Variant report

Variant	nsv832432
Chromosome Location	chr12:60801619-60968907
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:552)
CpG islands
(count:122)
Chromatin interactive
region (count:30)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:60845275-60845679	HepG2	liver:	n/a	n/a
2	CBX3	chr12:60809451-60809945	HCT-116	colon:	n/a	n/a
3	CEBPB	chr12:60929125-60929452	IMR90	lung:	n/a	chr12:60929276-60929287 chr12:60929276-60929289 chr12:60929384-60929397
4	CEBPB	chr12:60809236-60809610	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr12:60952470-60952769	A549	lung:	n/a	chr12:60952614-60952625 chr12:60952598-60952609
6	CEBPB	chr12:60920475-60920662	IMR90	lung:	n/a	n/a
7	CEBPB	chr12:60928839-60929460	Hela-S3	cervix:	n/a	chr12:60929276-60929287 chr12:60928882-60928891 chr12:60929276-60929289 chr12:60928882-60928891 chr12:60929384-60929397
8	CEBPB	chr12:60929135-60929446	A549	lung:	n/a	chr12:60929276-60929287 chr12:60929276-60929289 chr12:60929384-60929397
9	CEBPB	chr12:60952457-60952721	IMR90	lung:	n/a	chr12:60952614-60952625 chr12:60952598-60952609
10	CEBPB	chr12:60929118-60929449	HepG2	liver:	n/a	chr12:60929276-60929287 chr12:60929276-60929289 chr12:60929384-60929397
11	CEBPB	chr12:60952520-60952796	MCF-7	breast:	n/a	chr12:60952614-60952625 chr12:60952598-60952609
12	CEBPB	chr12:60962378-60962530	A549	lung:	n/a	n/a
13	CEBPB	chr12:60940872-60940935	HepG2	liver:	n/a	chr12:60940894-60940905
14	CEBPB	chr12:60952559-60952686	Hela-S3	cervix:	n/a	chr12:60952614-60952625 chr12:60952598-60952609
15	CEBPB	chr12:60809161-60809716	IMR90	lung:	n/a	n/a
16	CEBPB	chr12:60816968-60817098	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr12:60928897-60929468	MCF-7	breast:	n/a	chr12:60929276-60929287 chr12:60929276-60929289 chr12:60929384-60929397
18	CEBPB	chr12:60862032-60862201	HepG2	liver:	n/a	n/a
19	CEBPB	chr12:60913763-60913944	HepG2	liver:	n/a	chr12:60913919-60913932 chr12:60913814-60913825 chr12:60913814-60913827
20	CEBPB	chr12:60952451-60952786	HepG2	liver:	n/a	chr12:60952614-60952625 chr12:60952598-60952609
21	CHD2	chr12:60825933-60826115	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr12:60888095-60888370	Gliobla	brain:	n/a	n/a
23	CTCF	chr12:60887880-60888030	GM12864	blood:	n/a	n/a
24	CTCF	chr12:60895200-60895350	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr12:60887820-60887970	GM12867	blood:	n/a	n/a
26	CTCF	chr12:60888180-60888330	GM12878	blood:	n/a	n/a
27	CTCF	chr12:60887944-60888520	MCF-7	breast:	n/a	n/a
28	CTCF	chr12:60890582-60890643	GM13976	blood:	n/a	n/a
29	CTCF	chr12:60887840-60887990	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr12:60895220-60895370	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr12:60888117-60888284	A549	lung:	n/a	n/a
32	CTCF	chr12:60888200-60888350	HVMF	connective:	n/a	n/a
33	CTCF	chr12:60895220-60895370	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr12:60895220-60895370	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr12:60888140-60888290	SAEC	small airway:	n/a	n/a
36	CTCF	chr12:60895200-60895350	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr12:60895160-60895310	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr12:60888120-60888270	RPTEC	kidney:	n/a	n/a
39	CTCF	chr12:60815480-60815630	AoAF	blood vessel:	n/a	n/a
40	CTCF	chr12:60888080-60888230	K562	blood:	n/a	n/a
41	CTCF	chr12:60888160-60888310	GM12801	blood:	n/a	n/a
42	CTCF	chr12:60854449-60854452	GM13976	blood:	n/a	n/a
43	CTCF	chr12:60888080-60888230	BE2_C	brain:	n/a	n/a
44	CTCF	chr12:60895240-60895390	BJ	skin:	n/a	n/a
45	CTCF	chr12:60895160-60895310	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr12:60888120-60888270	GM12873	blood:	n/a	n/a
47	CTCF	chr12:60888160-60888310	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr12:60888180-60888330	GM12865	blood:	n/a	n/a
49	CTCF	chr12:60888140-60888290	HAc	cerebellar:	n/a	n/a
50	CTCF	chr12:60888120-60888270	HFF-Myc	foreskin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:60812268-60812318	GM12878	blood:	n/a
2	chr12:60812459-60812509	HRPEpiC	eye:	n/a
3	chr12:60812459-60812509	HL-60	blood:	n/a
4	chr12:60812459-60812509	GM12891	blood:	n/a
5	chr12:60812459-60812509	LNCaP	prostate:	n/a
6	chr12:60812459-60812509	GM19239	blood:	n/a
7	chr12:60812459-60812509	HRCEpiC	kidney:	n/a
8	chr12:60812459-60812509	HIPEpiC	eye:	n/a
9	chr12:60812459-60812509	HEEpiC	esophagus:	n/a
10	chr12:60812268-60812318	SKMC	muscle:	n/a
11	chr12:60812268-60812318	HUVEC	blood vessel:	n/a
12	chr12:60812459-60812509	BE2_C	brain:	n/a
13	chr12:60812268-60812318	MCF10A-Er-Src	breast:	n/a
14	chr12:60812268-60812318	ProgFib	skin:	n/a
15	chr12:60812459-60812509	SK-N-SH_RA	brain:	n/a
16	chr12:60812268-60812318	SK-N-MC	brain:	n/a
17	chr12:60812268-60812318	HEK293	kidney:	embryo
18	chr12:60812459-60812509	HUVEC	blood vessel:	n/a
19	chr12:60812459-60812509	GM12892	blood:	n/a
20	chr12:60812459-60812509	T-47D	breast:	n/a
21	chr12:60812459-60812509	AG10803	skin:	n/a
22	chr12:60812268-60812318	AG04450	lung:	fetal
23	chr12:60812268-60812318	HCT-116	colon:	n/a
24	chr12:60812459-60812509	MCF-7	breast:	n/a
25	chr12:60812459-60812509	NT2-D1	testis:	n/a
26	chr12:60812459-60812509	AoSMC	blood vessel:	n/a
27	chr12:60812459-60812509	HMEC	breast:	n/a
28	chr12:60812268-60812318	ovcar-3	ovarian:	n/a
29	chr12:60812268-60812318	SAEC	small airway:	n/a
30	chr12:60812268-60812318	NHDF-neo	bronchial:	n/a
31	chr12:60812268-60812318	HRCEpiC	kidney:	n/a
32	chr12:60812459-60812509	SKMC	muscle:	n/a
33	chr12:60812459-60812509	SK-N-MC	brain:	n/a
34	chr12:60812268-60812318	AG09309	skin:	n/a
35	chr12:60812268-60812318	BE2_C	brain:	n/a
36	chr12:60812459-60812509	MCF10A-Er-Src	breast:	n/a
37	chr12:60812459-60812509	Jurkat	blood:	n/a
38	chr12:60812459-60812509	RPTEC	kidney:	n/a
39	chr12:60812268-60812318	MCF-7	breast:	n/a
40	chr12:60812459-60812509	NB4	blood:	n/a
41	chr12:60812268-60812318	HL-60	blood:	n/a
42	chr12:60812459-60812509	HEK293	kidney:	embryo
43	chr12:60812268-60812318	HepG2	liver:	n/a
44	chr12:60812459-60812509	AG09319	gingival:	n/a
45	chr12:60812459-60812509	HAEpiC	amniotic membrane:	n/a
46	chr12:60812459-60812509	AG09309	skin:	n/a
47	chr12:60812268-60812318	SK-N-SH	brain:	n/a
48	chr12:60812268-60812318	RPTEC	kidney:	n/a
49	chr12:60812459-60812509	Hela-S3	cervix:	n/a
50	chr12:60812459-60812509	HCF	heart:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:60815890..60818055-chr12:60827289..60829095,2	MCF-7	breast:
2	chr12:60809569..60811831-chr12:60814159..60815747,2	MCF-7	breast:
3	chr12:60790028..60792410-chr12:60842301..60844281,2	MCF-7	breast:
4	chr12:60895016..60895740-chr12:61932467..61933383,2	MCF-7	breast:
5	chr12:60650536..60651477-chr12:60887538..60888726,4	MCF-7	breast:
6	chr12:60499782..60500621-chr12:60887467..60888321,3	MCF-7	breast:
7	chr12:60816031..60818279-chr12:60819257..60821950,2	K562	blood:
8	chr12:60891633..60893813-chr12:60898441..60900083,2	MCF-7	breast:
9	chr12:60816866..60819028-chr12:60821142..60823191,2	MCF-7	breast:
10	chr12:60800545..60802133-chr12:60807687..60809552,2	K562	blood:
11	chr12:60800545..60802133-chr12:60807687..60809552,2	K562	blood:
12	chr12:60822466..60825457-chr12:60830238..60832110,2	K562	blood:
13	chr12:60860993..60863300-chr12:60865584..60868066,2	K562	blood:
14	chr12:60815890..60818055-chr12:60827289..60829095,2	MCF-7	breast:
15	chr12:60860157..60861729-chr12:60880266..60882965,2	K562	blood:
16	chr12:60535718..60536628-chr12:60888012..60888523,2	MCF-7	breast:
17	chr12:60809569..60811831-chr12:60814159..60815747,2	MCF-7	breast:
18	chr12:60860157..60861729-chr12:60880266..60882965,2	K562	blood:
19	chr12:60868652..60870460-chr12:60874035..60876045,2	MCF-7	breast:
20	chr12:60816866..60819028-chr12:60821142..60823191,2	MCF-7	breast:
21	chr12:60846358..60847991-chr12:60852007..60854549,2	MCF-7	breast:
22	chr11:69453740..69456116-chr12:60840140..60842721,2	MCF-7	breast:
23	chr12:60795925..60797882-chr12:60800577..60802586,2	MCF-7	breast:
24	chr12:60868652..60870460-chr12:60874035..60876045,2	MCF-7	breast:
25	chr12:60860993..60863300-chr12:60865584..60868066,2	K562	blood:
26	chr12:60816031..60818279-chr12:60819257..60821950,2	K562	blood:
27	chr12:60894975..60895756-chr12:62387590..62388098,2	MCF-7	breast:
28	chr12:60846358..60847991-chr12:60852007..60854549,2	MCF-7	breast:
29	chr12:60891633..60893813-chr12:60898441..60900083,2	MCF-7	breast:
30	chr12:60822466..60825457-chr12:60830238..60832110,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-272B17.2.1-5	chr12:60803379-60803467	NONHSAT029064
2	lnc-RP11-272B17.2.1-6	chr12:60940686-60940908	expReg_chr12_6157_-
3	lnc-RP11-272B17.2.1-5	chr12:60806615-60806771	NONHSAT029064
4	lnc-SLC16A7-6	chr12:60812764-60813074	NONHSAT029065

No data

Variant related genes	Relation type
ENSG00000257865	TF binding region
ENSG00000257865	CpG island
ENSG00000110092	chromatin interactions

Extended variants
information (count: 1852 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1852 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554526375	chr12:60803401-60803402	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs191683116	chr12:60803405-60803406	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs117279473	chr12:60803409-60803410	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs536131956	chr12:60803432-60803433	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs556189006	chr12:60803459-60803460	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs536668520	chr12:60806625-60806626	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs530404810	chr12:60806661-60806662	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs74649816	chr12:60806679-60806680	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs576906331	chr12:60806700-60806701	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs368166271	chr12:60806739-60806740	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs539538115	chr12:60806816-60806817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs188878431	chr12:60806854-60806855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs62825262	chr12:60806861-60806862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201507009	chr12:60806890-60806891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs12426853	chr12:60806993-60806994	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs377020906	chr12:60807018-60807019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542013705	chr12:60807035-60807036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561858456	chr12:60807059-60807060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs76181367	chr12:60807077-60807078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147870502	chr12:60807085-60807086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368614500	chr12:60807123-60807124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35120936	chr12:60807176-60807177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs372853818	chr12:60807181-60807182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533310140	chr12:60807260-60807261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190873138	chr12:60807261-60807262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560170377	chr12:60807301-60807302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559760218	chr12:60807323-60807324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs115806561	chr12:60807330-60807331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532261842	chr12:60807361-60807362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375411250	chr12:60807413-60807414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182679649	chr12:60807450-60807451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538514586	chr12:60807451-60807452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369603441	chr12:60807468-60807469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550353009	chr12:60807487-60807488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73359642	chr12:60807491-60807492	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs539399328	chr12:60807534-60807535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553120210	chr12:60807571-60807572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572949886	chr12:60807580-60807581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535678204	chr12:60807685-60807686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142306948	chr12:60807686-60807687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2062867	chr12:60807705-60807706	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs150164784	chr12:60807759-60807760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564175786	chr12:60807766-60807767	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs138616242	chr12:60807775-60807776	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs540200019	chr12:60807811-60807812	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs187551015	chr12:60807813-60807814	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs529324103	chr12:60807917-60807918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs117764885	chr12:60807922-60807923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563095743	chr12:60807937-60807938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531767254	chr12:60807938-60807939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
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
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:60806600-60808800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:60808800-60810400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:60809400-60809600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
4	chr12:60810400-60819400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:60812200-60812400	Bivalent/Poised TSS	Aorta	Aorta
6	chr12:60830600-60832400	Enhancers	HUVEC	blood vessel
7	chr12:60845200-60846000	Enhancers	Fetal Intestine Small	intestine
8	chr12:60845400-60846600	Enhancers	HepG2	liver
9	chr12:60845600-60846800	Enhancers	Fetal Intestine Large	intestine
10	chr12:60868600-60870600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr12:60868800-60869800	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr12:60869000-60870600	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr12:60869000-60870600	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr12:60869200-60870200	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr12:60869200-60870200	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr12:60869400-60870600	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr12:60869600-60870600	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr12:60869800-60870200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr12:60870200-60870600	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr12:60872400-60887600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr12:60877600-60878000	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr12:60877800-60878200	Enhancers	H1 Cell Line	embryonic stem cell
23	chr12:60881600-60882000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr12:60882000-60882200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr12:60882000-60882400	Enhancers	Fetal Intestine Large	intestine
26	chr12:60887800-60888000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr12:60892000-60896000	Enhancers	Fetal Heart	heart
28	chr12:60892600-60893000	Enhancers	Hela-S3	cervix
29	chr12:60892600-60893400	Enhancers	HUVEC	blood vessel
30	chr12:60892800-60893200	Enhancers	Left Ventricle	heart
31	chr12:60893400-60893800	Weak transcription	HUVEC	blood vessel
32	chr12:60893800-60894000	Enhancers	HUVEC	blood vessel
33	chr12:60894000-60895000	Weak transcription	HUVEC	blood vessel
34	chr12:60895000-60895400	Enhancers	Aorta	Aorta
35	chr12:60895000-60895400	Enhancers	Pancreas	Pancrea
36	chr12:60895000-60895400	Enhancers	HUVEC	blood vessel
37	chr12:60895200-60896000	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr12:60895400-60896000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr12:60912000-60915800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr12:60915200-60916400	Enhancers	Brain Germinal Matrix	brain
41	chr12:60915800-60916200	Enhancers	Brain Cingulate Gyrus	brain
42	chr12:60915800-60916200	Enhancers	Brain Substantia Nigra	brain
43	chr12:60915800-60916400	Enhancers	Brain Anterior Caudate	brain
44	chr12:60915800-60917200	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr12:60915800-60917200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr12:60928600-60929800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr12:60928600-60929800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr12:60929800-60933200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr12:60933200-60933800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr12:60933200-60933800	Active TSS	Fetal Lung	lung

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