Variant report

Variant	nsv898762
Chromosome Location	chr12:10509383-10564329
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1531)
CpG islands
(count:552)
Chromatin interactive
region (count:26)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1531 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:10517306-10518105	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:10514385-10514386	K562	blood:	n/a	n/a
3	ARID3A	chr12:10513720-10513857	K562	blood:	n/a	n/a
4	ARID3A	chr12:10536954-10536986	K562	blood:	n/a	n/a
5	ARID3A	chr12:10515922-10516407	K562	blood:	n/a	n/a
6	ARID3A	chr12:10548121-10548681	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:10519484-10519894	HepG2	liver:	n/a	n/a
8	ARID3A	chr12:10563882-10564383	HepG2	liver:	n/a	n/a
9	ARID3A	chr12:10562084-10562332	K562	blood:	n/a	n/a
10	ATF1	chr12:10515987-10516344	K562	blood:	n/a	n/a
11	ATF1	chr12:10518006-10518279	K562	blood:	n/a	n/a
12	ATF1	chr12:10518698-10519024	K562	blood:	n/a	n/a
13	ATF1	chr12:10562095-10562363	K562	blood:	n/a	n/a
14	ATF2	chr12:10516736-10518064	GM12878	blood:	n/a	n/a
15	ATF2	chr12:10515391-10516378	GM12878	blood:	n/a	n/a
16	ATF2	chr12:10515378-10516482	GM12878	blood:	n/a	n/a
17	ATF2	chr12:10516513-10517982	GM12878	blood:	n/a	n/a
18	ATF2	chr12:10517788-10518192	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr12:10544776-10545621	GM12878	blood:	n/a	n/a
20	ATF2	chr12:10517765-10518225	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr12:10547858-10548386	GM12878	blood:	n/a	n/a
22	ATF3	chr12:10515933-10516347	K562	blood:	n/a	n/a
23	BACH1	chr12:10517085-10517124	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr12:10516901-10517786	GM12878	blood:	n/a	n/a
25	BCL11A	chr12:10544925-10545336	GM12878	blood:	n/a	n/a
26	BCL11A	chr12:10547875-10548349	GM12878	blood:	n/a	n/a
27	BCL11A	chr12:10517007-10517370	GM12878	blood:	n/a	n/a
28	BCL11A	chr12:10547793-10548282	GM12878	blood:	n/a	n/a
29	BCL11A	chr12:10544909-10545281	GM12878	blood:	n/a	n/a
30	BCL11A	chr12:10515491-10515913	GM12878	blood:	n/a	n/a
31	BCL11A	chr12:10516986-10517620	GM12878	blood:	n/a	n/a
32	BCL3	chr12:10515498-10515948	GM12878	blood:	n/a	n/a
33	BCLAF1	chr12:10516740-10517803	GM12878	blood:	n/a	n/a
34	BCLAF1	chr12:10516769-10517765	GM12878	blood:	n/a	n/a
35	BCLAF1	chr12:10516330-10516752	GM12878	blood:	n/a	n/a
36	BCLAF1	chr12:10544894-10545448	GM12878	blood:	n/a	n/a
37	BCLAF1	chr12:10547846-10548369	GM12878	blood:	n/a	n/a
38	BCLAF1	chr12:10544936-10545515	GM12878	blood:	n/a	chr12:10545490-10545499
39	BHLHE40	chr12:10516861-10517974	GM12878	blood:	n/a	n/a
40	BHLHE40	chr12:10559427-10559772	K562	blood:	n/a	n/a
41	BHLHE40	chr12:10516495-10517792	K562	blood:	n/a	n/a
42	BHLHE40	chr12:10515999-10516244	K562	blood:	n/a	n/a
43	BHLHE40	chr12:10547847-10548665	GM12878	blood:	n/a	n/a
44	BHLHE40	chr12:10562058-10562261	K562	blood:	n/a	n/a
45	BHLHE40	chr12:10559410-10559764	GM12878	blood:	n/a	n/a
46	BHLHE40	chr12:10515601-10515915	GM12878	blood:	n/a	n/a
47	BRCA1	chr12:10546999-10547736	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr12:10562044-10562186	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr12:10517548-10518007	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr12:10544899-10545539	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10516240-10516290	NH-A	brain:	n/a
2	chr12:10525233-10525283	GM06990	blood:	n/a
3	chr12:10543073-10543123	MCF-7	breast:	n/a
4	chr12:10516240-10516290	NH-A	brain:	n/a
5	chr12:10525233-10525283	GM06990	blood:	n/a
6	chr12:10543073-10543123	MCF-7	breast:	n/a
7	chr12:10532046-10532096	GM12891	blood:	n/a
8	chr12:10560602-10560652	GM12891	blood:	n/a
9	chr12:10532046-10532096	T-47D	breast:	n/a
10	chr12:10515574-10515624	HMEC	breast:	n/a
11	chr12:10560602-10560652	HMEC	breast:	n/a
12	chr12:10515091-10515141	HRCEpiC	kidney:	n/a
13	chr12:10545083-10545133	HMEC	breast:	n/a
14	chr12:10532046-10532096	HIPEpiC	eye:	n/a
15	chr12:10515091-10515141	HPAEpiC	pulmonary alveolar:	n/a
16	chr12:10543073-10543123	Hela-S3	cervix:	n/a
17	chr12:10543073-10543123	GM19239	blood:	n/a
18	chr12:10525233-10525283	HepG2	liver:	n/a
19	chr12:10544636-10544686	PANC-1	pancreas:	n/a
20	chr12:10545083-10545133	HCPEpiC	choroid plexus:	n/a
21	chr12:10516240-10516290	PrEC	prostate:	n/a
22	chr12:10516240-10516290	ovcar-3	ovarian:	n/a
23	chr12:10560602-10560652	ProgFib	skin:	n/a
24	chr12:10515091-10515141	HUVEC	blood vessel:	n/a
25	chr12:10560602-10560652	GM12892	blood:	n/a
26	chr12:10543073-10543123	BE2_C	brain:	n/a
27	chr12:10516240-10516290	HCPEpiC	choroid plexus:	n/a
28	chr12:10515574-10515624	HUVEC	blood vessel:	n/a
29	chr12:10532046-10532096	ovcar-3	ovarian:	n/a
30	chr12:10560602-10560652	PANC-1	pancreas:	n/a
31	chr12:10543073-10543123	PANC-1	pancreas:	n/a
32	chr12:10515091-10515141	NHBE	bronchial:	n/a
33	chr12:10515091-10515141	HIPEpiC	eye:	n/a
34	chr12:10560602-10560652	GM19239	blood:	n/a
35	chr12:10543073-10543123	SK-N-SH_RA	brain:	n/a
36	chr12:10532046-10532096	Hela-S3	cervix:	n/a
37	chr12:10525233-10525283	HIPEpiC	eye:	n/a
38	chr12:10532046-10532096	LNCaP	prostate:	n/a
39	chr12:10516240-10516290	NB4	blood:	n/a
40	chr12:10516240-10516290	HPAEpiC	pulmonary alveolar:	n/a
41	chr12:10515574-10515624	HL-60	blood:	n/a
42	chr12:10544636-10544686	HCM	heart:	n/a
43	chr12:10545083-10545133	U87	brain:	n/a
44	chr12:10544636-10544686	AG09309	skin:	n/a
45	chr12:10543073-10543123	ECC-1	luminal epithelium:	n/a
46	chr12:10544636-10544686	HRPEpiC	eye:	n/a
47	chr12:10543073-10543123	BJ	skin:	n/a
48	chr12:10543073-10543123	HCF	heart:	n/a
49	chr12:10544636-10544686	HCF	heart:	n/a
50	chr12:10544636-10544686	BE2_C	brain:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:10518506..10519182-chr16:20688297..20688797,2	HCT-116	colon:
2	chr12:10537029..10538774-chr12:10541549..10544546,2	K562	blood:
3	chr12:10561211..10561774-chr17:76182659..76183234,2	Hela-S3	cervix:
4	chr12:10436832..10439225-chr12:10509141..10511407,2	K562	blood:
5	chr12:10507526..10509637-chr12:10511583..10513205,2	K562	blood:
6	chr12:10509675..10512643-chr12:10514341..10517366,3	K562	blood:
7	chr12:10527378..10530229-chr12:10546803..10548399,2	K562	blood:
8	chr12:10547736..10550018-chr12:10555798..10557891,2	MCF-7	breast:
9	chr12:10554334..10554872-chr16:81477760..81478703,2	Hela-S3	cervix:
10	chr12:10516092..10519058-chr12:10537972..10540241,2	K562	blood:
11	chr12:10563346..10565218-chr12:11316267..11318781,2	K562	blood:
12	chr12:10534850..10537741-chr12:10540764..10542364,2	MCF-7	breast:
13	chr12:10515701..10519228-chr12:10526352..10529377,4	K562	blood:
14	chr12:10536735..10538905-chr12:10543028..10545121,2	MCF-7	breast:
15	chr12:10548044..10548696-chr9:117267865..117268396,2	Hela-S3	cervix:
16	chr12:10519323..10520144-chr12:10902384..10903013,2	MCF-7	breast:
17	chr12:10520202..10521817-chr12:10526312..10528193,2	K562	blood:
18	chr12:10515701..10517485-chr12:10526352..10529351,3	K562	blood:
19	chr12:10507526..10509637-chr12:10511583..10513205,2	K562	blood:
20	chr12:10559960..10560793-chrX:131351678..131352452,2	Hela-S3	cervix:
21	chr12:10528733..10530247-chr12:10762165..10764402,2	K562	blood:
22	chr12:10514090..10517702-chr12:10563594..10568036,4	K562	blood:
23	chr12:10547736..10550018-chr12:10555798..10557891,2	MCF-7	breast:
24	chr1:28974955..28975586-chr12:10563608..10564342,2	Hela-S3	cervix:
25	chr12:10527378..10530229-chr12:10546803..10548399,2	K562	blood:
26	chr12:10520202..10521817-chr12:10526312..10528193,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLRD1-1	chr12:10526634-10526735	ENSG00000245648
2	lnc-RP11-277P12.7.1-1	chr12:10511063-10511162	ENSG00000256155
3	lnc-KLRD1-1	chr12:10532301-10532435	ENSG00000245648
4	lnc-RP11-277P12.7.1-1	chr12:10513183-10513644	ENSG00000256155
5	lnc-KLRD1-1	chr12:10516368-10516632	ENSG00000245648
6	lnc-KLRD1-1	chr12:10548778-10551105	ENSG00000245648

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KLRK1	hsa-miR-9-5p	chr12:10525600-10525624

Variant related genes	Relation type
KLRK1	TF binding region
KLRC4	TF binding region
KLRC4-KLRK1	TF binding region
ENSG00000256155	TF binding region
ENSG00000245648	TF binding region
KLRK1	CpG island
KLRC4	CpG island
KLRC4-KLRK1	CpG island
ENSG00000256155	CpG island
ENSG00000245648	CpG island
ENSG00000270103	chromatin interactions
ENSG00000256888	chromatin interactions
ENSG00000167900	chromatin interactions
ENSG00000213809	chromatin interactions
ENSG00000245648	chromatin interactions
ENSG00000123728	chromatin interactions
ESR1	miRNA target sites
SMAD4	miRNA target sites
KIAA1967	miRNA target sites

Extended variants
information (count: 2183 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2183 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10734827	chr12:10509383-10509384	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs10734828	chr12:10509409-10509410	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs546683902	chr12:10509437-10509438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566524285	chr12:10509465-10509466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375249868	chr12:10509480-10509481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569192412	chr12:10509505-10509506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368677100	chr12:10509512-10509513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150680952	chr12:10509520-10509521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372406149	chr12:10509526-10509527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34897523	chr12:10509541-10509542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534014075	chr12:10509542-10509543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548788858	chr12:10509558-10509559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200930066	chr12:10509559-10509560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374585013	chr12:10509560-10509561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568801359	chr12:10509583-10509584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs374202549	chr12:10509669-10509670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183112947	chr12:10509695-10509696	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs576052619	chr12:10509758-10509759	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs545068631	chr12:10509759-10509760	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs557339794	chr12:10509771-10509772	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs114387319	chr12:10509783-10509784	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs372252929	chr12:10509803-10509804	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs539406708	chr12:10509844-10509845	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs370071504	chr12:10509847-10509848	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs572992810	chr12:10509857-10509858	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs1947763	chr12:10509916-10509917	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs530958283	chr12:10509988-10509989	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs187699733	chr12:10509990-10509991	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs544509464	chr12:10509991-10509992	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs564183886	chr12:10509995-10509996	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs140936941	chr12:10510111-10510112	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs540228377	chr12:10510143-10510144	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs560327465	chr12:10510145-10510146	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs528979057	chr12:10510154-10510155	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs548825673	chr12:10510155-10510156	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs568657469	chr12:10510171-10510172	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs192209550	chr12:10510180-10510181	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs577645158	chr12:10510191-10510192	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs144795172	chr12:10510197-10510198	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs55889207	chr12:10510198-10510199	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs1947764	chr12:10510201-10510202	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs182880140	chr12:10510205-10510206	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs201771525	chr12:10510238-10510239	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs192562100	chr12:10510292-10510293	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs184490416	chr12:10510300-10510301	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs575405661	chr12:10510318-10510319	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs536156077	chr12:10510353-10510354	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs369115438	chr12:10510383-10510384	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs558078006	chr12:10510432-10510433	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs577848087	chr12:10510447-10510448	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	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
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
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1740 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10507200-10513000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr12:10507400-10510200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr12:10507400-10512800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr12:10507400-10512800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr12:10507400-10513400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr12:10507400-10513400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr12:10507400-10513400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr12:10507400-10515800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr12:10507600-10513400	Weak transcription	HMEC	breast
10	chr12:10508000-10511400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr12:10508000-10515200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr12:10508200-10511400	Weak transcription	Hela-S3	cervix
13	chr12:10508800-10511400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr12:10509200-10513600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr12:10509600-10513600	Weak transcription	Fetal Kidney	kidney
16	chr12:10510200-10512600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr12:10510400-10512200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr12:10510800-10511400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
19	chr12:10511400-10511600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
20	chr12:10511400-10511600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr12:10511400-10511600	Enhancers	Primary T cells fromperipheralblood	blood
22	chr12:10511400-10511600	Enhancers	Gastric	stomach
23	chr12:10511400-10511800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr12:10511400-10511800	Enhancers	Hela-S3	cervix
25	chr12:10511400-10512200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr12:10511600-10511800	Enhancers	Thymus	Thymus
27	chr12:10511600-10512200	Enhancers	Primary T killer memory cells from peripheral blood	blood
28	chr12:10511600-10512800	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr12:10511600-10516400	Weak transcription	Gastric	stomach
30	chr12:10511800-10512800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr12:10511800-10513400	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr12:10511800-10513400	Weak transcription	Hela-S3	cervix
33	chr12:10511800-10514000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr12:10511800-10516200	Weak transcription	Thymus	Thymus
35	chr12:10512200-10513000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr12:10512200-10514000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr12:10512200-10515200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr12:10512600-10513400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr12:10512800-10513200	Active TSS	HUES6 Cell Line	embryonic stem cell
40	chr12:10512800-10513400	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr12:10512800-10513400	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr12:10512800-10515000	Weak transcription	Primary B cells from cord blood	blood
43	chr12:10512800-10515200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr12:10513000-10513800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
45	chr12:10513000-10513800	Enhancers	Brain Hippocampus Middle	brain
46	chr12:10513000-10514200	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr12:10513000-10514800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr12:10513000-10515600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr12:10513000-10516400	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr12:10513200-10513600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell

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