Variant report

Variant	nsv1045447
Chromosome Location	chr12:1959333-1993612
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	BHLHE40	chr12:1991971-1992232	K562	blood:	n/a	n/a
2	BHLHE40	chr12:1974549-1974700	K562	blood:	n/a	n/a
3	BHLHE40	chr12:1979460-1979468	K562	blood:	n/a	n/a
4	CEBPB	chr12:1960290-1960578	IMR90	lung:	n/a	n/a
5	CTCF	chr12:1966944-1966981	LNCaP	prostate:	n/a	n/a
6	CTCF	chr12:1980682-1980762	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr12:1980225-1980843	GM19239	blood:	n/a	n/a
8	CTCF	chr12:1980617-1980698	ProgFib	skin:	n/a	n/a
9	CTCF	chr12:1960540-1960690	AG10803	skin:	n/a	n/a
10	CTCF	chr12:1962700-1962850	GM12872	blood:	n/a	chr12:1962840-1962848
11	E2F4	chr12:1968881-1969065	MCF10A-Er-Src	breast:	n/a	n/a
12	ELF1	chr12:1974459-1974841	K562	blood:	n/a	chr12:1974668-1974679 chr12:1974667-1974680 chr12:1974668-1974679
13	ELF1	chr12:1974497-1974834	HepG2	liver:	n/a	chr12:1974668-1974679 chr12:1974667-1974680 chr12:1974668-1974679
14	ELF1	chr12:1974521-1974807	HepG2	liver:	n/a	chr12:1974668-1974679 chr12:1974667-1974680 chr12:1974668-1974679
15	EP300	chr12:1979216-1979485	T-47D	breast:	n/a	n/a
16	FOS	chr12:1961505-1961544	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr12:1960240-1960701	MCF10A-Er-Src	breast:	n/a	chr12:1960508-1960519
18	FOS	chr12:1968763-1969077	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr12:1968777-1969073	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr12:1968778-1969070	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr12:1960364-1960660	HUVEC	blood vessel:	n/a	chr12:1960508-1960519
22	FOS	chr12:1960260-1960690	MCF10A-Er-Src	breast:	n/a	chr12:1960508-1960519
23	FOS	chr12:1960240-1960731	MCF10A-Er-Src	breast:	n/a	chr12:1960508-1960519
24	FOS	chr12:1968778-1969078	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr12:1971920-1971943	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr12:1960227-1960683	MCF10A-Er-Src	breast:	n/a	chr12:1960508-1960519
27	FOSL2	chr12:1960283-1960747	SK-N-SH	brain:	n/a	n/a
28	FOXA1	chr12:1971224-1971579	T-47D	breast:	n/a	n/a
29	FOXA1	chr12:1991272-1991453	HepG2	liver:	n/a	n/a
30	FOXA1	chr12:1971298-1971541	T-47D	breast:	n/a	n/a
31	FOXA1	chr12:1968871-1969216	T-47D	breast:	n/a	n/a
32	FOXA1	chr12:1979174-1979614	T-47D	breast:	n/a	n/a
33	FOXA2	chr12:1991235-1991563	A549	lung:	n/a	n/a
34	GATA2	chr12:1972860-1973198	SH-SY5Y	brain:	n/a	n/a
35	GATA3	chr12:1972819-1973121	SH-SY5Y	brain:	n/a	n/a
36	GATA3	chr12:1979187-1979630	T-47D	breast:	n/a	n/a
37	GATA3	chr12:1979269-1979600	T-47D	breast:	n/a	n/a
38	GATA3	chr12:1968697-1969101	MCF-7	breast:	n/a	chr12:1969041-1969049
39	GATA3	chr12:1960335-1960780	SK-N-SH	brain:	n/a	n/a
40	JUN	chr12:1980723-1980931	H1-hESC	embryonic stem cell:	n/a	n/a
41	JUND	chr12:1989764-1989867	HepG2	liver:	n/a	chr12:1989816-1989824 chr12:1989816-1989824 chr12:1989817-1989824 chr12:1989815-1989825 chr12:1989814-1989825 chr12:1989814-1989826
42	KAP1	chr12:1968804-1969161	U2OS	brain:	n/a	n/a
43	KAP1	chr12:1964381-1964816	HEK293	kidney:	n/a	n/a
44	MAFF	chr12:1989700-1989976	HepG2	liver:	n/a	chr12:1989807-1989825
45	MAFF	chr12:1989660-1990005	K562	blood:	n/a	chr12:1989807-1989825
46	MAFK	chr12:1989718-1989855	H1-hESC	embryonic stem cell:	n/a	chr12:1989809-1989824 chr12:1989814-1989823 chr12:1989814-1989824
47	MAFK	chr12:1989655-1989990	K562	blood:	n/a	chr12:1989809-1989824 chr12:1989814-1989823 chr12:1989814-1989824
48	MAFK	chr12:1989688-1989946	HepG2	liver:	n/a	chr12:1989809-1989824 chr12:1989814-1989823 chr12:1989814-1989824
49	MAFK	chr12:1989689-1989965	HepG2	liver:	n/a	chr12:1989809-1989824 chr12:1989814-1989823 chr12:1989814-1989824
50	MAX	chr12:1991244-1991336	NB4	blood:	n/a	chr12:1991306-1991316

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1973237-1973287	HCT-116	colon:	n/a
2	chr12:1963310-1963360	NHBE	bronchial:	n/a
3	chr12:1973340-1973390	SAEC	small airway:	n/a
4	chr12:1964603-1964653	SK-N-MC	brain:	n/a
5	chr12:1964603-1964653	RPTEC	kidney:	n/a
6	chr12:1973208-1973258	ProgFib	skin:	n/a
7	chr12:1973208-1973258	GM19239	blood:	n/a
8	chr12:1978889-1978939	HCT-116	colon:	n/a
9	chr12:1963310-1963360	LNCaP	prostate:	n/a
10	chr12:1974814-1974864	AG10803	skin:	n/a
11	chr12:1973340-1973390	NHBE	bronchial:	n/a
12	chr12:1970170-1970220	T-47D	breast:	n/a
13	chr12:1974168-1974218	T-47D	breast:	n/a
14	chr12:1974168-1974218	BJ	skin:	n/a
15	chr12:1964603-1964653	HUVEC	blood vessel:	n/a
16	chr12:1976671-1976721	SK-N-SH_RA	brain:	n/a
17	chr12:1973208-1973258	BE2_C	brain:	n/a
18	chr12:1973208-1973258	NH-A	brain:	n/a
19	chr12:1973872-1973922	AG09319	gingival:	n/a
20	chr12:1974814-1974864	Hela-S3	cervix:	n/a
21	chr12:1974724-1974774	CMK	blood:	n/a
22	chr12:1974724-1974774	HAEpiC	amniotic membrane:	n/a
23	chr12:1974122-1974172	Hela-S3	cervix:	n/a
24	chr12:1978889-1978939	BJ	skin:	n/a
25	chr12:1974814-1974864	SK-N-SH_RA	brain:	n/a
26	chr12:1976671-1976721	HEEpiC	esophagus:	n/a
27	chr12:1978889-1978939	RPTEC	kidney:	n/a
28	chr12:1974122-1974172	A549	lung:	n/a
29	chr12:1964603-1964653	GM12891	blood:	n/a
30	chr12:1963310-1963360	Hepatocyte	liver:	n/a
31	chr12:1978889-1978939	HRPEpiC	eye:	n/a
32	chr12:1974168-1974218	HepG2	liver:	n/a
33	chr12:1974168-1974218	HRPEpiC	eye:	n/a
34	chr12:1970170-1970220	HCT-116	colon:	n/a
35	chr12:1973367-1973417	HEEpiC	esophagus:	n/a
36	chr12:1973367-1973417	HRCEpiC	kidney:	n/a
37	chr12:1978889-1978939	HUVEC	blood vessel:	n/a
38	chr12:1974814-1974864	HL-60	blood:	n/a
39	chr12:1973237-1973287	RPTEC	kidney:	n/a
40	chr12:1973452-1973502	AG10803	skin:	n/a
41	chr12:1974168-1974218	HCT-116	colon:	n/a
42	chr12:1973367-1973417	T-47D	breast:	n/a
43	chr12:1973872-1973922	HepG2	liver:	n/a
44	chr12:1974168-1974218	PrEC	prostate:	n/a
45	chr12:1973872-1973922	Jurkat	blood:	n/a
46	chr12:1976671-1976721	NT2-D1	testis:	n/a
47	chr12:1973452-1973502	HMEC	breast:	n/a
48	chr12:1973237-1973287	HNPCEpiC	eye:	n/a
49	chr12:1974814-1974864	IMR90	lung:	fetal
50	chr12:1973340-1973390	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:1950335..1952773-chr12:1969860..1971374,2	MCF-7	breast:
2	chr12:1978767..1980595-chr12:2025590..2028373,2	MCF-7	breast:
3	chr12:1982062..1983660-chr12:1991935..1993547,2	MCF-7	breast:
4	chr12:1962744..1965202-chr12:1987725..1990187,2	MCF-7	breast:
5	chr12:1982062..1983660-chr12:1991935..1993547,2	MCF-7	breast:
6	chr12:1947774..1950374-chr12:1986873..1988503,2	MCF-7	breast:
7	chr12:1976877..1978383-chr12:1995618..1998420,2	MCF-7	breast:
8	chr12:1968515..1969333-chr12:2041106..2041850,2	MCF-7	breast:
9	chr12:1968515..1969082-chr12:2040995..2041606,2	MCF-7	breast:
10	chr12:1956703..1959604-chr12:1963408..1966102,2	MCF-7	breast:
11	chr12:1947643..1951345-chr12:1957413..1959557,3	MCF-7	breast:
12	chr12:1956703..1959604-chr12:1963408..1966102,2	MCF-7	breast:
13	chr12:1953795..1956547-chr12:1969421..1971021,2	MCF-7	breast:
14	chr12:1959456..1961016-chr12:1962388..1965205,2	MCF-7	breast:
15	chr12:1945038..1946828-chr12:1971867..1974133,2	K562	blood:
16	chr12:1962397..1965390-chr12:1965944..1968413,2	K562	blood:

Variant related genes	Relation type
CACNA2D4	TF binding region
CACNA2D4	CpG island
ENSG00000151062	chromatin interactions
ENSG00000256706	chromatin interactions

Extended variants
information (count: 1294 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1294 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373584875	chr12:1959364-1959365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs570304662	chr12:1959427-1959428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs79639749	chr12:1959432-1959433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs145324095	chr12:1959436-1959437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565292283	chr12:1959437-1959438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191945417	chr12:1959466-1959467	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs566342558	chr12:1959532-1959533	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs536480833	chr12:1959552-1959553	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs532790850	chr12:1959570-1959571	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs200708861	chr12:1959572-1959573	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs73047927	chr12:1959639-1959640	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs117738252	chr12:1959640-1959641	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs537102486	chr12:1959649-1959650	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs569410804	chr12:1959664-1959665	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs536627703	chr12:1959719-1959720	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs73047930	chr12:1959752-1959753	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs577132998	chr12:1959754-1959755	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs577581556	chr12:1959757-1959758	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs184186645	chr12:1959772-1959773	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs74551806	chr12:1959774-1959775	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs574657767	chr12:1959791-1959792	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs542084903	chr12:1959796-1959797	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs563467087	chr12:1959798-1959799	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs530624351	chr12:1959799-1959800	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs185870122	chr12:1959808-1959809	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs566874341	chr12:1959836-1959837	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs533806175	chr12:1959837-1959838	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs564124173	chr12:1959845-1959846	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs113232452	chr12:1959870-1959871	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs182417693	chr12:1959878-1959879	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs566285858	chr12:1959883-1959884	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs543299289	chr12:1959906-1959907	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs145143436	chr12:1959973-1959974	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs112110254	chr12:1959996-1959997	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs112359717	chr12:1960042-1960043	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs546091435	chr12:1960047-1960048	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs574379620	chr12:1960048-1960049	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs3078857	chr12:1960064-1960065	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs79773400	chr12:1960066-1960067	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs114154622	chr12:1960072-1960073	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs576954145	chr12:1960099-1960100	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs187023613	chr12:1960103-1960104	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs537682885	chr12:1960162-1960163	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs555098940	chr12:1960185-1960186	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs376672441	chr12:1960196-1960197	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs555817477	chr12:1960208-1960209	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs574687873	chr12:1960220-1960221	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs10774000	chr12:1960237-1960238	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs557201924	chr12:1960257-1960258	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs575475868	chr12:1960264-1960265	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Urothelial carcinoma	21177765	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	22488967	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1955200-1960000	Weak transcription	Fetal Brain Male	brain
2	chr12:1958200-1962800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr12:1960000-1960600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr12:1960000-1961000	Enhancers	Osteobl	bone
5	chr12:1960000-1962000	Enhancers	Fetal Brain Male	brain
6	chr12:1960200-1960800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr12:1960200-1960800	Enhancers	Muscle Satellite Cultured Cells	--
8	chr12:1960600-1960800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr12:1960600-1961000	Enhancers	Dnd41	blood
10	chr12:1960800-1961600	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr12:1960800-1963800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr12:1963400-1964400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr12:1963800-1965600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr12:1964000-1965200	ZNF genes & repeats	Brain Cingulate Gyrus	brain
15	chr12:1964200-1964800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr12:1964200-1965200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr12:1964400-1964800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr12:1964400-1965000	ZNF genes & repeats	Aorta	Aorta
19	chr12:1964400-1965200	ZNF genes & repeats	Adipose Nuclei	Adipose
20	chr12:1964400-1965200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
21	chr12:1964600-1965800	ZNF genes & repeats	Stomach Smooth Muscle	stomach
22	chr12:1964800-1965200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr12:1965600-1966400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr12:1968600-1968800	Bivalent Enhancer	HepG2	liver
25	chr12:1969000-1969200	Bivalent Enhancer	Osteobl	bone
26	chr12:1969400-1969600	Bivalent Enhancer	Lung	lung
27	chr12:1972800-1973400	Weak transcription	Lung	lung
28	chr12:1973600-1974200	ZNF genes & repeats	Spleen	Spleen
29	chr12:1973800-1974000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr12:1973800-1974000	Bivalent Enhancer	Fetal Intestine Large	intestine
31	chr12:1973800-1974400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
32	chr12:1973800-1974600	Bivalent Enhancer	Fetal Stomach	stomach
33	chr12:1973800-1974800	ZNF genes & repeats	Lung	lung
34	chr12:1974000-1974200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr12:1974000-1974200	Bivalent Enhancer	Fetal Lung	lung
36	chr12:1974000-1974200	Bivalent Enhancer	Right Ventricle	heart
37	chr12:1974000-1974400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr12:1974000-1974400	Active TSS	Duodenum Mucosa	Duodenum
39	chr12:1974200-1974400	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr12:1974200-1974400	Bivalent Enhancer	Left Ventricle	heart
41	chr12:1974200-1974600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr12:1974200-1974600	ZNF genes & repeats	Pancreas	Pancrea
43	chr12:1974200-1974800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr12:1974200-1974800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr12:1974200-1974800	Enhancers	Gastric	stomach
46	chr12:1974400-1979200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr12:1974600-1974800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr12:1974800-1978400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr12:1978400-1978800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr12:1978800-1980200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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