Variant report

Variant	esv3375110
Chromosome Location	chr12:56956280-56965593
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	ARID3A	chr12:56959603-56959797	HepG2	liver:	n/a	n/a
2	ATF1	chr12:56959356-56959751	K562	blood:	n/a	n/a
3	BATF	chr12:56963882-56964209	GM12878	blood:	n/a	n/a
4	BHLHE40	chr12:56959486-56959769	K562	blood:	n/a	n/a
5	CEBPB	chr12:56963956-56964286	Hela-S3	cervix:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
6	CEBPB	chr12:56964021-56964260	K562	blood:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
7	CEBPB	chr12:56963867-56964428	ECC-1	luminal epithelium:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
8	CEBPB	chr12:56958291-56958384	A549	lung:	n/a	n/a
9	CEBPB	chr12:56963938-56964307	IMR90	lung:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
10	CEBPB	chr12:56963801-56964436	ECC-1	luminal epithelium:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
11	CEBPB	chr12:56963939-56964299	HepG2	liver:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
12	CEBPB	chr12:56963927-56964331	HepG2	liver:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
13	CEBPB	chr12:56963879-56964311	HepG2	liver:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
14	CEBPB	chr12:56964018-56964287	A549	lung:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
15	CEBPB	chr12:56964028-56964213	HepG2	liver:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
16	CEBPB	chr12:56964005-56964245	K562	blood:	n/a	chr12:56964129-56964142 chr12:56964130-56964141 chr12:56964106-56964117 chr12:56964103-56964114 chr12:56964131-56964140 chr12:56964102-56964115
17	CHD2	chr12:56959351-56959353	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr12:56959600-56959750	NHLF	lung:	n/a	n/a
19	CTCF	chr12:56959480-56959630	HVMF	connective:	n/a	n/a
20	CTCF	chr12:56959680-56959830	HPAF	blood vessel:	n/a	n/a
21	CTCF	chr12:56959720-56959870	HVMF	connective:	n/a	n/a
22	CTCF	chr12:56959680-56959830	HCFaa	heart:	n/a	n/a
23	CTCF	chr12:56959640-56959790	HVMF	connective:	n/a	n/a
24	CTCF	chr12:56959424-56959471	MCF-7	breast:	n/a	n/a
25	CTCF	chr12:56959420-56959570	GM12864	blood:	n/a	n/a
26	CTCF	chr12:56959620-56959770	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr12:56959360-56959510	A549	lung:	n/a	n/a
28	CTCF	chr12:56959640-56959790	BJ	skin:	n/a	n/a
29	CTCF	chr12:56959700-56959850	GM12866	blood:	n/a	n/a
30	CTCF	chr12:56959513-56959835	K562	blood:	n/a	n/a
31	CTCF	chr12:56963880-56964030	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr12:56959320-56959470	RPTEC	kidney:	n/a	n/a
33	CTCF	chr12:56959520-56959770	AG10803	skin:	n/a	n/a
34	CTCF	chr12:56959660-56959810	AoAF	blood vessel:	n/a	n/a
35	CTCF	chr12:56959660-56959810	HepG2	liver:	n/a	n/a
36	CTCF	chr12:56959380-56959530	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr12:56959300-56959450	BJ	skin:	n/a	n/a
38	CTCF	chr12:56959660-56959810	AG04449	skin:	n/a	n/a
39	CTCF	chr12:56959580-56959730	AG04450	lung:	n/a	n/a
40	CTCF	chr12:56959421-56959503	GM12892	blood:	n/a	n/a
41	CTCF	chr12:56959422-56959494	GM19239	blood:	n/a	n/a
42	CTCF	chr12:56959780-56959930	AG04450	lung:	n/a	n/a
43	CTCF	chr12:56959700-56959850	AG04449	skin:	n/a	n/a
44	CTCF	chr12:56959600-56959750	GM12873	blood:	n/a	n/a
45	CTCF	chr12:56959527-56959593	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr12:56959720-56959870	GM12872	blood:	n/a	n/a
47	CTCF	chr12:56963900-56964050	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr12:56959660-56959810	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr12:56959660-56959810	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr12:56959660-56959810	HUVEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:56959642-56959692	GM12892	blood:	n/a
2	chr12:56959642-56959692	AG10803	skin:	n/a
3	chr12:56959642-56959692	NHDF-neo	bronchial:	n/a
4	chr12:56959642-56959692	RPTEC	kidney:	n/a
5	chr12:56959642-56959692	GM06990	blood:	n/a
6	chr12:56959642-56959692	AG09319	gingival:	n/a
7	chr12:56959642-56959692	AG09309	skin:	n/a
8	chr12:56959642-56959692	HCM	heart:	n/a
9	chr12:56959642-56959692	MCF10A-Er-Src	breast:	n/a
10	chr12:56959642-56959692	AoSMC	blood vessel:	n/a
11	chr12:56959642-56959692	SK-N-SH_RA	brain:	n/a
12	chr12:56959642-56959692	Jurkat	blood:	n/a
13	chr12:56959642-56959692	HUVEC	blood vessel:	n/a
14	chr12:56959642-56959692	LNCaP	prostate:	n/a
15	chr12:56959642-56959692	GM12878	blood:	n/a
16	chr12:56959642-56959692	NH-A	brain:	n/a
17	chr12:56959642-56959692	HCF	heart:	n/a
18	chr12:56959642-56959692	HCT-116	colon:	n/a
19	chr12:56959642-56959692	HRPEpiC	eye:	n/a
20	chr12:56959642-56959692	GM19239	blood:	n/a
21	chr12:56959642-56959692	HEEpiC	esophagus:	n/a
22	chr12:56959642-56959692	Hela-S3	cervix:	n/a
23	chr12:56959642-56959692	H1-hESC	embryonic stem cell:	embryo
24	chr12:56959642-56959692	HMEC	breast:	n/a
25	chr12:56959642-56959692	HRE	kidney:	n/a
26	chr12:56959642-56959692	BE2_C	brain:	n/a
27	chr12:56959642-56959692	HIPEpiC	eye:	n/a
28	chr12:56959642-56959692	T-47D	breast:	n/a
29	chr12:56959642-56959692	HAEpiC	amniotic membrane:	n/a
30	chr12:56959642-56959692	NHBE	bronchial:	n/a
31	chr12:56959642-56959692	A549	lung:	n/a
32	chr12:56959642-56959692	MCF-7	breast:	n/a
33	chr12:56959642-56959692	AG04449	skin:	fetal
34	chr12:56959642-56959692	HepG2	liver:	n/a
35	chr12:56959642-56959692	SAEC	small airway:	n/a
36	chr12:56959642-56959692	HCPEpiC	choroid plexus:	n/a
37	chr12:56959642-56959692	Hepatocyte	liver:	n/a
38	chr12:56959642-56959692	HEK293	kidney:	embryo
39	chr12:56959642-56959692	ovcar-3	ovarian:	n/a
40	chr12:56959642-56959692	GM12891	blood:	n/a
41	chr12:56959642-56959692	ECC-1	luminal epithelium:	n/a
42	chr12:56959642-56959692	IMR90	lung:	fetal
43	chr12:56959642-56959692	K562	blood:	n/a
44	chr12:56959642-56959692	NB4	blood:	n/a
45	chr12:56959642-56959692	SKMC	muscle:	n/a
46	chr12:56959642-56959692	CMK	blood:	n/a
47	chr12:56959642-56959692	U87	brain:	n/a
48	chr12:56959642-56959692	NT2-D1	testis:	n/a
49	chr12:56959642-56959692	SK-N-MC	brain:	n/a
50	chr12:56959642-56959692	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:56959480..56961532-chr12:56961606..56964152,2	K562	blood:
2	chr12:56959480..56961532-chr12:56961606..56964152,2	K562	blood:
3	chr12:56907698..56908302-chr12:56959477..56960149,2	MCF-7	breast:
4	chr12:56959228..56960829-chr12:56962123..56963896,2	MCF-7	breast:
5	chr12:56870822..56872349-chr12:56963864..56966406,2	MCF-7	breast:
6	chr12:56959228..56960829-chr12:56962123..56963896,2	MCF-7	breast:
7	chr12:56582662..56585164-chr12:56962961..56964901,2	K562	blood:

Variant related genes	Relation type
RBMS2	TF binding region
RBMS2	CpG island
ENSG00000135423	chromatin interactions
ENSG00000139613	chromatin interactions
ENSG00000258199	chromatin interactions

Extended variants
information (count: 308 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563161140	chr12:56956294-56956295	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs138231675	chr12:56956315-56956316	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs150693575	chr12:56956321-56956322	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs201891574	chr12:56956367-56956368	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs140037879	chr12:56956368-56956369	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375382100	chr12:56956376-56956377	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs371757965	chr12:56956384-56956385	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369520171	chr12:56956387-56956388	Weak transcription Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs560187309	chr12:56956410-56956411	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs116982837	chr12:56956416-56956417	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs549084721	chr12:56956433-56956434	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs118006674	chr12:56956442-56956443	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs531507025	chr12:56956449-56956450	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs547941135	chr12:56956456-56956457	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs549823744	chr12:56956460-56956461	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs35580823	chr12:56956485-56956486	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs371704091	chr12:56956486-56956487	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs571480507	chr12:56956491-56956492	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs34567979	chr12:56956544-56956545	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs567790008	chr12:56956642-56956643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558182076	chr12:56956681-56956682	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs2888045	chr12:56956698-56956699	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs143117140	chr12:56956764-56956765	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs111584215	chr12:56956775-56956776	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185470684	chr12:56956776-56956777	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs141182263	chr12:56956782-56956783	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556580389	chr12:56956792-56956793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146214589	chr12:56956800-56956801	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs139093040	chr12:56956801-56956802	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545366991	chr12:56956832-56956833	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560224178	chr12:56956851-56956852	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs142398115	chr12:56956885-56956886	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371774272	chr12:56956890-56956891	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369847257	chr12:56956898-56956899	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560932335	chr12:56956909-56956910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531416068	chr12:56956959-56956960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs59950664	chr12:56957016-56957017	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs189830702	chr12:56957019-56957020	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558509578	chr12:56957120-56957121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532481126	chr12:56957141-56957142	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs78475403	chr12:56957168-56957169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566546972	chr12:56957254-56957255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146148823	chr12:56957269-56957270	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549073012	chr12:56957282-56957283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs61939871	chr12:56957303-56957304	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs140017944	chr12:56957327-56957328	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556756591	chr12:56957363-56957364	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149857087	chr12:56957450-56957451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145794598	chr12:56957455-56957456	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369407925	chr12:56957472-56957473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Wilms tumour	21544195	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
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
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Bladder cancer	21909424	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	20531469	CNVD
Rhabdomyosarcoma	16790082	CNVD
Renal cell carcinoma	18765545	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21138945	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	21509527	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glycogen storage disease	18421352	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD

Chromatin state (count:641 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:56917000-56958000	Weak transcription	Ovary	ovary
2	chr12:56917200-56959200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr12:56922400-56959200	Weak transcription	Fetal Kidney	kidney
4	chr12:56923800-56959400	Weak transcription	Aorta	Aorta
5	chr12:56924800-56959200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr12:56925000-56959200	Weak transcription	HSMMtube	muscle
7	chr12:56931400-56956800	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr12:56931400-56959400	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr12:56931600-56965000	Weak transcription	Hela-S3	cervix
10	chr12:56931800-56956400	Weak transcription	NHLF	lung
11	chr12:56932200-56959200	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr12:56933200-56959000	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr12:56933200-56959200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr12:56933400-56959200	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr12:56935600-56959200	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr12:56937200-56959200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr12:56939600-56957800	Weak transcription	HMEC	breast
18	chr12:56945400-56956800	Weak transcription	Colon Smooth Muscle	Colon
19	chr12:56946600-56959200	Weak transcription	Spleen	Spleen
20	chr12:56947000-56958000	Weak transcription	Lung	lung
21	chr12:56947200-56956400	Weak transcription	Left Ventricle	heart
22	chr12:56947200-56959200	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr12:56948200-56959200	Weak transcription	Colonic Mucosa	Colon
24	chr12:56948600-56981200	Weak transcription	Brain Cingulate Gyrus	brain
25	chr12:56950000-56959600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr12:56950800-56975000	Weak transcription	Esophagus	oesophagus
27	chr12:56951000-56959600	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr12:56951200-56959200	Weak transcription	Fetal Thymus	thymus
29	chr12:56951400-56957000	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr12:56951400-56959200	Weak transcription	Duodenum Mucosa	Duodenum
31	chr12:56951400-56963600	Weak transcription	Brain Anterior Caudate	brain
32	chr12:56952600-56966200	Weak transcription	Fetal Brain Female	brain
33	chr12:56952600-56974800	Weak transcription	Pancreas	Pancrea
34	chr12:56953200-56959200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr12:56953200-56981200	Weak transcription	Brain Substantia Nigra	brain
36	chr12:56954400-56974800	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr12:56954600-56958800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr12:56954600-56959000	Weak transcription	Rectal Smooth Muscle	rectum
39	chr12:56954600-56959200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr12:56954600-56993400	Weak transcription	Fetal Brain Male	brain
41	chr12:56954800-56957400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr12:56955000-56958600	Strong transcription	Fetal Intestine Small	intestine
43	chr12:56955000-56959000	Weak transcription	Primary hematopoietic stem cells	blood
44	chr12:56955000-56959200	Weak transcription	Fetal Heart	heart
45	chr12:56955000-56959400	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr12:56955000-56959400	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr12:56955600-56958800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr12:56955600-56958800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr12:56955800-56956800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr12:56955800-56957000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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