Variant report

Variant	nsv871430
Chromosome Location	chr1:70765659-70819912
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:521)
CpG islands
(count:183)
Chromatin interactive
region (count:56)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:521 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:70798955-70799186	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:70790022-70790087	K562	blood:	n/a	n/a
3	ATF1	chr1:70800211-70800382	K562	blood:	n/a	n/a
4	ATF2	chr1:70819127-70819590	GM12878	blood:	n/a	n/a
5	ATF3	chr1:70800053-70800510	HCT-116	colon:	n/a	n/a
6	ATF3	chr1:70800117-70800394	K562	blood:	n/a	n/a
7	BCL11A	chr1:70819289-70819660	GM12878	blood:	n/a	n/a
8	BCL11A	chr1:70819328-70819551	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:70819516-70819847	K562	blood:	n/a	n/a
10	BHLHE40	chr1:70819246-70820872	GM12878	blood:	n/a	chr1:70820349-70820365
11	BRCA1	chr1:70819787-70820855	HepG2	liver:	n/a	chr1:70820407-70820416
12	BRCA1	chr1:70819134-70820943	Hela-S3	cervix:	n/a	chr1:70820407-70820416
13	CBX3	chr1:70792873-70793458	HCT-116	colon:	n/a	n/a
14	CBX3	chr1:70785309-70785897	HCT-116	colon:	n/a	n/a
15	CCNT2	chr1:70818145-70818335	K562	blood:	n/a	n/a
16	CEBPB	chr1:70791359-70791562	HepG2	liver:	n/a	chr1:70791512-70791523
17	CEBPB	chr1:70781524-70781769	A549	lung:	n/a	chr1:70781678-70781691 chr1:70781678-70781689 chr1:70781678-70781691
18	CEBPB	chr1:70800096-70800427	A549	lung:	n/a	chr1:70800262-70800273
19	CEBPB	chr1:70780912-70781055	K562	blood:	n/a	chr1:70781025-70781036 chr1:70781023-70781036 chr1:70781023-70781036
20	CEBPB	chr1:70791390-70791623	K562	blood:	n/a	chr1:70791512-70791523
21	CEBPB	chr1:70795228-70795351	K562	blood:	n/a	chr1:70795259-70795268 chr1:70795257-70795270
22	CEBPB	chr1:70791352-70791560	K562	blood:	n/a	chr1:70791512-70791523
23	CEBPB	chr1:70800106-70800367	MCF-7	breast:	n/a	chr1:70800262-70800273
24	CEBPB	chr1:70792873-70793441	HCT-116	colon:	n/a	n/a
25	CEBPB	chr1:70800076-70800447	K562	blood:	n/a	chr1:70800262-70800273
26	CEBPB	chr1:70800126-70800381	Hela-S3	cervix:	n/a	chr1:70800262-70800273
27	CEBPB	chr1:70799961-70800557	HCT-116	colon:	n/a	chr1:70800262-70800273
28	CEBPB	chr1:70799922-70800654	HCT-116	colon:	n/a	chr1:70800262-70800273
29	CEBPB	chr1:70791367-70791572	IMR90	lung:	n/a	chr1:70791512-70791523
30	CEBPB	chr1:70800113-70800436	HepG2	liver:	n/a	chr1:70800262-70800273
31	CEBPB	chr1:70817879-70818079	K562	blood:	n/a	n/a
32	CEBPB	chr1:70791382-70791696	H1-hESC	embryonic stem cell:	n/a	chr1:70791512-70791523
33	CEBPB	chr1:70800073-70800451	K562	blood:	n/a	chr1:70800262-70800273
34	CEBPB	chr1:70800108-70800355	K562	blood:	n/a	chr1:70800262-70800273
35	CEBPB	chr1:70783872-70784474	HCT-116	colon:	n/a	n/a
36	CHD1	chr1:70813329-70813529	GM12878	blood:	n/a	n/a
37	CHD1	chr1:70819051-70821083	H1-hESC	embryonic stem cell:	n/a	chr1:70820407-70820416
38	CHD1	chr1:70819287-70821036	GM12878	blood:	n/a	chr1:70820407-70820416
39	CHD2	chr1:70819179-70820959	GM12878	blood:	n/a	chr1:70820407-70820416
40	CHD2	chr1:70819276-70821003	K562	blood:	n/a	chr1:70820407-70820416
41	CHD2	chr1:70819383-70820925	HepG2	liver:	n/a	chr1:70820407-70820416
42	CHD2	chr1:70819624-70820891	H1-hESC	embryonic stem cell:	n/a	chr1:70820407-70820416
43	CHD2	chr1:70819179-70820997	Hela-S3	cervix:	n/a	chr1:70820407-70820416
44	CREB1	chr1:70819831-70821147	HepG2	liver:	n/a	n/a
45	CREB1	chr1:70819881-70821116	GM12878	blood:	n/a	n/a
46	CREB1	chr1:70819272-70821228	GM12878	blood:	n/a	n/a
47	CTCF	chr1:70790544-70790616	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr1:70790380-70790530	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr1:70780765-70780846	Medullo	brain:	n/a	n/a
50	CTCF	chr1:70780460-70780610	HEEpiC	esophagus:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:70816768-70816818	SK-N-MC	brain:	n/a
2	chr1:70819839-70819889	HRE	kidney:	n/a
3	chr1:70819273-70819323	GM12891	blood:	n/a
4	chr1:70816768-70816818	HCF	heart:	n/a
5	chr1:70819839-70819889	HRPEpiC	eye:	n/a
6	chr1:70819839-70819889	GM19239	blood:	n/a
7	chr1:70819273-70819323	HUVEC	blood vessel:	n/a
8	chr1:70819273-70819323	ECC-1	luminal epithelium:	n/a
9	chr1:70816768-70816818	IMR90	lung:	fetal
10	chr1:70819839-70819889	H1-hESC	embryonic stem cell:	embryo
11	chr1:70819839-70819889	HepG2	liver:	n/a
12	chr1:70816768-70816818	T-47D	breast:	n/a
13	chr1:70819273-70819323	Caco-2	colon:	n/a
14	chr1:70816768-70816818	HRE	kidney:	n/a
15	chr1:70819273-70819323	ovcar-3	ovarian:	n/a
16	chr1:70816768-70816818	HUVEC	blood vessel:	n/a
17	chr1:70819839-70819889	NHBE	bronchial:	n/a
18	chr1:70819273-70819323	HPAEpiC	pulmonary alveolar:	n/a
19	chr1:70816768-70816818	Jurkat	blood:	n/a
20	chr1:70819839-70819889	Hela-S3	cervix:	n/a
21	chr1:70816768-70816818	AG09309	skin:	n/a
22	chr1:70816768-70816818	H1-hESC	embryonic stem cell:	embryo
23	chr1:70819839-70819889	NT2-D1	testis:	n/a
24	chr1:70816768-70816818	MCF-7	breast:	n/a
25	chr1:70816768-70816818	SKMC	muscle:	n/a
26	chr1:70816768-70816818	BE2_C	brain:	n/a
27	chr1:70819839-70819889	AoSMC	blood vessel:	n/a
28	chr1:70819273-70819323	HCPEpiC	choroid plexus:	n/a
29	chr1:70816768-70816818	ovcar-3	ovarian:	n/a
30	chr1:70819273-70819323	HRCEpiC	kidney:	n/a
31	chr1:70819273-70819323	SK-N-MC	brain:	n/a
32	chr1:70819273-70819323	SK-N-SH	brain:	n/a
33	chr1:70816768-70816818	HEEpiC	esophagus:	n/a
34	chr1:70819839-70819889	HMEC	breast:	n/a
35	chr1:70819839-70819889	SK-N-MC	brain:	n/a
36	chr1:70819839-70819889	AG09309	skin:	n/a
37	chr1:70819839-70819889	GM06990	blood:	n/a
38	chr1:70819839-70819889	HCM	heart:	n/a
39	chr1:70819273-70819323	H1-hESC	embryonic stem cell:	embryo
40	chr1:70819839-70819889	T-47D	breast:	n/a
41	chr1:70819273-70819323	HCM	heart:	n/a
42	chr1:70816768-70816818	AG09319	gingival:	n/a
43	chr1:70816768-70816818	HepG2	liver:	n/a
44	chr1:70819839-70819889	SK-N-SH_RA	brain:	n/a
45	chr1:70819273-70819323	HCF	heart:	n/a
46	chr1:70819839-70819889	BJ	skin:	n/a
47	chr1:70816768-70816818	HRPEpiC	eye:	n/a
48	chr1:70819273-70819323	LNCaP	prostate:	n/a
49	chr1:70819839-70819889	U87	brain:	n/a
50	chr1:70816768-70816818	HIPEpiC	eye:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:70783413..70785346-chr1:70819101..70821249,2	K562	blood:
2	chr1:70761212..70763376-chr1:70772596..70774368,2	K562	blood:
3	chr1:70796451..70799252-chr1:70818404..70820900,3	MCF-7	breast:
4	chr1:70769640..70771960-chr1:70781339..70784000,2	MCF-7	breast:
5	chr1:70670191..70673421-chr1:70819814..70822311,3	K562	blood:
6	chr1:70819015..70821620-chr1:70875663..70878848,3	MCF-7	breast:
7	chr1:70805309..70807484-chr1:70808987..70811577,3	K562	blood:
8	chr1:70803471..70806193-chr1:70890743..70892737,2	K562	blood:
9	chr1:70770014..70772421-chr1:70774036..70776596,3	K562	blood:
10	chr1:70798378..70801326-chr1:70805359..70808008,3	K562	blood:
11	chr1:70765373..70767402-chr1:70769005..70771192,2	K562	blood:
12	chr1:70779446..70781152-chr1:70876074..70878497,2	MCF-7	breast:
13	chr1:70686799..70688622-chr1:70819236..70822047,3	K562	blood:
14	chr1:70765373..70767402-chr1:70769005..70771192,2	K562	blood:
15	chr1:70803895..70805933-chr1:70875287..70878177,2	K562	blood:
16	chr1:70807888..70809434-chr1:70810416..70811940,2	K562	blood:
17	chr1:70818087..70822177-chr1:70874224..70879265,8	K562	blood:
18	chr1:70686767..70689766-chr1:70815216..70817430,2	K562	blood:
19	chr1:70800477..70802096-chr1:70818864..70821491,2	MCF-7	breast:
20	chr1:70814842..70821925-chr1:70874223..70879265,8	K562	blood:
21	chr1:70771700..70774695-chr1:70774871..70777365,2	MCF-7	breast:
22	chr1:70814864..70817394-chr1:70817734..70820008,3	MCF-7	breast:
23	chr1:70819774..70820742-chr19:2268884..2269581,2	Hela-S3	cervix:
24	chr1:70805309..70807484-chr1:70808987..70811577,3	K562	blood:
25	chr1:70770014..70772421-chr1:70774036..70776596,3	K562	blood:
26	chr1:70697900..70700190-chr1:70817863..70820129,2	MCF-7	breast:
27	chr1:70797297..70799237-chr1:70818892..70820445,2	K562	blood:
28	chr1:70690194..70693110-chr1:70772753..70775116,2	K562	blood:
29	chr1:70812176..70814577-chr1:70818800..70821744,3	MCF-7	breast:
30	chr1:70819842..70820538-chr21:44865952..44866901,2	Hela-S3	cervix:
31	chr1:70691837..70693690-chr1:70781962..70783731,2	K562	blood:
32	chr1:70799977..70802137-chr1:70803944..70806998,3	K562	blood:
33	chr1:70819013..70822302-chr1:70824014..70829303,9	MCF-7	breast:
34	chr1:70799533..70801212-chr1:70816344..70819008,2	K562	blood:
35	chr1:70794744..70797990-chr1:70798534..70802475,3	K562	blood:
36	chr1:70809714..70814478-chr1:70818976..70822377,5	MCF-7	breast:
37	chr1:70771700..70774695-chr1:70774871..70777365,2	MCF-7	breast:
38	chr1:70794744..70797990-chr1:70798534..70802475,3	K562	blood:
39	chr1:70817791..70820390-chr1:70876768..70878594,3	MCF-7	breast:
40	chr1:70801316..70804489-chr1:70807726..70811501,3	K562	blood:
41	chr1:70807888..70809434-chr1:70810416..70811940,2	K562	blood:
42	chr1:70819841..70820741-chr21:33765342..33765918,2	Hela-S3	cervix:
43	chr1:70686799..70689606-chr1:70818481..70820974,3	K562	blood:
44	chr1:70797127..70799237-chr1:70818945..70821123,3	K562	blood:
45	chr1:70814864..70817394-chr1:70817734..70820008,3	MCF-7	breast:
46	chr1:70801316..70804489-chr1:70807726..70811501,3	K562	blood:
47	chr1:70769640..70771960-chr1:70781339..70784000,2	MCF-7	breast:
48	chr1:70693400..70696286-chr1:70816820..70818777,2	K562	blood:
49	chr1:70814888..70817395-chr1:70819218..70821847,2	MCF-7	breast:
50	chr1:70786838..70788846-chr1:70818931..70822142,3	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC40-5	chr1:70781164-70781249	NONHSAT003855
2	lnc-LRRC40-5	chr1:70771369-70771640	NONHSAT003855
3	lnc-LRRC40-5	chr1:70790536-70790640	NONHSAT003855
4	lnc-LRRC40-5	chr1:70771907-70771973	NONHSAT003855

No data

Variant related genes	Relation type
HHLA3	TF binding region
ANKRD13C	TF binding region
HHLA3	CpG island
ANKRD13C	CpG island
ENSG00000197568	chromatin interactions
ENSG00000116761	chromatin interactions
ENSG00000118454	chromatin interactions
ENSG00000256073	chromatin interactions
ENSG00000066557	chromatin interactions
ENSG00000104904	chromatin interactions
ENSG00000226088	chromatin interactions
ENSG00000167476	chromatin interactions
ENSG00000116754	chromatin interactions
ENSG00000188660	chromatin interactions

Extended variants
information (count: 1756 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:1756 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12135469	chr1:70765659-70765660	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184098022	chr1:70765695-70765696	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs188504605	chr1:70765711-70765712	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs556892536	chr1:70765712-70765713	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs561544107	chr1:70765739-70765740	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs181747981	chr1:70765813-70765814	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs186778264	chr1:70765825-70765826	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs151278749	chr1:70765830-70765831	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs549769518	chr1:70765833-70765834	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs563261790	chr1:70765927-70765928	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs532191711	chr1:70765931-70765932	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs549227417	chr1:70765938-70765939	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs190471705	chr1:70765943-70765944	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs565912147	chr1:70765946-70765947	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs377567515	chr1:70765963-70765964	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs548111717	chr1:70765966-70765967	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs139520525	chr1:70765972-70765973	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs182239351	chr1:70766037-70766038	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs556472103	chr1:70766087-70766088	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs144181758	chr1:70766101-70766102	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs539165881	chr1:70766184-70766185	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs374672448	chr1:70766202-70766203	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs558782427	chr1:70766203-70766204	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs151067777	chr1:70766207-70766208	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs575356627	chr1:70766210-70766211	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs555318462	chr1:70766226-70766227	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs186379329	chr1:70766227-70766228	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs543055245	chr1:70766228-70766229	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs557628702	chr1:70766277-70766278	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs540141702	chr1:70766283-70766284	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs373884050	chr1:70766324-70766325	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs189952797	chr1:70766335-70766336	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs182279420	chr1:70766363-70766364	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs559167722	chr1:70766396-70766397	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs528283607	chr1:70766400-70766401	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs397864249	chr1:70766408-70766409	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs547951091	chr1:70766444-70766445	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs377512996	chr1:70766450-70766451	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs138861589	chr1:70766510-70766511	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs371581543	chr1:70766561-70766562	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs111323234	chr1:70766636-70766637	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs185867005	chr1:70766639-70766640	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs376961912	chr1:70766641-70766642	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs530674284	chr1:70766720-70766721	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs376941505	chr1:70766861-70766862	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs3839011	chr1:70766862-70766863	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs3795694	chr1:70766863-70766864	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
48	rs3795695	chr1:70766865-70766866	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs112457790	chr1:70766866-70766867	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs72092471	chr1:70766871-70766872	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal cancer	21851588	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1409 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:70688000-70819200	Weak transcription	Esophagus	oesophagus
2	chr1:70714000-70767000	Weak transcription	HSMMtube	muscle
3	chr1:70715600-70767800	Weak transcription	Small Intestine	intestine
4	chr1:70715800-70771000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr1:70716000-70775600	Weak transcription	Spleen	Spleen
6	chr1:70716200-70775200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr1:70716800-70769000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr1:70716800-70769400	Weak transcription	Right Ventricle	heart
9	chr1:70716800-70815800	Weak transcription	Brain Angular Gyrus	brain
10	chr1:70717600-70780400	Weak transcription	Brain Substantia Nigra	brain
11	chr1:70717800-70788200	Weak transcription	Brain Cingulate Gyrus	brain
12	chr1:70719200-70783800	Weak transcription	A549	lung
13	chr1:70733800-70773400	Weak transcription	Fetal Kidney	kidney
14	chr1:70734000-70769600	Weak transcription	Pancreas	Pancrea
15	chr1:70734000-70786000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr1:70734400-70786000	Weak transcription	Psoas Muscle	Psoas
17	chr1:70734400-70813000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr1:70740600-70767000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr1:70744800-70768400	Weak transcription	Stomach Mucosa	stomach
20	chr1:70747000-70769400	Weak transcription	Fetal Heart	heart
21	chr1:70750000-70771800	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr1:70752400-70767800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr1:70752800-70793400	Weak transcription	Gastric	stomach
24	chr1:70753600-70766600	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr1:70753600-70767800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr1:70753600-70768800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr1:70753600-70769000	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr1:70754200-70768800	Strong transcription	Primary T helper cells fromperipheralblood	blood
29	chr1:70754200-70780400	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr1:70754400-70767600	Strong transcription	Dnd41	blood
31	chr1:70754400-70767800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr1:70754600-70775400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr1:70755600-70767400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr1:70755600-70768800	Strong transcription	Primary monocytes fromperipheralblood	blood
35	chr1:70755800-70775400	Weak transcription	Primary neutrophils fromperipheralblood	blood
36	chr1:70756600-70767000	Weak transcription	NHEK	skin
37	chr1:70757000-70769200	Weak transcription	Colonic Mucosa	Colon
38	chr1:70757000-70799800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr1:70757400-70766400	Weak transcription	HepG2	liver
40	chr1:70757400-70768800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr1:70757400-70813200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr1:70757800-70786000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr1:70757800-70799400	Weak transcription	Brain Germinal Matrix	brain
44	chr1:70757800-70812400	Weak transcription	Fetal Brain Male	brain
45	chr1:70759200-70768800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr1:70759400-70767800	Strong transcription	Primary B cells from peripheral blood	blood
47	chr1:70759400-70785400	Weak transcription	HMEC	breast
48	chr1:70760000-70767000	Weak transcription	Stomach Smooth Muscle	stomach
49	chr1:70760200-70799800	Weak transcription	Lung	lung
50	chr1:70760400-70802400	Weak transcription	Brain Hippocampus Middle	brain

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