Variant report

Variant	nsv560460
Chromosome Location	chr12:122177322-122185780
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	chr12:122180751-122181242	K562	blood:	n/a	n/a
2	ARID3A	chr12:122179728-122179897	K562	blood:	n/a	n/a
3	ATF1	chr12:122180824-122181237	K562	blood:	n/a	n/a
4	ATF3	chr12:122180935-122181287	K562	blood:	n/a	n/a
5	BHLHE40	chr12:122180827-122181335	K562	blood:	n/a	n/a
6	CEBPB	chr12:122183550-122183687	IMR90	lung:	n/a	chr12:122183646-122183657
7	CEBPB	chr12:122183527-122183755	HepG2	liver:	n/a	chr12:122183646-122183657
8	CEBPB	chr12:122183515-122183798	K562	blood:	n/a	chr12:122183646-122183657
9	CEBPB	chr12:122182803-122182929	HepG2	liver:	n/a	chr12:122182884-122182895
10	CEBPB	chr12:122183471-122183812	K562	blood:	n/a	chr12:122183646-122183657
11	CTCF	chr12:122185083-122185150	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr12:122180172-122180261	Spleen_OC	spleen:	n/a	n/a
13	CUX1	chr12:122180972-122181178	K562	blood:	n/a	n/a
14	EP300	chr12:122180704-122181297	K562	blood:	n/a	n/a
15	FOS	chr12:122179806-122179854	MCF10A-Er-Src	breast:	n/a	chr12:122179821-122179831 chr12:122179821-122179831 chr12:122179821-122179831 chr12:122179821-122179830 chr12:122179821-122179831 chr12:122179820-122179832
16	FOS	chr12:122180950-122181330	HUVEC	blood vessel:	n/a	chr12:122181184-122181195
17	FOSL1	chr12:122181047-122181248	K562	blood:	n/a	chr12:122181184-122181195
18	FOSL1	chr12:122180969-122181301	K562	blood:	n/a	chr12:122181184-122181195
19	FOSL1	chr12:122179699-122179999	K562	blood:	n/a	chr12:122179821-122179831 chr12:122179821-122179831 chr12:122179821-122179831 chr12:122179821-122179830 chr12:122179821-122179831 chr12:122179820-122179832 chr12:122179783-122179793
20	FOSL2	chr12:122179559-122180006	A549	lung:	n/a	chr12:122179821-122179831 chr12:122179821-122179831 chr12:122179821-122179831 chr12:122179821-122179830 chr12:122179821-122179831 chr12:122179820-122179832 chr12:122179783-122179793
21	FOSL2	chr12:122180943-122181323	A549	lung:	n/a	n/a
22	FOSL2	chr12:122185664-122186169	HepG2	liver:	n/a	n/a
23	FOXA2	chr12:122179548-122180141	A549	lung:	n/a	n/a
24	GTF3C2	chr12:122180531-122181430	K562	blood:	n/a	n/a
25	HCFC1	chr12:122180874-122181195	K562	blood:	n/a	n/a
26	JUN	chr12:122179577-122180156	K562	blood:	n/a	chr12:122179821-122179831 chr12:122179821-122179831 chr12:122179821-122179831 chr12:122179821-122179830 chr12:122179821-122179831 chr12:122179820-122179832 chr12:122179783-122179793
27	JUN	chr12:122180694-122181897	K562	blood:	n/a	n/a
28	JUN	chr12:122179712-122179922	K562	blood:	n/a	chr12:122179821-122179831 chr12:122179821-122179831 chr12:122179821-122179831 chr12:122179821-122179830 chr12:122179821-122179831 chr12:122179820-122179832 chr12:122179783-122179793
29	JUN	chr12:122180959-122181287	K562	blood:	n/a	n/a
30	JUN	chr12:122175970-122177401	K562	blood:	n/a	n/a
31	JUND	chr12:122179682-122179965	H1-hESC	embryonic stem cell:	n/a	chr12:122179821-122179831 chr12:122179821-122179831 chr12:122179821-122179831 chr12:122179821-122179830 chr12:122179821-122179831 chr12:122179820-122179832 chr12:122179783-122179793
32	JUND	chr12:122179668-122179990	K562	blood:	n/a	chr12:122179821-122179831 chr12:122179821-122179831 chr12:122179821-122179831 chr12:122179821-122179830 chr12:122179821-122179831 chr12:122179820-122179832 chr12:122179783-122179793
33	JUND	chr12:122185730-122186095	HepG2	liver:	n/a	n/a
34	JUND	chr12:122180705-122181374	K562	blood:	n/a	n/a
35	KAP1	chr12:122180782-122181135	U2OS	brain:	n/a	n/a
36	MAZ	chr12:122180780-122181246	K562	blood:	n/a	n/a
37	MYC	chr12:122181085-122181159	K562	blood:	n/a	n/a
38	NR3C1	chr12:122185670-122187292	A549	lung:	n/a	chr12:122186880-122186906 chr12:122186593-122186600 chr12:122187002-122187011 chr12:122186622-122186631 chr12:122187227-122187240
39	NR3C1	chr12:122185755-122187151	A549	lung:	n/a	chr12:122186880-122186906 chr12:122186593-122186600 chr12:122187002-122187011 chr12:122186622-122186631
40	NR3C1	chr12:122185701-122187286	A549	lung:	n/a	chr12:122186880-122186906 chr12:122186593-122186600 chr12:122187002-122187011 chr12:122186622-122186631 chr12:122187227-122187240
41	PBX3	chr12:122185731-122186133	GM12878	blood:	n/a	n/a
42	POLR2A	chr12:122180901-122181267	HUVEC	blood vessel:	n/a	n/a
43	POLR2A	chr12:122185742-122186121	GM12878	blood:	n/a	n/a
44	POLR2A	chr12:122181147-122181205	HUVEC	blood vessel:	n/a	n/a
45	POLR2A	chr12:122182740-122182743	HepG2	liver:	n/a	n/a
46	POLR2A	chr12:122185723-122186718	A549	lung:	n/a	n/a
47	POLR2A	chr12:122185684-122186695	A549	lung:	n/a	n/a
48	POLR2A	chr12:122185725-122186175	A549	lung:	n/a	n/a
49	POLR2A	chr12:122182605-122182736	HepG2	liver:	n/a	n/a
50	POU2F2	chr12:122185692-122186194	GM12891	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:122148459..122151159-chr12:122185562..122188129,3	K562	blood:
2	chr12:122149421..122152814-chr12:122185119..122186671,3	MCF-7	breast:
3	chr12:122149138..122151891-chr12:122182134..122184327,2	MCF-7	breast:
4	chr12:122184924..122187179-chr12:122189642..122193871,5	K562	blood:
5	chr12:122180307..122182295-chr12:122185324..122187863,3	K562	blood:
6	chr12:122147215..122155218-chr12:122185094..122190846,22	MCF-7	breast:
7	chr12:122176347..122177868-chr12:122237550..122239759,2	K562	blood:
8	chr12:122133742..122136740-chr12:122185481..122187047,2	MCF-7	breast:
9	chr12:122180813..122182540-chr12:122189739..122192360,2	MCF-7	breast:
10	chr12:122185267..122187971-chr12:122239677..122241444,2	MCF-7	breast:
11	chr12:122175709..122178951-chr12:122179528..122184666,6	K562	blood:
12	chr12:122178967..122180494-chr12:122238861..122240682,2	K562	blood:
13	chr12:122182089..122184011-chr12:122191407..122193970,2	MCF-7	breast:
14	chr12:122184835..122196012-chr12:122235281..122245445,27	MCF-7	breast:
15	chr12:122180307..122183056-chr12:122185275..122189745,5	K562	blood:
16	chr12:122149726..122151344-chr12:122176465..122178233,2	K562	blood:
17	chr12:122184667..122189513-chr12:122211148..122219682,10	MCF-7	breast:
18	chr12:122176381..122178951-chr12:122179528..122182471,2	K562	blood:
19	chr12:122181727..122184365-chr12:122185006..122187114,3	MCF-7	breast:
20	chr12:122185243..122188214-chr12:122238983..122240823,2	K562	blood:
21	chr12:121836861..121838700-chr12:122185043..122186944,2	K562	blood:
22	chr12:122181727..122184365-chr12:122185006..122187114,3	MCF-7	breast:
23	chr12:122185135..122187179-chr12:122190114..122193871,4	K562	blood:
24	chr12:122177645..122180550-chr12:122180638..122183129,3	MCF-7	breast:
25	chr12:122181102..122183945-chr12:122184844..122187780,3	MCF-7	breast:

Variant related genes	Relation type
TMEM120B	TF binding region
ENSG00000139725	chromatin interactions
ENSG00000188735	chromatin interactions
ENSG00000170633	chromatin interactions
ENSG00000139718	chromatin interactions
ENSG00000272849	chromatin interactions
ENSG00000089053	chromatin interactions
ENSG00000212694	chromatin interactions

Extended variants
information (count: 394 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:394 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2669170	chr12:122177322-122177323	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181038211	chr12:122177330-122177331	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs150540267	chr12:122177341-122177342	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs185992765	chr12:122177366-122177367	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs34355410	chr12:122177383-122177384	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs112800675	chr12:122177386-122177387	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs79883279	chr12:122177396-122177397	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs61952254	chr12:122177398-122177399	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs372585596	chr12:122177404-122177405	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs555406838	chr12:122177503-122177504	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs573893509	chr12:122177517-122177518	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs370737495	chr12:122177524-122177525	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs564603053	chr12:122177532-122177533	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs552951778	chr12:122177585-122177586	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs577574960	chr12:122177588-122177589	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs113095488	chr12:122177611-122177612	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs113053848	chr12:122177645-122177646	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs190892592	chr12:122177662-122177663	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs200085137	chr12:122177705-122177706	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs183965717	chr12:122177773-122177774	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs144436716	chr12:122177777-122177778	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs372719928	chr12:122177787-122177788	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs561298199	chr12:122177824-122177825	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs528800157	chr12:122177833-122177834	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs547277195	chr12:122177835-122177836	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs188972058	chr12:122177842-122177843	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs565722517	chr12:122177843-122177844	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs12372742	chr12:122177869-122177870	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs190778874	chr12:122177921-122177922	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs551212727	chr12:122177934-122177935	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs183004592	chr12:122177978-122177979	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs528803676	chr12:122177980-122177981	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs187340124	chr12:122177984-122177985	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs575194814	chr12:122178033-122178034	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs555558615	chr12:122178042-122178043	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs7307946	chr12:122178082-122178083	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs567301546	chr12:122178111-122178112	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs191802302	chr12:122178117-122178118	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs61952255	chr12:122178145-122178146	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs9668439	chr12:122178188-122178189	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs9668440	chr12:122178197-122178198	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs9668619	chr12:122178211-122178212	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs9668727	chr12:122178234-122178235	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs58684387	chr12:122178250-122178251	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs544987919	chr12:122178256-122178257	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs146384883	chr12:122178263-122178264	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs575717458	chr12:122178282-122178283	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs370896171	chr12:122178305-122178306	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs184014215	chr12:122178331-122178332	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs561543026	chr12:122178362-122178363	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Autism	22495311	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
Urothelial carcinoma	21177765	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
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:220 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:122151600-122186200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr12:122152000-122182200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr12:122152000-122188000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr12:122152200-122181600	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr12:122152200-122181800	Weak transcription	Right Ventricle	heart
6	chr12:122152200-122186400	Weak transcription	Duodenum Mucosa	Duodenum
7	chr12:122152200-122188000	Weak transcription	Brain Germinal Matrix	brain
8	chr12:122152200-122188000	Weak transcription	Dnd41	blood
9	chr12:122152200-122191600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr12:122152200-122191600	Weak transcription	Rectal Smooth Muscle	rectum
11	chr12:122152200-122200200	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr12:122152400-122188000	Weak transcription	Stomach Smooth Muscle	stomach
13	chr12:122152800-122186200	Weak transcription	Pancreas	Pancrea
14	chr12:122154000-122182200	Weak transcription	Primary T cells from cord blood	blood
15	chr12:122154200-122200400	Weak transcription	Psoas Muscle	Psoas
16	chr12:122155200-122181600	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr12:122155200-122182400	Weak transcription	NHEK	skin
18	chr12:122155200-122186400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr12:122155400-122178600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr12:122155600-122186200	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr12:122157200-122179600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr12:122157200-122182400	Weak transcription	GM12878-XiMat	blood
23	chr12:122158800-122186200	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr12:122158800-122186200	Weak transcription	NHDF-Ad	bronchial
25	chr12:122158800-122186400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr12:122159000-122186200	Weak transcription	NH-A	brain
27	chr12:122159200-122181600	Weak transcription	NHLF	lung
28	chr12:122159200-122186400	Weak transcription	HSMM	muscle
29	chr12:122159400-122194800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr12:122159600-122181600	Weak transcription	Brain Angular Gyrus	brain
31	chr12:122161800-122181600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr12:122163400-122181400	Weak transcription	Fetal Stomach	stomach
33	chr12:122163400-122186200	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr12:122163600-122180400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr12:122163600-122182000	Weak transcription	Fetal Muscle Trunk	muscle
36	chr12:122163600-122186200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr12:122163600-122186200	Weak transcription	Liver	Liver
38	chr12:122163600-122186600	Weak transcription	HSMMtube	muscle
39	chr12:122163600-122188000	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr12:122163600-122188200	Weak transcription	Brain Anterior Caudate	brain
41	chr12:122163800-122182400	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr12:122163800-122186200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr12:122164200-122181400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr12:122164800-122188200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr12:122166800-122186200	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr12:122166800-122186200	Weak transcription	Thymus	Thymus
47	chr12:122166800-122186400	Weak transcription	Colon Smooth Muscle	Colon
48	chr12:122167200-122186400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr12:122167600-122186200	Weak transcription	Spleen	Spleen
50	chr12:122170400-122178600	Weak transcription	A549	lung

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