Variant report

Variant	nsv898619
Chromosome Location	chr12:4737715-4771456
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:509)
CpG islands
(count:855)
Chromatin interactive
region (count:23)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:509 , 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	chr12:4757999-4758491	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr12:4758070-4758634	GM12878	blood:	n/a	n/a
4	ATF2	chr12:4757972-4758620	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	chr12:4757362-4757603	GM12878	blood:	n/a	n/a
10	BHLHE40	chr12:4757761-4758471	K562	blood:	n/a	n/a
11	BRCA1	chr12:4757522-4758889	Hela-S3	cervix:	n/a	n/a
12	CCNT2	chr12:4757956-4758363	K562	blood:	n/a	n/a
13	CEBPB	chr12:4751163-4751331	HepG2	liver:	n/a	n/a
14	CEBPB	chr12:4757830-4757894	K562	blood:	n/a	n/a
15	CEBPB	chr12:4758026-4758412	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr12:4751161-4751189	K562	blood:	n/a	n/a
17	CEBPB	chr12:4760017-4760288	K562	blood:	n/a	chr12:4760126-4760137 chr12:4760126-4760139 chr12:4760127-4760138
18	CEBPB	chr12:4759436-4759663	HepG2	liver:	n/a	n/a
19	CEBPB	chr12:4759955-4760222	HepG2	liver:	n/a	chr12:4760126-4760137 chr12:4760126-4760139 chr12:4760127-4760138
20	CEBPD	chr12:4758143-4758473	HepG2	liver:	n/a	n/a
21	CHD1	chr12:4757476-4758871	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr12:4758193-4758446	HepG2	liver:	n/a	n/a
23	CHD2	chr12:4758078-4758446	GM12878	blood:	n/a	n/a
24	CHD2	chr12:4757626-4758623	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr12:4757737-4757887	K562	blood:	n/a	n/a
26	CHD2	chr12:4758021-4758466	H1-hESC	embryonic stem cell:	n/a	n/a
27	CREB1	chr12:4758078-4758323	A549	lung:	n/a	n/a
28	CREB1	chr12:4757960-4758541	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr12:4758112-4758477	A549	lung:	n/a	n/a
30	CREB1	chr12:4754210-4754564	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr12:4762380-4762530	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr12:4750293-4750337	Fibrobl	skin:	n/a	n/a
33	CTCF	chr12:4762460-4762610	RPTEC	kidney:	n/a	n/a
34	CTCF	chr12:4762400-4762550	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr12:4762380-4762530	Caco-2	colon:	n/a	n/a
36	CTCF	chr12:4758195-4758285	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr12:4762380-4762530	HMEC	breast:	n/a	n/a
38	CTCF	chr12:4757436-4757457	GM10266	blood:	n/a	n/a
39	CTCF	chr12:4762460-4762610	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr12:4757748-4757758	K562	blood:	n/a	n/a
41	CTCF	chr12:4758165-4758206	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr12:4762420-4762570	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr12:4762440-4762590	AG04449	skin:	n/a	n/a
44	CTCF	chr12:4764900-4765050	NHEK	skin:	n/a	n/a
45	CTCF	chr12:4757660-4757810	A549	lung:	n/a	n/a
46	CTCF	chr12:4762460-4762610	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr12:4740568-4740640	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr12:4758740-4758890	Caco-2	colon:	n/a	n/a
49	CTCF	chr12:4762420-4762570	HVMF	connective:	n/a	n/a
50	CTCF	chr12:4762500-4762650	AG10803	skin:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:4758272-4758322	Hepatocyte	liver:	n/a
2	chr12:4758272-4758322	Hepatocyte	liver:	n/a
3	chr12:4757759-4757809	HEK293	kidney:	embryo
4	chr12:4758424-4758474	HRCEpiC	kidney:	n/a
5	chr12:4755479-4755529	K562	blood:	n/a
6	chr12:4758272-4758322	GM12891	blood:	n/a
7	chr12:4755555-4755605	NB4	blood:	n/a
8	chr12:4762206-4762256	NHBE	bronchial:	n/a
9	chr12:4758424-4758474	GM12891	blood:	n/a
10	chr12:4757728-4757778	HPAEpiC	pulmonary alveolar:	n/a
11	chr12:4758201-4758251	MCF10A-Er-Src	breast:	n/a
12	chr12:4762206-4762256	SK-N-SH	brain:	n/a
13	chr12:4758496-4758546	SK-N-MC	brain:	n/a
14	chr12:4758250-4758300	H1-hESC	embryonic stem cell:	embryo
15	chr12:4757717-4757767	HCPEpiC	choroid plexus:	n/a
16	chr12:4757759-4757809	AG04449	skin:	fetal
17	chr12:4755555-4755605	HRCEpiC	kidney:	n/a
18	chr12:4757728-4757778	GM06990	blood:	n/a
19	chr12:4758496-4758546	CMK	blood:	n/a
20	chr12:4740542-4740592	AG04450	lung:	fetal
21	chr12:4758250-4758300	HAEpiC	amniotic membrane:	n/a
22	chr12:4758217-4758267	GM19239	blood:	n/a
23	chr12:4740542-4740592	K562	blood:	n/a
24	chr12:4762206-4762256	HRCEpiC	kidney:	n/a
25	chr12:4757728-4757778	NB4	blood:	n/a
26	chr12:4758250-4758300	Jurkat	blood:	n/a
27	chr12:4758272-4758322	SK-N-SH	brain:	n/a
28	chr12:4757728-4757778	SK-N-SH	brain:	n/a
29	chr12:4758217-4758267	HRPEpiC	eye:	n/a
30	chr12:4754247-4754297	Caco-2	colon:	n/a
31	chr12:4758272-4758322	AG04450	lung:	fetal
32	chr12:4758424-4758474	GM06990	blood:	n/a
33	chr12:4757728-4757778	GM19239	blood:	n/a
34	chr12:4755479-4755529	MCF10A-Er-Src	breast:	n/a
35	chr12:4740542-4740592	BJ	skin:	n/a
36	chr12:4757759-4757809	HEEpiC	esophagus:	n/a
37	chr12:4757759-4757809	SK-N-SH_RA	brain:	n/a
38	chr12:4758272-4758322	AoSMC	blood vessel:	n/a
39	chr12:4762206-4762256	HNPCEpiC	eye:	n/a
40	chr12:4755479-4755529	HIPEpiC	eye:	n/a
41	chr12:4758496-4758546	AG04449	skin:	fetal
42	chr12:4758424-4758474	Caco-2	colon:	n/a
43	chr12:4762206-4762256	Caco-2	colon:	n/a
44	chr12:4757759-4757809	AG09319	gingival:	n/a
45	chr12:4758272-4758322	HPAEpiC	pulmonary alveolar:	n/a
46	chr12:4757717-4757767	PrEC	prostate:	n/a
47	chr12:4740542-4740592	NH-A	brain:	n/a
48	chr12:4757728-4757778	PANC-1	pancreas:	n/a
49	chr12:4755555-4755605	AG10803	skin:	n/a
50	chr12:4755479-4755529	AG04450	lung:	fetal

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:4762342..4764303-chr12:4764418..4767058,2	K562	blood:
2	chr12:4758240..4760595-chr12:4768074..4769785,2	K562	blood:
3	chr12:4757537..4758351-chr2:9983167..9983703,2	Hela-S3	cervix:
4	chr12:4751073..4755821-chr12:4757118..4761577,5	MCF-7	breast:
5	chr12:4754845..4760714-chr12:4761830..4765057,7	MCF-7	breast:
6	chr12:4757018..4762059-chr12:4764285..4767290,6	K562	blood:
7	chr12:4762342..4764303-chr12:4764418..4767058,2	K562	blood:
8	chr12:4744167..4745708-chr12:4746619..4748785,2	K562	blood:
9	chr12:4758381..4761405-chr12:4778974..4782071,3	K562	blood:
10	chr12:4762857..4765662-chr12:4767685..4769794,2	K562	blood:
11	chr12:4756861..4759668-chr12:4760395..4765208,7	MCF-7	breast:
12	chr12:4757018..4762059-chr12:4764285..4767290,6	K562	blood:
13	chr12:4756861..4759668-chr12:4760395..4765208,7	MCF-7	breast:
14	chr12:4762857..4765662-chr12:4767685..4769794,2	K562	blood:
15	chr12:4757573..4759938-chr12:4760465..4764276,3	K562	blood:
16	chr12:4754845..4760714-chr12:4761830..4765057,7	MCF-7	breast:
17	chr12:4743724..4745923-chr12:4752293..4755038,2	K562	blood:
18	chr12:4757989..4759732-chr12:4759874..4761785,2	MCF-7	breast:
19	chr12:4757063..4759938-chr12:4760465..4764038,5	K562	blood:
20	chr12:4757573..4759938-chr12:4760465..4764276,3	K562	blood:
21	chr12:4757063..4759938-chr12:4760465..4764038,5	K562	blood:
22	chr12:4743724..4745923-chr12:4752293..4755038,2	K562	blood:
23	chr12:4751073..4755821-chr12:4757118..4761577,5	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 1332 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1332 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2072355	chr12:4737715-4737716	ZNF genes & repeats Enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs200125907	chr12:4737727-4737728	ZNF genes & repeats Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141858181	chr12:4737736-4737737	ZNF genes & repeats Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368342610	chr12:4737748-4737749	ZNF genes & repeats Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs36066195	chr12:4737808-4737809	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs200300900	chr12:4737825-4737826	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138303652	chr12:4737849-4737850	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs138233318	chr12:4737855-4737856	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558729195	chr12:4737879-4737880	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201140446	chr12:4737889-4737890	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs61755981	chr12:4737900-4737901	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559892469	chr12:4737910-4737911	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140648530	chr12:4737931-4737932	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs199966108	chr12:4737937-4737938	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372584198	chr12:4737967-4737968	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs142800348	chr12:4738006-4738007	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs192261158	chr12:4738015-4738016	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146054131	chr12:4738016-4738017	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs139826298	chr12:4738036-4738037	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185219274	chr12:4738045-4738046	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564915786	chr12:4738070-4738071	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373400255	chr12:4738084-4738085	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527975466	chr12:4738101-4738102	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149796240	chr12:4738153-4738154	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35049155	chr12:4738160-4738161	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs917566	chr12:4738181-4738182	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs564432850	chr12:4738222-4738223	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190500315	chr12:4738264-4738265	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182275158	chr12:4738270-4738271	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs114376555	chr12:4738310-4738311	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs917565	chr12:4738326-4738327	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs558894553	chr12:4738348-4738349	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115814863	chr12:4738369-4738370	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534719715	chr12:4738383-4738384	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201571935	chr12:4738423-4738424	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs144790702	chr12:4738430-4738431	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148547475	chr12:4738439-4738440	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556133717	chr12:4738473-4738474	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576080501	chr12:4738507-4738508	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544812543	chr12:4738515-4738516	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs11063267	chr12:4738595-4738596	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs11063268	chr12:4738611-4738612	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs541034989	chr12:4738655-4738656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565983415	chr12:4738656-4738657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561221062	chr12:4738661-4738662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372979849	chr12:4738666-4738667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561516082	chr12:4738717-4738718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145055194	chr12:4738730-4738731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs66871237	chr12:4738746-4738747	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs184415403	chr12:4738750-4738751	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:947 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:4724200-4756800	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr12:4725400-4752200	Weak transcription	Brain Hippocampus Middle	brain
3	chr12:4725600-4738400	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr12:4735800-4738400	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr12:4736800-4738600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
6	chr12:4737000-4737800	Strong transcription	Brain Anterior Caudate	brain
7	chr12:4737000-4737800	Strong transcription	Left Ventricle	heart
8	chr12:4737000-4738000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:4737200-4738200	Enhancers	HMEC	breast
10	chr12:4737600-4757400	Weak transcription	Pancreas	Pancrea
11	chr12:4737800-4742200	Weak transcription	Left Ventricle	heart
12	chr12:4737800-4757200	Weak transcription	Brain Anterior Caudate	brain
13	chr12:4738600-4739200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr12:4738800-4739200	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr12:4738800-4741600	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr12:4739000-4739200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr12:4739000-4739200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr12:4739000-4739200	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr12:4739000-4739400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr12:4739200-4740000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
21	chr12:4739200-4740000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
22	chr12:4739200-4740000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
23	chr12:4739200-4740000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr12:4739200-4741600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr12:4739400-4739800	Active TSS	HUES48 Cell Line	embryonic stem cell
26	chr12:4739400-4740400	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr12:4739600-4740000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr12:4739800-4740000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
29	chr12:4740000-4740200	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr12:4740000-4740600	Enhancers	H1 Cell Line	embryonic stem cell
31	chr12:4740000-4740800	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr12:4740000-4741000	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr12:4740000-4741400	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr12:4740000-4741600	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr12:4740200-4740400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr12:4740400-4741400	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr12:4742600-4743000	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr12:4745400-4757200	Weak transcription	Brain Substantia Nigra	brain
39	chr12:4746600-4757000	Weak transcription	Small Intestine	intestine
40	chr12:4747200-4748200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr12:4747400-4748200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr12:4752800-4754000	Enhancers	GM12878-XiMat	blood
43	chr12:4754000-4754800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr12:4754000-4755000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr12:4754000-4756600	Weak transcription	GM12878-XiMat	blood
46	chr12:4754200-4754400	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr12:4754200-4754600	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr12:4754200-4754800	Weak transcription	Aorta	Aorta
49	chr12:4754400-4757200	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr12:4754600-4754800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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