Variant report

Variant	nsv831204
Chromosome Location	chr1:120266449-120314091
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1003)
CpG islands
(count:737)
Chromatin interactive
region (count:85)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1003 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:120266970-120267873	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:120286725-120287101	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:120271521-120272115	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:120308359-120309408	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:120279845-120280184	K562	blood:	n/a	n/a
6	ARID3A	chr1:120275475-120275600	HepG2	liver:	n/a	n/a
7	ATF1	chr1:120306358-120306836	K562	blood:	n/a	n/a
8	ATF1	chr1:120286724-120287023	K562	blood:	n/a	n/a
9	ATF1	chr1:120270760-120270987	K562	blood:	n/a	n/a
10	ATF2	chr1:120286732-120287132	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr1:120295600-120295613	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr1:120279875-120280173	K562	blood:	n/a	n/a
13	BACH1	chr1:120280854-120280965	K562	blood:	n/a	n/a
14	BHLHE40	chr1:120279128-120280294	K562	blood:	n/a	n/a
15	BHLHE40	chr1:120286806-120287048	GM12878	blood:	n/a	n/a
16	BHLHE40	chr1:120281909-120282075	K562	blood:	n/a	n/a
17	BHLHE40	chr1:120286558-120287092	K562	blood:	n/a	n/a
18	BRCA1	chr1:120275857-120275863	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr1:120287588-120287684	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr1:120279818-120280275	K562	blood:	n/a	n/a
21	CBX3	chr1:120278672-120278915	K562	blood:	n/a	n/a
22	CBX3	chr1:120279180-120279658	K562	blood:	n/a	n/a
23	CBX3	chr1:120278995-120279592	K562	blood:	n/a	n/a
24	CCNT2	chr1:120279425-120280263	K562	blood:	n/a	chr1:120279992-120280012 chr1:120279906-120279915
25	CEBPB	chr1:120279891-120280230	K562	blood:	n/a	n/a
26	CEBPB	chr1:120302143-120302426	H1-hESC	embryonic stem cell:	n/a	chr1:120302279-120302290
27	CEBPB	chr1:120302129-120302444	HepG2	liver:	n/a	chr1:120302279-120302290
28	CEBPB	chr1:120271759-120272059	HepG2	liver:	n/a	n/a
29	CEBPB	chr1:120267438-120267765	HepG2	liver:	n/a	chr1:120267618-120267629 chr1:120267617-120267628 chr1:120267617-120267630
30	CEBPB	chr1:120267395-120267744	HepG2	liver:	n/a	chr1:120267618-120267629 chr1:120267617-120267628 chr1:120267617-120267630
31	CEBPB	chr1:120267318-120267836	HepG2	liver:	n/a	chr1:120267618-120267629 chr1:120267617-120267628 chr1:120267617-120267630
32	CEBPB	chr1:120267381-120267866	HepG2	liver:	n/a	chr1:120267618-120267629 chr1:120267617-120267628 chr1:120267617-120267630
33	CEBPB	chr1:120308931-120309289	HepG2	liver:	n/a	n/a
34	CEBPB	chr1:120272691-120272960	HepG2	liver:	n/a	chr1:120272815-120272826
35	CEBPD	chr1:120267421-120267793	HepG2	liver:	n/a	n/a
36	CEBPD	chr1:120279636-120280346	K562	blood:	n/a	n/a
37	CEBPD	chr1:120267413-120267767	HepG2	liver:	n/a	n/a
38	CEBPD	chr1:120286742-120287015	HepG2	liver:	n/a	n/a
39	CEBPD	chr1:120279682-120280282	K562	blood:	n/a	n/a
40	CEBPZ	chr1:120270899-120271055	HepG2	liver:	n/a	n/a
41	CEBPZ	chr1:120309578-120309646	HepG2	liver:	n/a	n/a
42	CHD1	chr1:120272360-120272426	GM12878	blood:	n/a	n/a
43	CHD2	chr1:120311585-120311801	HepG2	liver:	n/a	n/a
44	CHD2	chr1:120279806-120280121	K562	blood:	n/a	n/a
45	CHD2	chr1:120286706-120287102	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr1:120286706-120286912	GM12878	blood:	n/a	n/a
47	CHD2	chr1:120280313-120280314	HepG2	liver:	n/a	n/a
48	CREB1	chr1:120267248-120267851	HepG2	liver:	n/a	n/a
49	CREB1	chr1:120286645-120287120	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr1:120313738-120313963	H1-hESC	embryonic stem cell:	n/a	n/a

(count:737 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:120311653-120311703	GM12878	blood:	n/a
2	chr1:120311542-120311592	HRCEpiC	kidney:	n/a
3	chr1:120311439-120311489	LNCaP	prostate:	n/a
4	chr1:120312730-120312780	U87	brain:	n/a
5	chr1:120310021-120310071	AG09309	skin:	n/a
6	chr1:120311653-120311703	GM12878	blood:	n/a
7	chr1:120311542-120311592	HRCEpiC	kidney:	n/a
8	chr1:120311439-120311489	LNCaP	prostate:	n/a
9	chr1:120312730-120312780	U87	brain:	n/a
10	chr1:120310021-120310071	AG09309	skin:	n/a
11	chr1:120286814-120286864	AG10803	skin:	n/a
12	chr1:120272766-120272816	HUVEC	blood vessel:	n/a
13	chr1:120272766-120272816	SK-N-SH	brain:	n/a
14	chr1:120284868-120284918	NB4	blood:	n/a
15	chr1:120311653-120311703	HRCEpiC	kidney:	n/a
16	chr1:120311649-120311699	Jurkat	blood:	n/a
17	chr1:120284868-120284918	SKMC	muscle:	n/a
18	chr1:120311653-120311703	HNPCEpiC	eye:	n/a
19	chr1:120311542-120311592	RPTEC	kidney:	n/a
20	chr1:120284868-120284918	AG09319	gingival:	n/a
21	chr1:120292140-120292190	HRE	kidney:	n/a
22	chr1:120311542-120311592	HNPCEpiC	eye:	n/a
23	chr1:120272766-120272816	HRE	kidney:	n/a
24	chr1:120311542-120311592	GM19239	blood:	n/a
25	chr1:120292140-120292190	GM19239	blood:	n/a
26	chr1:120272766-120272816	HIPEpiC	eye:	n/a
27	chr1:120311649-120311699	SKMC	muscle:	n/a
28	chr1:120312730-120312780	HepG2	liver:	n/a
29	chr1:120289923-120289973	GM12878	blood:	n/a
30	chr1:120311653-120311703	HRPEpiC	eye:	n/a
31	chr1:120311653-120311703	HAEpiC	amniotic membrane:	n/a
32	chr1:120311439-120311489	AG09309	skin:	n/a
33	chr1:120284868-120284918	HMEC	breast:	n/a
34	chr1:120272766-120272816	AG09309	skin:	n/a
35	chr1:120310021-120310071	SK-N-SH	brain:	n/a
36	chr1:120292140-120292190	ovcar-3	ovarian:	n/a
37	chr1:120284868-120284918	HPAEpiC	pulmonary alveolar:	n/a
38	chr1:120312730-120312780	BE2_C	brain:	n/a
39	chr1:120292140-120292190	HEK293	kidney:	embryo
40	chr1:120310021-120310071	NHBE	bronchial:	n/a
41	chr1:120310021-120310071	HRCEpiC	kidney:	n/a
42	chr1:120311653-120311703	HPAEpiC	pulmonary alveolar:	n/a
43	chr1:120289923-120289973	Hela-S3	cervix:	n/a
44	chr1:120292140-120292190	HRCEpiC	kidney:	n/a
45	chr1:120292140-120292190	HIPEpiC	eye:	n/a
46	chr1:120289923-120289973	NT2-D1	testis:	n/a
47	chr1:120272766-120272816	HRPEpiC	eye:	n/a
48	chr1:120292140-120292190	Hela-S3	cervix:	n/a
49	chr1:120286814-120286864	PANC-1	pancreas:	n/a
50	chr1:120311439-120311489	HMEC	breast:	n/a

(count:85 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:120266054..120268534-chr1:120274257..120277960,3	MCF-7	breast:
2	chr1:120286524..120287134-chr1:120352493..120353035,2	MCF-7	breast:
3	chr1:120286664..120287293-chr1:120416745..120417547,2	MCF-7	breast:
4	chr1:120274619..120277352-chr1:120278861..120281353,2	K562	blood:
5	chr1:120286305..120287642-chr1:120412794..120414270,15	MCF-7	breast:
6	chr1:120286505..120288307-chr1:120292207..120294976,2	K562	blood:
7	chr1:120312850..120316176-chr1:120320921..120324121,3	MCF-7	breast:
8	chr1:120188673..120191126-chr1:120281749..120284526,2	K562	blood:
9	chr1:120283662..120285685-chr1:120414247..120416692,2	MCF-7	breast:
10	chr1:120265174..120267871-chr1:120268528..120272472,4	K562	blood:
11	chr1:120265675..120267293-chr1:120269685..120271741,2	MCF-7	breast:
12	chr1:120290128..120292064-chr1:120293501..120296398,3	MCF-7	breast:
13	chr1:120286420..120287121-chr1:232656270..232657169,2	MCF-7	breast:
14	chr1:120290128..120292064-chr1:120293501..120296398,3	MCF-7	breast:
15	chr1:120279084..120281873-chr1:120323241..120326193,2	MCF-7	breast:
16	chr1:120260236..120262587-chr1:120272790..120274476,2	K562	blood:
17	chr1:120306158..120308946-chr1:120309949..120314499,4	K562	blood:
18	chr1:120261924..120264165-chr1:120287525..120289595,2	K562	blood:
19	chr1:120300548..120303157-chr1:120311431..120313956,2	MCF-7	breast:
20	chr1:120278740..120281495-chr1:120284812..120287109,2	MCF-7	breast:
21	chr1:120307608..120310232-chr1:120312392..120315286,2	MCF-7	breast:
22	chr1:120264144..120265719-chr1:120292692..120294655,2	K562	blood:
23	chr1:120265675..120267293-chr1:120269685..120271741,2	MCF-7	breast:
24	chr1:120278363..120280873-chr1:120284153..120287954,3	K562	blood:
25	chr1:120300614..120303588-chr1:120307182..120308766,2	MCF-7	breast:
26	chr1:120272371..120274124-chr1:120277944..120279657,2	K562	blood:
27	chr1:120300614..120303588-chr1:120307182..120308766,2	MCF-7	breast:
28	chr1:120286779..120287318-chr1:120313731..120314350,3	MCF-7	breast:
29	chr1:120257304..120259977-chr1:120266897..120269007,2	K562	blood:
30	chr1:120286920..120290208-chr1:120298529..120301740,3	K562	blood:
31	chr1:120274366..120276361-chr1:120277887..120280067,2	MCF-7	breast:
32	chr1:120286779..120287318-chr1:120313731..120314350,3	MCF-7	breast:
33	chr1:120302494..120304014-chr1:120308491..120310237,2	K562	blood:
34	chr1:120272664..120274375-chr1:120275952..120277511,2	MCF-7	breast:
35	chr1:120272371..120274124-chr1:120277944..120279657,2	K562	blood:
36	chr1:120278483..120280232-chr1:120286168..120288570,2	K562	blood:
37	chr1:120305431..120308946-chr1:120308988..120311839,5	K562	blood:
38	chr1:120281402..120284311-chr1:120289109..120290703,2	MCF-7	breast:
39	chr1:120266399..120268566-chr1:120269981..120272303,2	MCF-7	breast:
40	chr1:120286454..120287367-chr1:120413250..120414231,6	MCF-7	breast:
41	chr1:120286666..120287316-chr1:120351262..120352219,4	MCF-7	breast:
42	chr1:120294870..120296469-chr1:120302172..120304814,2	K562	blood:
43	chr1:120286445..120287336-chr1:120428589..120429153,3	MCF-7	breast:
44	chr1:120288807..120290729-chr1:120293224..120295388,2	MCF-7	breast:
45	chr1:120278740..120281495-chr1:120284812..120287109,2	MCF-7	breast:
46	chr1:120282346..120286075-chr1:120287322..120291391,4	K562	blood:
47	chr1:120280233..120281890-chr1:120349060..120351958,2	K562	blood:
48	chr1:120240386..120241937-chr1:120285386..120286899,2	MCF-7	breast:
49	chr1:120286505..120288307-chr1:120292207..120294976,2	K562	blood:
50	chr1:120286920..120290208-chr1:120298529..120301740,3	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PHGDH	hsa-miR-107	chr1:120285636-120285656

Variant related genes	Relation type
PHGDH	TF binding region
HMGCS2	TF binding region
PHGDH	CpG island
HMGCS2	CpG island
ENSG00000134240	chromatin interactions
ENSG00000092621	chromatin interactions
ENSG00000134193	chromatin interactions
ENSG00000143067	chromatin interactions
ENSG00000226446	chromatin interactions

Extended variants
information (count: 1778 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1778 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587704731	chr1:120266462-120266463	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs587758661	chr1:120266483-120266484	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs587656546	chr1:120266584-120266585	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs183364265	chr1:120266615-120266616	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs187132811	chr1:120266791-120266792	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs376239217	chr1:120266855-120266856	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs587742081	chr1:120266874-120266875	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs662602	chr1:120266903-120266904	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs191952424	chr1:120266936-120266937	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs142961894	chr1:120266982-120266983	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs587618884	chr1:120266984-120266985	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs587659402	chr1:120266988-120266989	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs587738997	chr1:120267018-120267019	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs183376245	chr1:120267037-120267038	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs138003411	chr1:120267059-120267060	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs45488800	chr1:120267061-120267062	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs587753946	chr1:120267075-120267076	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs587627928	chr1:120267112-120267113	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs663807	chr1:120267118-120267119	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs587752123	chr1:120267171-120267172	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs569071	chr1:120267188-120267189	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs587755349	chr1:120267190-120267191	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs149483193	chr1:120267202-120267203	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs10923893	chr1:120267220-120267221	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs587776209	chr1:120267238-120267239	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs587666264	chr1:120267269-120267270	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs77330467	chr1:120267281-120267282	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs34327221	chr1:120267283-120267284	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs201607710	chr1:120267286-120267287	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs587745924	chr1:120267287-120267288	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs78415361	chr1:120267298-120267299	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs55897028	chr1:120267299-120267300	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs587599267	chr1:120267313-120267314	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs186629673	chr1:120267374-120267375	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs113575455	chr1:120267383-120267384	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs587699542	chr1:120267390-120267391	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs143891093	chr1:120267405-120267406	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs55899400	chr1:120267431-120267432	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs483180	chr1:120267505-120267506	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs11576585	chr1:120267510-120267511	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs1886736	chr1:120267544-120267545	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs587599714	chr1:120267548-120267549	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs373843231	chr1:120267594-120267595	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs3838425	chr1:120267598-120267599	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs398089568	chr1:120267599-120267600	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs587673630	chr1:120267624-120267625	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs148608236	chr1:120267639-120267640	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs10923894	chr1:120267643-120267644	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs587614457	chr1:120267645-120267646	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs142679679	chr1:120267648-120267649	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 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
Breast cancer	21364760	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	20164920	CNVD
Cancer	21272361	CNVD
Pancreatic cancer	17952125	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	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

Chromatin state (count:1122 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:120256200-120266600	Weak transcription	Primary B cells from cord blood	blood
2	chr1:120256200-120267400	Weak transcription	Lung	lung
3	chr1:120256200-120271800	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr1:120256400-120271800	Weak transcription	Gastric	stomach
5	chr1:120256400-120276800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr1:120256400-120284400	Weak transcription	GM12878-XiMat	blood
7	chr1:120256600-120275600	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr1:120257000-120271800	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr1:120257000-120277400	Weak transcription	Fetal Heart	heart
10	chr1:120257000-120278400	Weak transcription	Rectal Smooth Muscle	rectum
11	chr1:120257000-120278600	Weak transcription	HSMM	muscle
12	chr1:120257000-120282400	Weak transcription	A549	lung
13	chr1:120257200-120287000	Weak transcription	NH-A	brain
14	chr1:120257600-120268000	Weak transcription	Fetal Brain Male	brain
15	chr1:120258600-120267200	Weak transcription	Fetal Brain Female	brain
16	chr1:120258600-120289200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr1:120258800-120269400	Weak transcription	Spleen	Spleen
18	chr1:120258800-120275000	Weak transcription	Right Atrium	heart
19	chr1:120259200-120277800	Weak transcription	Right Ventricle	heart
20	chr1:120260400-120287600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr1:120261000-120274200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr1:120261000-120287200	Strong transcription	Hela-S3	cervix
23	chr1:120261200-120269400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr1:120261400-120268800	Weak transcription	Small Intestine	intestine
25	chr1:120261400-120274800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr1:120261600-120273600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr1:120261600-120288200	Strong transcription	HUES48 Cell Line	embryonic stem cell
28	chr1:120261800-120267800	Genic enhancers	HepG2	liver
29	chr1:120261800-120281600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr1:120261800-120287000	Strong transcription	HUES6 Cell Line	embryonic stem cell
31	chr1:120261800-120287600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
32	chr1:120262000-120273200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr1:120262000-120274600	Strong transcription	Fetal Muscle Trunk	muscle
34	chr1:120262000-120284600	Strong transcription	Fetal Stomach	stomach
35	chr1:120262000-120287200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
36	chr1:120262000-120287400	Strong transcription	HUES64 Cell Line	embryonic stem cell
37	chr1:120262000-120287400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
38	chr1:120262000-120287800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr1:120262000-120288200	Strong transcription	H1 Cell Line	embryonic stem cell
40	chr1:120262200-120273800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
41	chr1:120262200-120274400	Strong transcription	Fetal Muscle Leg	muscle
42	chr1:120262200-120284400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr1:120262400-120279200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr1:120262400-120283600	Strong transcription	ES-I3 Cell Line	embryonic stem cell
45	chr1:120262400-120285000	Strong transcription	NHEK	skin
46	chr1:120262400-120287400	Strong transcription	Dnd41	blood
47	chr1:120262400-120288200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr1:120262600-120271800	Genic enhancers	Fetal Intestine Small	intestine
49	chr1:120262600-120282800	Strong transcription	H9 Cell Line	embryonic stem cell
50	chr1:120262600-120283800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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