Variant report

Variant	nsv1024333
Chromosome Location	chr6:144468065-144502824
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:144472203-144472876	GM12878	blood:	n/a	n/a
2	ATF2	chr6:144472064-144473027	GM12878	blood:	n/a	n/a
3	ATF2	chr6:144471064-144471607	GM12878	blood:	n/a	n/a
4	BACH1	chr6:144470985-144472016	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr6:144501538-144501969	GM12878	blood:	n/a	n/a
6	BATF	chr6:144476674-144477035	GM12878	blood:	n/a	n/a
7	BATF	chr6:144472327-144472741	GM12878	blood:	n/a	chr6:144472549-144472560
8	BATF	chr6:144501557-144501859	GM12878	blood:	n/a	n/a
9	BATF	chr6:144472250-144472822	GM12878	blood:	n/a	chr6:144472549-144472560
10	BATF	chr6:144476638-144477020	GM12878	blood:	n/a	n/a
11	BCL11A	chr6:144472351-144472698	GM12878	blood:	n/a	chr6:144472552-144472561 chr6:144472525-144472533
12	BCL11A	chr6:144472229-144472724	GM12878	blood:	n/a	chr6:144472552-144472561 chr6:144472525-144472533 chr6:144472695-144472704
13	BCL11A	chr6:144471118-144471477	GM12878	blood:	n/a	chr6:144471297-144471310 chr6:144471350-144471359 chr6:144471329-144471342
14	BCL3	chr6:144471056-144471854	GM12878	blood:	n/a	chr6:144471297-144471310 chr6:144471350-144471359 chr6:144471727-144471740 chr6:144471717-144471730 chr6:144471664-144471673 chr6:144471563-144471572 chr6:144471627-144471636 chr6:144471557-144471570 chr6:144471329-144471342 chr6:144471661-144471670
15	BCL3	chr6:144472266-144472740	GM12878	blood:	n/a	chr6:144472552-144472561 chr6:144472525-144472533 chr6:144472695-144472704
16	BCLAF1	chr6:144470975-144472867	GM12878	blood:	n/a	chr6:144471297-144471310 chr6:144471868-144471877 chr6:144471350-144471359 chr6:144472552-144472561 chr6:144471727-144471740 chr6:144471717-144471730 chr6:144471664-144471673 chr6:144471563-144471572 chr6:144471921-144471930 chr6:144471627-144471636 chr6:144471557-144471570 chr6:144471848-144471857 chr6:144471329-144471342 chr6:144472525-144472533 chr6:144472695-144472704 chr6:144471661-144471670
17	BCLAF1	chr6:144472186-144472725	GM12878	blood:	n/a	chr6:144472552-144472561 chr6:144472525-144472533 chr6:144472695-144472704
18	BCLAF1	chr6:144471058-144471910	GM12878	blood:	n/a	chr6:144471297-144471310 chr6:144471868-144471877 chr6:144471350-144471359 chr6:144471727-144471740 chr6:144471717-144471730 chr6:144471664-144471673 chr6:144471563-144471572 chr6:144471627-144471636 chr6:144471557-144471570 chr6:144471848-144471857 chr6:144471329-144471342 chr6:144471661-144471670
19	BHLHE40	chr6:144471974-144472961	GM12878	blood:	n/a	n/a
20	BHLHE40	chr6:144471532-144471550	K562	blood:	n/a	n/a
21	BHLHE40	chr6:144499527-144499611	GM12878	blood:	n/a	n/a
22	BHLHE40	chr6:144470962-144471751	GM12878	blood:	n/a	chr6:144471557-144471573 chr6:144471709-144471725 chr6:144471495-144471511
23	BRCA1	chr6:144479289-144479632	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr6:144471330-144471659	K562	blood:	n/a	n/a
25	CCNT2	chr6:144471222-144471845	K562	blood:	n/a	n/a
26	CEBPB	chr6:144484226-144484381	K562	blood:	n/a	chr6:144484316-144484325 chr6:144484316-144484325 chr6:144484314-144484327 chr6:144484316-144484325
27	CEBPB	chr6:144471432-144471850	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr6:144477502-144477818	Hela-S3	cervix:	n/a	chr6:144477648-144477659 chr6:144477649-144477660 chr6:144477638-144477649 chr6:144477650-144477659
29	CEBPB	chr6:144499098-144499119	A549	lung:	n/a	n/a
30	CEBPB	chr6:144473631-144474003	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr6:144495344-144495390	IMR90	lung:	n/a	n/a
32	CEBPB	chr6:144484143-144484503	K562	blood:	n/a	chr6:144484316-144484325 chr6:144484316-144484325 chr6:144484314-144484327 chr6:144484316-144484325
33	CEBPB	chr6:144484177-144484453	IMR90	lung:	n/a	chr6:144484316-144484325 chr6:144484316-144484325 chr6:144484314-144484327 chr6:144484316-144484325
34	CEBPB	chr6:144479286-144479724	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr6:144470975-144471637	GM12878	blood:	n/a	n/a
36	CEBPB	chr6:144484105-144484392	K562	blood:	n/a	chr6:144484316-144484325 chr6:144484316-144484325 chr6:144484314-144484327 chr6:144484316-144484325
37	CEBPB	chr6:144472403-144473126	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr6:144484201-144484447	A549	lung:	n/a	chr6:144484316-144484325 chr6:144484316-144484325 chr6:144484314-144484327 chr6:144484316-144484325
39	CEBPB	chr6:144477494-144477828	IMR90	lung:	n/a	chr6:144477648-144477659 chr6:144477649-144477660 chr6:144477638-144477649 chr6:144477650-144477659
40	CEBPB	chr6:144477529-144477790	K562	blood:	n/a	chr6:144477648-144477659 chr6:144477649-144477660 chr6:144477638-144477649 chr6:144477650-144477659
41	CEBPB	chr6:144477541-144477802	A549	lung:	n/a	chr6:144477648-144477659 chr6:144477649-144477660 chr6:144477638-144477649 chr6:144477650-144477659
42	CEBPB	chr6:144477480-144477819	HepG2	liver:	n/a	chr6:144477648-144477659 chr6:144477649-144477660 chr6:144477638-144477649 chr6:144477650-144477659
43	CEBPB	chr6:144484153-144484451	HepG2	liver:	n/a	chr6:144484316-144484325 chr6:144484316-144484325 chr6:144484314-144484327 chr6:144484316-144484325
44	CHD1	chr6:144479495-144479518	GM12878	blood:	n/a	n/a
45	CHD1	chr6:144484229-144484369	GM12878	blood:	n/a	n/a
46	CHD1	chr6:144474088-144475011	GM12878	blood:	n/a	n/a
47	CHD1	chr6:144470863-144473498	GM12878	blood:	n/a	chr6:144471204-144471214 chr6:144471426-144471436
48	CHD2	chr6:144479345-144479709	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr6:144470993-144471833	GM12878	blood:	n/a	chr6:144471204-144471214 chr6:144471426-144471436
50	CHD2	chr6:144471283-144471728	Hela-S3	cervix:	n/a	chr6:144471426-144471436

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:144474807-144474857	HRE	kidney:	n/a
2	chr6:144471433-144471483	SK-N-SH_RA	brain:	n/a
3	chr6:144471433-144471483	MCF-7	breast:	n/a
4	chr6:144472333-144472383	AG09309	skin:	n/a
5	chr6:144479349-144479399	GM12878	blood:	n/a
6	chr6:144471198-144471248	K562	blood:	n/a
7	chr6:144471431-144471481	PANC-1	pancreas:	n/a
8	chr6:144471985-144472035	HEEpiC	esophagus:	n/a
9	chr6:144472355-144472405	GM19239	blood:	n/a
10	chr6:144471433-144471483	NT2-D1	testis:	n/a
11	chr6:144470511-144470561	Caco-2	colon:	n/a
12	chr6:144471431-144471481	HIPEpiC	eye:	n/a
13	chr6:144471798-144471848	HRE	kidney:	n/a
14	chr6:144471431-144471481	MCF10A-Er-Src	breast:	n/a
15	chr6:144471985-144472035	AG09309	skin:	n/a
16	chr6:144470511-144470561	GM12878	blood:	n/a
17	chr6:144471564-144471614	NHDF-neo	bronchial:	n/a
18	chr6:144472355-144472405	MCF-7	breast:	n/a
19	chr6:144471985-144472035	GM19239	blood:	n/a
20	chr6:144471431-144471481	IMR90	lung:	fetal
21	chr6:144474807-144474857	GM12891	blood:	n/a
22	chr6:144470511-144470561	PrEC	prostate:	n/a
23	chr6:144471985-144472035	HMEC	breast:	n/a
24	chr6:144471431-144471481	H1-hESC	embryonic stem cell:	embryo
25	chr6:144471431-144471481	GM12891	blood:	n/a
26	chr6:144471431-144471481	AG04449	skin:	fetal
27	chr6:144470511-144470561	GM06990	blood:	n/a
28	chr6:144471643-144471693	HCF	heart:	n/a
29	chr6:144471433-144471483	LNCaP	prostate:	n/a
30	chr6:144474807-144474857	AoSMC	blood vessel:	n/a
31	chr6:144472333-144472383	HRCEpiC	kidney:	n/a
32	chr6:144471798-144471848	GM06990	blood:	n/a
33	chr6:144479349-144479399	HepG2	liver:	n/a
34	chr6:144471198-144471248	ovcar-3	ovarian:	n/a
35	chr6:144479349-144479399	SAEC	small airway:	n/a
36	chr6:144471198-144471248	HEK293	kidney:	embryo
37	chr6:144471798-144471848	HL-60	blood:	n/a
38	chr6:144472355-144472405	SAEC	small airway:	n/a
39	chr6:144471643-144471693	A549	lung:	n/a
40	chr6:144470511-144470561	RPTEC	kidney:	n/a
41	chr6:144471798-144471848	Jurkat	blood:	n/a
42	chr6:144471643-144471693	GM12891	blood:	n/a
43	chr6:144471643-144471693	RPTEC	kidney:	n/a
44	chr6:144471431-144471481	AG09309	skin:	n/a
45	chr6:144479349-144479399	PANC-1	pancreas:	n/a
46	chr6:144474807-144474857	H1-hESC	embryonic stem cell:	embryo
47	chr6:144472333-144472383	SK-N-SH	brain:	n/a
48	chr6:144471564-144471614	HMEC	breast:	n/a
49	chr6:144470511-144470561	AG04449	skin:	fetal
50	chr6:144472333-144472383	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:144472179..144474149-chr6:144476552..144479484,2	K562	blood:
2	chr6:144474360..144477861-chr6:144491638..144494862,3	K562	blood:
3	chr6:144469135..144471504-chr6:144482402..144484343,2	K562	blood:
4	chr6:144470339..144473256-chr6:144473370..144475753,2	K562	blood:
5	chr6:144479875..144482204-chr6:144493372..144495029,2	K562	blood:
6	chr6:144469135..144471504-chr6:144482402..144484343,2	K562	blood:
7	chr6:144479875..144482204-chr6:144493372..144495029,2	K562	blood:
8	chr6:144492987..144496761-chr6:144536161..144539175,3	K562	blood:
9	chr6:144414051..144416949-chr6:144473098..144474790,2	K562	blood:
10	chr6:144477392..144479539-chr6:144497614..144499200,2	MCF-7	breast:
11	chr6:144499605..144501312-chr6:144540147..144541941,2	K562	blood:
12	chr6:144476586..144479088-chr6:144535900..144538153,2	MCF-7	breast:
13	chr6:144472179..144474149-chr6:144476552..144479484,2	K562	blood:
14	chr6:144494396..144496761-chr6:144536161..144538816,2	K562	blood:
15	chr6:144467428..144469078-chr6:144471354..144473087,2	MCF-7	breast:
16	chr6:144474360..144477861-chr6:144491638..144494862,3	K562	blood:
17	chr6:144477392..144479539-chr6:144497614..144499200,2	MCF-7	breast:

Variant related genes	Relation type
STX11	TF binding region
STX11	CpG island
ENSG00000169976	chromatin interactions
ENSG00000135604	chromatin interactions

Extended variants
information (count: 1260 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1260 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9390157	chr6:144468065-144468066	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs9496881	chr6:144468073-144468074	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs368677240	chr6:144468100-144468101	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs118186944	chr6:144468130-144468131	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs555236692	chr6:144468163-144468164	Genic enhancers Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs542669728	chr6:144468192-144468193	Genic enhancers Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs576788038	chr6:144468205-144468206	Genic enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs544176021	chr6:144468291-144468292	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs7763339	chr6:144468293-144468294	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs370377892	chr6:144468301-144468302	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs371131638	chr6:144468303-144468304	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs199765716	chr6:144468311-144468312	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs57924646	chr6:144468312-144468313	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs74914154	chr6:144468316-144468317	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs76872849	chr6:144468317-144468318	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs56897751	chr6:144468318-144468319	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs182587077	chr6:144468328-144468329	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs7745240	chr6:144468342-144468343	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs557191120	chr6:144468368-144468369	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs79704826	chr6:144468415-144468416	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs58084770	chr6:144468423-144468424	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs547957536	chr6:144468444-144468445	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs142230341	chr6:144468482-144468483	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs61249035	chr6:144468498-144468499	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs552061859	chr6:144468519-144468520	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs60762289	chr6:144468539-144468540	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs145872089	chr6:144468543-144468544	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs373823047	chr6:144468557-144468558	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs552757989	chr6:144468563-144468564	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs376733663	chr6:144468564-144468565	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs138230567	chr6:144468569-144468570	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs535572514	chr6:144468598-144468599	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs111520767	chr6:144468605-144468606	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs576751932	chr6:144468737-144468738	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs57063441	chr6:144468755-144468756	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs76511246	chr6:144468763-144468764	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs139770537	chr6:144468775-144468776	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs12173565	chr6:144468809-144468810	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs541433659	chr6:144468905-144468906	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs559513418	chr6:144468948-144468949	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs77020557	chr6:144468950-144468951	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs576269540	chr6:144468976-144468977	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs541959171	chr6:144469012-144469013	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs185829059	chr6:144469021-144469022	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs115055477	chr6:144469030-144469031	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs147400114	chr6:144469031-144469032	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs139793428	chr6:144469038-144469039	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs528408821	chr6:144469065-144469066	Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs546553541	chr6:144469123-144469124	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568010799	chr6:144469173-144469174	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17142309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:962 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:144463000-144470600	Weak transcription	GM12878-XiMat	blood
2	chr6:144463200-144470600	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr6:144466400-144470800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr6:144466600-144469400	Weak transcription	NHEK	skin
5	chr6:144466600-144470600	Genic enhancers	Primary neutrophils fromperipheralblood	blood
6	chr6:144467000-144470800	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr6:144467000-144470800	Weak transcription	HUVEC	blood vessel
8	chr6:144467400-144470000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr6:144467600-144470400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr6:144468000-144468200	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr6:144468200-144470800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr6:144469800-144470000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr6:144470000-144470200	Enhancers	NHLF	lung
14	chr6:144470000-144470600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr6:144470400-144470600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr6:144470400-144470600	Enhancers	Placenta	Placenta
17	chr6:144470400-144470800	Enhancers	Primary hematopoietic stem cells	blood
18	chr6:144470400-144470800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr6:144470400-144471000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr6:144470400-144471000	Enhancers	NHDF-Ad	bronchial
21	chr6:144470400-144473200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
22	chr6:144470600-144470800	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr6:144470600-144470800	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr6:144470600-144470800	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr6:144470600-144470800	Enhancers	Primary B cells from peripheral blood	blood
26	chr6:144470600-144470800	Enhancers	Primary T cells fromperipheralblood	blood
27	chr6:144470600-144470800	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr6:144470600-144470800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr6:144470600-144470800	Enhancers	Primary T helper cells fromperipheralblood	blood
30	chr6:144470600-144470800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
31	chr6:144470600-144470800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr6:144470600-144470800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr6:144470600-144470800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr6:144470600-144470800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr6:144470600-144470800	Enhancers	Adipose Nuclei	Adipose
36	chr6:144470600-144470800	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
37	chr6:144470600-144470800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
38	chr6:144470600-144470800	Enhancers	GM12878-XiMat	blood
39	chr6:144470600-144470800	Enhancers	Hela-S3	cervix
40	chr6:144470600-144470800	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr6:144470600-144470800	Bivalent Enhancer	NHEK	skin
42	chr6:144470600-144471000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
43	chr6:144470600-144471000	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr6:144470600-144471000	Bivalent Enhancer	Fetal Intestine Small	intestine
45	chr6:144470600-144471000	Bivalent Enhancer	Fetal Stomach	stomach
46	chr6:144470600-144471000	Enhancers	Lung	lung
47	chr6:144470600-144471000	Enhancers	Ovary	ovary
48	chr6:144470600-144471000	Enhancers	Sigmoid Colon	Sigmoid Colon
49	chr6:144470600-144471200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr6:144470600-144471200	Bivalent Enhancer	Fetal Kidney	kidney

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