Variant report

Variant	nsv606046
Chromosome Location	chr7:7913819-7970560
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:526)
CpG islands
(count:183)
Chromatin interactive
region (count:55)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:526 , 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	ATF2	chr7:7958625-7959819	GM12878	blood:	n/a	n/a
2	ATF2	chr7:7960070-7960623	GM12878	blood:	n/a	n/a
3	ATF2	chr7:7958697-7959462	GM12878	blood:	n/a	n/a
4	ATF2	chr7:7959982-7960638	GM12878	blood:	n/a	n/a
5	BATF	chr7:7959077-7959459	GM12878	blood:	n/a	n/a
6	BATF	chr7:7960171-7960572	GM12878	blood:	n/a	n/a
7	BATF	chr7:7960131-7960582	GM12878	blood:	n/a	n/a
8	BATF	chr7:7959098-7959450	GM12878	blood:	n/a	n/a
9	BATF	chr7:7958720-7959043	GM12878	blood:	n/a	n/a
10	BCL11A	chr7:7960150-7960494	GM12878	blood:	n/a	n/a
11	BCL11A	chr7:7958762-7959113	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:7960180-7960428	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	chr7:7958749-7959392	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:7960099-7960686	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	chr7:7961566-7961742	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr7:7916070-7916434	IMR90	lung:	n/a	chr7:7916238-7916249 chr7:7916238-7916251 chr7:7916240-7916249 chr7:7916240-7916249 chr7:7916240-7916249
23	CEBPB	chr7:7946927-7947202	A549	lung:	n/a	chr7:7947128-7947139
24	CEBPB	chr7:7962316-7962726	MCF-7	breast:	n/a	n/a
25	CEBPB	chr7:7931303-7931494	HepG2	liver:	n/a	chr7:7931359-7931370 chr7:7931461-7931472 chr7:7931465-7931476
26	CEBPB	chr7:7926416-7926676	IMR90	lung:	n/a	chr7:7926541-7926552
27	CEBPB	chr7:7930400-7930739	HepG2	liver:	n/a	chr7:7930559-7930570
28	CEBPB	chr7:7926447-7926695	A549	lung:	n/a	chr7:7926541-7926552
29	CEBPB	chr7:7950791-7951591	MCF-7	breast:	n/a	n/a
30	CEBPB	chr7:7931313-7931502	K562	blood:	n/a	chr7:7931359-7931370 chr7:7931461-7931472 chr7:7931465-7931476
31	CEBPB	chr7:7958412-7958729	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr7:7951010-7951401	HepG2	liver:	n/a	n/a
33	CEBPB	chr7:7916760-7916855	IMR90	lung:	n/a	chr7:7916817-7916828 chr7:7916815-7916828
34	CEBPB	chr7:7930431-7930664	K562	blood:	n/a	chr7:7930559-7930570
35	CEBPB	chr7:7958425-7958655	IMR90	lung:	n/a	n/a
36	CEBPB	chr7:7953116-7953416	IMR90	lung:	n/a	n/a
37	CEBPB	chr7:7950741-7951776	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr7:7930459-7930578	H1-hESC	embryonic stem cell:	n/a	chr7:7930559-7930570
39	CEBPB	chr7:7916084-7916418	A549	lung:	n/a	chr7:7916238-7916249 chr7:7916238-7916251 chr7:7916240-7916249 chr7:7916240-7916249 chr7:7916240-7916249
40	CEBPB	chr7:7951028-7951441	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr7:7953133-7953405	HepG2	liver:	n/a	n/a
42	CEBPB	chr7:7946979-7947288	Hela-S3	cervix:	n/a	chr7:7947128-7947139
43	CEBPB	chr7:7916067-7916396	Hela-S3	cervix:	n/a	chr7:7916238-7916249 chr7:7916238-7916251 chr7:7916240-7916249 chr7:7916240-7916249 chr7:7916240-7916249
44	CEBPB	chr7:7950970-7951399	IMR90	lung:	n/a	n/a
45	CEBPB	chr7:7951014-7951271	A549	lung:	n/a	n/a
46	CEBPB	chr7:7946981-7947242	MCF-7	breast:	n/a	chr7:7947128-7947139
47	CEBPB	chr7:7952970-7953850	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr7:7961525-7961725	A549	lung:	n/a	n/a
49	CEBPB	chr7:7931285-7931446	IMR90	lung:	n/a	chr7:7931359-7931370
50	CEBPB	chr7:7946968-7947295	IMR90	lung:	n/a	chr7:7947128-7947139

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:7959339-7959389	SK-N-MC	brain:	n/a
2	chr7:7936962-7937012	MCF-7	breast:	n/a
3	chr7:7962810-7962860	MCF-7	breast:	n/a
4	chr7:7962810-7962860	Hepatocyte	liver:	n/a
5	chr7:7936962-7937012	AG04449	skin:	fetal
6	chr7:7962810-7962860	ECC-1	luminal epithelium:	n/a
7	chr7:7936962-7937012	HEEpiC	esophagus:	n/a
8	chr7:7936962-7937012	HCPEpiC	choroid plexus:	n/a
9	chr7:7962810-7962860	AG09309	skin:	n/a
10	chr7:7962810-7962860	HRE	kidney:	n/a
11	chr7:7936962-7937012	CMK	blood:	n/a
12	chr7:7962810-7962860	SKMC	muscle:	n/a
13	chr7:7936962-7937012	HCM	heart:	n/a
14	chr7:7959339-7959389	SK-N-SH_RA	brain:	n/a
15	chr7:7959339-7959389	PANC-1	pancreas:	n/a
16	chr7:7962810-7962860	HMEC	breast:	n/a
17	chr7:7936962-7937012	AG09319	gingival:	n/a
18	chr7:7959339-7959389	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:7936962-7937012	Hela-S3	cervix:	n/a
20	chr7:7936962-7937012	Hepatocyte	liver:	n/a
21	chr7:7962810-7962860	HNPCEpiC	eye:	n/a
22	chr7:7962810-7962860	AG09319	gingival:	n/a
23	chr7:7936962-7937012	RPTEC	kidney:	n/a
24	chr7:7959339-7959389	ovcar-3	ovarian:	n/a
25	chr7:7959339-7959389	PFSK-1	brain:	n/a
26	chr7:7962810-7962860	T-47D	breast:	n/a
27	chr7:7962810-7962860	SAEC	small airway:	n/a
28	chr7:7936962-7937012	HepG2	liver:	n/a
29	chr7:7962810-7962860	IMR90	lung:	fetal
30	chr7:7959339-7959389	NT2-D1	testis:	n/a
31	chr7:7962810-7962860	BJ	skin:	n/a
32	chr7:7959339-7959389	PrEC	prostate:	n/a
33	chr7:7936962-7937012	Caco-2	colon:	n/a
34	chr7:7962810-7962860	SK-N-MC	brain:	n/a
35	chr7:7959339-7959389	NH-A	brain:	n/a
36	chr7:7962810-7962860	NHDF-neo	bronchial:	n/a
37	chr7:7936962-7937012	GM06990	blood:	n/a
38	chr7:7959339-7959389	HRPEpiC	eye:	n/a
39	chr7:7959339-7959389	HMEC	breast:	n/a
40	chr7:7959339-7959389	U87	brain:	n/a
41	chr7:7936962-7937012	U87	brain:	n/a
42	chr7:7962810-7962860	ovcar-3	ovarian:	n/a
43	chr7:7936962-7937012	HRCEpiC	kidney:	n/a
44	chr7:7959339-7959389	GM12891	blood:	n/a
45	chr7:7959339-7959389	A549	lung:	n/a
46	chr7:7962810-7962860	AoSMC	blood vessel:	n/a
47	chr7:7959339-7959389	CMK	blood:	n/a
48	chr7:7962810-7962860	HCT-116	colon:	n/a
49	chr7:7959339-7959389	HNPCEpiC	eye:	n/a
50	chr7:7962810-7962860	Jurkat	blood:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:7941789..7943515-chr7:8007285..8009574,2	MCF-7	breast:
2	chr7:7920545..7923153-chr7:7947615..7949685,2	MCF-7	breast:
3	chr7:7936554..7939221-chr7:8008179..8010269,3	MCF-7	breast:
4	chr7:7951069..7953394-chr7:7953998..7956483,2	K562	blood:
5	chr7:7935711..7938261-chr7:7941744..7943349,2	K562	blood:
6	chr7:7929818..7931482-chr7:7931522..7933853,2	MCF-7	breast:
7	chr7:7935831..7938842-chr7:8008024..8010603,3	MCF-7	breast:
8	chr7:7949577..7953346-chr7:7959266..7963720,5	MCF-7	breast:
9	chr7:7949350..7952293-chr7:7956418..7958594,2	MCF-7	breast:
10	chr6:36077762..36078586-chr7:7965279..7966158,2	MCF-7	breast:
11	chr7:7969976..7971625-chr7:7983223..7985791,2	MCF-7	breast:
12	chr7:7961731..7965503-chr7:8006784..8010279,5	MCF-7	breast:
13	chr7:7930260..7932176-chr7:7966125..7967661,2	K562	blood:
14	chr7:7908747..7911245-chr7:7915416..7917083,2	MCF-7	breast:
15	chr7:7947056..7948865-chr7:7950686..7953467,2	MCF-7	breast:
16	chr7:7908600..7910763-chr7:7934050..7936742,2	K562	blood:
17	chr7:7913240..7915292-chr7:7916036..7917887,2	K562	blood:
18	chr7:7946658..7949291-chr7:8008085..8010236,2	K562	blood:
19	chr7:7952035..7955913-chr7:7956512..7960009,4	MCF-7	breast:
20	chr7:7952035..7955913-chr7:7956512..7960009,4	MCF-7	breast:
21	chr7:7932645..7934651-chr7:7935237..7938092,2	K562	blood:
22	chr7:7959000..7960788-chr7:8011254..8013968,2	MCF-7	breast:
23	chr18:3245457..3248097-chr7:7961361..7963995,2	MCF-7	breast:
24	chr7:7911633..7914255-chr7:7920651..7923131,2	K562	blood:
25	chr7:7951350..7953467-chr7:8011566..8014289,2	MCF-7	breast:
26	chr7:7951218..7952780-chr7:7955913..7958820,2	K562	blood:
27	chr7:7953946..7955659-chr7:7959073..7960806,2	K562	blood:
28	chr1:151028007..151030723-chr7:7959783..7961888,2	MCF-7	breast:
29	chr7:7947370..7958537-chr7:8006160..8010935,22	MCF-7	breast:
30	chr7:7944145..7947023-chr7:7968614..7970373,2	K562	blood:
31	chr7:7958467..7959967-chr7:8328195..8331123,2	K562	blood:
32	chr7:7929818..7931482-chr7:7931522..7933853,2	MCF-7	breast:
33	chr7:7947056..7948865-chr7:7950686..7953467,2	MCF-7	breast:
34	chr7:7904713..7906723-chr7:7911764..7914696,2	K562	blood:
35	chr7:7912939..7915292-chr7:7916036..7918136,3	K562	blood:
36	chr7:7951069..7953394-chr7:7953998..7956483,2	K562	blood:
37	chr7:7932645..7934651-chr7:7935237..7938092,2	K562	blood:
38	chr7:7948433..7950272-chr7:7951772..7953401,2	MCF-7	breast:
39	chr7:7956835..7959922-chr7:8007692..8010316,3	MCF-7	breast:
40	chr1:65350348..65350931-chr7:7966977..7967736,2	MCF-7	breast:
41	chr7:7951218..7952780-chr7:7955913..7958820,2	K562	blood:
42	chr7:7953946..7955659-chr7:7959073..7960806,2	K562	blood:
43	chr7:7912939..7915292-chr7:7916036..7918136,3	K562	blood:
44	chr7:7913240..7915292-chr7:7916036..7917887,2	K562	blood:
45	chr7:7920545..7923153-chr7:7947615..7949685,2	MCF-7	breast:
46	chr7:7935711..7938261-chr7:7941744..7943349,2	K562	blood:
47	chr7:7950749..7951554-chr7:8008162..8008847,3	MCF-7	breast:
48	chr7:7911633..7914255-chr7:7920651..7923131,2	K562	blood:
49	chr7:7960248..7962002-chr7:8129033..8131831,2	MCF-7	breast:
50	chr7:7951059..7955946-chr7:8007279..8010658,10	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLCCI1-6	chr7:7938942-7939427	NONHSAT119135
2	lnc-ICA1-5	chr7:7951502-7951811	l_3361_chr7:7951501-7956400_thyroid
3	lnc-ICA1-5	chr7:7956828-7956865	NONHSAT119137
4	lnc-GLCCI1-6	chr7:7959367-7960001	NONHSAT119135
5	lnc-ICA1-5	chr7:7951815-7952442	l_3361_chr7:7951501-7956400_thyroid
6	lnc-ICA1-5	chr7:7956205-7956400	l_3361_chr7:7951501-7956400_thyroid
7	lnc-GLCCI1-6	chr7:7933669-7934024	NONHSAT119135
8	lnc-GLCCI1-6	chr7:7968360-7968895	NONHSAT119135
9	lnc-GLCCI1-6	chr7:7939478-7939517	NONHSAT119135
10	lnc-ICA1-5	chr7:7956100-7956171	l_3361_chr7:7951501-7956400_thyroid
11	lnc-ICA1-5	chr7:7956009-7956662	NONHSAT119137
12	lnc-GLCCI1-6	chr7:7935007-7935362	NONHSAT119135

No data

Variant related genes	Relation type
ENSG00000214998	TF binding region
RNU6-534P	TF binding region
ENSG00000214998	CpG island
RNU6-534P	CpG island
ENSG00000214998	chromatin interactions
ENSG00000201747	chromatin interactions
ENSG00000106415	chromatin interactions
ENSG00000101608	chromatin interactions
ENSG00000213190	chromatin interactions
ENSG00000272688	chromatin interactions
ENSG00000233108	chromatin interactions

Extended variants
information (count: 2332 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2332 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10255964	chr7:7913819-7913820	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs59988288	chr7:7913833-7913834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542837549	chr7:7913859-7913860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs578259345	chr7:7913866-7913867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545601129	chr7:7913890-7913891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs561105297	chr7:7913901-7913902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs10241098	chr7:7913945-7913946	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs187443884	chr7:7913963-7913964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs575620885	chr7:7913976-7913977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs112735506	chr7:7914035-7914036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs111424871	chr7:7914046-7914047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533186596	chr7:7914064-7914065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs116131871	chr7:7914072-7914073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs543122245	chr7:7914105-7914106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562086427	chr7:7914168-7914169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs74943926	chr7:7914169-7914170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112368484	chr7:7914185-7914186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567555432	chr7:7914246-7914247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs67462815	chr7:7914297-7914298	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs114552774	chr7:7914305-7914306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528488945	chr7:7914312-7914313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577533293	chr7:7914320-7914321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368143226	chr7:7914324-7914325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538267931	chr7:7914383-7914384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374195899	chr7:7914387-7914388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs55820070	chr7:7914429-7914430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575180931	chr7:7914437-7914438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs117744384	chr7:7914438-7914439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575437827	chr7:7914474-7914475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150214486	chr7:7914475-7914476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138766523	chr7:7914480-7914481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564823361	chr7:7914495-7914496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115118489	chr7:7914559-7914560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs532302246	chr7:7914561-7914562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550333778	chr7:7914594-7914595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs13438763	chr7:7914604-7914605	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs183859885	chr7:7914632-7914633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs13438161	chr7:7914685-7914686	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs111399367	chr7:7914695-7914696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539927557	chr7:7914700-7914701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531094477	chr7:7914721-7914722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142655261	chr7:7914723-7914724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs145953575	chr7:7914727-7914728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528678578	chr7:7914763-7914764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546636864	chr7:7914791-7914792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571259827	chr7:7914800-7914801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538764923	chr7:7914804-7914805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs556665374	chr7:7914821-7914822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561842698	chr7:7914840-7914841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568861074	chr7:7914857-7914858	Weak transcription	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
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:580 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7895400-7918000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:7897200-7923200	Weak transcription	Psoas Muscle	Psoas
3	chr7:7897200-7942400	Weak transcription	Aorta	Aorta
4	chr7:7901200-7915600	Weak transcription	Gastric	stomach
5	chr7:7907800-7915200	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr7:7908000-7919400	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr7:7908200-7918800	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr7:7908200-7921200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr7:7909000-7915600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr7:7909000-7922600	Weak transcription	Primary B cells from peripheral blood	blood
11	chr7:7909400-7922400	Weak transcription	Primary B cells from cord blood	blood
12	chr7:7909600-7924000	Weak transcription	Fetal Intestine Small	intestine
13	chr7:7909600-7942400	Weak transcription	Left Ventricle	heart
14	chr7:7910400-7916000	Weak transcription	Brain Hippocampus Middle	brain
15	chr7:7910600-7918000	Weak transcription	Right Atrium	heart
16	chr7:7910800-7914400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr7:7911400-7914400	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr7:7911600-7934800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr7:7911600-7934800	Weak transcription	Pancreas	Pancrea
20	chr7:7912200-7930000	Weak transcription	Esophagus	oesophagus
21	chr7:7912200-7934600	Weak transcription	Stomach Smooth Muscle	stomach
22	chr7:7912600-7924200	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr7:7913200-7942400	Weak transcription	Primary T cells from cord blood	blood
24	chr7:7913600-7914000	Enhancers	Brain Germinal Matrix	brain
25	chr7:7915400-7916000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr7:7915600-7915800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr7:7915600-7915800	Enhancers	Gastric	stomach
28	chr7:7915800-7916000	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
29	chr7:7915800-7943000	Weak transcription	Gastric	stomach
30	chr7:7916000-7917800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr7:7917000-7919600	Weak transcription	Fetal Intestine Large	intestine
32	chr7:7921200-7921400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr7:7921400-7921800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr7:7922400-7924800	Enhancers	Primary B cells from cord blood	blood
35	chr7:7922600-7924000	Enhancers	Primary B cells from peripheral blood	blood
36	chr7:7923000-7923400	Enhancers	Fetal Muscle Leg	muscle
37	chr7:7923000-7923400	Enhancers	Ovary	ovary
38	chr7:7923000-7923400	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr7:7923200-7923400	Enhancers	Psoas Muscle	Psoas
40	chr7:7923200-7923800	Enhancers	Colon Smooth Muscle	Colon
41	chr7:7923200-7926600	Weak transcription	Primary hematopoietic stem cells	blood
42	chr7:7923400-7924600	Weak transcription	Ovary	ovary
43	chr7:7923600-7925200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr7:7924200-7924800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr7:7924200-7925000	Enhancers	Muscle Satellite Cultured Cells	--
46	chr7:7924400-7924800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr7:7924400-7924800	Enhancers	Hela-S3	cervix
48	chr7:7924600-7925400	Enhancers	Ovary	ovary
49	chr7:7924800-7931200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr7:7924800-7932600	Weak transcription	Primary B cells from cord blood	blood

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