Variant report

Variant	nsv1043906
Chromosome Location	chr12:118991884-119087146
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:546)
CpG islands
(count:183)
Chromatin interactive
region (count:11)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:546 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:119041419-119041867	HepG2	liver:	n/a	n/a
2	ATF1	chr12:119044103-119044108	K562	blood:	n/a	n/a
3	ATF3	chr12:119056617-119056750	K562	blood:	n/a	n/a
4	ATF3	chr12:119056584-119056782	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr12:119056547-119056838	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr12:119041920-119042070	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr12:119071146-119071219	K562	blood:	n/a	n/a
8	BHLHE40	chr12:119041434-119041936	HepG2	liver:	n/a	n/a
9	BHLHE40	chr12:119049600-119049910	K562	blood:	n/a	n/a
10	BHLHE40	chr12:119063152-119063382	K562	blood:	n/a	n/a
11	CBX3	chr12:119063053-119063415	K562	blood:	n/a	n/a
12	CCNT2	chr12:119063165-119063384	K562	blood:	n/a	n/a
13	CEBPB	chr12:119031397-119031429	A549	lung:	n/a	n/a
14	CEBPB	chr12:119041325-119041395	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr12:119065571-119065739	K562	blood:	n/a	chr12:119065661-119065672
16	CEBPB	chr12:119041184-119041839	HepG2	liver:	n/a	n/a
17	CEBPB	chr12:119063079-119063461	K562	blood:	n/a	n/a
18	CEBPB	chr12:119004714-119004922	K562	blood:	n/a	n/a
19	CEBPB	chr12:119001653-119001776	A549	lung:	n/a	n/a
20	CEBPB	chr12:119041518-119041725	HepG2	liver:	n/a	n/a
21	CEBPB	chr12:119031399-119031496	HepG2	liver:	n/a	chr12:119031449-119031460
22	CEBPB	chr12:119049606-119049884	K562	blood:	n/a	n/a
23	CEBPB	chr12:119065607-119065774	HepG2	liver:	n/a	chr12:119065661-119065672
24	CEBPB	chr12:119031374-119031530	K562	blood:	n/a	chr12:119031449-119031460
25	CEBPB	chr12:119004698-119004887	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPD	chr12:119049617-119049997	K562	blood:	n/a	n/a
27	CEBPD	chr12:119049594-119049990	K562	blood:	n/a	n/a
28	CHD2	chr12:119041558-119041788	HepG2	liver:	n/a	n/a
29	CTCF	chr12:119060520-119060670	HCFaa	heart:	n/a	n/a
30	CTCF	chr12:119055177-119055242	GM13976	blood:	n/a	n/a
31	CTCF	chr12:119060520-119060670	AG09309	skin:	n/a	n/a
32	CTCF	chr12:119046890-119046980	K562	blood:	n/a	n/a
33	CTCF	chr12:119060356-119060877	K562	blood:	n/a	n/a
34	CTCF	chr12:119064820-119064970	GM12878	blood:	n/a	n/a
35	CTCF	chr12:119060408-119060768	MCF-7	breast:	n/a	n/a
36	CTCF	chr12:119046900-119047050	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr12:119046980-119047130	A549	lung:	n/a	n/a
38	CTCF	chr12:119060529-119060752	Gliobla	brain:	n/a	n/a
39	CTCF	chr12:119060487-119060717	K562	blood:	n/a	n/a
40	CTCF	chr12:119060520-119060670	GM12864	blood:	n/a	n/a
41	CTCF	chr12:119057020-119057170	WI-38	lung:	n/a	n/a
42	CTCF	chr12:119060580-119060730	GM12865	blood:	n/a	n/a
43	CTCF	chr12:119060425-119060727	HepG2	liver:	n/a	n/a
44	CTCF	chr12:119060820-119060970	A549	lung:	n/a	n/a
45	CTCF	chr12:119060501-119060769	MCF-7	breast:	n/a	n/a
46	CTCF	chr12:119046920-119047070	MCF-7	breast:	n/a	n/a
47	CTCF	chr12:119082309-119082381	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr12:119060542-119060741	GM19240	blood:	n/a	n/a
49	CTCF	chr12:119060934-119060976	LNCaP	prostate:	n/a	n/a
50	CTCF	chr12:119060540-119060690	GM12864	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:119034267-119034317	HPAEpiC	pulmonary alveolar:	n/a
2	chr12:119048988-119049038	RPTEC	kidney:	n/a
3	chr12:119034267-119034317	NH-A	brain:	n/a
4	chr12:119034267-119034317	NHDF-neo	bronchial:	n/a
5	chr12:119034267-119034317	GM12891	blood:	n/a
6	chr12:119034267-119034317	AG10803	skin:	n/a
7	chr12:119034267-119034317	SK-N-MC	brain:	n/a
8	chr12:119027591-119027641	IMR90	lung:	fetal
9	chr12:119027591-119027641	ECC-1	luminal epithelium:	n/a
10	chr12:119048988-119049038	HPAEpiC	pulmonary alveolar:	n/a
11	chr12:119034267-119034317	SK-N-SH_RA	brain:	n/a
12	chr12:119048988-119049038	HRCEpiC	kidney:	n/a
13	chr12:119048988-119049038	GM12891	blood:	n/a
14	chr12:119027591-119027641	NB4	blood:	n/a
15	chr12:119048988-119049038	Caco-2	colon:	n/a
16	chr12:119034267-119034317	BJ	skin:	n/a
17	chr12:119048988-119049038	ECC-1	luminal epithelium:	n/a
18	chr12:119034267-119034317	GM19239	blood:	n/a
19	chr12:119027591-119027641	PANC-1	pancreas:	n/a
20	chr12:119048988-119049038	AoSMC	blood vessel:	n/a
21	chr12:119048988-119049038	NH-A	brain:	n/a
22	chr12:119027591-119027641	AG04450	lung:	fetal
23	chr12:119034267-119034317	AG04450	lung:	fetal
24	chr12:119048988-119049038	GM12878	blood:	n/a
25	chr12:119048988-119049038	PrEC	prostate:	n/a
26	chr12:119048988-119049038	MCF-7	breast:	n/a
27	chr12:119027591-119027641	LNCaP	prostate:	n/a
28	chr12:119048988-119049038	K562	blood:	n/a
29	chr12:119034267-119034317	H1-hESC	embryonic stem cell:	embryo
30	chr12:119027591-119027641	T-47D	breast:	n/a
31	chr12:119034267-119034317	HMEC	breast:	n/a
32	chr12:119027591-119027641	SK-N-MC	brain:	n/a
33	chr12:119048988-119049038	HMEC	breast:	n/a
34	chr12:119034267-119034317	HNPCEpiC	eye:	n/a
35	chr12:119034267-119034317	HAEpiC	amniotic membrane:	n/a
36	chr12:119027591-119027641	HCT-116	colon:	n/a
37	chr12:119027591-119027641	HCPEpiC	choroid plexus:	n/a
38	chr12:119048988-119049038	ovcar-3	ovarian:	n/a
39	chr12:119027591-119027641	HAEpiC	amniotic membrane:	n/a
40	chr12:119048988-119049038	HRPEpiC	eye:	n/a
41	chr12:119027591-119027641	K562	blood:	n/a
42	chr12:119027591-119027641	HCM	heart:	n/a
43	chr12:119048988-119049038	HL-60	blood:	n/a
44	chr12:119027591-119027641	Hela-S3	cervix:	n/a
45	chr12:119034267-119034317	PANC-1	pancreas:	n/a
46	chr12:119034267-119034317	HCT-116	colon:	n/a
47	chr12:119034267-119034317	IMR90	lung:	fetal
48	chr12:119027591-119027641	AG10803	skin:	n/a
49	chr12:119048988-119049038	T-47D	breast:	n/a
50	chr12:119048988-119049038	HCPEpiC	choroid plexus:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:118999474..119001339-chr12:119002292..119005098,2	K562	blood:
2	chr12:118842493..118843365-chr12:119060157..119061106,4	MCF-7	breast:
3	chr12:119019620..119021400-chr12:119023440..119025159,2	K562	blood:
4	chr12:119035847..119037394-chr12:119041054..119043149,2	K562	blood:
5	chr12:119035847..119037394-chr12:119041054..119043149,2	K562	blood:
6	chr12:118883772..118884730-chr12:119060191..119061108,3	MCF-7	breast:
7	chr12:119026589..119028624-chr17:57915360..57917197,2	MCF-7	breast:
8	chr12:118903371..118904028-chr12:119060619..119061618,2	MCF-7	breast:
9	chr12:119019620..119021400-chr12:119023440..119025159,2	K562	blood:
10	chr12:118999474..119001339-chr12:119002292..119005098,2	K562	blood:
11	chr12:119025023..119026651-chr9:86161675..86163192,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TAOK3-2	chr12:119085680-119085759	ENSG00000255714
2	lnc-TAOK3-2	chr12:119082654-119083334	XLOC_010213
3	lnc-TAOK3-2	chr12:119083120-119083334	ENSG00000255714
4	lnc-TAOK3-2	chr12:119086289-119086529	ENSG00000255714
5	lnc-TAOK3-2	chr12:119083695-119083867	XLOC_010213

No data

Variant related genes	Relation type
ENSG00000255714	TF binding region
ENSG00000255714	CpG island

Extended variants
information (count: 2480 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2480 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11836667	chr12:118991884-118991885	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566186173	chr12:118991885-118991886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534701849	chr12:118991899-118991900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs11836672	chr12:118991911-118991912	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs568032502	chr12:118991937-118991938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs138277268	chr12:118991938-118991939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557249196	chr12:118991940-118991941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577067636	chr12:118991978-118991979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs114608275	chr12:118991998-118991999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs142819026	chr12:118992041-118992042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572987627	chr12:118992082-118992083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs75467677	chr12:118992104-118992105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs12309816	chr12:118992118-118992119	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs185688104	chr12:118992130-118992131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529997866	chr12:118992174-118992175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571875327	chr12:118992182-118992183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs12316828	chr12:118992217-118992218	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs190589033	chr12:118992227-118992228	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs118027325	chr12:118992232-118992233	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544549141	chr12:118992243-118992244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528753437	chr12:118992259-118992260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs79418789	chr12:118992272-118992273	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530343586	chr12:118992277-118992278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561221641	chr12:118992289-118992290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12311301	chr12:118992376-118992377	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs117827490	chr12:118992410-118992411	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs549504166	chr12:118992413-118992414	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548272092	chr12:118992419-118992420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568168125	chr12:118992460-118992461	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140018433	chr12:118992480-118992481	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12319707	chr12:118992485-118992486	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs540796265	chr12:118992497-118992498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183203263	chr12:118992533-118992534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188085885	chr12:118992539-118992540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560388952	chr12:118992545-118992546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532600362	chr12:118992578-118992579	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552696942	chr12:118992603-118992604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192707521	chr12:118992614-118992615	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182726583	chr12:118992616-118992617	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535278589	chr12:118992636-118992637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532225963	chr12:118992640-118992641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112899140	chr12:118992645-118992646	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs79313766	chr12:118992652-118992653	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146265343	chr12:118992754-118992755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563687551	chr12:118992780-118992781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs73411648	chr12:118992786-118992787	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs546450902	chr12:118992790-118992791	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569321556	chr12:118992798-118992799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559809942	chr12:118992811-118992812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528654335	chr12:118992824-118992825	Enhancers Weak transcription	n/a	n/a	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	17603634	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	16783165	CNVD
mental retardation	16760730	CNVD
Breast cancer	21509527	CNVD
Lung adenocarcinoma	21045234	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:211 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118991800-118992200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
2	chr12:118991800-118992200	Enhancers	H1 Cell Line	embryonic stem cell
3	chr12:118991800-118992200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr12:118991800-118992200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr12:118991800-118992200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr12:118991800-118992400	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr12:118991800-118992400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr12:118991800-118992400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr12:118991800-118992800	Enhancers	H9 Cell Line	embryonic stem cell
10	chr12:118991800-118993000	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr12:118992000-118992400	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr12:118992200-118993200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr12:118992200-118993200	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr12:118992200-118993400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr12:118992400-118993400	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr12:118992400-118993400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr12:118992400-118996600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr12:118993000-118993600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr12:118993200-118993600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
20	chr12:118993200-118993600	Enhancers	H9 Cell Line	embryonic stem cell
21	chr12:118993200-118994400	Enhancers	Fetal Brain Female	brain
22	chr12:118993400-118993600	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr12:118993400-118993600	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr12:118993400-118993800	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr12:118993400-118994200	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr12:118993600-118994000	Enhancers	Fetal Brain Male	brain
27	chr12:118993800-118994200	Enhancers	Brain Hippocampus Middle	brain
28	chr12:118994000-118998000	Weak transcription	Fetal Brain Male	brain
29	chr12:118994400-118996800	Weak transcription	Fetal Brain Female	brain
30	chr12:118994400-118996800	Weak transcription	Fetal Heart	heart
31	chr12:118995600-118995800	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr12:118996400-118997000	Enhancers	Brain Germinal Matrix	brain
33	chr12:118996600-118996800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr12:118996800-118997200	Enhancers	Fetal Brain Female	brain
35	chr12:118996800-118997400	Enhancers	Brain Hippocampus Middle	brain
36	chr12:118996800-118998200	Enhancers	Brain Substantia Nigra	brain
37	chr12:118996800-118999400	Enhancers	Fetal Heart	heart
38	chr12:118997200-118997600	Enhancers	Left Ventricle	heart
39	chr12:118997200-118999800	Enhancers	Colon Smooth Muscle	Colon
40	chr12:118997600-118997800	Weak transcription	Left Ventricle	heart
41	chr12:118997800-118998200	Enhancers	Left Ventricle	heart
42	chr12:118997800-118999200	Enhancers	Stomach Smooth Muscle	stomach
43	chr12:118998000-118998200	Enhancers	Fetal Brain Male	brain
44	chr12:118998000-118999400	Enhancers	Psoas Muscle	Psoas
45	chr12:118998200-118999000	Weak transcription	Left Ventricle	heart
46	chr12:118998200-118999200	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr12:118998400-118999200	Enhancers	Rectal Smooth Muscle	rectum
48	chr12:118998400-118999400	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr12:118999000-118999400	Enhancers	Left Ventricle	heart
50	chr12:119007600-119009800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links