Variant report

Variant	nsv898760
Chromosome Location	chr12:10492982-10564329
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1567)
CpG islands
(count:551)
Chromatin interactive
region (count:27)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1567 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:10563882-10564383	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:10536954-10536986	K562	blood:	n/a	n/a
3	ARID3A	chr12:10515922-10516407	K562	blood:	n/a	n/a
4	ARID3A	chr12:10562084-10562332	K562	blood:	n/a	n/a
5	ARID3A	chr12:10519484-10519894	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:10514385-10514386	K562	blood:	n/a	n/a
7	ARID3A	chr12:10517306-10518105	HepG2	liver:	n/a	n/a
8	ARID3A	chr12:10513720-10513857	K562	blood:	n/a	n/a
9	ARID3A	chr12:10548121-10548681	HepG2	liver:	n/a	n/a
10	ATF1	chr12:10562095-10562363	K562	blood:	n/a	n/a
11	ATF1	chr12:10518698-10519024	K562	blood:	n/a	n/a
12	ATF1	chr12:10518006-10518279	K562	blood:	n/a	n/a
13	ATF1	chr12:10515987-10516344	K562	blood:	n/a	n/a
14	ATF2	chr12:10515378-10516482	GM12878	blood:	n/a	n/a
15	ATF2	chr12:10515391-10516378	GM12878	blood:	n/a	n/a
16	ATF2	chr12:10516513-10517982	GM12878	blood:	n/a	n/a
17	ATF2	chr12:10547858-10548386	GM12878	blood:	n/a	n/a
18	ATF2	chr12:10516736-10518064	GM12878	blood:	n/a	n/a
19	ATF2	chr12:10517788-10518192	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr12:10517765-10518225	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr12:10544776-10545621	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	chr12:10547793-10548282	GM12878	blood:	n/a	n/a
26	BCL11A	chr12:10516986-10517620	GM12878	blood:	n/a	n/a
27	BCL11A	chr12:10544925-10545336	GM12878	blood:	n/a	n/a
28	BCL11A	chr12:10517007-10517370	GM12878	blood:	n/a	n/a
29	BCL11A	chr12:10515491-10515913	GM12878	blood:	n/a	n/a
30	BCL11A	chr12:10544909-10545281	GM12878	blood:	n/a	n/a
31	BCL11A	chr12:10547875-10548349	GM12878	blood:	n/a	n/a
32	BCL3	chr12:10515498-10515948	GM12878	blood:	n/a	n/a
33	BCLAF1	chr12:10547846-10548369	GM12878	blood:	n/a	n/a
34	BCLAF1	chr12:10516769-10517765	GM12878	blood:	n/a	n/a
35	BCLAF1	chr12:10516740-10517803	GM12878	blood:	n/a	n/a
36	BCLAF1	chr12:10544894-10545448	GM12878	blood:	n/a	n/a
37	BCLAF1	chr12:10516330-10516752	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	chr12:10547847-10548665	GM12878	blood:	n/a	n/a
42	BHLHE40	chr12:10516495-10517792	K562	blood:	n/a	n/a
43	BHLHE40	chr12:10562058-10562261	K562	blood:	n/a	n/a
44	BHLHE40	chr12:10515999-10516244	K562	blood:	n/a	n/a
45	BHLHE40	chr12:10515601-10515915	GM12878	blood:	n/a	n/a
46	BHLHE40	chr12:10559410-10559764	GM12878	blood:	n/a	n/a
47	BRCA1	chr12:10546999-10547736	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr12:10541035-10541418	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr12:10562044-10562186	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr12:10544899-10545539	Hela-S3	cervix:	n/a	n/a

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10545083-10545133	PFSK-1	brain:	n/a
2	chr12:10516240-10516290	HMEC	breast:	n/a
3	chr12:10545083-10545133	PFSK-1	brain:	n/a
4	chr12:10516240-10516290	HMEC	breast:	n/a
5	chr12:10525233-10525283	HCPEpiC	choroid plexus:	n/a
6	chr12:10515574-10515624	H1-hESC	embryonic stem cell:	embryo
7	chr12:10525233-10525283	LNCaP	prostate:	n/a
8	chr12:10545083-10545133	ovcar-3	ovarian:	n/a
9	chr12:10545083-10545133	BE2_C	brain:	n/a
10	chr12:10525233-10525283	NH-A	brain:	n/a
11	chr12:10544636-10544686	GM06990	blood:	n/a
12	chr12:10515574-10515624	AG04450	lung:	fetal
13	chr12:10560602-10560652	GM12892	blood:	n/a
14	chr12:10544636-10544686	CMK	blood:	n/a
15	chr12:10543073-10543123	SK-N-MC	brain:	n/a
16	chr12:10515574-10515624	HRPEpiC	eye:	n/a
17	chr12:10516240-10516290	K562	blood:	n/a
18	chr12:10560602-10560652	SK-N-SH_RA	brain:	n/a
19	chr12:10532046-10532096	SAEC	small airway:	n/a
20	chr12:10532046-10532096	PANC-1	pancreas:	n/a
21	chr12:10515574-10515624	HEK293	kidney:	embryo
22	chr12:10516240-10516290	AG04449	skin:	fetal
23	chr12:10516240-10516290	NHBE	bronchial:	n/a
24	chr12:10545083-10545133	AG09309	skin:	n/a
25	chr12:10544636-10544686	PFSK-1	brain:	n/a
26	chr12:10525233-10525283	HNPCEpiC	eye:	n/a
27	chr12:10545083-10545133	BJ	skin:	n/a
28	chr12:10544636-10544686	SK-N-SH	brain:	n/a
29	chr12:10525233-10525283	AoSMC	blood vessel:	n/a
30	chr12:10515574-10515624	GM12891	blood:	n/a
31	chr12:10543073-10543123	GM06990	blood:	n/a
32	chr12:10515574-10515624	HMEC	breast:	n/a
33	chr12:10525233-10525283	U87	brain:	n/a
34	chr12:10515091-10515141	Caco-2	colon:	n/a
35	chr12:10545083-10545133	NH-A	brain:	n/a
36	chr12:10560602-10560652	HPAEpiC	pulmonary alveolar:	n/a
37	chr12:10545083-10545133	Hepatocyte	liver:	n/a
38	chr12:10543073-10543123	U87	brain:	n/a
39	chr12:10543073-10543123	HL-60	blood:	n/a
40	chr12:10544636-10544686	NH-A	brain:	n/a
41	chr12:10515574-10515624	NT2-D1	testis:	n/a
42	chr12:10516240-10516290	HNPCEpiC	eye:	n/a
43	chr12:10516240-10516290	HRCEpiC	kidney:	n/a
44	chr12:10560602-10560652	HAEpiC	amniotic membrane:	n/a
45	chr12:10515574-10515624	AoSMC	blood vessel:	n/a
46	chr12:10515574-10515624	GM06990	blood:	n/a
47	chr12:10516240-10516290	SK-N-SH_RA	brain:	n/a
48	chr12:10560602-10560652	LNCaP	prostate:	n/a
49	chr12:10532046-10532096	HepG2	liver:	n/a
50	chr12:10545083-10545133	PANC-1	pancreas:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:10509675..10512643-chr12:10514341..10517366,3	K562	blood:
2	chr12:10534850..10537741-chr12:10540764..10542364,2	MCF-7	breast:
3	chr12:10536735..10538905-chr12:10543028..10545121,2	MCF-7	breast:
4	chr12:10514090..10517702-chr12:10563594..10568036,4	K562	blood:
5	chr12:10515701..10517485-chr12:10526352..10529351,3	K562	blood:
6	chr12:10506746..10508549-chr12:10514255..10516412,2	K562	blood:
7	chr12:10527378..10530229-chr12:10546803..10548399,2	K562	blood:
8	chr12:10547736..10550018-chr12:10555798..10557891,2	MCF-7	breast:
9	chr12:10436832..10439225-chr12:10509141..10511407,2	K562	blood:
10	chr12:10507526..10509637-chr12:10511583..10513205,2	K562	blood:
11	chr12:10559960..10560793-chrX:131351678..131352452,2	Hela-S3	cervix:
12	chr12:10561211..10561774-chr17:76182659..76183234,2	Hela-S3	cervix:
13	chr12:10537029..10538774-chr12:10541549..10544546,2	K562	blood:
14	chr12:10527378..10530229-chr12:10546803..10548399,2	K562	blood:
15	chr1:28974955..28975586-chr12:10563608..10564342,2	Hela-S3	cervix:
16	chr12:10520202..10521817-chr12:10526312..10528193,2	K562	blood:
17	chr12:10528733..10530247-chr12:10762165..10764402,2	K562	blood:
18	chr12:10519323..10520144-chr12:10902384..10903013,2	MCF-7	breast:
19	chr12:10516092..10519058-chr12:10537972..10540241,2	K562	blood:
20	chr12:10515701..10519228-chr12:10526352..10529377,4	K562	blood:
21	chr12:10518506..10519182-chr16:20688297..20688797,2	HCT-116	colon:
22	chr12:10554334..10554872-chr16:81477760..81478703,2	Hela-S3	cervix:
23	chr12:10520202..10521817-chr12:10526312..10528193,2	K562	blood:
24	chr12:10563346..10565218-chr12:11316267..11318781,2	K562	blood:
25	chr12:10507526..10509637-chr12:10511583..10513205,2	K562	blood:
26	chr12:10548044..10548696-chr9:117267865..117268396,2	Hela-S3	cervix:
27	chr12:10547736..10550018-chr12:10555798..10557891,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLRD1-1	chr12:10516368-10516632	ENSG00000245648
2	lnc-KLRD1-1	chr12:10526634-10526735	ENSG00000245648
3	lnc-KLRD1-1	chr12:10532301-10532435	ENSG00000245648
4	lnc-RP11-277P12.7.1-1	chr12:10513183-10513644	ENSG00000256155
5	lnc-RP11-277P12.7.1-1	chr12:10511063-10511162	ENSG00000256155
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
ENSG00000256288	TF binding region
KLRK1	TF binding region
KLRC4	TF binding region
KLRC4-KLRK1	TF binding region
ENSG00000256155	TF binding region
ENSG00000245648	TF binding region
ENSG00000256288	CpG island
KLRK1	CpG island
KLRC4	CpG island
KLRC4-KLRK1	CpG island
ENSG00000256155	CpG island
ENSG00000245648	CpG island
ENSG00000256888	chromatin interactions
ENSG00000245648	chromatin interactions
ENSG00000167900	chromatin interactions
ENSG00000123728	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000213809	chromatin interactions
SMAD4	miRNA target sites
KIAA1967	miRNA target sites
ESR1	miRNA target sites

Extended variants
information (count: 2948 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2948 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10845109	chr12:10492982-10492983	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs572480772	chr12:10493068-10493069	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs535061510	chr12:10493077-10493078	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs555473016	chr12:10493085-10493086	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs77950826	chr12:10493108-10493109	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs114891448	chr12:10493113-10493114	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs184422269	chr12:10493130-10493131	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs577625923	chr12:10493132-10493133	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs546491143	chr12:10493133-10493134	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs190413937	chr12:10493174-10493175	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs528527292	chr12:10493194-10493195	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs181765575	chr12:10493196-10493197	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs186173718	chr12:10493206-10493207	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs560981160	chr12:10493210-10493211	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs75933594	chr12:10493229-10493230	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs527628366	chr12:10493233-10493234	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs2617142	chr12:10493251-10493252	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs142183014	chr12:10493276-10493277	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs539372800	chr12:10493288-10493289	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs564111681	chr12:10493289-10493290	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs566414735	chr12:10493319-10493320	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs188942569	chr12:10493343-10493344	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs151193944	chr12:10493366-10493367	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs368070074	chr12:10493403-10493404	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs7306846	chr12:10493429-10493430	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs201906999	chr12:10493444-10493445	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs557552067	chr12:10493463-10493464	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs117295591	chr12:10493464-10493465	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs546403148	chr12:10493484-10493485	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs527777599	chr12:10493485-10493486	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs560127801	chr12:10493514-10493515	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs386760270	chr12:10493561-10493562	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186486119	chr12:10493562-10493563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191421281	chr12:10493627-10493628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs34232738	chr12:10493657-10493658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201045098	chr12:10493686-10493687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561890694	chr12:10493693-10493694	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531052135	chr12:10493695-10493696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147063652	chr12:10493770-10493771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564221595	chr12:10493808-10493809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532995702	chr12:10493839-10493840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546380144	chr12:10493840-10493841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs372364937	chr12:10493860-10493861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs529106343	chr12:10493865-10493866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs10772262	chr12:10493878-10493879	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs549643640	chr12:10493916-10493917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142351334	chr12:10493953-10493954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566364898	chr12:10493966-10493967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537825087	chr12:10493972-10493973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535348336	chr12:10493980-10493981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1802 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10491000-10493000	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr12:10491400-10493000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr12:10491400-10493000	Enhancers	Hela-S3	cervix
4	chr12:10491400-10493000	Enhancers	HSMM	muscle
5	chr12:10491400-10494800	Enhancers	HMEC	breast
6	chr12:10491600-10495000	Enhancers	HUVEC	blood vessel
7	chr12:10491800-10493000	Enhancers	A549	lung
8	chr12:10491800-10495800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr12:10492200-10493200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr12:10492200-10494400	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr12:10492400-10493800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr12:10492400-10494600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr12:10492800-10507000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr12:10493000-10493200	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr12:10493200-10493400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr12:10493800-10495000	Enhancers	Dnd41	blood
17	chr12:10494400-10495000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
18	chr12:10494400-10495000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
19	chr12:10494600-10495000	Enhancers	Primary B cells from peripheral blood	blood
20	chr12:10494600-10495000	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
21	chr12:10494600-10495000	Enhancers	Brain Hippocampus Middle	brain
22	chr12:10494600-10507000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
23	chr12:10504000-10504200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr12:10504200-10507000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr12:10505000-10505600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr12:10505600-10505800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr12:10505600-10507000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr12:10505800-10506800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr12:10506600-10506800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr12:10506800-10507200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
31	chr12:10506800-10507200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr12:10506800-10507200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr12:10506800-10507200	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr12:10506800-10507200	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr12:10506800-10507200	Enhancers	GM12878-XiMat	blood
36	chr12:10506800-10507400	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr12:10506800-10507400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
38	chr12:10506800-10507400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr12:10506800-10508000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr12:10506800-10508000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr12:10506800-10508200	Enhancers	Hela-S3	cervix
42	chr12:10507000-10507200	Enhancers	Gastric	stomach
43	chr12:10507000-10507200	Enhancers	Pancreas	Pancrea
44	chr12:10507000-10507400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr12:10507000-10507400	Enhancers	H1 Cell Line	embryonic stem cell
46	chr12:10507000-10507400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr12:10507000-10507400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr12:10507000-10507400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr12:10507000-10507400	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr12:10507000-10507400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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