Variant report

Variant	nsv557743
Chromosome Location	chr12:21670410-21688900
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:209)
CpG islands
(count:671)
Chromatin interactive
region (count:7)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:209 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr12:21678978-21679210	K562	blood:	n/a	n/a
2	BACH1	chr12:21674625-21674693	K562	blood:	n/a	n/a
3	BACH1	chr12:21680547-21680670	H1-hESC	embryonic stem cell:	n/a	n/a
4	CCNT2	chr12:21674469-21674678	K562	blood:	n/a	n/a
5	CEBPB	chr12:21678873-21679461	A549	lung:	n/a	chr12:21679146-21679157
6	CEBPB	chr12:21679034-21679406	MCF-7	breast:	n/a	chr12:21679146-21679157
7	CEBPB	chr12:21678967-21679310	IMR90	lung:	n/a	chr12:21679146-21679157
8	CEBPB	chr12:21676115-21676449	HepG2	liver:	n/a	n/a
9	CEBPB	chr12:21678928-21679487	HCT-116	colon:	n/a	chr12:21679146-21679157
10	CEBPB	chr12:21678916-21679400	A549	lung:	n/a	chr12:21679146-21679157
11	CEBPB	chr12:21678984-21679313	H1-hESC	embryonic stem cell:	n/a	chr12:21679146-21679157
12	CEBPB	chr12:21679036-21679285	K562	blood:	n/a	chr12:21679146-21679157
13	CEBPB	chr12:21678974-21679293	ECC-1	luminal epithelium:	n/a	chr12:21679146-21679157
14	CEBPB	chr12:21678966-21679339	Hela-S3	cervix:	n/a	chr12:21679146-21679157
15	CEBPB	chr12:21678961-21679327	HepG2	liver:	n/a	chr12:21679146-21679157
16	CEBPB	chr12:21679058-21679180	HepG2	liver:	n/a	chr12:21679146-21679157
17	CEBPB	chr12:21679071-21679242	K562	blood:	n/a	chr12:21679146-21679157
18	CEBPB	chr12:21678962-21679321	K562	blood:	n/a	chr12:21679146-21679157
19	CEBPB	chr12:21678952-21679350	A549	lung:	n/a	chr12:21679146-21679157
20	CHD1	chr12:21680481-21681094	H1-hESC	embryonic stem cell:	n/a	chr12:21680775-21680785
21	CHD2	chr12:21680662-21680690	GM12878	blood:	n/a	n/a
22	CHD2	chr12:21680859-21681129	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr12:21680383-21681134	A549	lung:	n/a	n/a
24	CREB1	chr12:21680585-21681121	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr12:21680598-21681094	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTBP2	chr12:21680322-21681135	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr12:21680800-21680950	AG04449	skin:	n/a	n/a
28	CTCF	chr12:21681000-21681150	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr12:21681080-21681230	A549	lung:	n/a	n/a
30	CTCF	chr12:21680900-21681050	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr12:21680960-21681110	HMF	breast:	n/a	n/a
32	CTCF	chr12:21680840-21680990	A549	lung:	n/a	n/a
33	CTCF	chr12:21680880-21681030	HepG2	liver:	n/a	n/a
34	CTCF	chr12:21680760-21680910	HRE	kidney:	n/a	n/a
35	CTCF	chr12:21681001-21681014	Fibrobl	skin:	n/a	n/a
36	CTCF	chr12:21680200-21680350	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr12:21680960-21681110	SAEC	small airway:	n/a	n/a
38	CTCF	chr12:21680940-21680989	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr12:21680954-21680958	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr12:21680782-21680844	A549	lung:	n/a	n/a
41	CTCF	chr12:21680855-21681151	GM12878	blood:	n/a	n/a
42	CTCF	chr12:21680940-21681090	HRE	kidney:	n/a	n/a
43	CTCF	chr12:21680700-21680850	GM12870	blood:	n/a	n/a
44	CTCF	chr12:21680975-21680988	MCF-7	breast:	n/a	n/a
45	CTCF	chr12:21680980-21681130	BJ	skin:	n/a	n/a
46	CTCF	chr12:21680942-21681084	A549	lung:	n/a	n/a
47	CTCF	chr12:21680940-21681090	SAEC	small airway:	n/a	n/a
48	CTCF	chr12:21680940-21681090	HCFaa	heart:	n/a	n/a
49	CUX1	chr12:21678796-21679127	K562	blood:	n/a	n/a
50	E2F4	chr12:21680790-21681022	MCF10A-Er-Src	breast:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:21679634-21679684	Hela-S3	cervix:	n/a
2	chr12:21680508-21680558	HRPEpiC	eye:	n/a
3	chr12:21680508-21680558	Caco-2	colon:	n/a
4	chr12:21679634-21679684	BE2_C	brain:	n/a
5	chr12:21678386-21678436	Jurkat	blood:	n/a
6	chr12:21680508-21680558	PANC-1	pancreas:	n/a
7	chr12:21680848-21680898	H1-hESC	embryonic stem cell:	embryo
8	chr12:21680220-21680270	HCF	heart:	n/a
9	chr12:21680426-21680476	Jurkat	blood:	n/a
10	chr12:21678044-21678094	Jurkat	blood:	n/a
11	chr12:21680409-21680459	HIPEpiC	eye:	n/a
12	chr12:21680220-21680270	HAEpiC	amniotic membrane:	n/a
13	chr12:21680848-21680898	HAEpiC	amniotic membrane:	n/a
14	chr12:21680508-21680558	CMK	blood:	n/a
15	chr12:21680220-21680270	ProgFib	skin:	n/a
16	chr12:21680409-21680459	HRCEpiC	kidney:	n/a
17	chr12:21679634-21679684	RPTEC	kidney:	n/a
18	chr12:21681006-21681056	SK-N-SH_RA	brain:	n/a
19	chr12:21678044-21678094	HRCEpiC	kidney:	n/a
20	chr12:21680508-21680558	SK-N-SH_RA	brain:	n/a
21	chr12:21681006-21681056	SKMC	muscle:	n/a
22	chr12:21681006-21681056	GM19239	blood:	n/a
23	chr12:21680848-21680898	Jurkat	blood:	n/a
24	chr12:21679634-21679684	GM12892	blood:	n/a
25	chr12:21680981-21681031	LNCaP	prostate:	n/a
26	chr12:21681006-21681056	Caco-2	colon:	n/a
27	chr12:21678044-21678094	HL-60	blood:	n/a
28	chr12:21679634-21679684	GM12878	blood:	n/a
29	chr12:21680848-21680898	PANC-1	pancreas:	n/a
30	chr12:21680220-21680270	Caco-2	colon:	n/a
31	chr12:21680848-21680898	HMEC	breast:	n/a
32	chr12:21679634-21679684	GM06990	blood:	n/a
33	chr12:21680409-21680459	HCPEpiC	choroid plexus:	n/a
34	chr12:21680508-21680558	HNPCEpiC	eye:	n/a
35	chr12:21680669-21680719	AG10803	skin:	n/a
36	chr12:21680508-21680558	Jurkat	blood:	n/a
37	chr12:21680981-21681031	HAEpiC	amniotic membrane:	n/a
38	chr12:21680508-21680558	NHBE	bronchial:	n/a
39	chr12:21681006-21681056	K562	blood:	n/a
40	chr12:21680220-21680270	HIPEpiC	eye:	n/a
41	chr12:21680981-21681031	AG09319	gingival:	n/a
42	chr12:21680508-21680558	BE2_C	brain:	n/a
43	chr12:21680848-21680898	LNCaP	prostate:	n/a
44	chr12:21678044-21678094	HUVEC	blood vessel:	n/a
45	chr12:21680981-21681031	GM12891	blood:	n/a
46	chr12:21681006-21681056	ProgFib	skin:	n/a
47	chr12:21680220-21680270	AoSMC	blood vessel:	n/a
48	chr12:21678386-21678436	AG04449	skin:	fetal
49	chr12:21680426-21680476	HPAEpiC	pulmonary alveolar:	n/a
50	chr12:21680426-21680476	A549	lung:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:21666099..21668505-chr12:21668536..21671439,2	K562	blood:
2	chr12:21667585..21669254-chr12:21672387..21674128,2	K562	blood:
3	chr12:21654473..21659052-chr12:21670057..21674835,6	K562	blood:
4	chr12:21685388..21686219-chr7:120328726..120329601,2	MCF-7	breast:
5	chr12:21671832..21674785-chr12:21687913..21690095,2	K562	blood:
6	chr12:21671832..21674785-chr12:21687913..21690095,2	K562	blood:
7	chr12:21659626..21662190-chr12:21669299..21671528,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GOLT1B-2	chr12:21681935-21682018	NONHSAT027254
2	lnc-GOLT1B-2	chr12:21680870-21681085	NONHSAT027254
3	lnc-GOLT1B-2	chr12:21684071-21685457	NONHSAT027254

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	GOLT1B	hsa-miR-16-5p	chr12:21670993-21670999
2	GOLT1B	hsa-miR-16-5p	chr12:21670982-21671000
3	GOLT1B	hsa-miR-155-5p	chr12:21670582-21670603
4	GOLT1B	hsa-miR-103a-3p	chr12:21670976-21670999

Variant related genes	Relation type
C12orf39	TF binding region
C12orf39	CpG island
ENSG00000004700	chromatin interactions
ENSG00000111711	chromatin interactions

Extended variants
information (count: 679 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:679 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10770819	chr12:21670410-21670411	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553065591	chr12:21670414-21670415	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs566550568	chr12:21670424-21670425	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs528034315	chr12:21670469-21670470	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs185837509	chr12:21670549-21670550	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs538856335	chr12:21670601-21670602	Weak transcription Strong transcription Enhancers	Chromatin interactive region miRNA target site	3 gene(s)	Overlapped CNVs	n/a
7	rs146393209	chr12:21670685-21670686	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs575620411	chr12:21670759-21670760	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs544448138	chr12:21670772-21670773	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs554567774	chr12:21670839-21670840	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs574021758	chr12:21670912-21670913	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs11555095	chr12:21670990-21670991	Weak transcription Strong transcription	Chromatin interactive region miRNA target site	3 gene(s)	Overlapped CNVs	n/a
13	rs34674091	chr12:21671082-21671083	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs374897103	chr12:21671089-21671090	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs80115468	chr12:21671107-21671108	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs559451272	chr12:21671135-21671136	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs73079391	chr12:21671141-21671142	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs116199620	chr12:21671165-21671166	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs536866072	chr12:21671173-21671174	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs565087412	chr12:21671179-21671180	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs139781385	chr12:21671180-21671181	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs1048617	chr12:21671191-21671192	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs3088178	chr12:21671193-21671194	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs529720811	chr12:21671213-21671214	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs546250055	chr12:21671219-21671220	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs183097316	chr12:21671253-21671254	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs186030251	chr12:21671281-21671282	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs558789451	chr12:21671322-21671323	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs569120889	chr12:21671365-21671366	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs537638242	chr12:21671399-21671400	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs554885533	chr12:21671406-21671407	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs75737884	chr12:21671441-21671442	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs12371654	chr12:21671506-21671507	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs552906669	chr12:21671525-21671526	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs573001338	chr12:21671540-21671541	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs545142387	chr12:21671554-21671555	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs2110162	chr12:21671566-21671567	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs143980666	chr12:21671569-21671570	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs377077708	chr12:21671570-21671571	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs561647584	chr12:21671625-21671626	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs145948444	chr12:21671719-21671720	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs546629801	chr12:21671730-21671731	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs556544309	chr12:21671784-21671785	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs73079397	chr12:21671803-21671804	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs190489179	chr12:21671836-21671837	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs532142905	chr12:21671891-21671892	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs139474042	chr12:21672005-21672006	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs2417994	chr12:21672022-21672023	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs182633646	chr12:21672027-21672028	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs548054946	chr12:21672028-21672029	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Malignant germ cell tumour	17285132	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21364760	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Lung cancer	21911935	CNVD
Breast cancer	22048815	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Heart disease	21282601	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Gastric cancer	24379144	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Gastric cancer	19545448	CNVD
Lung cancer	20031968	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung adenocarcinoma	19826477	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19826477	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	17504988	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	19671679	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:528 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:21655400-21674800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr12:21656000-21671800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr12:21656000-21672800	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr12:21656000-21674000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr12:21656000-21674600	Weak transcription	Fetal Kidney	kidney
6	chr12:21656200-21671800	Weak transcription	Thymus	Thymus
7	chr12:21656200-21680000	Weak transcription	Right Ventricle	heart
8	chr12:21656400-21680200	Weak transcription	Aorta	Aorta
9	chr12:21656800-21671400	Weak transcription	Fetal Heart	heart
10	chr12:21656800-21680000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr12:21657400-21680000	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr12:21657600-21675000	Weak transcription	Small Intestine	intestine
13	chr12:21657600-21675400	Weak transcription	Fetal Brain Male	brain
14	chr12:21657600-21679800	Weak transcription	Pancreas	Pancrea
15	chr12:21657600-21680000	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr12:21657600-21680400	Weak transcription	Gastric	stomach
17	chr12:21660000-21671600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr12:21660000-21672000	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr12:21660200-21671600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr12:21660200-21672600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr12:21660400-21671600	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr12:21660400-21672200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr12:21660600-21670800	Strong transcription	Osteobl	bone
24	chr12:21660600-21672600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr12:21660800-21671600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr12:21660800-21672400	Strong transcription	Liver	Liver
27	chr12:21661000-21670600	Strong transcription	Adipose Nuclei	Adipose
28	chr12:21661400-21670800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr12:21661400-21677200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr12:21662200-21672400	Strong transcription	HSMM	muscle
31	chr12:21663400-21671000	Strong transcription	GM12878-XiMat	blood
32	chr12:21664400-21671800	Strong transcription	Primary T helper cells PMA-I stimulated	--
33	chr12:21664600-21670600	Strong transcription	Rectal Mucosa Donor 31	rectum
34	chr12:21664800-21671600	Strong transcription	Primary T helper cells fromperipheralblood	blood
35	chr12:21664800-21672400	Strong transcription	NH-A	brain
36	chr12:21665000-21670600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
37	chr12:21665200-21670800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr12:21665600-21670600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr12:21665600-21670800	Strong transcription	Primary T cells fromperipheralblood	blood
40	chr12:21665800-21672400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr12:21666000-21671800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr12:21666000-21680200	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr12:21666800-21671600	Weak transcription	Brain Germinal Matrix	brain
44	chr12:21666800-21671600	Weak transcription	Ovary	ovary
45	chr12:21666800-21672800	Weak transcription	NHEK	skin
46	chr12:21666800-21675800	Weak transcription	HepG2	liver
47	chr12:21666800-21676800	Weak transcription	Fetal Brain Female	brain
48	chr12:21666800-21679800	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr12:21666800-21680000	Weak transcription	Psoas Muscle	Psoas
50	chr12:21666800-21680200	Weak transcription	Colonic Mucosa	Colon

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