Variant report

Variant	esv1792702
Chromosome Location	chr1:70755511-70818576
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:328)
CpG islands
(count:61)
Chromatin interactive
region (count:59)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:70790022-70790087	K562	blood:	n/a	n/a
2	ARID3A	chr1:70798955-70799186	HepG2	liver:	n/a	n/a
3	ATF1	chr1:70800211-70800382	K562	blood:	n/a	n/a
4	ATF3	chr1:70800053-70800510	HCT-116	colon:	n/a	n/a
5	ATF3	chr1:70800117-70800394	K562	blood:	n/a	n/a
6	BACH1	chr1:70758168-70758248	K562	blood:	n/a	n/a
7	CBX3	chr1:70792873-70793458	HCT-116	colon:	n/a	n/a
8	CBX3	chr1:70785309-70785897	HCT-116	colon:	n/a	n/a
9	CCNT2	chr1:70818145-70818335	K562	blood:	n/a	n/a
10	CEBPB	chr1:70756777-70756778	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr1:70799922-70800654	HCT-116	colon:	n/a	chr1:70800262-70800273
12	CEBPB	chr1:70795228-70795351	K562	blood:	n/a	chr1:70795259-70795268 chr1:70795257-70795270
13	CEBPB	chr1:70756770-70756796	Hela-S3	cervix:	n/a	chr1:70756771-70756782
14	CEBPB	chr1:70800096-70800427	A549	lung:	n/a	chr1:70800262-70800273
15	CEBPB	chr1:70791382-70791696	H1-hESC	embryonic stem cell:	n/a	chr1:70791512-70791523
16	CEBPB	chr1:70756750-70756815	HepG2	liver:	n/a	chr1:70756771-70756782
17	CEBPB	chr1:70791367-70791572	IMR90	lung:	n/a	chr1:70791512-70791523
18	CEBPB	chr1:70781524-70781769	A549	lung:	n/a	chr1:70781678-70781691 chr1:70781678-70781689 chr1:70781678-70781691
19	CEBPB	chr1:70791359-70791562	HepG2	liver:	n/a	chr1:70791512-70791523
20	CEBPB	chr1:70792873-70793441	HCT-116	colon:	n/a	n/a
21	CEBPB	chr1:70780912-70781055	K562	blood:	n/a	chr1:70781025-70781036 chr1:70781023-70781036 chr1:70781023-70781036
22	CEBPB	chr1:70756756-70756803	K562	blood:	n/a	chr1:70756771-70756782
23	CEBPB	chr1:70800113-70800436	HepG2	liver:	n/a	chr1:70800262-70800273
24	CEBPB	chr1:70800076-70800447	K562	blood:	n/a	chr1:70800262-70800273
25	CEBPB	chr1:70800106-70800367	MCF-7	breast:	n/a	chr1:70800262-70800273
26	CEBPB	chr1:70762571-70762743	HepG2	liver:	n/a	chr1:70762630-70762641 chr1:70762630-70762643 chr1:70762631-70762642 chr1:70762630-70762643
27	CEBPB	chr1:70799961-70800557	HCT-116	colon:	n/a	chr1:70800262-70800273
28	CEBPB	chr1:70783872-70784474	HCT-116	colon:	n/a	n/a
29	CEBPB	chr1:70791352-70791560	K562	blood:	n/a	chr1:70791512-70791523
30	CEBPB	chr1:70800108-70800355	K562	blood:	n/a	chr1:70800262-70800273
31	CEBPB	chr1:70817879-70818079	K562	blood:	n/a	n/a
32	CEBPB	chr1:70791390-70791623	K562	blood:	n/a	chr1:70791512-70791523
33	CEBPB	chr1:70800126-70800381	Hela-S3	cervix:	n/a	chr1:70800262-70800273
34	CEBPB	chr1:70800073-70800451	K562	blood:	n/a	chr1:70800262-70800273
35	CHD1	chr1:70813329-70813529	GM12878	blood:	n/a	n/a
36	CTCF	chr1:70794244-70794295	GM20000	blood:	n/a	n/a
37	CTCF	chr1:70780440-70780590	HCT-116	colon:	n/a	n/a
38	CTCF	chr1:70780480-70780630	HCFaa	heart:	n/a	n/a
39	CTCF	chr1:70780540-70780690	HVMF	connective:	n/a	n/a
40	CTCF	chr1:70790380-70790670	A549	lung:	n/a	n/a
41	CTCF	chr1:70780617-70780886	GM12878	blood:	n/a	n/a
42	CTCF	chr1:70790508-70790647	MCF-7	breast:	n/a	n/a
43	CTCF	chr1:70790480-70790630	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr1:70780480-70780630	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr1:70790521-70790634	NHEK	skin:	n/a	n/a
46	CTCF	chr1:70790521-70790625	A549	lung:	n/a	n/a
47	CTCF	chr1:70780644-70780892	K562	blood:	n/a	n/a
48	CTCF	chr1:70780480-70780630	HCT-116	colon:	n/a	n/a
49	CTCF	chr1:70780500-70780650	RPTEC	kidney:	n/a	n/a
50	CTCF	chr1:70780460-70780610	HMEC	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:70816768-70816818	HCF	heart:	n/a
2	chr1:70816768-70816818	AG09309	skin:	n/a
3	chr1:70816768-70816818	T-47D	breast:	n/a
4	chr1:70816768-70816818	HEK293	kidney:	embryo
5	chr1:70816768-70816818	SK-N-MC	brain:	n/a
6	chr1:70816768-70816818	LNCaP	prostate:	n/a
7	chr1:70816768-70816818	HCPEpiC	choroid plexus:	n/a
8	chr1:70816768-70816818	K562	blood:	n/a
9	chr1:70816768-70816818	HCM	heart:	n/a
10	chr1:70816768-70816818	Jurkat	blood:	n/a
11	chr1:70816768-70816818	SKMC	muscle:	n/a
12	chr1:70816768-70816818	HUVEC	blood vessel:	n/a
13	chr1:70816768-70816818	HRCEpiC	kidney:	n/a
14	chr1:70816768-70816818	HCT-116	colon:	n/a
15	chr1:70816768-70816818	PFSK-1	brain:	n/a
16	chr1:70816768-70816818	A549	lung:	n/a
17	chr1:70816768-70816818	MCF10A-Er-Src	breast:	n/a
18	chr1:70816768-70816818	GM12892	blood:	n/a
19	chr1:70816768-70816818	HAEpiC	amniotic membrane:	n/a
20	chr1:70816768-70816818	HEEpiC	esophagus:	n/a
21	chr1:70816768-70816818	GM06990	blood:	n/a
22	chr1:70816768-70816818	HIPEpiC	eye:	n/a
23	chr1:70816768-70816818	SAEC	small airway:	n/a
24	chr1:70816768-70816818	NH-A	brain:	n/a
25	chr1:70816768-70816818	AG04449	skin:	fetal
26	chr1:70816768-70816818	AG09319	gingival:	n/a
27	chr1:70816768-70816818	HRE	kidney:	n/a
28	chr1:70816768-70816818	AG10803	skin:	n/a
29	chr1:70816768-70816818	RPTEC	kidney:	n/a
30	chr1:70816768-70816818	HL-60	blood:	n/a
31	chr1:70816768-70816818	NB4	blood:	n/a
32	chr1:70816768-70816818	ProgFib	skin:	n/a
33	chr1:70816768-70816818	ovcar-3	ovarian:	n/a
34	chr1:70816768-70816818	ECC-1	luminal epithelium:	n/a
35	chr1:70816768-70816818	BE2_C	brain:	n/a
36	chr1:70816768-70816818	NHDF-neo	bronchial:	n/a
37	chr1:70816768-70816818	U87	brain:	n/a
38	chr1:70816768-70816818	CMK	blood:	n/a
39	chr1:70816768-70816818	GM12891	blood:	n/a
40	chr1:70816768-70816818	Caco-2	colon:	n/a
41	chr1:70816768-70816818	HRPEpiC	eye:	n/a
42	chr1:70816768-70816818	H1-hESC	embryonic stem cell:	embryo
43	chr1:70816768-70816818	PANC-1	pancreas:	n/a
44	chr1:70816768-70816818	Hela-S3	cervix:	n/a
45	chr1:70816768-70816818	NHBE	bronchial:	n/a
46	chr1:70816768-70816818	NT2-D1	testis:	n/a
47	chr1:70816768-70816818	GM12878	blood:	n/a
48	chr1:70816768-70816818	IMR90	lung:	fetal
49	chr1:70816768-70816818	PrEC	prostate:	n/a
50	chr1:70816768-70816818	GM19239	blood:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:70765373..70767402-chr1:70769005..70771192,2	K562	blood:
2	chr1:70798378..70801326-chr1:70805359..70808008,3	K562	blood:
3	chr1:70812176..70814908-chr1:70864607..70866509,2	K562	blood:
4	chr1:70794744..70797990-chr1:70798534..70802475,3	K562	blood:
5	chr1:70803895..70805933-chr1:70875287..70878177,2	K562	blood:
6	chr1:70799977..70802137-chr1:70803944..70806998,3	K562	blood:
7	chr1:70818087..70822177-chr1:70874224..70879265,8	K562	blood:
8	chr1:70797297..70799237-chr1:70818892..70820445,2	K562	blood:
9	chr1:70761212..70763376-chr1:70772596..70774368,2	K562	blood:
10	chr1:70796451..70799252-chr1:70818404..70820900,3	MCF-7	breast:
11	chr1:70797127..70799237-chr1:70818945..70821123,3	K562	blood:
12	chr1:70807888..70809434-chr1:70810416..70811940,2	K562	blood:
13	chr1:70769640..70771960-chr1:70781339..70784000,2	MCF-7	breast:
14	chr1:70814864..70817394-chr1:70817734..70820008,3	MCF-7	breast:
15	chr1:70817791..70820390-chr1:70876768..70878594,3	MCF-7	breast:
16	chr1:70758382..70760843-chr1:70761475..70764285,2	K562	blood:
17	chr1:70814888..70817395-chr1:70819218..70821847,2	MCF-7	breast:
18	chr1:70805309..70807484-chr1:70808987..70811577,3	K562	blood:
19	chr1:70786838..70788846-chr1:70818931..70822142,3	MCF-7	breast:
20	chr1:70753569..70756321-chr1:70876105..70877838,2	K562	blood:
21	chr1:70805309..70807484-chr1:70808987..70811577,3	K562	blood:
22	chr1:70686799..70689606-chr1:70818481..70820974,3	K562	blood:
23	chr1:70771700..70774695-chr1:70774871..70777365,2	MCF-7	breast:
24	chr1:70799533..70801212-chr1:70816344..70819008,2	K562	blood:
25	chr1:70798378..70801326-chr1:70805359..70808008,3	K562	blood:
26	chr1:70799977..70802137-chr1:70803944..70806998,3	K562	blood:
27	chr1:70754539..70757026-chr1:70759738..70761515,2	K562	blood:
28	chr1:70765373..70767402-chr1:70769005..70771192,2	K562	blood:
29	chr1:70761212..70763376-chr1:70772596..70774368,2	K562	blood:
30	chr1:70812176..70814577-chr1:70818800..70821744,3	MCF-7	breast:
31	chr1:70770014..70772421-chr1:70774036..70776596,3	K562	blood:
32	chr1:70809714..70814478-chr1:70818976..70822377,5	MCF-7	breast:
33	chr1:70783413..70785346-chr1:70819101..70821249,2	K562	blood:
34	chr1:70693400..70696286-chr1:70816820..70818777,2	K562	blood:
35	chr1:70771700..70774695-chr1:70774871..70777365,2	MCF-7	breast:
36	chr1:70690194..70693110-chr1:70772753..70775116,2	K562	blood:
37	chr1:70800642..70802626-chr1:70820402..70821912,2	K562	blood:
38	chr1:70759212..70761172-chr1:70763174..70765295,2	MCF-7	breast:
39	chr1:70803471..70806193-chr1:70890743..70892737,2	K562	blood:
40	chr1:70800477..70802096-chr1:70818864..70821491,2	MCF-7	breast:
41	chr1:70697900..70700190-chr1:70817863..70820129,2	MCF-7	breast:
42	chr1:70759212..70761172-chr1:70763174..70765295,2	MCF-7	breast:
43	chr1:70799533..70801212-chr1:70816344..70819008,2	K562	blood:
44	chr1:70801316..70804489-chr1:70807726..70811501,3	K562	blood:
45	chr1:70801316..70804489-chr1:70807726..70811501,3	K562	blood:
46	chr1:70814842..70821925-chr1:70874223..70879265,8	K562	blood:
47	chr1:70758382..70760843-chr1:70761475..70764285,2	K562	blood:
48	chr1:70670547..70673150-chr1:70760929..70763801,2	K562	blood:
49	chr1:70814864..70817394-chr1:70817734..70820008,3	MCF-7	breast:
50	chr1:70794744..70797990-chr1:70798534..70802475,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC40-5	chr1:70771369-70771640	NONHSAT003855
2	lnc-LRRC40-5	chr1:70790536-70790640	NONHSAT003855
3	lnc-LRRC40-5	chr1:70781164-70781249	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
ENSG00000116754	chromatin interactions
ENSG00000197568	chromatin interactions
ENSG00000118454	chromatin interactions
ENSG00000116761	chromatin interactions
ENSG00000066557	chromatin interactions

Extended variants
information (count: 2037 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2037 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4612579	chr1:70755511-70755512	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs573686262	chr1:70755560-70755561	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs187509595	chr1:70755633-70755634	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs192944820	chr1:70755634-70755635	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs184885315	chr1:70755709-70755710	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs538844342	chr1:70755719-70755720	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs188249601	chr1:70755729-70755730	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs192311622	chr1:70755806-70755807	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs199963100	chr1:70755812-70755813	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs386632245	chr1:70755815-70755816	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs55823240	chr1:70755816-70755817	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs565211896	chr1:70755818-70755819	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs375469597	chr1:70755821-70755822	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs149140548	chr1:70755851-70755852	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs114987978	chr1:70755949-70755950	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs529279088	chr1:70756013-70756014	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs549113702	chr1:70756116-70756117	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs184375474	chr1:70756135-70756136	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs562621374	chr1:70756137-70756138	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs189470747	chr1:70756154-70756155	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs562151151	chr1:70756192-70756193	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs114265606	chr1:70756193-70756194	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs572383045	chr1:70756233-70756234	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs78554751	chr1:70756236-70756237	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs78228095	chr1:70756237-70756238	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs1138751	chr1:70756303-70756304	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs542924529	chr1:70756317-70756318	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs534183279	chr1:70756356-70756357	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs527850241	chr1:70756381-70756382	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567188807	chr1:70756382-70756383	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs536249796	chr1:70756391-70756392	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs114725340	chr1:70756396-70756397	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs28403019	chr1:70756413-70756414	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs146823152	chr1:70756420-70756421	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538851771	chr1:70756508-70756509	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558438882	chr1:70756560-70756561	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs1551389	chr1:70756561-70756562	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs374335197	chr1:70756563-70756564	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs141804134	chr1:70756601-70756602	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs541009217	chr1:70756663-70756664	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554844973	chr1:70756699-70756700	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs140626103	chr1:70756709-70756710	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs374607675	chr1:70756714-70756715	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs542596759	chr1:70756725-70756726	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562660034	chr1:70756738-70756739	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs181829400	chr1:70756776-70756777	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545203611	chr1:70756780-70756781	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs72929259	chr1:70756810-70756811	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs386632246	chr1:70756836-70756837	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184526129	chr1:70756838-70756839	Weak transcription Strong transcription Genic enhancers	n/a	n/a	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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1580 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:70688000-70819200	Weak transcription	Esophagus	oesophagus
2	chr1:70710800-70756200	Weak transcription	Aorta	Aorta
3	chr1:70714000-70767000	Weak transcription	HSMMtube	muscle
4	chr1:70714200-70756000	Weak transcription	Colonic Mucosa	Colon
5	chr1:70715600-70767800	Weak transcription	Small Intestine	intestine
6	chr1:70715800-70756200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr1:70715800-70771000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr1:70716000-70775600	Weak transcription	Spleen	Spleen
9	chr1:70716200-70775200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr1:70716800-70769000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr1:70716800-70769400	Weak transcription	Right Ventricle	heart
12	chr1:70716800-70815800	Weak transcription	Brain Angular Gyrus	brain
13	chr1:70717000-70755600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr1:70717000-70759000	Weak transcription	Rectal Smooth Muscle	rectum
15	chr1:70717200-70759000	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr1:70717600-70765000	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr1:70717600-70780400	Weak transcription	Brain Substantia Nigra	brain
18	chr1:70717800-70758000	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr1:70717800-70761200	Weak transcription	NHLF	lung
20	chr1:70717800-70765000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr1:70717800-70788200	Weak transcription	Brain Cingulate Gyrus	brain
22	chr1:70718200-70755800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
23	chr1:70719000-70758800	Weak transcription	HMEC	breast
24	chr1:70719200-70783800	Weak transcription	A549	lung
25	chr1:70723600-70756800	Weak transcription	Lung	lung
26	chr1:70728600-70756200	Weak transcription	NH-A	brain
27	chr1:70728600-70761400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr1:70731400-70756800	Weak transcription	Left Ventricle	heart
29	chr1:70733800-70773400	Weak transcription	Fetal Kidney	kidney
30	chr1:70734000-70769600	Weak transcription	Pancreas	Pancrea
31	chr1:70734000-70786000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr1:70734400-70755800	Weak transcription	Fetal Brain Female	brain
33	chr1:70734400-70756200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr1:70734400-70756200	Weak transcription	Brain Germinal Matrix	brain
35	chr1:70734400-70756800	Weak transcription	Thymus	Thymus
36	chr1:70734400-70786000	Weak transcription	Psoas Muscle	Psoas
37	chr1:70734400-70813000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr1:70734800-70755600	Weak transcription	Ovary	ovary
39	chr1:70736200-70762000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr1:70736600-70755600	Weak transcription	Stomach Smooth Muscle	stomach
41	chr1:70736800-70755800	Weak transcription	Primary hematopoietic stem cells	blood
42	chr1:70737400-70756800	Weak transcription	HSMM	muscle
43	chr1:70737800-70755600	Weak transcription	HUVEC	blood vessel
44	chr1:70738000-70756600	Weak transcription	HepG2	liver
45	chr1:70739800-70756200	Weak transcription	Placenta	Placenta
46	chr1:70740600-70755800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr1:70740600-70756600	Weak transcription	Osteobl	bone
48	chr1:70740600-70759600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr1:70740600-70767000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr1:70741400-70756000	Weak transcription	Muscle Satellite Cultured Cells	--

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