Variant report

Variant	esv2757517
Chromosome Location	chr12:124110122-124195856
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1392)
CpG islands
(count:1895)
Chromatin interactive
region (count:136)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1392 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:124118202-124118430	K562	blood:	n/a	n/a
2	ARID3A	chr12:124118134-124118531	HepG2	liver:	n/a	n/a
3	ATF1	chr12:124118054-124118572	K562	blood:	n/a	n/a
4	ATF2	chr12:124118041-124118671	GM12878	blood:	n/a	n/a
5	ATF2	chr12:124118102-124118636	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr12:124172381-124172960	GM12878	blood:	n/a	n/a
7	ATF2	chr12:124118133-124118718	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr12:124144752-124145277	GM12878	blood:	n/a	n/a
9	ATF2	chr12:124165973-124166596	GM12878	blood:	n/a	n/a
10	ATF2	chr12:124165813-124166609	GM12878	blood:	n/a	n/a
11	ATF2	chr12:124172426-124172866	GM12878	blood:	n/a	n/a
12	ATF2	chr12:124117993-124118726	GM12878	blood:	n/a	n/a
13	ATF3	chr12:124117986-124118648	A549	lung:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
14	ATF3	chr12:124118056-124118549	K562	blood:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
15	ATF3	chr12:124118070-124118525	K562	blood:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
16	ATF3	chr12:124117981-124118734	A549	lung:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
17	ATF3	chr12:124118039-124118550	H1-hESC	embryonic stem cell:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
18	ATF3	chr12:124117982-124118633	HepG2	liver:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
19	ATF3	chr12:124190442-124190745	K562	blood:	n/a	n/a
20	ATF3	chr12:124118087-124118409	GM12878	blood:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
21	ATF3	chr12:124118019-124118526	HepG2	liver:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
22	ATF3	chr12:124118016-124118688	GM12878	blood:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
23	ATF3	chr12:124190540-124190739	K562	blood:	n/a	n/a
24	ATF3	chr12:124118086-124118563	K562	blood:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
25	ATF3	chr12:124118019-124118591	H1-hESC	embryonic stem cell:	n/a	chr12:124118170-124118179 chr12:124118312-124118332
26	BACH1	chr12:124118432-124118786	K562	blood:	n/a	n/a
27	BATF	chr12:124144904-124145195	GM12878	blood:	n/a	chr12:124145072-124145083
28	BATF	chr12:124144875-124145201	GM12878	blood:	n/a	chr12:124145072-124145083
29	BATF	chr12:124172484-124172812	GM12878	blood:	n/a	n/a
30	BATF	chr12:124166147-124166490	GM12878	blood:	n/a	n/a
31	BATF	chr12:124166177-124166501	GM12878	blood:	n/a	n/a
32	BATF	chr12:124118055-124118499	GM12878	blood:	n/a	n/a
33	BATF	chr12:124172432-124172890	GM12878	blood:	n/a	n/a
34	BCL11A	chr12:124172540-124172846	GM12878	blood:	n/a	n/a
35	BCL11A	chr12:124172504-124172853	GM12878	blood:	n/a	n/a
36	BCL11A	chr12:124166091-124166461	GM12878	blood:	n/a	n/a
37	BCL3	chr12:124117744-124118749	A549	lung:	n/a	n/a
38	BCL3	chr12:124117820-124118863	A549	lung:	n/a	n/a
39	BCL3	chr12:124117997-124118571	GM12878	blood:	n/a	n/a
40	BCLAF1	chr12:124117968-124118680	GM12878	blood:	n/a	n/a
41	BCLAF1	chr12:124166045-124166526	GM12878	blood:	n/a	n/a
42	BCLAF1	chr12:124117938-124119147	K562	blood:	n/a	chr12:124119093-124119101
43	BCLAF1	chr12:124172411-124172914	GM12878	blood:	n/a	n/a
44	BCLAF1	chr12:124139925-124140367	GM12878	blood:	n/a	n/a
45	BCLAF1	chr12:124117899-124118589	GM12878	blood:	n/a	n/a
46	BHLHE40	chr12:124117548-124118596	K562	blood:	n/a	n/a
47	BHLHE40	chr12:124146182-124146377	GM12878	blood:	n/a	n/a
48	BHLHE40	chr12:124166226-124166361	GM12878	blood:	n/a	n/a
49	BHLHE40	chr12:124155699-124155729	K562	blood:	n/a	n/a
50	BHLHE40	chr12:124172483-124172783	GM12878	blood:	n/a	n/a

(count:1895 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:124119250-124119300	HRPEpiC	eye:	n/a
2	chr12:124118386-124118436	HCM	heart:	n/a
3	chr12:124155579-124155629	HEEpiC	esophagus:	n/a
4	chr12:124155451-124155501	T-47D	breast:	n/a
5	chr12:124119250-124119300	HRPEpiC	eye:	n/a
6	chr12:124118386-124118436	HCM	heart:	n/a
7	chr12:124155579-124155629	HEEpiC	esophagus:	n/a
8	chr12:124155451-124155501	T-47D	breast:	n/a
9	chr12:124155458-124155508	HEEpiC	esophagus:	n/a
10	chr12:124145110-124145160	H1-hESC	embryonic stem cell:	embryo
11	chr12:124118264-124118314	HUVEC	blood vessel:	n/a
12	chr12:124156170-124156220	HL-60	blood:	n/a
13	chr12:124155880-124155930	SKMC	muscle:	n/a
14	chr12:124118386-124118436	A549	lung:	n/a
15	chr12:124121050-124121100	NHDF-neo	bronchial:	n/a
16	chr12:124192819-124192869	AG09319	gingival:	n/a
17	chr12:124118052-124118102	ProgFib	skin:	n/a
18	chr12:124155458-124155508	Hepatocyte	liver:	n/a
19	chr12:124155451-124155501	GM19239	blood:	n/a
20	chr12:124154378-124154428	GM19239	blood:	n/a
21	chr12:124156170-124156220	GM06990	blood:	n/a
22	chr12:124121050-124121100	SK-N-MC	brain:	n/a
23	chr12:124155579-124155629	RPTEC	kidney:	n/a
24	chr12:124119053-124119103	NB4	blood:	n/a
25	chr12:124118184-124118234	RPTEC	kidney:	n/a
26	chr12:124118360-124118410	HRCEpiC	kidney:	n/a
27	chr12:124144432-124144482	AG04450	lung:	fetal
28	chr12:124156170-124156220	K562	blood:	n/a
29	chr12:124155594-124155644	SK-N-SH	brain:	n/a
30	chr12:124155451-124155501	A549	lung:	n/a
31	chr12:124158499-124158549	SAEC	small airway:	n/a
32	chr12:124115280-124115330	NB4	blood:	n/a
33	chr12:124154378-124154428	GM12878	blood:	n/a
34	chr12:124118386-124118436	HCPEpiC	choroid plexus:	n/a
35	chr12:124118329-124118379	K562	blood:	n/a
36	chr12:124158499-124158549	NH-A	brain:	n/a
37	chr12:124155712-124155762	AG10803	skin:	n/a
38	chr12:124118326-124118376	LNCaP	prostate:	n/a
39	chr12:124118329-124118379	NH-A	brain:	n/a
40	chr12:124115280-124115330	AoSMC	blood vessel:	n/a
41	chr12:124154378-124154428	HEEpiC	esophagus:	n/a
42	chr12:124118326-124118376	U87	brain:	n/a
43	chr12:124116920-124116970	ovcar-3	ovarian:	n/a
44	chr12:124158499-124158549	HL-60	blood:	n/a
45	chr12:124118326-124118376	A549	lung:	n/a
46	chr12:124118386-124118436	IMR90	lung:	fetal
47	chr12:124145110-124145160	HIPEpiC	eye:	n/a
48	chr12:124155579-124155629	NT2-D1	testis:	n/a
49	chr12:124116920-124116970	HEK293	kidney:	embryo
50	chr12:124155579-124155629	SK-N-SH_RA	brain:	n/a

(count:136 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:123753793..123756876-chr12:124117523..124121813,4	K562	blood:
2	chr12:124131124..124134135-chr12:124154416..124157411,3	K562	blood:
3	chr12:124116825..124119400-chr12:124154444..124157055,3	MCF-7	breast:
4	chr12:124125615..124128872-chr12:124133075..124135751,3	MCF-7	breast:
5	chr12:124157620..124159905-chr12:124196914..124199226,2	K562	blood:
6	chr12:124116659..124120709-chr12:124455290..124460616,5	K562	blood:
7	chr12:124189784..124191716-chr12:124194882..124197193,2	K562	blood:
8	chr12:124105043..124107387-chr12:124113363..124115205,2	K562	blood:
9	chr12:124188235..124191139-chr12:124193941..124195953,3	MCF-7	breast:
10	chr12:124157024..124160371-chr12:124188986..124191737,3	MCF-7	breast:
11	chr12:124105734..124108451-chr12:124133249..124135719,2	K562	blood:
12	chr12:124127308..124129753-chr12:124158031..124160799,2	K562	blood:
13	chr12:124157962..124160129-chr12:124161284..124163771,2	MCF-7	breast:
14	chr12:124109158..124110697-chr12:124113991..124116759,2	K562	blood:
15	chr12:123753772..123755288-chr12:124118042..124119686,2	MCF-7	breast:
16	chr12:124105722..124107597-chr12:124119086..124122015,4	K562	blood:
17	chr12:124155436..124158746-chr12:124195101..124198299,4	MCF-7	breast:
18	chr12:124150219..124152252-chr12:124155815..124157987,2	MCF-7	breast:
19	chr12:124107998..124110847-chr12:124196796..124199749,2	MCF-7	breast:
20	chr12:124143980..124146532-chr12:124155769..124157495,2	MCF-7	breast:
21	chr12:124084509..124086598-chr12:124112180..124115159,2	K562	blood:
22	chr12:124115420..124119615-chr12:124195159..124199573,8	MCF-7	breast:
23	chr12:124117633..124120865-chr12:124133499..124139438,5	K562	blood:
24	chr12:124157962..124160129-chr12:124161284..124163771,2	MCF-7	breast:
25	chr12:124116424..124121252-chr12:124194298..124198817,7	K562	blood:
26	chr12:124188235..124191139-chr12:124193941..124195953,3	MCF-7	breast:
27	chr12:124172137..124174302-chr12:124194954..124197751,2	MCF-7	breast:
28	chr12:124155020..124157089-chr12:124215035..124217819,2	MCF-7	breast:
29	chr12:124130507..124132191-chr12:124132895..124134450,2	MCF-7	breast:
30	chr12:124176790..124178829-chr12:124179921..124182332,2	K562	blood:
31	chr12:124130618..124132144-chr12:124154341..124156246,2	MCF-7	breast:
32	chr12:124125615..124128872-chr12:124133075..124135751,3	MCF-7	breast:
33	chr12:123875063..123876805-chr12:124118427..124120711,2	K562	blood:
34	chr12:124085496..124088026-chr12:124116630..124119648,4	MCF-7	breast:
35	chr12:124195749..124198082-chr12:124236149..124239807,3	MCF-7	breast:
36	chr12:124117633..124119272-chr12:124133499..124136176,2	K562	blood:
37	chr12:124186888..124189233-chr12:124196275..124198488,2	MCF-7	breast:
38	chr12:123755830..123757417-chr12:124116609..124118455,2	MCF-7	breast:
39	chr12:124157024..124160371-chr12:124188986..124191737,3	MCF-7	breast:
40	chr12:124117557..124118523-chr17:78120518..78121066,2	Hela-S3	cervix:
41	chr12:124171218..124172882-chr12:124173161..124174693,2	K562	blood:
42	chr12:124119318..124121767-chr12:124194183..124197056,2	MCF-7	breast:
43	chr12:124117107..124120837-chr12:124123304..124127842,5	MCF-7	breast:
44	chr12:124068831..124072178-chr12:124116882..124120107,5	K562	blood:
45	chr12:124185897..124191093-chr12:124195290..124198994,7	MCF-7	breast:
46	chr12:124181824..124184450-chr12:124186002..124188364,2	K562	blood:
47	chr12:124173898..124176239-chr12:124177848..124179680,2	MCF-7	breast:
48	chr12:124084914..124087862-chr12:124122413..124125179,2	K562	blood:
49	chr12:124176790..124178829-chr12:124179921..124182332,2	K562	blood:
50	chr12:123847883..123849879-chr12:124118467..124120545,3	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
GTF2H3	TF binding region
TCTN2	TF binding region
ENSG00000255839	TF binding region
EIF2B1	TF binding region
ATP6V0A2	TF binding region
GTF2H3	CpG island
TCTN2	CpG island
ENSG00000255839	CpG island
EIF2B1	CpG island
ATP6V0A2	CpG island
ENSG00000136450	chromatin interactions
ENSG00000184575	chromatin interactions
ENSG00000111361	chromatin interactions
ENSG00000256092	chromatin interactions
ENSG00000247373	chromatin interactions
ENSG00000119242	chromatin interactions
ENSG00000051825	chromatin interactions
ENSG00000270095	chromatin interactions
ENSG00000111358	chromatin interactions
ENSG00000111364	chromatin interactions
ENSG00000168778	chromatin interactions
ENSG00000111328	chromatin interactions
ENSG00000139697	chromatin interactions
ENSG00000185344	chromatin interactions
ENSG00000178882	chromatin interactions
ENSG00000179195	chromatin interactions
ENSG00000130921	chromatin interactions
ENSG00000183955	chromatin interactions
ENSG00000255839	chromatin interactions
ENSG00000188026	chromatin interactions
ENSG00000086598	chromatin interactions
ENSG00000141543	chromatin interactions

Extended variants
information (count: 3443 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:3443 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1060637	chr12:124110122-124110123	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs373611459	chr12:124110135-124110136	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs3789968	chr12:124110161-124110162	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs192080943	chr12:124110203-124110204	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs538210295	chr12:124110221-124110222	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs142764242	chr12:124110235-124110236	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs569159521	chr12:124110311-124110312	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs184112835	chr12:124110336-124110337	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs555293285	chr12:124110420-124110421	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs573337551	chr12:124110444-124110445	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs540859664	chr12:124110515-124110516	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs186680021	chr12:124110536-124110537	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs147396112	chr12:124110552-124110553	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs369495379	chr12:124110556-124110557	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs191447204	chr12:124110599-124110600	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs562882072	chr12:124110617-124110618	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs182533252	chr12:124110621-124110622	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs11831129	chr12:124110675-124110676	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs141248531	chr12:124110691-124110692	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs531166408	chr12:124110699-124110700	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs367702612	chr12:124110702-124110703	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs561263860	chr12:124110726-124110727	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs528258359	chr12:124110793-124110794	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs71458809	chr12:124110798-124110799	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs546785529	chr12:124110799-124110800	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs369139045	chr12:124110802-124110803	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs564608300	chr12:124110815-124110816	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs149944921	chr12:124110861-124110862	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs73414295	chr12:124110885-124110886	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs568510703	chr12:124110892-124110893	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs536275457	chr12:124110902-124110903	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs373489547	chr12:124110914-124110915	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs3704	chr12:124110934-124110935	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs375884336	chr12:124110941-124110942	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs368908018	chr12:124110946-124110947	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs373998526	chr12:124110950-124110951	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs199673798	chr12:124110957-124110958	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs139071270	chr12:124110974-124110975	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs201342513	chr12:124111006-124111007	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs112623314	chr12:124111012-124111013	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs559110064	chr12:124111052-124111053	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs79606093	chr12:124111062-124111063	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs538334370	chr12:124111095-124111096	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs563789582	chr12:124111109-124111110	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs529385739	chr12:124111149-124111150	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs187318234	chr12:124111199-124111200	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs542242816	chr12:124111329-124111330	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs144193478	chr12:124111343-124111344	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs201561704	chr12:124111347-124111348	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs573111325	chr12:124111351-124111352	Weak transcription Strong transcription	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:3164 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:124088200-124116000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr12:124088200-124117000	Strong transcription	Fetal Stomach	stomach
3	chr12:124088400-124116000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr12:124088400-124116000	Strong transcription	HUES48 Cell Line	embryonic stem cell
5	chr12:124088400-124116000	Strong transcription	HUES64 Cell Line	embryonic stem cell
6	chr12:124088400-124116000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr12:124088400-124116000	Strong transcription	Sigmoid Colon	Sigmoid Colon
8	chr12:124088400-124116200	Strong transcription	HUES6 Cell Line	embryonic stem cell
9	chr12:124088400-124116800	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr12:124088400-124117000	Strong transcription	Fetal Intestine Small	intestine
11	chr12:124088600-124116000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr12:124088600-124116000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
13	chr12:124088600-124116000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
14	chr12:124088600-124116000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr12:124088600-124116000	Strong transcription	Duodenum Smooth Muscle	Duodenum
16	chr12:124088600-124116000	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr12:124088600-124116200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr12:124088600-124116200	Strong transcription	Fetal Thymus	thymus
19	chr12:124088600-124116800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr12:124088600-124116800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr12:124088600-124116800	Strong transcription	Fetal Muscle Trunk	muscle
22	chr12:124088600-124117000	Strong transcription	Primary B cells from peripheral blood	blood
23	chr12:124088800-124116000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr12:124088800-124116000	Strong transcription	Cortex derived primary cultured neurospheres	brain
25	chr12:124088800-124116000	Strong transcription	Fetal Intestine Large	intestine
26	chr12:124089000-124116000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr12:124089000-124116200	Strong transcription	Brain Germinal Matrix	brain
28	chr12:124089200-124115400	Strong transcription	Primary T helper cells fromperipheralblood	blood
29	chr12:124089200-124116000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr12:124089200-124116000	Strong transcription	Primary T helper cells PMA-I stimulated	--
31	chr12:124089200-124116000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr12:124089200-124116200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr12:124089200-124116400	Strong transcription	Liver	Liver
34	chr12:124089200-124116600	Strong transcription	Stomach Smooth Muscle	stomach
35	chr12:124089600-124116000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr12:124089600-124116000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr12:124089600-124116000	Strong transcription	Duodenum Mucosa	Duodenum
38	chr12:124089800-124116200	Strong transcription	Thymus	Thymus
39	chr12:124089800-124117000	Strong transcription	Placenta	Placenta
40	chr12:124090000-124115600	Strong transcription	GM12878-XiMat	blood
41	chr12:124090000-124116000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
42	chr12:124090000-124116000	Strong transcription	Primary B cells from cord blood	blood
43	chr12:124090000-124116000	Strong transcription	Primary T cells from cord blood	blood
44	chr12:124090200-124116000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr12:124090200-124116000	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr12:124090200-124116000	Strong transcription	Rectal Smooth Muscle	rectum
47	chr12:124090200-124116200	Strong transcription	Primary neutrophils fromperipheralblood	blood
48	chr12:124090200-124116200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr12:124090200-124116200	Strong transcription	Brain Anterior Caudate	brain
50	chr12:124090200-124116800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood

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