Variant report

Variant	esv1801139
Chromosome Location	chr12:121228410-121241933
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:137)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:137 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:121237337-121237617	HepG2	liver:	n/a	n/a
2	BATF	chr12:121238482-121238807	GM12878	blood:	n/a	n/a
3	BCLAF1	chr12:121235590-121236252	GM12878	blood:	n/a	chr12:121235908-121235916
4	BHLHE40	chr12:121235915-121236297	GM12878	blood:	n/a	n/a
5	CBX3	chr12:121233504-121233974	K562	blood:	n/a	n/a
6	CBX3	chr12:121233519-121233991	HCT-116	colon:	n/a	n/a
7	CBX3	chr12:121233590-121233961	K562	blood:	n/a	n/a
8	CHD1	chr12:121235759-121237028	GM12878	blood:	n/a	n/a
9	CHD2	chr12:121236047-121236528	GM12878	blood:	n/a	n/a
10	CTCF	chr12:121235760-121235910	GM12869	blood:	n/a	n/a
11	CTCF	chr12:121239120-121239270	MCF-7	breast:	n/a	n/a
12	CTCF	chr12:121232208-121232288	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr12:121238600-121238750	HCPEpiC	choroid plexus:	n/a	n/a
14	CTCF	chr12:121233340-121233490	GM12875	blood:	n/a	n/a
15	CTCF	chr12:121233360-121233510	AoAF	blood vessel:	n/a	n/a
16	CTCF	chr12:121235780-121235930	GM12801	blood:	n/a	n/a
17	CTCF	chr12:121235760-121235910	GM12865	blood:	n/a	n/a
18	CTCF	chr12:121233380-121233530	GM12864	blood:	n/a	n/a
19	CTCF	chr12:121235760-121236030	GM12871	blood:	n/a	n/a
20	CTCF	chr12:121235863-121235962	GM19240	blood:	n/a	n/a
21	CTCF	chr12:121235820-121235970	GM12872	blood:	n/a	n/a
22	CTCF	chr12:121235780-121235930	GM12866	blood:	n/a	n/a
23	CTCF	chr12:121239155-121239180	MCF-7	breast:	n/a	n/a
24	CTCF	chr12:121233420-121233570	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr12:121228689-121228757	Fibrobl	skin:	n/a	n/a
26	CTCF	chr12:121235832-121235949	GM13977	blood:	n/a	n/a
27	CTCF	chr12:121233320-121233470	MCF-7	breast:	n/a	n/a
28	CTCF	chr12:121235820-121235970	GM12873	blood:	n/a	n/a
29	CTCF	chr12:121233340-121233490	MCF-7	breast:	n/a	n/a
30	CTCF	chr12:121235840-121235990	GM12864	blood:	n/a	n/a
31	CTCF	chr12:121235819-121235967	GM19238	blood:	n/a	n/a
32	CTCF	chr12:121235894-121235918	MCF-7	breast:	n/a	n/a
33	CTCF	chr12:121236280-121236430	GM06990	blood:	n/a	n/a
34	CTCF	chr12:121233040-121233190	GM12873	blood:	n/a	n/a
35	CTCF	chr12:121235800-121235950	GM12873	blood:	n/a	n/a
36	CTCF	chr12:121233360-121233510	HCFaa	heart:	n/a	n/a
37	CTCF	chr12:121235720-121235870	GM12875	blood:	n/a	n/a
38	CTCF	chr12:121235820-121235970	GM12866	blood:	n/a	n/a
39	CTCF	chr12:121235880-121236030	GM12874	blood:	n/a	n/a
40	CTCF	chr12:121235879-121235920	GM10248	blood:	n/a	n/a
41	CTCF	chr12:121235740-121235890	GM12868	blood:	n/a	n/a
42	CTCF	chr12:121235704-121236063	GM12878	blood:	n/a	n/a
43	CTCF	chr12:121239151-121239196	MCF-7	breast:	n/a	n/a
44	CTCF	chr12:121233340-121233490	GM12873	blood:	n/a	n/a
45	CTCF	chr12:121235840-121235990	GM12871	blood:	n/a	n/a
46	CTCF	chr12:121235876-121235925	MCF-7	breast:	n/a	n/a
47	CTCF	chr12:121235825-121235947	GM10266	blood:	n/a	n/a
48	CTCF	chr12:121235833-121235942	GM19239	blood:	n/a	n/a
49	CTCF	chr12:121235838-121235972	GM12892	blood:	n/a	n/a
50	CTCF	chr12:121233380-121233530	A549	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:121239400-121239450	PrEC	prostate:	n/a
2	chr12:121239400-121239450	GM12892	blood:	n/a
3	chr12:121239400-121239450	NHDF-neo	bronchial:	n/a
4	chr12:121239400-121239450	MCF10A-Er-Src	breast:	n/a
5	chr12:121239400-121239450	HCM	heart:	n/a
6	chr12:121239400-121239450	H1-hESC	embryonic stem cell:	embryo
7	chr12:121239400-121239450	A549	lung:	n/a
8	chr12:121239400-121239450	Jurkat	blood:	n/a
9	chr12:121239400-121239450	U87	brain:	n/a
10	chr12:121239400-121239450	HMEC	breast:	n/a
11	chr12:121239400-121239450	SK-N-SH_RA	brain:	n/a
12	chr12:121239400-121239450	GM12891	blood:	n/a
13	chr12:121239400-121239450	BJ	skin:	n/a
14	chr12:121239400-121239450	ovcar-3	ovarian:	n/a
15	chr12:121239400-121239450	NH-A	brain:	n/a
16	chr12:121239400-121239450	RPTEC	kidney:	n/a
17	chr12:121239400-121239450	Hepatocyte	liver:	n/a
18	chr12:121239400-121239450	HRPEpiC	eye:	n/a
19	chr12:121239400-121239450	AG10803	skin:	n/a
20	chr12:121239400-121239450	AG09309	skin:	n/a
21	chr12:121239400-121239450	GM06990	blood:	n/a
22	chr12:121239400-121239450	NT2-D1	testis:	n/a
23	chr12:121239400-121239450	HNPCEpiC	eye:	n/a
24	chr12:121239400-121239450	HIPEpiC	eye:	n/a
25	chr12:121239400-121239450	Hela-S3	cervix:	n/a
26	chr12:121239400-121239450	HepG2	liver:	n/a
27	chr12:121239400-121239450	AG04449	skin:	fetal
28	chr12:121239400-121239450	HAEpiC	amniotic membrane:	n/a
29	chr12:121239400-121239450	GM12878	blood:	n/a
30	chr12:121239400-121239450	SAEC	small airway:	n/a
31	chr12:121239400-121239450	PFSK-1	brain:	n/a
32	chr12:121239400-121239450	LNCaP	prostate:	n/a
33	chr12:121239400-121239450	CMK	blood:	n/a
34	chr12:121239400-121239450	HRCEpiC	kidney:	n/a
35	chr12:121239400-121239450	IMR90	lung:	fetal
36	chr12:121239400-121239450	ECC-1	luminal epithelium:	n/a
37	chr12:121239400-121239450	HL-60	blood:	n/a
38	chr12:121239400-121239450	ProgFib	skin:	n/a
39	chr12:121239400-121239450	Caco-2	colon:	n/a
40	chr12:121239400-121239450	BE2_C	brain:	n/a
41	chr12:121239400-121239450	HEK293	kidney:	embryo
42	chr12:121239400-121239450	PANC-1	pancreas:	n/a
43	chr12:121239400-121239450	K562	blood:	n/a
44	chr12:121239400-121239450	GM19239	blood:	n/a
45	chr12:121239400-121239450	MCF-7	breast:	n/a
46	chr12:121239400-121239450	HUVEC	blood vessel:	n/a
47	chr12:121239400-121239450	HEEpiC	esophagus:	n/a
48	chr12:121239400-121239450	AG09319	gingival:	n/a
49	chr12:121239400-121239450	AoSMC	blood vessel:	n/a
50	chr12:121239400-121239450	SK-N-MC	brain:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:121227665..121229362-chr12:121229925..121232592,2	MCF-7	breast:
2	chr12:121224775..121227076-chr12:121227465..121229261,2	K562	blood:
3	chr12:121226286..121228196-chr12:121235174..121237034,2	K562	blood:
4	chr12:121223533..121225993-chr12:121234568..121236764,2	K562	blood:
5	chr12:121238531..121240722-chr12:121246425..121248105,2	K562	blood:
6	chr12:121233943..121235846-chr12:121237594..121239607,2	K562	blood:
7	chr12:121239385..121241045-chr12:121266410..121269390,2	K562	blood:
8	chr12:121230474..121232207-chr12:121234744..121236452,2	K562	blood:
9	chr12:121230474..121232207-chr12:121234744..121236452,2	K562	blood:
10	chr12:121240989..121243362-chr12:121247289..121249209,3	K562	blood:
11	chr12:121227665..121229362-chr12:121229925..121232592,2	MCF-7	breast:
12	chr12:120729295..120732240-chr12:121229424..121231608,2	K562	blood:
13	chr12:121233943..121235846-chr12:121237594..121239607,2	K562	blood:

No data

Variant related genes	Relation type
SPPL3	TF binding region
SPPL3	CpG island
ENSG00000202538	chromatin interactions
ENSG00000200795	chromatin interactions

Extended variants
information (count: 531 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:531 , 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	rs6489780	chr12:121228410-121228411	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs150590124	chr12:121228504-121228505	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552332958	chr12:121228566-121228567	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566081500	chr12:121228599-121228600	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs35743748	chr12:121228629-121228630	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs10744754	chr12:121228647-121228648	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs548294958	chr12:121228672-121228673	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568414738	chr12:121228700-121228701	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537356742	chr12:121228780-121228781	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs557324585	chr12:121228784-121228785	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs708785	chr12:121228791-121228792	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs544704571	chr12:121228811-121228812	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs191782084	chr12:121228824-121228825	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553124914	chr12:121228843-121228844	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565450177	chr12:121228953-121228954	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs80020934	chr12:121228955-121228956	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374117566	chr12:121228987-121228988	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572862301	chr12:121228991-121228992	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541865862	chr12:121229008-121229009	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559772541	chr12:121229010-121229011	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183996441	chr12:121229042-121229043	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs114971060	chr12:121229055-121229056	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376390908	chr12:121229071-121229072	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530034538	chr12:121229083-121229084	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528316698	chr12:121229088-121229089	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544138208	chr12:121229124-121229125	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543789941	chr12:121229155-121229156	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563668521	chr12:121229169-121229170	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532656284	chr12:121229208-121229209	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112563251	chr12:121229211-121229212	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186980151	chr12:121229213-121229214	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs77723057	chr12:121229225-121229226	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548627284	chr12:121229242-121229243	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568443132	chr12:121229253-121229254	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35374564	chr12:121229259-121229260	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147398053	chr12:121229327-121229328	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561253659	chr12:121229331-121229332	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529244777	chr12:121229344-121229345	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs374927561	chr12:121229380-121229381	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550988844	chr12:121229387-121229388	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570802422	chr12:121229408-121229409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs368470188	chr12:121229409-121229410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs562282255	chr12:121229489-121229490	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs552898645	chr12:121229490-121229491	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs371491227	chr12:121229537-121229538	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs639343	chr12:121229569-121229570	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs535212891	chr12:121229591-121229592	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs555472989	chr12:121229625-121229626	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs559825307	chr12:121229630-121229631	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs369216747	chr12:121229633-121229634	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	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	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	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	chr12:121206200-121238600	Weak transcription	Small Intestine	intestine
2	chr12:121207200-121233000	Weak transcription	HSMMtube	muscle
3	chr12:121209400-121236800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr12:121211400-121260800	Weak transcription	Gastric	stomach
5	chr12:121212600-121229600	Weak transcription	Right Atrium	heart
6	chr12:121212600-121229800	Weak transcription	Right Ventricle	heart
7	chr12:121212600-121236600	Weak transcription	Fetal Heart	heart
8	chr12:121213200-121231200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr12:121221000-121250000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr12:121221200-121229600	Weak transcription	Osteobl	bone
11	chr12:121221200-121233000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr12:121221200-121233600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr12:121221200-121249400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr12:121221400-121229800	Weak transcription	NHDF-Ad	bronchial
15	chr12:121221400-121230400	Weak transcription	HMEC	breast
16	chr12:121221400-121231000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr12:121221400-121232800	Weak transcription	A549	lung
18	chr12:121221400-121235800	Weak transcription	Hela-S3	cervix
19	chr12:121221400-121240800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr12:121221600-121238800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr12:121222000-121229400	Weak transcription	Brain Anterior Caudate	brain
22	chr12:121222000-121233200	Weak transcription	NHEK	skin
23	chr12:121222000-121233800	Weak transcription	Fetal Stomach	stomach
24	chr12:121222200-121229400	Weak transcription	HepG2	liver
25	chr12:121222200-121230200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr12:121222200-121231200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr12:121222200-121231200	Weak transcription	Fetal Brain Female	brain
28	chr12:121222200-121237200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr12:121222200-121274000	Weak transcription	Lung	lung
30	chr12:121222400-121229600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr12:121222400-121231200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr12:121222400-121238800	Weak transcription	Placenta	Placenta
33	chr12:121222400-121240400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr12:121222600-121229400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr12:121222600-121229600	Weak transcription	Colonic Mucosa	Colon
36	chr12:121222600-121229600	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr12:121222600-121229800	Weak transcription	Colon Smooth Muscle	Colon
38	chr12:121222600-121230600	Weak transcription	Adipose Nuclei	Adipose
39	chr12:121222600-121231000	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr12:121222600-121231200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr12:121222600-121232200	Weak transcription	Fetal Muscle Trunk	muscle
42	chr12:121222600-121233200	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr12:121222600-121237200	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr12:121222600-121249200	Weak transcription	Rectal Smooth Muscle	rectum
45	chr12:121222600-121259000	Weak transcription	Ovary	ovary
46	chr12:121222600-121260800	Weak transcription	Spleen	Spleen
47	chr12:121222600-121268600	Weak transcription	Esophagus	oesophagus
48	chr12:121222600-121268600	Weak transcription	Stomach Smooth Muscle	stomach
49	chr12:121222800-121228800	Weak transcription	Fetal Intestine Large	intestine
50	chr12:121222800-121229200	Weak transcription	Rectal Mucosa Donor 29	rectum

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