Variant report

Variant	nsv557522
Chromosome Location	chr12:11242096-11279407
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:65)
CpG islands
(count:122)
Chromatin interactive
region (count:4)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:65 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr12:11263799-11264109	GM12878	blood:	n/a	n/a
2	BATF	chr12:11247547-11247827	GM12878	blood:	n/a	n/a
3	BATF	chr12:11263857-11264113	GM12878	blood:	n/a	n/a
4	BATF	chr12:11247482-11247799	GM12878	blood:	n/a	n/a
5	BCL11A	chr12:11247500-11247829	GM12878	blood:	n/a	n/a
6	BCL11A	chr12:11263900-11264159	GM12878	blood:	n/a	n/a
7	CEBPB	chr12:11260954-11260970	HepG2	liver:	n/a	n/a
8	CTCF	chr12:11265530-11265560	GM13976	blood:	n/a	n/a
9	CTCF	chr12:11248748-11248798	Kidney_OC	kidney:	n/a	n/a
10	CTCF	chr12:11270380-11270463	GM13977	blood:	n/a	n/a
11	CTCF	chr12:11257042-11257094	GM20000	blood:	n/a	n/a
12	CTCF	chr12:11247641-11247704	GM20000	blood:	n/a	n/a
13	E2F4	chr12:11278096-11278419	MCF10A-Er-Src	breast:	n/a	n/a
14	ELF1	chr12:11261505-11261735	K562	blood:	n/a	n/a
15	ELK1	chr12:11278900-11278906	GM12878	blood:	n/a	n/a
16	GATA3	chr12:11270848-11270991	SH-SY5Y	brain:	n/a	n/a
17	HCFC1	chr12:11260107-11260159	K562	blood:	n/a	n/a
18	IRF1	chr12:11274892-11274895	K562	blood:	n/a	n/a
19	IRF4	chr12:11247559-11247865	GM12878	blood:	n/a	n/a
20	IRF4	chr12:11263795-11264158	GM12878	blood:	n/a	n/a
21	IRF4	chr12:11247411-11247911	GM12878	blood:	n/a	n/a
22	KAP1	chr12:11279200-11279719	K562	blood:	n/a	n/a
23	KAP1	chr12:11258085-11258322	K562	blood:	n/a	n/a
24	MAFK	chr12:11262928-11263070	IMR90	lung:	n/a	n/a
25	MAFK	chr12:11262939-11263117	HepG2	liver:	n/a	n/a
26	MAFK	chr12:11263010-11263067	HepG2	liver:	n/a	n/a
27	MAFK	chr12:11254181-11254247	HepG2	liver:	n/a	n/a
28	NFIC	chr12:11247511-11247905	GM12878	blood:	n/a	n/a
29	POLR2A	chr12:11267800-11267937	ProgFib	skin:	n/a	n/a
30	POLR2A	chr12:11248155-11248217	ProgFib	skin:	n/a	n/a
31	POLR2A	chr12:11250369-11250399	MCF-7	breast:	n/a	n/a
32	POLR2A	chr12:11245104-11245259	ProgFib	skin:	n/a	n/a
33	POLR2A	chr12:11247430-11247491	MCF-7	breast:	n/a	n/a
34	POLR2A	chr12:11250498-11250548	MCF-7	breast:	n/a	n/a
35	POLR2A	chr12:11245835-11245949	ProgFib	skin:	n/a	n/a
36	POLR2A	chr12:11272427-11272525	MCF10A-Er-Src	breast:	n/a	n/a
37	POLR2A	chr12:11278688-11278750	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr12:11261543-11261632	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr12:11278109-11278154	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr12:11250420-11250426	MCF-7	breast:	n/a	n/a
41	POLR2A	chr12:11253951-11254012	Gliobla	brain:	n/a	n/a
42	POLR2A	chr12:11248225-11248247	ProgFib	skin:	n/a	n/a
43	POLR2A	chr12:11273503-11273513	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr12:11268417-11268535	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr12:11245075-11245101	ProgFib	skin:	n/a	n/a
46	POLR2A	chr12:11253056-11253167	Hela-S3	cervix:	n/a	n/a
47	RFX5	chr12:11274302-11274497	K562	blood:	n/a	n/a
48	RUNX3	chr12:11263854-11264165	GM12878	blood:	n/a	n/a
49	RUNX3	chr12:11263840-11264161	GM12878	blood:	n/a	n/a
50	SETDB1	chr12:11276174-11276738	U2OS	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11244899-11244949	BE2_C	brain:	n/a
2	chr12:11244899-11244949	HNPCEpiC	eye:	n/a
3	chr12:11244899-11244949	HAEpiC	amniotic membrane:	n/a
4	chr12:11244899-11244949	HRE	kidney:	n/a
5	chr12:11244939-11244989	IMR90	lung:	fetal
6	chr12:11244939-11244989	AG04449	skin:	fetal
7	chr12:11244899-11244949	HEEpiC	esophagus:	n/a
8	chr12:11244899-11244949	LNCaP	prostate:	n/a
9	chr12:11244939-11244989	MCF-7	breast:	n/a
10	chr12:11244899-11244949	HEK293	kidney:	embryo
11	chr12:11244899-11244949	NHBE	bronchial:	n/a
12	chr12:11244939-11244989	HAEpiC	amniotic membrane:	n/a
13	chr12:11244899-11244949	K562	blood:	n/a
14	chr12:11244939-11244989	GM12892	blood:	n/a
15	chr12:11244939-11244989	SK-N-SH	brain:	n/a
16	chr12:11244899-11244949	GM12891	blood:	n/a
17	chr12:11244939-11244989	SKMC	muscle:	n/a
18	chr12:11244939-11244989	SK-N-SH_RA	brain:	n/a
19	chr12:11244899-11244949	PrEC	prostate:	n/a
20	chr12:11244939-11244989	AG10803	skin:	n/a
21	chr12:11244939-11244989	RPTEC	kidney:	n/a
22	chr12:11244899-11244949	SKMC	muscle:	n/a
23	chr12:11244899-11244949	NH-A	brain:	n/a
24	chr12:11244899-11244949	ovcar-3	ovarian:	n/a
25	chr12:11244939-11244989	HIPEpiC	eye:	n/a
26	chr12:11244939-11244989	AG09319	gingival:	n/a
27	chr12:11244899-11244949	SK-N-SH	brain:	n/a
28	chr12:11244939-11244989	LNCaP	prostate:	n/a
29	chr12:11244899-11244949	PFSK-1	brain:	n/a
30	chr12:11244939-11244989	Jurkat	blood:	n/a
31	chr12:11244899-11244949	U87	brain:	n/a
32	chr12:11244899-11244949	RPTEC	kidney:	n/a
33	chr12:11244899-11244949	HIPEpiC	eye:	n/a
34	chr12:11244899-11244949	GM19239	blood:	n/a
35	chr12:11244899-11244949	GM06990	blood:	n/a
36	chr12:11244939-11244989	HCPEpiC	choroid plexus:	n/a
37	chr12:11244899-11244949	A549	lung:	n/a
38	chr12:11244939-11244989	GM19239	blood:	n/a
39	chr12:11244899-11244949	HCT-116	colon:	n/a
40	chr12:11244939-11244989	HCT-116	colon:	n/a
41	chr12:11244939-11244989	CMK	blood:	n/a
42	chr12:11244939-11244989	HPAEpiC	pulmonary alveolar:	n/a
43	chr12:11244899-11244949	HMEC	breast:	n/a
44	chr12:11244899-11244949	NHDF-neo	bronchial:	n/a
45	chr12:11244899-11244949	Jurkat	blood:	n/a
46	chr12:11244939-11244989	HRCEpiC	kidney:	n/a
47	chr12:11244939-11244989	HCM	heart:	n/a
48	chr12:11244899-11244949	CMK	blood:	n/a
49	chr12:11244939-11244989	NH-A	brain:	n/a
50	chr12:11244939-11244989	A549	lung:	n/a

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

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRH1-1	chr12:11273435-11273779	NONHSAT026920
2	lnc-PRH1-1	chr12:11273609-11273779	NONHSAT026916

No data

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

Extended variants
information (count: 1704 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1704 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1965231	chr12:11242096-11242097	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs112818078	chr12:11242105-11242106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558908658	chr12:11242126-11242127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs73064954	chr12:11242161-11242162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs183580733	chr12:11242162-11242163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368838380	chr12:11242166-11242167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541279259	chr12:11242188-11242189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs138931602	chr12:11242228-11242229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554469613	chr12:11242229-11242230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560848099	chr12:11242255-11242256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543556181	chr12:11242256-11242257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563405021	chr12:11242262-11242263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530313386	chr12:11242275-11242276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113233989	chr12:11242293-11242294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138263172	chr12:11242297-11242298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532221676	chr12:11242317-11242318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143455255	chr12:11242320-11242321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201732725	chr12:11242346-11242347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs117530547	chr12:11242409-11242410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112365716	chr12:11242424-11242425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527981688	chr12:11242447-11242448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187878013	chr12:11242471-11242472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548043481	chr12:11242480-11242481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567536908	chr12:11242523-11242524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs530266964	chr12:11242524-11242525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192602280	chr12:11242550-11242551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs549941504	chr12:11242558-11242559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138257714	chr12:11242568-11242569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs74062433	chr12:11242619-11242620	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs111663719	chr12:11242622-11242623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs117979497	chr12:11242635-11242636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146990489	chr12:11242640-11242641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569785790	chr12:11242652-11242653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184541836	chr12:11242671-11242672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190240842	chr12:11242685-11242686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181708127	chr12:11242686-11242687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375182912	chr12:11242709-11242710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566017194	chr12:11242778-11242779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534633258	chr12:11242784-11242785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552466644	chr12:11242813-11242814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554868213	chr12:11242857-11242858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112872106	chr12:11242865-11242866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368471105	chr12:11242883-11242884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543667974	chr12:11242888-11242889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145982706	chr12:11242896-11242897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs111950832	chr12:11242897-11242898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576877446	chr12:11242902-11242903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371601346	chr12:11242903-11242904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545839054	chr12:11242906-11242907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568892667	chr12:11242975-11242976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Acute myeloid leukemia	17237825	CNVD
Acute myeloid leukemia	20729466	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:505 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11203800-11261200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr12:11204800-11247600	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr12:11205800-11269200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr12:11208600-11259600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr12:11218200-11256800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr12:11221200-11259600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr12:11225200-11261000	Weak transcription	Fetal Stomach	stomach
8	chr12:11233800-11243400	Weak transcription	Fetal Heart	heart
9	chr12:11233800-11252200	Weak transcription	Primary hematopoietic stem cells	blood
10	chr12:11234400-11261200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr12:11234400-11261400	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr12:11237000-11243600	Weak transcription	Fetal Muscle Trunk	muscle
13	chr12:11237200-11256400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr12:11237200-11262200	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr12:11237800-11246400	Weak transcription	Fetal Muscle Leg	muscle
16	chr12:11238800-11243800	Weak transcription	Primary B cells from peripheral blood	blood
17	chr12:11239200-11283600	Weak transcription	Fetal Thymus	thymus
18	chr12:11239600-11261600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr12:11239800-11243800	Weak transcription	Fetal Intestine Small	intestine
20	chr12:11239800-11261400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr12:11240200-11244600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr12:11240200-11253800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:11241800-11259400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr12:11242000-11243800	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr12:11242000-11244200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr12:11242000-11257200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr12:11243800-11244800	Strong transcription	Primary B cells from peripheral blood	blood
28	chr12:11244200-11245000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr12:11244800-11261400	Weak transcription	Primary B cells from peripheral blood	blood
30	chr12:11245000-11250800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr12:11245200-11286000	Weak transcription	Ovary	ovary
32	chr12:11246400-11246600	ZNF genes & repeats	Fetal Muscle Leg	muscle
33	chr12:11246600-11251800	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr12:11249400-11255600	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr12:11249600-11261600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr12:11249800-11253800	Weak transcription	Fetal Intestine Large	intestine
37	chr12:11249800-11261600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr12:11250600-11255600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr12:11250800-11251400	ZNF genes & repeats	Primary B cells from cord blood	blood
40	chr12:11250800-11251400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
41	chr12:11250800-11254000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr12:11251000-11256600	Weak transcription	Fetal Lung	lung
43	chr12:11251000-11276200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr12:11251200-11251400	ZNF genes & repeats	A549	lung
45	chr12:11251200-11259600	Weak transcription	Thymus	Thymus
46	chr12:11251200-11269800	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr12:11251400-11252600	Weak transcription	Primary T cells from cord blood	blood
48	chr12:11251400-11259200	Weak transcription	Primary B cells from cord blood	blood
49	chr12:11251400-11259600	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr12:11251400-11260000	Weak transcription	A549	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links