Variant report

Variant	nsv973993
Chromosome Location	chr12:116861012-116874861
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:821)
CpG islands
(count:122)
Chromatin interactive
region (count:45)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:821 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:116872197-116872228	K562	blood:	n/a	n/a
2	ARID3A	chr12:116874680-116875049	HepG2	liver:	n/a	n/a
3	ATF2	chr12:116864803-116865520	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr12:116864913-116865733	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr12:116871894-116872876	A549	lung:	n/a	n/a
6	ATF3	chr12:116863970-116864617	A549	lung:	n/a	n/a
7	ATF3	chr12:116864952-116865510	A549	lung:	n/a	n/a
8	ATF3	chr12:116864003-116864755	A549	lung:	n/a	n/a
9	BACH1	chr12:116872047-116872277	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr12:116871806-116872963	A549	lung:	n/a	chr12:116872573-116872582
11	BCL3	chr12:116863769-116864695	A549	lung:	n/a	n/a
12	BCL3	chr12:116871856-116872879	A549	lung:	n/a	chr12:116872573-116872582
13	BCL3	chr12:116864845-116865875	A549	lung:	n/a	n/a
14	BCL3	chr12:116864898-116865546	A549	lung:	n/a	n/a
15	BCL3	chr12:116863937-116864646	A549	lung:	n/a	n/a
16	BHLHE40	chr12:116864206-116864719	K562	blood:	n/a	n/a
17	BHLHE40	chr12:116871917-116872292	K562	blood:	n/a	n/a
18	BHLHE40	chr12:116872018-116872249	HepG2	liver:	n/a	n/a
19	BHLHE40	chr12:116866275-116866376	K562	blood:	n/a	n/a
20	BHLHE40	chr12:116872051-116872836	A549	lung:	n/a	n/a
21	BRCA1	chr12:116872092-116872374	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr12:116871787-116873041	HCT-116	colon:	n/a	n/a
23	CBX3	chr12:116870124-116870667	K562	blood:	n/a	n/a
24	CBX3	chr12:116863928-116864740	HCT-116	colon:	n/a	n/a
25	CBX3	chr12:116864165-116864797	K562	blood:	n/a	n/a
26	CBX3	chr12:116870267-116870601	K562	blood:	n/a	n/a
27	CCNT2	chr12:116864278-116864710	K562	blood:	n/a	n/a
28	CCNT2	chr12:116872121-116872283	K562	blood:	n/a	n/a
29	CCNT2	chr12:116860858-116861038	K562	blood:	n/a	n/a
30	CEBPB	chr12:116866542-116866739	Hela-S3	cervix:	n/a	chr12:116866641-116866652
31	CEBPB	chr12:116869798-116870002	HepG2	liver:	n/a	n/a
32	CEBPB	chr12:116869583-116870159	A549	lung:	n/a	n/a
33	CEBPB	chr12:116872051-116872538	K562	blood:	n/a	chr12:116872251-116872262 chr12:116872250-116872263
34	CEBPB	chr12:116864200-116864563	A549	lung:	n/a	n/a
35	CEBPB	chr12:116874428-116875035	HepG2	liver:	n/a	n/a
36	CEBPB	chr12:116860864-116861421	A549	lung:	n/a	chr12:116861120-116861131 chr12:116861122-116861133 chr12:116861120-116861133
37	CEBPB	chr12:116869712-116870078	A549	lung:	n/a	n/a
38	CEBPB	chr12:116867611-116867725	HepG2	liver:	n/a	chr12:116867654-116867665 chr12:116867652-116867663
39	CEBPB	chr12:116869647-116870132	MCF-7	breast:	n/a	n/a
40	CEBPB	chr12:116869722-116870086	IMR90	lung:	n/a	n/a
41	CEBPB	chr12:116861096-116861176	K562	blood:	n/a	chr12:116861120-116861131 chr12:116861122-116861133 chr12:116861120-116861133
42	CEBPB	chr12:116871913-116872766	A549	lung:	n/a	chr12:116872251-116872262 chr12:116872250-116872263
43	CEBPB	chr12:116869711-116870080	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr12:116869738-116870077	A549	lung:	n/a	n/a
45	CEBPB	chr12:116866549-116866881	MCF-7	breast:	n/a	chr12:116866641-116866652
46	CEBPB	chr12:116866459-116866833	HepG2	liver:	n/a	chr12:116866641-116866652
47	CEBPB	chr12:116866485-116866884	MCF-7	breast:	n/a	chr12:116866641-116866652
48	CEBPB	chr12:116866318-116866847	K562	blood:	n/a	chr12:116866641-116866652
49	CEBPB	chr12:116871994-116872641	IMR90	lung:	n/a	chr12:116872251-116872262 chr12:116872250-116872263
50	CEBPB	chr12:116860986-116861264	A549	lung:	n/a	chr12:116861120-116861131 chr12:116861122-116861133 chr12:116861120-116861133

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:116872185-116872235	AG10803	skin:	n/a
2	chr12:116864616-116864666	HIPEpiC	eye:	n/a
3	chr12:116872185-116872235	SAEC	small airway:	n/a
4	chr12:116864616-116864666	PANC-1	pancreas:	n/a
5	chr12:116872185-116872235	HUVEC	blood vessel:	n/a
6	chr12:116864616-116864666	ProgFib	skin:	n/a
7	chr12:116872185-116872235	MCF10A-Er-Src	breast:	n/a
8	chr12:116864616-116864666	H1-hESC	embryonic stem cell:	embryo
9	chr12:116872185-116872235	HIPEpiC	eye:	n/a
10	chr12:116864616-116864666	HCF	heart:	n/a
11	chr12:116872185-116872235	SK-N-MC	brain:	n/a
12	chr12:116864616-116864666	HL-60	blood:	n/a
13	chr12:116864616-116864666	GM12891	blood:	n/a
14	chr12:116872185-116872235	HRCEpiC	kidney:	n/a
15	chr12:116864616-116864666	HEK293	kidney:	embryo
16	chr12:116872185-116872235	BE2_C	brain:	n/a
17	chr12:116864616-116864666	AG04450	lung:	fetal
18	chr12:116872185-116872235	K562	blood:	n/a
19	chr12:116872185-116872235	NHBE	bronchial:	n/a
20	chr12:116864616-116864666	Caco-2	colon:	n/a
21	chr12:116864616-116864666	Hepatocyte	liver:	n/a
22	chr12:116872185-116872235	Hela-S3	cervix:	n/a
23	chr12:116864616-116864666	BJ	skin:	n/a
24	chr12:116864616-116864666	HMEC	breast:	n/a
25	chr12:116864616-116864666	CMK	blood:	n/a
26	chr12:116872185-116872235	GM12878	blood:	n/a
27	chr12:116872185-116872235	PrEC	prostate:	n/a
28	chr12:116872185-116872235	NB4	blood:	n/a
29	chr12:116872185-116872235	HNPCEpiC	eye:	n/a
30	chr12:116864616-116864666	AG09319	gingival:	n/a
31	chr12:116864616-116864666	HUVEC	blood vessel:	n/a
32	chr12:116872185-116872235	Jurkat	blood:	n/a
33	chr12:116872185-116872235	HRPEpiC	eye:	n/a
34	chr12:116872185-116872235	Caco-2	colon:	n/a
35	chr12:116864616-116864666	ovcar-3	ovarian:	n/a
36	chr12:116872185-116872235	HL-60	blood:	n/a
37	chr12:116872185-116872235	H1-hESC	embryonic stem cell:	embryo
38	chr12:116872185-116872235	AG09309	skin:	n/a
39	chr12:116872185-116872235	PANC-1	pancreas:	n/a
40	chr12:116864616-116864666	K562	blood:	n/a
41	chr12:116864616-116864666	IMR90	lung:	fetal
42	chr12:116872185-116872235	LNCaP	prostate:	n/a
43	chr12:116872185-116872235	Hepatocyte	liver:	n/a
44	chr12:116872185-116872235	AG04450	lung:	fetal
45	chr12:116872185-116872235	NH-A	brain:	n/a
46	chr12:116864616-116864666	AG09309	skin:	n/a
47	chr12:116872185-116872235	HRE	kidney:	n/a
48	chr12:116864616-116864666	U87	brain:	n/a
49	chr12:116872185-116872235	HCT-116	colon:	n/a
50	chr12:116864616-116864666	Jurkat	blood:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:116855904..116857605-chr12:116861971..116863958,2	MCF-7	breast:
2	chr12:116714988..116717524-chr12:116861718..116863964,2	MCF-7	breast:
3	chr12:116827904..116828800-chr12:116863907..116864920,4	MCF-7	breast:
4	chr12:116831911..116834064-chr12:116861978..116863486,2	MCF-7	breast:
5	chr12:116714201..116716433-chr12:116870106..116872016,2	MCF-7	breast:
6	chr12:116842855..116845952-chr12:116869498..116873859,6	MCF-7	breast:
7	chr12:116865048..116865848-chr12:116932283..116933175,2	MCF-7	breast:
8	chr12:116862815..116867258-chr12:116867688..116873665,8	MCF-7	breast:
9	chr12:116868461..116874518-chr12:116929408..116934961,8	MCF-7	breast:
10	chr12:116854677..116856418-chr12:116858320..116861073,2	MCF-7	breast:
11	chr12:116827133..116831140-chr12:116860978..116865806,7	MCF-7	breast:
12	chr12:116857980..116859538-chr12:116859548..116861862,2	MCF-7	breast:
13	chr12:116862474..116864567-chr12:116876098..116878521,3	MCF-7	breast:
14	chr12:116862734..116864290-chr12:117037088..117038676,2	MCF-7	breast:
15	chr12:116828032..116828554-chr12:116865121..116865691,2	MCF-7	breast:
16	chr12:116842396..116845943-chr12:116861127..116865065,6	MCF-7	breast:
17	chr12:116870822..116873673-chr12:116997281..116998903,2	MCF-7	breast:
18	chr12:116713840..116716217-chr12:116869656..116871924,3	MCF-7	breast:
19	chr12:116827950..116828800-chr12:116863907..116864697,2	MCF-7	breast:
20	chr12:116849525..116852471-chr12:116871816..116874703,2	MCF-7	breast:
21	chr12:116867357..116868122-chr3:139445836..139446358,2	MCF-7	breast:
22	chr12:116862737..116864575-chr12:117134402..117135902,2	MCF-7	breast:
23	chr12:116715734..116717638-chr12:116859519..116862412,2	K562	blood:
24	chr12:116714942..116716969-chr12:116873241..116875497,2	MCF-7	breast:
25	chr12:116863823..116865402-chr12:116870010..116872543,2	K562	blood:
26	chr12:116871920..116874112-chr12:116939514..116942130,2	MCF-7	breast:
27	chr12:116869767..116872819-chr12:116879197..116881909,3	MCF-7	breast:
28	chr12:116874818..116876766-chr12:116892602..116894853,2	K562	blood:
29	chr12:116858970..116860681-chr12:116862728..116865463,2	MCF-7	breast:
30	chr12:116858356..116860792-chr12:116870655..116872690,2	MCF-7	breast:
31	chr12:116772348..116774581-chr12:116862812..116865326,2	MCF-7	breast:
32	chr12:116843058..116845423-chr12:116858142..116861084,3	MCF-7	breast:
33	chr12:116863823..116865402-chr12:116870010..116872543,2	K562	blood:
34	chr12:116713061..116717108-chr12:116860033..116868382,13	MCF-7	breast:
35	chr12:116870032..116871655-chr12:116975308..116976857,2	MCF-7	breast:
36	chr12:116844478..116845227-chr12:116863820..116864567,2	MCF-7	breast:
37	chr12:116861189..116865677-chr12:116930751..116933434,4	MCF-7	breast:
38	chr12:116713188..116716482-chr12:116864125..116866689,4	MCF-7	breast:
39	chr12:116872492..116874350-chr12:116885501..116887800,2	MCF-7	breast:
40	chr12:116858487..116861444-chr12:116862668..116866712,3	K562	blood:
41	chr12:116847212..116851109-chr12:116861228..116866038,6	MCF-7	breast:
42	chr12:116827236..116830738-chr12:116867857..116873341,7	MCF-7	breast:
43	chr12:116867559..116869139-chr12:116884102..116886241,2	MCF-7	breast:
44	chr12:116828068..116829010-chr12:116865125..116865728,2	MCF-7	breast:
45	chr10:12961921..12963741-chr12:116863676..116865934,2	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4472	chr12:116866099-116866116	MIMAT0018999

No data

Variant related genes	Relation type
MIR4472-2	TF binding region
MIR4472-2	CpG island
ENSG00000123066	chromatin interactions
ENSG00000264037	chromatin interactions

Extended variants
information (count: 590 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:590 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192266306	chr12:116861086-116861087	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs537737548	chr12:116861088-116861089	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs554443991	chr12:116861113-116861114	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs557327738	chr12:116861122-116861123	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs577468034	chr12:116861132-116861133	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs545762197	chr12:116861175-116861176	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs370201607	chr12:116861207-116861208	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs559336593	chr12:116861208-116861209	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs577208069	chr12:116861209-116861210	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs572985131	chr12:116861259-116861260	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs184074223	chr12:116861284-116861285	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs561133553	chr12:116861365-116861366	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs529810029	chr12:116861387-116861388	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs549951142	chr12:116861402-116861403	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs188607421	chr12:116861430-116861431	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs532465333	chr12:116861476-116861477	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs112755508	chr12:116861489-116861490	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs117860896	chr12:116861544-116861545	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs376603110	chr12:116861575-116861576	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs111746508	chr12:116861608-116861609	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs565709969	chr12:116861630-116861631	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs10850629	chr12:116861641-116861642	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs543925513	chr12:116861657-116861658	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs531862063	chr12:116861659-116861660	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs542305597	chr12:116861681-116861682	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs561097038	chr12:116861717-116861718	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs148613105	chr12:116861719-116861720	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs568155170	chr12:116861743-116861744	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs187313126	chr12:116861758-116861759	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs200130654	chr12:116861761-116861762	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs369725952	chr12:116861762-116861763	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs201962935	chr12:116861766-116861767	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs72163907	chr12:116861767-116861768	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs398070191	chr12:116861768-116861769	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs200071563	chr12:116861769-116861770	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs201013969	chr12:116861770-116861771	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs71095534	chr12:116861776-116861777	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs111281624	chr12:116861864-116861865	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs562203270	chr12:116861920-116861921	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs191710964	chr12:116861927-116861928	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs71469760	chr12:116861931-116861932	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs142055216	chr12:116861952-116861953	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs112359365	chr12:116861965-116861966	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs182578791	chr12:116861990-116861991	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs542217368	chr12:116862035-116862036	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs527565944	chr12:116862037-116862038	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs140275409	chr12:116862189-116862190	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs34225760	chr12:116862202-116862203	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs543219076	chr12:116862203-116862204	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs145314902	chr12:116862223-116862224	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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

Chromatin state (count:600 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:116844800-116862400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr12:116854200-116864000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr12:116854400-116863600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr12:116855000-116863200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr12:116859000-116863200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr12:116860200-116863000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr12:116860200-116863200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr12:116860200-116864400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr12:116860600-116861400	Enhancers	Colon Smooth Muscle	Colon
10	chr12:116860600-116861400	Enhancers	Fetal Stomach	stomach
11	chr12:116860600-116861400	Enhancers	NHDF-Ad	bronchial
12	chr12:116860600-116861600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr12:116860600-116861600	Enhancers	Fetal Intestine Large	intestine
14	chr12:116860800-116861200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr12:116860800-116861400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr12:116860800-116861400	Enhancers	Fetal Intestine Small	intestine
17	chr12:116860800-116861400	Enhancers	Fetal Lung	lung
18	chr12:116860800-116861400	Enhancers	Placenta	Placenta
19	chr12:116860800-116861400	Enhancers	Ovary	ovary
20	chr12:116860800-116861400	Enhancers	Osteobl	bone
21	chr12:116860800-116861600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr12:116860800-116861600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr12:116860800-116861800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr12:116861000-116861200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr12:116861000-116861200	Enhancers	A549	lung
26	chr12:116861000-116861400	Enhancers	Muscle Satellite Cultured Cells	--
27	chr12:116861000-116863600	Weak transcription	NHLF	lung
28	chr12:116861200-116861400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr12:116861200-116861800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr12:116861200-116862400	Weak transcription	A549	lung
31	chr12:116861200-116864000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr12:116861400-116862400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr12:116861400-116862800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr12:116861400-116863000	Weak transcription	Placenta	Placenta
35	chr12:116861400-116863200	Weak transcription	Osteobl	bone
36	chr12:116861400-116863400	Weak transcription	NHDF-Ad	bronchial
37	chr12:116861400-116863600	Weak transcription	Ovary	ovary
38	chr12:116861400-116863800	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr12:116861400-116863800	Weak transcription	Fetal Stomach	stomach
40	chr12:116861400-116864000	Weak transcription	Fetal Lung	lung
41	chr12:116861400-116864800	Weak transcription	Fetal Intestine Small	intestine
42	chr12:116861600-116862400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr12:116861600-116863000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr12:116861600-116863400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr12:116861600-116864200	Weak transcription	Fetal Intestine Large	intestine
46	chr12:116861800-116863200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr12:116861800-116863600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr12:116862400-116862600	Enhancers	Placenta Amnion	Placenta Amnion
49	chr12:116862400-116863800	Enhancers	A549	lung
50	chr12:116862400-116865600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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