:8225856..8231601,6	K562	blood:
8	chr7:8211099..8214068-chr7:8215795..8217513,2	K562	blood:
9	chr7:8202112..8204427-chr7:8208191..8210317,2	MCF-7	breast:
10	chr7:8215446..8217652-chr7:8225856..8228822,2	K562	blood:
11	chr7:8215446..8217652-chr7:8225856..8228822,2	K562	blood:
12	chr7:8209481..8211685-chr7:8214647..8216903,2	K562	blood:
13	chr7:8209481..8211685-chr7:8214647..8216903,2	K562	blood:
14	chr2:182755000..182757642-chr7:8220780..8223755,2	MCF-7	breast:
15	chr7:8215446..8219264-chr7:8225856..8231601,6	K562	blood:
16	chr7:8222291..8223981-chr7:8225948..8229409,3	K562	blood:
17	chr7:8211099..8214068-chr7:8215795..8217513,2	K562	blood:
18	chr7:8222291..8223981-chr7:8225948..8229409,3	K562	blood:

No data

Variant related genes	Relation type
ICA1	TF binding region
ICA1	CpG island
ENSG00000106415	chromatin interactions
ENSG00000233108	chromatin interactions
ENSG00000138434	chromatin interactions
ENSG00000260742	chromatin interactions

Extended variants
information (count: 1201 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1201 , 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	rs7799828	chr7:8202132-8202133	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs547505756	chr7:8202197-8202198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs115077045	chr7:8202209-8202210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116616480	chr7:8202222-8202223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113418579	chr7:8202251-8202252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs73232272	chr7:8202267-8202268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536963895	chr7:8202327-8202328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs6463774	chr7:8202361-8202362	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs181310226	chr7:8202379-8202380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146386715	chr7:8202418-8202419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139564514	chr7:8202424-8202425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs144197207	chr7:8202425-8202426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185841205	chr7:8202459-8202460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563768386	chr7:8202464-8202465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs575846325	chr7:8202475-8202476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113933952	chr7:8202511-8202512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561126713	chr7:8202515-8202516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374663031	chr7:8202591-8202592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544157816	chr7:8202597-8202598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562128600	chr7:8202614-8202615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529530358	chr7:8202634-8202635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs6463775	chr7:8202637-8202638	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs565719901	chr7:8202639-8202640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs148744589	chr7:8202641-8202642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs202005113	chr7:8202651-8202652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565214579	chr7:8202674-8202675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs117619938	chr7:8202675-8202676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114256237	chr7:8202685-8202686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370681886	chr7:8202688-8202689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190697154	chr7:8202691-8202692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544836661	chr7:8202702-8202703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532174797	chr7:8202707-8202708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs142316798	chr7:8202714-8202715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552901099	chr7:8202744-8202745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572537360	chr7:8202839-8202840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546343926	chr7:8202846-8202847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs151199909	chr7:8202858-8202859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs111322508	chr7:8202873-8202874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550405018	chr7:8202906-8202907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543750490	chr7:8203025-8203026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562450312	chr7:8203042-8203043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529562356	chr7:8203049-8203050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114698245	chr7:8203117-8203118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181566259	chr7:8203162-8203163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532834706	chr7:8203163-8203164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs140283238	chr7:8203190-8203191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs147017909	chr7:8203300-8203301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147641280	chr7:8203328-8203329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs548706532	chr7:8203346-8203347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs80155031	chr7:8203351-8203352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Melanoma	18172304	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
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Williams Syndrome	20824207	CNVD
Renal cell carcinoma	18194544	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:520 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:8172400-8215800	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr7:8186800-8208600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr7:8190600-8214000	Weak transcription	Primary B cells from cord blood	blood
4	chr7:8192400-8217800	Weak transcription	Psoas Muscle	Psoas
5	chr7:8192400-8226600	Weak transcription	Fetal Stomach	stomach
6	chr7:8192600-8203200	Weak transcription	Right Ventricle	heart
7	chr7:8192600-8207400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr7:8192800-8205200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr7:8192800-8241400	Weak transcription	Pancreas	Pancrea
10	chr7:8194800-8214600	Weak transcription	Primary hematopoietic stem cells	blood
11	chr7:8196200-8215400	Weak transcription	Fetal Intestine Large	intestine
12	chr7:8197200-8214400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr7:8198000-8213600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:8199800-8208200	Weak transcription	Adipose Nuclei	Adipose
15	chr7:8200000-8202200	Enhancers	Fetal Heart	heart
16	chr7:8201000-8204600	Weak transcription	Brain Angular Gyrus	brain
17	chr7:8201400-8202400	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr7:8201400-8204400	Weak transcription	Left Ventricle	heart
19	chr7:8201400-8214600	Weak transcription	Fetal Intestine Small	intestine
20	chr7:8201400-8215400	Weak transcription	Spleen	Spleen
21	chr7:8201400-8218400	Weak transcription	Gastric	stomach
22	chr7:8201600-8203000	Weak transcription	K562	blood
23	chr7:8201600-8205600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr7:8201600-8207000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr7:8201600-8207400	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr7:8201600-8217400	Weak transcription	Brain Anterior Caudate	brain
27	chr7:8201800-8207400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr7:8201800-8208800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr7:8202000-8202600	Weak transcription	HSMMtube	muscle
30	chr7:8202200-8204600	Weak transcription	Fetal Heart	heart
31	chr7:8203200-8203400	Enhancers	Right Ventricle	heart
32	chr7:8203400-8203600	Enhancers	HSMMtube	muscle
33	chr7:8203400-8203600	Enhancers	K562	blood
34	chr7:8204400-8205200	Enhancers	Left Ventricle	heart
35	chr7:8204600-8204800	Enhancers	Brain Angular Gyrus	brain
36	chr7:8204600-8205000	Enhancers	Primary B cells from peripheral blood	blood
37	chr7:8204600-8205200	Enhancers	Fetal Heart	heart
38	chr7:8205200-8206600	Weak transcription	Fetal Heart	heart
39	chr7:8205200-8215800	Weak transcription	Left Ventricle	heart
40	chr7:8206600-8208400	Enhancers	Fetal Heart	heart
41	chr7:8207000-8207800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr7:8207200-8208200	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr7:8207400-8208000	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr7:8207400-8208000	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr7:8207400-8208000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr7:8207400-8208200	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr7:8207400-8208400	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr7:8207600-8208000	Enhancers	H1 Cell Line	embryonic stem cell
49	chr7:8207600-8208200	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr7:8207600-8208400	Enhancers	Liver	Liver

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