Variant report

Variant	esv1806956
Chromosome Location	chr6:166928580-166938431
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	ATF1	chr6:166928991-166929159	K562	blood:	n/a	n/a
2	BACH1	chr6:166928717-166928821	H1-hESC	embryonic stem cell:	n/a	chr6:166928759-166928773
3	CBX3	chr6:166931184-166931428	K562	blood:	n/a	n/a
4	CBX3	chr6:166931210-166931373	K562	blood:	n/a	n/a
5	CEBPB	chr6:166928607-166929177	IMR90	lung:	n/a	n/a
6	CEBPB	chr6:166928642-166928852	Hela-S3	cervix:	n/a	n/a
7	CHD2	chr6:166930360-166930361	K562	blood:	n/a	n/a
8	CHD2	chr6:166932271-166932302	HepG2	liver:	n/a	n/a
9	CTCF	chr6:166928640-166928790	HMF	breast:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
10	CTCF	chr6:166928600-166928750	HVMF	connective:	n/a	chr6:166928722-166928731
11	CTCF	chr6:166928620-166928770	AoAF	blood vessel:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
12	CTCF	chr6:166928640-166928790	GM12875	blood:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
13	CTCF	chr6:166928700-166928850	A549	lung:	n/a	chr6:166928822-166928835 chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
14	CTCF	chr6:166928596-166928797	SK-N-SH_RA	brain:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
15	CTCF	chr6:166928580-166928730	BE2_C	brain:	n/a	n/a
16	CTCF	chr6:166928680-166928830	HepG2	liver:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
17	CTCF	chr6:166928640-166928790	AG09309	skin:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
18	CTCF	chr6:166928700-166928850	RPTEC	kidney:	n/a	chr6:166928822-166928835 chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
19	CTCF	chr6:166928587-166928844	Gliobla	brain:	n/a	chr6:166928822-166928835 chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
20	CTCF	chr6:166928640-166928790	AG10803	skin:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
21	CTCF	chr6:166928640-166928790	HBMEC	blood vessel:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
22	CTCF	chr6:166928680-166928830	HVMF	connective:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
23	CTCF	chr6:166928620-166928770	AG04450	lung:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
24	CTCF	chr6:166928640-166928790	HCPEpiC	choroid plexus:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
25	CTCF	chr6:166928640-166928790	AG04450	lung:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
26	CTCF	chr6:166928601-166928831	MCF-7	breast:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
27	CTCF	chr6:166928600-166928750	SK-N-SH_RA	brain:	n/a	chr6:166928722-166928731
28	CTCF	chr6:166928580-166928730	HFF-Myc	foreskin:	n/a	n/a
29	CTCF	chr6:166928640-166928790	HEK293	kidney:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
30	CTCF	chr6:166928640-166928790	HRPEpiC	eye:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
31	CTCF	chr6:166928660-166928810	HEK293	kidney:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
32	CTCF	chr6:166928680-166928830	GM12865	blood:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
33	CTCF	chr6:166928640-166928790	AG04449	skin:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
34	CTCF	chr6:166928660-166928810	WI-38	lung:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
35	CTCF	chr6:166928680-166928830	AG09319	gingival:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
36	CTCF	chr6:166928680-166928830	NHDF-neo	bronchial:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
37	CTCF	chr6:166928660-166928810	AoAF	blood vessel:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
38	CTCF	chr6:166928773-166928787	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr6:166928640-166928790	WERI-Rb-1	eye:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
40	CTCF	chr6:166928640-166928790	NHLF	lung:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
41	CTCF	chr6:166928660-166928810	RPTEC	kidney:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
42	CTCF	chr6:166928660-166928810	AG10803	skin:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
43	CTCF	chr6:166928660-166928810	GM12878	blood:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
44	CTCF	chr6:166928620-166928770	HEEpiC	esophagus:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
45	CTCF	chr6:166928632-166928827	MCF-7	breast:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
46	CTCF	chr6:166928600-166928750	HMEC	breast:	n/a	chr6:166928722-166928731
47	CTCF	chr6:166928620-166928770	HRPEpiC	eye:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
48	CTCF	chr6:166928680-166928830	HA-sp	spinal cord:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
49	CTCF	chr6:166928656-166928811	GM12891	blood:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755
50	CTCF	chr6:166928640-166928790	BJ	skin:	n/a	chr6:166928742-166928755 chr6:166928722-166928731 chr6:166928746-166928755

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:166929057-166929107	HRE	kidney:	n/a
2	chr6:166929057-166929107	HIPEpiC	eye:	n/a
3	chr6:166929057-166929107	HUVEC	blood vessel:	n/a
4	chr6:166929057-166929107	T-47D	breast:	n/a
5	chr6:166929057-166929107	NH-A	brain:	n/a
6	chr6:166929057-166929107	RPTEC	kidney:	n/a
7	chr6:166929057-166929107	NHDF-neo	bronchial:	n/a
8	chr6:166929057-166929107	ProgFib	skin:	n/a
9	chr6:166929057-166929107	ovcar-3	ovarian:	n/a
10	chr6:166929057-166929107	HAEpiC	amniotic membrane:	n/a
11	chr6:166929057-166929107	AG04450	lung:	fetal
12	chr6:166929057-166929107	BE2_C	brain:	n/a
13	chr6:166929057-166929107	LNCaP	prostate:	n/a
14	chr6:166929057-166929107	HepG2	liver:	n/a
15	chr6:166929057-166929107	SAEC	small airway:	n/a
16	chr6:166929057-166929107	GM12891	blood:	n/a
17	chr6:166929057-166929107	HRPEpiC	eye:	n/a
18	chr6:166929057-166929107	GM19239	blood:	n/a
19	chr6:166929057-166929107	HEEpiC	esophagus:	n/a
20	chr6:166929057-166929107	HRCEpiC	kidney:	n/a
21	chr6:166929057-166929107	ECC-1	luminal epithelium:	n/a
22	chr6:166929057-166929107	MCF10A-Er-Src	breast:	n/a
23	chr6:166929057-166929107	HMEC	breast:	n/a
24	chr6:166929057-166929107	AG04449	skin:	fetal
25	chr6:166929057-166929107	H1-hESC	embryonic stem cell:	embryo
26	chr6:166929057-166929107	HCM	heart:	n/a
27	chr6:166929057-166929107	Hepatocyte	liver:	n/a
28	chr6:166929057-166929107	Caco-2	colon:	n/a
29	chr6:166929057-166929107	HCT-116	colon:	n/a
30	chr6:166929057-166929107	HL-60	blood:	n/a
31	chr6:166929057-166929107	A549	lung:	n/a
32	chr6:166929057-166929107	HPAEpiC	pulmonary alveolar:	n/a
33	chr6:166929057-166929107	GM06990	blood:	n/a
34	chr6:166929057-166929107	SK-N-SH_RA	brain:	n/a
35	chr6:166929057-166929107	K562	blood:	n/a
36	chr6:166929057-166929107	Hela-S3	cervix:	n/a
37	chr6:166929057-166929107	NB4	blood:	n/a
38	chr6:166929057-166929107	HCPEpiC	choroid plexus:	n/a
39	chr6:166929057-166929107	NHBE	bronchial:	n/a
40	chr6:166929057-166929107	Jurkat	blood:	n/a
41	chr6:166929057-166929107	SKMC	muscle:	n/a
42	chr6:166929057-166929107	BJ	skin:	n/a
43	chr6:166929057-166929107	AG10803	skin:	n/a
44	chr6:166929057-166929107	PrEC	prostate:	n/a
45	chr6:166929057-166929107	AoSMC	blood vessel:	n/a
46	chr6:166929057-166929107	PANC-1	pancreas:	n/a
47	chr6:166929057-166929107	SK-N-MC	brain:	n/a
48	chr6:166929057-166929107	GM12878	blood:	n/a
49	chr6:166929057-166929107	HNPCEpiC	eye:	n/a
50	chr6:166929057-166929107	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr6:166932943..166934797-chr6:166936117..166937896,2	K562	blood:
2	chr6:166935159..166937591-chr6:166943431..166946372,2	K562	blood:
3	chr6:166928469..166930058-chr6:167040238..167042581,2	MCF-7	breast:
4	chr6:166938386..166940136-chr6:166942749..166944700,2	K562	blood:
5	chr6:166928192..166929030-chr6:167027760..167028686,4	MCF-7	breast:
6	chr6:166869518..166870276-chr6:166927954..166928779,2	MCF-7	breast:
7	chr6:166932943..166934797-chr6:166936117..166937896,2	K562	blood:

Variant related genes	Relation type
RPS6KA2	TF binding region
RPS6KA2	CpG island
ENSG00000071242	chromatin interactions
ENSG00000269048	chromatin interactions

Extended variants
information (count: 422 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:422 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs378373	chr6:166928580-166928581	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs191725211	chr6:166928622-166928623	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs535052775	chr6:166928627-166928628	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs553321072	chr6:166928641-166928642	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs574750583	chr6:166928689-166928690	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs3778418	chr6:166928704-166928705	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs557056183	chr6:166928725-166928726	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs12212961	chr6:166928728-166928729	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs372289516	chr6:166928774-166928775	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs543199429	chr6:166928788-166928789	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs564767877	chr6:166928805-166928806	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs532435827	chr6:166928817-166928818	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs566645399	chr6:166928828-166928829	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs559264299	chr6:166928854-166928855	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs181737671	chr6:166928978-166928979	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs78545381	chr6:166929000-166929001	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs569748229	chr6:166929003-166929004	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs146635988	chr6:166929045-166929046	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs371405440	chr6:166929058-166929059	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs185858716	chr6:166929062-166929063	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs369348200	chr6:166929063-166929064	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs4473841	chr6:166929074-166929075	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs553400221	chr6:166929099-166929100	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs16899050	chr6:166929100-166929101	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs562269693	chr6:166929107-166929108	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs535477940	chr6:166929116-166929117	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs111492326	chr6:166929120-166929121	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs375752791	chr6:166929122-166929123	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs115426493	chr6:166929138-166929139	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs17505698	chr6:166929190-166929191	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs4327671	chr6:166929202-166929203	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs558326023	chr6:166929290-166929291	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs576965400	chr6:166929307-166929308	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs148320403	chr6:166929314-166929315	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs559413042	chr6:166929320-166929321	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs530034049	chr6:166929322-166929323	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs541833514	chr6:166929326-166929327	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs145922904	chr6:166929337-166929338	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs530620293	chr6:166929341-166929342	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs61063421	chr6:166929385-166929386	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs533505427	chr6:166929386-166929387	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs564662879	chr6:166929395-166929396	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs141428382	chr6:166929433-166929434	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs552489451	chr6:166929464-166929465	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs182313121	chr6:166929478-166929479	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs150394571	chr6:166929483-166929484	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs375514691	chr6:166929732-166929733	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs138654287	chr6:166929780-166929781	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs141806979	chr6:166929873-166929874	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs539499296	chr6:166929927-166929928	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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
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
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	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
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ependymoma	20639864	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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166899400-166929400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:166901000-166954800	Weak transcription	Rectal Smooth Muscle	rectum
3	chr6:166902200-166954400	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr6:166902600-166952800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr6:166909600-166943800	Weak transcription	Colonic Mucosa	Colon
6	chr6:166912200-166931200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:166913000-166929000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:166913000-166952000	Weak transcription	Primary T cells from cord blood	blood
9	chr6:166916200-166954200	Weak transcription	Right Atrium	heart
10	chr6:166916400-166940400	Weak transcription	Fetal Heart	heart
11	chr6:166917200-166932000	Weak transcription	Primary B cells from cord blood	blood
12	chr6:166918000-166928600	Weak transcription	HUVEC	blood vessel
13	chr6:166918200-166928600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr6:166918400-166931400	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr6:166919200-166928600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr6:166921200-166930000	Weak transcription	Fetal Intestine Large	intestine
17	chr6:166921400-166930000	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr6:166921400-166930200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr6:166921400-166943600	Weak transcription	Fetal Lung	lung
20	chr6:166921600-166932000	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr6:166921600-166932000	Weak transcription	Fetal Kidney	kidney
22	chr6:166921600-166937400	Weak transcription	Fetal Brain Male	brain
23	chr6:166922400-166928600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr6:166922400-166929400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr6:166923000-166930000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr6:166923000-166930000	Weak transcription	Esophagus	oesophagus
27	chr6:166923000-166931400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr6:166923000-166937200	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr6:166923000-166940400	Weak transcription	Aorta	Aorta
30	chr6:166923000-166943800	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr6:166923200-166931200	Weak transcription	Brain Germinal Matrix	brain
32	chr6:166923200-166932200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr6:166923200-166940200	Weak transcription	Ovary	ovary
34	chr6:166923200-166943200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr6:166923200-166943800	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr6:166923600-166928600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr6:166923600-166936800	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr6:166923800-166930000	Weak transcription	Placenta	Placenta
39	chr6:166923800-166944400	Weak transcription	Psoas Muscle	Psoas
40	chr6:166923800-166953000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr6:166924600-166928800	Weak transcription	HSMMtube	muscle
42	chr6:166925000-166940400	Weak transcription	Adipose Nuclei	Adipose
43	chr6:166926200-166928600	Weak transcription	Osteobl	bone
44	chr6:166926200-166929000	Strong transcription	Fetal Muscle Trunk	muscle
45	chr6:166926200-166930400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr6:166926200-166930400	Strong transcription	Fetal Stomach	stomach
47	chr6:166926400-166929200	Strong transcription	Fetal Muscle Leg	muscle
48	chr6:166926600-166928800	Strong transcription	Pancreas	Pancrea
49	chr6:166926600-166928800	Strong transcription	Skeletal Muscle Male	skeletal muscle
50	chr6:166927000-166929000	Strong transcription	Primary neutrophils fromperipheralblood	blood

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