Variant report

Variant	nsv1044587
Chromosome Location	chr12:10029514-10123414
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:820)
CpG islands
(count:1038)
Chromatin interactive
region (count:29)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:820 , 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	chr12:10078546-10078669	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:10034714-10034802	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:10047765-10048421	K562	blood:	n/a	n/a
4	ATF1	chr12:10047881-10048148	K562	blood:	n/a	n/a
5	ATF2	chr12:10060131-10064176	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr12:10101171-10101624	GM12878	blood:	n/a	n/a
7	ATF2	chr12:10060655-10064138	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr12:10100251-10100605	GM12878	blood:	n/a	n/a
9	BATF	chr12:10086322-10086608	GM12878	blood:	n/a	n/a
10	BATF	chr12:10100345-10100573	GM12878	blood:	n/a	n/a
11	BATF	chr12:10100260-10100612	GM12878	blood:	n/a	n/a
12	BATF	chr12:10101211-10101544	GM12878	blood:	n/a	n/a
13	BATF	chr12:10101190-10101497	GM12878	blood:	n/a	n/a
14	BATF	chr12:10086281-10086610	GM12878	blood:	n/a	n/a
15	BCL11A	chr12:10101225-10101619	GM12878	blood:	n/a	n/a
16	BCL11A	chr12:10101277-10101453	GM12878	blood:	n/a	n/a
17	BCL11A	chr12:10100277-10100640	GM12878	blood:	n/a	n/a
18	BCL3	chr12:10079494-10079845	GM12878	blood:	n/a	n/a
19	BCL3	chr12:10079569-10079849	GM12878	blood:	n/a	n/a
20	BCLAF1	chr12:10101143-10101621	GM12878	blood:	n/a	n/a
21	BHLHE40	chr12:10089360-10089741	GM12878	blood:	n/a	n/a
22	BRCA1	chr12:10061177-10063441	H1-hESC	embryonic stem cell:	n/a	n/a
23	CBX3	chr12:10063399-10063744	K562	blood:	n/a	n/a
24	CBX3	chr12:10063365-10063823	K562	blood:	n/a	n/a
25	CBX3	chr12:10055133-10055462	K562	blood:	n/a	n/a
26	CBX3	chr12:10055120-10055563	K562	blood:	n/a	n/a
27	CCNT2	chr12:10047826-10048458	K562	blood:	n/a	n/a
28	CEBPB	chr12:10063884-10064089	IMR90	lung:	n/a	chr12:10063963-10063974
29	CEBPB	chr12:10063891-10063997	A549	lung:	n/a	chr12:10063963-10063974
30	CEBPB	chr12:10043207-10043517	IMR90	lung:	n/a	n/a
31	CEBPB	chr12:10062884-10062902	HepG2	liver:	n/a	n/a
32	CEBPB	chr12:10051831-10052164	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr12:10063831-10063999	K562	blood:	n/a	chr12:10063963-10063974
34	CEBPB	chr12:10063798-10064128	HepG2	liver:	n/a	chr12:10063963-10063974
35	CEBPB	chr12:10069869-10070069	HepG2	liver:	n/a	n/a
36	CEBPB	chr12:10043214-10043562	A549	lung:	n/a	n/a
37	CEBPB	chr12:10063671-10064167	H1-hESC	embryonic stem cell:	n/a	chr12:10063963-10063974
38	CEBPB	chr12:10043218-10043526	HepG2	liver:	n/a	n/a
39	CEBPB	chr12:10043218-10043524	K562	blood:	n/a	n/a
40	CEBPB	chr12:10079831-10080031	A549	lung:	n/a	n/a
41	CEBPD	chr12:10047684-10048332	K562	blood:	n/a	n/a
42	CEBPD	chr12:10047730-10048504	K562	blood:	n/a	n/a
43	CHD1	chr12:10058739-10058975	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr12:10060502-10064476	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD1	chr12:10059944-10060186	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr12:10033385-10033602	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr12:10059985-10064107	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr12:10063573-10064204	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr12:10093080-10093230	HPF	lung:	n/a	n/a
50	CTCF	chr12:10078553-10078652	GM20000	blood:	n/a	chr12:10078583-10078601 chr12:10078584-10078600 chr12:10078578-10078599 chr12:10078586-10078596

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10122522-10122572	RPTEC	kidney:	n/a
2	chr12:10122522-10122572	RPTEC	kidney:	n/a
3	chr12:10086277-10086327	HCM	heart:	n/a
4	chr12:10096112-10096162	HCF	heart:	n/a
5	chr12:10085174-10085224	HMEC	breast:	n/a
6	chr12:10122522-10122572	BJ	skin:	n/a
7	chr12:10095997-10096047	HEEpiC	esophagus:	n/a
8	chr12:10085174-10085224	ECC-1	luminal epithelium:	n/a
9	chr12:10095902-10095952	HRCEpiC	kidney:	n/a
10	chr12:10086353-10086403	AG04450	lung:	fetal
11	chr12:10096118-10096168	HRCEpiC	kidney:	n/a
12	chr12:10107302-10107352	HCF	heart:	n/a
13	chr12:10096112-10096162	SK-N-SH_RA	brain:	n/a
14	chr12:10096112-10096162	NH-A	brain:	n/a
15	chr12:10095902-10095952	LNCaP	prostate:	n/a
16	chr12:10103165-10103215	AG09309	skin:	n/a
17	chr12:10103812-10103862	GM19239	blood:	n/a
18	chr12:10096152-10096202	HPAEpiC	pulmonary alveolar:	n/a
19	chr12:10086353-10086403	H1-hESC	embryonic stem cell:	embryo
20	chr12:10084936-10084986	SK-N-MC	brain:	n/a
21	chr12:10103812-10103862	HMEC	breast:	n/a
22	chr12:10095997-10096047	NB4	blood:	n/a
23	chr12:10095997-10096047	GM19239	blood:	n/a
24	chr12:10103812-10103862	T-47D	breast:	n/a
25	chr12:10065986-10066036	ProgFib	skin:	n/a
26	chr12:10095902-10095952	AG09309	skin:	n/a
27	chr12:10095997-10096047	HMEC	breast:	n/a
28	chr12:10103165-10103215	HL-60	blood:	n/a
29	chr12:10107302-10107352	HEEpiC	esophagus:	n/a
30	chr12:10084936-10084986	CMK	blood:	n/a
31	chr12:10085174-10085224	PANC-1	pancreas:	n/a
32	chr12:10102820-10102870	Jurkat	blood:	n/a
33	chr12:10107302-10107352	SK-N-MC	brain:	n/a
34	chr12:10095997-10096047	HRCEpiC	kidney:	n/a
35	chr12:10065986-10066036	GM12878	blood:	n/a
36	chr12:10095997-10096047	HepG2	liver:	n/a
37	chr12:10096794-10096844	HL-60	blood:	n/a
38	chr12:10096152-10096202	T-47D	breast:	n/a
39	chr12:10086353-10086403	HCT-116	colon:	n/a
40	chr12:10122522-10122572	Jurkat	blood:	n/a
41	chr12:10096794-10096844	Hepatocyte	liver:	n/a
42	chr12:10103812-10103862	RPTEC	kidney:	n/a
43	chr12:10095997-10096047	MCF10A-Er-Src	breast:	n/a
44	chr12:10084936-10084986	HCPEpiC	choroid plexus:	n/a
45	chr12:10085174-10085224	SK-N-SH_RA	brain:	n/a
46	chr12:10096794-10096844	HAEpiC	amniotic membrane:	n/a
47	chr12:10103812-10103862	GM12892	blood:	n/a
48	chr12:10103165-10103215	HEK293	kidney:	embryo
49	chr12:10084943-10084993	AG09319	gingival:	n/a
50	chr12:10103165-10103215	HCPEpiC	choroid plexus:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:9966552..9967437-chr12:10060979..10062470,4	K562	blood:
2	chr12:9903036..9905179-chr12:10078668..10080707,2	K562	blood:
3	chr12:9909065..9911051-chr12:10072172..10073790,2	K562	blood:
4	chr12:9903079..9903979-chr12:10078128..10079168,4	K562	blood:
5	chr12:9966403..9967529-chr12:10077074..10079200,18	MCF-7	breast:
6	chr12:10035043..10038365-chr12:10041988..10044335,3	MCF-7	breast:
7	chr12:10035043..10038365-chr12:10041988..10044335,3	MCF-7	breast:
8	chr12:10074227..10076810-chr12:10077015..10079502,2	K562	blood:
9	chr12:10020631..10023050-chr12:10030777..10032743,2	K562	blood:
10	chr12:10083355..10085342-chr12:10088920..10091712,2	K562	blood:
11	chr12:9966509..9967473-chr12:10078086..10079366,6	K562	blood:
12	chr12:9903072..9904066-chr12:10078179..10078803,2	MCF-7	breast:
13	chr12:9907055..9909270-chr12:10093617..10095503,2	K562	blood:
14	chr12:10111543..10114213-chr12:10132287..10134141,2	K562	blood:
15	chr12:10048238..10050006-chr12:10050229..10052826,2	K562	blood:
16	chr12:10040241..10042758-chr12:10046843..10049841,3	K562	blood:
17	chr12:10034768..10037295-chr12:10040504..10042625,2	K562	blood:
18	chr12:9965884..9968013-chr12:10078190..10080752,2	MCF-7	breast:
19	chr12:10024036..10026643-chr12:10029276..10031174,3	K562	blood:
20	chr12:10034768..10037295-chr12:10040504..10042625,2	K562	blood:
21	chr12:9908521..9910612-chr12:10055343..10056923,2	K562	blood:
22	chr12:9907740..9910735-chr12:10101487..10103775,2	K562	blood:
23	chr12:10040241..10042758-chr12:10046843..10049841,3	K562	blood:
24	chr12:10024279..10026522-chr12:10046207..10048850,2	K562	blood:
25	chr12:9966658..9967409-chr12:10077781..10079121,6	MCF-7	breast:
26	chr12:9903679..9905880-chr12:10079207..10081404,2	K562	blood:
27	chr12:10114461..10116965-chr12:10125225..10126914,2	K562	blood:
28	chr12:10074227..10076810-chr12:10077015..10079502,2	K562	blood:
29	chr12:10048238..10050006-chr12:10050229..10052826,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC2A-1	chr12:10091662-10091769	XLOC_010013
2	lnc-CLEC2A-1	chr12:10095088-10095171	XLOC_010013
3	lnc-CLEC2A-1	chr12:10091662-10091769	XLOC_010013
4	lnc-CLEC2A-1	chr12:10095088-10095171	XLOC_010013
5	lnc-CLEC2A-1	chr12:10089216-10089413	XLOC_010013
6	lnc-CLEC2A-1	chr12:10092508-10092692	XLOC_010013
7	lnc-CLEC2A-1	chr12:10089216-10089481	XLOC_010013
8	lnc-CLEC2A-1	chr12:10092508-10092692	XLOC_010013

No data

Variant related genes	Relation type
ENSG00000231560	TF binding region
CLEC2A	TF binding region
KLRF2	TF binding region
ENSG00000225231	TF binding region
CLEC12A	TF binding region
ENSG00000231560	CpG island
CLEC2A	CpG island
KLRF2	CpG island
ENSG00000225231	CpG island
CLEC12A	CpG island
ENSG00000188393	chromatin interactions
ENSG00000110852	chromatin interactions
BCL6	miRNA target sites
BCL2L11	miRNA target sites
BCL2L2	miRNA target sites

Extended variants
information (count: 3841 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:3841 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7313246	chr12:10029514-10029515	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs527275519	chr12:10029519-10029520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs11609546	chr12:10029521-10029522	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs567014414	chr12:10029558-10029559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs116325289	chr12:10029578-10029579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181833587	chr12:10029587-10029588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376470794	chr12:10029629-10029630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112267088	chr12:10029631-10029632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369320681	chr12:10029644-10029645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539743140	chr12:10029648-10029649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs149924235	chr12:10029651-10029652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs184544784	chr12:10029672-10029673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556164166	chr12:10029693-10029694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372018712	chr12:10029695-10029696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs578257293	chr12:10029754-10029755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145250045	chr12:10029811-10029812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs149154830	chr12:10029833-10029834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574008840	chr12:10029901-10029902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543110255	chr12:10029916-10029917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188907683	chr12:10029919-10029920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs76127080	chr12:10029952-10029953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143635607	chr12:10029954-10029955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181789436	chr12:10029961-10029962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186483489	chr12:10029962-10029963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555489602	chr12:10029965-10029966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546949962	chr12:10030005-10030006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs58312580	chr12:10030017-10030018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529729064	chr12:10030025-10030026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549863278	chr12:10030030-10030031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs117630176	chr12:10030055-10030056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556159660	chr12:10030072-10030073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113054285	chr12:10030075-10030076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369221749	chr12:10030096-10030097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571959242	chr12:10030148-10030149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112137973	chr12:10030159-10030160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369621611	chr12:10030170-10030171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373448396	chr12:10030197-10030198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs180930407	chr12:10030200-10030201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574481852	chr12:10030204-10030205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541089474	chr12:10030208-10030209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536311060	chr12:10030234-10030235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184971257	chr12:10030296-10030297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566918188	chr12:10030328-10030329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576486560	chr12:10030329-10030330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377441683	chr12:10030341-10030342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544798615	chr12:10030425-10030426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190916677	chr12:10030441-10030442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571965624	chr12:10030497-10030498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372625845	chr12:10030520-10030521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs146779925	chr12:10030537-10030538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	21248843	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
Cancer	20164919	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10025600-10033400	Weak transcription	Primary hematopoietic stem cells	blood
2	chr12:10029200-10029600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr12:10032800-10033600	Enhancers	Hela-S3	cervix
4	chr12:10033000-10033400	Enhancers	H1 Cell Line	embryonic stem cell
5	chr12:10033000-10033400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr12:10033000-10033600	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr12:10033000-10033600	Enhancers	H9 Cell Line	embryonic stem cell
8	chr12:10033000-10034400	Enhancers	Dnd41	blood
9	chr12:10033200-10033800	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr12:10033200-10033800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr12:10033200-10034400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr12:10033200-10035000	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr12:10033200-10035000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr12:10033400-10033800	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr12:10033400-10033800	Enhancers	Primary hematopoietic stem cells	blood
16	chr12:10033400-10034600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr12:10034000-10034600	Enhancers	Primary T cells from cord blood	blood
18	chr12:10034000-10035200	Enhancers	HepG2	liver
19	chr12:10034600-10035400	Enhancers	Liver	Liver
20	chr12:10034600-10037600	Weak transcription	Primary T cells from cord blood	blood
21	chr12:10034800-10035000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr12:10035400-10035800	Weak transcription	Liver	Liver
23	chr12:10035400-10036400	Enhancers	NHEK	skin
24	chr12:10035600-10036200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr12:10035600-10036200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr12:10035600-10036200	Enhancers	HMEC	breast
27	chr12:10035800-10036200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr12:10035800-10036400	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr12:10035800-10036600	Enhancers	Liver	Liver
30	chr12:10036000-10036600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr12:10036200-10041400	Weak transcription	HMEC	breast
32	chr12:10036200-10043000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr12:10036400-10041400	Weak transcription	NHEK	skin
34	chr12:10036600-10041400	Weak transcription	Liver	Liver
35	chr12:10037600-10038400	Enhancers	Primary T cells from cord blood	blood
36	chr12:10038000-10038400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr12:10038400-10041400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr12:10041400-10041800	Enhancers	Primary T cells fromperipheralblood	blood
39	chr12:10041400-10041800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
40	chr12:10041400-10041800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr12:10041400-10041800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr12:10041400-10041800	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr12:10041400-10041800	Enhancers	Liver	Liver
44	chr12:10041400-10041800	Enhancers	Esophagus	oesophagus
45	chr12:10041400-10041800	Enhancers	Stomach Mucosa	stomach
46	chr12:10041400-10041800	Enhancers	HMEC	breast
47	chr12:10041400-10041800	Enhancers	NHEK	skin
48	chr12:10041400-10042000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr12:10041400-10042200	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr12:10041400-10042200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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