Variant report

Variant	nsv1053417
Chromosome Location	chr12:118688969-118808530
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1488)
CpG islands
(count:366)
Chromatin interactive
region (count:121)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1488 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:118783078-118783600	K562	blood:	n/a	chr12:118783100-118783116
2	ARID3A	chr12:118747592-118747909	K562	blood:	n/a	n/a
3	ARID3A	chr12:118775006-118775188	K562	blood:	n/a	n/a
4	ARID3A	chr12:118725664-118726444	K562	blood:	n/a	n/a
5	ARID3A	chr12:118808416-118809065	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:118785125-118785126	K562	blood:	n/a	n/a
7	ARID3A	chr12:118794909-118797601	K562	blood:	n/a	chr12:118795855-118795871 chr12:118795856-118795872
8	ARID3A	chr12:118767517-118768711	K562	blood:	n/a	n/a
9	ARID3A	chr12:118757499-118757759	K562	blood:	n/a	n/a
10	ARID3A	chr12:118776752-118776947	K562	blood:	n/a	n/a
11	ARID3A	chr12:118789073-118789336	HepG2	liver:	n/a	n/a
12	ARID3A	chr12:118798421-118799202	K562	blood:	n/a	n/a
13	ATF1	chr12:118747580-118747681	K562	blood:	n/a	n/a
14	ATF1	chr12:118726099-118726318	K562	blood:	n/a	n/a
15	ATF1	chr12:118770412-118770654	K562	blood:	n/a	n/a
16	ATF1	chr12:118768175-118768520	K562	blood:	n/a	n/a
17	ATF1	chr12:118795123-118795665	K562	blood:	n/a	n/a
18	ATF2	chr12:118794992-118795693	GM12878	blood:	n/a	n/a
19	ATF2	chr12:118792682-118793158	GM12878	blood:	n/a	n/a
20	ATF2	chr12:118744751-118745630	GM12878	blood:	n/a	n/a
21	ATF2	chr12:118794642-118795906	GM12878	blood:	n/a	n/a
22	ATF2	chr12:118750243-118750781	GM12878	blood:	n/a	n/a
23	ATF2	chr12:118750304-118750819	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	chr12:118783167-118783299	K562	blood:	n/a	n/a
27	BACH1	chr12:118757434-118757824	K562	blood:	n/a	n/a
28	BACH1	chr12:118715665-118716093	K562	blood:	n/a	n/a
29	BATF	chr12:118765637-118765993	GM12878	blood:	n/a	chr12:118765770-118765781
30	BATF	chr12:118689417-118689668	GM12878	blood:	n/a	n/a
31	BATF	chr12:118744836-118745142	GM12878	blood:	n/a	chr12:118744998-118745009
32	BATF	chr12:118750332-118750730	GM12878	blood:	n/a	n/a
33	BATF	chr12:118741985-118742269	GM12878	blood:	n/a	n/a
34	BATF	chr12:118750339-118750660	GM12878	blood:	n/a	n/a
35	BATF	chr12:118744771-118745254	GM12878	blood:	n/a	chr12:118744998-118745009
36	BATF	chr12:118765710-118765913	GM12878	blood:	n/a	chr12:118765770-118765781
37	BCL11A	chr12:118744829-118745165	GM12878	blood:	n/a	n/a
38	BCL11A	chr12:118750375-118750755	GM12878	blood:	n/a	n/a
39	BCL11A	chr12:118750417-118750694	GM12878	blood:	n/a	n/a
40	BCLAF1	chr12:118744805-118745730	GM12878	blood:	n/a	n/a
41	BCLAF1	chr12:118750273-118750876	GM12878	blood:	n/a	n/a
42	BCLAF1	chr12:118765522-118765946	GM12878	blood:	n/a	n/a
43	BHLHE40	chr12:118795076-118795764	K562	blood:	n/a	n/a
44	BHLHE40	chr12:118796819-118797369	GM12878	blood:	n/a	n/a
45	BHLHE40	chr12:118784671-118785194	GM12878	blood:	n/a	n/a
46	BHLHE40	chr12:118744671-118745674	GM12878	blood:	n/a	n/a
47	BHLHE40	chr12:118768135-118768478	K562	blood:	n/a	n/a
48	BHLHE40	chr12:118737807-118738444	GM12878	blood:	n/a	n/a
49	BHLHE40	chr12:118783163-118783489	K562	blood:	n/a	n/a
50	BHLHE40	chr12:118795037-118795902	GM12878	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:118797027-118797077	BE2_C	brain:	n/a
2	chr12:118728016-118728066	NB4	blood:	n/a
3	chr12:118806439-118806489	BE2_C	brain:	n/a
4	chr12:118782453-118782503	HUVEC	blood vessel:	n/a
5	chr12:118808298-118808348	HNPCEpiC	eye:	n/a
6	chr12:118782453-118782503	HCM	heart:	n/a
7	chr12:118782453-118782503	RPTEC	kidney:	n/a
8	chr12:118782453-118782503	SK-N-MC	brain:	n/a
9	chr12:118808298-118808348	HRPEpiC	eye:	n/a
10	chr12:118808298-118808348	GM12892	blood:	n/a
11	chr12:118808298-118808348	HUVEC	blood vessel:	n/a
12	chr12:118808298-118808348	AG04450	lung:	fetal
13	chr12:118808298-118808348	SK-N-MC	brain:	n/a
14	chr12:118782453-118782503	HRCEpiC	kidney:	n/a
15	chr12:118728016-118728066	SK-N-MC	brain:	n/a
16	chr12:118806439-118806489	HCT-116	colon:	n/a
17	chr12:118806439-118806489	PANC-1	pancreas:	n/a
18	chr12:118728016-118728066	GM19239	blood:	n/a
19	chr12:118775197-118775247	AG04450	lung:	fetal
20	chr12:118806439-118806489	HRE	kidney:	n/a
21	chr12:118808298-118808348	HCF	heart:	n/a
22	chr12:118808298-118808348	NT2-D1	testis:	n/a
23	chr12:118782453-118782503	NT2-D1	testis:	n/a
24	chr12:118797027-118797077	HCM	heart:	n/a
25	chr12:118806439-118806489	AoSMC	blood vessel:	n/a
26	chr12:118728016-118728066	ECC-1	luminal epithelium:	n/a
27	chr12:118782453-118782503	HCPEpiC	choroid plexus:	n/a
28	chr12:118806439-118806489	Caco-2	colon:	n/a
29	chr12:118806439-118806489	SK-N-MC	brain:	n/a
30	chr12:118808298-118808348	ovcar-3	ovarian:	n/a
31	chr12:118797027-118797077	BJ	skin:	n/a
32	chr12:118728016-118728066	HRE	kidney:	n/a
33	chr12:118808298-118808348	RPTEC	kidney:	n/a
34	chr12:118806439-118806489	GM12891	blood:	n/a
35	chr12:118775197-118775247	HEK293	kidney:	embryo
36	chr12:118728016-118728066	IMR90	lung:	fetal
37	chr12:118808298-118808348	GM12891	blood:	n/a
38	chr12:118808298-118808348	K562	blood:	n/a
39	chr12:118808298-118808348	NH-A	brain:	n/a
40	chr12:118808298-118808348	Caco-2	colon:	n/a
41	chr12:118808298-118808348	NHDF-neo	bronchial:	n/a
42	chr12:118808298-118808348	BJ	skin:	n/a
43	chr12:118808298-118808348	BE2_C	brain:	n/a
44	chr12:118782453-118782503	ECC-1	luminal epithelium:	n/a
45	chr12:118782453-118782503	HEEpiC	esophagus:	n/a
46	chr12:118782453-118782503	Hepatocyte	liver:	n/a
47	chr12:118806439-118806489	Hepatocyte	liver:	n/a
48	chr12:118797027-118797077	PANC-1	pancreas:	n/a
49	chr12:118728016-118728066	H1-hESC	embryonic stem cell:	embryo
50	chr12:118797027-118797077	NHDF-neo	bronchial:	n/a

(count:121 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:118756520..118758631-chr12:118810566..118812183,2	K562	blood:
2	chr12:118691774..118694683-chr12:118713486..118715660,2	K562	blood:
3	chr12:118727163..118729495-chr12:118743311..118746203,2	K562	blood:
4	chr12:118774312..118778410-chr12:118809648..118812658,5	K562	blood:
5	chr12:118750220..118752210-chr12:118752581..118754741,2	K562	blood:
6	chr12:118792933..118800473-chr12:118805927..118813309,24	K562	blood:
7	chr12:118751643..118753393-chr12:118756511..118758342,2	K562	blood:
8	chr12:118794409..118797203-chr12:118798359..118800933,4	K562	blood:
9	chr12:118766497..118768322-chr12:118773115..118775978,2	MCF-7	breast:
10	chr12:118744025..118746291-chr12:118766645..118768402,2	K562	blood:
11	chr12:118760395..118762832-chr12:118765688..118768481,2	K562	blood:
12	chr12:118744293..118746408-chr12:118812184..118814602,2	K562	blood:
13	chr12:118685088..118687913-chr12:118695342..118697547,2	MCF-7	breast:
14	chr12:118764873..118767351-chr12:118794759..118796919,2	MCF-7	breast:
15	chr12:118756336..118758349-chr12:118762596..118765319,2	K562	blood:
16	chr12:118697555..118699270-chr12:118703351..118704934,2	K562	blood:
17	chr12:118789460..118791189-chr12:118792284..118794787,2	K562	blood:
18	chr12:118742809..118745415-chr12:118767577..118770424,2	MCF-7	breast:
19	chr12:118791808..118793496-chr12:118793653..118795159,2	K562	blood:
20	chr12:118744025..118746291-chr12:118766645..118768402,2	K562	blood:
21	chr12:118734540..118737198-chr12:118753969..118757763,3	K562	blood:
22	chr12:118746730..118750377-chr12:118808240..118815610,7	K562	blood:
23	chr12:118758501..118762498-chr12:118764368..118769658,5	K562	blood:
24	chr12:118497374..118499405-chr12:118794577..118796696,2	K562	blood:
25	chr12:118746730..118749165-chr12:118809879..118812657,2	K562	blood:
26	chr12:118787708..118789568-chr12:118793165..118794977,2	MCF-7	breast:
27	chr12:118764089..118768365-chr12:118776795..118780945,4	K562	blood:
28	chr12:118789693..118801109-chr12:118805205..118813455,21	K562	blood:
29	chr12:118755879..118758733-chr12:118792249..118794715,2	K562	blood:
30	chr12:118763801..118766450-chr12:118767353..118769145,2	MCF-7	breast:
31	chr12:118756336..118758349-chr12:118762596..118765319,2	K562	blood:
32	chr12:118795210..118796886-chr12:118801131..118803860,2	K562	blood:
33	chr12:118693183..118695711-chr12:118713486..118715478,2	K562	blood:
34	chr12:118763801..118766450-chr12:118767353..118769145,2	MCF-7	breast:
35	chr12:118729613..118732493-chr12:118733521..118736057,3	K562	blood:
36	chr12:118751783..118754702-chr12:118810776..118812505,2	K562	blood:
37	chr12:118751643..118753393-chr12:118756511..118758342,2	K562	blood:
38	chr12:118688074..118690965-chr12:118809730..118812650,2	MCF-7	breast:
39	chr12:118787708..118789568-chr12:118793165..118794977,2	MCF-7	breast:
40	chr12:118702115..118703635-chr12:118708440..118710565,2	MCF-7	breast:
41	chr12:118766254..118768357-chr12:118781756..118783461,2	K562	blood:
42	chr12:118730543..118732493-chr12:118733563..118736057,4	K562	blood:
43	chr12:118791019..118798938-chr12:118809011..118813946,9	MCF-7	breast:
44	chr12:118690956..118692482-chr12:118706042..118708057,2	K562	blood:
45	chr12:118789460..118791189-chr12:118792284..118794787,2	K562	blood:
46	chr12:118765311..118767097-chr12:118807777..118809983,2	K562	blood:
47	chr12:118734540..118737198-chr12:118753969..118757763,3	K562	blood:
48	chr12:118769840..118772299-chr12:118773949..118776713,2	K562	blood:
49	chr12:118626469..118629447-chr12:118780334..118782967,2	K562	blood:
50	chr12:118694521..118696349-chr12:118811517..118814148,3	K562	blood:

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

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

No data

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

Extended variants
information (count: 3912 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3912 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540155249	chr12:118688972-118688973	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs369092256	chr12:118689012-118689013	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs113686046	chr12:118689028-118689029	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs572513267	chr12:118689120-118689121	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs541377675	chr12:118689138-118689139	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs58113338	chr12:118689140-118689141	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs184305527	chr12:118689176-118689177	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs141950025	chr12:118689236-118689237	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs564330676	chr12:118689270-118689271	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs543307876	chr12:118689296-118689297	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs532977230	chr12:118689304-118689305	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs201242096	chr12:118689305-118689306	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs376625990	chr12:118689310-118689311	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs375194188	chr12:118689333-118689334	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs370990490	chr12:118689414-118689415	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs16948199	chr12:118689440-118689441	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs560449847	chr12:118689457-118689458	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs528499895	chr12:118689466-118689467	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs548576889	chr12:118689499-118689500	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs146317100	chr12:118689500-118689501	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs537585860	chr12:118689510-118689511	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs188749953	chr12:118689515-118689516	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs75644537	chr12:118689544-118689545	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs180769742	chr12:118689563-118689564	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs553253886	chr12:118689576-118689577	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs528697580	chr12:118689585-118689586	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs373173461	chr12:118689610-118689611	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs75258628	chr12:118689644-118689645	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs77332445	chr12:118689645-118689646	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs573171931	chr12:118689717-118689718	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs377648527	chr12:118689720-118689721	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs466600	chr12:118689727-118689728	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs554976073	chr12:118689772-118689773	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs373399053	chr12:118689776-118689777	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs464781	chr12:118689816-118689817	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs544338771	chr12:118689858-118689859	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs564013892	chr12:118689900-118689901	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs577779505	chr12:118689904-118689905	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs370137926	chr12:118689905-118689906	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs551974276	chr12:118689907-118689908	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs530908651	chr12:118689916-118689917	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs540008500	chr12:118689934-118689935	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs560471800	chr12:118690002-118690003	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs183792515	chr12:118690061-118690062	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs80017233	chr12:118690064-118690065	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs571875851	chr12:118690153-118690154	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs61945212	chr12:118690156-118690157	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs12578471	chr12:118690192-118690193	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs530808073	chr12:118690229-118690230	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs78699582	chr12:118690230-118690231	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	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:2553 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118628400-118697200	Weak transcription	Psoas Muscle	Psoas
2	chr12:118636800-118695000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr12:118637200-118700600	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr12:118637200-118700800	Weak transcription	Fetal Muscle Leg	muscle
5	chr12:118637400-118694200	Weak transcription	Brain Angular Gyrus	brain
6	chr12:118637400-118701400	Weak transcription	Spleen	Spleen
7	chr12:118637400-118703800	Weak transcription	Esophagus	oesophagus
8	chr12:118637400-118724000	Weak transcription	Aorta	Aorta
9	chr12:118650400-118690400	Weak transcription	Stomach Mucosa	stomach
10	chr12:118652200-118727800	Weak transcription	NHLF	lung
11	chr12:118659000-118693800	Weak transcription	Brain Cingulate Gyrus	brain
12	chr12:118666800-118701000	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr12:118667200-118704600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr12:118669000-118709000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr12:118669000-118725200	Weak transcription	K562	blood
16	chr12:118671200-118701800	Weak transcription	Right Ventricle	heart
17	chr12:118673200-118698800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr12:118673200-118701600	Weak transcription	Rectal Smooth Muscle	rectum
19	chr12:118673400-118692000	Weak transcription	Brain Anterior Caudate	brain
20	chr12:118673400-118705400	Weak transcription	Colonic Mucosa	Colon
21	chr12:118673400-118710400	Weak transcription	Placenta	Placenta
22	chr12:118673400-118737600	Weak transcription	Brain Hippocampus Middle	brain
23	chr12:118673600-118712000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr12:118673800-118691400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr12:118673800-118694200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr12:118673800-118703000	Weak transcription	Thymus	Thymus
27	chr12:118673800-118709200	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr12:118673800-118737800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr12:118674000-118692000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr12:118674000-118700800	Weak transcription	Stomach Smooth Muscle	stomach
31	chr12:118674000-118706200	Weak transcription	Left Ventricle	heart
32	chr12:118674000-118726200	Weak transcription	Lung	lung
33	chr12:118675200-118692200	Weak transcription	Osteobl	bone
34	chr12:118675400-118691600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr12:118676000-118692000	Weak transcription	Adipose Nuclei	Adipose
36	chr12:118676000-118745200	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr12:118676200-118692000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
38	chr12:118676200-118694000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr12:118676200-118707400	Weak transcription	HSMM	muscle
40	chr12:118676400-118705000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr12:118676400-118718400	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr12:118676800-118720400	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr12:118677000-118690800	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr12:118677000-118691800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr12:118677000-118695400	Weak transcription	HMEC	breast
46	chr12:118677000-118708000	Weak transcription	NHEK	skin
47	chr12:118677000-118708800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr12:118677000-118739800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
49	chr12:118678000-118692000	Weak transcription	Primary B cells from peripheral blood	blood
50	chr12:118679000-118694200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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