Variant report

Variant	nsv898618
Chromosome Location	chr12:4726068-4764137
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:521)
CpG islands
(count:919)
Chromatin interactive
region (count:22)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:521 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:4757430-4758315	K562	blood:	n/a	n/a
2	ATF2	chr12:4757972-4758620	GM12878	blood:	n/a	n/a
3	ATF2	chr12:4757999-4758491	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr12:4758070-4758634	GM12878	blood:	n/a	n/a
5	BCL11A	chr12:4739499-4739759	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCLAF1	chr12:4757941-4758505	GM12878	blood:	n/a	chr12:4758114-4758123
7	BCLAF1	chr12:4757913-4758630	GM12878	blood:	n/a	chr12:4758114-4758123
8	BHLHE40	chr12:4758013-4758504	GM12878	blood:	n/a	n/a
9	BHLHE40	chr12:4757761-4758471	K562	blood:	n/a	n/a
10	BHLHE40	chr12:4757362-4757603	GM12878	blood:	n/a	n/a
11	BRCA1	chr12:4757522-4758889	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr12:4737530-4737649	Hela-S3	cervix:	n/a	n/a
13	CCNT2	chr12:4757956-4758363	K562	blood:	n/a	n/a
14	CEBPB	chr12:4757830-4757894	K562	blood:	n/a	n/a
15	CEBPB	chr12:4759436-4759663	HepG2	liver:	n/a	n/a
16	CEBPB	chr12:4760017-4760288	K562	blood:	n/a	chr12:4760126-4760137 chr12:4760126-4760139 chr12:4760127-4760138
17	CEBPB	chr12:4758026-4758412	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr12:4751163-4751331	HepG2	liver:	n/a	n/a
19	CEBPB	chr12:4751161-4751189	K562	blood:	n/a	n/a
20	CEBPB	chr12:4734656-4734801	HepG2	liver:	n/a	chr12:4734734-4734745
21	CEBPB	chr12:4759955-4760222	HepG2	liver:	n/a	chr12:4760126-4760137 chr12:4760126-4760139 chr12:4760127-4760138
22	CEBPD	chr12:4758143-4758473	HepG2	liver:	n/a	n/a
23	CHD1	chr12:4757476-4758871	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr12:4758021-4758466	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr12:4757626-4758623	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr12:4758078-4758446	GM12878	blood:	n/a	n/a
27	CHD2	chr12:4758193-4758446	HepG2	liver:	n/a	n/a
28	CHD2	chr12:4757737-4757887	K562	blood:	n/a	n/a
29	CREB1	chr12:4758078-4758323	A549	lung:	n/a	n/a
30	CREB1	chr12:4757960-4758541	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr12:4758112-4758477	A549	lung:	n/a	n/a
32	CREB1	chr12:4754210-4754564	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr12:4762380-4762530	HMEC	breast:	n/a	n/a
34	CTCF	chr12:4762420-4762570	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr12:4758162-4758291	GM12878	blood:	n/a	n/a
36	CTCF	chr12:4757436-4757457	GM10266	blood:	n/a	n/a
37	CTCF	chr12:4762380-4762530	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr12:4758740-4758890	Caco-2	colon:	n/a	n/a
39	CTCF	chr12:4762440-4762590	AG04449	skin:	n/a	n/a
40	CTCF	chr12:4750293-4750337	Fibrobl	skin:	n/a	n/a
41	CTCF	chr12:4762400-4762550	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr12:4762460-4762610	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr12:4762460-4762610	RPTEC	kidney:	n/a	n/a
44	CTCF	chr12:4740568-4740640	Pancreas_OC	pancreas:	n/a	n/a
45	CTCF	chr12:4762420-4762570	HVMF	connective:	n/a	n/a
46	CTCF	chr12:4757748-4757758	K562	blood:	n/a	n/a
47	CTCF	chr12:4762360-4762510	AG04450	lung:	n/a	n/a
48	CTCF	chr12:4758165-4758206	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr12:4762380-4762530	Caco-2	colon:	n/a	n/a
50	CTCF	chr12:4757660-4757810	A549	lung:	n/a	n/a

(count:919 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:4754247-4754297	SK-N-SH_RA	brain:	n/a
2	chr12:4758496-4758546	GM19239	blood:	n/a
3	chr12:4758217-4758267	HepG2	liver:	n/a
4	chr12:4758250-4758300	HMEC	breast:	n/a
5	chr12:4754247-4754297	SK-N-SH_RA	brain:	n/a
6	chr12:4758496-4758546	GM19239	blood:	n/a
7	chr12:4758217-4758267	HepG2	liver:	n/a
8	chr12:4758250-4758300	HMEC	breast:	n/a
9	chr12:4736730-4736780	ECC-1	luminal epithelium:	n/a
10	chr12:4755555-4755605	GM12891	blood:	n/a
11	chr12:4755479-4755529	NHBE	bronchial:	n/a
12	chr12:4758272-4758322	HRE	kidney:	n/a
13	chr12:4758250-4758300	HAEpiC	amniotic membrane:	n/a
14	chr12:4757717-4757767	HRPEpiC	eye:	n/a
15	chr12:4736730-4736780	HCF	heart:	n/a
16	chr12:4758424-4758474	Hepatocyte	liver:	n/a
17	chr12:4757728-4757778	GM12891	blood:	n/a
18	chr12:4757728-4757778	HMEC	breast:	n/a
19	chr12:4755479-4755529	GM12891	blood:	n/a
20	chr12:4740542-4740592	Hela-S3	cervix:	n/a
21	chr12:4755555-4755605	HMEC	breast:	n/a
22	chr12:4758217-4758267	T-47D	breast:	n/a
23	chr12:4758201-4758251	NT2-D1	testis:	n/a
24	chr12:4758424-4758474	HRE	kidney:	n/a
25	chr12:4755479-4755529	HRCEpiC	kidney:	n/a
26	chr12:4758217-4758267	GM12892	blood:	n/a
27	chr12:4762206-4762256	Jurkat	blood:	n/a
28	chr12:4758496-4758546	PANC-1	pancreas:	n/a
29	chr12:4758272-4758322	SK-N-SH	brain:	n/a
30	chr12:4762206-4762256	MCF10A-Er-Src	breast:	n/a
31	chr12:4758496-4758546	HUVEC	blood vessel:	n/a
32	chr12:4757728-4757778	Hepatocyte	liver:	n/a
33	chr12:4758496-4758546	NHBE	bronchial:	n/a
34	chr12:4758272-4758322	SK-N-SH_RA	brain:	n/a
35	chr12:4762206-4762256	HCPEpiC	choroid plexus:	n/a
36	chr12:4757728-4757778	SK-N-SH_RA	brain:	n/a
37	chr12:4758272-4758322	HepG2	liver:	n/a
38	chr12:4754247-4754297	HEK293	kidney:	embryo
39	chr12:4757728-4757778	NH-A	brain:	n/a
40	chr12:4755479-4755529	SAEC	small airway:	n/a
41	chr12:4740542-4740592	CMK	blood:	n/a
42	chr12:4740542-4740592	AG04450	lung:	fetal
43	chr12:4755479-4755529	BJ	skin:	n/a
44	chr12:4758250-4758300	T-47D	breast:	n/a
45	chr12:4758424-4758474	T-47D	breast:	n/a
46	chr12:4758424-4758474	HCT-116	colon:	n/a
47	chr12:4757717-4757767	MCF10A-Er-Src	breast:	n/a
48	chr12:4757759-4757809	HL-60	blood:	n/a
49	chr12:4762206-4762256	Caco-2	colon:	n/a
50	chr12:4758424-4758474	HCM	heart:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:4717083..4718773-chr12:4723734..4726455,2	K562	blood:
2	chr12:4756861..4759668-chr12:4760395..4765208,7	MCF-7	breast:
3	chr12:4743724..4745923-chr12:4752293..4755038,2	K562	blood:
4	chr12:4744167..4745708-chr12:4746619..4748785,2	K562	blood:
5	chr12:4757063..4759938-chr12:4760465..4764038,5	K562	blood:
6	chr12:4751073..4755821-chr12:4757118..4761577,5	MCF-7	breast:
7	chr12:4762342..4764303-chr12:4764418..4767058,2	K562	blood:
8	chr12:4754845..4760714-chr12:4761830..4765057,7	MCF-7	breast:
9	chr12:4751073..4755821-chr12:4757118..4761577,5	MCF-7	breast:
10	chr12:4727784..4729358-chr12:4757590..4759255,2	MCF-7	breast:
11	chr12:4724909..4726859-chr12:4756521..4758491,2	K562	blood:
12	chr12:4757063..4759938-chr12:4760465..4764038,5	K562	blood:
13	chr12:4758381..4761405-chr12:4778974..4782071,3	K562	blood:
14	chr12:4757537..4758351-chr2:9983167..9983703,2	Hela-S3	cervix:
15	chr12:4757018..4762059-chr12:4764285..4767290,6	K562	blood:
16	chr12:4756861..4759668-chr12:4760395..4765208,7	MCF-7	breast:
17	chr12:4762857..4765662-chr12:4767685..4769794,2	K562	blood:
18	chr12:4743724..4745923-chr12:4752293..4755038,2	K562	blood:
19	chr12:4757989..4759732-chr12:4759874..4761785,2	MCF-7	breast:
20	chr12:4757573..4759938-chr12:4760465..4764276,3	K562	blood:
21	chr12:4754845..4760714-chr12:4761830..4765057,7	MCF-7	breast:
22	chr12:4757573..4759938-chr12:4760465..4764276,3	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKAP3-3	chr12:4757620-4758174	NONHSAT025968
2	lnc-AKAP3-3	chr12:4751152-4751170	NONHSAT025968
3	lnc-AKAP3-3	chr12:4751065-4751170	NONHSAT025967
4	lnc-RP11-234B24.6.1-1	chr12:4757002-4757193	ENSG00000256381
5	lnc-AKAP3-3	chr12:4754221-4754358	NONHSAT025967
6	lnc-RP11-234B24.6.1-1	chr12:4754662-4755041	ENSG00000256381
7	lnc-AKAP3-3	chr12:4756240-4758165	NONHSAT025970
8	lnc-AKAP3-3	chr12:4757911-4758213	NONHSAT025967

No data

Variant related genes	Relation type
ENSG00000256381	TF binding region
NDUFA9	TF binding region
AKAP3	TF binding region
ENSG00000256799	TF binding region
ENSG00000255639	TF binding region
ENSG00000256381	CpG island
NDUFA9	CpG island
AKAP3	CpG island
ENSG00000256799	CpG island
ENSG00000255639	CpG island
ENSG00000115750	chromatin interactions
ENSG00000111254	chromatin interactions
ENSG00000256799	chromatin interactions
ENSG00000139180	chromatin interactions
ENSG00000256381	chromatin interactions
ENSG00000255639	chromatin interactions

Extended variants
information (count: 1521 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1521 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11063261	chr12:4726068-4726069	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532881189	chr12:4726114-4726115	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs543586716	chr12:4726166-4726167	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs139814738	chr12:4726174-4726175	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs551377663	chr12:4726193-4726194	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs532175603	chr12:4726205-4726206	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs188034015	chr12:4726208-4726209	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs559963433	chr12:4726259-4726260	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs528792576	chr12:4726271-4726272	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs12829711	chr12:4726297-4726298	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs12828416	chr12:4726359-4726360	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs201835408	chr12:4726459-4726460	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs550652163	chr12:4726464-4726465	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs11614502	chr12:4726490-4726491	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs192450735	chr12:4726519-4726520	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs549294570	chr12:4726576-4726577	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs570631331	chr12:4726584-4726585	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs539785445	chr12:4726599-4726600	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs183876237	chr12:4726628-4726629	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs536461685	chr12:4726640-4726641	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs75473126	chr12:4726654-4726655	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs534654332	chr12:4726657-4726658	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs554738254	chr12:4726661-4726662	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs552820018	chr12:4726698-4726699	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs10744656	chr12:4726748-4726749	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs139666928	chr12:4726764-4726765	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs149803818	chr12:4726810-4726811	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs566414743	chr12:4726817-4726818	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs545744769	chr12:4726825-4726826	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs2884671	chr12:4726832-4726833	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs10774248	chr12:4726841-4726842	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs200061868	chr12:4726917-4726918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542187422	chr12:4726918-4726919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs116621246	chr12:4726932-4726933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs71061196	chr12:4726934-4726935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs34087017	chr12:4726943-4726944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs73257493	chr12:4726955-4726956	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs530980392	chr12:4726964-4726965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189044718	chr12:4727114-4727115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78955094	chr12:4727301-4727302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113240806	chr12:4727326-4727327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs59797873	chr12:4727331-4727332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs116843616	chr12:4727344-4727345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192937273	chr12:4727368-4727369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534905454	chr12:4727454-4727455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554934546	chr12:4727506-4727507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568387009	chr12:4727528-4727529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537209880	chr12:4727550-4727551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184567940	chr12:4727555-4727556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs146605073	chr12:4727580-4727581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Epilepsy	21858020	CNVD
Colorectal cancer	19359472	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:951 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:4714400-4726400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:4714600-4726200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr12:4714600-4726800	Weak transcription	Right Ventricle	heart
4	chr12:4714800-4726600	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr12:4715200-4726400	Weak transcription	Fetal Heart	heart
6	chr12:4716000-4726400	Weak transcription	HUVEC	blood vessel
7	chr12:4716000-4726400	Weak transcription	NHDF-Ad	bronchial
8	chr12:4716400-4726400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr12:4716400-4727200	Weak transcription	HepG2	liver
10	chr12:4720400-4726600	Weak transcription	NHEK	skin
11	chr12:4721200-4727200	Weak transcription	Psoas Muscle	Psoas
12	chr12:4723200-4726600	Weak transcription	Placenta	Placenta
13	chr12:4723200-4726600	Weak transcription	Small Intestine	intestine
14	chr12:4723400-4726200	Weak transcription	Colon Smooth Muscle	Colon
15	chr12:4723400-4726800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr12:4723600-4726400	Weak transcription	Fetal Muscle Trunk	muscle
17	chr12:4723600-4726800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr12:4723600-4726800	Weak transcription	Fetal Stomach	stomach
19	chr12:4723600-4727000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr12:4723600-4727200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr12:4723600-4728200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr12:4723600-4735600	Weak transcription	HMEC	breast
23	chr12:4723800-4726800	Weak transcription	Thymus	Thymus
24	chr12:4723800-4727000	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr12:4723800-4727400	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr12:4723800-4728000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr12:4723800-4728600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr12:4723800-4732000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr12:4724000-4727000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr12:4724000-4727000	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr12:4724000-4727200	Weak transcription	Brain Germinal Matrix	brain
32	chr12:4724200-4726600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr12:4724200-4726800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr12:4724200-4726800	Weak transcription	Rectal Smooth Muscle	rectum
35	chr12:4724200-4727400	Weak transcription	Fetal Thymus	thymus
36	chr12:4724200-4735600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr12:4724200-4756800	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr12:4724400-4726600	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr12:4724400-4727200	Weak transcription	Osteobl	bone
40	chr12:4724400-4727600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr12:4724600-4726800	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr12:4724800-4726400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr12:4724800-4727200	Weak transcription	Ovary	ovary
44	chr12:4724800-4727400	Weak transcription	HSMMtube	muscle
45	chr12:4724800-4729000	Weak transcription	Primary hematopoietic stem cells	blood
46	chr12:4725000-4726800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr12:4725000-4726800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr12:4725000-4727200	Weak transcription	Fetal Brain Female	brain
49	chr12:4725000-4727600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr12:4725200-4726800	Weak transcription	Primary B cells from peripheral blood	blood

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