Variant report

Variant	nsv1052801
Chromosome Location	chr13:50116407-50144995
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:452)
CpG islands
(count:183)
Chromatin interactive
region (count:34)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:452 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:50134434-50134784	HepG2	liver:	n/a	n/a
2	BATF	chr13:50144463-50144729	GM12878	blood:	n/a	chr13:50144518-50144527
3	BHLHE40	chr13:50134491-50134757	HepG2	liver:	n/a	n/a
4	BHLHE40	chr13:50141587-50141920	K562	blood:	n/a	n/a
5	CBX3	chr13:50141604-50141930	K562	blood:	n/a	n/a
6	CEBPB	chr13:50137719-50137986	MCF-7	breast:	n/a	n/a
7	CEBPB	chr13:50137698-50137998	K562	blood:	n/a	n/a
8	CEBPB	chr13:50134407-50134773	IMR90	lung:	n/a	chr13:50134589-50134601
9	CEBPB	chr13:50137681-50138029	K562	blood:	n/a	n/a
10	CEBPB	chr13:50137661-50138023	A549	lung:	n/a	n/a
11	CEBPB	chr13:50144145-50144564	Hela-S3	cervix:	n/a	chr13:50144394-50144411
12	CEBPB	chr13:50137039-50137174	A549	lung:	n/a	n/a
13	CEBPB	chr13:50134505-50134649	HepG2	liver:	n/a	chr13:50134589-50134601
14	CEBPB	chr13:50134453-50134639	K562	blood:	n/a	chr13:50134589-50134601
15	CEBPB	chr13:50137682-50138030	HepG2	liver:	n/a	n/a
16	CEBPB	chr13:50134464-50134743	MCF-7	breast:	n/a	chr13:50134589-50134601
17	CEBPB	chr13:50144187-50144589	MCF-7	breast:	n/a	chr13:50144394-50144411
18	CEBPB	chr13:50144217-50144417	IMR90	lung:	n/a	chr13:50144394-50144411
19	CEBPB	chr13:50137134-50137172	IMR90	lung:	n/a	n/a
20	CEBPB	chr13:50137673-50138025	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr13:50134496-50134718	K562	blood:	n/a	chr13:50134589-50134601
22	CEBPB	chr13:50134436-50134731	A549	lung:	n/a	chr13:50134589-50134601
23	CEBPB	chr13:50143875-50144532	MCF-7	breast:	n/a	chr13:50144394-50144411
24	CEBPB	chr13:50137666-50138026	IMR90	lung:	n/a	n/a
25	CEBPB	chr13:50137785-50138001	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr13:50137123-50137234	HepG2	liver:	n/a	n/a
27	CEBPB	chr13:50134431-50134724	HepG2	liver:	n/a	chr13:50134589-50134601
28	CTCF	chr13:50123480-50123630	HFF-Myc	foreskin:	n/a	n/a
29	CTCF	chr13:50134580-50134730	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr13:50123520-50123670	Caco-2	colon:	n/a	n/a
31	CTCF	chr13:50123520-50123670	HVMF	connective:	n/a	n/a
32	CTCF	chr13:50123500-50123650	RPTEC	kidney:	n/a	n/a
33	CTCF	chr13:50128660-50128810	AG04449	skin:	n/a	n/a
34	CTCF	chr13:50134560-50134710	HepG2	liver:	n/a	n/a
35	CTCF	chr13:50123520-50123670	NHDF-neo	bronchial:	n/a	n/a
36	CTCF	chr13:50134534-50134715	LNCaP	prostate:	n/a	n/a
37	CTCF	chr13:50123453-50123746	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr13:50134480-50134630	GM12873	blood:	n/a	n/a
39	CTCF	chr13:50123520-50123670	MCF-7	breast:	n/a	n/a
40	CTCF	chr13:50128650-50128882	MCF-7	breast:	n/a	n/a
41	CTCF	chr13:50134560-50134710	GM12873	blood:	n/a	n/a
42	CTCF	chr13:50123440-50123590	HMEC	breast:	n/a	n/a
43	CTCF	chr13:50134480-50134630	GM12871	blood:	n/a	n/a
44	CTCF	chr13:50123460-50123610	HAc	cerebellar:	n/a	n/a
45	CTCF	chr13:50134540-50134690	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr13:50128686-50128785	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr13:50134501-50134750	K562	blood:	n/a	n/a
48	CTCF	chr13:50123440-50123590	HVMF	connective:	n/a	n/a
49	CTCF	chr13:50123540-50123690	RPTEC	kidney:	n/a	n/a
50	CTCF	chr13:50123531-50123723	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:50123645-50123695	HCPEpiC	choroid plexus:	n/a
2	chr13:50123645-50123695	HL-60	blood:	n/a
3	chr13:50134640-50134690	ECC-1	luminal epithelium:	n/a
4	chr13:50134640-50134690	T-47D	breast:	n/a
5	chr13:50123613-50123663	NB4	blood:	n/a
6	chr13:50123645-50123695	RPTEC	kidney:	n/a
7	chr13:50134640-50134690	AG09319	gingival:	n/a
8	chr13:50123613-50123663	GM12892	blood:	n/a
9	chr13:50134640-50134690	BJ	skin:	n/a
10	chr13:50123613-50123663	HRCEpiC	kidney:	n/a
11	chr13:50134640-50134690	SK-N-SH	brain:	n/a
12	chr13:50123613-50123663	IMR90	lung:	fetal
13	chr13:50123645-50123695	HEEpiC	esophagus:	n/a
14	chr13:50123645-50123695	GM06990	blood:	n/a
15	chr13:50134640-50134690	PANC-1	pancreas:	n/a
16	chr13:50123645-50123695	U87	brain:	n/a
17	chr13:50123645-50123695	Hela-S3	cervix:	n/a
18	chr13:50123645-50123695	HRCEpiC	kidney:	n/a
19	chr13:50123645-50123695	BE2_C	brain:	n/a
20	chr13:50123645-50123695	HAEpiC	amniotic membrane:	n/a
21	chr13:50123613-50123663	HPAEpiC	pulmonary alveolar:	n/a
22	chr13:50123645-50123695	AG09319	gingival:	n/a
23	chr13:50123645-50123695	AoSMC	blood vessel:	n/a
24	chr13:50123645-50123695	CMK	blood:	n/a
25	chr13:50134640-50134690	ProgFib	skin:	n/a
26	chr13:50123645-50123695	SK-N-MC	brain:	n/a
27	chr13:50134640-50134690	AG09309	skin:	n/a
28	chr13:50123613-50123663	PFSK-1	brain:	n/a
29	chr13:50134640-50134690	HCPEpiC	choroid plexus:	n/a
30	chr13:50134640-50134690	NHDF-neo	bronchial:	n/a
31	chr13:50134640-50134690	HNPCEpiC	eye:	n/a
32	chr13:50123613-50123663	NHDF-neo	bronchial:	n/a
33	chr13:50123645-50123695	MCF-7	breast:	n/a
34	chr13:50123613-50123663	SK-N-SH_RA	brain:	n/a
35	chr13:50123645-50123695	SK-N-SH	brain:	n/a
36	chr13:50123645-50123695	PFSK-1	brain:	n/a
37	chr13:50123613-50123663	BJ	skin:	n/a
38	chr13:50123645-50123695	HepG2	liver:	n/a
39	chr13:50134640-50134690	U87	brain:	n/a
40	chr13:50123613-50123663	SK-N-MC	brain:	n/a
41	chr13:50134640-50134690	HRCEpiC	kidney:	n/a
42	chr13:50134640-50134690	HEK293	kidney:	embryo
43	chr13:50134640-50134690	HRE	kidney:	n/a
44	chr13:50123613-50123663	NH-A	brain:	n/a
45	chr13:50123645-50123695	H1-hESC	embryonic stem cell:	embryo
46	chr13:50123645-50123695	GM12892	blood:	n/a
47	chr13:50134640-50134690	GM19239	blood:	n/a
48	chr13:50123645-50123695	PrEC	prostate:	n/a
49	chr13:50134640-50134690	Jurkat	blood:	n/a
50	chr13:50123613-50123663	ProgFib	skin:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:50137662..50139363-chr13:50159195..50160839,2	MCF-7	breast:
2	chr13:50038641..50040451-chr13:50143314..50145864,2	MCF-7	breast:
3	chr13:50134986..50135758-chr13:50143919..50144828,2	MCF-7	breast:
4	chr13:50134505..50135459-chr13:50143778..50144515,3	MCF-7	breast:
5	chr13:50068598..50070239-chr13:50135700..50137416,2	MCF-7	breast:
6	chr13:50134458..50136628-chr13:50139261..50141252,2	MCF-7	breast:
7	chr13:50134779..50137828-chr13:50140921..50142745,3	MCF-7	breast:
8	chr13:50016440..50019751-chr13:50141127..50144444,4	MCF-7	breast:
9	chr13:50134986..50135758-chr13:50143919..50144828,2	MCF-7	breast:
10	chr13:50017307..50019773-chr13:50138937..50140601,2	MCF-7	breast:
11	chr13:50133873..50136164-chr13:50144707..50146572,2	MCF-7	breast:
12	chr13:50124973..50127457-chr13:50130944..50133269,2	MCF-7	breast:
13	chr13:50132996..50135368-chr13:50158926..50161457,2	MCF-7	breast:
14	chr13:50016553..50018688-chr13:50135233..50137955,2	K562	blood:
15	chr13:50132912..50136766-chr13:50158156..50162933,6	MCF-7	breast:
16	chr13:50127837..50130111-chr13:50134111..50136962,3	MCF-7	breast:
17	chr13:50134505..50135459-chr13:50143778..50144515,3	MCF-7	breast:
18	chr13:50017247..50020200-chr13:50127013..50128782,3	MCF-7	breast:
19	chr13:50126796..50128354-chr13:50131796..50134070,2	MCF-7	breast:
20	chr13:50140129..50142488-chr13:50158778..50160378,3	MCF-7	breast:
21	chr13:50129638..50131635-chr13:50134638..50136314,2	MCF-7	breast:
22	chr13:50143614..50146624-chr13:50158019..50161696,4	MCF-7	breast:
23	chr13:49875014..49875947-chr13:50128275..50129099,3	MCF-7	breast:
24	chr13:50143262..50147042-chr13:50150087..50153613,4	MCF-7	breast:
25	chr13:50133873..50136164-chr13:50144707..50146572,2	MCF-7	breast:
26	chr13:50119828..50121736-chr13:50158802..50160343,2	MCF-7	breast:
27	chr13:50129638..50131635-chr13:50134638..50136314,2	MCF-7	breast:
28	chr13:50142756..50146527-chr13:50158016..50161593,4	MCF-7	breast:
29	chr13:50123244..50123850-chr13:50179491..50180112,2	MCF-7	breast:
30	chr13:50068857..50071479-chr13:50143285..50145487,2	MCF-7	breast:
31	chr13:50127837..50130111-chr13:50134111..50136962,3	MCF-7	breast:
32	chr13:50126796..50128354-chr13:50131796..50134070,2	MCF-7	breast:
33	chr13:50022863..50025187-chr13:50116857..50119478,2	K562	blood:
34	chr13:50134458..50136628-chr13:50139261..50141252,2	MCF-7	breast:

No data

Variant related genes	Relation type
RCBTB1	TF binding region
RCBTB1	CpG island
ENSG00000136144	chromatin interactions
ENSG00000136169	chromatin interactions
ENSG00000136147	chromatin interactions
ENSG00000102547	chromatin interactions

Extended variants
information (count: 1235 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:1235 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9596137	chr13:50116435-50116436	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535111926	chr13:50116440-50116441	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs372827262	chr13:50116443-50116444	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556503346	chr13:50116458-50116459	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575015481	chr13:50116528-50116529	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545542852	chr13:50116557-50116558	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs557827335	chr13:50116566-50116567	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs17073112	chr13:50116571-50116572	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs541594814	chr13:50116574-50116575	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs560123958	chr13:50116603-50116604	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs530382798	chr13:50116623-50116624	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs4942844	chr13:50116652-50116653	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs372804080	chr13:50116666-50116667	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs563627960	chr13:50116682-50116683	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs531042079	chr13:50116701-50116702	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs543343068	chr13:50116722-50116723	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs552430570	chr13:50116794-50116795	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs75091607	chr13:50116854-50116855	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570921610	chr13:50116856-50116857	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191923058	chr13:50116886-50116887	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529161590	chr13:50116892-50116893	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369656790	chr13:50116908-50116909	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184525744	chr13:50116961-50116962	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189187520	chr13:50116991-50116992	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138657706	chr13:50117033-50117034	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs7317140	chr13:50117036-50117037	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs116118979	chr13:50117090-50117091	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs181881189	chr13:50117091-50117092	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs571285661	chr13:50117115-50117116	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534922821	chr13:50117140-50117141	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558400100	chr13:50117165-50117166	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs377736935	chr13:50117195-50117196	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs575215219	chr13:50117199-50117200	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149317656	chr13:50117259-50117260	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs56856971	chr13:50117260-50117261	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs185618352	chr13:50117326-50117327	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs373469529	chr13:50117356-50117357	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs1409013	chr13:50117390-50117391	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs573307461	chr13:50117489-50117490	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146312408	chr13:50117503-50117504	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189343513	chr13:50117527-50117528	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556629637	chr13:50117626-50117627	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs180870149	chr13:50117635-50117636	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs529046537	chr13:50117648-50117649	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs75419616	chr13:50117691-50117692	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs569115236	chr13:50117704-50117705	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186335625	chr13:50117736-50117737	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551323387	chr13:50117751-50117752	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138203444	chr13:50117794-50117795	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555026426	chr13:50117833-50117834	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Sezary syndrome	18413736	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21990379	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute promyelocytic leukemia	19109227	CNVD

Chromatin state (count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50075000-50143800	Weak transcription	Small Intestine	intestine
2	chr13:50088400-50151000	Weak transcription	Psoas Muscle	Psoas
3	chr13:50088600-50134200	Weak transcription	Stomach Mucosa	stomach
4	chr13:50090000-50122800	Weak transcription	Ovary	ovary
5	chr13:50090000-50123600	Weak transcription	Esophagus	oesophagus
6	chr13:50090200-50117800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr13:50091400-50138800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr13:50094600-50120000	Weak transcription	Spleen	Spleen
9	chr13:50094600-50141600	Weak transcription	Right Ventricle	heart
10	chr13:50095000-50120400	Weak transcription	A549	lung
11	chr13:50097800-50135000	Weak transcription	Colonic Mucosa	Colon
12	chr13:50101600-50142800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr13:50104600-50143800	Weak transcription	Hela-S3	cervix
14	chr13:50106600-50133200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr13:50108600-50158800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr13:50109200-50121600	Weak transcription	Brain Germinal Matrix	brain
17	chr13:50110400-50134400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr13:50110600-50124800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr13:50110800-50126800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
20	chr13:50111400-50127600	Weak transcription	Fetal Heart	heart
21	chr13:50111600-50136600	Strong transcription	Dnd41	blood
22	chr13:50111800-50133200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr13:50112000-50118200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr13:50112000-50118400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr13:50112000-50135000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr13:50112200-50118200	Strong transcription	Fetal Muscle Leg	muscle
27	chr13:50112200-50121200	Strong transcription	Fetal Intestine Large	intestine
28	chr13:50112200-50134200	Strong transcription	HUES48 Cell Line	embryonic stem cell
29	chr13:50112200-50138400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr13:50112400-50116600	Strong transcription	Fetal Stomach	stomach
31	chr13:50112400-50118200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr13:50113200-50118200	Strong transcription	NHEK	skin
33	chr13:50113200-50121400	Strong transcription	HMEC	breast
34	chr13:50113200-50127200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr13:50113400-50116800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr13:50113400-50117800	Strong transcription	Osteobl	bone
37	chr13:50113600-50123400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr13:50113800-50116600	Strong transcription	Muscle Satellite Cultured Cells	--
39	chr13:50114000-50125800	Strong transcription	Stomach Smooth Muscle	stomach
40	chr13:50114000-50126600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
41	chr13:50114200-50116600	Strong transcription	Brain Substantia Nigra	brain
42	chr13:50114200-50120000	Weak transcription	Brain Anterior Caudate	brain
43	chr13:50114800-50116600	Weak transcription	NHDF-Ad	bronchial
44	chr13:50114800-50118000	Strong transcription	Fetal Intestine Small	intestine
45	chr13:50115000-50117800	Strong transcription	HUES6 Cell Line	embryonic stem cell
46	chr13:50115000-50118800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr13:50115000-50119400	Weak transcription	Primary neutrophils fromperipheralblood	blood
48	chr13:50115000-50119400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr13:50115000-50119400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr13:50115000-50119800	Weak transcription	Pancreatic Islets	Pancreatic Islet

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