Variant report

Variant	esv3444473
Chromosome Location	chr12:11210415-11240825
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:107)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:107 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:11224069-11224255	HepG2	liver:	n/a	n/a
2	ATF2	chr12:11238009-11238486	GM12878	blood:	n/a	n/a
3	ATF2	chr12:11237956-11238445	GM12878	blood:	n/a	n/a
4	BATF	chr12:11225254-11225547	GM12878	blood:	n/a	n/a
5	BATF	chr12:11228218-11228560	GM12878	blood:	n/a	n/a
6	BATF	chr12:11216721-11217010	GM12878	blood:	n/a	n/a
7	BATF	chr12:11238012-11238373	GM12878	blood:	n/a	n/a
8	BATF	chr12:11238084-11238352	GM12878	blood:	n/a	n/a
9	BCL11A	chr12:11238061-11238356	GM12878	blood:	n/a	chr12:11238263-11238272
10	BCL11A	chr12:11228248-11228517	GM12878	blood:	n/a	n/a
11	BHLHE40	chr12:11228293-11228667	GM12878	blood:	n/a	n/a
12	CEBPB	chr12:11226186-11226481	HepG2	liver:	n/a	n/a
13	CEBPB	chr12:11223987-11224332	HepG2	liver:	n/a	n/a
14	CEBPB	chr12:11222658-11222813	HepG2	liver:	n/a	n/a
15	CHD2	chr12:11238132-11238304	GM12878	blood:	n/a	n/a
16	CTCF	chr12:11230498-11230623	Lung_OC	lung:	n/a	n/a
17	CUX1	chr12:11238241-11238349	GM12878	blood:	n/a	n/a
18	E2F4	chr12:11220752-11221188	MCF10A-Er-Src	breast:	n/a	n/a
19	EBF1	chr12:11226243-11226583	GM12878	blood:	n/a	chr12:11226441-11226451 chr12:11226441-11226450 chr12:11226439-11226452
20	EP300	chr12:11238133-11238438	GM12878	blood:	n/a	n/a
21	EP300	chr12:11228364-11228516	GM12878	blood:	n/a	n/a
22	EP300	chr12:11223962-11224277	HepG2	liver:	n/a	n/a
23	EP300	chr12:11238104-11238440	GM12878	blood:	n/a	n/a
24	FOXA1	chr12:11223802-11224380	HepG2	liver:	n/a	n/a
25	FOXA1	chr12:11223913-11224415	HepG2	liver:	n/a	n/a
26	FOXA1	chr12:11223940-11224452	HepG2	liver:	n/a	n/a
27	FOXA1	chr12:11223974-11224466	HepG2	liver:	n/a	n/a
28	FOXA2	chr12:11223986-11224245	A549	lung:	n/a	n/a
29	FOXA2	chr12:11223617-11224724	HepG2	liver:	n/a	n/a
30	FOXA2	chr12:11223920-11224357	HepG2	liver:	n/a	n/a
31	FOXM1	chr12:11238005-11238472	GM12878	blood:	n/a	n/a
32	GATA3	chr12:11221936-11222225	MCF-7	breast:	n/a	n/a
33	HDAC2	chr12:11223990-11224345	HepG2	liver:	n/a	n/a
34	IKZF1	chr12:11238336-11238561	GM12878	blood:	n/a	n/a
35	JUN	chr12:11212501-11212751	HepG2	liver:	n/a	chr12:11212602-11212615
36	JUND	chr12:11212422-11212743	HepG2	liver:	n/a	n/a
37	JUND	chr12:11224111-11224296	HepG2	liver:	n/a	n/a
38	KAP1	chr12:11233595-11233844	HEK293	kidney:	n/a	n/a
39	MAFF	chr12:11234615-11234942	HepG2	liver:	n/a	n/a
40	MAFK	chr12:11234617-11234968	IMR90	lung:	n/a	chr12:11234789-11234806
41	MAFK	chr12:11234630-11234922	HepG2	liver:	n/a	chr12:11234789-11234806
42	MAFK	chr12:11220562-11220586	HepG2	liver:	n/a	n/a
43	MAFK	chr12:11230418-11230581	HepG2	liver:	n/a	chr12:11230570-11230581 chr12:11230528-11230539 chr12:11230527-11230538 chr12:11230527-11230538 chr12:11230570-11230581
44	MAFK	chr12:11234655-11234917	H1-hESC	embryonic stem cell:	n/a	chr12:11234789-11234806
45	MAFK	chr12:11234616-11234980	HepG2	liver:	n/a	chr12:11234789-11234806
46	MXI1	chr12:11238156-11238251	GM12878	blood:	n/a	n/a
47	MYC	chr12:11226626-11226646	H1-hESC	embryonic stem cell:	n/a	n/a
48	NANOG	chr12:11224022-11224335	H1-hESC	embryonic stem cell:	n/a	n/a
49	NFATC1	chr12:11237942-11238414	GM12878	blood:	n/a	n/a
50	NFATC1	chr12:11238014-11238349	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11216351-11216401	HRCEpiC	kidney:	n/a
2	chr12:11216351-11216401	K562	blood:	n/a
3	chr12:11215083-11215133	HMEC	breast:	n/a
4	chr12:11216351-11216401	GM12891	blood:	n/a
5	chr12:11215083-11215133	PFSK-1	brain:	n/a
6	chr12:11215083-11215133	NB4	blood:	n/a
7	chr12:11215083-11215133	HL-60	blood:	n/a
8	chr12:11216351-11216401	PANC-1	pancreas:	n/a
9	chr12:11216351-11216401	SK-N-MC	brain:	n/a
10	chr12:11216351-11216401	AG04450	lung:	fetal
11	chr12:11215083-11215133	SKMC	muscle:	n/a
12	chr12:11215083-11215133	BE2_C	brain:	n/a
13	chr12:11215083-11215133	T-47D	breast:	n/a
14	chr12:11216351-11216401	HMEC	breast:	n/a
15	chr12:11215083-11215133	HPAEpiC	pulmonary alveolar:	n/a
16	chr12:11215083-11215133	SK-N-SH_RA	brain:	n/a
17	chr12:11215083-11215133	HNPCEpiC	eye:	n/a
18	chr12:11215083-11215133	U87	brain:	n/a
19	chr12:11215083-11215133	SAEC	small airway:	n/a
20	chr12:11215083-11215133	Hepatocyte	liver:	n/a
21	chr12:11215083-11215133	HAEpiC	amniotic membrane:	n/a
22	chr12:11216351-11216401	HEK293	kidney:	embryo
23	chr12:11216351-11216401	GM12878	blood:	n/a
24	chr12:11215083-11215133	IMR90	lung:	fetal
25	chr12:11215083-11215133	ECC-1	luminal epithelium:	n/a
26	chr12:11216351-11216401	HRPEpiC	eye:	n/a
27	chr12:11216351-11216401	A549	lung:	n/a
28	chr12:11216351-11216401	HepG2	liver:	n/a
29	chr12:11216351-11216401	ovcar-3	ovarian:	n/a
30	chr12:11216351-11216401	BJ	skin:	n/a
31	chr12:11215083-11215133	AG04450	lung:	fetal
32	chr12:11216351-11216401	NB4	blood:	n/a
33	chr12:11216351-11216401	Hela-S3	cervix:	n/a
34	chr12:11216351-11216401	NT2-D1	testis:	n/a
35	chr12:11216351-11216401	NHDF-neo	bronchial:	n/a
36	chr12:11215083-11215133	CMK	blood:	n/a
37	chr12:11215083-11215133	AG04449	skin:	fetal
38	chr12:11215083-11215133	GM06990	blood:	n/a
39	chr12:11215083-11215133	HRE	kidney:	n/a
40	chr12:11216351-11216401	SKMC	muscle:	n/a
41	chr12:11216351-11216401	HCPEpiC	choroid plexus:	n/a
42	chr12:11215083-11215133	AG09319	gingival:	n/a
43	chr12:11216351-11216401	HPAEpiC	pulmonary alveolar:	n/a
44	chr12:11216351-11216401	Hepatocyte	liver:	n/a
45	chr12:11215083-11215133	NHDF-neo	bronchial:	n/a
46	chr12:11215083-11215133	HEK293	kidney:	embryo
47	chr12:11215083-11215133	A549	lung:	n/a
48	chr12:11215083-11215133	H1-hESC	embryonic stem cell:	embryo
49	chr12:11216351-11216401	AoSMC	blood vessel:	n/a
50	chr12:11215083-11215133	HRCEpiC	kidney:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:11210669..11211248-chr5:109800405..109801099,2	MCF-7	breast:
2	chr12:11237724..11239418-chr12:11252570..11254241,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TAS2R43-1	chr12:11229368-11231770	NONHSAT026918
2	lnc-TAS2R43-1	chr12:11229915-11230841	NONHSAT140056

No data

Variant related genes	Relation type
TAS2R46	TF binding region
TAS2R64P	TF binding region
TAS2R46	CpG island
TAS2R64P	CpG island

Extended variants
information (count: 1994 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1994 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199987596	chr12:11210431-11210432	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs72477408	chr12:11210440-11210441	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs74413754	chr12:11210487-11210488	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs35605594	chr12:11210488-11210489	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs75569441	chr12:11210504-11210505	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150490188	chr12:11210526-11210527	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs75010210	chr12:11210555-11210556	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs77814832	chr12:11210566-11210567	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs78028591	chr12:11210567-11210568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554035386	chr12:11210583-11210584	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187022269	chr12:11210587-11210588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112713988	chr12:11210663-11210664	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs77604725	chr12:11210672-11210673	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs555989469	chr12:11210747-11210748	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs191893950	chr12:11210770-11210771	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183381342	chr12:11210779-11210780	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs565672864	chr12:11210812-11210813	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs187143061	chr12:11210826-11210827	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs190011689	chr12:11210892-11210893	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560849125	chr12:11210912-11210913	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs368583040	chr12:11210981-11210982	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529606331	chr12:11210999-11211000	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs200664432	chr12:11211003-11211004	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs138432187	chr12:11211020-11211021	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs79095756	chr12:11211054-11211055	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs76032018	chr12:11211059-11211060	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs79585361	chr12:11211081-11211082	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs551925294	chr12:11211092-11211093	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs76815507	chr12:11211096-11211097	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs578097604	chr12:11211128-11211129	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs74200682	chr12:11211129-11211130	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs78708533	chr12:11211135-11211136	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs77087349	chr12:11211166-11211167	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs73053037	chr12:11211185-11211186	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs182426132	chr12:11211189-11211190	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs73053039	chr12:11211190-11211191	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527692277	chr12:11211206-11211207	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186705281	chr12:11211229-11211230	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs368354969	chr12:11211233-11211234	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536172685	chr12:11211254-11211255	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs138178614	chr12:11211261-11211262	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs200643412	chr12:11211282-11211283	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs569532821	chr12:11211308-11211309	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149540511	chr12:11211426-11211427	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs368893429	chr12:11211486-11211487	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs558234359	chr12:11211487-11211488	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs371479899	chr12:11211535-11211536	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs192170564	chr12:11211538-11211539	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs372597253	chr12:11211548-11211549	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs144179259	chr12:11211599-11211600	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Acute myeloid leukemia	17237825	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Acute myeloid leukemia	20729466	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:231 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11169400-11219400	Weak transcription	HUVEC	blood vessel
2	chr12:11171000-11225600	Weak transcription	HSMMtube	muscle
3	chr12:11176400-11211200	Weak transcription	Aorta	Aorta
4	chr12:11179000-11223800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr12:11179400-11222000	Weak transcription	Fetal Kidney	kidney
6	chr12:11181000-11217400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr12:11181000-11220000	Weak transcription	Gastric	stomach
8	chr12:11181000-11224800	Weak transcription	Fetal Stomach	stomach
9	chr12:11184200-11213000	Weak transcription	Thymus	Thymus
10	chr12:11193200-11224200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr12:11196600-11211400	Weak transcription	Fetal Heart	heart
12	chr12:11196600-11215000	Weak transcription	NHLF	lung
13	chr12:11198000-11230200	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr12:11199600-11214200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr12:11199800-11222800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr12:11201400-11210600	Weak transcription	Left Ventricle	heart
17	chr12:11201600-11227800	Weak transcription	HSMM	muscle
18	chr12:11203200-11211600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr12:11203600-11216800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr12:11203600-11240000	Weak transcription	Ovary	ovary
21	chr12:11203800-11211200	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr12:11203800-11211400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr12:11203800-11211600	Weak transcription	Hela-S3	cervix
24	chr12:11203800-11212200	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr12:11203800-11212400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr12:11203800-11261200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr12:11204600-11224000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr12:11204600-11227600	Weak transcription	Fetal Lung	lung
29	chr12:11204800-11247600	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr12:11205800-11218200	Weak transcription	Primary B cells from cord blood	blood
31	chr12:11205800-11269200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr12:11206000-11221600	Weak transcription	Fetal Muscle Leg	muscle
33	chr12:11207000-11223000	Weak transcription	HepG2	liver
34	chr12:11207000-11224200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr12:11208400-11214400	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr12:11208600-11213200	Weak transcription	A549	lung
37	chr12:11208600-11218400	Weak transcription	Primary T cells from cord blood	blood
38	chr12:11208600-11228000	Weak transcription	Dnd41	blood
39	chr12:11208600-11232400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr12:11208600-11259600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr12:11209200-11211800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr12:11209400-11211000	Weak transcription	Primary hematopoietic stem cells	blood
43	chr12:11209400-11211200	Weak transcription	Right Ventricle	heart
44	chr12:11209600-11214200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr12:11210000-11211200	Weak transcription	Right Atrium	heart
46	chr12:11210000-11211400	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr12:11210200-11214000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr12:11210600-11211600	Enhancers	Left Ventricle	heart
49	chr12:11211000-11211800	Strong transcription	Primary hematopoietic stem cells	blood
50	chr12:11211200-11211600	ZNF genes & repeats	Aorta	Aorta

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