Variant report

Variant	nsv606049
Chromosome Location	chr7:7949059-7967424
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:339)
CpG islands
(count:122)
Chromatin interactive
region (count:31)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:339 , 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	ATF2	chr7:7958625-7959819	GM12878	blood:	n/a	n/a
2	ATF2	chr7:7958697-7959462	GM12878	blood:	n/a	n/a
3	ATF2	chr7:7959982-7960638	GM12878	blood:	n/a	n/a
4	ATF2	chr7:7960070-7960623	GM12878	blood:	n/a	n/a
5	BATF	chr7:7960171-7960572	GM12878	blood:	n/a	n/a
6	BATF	chr7:7958720-7959043	GM12878	blood:	n/a	n/a
7	BATF	chr7:7959077-7959459	GM12878	blood:	n/a	n/a
8	BATF	chr7:7960131-7960582	GM12878	blood:	n/a	n/a
9	BATF	chr7:7959098-7959450	GM12878	blood:	n/a	n/a
10	BCL11A	chr7:7958762-7959113	GM12878	blood:	n/a	n/a
11	BCL11A	chr7:7960180-7960428	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:7960150-7960494	GM12878	blood:	n/a	n/a
13	BCL11A	chr7:7959156-7959459	GM12878	blood:	n/a	n/a
14	BCL3	chr7:7960150-7960591	GM12878	blood:	n/a	n/a
15	BCLAF1	chr7:7960024-7960613	GM12878	blood:	n/a	n/a
16	BCLAF1	chr7:7958610-7959527	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:7960099-7960686	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:7958749-7959392	GM12878	blood:	n/a	n/a
19	BRCA1	chr7:7952755-7953845	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr7:7950678-7951759	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr7:7952970-7953850	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr7:7950896-7951590	MCF-7	breast:	n/a	n/a
23	CEBPB	chr7:7958504-7958634	A549	lung:	n/a	n/a
24	CEBPB	chr7:7950791-7951591	MCF-7	breast:	n/a	n/a
25	CEBPB	chr7:7961525-7961725	A549	lung:	n/a	n/a
26	CEBPB	chr7:7951028-7951441	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr7:7950970-7951399	IMR90	lung:	n/a	n/a
28	CEBPB	chr7:7951010-7951401	HepG2	liver:	n/a	n/a
29	CEBPB	chr7:7953116-7953416	IMR90	lung:	n/a	n/a
30	CEBPB	chr7:7961566-7961742	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr7:7958425-7958655	IMR90	lung:	n/a	n/a
32	CEBPB	chr7:7958412-7958729	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr7:7962316-7962726	MCF-7	breast:	n/a	n/a
34	CEBPB	chr7:7958547-7958660	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr7:7953133-7953405	HepG2	liver:	n/a	n/a
36	CEBPB	chr7:7951014-7951271	A549	lung:	n/a	n/a
37	CEBPB	chr7:7950741-7951776	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr7:7960080-7960545	GM12878	blood:	n/a	n/a
39	CHD2	chr7:7953068-7953596	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr7:7958748-7959073	GM12878	blood:	n/a	n/a
41	CHD2	chr7:7950949-7951776	Hela-S3	cervix:	n/a	n/a
42	CREB1	chr7:7950935-7951373	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr7:7958797-7959561	GM12878	blood:	n/a	n/a
44	CTCF	chr7:7953220-7953370	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr7:7965508-7965555	MCF-7	breast:	n/a	n/a
46	CUX1	chr7:7958758-7959513	GM12878	blood:	n/a	n/a
47	CUX1	chr7:7963377-7963428	GM12878	blood:	n/a	n/a
48	CUX1	chr7:7959986-7960662	GM12878	blood:	n/a	n/a
49	E2F4	chr7:7966379-7966428	MCF10A-Er-Src	breast:	n/a	n/a
50	EBF1	chr7:7960140-7960431	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	chr7:7962810-7962860	H1-hESC	embryonic stem cell:	embryo
2	chr7:7959339-7959389	HEK293	kidney:	embryo
3	chr7:7962810-7962860	Hela-S3	cervix:	n/a
4	chr7:7959339-7959389	AG09319	gingival:	n/a
5	chr7:7962810-7962860	AG10803	skin:	n/a
6	chr7:7962810-7962860	HL-60	blood:	n/a
7	chr7:7959339-7959389	IMR90	lung:	fetal
8	chr7:7962810-7962860	MCF-7	breast:	n/a
9	chr7:7962810-7962860	GM12891	blood:	n/a
10	chr7:7962810-7962860	T-47D	breast:	n/a
11	chr7:7962810-7962860	HRCEpiC	kidney:	n/a
12	chr7:7959339-7959389	AG10803	skin:	n/a
13	chr7:7962810-7962860	Caco-2	colon:	n/a
14	chr7:7962810-7962860	HAEpiC	amniotic membrane:	n/a
15	chr7:7962810-7962860	HRPEpiC	eye:	n/a
16	chr7:7959339-7959389	HRPEpiC	eye:	n/a
17	chr7:7962810-7962860	SK-N-SH	brain:	n/a
18	chr7:7959339-7959389	MCF-7	breast:	n/a
19	chr7:7959339-7959389	BJ	skin:	n/a
20	chr7:7962810-7962860	SKMC	muscle:	n/a
21	chr7:7962810-7962860	HEEpiC	esophagus:	n/a
22	chr7:7959339-7959389	Hepatocyte	liver:	n/a
23	chr7:7959339-7959389	AG09309	skin:	n/a
24	chr7:7959339-7959389	GM12878	blood:	n/a
25	chr7:7962810-7962860	PANC-1	pancreas:	n/a
26	chr7:7959339-7959389	HCPEpiC	choroid plexus:	n/a
27	chr7:7962810-7962860	U87	brain:	n/a
28	chr7:7962810-7962860	PrEC	prostate:	n/a
29	chr7:7962810-7962860	HMEC	breast:	n/a
30	chr7:7959339-7959389	T-47D	breast:	n/a
31	chr7:7962810-7962860	IMR90	lung:	fetal
32	chr7:7959339-7959389	H1-hESC	embryonic stem cell:	embryo
33	chr7:7962810-7962860	NB4	blood:	n/a
34	chr7:7959339-7959389	HCT-116	colon:	n/a
35	chr7:7959339-7959389	HPAEpiC	pulmonary alveolar:	n/a
36	chr7:7962810-7962860	NT2-D1	testis:	n/a
37	chr7:7959339-7959389	HL-60	blood:	n/a
38	chr7:7962810-7962860	GM12878	blood:	n/a
39	chr7:7959339-7959389	SK-N-SH	brain:	n/a
40	chr7:7962810-7962860	SAEC	small airway:	n/a
41	chr7:7959339-7959389	AoSMC	blood vessel:	n/a
42	chr7:7962810-7962860	AG09309	skin:	n/a
43	chr7:7959339-7959389	NT2-D1	testis:	n/a
44	chr7:7959339-7959389	HIPEpiC	eye:	n/a
45	chr7:7959339-7959389	LNCaP	prostate:	n/a
46	chr7:7962810-7962860	MCF10A-Er-Src	breast:	n/a
47	chr7:7959339-7959389	AG04450	lung:	fetal
48	chr7:7959339-7959389	ovcar-3	ovarian:	n/a
49	chr7:7962810-7962860	NH-A	brain:	n/a
50	chr7:7959339-7959389	RPTEC	kidney:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:7958223..7960322-chr7:7962105..7964489,3	MCF-7	breast:
2	chr7:7960775..7968037-chr7:8006243..8012214,13	MCF-7	breast:
3	chr1:151028007..151030723-chr7:7959783..7961888,2	MCF-7	breast:
4	chr7:7953946..7955659-chr7:7959073..7960806,2	K562	blood:
5	chr7:7959000..7960788-chr7:8011254..8013968,2	MCF-7	breast:
6	chr7:7958467..7959967-chr7:8328195..8331123,2	K562	blood:
7	chr7:7948433..7950272-chr7:7951772..7953401,2	MCF-7	breast:
8	chr7:7961731..7965503-chr7:8006784..8010279,5	MCF-7	breast:
9	chr7:7949577..7953346-chr7:7959266..7963720,5	MCF-7	breast:
10	chr7:7951069..7953394-chr7:7953998..7956483,2	K562	blood:
11	chr7:7951218..7952780-chr7:7955913..7958820,2	K562	blood:
12	chr7:7930260..7932176-chr7:7966125..7967661,2	K562	blood:
13	chr7:7920545..7923153-chr7:7947615..7949685,2	MCF-7	breast:
14	chr7:7956835..7959922-chr7:8007692..8010316,3	MCF-7	breast:
15	chr7:7951059..7955946-chr7:8007279..8010658,10	MCF-7	breast:
16	chr7:7960248..7962002-chr7:8129033..8131831,2	MCF-7	breast:
17	chr7:7953946..7955659-chr7:7959073..7960806,2	K562	blood:
18	chr7:7947370..7958537-chr7:8006160..8010935,22	MCF-7	breast:
19	chr18:3245457..3248097-chr7:7961361..7963995,2	MCF-7	breast:
20	chr1:65350348..65350931-chr7:7966977..7967736,2	MCF-7	breast:
21	chr7:7951350..7953467-chr7:8011566..8014289,2	MCF-7	breast:
22	chr7:7952035..7955913-chr7:7956512..7960009,4	MCF-7	breast:
23	chr7:7958223..7960322-chr7:7962105..7964489,3	MCF-7	breast:
24	chr6:36077762..36078586-chr7:7965279..7966158,2	MCF-7	breast:
25	chr7:7950749..7951554-chr7:8008162..8008847,3	MCF-7	breast:
26	chr7:7947056..7948865-chr7:7950686..7953467,2	MCF-7	breast:
27	chr7:7949350..7952293-chr7:7956418..7958594,2	MCF-7	breast:
28	chr7:7946658..7949291-chr7:8008085..8010236,2	K562	blood:
29	chr7:7951069..7953394-chr7:7953998..7956483,2	K562	blood:
30	chr7:7952035..7955913-chr7:7956512..7960009,4	MCF-7	breast:
31	chr7:7951218..7952780-chr7:7955913..7958820,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ICA1-5	chr7:7956100-7956171	l_3361_chr7:7951501-7956400_thyroid
2	lnc-ICA1-5	chr7:7956828-7956865	NONHSAT119137
3	lnc-ICA1-5	chr7:7951815-7952442	l_3361_chr7:7951501-7956400_thyroid
4	lnc-GLCCI1-6	chr7:7959367-7960001	NONHSAT119135
5	lnc-ICA1-5	chr7:7951502-7951811	l_3361_chr7:7951501-7956400_thyroid
6	lnc-ICA1-5	chr7:7956205-7956400	l_3361_chr7:7951501-7956400_thyroid
7	lnc-ICA1-5	chr7:7956009-7956662	NONHSAT119137

No data

Variant related genes	Relation type
ENSG00000214998	TF binding region
ENSG00000214998	CpG island
ENSG00000214998	chromatin interactions
ENSG00000272688	chromatin interactions
ENSG00000106415	chromatin interactions
ENSG00000101608	chromatin interactions
ENSG00000233108	chromatin interactions
ENSG00000213190	chromatin interactions

Extended variants
information (count: 678 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:678 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3919526	chr7:7949059-7949060	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs140450500	chr7:7949086-7949087	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs569345188	chr7:7949106-7949107	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs528814585	chr7:7949123-7949124	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs112068834	chr7:7949167-7949168	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs571881990	chr7:7949185-7949186	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs539282161	chr7:7949230-7949231	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs568983587	chr7:7949237-7949238	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs61741163	chr7:7949295-7949296	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs568890142	chr7:7949296-7949297	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs369295238	chr7:7949311-7949312	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs61749478	chr7:7949329-7949330	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs73674723	chr7:7949336-7949337	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs566402675	chr7:7949342-7949343	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs539506613	chr7:7949363-7949364	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs556704078	chr7:7949383-7949384	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs180816291	chr7:7949386-7949387	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs74789685	chr7:7949406-7949407	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs570295119	chr7:7949491-7949492	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs185911884	chr7:7949501-7949502	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs557409357	chr7:7949579-7949580	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs575662060	chr7:7949584-7949585	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs542977469	chr7:7949614-7949615	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs188290306	chr7:7949618-7949619	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs552488788	chr7:7949631-7949632	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs12702675	chr7:7949666-7949667	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs111530332	chr7:7949699-7949700	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs10243568	chr7:7949712-7949713	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs181157233	chr7:7949749-7949750	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs138083683	chr7:7949762-7949763	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs541682665	chr7:7949799-7949800	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs61748868	chr7:7949801-7949802	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs7780510	chr7:7949814-7949815	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs12702676	chr7:7949823-7949824	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs548123541	chr7:7949828-7949829	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs566120485	chr7:7949883-7949884	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs12702677	chr7:7949890-7949891	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs558408487	chr7:7949918-7949919	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs12668922	chr7:7949986-7949987	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs538007431	chr7:7950000-7950001	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs185756984	chr7:7950016-7950017	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs112658568	chr7:7950115-7950116	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs190571837	chr7:7950118-7950119	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs563549709	chr7:7950176-7950177	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs111621056	chr7:7950203-7950204	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs187171690	chr7:7950324-7950325	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs192471158	chr7:7950325-7950326	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs183925032	chr7:7950353-7950354	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs186472895	chr7:7950400-7950401	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs565564783	chr7:7950407-7950408	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7930200-7951000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:7935000-7951600	Weak transcription	Pancreas	Pancrea
3	chr7:7935400-7952600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr7:7938800-7950600	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr7:7942600-7963600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:7943000-7958800	Weak transcription	Aorta	Aorta
7	chr7:7944400-7959600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr7:7944800-7949200	Weak transcription	Psoas Muscle	Psoas
9	chr7:7947600-7950200	Enhancers	Fetal Stomach	stomach
10	chr7:7947800-7949200	Enhancers	Thymus	Thymus
11	chr7:7947800-7950000	Enhancers	Fetal Thymus	thymus
12	chr7:7948200-7949200	Enhancers	Primary B cells from cord blood	blood
13	chr7:7948200-7949600	Enhancers	Primary B cells from peripheral blood	blood
14	chr7:7948400-7949600	Enhancers	H9 Cell Line	embryonic stem cell
15	chr7:7948400-7949800	Enhancers	Fetal Lung	lung
16	chr7:7948400-7950000	Enhancers	Colon Smooth Muscle	Colon
17	chr7:7948600-7949200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr7:7948600-7952800	Weak transcription	Stomach Smooth Muscle	stomach
19	chr7:7948800-7949200	Enhancers	Rectal Smooth Muscle	rectum
20	chr7:7948800-7949600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr7:7948800-7951400	Enhancers	Hela-S3	cervix
22	chr7:7949000-7949200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr7:7949000-7949200	Enhancers	HSMM	muscle
24	chr7:7949000-7949400	Enhancers	Ovary	ovary
25	chr7:7949000-7949800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr7:7949000-7950000	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr7:7949000-7950000	Enhancers	Placenta	Placenta
28	chr7:7949200-7949600	Enhancers	Psoas Muscle	Psoas
29	chr7:7949200-7950600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr7:7949200-7952600	Weak transcription	HSMM	muscle
31	chr7:7949200-7960200	Weak transcription	Rectal Smooth Muscle	rectum
32	chr7:7949400-7949600	Enhancers	HSMMtube	muscle
33	chr7:7949400-7949800	Weak transcription	Ovary	ovary
34	chr7:7949600-7950000	Enhancers	Placenta Amnion	Placenta Amnion
35	chr7:7949600-7950800	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr7:7949600-7952400	Weak transcription	HSMMtube	muscle
37	chr7:7949600-7953000	Weak transcription	Psoas Muscle	Psoas
38	chr7:7949800-7950000	Enhancers	Ovary	ovary
39	chr7:7949800-7950800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr7:7949800-7951000	Weak transcription	Fetal Lung	lung
41	chr7:7950000-7950400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr7:7950000-7950800	Weak transcription	Placenta	Placenta
43	chr7:7950000-7951400	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr7:7950000-7953000	Weak transcription	Colon Smooth Muscle	Colon
45	chr7:7950000-7953600	Weak transcription	Ovary	ovary
46	chr7:7950200-7953000	Weak transcription	Fetal Stomach	stomach
47	chr7:7950400-7954400	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr7:7950600-7950800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:7950600-7950800	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr7:7950600-7951400	Enhancers	iPS-18 Cell Line	embryonic stem cell

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