Variant report

Variant	nsv528912
Chromosome Location	chr12:12253591-12266041
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:130)
CpG islands
(count:183)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:130 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr12:12263903-12264159	GM12878	blood:	n/a	n/a
2	BCL11A	chr12:12263900-12264228	GM12878	blood:	n/a	n/a
3	BCL11A	chr12:12263916-12264097	GM12878	blood:	n/a	n/a
4	CEBPB	chr12:12257452-12257725	IMR90	lung:	n/a	chr12:12257591-12257602
5	CEBPB	chr12:12257494-12257665	K562	blood:	n/a	chr12:12257591-12257602
6	CEBPB	chr12:12257452-12257771	A549	lung:	n/a	chr12:12257591-12257602
7	CEBPB	chr12:12253520-12253669	HepG2	liver:	n/a	chr12:12253564-12253575
8	CEBPB	chr12:12257446-12257772	HepG2	liver:	n/a	chr12:12257591-12257602
9	CEBPB	chr12:12257451-12257773	Hela-S3	cervix:	n/a	chr12:12257591-12257602
10	CTCF	chr12:12264130-12264206	GM10266	blood:	n/a	n/a
11	CTCF	chr12:12264011-12264099	GM13976	blood:	n/a	n/a
12	CTCF	chr12:12258820-12258970	GM12868	blood:	n/a	n/a
13	CTCF	chr12:12264276-12264328	Kidney_OC	kidney:	n/a	n/a
14	CTCF	chr12:12264116-12264199	Kidney_OC	kidney:	n/a	n/a
15	EBF1	chr12:12264363-12264681	GM12878	blood:	n/a	n/a
16	EBF1	chr12:12264323-12264643	GM12878	blood:	n/a	n/a
17	EP300	chr12:12253407-12254948	SK-N-SH	brain:	n/a	n/a
18	EP300	chr12:12253834-12254159	SK-N-SH_RA	brain:	n/a	n/a
19	FOS	chr12:12261635-12261703	MCF10A-Er-Src	breast:	n/a	n/a
20	FOSL2	chr12:12263793-12264168	HepG2	liver:	n/a	n/a
21	GATA3	chr12:12253734-12254321	SK-N-SH	brain:	n/a	n/a
22	GATA3	chr12:12253885-12254076	SH-SY5Y	brain:	n/a	n/a
23	GATA3	chr12:12253758-12254235	SK-N-SH	brain:	n/a	n/a
24	HEY1	chr12:12264921-12265145	K562	blood:	n/a	n/a
25	HEY1	chr12:12263868-12264172	HepG2	liver:	n/a	n/a
26	HEY1	chr12:12263743-12264249	HepG2	liver:	n/a	n/a
27	HEY1	chr12:12264338-12264656	K562	blood:	n/a	n/a
28	HEY1	chr12:12263805-12264259	K562	blood:	n/a	n/a
29	HEY1	chr12:12263801-12264171	K562	blood:	n/a	n/a
30	JUND	chr12:12263896-12264090	HepG2	liver:	n/a	n/a
31	MAFF	chr12:12257979-12258169	HepG2	liver:	n/a	n/a
32	MAFF	chr12:12265007-12265113	HepG2	liver:	n/a	n/a
33	MAFK	chr12:12265082-12265151	HepG2	liver:	n/a	chr12:12265085-12265096 chr12:12265085-12265096
34	MAFK	chr12:12257949-12258213	HepG2	liver:	n/a	n/a
35	MAFK	chr12:12257979-12258164	HepG2	liver:	n/a	n/a
36	PAX5	chr12:12264416-12264613	GM12878	blood:	n/a	n/a
37	PAX5	chr12:12263901-12264123	GM12878	blood:	n/a	n/a
38	PBX3	chr12:12263925-12264103	GM12878	blood:	n/a	n/a
39	POLR2A	chr12:12263869-12264021	Gliobla	brain:	n/a	n/a
40	POLR2A	chr12:12264339-12264642	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr12:12263850-12264221	A549	lung:	n/a	n/a
42	POLR2A	chr12:12263788-12264024	MCF-7	breast:	n/a	n/a
43	POLR2A	chr12:12263843-12264145	HepG2	liver:	n/a	n/a
44	POLR2A	chr12:12264308-12264352	K562	blood:	n/a	n/a
45	POLR2A	chr12:12263810-12264737	GM12892	blood:	n/a	n/a
46	POLR2A	chr12:12263848-12264181	GM12878	blood:	n/a	n/a
47	POLR2A	chr12:12263804-12264314	GM12892	blood:	n/a	n/a
48	POLR2A	chr12:12260384-12260557	MCF-7	breast:	n/a	n/a
49	POLR2A	chr12:12263795-12264094	K562	blood:	n/a	n/a
50	POLR2A	chr12:12263887-12264134	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:12264176-12264226	NT2-D1	testis:	n/a
2	chr12:12264075-12264125	Hepatocyte	liver:	n/a
3	chr12:12264176-12264226	PANC-1	pancreas:	n/a
4	chr12:12264176-12264226	HNPCEpiC	eye:	n/a
5	chr12:12264390-12264440	HCF	heart:	n/a
6	chr12:12264390-12264440	U87	brain:	n/a
7	chr12:12264075-12264125	HepG2	liver:	n/a
8	chr12:12264176-12264226	AG09319	gingival:	n/a
9	chr12:12264075-12264125	Hela-S3	cervix:	n/a
10	chr12:12264176-12264226	HEEpiC	esophagus:	n/a
11	chr12:12264075-12264125	GM12892	blood:	n/a
12	chr12:12264176-12264226	SKMC	muscle:	n/a
13	chr12:12264075-12264125	HPAEpiC	pulmonary alveolar:	n/a
14	chr12:12264176-12264226	PrEC	prostate:	n/a
15	chr12:12264176-12264226	SK-N-SH	brain:	n/a
16	chr12:12264176-12264226	HL-60	blood:	n/a
17	chr12:12264176-12264226	Jurkat	blood:	n/a
18	chr12:12264176-12264226	Hela-S3	cervix:	n/a
19	chr12:12264176-12264226	NH-A	brain:	n/a
20	chr12:12264075-12264125	PANC-1	pancreas:	n/a
21	chr12:12264390-12264440	AoSMC	blood vessel:	n/a
22	chr12:12264176-12264226	ovcar-3	ovarian:	n/a
23	chr12:12264390-12264440	AG04449	skin:	fetal
24	chr12:12264176-12264226	GM06990	blood:	n/a
25	chr12:12264075-12264125	GM12878	blood:	n/a
26	chr12:12264176-12264226	U87	brain:	n/a
27	chr12:12264176-12264226	LNCaP	prostate:	n/a
28	chr12:12264176-12264226	HepG2	liver:	n/a
29	chr12:12264176-12264226	GM12878	blood:	n/a
30	chr12:12264075-12264125	HCM	heart:	n/a
31	chr12:12264176-12264226	NHBE	bronchial:	n/a
32	chr12:12264075-12264125	PrEC	prostate:	n/a
33	chr12:12264176-12264226	MCF-7	breast:	n/a
34	chr12:12264176-12264226	HCPEpiC	choroid plexus:	n/a
35	chr12:12264390-12264440	SKMC	muscle:	n/a
36	chr12:12264390-12264440	Jurkat	blood:	n/a
37	chr12:12264390-12264440	HRE	kidney:	n/a
38	chr12:12264075-12264125	SKMC	muscle:	n/a
39	chr12:12264390-12264440	HUVEC	blood vessel:	n/a
40	chr12:12264176-12264226	BJ	skin:	n/a
41	chr12:12264075-12264125	K562	blood:	n/a
42	chr12:12264075-12264125	U87	brain:	n/a
43	chr12:12264390-12264440	HCM	heart:	n/a
44	chr12:12264176-12264226	HIPEpiC	eye:	n/a
45	chr12:12264075-12264125	HRCEpiC	kidney:	n/a
46	chr12:12264176-12264226	PFSK-1	brain:	n/a
47	chr12:12264390-12264440	AG09319	gingival:	n/a
48	chr12:12264176-12264226	GM19239	blood:	n/a
49	chr12:12264176-12264226	SAEC	small airway:	n/a
50	chr12:12264075-12264125	SK-N-MC	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:12261824..12262324-chr15:80352071..80352800,2	Hela-S3	cervix:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1244	chr12:12264940-12264965	MIMAT0005896_1

No data

Variant related genes	Relation type
ENSG00000198134	TF binding region
ENSG00000198134	CpG island
ENSG00000086666	chromatin interactions

Extended variants
information (count: 514 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:514 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4763780	chr12:12253591-12253592	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs569200084	chr12:12253593-12253594	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs377686051	chr12:12253646-12253647	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs56390212	chr12:12253647-12253648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560997680	chr12:12253675-12253676	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554946387	chr12:12253681-12253682	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573261644	chr12:12253694-12253695	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143948654	chr12:12253722-12253723	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552768031	chr12:12253782-12253783	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577797907	chr12:12253790-12253791	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544863254	chr12:12253820-12253821	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181030708	chr12:12253900-12253901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185654121	chr12:12253915-12253916	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs17758082	chr12:12253947-12253948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs147299181	chr12:12253951-12253952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191307128	chr12:12253958-12253959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561281552	chr12:12253977-12253978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528447596	chr12:12254053-12254054	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547098810	chr12:12254056-12254057	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2448032	chr12:12254075-12254076	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs74061103	chr12:12254091-12254092	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs550759572	chr12:12254097-12254098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34093785	chr12:12254103-12254104	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569063161	chr12:12254148-12254149	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536558630	chr12:12254150-12254151	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201382482	chr12:12254163-12254164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs76148261	chr12:12254164-12254165	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs79090477	chr12:12254176-12254177	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs548442011	chr12:12254195-12254196	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376924733	chr12:12254240-12254241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567278425	chr12:12254255-12254256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370107217	chr12:12254256-12254257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546691419	chr12:12254267-12254268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs144668269	chr12:12254286-12254287	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76668266	chr12:12254294-12254295	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs373071299	chr12:12254296-12254297	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs4763781	chr12:12254476-12254477	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs148520721	chr12:12254503-12254504	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565191393	chr12:12254564-12254565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142867154	chr12:12254597-12254598	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113358005	chr12:12254628-12254629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575473777	chr12:12254650-12254651	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146079811	chr12:12254687-12254688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370797454	chr12:12254716-12254717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561144547	chr12:12254720-12254721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573222027	chr12:12254726-12254727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs4763782	chr12:12254756-12254757	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs565425616	chr12:12254759-12254760	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181704223	chr12:12254772-12254773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186836850	chr12:12254774-12254775	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
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
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	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 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
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:275 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:12225000-12255000	Weak transcription	Small Intestine	intestine
2	chr12:12232800-12257000	Weak transcription	HSMMtube	muscle
3	chr12:12234800-12259600	Weak transcription	Aorta	Aorta
4	chr12:12235400-12260200	Weak transcription	Gastric	stomach
5	chr12:12235400-12260800	Weak transcription	Stomach Smooth Muscle	stomach
6	chr12:12235400-12278800	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr12:12237400-12259800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr12:12240400-12254200	Weak transcription	Stomach Mucosa	stomach
9	chr12:12240600-12256800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr12:12241000-12260600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr12:12241000-12273400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr12:12241200-12256800	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr12:12241200-12261000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr12:12241400-12272600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr12:12241800-12260400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr12:12242000-12257000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr12:12245600-12253600	Weak transcription	Colonic Mucosa	Colon
18	chr12:12245600-12257000	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr12:12245600-12260400	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr12:12245600-12260400	Weak transcription	Fetal Brain Female	brain
21	chr12:12245600-12260600	Weak transcription	Psoas Muscle	Psoas
22	chr12:12245800-12255600	Weak transcription	Brain Substantia Nigra	brain
23	chr12:12245800-12256600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr12:12245800-12256600	Weak transcription	Lung	lung
25	chr12:12245800-12260400	Weak transcription	Brain Germinal Matrix	brain
26	chr12:12245800-12260400	Weak transcription	Fetal Muscle Trunk	muscle
27	chr12:12245800-12260600	Weak transcription	Brain Hippocampus Middle	brain
28	chr12:12245800-12263800	Weak transcription	Pancreas	Pancrea
29	chr12:12245800-12266200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr12:12246000-12254400	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr12:12246000-12256600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr12:12246200-12253600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr12:12246200-12253600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr12:12246200-12256000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr12:12246200-12260400	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr12:12246200-12260400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr12:12246400-12257000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr12:12246400-12272000	Weak transcription	Osteobl	bone
39	chr12:12247600-12261400	Weak transcription	Colon Smooth Muscle	Colon
40	chr12:12248200-12271800	Weak transcription	Fetal Kidney	kidney
41	chr12:12248400-12260800	Weak transcription	Hela-S3	cervix
42	chr12:12248400-12261000	Weak transcription	NH-A	brain
43	chr12:12248800-12256600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr12:12248800-12256600	Weak transcription	Fetal Stomach	stomach
45	chr12:12249200-12256000	Weak transcription	Fetal Intestine Small	intestine
46	chr12:12249400-12256600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr12:12250000-12261400	Weak transcription	Primary T cells from cord blood	blood
48	chr12:12250200-12254400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr12:12250800-12260600	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr12:12251000-12254800	Strong transcription	Liver	Liver

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