Variant report

Variant	nsv1040904
Chromosome Location	chr12:116999897-117033944
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:387)
CpG islands
(count:245)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:387 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:117001136-117001352	K562	blood:	n/a	n/a
2	ARID3A	chr12:117020384-117020957	K562	blood:	n/a	n/a
3	ARID3A	chr12:117015004-117015510	K562	blood:	n/a	n/a
4	ARID3A	chr12:117029442-117029733	K562	blood:	n/a	n/a
5	ATF1	chr12:117014905-117015354	K562	blood:	n/a	n/a
6	BACH1	chr12:117015018-117015204	K562	blood:	n/a	n/a
7	BACH1	chr12:117020510-117020646	K562	blood:	n/a	n/a
8	BHLHE40	chr12:117032089-117032352	K562	blood:	n/a	n/a
9	BHLHE40	chr12:117020380-117020760	K562	blood:	n/a	n/a
10	BHLHE40	chr12:117006178-117006266	K562	blood:	n/a	n/a
11	BHLHE40	chr12:117015069-117015269	K562	blood:	n/a	n/a
12	CBX3	chr12:117002951-117003633	K562	blood:	n/a	n/a
13	CBX3	chr12:117022677-117023145	K562	blood:	n/a	n/a
14	CBX3	chr12:117001900-117002280	K562	blood:	n/a	n/a
15	CBX3	chr12:117029397-117029723	K562	blood:	n/a	n/a
16	CBX3	chr12:117020200-117020923	K562	blood:	n/a	n/a
17	CBX3	chr12:117001030-117001544	K562	blood:	n/a	n/a
18	CBX3	chr12:117001001-117001526	HCT-116	colon:	n/a	n/a
19	CBX3	chr12:117031299-117031634	K562	blood:	n/a	n/a
20	CBX3	chr12:116999246-117000598	K562	blood:	n/a	n/a
21	CBX3	chr12:117022776-117023075	K562	blood:	n/a	n/a
22	CBX3	chr12:117000946-117001511	K562	blood:	n/a	n/a
23	CCNT2	chr12:117014932-117015399	K562	blood:	n/a	n/a
24	CEBPB	chr12:117001172-117001355	K562	blood:	n/a	n/a
25	CEBPB	chr12:117033138-117033363	HepG2	liver:	n/a	chr12:117033220-117033231
26	CEBPB	chr12:117030656-117030799	HepG2	liver:	n/a	chr12:117030756-117030767
27	CEBPB	chr12:117019942-117020142	K562	blood:	n/a	n/a
28	CEBPB	chr12:117028433-117028803	MCF-7	breast:	n/a	n/a
29	CEBPB	chr12:117028412-117028776	A549	lung:	n/a	n/a
30	CEBPB	chr12:117015027-117015388	HepG2	liver:	n/a	chr12:117015211-117015222
31	CEBPB	chr12:117018650-117018830	K562	blood:	n/a	n/a
32	CEBPB	chr12:117015045-117015375	A549	lung:	n/a	chr12:117015211-117015222
33	CEBPB	chr12:117028403-117028738	A549	lung:	n/a	n/a
34	CEBPB	chr12:117030678-117030900	K562	blood:	n/a	chr12:117030756-117030767
35	CEBPB	chr12:117028494-117028679	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr12:117009040-117009320	HepG2	liver:	n/a	chr12:117009151-117009162
37	CEBPB	chr12:117014801-117015401	K562	blood:	n/a	chr12:117015211-117015222
38	CEBPB	chr12:117028391-117028710	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr12:117028392-117028746	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr12:117015009-117015350	MCF-7	breast:	n/a	chr12:117015211-117015222
41	CEBPB	chr12:117014817-117015411	K562	blood:	n/a	chr12:117015211-117015222
42	CEBPB	chr12:117014955-117015256	K562	blood:	n/a	chr12:117015211-117015222
43	CEBPB	chr12:117002026-117002037	K562	blood:	n/a	n/a
44	CEBPB	chr12:117033092-117033330	A549	lung:	n/a	chr12:117033220-117033231
45	CEBPB	chr12:117014877-117015392	IMR90	lung:	n/a	chr12:117015211-117015222
46	CEBPB	chr12:117009001-117009297	K562	blood:	n/a	chr12:117009151-117009162
47	CEBPB	chr12:117028250-117028825	A549	lung:	n/a	n/a
48	CEBPD	chr12:117014775-117015444	K562	blood:	n/a	n/a
49	CEBPD	chr12:117014897-117015476	K562	blood:	n/a	n/a
50	CHD2	chr12:116999817-116999944	K562	blood:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:117029821-117029871	GM12891	blood:	n/a
2	chr12:117029821-117029871	GM12891	blood:	n/a
3	chr12:117013718-117013768	SAEC	small airway:	n/a
4	chr12:117013718-117013768	PFSK-1	brain:	n/a
5	chr12:117013817-117013867	PrEC	prostate:	n/a
6	chr12:117013817-117013867	AG10803	skin:	n/a
7	chr12:117013755-117013805	HCPEpiC	choroid plexus:	n/a
8	chr12:117013755-117013805	AG04449	skin:	fetal
9	chr12:117013718-117013768	BJ	skin:	n/a
10	chr12:117029821-117029871	GM12892	blood:	n/a
11	chr12:117029821-117029871	GM06990	blood:	n/a
12	chr12:117013817-117013867	HEEpiC	esophagus:	n/a
13	chr12:117013755-117013805	AG09319	gingival:	n/a
14	chr12:117013817-117013867	NH-A	brain:	n/a
15	chr12:117029821-117029871	SAEC	small airway:	n/a
16	chr12:117029821-117029871	HL-60	blood:	n/a
17	chr12:117013817-117013867	PANC-1	pancreas:	n/a
18	chr12:117013755-117013805	HepG2	liver:	n/a
19	chr12:117013755-117013805	NHDF-neo	bronchial:	n/a
20	chr12:117013718-117013768	GM19239	blood:	n/a
21	chr12:117013817-117013867	HUVEC	blood vessel:	n/a
22	chr12:117029821-117029871	SK-N-MC	brain:	n/a
23	chr12:117013718-117013768	A549	lung:	n/a
24	chr12:117013755-117013805	NHBE	bronchial:	n/a
25	chr12:117013817-117013867	GM12878	blood:	n/a
26	chr12:117029821-117029871	T-47D	breast:	n/a
27	chr12:117013755-117013805	MCF10A-Er-Src	breast:	n/a
28	chr12:117013755-117013805	PANC-1	pancreas:	n/a
29	chr12:117029821-117029871	HMEC	breast:	n/a
30	chr12:117013817-117013867	SK-N-SH_RA	brain:	n/a
31	chr12:117013817-117013867	GM12891	blood:	n/a
32	chr12:117013755-117013805	H1-hESC	embryonic stem cell:	embryo
33	chr12:117013755-117013805	HCM	heart:	n/a
34	chr12:117013755-117013805	HNPCEpiC	eye:	n/a
35	chr12:117029821-117029871	MCF10A-Er-Src	breast:	n/a
36	chr12:117013718-117013768	HCPEpiC	choroid plexus:	n/a
37	chr12:117013755-117013805	BE2_C	brain:	n/a
38	chr12:117013755-117013805	Jurkat	blood:	n/a
39	chr12:117013817-117013867	HEK293	kidney:	embryo
40	chr12:117029821-117029871	AG04450	lung:	fetal
41	chr12:117029821-117029871	A549	lung:	n/a
42	chr12:117013817-117013867	H1-hESC	embryonic stem cell:	embryo
43	chr12:117013718-117013768	GM12878	blood:	n/a
44	chr12:117013817-117013867	U87	brain:	n/a
45	chr12:117029821-117029871	MCF-7	breast:	n/a
46	chr12:117029821-117029871	NB4	blood:	n/a
47	chr12:117013755-117013805	HRE	kidney:	n/a
48	chr12:117013718-117013768	RPTEC	kidney:	n/a
49	chr12:117013718-117013768	PrEC	prostate:	n/a
50	chr12:117029821-117029871	CMK	blood:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:116998103..117000799-chr12:117011833..117013423,2	MCF-7	breast:
2	chr12:117019845..117021586-chr12:117030013..117032301,2	K562	blood:
3	chr12:116995728..116997735-chr12:117003472..117005599,2	MCF-7	breast:
4	chr12:116996410..116999270-chr12:117014389..117017088,2	K562	blood:
5	chr12:116999930..117002030-chr12:117019676..117022158,2	K562	blood:
6	chr12:116827531..116830730-chr12:117032001..117035622,5	MCF-7	breast:
7	chr12:117019845..117021586-chr12:117030013..117032301,2	K562	blood:
8	chr12:117028250..117028857-chr12:117146681..117147589,2	MCF-7	breast:
9	chr12:116999859..117002706-chr12:117013577..117016502,2	MCF-7	breast:
10	chr12:116998103..117000799-chr12:117011833..117013423,2	MCF-7	breast:
11	chr12:117028443..117029039-chr12:117037442..117038001,2	MCF-7	breast:
12	chr12:117002841..117005403-chr12:117005635..117007763,2	MCF-7	breast:
13	chr12:117032171..117034529-chr12:117035263..117037602,2	MCF-7	breast:
14	chr12:117002841..117005403-chr12:117005635..117007763,2	MCF-7	breast:
15	chr12:116996783..116999967-chr12:117023571..117027055,3	K562	blood:
16	chr12:116969803..116971986-chr12:117002739..117004587,2	K562	blood:
17	chr12:117008681..117011490-chr12:117013979..117015609,2	MCF-7	breast:
18	chr12:116996783..116999967-chr12:117023571..117027055,4	K562	blood:
19	chr12:117004610..117007092-chr12:117013364..117015752,2	K562	blood:
20	chr12:116999930..117002030-chr12:117019676..117022158,2	K562	blood:
21	chr12:117028125..117029029-chr12:117125531..117126255,2	MCF-7	breast:
22	chr12:116715441..116716981-chr12:117020460..117023369,2	MCF-7	breast:
23	chr12:117008681..117011490-chr12:117013979..117015609,2	MCF-7	breast:

No data

Variant related genes	Relation type
MAP1LC3B2	TF binding region
ENSG00000258249	TF binding region
MAP1LC3B2	CpG island
ENSG00000258249	CpG island
ENSG00000171471	chromatin interactions
ENSG00000196668	chromatin interactions
ENSG00000258249	chromatin interactions

Extended variants
information (count: 1239 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1239 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8181728	chr12:116999897-116999898	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs8181752	chr12:116999936-116999937	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs8181730	chr12:116999958-116999959	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs189259746	chr12:116999989-116999990	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs539333353	chr12:117000001-117000002	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs10161436	chr12:117000032-117000033	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs548145977	chr12:117000057-117000058	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs560946567	chr12:117000096-117000097	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs148591439	chr12:117000097-117000098	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs78683855	chr12:117000110-117000111	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs116629242	chr12:117000120-117000121	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs8181768	chr12:117000196-117000197	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs571058991	chr12:117000235-117000236	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs74882810	chr12:117000344-117000345	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs540009809	chr12:117000438-117000439	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs533700739	chr12:117000479-117000480	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs571235643	chr12:117000508-117000509	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs182225148	chr12:117000546-117000547	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs151038731	chr12:117000562-117000563	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs78366688	chr12:117000565-117000566	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs186854036	chr12:117000566-117000567	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs12312811	chr12:117000575-117000576	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs371782114	chr12:117000632-117000633	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs576660273	chr12:117000692-117000693	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs550396917	chr12:117000693-117000694	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs541887441	chr12:117000695-117000696	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs570278209	chr12:117000747-117000748	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs11068075	chr12:117000755-117000756	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs552801917	chr12:117000792-117000793	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs142336360	chr12:117000807-117000808	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs535148273	chr12:117000811-117000812	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs144751933	chr12:117000813-117000814	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs147899491	chr12:117000829-117000830	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs117482585	chr12:117000830-117000831	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs558396958	chr12:117000849-117000850	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs555468966	chr12:117000885-117000886	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs578194773	chr12:117000891-117000892	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs376749564	chr12:117000905-117000906	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs567404813	chr12:117000917-117000918	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs540928644	chr12:117000964-117000965	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs372600869	chr12:117000969-117000970	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs560727275	chr12:117000996-117000997	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs368877520	chr12:117001011-117001012	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs539500193	chr12:117001015-117001016	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs564197882	chr12:117001027-117001028	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs532199186	chr12:117001078-117001079	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs373005277	chr12:117001102-117001103	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs191651499	chr12:117001103-117001104	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs201710519	chr12:117001121-117001122	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs202061781	chr12:117001126-117001127	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Neuroblastoma	20406844	CNVD
Medulloblastoma	16783165	CNVD
mental retardation	16760730	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Lung adenocarcinoma	21045234	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:433 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:116997400-117001800	Weak transcription	Fetal Lung	lung
2	chr12:116997600-117000000	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr12:116997600-117000000	Enhancers	Primary hematopoietic stem cells	blood
4	chr12:116997800-117000000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr12:116997800-117000000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr12:116997800-117000200	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr12:116997800-117000200	Enhancers	Primary T killer memory cells from peripheral blood	blood
8	chr12:116997800-117000600	Weak transcription	Stomach Mucosa	stomach
9	chr12:116998000-117000000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr12:116998000-117000000	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr12:116998000-117001800	Weak transcription	NHEK	skin
12	chr12:116998200-117000200	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr12:116998400-117000000	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr12:116998600-117000000	Enhancers	Right Atrium	heart
15	chr12:116998600-117000400	Enhancers	Dnd41	blood
16	chr12:116998800-117000600	Weak transcription	Thymus	Thymus
17	chr12:116999600-117000000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr12:116999600-117000200	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr12:116999600-117000400	Enhancers	K562	blood
20	chr12:116999800-117000000	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr12:117000200-117002400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr12:117000400-117001200	Weak transcription	Dnd41	blood
23	chr12:117001200-117003600	ZNF genes & repeats	Dnd41	blood
24	chr12:117001400-117003800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr12:117002000-117002800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
26	chr12:117002400-117005000	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr12:117003200-117003600	Enhancers	Esophagus	oesophagus
28	chr12:117003200-117004400	Enhancers	NHEK	skin
29	chr12:117003400-117004000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr12:117003600-117004200	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr12:117003600-117005000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr12:117003600-117005800	Weak transcription	Dnd41	blood
33	chr12:117005000-117005800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr12:117005800-117006200	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr12:117005800-117006400	Enhancers	Dnd41	blood
36	chr12:117011400-117012000	Enhancers	Fetal Brain Male	brain
37	chr12:117011600-117012400	Enhancers	Primary B cells from peripheral blood	blood
38	chr12:117013400-117013600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr12:117013600-117013800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr12:117013800-117022600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr12:117014400-117015600	Enhancers	K562	blood
42	chr12:117015000-117015600	Enhancers	Osteobl	bone
43	chr12:117015200-117015400	Enhancers	Muscle Satellite Cultured Cells	--
44	chr12:117015200-117015800	Enhancers	Stomach Mucosa	stomach
45	chr12:117015600-117017600	Weak transcription	K562	blood
46	chr12:117015800-117020200	Weak transcription	Stomach Mucosa	stomach
47	chr12:117017200-117017600	Enhancers	Fetal Thymus	thymus
48	chr12:117017600-117020200	Enhancers	K562	blood
49	chr12:117018200-117018400	Enhancers	Aorta	Aorta
50	chr12:117018400-117019000	Enhancers	Monocytes-CD14+_RO01746	blood

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