Variant report

Variant	nsv968861
Chromosome Location	chr5:178251700-178275142
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	ARID3A	chr5:178266442-178266591	HepG2	liver:	n/a	n/a
2	ATF1	chr5:178265901-178266202	K562	blood:	n/a	n/a
3	BACH1	chr5:178259949-178259966	K562	blood:	n/a	n/a
4	BACH1	chr5:178254765-178254792	K562	blood:	n/a	n/a
5	BHLHE40	chr5:178259661-178259927	K562	blood:	n/a	n/a
6	BHLHE40	chr5:178266386-178266649	HepG2	liver:	n/a	n/a
7	BHLHE40	chr5:178266434-178266669	K562	blood:	n/a	n/a
8	BRCA1	chr5:178266539-178266607	HepG2	liver:	n/a	n/a
9	CEBPB	chr5:178257724-178257754	HepG2	liver:	n/a	n/a
10	CEBPB	chr5:178266040-178266088	K562	blood:	n/a	n/a
11	CHD2	chr5:178259461-178260123	K562	blood:	n/a	n/a
12	CTCF	chr5:178266407-178266700	NHEK	skin:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
13	CTCF	chr5:178266490-178266644	HUVEC	blood vessel:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
14	CTCF	chr5:178266460-178266610	AG04449	skin:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
15	CTCF	chr5:178258120-178258363	MCF-7	breast:	n/a	chr5:178258242-178258260
16	CTCF	chr5:178266500-178266650	HCFaa	heart:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
17	CTCF	chr5:178266367-178266710	MCF-7	breast:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
18	CTCF	chr5:178266500-178266650	GM12873	blood:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
19	CTCF	chr5:178266387-178266700	MCF-7	breast:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
20	CTCF	chr5:178266540-178266690	GM06990	blood:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266550-178266559
21	CTCF	chr5:178266440-178266590	GM12869	blood:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
22	CTCF	chr5:178258180-178258330	GM12873	blood:	n/a	chr5:178258242-178258260
23	CTCF	chr5:178266217-178266761	MCF-7	breast:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
24	CTCF	chr5:178266540-178266690	MCF-7	breast:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266550-178266559
25	CTCF	chr5:178258863-178259012	MCF-7	breast:	n/a	n/a
26	CTCF	chr5:178253340-178253490	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr5:178266480-178266630	AG10803	skin:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
28	CTCF	chr5:178266420-178266570	HBMEC	blood vessel:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
29	CTCF	chr5:178258120-178258270	K562	blood:	n/a	chr5:178258242-178258260
30	CTCF	chr5:178266477-178266635	GM19240	blood:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
31	CTCF	chr5:178258582-178258969	K562	blood:	n/a	n/a
32	CTCF	chr5:178266440-178266590	MCF-7	breast:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
33	CTCF	chr5:178266480-178266630	GM06990	blood:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
34	CTCF	chr5:178253371-178253446	NHEK	skin:	n/a	n/a
35	CTCF	chr5:178257620-178257770	HEEpiC	esophagus:	n/a	chr5:178257730-178257743
36	CTCF	chr5:178266417-178266689	H1-hESC	embryonic stem cell:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
37	CTCF	chr5:178266460-178266610	GM12874	blood:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
38	CTCF	chr5:178266480-178266630	Hela-S3	cervix:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
39	CTCF	chr5:178266344-178266615	A549	lung:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
40	CTCF	chr5:178266481-178266631	GM19238	blood:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
41	CTCF	chr5:178266460-178266610	HPF	lung:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
42	CTCF	chr5:178266349-178266717	T-47D	breast:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
43	CTCF	chr5:178258180-178258330	HEEpiC	esophagus:	n/a	chr5:178258242-178258260
44	CTCF	chr5:178266540-178266690	HAc	cerebellar:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266550-178266559
45	CTCF	chr5:178258155-178258354	H1-hESC	embryonic stem cell:	n/a	chr5:178258242-178258260
46	CTCF	chr5:178266440-178266590	BJ	skin:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
47	CTCF	chr5:178266500-178266650	HMF	breast:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559
48	CTCF	chr5:178257679-178257772	NHEK	skin:	n/a	chr5:178257730-178257743
49	CTCF	chr5:178258200-178258350	Hela-S3	cervix:	n/a	chr5:178258242-178258260
50	CTCF	chr5:178266429-178266704	LNCaP	prostate:	n/a	chr5:178266544-178266562 chr5:178266546-178266559 chr5:178266547-178266557 chr5:178266545-178266561 chr5:178266539-178266560 chr5:178266550-178266559

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178266137-178266187	AG10803	skin:	n/a
2	chr5:178266137-178266187	AG10803	skin:	n/a
3	chr5:178266060-178266110	HPAEpiC	pulmonary alveolar:	n/a
4	chr5:178266060-178266110	Jurkat	blood:	n/a
5	chr5:178266137-178266187	T-47D	breast:	n/a
6	chr5:178266175-178266225	RPTEC	kidney:	n/a
7	chr5:178266137-178266187	GM19239	blood:	n/a
8	chr5:178266060-178266110	GM12891	blood:	n/a
9	chr5:178266060-178266110	HNPCEpiC	eye:	n/a
10	chr5:178266175-178266225	HUVEC	blood vessel:	n/a
11	chr5:178266060-178266110	HepG2	liver:	n/a
12	chr5:178266060-178266110	ovcar-3	ovarian:	n/a
13	chr5:178266137-178266187	BE2_C	brain:	n/a
14	chr5:178266060-178266110	AG09309	skin:	n/a
15	chr5:178266175-178266225	SK-N-MC	brain:	n/a
16	chr5:178266137-178266187	HRE	kidney:	n/a
17	chr5:178266060-178266110	HCT-116	colon:	n/a
18	chr5:178266137-178266187	ovcar-3	ovarian:	n/a
19	chr5:178266060-178266110	GM12878	blood:	n/a
20	chr5:178266060-178266110	PrEC	prostate:	n/a
21	chr5:178266060-178266110	MCF-7	breast:	n/a
22	chr5:178266060-178266110	HUVEC	blood vessel:	n/a
23	chr5:178266137-178266187	SKMC	muscle:	n/a
24	chr5:178266175-178266225	ovcar-3	ovarian:	n/a
25	chr5:178266175-178266225	MCF10A-Er-Src	breast:	n/a
26	chr5:178266060-178266110	Hela-S3	cervix:	n/a
27	chr5:178266175-178266225	ProgFib	skin:	n/a
28	chr5:178266137-178266187	GM12891	blood:	n/a
29	chr5:178266060-178266110	GM06990	blood:	n/a
30	chr5:178266137-178266187	Hepatocyte	liver:	n/a
31	chr5:178266137-178266187	PFSK-1	brain:	n/a
32	chr5:178266175-178266225	BJ	skin:	n/a
33	chr5:178266060-178266110	PANC-1	pancreas:	n/a
34	chr5:178266137-178266187	HAEpiC	amniotic membrane:	n/a
35	chr5:178266175-178266225	GM06990	blood:	n/a
36	chr5:178266175-178266225	MCF-7	breast:	n/a
37	chr5:178266137-178266187	SAEC	small airway:	n/a
38	chr5:178266060-178266110	HCF	heart:	n/a
39	chr5:178266137-178266187	MCF10A-Er-Src	breast:	n/a
40	chr5:178266137-178266187	GM12892	blood:	n/a
41	chr5:178266175-178266225	Hela-S3	cervix:	n/a
42	chr5:178266137-178266187	IMR90	lung:	fetal
43	chr5:178266175-178266225	NH-A	brain:	n/a
44	chr5:178266060-178266110	PFSK-1	brain:	n/a
45	chr5:178266175-178266225	Hepatocyte	liver:	n/a
46	chr5:178266175-178266225	K562	blood:	n/a
47	chr5:178266137-178266187	BJ	skin:	n/a
48	chr5:178266137-178266187	GM06990	blood:	n/a
49	chr5:178266060-178266110	ProgFib	skin:	n/a
50	chr5:178266175-178266225	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:178248233..178250497-chr5:178253238..178254765,2	K562	blood:
2	chr5:178250159..178253046-chr5:178256116..178259012,3	MCF-7	breast:
3	chr5:178219935..178220578-chr5:178266097..178266710,3	MCF-7	breast:
4	chr5:178251481..178253894-chr5:178255525..178257493,2	K562	blood:
5	chr5:178156362..178158364-chr5:178252776..178254974,2	K562	blood:
6	chr5:178228775..178231759-chr5:178257850..178260513,2	MCF-7	breast:
7	chr5:178157367..178158168-chr5:178266123..178266937,3	MCF-7	breast:
8	chr5:178258610..178261483-chr5:178285999..178288925,2	K562	blood:
9	chr5:178256899..178257517-chr5:178489612..178490272,2	K562	blood:
10	chr5:177706663..177708953-chr5:178261165..178263624,2	MCF-7	breast:
11	chr5:178250159..178253046-chr5:178256116..178259012,3	MCF-7	breast:
12	chr5:177661743..177662668-chr5:178266372..178266966,2	K562	blood:
13	chr5:178223973..178226497-chr5:178266303..178268866,2	MCF-7	breast:
14	chr5:178053047..178055636-chr5:178260492..178262068,2	K562	blood:
15	chr5:178252394..178254113-chr5:178255346..178258174,3	K562	blood:
16	chr5:178264186..178266313-chr5:178270488..178273068,2	MCF-7	breast:
17	chr5:178251481..178253894-chr5:178255525..178257493,2	K562	blood:
18	chr5:178262543..178264784-chr5:178273613..178275521,2	K562	blood:
19	chr5:178250289..178252809-chr5:178285949..178288752,2	K562	blood:
20	chr5:178219826..178220832-chr5:178266011..178266987,10	MCF-7	breast:
21	chr5:177661196..177662135-chr5:178266134..178266915,2	MCF-7	breast:
22	chr5:178157414..178158390-chr5:178265741..178266981,10	MCF-7	breast:
23	chr5:178050940..178053910-chr5:178263858..178266243,2	MCF-7	breast:
24	chr5:178262543..178264784-chr5:178273613..178275521,2	K562	blood:
25	chr5:178251204..178253302-chr5:178256012..178257744,2	MCF-7	breast:
26	chr5:178264186..178266313-chr5:178270488..178273068,2	MCF-7	breast:
27	chr5:178251204..178253302-chr5:178256012..178257744,2	MCF-7	breast:
28	chr5:177706757..177707961-chr5:178266041..178266913,4	MCF-7	breast:
29	chr5:177710796..177711682-chr5:178266072..178266614,2	K562	blood:
30	chr5:178219910..178220433-chr5:178257274..178257901,2	MCF-7	breast:
31	chr5:178252394..178254113-chr5:178255346..178258174,3	K562	blood:
32	chr5:178214124..178214763-chr5:178265905..178266637,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000253725	TF binding region
ENSG00000253725	CpG island
ENSG00000169131	chromatin interactions
ENSG00000250420	chromatin interactions
ENSG00000178338	chromatin interactions
ENSG00000113240	chromatin interactions

Extended variants
information (count: 1335 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1335 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138509217	chr5:178251719-178251720	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs187634428	chr5:178251732-178251733	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs115502266	chr5:178251837-178251838	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs115659013	chr5:178251838-178251839	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs67044608	chr5:178251851-178251852	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs80322687	chr5:178251860-178251861	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs117947677	chr5:178251867-178251868	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs143996405	chr5:178251874-178251875	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs62393010	chr5:178251877-178251878	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs555257834	chr5:178251912-178251913	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs191563722	chr5:178251914-178251915	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs534321762	chr5:178251919-178251920	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs183500597	chr5:178251939-178251940	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs538909838	chr5:178251953-178251954	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs188443992	chr5:178251954-178251955	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs375820369	chr5:178251962-178251963	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs564677689	chr5:178251971-178251972	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs368297234	chr5:178251978-178251979	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs576741774	chr5:178252000-178252001	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs544092602	chr5:178252005-178252006	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs6869023	chr5:178252009-178252010	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs386695524	chr5:178252021-178252022	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs547763188	chr5:178252032-178252033	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs559535962	chr5:178252038-178252039	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs558873294	chr5:178252041-178252042	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs13158576	chr5:178252052-178252053	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs191683370	chr5:178252080-178252081	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs530640217	chr5:178252085-178252086	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs548818824	chr5:178252090-178252091	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs567232361	chr5:178252098-178252099	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs6884341	chr5:178252127-178252128	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs552928686	chr5:178252135-178252136	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs10716034	chr5:178252149-178252150	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs60335833	chr5:178252156-178252157	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs10075819	chr5:178252157-178252158	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs371845375	chr5:178252158-178252159	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs115228832	chr5:178252159-178252160	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs200936517	chr5:178252166-178252167	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs60801811	chr5:178252167-178252168	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs56748548	chr5:178252168-178252169	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs59711935	chr5:178252170-178252171	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs538708673	chr5:178252212-178252213	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs148687384	chr5:178252213-178252214	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs557742826	chr5:178252236-178252237	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs112328559	chr5:178252294-178252295	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs576678454	chr5:178252312-178252313	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs544042299	chr5:178252336-178252337	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs556039044	chr5:178252363-178252364	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs10068395	chr5:178252366-178252367	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs142573217	chr5:178252377-178252378	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	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
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178236800-178255800	Weak transcription	K562	blood
2	chr5:178241200-178252400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr5:178251800-178252400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr5:178252200-178253200	Enhancers	H9 Cell Line	embryonic stem cell
5	chr5:178252400-178252600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr5:178252400-178253200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr5:178252400-178253400	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr5:178252400-178254000	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr5:178252400-178254600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr5:178252400-178255000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr5:178252600-178253000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr5:178252600-178253200	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr5:178252600-178254200	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr5:178252600-178254400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr5:178252600-178254400	Enhancers	HMEC	breast
16	chr5:178252600-178254600	Enhancers	NHEK	skin
17	chr5:178252600-178255000	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr5:178252800-178253400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr5:178252800-178254000	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr5:178252800-178254400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr5:178253000-178253200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr5:178253200-178255800	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr5:178253200-178256000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr5:178253200-178257000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr5:178253200-178257800	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr5:178253400-178253800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr5:178253400-178254000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr5:178253800-178255000	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr5:178254000-178254200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr5:178254000-178255800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr5:178254000-178259400	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr5:178254200-178259400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr5:178254400-178258200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr5:178254600-178256800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr5:178255000-178255800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr5:178255000-178256000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr5:178255000-178257000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr5:178255800-178256000	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr5:178255800-178256400	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr5:178255800-178256600	Strong transcription	K562	blood
41	chr5:178255800-178257200	Enhancers	H9 Cell Line	embryonic stem cell
42	chr5:178255800-178257200	Bivalent Enhancer	Fetal Brain Male	brain
43	chr5:178255800-178257600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr5:178256000-178256600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr5:178256000-178256800	Enhancers	Adipose Nuclei	Adipose
46	chr5:178256000-178257200	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr5:178256400-178257200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr5:178256400-178258600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr5:178256600-178257000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr5:178256600-178258200	Weak transcription	K562	blood

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