Variant report

Variant	nsv873163
Chromosome Location	chr1:212629935-212669475
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1300)
CpG islands
(count:308)
Chromatin interactive
region (count:105)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1300 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:212659393-212659732	HepG2	liver:	n/a	n/a
2	ATF1	chr1:212668358-212668386	K562	blood:	n/a	n/a
3	ATF1	chr1:212659036-212659611	K562	blood:	n/a	n/a
4	ATF1	chr1:212661868-212662226	K562	blood:	n/a	n/a
5	ATF1	chr1:212658290-212658394	K562	blood:	n/a	n/a
6	ATF2	chr1:212661770-212662307	GM12878	blood:	n/a	n/a
7	ATF2	chr1:212650470-212650862	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr1:212661748-212662394	GM12878	blood:	n/a	n/a
9	ATF2	chr1:212650336-212650867	GM12878	blood:	n/a	n/a
10	ATF2	chr1:212650373-212650759	GM12878	blood:	n/a	n/a
11	ATF3	chr1:212656204-212656383	K562	blood:	n/a	n/a
12	ATF3	chr1:212661819-212662229	K562	blood:	n/a	chr1:212662175-212662184 chr1:212662044-212662057
13	ATF3	chr1:212659232-212659872	A549	lung:	n/a	n/a
14	ATF3	chr1:212650361-212650925	A549	lung:	n/a	n/a
15	ATF3	chr1:212659231-212659657	K562	blood:	n/a	n/a
16	ATF3	chr1:212661716-212662272	A549	lung:	n/a	chr1:212662175-212662184 chr1:212662044-212662057
17	ATF3	chr1:212658110-212658687	A549	lung:	n/a	n/a
18	ATF3	chr1:212659306-212659554	K562	blood:	n/a	n/a
19	BCL3	chr1:212658044-212658583	A549	lung:	n/a	n/a
20	BCL3	chr1:212661631-212662423	A549	lung:	n/a	chr1:212662097-212662106
21	BCL3	chr1:212658000-212658641	A549	lung:	n/a	n/a
22	BCL3	chr1:212655728-212656536	A549	lung:	n/a	n/a
23	BCL3	chr1:212659159-212659906	A549	lung:	n/a	n/a
24	BCL3	chr1:212661819-212662294	GM12878	blood:	n/a	chr1:212662097-212662106
25	BCL3	chr1:212659099-212659996	A549	lung:	n/a	n/a
26	BCL3	chr1:212661706-212662421	A549	lung:	n/a	chr1:212662097-212662106
27	BCLAF1	chr1:212650451-212650848	GM12878	blood:	n/a	chr1:212650705-212650714
28	BCLAF1	chr1:212650363-212650872	GM12878	blood:	n/a	chr1:212650705-212650714
29	BHLHE40	chr1:212650582-212650783	HepG2	liver:	n/a	n/a
30	BHLHE40	chr1:212661948-212662312	GM12878	blood:	n/a	n/a
31	BHLHE40	chr1:212656127-212656440	A549	lung:	n/a	n/a
32	BHLHE40	chr1:212656184-212656438	GM12878	blood:	n/a	n/a
33	BHLHE40	chr1:212631181-212631342	K562	blood:	n/a	n/a
34	BHLHE40	chr1:212669275-212669461	K562	blood:	n/a	n/a
35	BHLHE40	chr1:212633871-212634123	K562	blood:	n/a	n/a
36	BHLHE40	chr1:212658371-212658556	K562	blood:	n/a	n/a
37	BHLHE40	chr1:212661867-212662382	K562	blood:	n/a	n/a
38	BHLHE40	chr1:212659292-212659506	GM12878	blood:	n/a	n/a
39	BHLHE40	chr1:212656136-212656496	K562	blood:	n/a	n/a
40	BHLHE40	chr1:212659044-212659826	K562	blood:	n/a	n/a
41	BHLHE40	chr1:212631302-212631304	GM12878	blood:	n/a	n/a
42	BHLHE40	chr1:212643471-212643619	K562	blood:	n/a	n/a
43	BHLHE40	chr1:212650516-212650812	K562	blood:	n/a	n/a
44	BHLHE40	chr1:212661999-212662260	HepG2	liver:	n/a	n/a
45	BRCA1	chr1:212650500-212650839	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr1:212631178-212631403	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr1:212650636-212650771	HepG2	liver:	n/a	n/a
48	BRCA1	chr1:212658995-212659938	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr1:212645114-212645188	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr1:212661713-212662547	Hela-S3	cervix:	n/a	chr1:212662143-212662150

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:212658636-212658686	MCF10A-Er-Src	breast:	n/a
2	chr1:212643521-212643571	Jurkat	blood:	n/a
3	chr1:212656756-212656806	T-47D	breast:	n/a
4	chr1:212658636-212658686	MCF10A-Er-Src	breast:	n/a
5	chr1:212643521-212643571	Jurkat	blood:	n/a
6	chr1:212656756-212656806	T-47D	breast:	n/a
7	chr1:212662017-212662067	NHDF-neo	bronchial:	n/a
8	chr1:212643521-212643571	GM12891	blood:	n/a
9	chr1:212635804-212635854	ProgFib	skin:	n/a
10	chr1:212656756-212656806	BJ	skin:	n/a
11	chr1:212656756-212656806	AG09309	skin:	n/a
12	chr1:212662017-212662067	NHBE	bronchial:	n/a
13	chr1:212635804-212635854	T-47D	breast:	n/a
14	chr1:212635804-212635854	Hepatocyte	liver:	n/a
15	chr1:212643521-212643571	NHDF-neo	bronchial:	n/a
16	chr1:212658636-212658686	HIPEpiC	eye:	n/a
17	chr1:212656756-212656806	LNCaP	prostate:	n/a
18	chr1:212662017-212662067	HepG2	liver:	n/a
19	chr1:212662017-212662067	MCF-7	breast:	n/a
20	chr1:212662017-212662067	SK-N-SH_RA	brain:	n/a
21	chr1:212643521-212643571	HEEpiC	esophagus:	n/a
22	chr1:212662017-212662067	HAEpiC	amniotic membrane:	n/a
23	chr1:212656756-212656806	NHDF-neo	bronchial:	n/a
24	chr1:212635804-212635854	SK-N-SH_RA	brain:	n/a
25	chr1:212635804-212635854	HNPCEpiC	eye:	n/a
26	chr1:212658636-212658686	SK-N-MC	brain:	n/a
27	chr1:212635804-212635854	GM19239	blood:	n/a
28	chr1:212658636-212658686	HEK293	kidney:	embryo
29	chr1:212643521-212643571	PrEC	prostate:	n/a
30	chr1:212662017-212662067	PFSK-1	brain:	n/a
31	chr1:212656756-212656806	AG09319	gingival:	n/a
32	chr1:212658636-212658686	NB4	blood:	n/a
33	chr1:212656756-212656806	HCM	heart:	n/a
34	chr1:212662017-212662067	AG04450	lung:	fetal
35	chr1:212656756-212656806	Caco-2	colon:	n/a
36	chr1:212662017-212662067	HEK293	kidney:	embryo
37	chr1:212656756-212656806	GM19239	blood:	n/a
38	chr1:212643521-212643571	HCM	heart:	n/a
39	chr1:212635804-212635854	HL-60	blood:	n/a
40	chr1:212635804-212635854	HCT-116	colon:	n/a
41	chr1:212656756-212656806	CMK	blood:	n/a
42	chr1:212658636-212658686	GM12892	blood:	n/a
43	chr1:212658636-212658686	NT2-D1	testis:	n/a
44	chr1:212643521-212643571	RPTEC	kidney:	n/a
45	chr1:212662017-212662067	LNCaP	prostate:	n/a
46	chr1:212658636-212658686	SK-N-SH_RA	brain:	n/a
47	chr1:212635804-212635854	HAEpiC	amniotic membrane:	n/a
48	chr1:212658636-212658686	PFSK-1	brain:	n/a
49	chr1:212635804-212635854	HCF	heart:	n/a
50	chr1:212656756-212656806	IMR90	lung:	fetal

(count:105 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:212622646..212625445-chr1:212627199..212631249,4	K562	blood:
2	chr1:212642565..212644909-chr1:212645772..212647720,2	K562	blood:
3	chr1:212626698..212637479-chr1:212779685..212784714,19	K562	blood:
4	chr1:212636838..212639720-chr1:212643460..212645324,2	K562	blood:
5	chr1:212661862..212663764-chr1:212729767..212731611,2	K562	blood:
6	chr1:212630852..212631355-chr1:212641154..212641815,2	K562	blood:
7	chr1:212641496..212643517-chr1:212649175..212651881,2	K562	blood:
8	chr1:212645024..212669819-chr1:212778382..212791615,68	K562	blood:
9	chr1:212657965..212660283-chr1:212780837..212783197,2	MCF-7	breast:
10	chr1:212658367..212661601-chr1:212781233..212783647,4	MCF-7	breast:
11	chr1:212654477..212657612-chr1:212658521..212662499,5	K562	blood:
12	chr1:212548749..212550698-chr1:212631997..212633826,2	K562	blood:
13	chr1:212641496..212643517-chr1:212649175..212651881,2	K562	blood:
14	chr1:212634490..212636091-chr1:212645524..212647172,2	K562	blood:
15	chr1:212650902..212653623-chr1:212731690..212733930,2	K562	blood:
16	chr1:212641004..212643308-chr1:212781641..212784619,3	K562	blood:
17	chr1:212650264..212651134-chr1:212782287..212782879,2	MCF-7	breast:
18	chr1:212646206..212648127-chr1:212778382..212780130,2	K562	blood:
19	chr1:212185000..212185952-chr1:212629353..212630011,4	K562	blood:
20	chr1:212657477..212661646-chr1:212730263..212734721,4	K562	blood:
21	chr1:212634664..212637460-chr1:212638255..212640310,2	MCF-7	breast:
22	chr1:212634967..212638975-chr1:212780720..212784132,4	K562	blood:
23	chr1:212650198..212651416-chr1:212803125..212803807,3	MCF-7	breast:
24	chr1:212663057..212665371-chr1:212783064..212784989,2	MCF-7	breast:
25	chr1:212639292..212640942-chr1:212781990..212784541,2	K562	blood:
26	chr1:212230913..212233313-chr1:212635726..212638248,2	K562	blood:
27	chr1:212630980..212631781-chr1:212955510..212956087,2	K562	blood:
28	chr1:212650238..212651131-chr1:212955932..212956435,2	K562	blood:
29	chr1:212645805..212648932-chr1:212650111..212654210,5	K562	blood:
30	chr1:212663187..212667039-chr1:212686323..212689300,3	K562	blood:
31	chr1:212657352..212659830-chr1:212670221..212673074,2	K562	blood:
32	chr1:212606882..212608476-chr1:212631103..212632696,2	MCF-7	breast:
33	chr1:212648507..212667078-chr1:212779147..212787651,52	K562	blood:
34	chr1:212639889..212643172-chr1:212795709..212798826,3	K562	blood:
35	chr1:212654477..212657612-chr1:212658521..212662499,5	K562	blood:
36	chr1:212646367..212648750-chr1:212657386..212659832,2	K562	blood:
37	chr1:212644101..212647867-chr1:212656026..212658886,3	K562	blood:
38	chr1:212630808..212631798-chr1:213168552..213169259,4	K562	blood:
39	chr1:212634664..212637460-chr1:212638255..212640310,2	MCF-7	breast:
40	chr1:212652289..212653872-chr1:212658480..212660402,2	K562	blood:
41	chr1:212540519..212541569-chr1:212628751..212630135,3	K562	blood:
42	chr1:212243790..212245029-chr1:212629216..212630156,6	K562	blood:
43	chr1:212656091..212658082-chr1:212788332..212791043,2	K562	blood:
44	chr1:212645805..212648932-chr1:212650111..212654210,5	K562	blood:
45	chr1:212650175..212651195-chr1:212803104..212804056,5	K562	blood:
46	chr1:212650603..212651105-chr1:212842126..212842894,2	K562	blood:
47	chr1:212635848..212638507-chr1:212642034..212643626,2	MCF-7	breast:
48	chr1:212589362..212592084-chr1:212630605..212632407,2	K562	blood:
49	chr1:212648977..212651974-chr1:212781395..212783104,2	MCF-7	breast:
50	chr1:212644101..212647867-chr1:212656026..212658886,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM206-2	chr1:212640158-212640439	XLOC_001193
2	lnc-TMEM206-2	chr1:212641009-212641085	XLOC_001193

No data

Variant related genes	Relation type
ENSG00000224535	TF binding region
ENSG00000224535	CpG island
ENSG00000224535	chromatin interactions
ENSG00000260805	chromatin interactions
ENSG00000162771	chromatin interactions
ENSG00000074800	chromatin interactions
ENSG00000237980	chromatin interactions
ENSG00000264590	chromatin interactions
ENSG00000162772	chromatin interactions
ENSG00000117691	chromatin interactions

Extended variants
information (count: 1534 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1534 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs479564	chr1:212629935-212629936	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs192051294	chr1:212629978-212629979	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs369630452	chr1:212630021-212630022	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs146364152	chr1:212630054-212630055	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs543985918	chr1:212630146-212630147	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs531822405	chr1:212630153-212630154	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs573635049	chr1:212630163-212630164	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs74140023	chr1:212630174-212630175	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs559425900	chr1:212630218-212630219	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs536474049	chr1:212630256-212630257	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs532937504	chr1:212630257-212630258	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs545370287	chr1:212630298-212630299	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs183317421	chr1:212630349-212630350	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs12741513	chr1:212630389-212630390	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs576444666	chr1:212630390-212630391	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs373200991	chr1:212630402-212630403	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs372617904	chr1:212630419-212630420	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs549117110	chr1:212630425-212630426	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs73088538	chr1:212630442-212630443	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs374857916	chr1:212630445-212630446	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs144300108	chr1:212630453-212630454	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs186973813	chr1:212630460-212630461	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs78075059	chr1:212630485-212630486	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs61830682	chr1:212630489-212630490	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs28445869	chr1:212630519-212630520	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs148709458	chr1:212630557-212630558	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs200881644	chr1:212630579-212630580	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs558068913	chr1:212630599-212630600	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs398074616	chr1:212630608-212630609	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs191242649	chr1:212630635-212630636	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs376383853	chr1:212630665-212630666	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs540654770	chr1:212630685-212630686	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs570289089	chr1:212630699-212630700	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs537250179	chr1:212630710-212630711	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs555894828	chr1:212630721-212630722	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs55816718	chr1:212630762-212630763	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs187851930	chr1:212630784-212630785	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs193178253	chr1:212630955-212630956	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs577754944	chr1:212630963-212630964	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs544982506	chr1:212630986-212630987	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs544037563	chr1:212631058-212631059	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs185289948	chr1:212631089-212631090	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs10863968	chr1:212631140-212631141	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs80160597	chr1:212631145-212631146	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs534119512	chr1:212631228-212631229	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs492231	chr1:212631290-212631291	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs80197781	chr1:212631309-212631310	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs75146892	chr1:212631311-212631312	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs147838980	chr1:212631350-212631351	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs547531099	chr1:212631364-212631365	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Liposarcoma	21253554	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
Breast cancer	21858162	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	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
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	17060936	CNVD
Atypical hemolytic uremic syndrome	19861685	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:866 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:212614400-212636800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr1:212619600-212636800	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr1:212620000-212631000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:212620200-212631400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr1:212622400-212631000	Enhancers	Fetal Muscle Leg	muscle
6	chr1:212624800-212630000	Weak transcription	Esophagus	oesophagus
7	chr1:212627400-212631600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr1:212627400-212631600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr1:212627400-212631800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr1:212628400-212631800	Enhancers	Brain Hippocampus Middle	brain
11	chr1:212628600-212630800	Enhancers	Brain Angular Gyrus	brain
12	chr1:212628800-212631200	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr1:212628800-212631200	Enhancers	Brain Substantia Nigra	brain
14	chr1:212628800-212632600	Enhancers	Brain Anterior Caudate	brain
15	chr1:212629000-212630000	Enhancers	Fetal Brain Male	brain
16	chr1:212629000-212630000	Enhancers	HepG2	liver
17	chr1:212629000-212630600	Enhancers	Fetal Muscle Trunk	muscle
18	chr1:212629000-212631400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
19	chr1:212629200-212630000	Enhancers	Adipose Nuclei	Adipose
20	chr1:212629200-212630000	Enhancers	NHDF-Ad	bronchial
21	chr1:212629200-212630400	Enhancers	Left Ventricle	heart
22	chr1:212629400-212630000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:212629400-212630000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr1:212629400-212630000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:212629400-212630000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
26	chr1:212629400-212630200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
27	chr1:212629400-212631400	Weak transcription	Dnd41	blood
28	chr1:212629400-212631800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr1:212629400-212631800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr1:212629600-212630000	Enhancers	Fetal Lung	lung
31	chr1:212629600-212630000	Flanking Active TSS	HSMMtube	muscle
32	chr1:212629600-212630200	Enhancers	Fetal Stomach	stomach
33	chr1:212629600-212630200	Enhancers	Right Atrium	heart
34	chr1:212629800-212630000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:212629800-212630000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr1:212629800-212630000	Weak transcription	Psoas Muscle	Psoas
37	chr1:212629800-212630000	Enhancers	HSMM	muscle
38	chr1:212629800-212630200	Enhancers	Osteobl	bone
39	chr1:212629800-212631400	Enhancers	Brain Cingulate Gyrus	brain
40	chr1:212629800-212640000	Weak transcription	Pancreas	Pancrea
41	chr1:212629800-212642600	Weak transcription	Stomach Smooth Muscle	stomach
42	chr1:212629800-212643200	Weak transcription	Rectal Smooth Muscle	rectum
43	chr1:212630000-212630200	Enhancers	HSMMtube	muscle
44	chr1:212630000-212630400	Enhancers	Psoas Muscle	Psoas
45	chr1:212630000-212631400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr1:212630000-212632000	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr1:212630200-212631000	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr1:212630600-212631800	Weak transcription	Fetal Muscle Trunk	muscle
49	chr1:212630800-212631600	Weak transcription	Brain Angular Gyrus	brain
50	chr1:212631000-212632000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived

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