Variant report

Variant	nsv975443
Chromosome Location	chr12:9596751-9601469
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr12:9600477-9600495	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr12:9600846-9601058	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr12:9600026-9601051	GM12878	blood:	n/a	n/a
4	BATF	chr12:9599060-9599517	GM12878	blood:	n/a	chr12:9599254-9599262
5	BATF	chr12:9599040-9599656	GM12878	blood:	n/a	chr12:9599254-9599262
6	BCL11A	chr12:9599028-9599550	GM12878	blood:	n/a	n/a
7	BCL11A	chr12:9599859-9600445	GM12878	blood:	n/a	chr12:9600117-9600126
8	BCL11A	chr12:9599928-9600111	GM12878	blood:	n/a	n/a
9	BCL11A	chr12:9600546-9600932	GM12878	blood:	n/a	chr12:9600809-9600818 chr12:9600810-9600823
10	BCL11A	chr12:9600168-9600488	GM12878	blood:	n/a	n/a
11	BCL11A	chr12:9600454-9600822	GM12878	blood:	n/a	chr12:9600809-9600818
12	BCL11A	chr12:9598941-9599450	GM12878	blood:	n/a	chr12:9599009-9599018
13	BHLHE40	chr12:9600844-9601336	K562	blood:	n/a	chr12:9600944-9600960
14	BRCA1	chr12:9600585-9600802	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr12:9599960-9601079	K562	blood:	n/a	n/a
16	CEBPB	chr12:9600111-9600908	GM12878	blood:	n/a	chr12:9600576-9600588
17	CEBPB	chr12:9600431-9601043	Hela-S3	cervix:	n/a	chr12:9600576-9600588
18	CEBPD	chr12:9600756-9601125	K562	blood:	n/a	n/a
19	CEBPD	chr12:9600207-9600646	K562	blood:	n/a	n/a
20	CHD2	chr12:9600600-9600659	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr12:9600363-9601066	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr12:9600478-9601040	GM12878	blood:	n/a	n/a
23	CTCF	chr12:9600040-9600190	AoAF	blood vessel:	n/a	n/a
24	CTCF	chr12:9599967-9600069	MCF-7	breast:	n/a	chr12:9599973-9599986
25	CTCF	chr12:9599867-9600056	K562	blood:	n/a	chr12:9599973-9599986
26	CTCF	chr12:9600002-9600065	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr12:9600023-9600067	GM19239	blood:	n/a	n/a
28	CTCF	chr12:9599960-9600110	GM12868	blood:	n/a	chr12:9599973-9599986
29	CTCF	chr12:9599913-9600037	GM13976	blood:	n/a	chr12:9599973-9599986
30	CTCF	chr12:9600770-9600895	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr12:9599974-9599998	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr12:9600840-9600990	HUVEC	blood vessel:	n/a	chr12:9600940-9600953
33	E2F1	chr12:9600412-9601092	Hela-S3	cervix:	n/a	chr12:9600732-9600742 chr12:9600552-9600559 chr12:9600838-9600849 chr12:9600552-9600559 chr12:9600820-9600829 chr12:9600552-9600559 chr12:9600551-9600563
34	E2F4	chr12:9600366-9601170	MCF10A-Er-Src	breast:	n/a	chr12:9600732-9600742 chr12:9600552-9600559 chr12:9600552-9600559 chr12:9600820-9600829 chr12:9600552-9600559 chr12:9600551-9600563
35	E2F4	chr12:9600366-9601161	Hela-S3	cervix:	n/a	chr12:9600732-9600742 chr12:9600552-9600559 chr12:9600552-9600559 chr12:9600820-9600829 chr12:9600552-9600559 chr12:9600551-9600563
36	E2F4	chr12:9600535-9601068	K562	blood:	n/a	chr12:9600732-9600742 chr12:9600552-9600559 chr12:9600552-9600559 chr12:9600820-9600829 chr12:9600552-9600559 chr12:9600551-9600563
37	E2F4	chr12:9600593-9600980	GM12878	blood:	n/a	chr12:9600732-9600742 chr12:9600820-9600829
38	E2F6	chr12:9600287-9601085	K562	blood:	n/a	chr12:9600732-9600742 chr12:9600552-9600559 chr12:9600552-9600559 chr12:9600820-9600829 chr12:9600552-9600559 chr12:9600551-9600563
39	E2F6	chr12:9600706-9600976	K562	blood:	n/a	chr12:9600732-9600742 chr12:9600820-9600829
40	E2F6	chr12:9600678-9601055	A549	lung:	n/a	chr12:9600732-9600742 chr12:9600820-9600829
41	E2F6	chr12:9600387-9600655	K562	blood:	n/a	chr12:9600552-9600559 chr12:9600552-9600559 chr12:9600552-9600559 chr12:9600551-9600563
42	EBF1	chr12:9599420-9599686	GM12878	blood:	n/a	n/a
43	EBF1	chr12:9600888-9601155	GM12878	blood:	n/a	n/a
44	EBF1	chr12:9600892-9601128	GM12878	blood:	n/a	n/a
45	EBF1	chr12:9599032-9601315	GM12878	blood:	n/a	n/a
46	EBF1	chr12:9599719-9600094	GM12878	blood:	n/a	n/a
47	EGR1	chr12:9600404-9600642	K562	blood:	n/a	n/a
48	ELF1	chr12:9600382-9600649	K562	blood:	n/a	n/a
49	ELF1	chr12:9600691-9600885	K562	blood:	n/a	chr12:9600809-9600821
50	ELF1	chr12:9600365-9601049	GM12878	blood:	n/a	chr12:9600809-9600821

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9600941-9600991	Jurkat	blood:	n/a
2	chr12:9600941-9600991	Jurkat	blood:	n/a
3	chr12:9597637-9597687	BE2_C	brain:	n/a
4	chr12:9600060-9600110	GM12878	blood:	n/a
5	chr12:9601031-9601081	ECC-1	luminal epithelium:	n/a
6	chr12:9600941-9600991	AG10803	skin:	n/a
7	chr12:9600875-9600925	GM12878	blood:	n/a
8	chr12:9600950-9601000	HEK293	kidney:	embryo
9	chr12:9600060-9600110	AG10803	skin:	n/a
10	chr12:9600886-9600936	NB4	blood:	n/a
11	chr12:9601066-9601116	K562	blood:	n/a
12	chr12:9601149-9601199	HRE	kidney:	n/a
13	chr12:9600060-9600110	NHDF-neo	bronchial:	n/a
14	chr12:9597637-9597687	NHBE	bronchial:	n/a
15	chr12:9600886-9600936	GM12878	blood:	n/a
16	chr12:9600884-9600934	MCF-7	breast:	n/a
17	chr12:9600950-9601000	PrEC	prostate:	n/a
18	chr12:9601149-9601199	HIPEpiC	eye:	n/a
19	chr12:9600888-9600938	PFSK-1	brain:	n/a
20	chr12:9600756-9600806	IMR90	lung:	fetal
21	chr12:9600888-9600938	HRE	kidney:	n/a
22	chr12:9600941-9600991	HRPEpiC	eye:	n/a
23	chr12:9600453-9600503	SK-N-SH_RA	brain:	n/a
24	chr12:9601031-9601081	MCF-7	breast:	n/a
25	chr12:9600453-9600503	PrEC	prostate:	n/a
26	chr12:9600941-9600991	GM19239	blood:	n/a
27	chr12:9600950-9601000	ProgFib	skin:	n/a
28	chr12:9600453-9600503	IMR90	lung:	fetal
29	chr12:9600888-9600938	T-47D	breast:	n/a
30	chr12:9600060-9600110	HMEC	breast:	n/a
31	chr12:9600060-9600110	AG09319	gingival:	n/a
32	chr12:9600453-9600503	NB4	blood:	n/a
33	chr12:9601066-9601116	ovcar-3	ovarian:	n/a
34	chr12:9600801-9600851	AG04449	skin:	fetal
35	chr12:9597637-9597687	GM19239	blood:	n/a
36	chr12:9600756-9600806	SAEC	small airway:	n/a
37	chr12:9601066-9601116	HepG2	liver:	n/a
38	chr12:9601149-9601199	Hela-S3	cervix:	n/a
39	chr12:9600875-9600925	PANC-1	pancreas:	n/a
40	chr12:9601066-9601116	HCF	heart:	n/a
41	chr12:9600756-9600806	GM19239	blood:	n/a
42	chr12:9600453-9600503	U87	brain:	n/a
43	chr12:9601066-9601116	GM06990	blood:	n/a
44	chr12:9600875-9600925	MCF10A-Er-Src	breast:	n/a
45	chr12:9600888-9600938	CMK	blood:	n/a
46	chr12:9601149-9601199	LNCaP	prostate:	n/a
47	chr12:9600453-9600503	K562	blood:	n/a
48	chr12:9600886-9600936	Jurkat	blood:	n/a
49	chr12:9600884-9600934	SK-N-SH	brain:	n/a
50	chr12:9601149-9601199	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr12:9436150..9437103-chr12:9600374..9601086,2	Hela-S3	cervix:
2	chr12:9436185..9436710-chr12:9599925..9600582,2	MCF-7	breast:
3	chr12:9436030..9436711-chr12:9600583..9601103,2	HCT-116	colon:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC2D-2	chr12:9600944-9601474	FPKM1_group_5754_transcript_1
2	lnc-KLRB1-3	chr12:9600578-9600808	NONHSAT026827
3	lnc-CLEC2D-2	chr12:9600969-9601474	XLOC_009653

Variant related genes	Relation type
ENSG00000212432	TF binding region
DDX12P	TF binding region
ENSG00000212432	CpG island
DDX12P	CpG island
ENSG00000111788	chromatin interactions
CASP7	miRNA target sites

Extended variants
information (count: 105 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:105 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201701969	chr12:9596804-9596805	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs555506302	chr12:9596929-9596930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2433005	chr12:9596932-9596933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112758009	chr12:9596957-9596958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572097651	chr12:9596960-9596961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370409627	chr12:9596971-9596972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200381699	chr12:9596985-9596986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370721299	chr12:9597000-9597001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs61914747	chr12:9597026-9597027	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
10	rs199689667	chr12:9597046-9597047	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs200333296	chr12:9597098-9597099	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs146684183	chr12:9597101-9597102	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs368349138	chr12:9597105-9597106	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs371389057	chr12:9597122-9597123	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs112088413	chr12:9597254-9597255	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs188831737	chr12:9597281-9597282	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs564085924	chr12:9597307-9597308	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs75023288	chr12:9597341-9597342	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs72656615	chr12:9597347-9597348	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs111629659	chr12:9597352-9597353	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs146279652	chr12:9597363-9597364	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs201361076	chr12:9597377-9597378	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs138091477	chr12:9597392-9597393	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs199551084	chr12:9597402-9597403	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs113745374	chr12:9597426-9597427	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs74822933	chr12:9597437-9597438	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs201885865	chr12:9597519-9597520	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs139266573	chr12:9597630-9597631	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs200055999	chr12:9597637-9597638	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs79840418	chr12:9597673-9597674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372050502	chr12:9597727-9597728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192905500	chr12:9597735-9597736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115182234	chr12:9597776-9597777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs142706032	chr12:9597813-9597814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200941502	chr12:9597848-9597849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs61914749	chr12:9598412-9598413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs61914750	chr12:9598458-9598459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112553795	chr12:9598796-9598797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375862550	chr12:9599110-9599111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200773432	chr12:9599148-9599149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373507147	chr12:9599179-9599180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200748029	chr12:9599220-9599221	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs375283444	chr12:9599296-9599297	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs202112149	chr12:9599363-9599364	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs200526332	chr12:9599376-9599377	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs563212738	chr12:9599395-9599396	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs377387483	chr12:9599588-9599589	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs61081947	chr12:9599642-9599643	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs397834882	chr12:9599734-9599735	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs3882941	chr12:9599813-9599814	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance

Variant related diseases (count:90)

Disease	PMID	Source
Breast cancer	17133270	CNVD
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
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21611746	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Obesity	21131291	CNVD
small cell lung cancer	20016488	CNVD
Incontinentia Pigmenti	22033527	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Cancer	21272361	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:314 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9559200-9599600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr12:9560000-9599800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:9560200-9599600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr12:9560400-9599600	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr12:9560400-9599600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr12:9565000-9599800	Weak transcription	Esophagus	oesophagus
7	chr12:9567000-9599400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr12:9567000-9599400	Weak transcription	HepG2	liver
9	chr12:9567000-9599600	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr12:9567000-9599800	Weak transcription	Spleen	Spleen
11	chr12:9567200-9599800	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr12:9569400-9599800	Weak transcription	Gastric	stomach
13	chr12:9571000-9599800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr12:9572400-9600400	Weak transcription	Small Intestine	intestine
15	chr12:9572600-9599600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr12:9573400-9599200	Weak transcription	Hela-S3	cervix
17	chr12:9573600-9599600	Weak transcription	Fetal Muscle Leg	muscle
18	chr12:9577000-9599600	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr12:9577200-9599600	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr12:9577200-9599800	Weak transcription	Fetal Muscle Trunk	muscle
21	chr12:9577200-9599800	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr12:9577400-9599600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr12:9579200-9599400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr12:9579400-9599600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr12:9580400-9599400	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr12:9581800-9599800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr12:9581800-9600400	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr12:9583400-9599600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr12:9583400-9599800	Weak transcription	Fetal Intestine Small	intestine
30	chr12:9583400-9599800	Weak transcription	Fetal Stomach	stomach
31	chr12:9583600-9599600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr12:9585600-9599600	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr12:9585800-9599600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr12:9586800-9599400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr12:9586800-9599600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr12:9588600-9599400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr12:9588600-9599600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr12:9590600-9599400	Weak transcription	Dnd41	blood
39	chr12:9590800-9599600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr12:9593800-9599800	Weak transcription	Left Ventricle	heart
41	chr12:9594400-9599600	Weak transcription	Fetal Thymus	thymus
42	chr12:9599200-9600000	Flanking Active TSS	Hela-S3	cervix
43	chr12:9599400-9599600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr12:9599400-9599600	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr12:9599400-9599600	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr12:9599400-9599600	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr12:9599400-9599600	Active TSS	Primary T helper cells PMA-I stimulated	--
48	chr12:9599400-9599600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr12:9599400-9599600	Enhancers	Fetal Lung	lung
50	chr12:9599400-9599600	Flanking Active TSS	HepG2	liver

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