Variant report

Variant	nsv1040061
Chromosome Location	chr12:118648415-118800437
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1662)
CpG islands
(count:305)
Chromatin interactive
region (count:129)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1662 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:118776752-118776947	K562	blood:	n/a	n/a
2	ARID3A	chr12:118775006-118775188	K562	blood:	n/a	n/a
3	ARID3A	chr12:118757499-118757759	K562	blood:	n/a	n/a
4	ARID3A	chr12:118794909-118797601	K562	blood:	n/a	chr12:118795855-118795871 chr12:118795856-118795872
5	ARID3A	chr12:118659728-118660141	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:118767517-118768711	K562	blood:	n/a	n/a
7	ARID3A	chr12:118785125-118785126	K562	blood:	n/a	n/a
8	ARID3A	chr12:118798421-118799202	K562	blood:	n/a	n/a
9	ARID3A	chr12:118789073-118789336	HepG2	liver:	n/a	n/a
10	ARID3A	chr12:118725664-118726444	K562	blood:	n/a	n/a
11	ARID3A	chr12:118747592-118747909	K562	blood:	n/a	n/a
12	ARID3A	chr12:118783078-118783600	K562	blood:	n/a	chr12:118783100-118783116
13	ATF1	chr12:118770412-118770654	K562	blood:	n/a	n/a
14	ATF1	chr12:118747580-118747681	K562	blood:	n/a	n/a
15	ATF1	chr12:118795123-118795665	K562	blood:	n/a	n/a
16	ATF1	chr12:118768175-118768520	K562	blood:	n/a	n/a
17	ATF1	chr12:118726099-118726318	K562	blood:	n/a	n/a
18	ATF2	chr12:118792682-118793158	GM12878	blood:	n/a	n/a
19	ATF2	chr12:118794642-118795906	GM12878	blood:	n/a	n/a
20	ATF2	chr12:118794992-118795693	GM12878	blood:	n/a	n/a
21	ATF2	chr12:118744751-118745630	GM12878	blood:	n/a	n/a
22	ATF2	chr12:118750304-118750819	GM12878	blood:	n/a	n/a
23	ATF2	chr12:118750243-118750781	GM12878	blood:	n/a	n/a
24	ATF3	chr12:118798626-118798938	K562	blood:	n/a	n/a
25	ATF3	chr12:118760680-118760999	K562	blood:	n/a	n/a
26	BACH1	chr12:118757434-118757824	K562	blood:	n/a	n/a
27	BACH1	chr12:118715665-118716093	K562	blood:	n/a	n/a
28	BACH1	chr12:118783167-118783299	K562	blood:	n/a	n/a
29	BATF	chr12:118750339-118750660	GM12878	blood:	n/a	n/a
30	BATF	chr12:118750332-118750730	GM12878	blood:	n/a	n/a
31	BATF	chr12:118765637-118765993	GM12878	blood:	n/a	chr12:118765770-118765781
32	BATF	chr12:118689417-118689668	GM12878	blood:	n/a	n/a
33	BATF	chr12:118741985-118742269	GM12878	blood:	n/a	n/a
34	BATF	chr12:118765710-118765913	GM12878	blood:	n/a	chr12:118765770-118765781
35	BATF	chr12:118744771-118745254	GM12878	blood:	n/a	chr12:118744998-118745009
36	BATF	chr12:118744836-118745142	GM12878	blood:	n/a	chr12:118744998-118745009
37	BCL11A	chr12:118750375-118750755	GM12878	blood:	n/a	n/a
38	BCL11A	chr12:118674790-118675224	GM12878	blood:	n/a	chr12:118675058-118675067
39	BCL11A	chr12:118674866-118675185	GM12878	blood:	n/a	chr12:118675058-118675067
40	BCL11A	chr12:118750417-118750694	GM12878	blood:	n/a	n/a
41	BCL11A	chr12:118744829-118745165	GM12878	blood:	n/a	n/a
42	BCL3	chr12:118658664-118658891	GM12878	blood:	n/a	n/a
43	BCLAF1	chr12:118765522-118765946	GM12878	blood:	n/a	n/a
44	BCLAF1	chr12:118674680-118675262	GM12878	blood:	n/a	chr12:118675058-118675067
45	BCLAF1	chr12:118750273-118750876	GM12878	blood:	n/a	n/a
46	BCLAF1	chr12:118744805-118745730	GM12878	blood:	n/a	n/a
47	BHLHE40	chr12:118737807-118738444	GM12878	blood:	n/a	n/a
48	BHLHE40	chr12:118795037-118795902	GM12878	blood:	n/a	n/a
49	BHLHE40	chr12:118784671-118785194	GM12878	blood:	n/a	n/a
50	BHLHE40	chr12:118744671-118745674	GM12878	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:118782453-118782503	AoSMC	blood vessel:	n/a
2	chr12:118683952-118684002	Caco-2	colon:	n/a
3	chr12:118782453-118782503	NHDF-neo	bronchial:	n/a
4	chr12:118728016-118728066	HAEpiC	amniotic membrane:	n/a
5	chr12:118728016-118728066	NB4	blood:	n/a
6	chr12:118775197-118775247	NT2-D1	testis:	n/a
7	chr12:118683952-118684002	HCM	heart:	n/a
8	chr12:118797027-118797077	AG10803	skin:	n/a
9	chr12:118797027-118797077	HAEpiC	amniotic membrane:	n/a
10	chr12:118775197-118775247	T-47D	breast:	n/a
11	chr12:118683952-118684002	SK-N-SH_RA	brain:	n/a
12	chr12:118775197-118775247	A549	lung:	n/a
13	chr12:118775197-118775247	AoSMC	blood vessel:	n/a
14	chr12:118782453-118782503	ProgFib	skin:	n/a
15	chr12:118797027-118797077	HIPEpiC	eye:	n/a
16	chr12:118683952-118684002	ovcar-3	ovarian:	n/a
17	chr12:118797027-118797077	HRPEpiC	eye:	n/a
18	chr12:118782453-118782503	LNCaP	prostate:	n/a
19	chr12:118775197-118775247	HRPEpiC	eye:	n/a
20	chr12:118775197-118775247	HCT-116	colon:	n/a
21	chr12:118797027-118797077	A549	lung:	n/a
22	chr12:118683952-118684002	HRPEpiC	eye:	n/a
23	chr12:118782453-118782503	GM06990	blood:	n/a
24	chr12:118683952-118684002	CMK	blood:	n/a
25	chr12:118782453-118782503	Hepatocyte	liver:	n/a
26	chr12:118782453-118782503	Jurkat	blood:	n/a
27	chr12:118728016-118728066	BJ	skin:	n/a
28	chr12:118683952-118684002	HMEC	breast:	n/a
29	chr12:118797027-118797077	HL-60	blood:	n/a
30	chr12:118782453-118782503	GM19239	blood:	n/a
31	chr12:118683952-118684002	GM19239	blood:	n/a
32	chr12:118782453-118782503	NHBE	bronchial:	n/a
33	chr12:118797027-118797077	NT2-D1	testis:	n/a
34	chr12:118683952-118684002	RPTEC	kidney:	n/a
35	chr12:118728016-118728066	HRE	kidney:	n/a
36	chr12:118782453-118782503	HAEpiC	amniotic membrane:	n/a
37	chr12:118683952-118684002	NHDF-neo	bronchial:	n/a
38	chr12:118775197-118775247	IMR90	lung:	fetal
39	chr12:118797027-118797077	PANC-1	pancreas:	n/a
40	chr12:118797027-118797077	AG04450	lung:	fetal
41	chr12:118782453-118782503	HCF	heart:	n/a
42	chr12:118683952-118684002	NHBE	bronchial:	n/a
43	chr12:118683952-118684002	MCF-7	breast:	n/a
44	chr12:118728016-118728066	SAEC	small airway:	n/a
45	chr12:118775197-118775247	HNPCEpiC	eye:	n/a
46	chr12:118782453-118782503	HepG2	liver:	n/a
47	chr12:118797027-118797077	SK-N-SH_RA	brain:	n/a
48	chr12:118782453-118782503	HRE	kidney:	n/a
49	chr12:118782453-118782503	AG10803	skin:	n/a
50	chr12:118775197-118775247	PFSK-1	brain:	n/a

(count:129 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:118796352..118799029-chr12:118814094..118816699,2	K562	blood:
2	chr12:118778728..118784992-chr12:118810812..118815576,8	K562	blood:
3	chr12:118673323..118676031-chr12:118677378..118679199,2	MCF-7	breast:
4	chr12:118755879..118758733-chr12:118792249..118794715,2	K562	blood:
5	chr12:118781789..118783581-chr12:118812715..118814599,2	K562	blood:
6	chr12:118766497..118768322-chr12:118773115..118775978,2	MCF-7	breast:
7	chr12:118718803..118721131-chr12:118813506..118815349,2	K562	blood:
8	chr12:118775460..118777770-chr12:118780003..118783654,3	K562	blood:
9	chr12:118760395..118762832-chr12:118765688..118768481,2	K562	blood:
10	chr12:118737392..118738010-chr12:118813657..118814370,2	MCF-7	breast:
11	chr12:118687145..118690867-chr12:118809484..118812867,4	K562	blood:
12	chr12:118751643..118753393-chr12:118756511..118758342,2	K562	blood:
13	chr12:118764873..118767351-chr12:118794759..118796919,2	MCF-7	breast:
14	chr12:118750220..118752210-chr12:118752581..118754741,2	K562	blood:
15	chr12:118758501..118762498-chr12:118764368..118769658,5	K562	blood:
16	chr12:118794409..118797203-chr12:118798359..118800933,4	K562	blood:
17	chr12:118764089..118768365-chr12:118776795..118780945,4	K562	blood:
18	chr12:118746730..118749165-chr12:118809879..118812657,2	K562	blood:
19	chr12:118756336..118758349-chr12:118762596..118765319,2	K562	blood:
20	chr12:118742809..118745415-chr12:118767577..118770424,2	MCF-7	breast:
21	chr12:118674498..118676641-chr12:118709744..118711259,2	MCF-7	breast:
22	chr12:118737762..118738300-chr12:118813548..118814079,2	K562	blood:
23	chr12:118789460..118791189-chr12:118792284..118794787,2	K562	blood:
24	chr12:118766254..118768357-chr12:118781756..118783461,2	K562	blood:
25	chr12:118712134..118713954-chr12:118730833..118733395,2	MCF-7	breast:
26	chr12:118750220..118752210-chr12:118752581..118754741,2	K562	blood:
27	chr12:118694521..118696349-chr12:118811517..118814148,3	K562	blood:
28	chr12:118779976..118782774-chr12:118809831..118812312,2	K562	blood:
29	chr12:118676214..118678466-chr12:118707560..118709083,2	MCF-7	breast:
30	chr12:118686747..118689225-chr12:118810170..118812867,3	K562	blood:
31	chr12:118728193..118730845-chr12:118739160..118741836,2	K562	blood:
32	chr12:118787708..118789568-chr12:118793165..118794977,2	MCF-7	breast:
33	chr12:118769840..118772299-chr12:118773949..118776713,2	K562	blood:
34	chr12:118775460..118777770-chr12:118780003..118783654,3	K562	blood:
35	chr12:118734078..118737049-chr12:118810248..118811889,2	MCF-7	breast:
36	chr12:118690956..118692482-chr12:118706042..118708057,2	K562	blood:
37	chr12:118691774..118694683-chr12:118713486..118715660,2	K562	blood:
38	chr12:118763625..118770467-chr12:118808483..118814296,9	K562	blood:
39	chr12:118773930..118776516-chr12:118779431..118781891,3	K562	blood:
40	chr12:118702115..118703635-chr12:118708440..118710565,2	MCF-7	breast:
41	chr12:118787708..118789568-chr12:118793165..118794977,2	MCF-7	breast:
42	chr11:62432316..62432909-chr12:118794399..118795229,2	NB4	blood:
43	chr12:118637134..118639756-chr12:118657925..118660314,3	MCF-7	breast:
44	chr12:118754566..118756895-chr12:118766418..118769131,2	K562	blood:
45	chr12:118791019..118798938-chr12:118809011..118813946,9	MCF-7	breast:
46	chr12:118778728..118780877-chr12:118813193..118815933,2	K562	blood:
47	chr12:118795944..118799029-chr12:118813367..118816891,5	K562	blood:
48	chr12:118777906..118781488-chr12:118782215..118786255,6	K562	blood:
49	chr12:118685088..118687913-chr12:118695342..118697547,2	MCF-7	breast:
50	chr12:118749913..118751885-chr12:118794829..118796895,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VSIG10-4	chr12:118699302-118699478	NONHSAT031036
2	lnc-VSIG10-4	chr12:118693401-118693460	NONHSAT031036
3	lnc-VSIG10-4	chr12:118704460-118704564	NONHSAT031036

No data

Variant related genes	Relation type
RPS2P5	TF binding region
TAOK3	TF binding region
RPS2P5	CpG island
TAOK3	CpG island
ENSG00000214756	chromatin interactions
ENSG00000255432	chromatin interactions
ENSG00000206597	chromatin interactions
ENSG00000176834	chromatin interactions
ENSG00000135090	chromatin interactions
ENSG00000089220	chromatin interactions
ENSG00000270482	chromatin interactions
ENSG00000176871	chromatin interactions
ENSG00000162194	chromatin interactions
ENSG00000111707	chromatin interactions

Extended variants
information (count: 4957 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:4957 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555411674	chr12:118648420-118648421	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs572234833	chr12:118648460-118648461	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192725806	chr12:118648462-118648463	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs537692709	chr12:118648467-118648468	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562284726	chr12:118648517-118648518	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557516951	chr12:118648542-118648543	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs199626806	chr12:118648545-118648546	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376370236	chr12:118648575-118648576	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142901738	chr12:118648587-118648588	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558179998	chr12:118648629-118648630	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559505250	chr12:118648630-118648631	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577962270	chr12:118648668-118648669	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs546038929	chr12:118648679-118648680	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184426587	chr12:118648732-118648733	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs541838196	chr12:118648817-118648818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562211837	chr12:118648822-118648823	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189354043	chr12:118648828-118648829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs114833827	chr12:118648838-118648839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs353889	chr12:118648847-118648848	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs576159690	chr12:118648868-118648869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182288874	chr12:118648882-118648883	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567037009	chr12:118648884-118648885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs80241602	chr12:118649082-118649083	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533091521	chr12:118649122-118649123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76654443	chr12:118649132-118649133	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs57556064	chr12:118649157-118649158	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537504806	chr12:118649271-118649272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs17512219	chr12:118649273-118649274	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs577735898	chr12:118649277-118649278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533734793	chr12:118649278-118649279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs115786049	chr12:118649316-118649317	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570137775	chr12:118649325-118649326	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573851897	chr12:118649373-118649374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542285051	chr12:118649396-118649397	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184826453	chr12:118649399-118649400	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575811690	chr12:118649411-118649412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs5801272	chr12:118649419-118649420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs398021270	chr12:118649434-118649435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544689685	chr12:118649521-118649522	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138817569	chr12:118649566-118649567	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201290565	chr12:118649597-118649598	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs199597359	chr12:118649627-118649628	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs55798136	chr12:118649663-118649664	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs189395057	chr12:118649778-118649779	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs16948185	chr12:118649814-118649815	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs564061244	chr12:118649837-118649838	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs144631523	chr12:118649850-118649851	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529548388	chr12:118649868-118649869	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2280711	chr12:118649954-118649955	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs568487917	chr12:118649981-118649982	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Autism	22495311	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	17603634	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Neuroblastoma	20406844	CNVD
Medulloblastoma	16783165	CNVD
mental retardation	16760730	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Lung adenocarcinoma	21045234	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Pancreatic cancer	17952125	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	18511947	CNVD

Chromatin state (count:3004 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118620200-118656400	Weak transcription	HepG2	liver
2	chr12:118621000-118682600	Weak transcription	A549	lung
3	chr12:118628400-118697200	Weak transcription	Psoas Muscle	Psoas
4	chr12:118628800-118650000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr12:118628800-118672600	Weak transcription	Colon Smooth Muscle	Colon
6	chr12:118628800-118673000	Weak transcription	NH-A	brain
7	chr12:118629800-118652400	Strong transcription	Primary T helper cells fromperipheralblood	blood
8	chr12:118630800-118650000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr12:118636800-118658600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr12:118636800-118695000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr12:118637000-118652200	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr12:118637200-118654400	Weak transcription	Stomach Smooth Muscle	stomach
13	chr12:118637200-118700600	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr12:118637200-118700800	Weak transcription	Fetal Muscle Leg	muscle
15	chr12:118637400-118649200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr12:118637400-118653600	Weak transcription	Ovary	ovary
17	chr12:118637400-118658200	Weak transcription	Brain Anterior Caudate	brain
18	chr12:118637400-118671400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr12:118637400-118672400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr12:118637400-118684200	Weak transcription	Pancreas	Pancrea
21	chr12:118637400-118694200	Weak transcription	Brain Angular Gyrus	brain
22	chr12:118637400-118701400	Weak transcription	Spleen	Spleen
23	chr12:118637400-118703800	Weak transcription	Esophagus	oesophagus
24	chr12:118637400-118724000	Weak transcription	Aorta	Aorta
25	chr12:118637600-118673000	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr12:118637800-118650000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
27	chr12:118638600-118650200	Weak transcription	HUVEC	blood vessel
28	chr12:118638600-118651400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr12:118638800-118651400	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr12:118638800-118651600	Weak transcription	Lung	lung
31	chr12:118638800-118654400	Weak transcription	Colonic Mucosa	Colon
32	chr12:118638800-118687800	Weak transcription	Gastric	stomach
33	chr12:118639000-118650000	Weak transcription	Fetal Lung	lung
34	chr12:118639000-118672200	Weak transcription	Placenta	Placenta
35	chr12:118639000-118672200	Weak transcription	Left Ventricle	heart
36	chr12:118639000-118672800	Weak transcription	Small Intestine	intestine
37	chr12:118639200-118649800	Weak transcription	Adipose Nuclei	Adipose
38	chr12:118639200-118650200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr12:118639200-118650800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr12:118639200-118651400	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr12:118639200-118651600	Weak transcription	Fetal Thymus	thymus
42	chr12:118639200-118658000	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr12:118639200-118658200	Weak transcription	Brain Cingulate Gyrus	brain
44	chr12:118639400-118651400	Weak transcription	NHEK	skin
45	chr12:118639400-118660800	Weak transcription	HSMMtube	muscle
46	chr12:118639400-118661800	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr12:118639400-118674800	Weak transcription	HMEC	breast
48	chr12:118639800-118649200	Weak transcription	HSMM	muscle
49	chr12:118639800-118649400	Weak transcription	NHLF	lung
50	chr12:118639800-118649800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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