Variant report

Variant	nsv826535
Chromosome Location	chr12:124495436-124500803
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:52)
CpG islands
(count:122)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:52 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:124497599-124497959	K562	blood:	n/a	n/a
2	BHLHE40	chr12:124497837-124498004	K562	blood:	n/a	n/a
3	CEBPB	chr12:124497464-124497738	K562	blood:	n/a	n/a
4	CEBPB	chr12:124497473-124497732	HepG2	liver:	n/a	n/a
5	CTCF	chr12:124497831-124497899	K562	blood:	n/a	n/a
6	CTCF	chr12:124497693-124497996	K562	blood:	n/a	n/a
7	CTCF	chr12:124497720-124497870	HL-60	blood:	n/a	n/a
8	E2F4	chr12:124498374-124498578	MCF10A-Er-Src	breast:	n/a	n/a
9	EP300	chr12:124500703-124500953	K562	blood:	n/a	n/a
10	FOS	chr12:124497901-124498122	MCF10A-Er-Src	breast:	n/a	n/a
11	HMGN3	chr12:124500367-124500475	K562	blood:	n/a	n/a
12	JUND	chr12:124497830-124497906	K562	blood:	n/a	n/a
13	JUND	chr12:124497932-124498213	HepG2	liver:	n/a	chr12:124498068-124498079
14	MAFF	chr12:124496279-124496451	HepG2	liver:	n/a	n/a
15	MAFK	chr12:124497802-124497928	K562	blood:	n/a	n/a
16	MAFK	chr12:124496227-124496498	IMR90	lung:	n/a	n/a
17	MAFK	chr12:124496257-124496457	HepG2	liver:	n/a	n/a
18	MAFK	chr12:124496206-124496521	HepG2	liver:	n/a	n/a
19	MYC	chr12:124500507-124500517	MCF-7	breast:	n/a	n/a
20	NR3C1	chr12:124495218-124495600	A549	lung:	n/a	n/a
21	NR3C1	chr12:124495211-124495604	A549	lung:	n/a	n/a
22	POLR2A	chr12:124500787-124500895	K562	blood:	n/a	n/a
23	POLR2A	chr12:124498253-124498507	Hela-S3	cervix:	n/a	n/a
24	POLR2A	chr12:124500239-124500459	HepG2	liver:	n/a	n/a
25	POLR2A	chr12:124500463-124500539	A549	lung:	n/a	n/a
26	POLR2A	chr12:124498784-124498968	MCF-7	breast:	n/a	n/a
27	POLR2A	chr12:124500732-124500954	ECC-1	luminal epithelium:	n/a	n/a
28	POLR2A	chr12:124499428-124499533	HepG2	liver:	n/a	n/a
29	POLR2A	chr12:124500187-124500303	K562	blood:	n/a	n/a
30	POLR2A	chr12:124497558-124499057	K562	blood:	n/a	n/a
31	POLR2A	chr12:124499979-124500967	MCF-7	breast:	n/a	n/a
32	POLR2A	chr12:124498689-124498967	Hela-S3	cervix:	n/a	n/a
33	POLR2A	chr12:124500477-124500510	HepG2	liver:	n/a	n/a
34	POLR2A	chr12:124497072-124497188	K562	blood:	n/a	n/a
35	POLR2A	chr12:124499262-124501208	K562	blood:	n/a	n/a
36	POLR2A	chr12:124498433-124498687	HepG2	liver:	n/a	n/a
37	POLR2A	chr12:124497574-124497597	MCF-7	breast:	n/a	n/a
38	POLR2A	chr12:124500028-124500169	HepG2	liver:	n/a	n/a
39	POLR2A	chr12:124498902-124498971	K562	blood:	n/a	n/a
40	POLR2A	chr12:124500324-124500341	K562	blood:	n/a	n/a
41	POLR2A	chr12:124500024-124500981	Hela-S3	cervix:	n/a	n/a
42	POLR2A	chr12:124500356-124501082	Hela-S3	cervix:	n/a	n/a
43	POLR2A	chr12:124500436-124500631	GM12878	blood:	n/a	n/a
44	POLR2A	chr12:124500706-124501193	HepG2	liver:	n/a	n/a
45	POLR2A	chr12:124500213-124500233	HepG2	liver:	n/a	n/a
46	POLR2A	chr12:124499138-124499149	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr12:124499425-124499560	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr12:124500682-124500772	K562	blood:	n/a	n/a
49	POLR2A	chr12:124497631-124497810	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr12:124500090-124500337	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:124497713-124497763	HRE	kidney:	n/a
2	chr12:124497713-124497763	PrEC	prostate:	n/a
3	chr12:124497713-124497763	AoSMC	blood vessel:	n/a
4	chr12:124497105-124497155	LNCaP	prostate:	n/a
5	chr12:124497105-124497155	GM19239	blood:	n/a
6	chr12:124497713-124497763	HL-60	blood:	n/a
7	chr12:124497105-124497155	H1-hESC	embryonic stem cell:	embryo
8	chr12:124497713-124497763	ovcar-3	ovarian:	n/a
9	chr12:124497105-124497155	SAEC	small airway:	n/a
10	chr12:124497105-124497155	AG09309	skin:	n/a
11	chr12:124497105-124497155	HRCEpiC	kidney:	n/a
12	chr12:124497713-124497763	A549	lung:	n/a
13	chr12:124497713-124497763	NT2-D1	testis:	n/a
14	chr12:124497105-124497155	SKMC	muscle:	n/a
15	chr12:124497105-124497155	AG10803	skin:	n/a
16	chr12:124497105-124497155	NB4	blood:	n/a
17	chr12:124497713-124497763	BE2_C	brain:	n/a
18	chr12:124497713-124497763	HCT-116	colon:	n/a
19	chr12:124497713-124497763	CMK	blood:	n/a
20	chr12:124497105-124497155	NH-A	brain:	n/a
21	chr12:124497713-124497763	GM06990	blood:	n/a
22	chr12:124497105-124497155	RPTEC	kidney:	n/a
23	chr12:124497105-124497155	Hepatocyte	liver:	n/a
24	chr12:124497105-124497155	Hela-S3	cervix:	n/a
25	chr12:124497713-124497763	U87	brain:	n/a
26	chr12:124497105-124497155	NHBE	bronchial:	n/a
27	chr12:124497713-124497763	HMEC	breast:	n/a
28	chr12:124497105-124497155	K562	blood:	n/a
29	chr12:124497713-124497763	HRPEpiC	eye:	n/a
30	chr12:124497713-124497763	LNCaP	prostate:	n/a
31	chr12:124497713-124497763	ECC-1	luminal epithelium:	n/a
32	chr12:124497713-124497763	SK-N-SH_RA	brain:	n/a
33	chr12:124497105-124497155	AoSMC	blood vessel:	n/a
34	chr12:124497713-124497763	SK-N-MC	brain:	n/a
35	chr12:124497105-124497155	NHDF-neo	bronchial:	n/a
36	chr12:124497105-124497155	HEEpiC	esophagus:	n/a
37	chr12:124497105-124497155	IMR90	lung:	fetal
38	chr12:124497713-124497763	NB4	blood:	n/a
39	chr12:124497713-124497763	HCPEpiC	choroid plexus:	n/a
40	chr12:124497713-124497763	GM12891	blood:	n/a
41	chr12:124497105-124497155	MCF-7	breast:	n/a
42	chr12:124497105-124497155	AG04449	skin:	fetal
43	chr12:124497713-124497763	SKMC	muscle:	n/a
44	chr12:124497713-124497763	HPAEpiC	pulmonary alveolar:	n/a
45	chr12:124497105-124497155	HCM	heart:	n/a
46	chr12:124497713-124497763	HUVEC	blood vessel:	n/a
47	chr12:124497105-124497155	HPAEpiC	pulmonary alveolar:	n/a
48	chr12:124497713-124497763	SAEC	small airway:	n/a
49	chr12:124497713-124497763	NHBE	bronchial:	n/a
50	chr12:124497713-124497763	Hela-S3	cervix:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:124491034..124493507-chr12:124494589..124496940,2	MCF-7	breast:
2	chr12:124492436..124495836-chr12:124497804..124500865,3	K562	blood:
3	chr12:124492436..124495836-chr12:124497804..124500865,3	K562	blood:
4	chr12:124440660..124443329-chr12:124494503..124496915,2	K562	blood:
5	chr12:124493164..124494909-chr12:124500524..124502478,2	MCF-7	breast:
6	chr12:124196789..124198496-chr12:124499802..124501638,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000256827	TF binding region
ENSG00000256827	CpG island
ENSG00000185344	chromatin interactions

Extended variants
information (count: 228 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:228 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570141128	chr12:124495455-124495456	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs563301917	chr12:124495518-124495519	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs577649103	chr12:124495550-124495551	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs184533392	chr12:124495569-124495570	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs370075094	chr12:124495624-124495625	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs79839869	chr12:124495655-124495656	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535341575	chr12:124495661-124495662	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554031302	chr12:124495678-124495679	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs139678070	chr12:124495700-124495701	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs545576489	chr12:124495704-124495705	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs557459624	chr12:124495705-124495706	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs149949898	chr12:124495720-124495721	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs530752816	chr12:124495737-124495738	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145093885	chr12:124495760-124495761	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs561485427	chr12:124495778-124495779	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574280400	chr12:124495794-124495795	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563685149	chr12:124495810-124495811	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35059531	chr12:124495824-124495825	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs180734494	chr12:124495921-124495922	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs61448249	chr12:124495963-124495964	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs559987177	chr12:124495986-124495987	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs375649820	chr12:124496097-124496098	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186087904	chr12:124496098-124496099	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551974398	chr12:124496133-124496134	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs35572207	chr12:124496153-124496154	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563787120	chr12:124496241-124496242	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530983121	chr12:124496277-124496278	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs549360009	chr12:124496289-124496290	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs567600138	chr12:124496291-124496292	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs535007831	chr12:124496301-124496302	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs1054852	chr12:124496316-124496317	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs565615287	chr12:124496354-124496355	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189757125	chr12:124496355-124496356	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551490961	chr12:124496371-124496372	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181442942	chr12:124496420-124496421	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs142294299	chr12:124496428-124496429	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs564866999	chr12:124496449-124496450	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs536701234	chr12:124496474-124496475	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs555440431	chr12:124496482-124496483	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs530570710	chr12:124496518-124496519	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573597891	chr12:124496519-124496520	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs541008757	chr12:124496520-124496521	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550849956	chr12:124496559-124496560	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs578240940	chr12:124496582-124496583	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs186047104	chr12:124496587-124496588	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563822718	chr12:124496622-124496623	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs376791554	chr12:124496644-124496645	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs200362520	chr12:124496656-124496657	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs117061283	chr12:124496664-124496665	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs202221802	chr12:124496670-124496671	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
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
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 ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Developmental delay	19490664	CNVD

Chromatin state (count:342 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:124461200-124496800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr12:124480600-124496200	Weak transcription	Small Intestine	intestine
3	chr12:124484400-124498400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr12:124485000-124498800	Strong transcription	Hela-S3	cervix
5	chr12:124486000-124496400	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr12:124486400-124496200	Weak transcription	HMEC	breast
7	chr12:124486800-124496200	Weak transcription	Rectal Smooth Muscle	rectum
8	chr12:124486800-124496200	Weak transcription	NHLF	lung
9	chr12:124487000-124495800	Weak transcription	Ovary	ovary
10	chr12:124488400-124498400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr12:124489200-124510400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr12:124489800-124496200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr12:124490400-124498800	Strong transcription	Rectal Mucosa Donor 29	rectum
14	chr12:124490400-124500400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr12:124490800-124496000	Weak transcription	Colon Smooth Muscle	Colon
16	chr12:124491000-124496200	Weak transcription	Gastric	stomach
17	chr12:124491000-124497000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr12:124491000-124497600	Weak transcription	Colonic Mucosa	Colon
19	chr12:124491200-124496200	Weak transcription	NHEK	skin
20	chr12:124491600-124498400	Strong transcription	Placenta	Placenta
21	chr12:124491600-124499400	Strong transcription	Duodenum Mucosa	Duodenum
22	chr12:124491800-124495800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr12:124491800-124496200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr12:124491800-124497800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr12:124492000-124496200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr12:124492000-124496200	Weak transcription	Spleen	Spleen
27	chr12:124492200-124496000	Weak transcription	HSMMtube	muscle
28	chr12:124492200-124496800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr12:124492200-124498000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr12:124492600-124496400	Weak transcription	Aorta	Aorta
31	chr12:124492600-124499200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr12:124492800-124496000	Weak transcription	GM12878-XiMat	blood
33	chr12:124492800-124496200	Weak transcription	HepG2	liver
34	chr12:124493000-124495600	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr12:124493000-124495800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr12:124493000-124496000	Weak transcription	Stomach Smooth Muscle	stomach
37	chr12:124493000-124496200	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr12:124493000-124496400	Weak transcription	Fetal Heart	heart
39	chr12:124493000-124500200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr12:124493000-124501400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr12:124493000-124501600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr12:124493000-124503200	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr12:124493200-124495600	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr12:124493200-124495600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr12:124493200-124495600	Genic enhancers	Fetal Thymus	thymus
46	chr12:124493200-124496800	Weak transcription	Stomach Mucosa	stomach
47	chr12:124493200-124501200	Strong transcription	Fetal Stomach	stomach
48	chr12:124493400-124495600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr12:124493400-124495800	Weak transcription	Primary T cells from cord blood	blood
50	chr12:124493400-124496200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links