Variant report

Variant	nsv887451
Chromosome Location	chr7:6779270-6985071
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2326)
CpG islands
(count:4397)
Chromatin interactive
region (count:9)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2326 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:6962881-6963081	K562	blood:	n/a	n/a
2	BACH1	chr7:6897551-6897628	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr7:6959520-6959921	GM12878	blood:	n/a	chr7:6959720-6959731
4	BATF	chr7:6911365-6911638	GM12878	blood:	n/a	n/a
5	BATF	chr7:6897373-6897774	GM12878	blood:	n/a	n/a
6	BATF	chr7:6865157-6865489	GM12878	blood:	n/a	n/a
7	BATF	chr7:6865860-6866054	GM12878	blood:	n/a	n/a
8	BATF	chr7:6967256-6967613	GM12878	blood:	n/a	n/a
9	BATF	chr7:6965828-6966219	GM12878	blood:	n/a	n/a
10	BATF	chr7:6882514-6882830	GM12878	blood:	n/a	n/a
11	BATF	chr7:6911459-6911623	GM12878	blood:	n/a	n/a
12	BATF	chr7:6965792-6966222	GM12878	blood:	n/a	n/a
13	BATF	chr7:6930048-6930266	GM12878	blood:	n/a	chr7:6930144-6930155
14	BATF	chr7:6970367-6970679	GM12878	blood:	n/a	n/a
15	BATF	chr7:6967768-6968127	GM12878	blood:	n/a	n/a
16	BATF	chr7:6959640-6959863	GM12878	blood:	n/a	chr7:6959720-6959731
17	BATF	chr7:6967778-6968070	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:6865814-6866066	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:6966697-6966858	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:6967360-6967540	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:6897283-6897636	GM12878	blood:	n/a	chr7:6897421-6897434
22	BCL11A	chr7:6965815-6966145	GM12878	blood:	n/a	chr7:6966028-6966037
23	BCL11A	chr7:6967281-6967607	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:6965764-6966259	GM12878	blood:	n/a	chr7:6966028-6966037
25	BCL11A	chr7:6968204-6968549	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:6970443-6970693	GM12878	blood:	n/a	n/a
27	BCL3	chr7:6928564-6929398	GM12878	blood:	n/a	n/a
28	BCL3	chr7:6928637-6929472	GM12878	blood:	n/a	n/a
29	BCL3	chr7:6870972-6871253	GM12878	blood:	n/a	n/a
30	BCL3	chr7:6873151-6873685	GM12878	blood:	n/a	n/a
31	BCL3	chr7:6916434-6916785	GM12878	blood:	n/a	n/a
32	BCL3	chr7:6872794-6873775	GM12878	blood:	n/a	n/a
33	BCLAF1	chr7:6897456-6897677	GM12878	blood:	n/a	n/a
34	BHLHE40	chr7:6897488-6897590	GM12878	blood:	n/a	n/a
35	BHLHE40	chr7:6865906-6866108	K562	blood:	n/a	n/a
36	BHLHE40	chr7:6962913-6963006	K562	blood:	n/a	n/a
37	BHLHE40	chr7:6967280-6967585	GM12878	blood:	n/a	n/a
38	BHLHE40	chr7:6968034-6968094	GM12878	blood:	n/a	n/a
39	BHLHE40	chr7:6832293-6832495	HepG2	liver:	n/a	n/a
40	BHLHE40	chr7:6929175-6929309	K562	blood:	n/a	n/a
41	BHLHE40	chr7:6832136-6832415	HepG2	liver:	n/a	n/a
42	BHLHE40	chr7:6865917-6866116	GM12878	blood:	n/a	n/a
43	BHLHE40	chr7:6943039-6943099	GM12878	blood:	n/a	n/a
44	CBX3	chr7:6803410-6803703	K562	blood:	n/a	n/a
45	CBX3	chr7:6962801-6963079	K562	blood:	n/a	n/a
46	CBX3	chr7:6864785-6865473	K562	blood:	n/a	n/a
47	CBX3	chr7:6866895-6867260	K562	blood:	n/a	n/a
48	CBX3	chr7:6965814-6966339	K562	blood:	n/a	n/a
49	CBX3	chr7:6865752-6866597	K562	blood:	n/a	n/a
50	CBX3	chr7:6977915-6978267	K562	blood:	n/a	n/a

(count:4397 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6897353-6897403	H1-hESC	embryonic stem cell:	embryo
2	chr7:6893553-6893603	HCT-116	colon:	n/a
3	chr7:6915508-6915558	LNCaP	prostate:	n/a
4	chr7:6865915-6865965	HIPEpiC	eye:	n/a
5	chr7:6887294-6887344	Hepatocyte	liver:	n/a
6	chr7:6897353-6897403	H1-hESC	embryonic stem cell:	embryo
7	chr7:6893553-6893603	HCT-116	colon:	n/a
8	chr7:6915508-6915558	LNCaP	prostate:	n/a
9	chr7:6865915-6865965	HIPEpiC	eye:	n/a
10	chr7:6887294-6887344	Hepatocyte	liver:	n/a
11	chr7:6974956-6975006	NH-A	brain:	n/a
12	chr7:6861742-6861792	Hepatocyte	liver:	n/a
13	chr7:6894869-6894919	NT2-D1	testis:	n/a
14	chr7:6885539-6885589	HPAEpiC	pulmonary alveolar:	n/a
15	chr7:6885539-6885589	HEK293	kidney:	embryo
16	chr7:6921561-6921611	NHBE	bronchial:	n/a
17	chr7:6865960-6866010	ProgFib	skin:	n/a
18	chr7:6886021-6886071	HCPEpiC	choroid plexus:	n/a
19	chr7:6921561-6921611	IMR90	lung:	fetal
20	chr7:6886021-6886071	MCF-7	breast:	n/a
21	chr7:6797497-6797547	HUVEC	blood vessel:	n/a
22	chr7:6793977-6794027	GM12891	blood:	n/a
23	chr7:6867074-6867124	HPAEpiC	pulmonary alveolar:	n/a
24	chr7:6885918-6885968	GM12891	blood:	n/a
25	chr7:6882194-6882244	CMK	blood:	n/a
26	chr7:6866072-6866122	MCF10A-Er-Src	breast:	n/a
27	chr7:6887187-6887237	RPTEC	kidney:	n/a
28	chr7:6974758-6974808	AG04449	skin:	fetal
29	chr7:6915508-6915558	HRPEpiC	eye:	n/a
30	chr7:6864491-6864541	HEEpiC	esophagus:	n/a
31	chr7:6892911-6892961	HCPEpiC	choroid plexus:	n/a
32	chr7:6897353-6897403	HRE	kidney:	n/a
33	chr7:6797497-6797547	MCF-7	breast:	n/a
34	chr7:6893572-6893622	NHDF-neo	bronchial:	n/a
35	chr7:6819532-6819582	Hepatocyte	liver:	n/a
36	chr7:6797497-6797547	HEK293	kidney:	embryo
37	chr7:6977556-6977606	HCPEpiC	choroid plexus:	n/a
38	chr7:6865960-6866010	MCF10A-Er-Src	breast:	n/a
39	chr7:6861742-6861792	ProgFib	skin:	n/a
40	chr7:6886021-6886071	SK-N-SH	brain:	n/a
41	chr7:6865886-6865936	HCPEpiC	choroid plexus:	n/a
42	chr7:6865970-6866020	AG09309	skin:	n/a
43	chr7:6886021-6886071	HCT-116	colon:	n/a
44	chr7:6865965-6866015	Jurkat	blood:	n/a
45	chr7:6888133-6888183	PFSK-1	brain:	n/a
46	chr7:6897353-6897403	GM12878	blood:	n/a
47	chr7:6790012-6790062	PrEC	prostate:	n/a
48	chr7:6800488-6800538	U87	brain:	n/a
49	chr7:6910741-6910791	AG04449	skin:	fetal
50	chr7:6892911-6892961	A549	lung:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:6629513..6630064-chr7:6897112..6897752,3	MCF-7	breast:
2	chr7:6766860..6769459-chr7:6864426..6866111,2	MCF-7	breast:
3	chr7:6362339..6362861-chr7:6969838..6970665,2	K562	blood:
4	chr7:6865395..6868378-chr7:6875321..6876917,2	MCF-7	breast:
5	chr7:6144018..6145898-chr7:6967333..6970236,2	K562	blood:
6	chr7:6628333..6631201-chr7:6866874..6868650,2	MCF-7	breast:
7	chr7:6865395..6868378-chr7:6875321..6876917,2	MCF-7	breast:
8	chr7:6865923..6867484-chr7:6871034..6873441,2	MCF-7	breast:
9	chr7:6487483..6489084-chr7:6871444..6873922,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RSPH10B2-1	chr7:6792653-6793492	NONHSAT119063
2	lnc-CCZ1B-1	chr7:6836407-6836567	NONHSAT119073
3	lnc-CCZ1B-5	chr7:6963709-6964144	NONHSAT119086
4	lnc-CCZ1B-1	chr7:6836264-6836309	NONHSAT119073
5	lnc-CCZ1B-1	chr7:6833772-6834166	NONHSAT119073

No data

Variant related genes	Relation type
RSPH10B2	TF binding region
ALG1L5P	TF binding region
FAM86LP	TF binding region
ENSG00000241539	TF binding region
OR7E136P	TF binding region
CCZ1B	TF binding region
ENSG00000263457	TF binding region
ENSG00000243531	TF binding region
UNC93B2	TF binding region
OR7E59P	TF binding region
OR7E39P	TF binding region
RSPH10B2	CpG island
ALG1L5P	CpG island
FAM86LP	CpG island
ENSG00000241539	CpG island
OR7E136P	CpG island
CCZ1B	CpG island
ENSG00000263457	CpG island
ENSG00000243531	CpG island
UNC93B2	CpG island
OR7E59P	CpG island
OR7E39P	CpG island
ENSG00000273252	chromatin interactions
ENSG00000106346	chromatin interactions
ENSG00000146574	chromatin interactions
ENSG00000146576	chromatin interactions
ENSG00000164535	chromatin interactions
ENSG00000187953	chromatin interactions
ENSG00000232581	chromatin interactions

Extended variants
information (count: 8476 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:8476 , 50 per page) page: 1 2 3 4 5 6 7 ... 170

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7779296	chr7:6779270-6779271	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553603745	chr7:6779296-6779297	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572057568	chr7:6779398-6779399	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138969533	chr7:6779432-6779433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557704784	chr7:6779586-6779587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576068197	chr7:6779587-6779588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142968665	chr7:6779608-6779609	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561834710	chr7:6779623-6779624	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573637652	chr7:6779624-6779625	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547056140	chr7:6779633-6779634	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112940427	chr7:6779660-6779661	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186827201	chr7:6779662-6779663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376245879	chr7:6779695-6779696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191589505	chr7:6779730-6779731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139673105	chr7:6779751-6779752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182673693	chr7:6779797-6779798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs62439737	chr7:6779810-6779811	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs187285573	chr7:6779834-6779835	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147890389	chr7:6779875-6779876	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567425235	chr7:6779876-6779877	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs62439738	chr7:6779896-6779897	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs192103485	chr7:6779901-6779902	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs145266107	chr7:6779941-6779942	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565625365	chr7:6779947-6779948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539382396	chr7:6779948-6779949	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375541589	chr7:6780013-6780014	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs149119078	chr7:6780042-6780043	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs185242679	chr7:6780056-6780057	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190535998	chr7:6780063-6780064	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573825000	chr7:6780155-6780156	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs193104035	chr7:6780175-6780176	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553036596	chr7:6780203-6780204	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs10215807	chr7:6780231-6780232	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs545348459	chr7:6780235-6780236	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs564018306	chr7:6780248-6780249	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530961303	chr7:6780258-6780259	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs543254148	chr7:6780294-6780295	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs529414262	chr7:6780303-6780304	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs137969747	chr7:6780306-6780307	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs528600081	chr7:6780338-6780339	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs546570112	chr7:6780360-6780361	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs571282103	chr7:6780361-6780362	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532557566	chr7:6780362-6780363	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs112453795	chr7:6780480-6780481	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112080835	chr7:6780485-6780486	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185833785	chr7:6780493-6780494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371996328	chr7:6780519-6780520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188074840	chr7:6780532-6780533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181022341	chr7:6780533-6780534	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536848869	chr7:6780576-6780577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
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
Glioblastoma multiforme	21525872	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1497 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6770000-6783400	Weak transcription	Aorta	Aorta
2	chr7:6770200-6782600	Weak transcription	Small Intestine	intestine
3	chr7:6770400-6784800	Weak transcription	NHLF	lung
4	chr7:6770800-6786400	Weak transcription	Fetal Brain Male	brain
5	chr7:6771000-6782000	Strong transcription	Fetal Stomach	stomach
6	chr7:6771000-6786200	Weak transcription	HUVEC	blood vessel
7	chr7:6771000-6786400	Weak transcription	Primary B cells from cord blood	blood
8	chr7:6771200-6780200	Weak transcription	Right Atrium	heart
9	chr7:6771200-6781400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr7:6771200-6792400	Weak transcription	NHEK	skin
11	chr7:6771600-6781800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr7:6771800-6780400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr7:6771800-6783400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:6772000-6780400	Strong transcription	Fetal Muscle Trunk	muscle
15	chr7:6772000-6780400	Strong transcription	Fetal Thymus	thymus
16	chr7:6772000-6781600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr7:6772000-6782000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr7:6772000-6782600	Strong transcription	Primary neutrophils fromperipheralblood	blood
19	chr7:6772000-6782600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr7:6772200-6780600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr7:6772400-6780600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr7:6772400-6780600	Strong transcription	Placenta	Placenta
23	chr7:6772400-6783200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr7:6772600-6780400	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr7:6772800-6787000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr7:6773000-6783200	Weak transcription	Brain Cingulate Gyrus	brain
27	chr7:6773000-6786400	Weak transcription	Rectal Smooth Muscle	rectum
28	chr7:6773200-6780200	Strong transcription	Lung	lung
29	chr7:6773400-6788200	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr7:6773600-6784400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr7:6774000-6782000	Weak transcription	Hela-S3	cervix
32	chr7:6774600-6780400	Strong transcription	Adipose Nuclei	Adipose
33	chr7:6774600-6780400	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr7:6775400-6781800	Weak transcription	HMEC	breast
35	chr7:6775800-6785000	Weak transcription	NH-A	brain
36	chr7:6776200-6783200	Weak transcription	Right Ventricle	heart
37	chr7:6777000-6780200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr7:6777200-6780200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr7:6777200-6784000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr7:6777200-6784800	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr7:6777200-6785000	Weak transcription	HSMM	muscle
42	chr7:6777200-6786600	Weak transcription	HSMMtube	muscle
43	chr7:6777400-6779400	Weak transcription	Duodenum Mucosa	Duodenum
44	chr7:6777400-6779600	Weak transcription	Thymus	Thymus
45	chr7:6777400-6779800	Weak transcription	Primary T cells from cord blood	blood
46	chr7:6777400-6779800	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chr7:6777400-6779800	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr7:6777400-6779800	Weak transcription	Stomach Smooth Muscle	stomach
49	chr7:6777400-6780400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr7:6777400-6781800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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