Variant report

Variant	nsv605
Chromosome Location	chr12:10448638-10494208
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:383)
CpG islands
(count:552)
Chromatin interactive
region (count:12)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:383 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:10456577-10457005	GM12878	blood:	n/a	n/a
2	ATF2	chr12:10470709-10471203	GM12878	blood:	n/a	n/a
3	ATF2	chr12:10470741-10471136	GM12878	blood:	n/a	n/a
4	ATF2	chr12:10473155-10473759	GM12878	blood:	n/a	n/a
5	BATF	chr12:10470851-10471221	GM12878	blood:	n/a	chr12:10471022-10471030
6	BATF	chr12:10456621-10457029	GM12878	blood:	n/a	n/a
7	BATF	chr12:10473160-10473741	GM12878	blood:	n/a	n/a
8	BATF	chr12:10473216-10473419	GM12878	blood:	n/a	n/a
9	BATF	chr12:10455627-10455902	GM12878	blood:	n/a	chr12:10455749-10455760
10	BATF	chr12:10473434-10473653	GM12878	blood:	n/a	n/a
11	BCL11A	chr12:10473293-10473615	GM12878	blood:	n/a	n/a
12	BCL3	chr12:10470815-10471173	GM12878	blood:	n/a	chr12:10470997-10471006
13	BCL3	chr12:10456668-10457144	GM12878	blood:	n/a	n/a
14	BCLAF1	chr12:10470778-10471247	GM12878	blood:	n/a	chr12:10470997-10471006
15	BCLAF1	chr12:10473313-10473710	GM12878	blood:	n/a	n/a
16	BHLHE40	chr12:10484273-10484556	GM12878	blood:	n/a	n/a
17	BHLHE40	chr12:10472918-10473181	GM12878	blood:	n/a	n/a
18	BHLHE40	chr12:10456938-10456948	GM12878	blood:	n/a	n/a
19	CEBPB	chr12:10487581-10487803	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr12:10456678-10457101	IMR90	lung:	n/a	n/a
21	CEBPB	chr12:10469048-10469179	Hela-S3	cervix:	n/a	chr12:10469057-10469068
22	CEBPB	chr12:10474613-10474641	HepG2	liver:	n/a	n/a
23	CEBPB	chr12:10468976-10469243	HepG2	liver:	n/a	chr12:10469057-10469068
24	CEBPB	chr12:10469010-10469209	A549	lung:	n/a	chr12:10469057-10469068
25	CEBPB	chr12:10456755-10457020	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr12:10460969-10461135	HepG2	liver:	n/a	n/a
27	CEBPB	chr12:10453905-10454072	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr12:10468932-10469198	K562	blood:	n/a	chr12:10469057-10469068
29	CEBPB	chr12:10468993-10469151	MCF-7	breast:	n/a	chr12:10469057-10469068
30	CEBPB	chr12:10463938-10464283	Hela-S3	cervix:	n/a	n/a
31	CHD1	chr12:10456543-10457321	IMR90	lung:	n/a	n/a
32	CTCF	chr12:10484380-10484530	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr12:10484380-10484530	AG04449	skin:	n/a	n/a
34	CTCF	chr12:10484380-10484530	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr12:10484400-10484550	BJ	skin:	n/a	n/a
36	CTCF	chr12:10484360-10484510	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr12:10484296-10484554	Gliobla	brain:	n/a	n/a
38	CTCF	chr12:10484360-10484510	AG04450	lung:	n/a	n/a
39	CTCF	chr12:10484340-10484490	GM12865	blood:	n/a	n/a
40	CTCF	chr12:10484327-10484551	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr12:10455311-10455317	GM13977	blood:	n/a	n/a
42	CTCF	chr12:10484320-10484536	NHEK	skin:	n/a	n/a
43	CTCF	chr12:10484241-10484534	A549	lung:	n/a	n/a
44	CTCF	chr12:10484340-10484490	AG09319	gingival:	n/a	n/a
45	CTCF	chr12:10484288-10484710	K562	blood:	n/a	n/a
46	CTCF	chr12:10484380-10484530	AG09309	skin:	n/a	n/a
47	CTCF	chr12:10484340-10484490	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr12:10484300-10484450	GM12865	blood:	n/a	n/a
49	CTCF	chr12:10484314-10484569	GM12878	blood:	n/a	n/a
50	CTCF	chr12:10484400-10484550	GM06990	blood:	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	chr12:10460612-10460662	MCF-7	breast:	n/a
2	chr12:10460639-10460689	Caco-2	colon:	n/a
3	chr12:10460612-10460662	AoSMC	blood vessel:	n/a
4	chr12:10460612-10460662	MCF-7	breast:	n/a
5	chr12:10460639-10460689	Caco-2	colon:	n/a
6	chr12:10460612-10460662	AoSMC	blood vessel:	n/a
7	chr12:10459972-10460022	T-47D	breast:	n/a
8	chr12:10456885-10456935	HCPEpiC	choroid plexus:	n/a
9	chr12:10465272-10465322	Caco-2	colon:	n/a
10	chr12:10459923-10459973	ovcar-3	ovarian:	n/a
11	chr12:10459972-10460022	SK-N-SH	brain:	n/a
12	chr12:10456885-10456935	PrEC	prostate:	n/a
13	chr12:10465272-10465322	GM12878	blood:	n/a
14	chr12:10456885-10456935	SK-N-MC	brain:	n/a
15	chr12:10459912-10459962	NT2-D1	testis:	n/a
16	chr12:10459972-10460022	MCF-7	breast:	n/a
17	chr12:10459972-10460022	NH-A	brain:	n/a
18	chr12:10459912-10459962	SK-N-SH_RA	brain:	n/a
19	chr12:10459912-10459962	K562	blood:	n/a
20	chr12:10460639-10460689	NHDF-neo	bronchial:	n/a
21	chr12:10459923-10459973	GM12892	blood:	n/a
22	chr12:10459972-10460022	HNPCEpiC	eye:	n/a
23	chr12:10460639-10460689	HEEpiC	esophagus:	n/a
24	chr12:10459912-10459962	MCF10A-Er-Src	breast:	n/a
25	chr12:10456885-10456935	LNCaP	prostate:	n/a
26	chr12:10459923-10459973	HRPEpiC	eye:	n/a
27	chr12:10460612-10460662	IMR90	lung:	fetal
28	chr12:10456885-10456935	ProgFib	skin:	n/a
29	chr12:10459923-10459973	AG04450	lung:	fetal
30	chr12:10469147-10469197	SAEC	small airway:	n/a
31	chr12:10459923-10459973	GM06990	blood:	n/a
32	chr12:10469147-10469197	HRPEpiC	eye:	n/a
33	chr12:10460612-10460662	HAEpiC	amniotic membrane:	n/a
34	chr12:10460612-10460662	HEK293	kidney:	embryo
35	chr12:10460612-10460662	HRCEpiC	kidney:	n/a
36	chr12:10459923-10459973	IMR90	lung:	fetal
37	chr12:10459912-10459962	GM19239	blood:	n/a
38	chr12:10456885-10456935	SK-N-SH_RA	brain:	n/a
39	chr12:10455788-10455838	HCF	heart:	n/a
40	chr12:10459923-10459973	ECC-1	luminal epithelium:	n/a
41	chr12:10465272-10465322	GM19239	blood:	n/a
42	chr12:10465272-10465322	ProgFib	skin:	n/a
43	chr12:10459923-10459973	HAEpiC	amniotic membrane:	n/a
44	chr12:10455788-10455838	HepG2	liver:	n/a
45	chr12:10455788-10455838	PANC-1	pancreas:	n/a
46	chr12:10460612-10460662	HRPEpiC	eye:	n/a
47	chr12:10469147-10469197	NT2-D1	testis:	n/a
48	chr12:10459923-10459973	ProgFib	skin:	n/a
49	chr12:10456885-10456935	AG09319	gingival:	n/a
50	chr12:10465272-10465322	T-47D	breast:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:10442366..10444908-chr12:10450816..10453146,2	K562	blood:
2	chr12:10484385..10484963-chr12:10714626..10715246,2	MCF-7	breast:
3	chr12:10453243..10455277-chr12:10460503..10462364,2	K562	blood:
4	chr12:10484283..10485072-chr12:10714510..10715568,4	K562	blood:
5	chr12:10470749..10472594-chr12:10475991..10477834,2	K562	blood:
6	chr12:10483978..10484906-chr12:10714545..10715159,3	MCF-7	breast:
7	chr12:10484044..10484911-chr12:10711156..10712037,3	MCF-7	breast:
8	chr12:10470749..10472594-chr12:10475991..10477834,2	K562	blood:
9	chr12:10445022..10447315-chr12:10448355..10450390,2	K562	blood:
10	chr12:10484518..10485026-chr12:10826902..10827419,2	MCF-7	breast:
11	chr12:10483953..10484953-chr12:10826469..10827411,2	K562	blood:
12	chr12:10484099..10484956-chr12:10652861..10653779,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GABARAPL1-3	chr12:10460544-10460683	NONHSAT026878
2	lnc-GABARAPL1-3	chr12:10464063-10464282	NONHSAT026878
3	lnc-GABARAPL1-3	chr12:10464063-10464214	NONHSAT026875
4	lnc-GABARAPL1-3	chr12:10466009-10466112	NONHSAT026875
5	lnc-GABARAPL1-3	chr12:10462225-10462287	NONHSAT026878
6	lnc-GABARAPL1-3	chr12:10467272-10467608	NONHSAT026875
7	lnc-RP11-277P12.7.1-2	chr12:10488711-10488908	ENSG00000256288
8	lnc-RP11-277P12.7.1-2	chr12:10485460-10485662	ENSG00000256288
9	lnc-RP11-277P12.7.1-2	chr12:10490644-10490891	ENSG00000256288
10	lnc-GABARAPL1-3	chr12:10457065-10457146	NONHSAT026875
11	lnc-GABARAPL1-3	chr12:10460577-10462287	NONHSAT026875

No data

Variant related genes	Relation type
ENSG00000256288	TF binding region
KLRD1	TF binding region
ENSG00000256288	CpG island
KLRD1	CpG island
ENSG00000134539	chromatin interactions
ENSG00000060140	chromatin interactions
NFIB	miRNA target sites
LPHN2	miRNA target sites
RNF111	miRNA target sites

Extended variants
information (count: 2010 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2010 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535668364	chr12:10448656-10448657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs555717063	chr12:10448685-10448686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2537785	chr12:10448708-10448709	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs2537784	chr12:10448754-10448755	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs115263699	chr12:10448755-10448756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188204311	chr12:10448802-10448803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs578075563	chr12:10448825-10448826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs540588720	chr12:10448837-10448838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs117569667	chr12:10448838-10448839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563754238	chr12:10448843-10448844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs529433888	chr12:10448845-10448846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs560926157	chr12:10448852-10448853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs375458620	chr12:10448886-10448887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs373983949	chr12:10448898-10448899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs12814085	chr12:10448911-10448912	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs562571354	chr12:10448984-10448985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs139639121	chr12:10449039-10449040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs372613175	chr12:10449041-10449042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs551429110	chr12:10449063-10449064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568201974	chr12:10449080-10449081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192915220	chr12:10449101-10449102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs113495601	chr12:10449110-10449111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542167116	chr12:10449135-10449136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546953758	chr12:10449142-10449143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs146076054	chr12:10449144-10449145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs374602895	chr12:10449152-10449153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs76131228	chr12:10449203-10449204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs182563022	chr12:10449225-10449226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556218295	chr12:10449262-10449263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372206077	chr12:10449286-10449287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs374340471	chr12:10449313-10449314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs34666383	chr12:10449341-10449342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs538393227	chr12:10449343-10449344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs148718182	chr12:10449381-10449382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs578243548	chr12:10449385-10449386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs7307026	chr12:10449431-10449432	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs186835223	chr12:10449432-10449433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs117891507	chr12:10449450-10449451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs570079909	chr12:10449457-10449458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs560041345	chr12:10449464-10449465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542801979	chr12:10449500-10449501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562991182	chr12:10449535-10449536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs142252127	chr12:10449562-10449563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545158466	chr12:10449563-10449564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs148998209	chr12:10449695-10449696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs564849718	chr12:10449762-10449763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs527614576	chr12:10449777-10449778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs547265838	chr12:10449827-10449828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs117117730	chr12:10449850-10449851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529680079	chr12:10449971-10449972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD

Chromatin state (count:182 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10447000-10453600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr12:10447400-10448800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr12:10447400-10455000	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr12:10447600-10449000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr12:10447800-10453600	Weak transcription	Primary T cells from cord blood	blood
6	chr12:10447800-10456600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr12:10448800-10449600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr12:10449000-10449800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
9	chr12:10449600-10453800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr12:10449800-10453200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr12:10453200-10454400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr12:10453200-10461000	Weak transcription	Placenta	Placenta
13	chr12:10453400-10454600	Enhancers	Thymus	Thymus
14	chr12:10453400-10457000	Enhancers	Placenta Amnion	Placenta Amnion
15	chr12:10453600-10454200	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr12:10453600-10454400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr12:10453600-10454400	Enhancers	Fetal Thymus	thymus
18	chr12:10453600-10454400	Enhancers	Dnd41	blood
19	chr12:10453600-10454600	Enhancers	Primary T cells from cord blood	blood
20	chr12:10453800-10457200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr12:10454000-10454400	Enhancers	Muscle Satellite Cultured Cells	--
22	chr12:10454200-10458000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr12:10454400-10455600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr12:10454600-10455200	Weak transcription	Thymus	Thymus
25	chr12:10454800-10474400	Weak transcription	Left Ventricle	heart
26	chr12:10455000-10456000	Enhancers	Primary T cells fromperipheralblood	blood
27	chr12:10455200-10455400	ZNF genes & repeats	Thymus	Thymus
28	chr12:10455600-10455800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr12:10455800-10456200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr12:10456000-10457000	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr12:10456200-10456400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr12:10456200-10457200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr12:10456400-10457200	Enhancers	Muscle Satellite Cultured Cells	--
34	chr12:10456400-10457800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr12:10456600-10457200	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr12:10457000-10457400	Enhancers	Primary T cells fromperipheralblood	blood
37	chr12:10457200-10457600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr12:10457200-10458000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
39	chr12:10457400-10458000	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr12:10457400-10458000	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr12:10457600-10458200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr12:10457600-10458200	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr12:10457600-10458200	Enhancers	Primary T killer memory cells from peripheral blood	blood
44	chr12:10457600-10458400	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr12:10457800-10458400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr12:10458000-10458400	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr12:10458000-10458400	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
48	chr12:10458000-10464200	Active TSS	Primary T cells fromperipheralblood	blood
49	chr12:10458200-10460600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
50	chr12:10458400-10458800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood

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