Variant report

Variant	nsv1040964
Chromosome Location	chr11:26998213-27223388
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1664)
CpG islands
(count:1160)
Chromatin interactive
region (count:42)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1664 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:27223146-27223932	K562	blood:	n/a	n/a
2	ARID3A	chr11:27223258-27223908	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:27180369-27180629	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:27046863-27047194	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:27076369-27077106	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:27196470-27196721	HepG2	liver:	n/a	n/a
7	ATF1	chr11:27223031-27223468	K562	blood:	n/a	n/a
8	ATF3	chr11:27180331-27180589	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr11:27180266-27180705	K562	blood:	n/a	n/a
10	ATF3	chr11:27179905-27180741	A549	lung:	n/a	n/a
11	ATF3	chr11:27179915-27180632	A549	lung:	n/a	n/a
12	ATF3	chr11:27223124-27223791	A549	lung:	n/a	n/a
13	ATF3	chr11:27180379-27180595	K562	blood:	n/a	n/a
14	ATF3	chr11:27180365-27180557	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr11:27180294-27180574	GM12878	blood:	n/a	n/a
16	BCL3	chr11:27223194-27223948	A549	lung:	n/a	n/a
17	BCL3	chr11:27204270-27204518	GM12878	blood:	n/a	n/a
18	BDP1	chr11:27180003-27180578	Hela-S3	cervix:	n/a	n/a
19	BHLHE40	chr11:27180438-27180713	GM12878	blood:	n/a	n/a
20	BHLHE40	chr11:27223103-27223970	K562	blood:	n/a	n/a
21	BHLHE40	chr11:27076685-27077064	HepG2	liver:	n/a	n/a
22	BRCA1	chr11:27180331-27180690	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr11:27140734-27140760	H1-hESC	embryonic stem cell:	n/a	n/a
24	CBX3	chr11:27223068-27223510	K562	blood:	n/a	n/a
25	CBX3	chr11:27163163-27163370	K562	blood:	n/a	n/a
26	CEBPB	chr11:27223113-27223432	K562	blood:	n/a	n/a
27	CEBPB	chr11:27119184-27119499	A549	lung:	n/a	n/a
28	CEBPB	chr11:27062301-27062649	H1-hESC	embryonic stem cell:	n/a	chr11:27062468-27062481 chr11:27062470-27062479 chr11:27062469-27062480 chr11:27062468-27062479
29	CEBPB	chr11:27114300-27114344	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr11:27013506-27013842	A549	lung:	n/a	chr11:27013752-27013765 chr11:27013643-27013656 chr11:27013752-27013765 chr11:27013644-27013655 chr11:27013643-27013654
31	CEBPB	chr11:27015433-27015769	IMR90	lung:	n/a	n/a
32	CEBPB	chr11:27063948-27063974	Hela-S3	cervix:	n/a	chr11:27063955-27063966
33	CEBPB	chr11:27119275-27119383	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr11:27046927-27047231	HepG2	liver:	n/a	n/a
35	CEBPB	chr11:27062323-27062641	Hela-S3	cervix:	n/a	chr11:27062468-27062481 chr11:27062470-27062479 chr11:27062469-27062480 chr11:27062468-27062479
36	CEBPB	chr11:27105338-27105516	HepG2	liver:	n/a	n/a
37	CEBPB	chr11:27215132-27215381	K562	blood:	n/a	n/a
38	CEBPB	chr11:27069501-27069701	HepG2	liver:	n/a	chr11:27069586-27069597
39	CEBPB	chr11:27223169-27223496	K562	blood:	n/a	n/a
40	CEBPB	chr11:27196501-27196659	A549	lung:	n/a	n/a
41	CEBPB	chr11:27076591-27076974	HepG2	liver:	n/a	n/a
42	CEBPB	chr11:27195319-27195916	MCF-7	breast:	n/a	chr11:27195539-27195552
43	CEBPB	chr11:27180303-27180665	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr11:27062301-27062658	HepG2	liver:	n/a	chr11:27062468-27062481 chr11:27062470-27062479 chr11:27062469-27062480 chr11:27062468-27062479
45	CEBPB	chr11:27223210-27224000	A549	lung:	n/a	n/a
46	CEBPB	chr11:27196387-27196771	HepG2	liver:	n/a	n/a
47	CEBPB	chr11:27196453-27196695	HepG2	liver:	n/a	n/a
48	CEBPB	chr11:27116809-27116915	A549	lung:	n/a	chr11:27116811-27116822 chr11:27116809-27116822
49	CEBPB	chr11:27206332-27206637	HepG2	liver:	n/a	n/a
50	CEBPB	chr11:27206434-27206588	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:27061533-27061583	HMEC	breast:	n/a
2	chr11:27061533-27061583	HMEC	breast:	n/a
3	chr11:27017005-27017055	Jurkat	blood:	n/a
4	chr11:27015813-27015863	ProgFib	skin:	n/a
5	chr11:27015813-27015863	PFSK-1	brain:	n/a
6	chr11:27016671-27016721	AoSMC	blood vessel:	n/a
7	chr11:27145585-27145635	AG10803	skin:	n/a
8	chr11:27017005-27017055	AG09319	gingival:	n/a
9	chr11:27017005-27017055	HEEpiC	esophagus:	n/a
10	chr11:27015991-27016041	SK-N-MC	brain:	n/a
11	chr11:27015991-27016041	U87	brain:	n/a
12	chr11:27015872-27015922	AG04449	skin:	fetal
13	chr11:27062963-27063013	GM06990	blood:	n/a
14	chr11:27061899-27061949	SKMC	muscle:	n/a
15	chr11:27062416-27062466	BJ	skin:	n/a
16	chr11:27062416-27062466	NHBE	bronchial:	n/a
17	chr11:27105814-27105864	HepG2	liver:	n/a
18	chr11:27015808-27015858	HCPEpiC	choroid plexus:	n/a
19	chr11:27015656-27015706	U87	brain:	n/a
20	chr11:27061533-27061583	NT2-D1	testis:	n/a
21	chr11:27015991-27016041	GM19239	blood:	n/a
22	chr11:27062963-27063013	IMR90	lung:	fetal
23	chr11:27097023-27097073	Caco-2	colon:	n/a
24	chr11:27145585-27145635	HMEC	breast:	n/a
25	chr11:27062963-27063013	HCPEpiC	choroid plexus:	n/a
26	chr11:27016671-27016721	SKMC	muscle:	n/a
27	chr11:27015991-27016041	HCF	heart:	n/a
28	chr11:27160935-27160985	SK-N-SH	brain:	n/a
29	chr11:27015813-27015863	PrEC	prostate:	n/a
30	chr11:27015656-27015706	ECC-1	luminal epithelium:	n/a
31	chr11:27034225-27034275	Jurkat	blood:	n/a
32	chr11:27017005-27017055	HIPEpiC	eye:	n/a
33	chr11:27145585-27145635	ProgFib	skin:	n/a
34	chr11:27061899-27061949	GM12892	blood:	n/a
35	chr11:27105814-27105864	CMK	blood:	n/a
36	chr11:27015991-27016041	HepG2	liver:	n/a
37	chr11:27015592-27015642	CMK	blood:	n/a
38	chr11:27015813-27015863	MCF10A-Er-Src	breast:	n/a
39	chr11:27015991-27016041	HEEpiC	esophagus:	n/a
40	chr11:27160935-27160985	HPAEpiC	pulmonary alveolar:	n/a
41	chr11:27015808-27015858	SK-N-MC	brain:	n/a
42	chr11:27017005-27017055	SK-N-MC	brain:	n/a
43	chr11:27160935-27160985	CMK	blood:	n/a
44	chr11:27145585-27145635	GM12892	blood:	n/a
45	chr11:27062963-27063013	HPAEpiC	pulmonary alveolar:	n/a
46	chr11:27061533-27061583	CMK	blood:	n/a
47	chr11:27062963-27063013	A549	lung:	n/a
48	chr11:27160935-27160985	GM12892	blood:	n/a
49	chr11:27097023-27097073	SK-N-SH_RA	brain:	n/a
50	chr11:27015813-27015863	AG04449	skin:	fetal

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:27206362..27207013-chr11:27317950..27318581,2	MCF-7	breast:
2	chr11:27016139..27017650-chr11:27021439..27023753,2	K562	blood:
3	chr11:27205592..27206109-chr11:27518894..27519608,2	K562	blood:
4	chr11:27050228..27052948-chr11:27053328..27055109,2	MCF-7	breast:
5	chr11:27173133..27174774-chr11:27180444..27183032,2	K562	blood:
6	chr11:27205192..27206125-chr11:27317809..27318532,3	MCF-7	breast:
7	chr11:26306569..26307360-chr11:27180028..27180570,2	K562	blood:
8	chr11:27050228..27052948-chr11:27053328..27055109,2	MCF-7	breast:
9	chr11:26775214..26776083-chr11:27180054..27180898,5	MCF-7	breast:
10	chr11:27205188..27206173-chr11:27507158..27508421,10	K562	blood:
11	chr11:27205289..27206114-chr11:27232993..27233660,2	MCF-7	breast:
12	chr11:27222753..27224767-chr11:27527380..27529573,2	K562	blood:
13	chr11:27195294..27197746-chr11:27526620..27528329,2	MCF-7	breast:
14	chr11:27204301..27206366-chr11:27223714..27225288,2	MCF-7	breast:
15	chr11:27046527..27047233-chr8:129115547..129116417,2	MCF-7	breast:
16	chr11:27199376..27201905-chr11:27487180..27488680,2	MCF-7	breast:
17	chr11:27215715..27217258-chr11:27219758..27222636,2	K562	blood:
18	chr11:27222710..27225256-chr11:27227598..27230568,2	K562	blood:
19	chr11:26774919..26776345-chr11:27179975..27180962,4	MCF-7	breast:
20	chr11:27217010..27219273-chr11:27415722..27417887,2	K562	blood:
21	chr11:27222741..27229054-chr11:27229384..27235549,8	K562	blood:
22	chr11:27199374..27201790-chr11:27208479..27210287,2	K562	blood:
23	chr11:27173133..27174774-chr11:27180444..27183032,2	K562	blood:
24	chr11:27215715..27217258-chr11:27219758..27222636,2	K562	blood:
25	chr11:27199374..27201117-chr11:27208388..27209979,2	K562	blood:
26	chr11:27199374..27201790-chr11:27208479..27210287,2	K562	blood:
27	chr11:27217202..27219718-chr11:27226989..27229921,2	MCF-7	breast:
28	chr11:26775142..26776062-chr11:27146200..27147224,6	MCF-7	breast:
29	chr11:27205266..27206256-chr11:27507177..27508122,4	MCF-7	breast:
30	chr11:27217663..27219197-chr11:27221701..27223639,2	MCF-7	breast:
31	chr11:27212584..27215226-chr11:27218417..27220419,2	K562	blood:
32	chr11:27217663..27219197-chr11:27221701..27223639,2	MCF-7	breast:
33	chr11:27016139..27017650-chr11:27021439..27023753,2	K562	blood:
34	chr11:27223288..27224844-chr11:27234778..27236414,2	MCF-7	breast:
35	chr11:26307690..26308295-chr11:27180273..27180978,2	K562	blood:
36	chr11:27205070..27206237-chr11:27507034..27508588,8	MCF-7	breast:
37	chr11:26353203..26353841-chr11:27180057..27180963,2	K562	blood:
38	chr11:27207294..27208926-chr11:27210575..27212160,2	MCF-7	breast:
39	chr11:27015097..27016903-chr11:27033368..27035440,2	K562	blood:
40	chr11:27207294..27208926-chr11:27210575..27212160,2	MCF-7	breast:
41	chr11:27199374..27201117-chr11:27208388..27209979,2	K562	blood:
42	chr11:27212584..27215226-chr11:27218417..27220419,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC34-1	chr11:27172597-27172699	ENSG00000254560.1
2	lnc-CCDC34-1	chr11:27088039-27088209	ENSG00000254560.1
3	lnc-FIBIN-2	chr11:27148999-27149235	NONHSAT018479
4	lnc-FIBIN-1	chr11:27062418-27062566	NONHSAT018464
5	lnc-CCDC34-1	chr11:27084530-27084607	ENSG00000254560.1
6	lnc-FIBIN-1	chr11:27062763-27063025	NONHSAT018464
7	lnc-CCDC34-1	chr11:27068733-27068859	ENSG00000254560.1
8	lnc-CCDC34-1	chr11:27172597-27172699	ENSG00000254560.1
9	lnc-FIBIN-1	chr11:27067789-27067833	NONHSAT018464

No data

Variant related genes	Relation type
FIBIN	TF binding region
BBOX1	TF binding region
FIBIN	CpG island
BBOX1	CpG island
ENSG00000148943	chromatin interactions
ENSG00000245573	chromatin interactions
ENSG00000134343	chromatin interactions
ENSG00000176971	chromatin interactions

Extended variants
information (count: 8320 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:8320 , 50 per page) page: 1 2 3 4 5 6 7 ... 167

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183555136	chr11:26998222-26998223	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs542990183	chr11:26998225-26998226	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs561248749	chr11:26998281-26998282	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs531765740	chr11:26998324-26998325	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs543905340	chr11:26998327-26998328	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs377411133	chr11:26998329-26998330	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs565391655	chr11:26998334-26998335	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs540955232	chr11:26998354-26998355	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs553529960	chr11:26998398-26998399	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs565562449	chr11:26998433-26998434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551552530	chr11:26998438-26998439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs566592257	chr11:26998462-26998463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs145169802	chr11:26998468-26998469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187470075	chr11:26998481-26998482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566896017	chr11:26998483-26998484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571957722	chr11:26998598-26998599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537464442	chr11:26998609-26998610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555799509	chr11:26998615-26998616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372704915	chr11:26998633-26998634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571322285	chr11:26998637-26998638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539066608	chr11:26998639-26998640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555717206	chr11:26998642-26998643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538401534	chr11:26998643-26998644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554333561	chr11:26998680-26998681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11603310	chr11:26998681-26998682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543318871	chr11:26998683-26998684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564416172	chr11:26998693-26998694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532358323	chr11:26998694-26998695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576467829	chr11:26998697-26998698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556232867	chr11:26998700-26998701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543845416	chr11:26998722-26998723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190507656	chr11:26998723-26998724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577261026	chr11:26998726-26998727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541202320	chr11:26998732-26998733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs11605261	chr11:26998738-26998739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs377266319	chr11:26998782-26998783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560275477	chr11:26998816-26998817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs145017948	chr11:26998856-26998857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138105584	chr11:26998864-26998865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142707309	chr11:26998868-26998869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531162557	chr11:26998869-26998870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182760099	chr11:26998875-26998876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571194657	chr11:26998879-26998880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544617744	chr11:26998932-26998933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186999145	chr11:26998956-26998957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547201412	chr11:26998969-26998970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566234132	chr11:26998972-26998973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536850050	chr11:26998993-26998994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs75260549	chr11:26999009-26999010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192369748	chr11:26999035-26999036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Neuroticism	17667963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
early-passage human iPS cells	21368824	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:1418 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:26997200-26998400	Enhancers	Fetal Stomach	stomach
2	chr11:26997200-26998400	Enhancers	Ovary	ovary
3	chr11:26997200-26998400	Enhancers	Rectal Smooth Muscle	rectum
4	chr11:26997200-26998400	Enhancers	NH-A	brain
5	chr11:26997400-26998400	Enhancers	Osteobl	bone
6	chr11:26997600-26998400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr11:26997800-26998400	Enhancers	Stomach Smooth Muscle	stomach
8	chr11:26997800-26998400	Active TSS	A549	lung
9	chr11:26998000-26998400	Enhancers	HSMMtube	muscle
10	chr11:26998200-26998400	Active TSS	Colon Smooth Muscle	Colon
11	chr11:26998200-26998400	Enhancers	Hela-S3	cervix
12	chr11:26998200-27008600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr11:27004800-27010400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr11:27005000-27005600	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr11:27005200-27005600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr11:27005400-27005600	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr11:27005400-27005800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr11:27006000-27006200	Enhancers	Duodenum Smooth Muscle	Duodenum
19	chr11:27006200-27014800	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr11:27006400-27009400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr11:27006600-27008000	Enhancers	NHDF-Ad	bronchial
22	chr11:27007000-27007200	Enhancers	Rectal Smooth Muscle	rectum
23	chr11:27007000-27008200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr11:27007000-27009600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr11:27007200-27007800	Weak transcription	Rectal Smooth Muscle	rectum
26	chr11:27007200-27008000	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr11:27007200-27008000	Enhancers	Osteobl	bone
28	chr11:27007200-27010400	Enhancers	Fetal Lung	lung
29	chr11:27007400-27008000	Enhancers	Aorta	Aorta
30	chr11:27007800-27008000	Enhancers	Rectal Smooth Muscle	rectum
31	chr11:27008000-27012200	Weak transcription	NHDF-Ad	bronchial
32	chr11:27008000-27012800	Weak transcription	Aorta	Aorta
33	chr11:27008000-27013000	Weak transcription	Osteobl	bone
34	chr11:27008000-27013400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr11:27008000-27015400	Weak transcription	Rectal Smooth Muscle	rectum
36	chr11:27008200-27012800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr11:27008600-27010200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr11:27008800-27009600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr11:27008800-27009600	Enhancers	Muscle Satellite Cultured Cells	--
40	chr11:27008800-27010000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr11:27009400-27012800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr11:27009600-27012800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr11:27009600-27013000	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr11:27009600-27013200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr11:27010000-27013000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr11:27010200-27010600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr11:27010400-27010600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr11:27010400-27010600	Flanking Active TSS	Fetal Lung	lung
49	chr11:27010600-27010800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr11:27010600-27011200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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