Variant report

Variant	nsv1048328
Chromosome Location	chr11:56471984-56649908
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:855)
CpG islands
(count:732)
Chromatin interactive
region (count:18)
LncRNA
region (count:18)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:56483721-56484112	GM12878	blood:	n/a	n/a
2	ATF3	chr11:56517803-56518031	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr11:56615460-56615977	A549	lung:	n/a	n/a
4	ATF3	chr11:56615453-56615997	A549	lung:	n/a	n/a
5	BACH1	chr11:56646070-56646184	K562	blood:	n/a	n/a
6	BATF	chr11:56483790-56484093	GM12878	blood:	n/a	chr11:56483931-56483942
7	BATF	chr11:56483821-56484012	GM12878	blood:	n/a	chr11:56483931-56483942
8	BCL3	chr11:56615347-56616338	A549	lung:	n/a	n/a
9	BCL3	chr11:56615380-56615997	A549	lung:	n/a	n/a
10	CEBPB	chr11:56484043-56484454	MCF-7	breast:	n/a	chr11:56484335-56484346
11	CEBPB	chr11:56617323-56617647	A549	lung:	n/a	chr11:56617512-56617523
12	CEBPB	chr11:56517634-56517959	IMR90	lung:	n/a	chr11:56517867-56517884
13	CEBPB	chr11:56617279-56617787	A549	lung:	n/a	chr11:56617512-56617523
14	CEBPB	chr11:56643958-56644540	A549	lung:	n/a	n/a
15	CEBPB	chr11:56517651-56518070	H1-hESC	embryonic stem cell:	n/a	chr11:56517867-56517884
16	CEBPB	chr11:56644870-56645190	A549	lung:	n/a	chr11:56645019-56645030
17	CEBPB	chr11:56545897-56545901	A549	lung:	n/a	n/a
18	CEBPB	chr11:56568286-56568976	HepG2	liver:	n/a	chr11:56568406-56568417 chr11:56568834-56568843 chr11:56568834-56568843 chr11:56568834-56568843 chr11:56568405-56568416 chr11:56568832-56568845 chr11:56568405-56568418
19	CEBPB	chr11:56644885-56645198	HepG2	liver:	n/a	chr11:56645019-56645030
20	CEBPB	chr11:56644882-56645189	IMR90	lung:	n/a	chr11:56645019-56645030
21	CEBPB	chr11:56517644-56518052	HepG2	liver:	n/a	chr11:56517867-56517884
22	CEBPB	chr11:56568845-56568849	A549	lung:	n/a	n/a
23	CEBPB	chr11:56568768-56568903	K562	blood:	n/a	chr11:56568834-56568843 chr11:56568834-56568843 chr11:56568834-56568843 chr11:56568832-56568845
24	CEBPB	chr11:56484051-56484477	HepG2	liver:	n/a	chr11:56484335-56484346
25	CEBPB	chr11:56517761-56517904	HepG2	liver:	n/a	chr11:56517867-56517884
26	CEBPB	chr11:56517620-56518023	HepG2	liver:	n/a	chr11:56517867-56517884
27	CEBPB	chr11:56517722-56518003	MCF-7	breast:	n/a	chr11:56517867-56517884
28	CEBPB	chr11:56615462-56616086	A549	lung:	n/a	n/a
29	CEBPB	chr11:56608674-56609010	A549	lung:	n/a	n/a
30	CEBPB	chr11:56517717-56517991	A549	lung:	n/a	chr11:56517867-56517884
31	CEBPB	chr11:56594865-56595180	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr11:56565598-56565920	A549	lung:	n/a	n/a
33	CEBPB	chr11:56568334-56568570	A549	lung:	n/a	chr11:56568406-56568417 chr11:56568405-56568416 chr11:56568405-56568418
34	CEBPB	chr11:56588032-56588235	HepG2	liver:	n/a	chr11:56588126-56588137
35	CEBPB	chr11:56568721-56568994	IMR90	lung:	n/a	chr11:56568834-56568843 chr11:56568834-56568843 chr11:56568834-56568843 chr11:56568832-56568845
36	CEBPB	chr11:56617430-56617625	HepG2	liver:	n/a	chr11:56617512-56617523
37	CEBPB	chr11:56616784-56617073	A549	lung:	n/a	n/a
38	CEBPB	chr11:56488019-56488253	HepG2	liver:	n/a	chr11:56488133-56488144
39	CEBPB	chr11:56517810-56517951	K562	blood:	n/a	chr11:56517867-56517884
40	CEBPB	chr11:56484117-56484430	A549	lung:	n/a	chr11:56484335-56484346
41	CREB1	chr11:56608671-56608988	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr11:56615573-56615779	A549	lung:	n/a	n/a
43	CTCF	chr11:56608800-56608950	RPTEC	kidney:	n/a	chr11:56608871-56608889
44	CTCF	chr11:56551020-56551170	NHDF-neo	bronchial:	n/a	chr11:56551112-56551128 chr11:56551106-56551127 chr11:56551116-56551124 chr11:56551111-56551129
45	CTCF	chr11:56517741-56517991	H1-hESC	embryonic stem cell:	n/a	chr11:56517900-56517918
46	CTCF	chr11:56608780-56608930	GM12869	blood:	n/a	chr11:56608871-56608889
47	CTCF	chr11:56551020-56551170	BJ	skin:	n/a	chr11:56551112-56551128 chr11:56551106-56551127 chr11:56551116-56551124 chr11:56551111-56551129
48	CTCF	chr11:56551060-56551210	GM12865	blood:	n/a	chr11:56551112-56551128 chr11:56551106-56551127 chr11:56551116-56551124 chr11:56551111-56551129
49	CTCF	chr11:56608744-56608965	SK-N-SH_RA	brain:	n/a	chr11:56608871-56608889
50	CTCF	chr11:56579480-56579630	NHLF	lung:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:56587212-56587262	AG04450	lung:	fetal
2	chr11:56511965-56512015	IMR90	lung:	fetal
3	chr11:56545039-56545089	SK-N-SH_RA	brain:	n/a
4	chr11:56545039-56545089	BE2_C	brain:	n/a
5	chr11:56512503-56512553	BE2_C	brain:	n/a
6	chr11:56511965-56512015	A549	lung:	n/a
7	chr11:56615879-56615929	PrEC	prostate:	n/a
8	chr11:56587595-56587645	Hepatocyte	liver:	n/a
9	chr11:56512503-56512553	ECC-1	luminal epithelium:	n/a
10	chr11:56545039-56545089	CMK	blood:	n/a
11	chr11:56511965-56512015	H1-hESC	embryonic stem cell:	embryo
12	chr11:56511965-56512015	HCT-116	colon:	n/a
13	chr11:56643145-56643195	HMEC	breast:	n/a
14	chr11:56615725-56615775	GM12891	blood:	n/a
15	chr11:56545039-56545089	HCM	heart:	n/a
16	chr11:56587256-56587306	AG04449	skin:	fetal
17	chr11:56511965-56512015	HAEpiC	amniotic membrane:	n/a
18	chr11:56643145-56643195	NB4	blood:	n/a
19	chr11:56512503-56512553	AG10803	skin:	n/a
20	chr11:56614928-56614978	AG10803	skin:	n/a
21	chr11:56587595-56587645	NB4	blood:	n/a
22	chr11:56511965-56512015	NB4	blood:	n/a
23	chr11:56511248-56511298	NB4	blood:	n/a
24	chr11:56545039-56545089	HCF	heart:	n/a
25	chr11:56511248-56511298	MCF-7	breast:	n/a
26	chr11:56615879-56615929	HUVEC	blood vessel:	n/a
27	chr11:56512503-56512553	U87	brain:	n/a
28	chr11:56545039-56545089	NHDF-neo	bronchial:	n/a
29	chr11:56643145-56643195	HCF	heart:	n/a
30	chr11:56587595-56587645	PFSK-1	brain:	n/a
31	chr11:56614928-56614978	CMK	blood:	n/a
32	chr11:56511248-56511298	HEK293	kidney:	embryo
33	chr11:56615725-56615775	AG10803	skin:	n/a
34	chr11:56614928-56614978	AG09309	skin:	n/a
35	chr11:56510971-56511021	HRPEpiC	eye:	n/a
36	chr11:56587256-56587306	GM12878	blood:	n/a
37	chr11:56511248-56511298	HepG2	liver:	n/a
38	chr11:56587212-56587262	ProgFib	skin:	n/a
39	chr11:56511965-56512015	HCPEpiC	choroid plexus:	n/a
40	chr11:56587256-56587306	ECC-1	luminal epithelium:	n/a
41	chr11:56643145-56643195	H1-hESC	embryonic stem cell:	embryo
42	chr11:56587595-56587645	BE2_C	brain:	n/a
43	chr11:56545039-56545089	H1-hESC	embryonic stem cell:	embryo
44	chr11:56545039-56545089	HCT-116	colon:	n/a
45	chr11:56614928-56614978	BE2_C	brain:	n/a
46	chr11:56510971-56511021	GM12892	blood:	n/a
47	chr11:56643145-56643195	SK-N-MC	brain:	n/a
48	chr11:56615879-56615929	U87	brain:	n/a
49	chr11:56510971-56511021	HEEpiC	esophagus:	n/a
50	chr11:56511248-56511298	ovcar-3	ovarian:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:56618059..56620569-chr11:56629242..56631002,2	K562	blood:
2	chr11:56604071..56605908-chr11:56606591..56609227,2	K562	blood:
3	chr11:56640294..56642115-chr11:56642674..56646805,4	K562	blood:
4	chr11:56391852..56392531-chr11:56550628..56551135,2	MCF-7	breast:
5	chr11:56628427..56630548-chr11:56631596..56633931,2	K562	blood:
6	chr11:56628427..56630548-chr11:56631596..56633931,2	K562	blood:
7	chr11:56640294..56642115-chr11:56642674..56646805,4	K562	blood:
8	chr11:56646465..56649384-chr11:56653182..56655132,3	K562	blood:
9	chr11:56489679..56491375-chr11:56501753..56504134,2	K562	blood:
10	chr11:56608365..56609372-chr11:57017133..57018075,3	MCF-7	breast:
11	chr11:56288968..56289520-chr11:56550857..56551450,2	MCF-7	breast:
12	chr11:56608383..56609306-chr11:57016176..57017128,2	MCF-7	breast:
13	chr11:56562414..56565346-chr11:56565920..56568664,2	K562	blood:
14	chr11:56618059..56620569-chr11:56629242..56631002,2	K562	blood:
15	chr11:56608400..56609354-chr11:57016455..57017401,5	MCF-7	breast:
16	chr11:56604071..56605908-chr11:56606591..56609227,2	K562	blood:
17	chr11:56608476..56609545-chr11:57016926..57017835,4	K562	blood:
18	chr11:56562414..56565346-chr11:56565920..56568664,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR5AK2-1	chr11:56638567-56638727	ENSG00000255433
2	lnc-OR5AK2-1	chr11:56643073-56645554	NR_110136
3	lnc-OR5AK2-1	chr11:56643073-56645554	ENSG00000255433
4	lnc-OR5AK2-1	chr11:56615954-56616091	NR_110136
5	lnc-OR9G4-1	chr11:56587057-56587123	NONHSAT021395
6	lnc-OR5AK2-1	chr11:56642200-56642319	NR_110136
7	lnc-OR9G4-1	chr11:56570001-56570030	NONHSAT021395
8	lnc-OR5AK2-1	chr11:56638567-56638727	NR_110136
9	lnc-OR5AK2-1	chr11:56643073-56644687	ENSG00000255433
10	lnc-OR9G4-1	chr11:56569552-56569670	NONHSAT021395
11	lnc-OR5AK2-1	chr11:56638567-56638727	XLOC_009132
12	lnc-OR5AK2-1	chr11:56615954-56616091	XLOC_009132
13	lnc-OR5AK2-1	chr11:56642200-56642319	ENSG00000255433
14	lnc-OR5AK2-1	chr11:56615954-56616091	ENSG00000255433
15	lnc-OR5AK2-1	chr11:56616044-56616091	ENSG00000255433
16	lnc-OR5AK2-1	chr11:56638567-56638727	ENSG00000255433
17	lnc-OR5AK2-1	chr11:56643073-56645554	XLOC_009132
18	lnc-OR9G4-1	chr11:56570184-56570284	NONHSAT021395

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6128	chr11:56511419-56511437	MIMAT0024611

No data

Variant related genes	Relation type
OR5G1P	TF binding region
OR9G2P	TF binding region
ENSG00000255433	TF binding region
OR5G3	TF binding region
ENSG00000254953	TF binding region
OR9G3P	TF binding region
OR9G4	TF binding region
OR5G5P	TF binding region
OR5G4P	TF binding region
OR5G1P	CpG island
OR9G2P	CpG island
ENSG00000255433	CpG island
OR5G3	CpG island
ENSG00000254953	CpG island
OR9G3P	CpG island
OR9G4	CpG island
OR5G5P	CpG island
OR5G4P	CpG island
ENSG00000254953	chromatin interactions

Extended variants
information (count: 3596 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3596 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532423006	chr11:56471991-56471992	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs200474500	chr11:56472000-56472001	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs547395167	chr11:56472006-56472007	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs374770907	chr11:56472013-56472014	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs74212830	chr11:56472023-56472024	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs565700724	chr11:56472037-56472038	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs370594714	chr11:56472087-56472088	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs200634436	chr11:56472096-56472097	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs555660659	chr11:56472118-56472119	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs201360722	chr11:56472126-56472127	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs202197347	chr11:56472147-56472148	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs513366	chr11:56472149-56472150	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs75042793	chr11:56472151-56472152	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs182413822	chr11:56472156-56472157	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs78634608	chr11:56472167-56472168	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs74587983	chr11:56472172-56472173	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs75239012	chr11:56472177-56472178	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs80299446	chr11:56472181-56472182	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs77926496	chr11:56472189-56472190	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs77699856	chr11:56472196-56472197	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs371566792	chr11:56472202-56472203	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs74421489	chr11:56472214-56472215	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs556041466	chr11:56472216-56472217	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs77078259	chr11:56472217-56472218	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs80038107	chr11:56472223-56472224	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs78160366	chr11:56472226-56472227	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs76810610	chr11:56472256-56472257	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs74374296	chr11:56472261-56472262	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs79224037	chr11:56472266-56472267	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs61904579	chr11:56472268-56472269	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs75751300	chr11:56472272-56472273	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs75978293	chr11:56472277-56472278	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs76155244	chr11:56472284-56472285	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs78403381	chr11:56472287-56472288	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs545091738	chr11:56472306-56472307	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs77003419	chr11:56472308-56472309	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs553825691	chr11:56472310-56472311	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs74715073	chr11:56472314-56472315	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs369576286	chr11:56472323-56472324	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs79811763	chr11:56472330-56472331	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs75964845	chr11:56472339-56472340	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs76537897	chr11:56472346-56472347	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs78829560	chr11:56472357-56472358	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs78495035	chr11:56472375-56472376	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs78961465	chr11:56472389-56472390	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs77513540	chr11:56472391-56472392	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs147409131	chr11:56472393-56472394	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs75545072	chr11:56472397-56472398	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs531907592	chr11:56472419-56472420	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs77022129	chr11:56472421-56472422	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:262 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:56468200-56473200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr11:56468600-56473200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:56468600-56473200	Weak transcription	HMEC	breast
4	chr11:56468600-56473600	Weak transcription	NHEK	skin
5	chr11:56468800-56472600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr11:56470200-56473200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr11:56471800-56474200	Flanking Active TSS	Dnd41	blood
8	chr11:56472000-56473800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr11:56472600-56473600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr11:56473200-56473800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr11:56473200-56474000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr11:56473200-56474600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr11:56473200-56474600	Enhancers	HMEC	breast
14	chr11:56473600-56474400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr11:56473600-56474400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr11:56473600-56474400	Enhancers	NHEK	skin
17	chr11:56473800-56474200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr11:56473800-56474200	Enhancers	H9 Cell Line	embryonic stem cell
19	chr11:56474200-56475000	Enhancers	Dnd41	blood
20	chr11:56480800-56482600	Enhancers	Dnd41	blood
21	chr11:56482000-56482200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr11:56482200-56484000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr11:56482600-56483400	Weak transcription	Dnd41	blood
24	chr11:56483400-56484400	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr11:56483400-56484400	Enhancers	Dnd41	blood
26	chr11:56484000-56484400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr11:56484400-56487200	Weak transcription	Dnd41	blood
28	chr11:56485600-56486000	Enhancers	Fetal Intestine Small	intestine
29	chr11:56487200-56491800	Enhancers	Dnd41	blood
30	chr11:56504800-56505200	Enhancers	Fetal Brain Male	brain
31	chr11:56519000-56519200	ZNF genes & repeats	Spleen	Spleen
32	chr11:56520000-56520400	Enhancers	Dnd41	blood
33	chr11:56520400-56524600	Weak transcription	Dnd41	blood
34	chr11:56521600-56521800	Enhancers	H1 Cell Line	embryonic stem cell
35	chr11:56521800-56522800	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr11:56521800-56523600	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr11:56522000-56523600	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr11:56522400-56522800	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr11:56522400-56523400	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr11:56522600-56522800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr11:56522600-56523000	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr11:56522800-56523000	Enhancers	H1 Cell Line	embryonic stem cell
43	chr11:56522800-56523200	Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr11:56523000-56523600	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr11:56523600-56523800	Enhancers	H1 Cell Line	embryonic stem cell
46	chr11:56523800-56525200	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr11:56524600-56525800	Enhancers	Dnd41	blood
48	chr11:56525200-56525400	Enhancers	H1 Cell Line	embryonic stem cell
49	chr11:56532400-56533000	Enhancers	A549	lung
50	chr11:56541800-56542200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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