Variant report

Variant	nsv872548
Chromosome Location	chr1:172518012-172551724
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:152)
CpG islands
(count:185)
Chromatin interactive
region (count:58)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:152 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:172526452-172526912	HepG2	liver:	n/a	chr1:172526750-172526766
2	ARID3A	chr1:172536592-172536681	K562	blood:	n/a	n/a
3	ARID3A	chr1:172519144-172519422	K562	blood:	n/a	n/a
4	ATF3	chr1:172535369-172535700	K562	blood:	n/a	n/a
5	CCNT2	chr1:172519174-172519339	K562	blood:	n/a	n/a
6	CCNT2	chr1:172520515-172520578	K562	blood:	n/a	n/a
7	CEBPB	chr1:172535330-172535652	HepG2	liver:	n/a	chr1:172535507-172535518
8	CEBPB	chr1:172525745-172525882	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:172535283-172535703	K562	blood:	n/a	chr1:172535507-172535518
10	CEBPB	chr1:172535366-172535612	H1-hESC	embryonic stem cell:	n/a	chr1:172535507-172535518
11	CEBPB	chr1:172535344-172535644	MCF-7	breast:	n/a	chr1:172535507-172535518
12	CEBPB	chr1:172535340-172535667	A549	lung:	n/a	chr1:172535507-172535518
13	CEBPB	chr1:172535319-172535704	K562	blood:	n/a	chr1:172535507-172535518
14	CEBPB	chr1:172535348-172535669	Hela-S3	cervix:	n/a	chr1:172535507-172535518
15	CEBPB	chr1:172525739-172525917	K562	blood:	n/a	n/a
16	CEBPB	chr1:172535332-172535669	IMR90	lung:	n/a	chr1:172535507-172535518
17	CEBPB	chr1:172535329-172535571	K562	blood:	n/a	chr1:172535507-172535518
18	CTCF	chr1:172537218-172537278	Medullo	brain:	n/a	n/a
19	E2F4	chr1:172551595-172552308	MCF10A-Er-Src	breast:	n/a	n/a
20	EP300	chr1:172526432-172526787	HepG2	liver:	n/a	n/a
21	EP300	chr1:172544630-172544743	GM12878	blood:	n/a	n/a
22	EP300	chr1:172526409-172526842	HepG2	liver:	n/a	n/a
23	EP300	chr1:172536769-172536796	K562	blood:	n/a	n/a
24	FOXA1	chr1:172526339-172526903	HepG2	liver:	n/a	n/a
25	FOXA1	chr1:172520196-172520481	T-47D	breast:	n/a	n/a
26	FOXA1	chr1:172526422-172526743	HepG2	liver:	n/a	n/a
27	FOXA1	chr1:172526352-172526883	HepG2	liver:	n/a	n/a
28	FOXA1	chr1:172526432-172526754	HepG2	liver:	n/a	n/a
29	FOXA2	chr1:172526380-172526922	HepG2	liver:	n/a	n/a
30	FOXA2	chr1:172526420-172526831	HepG2	liver:	n/a	n/a
31	GATA2	chr1:172519100-172519300	SH-SY5Y	brain:	n/a	n/a
32	GATA3	chr1:172533035-172533287	MCF-7	breast:	n/a	n/a
33	GATA3	chr1:172550827-172550918	SH-SY5Y	brain:	n/a	n/a
34	GATA3	chr1:172546570-172546581	SH-SY5Y	brain:	n/a	n/a
35	GATA3	chr1:172519271-172519295	SH-SY5Y	brain:	n/a	n/a
36	GATA3	chr1:172530293-172530769	SK-N-SH	brain:	n/a	n/a
37	GATA3	chr1:172542867-172542987	SH-SY5Y	brain:	n/a	n/a
38	HNF4A	chr1:172526405-172526675	HepG2	liver:	n/a	n/a
39	IRF1	chr1:172527460-172527472	K562	blood:	n/a	n/a
40	IRF1	chr1:172520526-172521139	K562	blood:	n/a	chr1:172520609-172520623 chr1:172520599-172520613 chr1:172520605-172520619 chr1:172520603-172520617 chr1:172520603-172520613 chr1:172520609-172520619 chr1:172520601-172520621
41	IRF1	chr1:172548254-172548467	K562	blood:	n/a	chr1:172548320-172548334 chr1:172548319-172548333 chr1:172548314-172548331 chr1:172548325-172548337 chr1:172548323-172548337 chr1:172548319-172548332 chr1:172548322-172548336 chr1:172548318-172548338
42	IRF1	chr1:172529537-172529566	K562	blood:	n/a	n/a
43	IRF1	chr1:172550425-172550514	K562	blood:	n/a	n/a
44	IRF1	chr1:172518877-172519178	K562	blood:	n/a	chr1:172519062-172519073 chr1:172519059-172519072 chr1:172519060-172519077
45	IRF1	chr1:172527476-172527486	K562	blood:	n/a	n/a
46	IRF1	chr1:172520936-172521125	K562	blood:	n/a	n/a
47	JUN	chr1:172547111-172547188	K562	blood:	n/a	chr1:172547166-172547175
48	JUN	chr1:172547883-172548046	K562	blood:	n/a	n/a
49	JUND	chr1:172535357-172535660	K562	blood:	n/a	n/a
50	KAP1	chr1:172538264-172538701	K562	blood:	n/a	n/a

(count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:172541012-172541062	T-47D	breast:	n/a
2	chr1:172541012-172541062	HCPEpiC	choroid plexus:	n/a
3	chr1:172541012-172541062	T-47D	breast:	n/a
4	chr1:172541012-172541062	HCPEpiC	choroid plexus:	n/a
5	chr1:172540913-172540963	SAEC	small airway:	n/a
6	chr1:172540913-172540963	K562	blood:	n/a
7	chr1:172541012-172541062	AG09309	skin:	n/a
8	chr1:172543864-172543914	AG09309	skin:	n/a
9	chr1:172540913-172540963	U87	brain:	n/a
10	chr1:172540913-172540963	Hepatocyte	liver:	n/a
11	chr1:172541012-172541062	HMEC	breast:	n/a
12	chr1:172540913-172540963	Caco-2	colon:	n/a
13	chr1:172541012-172541062	NHBE	bronchial:	n/a
14	chr1:172541012-172541062	NT2-D1	testis:	n/a
15	chr1:172543864-172543914	T-47D	breast:	n/a
16	chr1:172541012-172541062	MCF10A-Er-Src	breast:	n/a
17	chr1:172540913-172540963	HPAEpiC	pulmonary alveolar:	n/a
18	chr1:172541012-172541062	HEK293	kidney:	embryo
19	chr1:172543864-172543914	HEK293	kidney:	embryo
20	chr1:172543864-172543914	HL-60	blood:	n/a
21	chr1:172540913-172540963	SKMC	muscle:	n/a
22	chr1:172540913-172540963	H1-hESC	embryonic stem cell:	embryo
23	chr1:172540913-172540963	NHBE	bronchial:	n/a
24	chr1:172541012-172541062	GM06990	blood:	n/a
25	chr1:172540913-172540963	HIPEpiC	eye:	n/a
26	chr1:172541012-172541062	SK-N-MC	brain:	n/a
27	chr1:172543864-172543914	ovcar-3	ovarian:	n/a
28	chr1:172543864-172543914	GM12892	blood:	n/a
29	chr1:172540913-172540963	PANC-1	pancreas:	n/a
30	chr1:172541012-172541062	HPAEpiC	pulmonary alveolar:	n/a
31	chr1:172543864-172543914	GM12878	blood:	n/a
32	chr1:172543864-172543914	HMEC	breast:	n/a
33	chr1:172541012-172541062	LNCaP	prostate:	n/a
34	chr1:172543864-172543914	ECC-1	luminal epithelium:	n/a
35	chr1:172540913-172540963	MCF10A-Er-Src	breast:	n/a
36	chr1:172543864-172543914	ProgFib	skin:	n/a
37	chr1:172541012-172541062	HRPEpiC	eye:	n/a
38	chr1:172541012-172541062	H1-hESC	embryonic stem cell:	embryo
39	chr1:172543864-172543914	U87	brain:	n/a
40	chr1:172540913-172540963	A549	lung:	n/a
41	chr1:172543864-172543914	MCF-7	breast:	n/a
42	chr1:172540913-172540963	AG04449	skin:	fetal
43	chr1:172543864-172543914	NB4	blood:	n/a
44	chr1:172541012-172541062	HCT-116	colon:	n/a
45	chr1:172543864-172543914	PANC-1	pancreas:	n/a
46	chr1:172541012-172541062	A549	lung:	n/a
47	chr1:172541012-172541062	HAEpiC	amniotic membrane:	n/a
48	chr1:172541012-172541062	SK-N-SH	brain:	n/a
49	chr1:172543864-172543914	SAEC	small airway:	n/a
50	chr1:172540913-172540963	GM06990	blood:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:172499376..172501667-chr1:172538683..172540537,2	K562	blood:
2	chr1:172500935..172503676-chr1:172549899..172554092,3	MCF-7	breast:
3	chr1:172501396..172504430-chr1:172536696..172538886,3	MCF-7	breast:
4	chr1:172518503..172521143-chr1:172524413..172526637,2	K562	blood:
5	chr1:172530178..172532792-chr1:172534437..172536976,3	K562	blood:
6	chr1:172520454..172524675-chr1:172533729..172536639,3	K562	blood:
7	chr1:172530178..172532826-chr1:172534437..172536976,3	K562	blood:
8	chr1:172518008..172521748-chr1:172521862..172526550,7	K562	blood:
9	chr1:172536299..172538930-chr1:172539967..172542813,2	MCF-7	breast:
10	chr1:172499376..172501724-chr1:172539037..172541418,2	K562	blood:
11	chr1:172540565..172542685-chr1:172550671..172552538,2	K562	blood:
12	chr1:172524779..172527328-chr1:172528773..172530813,3	K562	blood:
13	chr1:172518787..172521238-chr1:172523963..172525755,2	MCF-7	breast:
14	chr1:172533299..172534999-chr1:172535109..172538092,2	K562	blood:
15	chr1:172542019..172544781-chr1:172548161..172550127,2	K562	blood:
16	chr1:172530178..172532826-chr1:172534437..172536976,3	K562	blood:
17	chr1:172499469..172503029-chr1:172527261..172529453,3	K562	blood:
18	chr1:172418505..172419330-chr1:172551492..172552290,2	MCF-7	breast:
19	chr1:172518503..172521143-chr1:172524413..172526637,2	K562	blood:
20	chr1:172501069..172504087-chr1:172524963..172528028,4	MCF-7	breast:
21	chr1:172501115..172503585-chr1:172541113..172543776,2	K562	blood:
22	chr1:172503248..172504952-chr1:172533651..172536311,2	K562	blood:
23	chr1:172511443..172515146-chr1:172549683..172552996,3	K562	blood:
24	chr1:172520824..172522644-chr1:172528724..172530286,2	K562	blood:
25	chr1:172549201..172550715-chr1:172556129..172558563,2	K562	blood:
26	chr1:172529012..172530791-chr1:172538139..172539734,2	K562	blood:
27	chr1:172524779..172527801-chr1:172528773..172532155,3	K562	blood:
28	chr1:172503233..172505429-chr1:172517362..172521428,4	MCF-7	breast:
29	chr1:172417892..172422705-chr1:172522786..172525518,5	MCF-7	breast:
30	chr1:172509695..172512146-chr1:172529892..172531866,2	K562	blood:
31	chr1:172527755..172529471-chr1:172533973..172536807,2	K562	blood:
32	chr1:172500260..172503470-chr1:172516553..172520247,3	MCF-7	breast:
33	chr1:172533299..172534999-chr1:172535109..172538092,2	K562	blood:
34	chr1:172417587..172421346-chr1:172527795..172529688,3	MCF-7	breast:
35	chr1:172519187..172521470-chr1:172549104..172550723,2	K562	blood:
36	chr1:172500340..172502764-chr1:172523653..172526492,2	K562	blood:
37	chr1:172548978..172551099-chr1:172556129..172558603,3	K562	blood:
38	chr1:172500697..172503568-chr1:172528002..172531240,3	MCF-7	breast:
39	chr1:172519187..172521470-chr1:172549104..172550723,2	K562	blood:
40	chr1:172510611..172514641-chr1:172517107..172521407,5	K562	blood:
41	chr1:172528364..172530709-chr1:172549872..172552272,2	K562	blood:
42	chr1:172527755..172529471-chr1:172533973..172536807,2	K562	blood:
43	chr1:172528364..172530709-chr1:172549872..172552272,2	K562	blood:
44	chr1:172542019..172544781-chr1:172548161..172550127,2	K562	blood:
45	chr1:172524779..172527328-chr1:172528773..172530813,3	K562	blood:
46	chr1:172530178..172532792-chr1:172534437..172536976,3	K562	blood:
47	chr1:172499192..172502524-chr1:172551121..172556401,4	MCF-7	breast:
48	chr1:172500667..172503739-chr1:172526545..172530565,4	K562	blood:
49	chr1:172520150..172522644-chr1:172528070..172530577,3	K562	blood:
50	chr1:172513266..172515531-chr1:172525208..172528046,2	K562	blood:

No data

Variant related genes	Relation type
SUCO	TF binding region
SUCO	CpG island
ENSG00000094975	chromatin interactions
ENSG00000180999	chromatin interactions

Extended variants
information (count: 1199 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1199 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2472551	chr1:172518012-172518013	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535589013	chr1:172518085-172518086	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs551009550	chr1:172518104-172518105	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs568749659	chr1:172518121-172518122	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs142398617	chr1:172518146-172518147	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs368626308	chr1:172518152-172518153	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs191127322	chr1:172518156-172518157	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs183611421	chr1:172518203-172518204	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs188314132	chr1:172518222-172518223	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs181826946	chr1:172518269-172518270	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs555078092	chr1:172518278-172518279	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs151275305	chr1:172518456-172518457	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs184797931	chr1:172518462-172518463	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs556214438	chr1:172518585-172518586	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs114636949	chr1:172518643-172518644	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs546399018	chr1:172518692-172518693	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs190121400	chr1:172518704-172518705	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs139291749	chr1:172518735-172518736	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs71637445	chr1:172518763-172518764	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs561944561	chr1:172518812-172518813	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs372212333	chr1:172518836-172518837	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs181770609	chr1:172518861-172518862	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs146557894	chr1:172518887-172518888	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs12758548	chr1:172518896-172518897	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs551176713	chr1:172518897-172518898	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs141198548	chr1:172518955-172518956	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs368965432	chr1:172518967-172518968	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs555632169	chr1:172518969-172518970	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs74124236	chr1:172518983-172518984	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs144932088	chr1:172518990-172518991	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs146754556	chr1:172519002-172519003	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs202208754	chr1:172519027-172519028	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs199546773	chr1:172519028-172519029	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs60802914	chr1:172519031-172519032	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs577835360	chr1:172519032-172519033	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs397709956	chr1:172519045-172519046	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs534406701	chr1:172519130-172519131	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs61806142	chr1:172519195-172519196	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs573430047	chr1:172519197-172519198	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs186326192	chr1:172519241-172519242	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs570691583	chr1:172519297-172519298	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs2516063	chr1:172519301-172519302	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs191182829	chr1:172519315-172519316	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs377279934	chr1:172519361-172519362	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs533076038	chr1:172519398-172519399	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs549292618	chr1:172519399-172519400	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs181434653	chr1:172519503-172519504	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs544613625	chr1:172519517-172519518	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs539669472	chr1:172519524-172519525	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs562507592	chr1:172519665-172519666	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	20409316	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1145 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:172503400-172528600	Weak transcription	Aorta	Aorta
2	chr1:172503400-172528600	Weak transcription	Lung	lung
3	chr1:172503600-172520200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr1:172503600-172531600	Weak transcription	Esophagus	oesophagus
5	chr1:172503800-172529000	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr1:172503800-172534200	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr1:172504000-172524400	Weak transcription	HSMM	muscle
8	chr1:172504200-172527000	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr1:172504400-172519400	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr1:172505200-172518800	Weak transcription	Brain Angular Gyrus	brain
11	chr1:172505800-172519600	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr1:172506000-172519000	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr1:172506000-172532600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr1:172506200-172525000	Weak transcription	Duodenum Mucosa	Duodenum
15	chr1:172506200-172526200	Weak transcription	Fetal Intestine Large	intestine
16	chr1:172506200-172528400	Weak transcription	Fetal Stomach	stomach
17	chr1:172507200-172518400	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr1:172507400-172518400	Weak transcription	NHEK	skin
19	chr1:172507400-172523000	Weak transcription	NHDF-Ad	bronchial
20	chr1:172507400-172526400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr1:172507400-172528600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr1:172508200-172519200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr1:172508200-172526400	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr1:172509400-172530800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr1:172510000-172518200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr1:172510000-172524000	Weak transcription	Dnd41	blood
27	chr1:172510000-172525000	Weak transcription	Left Ventricle	heart
28	chr1:172511800-172524800	Weak transcription	Liver	Liver
29	chr1:172511800-172528600	Weak transcription	Stomach Smooth Muscle	stomach
30	chr1:172511800-172557800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr1:172512000-172518400	Weak transcription	Brain Substantia Nigra	brain
32	chr1:172512000-172523400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr1:172512000-172529000	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr1:172512000-172534200	Weak transcription	Gastric	stomach
35	chr1:172512200-172519000	Weak transcription	Brain Anterior Caudate	brain
36	chr1:172512400-172524200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr1:172513400-172518400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr1:172513400-172518400	Weak transcription	HepG2	liver
39	chr1:172513600-172524600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr1:172513800-172525000	Weak transcription	Fetal Thymus	thymus
41	chr1:172514200-172558800	Weak transcription	Small Intestine	intestine
42	chr1:172514400-172526200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr1:172514600-172519000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr1:172514600-172524200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr1:172514800-172518400	Weak transcription	Placenta Amnion	Placenta Amnion
46	chr1:172514800-172518800	Weak transcription	Psoas Muscle	Psoas
47	chr1:172514800-172528600	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr1:172514800-172530200	Weak transcription	Thymus	Thymus
49	chr1:172515000-172523400	Weak transcription	Primary hematopoietic stem cells	blood
50	chr1:172515000-172524400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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