Variant report

Variant	nsv1045516
Chromosome Location	chr12:40543200-40589557
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:485)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:485 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:40546628-40546911	K562	blood:	n/a	n/a
2	ATF2	chr12:40586416-40587052	GM12878	blood:	n/a	n/a
3	ATF2	chr12:40562547-40563179	GM12878	blood:	n/a	n/a
4	ATF2	chr12:40586412-40587192	GM12878	blood:	n/a	n/a
5	ATF2	chr12:40562517-40563164	GM12878	blood:	n/a	n/a
6	ATF2	chr12:40561772-40562281	GM12878	blood:	n/a	n/a
7	ATF2	chr12:40561760-40562320	GM12878	blood:	n/a	n/a
8	BATF	chr12:40562718-40563113	GM12878	blood:	n/a	n/a
9	BATF	chr12:40586494-40587027	GM12878	blood:	n/a	n/a
10	BATF	chr12:40562763-40563054	GM12878	blood:	n/a	n/a
11	BATF	chr12:40561861-40562191	GM12878	blood:	n/a	chr12:40562020-40562031
12	BATF	chr12:40561850-40562111	GM12878	blood:	n/a	chr12:40562020-40562031
13	BCL11A	chr12:40561855-40562181	GM12878	blood:	n/a	chr12:40562020-40562029 chr12:40562019-40562028
14	BCL11A	chr12:40562744-40562991	GM12878	blood:	n/a	chr12:40562817-40562826
15	BCL11A	chr12:40562639-40563067	GM12878	blood:	n/a	chr12:40562817-40562826
16	BCL11A	chr12:40586564-40587015	GM12878	blood:	n/a	n/a
17	BCL11A	chr12:40586465-40587065	GM12878	blood:	n/a	n/a
18	BCL3	chr12:40586697-40586979	GM12878	blood:	n/a	n/a
19	BCLAF1	chr12:40586463-40586857	GM12878	blood:	n/a	n/a
20	BCLAF1	chr12:40586427-40586922	GM12878	blood:	n/a	n/a
21	BCLAF1	chr12:40562599-40563097	GM12878	blood:	n/a	chr12:40562817-40562826
22	BHLHE40	chr12:40586473-40587331	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:40561787-40563459	GM12878	blood:	n/a	n/a
24	CBX3	chr12:40582787-40583006	K562	blood:	n/a	n/a
25	CEBPB	chr12:40558987-40559278	HepG2	liver:	n/a	n/a
26	CEBPB	chr12:40562546-40563162	GM12878	blood:	n/a	n/a
27	CEBPB	chr12:40565470-40565502	A549	lung:	n/a	n/a
28	CEBPB	chr12:40552448-40552556	A549	lung:	n/a	n/a
29	CEBPB	chr12:40543731-40544102	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr12:40564027-40564186	A549	lung:	n/a	chr12:40564105-40564116
31	CEBPB	chr12:40551397-40551659	A549	lung:	n/a	chr12:40551504-40551513 chr12:40551502-40551515
32	CEBPB	chr12:40543763-40544037	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr12:40558991-40559285	A549	lung:	n/a	n/a
34	CHD1	chr12:40586562-40587281	GM12878	blood:	n/a	n/a
35	CHD1	chr12:40552572-40552917	GM12878	blood:	n/a	n/a
36	CHD2	chr12:40586158-40587275	GM12878	blood:	n/a	n/a
37	CHD2	chr12:40562672-40563107	GM12878	blood:	n/a	n/a
38	CHD2	chr12:40549674-40549874	GM12878	blood:	n/a	n/a
39	CHD2	chr12:40570471-40570477	GM12878	blood:	n/a	n/a
40	CREB1	chr12:40561823-40562211	GM12878	blood:	n/a	n/a
41	CREB1	chr12:40562700-40563169	GM12878	blood:	n/a	n/a
42	CREB1	chr12:40586494-40587106	GM12878	blood:	n/a	n/a
43	CTCF	chr12:40546720-40546870	HPAF	blood vessel:	n/a	chr12:40546776-40546792 chr12:40546777-40546798 chr12:40546778-40546791 chr12:40546775-40546793
44	CTCF	chr12:40547460-40547610	GM12873	blood:	n/a	n/a
45	CTCF	chr12:40546720-40546870	GM12871	blood:	n/a	chr12:40546776-40546792 chr12:40546777-40546798 chr12:40546778-40546791 chr12:40546775-40546793
46	CTCF	chr12:40546700-40546850	HCPEpiC	choroid plexus:	n/a	chr12:40546776-40546792 chr12:40546777-40546798 chr12:40546778-40546791 chr12:40546775-40546793
47	CTCF	chr12:40546680-40546830	GM12872	blood:	n/a	chr12:40546776-40546792 chr12:40546777-40546798 chr12:40546778-40546791 chr12:40546775-40546793
48	CTCF	chr12:40546634-40546891	GM10266	blood:	n/a	chr12:40546776-40546792 chr12:40546777-40546798 chr12:40546778-40546791 chr12:40546775-40546793
49	CTCF	chr12:40546720-40546870	HAc	cerebellar:	n/a	chr12:40546776-40546792 chr12:40546777-40546798 chr12:40546778-40546791 chr12:40546775-40546793
50	CTCF	chr12:40546680-40546830	WERI-Rb-1	eye:	n/a	chr12:40546776-40546792 chr12:40546777-40546798 chr12:40546778-40546791 chr12:40546775-40546793

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:40548738-40548788	ECC-1	luminal epithelium:	n/a
2	chr12:40548738-40548788	AG04449	skin:	fetal
3	chr12:40548738-40548788	NHDF-neo	bronchial:	n/a
4	chr12:40548738-40548788	HRE	kidney:	n/a
5	chr12:40548738-40548788	GM19239	blood:	n/a
6	chr12:40548738-40548788	HMEC	breast:	n/a
7	chr12:40548738-40548788	GM12891	blood:	n/a
8	chr12:40548738-40548788	BJ	skin:	n/a
9	chr12:40548738-40548788	AG04450	lung:	fetal
10	chr12:40548738-40548788	T-47D	breast:	n/a
11	chr12:40548738-40548788	SAEC	small airway:	n/a
12	chr12:40548738-40548788	CMK	blood:	n/a
13	chr12:40548738-40548788	IMR90	lung:	fetal
14	chr12:40548738-40548788	SKMC	muscle:	n/a
15	chr12:40548738-40548788	HRPEpiC	eye:	n/a
16	chr12:40548738-40548788	AoSMC	blood vessel:	n/a
17	chr12:40548738-40548788	HCM	heart:	n/a
18	chr12:40548738-40548788	HEK293	kidney:	embryo
19	chr12:40548738-40548788	Jurkat	blood:	n/a
20	chr12:40548738-40548788	HCT-116	colon:	n/a
21	chr12:40548738-40548788	HNPCEpiC	eye:	n/a
22	chr12:40548738-40548788	PANC-1	pancreas:	n/a
23	chr12:40548738-40548788	AG10803	skin:	n/a
24	chr12:40548738-40548788	SK-N-MC	brain:	n/a
25	chr12:40548738-40548788	MCF10A-Er-Src	breast:	n/a
26	chr12:40548738-40548788	BE2_C	brain:	n/a
27	chr12:40548738-40548788	NH-A	brain:	n/a
28	chr12:40548738-40548788	PFSK-1	brain:	n/a
29	chr12:40548738-40548788	A549	lung:	n/a
30	chr12:40548738-40548788	HCF	heart:	n/a
31	chr12:40548738-40548788	HCPEpiC	choroid plexus:	n/a
32	chr12:40548738-40548788	NHBE	bronchial:	n/a
33	chr12:40548738-40548788	HRCEpiC	kidney:	n/a
34	chr12:40548738-40548788	RPTEC	kidney:	n/a
35	chr12:40548738-40548788	ovcar-3	ovarian:	n/a
36	chr12:40548738-40548788	Hepatocyte	liver:	n/a
37	chr12:40548738-40548788	PrEC	prostate:	n/a
38	chr12:40548738-40548788	Hela-S3	cervix:	n/a
39	chr12:40548738-40548788	Caco-2	colon:	n/a
40	chr12:40548738-40548788	HL-60	blood:	n/a
41	chr12:40548738-40548788	K562	blood:	n/a
42	chr12:40548738-40548788	AG09319	gingival:	n/a
43	chr12:40548738-40548788	NT2-D1	testis:	n/a
44	chr12:40548738-40548788	HepG2	liver:	n/a
45	chr12:40548738-40548788	ProgFib	skin:	n/a
46	chr12:40548738-40548788	HIPEpiC	eye:	n/a
47	chr12:40548738-40548788	U87	brain:	n/a
48	chr12:40548738-40548788	H1-hESC	embryonic stem cell:	embryo
49	chr12:40548738-40548788	NB4	blood:	n/a
50	chr12:40548738-40548788	HAEpiC	amniotic membrane:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:40536767..40538493-chr12:40545018..40546756,2	K562	blood:
2	chr12:40543659..40545848-chr12:40705219..40707677,2	MCF-7	breast:
3	12:40551632-40552246..12:40703633-40711447	GM12878	blood:
4	chr12:40546236..40547437-chr12:40706403..40707441,12	MCF-7	breast:
5	12:40570708-40576790..12:40703633-40711447	K562	blood:
6	12:40543943-40545640..12:40703633-40711447	GM12878	blood:
7	12:40583667-40584606..12:40703633-40711447	GM12878	blood:
8	chr12:40546299..40547451-chr12:40706483..40707430,5	MCF-7	breast:
9	chr10:125795379..125796137-chr12:40561478..40561982,2	MCF-7	breast:
10	12:40560427-40561510..12:40703633-40711447	GM12878	blood:
11	chr12:40158520..40159448-chr12:40546284..40547792,5	MCF-7	breast:
12	12:40551632-40552246..12:40691796-40694737	GM12878	blood:
13	12:40545640-40549031..12:40691796-40694737	GM12878	blood:
14	12:40545640-40549031..12:40703633-40711447	GM12878	blood:
15	chr12:40546325..40546967-chr12:40662693..40663558,3	MCF-7	breast:
16	12:40570708-40576790..12:40691796-40694737	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC2A13-1	chr12:40551656-40551857	XLOC_010052
2	lnc-LRRK2-1	chr12:40561049-40561678	NONHSAT027720
3	lnc-SLC2A13-1	chr12:40545831-40545945	XLOC_010052
4	lnc-LRRK2-1	chr12:40560054-40560152	XLOC_009712
5	lnc-SLC2A13-2	chr12:40584055-40584196	XLOC_010053
6	lnc-LRRK2-1	chr12:40561050-40561414	XLOC_009712
7	lnc-SLC2A13-1	chr12:40552238-40552325	XLOC_010052
8	lnc-SLC2A13-2	chr12:40582885-40583007	XLOC_010053
9	lnc-SLC2A13-1	chr12:40552238-40552325	XLOC_010052
10	lnc-LRRK2-1	chr12:40561050-40561509	XLOC_009712
11	lnc-SLC2A13-1	chr12:40551656-40551857	XLOC_010052
12	lnc-LRRK2-1	chr12:40549559-40550164	NONHSAT027720
13	lnc-LRRK2-1	chr12:40560053-40560152	NONHSAT027720
14	lnc-SLC2A13-2	chr12:40579811-40579985	XLOC_010053
15	lnc-SLC2A13-1	chr12:40545831-40545945	XLOC_010052
16	lnc-LRRK2-1	chr12:40550041-40550145	XLOC_009712

No data

Variant related genes	Relation type
LRRK2	TF binding region
ENSG00000223914	TF binding region
LRRK2	CpG island
ENSG00000223914	CpG island
ENSG00000188906	chromatin interactions
SDCBP	miRNA target sites
BRWD1	miRNA target sites
BRSK1	miRNA target sites
NR3C1	miRNA target sites

Extended variants
information (count: 1613 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1613 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529942035	chr12:40543220-40543221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs368406545	chr12:40543236-40543237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547942650	chr12:40543329-40543330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185332685	chr12:40543340-40543341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs527538527	chr12:40543372-40543373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs552618062	chr12:40543389-40543390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs74380646	chr12:40543431-40543432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs35450753	chr12:40543434-40543435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538202502	chr12:40543441-40543442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs2708463	chr12:40543454-40543455	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs76484463	chr12:40543502-40543503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536163928	chr12:40543542-40543543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs17458808	chr12:40543545-40543546	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs572579721	chr12:40543565-40543566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs564796668	chr12:40543566-40543567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546117988	chr12:40543581-40543582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs139091286	chr12:40543585-40543586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147889531	chr12:40543600-40543601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs74586119	chr12:40543606-40543607	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576887778	chr12:40543608-40543609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1463719	chr12:40543693-40543694	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs2638267	chr12:40543733-40543734	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs17442832	chr12:40543768-40543769	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs17461323	chr12:40543772-40543773	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs17490006	chr12:40543814-40543815	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs568850338	chr12:40543838-40543839	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs191779057	chr12:40543844-40543845	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs541717965	chr12:40543867-40543868	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs560215359	chr12:40543888-40543889	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs17490013	chr12:40543912-40543913	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs552101849	chr12:40543920-40543921	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs11175344	chr12:40543963-40543964	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs531843455	chr12:40544088-40544089	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs550156894	chr12:40544149-40544150	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs17461330	chr12:40544204-40544205	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs536136023	chr12:40544212-40544213	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs184322546	chr12:40544247-40544248	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs5797654	chr12:40544253-40544254	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs554491741	chr12:40544283-40544284	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs566262862	chr12:40544312-40544313	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs28365189	chr12:40544323-40544324	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs17461337	chr12:40544344-40544345	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs558073067	chr12:40544395-40544396	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs722817	chr12:40544443-40544444	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs374669482	chr12:40544471-40544472	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs540805686	chr12:40544487-40544488	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs573714596	chr12:40544601-40544602	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs555889047	chr12:40544636-40544637	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs2638266	chr12:40544639-40544640	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs17442846	chr12:40544647-40544648	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	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
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40532800-40543800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:40541400-40546600	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr12:40541800-40546600	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr12:40543400-40544000	Enhancers	Adipose Nuclei	Adipose
5	chr12:40543400-40544200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr12:40543600-40543800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr12:40543600-40544000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr12:40543600-40544000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr12:40543600-40544000	Enhancers	Hela-S3	cervix
10	chr12:40543800-40544200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr12:40543800-40544200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr12:40543800-40544200	Enhancers	A549	lung
13	chr12:40543800-40544200	Enhancers	NHEK	skin
14	chr12:40543800-40547200	Weak transcription	HMEC	breast
15	chr12:40544000-40547400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr12:40544200-40546600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr12:40544200-40546600	Weak transcription	A549	lung
18	chr12:40544200-40547000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr12:40544200-40547200	Weak transcription	NHEK	skin
20	chr12:40545600-40545800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr12:40546200-40547400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr12:40546600-40546800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:40546600-40547200	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr12:40546600-40547800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr12:40546600-40547800	Enhancers	A549	lung
26	chr12:40546600-40548400	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr12:40546800-40547200	Enhancers	Liver	Liver
28	chr12:40546800-40548400	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr12:40547000-40547200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr12:40547000-40547800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr12:40547000-40547800	Enhancers	Primary B cells from peripheral blood	blood
32	chr12:40547000-40548000	Enhancers	Primary B cells from cord blood	blood
33	chr12:40547200-40547400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr12:40547200-40547400	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr12:40547200-40547600	Enhancers	HUVEC	blood vessel
36	chr12:40547200-40547600	Enhancers	NHEK	skin
37	chr12:40547200-40547800	Enhancers	HMEC	breast
38	chr12:40547200-40548000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
39	chr12:40547200-40558600	Weak transcription	Liver	Liver
40	chr12:40547400-40547800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr12:40547400-40547800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr12:40547400-40547800	Enhancers	GM12878-XiMat	blood
43	chr12:40547400-40548400	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr12:40547400-40548600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr12:40547600-40551800	Weak transcription	NHEK	skin
46	chr12:40547800-40549600	Weak transcription	Primary B cells from peripheral blood	blood
47	chr12:40547800-40549600	Weak transcription	GM12878-XiMat	blood
48	chr12:40547800-40551200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr12:40547800-40551200	Weak transcription	HMEC	breast
50	chr12:40547800-40551800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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