Variant report

Variant	nsv436325
Chromosome Location	chr1:120390914-120471049
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1066)
CpG islands
(count:1099)
Chromatin interactive
region (count:72)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:12)

(count:1066 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:120422885-120422997	K562	blood:	n/a	n/a
2	ARID3A	chr1:120416643-120417039	K562	blood:	n/a	n/a
3	ARID3A	chr1:120392364-120392392	K562	blood:	n/a	n/a
4	ARID3A	chr1:120413558-120413989	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:120413559-120413886	K562	blood:	n/a	n/a
6	ARID3A	chr1:120402048-120402592	K562	blood:	n/a	n/a
7	ARID3A	chr1:120441825-120442392	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:120425053-120425244	K562	blood:	n/a	n/a
9	ATF1	chr1:120462961-120463475	K562	blood:	n/a	n/a
10	ATF1	chr1:120402001-120402616	K562	blood:	n/a	n/a
11	ATF1	chr1:120398236-120398340	K562	blood:	n/a	n/a
12	ATF1	chr1:120426630-120426696	K562	blood:	n/a	n/a
13	ATF1	chr1:120410011-120410219	K562	blood:	n/a	n/a
14	ATF1	chr1:120391966-120392057	K562	blood:	n/a	n/a
15	ATF3	chr1:120402162-120402649	K562	blood:	n/a	n/a
16	BACH1	chr1:120431362-120431386	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr1:120416965-120417243	K562	blood:	n/a	chr1:120417090-120417104
18	BACH1	chr1:120412409-120412437	K562	blood:	n/a	n/a
19	BACH1	chr1:120430266-120430308	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr1:120416320-120416558	GM12878	blood:	n/a	chr1:120416427-120416438 chr1:120416428-120416438
21	BHLHE40	chr1:120413529-120413860	K562	blood:	n/a	n/a
22	BHLHE40	chr1:120425148-120425279	K562	blood:	n/a	n/a
23	BHLHE40	chr1:120416411-120417211	K562	blood:	n/a	n/a
24	BHLHE40	chr1:120462981-120463318	K562	blood:	n/a	n/a
25	BHLHE40	chr1:120414214-120414217	K562	blood:	n/a	n/a
26	BHLHE40	chr1:120402075-120402625	K562	blood:	n/a	n/a
27	BRCA1	chr1:120413720-120413825	HepG2	liver:	n/a	n/a
28	BRCA1	chr1:120413878-120413886	GM12878	blood:	n/a	n/a
29	BRCA1	chr1:120413508-120413986	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr1:120402018-120402716	K562	blood:	n/a	n/a
31	CCNT2	chr1:120416779-120417077	K562	blood:	n/a	n/a
32	CCNT2	chr1:120422520-120423032	K562	blood:	n/a	n/a
33	CCNT2	chr1:120438960-120439212	K562	blood:	n/a	n/a
34	CEBPB	chr1:120413556-120414068	Hela-S3	cervix:	n/a	chr1:120413914-120413927
35	CEBPB	chr1:120408184-120408568	IMR90	lung:	n/a	n/a
36	CEBPB	chr1:120435966-120436164	HepG2	liver:	n/a	n/a
37	CEBPB	chr1:120413598-120413872	K562	blood:	n/a	n/a
38	CEBPB	chr1:120413621-120413890	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr1:120425874-120425955	HepG2	liver:	n/a	n/a
40	CEBPB	chr1:120412709-120412901	K562	blood:	n/a	chr1:120412787-120412798
41	CEBPB	chr1:120413574-120414012	IMR90	lung:	n/a	chr1:120413914-120413927
42	CEBPB	chr1:120413514-120414026	MCF-7	breast:	n/a	chr1:120413914-120413927
43	CEBPB	chr1:120402260-120402530	K562	blood:	n/a	n/a
44	CEBPB	chr1:120437715-120437953	A549	lung:	n/a	chr1:120437871-120437882
45	CEBPB	chr1:120413569-120413925	K562	blood:	n/a	n/a
46	CEBPB	chr1:120413569-120413985	HepG2	liver:	n/a	chr1:120413914-120413927
47	CEBPB	chr1:120438377-120438610	H1-hESC	embryonic stem cell:	n/a	chr1:120438422-120438433
48	CEBPB	chr1:120436959-120437216	HepG2	liver:	n/a	n/a
49	CEBPB	chr1:120413598-120413996	H1-hESC	embryonic stem cell:	n/a	chr1:120413914-120413927
50	CEBPB	chr1:120413596-120413965	A549	lung:	n/a	chr1:120413914-120413927

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:120438925-120438975	PANC-1	pancreas:	n/a
2	chr1:120438925-120438975	PANC-1	pancreas:	n/a
3	chr1:120439396-120439446	RPTEC	kidney:	n/a
4	chr1:120395857-120395907	HEEpiC	esophagus:	n/a
5	chr1:120438925-120438975	Hepatocyte	liver:	n/a
6	chr1:120440230-120440280	MCF10A-Er-Src	breast:	n/a
7	chr1:120395943-120395993	A549	lung:	n/a
8	chr1:120396074-120396124	AoSMC	blood vessel:	n/a
9	chr1:120394120-120394170	AG09309	skin:	n/a
10	chr1:120439522-120439572	HAEpiC	amniotic membrane:	n/a
11	chr1:120439036-120439086	IMR90	lung:	fetal
12	chr1:120435245-120435295	HRCEpiC	kidney:	n/a
13	chr1:120439396-120439446	T-47D	breast:	n/a
14	chr1:120395857-120395907	HCPEpiC	choroid plexus:	n/a
15	chr1:120441702-120441752	AG04449	skin:	fetal
16	chr1:120437090-120437140	Hela-S3	cervix:	n/a
17	chr1:120396074-120396124	NHDF-neo	bronchial:	n/a
18	chr1:120439014-120439064	HCT-116	colon:	n/a
19	chr1:120395857-120395907	GM12891	blood:	n/a
20	chr1:120396167-120396217	HEEpiC	esophagus:	n/a
21	chr1:120395857-120395907	MCF10A-Er-Src	breast:	n/a
22	chr1:120396074-120396124	NHBE	bronchial:	n/a
23	chr1:120395943-120395993	GM12891	blood:	n/a
24	chr1:120457856-120457906	HPAEpiC	pulmonary alveolar:	n/a
25	chr1:120396167-120396217	IMR90	lung:	fetal
26	chr1:120441702-120441752	BE2_C	brain:	n/a
27	chr1:120395857-120395907	CMK	blood:	n/a
28	chr1:120438925-120438975	NB4	blood:	n/a
29	chr1:120441702-120441752	PrEC	prostate:	n/a
30	chr1:120439522-120439572	IMR90	lung:	fetal
31	chr1:120439812-120439862	CMK	blood:	n/a
32	chr1:120394120-120394170	HRCEpiC	kidney:	n/a
33	chr1:120439396-120439446	LNCaP	prostate:	n/a
34	chr1:120439522-120439572	CMK	blood:	n/a
35	chr1:120439036-120439086	BE2_C	brain:	n/a
36	chr1:120395943-120395993	AG10803	skin:	n/a
37	chr1:120438925-120438975	HepG2	liver:	n/a
38	chr1:120439036-120439086	NHDF-neo	bronchial:	n/a
39	chr1:120438925-120438975	HRE	kidney:	n/a
40	chr1:120396167-120396217	NHDF-neo	bronchial:	n/a
41	chr1:120395857-120395907	GM06990	blood:	n/a
42	chr1:120439870-120439920	HepG2	liver:	n/a
43	chr1:120439036-120439086	NB4	blood:	n/a
44	chr1:120437090-120437140	HPAEpiC	pulmonary alveolar:	n/a
45	chr1:120457856-120457906	HEK293	kidney:	embryo
46	chr1:120441702-120441752	NH-A	brain:	n/a
47	chr1:120440230-120440280	AG09319	gingival:	n/a
48	chr1:120439522-120439572	HRPEpiC	eye:	n/a
49	chr1:120438925-120438975	HCF	heart:	n/a
50	chr1:120439812-120439862	T-47D	breast:	n/a

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:120467969..120469676-chr1:120469960..120472021,2	MCF-7	breast:
2	chr1:120413136..120413983-chr1:120688071..120688676,2	MCF-7	breast:
3	chr1:120401746..120405481-chr1:120411089..120413247,3	K562	blood:
4	chr1:120395990..120398388-chr1:120402021..120403587,2	MCF-7	breast:
5	chr1:120436002..120438494-chr1:120462381..120464792,2	MCF-7	breast:
6	chr1:120402254..120403816-chr1:120407208..120410128,2	K562	blood:
7	chr1:120401746..120405481-chr1:120411089..120413247,3	K562	blood:
8	chr1:120423918..120425680-chr1:120436272..120439121,2	MCF-7	breast:
9	chr1:120418108..120420046-chr1:120426415..120428973,2	MCF-7	breast:
10	chr1:120401899..120403872-chr1:120404616..120406616,2	K562	blood:
11	chr1:120414299..120416081-chr1:120419114..120421121,2	MCF-7	breast:
12	chr1:120413185..120414823-chr1:120510316..120511509,11	K562	blood:
13	chr1:120454474..120456790-chr1:120460931..120463931,3	MCF-7	breast:
14	chr1:120395050..120396919-chr1:120400456..120403382,2	K562	blood:
15	chr1:120414299..120416081-chr1:120419114..120421121,2	MCF-7	breast:
16	chr1:120396123..120397960-chr1:120398634..120401481,2	MCF-7	breast:
17	chr1:120449760..120452245-chrX:18130620..18132924,2	MCF-7	breast:
18	chr1:120413290..120414192-chr1:145061552..145062410,3	MCF-7	breast:
19	chr1:120402638..120409843-chr1:120411143..120414879,6	K562	blood:
20	chr1:120400389..120402381-chr1:120411990..120414876,2	MCF-7	breast:
21	chr1:120286454..120287367-chr1:120413250..120414231,6	MCF-7	breast:
22	chr1:120400878..120403434-chr1:120429544..120432344,2	MCF-7	breast:
23	chr1:120356024..120358010-chr1:120414554..120416804,2	MCF-7	breast:
24	chr1:120456262..120460550-chr1:120460767..120463877,3	K562	blood:
25	chr1:120412006..120414446-chr20:39570090..39572688,2	MCF-7	breast:
26	chr1:120436002..120438494-chr1:120462381..120464792,2	MCF-7	breast:
27	chr1:120411363..120413507-chr1:120488348..120490535,2	MCF-7	breast:
28	chr1:120461834..120464698-chr1:120475865..120478415,2	MCF-7	breast:
29	chr1:120402638..120409843-chr1:120411143..120414879,6	K562	blood:
30	chr1:120447256..120450228-chr1:120525932..120527487,2	K562	blood:
31	chr1:120450368..120452473-chr1:120481049..120483944,2	K562	blood:
32	chr1:120407227..120409866-chr1:120411448..120413775,3	K562	blood:
33	chr1:120426879..120429312-chr1:120432285..120434673,2	MCF-7	breast:
34	chr1:120440889..120443240-chr12:109181998..109184664,2	MCF-7	breast:
35	chr1:120466619..120469104-chr1:120488906..120491795,2	K562	blood:
36	chr1:120449201..120451980-chr1:120452971..120455460,2	MCF-7	breast:
37	chr1:120445668..120448303-chr1:120496593..120499239,2	MCF-7	breast:
38	chr1:120444002..120446345-chr1:120453344..120455730,3	MCF-7	breast:
39	chr1:120407227..120409866-chr1:120411448..120413775,3	K562	blood:
40	chr1:120283662..120285685-chr1:120414247..120416692,2	MCF-7	breast:
41	chr1:120467969..120469676-chr1:120469960..120472021,2	MCF-7	breast:
42	chr1:120395990..120398388-chr1:120402021..120403587,2	MCF-7	breast:
43	chr1:120454474..120456790-chr1:120460931..120463931,3	MCF-7	breast:
44	chr1:120415380..120417252-chr1:120419705..120421927,2	K562	blood:
45	chr1:120461841..120464545-chr1:120468138..120469880,2	MCF-7	breast:
46	chr1:120455729..120458677-chr1:120465147..120468544,4	MCF-7	breast:
47	chr1:120444002..120446345-chr1:120453344..120455730,3	MCF-7	breast:
48	chr1:120402254..120403816-chr1:120407208..120410128,2	K562	blood:
49	chr1:120445705..120448547-chr1:120448757..120452152,3	MCF-7	breast:
50	chr1:120370478..120372574-chr1:120394062..120395720,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NOTCH2-1	chr1:120451878-120453236	ENSG00000261662.1
2	lnc-ADAM30-1	chr1:120390862-120391484	ENSG00000247433

No data

(count:12 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	NOTCH2	hsa-miR-107	chr1:120457885-120457879
2	NOTCH2	hsa-miR-16-5p	chr1:120457878-120457901
3	NOTCH2	hsa-miR-1	chr1:120454297-120454318
4	NOTCH2	hsa-miR-326	chr1:120454916-120454935
5	NOTCH2	hsa-miR-34a-5p	chr1:120455462-120455456
6	NOTCH2	hsa-miR-181c-5p	chr1:120454955-120454976
7	NOTCH2	hsa-miR-181a-5p	chr1:120454955-120454976
8	NOTCH2	hsa-miR-107	chr1:120457879-120457900
9	NOTCH2	hsa-miR-16-5p	chr1:120457884-120457878
10	NOTCH2	hsa-miR-181a-5p	chr1:120454961-120454954
11	NOTCH2	hsa-miR-181c-5p	chr1:120454961-120454954
12	NOTCH2	hsa-miR-34a-5p	chr1:120455456-120455477

Variant related genes	Relation type
NOTCH2	TF binding region
ADAM30	TF binding region
ENSG00000261662	TF binding region
NOTCH2P1	TF binding region
NBPF7	TF binding region
PFN1P9	TF binding region
NOTCH2	CpG island
ADAM30	CpG island
ENSG00000261662	CpG island
NOTCH2P1	CpG island
NBPF7	CpG island
PFN1P9	CpG island
ENSG00000227205	chromatin interactions
ENSG00000134193	chromatin interactions
ENSG00000134250	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000134249	chromatin interactions
ENSG00000226446	chromatin interactions
ENSG00000261662	chromatin interactions
ZDHHC2	miRNA target sites

Extended variants
information (count: 2644 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:2644 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587632178	chr1:120390928-120390929	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs587683100	chr1:120390967-120390968	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs587743634	chr1:120390969-120390970	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs587612928	chr1:120390972-120390973	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs111919742	chr1:120391008-120391009	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs10923912	chr1:120391026-120391027	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs587702571	chr1:120391038-120391039	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs587761702	chr1:120391050-120391051	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs587657053	chr1:120391111-120391112	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs10923913	chr1:120391118-120391119	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs587753538	chr1:120391138-120391139	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs587648432	chr1:120391205-120391206	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs182376017	chr1:120391206-120391207	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs587699385	chr1:120391265-120391266	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs74115376	chr1:120391281-120391282	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs587633265	chr1:120391282-120391283	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs190082229	chr1:120391296-120391297	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs56215403	chr1:120391311-120391312	Inactive region	TF binding region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs201420244	chr1:120391328-120391329	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs181691965	chr1:120391340-120391341	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs78278658	chr1:120391388-120391389	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs76489050	chr1:120391399-120391400	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs75954033	chr1:120391408-120391409	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs186396265	chr1:120391415-120391416	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs587605470	chr1:120391418-120391419	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs138825062	chr1:120391446-120391447	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs74890811	chr1:120391463-120391464	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs199743149	chr1:120391465-120391466	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs587738517	chr1:120391467-120391468	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs75596365	chr1:120391471-120391472	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs587703960	chr1:120391477-120391478	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs76715253	chr1:120391484-120391485	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
33	rs371146497	chr1:120391498-120391499	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs148584741	chr1:120391505-120391506	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs78219737	chr1:120391507-120391508	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs587695904	chr1:120391512-120391513	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs115640426	chr1:120391523-120391524	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs76057243	chr1:120391537-120391538	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs375057702	chr1:120391542-120391543	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs587641333	chr1:120391553-120391554	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs587680303	chr1:120391555-120391556	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs115830460	chr1:120391573-120391574	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs150667479	chr1:120391582-120391583	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs116270480	chr1:120391583-120391584	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs189623592	chr1:120391594-120391595	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs115526337	chr1:120391598-120391599	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs115799587	chr1:120391608-120391609	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs180881386	chr1:120391628-120391629	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs200982555	chr1:120391651-120391652	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs587738105	chr1:120391670-120391671	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Wilms tumour	21544195	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
Glioblastoma multiforme	21080181	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Aetanephric adenomas	20802469	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Systemic lupus erythematosus	21956041	CNVD
Breast cancer	21804112	CNVD
Mental retardation	21062444	CNVD
Myelofibrosis	22110671	CNVD
Emphysema	19352772	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	21272361	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ependymoma	19289631	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:850 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:120395000-120400400	Weak transcription	Fetal Intestine Small	intestine
2	chr1:120395800-120396000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:120395800-120396200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:120396000-120402400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr1:120397800-120398000	Enhancers	K562	blood
6	chr1:120398000-120398200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr1:120398200-120398600	Enhancers	HepG2	liver
8	chr1:120398200-120400600	Weak transcription	K562	blood
9	chr1:120398600-120400600	Weak transcription	HepG2	liver
10	chr1:120398600-120400800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr1:120400200-120402400	Enhancers	Fetal Intestine Large	intestine
12	chr1:120400400-120402600	Enhancers	Fetal Intestine Small	intestine
13	chr1:120400600-120401000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr1:120400600-120401000	Enhancers	Sigmoid Colon	Sigmoid Colon
15	chr1:120400600-120401400	Enhancers	HepG2	liver
16	chr1:120400600-120401800	Enhancers	K562	blood
17	chr1:120400800-120401000	Enhancers	Duodenum Mucosa	Duodenum
18	chr1:120400800-120401000	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr1:120400800-120401800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr1:120400800-120401800	Enhancers	Dnd41	blood
21	chr1:120400800-120402400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr1:120400800-120403200	Enhancers	HUVEC	blood vessel
23	chr1:120400800-120404000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr1:120400800-120404200	Enhancers	Fetal Muscle Leg	muscle
25	chr1:120400800-120405000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr1:120401000-120401400	Enhancers	Fetal Kidney	kidney
27	chr1:120401000-120402000	Weak transcription	Duodenum Mucosa	Duodenum
28	chr1:120401000-120402000	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr1:120401000-120402200	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr1:120401000-120404800	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr1:120401200-120401400	Enhancers	Small Intestine	intestine
32	chr1:120401200-120401600	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr1:120401200-120403200	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr1:120401400-120401600	Enhancers	Fetal Muscle Trunk	muscle
35	chr1:120401400-120402400	Enhancers	Primary hematopoietic stem cells	blood
36	chr1:120401400-120403400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr1:120401400-120415000	Weak transcription	Fetal Kidney	kidney
38	chr1:120401600-120402600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
39	chr1:120401600-120403000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr1:120401800-120402000	Enhancers	Muscle Satellite Cultured Cells	--
41	chr1:120401800-120402200	Flanking Active TSS	Dnd41	blood
42	chr1:120401800-120402600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr1:120401800-120402600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr1:120401800-120402600	Enhancers	Osteobl	bone
45	chr1:120401800-120402800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr1:120401800-120402800	Enhancers	HMEC	breast
47	chr1:120401800-120402800	Enhancers	HSMMtube	muscle
48	chr1:120401800-120402800	Flanking Active TSS	K562	blood
49	chr1:120401800-120402800	Enhancers	NH-A	brain
50	chr1:120401800-120403000	Weak transcription	Fetal Muscle Trunk	muscle

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