Variant report

Variant	nsv947130
Chromosome Location	chr1:150878115-150899504
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:919)
CpG islands
(count:733)
Chromatin interactive
region (count:47)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:919 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:150898472-150898951	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:150894917-150895265	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:150894961-150895298	K562	blood:	n/a	n/a
4	ATF1	chr1:150894991-150895261	K562	blood:	n/a	n/a
5	ATF1	chr1:150898565-150899013	K562	blood:	n/a	n/a
6	ATF2	chr1:150898413-150899138	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr1:150898591-150899092	GM12878	blood:	n/a	n/a
8	ATF2	chr1:150894987-150895482	GM12878	blood:	n/a	n/a
9	ATF2	chr1:150898473-150899122	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr1:150894909-150895330	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr1:150894950-150895216	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr1:150898474-150899074	GM12878	blood:	n/a	n/a
13	ATF2	chr1:150894905-150895445	GM12878	blood:	n/a	n/a
14	ATF3	chr1:150898530-150899028	A549	lung:	n/a	n/a
15	ATF3	chr1:150898597-150898959	K562	blood:	n/a	n/a
16	BACH1	chr1:150879981-150880181	K562	blood:	n/a	n/a
17	BATF	chr1:150894977-150895400	GM12878	blood:	n/a	chr1:150895192-150895203 chr1:150895153-150895164
18	BATF	chr1:150895019-150895431	GM12878	blood:	n/a	chr1:150895192-150895203 chr1:150895153-150895164
19	BCL11A	chr1:150895030-150895385	GM12878	blood:	n/a	n/a
20	BCL11A	chr1:150895108-150895385	GM12878	blood:	n/a	n/a
21	BCL3	chr1:150894983-150895454	GM12878	blood:	n/a	n/a
22	BCL3	chr1:150898446-150899338	A549	lung:	n/a	n/a
23	BCLAF1	chr1:150898524-150899178	GM12878	blood:	n/a	n/a
24	BCLAF1	chr1:150894856-150895445	GM12878	blood:	n/a	n/a
25	BCLAF1	chr1:150894903-150895435	GM12878	blood:	n/a	n/a
26	BHLHE40	chr1:150898376-150899025	HepG2	liver:	n/a	n/a
27	BHLHE40	chr1:150894980-150895342	GM12878	blood:	n/a	n/a
28	BHLHE40	chr1:150898533-150898904	A549	lung:	n/a	n/a
29	BHLHE40	chr1:150898371-150899001	K562	blood:	n/a	n/a
30	BHLHE40	chr1:150898437-150899051	GM12878	blood:	n/a	n/a
31	BRCA1	chr1:150898355-150898974	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr1:150898577-150898930	HepG2	liver:	n/a	n/a
33	BRCA1	chr1:150898779-150899057	GM12878	blood:	n/a	n/a
34	CBX3	chr1:150898236-150899275	K562	blood:	n/a	n/a
35	CCNT2	chr1:150898555-150898940	K562	blood:	n/a	n/a
36	CEBPB	chr1:150898417-150898990	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr1:150898532-150898780	HepG2	liver:	n/a	n/a
38	CEBPB	chr1:150894963-150895339	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr1:150885253-150885254	HepG2	liver:	n/a	n/a
40	CEBPB	chr1:150895052-150895327	IMR90	lung:	n/a	n/a
41	CEBPB	chr1:150880068-150880360	K562	blood:	n/a	n/a
42	CEBPB	chr1:150898626-150899334	GM12878	blood:	n/a	n/a
43	CEBPB	chr1:150879997-150880357	K562	blood:	n/a	n/a
44	CEBPD	chr1:150898737-150899231	K562	blood:	n/a	n/a
45	CEBPD	chr1:150898578-150899249	HepG2	liver:	n/a	n/a
46	CHD1	chr1:150898925-150899603	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr1:150898515-150898989	GM12878	blood:	n/a	n/a
48	CHD2	chr1:150898572-150899107	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr1:150898556-150899051	HepG2	liver:	n/a	n/a
50	CHD2	chr1:150898544-150899156	K562	blood:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:150898663-150898713	ECC-1	luminal epithelium:	n/a
2	chr1:150898663-150898713	ECC-1	luminal epithelium:	n/a
3	chr1:150898638-150898688	AG04450	lung:	fetal
4	chr1:150897856-150897906	HCM	heart:	n/a
5	chr1:150898620-150898670	HCPEpiC	choroid plexus:	n/a
6	chr1:150898635-150898685	PANC-1	pancreas:	n/a
7	chr1:150898638-150898688	Hela-S3	cervix:	n/a
8	chr1:150898663-150898713	Hela-S3	cervix:	n/a
9	chr1:150899251-150899301	NB4	blood:	n/a
10	chr1:150898638-150898688	SK-N-MC	brain:	n/a
11	chr1:150884890-150884940	GM12892	blood:	n/a
12	chr1:150898620-150898670	HNPCEpiC	eye:	n/a
13	chr1:150898693-150898743	SK-N-SH_RA	brain:	n/a
14	chr1:150898638-150898688	GM12891	blood:	n/a
15	chr1:150898693-150898743	ECC-1	luminal epithelium:	n/a
16	chr1:150898620-150898670	HUVEC	blood vessel:	n/a
17	chr1:150898727-150898777	BJ	skin:	n/a
18	chr1:150898727-150898777	T-47D	breast:	n/a
19	chr1:150899251-150899301	HepG2	liver:	n/a
20	chr1:150898761-150898811	SAEC	small airway:	n/a
21	chr1:150898620-150898670	A549	lung:	n/a
22	chr1:150898437-150898487	Caco-2	colon:	n/a
23	chr1:150899251-150899301	BJ	skin:	n/a
24	chr1:150898620-150898670	HCF	heart:	n/a
25	chr1:150898437-150898487	HEK293	kidney:	embryo
26	chr1:150898761-150898811	HCM	heart:	n/a
27	chr1:150898620-150898670	AoSMC	blood vessel:	n/a
28	chr1:150898638-150898688	PANC-1	pancreas:	n/a
29	chr1:150898620-150898670	SK-N-SH	brain:	n/a
30	chr1:150898693-150898743	HL-60	blood:	n/a
31	chr1:150898761-150898811	GM06990	blood:	n/a
32	chr1:150899163-150899213	HCM	heart:	n/a
33	chr1:150897856-150897906	A549	lung:	n/a
34	chr1:150898620-150898670	H1-hESC	embryonic stem cell:	embryo
35	chr1:150898437-150898487	Hela-S3	cervix:	n/a
36	chr1:150898727-150898777	HAEpiC	amniotic membrane:	n/a
37	chr1:150898727-150898777	HRE	kidney:	n/a
38	chr1:150898663-150898713	HEEpiC	esophagus:	n/a
39	chr1:150899251-150899301	Hela-S3	cervix:	n/a
40	chr1:150898635-150898685	ovcar-3	ovarian:	n/a
41	chr1:150898761-150898811	HRCEpiC	kidney:	n/a
42	chr1:150898437-150898487	IMR90	lung:	fetal
43	chr1:150898693-150898743	U87	brain:	n/a
44	chr1:150898693-150898743	RPTEC	kidney:	n/a
45	chr1:150898761-150898811	AG09309	skin:	n/a
46	chr1:150884890-150884940	HRE	kidney:	n/a
47	chr1:150898638-150898688	NT2-D1	testis:	n/a
48	chr1:150899163-150899213	Hela-S3	cervix:	n/a
49	chr1:150898638-150898688	Caco-2	colon:	n/a
50	chr1:150884890-150884940	GM19239	blood:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:150335444..150338410-chr1:150897207..150899165,2	MCF-7	breast:
2	chr1:150897581..150900279-chr1:150934565..150936945,2	K562	blood:
3	chr1:150898231..150898792-chr19:37701107..37701818,2	HCT-116	colon:
4	chr1:150533128..150536071-chr1:150896850..150898729,2	MCF-7	breast:
5	chr1:150824355..150826588-chr1:150896874..150898598,2	MCF-7	breast:
6	chr1:150888318..150890863-chr1:150893491..150895097,2	K562	blood:
7	chr1:150877283..150879552-chr1:150896139..150898336,2	MCF-7	breast:
8	chr1:150877283..150879552-chr1:150896139..150898336,2	MCF-7	breast:
9	chr1:150847391..150850807-chr1:150896212..150900555,5	MCF-7	breast:
10	chr1:150801858..150802888-chr1:150894612..150895566,5	MCF-7	breast:
11	chr1:150878790..150879531-chr1:150895034..150895606,2	MCF-7	breast:
12	chr1:150846958..150850554-chr1:150897225..150899118,3	K562	blood:
13	chr1:150524437..150526621-chr1:150884840..150887292,2	K562	blood:
14	chr1:150842114..150842998-chr1:150894692..150895584,2	MCF-7	breast:
15	chr1:150888096..150891022-chr1:150892225..150894393,2	K562	blood:
16	chr1:150849390..150851277-chr1:150877417..150879109,2	MCF-7	breast:
17	chr1:150883932..150886326-chr1:150890784..150892342,2	K562	blood:
18	chr1:150877469..150879238-chr1:150945811..150948116,2	MCF-7	breast:
19	chr1:150542198..150544708-chr1:150893350..150895206,2	K562	blood:
20	chr1:150884570..150885222-chr1:150894644..150895459,2	K562	blood:
21	chr1:150720840..150722838-chr1:150897246..150898815,2	K562	blood:
22	chr1:150833034..150834880-chr1:150896900..150898659,2	MCF-7	breast:
23	chr1:150898462..150900740-chr1:151030523..151033024,2	MCF-7	breast:
24	chr1:150898343..150899070-chr7:73256729..73257419,2	NB4	blood:
25	chr1:150878790..150879531-chr1:150895034..150895606,2	MCF-7	breast:
26	chr1:150800480..150802144-chr1:150885516..150887920,2	MCF-7	breast:
27	chr1:150883932..150886326-chr1:150890784..150892342,2	K562	blood:
28	chr1:150888318..150890863-chr1:150893491..150895097,2	K562	blood:
29	chr1:150541549..150544184-chr1:150897269..150900025,2	K562	blood:
30	chr1:150884570..150885222-chr1:150894644..150895459,2	K562	blood:
31	chr1:150888096..150891022-chr1:150892225..150894393,2	K562	blood:
32	chr1:150897692..150900384-chr1:150944923..150947345,3	K562	blood:
33	chr1:150887871..150890031-chr1:150893806..150895331,2	MCF-7	breast:
34	chr1:150808768..150811697-chr1:150895772..150898745,2	MCF-7	breast:
35	chr1:150894801..150896695-chr1:150898996..150900793,2	MCF-7	breast:
36	chr1:150825294..150827430-chr1:150885825..150887706,2	MCF-7	breast:
37	chr1:150890944..150896725-chr1:150896868..150900962,8	MCF-7	breast:
38	chr1:150889960..150892328-chr1:150896397..150898404,2	MCF-7	breast:
39	chr1:150887871..150890031-chr1:150893806..150895331,2	MCF-7	breast:
40	chr1:150889960..150892328-chr1:150896397..150898404,2	MCF-7	breast:
41	chr1:150848726..150850805-chr1:150878853..150880378,2	MCF-7	breast:
42	chr1:150892976..150894840-chr1:150949265..150951717,2	K562	blood:
43	chr1:150601346..150603290-chr1:150894418..150896629,2	MCF-7	breast:
44	chr1:150894686..150895203-chr1:150952093..150952665,2	MCF-7	breast:
45	chr1:150848716..150851402-chr1:150897221..150900291,3	MCF-7	breast:
46	chr1:150847503..150849791-chr1:150897618..150900781,3	K562	blood:
47	chr1:150436622..150437343-chr1:150894926..150895550,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SETDB1-2	chr1:150894577-150894647	NONHSAT006338
2	lnc-SETDB1-2	chr1:150895411-150895438	NONHSAT006338
3	lnc-SETDB1-2	chr1:150895702-150895904	NONHSAT006338

No data

Variant related genes	Relation type
SETDB1	TF binding region
SETDB1	CpG island
ENSG00000165171	chromatin interactions
ENSG00000203804	chromatin interactions
ENSG00000143379	chromatin interactions
ENSG00000143382	chromatin interactions
ENSG00000231073	chromatin interactions
ENSG00000264584	chromatin interactions
ENSG00000163131	chromatin interactions
ENSG00000245680	chromatin interactions
ENSG00000197622	chromatin interactions
ENSG00000267360	chromatin interactions
ENSG00000143418	chromatin interactions
ENSG00000143437	chromatin interactions
ENSG00000163125	chromatin interactions
ENSG00000143420	chromatin interactions

Extended variants
information (count: 654 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:654 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587734484	chr1:150878172-150878173	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs12072214	chr1:150878186-150878187	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs12082683	chr1:150878188-150878189	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs367991601	chr1:150878191-150878192	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs186482598	chr1:150878192-150878193	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs587653806	chr1:150878233-150878234	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs587713139	chr1:150878237-150878238	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs112419423	chr1:150878240-150878241	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs192939760	chr1:150878282-150878283	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs587768438	chr1:150878294-150878295	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs182903927	chr1:150878323-150878324	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs372180357	chr1:150878363-150878364	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs587696711	chr1:150878369-150878370	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs587752468	chr1:150878371-150878372	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs587654504	chr1:150878372-150878373	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs587691105	chr1:150878390-150878391	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs188803475	chr1:150878391-150878392	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs587652908	chr1:150878444-150878445	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs192889199	chr1:150878445-150878446	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs112438908	chr1:150878453-150878454	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs587631138	chr1:150878469-150878470	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs56259054	chr1:150878475-150878476	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs587716831	chr1:150878494-150878495	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs115298177	chr1:150878649-150878650	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs587678112	chr1:150878683-150878684	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs587661806	chr1:150878692-150878693	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs587747812	chr1:150878697-150878698	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs587758464	chr1:150878706-150878707	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs142346627	chr1:150878711-150878712	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs116021207	chr1:150878767-150878768	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs587764607	chr1:150878804-150878805	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs587621702	chr1:150878820-150878821	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs587693640	chr1:150878837-150878838	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs587741421	chr1:150878852-150878853	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs146830236	chr1:150878868-150878869	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs587698144	chr1:150878901-150878902	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs587755711	chr1:150878944-150878945	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs587648898	chr1:150879097-150879098	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs897815	chr1:150879101-150879102	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs587764093	chr1:150879119-150879120	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs140605445	chr1:150879123-150879124	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs376153757	chr1:150879190-150879191	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs200656415	chr1:150879202-150879203	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs587719770	chr1:150879204-150879205	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs367893991	chr1:150879212-150879213	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs34312281	chr1:150879232-150879233	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs587757181	chr1:150879249-150879250	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs185885927	chr1:150879252-150879253	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs587733961	chr1:150879305-150879306	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs111800876	chr1:150879308-150879309	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	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
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:398 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:150875400-150879000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr1:150877800-150879400	Enhancers	Placenta	Placenta
3	chr1:150879000-150879200	Enhancers	Placenta Amnion	Placenta Amnion
4	chr1:150879200-150879400	Enhancers	K562	blood
5	chr1:150879200-150880200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr1:150879200-150898200	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr1:150879400-150880400	Weak transcription	Placenta	Placenta
8	chr1:150880000-150880200	Enhancers	K562	blood
9	chr1:150880400-150880800	Enhancers	Placenta	Placenta
10	chr1:150881800-150882400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
11	chr1:150882200-150883200	Enhancers	Primary B cells from peripheral blood	blood
12	chr1:150882400-150882600	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr1:150882600-150883200	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr1:150884600-150885600	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr1:150884800-150885000	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr1:150884800-150885200	Enhancers	H1 Cell Line	embryonic stem cell
17	chr1:150884800-150885400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr1:150884800-150885400	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr1:150884800-150885600	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr1:150884800-150885600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr1:150884800-150885800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr1:150884800-150885800	Enhancers	H9 Cell Line	embryonic stem cell
23	chr1:150884800-150885800	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr1:150884800-150885800	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr1:150885000-150885400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr1:150885400-150885600	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr1:150885400-150887200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr1:150885600-150887200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr1:150886400-150888000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr1:150886600-150888000	Enhancers	NHDF-Ad	bronchial
31	chr1:150887200-150887800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr1:150887200-150888000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr1:150887400-150887800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr1:150887400-150887800	Enhancers	Muscle Satellite Cultured Cells	--
35	chr1:150887400-150888000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr1:150887600-150888000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:150887800-150890400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr1:150888000-150894800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr1:150890400-150890600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr1:150891200-150894800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr1:150894400-150894800	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr1:150894600-150894800	Enhancers	GM12878-XiMat	blood
43	chr1:150894600-150895000	Enhancers	Primary T killer memory cells from peripheral blood	blood
44	chr1:150894600-150895000	Enhancers	Rectal Mucosa Donor 29	rectum
45	chr1:150894600-150895400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr1:150894600-150895400	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr1:150894600-150895600	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr1:150894600-150895600	Enhancers	NHDF-Ad	bronchial
49	chr1:150894600-150895600	Enhancers	Osteobl	bone
50	chr1:150894600-150895800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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