Variant report

Variant	nsv1045889
Chromosome Location	chr11:56624365-56737435
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:523)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:523 , 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	ATF3	chr11:56700281-56700715	HCT-116	colon:	n/a	n/a
2	ATF3	chr11:56677422-56678255	A549	lung:	n/a	n/a
3	ATF3	chr11:56700116-56700807	A549	lung:	n/a	n/a
4	ATF3	chr11:56674119-56674737	A549	lung:	n/a	n/a
5	ATF3	chr11:56677375-56678070	A549	lung:	n/a	n/a
6	ATF3	chr11:56700056-56700856	A549	lung:	n/a	n/a
7	BACH1	chr11:56646070-56646184	K562	blood:	n/a	n/a
8	BCL3	chr11:56677385-56678346	A549	lung:	n/a	n/a
9	BCL3	chr11:56700090-56700807	A549	lung:	n/a	n/a
10	BCL3	chr11:56699810-56701075	A549	lung:	n/a	n/a
11	BCL3	chr11:56673973-56674803	A549	lung:	n/a	n/a
12	BCL3	chr11:56677223-56678627	A549	lung:	n/a	chr11:56678412-56678421 chr11:56678413-56678422
13	BCL3	chr11:56673648-56674760	A549	lung:	n/a	n/a
14	CBX3	chr11:56700195-56700768	HCT-116	colon:	n/a	n/a
15	CEBPB	chr11:56700165-56700906	A549	lung:	n/a	n/a
16	CEBPB	chr11:56692208-56692478	HepG2	liver:	n/a	chr11:56692374-56692386 chr11:56692343-56692354
17	CEBPB	chr11:56644885-56645198	HepG2	liver:	n/a	chr11:56645019-56645030
18	CEBPB	chr11:56653963-56654311	A549	lung:	n/a	chr11:56654140-56654153
19	CEBPB	chr11:56644870-56645190	A549	lung:	n/a	chr11:56645019-56645030
20	CEBPB	chr11:56666303-56666724	A549	lung:	n/a	n/a
21	CEBPB	chr11:56644882-56645189	IMR90	lung:	n/a	chr11:56645019-56645030
22	CEBPB	chr11:56677062-56678333	A549	lung:	n/a	chr11:56677154-56677166
23	CEBPB	chr11:56672207-56672605	A549	lung:	n/a	chr11:56672486-56672499 chr11:56672488-56672499 chr11:56672488-56672499
24	CEBPB	chr11:56699438-56699655	A549	lung:	n/a	chr11:56699596-56699607
25	CEBPB	chr11:56693610-56693866	A549	lung:	n/a	chr11:56693693-56693704 chr11:56693692-56693703 chr11:56693692-56693705
26	CEBPB	chr11:56700263-56700810	HCT-116	colon:	n/a	n/a
27	CEBPB	chr11:56673532-56674712	A549	lung:	n/a	n/a
28	CEBPB	chr11:56681837-56681985	HepG2	liver:	n/a	chr11:56681902-56681913 chr11:56681904-56681913 chr11:56681903-56681914
29	CEBPB	chr11:56689927-56690256	HepG2	liver:	n/a	chr11:56690086-56690097 chr11:56690086-56690099
30	CEBPB	chr11:56700192-56700845	A549	lung:	n/a	n/a
31	CEBPB	chr11:56699986-56701097	A549	lung:	n/a	n/a
32	CEBPB	chr11:56700378-56700640	MCF-7	breast:	n/a	n/a
33	CEBPB	chr11:56699562-56699629	HepG2	liver:	n/a	chr11:56699596-56699607
34	CEBPB	chr11:56672226-56672606	HepG2	liver:	n/a	chr11:56672486-56672499 chr11:56672488-56672499 chr11:56672488-56672499
35	CEBPB	chr11:56674000-56675226	A549	lung:	n/a	n/a
36	CEBPB	chr11:56653864-56654402	A549	lung:	n/a	chr11:56654140-56654153
37	CEBPB	chr11:56700255-56700726	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr11:56675074-56675163	A549	lung:	n/a	n/a
39	CEBPB	chr11:56677145-56679193	A549	lung:	n/a	chr11:56677154-56677166
40	CEBPB	chr11:56692200-56692499	A549	lung:	n/a	chr11:56692374-56692386 chr11:56692343-56692354
41	CEBPB	chr11:56664891-56665471	HepG2	liver:	n/a	chr11:56665031-56665042
42	CEBPB	chr11:56677430-56678043	A549	lung:	n/a	n/a
43	CEBPB	chr11:56700226-56700811	HCT-116	colon:	n/a	n/a
44	CEBPB	chr11:56693584-56693847	HepG2	liver:	n/a	chr11:56693693-56693704 chr11:56693692-56693703 chr11:56693692-56693705
45	CEBPB	chr11:56643958-56644540	A549	lung:	n/a	n/a
46	CEBPB	chr11:56692190-56692508	Hela-S3	cervix:	n/a	chr11:56692374-56692386 chr11:56692343-56692354
47	CEBPB	chr11:56700358-56700682	IMR90	lung:	n/a	n/a
48	CEBPB	chr11:56678719-56679324	A549	lung:	n/a	n/a
49	CEBPB	chr11:56653973-56654278	HepG2	liver:	n/a	chr11:56654140-56654153
50	CREB1	chr11:56677569-56677946	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:56643145-56643195	HEK293	kidney:	embryo
2	chr11:56643145-56643195	HCM	heart:	n/a
3	chr11:56643145-56643195	Hepatocyte	liver:	n/a
4	chr11:56643145-56643195	PFSK-1	brain:	n/a
5	chr11:56643145-56643195	GM19239	blood:	n/a
6	chr11:56643145-56643195	GM06990	blood:	n/a
7	chr11:56643145-56643195	K562	blood:	n/a
8	chr11:56643145-56643195	ECC-1	luminal epithelium:	n/a
9	chr11:56643145-56643195	AG04450	lung:	fetal
10	chr11:56643145-56643195	HRPEpiC	eye:	n/a
11	chr11:56643145-56643195	LNCaP	prostate:	n/a
12	chr11:56643145-56643195	HCT-116	colon:	n/a
13	chr11:56643145-56643195	Hela-S3	cervix:	n/a
14	chr11:56643145-56643195	Caco-2	colon:	n/a
15	chr11:56643145-56643195	BE2_C	brain:	n/a
16	chr11:56643145-56643195	AG09309	skin:	n/a
17	chr11:56643145-56643195	GM12892	blood:	n/a
18	chr11:56643145-56643195	GM12891	blood:	n/a
19	chr11:56643145-56643195	NH-A	brain:	n/a
20	chr11:56643145-56643195	HAEpiC	amniotic membrane:	n/a
21	chr11:56643145-56643195	AoSMC	blood vessel:	n/a
22	chr11:56643145-56643195	MCF-7	breast:	n/a
23	chr11:56643145-56643195	AG10803	skin:	n/a
24	chr11:56643145-56643195	HEEpiC	esophagus:	n/a
25	chr11:56643145-56643195	HMEC	breast:	n/a
26	chr11:56643145-56643195	GM12878	blood:	n/a
27	chr11:56643145-56643195	PrEC	prostate:	n/a
28	chr11:56643145-56643195	HepG2	liver:	n/a
29	chr11:56643145-56643195	HRE	kidney:	n/a
30	chr11:56643145-56643195	IMR90	lung:	fetal
31	chr11:56643145-56643195	BJ	skin:	n/a
32	chr11:56643145-56643195	A549	lung:	n/a
33	chr11:56643145-56643195	SAEC	small airway:	n/a
34	chr11:56643145-56643195	HCF	heart:	n/a
35	chr11:56643145-56643195	HPAEpiC	pulmonary alveolar:	n/a
36	chr11:56643145-56643195	PANC-1	pancreas:	n/a
37	chr11:56643145-56643195	CMK	blood:	n/a
38	chr11:56643145-56643195	Jurkat	blood:	n/a
39	chr11:56643145-56643195	NHBE	bronchial:	n/a
40	chr11:56643145-56643195	SKMC	muscle:	n/a
41	chr11:56643145-56643195	HIPEpiC	eye:	n/a
42	chr11:56643145-56643195	ovcar-3	ovarian:	n/a
43	chr11:56643145-56643195	HNPCEpiC	eye:	n/a
44	chr11:56643145-56643195	NT2-D1	testis:	n/a
45	chr11:56643145-56643195	NB4	blood:	n/a
46	chr11:56643145-56643195	SK-N-SH_RA	brain:	n/a
47	chr11:56643145-56643195	U87	brain:	n/a
48	chr11:56643145-56643195	SK-N-SH	brain:	n/a
49	chr11:56643145-56643195	T-47D	breast:	n/a
50	chr11:56643145-56643195	RPTEC	kidney:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:56640294..56642115-chr11:56642674..56646805,4	K562	blood:
2	chr11:56628427..56630548-chr11:56631596..56633931,2	K562	blood:
3	chr11:56664007..56666719-chr11:56666908..56669064,2	K562	blood:
4	chr11:56728699..56729199-chr12:122984833..122985494,2	Hela-S3	cervix:
5	chr11:56646465..56649384-chr11:56653182..56655132,3	K562	blood:
6	chr11:56640294..56642115-chr11:56642674..56646805,4	K562	blood:
7	chr11:56664007..56666719-chr11:56666908..56669064,2	K562	blood:
8	chr11:56628427..56630548-chr11:56631596..56633931,2	K562	blood:
9	chr11:56646465..56649384-chr11:56653182..56655132,3	K562	blood:
10	chr11:56618059..56620569-chr11:56629242..56631002,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR5AK2-1	chr11:56642200-56642319	ENSG00000255433
2	lnc-OR5AK2-1	chr11:56638567-56638727	ENSG00000255433
3	lnc-OR5AK2-1	chr11:56638567-56638727	ENSG00000255433
4	lnc-OR5AK2-1	chr11:56643073-56645554	ENSG00000255433
5	lnc-OR5AK2-1	chr11:56643073-56644687	ENSG00000255433
6	lnc-OR5AK2-1	chr11:56638567-56638727	NR_110136
7	lnc-OR5AK2-1	chr11:56643073-56645554	XLOC_009132
8	lnc-OR5AK2-1	chr11:56638567-56638727	XLOC_009132
9	lnc-OR5AK2-1	chr11:56643073-56645554	NR_110136
10	lnc-OR5AK2-1	chr11:56642200-56642319	NR_110136

No data

Variant related genes	Relation type
OR5AK3P	TF binding region
OR5AK3P	CpG island
ENSG00000033030	chromatin interactions

Extended variants
information (count: 3683 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:3683 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528836233	chr11:56624391-56624392	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs151255647	chr11:56624418-56624419	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs114648007	chr11:56624461-56624462	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs140444825	chr11:56624481-56624482	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs557908943	chr11:56624513-56624514	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs150440442	chr11:56624528-56624529	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs187279702	chr11:56624539-56624540	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs555784081	chr11:56624540-56624541	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs544123571	chr11:56624580-56624581	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs539945113	chr11:56624600-56624601	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs573972276	chr11:56624622-56624623	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs556571621	chr11:56624641-56624642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs61889109	chr11:56624663-56624664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191772085	chr11:56624690-56624691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554310752	chr11:56624701-56624702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575585890	chr11:56624735-56624736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574563029	chr11:56624748-56624749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11228820	chr11:56624766-56624767	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs138356841	chr11:56624825-56624826	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181636835	chr11:56624878-56624879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539957623	chr11:56624885-56624886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554574	chr11:56624910-56624911	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs546452622	chr11:56624915-56624916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs185487922	chr11:56624950-56624951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576487	chr11:56624971-56624972	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs573296658	chr11:56624974-56624975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189999470	chr11:56625042-56625043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565283586	chr11:56625047-56625048	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182256927	chr11:56625058-56625059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370500538	chr11:56625174-56625175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551616873	chr11:56625234-56625235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566955327	chr11:56625318-56625319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534374414	chr11:56625369-56625370	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs142557992	chr11:56625375-56625376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186783506	chr11:56625393-56625394	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531195033	chr11:56625398-56625399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551279385	chr11:56625405-56625406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs139228048	chr11:56625410-56625411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575647313	chr11:56625429-56625430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546131108	chr11:56625479-56625480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561595722	chr11:56625618-56625619	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149438329	chr11:56625625-56625626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572977032	chr11:56625666-56625667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs143815616	chr11:56625669-56625670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs73480469	chr11:56625728-56625729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530312962	chr11:56625729-56625730	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546916507	chr11:56625757-56625758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78437428	chr11:56625760-56625761	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2096581	chr11:56625775-56625776	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538357670	chr11:56625786-56625787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Breast cancer	17142309	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:290 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:56618800-56626600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr11:56620600-56624600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:56623000-56629400	Weak transcription	Stomach Mucosa	stomach
4	chr11:56624200-56624400	Active TSS	A549	lung
5	chr11:56624400-56624600	Flanking Active TSS	A549	lung
6	chr11:56624600-56624800	Enhancers	HMEC	breast
7	chr11:56624600-56625200	Enhancers	A549	lung
8	chr11:56624600-56625400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr11:56625600-56626000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr11:56626600-56626800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr11:56626800-56634200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr11:56629400-56630200	Enhancers	Stomach Mucosa	stomach
13	chr11:56630200-56637000	Weak transcription	Stomach Mucosa	stomach
14	chr11:56631200-56631600	Enhancers	Psoas Muscle	Psoas
15	chr11:56632400-56633000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr11:56634200-56635600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr11:56634400-56634800	Enhancers	Fetal Lung	lung
18	chr11:56635600-56640200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr11:56637000-56637200	Enhancers	Stomach Mucosa	stomach
20	chr11:56637200-56638000	Weak transcription	Stomach Mucosa	stomach
21	chr11:56638000-56638600	Enhancers	Stomach Mucosa	stomach
22	chr11:56638600-56642000	Weak transcription	Stomach Mucosa	stomach
23	chr11:56640000-56644000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr11:56640200-56640600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr11:56640600-56642800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr11:56642000-56645200	Enhancers	Stomach Mucosa	stomach
27	chr11:56642600-56642800	Enhancers	Fetal Intestine Small	intestine
28	chr11:56642800-56643200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr11:56642800-56646000	Weak transcription	Fetal Intestine Small	intestine
30	chr11:56643200-56644400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr11:56643600-56643800	Weak transcription	A549	lung
32	chr11:56643600-56645000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr11:56643600-56646000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr11:56643800-56644600	Enhancers	NHDF-Ad	bronchial
35	chr11:56643800-56644800	Enhancers	Duodenum Smooth Muscle	Duodenum
36	chr11:56643800-56644800	Enhancers	Fetal Lung	lung
37	chr11:56643800-56645200	Enhancers	A549	lung
38	chr11:56644000-56644400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr11:56644000-56644800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr11:56644200-56644600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr11:56644200-56644600	Enhancers	Gastric	stomach
42	chr11:56644200-56644600	Enhancers	HMEC	breast
43	chr11:56644200-56644600	Enhancers	NHEK	skin
44	chr11:56644400-56644600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
45	chr11:56644400-56644600	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr11:56644400-56644800	Enhancers	Right Atrium	heart
47	chr11:56644400-56645600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr11:56644600-56652600	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr11:56645000-56652600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr11:56645200-56645600	Weak transcription	Stomach Mucosa	stomach

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