Variant report

Variant	nsv560498
Chromosome Location	chr12:124129924-124195856
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:606)
CpG islands
(count:856)
Chromatin interactive
region (count:84)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:606 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:124172381-124172960	GM12878	blood:	n/a	n/a
2	ATF2	chr12:124172426-124172866	GM12878	blood:	n/a	n/a
3	ATF2	chr12:124144752-124145277	GM12878	blood:	n/a	n/a
4	ATF2	chr12:124165973-124166596	GM12878	blood:	n/a	n/a
5	ATF2	chr12:124165813-124166609	GM12878	blood:	n/a	n/a
6	ATF3	chr12:124190442-124190745	K562	blood:	n/a	n/a
7	ATF3	chr12:124190540-124190739	K562	blood:	n/a	n/a
8	BATF	chr12:124166147-124166490	GM12878	blood:	n/a	n/a
9	BATF	chr12:124172432-124172890	GM12878	blood:	n/a	n/a
10	BATF	chr12:124172484-124172812	GM12878	blood:	n/a	n/a
11	BATF	chr12:124144875-124145201	GM12878	blood:	n/a	chr12:124145072-124145083
12	BATF	chr12:124144904-124145195	GM12878	blood:	n/a	chr12:124145072-124145083
13	BATF	chr12:124166177-124166501	GM12878	blood:	n/a	n/a
14	BCL11A	chr12:124172504-124172853	GM12878	blood:	n/a	n/a
15	BCL11A	chr12:124172540-124172846	GM12878	blood:	n/a	n/a
16	BCL11A	chr12:124166091-124166461	GM12878	blood:	n/a	n/a
17	BCLAF1	chr12:124166045-124166526	GM12878	blood:	n/a	n/a
18	BCLAF1	chr12:124139925-124140367	GM12878	blood:	n/a	n/a
19	BCLAF1	chr12:124172411-124172914	GM12878	blood:	n/a	n/a
20	BHLHE40	chr12:124139600-124140393	GM12878	blood:	n/a	n/a
21	BHLHE40	chr12:124146182-124146377	GM12878	blood:	n/a	n/a
22	BHLHE40	chr12:124155699-124155729	K562	blood:	n/a	n/a
23	BHLHE40	chr12:124166226-124166361	GM12878	blood:	n/a	n/a
24	BHLHE40	chr12:124172483-124172783	GM12878	blood:	n/a	n/a
25	BRCA1	chr12:124133994-124134134	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr12:124147878-124148212	K562	blood:	n/a	n/a
27	CEBPB	chr12:124188933-124189113	A549	lung:	n/a	n/a
28	CEBPB	chr12:124155361-124155613	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr12:124166212-124166455	A549	lung:	n/a	chr12:124166370-124166381
30	CEBPB	chr12:124144946-124145307	A549	lung:	n/a	n/a
31	CEBPB	chr12:124166291-124166506	HepG2	liver:	n/a	chr12:124166370-124166381
32	CEBPB	chr12:124146435-124146820	MCF-7	breast:	n/a	chr12:124146632-124146643
33	CEBPB	chr12:124144941-124145298	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr12:124163883-124164027	K562	blood:	n/a	chr12:124163964-124163975
35	CEBPB	chr12:124144925-124145317	IMR90	lung:	n/a	n/a
36	CEBPB	chr12:124163947-124163977	HepG2	liver:	n/a	chr12:124163964-124163975
37	CEBPB	chr12:124146622-124146730	HepG2	liver:	n/a	chr12:124146632-124146643
38	CEBPB	chr12:124188889-124189157	HepG2	liver:	n/a	n/a
39	CEBPB	chr12:124144964-124145165	K562	blood:	n/a	n/a
40	CEBPB	chr12:124166279-124166491	IMR90	lung:	n/a	chr12:124166370-124166381
41	CEBPB	chr12:124166289-124166474	K562	blood:	n/a	chr12:124166370-124166381
42	CEBPB	chr12:124155348-124155869	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr12:124144969-124145294	K562	blood:	n/a	n/a
44	CEBPB	chr12:124155498-124155638	K562	blood:	n/a	n/a
45	CEBPB	chr12:124146558-124146645	K562	blood:	n/a	chr12:124146632-124146643
46	CEBPB	chr12:124144822-124145387	A549	lung:	n/a	n/a
47	CEBPB	chr12:124144926-124145288	MCF-7	breast:	n/a	n/a
48	CEBPB	chr12:124172369-124173000	GM12878	blood:	n/a	n/a
49	CEBPB	chr12:124155414-124155714	HepG2	liver:	n/a	n/a
50	CHD2	chr12:124155500-124155791	H1-hESC	embryonic stem cell:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:124154378-124154428	HRPEpiC	eye:	n/a
2	chr12:124156170-124156220	HNPCEpiC	eye:	n/a
3	chr12:124154378-124154428	HRPEpiC	eye:	n/a
4	chr12:124156170-124156220	HNPCEpiC	eye:	n/a
5	chr12:124145110-124145160	HEK293	kidney:	embryo
6	chr12:124158499-124158549	HRE	kidney:	n/a
7	chr12:124155712-124155762	IMR90	lung:	fetal
8	chr12:124155880-124155930	GM12892	blood:	n/a
9	chr12:124192819-124192869	SK-N-SH_RA	brain:	n/a
10	chr12:124154378-124154428	GM19239	blood:	n/a
11	chr12:124154378-124154428	Jurkat	blood:	n/a
12	chr12:124155712-124155762	BJ	skin:	n/a
13	chr12:124155620-124155670	U87	brain:	n/a
14	chr12:124192819-124192869	MCF10A-Er-Src	breast:	n/a
15	chr12:124158499-124158549	SKMC	muscle:	n/a
16	chr12:124155458-124155508	Hepatocyte	liver:	n/a
17	chr12:124192819-124192869	HepG2	liver:	n/a
18	chr12:124155712-124155762	AG09309	skin:	n/a
19	chr12:124144432-124144482	SAEC	small airway:	n/a
20	chr12:124156159-124156209	HRPEpiC	eye:	n/a
21	chr12:124155451-124155501	U87	brain:	n/a
22	chr12:124154378-124154428	AG09309	skin:	n/a
23	chr12:124155451-124155501	AG04450	lung:	fetal
24	chr12:124144432-124144482	HEEpiC	esophagus:	n/a
25	chr12:124155451-124155501	HRE	kidney:	n/a
26	chr12:124155712-124155762	HAEpiC	amniotic membrane:	n/a
27	chr12:124144432-124144482	Hepatocyte	liver:	n/a
28	chr12:124156159-124156209	SAEC	small airway:	n/a
29	chr12:124155712-124155762	NB4	blood:	n/a
30	chr12:124155712-124155762	LNCaP	prostate:	n/a
31	chr12:124144432-124144482	PrEC	prostate:	n/a
32	chr12:124156159-124156209	RPTEC	kidney:	n/a
33	chr12:124155880-124155930	HAEpiC	amniotic membrane:	n/a
34	chr12:124155579-124155629	HUVEC	blood vessel:	n/a
35	chr12:124156170-124156220	HMEC	breast:	n/a
36	chr12:124155594-124155644	Hela-S3	cervix:	n/a
37	chr12:124155579-124155629	BE2_C	brain:	n/a
38	chr12:124145110-124145160	ovcar-3	ovarian:	n/a
39	chr12:124145110-124145160	HepG2	liver:	n/a
40	chr12:124155458-124155508	MCF-7	breast:	n/a
41	chr12:124155451-124155501	AG10803	skin:	n/a
42	chr12:124154378-124154428	GM12891	blood:	n/a
43	chr12:124156159-124156209	AG04450	lung:	fetal
44	chr12:124155579-124155629	HL-60	blood:	n/a
45	chr12:124155451-124155501	HCPEpiC	choroid plexus:	n/a
46	chr12:124154378-124154428	HMEC	breast:	n/a
47	chr12:124155712-124155762	SK-N-SH_RA	brain:	n/a
48	chr12:124155620-124155670	SK-N-MC	brain:	n/a
49	chr12:124158499-124158549	NHDF-neo	bronchial:	n/a
50	chr12:124155458-124155508	GM12892	blood:	n/a

(count:84 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:124137919..124140915-chr12:124140949..124142983,2	MCF-7	breast:
2	chr12:124118193..124121025-chr12:124132767..124136539,4	MCF-7	breast:
3	chr12:124195139..124196741-chr12:124216677..124218308,2	MCF-7	breast:
4	chr12:124131124..124134135-chr12:124154416..124157411,3	K562	blood:
5	chr12:124150219..124152252-chr12:124155815..124157987,2	MCF-7	breast:
6	chr12:124157024..124160371-chr12:124188986..124191737,3	MCF-7	breast:
7	chr12:124157962..124160129-chr12:124161284..124163771,2	MCF-7	breast:
8	chr12:124125615..124128872-chr12:124133075..124135751,3	MCF-7	breast:
9	chr12:123847805..123850449-chr12:124195534..124198038,2	K562	blood:
10	chr12:124116825..124119400-chr12:124154444..124157055,3	MCF-7	breast:
11	chr12:124131124..124134135-chr12:124154416..124157411,3	K562	blood:
12	chr12:124155436..124158746-chr12:124195101..124198299,4	MCF-7	breast:
13	chr12:124150219..124152252-chr12:124155815..124157987,2	MCF-7	breast:
14	chr12:124143980..124146532-chr12:124155769..124157495,2	MCF-7	breast:
15	chr12:124127308..124129753-chr12:124158031..124160799,2	K562	blood:
16	chr12:124150313..124152080-chr12:124154611..124157419,2	MCF-7	breast:
17	chr12:124117774..124119426-chr12:124160532..124162075,2	K562	blood:
18	chr12:124116424..124121252-chr12:124194298..124198817,7	K562	blood:
19	chr12:124155020..124157089-chr12:124215035..124217819,2	MCF-7	breast:
20	chr12:124187896..124189887-chr12:124195478..124197199,2	K562	blood:
21	chr12:124141910..124144216-chr12:124195360..124197441,2	MCF-7	breast:
22	chr12:124176790..124178829-chr12:124179921..124182332,2	K562	blood:
23	chr12:124134030..124137334-chr12:124197093..124199913,4	MCF-7	breast:
24	chr12:124115420..124119615-chr12:124195159..124199573,8	MCF-7	breast:
25	chr12:124120951..124123869-chr12:124130412..124132116,2	K562	blood:
26	chr12:124128608..124131370-chr12:124135245..124137740,4	K562	blood:
27	chr12:124191295..124193347-chr12:124194777..124198625,4	MCF-7	breast:
28	chr12:124123949..124126710-chr12:124128875..124131426,2	K562	blood:
29	chr12:124157962..124160129-chr12:124161284..124163771,2	MCF-7	breast:
30	chr12:124185982..124187602-chr12:124193943..124196577,2	K562	blood:
31	chr12:124105734..124108451-chr12:124133249..124135719,2	K562	blood:
32	chr12:124143980..124146532-chr12:124155769..124157495,2	MCF-7	breast:
33	chr12:124195456..124198460-chr12:124455550..124458339,3	MCF-7	breast:
34	chr12:124154048..124155942-chr12:124162322..124165220,2	K562	blood:
35	chr12:123716636..123719388-chr12:124194108..124196844,2	K562	blood:
36	chr12:124177268..124179844-chr12:124184486..124185994,2	K562	blood:
37	chr12:124154972..124157295-chr12:124158575..124161176,3	K562	blood:
38	chr12:123755242..123756973-chr12:124144725..124146660,2	K562	blood:
39	chr12:124194853..124196399-chr12:124201524..124203920,2	K562	blood:
40	chr12:124155376..124157580-chr12:124194948..124197481,2	K562	blood:
41	chr12:124195458..124197705-chr12:124223204..124225071,2	MCF-7	breast:
42	chr12:124095180..124096998-chr12:124140972..124143607,2	MCF-7	breast:
43	chr12:124190696..124192494-chr12:124194252..124196865,2	K562	blood:
44	chr12:124130618..124132144-chr12:124154341..124156246,2	MCF-7	breast:
45	chr12:124171218..124172882-chr12:124173161..124174693,2	K562	blood:
46	chr12:124155686..124156232-chr17:56084289..56085093,2	HCT-116	colon:
47	chr12:124128608..124131370-chr12:124135245..124137740,4	K562	blood:
48	chr12:124120301..124122353-chr12:124128299..124130201,3	K562	blood:
49	chr12:124173898..124176239-chr12:124177848..124179680,2	MCF-7	breast:
50	chr12:124157620..124159905-chr12:124196914..124199226,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF2B1-3	chr12:124192789-124192933	ENSG00000255839
2	lnc-EIF2B1-3	chr12:124192149-124192324	ENSG00000255839

No data

Variant related genes	Relation type
ENSG00000255839	TF binding region
GTF2H3	TF binding region
ATP6V0A2	TF binding region
TCTN2	TF binding region
ENSG00000255839	CpG island
GTF2H3	CpG island
ATP6V0A2	CpG island
TCTN2	CpG island
ENSG00000130921	chromatin interactions
ENSG00000179195	chromatin interactions
ENSG00000119242	chromatin interactions
ENSG00000139697	chromatin interactions
ENSG00000168778	chromatin interactions
ENSG00000111328	chromatin interactions
ENSG00000256092	chromatin interactions
ENSG00000185344	chromatin interactions
ENSG00000270095	chromatin interactions
ENSG00000178882	chromatin interactions
ENSG00000111358	chromatin interactions
ENSG00000136450	chromatin interactions
ENSG00000111361	chromatin interactions
ENSG00000255839	chromatin interactions
ENSG00000051825	chromatin interactions

Extended variants
information (count: 2623 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:2623 , 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	rs11057315	chr12:124129924-124129925	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371943448	chr12:124129952-124129953	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs3817308	chr12:124129969-124129970	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs79670068	chr12:124129994-124129995	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs374884792	chr12:124129995-124129996	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs141727968	chr12:124130020-124130021	Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs376533282	chr12:124130029-124130030	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs147119955	chr12:124130049-124130050	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs372822888	chr12:124130055-124130056	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs138518883	chr12:124130059-124130060	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs183940144	chr12:124130064-124130065	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs530270065	chr12:124130065-124130066	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs2292702	chr12:124130128-124130129	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs377205247	chr12:124130153-124130154	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs560775605	chr12:124130183-124130184	Strong transcription Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs527778791	chr12:124130205-124130206	Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs547857880	chr12:124130231-124130232	Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs552664901	chr12:124130317-124130318	Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs112899428	chr12:124130369-124130370	Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs186678000	chr12:124130382-124130383	Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs11572953	chr12:124130385-124130386	Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs550435826	chr12:124130386-124130387	Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs10846535	chr12:124130388-124130389	Strong transcription Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs11572954	chr12:124130407-124130408	Strong transcription Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs191438980	chr12:124130433-124130434	Strong transcription Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs10846536	chr12:124130480-124130481	Strong transcription Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs182521093	chr12:124130535-124130536	Strong transcription Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs558653846	chr12:124130538-124130539	Strong transcription Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs576735089	chr12:124130549-124130550	Strong transcription Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs569978710	chr12:124130609-124130610	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs544230625	chr12:124130627-124130628	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs11572955	chr12:124130631-124130632	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs575174451	chr12:124130650-124130651	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs542589902	chr12:124130691-124130692	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs560456947	chr12:124130692-124130693	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs527918073	chr12:124130744-124130745	Strong transcription Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs11572956	chr12:124130802-124130803	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs34427180	chr12:124130803-124130804	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs398040222	chr12:124130820-124130821	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs201230414	chr12:124130843-124130844	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs187312656	chr12:124130885-124130886	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs531553840	chr12:124130886-124130887	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs113187553	chr12:124130925-124130926	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs549774277	chr12:124131032-124131033	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs568157033	chr12:124131043-124131044	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs574683515	chr12:124131044-124131045	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs11572957	chr12:124131049-124131050	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs566534024	chr12:124131064-124131065	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs534012782	chr12:124131125-124131126	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs558322407	chr12:124131183-124131184	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2132 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:124119200-124130000	Weak transcription	Pancreas	Pancrea
2	chr12:124119200-124130200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:124119200-124130200	Weak transcription	Right Ventricle	heart
4	chr12:124119200-124141000	Weak transcription	Aorta	Aorta
5	chr12:124119200-124155200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr12:124119400-124130200	Weak transcription	Fetal Kidney	kidney
7	chr12:124119400-124130200	Weak transcription	Gastric	stomach
8	chr12:124119400-124131200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr12:124119400-124132000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr12:124119600-124130000	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr12:124119600-124139000	Weak transcription	Fetal Heart	heart
12	chr12:124119600-124140600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr12:124119600-124143000	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr12:124119800-124130000	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr12:124119800-124130200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr12:124119800-124130200	Weak transcription	Spleen	Spleen
17	chr12:124119800-124134000	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr12:124119800-124134800	Weak transcription	Brain Germinal Matrix	brain
19	chr12:124119800-124146200	Weak transcription	Psoas Muscle	Psoas
20	chr12:124119800-124155200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr12:124121400-124144000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr12:124123200-124142600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr12:124123800-124137200	Strong transcription	Fetal Muscle Trunk	muscle
24	chr12:124123800-124142600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr12:124124000-124145600	Strong transcription	HUES64 Cell Line	embryonic stem cell
26	chr12:124124000-124146400	Strong transcription	Fetal Thymus	thymus
27	chr12:124124000-124148200	Strong transcription	Primary T cells from cord blood	blood
28	chr12:124124200-124136600	Strong transcription	Fetal Stomach	stomach
29	chr12:124124400-124136200	Strong transcription	Fetal Intestine Small	intestine
30	chr12:124124400-124136600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr12:124124400-124138200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr12:124124600-124130000	Weak transcription	Osteobl	bone
33	chr12:124124800-124130000	Weak transcription	Brain Angular Gyrus	brain
34	chr12:124124800-124130000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr12:124124800-124130000	Weak transcription	NH-A	brain
36	chr12:124125000-124146600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr12:124125600-124146800	Weak transcription	Small Intestine	intestine
38	chr12:124126200-124142600	Strong transcription	HUES6 Cell Line	embryonic stem cell
39	chr12:124126200-124148200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr12:124126400-124132600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr12:124126400-124142400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr12:124126600-124137600	Strong transcription	Duodenum Mucosa	Duodenum
43	chr12:124126800-124134000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr12:124126800-124137200	Strong transcription	Primary T cells fromperipheralblood	blood
45	chr12:124126800-124137200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr12:124126800-124142600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr12:124126800-124145800	Strong transcription	Primary T helper cells fromperipheralblood	blood
48	chr12:124126800-124148000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr12:124127000-124136400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr12:124127000-124137000	Strong transcription	K562	blood

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