Variant report

Variant	nsv976460
Chromosome Location	chr11:64727780-64743097
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:64736759-64736812	K562	blood:	n/a	n/a
2	ATF1	chr11:64730898-64730905	K562	blood:	n/a	n/a
3	BHLHE40	chr11:64739311-64739723	K562	blood:	n/a	n/a
4	BHLHE40	chr11:64739364-64739740	GM12878	blood:	n/a	n/a
5	CBX3	chr11:64739210-64739926	K562	blood:	n/a	n/a
6	CCNT2	chr11:64739470-64739836	K562	blood:	n/a	n/a
7	CCNT2	chr11:64728162-64728412	K562	blood:	n/a	n/a
8	CEBPB	chr11:64740377-64740458	K562	blood:	n/a	n/a
9	CEBPB	chr11:64740368-64740488	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr11:64739571-64739573	K562	blood:	n/a	n/a
11	CEBPB	chr11:64730811-64731123	K562	blood:	n/a	n/a
12	CEBPB	chr11:64730777-64731139	K562	blood:	n/a	n/a
13	CEBPB	chr11:64738226-64738398	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr11:64730810-64731034	K562	blood:	n/a	n/a
15	CEBPD	chr11:64728169-64728588	K562	blood:	n/a	n/a
16	CEBPD	chr11:64728138-64728590	K562	blood:	n/a	n/a
17	CEBPZ	chr11:64735440-64735526	HepG2	liver:	n/a	n/a
18	CTCF	chr11:64739578-64739689	Lung_OC	lung:	n/a	n/a
19	CTCF	chr11:64739520-64739670	GM12867	blood:	n/a	n/a
20	CTCF	chr11:64739500-64739650	AG04449	skin:	n/a	n/a
21	CTCF	chr11:64735100-64735250	AG04449	skin:	n/a	n/a
22	CTCF	chr11:64739559-64739623	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr11:64734876-64734972	Medullo	brain:	n/a	n/a
24	CTCF	chr11:64739527-64739674	Spleen_OC	spleen:	n/a	n/a
25	CUX1	chr11:64739637-64739651	GM12878	blood:	n/a	n/a
26	CUX1	chr11:64730621-64730967	K562	blood:	n/a	n/a
27	E2F4	chr11:64738218-64738494	MCF10A-Er-Src	breast:	n/a	chr11:64738336-64738345
28	E2F6	chr11:64739264-64739801	K562	blood:	n/a	chr11:64739629-64739638 chr11:64739565-64739574 chr11:64739711-64739718 chr11:64739711-64739718 chr11:64739710-64739719 chr11:64739711-64739718
29	E2F6	chr11:64739155-64739887	A549	lung:	n/a	chr11:64739629-64739638 chr11:64739565-64739574 chr11:64739711-64739718 chr11:64739711-64739718 chr11:64739710-64739719 chr11:64739711-64739718
30	E2F6	chr11:64739024-64739926	K562	blood:	n/a	chr11:64739629-64739638 chr11:64739565-64739574 chr11:64739711-64739718 chr11:64739711-64739718 chr11:64739710-64739719 chr11:64739711-64739718
31	E2F6	chr11:64739163-64739982	H1-hESC	embryonic stem cell:	n/a	chr11:64739629-64739638 chr11:64739565-64739574 chr11:64739711-64739718 chr11:64739711-64739718 chr11:64739710-64739719 chr11:64739711-64739718
32	E2F6	chr11:64738937-64740067	H1-hESC	embryonic stem cell:	n/a	chr11:64739629-64739638 chr11:64739565-64739574 chr11:64739711-64739718 chr11:64739711-64739718 chr11:64739710-64739719 chr11:64739711-64739718 chr11:64738938-64738947 chr11:64738938-64738950
33	E2F6	chr11:64739053-64739843	K562	blood:	n/a	chr11:64739629-64739638 chr11:64739565-64739574 chr11:64739711-64739718 chr11:64739711-64739718 chr11:64739710-64739719 chr11:64739711-64739718
34	E2F6	chr11:64739077-64739985	A549	lung:	n/a	chr11:64739629-64739638 chr11:64739565-64739574 chr11:64739711-64739718 chr11:64739711-64739718 chr11:64739710-64739719 chr11:64739711-64739718
35	ELF1	chr11:64738958-64739755	GM12878	blood:	n/a	n/a
36	EP300	chr11:64728107-64728498	K562	blood:	n/a	chr11:64728406-64728420
37	EP300	chr11:64727815-64728759	SK-N-SH	brain:	n/a	chr11:64728406-64728420
38	EP300	chr11:64730752-64730999	K562	blood:	n/a	chr11:64730765-64730772
39	EP300	chr11:64728222-64728420	SK-N-SH_RA	brain:	n/a	chr11:64728406-64728420
40	EP300	chr11:64739636-64739653	K562	blood:	n/a	n/a
41	EP300	chr11:64728147-64728425	SK-N-SH_RA	brain:	n/a	chr11:64728406-64728420
42	FOS	chr11:64738091-64738604	MCF10A-Er-Src	breast:	n/a	chr11:64738283-64738291 chr11:64738283-64738290 chr11:64738283-64738292
43	FOS	chr11:64736560-64737008	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr11:64738109-64738559	MCF10A-Er-Src	breast:	n/a	chr11:64738283-64738291 chr11:64738283-64738290 chr11:64738283-64738292
45	FOS	chr11:64736509-64737051	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr11:64738094-64738569	MCF10A-Er-Src	breast:	n/a	chr11:64738283-64738291 chr11:64738283-64738290 chr11:64738283-64738292
47	FOS	chr11:64736592-64736967	HUVEC	blood vessel:	n/a	n/a
48	FOS	chr11:64736521-64736970	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr11:64738113-64738498	MCF10A-Er-Src	breast:	n/a	chr11:64738283-64738291 chr11:64738283-64738290 chr11:64738283-64738292
50	FOS	chr11:64736552-64736986	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:64739253-64739303	AG10803	skin:	n/a
2	chr11:64739374-64739424	SAEC	small airway:	n/a
3	chr11:64739343-64739393	ECC-1	luminal epithelium:	n/a
4	chr11:64739852-64739902	SAEC	small airway:	n/a
5	chr11:64739852-64739902	HepG2	liver:	n/a
6	chr11:64739320-64739370	HNPCEpiC	eye:	n/a
7	chr11:64739374-64739424	HCM	heart:	n/a
8	chr11:64728445-64728495	HMEC	breast:	n/a
9	chr11:64727755-64727805	U87	brain:	n/a
10	chr11:64739320-64739370	Jurkat	blood:	n/a
11	chr11:64739343-64739393	GM12891	blood:	n/a
12	chr11:64739253-64739303	HRCEpiC	kidney:	n/a
13	chr11:64739336-64739386	HUVEC	blood vessel:	n/a
14	chr11:64728559-64728609	GM12891	blood:	n/a
15	chr11:64739343-64739393	HRPEpiC	eye:	n/a
16	chr11:64742882-64742932	SK-N-SH_RA	brain:	n/a
17	chr11:64727755-64727805	GM12891	blood:	n/a
18	chr11:64739320-64739370	A549	lung:	n/a
19	chr11:64742882-64742932	GM19239	blood:	n/a
20	chr11:64727755-64727805	Hela-S3	cervix:	n/a
21	chr11:64739714-64739764	SK-N-SH	brain:	n/a
22	chr11:64739343-64739393	AG09309	skin:	n/a
23	chr11:64739253-64739303	HUVEC	blood vessel:	n/a
24	chr11:64739336-64739386	AG09319	gingival:	n/a
25	chr11:64736754-64736804	MCF-7	breast:	n/a
26	chr11:64739343-64739393	MCF-7	breast:	n/a
27	chr11:64728559-64728609	BJ	skin:	n/a
28	chr11:64739374-64739424	HRCEpiC	kidney:	n/a
29	chr11:64727755-64727805	K562	blood:	n/a
30	chr11:64739714-64739764	HCF	heart:	n/a
31	chr11:64739484-64739534	HIPEpiC	eye:	n/a
32	chr11:64739484-64739534	NT2-D1	testis:	n/a
33	chr11:64742882-64742932	HL-60	blood:	n/a
34	chr11:64742882-64742932	HCM	heart:	n/a
35	chr11:64727755-64727805	HCM	heart:	n/a
36	chr11:64739714-64739764	AoSMC	blood vessel:	n/a
37	chr11:64739714-64739764	CMK	blood:	n/a
38	chr11:64739484-64739534	HRPEpiC	eye:	n/a
39	chr11:64727755-64727805	HRPEpiC	eye:	n/a
40	chr11:64739343-64739393	U87	brain:	n/a
41	chr11:64739852-64739902	HEEpiC	esophagus:	n/a
42	chr11:64739343-64739393	HPAEpiC	pulmonary alveolar:	n/a
43	chr11:64739253-64739303	SK-N-SH	brain:	n/a
44	chr11:64736754-64736804	PANC-1	pancreas:	n/a
45	chr11:64728559-64728609	MCF10A-Er-Src	breast:	n/a
46	chr11:64739484-64739534	HUVEC	blood vessel:	n/a
47	chr11:64739343-64739393	LNCaP	prostate:	n/a
48	chr11:64739320-64739370	HUVEC	blood vessel:	n/a
49	chr11:64739253-64739303	AG09319	gingival:	n/a
50	chr11:64736754-64736804	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:64737496..64741049-chr11:64742327..64745214,4	K562	blood:
2	chr11:64728080..64729823-chr11:64778498..64780871,2	MCF-7	breast:
3	chr11:64690400..64694324-chr11:64737120..64740822,5	K562	blood:
4	chr11:64739428..64743212-chr11:64780553..64782608,3	K562	blood:
5	chr11:64727356..64729952-chr11:64739370..64742304,2	K562	blood:
6	chr11:64710573..64712542-chr11:64732691..64735611,2	K562	blood:
7	chr11:64717890..64720243-chr11:64735642..64738070,2	MCF-7	breast:
8	chr11:64726169..64728205-chr11:64729834..64731770,2	K562	blood:
9	chr11:64716620..64718841-chr11:64735458..64738436,2	K562	blood:
10	chr11:64690400..64693254-chr11:64737120..64738862,2	K562	blood:
11	chr11:64730697..64733049-chr11:64734062..64736820,2	K562	blood:
12	chr11:64739549..64741143-chr11:64741750..64744421,2	K562	blood:
13	chr11:64736057..64738155-chr11:64877720..64880026,2	K562	blood:
14	chr11:64689666..64692617-chr11:64726636..64729077,2	K562	blood:
15	chr11:64730697..64733049-chr11:64734062..64736820,2	K562	blood:
16	chr11:64691117..64693562-chr11:64726636..64728966,2	K562	blood:
17	chr11:64727356..64729952-chr11:64739370..64742304,2	K562	blood:

Variant related genes	Relation type
C11orf85	TF binding region
C11orf85	CpG island
ENSG00000149823	chromatin interactions
ENSG00000068971	chromatin interactions
ENSG00000149809	chromatin interactions
ENSG00000254501	chromatin interactions
ENSG00000273003	chromatin interactions
ENSG00000168070	chromatin interactions
ENSG00000213465	chromatin interactions

Extended variants
information (count: 578 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:578 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567143381	chr11:64727823-64727824	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs375677561	chr11:64727828-64727829	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs567191142	chr11:64727861-64727862	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs535677318	chr11:64727873-64727874	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs549116194	chr11:64727952-64727953	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs568636502	chr11:64728105-64728106	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs17146511	chr11:64728107-64728108	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs557418497	chr11:64728114-64728115	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs556255967	chr11:64728204-64728205	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs533781630	chr11:64728231-64728232	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs553824072	chr11:64728264-64728265	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs573839585	chr11:64728341-64728342	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs542847569	chr11:64728398-64728399	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs562638466	chr11:64728434-64728435	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs371866464	chr11:64728494-64728495	Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs375043244	chr11:64728520-64728521	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs561627933	chr11:64728534-64728535	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs17146515	chr11:64728538-64728539	Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs183578	chr11:64728586-64728587	Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs17146519	chr11:64728611-64728612	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs4297469	chr11:64728634-64728635	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs533209210	chr11:64728644-64728645	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs533022844	chr11:64728645-64728646	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs375640179	chr11:64728675-64728676	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs140044476	chr11:64728689-64728690	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs193077148	chr11:64728708-64728709	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs529561307	chr11:64728743-64728744	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs549183574	chr11:64728812-64728813	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs372309787	chr11:64728828-64728829	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs538029286	chr11:64728855-64728856	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs143689314	chr11:64728867-64728868	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs558335374	chr11:64728879-64728880	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs11231909	chr11:64728885-64728886	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs185867562	chr11:64728890-64728891	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs189800378	chr11:64728891-64728892	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs111482619	chr11:64728934-64728935	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs36053356	chr11:64728939-64728940	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs578115386	chr11:64728940-64728941	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs57402534	chr11:64728964-64728965	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs539039554	chr11:64728965-64728966	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs553682258	chr11:64728974-64728975	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs240568	chr11:64729034-64729035	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs536583816	chr11:64729072-64729073	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs556473516	chr11:64729108-64729109	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs182004125	chr11:64729109-64729110	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs545212415	chr11:64729139-64729140	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs564431060	chr11:64729146-64729147	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs578009205	chr11:64729152-64729153	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs540288306	chr11:64729188-64729189	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs560505861	chr11:64729190-64729191	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	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
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Prostate cancer	18779856	CNVD
Cancer	17160897	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:300 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64726600-64728600	Enhancers	NHEK	skin
2	chr11:64726800-64728000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr11:64727000-64728600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr11:64727000-64728600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr11:64727000-64728800	Enhancers	K562	blood
6	chr11:64727400-64728400	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr11:64727600-64728400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr11:64727800-64728600	Enhancers	Fetal Intestine Small	intestine
9	chr11:64728000-64728600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr11:64728000-64728600	Enhancers	HepG2	liver
11	chr11:64728400-64728600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr11:64728600-64736400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr11:64730200-64738400	Weak transcription	Stomach Mucosa	stomach
14	chr11:64731800-64732400	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr11:64731800-64732800	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr11:64735000-64735200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
17	chr11:64735000-64735200	Enhancers	GM12878-XiMat	blood
18	chr11:64735200-64739000	Weak transcription	GM12878-XiMat	blood
19	chr11:64735800-64736000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr11:64736000-64739000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr11:64736200-64738400	Enhancers	NHEK	skin
22	chr11:64736200-64739000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr11:64736400-64736800	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr11:64736400-64737000	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr11:64736400-64737800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr11:64736400-64739200	Enhancers	HMEC	breast
27	chr11:64736600-64737600	Enhancers	HUVEC	blood vessel
28	chr11:64736600-64737800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr11:64736800-64737000	Enhancers	Fetal Brain Male	brain
30	chr11:64736800-64737000	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr11:64736800-64737400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr11:64737000-64737200	Enhancers	Brain Cingulate Gyrus	brain
33	chr11:64737000-64737200	Enhancers	Fetal Intestine Small	intestine
34	chr11:64737000-64737200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
35	chr11:64737000-64737200	Enhancers	NH-A	brain
36	chr11:64737000-64737400	Enhancers	Placenta	Placenta
37	chr11:64737000-64737400	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr11:64737200-64737400	Enhancers	Colonic Mucosa	Colon
39	chr11:64737200-64737600	Active TSS	Rectal Mucosa Donor 29	rectum
40	chr11:64737200-64738800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr11:64737200-64739000	Weak transcription	Fetal Brain Male	brain
42	chr11:64737400-64737600	Enhancers	Esophagus	oesophagus
43	chr11:64737400-64738200	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr11:64737400-64739000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr11:64737400-64739000	Weak transcription	Colonic Mucosa	Colon
46	chr11:64737400-64739000	Weak transcription	NH-A	brain
47	chr11:64737400-64739200	Weak transcription	Placenta	Placenta
48	chr11:64737600-64738000	Weak transcription	HUVEC	blood vessel
49	chr11:64737600-64738400	Weak transcription	Rectal Mucosa Donor 29	rectum
50	chr11:64737800-64738200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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