Variant report

Variant	nsv981398
Chromosome Location	chr7:66138644-66147890
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:617)
CpG islands
(count:367)
Chromatin interactive
region (count:29)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:617 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:66146912-66146994	K562	blood:	n/a	n/a
2	ARID3A	chr7:66146925-66147085	HepG2	liver:	n/a	n/a
3	ATF1	chr7:66146843-66147259	K562	blood:	n/a	n/a
4	ATF2	chr7:66146901-66147280	GM12878	blood:	n/a	n/a
5	ATF2	chr7:66146785-66147102	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr7:66146428-66147281	GM12878	blood:	n/a	n/a
7	BACH1	chr7:66146150-66146295	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:66146843-66146847	K562	blood:	n/a	n/a
9	BACH1	chr7:66147108-66147386	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr7:66146732-66147074	GM12878	blood:	n/a	n/a
11	BCL3	chr7:66146800-66147433	A549	lung:	n/a	chr7:66147274-66147287 chr7:66146867-66146876
12	BCL3	chr7:66146714-66147505	A549	lung:	n/a	chr7:66147274-66147287 chr7:66146867-66146876
13	BCL3	chr7:66146714-66147567	GM12878	blood:	n/a	chr7:66147274-66147287 chr7:66146867-66146876
14	BCLAF1	chr7:66146640-66147288	GM12878	blood:	n/a	chr7:66147274-66147287 chr7:66146867-66146876
15	BHLHE40	chr7:66146791-66147468	K562	blood:	n/a	n/a
16	BHLHE40	chr7:66146815-66147330	HepG2	liver:	n/a	n/a
17	BHLHE40	chr7:66146781-66147502	GM12878	blood:	n/a	n/a
18	BRCA1	chr7:66146848-66147364	GM12878	blood:	n/a	n/a
19	BRCA1	chr7:66146848-66147257	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr7:66146708-66147277	HepG2	liver:	n/a	n/a
21	CBX3	chr7:66146127-66148017	K562	blood:	n/a	n/a
22	CCNT2	chr7:66146708-66147651	K562	blood:	n/a	n/a
23	CCNT2	chr7:66143845-66144112	K562	blood:	n/a	n/a
24	CEBPB	chr7:66147839-66148014	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr7:66146962-66147162	K562	blood:	n/a	n/a
26	CEBPB	chr7:66145917-66146277	K562	blood:	n/a	n/a
27	CEBPB	chr7:66146808-66147565	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr7:66147795-66148169	IMR90	lung:	n/a	n/a
29	CEBPB	chr7:66145948-66146273	K562	blood:	n/a	n/a
30	CEBPD	chr7:66146795-66147330	HepG2	liver:	n/a	n/a
31	CEBPD	chr7:66146524-66147442	K562	blood:	n/a	n/a
32	CHD1	chr7:66146109-66149232	IMR90	lung:	n/a	n/a
33	CHD1	chr7:66146811-66147637	GM12878	blood:	n/a	n/a
34	CHD2	chr7:66146690-66147500	GM12878	blood:	n/a	n/a
35	CHD2	chr7:66146747-66147518	K562	blood:	n/a	n/a
36	CHD2	chr7:66146825-66147744	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr7:66146685-66147276	HepG2	liver:	n/a	n/a
38	CREB1	chr7:66146734-66147306	ECC-1	luminal epithelium:	n/a	n/a
39	CREB1	chr7:66146598-66147654	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr7:66146675-66147674	HepG2	liver:	n/a	n/a
41	CREB1	chr7:66146611-66147660	GM12878	blood:	n/a	n/a
42	CREB1	chr7:66146698-66147654	A549	lung:	n/a	n/a
43	CREB1	chr7:66146717-66147655	K562	blood:	n/a	n/a
44	CREB1	chr7:66146799-66147588	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr7:66146578-66147595	K562	blood:	n/a	n/a
46	CREB1	chr7:66146757-66147259	A549	lung:	n/a	n/a
47	CREB1	chr7:66146779-66147393	ECC-1	luminal epithelium:	n/a	n/a
48	CREB1	chr7:66146606-66147743	HepG2	liver:	n/a	n/a
49	CTCF	chr7:66146900-66147050	SAEC	small airway:	n/a	n/a
50	CTCF	chr7:66146770-66146822	MCF-7	breast:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:66146628-66146678	ECC-1	luminal epithelium:	n/a
2	chr7:66146628-66146678	ECC-1	luminal epithelium:	n/a
3	chr7:66147017-66147067	HepG2	liver:	n/a
4	chr7:66147509-66147559	CMK	blood:	n/a
5	chr7:66144066-66144116	ECC-1	luminal epithelium:	n/a
6	chr7:66147174-66147224	ECC-1	luminal epithelium:	n/a
7	chr7:66146628-66146678	K562	blood:	n/a
8	chr7:66144066-66144116	AG04450	lung:	fetal
9	chr7:66144066-66144116	HAEpiC	amniotic membrane:	n/a
10	chr7:66144066-66144116	Hepatocyte	liver:	n/a
11	chr7:66144066-66144116	ProgFib	skin:	n/a
12	chr7:66147081-66147131	PANC-1	pancreas:	n/a
13	chr7:66147017-66147067	AoSMC	blood vessel:	n/a
14	chr7:66144066-66144116	Jurkat	blood:	n/a
15	chr7:66147174-66147224	Hepatocyte	liver:	n/a
16	chr7:66146628-66146678	HRCEpiC	kidney:	n/a
17	chr7:66147509-66147559	U87	brain:	n/a
18	chr7:66147081-66147131	HepG2	liver:	n/a
19	chr7:66147017-66147067	Jurkat	blood:	n/a
20	chr7:66147081-66147131	Hepatocyte	liver:	n/a
21	chr7:66147017-66147067	MCF-7	breast:	n/a
22	chr7:66147509-66147559	PFSK-1	brain:	n/a
23	chr7:66147081-66147131	NHDF-neo	bronchial:	n/a
24	chr7:66147509-66147559	ProgFib	skin:	n/a
25	chr7:66146628-66146678	HRPEpiC	eye:	n/a
26	chr7:66147081-66147131	HRCEpiC	kidney:	n/a
27	chr7:66147017-66147067	LNCaP	prostate:	n/a
28	chr7:66147174-66147224	MCF-7	breast:	n/a
29	chr7:66147174-66147224	SAEC	small airway:	n/a
30	chr7:66147081-66147131	AG04449	skin:	fetal
31	chr7:66147509-66147559	AG04449	skin:	fetal
32	chr7:66147509-66147559	SK-N-MC	brain:	n/a
33	chr7:66146628-66146678	HepG2	liver:	n/a
34	chr7:66144066-66144116	PrEC	prostate:	n/a
35	chr7:66144066-66144116	HRCEpiC	kidney:	n/a
36	chr7:66147174-66147224	HAEpiC	amniotic membrane:	n/a
37	chr7:66144066-66144116	HepG2	liver:	n/a
38	chr7:66147017-66147067	AG04450	lung:	fetal
39	chr7:66147174-66147224	AG04449	skin:	fetal
40	chr7:66147174-66147224	GM12892	blood:	n/a
41	chr7:66147081-66147131	AG09309	skin:	n/a
42	chr7:66147017-66147067	MCF10A-Er-Src	breast:	n/a
43	chr7:66147081-66147131	SK-N-SH	brain:	n/a
44	chr7:66147017-66147067	ovcar-3	ovarian:	n/a
45	chr7:66146628-66146678	AG09309	skin:	n/a
46	chr7:66147081-66147131	GM19239	blood:	n/a
47	chr7:66147509-66147559	HNPCEpiC	eye:	n/a
48	chr7:66144066-66144116	NT2-D1	testis:	n/a
49	chr7:66144066-66144116	NHBE	bronchial:	n/a
50	chr7:66146628-66146678	Jurkat	blood:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:66142067..66143844-chr7:66145620..66147902,2	K562	blood:
2	chr7:66146728..66147607-chr7:66205638..66206158,2	NB4	blood:
3	chr7:66147345..66148941-chr7:66150960..66153085,3	K562	blood:
4	chr7:66145930..66148922-chr7:66213233..66215140,2	MCF-7	breast:
5	chr19:38826520..38827474-chr7:66146585..66147505,2	Hela-S3	cervix:
6	chr7:66119464..66119965-chr7:66146773..66147348,2	MCF-7	breast:
7	chr7:66118965..66120049-chr7:66146710..66147584,5	MCF-7	breast:
8	chr5:149829161..149829687-chr7:66146493..66147190,2	Hela-S3	cervix:
9	chr7:66118759..66121837-chr7:66141888..66144754,3	K562	blood:
10	chr7:66145819..66148736-chr7:66203770..66205462,3	MCF-7	breast:
11	chr1:180123619..180124402-chr7:66147119..66147881,2	NB4	blood:
12	chr7:66134305..66137456-chr7:66140702..66144674,4	K562	blood:
13	chr7:66140247..66145111-chr7:66145587..66148696,5	K562	blood:
14	chr1:25573287..25574307-chr7:66146290..66147502,3	Hela-S3	cervix:
15	chr7:66121223..66123141-chr7:66144196..66146928,3	MCF-7	breast:
16	chr7:66118403..66121534-chr7:66142637..66144652,3	K562	blood:
17	chr7:66133503..66137997-chr7:66139253..66143655,5	MCF-7	breast:
18	chr7:66137517..66139901-chr7:66146060..66148754,2	K562	blood:
19	chr1:36396098..36396815-chr7:66147191..66147691,2	Hela-S3	cervix:
20	chr7:66140006..66143902-chr7:66147034..66148710,3	MCF-7	breast:
21	chr7:66119490..66121348-chr7:66145844..66148158,2	K562	blood:
22	chr7:66145800..66148420-chr7:66309175..66311369,3	MCF-7	breast:
23	chr7:66144717..66148625-chr7:66203954..66207507,5	K562	blood:
24	chr7:66144088..66147004-chr7:66459962..66461648,2	MCF-7	breast:
25	chr19:49468432..49469010-chr7:66147016..66147572,2	Hela-S3	cervix:
26	chr7:66056772..66058576-chr7:66145183..66146865,2	MCF-7	breast:
27	chr7:66147119..66147718-chr7:66386034..66386593,2	Hela-S3	cervix:
28	chr7:66144687..66148625-chr7:66203954..66207507,6	K562	blood:
29	chr7:66118152..66121117-chr7:66145225..66147766,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RABGEF1-3	chr7:66147132-66147245	NONHSAT121219
2	lnc-RABGEF1-3	chr7:66147078-66147245	NR_104676
3	lnc-RABGEF1-3	chr7:66147150-66147245	NONHSAT121220

No data

Variant related genes	Relation type
RABGEF1	TF binding region
RABGEF1	CpG island
ENSG00000154710	chromatin interactions
ENSG00000126070	chromatin interactions
ENSG00000243335	chromatin interactions
ENSG00000099338	chromatin interactions
ENSG00000198874	chromatin interactions
ENSG00000272831	chromatin interactions
ENSG00000126524	chromatin interactions
ENSG00000164587	chromatin interactions
ENSG00000232559	chromatin interactions
ENSG00000106609	chromatin interactions
ENSG00000087086	chromatin interactions
ENSG00000116260	chromatin interactions
ENSG00000271064	chromatin interactions
ENSG00000117616	chromatin interactions
ENSG00000226824	chromatin interactions
ENSG00000230583	chromatin interactions

Extended variants
information (count: 400 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:400 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575109031	chr7:66138744-66138745	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs546792089	chr7:66138780-66138781	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs368519416	chr7:66138781-66138782	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs397804163	chr7:66138853-66138854	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs554566897	chr7:66138854-66138855	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs560871788	chr7:66138873-66138874	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs1612694	chr7:66138957-66138958	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs529217394	chr7:66138960-66138961	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs7785213	chr7:66138978-66138979	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs559533679	chr7:66138986-66138987	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs12537545	chr7:66139073-66139074	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs183666410	chr7:66139104-66139105	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs571822798	chr7:66139105-66139106	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs577013179	chr7:66139124-66139125	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs12534355	chr7:66139170-66139171	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs373217673	chr7:66139171-66139172	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs199512819	chr7:66139178-66139179	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs7789419	chr7:66139180-66139181	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs75898109	chr7:66139195-66139196	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs528795659	chr7:66139248-66139249	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs11765921	chr7:66139287-66139288	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
22	rs536972837	chr7:66139335-66139336	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs115560368	chr7:66139362-66139363	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs12234826	chr7:66139365-66139366	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs141480643	chr7:66139373-66139374	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs558375260	chr7:66139375-66139376	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs188035440	chr7:66139387-66139388	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs544018701	chr7:66139418-66139419	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs373384191	chr7:66139426-66139427	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs142668411	chr7:66139476-66139477	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs540198817	chr7:66139480-66139481	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs372277500	chr7:66139487-66139488	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs566341805	chr7:66139492-66139493	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs528479580	chr7:66139498-66139499	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs551082678	chr7:66139524-66139525	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs182228358	chr7:66139607-66139608	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs545453129	chr7:66139647-66139648	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs187298483	chr7:66139665-66139666	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs571002057	chr7:66139680-66139681	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs150940365	chr7:66139697-66139698	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs551172542	chr7:66139699-66139700	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs567906610	chr7:66139754-66139755	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs530413482	chr7:66139783-66139784	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs111242469	chr7:66139799-66139800	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs191752050	chr7:66139858-66139859	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs538278075	chr7:66139875-66139876	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs199895919	chr7:66139939-66139940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201085896	chr7:66139940-66139941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs72372036	chr7:66139950-66139951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs36102540	chr7:66139955-66139956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
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
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
Hodgkin''s lymphoma	18641027	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
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	18632612	CNVD
Schizophrenia	21346763	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:535 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:66120600-66146000	Weak transcription	Primary T cells from cord blood	blood
2	chr7:66120600-66146200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr7:66120800-66143600	Weak transcription	GM12878-XiMat	blood
4	chr7:66120800-66146000	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr7:66121000-66139400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr7:66121000-66143600	Weak transcription	Primary B cells from peripheral blood	blood
7	chr7:66121000-66144000	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr7:66121000-66146200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr7:66121000-66146200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr7:66121400-66139800	Weak transcription	Rectal Smooth Muscle	rectum
11	chr7:66121400-66146000	Weak transcription	Adipose Nuclei	Adipose
12	chr7:66121400-66146000	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr7:66121600-66144000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr7:66121600-66145400	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr7:66121600-66146200	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr7:66121600-66146200	Weak transcription	HSMMtube	muscle
17	chr7:66121800-66144000	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr7:66122600-66146000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr7:66127800-66146000	Weak transcription	A549	lung
20	chr7:66128000-66144000	Weak transcription	Pancreas	Pancrea
21	chr7:66128000-66144000	Weak transcription	Spleen	Spleen
22	chr7:66128000-66145800	Weak transcription	Primary B cells from cord blood	blood
23	chr7:66128000-66146000	Weak transcription	Duodenum Mucosa	Duodenum
24	chr7:66128000-66146000	Weak transcription	Fetal Lung	lung
25	chr7:66128000-66146000	Weak transcription	HSMM	muscle
26	chr7:66128000-66146200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr7:66128000-66146200	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr7:66128000-66146400	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr7:66131200-66146000	Weak transcription	Stomach Smooth Muscle	stomach
30	chr7:66132400-66146000	Weak transcription	Colon Smooth Muscle	Colon
31	chr7:66133600-66146000	Weak transcription	Primary hematopoietic stem cells	blood
32	chr7:66134400-66143800	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr7:66134400-66146000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr7:66134400-66146400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr7:66134600-66141400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr7:66134600-66143800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr7:66134600-66145800	Weak transcription	Thymus	Thymus
38	chr7:66135000-66144800	Weak transcription	Dnd41	blood
39	chr7:66135000-66145800	Weak transcription	Placenta	Placenta
40	chr7:66135000-66146000	Weak transcription	Brain Germinal Matrix	brain
41	chr7:66135200-66139400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr7:66135200-66143800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr7:66135200-66144400	Weak transcription	Fetal Muscle Leg	muscle
44	chr7:66135200-66145800	Weak transcription	Fetal Muscle Trunk	muscle
45	chr7:66135200-66146200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr7:66135200-66146200	Weak transcription	Fetal Brain Female	brain
47	chr7:66135200-66146200	Weak transcription	NHLF	lung
48	chr7:66135200-66146400	Weak transcription	Lung	lung
49	chr7:66135200-66146400	Weak transcription	Ovary	ovary
50	chr7:66135400-66143600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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