Variant report

Variant	nsv889121
Chromosome Location	chr7:120747228-120869464
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1065)
CpG islands
(count:61)
Chromatin interactive
region (count:138)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1065 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:120800023-120800487	K562	blood:	n/a	n/a
2	ARID3A	chr7:120778432-120778625	K562	blood:	n/a	n/a
3	ARID3A	chr7:120747983-120748273	K562	blood:	n/a	n/a
4	ATF1	chr7:120799677-120800576	K562	blood:	n/a	n/a
5	ATF1	chr7:120778322-120778731	K562	blood:	n/a	n/a
6	ATF2	chr7:120778277-120778721	GM12878	blood:	n/a	n/a
7	ATF2	chr7:120778230-120778840	GM12878	blood:	n/a	n/a
8	ATF2	chr7:120820324-120820939	GM12878	blood:	n/a	n/a
9	ATF2	chr7:120820349-120820987	GM12878	blood:	n/a	n/a
10	ATF3	chr7:120800134-120800510	K562	blood:	n/a	n/a
11	ATF3	chr7:120778265-120778713	K562	blood:	n/a	n/a
12	BACH1	chr7:120808205-120808275	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr7:120779259-120779282	K562	blood:	n/a	n/a
14	BACH1	chr7:120771434-120771460	K562	blood:	n/a	n/a
15	BACH1	chr7:120830804-120830897	K562	blood:	n/a	n/a
16	BATF	chr7:120820490-120820786	GM12878	blood:	n/a	n/a
17	BCL11A	chr7:120820486-120820825	GM12878	blood:	n/a	n/a
18	BCL3	chr7:120820455-120820804	GM12878	blood:	n/a	n/a
19	BCLAF1	chr7:120820473-120821033	GM12878	blood:	n/a	n/a
20	BHLHE40	chr7:120777877-120777906	K562	blood:	n/a	n/a
21	BHLHE40	chr7:120778436-120778667	K562	blood:	n/a	n/a
22	BHLHE40	chr7:120820459-120820914	GM12878	blood:	n/a	n/a
23	BHLHE40	chr7:120800243-120800443	K562	blood:	n/a	n/a
24	BHLHE40	chr7:120748070-120748317	GM12878	blood:	n/a	n/a
25	BHLHE40	chr7:120778337-120778832	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:120851610-120851680	K562	blood:	n/a	n/a
27	BRCA1	chr7:120763041-120763396	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr7:120766937-120767255	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr7:120760594-120761193	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr7:120844643-120844790	Hela-S3	cervix:	n/a	n/a
31	CCNT2	chr7:120782286-120782299	K562	blood:	n/a	n/a
32	CCNT2	chr7:120822723-120822729	K562	blood:	n/a	n/a
33	CCNT2	chr7:120851534-120851936	K562	blood:	n/a	n/a
34	CCNT2	chr7:120794292-120794305	K562	blood:	n/a	n/a
35	CCNT2	chr7:120746907-120747235	K562	blood:	n/a	n/a
36	CCNT2	chr7:120778435-120778703	K562	blood:	n/a	n/a
37	CCNT2	chr7:120868852-120868936	K562	blood:	n/a	n/a
38	CCNT2	chr7:120809085-120809113	K562	blood:	n/a	n/a
39	CCNT2	chr7:120756098-120756199	K562	blood:	n/a	n/a
40	CCNT2	chr7:120800247-120800550	K562	blood:	n/a	n/a
41	CCNT2	chr7:120850727-120850917	K562	blood:	n/a	n/a
42	CEBPB	chr7:120749195-120749605	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr7:120827720-120828104	K562	blood:	n/a	chr7:120827929-120827940 chr7:120827961-120827972
44	CEBPB	chr7:120842695-120842983	IMR90	lung:	n/a	n/a
45	CEBPB	chr7:120844891-120845145	K562	blood:	n/a	chr7:120844976-120844987 chr7:120844976-120844987
46	CEBPB	chr7:120778239-120778870	HCT-116	colon:	n/a	n/a
47	CEBPB	chr7:120778391-120778759	K562	blood:	n/a	n/a
48	CEBPB	chr7:120844737-120845132	Hela-S3	cervix:	n/a	chr7:120844976-120844987 chr7:120844976-120844987
49	CEBPB	chr7:120800108-120800673	K562	blood:	n/a	chr7:120800304-120800315
50	CEBPB	chr7:120759061-120759454	K562	blood:	n/a	chr7:120759258-120759269

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:120852287-120852337	AG09309	skin:	n/a
2	chr7:120852287-120852337	K562	blood:	n/a
3	chr7:120852287-120852337	Hepatocyte	liver:	n/a
4	chr7:120852287-120852337	PrEC	prostate:	n/a
5	chr7:120852287-120852337	RPTEC	kidney:	n/a
6	chr7:120852287-120852337	SK-N-SH	brain:	n/a
7	chr7:120852287-120852337	AoSMC	blood vessel:	n/a
8	chr7:120852287-120852337	LNCaP	prostate:	n/a
9	chr7:120852287-120852337	HNPCEpiC	eye:	n/a
10	chr7:120852287-120852337	NHDF-neo	bronchial:	n/a
11	chr7:120852287-120852337	MCF10A-Er-Src	breast:	n/a
12	chr7:120852287-120852337	MCF-7	breast:	n/a
13	chr7:120852287-120852337	BJ	skin:	n/a
14	chr7:120852287-120852337	HUVEC	blood vessel:	n/a
15	chr7:120852287-120852337	NB4	blood:	n/a
16	chr7:120852287-120852337	AG10803	skin:	n/a
17	chr7:120852287-120852337	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:120852287-120852337	AG04450	lung:	fetal
19	chr7:120852287-120852337	BE2_C	brain:	n/a
20	chr7:120852287-120852337	HCF	heart:	n/a
21	chr7:120852287-120852337	H1-hESC	embryonic stem cell:	embryo
22	chr7:120852287-120852337	ProgFib	skin:	n/a
23	chr7:120852287-120852337	HRCEpiC	kidney:	n/a
24	chr7:120852287-120852337	HCT-116	colon:	n/a
25	chr7:120852287-120852337	ECC-1	luminal epithelium:	n/a
26	chr7:120852287-120852337	HRPEpiC	eye:	n/a
27	chr7:120852287-120852337	GM06990	blood:	n/a
28	chr7:120852287-120852337	NHBE	bronchial:	n/a
29	chr7:120852287-120852337	NH-A	brain:	n/a
30	chr7:120852287-120852337	HEEpiC	esophagus:	n/a
31	chr7:120852287-120852337	HAEpiC	amniotic membrane:	n/a
32	chr7:120852287-120852337	SK-N-MC	brain:	n/a
33	chr7:120852287-120852337	HCPEpiC	choroid plexus:	n/a
34	chr7:120852287-120852337	HRE	kidney:	n/a
35	chr7:120852287-120852337	AG09319	gingival:	n/a
36	chr7:120852287-120852337	A549	lung:	n/a
37	chr7:120852287-120852337	IMR90	lung:	fetal
38	chr7:120852287-120852337	GM12892	blood:	n/a
39	chr7:120852287-120852337	PANC-1	pancreas:	n/a
40	chr7:120852287-120852337	SK-N-SH_RA	brain:	n/a
41	chr7:120852287-120852337	GM12891	blood:	n/a
42	chr7:120852287-120852337	HEK293	kidney:	embryo
43	chr7:120852287-120852337	U87	brain:	n/a
44	chr7:120852287-120852337	GM19239	blood:	n/a
45	chr7:120852287-120852337	AG04449	skin:	fetal
46	chr7:120852287-120852337	NT2-D1	testis:	n/a
47	chr7:120852287-120852337	PFSK-1	brain:	n/a
48	chr7:120852287-120852337	SAEC	small airway:	n/a
49	chr7:120852287-120852337	HepG2	liver:	n/a
50	chr7:120852287-120852337	ovcar-3	ovarian:	n/a

(count:138 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:120848400..120850146-chr7:120867197..120869985,2	K562	blood:
2	chr7:120854329..120856810-chr7:120876127..120877752,2	K562	blood:
3	chr7:120836253..120841319-chr7:120841811..120848062,9	K562	blood:
4	chr7:120776773..120780025-chr7:120780036..120783879,5	K562	blood:
5	chr7:120856242..120858668-chr7:120894112..120895725,2	K562	blood:
6	chr7:120849619..120853631-chr7:120859182..120861121,3	K562	blood:
7	chr7:120848908..120852746-chr7:120854048..120856854,5	K562	blood:
8	chr7:120627349..120628383-chr7:120747676..120749167,11	K562	blood:
9	chr7:120788426..120790789-chr7:120791125..120793163,2	K562	blood:
10	chr7:120753655..120756147-chr7:120756373..120757912,2	K562	blood:
11	chr7:120764507..120766599-chr7:120781831..120784588,2	K562	blood:
12	chr7:120561753..120563679-chr7:120747463..120748993,2	K562	blood:
13	chr7:120773227..120776221-chr7:120776532..120780949,5	K562	blood:
14	chr7:120741938..120744145-chr7:120762816..120764575,2	K562	blood:
15	chr7:120867657..120869346-chr7:120882060..120884535,2	K562	blood:
16	chr7:120742066..120743891-chr7:120758680..120761342,2	K562	blood:
17	chr7:120590916..120593428-chr7:120771496..120774928,3	K562	blood:
18	chr7:120836283..120838682-chr7:120872699..120875576,2	K562	blood:
19	chr7:120778509..120781370-chr7:120785067..120788347,3	K562	blood:
20	chr7:120744759..120747111-chr7:120748384..120750272,2	K562	blood:
21	chr7:120778481..120780848-chr7:120786003..120787680,2	K562	blood:
22	chr7:120770037..120772769-chr7:120796157..120798436,2	K562	blood:
23	chr7:120795773..120797824-chr7:120798929..120800429,2	K562	blood:
24	chr7:120742066..120745673-chr7:120758680..120764316,5	K562	blood:
25	chr7:120841468..120846547-chr7:120846758..120854034,8	K562	blood:
26	chr7:120773227..120776221-chr7:120776532..120780949,5	K562	blood:
27	chr7:120750275..120752757-chr7:120754885..120757852,3	K562	blood:
28	chr7:120787470..120791175-chr7:120804388..120809200,4	K562	blood:
29	chr7:120762968..120765297-chr7:120774508..120778182,3	K562	blood:
30	chr7:120748117..120751439-chr7:120760191..120762453,3	K562	blood:
31	chr7:120745612..120749676-chr7:120751128..120754629,5	K562	blood:
32	chr7:120770037..120772769-chr7:120796157..120798436,2	K562	blood:
33	chr7:120628746..120630644-chr7:120748164..120750985,2	K562	blood:
34	chr7:120736484..120739000-chr7:120756875..120758692,2	K562	blood:
35	chr7:120713720..120716672-chr7:120804546..120807169,2	K562	blood:
36	chr7:120811142..120813179-chr7:120814507..120817821,3	K562	blood:
37	chr7:120819870..120822812-chr7:120840045..120842182,2	K562	blood:
38	chr7:120739132..120740761-chr7:120746818..120749642,2	K562	blood:
39	chr7:120766449..120767437-chr7:120977220..120978039,4	MCF-7	breast:
40	chr7:120774713..120776221-chr7:120777852..120779454,2	K562	blood:
41	chr7:120750275..120752757-chr7:120754885..120757852,3	K562	blood:
42	chr7:120775298..120777729-chr7:120784980..120787236,2	K562	blood:
43	chr7:120589479..120591049-chr7:120760761..120762508,2	MCF-7	breast:
44	chr7:120762968..120765297-chr7:120774508..120778182,3	K562	blood:
45	chr7:120764507..120766599-chr7:120781831..120784588,2	K562	blood:
46	chr7:120431798..120432733-chr7:120748046..120748607,2	K562	blood:
47	chr7:120858530..120860172-chr7:120865997..120868025,2	K562	blood:
48	chr7:120815326..120817520-chr7:120824597..120827177,2	K562	blood:
49	chr7:120842227..120844085-chr7:120858166..120859847,2	K562	blood:
50	chr7:120718771..120721283-chr7:120791408..120793421,2	K562	blood:

No data

Variant related genes	Relation type
RNU6-517P	TF binding region
CPED1	TF binding region
RNU6-517P	CpG island
CPED1	CpG island
ENSG00000207090	chromatin interactions
ENSG00000106034	chromatin interactions
ENSG00000196937	chromatin interactions
ENSG00000071243	chromatin interactions

Extended variants
information (count: 4356 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:4356 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs798939	chr7:120747228-120747229	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs111974361	chr7:120747233-120747234	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs183484094	chr7:120747259-120747260	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs13223036	chr7:120747308-120747309	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	disease
5	rs557464555	chr7:120747315-120747316	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs549694128	chr7:120747320-120747321	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs563231196	chr7:120747332-120747333	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs529132973	chr7:120747333-120747334	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs548963307	chr7:120747377-120747378	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs372629208	chr7:120747383-120747384	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs139707310	chr7:120747385-120747386	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs113552760	chr7:120747529-120747530	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs565509354	chr7:120747545-120747546	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs117206111	chr7:120747546-120747547	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs115376337	chr7:120747548-120747549	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs113979290	chr7:120747550-120747551	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs555606257	chr7:120747558-120747559	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs537637408	chr7:120747560-120747561	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs557728236	chr7:120747564-120747565	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs574397972	chr7:120747612-120747613	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs577386967	chr7:120747679-120747680	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs536499225	chr7:120747690-120747691	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs149370669	chr7:120747702-120747703	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs573122906	chr7:120747703-120747704	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs545521955	chr7:120747705-120747706	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs12671108	chr7:120747749-120747750	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs75212905	chr7:120747780-120747781	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs535322876	chr7:120747843-120747844	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs369853906	chr7:120747854-120747855	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs188484954	chr7:120747858-120747859	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs192900634	chr7:120747859-120747860	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs572332407	chr7:120747874-120747875	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs144802893	chr7:120747986-120747987	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs75656428	chr7:120748109-120748110	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs529206593	chr7:120748126-120748127	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs556876054	chr7:120748171-120748172	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs13226812	chr7:120748257-120748258	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs117374763	chr7:120748264-120748265	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs185855067	chr7:120748286-120748287	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs113889977	chr7:120748317-120748318	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs143108052	chr7:120748345-120748346	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs530581191	chr7:120748403-120748404	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs543140492	chr7:120748435-120748436	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs146138638	chr7:120748448-120748449	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs371664607	chr7:120748505-120748506	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs79149543	chr7:120748534-120748535	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs536970513	chr7:120748542-120748543	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs10247551	chr7:120748564-120748565	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs566888373	chr7:120748566-120748567	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs538646211	chr7:120748599-120748600	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	21115979	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:677 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:120711400-120790600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr7:120725800-120761800	Weak transcription	Fetal Stomach	stomach
3	chr7:120727800-120756400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr7:120731200-120747800	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr7:120733000-120747800	Weak transcription	Spleen	Spleen
6	chr7:120735400-120784000	Weak transcription	Right Ventricle	heart
7	chr7:120737400-120747400	Strong transcription	Liver	Liver
8	chr7:120738200-120749200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr7:120740400-120753000	Weak transcription	Osteobl	bone
10	chr7:120740600-120758800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr7:120740800-120786000	Weak transcription	Fetal Lung	lung
12	chr7:120741400-120782200	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr7:120741800-120765600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr7:120742000-120810000	Weak transcription	Psoas Muscle	Psoas
15	chr7:120742400-120748200	Weak transcription	Colon Smooth Muscle	Colon
16	chr7:120742800-120752000	Weak transcription	Aorta	Aorta
17	chr7:120742800-120765000	Weak transcription	NHDF-Ad	bronchial
18	chr7:120742800-120771800	Weak transcription	Stomach Smooth Muscle	stomach
19	chr7:120743000-120748000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr7:120743000-120750600	Weak transcription	Ovary	ovary
21	chr7:120743000-120765400	Weak transcription	Left Ventricle	heart
22	chr7:120743000-120784200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr7:120743400-120778200	Strong transcription	K562	blood
24	chr7:120743600-120749000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr7:120743600-120752800	Weak transcription	HMEC	breast
26	chr7:120743800-120748800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr7:120743800-120753200	Weak transcription	HSMMtube	muscle
28	chr7:120743800-120765600	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr7:120745600-120747800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:120745600-120747800	Weak transcription	Adipose Nuclei	Adipose
31	chr7:120745600-120749200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr7:120746200-120768000	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr7:120746200-120777800	Weak transcription	Rectal Smooth Muscle	rectum
34	chr7:120746400-120747400	Weak transcription	HSMM	muscle
35	chr7:120746400-120750200	Weak transcription	NHLF	lung
36	chr7:120747400-120747600	Enhancers	HSMM	muscle
37	chr7:120747400-120752000	Weak transcription	Liver	Liver
38	chr7:120747600-120747800	Weak transcription	HSMM	muscle
39	chr7:120747800-120748000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr7:120747800-120748000	Genic enhancers	HSMM	muscle
41	chr7:120747800-120748200	Enhancers	Muscle Satellite Cultured Cells	--
42	chr7:120747800-120748200	Enhancers	Adipose Nuclei	Adipose
43	chr7:120748000-120748800	Weak transcription	HSMM	muscle
44	chr7:120748000-120749800	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr7:120748000-120750000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr7:120748200-120749200	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr7:120748200-120752600	Weak transcription	Adipose Nuclei	Adipose
48	chr7:120748800-120749200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr7:120748800-120749600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:120748800-120750200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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