Variant report

Variant	nsv898591
Chromosome Location	chr12:1745208-1755960
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:74)
CpG islands
(count:979)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:74 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr12:1751637-1752006	K562	blood:	n/a	chr12:1751802-1751811
2	BHLHE40	chr12:1755884-1756045	K562	blood:	n/a	n/a
3	CEBPB	chr12:1754187-1754499	IMR90	lung:	n/a	n/a
4	CEBPB	chr12:1754325-1754418	HepG2	liver:	n/a	n/a
5	CTCF	chr12:1747372-1747390	Kidney_OC	kidney:	n/a	n/a
6	CTCF	chr12:1754100-1754250	HAc	cerebellar:	n/a	n/a
7	CTCF	chr12:1753960-1754110	GM12864	blood:	n/a	n/a
8	CTCF	chr12:1749780-1749930	HepG2	liver:	n/a	n/a
9	CTCF	chr12:1753960-1754110	AG10803	skin:	n/a	n/a
10	CTCF	chr12:1754020-1754170	AG04449	skin:	n/a	n/a
11	CTCF	chr12:1749823-1749863	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr12:1754037-1754203	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr12:1753980-1754130	BE2_C	brain:	n/a	n/a
14	CTCF	chr12:1749802-1749902	HepG2	liver:	n/a	n/a
15	CTCF	chr12:1754040-1754190	AG09319	gingival:	n/a	n/a
16	CTCF	chr12:1749855-1749869	MCF-7	breast:	n/a	n/a
17	CTCF	chr12:1749700-1749850	WERI-Rb-1	eye:	n/a	n/a
18	E2F6	chr12:1748572-1749248	H1-hESC	embryonic stem cell:	n/a	n/a
19	E2F6	chr12:1748675-1749158	H1-hESC	embryonic stem cell:	n/a	n/a
20	EP300	chr12:1751039-1751588	MCF-7	breast:	n/a	n/a
21	EP300	chr12:1753683-1753946	SK-N-SH_RA	brain:	n/a	n/a
22	EP300	chr12:1753704-1754040	SK-N-SH_RA	brain:	n/a	n/a
23	FOS	chr12:1753805-1753959	MCF10A-Er-Src	breast:	n/a	n/a
24	FOXM1	chr12:1751040-1751530	MCF-7	breast:	n/a	n/a
25	GABPA	chr12:1748671-1749019	H1-hESC	embryonic stem cell:	n/a	n/a
26	GATA2	chr12:1753012-1754336	SH-SY5Y	brain:	n/a	n/a
27	GATA3	chr12:1753587-1753837	SH-SY5Y	brain:	n/a	n/a
28	GATA3	chr12:1751115-1751575	MCF-7	breast:	n/a	n/a
29	GATA3	chr12:1752997-1753364	SH-SY5Y	brain:	n/a	n/a
30	GATA3	chr12:1750940-1751533	MCF-7	breast:	n/a	n/a
31	GATA3	chr12:1750984-1751591	MCF-7	breast:	n/a	n/a
32	HDAC2	chr12:1751181-1751526	MCF-7	breast:	n/a	n/a
33	IRF1	chr12:1754595-1754602	K562	blood:	n/a	n/a
34	IRF1	chr12:1754671-1754844	K562	blood:	n/a	chr12:1754695-1754705 chr12:1754693-1754706 chr12:1754672-1754686 chr12:1754696-1754707 chr12:1754691-1754705 chr12:1754693-1754706 chr12:1754695-1754706 chr12:1754695-1754709 chr12:1754693-1754706
35	JUND	chr12:1747544-1747551	K562	blood:	n/a	n/a
36	MAFF	chr12:1751017-1751183	K562	blood:	n/a	n/a
37	MAFF	chr12:1746901-1747084	K562	blood:	n/a	chr12:1747021-1747039
38	MAFF	chr12:1746902-1747100	HepG2	liver:	n/a	chr12:1747021-1747039
39	MAFK	chr12:1746955-1747106	HepG2	liver:	n/a	chr12:1747023-1747038
40	MAFK	chr12:1746873-1747165	HepG2	liver:	n/a	chr12:1747023-1747038
41	MAFK	chr12:1753897-1754011	HepG2	liver:	n/a	n/a
42	MAFK	chr12:1747465-1747481	IMR90	lung:	n/a	n/a
43	MAFK	chr12:1753742-1754084	IMR90	lung:	n/a	n/a
44	MAFK	chr12:1747411-1747694	K562	blood:	n/a	n/a
45	MAFK	chr12:1746944-1747116	IMR90	lung:	n/a	chr12:1747023-1747038
46	MAX	chr12:1755686-1756666	NB4	blood:	n/a	n/a
47	MAX	chr12:1748692-1749124	H1-hESC	embryonic stem cell:	n/a	n/a
48	MAX	chr12:1748680-1749125	H1-hESC	embryonic stem cell:	n/a	n/a
49	MAX	chr12:1753643-1754148	SK-N-SH	brain:	n/a	chr12:1753890-1753899
50	MXI1	chr12:1753051-1754439	SK-N-SH	brain:	n/a	n/a

(count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1755143-1755193	Hepatocyte	liver:	n/a
2	chr12:1747274-1747324	GM06990	blood:	n/a
3	chr12:1755068-1755118	HEK293	kidney:	embryo
4	chr12:1755143-1755193	Hepatocyte	liver:	n/a
5	chr12:1747274-1747324	GM06990	blood:	n/a
6	chr12:1755068-1755118	HEK293	kidney:	embryo
7	chr12:1754980-1755030	ovcar-3	ovarian:	n/a
8	chr12:1748816-1748866	CMK	blood:	n/a
9	chr12:1751897-1751947	H1-hESC	embryonic stem cell:	embryo
10	chr12:1753440-1753490	GM12892	blood:	n/a
11	chr12:1747274-1747324	CMK	blood:	n/a
12	chr12:1747274-1747324	HRCEpiC	kidney:	n/a
13	chr12:1755162-1755212	AG04450	lung:	fetal
14	chr12:1755162-1755212	HRE	kidney:	n/a
15	chr12:1749013-1749063	AG10803	skin:	n/a
16	chr12:1749159-1749209	Jurkat	blood:	n/a
17	chr12:1753440-1753490	GM19239	blood:	n/a
18	chr12:1753866-1753916	ECC-1	luminal epithelium:	n/a
19	chr12:1755162-1755212	HCM	heart:	n/a
20	chr12:1753440-1753490	A549	lung:	n/a
21	chr12:1755068-1755118	PrEC	prostate:	n/a
22	chr12:1749013-1749063	U87	brain:	n/a
23	chr12:1749013-1749063	K562	blood:	n/a
24	chr12:1751897-1751947	NH-A	brain:	n/a
25	chr12:1747274-1747324	SK-N-MC	brain:	n/a
26	chr12:1749159-1749209	HAEpiC	amniotic membrane:	n/a
27	chr12:1755322-1755372	AG10803	skin:	n/a
28	chr12:1753440-1753490	BJ	skin:	n/a
29	chr12:1751357-1751407	AoSMC	blood vessel:	n/a
30	chr12:1755143-1755193	NT2-D1	testis:	n/a
31	chr12:1753866-1753916	LNCaP	prostate:	n/a
32	chr12:1754980-1755030	HAEpiC	amniotic membrane:	n/a
33	chr12:1755143-1755193	Caco-2	colon:	n/a
34	chr12:1751357-1751407	HCF	heart:	n/a
35	chr12:1753440-1753490	T-47D	breast:	n/a
36	chr12:1751897-1751947	AoSMC	blood vessel:	n/a
37	chr12:1751897-1751947	MCF-7	breast:	n/a
38	chr12:1747274-1747324	AG04450	lung:	fetal
39	chr12:1754156-1754206	Hela-S3	cervix:	n/a
40	chr12:1754156-1754206	NB4	blood:	n/a
41	chr12:1753440-1753490	HCT-116	colon:	n/a
42	chr12:1751897-1751947	ProgFib	skin:	n/a
43	chr12:1755143-1755193	BJ	skin:	n/a
44	chr12:1754750-1754800	GM12891	blood:	n/a
45	chr12:1755068-1755118	HRE	kidney:	n/a
46	chr12:1753440-1753490	HepG2	liver:	n/a
47	chr12:1751357-1751407	HepG2	liver:	n/a
48	chr12:1751357-1751407	HL-60	blood:	n/a
49	chr12:1748816-1748866	NH-A	brain:	n/a
50	chr12:1747274-1747324	A549	lung:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:1739520..1741562-chr12:1747330..1749766,2	MCF-7	breast:
2	chr12:1738742..1741489-chr12:1743344..1746284,2	K562	blood:
3	chr12:1745580..1751053-chr12:1752530..1755627,4	K562	blood:
4	chr12:1748743..1751681-chr12:1751691..1754305,2	MCF-7	breast:
5	chr12:1751543..1753813-chr12:1771357..1773090,2	K562	blood:
6	chr12:1750618..1752879-chr12:1756177..1759095,2	K562	blood:
7	chr12:1746984..1749673-chr12:1753092..1755153,3	K562	blood:
8	chr12:1702532..1704125-chr12:1743682..1745521,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	WNT5B	hsa-miR-185-5p	chr12:1755626-1755648
2	WNT5B	hsa-miR-185-5p	chr12:1755591-1755614

Variant related genes	Relation type
WNT5B	TF binding region
WNT5B	CpG island
ENSG00000111186	chromatin interactions
ENSG00000171823	chromatin interactions

Extended variants
information (count: 500 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:500 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28384806	chr12:1745208-1745209	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs140678118	chr12:1745225-1745226	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs377059551	chr12:1745264-1745265	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs150070150	chr12:1745274-1745275	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs371249627	chr12:1745350-1745351	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs575154873	chr12:1745390-1745391	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs113902131	chr12:1745461-1745462	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs563408738	chr12:1745468-1745469	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs373372551	chr12:1745487-1745488	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs185099686	chr12:1745500-1745501	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs553164006	chr12:1745510-1745511	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs11061884	chr12:1745559-1745560	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs146632618	chr12:1745585-1745586	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs111665549	chr12:1745637-1745638	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs377377750	chr12:1745651-1745652	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs181029446	chr12:1745654-1745655	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs143065723	chr12:1745664-1745665	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs201812987	chr12:1745675-1745676	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs56884302	chr12:1745676-1745677	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs200040873	chr12:1745677-1745678	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs61672089	chr12:1745678-1745679	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs56095993	chr12:1745696-1745697	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs58601982	chr12:1745700-1745701	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs71055175	chr12:1745707-1745708	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs55956039	chr12:1745709-1745710	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs554544452	chr12:1745778-1745779	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs564179766	chr12:1745821-1745822	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs141372878	chr12:1745825-1745826	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs375013084	chr12:1745868-1745869	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs148254573	chr12:1745869-1745870	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs577434559	chr12:1745873-1745874	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs397955602	chr12:1745899-1745900	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs145110731	chr12:1746023-1746024	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs112420958	chr12:1746027-1746028	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs528978748	chr12:1746030-1746031	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs550745820	chr12:1746089-1746090	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs568828133	chr12:1746094-1746095	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs184656578	chr12:1746109-1746110	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs532753779	chr12:1746153-1746154	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs551376615	chr12:1746154-1746155	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs535292413	chr12:1746155-1746156	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs553717565	chr12:1746165-1746166	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs138924418	chr12:1746166-1746167	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs370178254	chr12:1746185-1746186	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs114476580	chr12:1746269-1746270	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs535543428	chr12:1746286-1746287	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs551433977	chr12:1746307-1746308	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs575697252	chr12:1746339-1746340	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs545851622	chr12:1746362-1746363	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs372689358	chr12:1746372-1746373	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	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
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	21935476	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:442 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1739800-1753800	Weak transcription	Esophagus	oesophagus
2	chr12:1740000-1748800	Weak transcription	Pancreas	Pancrea
3	chr12:1740000-1749000	Weak transcription	Ovary	ovary
4	chr12:1740600-1745600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr12:1740600-1748800	Weak transcription	Gastric	stomach
6	chr12:1740600-1753400	Strong transcription	Osteobl	bone
7	chr12:1740600-1755000	Weak transcription	Spleen	Spleen
8	chr12:1740800-1747200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr12:1740800-1751000	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr12:1740800-1753200	Weak transcription	NH-A	brain
11	chr12:1740800-1753600	Weak transcription	Placenta	Placenta
12	chr12:1740800-1757400	Weak transcription	GM12878-XiMat	blood
13	chr12:1741000-1749200	Weak transcription	HSMMtube	muscle
14	chr12:1741400-1745600	Enhancers	Liver	Liver
15	chr12:1741400-1752800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr12:1741800-1746000	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr12:1742000-1753400	Weak transcription	NHEK	skin
18	chr12:1742200-1749400	Weak transcription	Stomach Smooth Muscle	stomach
19	chr12:1742400-1747400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr12:1742800-1747000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr12:1743000-1749400	Weak transcription	Fetal Lung	lung
22	chr12:1743600-1759000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr12:1743800-1745600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr12:1743800-1745600	Strong transcription	NHDF-Ad	bronchial
25	chr12:1743800-1749400	Weak transcription	Stomach Mucosa	stomach
26	chr12:1744000-1745400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
27	chr12:1744000-1749200	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr12:1744000-1753000	Weak transcription	Colon Smooth Muscle	Colon
29	chr12:1744000-1753200	Weak transcription	Colonic Mucosa	Colon
30	chr12:1744200-1746000	Strong transcription	HSMM	muscle
31	chr12:1744200-1749000	Weak transcription	Fetal Intestine Small	intestine
32	chr12:1744200-1751600	Weak transcription	Duodenum Mucosa	Duodenum
33	chr12:1744200-1753400	Weak transcription	Adipose Nuclei	Adipose
34	chr12:1744400-1747000	Strong transcription	Fetal Muscle Leg	muscle
35	chr12:1744400-1747200	Weak transcription	Fetal Heart	heart
36	chr12:1744400-1747200	Weak transcription	K562	blood
37	chr12:1744400-1748600	Weak transcription	Fetal Brain Male	brain
38	chr12:1744400-1752000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr12:1744400-1753000	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr12:1744400-1753200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr12:1744400-1753200	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr12:1744400-1759000	Weak transcription	Right Ventricle	heart
43	chr12:1744600-1753000	Weak transcription	Brain Cingulate Gyrus	brain
44	chr12:1744600-1753000	Weak transcription	Brain Substantia Nigra	brain
45	chr12:1744600-1758000	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr12:1744800-1745400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr12:1745000-1745600	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr12:1745000-1746200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr12:1745000-1748400	Weak transcription	Fetal Stomach	stomach
50	chr12:1745000-1748600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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