Variant report

Variant	esv6373
Chromosome Location	chr12:11209985-11282106
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:183)
CpG islands
(count:244)
Chromatin interactive
region (count:7)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:183 , 50 per page) page: 1 2 3 4

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	chr12:11247482-11247799	GM12878	blood:	n/a	n/a
5	BATF	chr12:11263857-11264113	GM12878	blood:	n/a	n/a
6	BATF	chr12:11238012-11238373	GM12878	blood:	n/a	n/a
7	BATF	chr12:11228218-11228560	GM12878	blood:	n/a	n/a
8	BATF	chr12:11216721-11217010	GM12878	blood:	n/a	n/a
9	BATF	chr12:11247547-11247827	GM12878	blood:	n/a	n/a
10	BATF	chr12:11238084-11238352	GM12878	blood:	n/a	n/a
11	BATF	chr12:11263799-11264109	GM12878	blood:	n/a	n/a
12	BATF	chr12:11225254-11225547	GM12878	blood:	n/a	n/a
13	BCL11A	chr12:11247500-11247829	GM12878	blood:	n/a	n/a
14	BCL11A	chr12:11238061-11238356	GM12878	blood:	n/a	chr12:11238263-11238272
15	BCL11A	chr12:11263900-11264159	GM12878	blood:	n/a	n/a
16	BCL11A	chr12:11228248-11228517	GM12878	blood:	n/a	n/a
17	BHLHE40	chr12:11228293-11228667	GM12878	blood:	n/a	n/a
18	CEBPB	chr12:11222658-11222813	HepG2	liver:	n/a	n/a
19	CEBPB	chr12:11226186-11226481	HepG2	liver:	n/a	n/a
20	CEBPB	chr12:11260954-11260970	HepG2	liver:	n/a	n/a
21	CEBPB	chr12:11223987-11224332	HepG2	liver:	n/a	n/a
22	CHD2	chr12:11238132-11238304	GM12878	blood:	n/a	n/a
23	CTCF	chr12:11247641-11247704	GM20000	blood:	n/a	n/a
24	CTCF	chr12:11230498-11230623	Lung_OC	lung:	n/a	n/a
25	CTCF	chr12:11209880-11210030	GM12872	blood:	n/a	n/a
26	CTCF	chr12:11270380-11270463	GM13977	blood:	n/a	n/a
27	CTCF	chr12:11281909-11281930	Spleen_OC	spleen:	n/a	n/a
28	CTCF	chr12:11257042-11257094	GM20000	blood:	n/a	n/a
29	CTCF	chr12:11248748-11248798	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr12:11281056-11281182	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr12:11265530-11265560	GM13976	blood:	n/a	n/a
32	CUX1	chr12:11238241-11238349	GM12878	blood:	n/a	n/a
33	E2F4	chr12:11220752-11221188	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr12:11278096-11278419	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr12:11282076-11282276	MCF10A-Er-Src	breast:	n/a	n/a
36	EBF1	chr12:11226243-11226583	GM12878	blood:	n/a	chr12:11226441-11226451 chr12:11226441-11226450 chr12:11226439-11226452
37	ELF1	chr12:11261505-11261735	K562	blood:	n/a	n/a
38	ELK1	chr12:11278900-11278906	GM12878	blood:	n/a	n/a
39	EP300	chr12:11238133-11238438	GM12878	blood:	n/a	n/a
40	EP300	chr12:11238104-11238440	GM12878	blood:	n/a	n/a
41	EP300	chr12:11228364-11228516	GM12878	blood:	n/a	n/a
42	EP300	chr12:11223962-11224277	HepG2	liver:	n/a	n/a
43	FOXA1	chr12:11223913-11224415	HepG2	liver:	n/a	n/a
44	FOXA1	chr12:11223802-11224380	HepG2	liver:	n/a	n/a
45	FOXA1	chr12:11223974-11224466	HepG2	liver:	n/a	n/a
46	FOXA1	chr12:11223940-11224452	HepG2	liver:	n/a	n/a
47	FOXA2	chr12:11223986-11224245	A549	lung:	n/a	n/a
48	FOXA2	chr12:11223920-11224357	HepG2	liver:	n/a	n/a
49	FOXA2	chr12:11223617-11224724	HepG2	liver:	n/a	n/a
50	FOXM1	chr12:11238005-11238472	GM12878	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11244899-11244949	HPAEpiC	pulmonary alveolar:	n/a
2	chr12:11244899-11244949	HRCEpiC	kidney:	n/a
3	chr12:11216351-11216401	PrEC	prostate:	n/a
4	chr12:11244939-11244989	PrEC	prostate:	n/a
5	chr12:11215083-11215133	HUVEC	blood vessel:	n/a
6	chr12:11216351-11216401	CMK	blood:	n/a
7	chr12:11244899-11244949	SK-N-SH_RA	brain:	n/a
8	chr12:11215083-11215133	HNPCEpiC	eye:	n/a
9	chr12:11244939-11244989	SK-N-MC	brain:	n/a
10	chr12:11215083-11215133	RPTEC	kidney:	n/a
11	chr12:11215083-11215133	AG04449	skin:	fetal
12	chr12:11244899-11244949	HEEpiC	esophagus:	n/a
13	chr12:11216351-11216401	SK-N-SH_RA	brain:	n/a
14	chr12:11244939-11244989	HCM	heart:	n/a
15	chr12:11215083-11215133	MCF-7	breast:	n/a
16	chr12:11244939-11244989	IMR90	lung:	fetal
17	chr12:11216351-11216401	SK-N-SH	brain:	n/a
18	chr12:11215083-11215133	NB4	blood:	n/a
19	chr12:11244899-11244949	HCPEpiC	choroid plexus:	n/a
20	chr12:11215083-11215133	SK-N-MC	brain:	n/a
21	chr12:11244899-11244949	HepG2	liver:	n/a
22	chr12:11244939-11244989	Hepatocyte	liver:	n/a
23	chr12:11244899-11244949	SK-N-MC	brain:	n/a
24	chr12:11244939-11244989	HEK293	kidney:	embryo
25	chr12:11244899-11244949	AG04450	lung:	fetal
26	chr12:11244939-11244989	GM12878	blood:	n/a
27	chr12:11216351-11216401	AG04449	skin:	fetal
28	chr12:11215083-11215133	LNCaP	prostate:	n/a
29	chr12:11244899-11244949	SAEC	small airway:	n/a
30	chr12:11216351-11216401	SKMC	muscle:	n/a
31	chr12:11215083-11215133	HRE	kidney:	n/a
32	chr12:11216351-11216401	GM12891	blood:	n/a
33	chr12:11244939-11244989	HRCEpiC	kidney:	n/a
34	chr12:11244899-11244949	T-47D	breast:	n/a
35	chr12:11216351-11216401	ProgFib	skin:	n/a
36	chr12:11215083-11215133	HRCEpiC	kidney:	n/a
37	chr12:11215083-11215133	Hepatocyte	liver:	n/a
38	chr12:11244899-11244949	NT2-D1	testis:	n/a
39	chr12:11244939-11244989	AoSMC	blood vessel:	n/a
40	chr12:11215083-11215133	AG09309	skin:	n/a
41	chr12:11244939-11244989	HUVEC	blood vessel:	n/a
42	chr12:11215083-11215133	HepG2	liver:	n/a
43	chr12:11216351-11216401	IMR90	lung:	fetal
44	chr12:11244939-11244989	AG09309	skin:	n/a
45	chr12:11244939-11244989	PFSK-1	brain:	n/a
46	chr12:11216351-11216401	Jurkat	blood:	n/a
47	chr12:11244899-11244949	SKMC	muscle:	n/a
48	chr12:11216351-11216401	HEEpiC	esophagus:	n/a
49	chr12:11215083-11215133	GM12892	blood:	n/a
50	chr12:11215083-11215133	ProgFib	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:11253040..11255708-chr12:11259363..11262255,2	K562	blood:
2	chr12:11271454..11274346-chr12:11279643..11282306,2	MCF-7	breast:
3	chr12:11237724..11239418-chr12:11252570..11254241,2	MCF-7	breast:
4	chr12:11271454..11274346-chr12:11279643..11282306,2	MCF-7	breast:
5	chr12:11253040..11255708-chr12:11259363..11262255,2	K562	blood:
6	chr12:11237724..11239418-chr12:11252570..11254241,2	MCF-7	breast:
7	chr12:11210669..11211248-chr5:109800405..109801099,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRH1-1	chr12:11273609-11273779	NONHSAT026916
2	lnc-TAS2R43-1	chr12:11229915-11230841	NONHSAT140056
3	lnc-PRH1-1	chr12:11273435-11273779	NONHSAT026920
4	lnc-TAS2R43-1	chr12:11229368-11231770	NONHSAT026918

No data

Variant related genes	Relation type
TAS2R46	TF binding region
ENSG00000256400	TF binding region
TAS2R43	TF binding region
TAS2R64P	TF binding region
TAS2R46	CpG island
ENSG00000256400	CpG island
TAS2R43	CpG island
TAS2R64P	CpG island

Extended variants
information (count: 3932 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:3932 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77914777	chr12:11209997-11209998	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs374673434	chr12:11210004-11210005	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77995910	chr12:11210009-11210010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368420855	chr12:11210123-11210124	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551858818	chr12:11210142-11210143	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs200260449	chr12:11210145-11210146	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374627775	chr12:11210154-11210155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547288310	chr12:11210178-11210179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570527926	chr12:11210187-11210188	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs111930430	chr12:11210202-11210203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs2708384	chr12:11210213-11210214	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs2598001	chr12:11210226-11210227	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs370188316	chr12:11210227-11210228	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549558124	chr12:11210240-11210241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372337170	chr12:11210272-11210273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199666613	chr12:11210273-11210274	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs79824370	chr12:11210381-11210382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76448825	chr12:11210395-11210396	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs199987596	chr12:11210431-11210432	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs72477408	chr12:11210440-11210441	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs74413754	chr12:11210487-11210488	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35605594	chr12:11210488-11210489	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs75569441	chr12:11210504-11210505	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs150490188	chr12:11210526-11210527	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs75010210	chr12:11210555-11210556	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs77814832	chr12:11210566-11210567	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs78028591	chr12:11210567-11210568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554035386	chr12:11210583-11210584	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187022269	chr12:11210587-11210588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112713988	chr12:11210663-11210664	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs77604725	chr12:11210672-11210673	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555989469	chr12:11210747-11210748	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191893950	chr12:11210770-11210771	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183381342	chr12:11210779-11210780	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs565672864	chr12:11210812-11210813	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187143061	chr12:11210826-11210827	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190011689	chr12:11210892-11210893	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560849125	chr12:11210912-11210913	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs368583040	chr12:11210981-11210982	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529606331	chr12:11210999-11211000	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200664432	chr12:11211003-11211004	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs138432187	chr12:11211020-11211021	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs79095756	chr12:11211054-11211055	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs76032018	chr12:11211059-11211060	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs79585361	chr12:11211081-11211082	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs551925294	chr12:11211092-11211093	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs76815507	chr12:11211096-11211097	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs578097604	chr12:11211128-11211129	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs74200682	chr12:11211129-11211130	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs78708533	chr12:11211135-11211136	Weak transcription Strong transcription Enhancers	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:783 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11166200-11210000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr12:11169400-11219400	Weak transcription	HUVEC	blood vessel
3	chr12:11171000-11225600	Weak transcription	HSMMtube	muscle
4	chr12:11176400-11211200	Weak transcription	Aorta	Aorta
5	chr12:11179000-11223800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr12:11179400-11222000	Weak transcription	Fetal Kidney	kidney
7	chr12:11181000-11217400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr12:11181000-11220000	Weak transcription	Gastric	stomach
9	chr12:11181000-11224800	Weak transcription	Fetal Stomach	stomach
10	chr12:11184200-11213000	Weak transcription	Thymus	Thymus
11	chr12:11193200-11224200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr12:11194600-11210000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr12:11196600-11211400	Weak transcription	Fetal Heart	heart
14	chr12:11196600-11215000	Weak transcription	NHLF	lung
15	chr12:11198000-11230200	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr12:11199600-11214200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr12:11199800-11222800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr12:11201400-11210600	Weak transcription	Left Ventricle	heart
19	chr12:11201600-11227800	Weak transcription	HSMM	muscle
20	chr12:11203200-11211600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr12:11203600-11216800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr12:11203600-11240000	Weak transcription	Ovary	ovary
23	chr12:11203800-11211200	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr12:11203800-11211400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr12:11203800-11211600	Weak transcription	Hela-S3	cervix
26	chr12:11203800-11212200	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr12:11203800-11212400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr12:11203800-11261200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr12:11204600-11224000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr12:11204600-11227600	Weak transcription	Fetal Lung	lung
31	chr12:11204800-11247600	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr12:11205800-11218200	Weak transcription	Primary B cells from cord blood	blood
33	chr12:11205800-11269200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr12:11206000-11221600	Weak transcription	Fetal Muscle Leg	muscle
35	chr12:11207000-11223000	Weak transcription	HepG2	liver
36	chr12:11207000-11224200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr12:11208400-11214400	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr12:11208600-11213200	Weak transcription	A549	lung
39	chr12:11208600-11218400	Weak transcription	Primary T cells from cord blood	blood
40	chr12:11208600-11228000	Weak transcription	Dnd41	blood
41	chr12:11208600-11232400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr12:11208600-11259600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr12:11209200-11211800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
44	chr12:11209400-11211000	Weak transcription	Primary hematopoietic stem cells	blood
45	chr12:11209400-11211200	Weak transcription	Right Ventricle	heart
46	chr12:11209600-11214200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr12:11209800-11210000	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr12:11209800-11210000	Enhancers	Right Atrium	heart
49	chr12:11210000-11211200	Weak transcription	Right Atrium	heart
50	chr12:11210000-11211400	Weak transcription	Brain Inferior Temporal Lobe	brain

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