Variant report

Variant	nsv508664
Chromosome Location	chr12:8450876-8604691
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1140)
CpG islands
(count:2993)
Chromatin interactive
region (count:0)
LncRNA
region (count:32)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1140 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:8477801-8477893	K562	blood:	n/a	n/a
2	ATF1	chr12:8477835-8478036	K562	blood:	n/a	n/a
3	BACH1	chr12:8549275-8549403	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr12:8472837-8473049	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr12:8465287-8465850	GM12878	blood:	n/a	chr12:8465611-8465619
6	BATF	chr12:8495383-8495701	GM12878	blood:	n/a	n/a
7	BATF	chr12:8472176-8472570	GM12878	blood:	n/a	n/a
8	BATF	chr12:8516441-8516876	GM12878	blood:	n/a	n/a
9	BATF	chr12:8472172-8472739	GM12878	blood:	n/a	n/a
10	BATF	chr12:8465483-8465876	GM12878	blood:	n/a	chr12:8465611-8465619
11	BATF	chr12:8486977-8487298	GM12878	blood:	n/a	n/a
12	BATF	chr12:8473299-8473507	GM12878	blood:	n/a	n/a
13	BATF	chr12:8495427-8495677	GM12878	blood:	n/a	n/a
14	BATF	chr12:8468528-8469314	GM12878	blood:	n/a	n/a
15	BATF	chr12:8572227-8572466	GM12878	blood:	n/a	n/a
16	BATF	chr12:8468641-8469136	GM12878	blood:	n/a	n/a
17	BATF	chr12:8529405-8529600	GM12878	blood:	n/a	n/a
18	BCL11A	chr12:8529324-8529698	GM12878	blood:	n/a	n/a
19	BCL11A	chr12:8471330-8471501	GM12878	blood:	n/a	n/a
20	BCL11A	chr12:8465466-8465929	GM12878	blood:	n/a	chr12:8465696-8465705
21	BCL11A	chr12:8472450-8472705	GM12878	blood:	n/a	n/a
22	BCL11A	chr12:8516727-8516902	GM12878	blood:	n/a	n/a
23	BCL11A	chr12:8495513-8495666	GM12878	blood:	n/a	chr12:8495622-8495631
24	BCL11A	chr12:8495462-8495734	GM12878	blood:	n/a	chr12:8495622-8495631
25	BCL11A	chr12:8473294-8473468	GM12878	blood:	n/a	n/a
26	BCL11A	chr12:8468528-8469107	GM12878	blood:	n/a	n/a
27	BCL11A	chr12:8472509-8472704	GM12878	blood:	n/a	n/a
28	BCL11A	chr12:8464258-8464453	GM12878	blood:	n/a	n/a
29	BCL11A	chr12:8529379-8529680	GM12878	blood:	n/a	n/a
30	BCL11A	chr12:8487014-8487435	GM12878	blood:	n/a	n/a
31	BCL11A	chr12:8468494-8469161	GM12878	blood:	n/a	n/a
32	BCL11A	chr12:8474618-8474785	GM12878	blood:	n/a	n/a
33	BCL11A	chr12:8465300-8465536	GM12878	blood:	n/a	n/a
34	BHLHE40	chr12:8549365-8549435	GM12878	blood:	n/a	n/a
35	BHLHE40	chr12:8468724-8468924	GM12878	blood:	n/a	n/a
36	BHLHE40	chr12:8543218-8543226	GM12878	blood:	n/a	n/a
37	CBX3	chr12:8466618-8466989	K562	blood:	n/a	chr12:8466977-8466988
38	CBX3	chr12:8477654-8478198	K562	blood:	n/a	n/a
39	CBX3	chr12:8481207-8481769	K562	blood:	n/a	n/a
40	CBX3	chr12:8481269-8481471	K562	blood:	n/a	n/a
41	CEBPB	chr12:8477125-8477527	K562	blood:	n/a	n/a
42	CEBPB	chr12:8550579-8550720	HepG2	liver:	n/a	chr12:8550656-8550665 chr12:8550654-8550665 chr12:8550654-8550667
43	CEBPB	chr12:8477720-8478067	K562	blood:	n/a	n/a
44	CEBPB	chr12:8550591-8550718	IMR90	lung:	n/a	chr12:8550656-8550665 chr12:8550654-8550665 chr12:8550654-8550667
45	CEBPB	chr12:8477687-8478095	K562	blood:	n/a	n/a
46	CEBPB	chr12:8477563-8478145	K562	blood:	n/a	n/a
47	CEBPD	chr12:8477087-8478154	K562	blood:	n/a	n/a
48	CHD2	chr12:8543173-8543243	GM12878	blood:	n/a	n/a
49	CTCF	chr12:8526532-8526576	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr12:8526460-8526610	AG09309	skin:	n/a	n/a

(count:2993 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:8596320-8596370	HPAEpiC	pulmonary alveolar:	n/a
2	chr12:8596320-8596370	MCF-7	breast:	n/a
3	chr12:8542524-8542574	BJ	skin:	n/a
4	chr12:8542524-8542574	AG10803	skin:	n/a
5	chr12:8596320-8596370	HPAEpiC	pulmonary alveolar:	n/a
6	chr12:8596320-8596370	MCF-7	breast:	n/a
7	chr12:8542524-8542574	BJ	skin:	n/a
8	chr12:8542524-8542574	AG10803	skin:	n/a
9	chr12:8575691-8575741	NB4	blood:	n/a
10	chr12:8599404-8599454	NB4	blood:	n/a
11	chr12:8548978-8549028	HAEpiC	amniotic membrane:	n/a
12	chr12:8571692-8571742	Hepatocyte	liver:	n/a
13	chr12:8575139-8575189	IMR90	lung:	fetal
14	chr12:8544796-8544846	GM12892	blood:	n/a
15	chr12:8548923-8548973	ECC-1	luminal epithelium:	n/a
16	chr12:8599149-8599199	ProgFib	skin:	n/a
17	chr12:8544796-8544846	SK-N-MC	brain:	n/a
18	chr12:8551501-8551551	HRE	kidney:	n/a
19	chr12:8539716-8539766	HepG2	liver:	n/a
20	chr12:8576728-8576778	GM19239	blood:	n/a
21	chr12:8599952-8600002	A549	lung:	n/a
22	chr12:8600287-8600337	A549	lung:	n/a
23	chr12:8542756-8542806	AG09309	skin:	n/a
24	chr12:8599952-8600002	HRCEpiC	kidney:	n/a
25	chr12:8544796-8544846	HRE	kidney:	n/a
26	chr12:8542756-8542806	SK-N-MC	brain:	n/a
27	chr12:8541476-8541526	HPAEpiC	pulmonary alveolar:	n/a
28	chr12:8474082-8474132	HRPEpiC	eye:	n/a
29	chr12:8548618-8548668	HNPCEpiC	eye:	n/a
30	chr12:8596320-8596370	HNPCEpiC	eye:	n/a
31	chr12:8542756-8542806	Jurkat	blood:	n/a
32	chr12:8597719-8597769	A549	lung:	n/a
33	chr12:8571374-8571424	GM19239	blood:	n/a
34	chr12:8570210-8570260	NT2-D1	testis:	n/a
35	chr12:8549446-8549496	Hepatocyte	liver:	n/a
36	chr12:8576728-8576778	HIPEpiC	eye:	n/a
37	chr12:8601085-8601135	Hela-S3	cervix:	n/a
38	chr12:8599952-8600002	BE2_C	brain:	n/a
39	chr12:8599404-8599454	IMR90	lung:	fetal
40	chr12:8559628-8559678	HRCEpiC	kidney:	n/a
41	chr12:8546330-8546380	AG10803	skin:	n/a
42	chr12:8549511-8549561	PrEC	prostate:	n/a
43	chr12:8548978-8549028	HPAEpiC	pulmonary alveolar:	n/a
44	chr12:8562937-8562987	GM19239	blood:	n/a
45	chr12:8601160-8601210	GM19239	blood:	n/a
46	chr12:8548978-8549028	U87	brain:	n/a
47	chr12:8597997-8598047	AG04449	skin:	fetal
48	chr12:8542756-8542806	GM06990	blood:	n/a
49	chr12:8559628-8559678	HAEpiC	amniotic membrane:	n/a
50	chr12:8570210-8570260	MCF-7	breast:	n/a

No data

(count:32 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC4E-2	chr12:8536701-8537017	ENSG00000226091.2
2	lnc-CLEC6A-2	chr12:8521588-8521956	NONHSAT026334
3	lnc-CLEC4E-2	chr12:8509559-8509737	ENSG00000226091.2
4	lnc-CLEC4E-2	chr12:8522809-8523025	ENSG00000226091.2
5	lnc-CLEC4E-2	chr12:8542866-8543107	NONHSAT026335
6	lnc-CLEC4E-2	chr12:8549019-8549212	NONHSAT026335
7	lnc-CLEC6A-2	chr12:8472977-8473022	ENSG00000256552.1
8	lnc-CLEC4E-2	chr12:8542866-8543348	NR_024420
9	lnc-CLEC4E-2	chr12:8535440-8535671	ENSG00000226091.2
10	lnc-CLEC6A-2	chr12:8521578-8522151	ENSG00000256552.1
11	lnc-CLEC4E-2	chr12:8542866-8543398	NONHSAT026332
12	lnc-CLEC4E-2	chr12:8543498-8543565	ENSG00000226091.2
13	lnc-CLEC4E-2	chr12:8522809-8523025	ENSG00000226091.2
14	lnc-CLEC6A-1	chr12:8475457-8475704	ENSG00000256101
15	lnc-CLEC6A-1	chr12:8481993-8482210	ENSG00000256101
16	lnc-CLEC4E-2	chr12:8539359-8540500	ENSG00000226091.2
17	lnc-CLEC4E-2	chr12:8538284-8538442	ENSG00000226091.2
18	lnc-CLEC4E-2	chr12:8509708-8509737	NONHSAT026332
19	lnc-CLEC4E-2	chr12:8522809-8523025	NONHSAT026332
20	lnc-CLEC4E-2	chr12:8542866-8543348	ENSG00000226091.2
21	lnc-CLEC4E-2	chr12:8549019-8549091	ENSG00000226091.2
22	lnc-CLEC6A-1	chr12:8474549-8474684	ENSG00000256101
23	lnc-CLEC4E-2	chr12:8542866-8543107	ENSG00000226091.2
24	lnc-CLEC4E-2	chr12:8537740-8537895	ENSG00000226091.2
25	lnc-CLEC4E-2	chr12:8542883-8542933	ENSG00000226091.2
26	lnc-CLEC4E-2	chr12:8522931-8523025	NONHSAT026335
27	lnc-CLEC4E-2	chr12:8523906-8524036	ENSG00000226091.2
28	lnc-CLEC4E-2	chr12:8509559-8509737	ENSG00000226091.2
29	lnc-CLEC4E-2	chr12:8538284-8538323	ENSG00000226091.2
30	lnc-CLEC4E-2	chr12:8527013-8527109	ENSG00000226091.2
31	lnc-CLEC4E-2	chr12:8509560-8509737	NR_024420
32	lnc-CLEC4E-2	chr12:8509559-8509737	ENSG00000226091.2

No data

Variant related genes	Relation type
OR7E140P	TF binding region
ENPP7P5	TF binding region
ENSG00000256552	TF binding region
ENSG00000256101	TF binding region
ENSG00000266218	TF binding region
ENSG00000221104	TF binding region
LINC00937	TF binding region
ENSG00000221307	TF binding region
OR7E148P	TF binding region
ENSG00000256136	TF binding region
CLEC6A	TF binding region
RPS3AP43	TF binding region
OR7E149P	TF binding region
OR7E140P	CpG island
ENPP7P5	CpG island
ENSG00000256552	CpG island
ENSG00000256101	CpG island
ENSG00000266218	CpG island
ENSG00000221104	CpG island
LINC00937	CpG island
ENSG00000221307	CpG island
OR7E148P	CpG island
ENSG00000256136	CpG island
CLEC6A	CpG island
RPS3AP43	CpG island
OR7E149P	CpG island

Extended variants
information (count: 3780 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:3780 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200431646	chr12:8450974-8450975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs202142244	chr12:8450976-8450977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144883126	chr12:8450977-8450978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs61922864	chr12:8450978-8450979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201219170	chr12:8450980-8450981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376646243	chr12:8450981-8450982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs57333779	chr12:8451015-8451016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371159718	chr12:8451016-8451017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs397958220	chr12:8451031-8451032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200261244	chr12:8451032-8451033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201330890	chr12:8451033-8451034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs145777780	chr12:8451056-8451057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs540243923	chr12:8451073-8451074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192588445	chr12:8451077-8451078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4882926	chr12:8451085-8451086	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
16	rs4883118	chr12:8451114-8451115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs61922865	chr12:8451181-8451182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs367812041	chr12:8451184-8451185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185146458	chr12:8451223-8451224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371064483	chr12:8451224-8451225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188412628	chr12:8451230-8451231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs4883119	chr12:8451233-8451234	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs4882927	chr12:8451328-8451329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112360688	chr12:8451333-8451334	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
25	rs10743306	chr12:8451337-8451338	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs4882928	chr12:8451343-8451344	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs10770449	chr12:8451352-8451353	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs58905789	chr12:8451381-8451382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs61922866	chr12:8451384-8451385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs12426746	chr12:8451416-8451417	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs12426753	chr12:8451459-8451460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs61922867	chr12:8451492-8451493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192819643	chr12:8451501-8451502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372769113	chr12:8451525-8451526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564408625	chr12:8451576-8451577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374810234	chr12:8451604-8451605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7307831	chr12:8451622-8451623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533708294	chr12:8451661-8451662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371701330	chr12:8451697-8451698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188111924	chr12:8451708-8451709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs80033431	chr12:8451747-8451748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111733358	chr12:8451760-8451761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191410786	chr12:8451761-8451762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs71042363	chr12:8451779-8451780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12227462	chr12:8451789-8451790	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs199735819	chr12:8451804-8451805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs71042364	chr12:8451819-8451820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs75115360	chr12:8451820-8451821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs74344186	chr12:8451822-8451823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577314964	chr12:8451834-8451835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
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
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
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:664 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:8433200-8463000	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr12:8447600-8473000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr12:8458200-8471600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr12:8459000-8460400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
5	chr12:8460400-8471600	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr12:8465000-8465200	Enhancers	Fetal Thymus	thymus
7	chr12:8465200-8465600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
8	chr12:8465200-8466000	Weak transcription	Fetal Thymus	thymus
9	chr12:8466000-8466600	Enhancers	Fetal Thymus	thymus
10	chr12:8466600-8471400	Weak transcription	Fetal Thymus	thymus
11	chr12:8468400-8468800	Enhancers	GM12878-XiMat	blood
12	chr12:8468800-8471800	Weak transcription	GM12878-XiMat	blood
13	chr12:8469800-8470200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr12:8470000-8470600	Enhancers	Fetal Lung	lung
15	chr12:8470200-8471600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr12:8470600-8473000	Weak transcription	Fetal Lung	lung
17	chr12:8470800-8472000	Enhancers	K562	blood
18	chr12:8471400-8471600	Enhancers	Fetal Intestine Large	intestine
19	chr12:8471400-8472800	Enhancers	Fetal Thymus	thymus
20	chr12:8471400-8473800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr12:8471400-8475800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr12:8471600-8471800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr12:8471600-8471800	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr12:8471600-8472000	Enhancers	H1 Cell Line	embryonic stem cell
25	chr12:8471600-8472000	Enhancers	H9 Cell Line	embryonic stem cell
26	chr12:8471600-8472800	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr12:8471600-8472800	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr12:8471600-8473800	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr12:8471600-8473800	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr12:8471600-8474000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr12:8471600-8474400	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr12:8471800-8472200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr12:8471800-8472800	Weak transcription	Primary neutrophils fromperipheralblood	blood
34	chr12:8471800-8472800	Enhancers	Dnd41	blood
35	chr12:8471800-8473600	Enhancers	GM12878-XiMat	blood
36	chr12:8471800-8473800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr12:8472000-8472200	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr12:8472000-8472800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr12:8472000-8473000	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr12:8472000-8473000	Weak transcription	K562	blood
41	chr12:8472200-8472400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr12:8472200-8472400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
43	chr12:8472200-8472600	Enhancers	H9 Cell Line	embryonic stem cell
44	chr12:8472200-8472600	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr12:8472200-8472600	Enhancers	Duodenum Mucosa	Duodenum
46	chr12:8472200-8472800	Enhancers	Primary T cells fromperipheralblood	blood
47	chr12:8472200-8473600	Enhancers	Primary T killer memory cells from peripheral blood	blood
48	chr12:8472200-8473800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr12:8472200-8473800	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr12:8472200-8473800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links