Variant report

Variant	nsv871057
Chromosome Location	chr1:94513142-94577286
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1252)
CpG islands
(count:551)
Chromatin interactive
region (count:57)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1252 , 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	chr1:94527623-94527960	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:94533701-94534898	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:94528881-94529252	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:94527001-94527344	HepG2	liver:	n/a	n/a
5	BACH1	chr1:94559679-94560184	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr1:94544546-94544923	GM12878	blood:	n/a	n/a
7	BATF	chr1:94544643-94544810	GM12878	blood:	n/a	n/a
8	BCL3	chr1:94560498-94560825	GM12878	blood:	n/a	n/a
9	BCL3	chr1:94570392-94570649	GM12878	blood:	n/a	n/a
10	BCL3	chr1:94570394-94570713	GM12878	blood:	n/a	n/a
11	BCLAF1	chr1:94527017-94527373	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:94527098-94527320	K562	blood:	n/a	n/a
13	BHLHE40	chr1:94576890-94577028	HepG2	liver:	n/a	n/a
14	BHLHE40	chr1:94572389-94572585	HepG2	liver:	n/a	n/a
15	BHLHE40	chr1:94527094-94527326	GM12878	blood:	n/a	n/a
16	BRCA1	chr1:94528983-94529075	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr1:94527097-94527338	HepG2	liver:	n/a	n/a
18	BRCA1	chr1:94527009-94527289	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr1:94533607-94534251	HCT-116	colon:	n/a	n/a
20	CBX3	chr1:94533433-94534347	HCT-116	colon:	n/a	n/a
21	CEBPB	chr1:94527634-94527873	HepG2	liver:	n/a	n/a
22	CEBPB	chr1:94547478-94547877	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr1:94533394-94534173	ECC-1	luminal epithelium:	n/a	chr1:94533522-94533533
24	CEBPB	chr1:94528769-94529093	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:94562436-94562877	HepG2	liver:	n/a	n/a
26	CEBPB	chr1:94533513-94534292	HCT-116	colon:	n/a	chr1:94533522-94533533 chr1:94534248-94534261
27	CEBPB	chr1:94547419-94547926	IMR90	lung:	n/a	n/a
28	CEBPB	chr1:94563285-94563453	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr1:94548373-94548418	HepG2	liver:	n/a	chr1:94548394-94548405 chr1:94548393-94548406 chr1:94548393-94548404
30	CEBPB	chr1:94527621-94527898	MCF-7	breast:	n/a	n/a
31	CEBPB	chr1:94559676-94559955	IMR90	lung:	n/a	n/a
32	CEBPB	chr1:94529020-94529087	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr1:94513992-94514301	HepG2	liver:	n/a	n/a
34	CEBPB	chr1:94548234-94548526	IMR90	lung:	n/a	chr1:94548394-94548405 chr1:94548393-94548406 chr1:94548393-94548404
35	CEBPB	chr1:94560557-94561243	IMR90	lung:	n/a	n/a
36	CEBPB	chr1:94527586-94527971	HepG2	liver:	n/a	n/a
37	CEBPB	chr1:94533932-94534258	A549	lung:	n/a	n/a
38	CEBPB	chr1:94527684-94527801	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr1:94548333-94548538	A549	lung:	n/a	chr1:94548394-94548405 chr1:94548393-94548406 chr1:94548393-94548404
40	CEBPB	chr1:94527649-94527834	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr1:94533752-94534155	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr1:94562691-94563088	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr1:94527540-94527953	HepG2	liver:	n/a	n/a
44	CEBPB	chr1:94527581-94527977	HepG2	liver:	n/a	n/a
45	CEBPB	chr1:94533842-94534042	HepG2	liver:	n/a	n/a
46	CEBPB	chr1:94562570-94563061	IMR90	lung:	n/a	n/a
47	CEBPB	chr1:94527649-94527935	A549	lung:	n/a	n/a
48	CEBPB	chr1:94547546-94547800	A549	lung:	n/a	n/a
49	CEBPB	chr1:94562672-94563040	ECC-1	luminal epithelium:	n/a	n/a
50	CEBPB	chr1:94533776-94534285	HepG2	liver:	n/a	chr1:94534248-94534261

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:94571619-94571669	NHDF-neo	bronchial:	n/a
2	chr1:94560697-94560747	PrEC	prostate:	n/a
3	chr1:94571619-94571669	NHDF-neo	bronchial:	n/a
4	chr1:94560697-94560747	PrEC	prostate:	n/a
5	chr1:94571619-94571669	HepG2	liver:	n/a
6	chr1:94561088-94561138	HUVEC	blood vessel:	n/a
7	chr1:94559714-94559764	AG04449	skin:	fetal
8	chr1:94561065-94561115	HL-60	blood:	n/a
9	chr1:94561088-94561138	HNPCEpiC	eye:	n/a
10	chr1:94561088-94561138	HRE	kidney:	n/a
11	chr1:94534645-94534695	SKMC	muscle:	n/a
12	chr1:94559714-94559764	AG09309	skin:	n/a
13	chr1:94560697-94560747	HRPEpiC	eye:	n/a
14	chr1:94561088-94561138	NHDF-neo	bronchial:	n/a
15	chr1:94528115-94528165	HCM	heart:	n/a
16	chr1:94528115-94528165	PANC-1	pancreas:	n/a
17	chr1:94560851-94560901	SKMC	muscle:	n/a
18	chr1:94560851-94560901	NH-A	brain:	n/a
19	chr1:94514548-94514598	HUVEC	blood vessel:	n/a
20	chr1:94514548-94514598	HepG2	liver:	n/a
21	chr1:94571619-94571669	HCF	heart:	n/a
22	chr1:94528115-94528165	GM12891	blood:	n/a
23	chr1:94571619-94571669	AG09309	skin:	n/a
24	chr1:94560697-94560747	HIPEpiC	eye:	n/a
25	chr1:94559714-94559764	A549	lung:	n/a
26	chr1:94571619-94571669	SAEC	small airway:	n/a
27	chr1:94528115-94528165	CMK	blood:	n/a
28	chr1:94559714-94559764	HCPEpiC	choroid plexus:	n/a
29	chr1:94534645-94534695	AG04450	lung:	fetal
30	chr1:94528115-94528165	MCF10A-Er-Src	breast:	n/a
31	chr1:94560851-94560901	Hepatocyte	liver:	n/a
32	chr1:94514548-94514598	Hepatocyte	liver:	n/a
33	chr1:94514548-94514598	AG09309	skin:	n/a
34	chr1:94560697-94560747	SK-N-SH_RA	brain:	n/a
35	chr1:94528115-94528165	HCPEpiC	choroid plexus:	n/a
36	chr1:94561065-94561115	GM19239	blood:	n/a
37	chr1:94561065-94561115	NHDF-neo	bronchial:	n/a
38	chr1:94514548-94514598	K562	blood:	n/a
39	chr1:94514548-94514598	U87	brain:	n/a
40	chr1:94571619-94571669	HEK293	kidney:	embryo
41	chr1:94560697-94560747	SAEC	small airway:	n/a
42	chr1:94571619-94571669	HIPEpiC	eye:	n/a
43	chr1:94571619-94571669	HMEC	breast:	n/a
44	chr1:94514548-94514598	GM12892	blood:	n/a
45	chr1:94571619-94571669	AG04450	lung:	fetal
46	chr1:94514548-94514598	NHBE	bronchial:	n/a
47	chr1:94514548-94514598	HL-60	blood:	n/a
48	chr1:94560851-94560901	HepG2	liver:	n/a
49	chr1:94559714-94559764	BE2_C	brain:	n/a
50	chr1:94571619-94571669	AG09319	gingival:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:94570362..94572497-chr1:94572794..94574672,2	MCF-7	breast:
2	chr1:94565667..94567409-chr1:94572169..94573688,2	MCF-7	breast:
3	chr1:94546449..94548986-chr1:94550186..94552023,2	K562	blood:
4	chr1:94527833..94529893-chr1:94702894..94705764,2	MCF-7	breast:
5	chr1:94567418..94570803-chr1:94581520..94584135,4	MCF-7	breast:
6	chr1:94548149..94550772-chr1:94556316..94558558,2	K562	blood:
7	chr1:94528533..94530442-chr1:94567755..94569846,3	MCF-7	breast:
8	chr1:94569570..94572395-chr1:94575385..94578285,2	MCF-7	breast:
9	chr1:94532845..94535328-chr1:94609574..94612339,2	MCF-7	breast:
10	chr1:94517264..94519171-chr1:94520165..94522225,2	K562	blood:
11	chr1:94546449..94548986-chr1:94550186..94552023,2	K562	blood:
12	chr1:94570013..94571668-chr1:94572393..94574114,2	MCF-7	breast:
13	chr1:94569733..94572105-chr1:94572652..94574259,3	K562	blood:
14	chr1:61547567..61548283-chr1:94576374..94576896,2	MCF-7	breast:
15	chr1:94529817..94533865-chr1:94534670..94536843,3	MCF-7	breast:
16	chr1:94527081..94529532-chr1:94702506..94704195,2	MCF-7	breast:
17	chr1:94573501..94575707-chr1:94575840..94578707,2	MCF-7	breast:
18	chr1:94561960..94563528-chr1:94582281..94584718,2	MCF-7	breast:
19	chr1:94564934..94567258-chr1:94582385..94584556,2	MCF-7	breast:
20	chr1:94541971..94545495-chr1:94547470..94549927,3	MCF-7	breast:
21	chr1:94565667..94567409-chr1:94572169..94573688,2	MCF-7	breast:
22	chr1:94527285..94528858-chr1:94532743..94535509,2	MCF-7	breast:
23	chr1:94524835..94527724-chr1:94798552..94800345,2	MCF-7	breast:
24	chr1:94565431..94568158-chr1:94701481..94704374,2	MCF-7	breast:
25	chr1:94556014..94558247-chr1:94558375..94560976,2	MCF-7	breast:
26	chr1:94528533..94530442-chr1:94567755..94569846,3	MCF-7	breast:
27	chr1:94556014..94558247-chr1:94558375..94560976,2	MCF-7	breast:
28	chr1:94532251..94537168-chr1:94582958..94586481,4	MCF-7	breast:
29	chr1:94573941..94577939-chr1:94585857..94589392,3	K562	blood:
30	chr1:94502330..94505107-chr1:94527585..94529424,2	MCF-7	breast:
31	chr1:94529817..94533865-chr1:94534670..94536843,3	MCF-7	breast:
32	chr1:94541971..94545495-chr1:94547470..94549927,3	MCF-7	breast:
33	chr1:94509075..94510685-chr1:94516003..94517889,2	MCF-7	breast:
34	chr1:94570362..94572497-chr1:94572794..94574672,2	MCF-7	breast:
35	chr1:94533904..94535691-chr1:94564792..94567232,2	MCF-7	breast:
36	chr1:94573713..94576246-chr1:94579221..94581547,2	MCF-7	breast:
37	chr1:94569570..94572395-chr1:94575385..94578285,2	MCF-7	breast:
38	chr1:94564366..94567195-chr1:94607779..94609670,2	MCF-7	breast:
39	chr1:94571469..94574892-chr1:94577789..94583222,4	K562	blood:
40	chr1:94567017..94567580-chr1:94583611..94584143,2	MCF-7	breast:
41	chr1:94532482..94534156-chr1:94582374..94584202,2	MCF-7	breast:
42	chr1:94532586..94535624-chr1:94566931..94569461,4	MCF-7	breast:
43	chr1:94573501..94575707-chr1:94575840..94578707,2	MCF-7	breast:
44	chr1:94526671..94528632-chr1:94533088..94535694,2	K562	blood:
45	chr1:94560214..94561880-chr1:94564179..94567111,2	MCF-7	breast:
46	chr1:94527285..94528858-chr1:94532743..94535509,2	MCF-7	breast:
47	chr1:94522843..94524816-chr1:94526964..94529105,2	K562	blood:
48	chr1:94532586..94535624-chr1:94566931..94569461,4	MCF-7	breast:
49	chr1:94570013..94571668-chr1:94572393..94574114,2	MCF-7	breast:
50	chr1:94569733..94572105-chr1:94572652..94574259,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGAP29-3	chr1:94562551-94562713	NONHSAT004569
2	lnc-ABCD3-7	chr1:94571411-94571553	NONHSAT004570
3	lnc-ARHGAP29-3	chr1:94556623-94557051	NONHSAT004569
4	lnc-ABCD3-7	chr1:94572656-94572992	NONHSAT004570

No data

Variant related genes	Relation type
ABCA4	TF binding region
ABCA4	CpG island
ENSG00000233482	chromatin interactions
ENSG00000137962	chromatin interactions
ENSG00000162599	chromatin interactions
ENSG00000198691	chromatin interactions
ENSG00000226835	chromatin interactions

Extended variants
information (count: 2753 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2753 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4147837	chr1:94513142-94513143	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560530789	chr1:94513163-94513164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs527704993	chr1:94513208-94513209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78061958	chr1:94513226-94513227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs148894708	chr1:94513314-94513315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs147016014	chr1:94513370-94513371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs75631840	chr1:94513407-94513408	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs571414907	chr1:94513450-94513451	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs532158020	chr1:94513451-94513452	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs539435	chr1:94513493-94513494	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs143640593	chr1:94513531-94513532	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs535865709	chr1:94513532-94513533	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs147203557	chr1:94513537-94513538	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs148112529	chr1:94513538-94513539	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs370840731	chr1:94513550-94513551	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs141906232	chr1:94513566-94513567	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs578131738	chr1:94513576-94513577	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs182950122	chr1:94513621-94513622	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs567918266	chr1:94513631-94513632	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs554332279	chr1:94513643-94513644	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs187463016	chr1:94513689-94513690	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs543080619	chr1:94513755-94513756	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs192878337	chr1:94513767-94513768	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs183162061	chr1:94513770-94513771	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs543701412	chr1:94513806-94513807	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs150610936	chr1:94513807-94513808	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs532350809	chr1:94513846-94513847	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs201462748	chr1:94513854-94513855	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs74968378	chr1:94513859-94513860	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs79760310	chr1:94513907-94513908	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs139700211	chr1:94513910-94513911	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs3789400	chr1:94513952-94513953	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs569637363	chr1:94514005-94514006	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs536603087	chr1:94514020-94514021	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs550466516	chr1:94514040-94514041	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs55712710	chr1:94514070-94514071	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs17392417	chr1:94514082-94514083	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs554393521	chr1:94514083-94514084	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs572615263	chr1:94514132-94514133	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs536739000	chr1:94514142-94514143	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs555052607	chr1:94514214-94514215	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537611922	chr1:94514220-94514221	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370388978	chr1:94514223-94514224	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576391876	chr1:94514252-94514253	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114681343	chr1:94514269-94514270	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146393869	chr1:94514280-94514281	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577041461	chr1:94514307-94514308	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs61665830	chr1:94514327-94514328	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs55711648	chr1:94514334-94514335	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540860736	chr1:94514361-94514362	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
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
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
Medulloblastoma	21979893	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
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1615 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:94505600-94514200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr1:94505800-94523600	Weak transcription	Psoas Muscle	Psoas
3	chr1:94506600-94513200	Weak transcription	Fetal Heart	heart
4	chr1:94508800-94513600	Enhancers	HUVEC	blood vessel
5	chr1:94509600-94516800	Enhancers	Fetal Muscle Leg	muscle
6	chr1:94509800-94514800	Enhancers	Placenta	Placenta
7	chr1:94509800-94515800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr1:94509800-94516800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr1:94510000-94514600	Enhancers	Left Ventricle	heart
10	chr1:94510000-94517400	Enhancers	NHDF-Ad	bronchial
11	chr1:94510400-94515200	Weak transcription	Fetal Lung	lung
12	chr1:94511000-94513800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:94511200-94513800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr1:94511600-94513200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr1:94511600-94513200	Weak transcription	Spleen	Spleen
16	chr1:94511600-94513400	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr1:94511600-94513400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr1:94511600-94513600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr1:94511600-94513600	Weak transcription	Aorta	Aorta
20	chr1:94511600-94513800	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr1:94511600-94513800	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr1:94511600-94513800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr1:94511600-94513800	Enhancers	Fetal Muscle Trunk	muscle
24	chr1:94511600-94514000	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr1:94511600-94514000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:94511600-94514000	Weak transcription	Pancreas	Pancrea
27	chr1:94511600-94514200	Weak transcription	HSMMtube	muscle
28	chr1:94511600-94514400	Weak transcription	Fetal Intestine Small	intestine
29	chr1:94511600-94515400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr1:94511600-94515400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr1:94511600-94515400	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr1:94511600-94515400	Weak transcription	A549	lung
33	chr1:94511600-94515800	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr1:94511600-94515800	Weak transcription	Stomach Mucosa	stomach
35	chr1:94511600-94515800	Weak transcription	NHLF	lung
36	chr1:94511600-94520800	Weak transcription	Brain Angular Gyrus	brain
37	chr1:94511800-94513200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr1:94511800-94513200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr1:94511800-94513200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr1:94511800-94513200	Weak transcription	Fetal Kidney	kidney
41	chr1:94511800-94513400	Weak transcription	HSMM	muscle
42	chr1:94511800-94513400	Weak transcription	Osteobl	bone
43	chr1:94511800-94513600	Weak transcription	NH-A	brain
44	chr1:94511800-94514200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr1:94511800-94515200	Weak transcription	HMEC	breast
46	chr1:94511800-94515200	Weak transcription	NHEK	skin
47	chr1:94511800-94515400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr1:94511800-94515800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr1:94511800-94518000	Weak transcription	Fetal Stomach	stomach
50	chr1:94512200-94513400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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