Variant report

Variant	nsv521511
Chromosome Location	chr11:17749028-17771487
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:813)
CpG islands
(count:1099)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:813 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:17752734-17752850	HepG2	liver:	n/a	n/a
2	BACH1	chr11:17756192-17756315	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr11:17752607-17752898	GM12878	blood:	n/a	n/a
4	BHLHE40	chr11:17756560-17756818	HepG2	liver:	n/a	chr11:17756644-17756660
5	BHLHE40	chr11:17756580-17756727	K562	blood:	n/a	chr11:17756644-17756660
6	BHLHE40	chr11:17756573-17756763	GM12878	blood:	n/a	chr11:17756644-17756660
7	BRCA1	chr11:17752729-17752836	HepG2	liver:	n/a	n/a
8	BRCA1	chr11:17752601-17752887	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr11:17752773-17752833	GM12878	blood:	n/a	n/a
10	CEBPB	chr11:17752607-17752941	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr11:17752665-17752866	HepG2	liver:	n/a	n/a
12	CEBPB	chr11:17756623-17756736	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr11:17752652-17752914	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD1	chr11:17752611-17752799	GM12878	blood:	n/a	n/a
15	CHD1	chr11:17756611-17756687	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD1	chr11:17752489-17753087	IMR90	lung:	n/a	n/a
17	CHD2	chr11:17752390-17752860	GM12878	blood:	n/a	n/a
18	CHD2	chr11:17756640-17756806	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr11:17757402-17757762	H1-hESC	embryonic stem cell:	n/a	chr11:17757442-17757452
20	CTCF	chr11:17752160-17752310	GM12872	blood:	n/a	n/a
21	CTCF	chr11:17757420-17757570	HBMEC	blood vessel:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
22	CTCF	chr11:17752200-17752350	GM12878	blood:	n/a	n/a
23	CTCF	chr11:17751880-17752030	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr11:17752640-17752790	A549	lung:	n/a	chr11:17752746-17752764 chr11:17752747-17752763 chr11:17752748-17752769 chr11:17752769-17752778
25	CTCF	chr11:17752530-17752901	MCF-7	breast:	n/a	chr11:17752746-17752764 chr11:17752747-17752763 chr11:17752748-17752769 chr11:17752769-17752778
26	CTCF	chr11:17752200-17752350	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr11:17752209-17752330	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr11:17757462-17757569	LNCaP	prostate:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
29	CTCF	chr11:17757400-17757550	AG09319	gingival:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
30	CTCF	chr11:17752220-17752370	AG04450	lung:	n/a	n/a
31	CTCF	chr11:17752220-17752370	GM12878	blood:	n/a	n/a
32	CTCF	chr11:17757200-17757350	HPF	lung:	n/a	n/a
33	CTCF	chr11:17752180-17752330	GM12801	blood:	n/a	n/a
34	CTCF	chr11:17752180-17752330	GM12865	blood:	n/a	n/a
35	CTCF	chr11:17752280-17752430	HAc	cerebellar:	n/a	n/a
36	CTCF	chr11:17752240-17752390	NHLF	lung:	n/a	n/a
37	CTCF	chr11:17760564-17760685	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr11:17757240-17757530	AG09309	skin:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
39	CTCF	chr11:17752200-17752350	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr11:17756100-17756253	HepG2	liver:	n/a	n/a
41	CTCF	chr11:17752240-17752390	SAEC	small airway:	n/a	n/a
42	CTCF	chr11:17752680-17752830	MCF-7	breast:	n/a	chr11:17752746-17752764 chr11:17752747-17752763 chr11:17752748-17752769 chr11:17752769-17752778
43	CTCF	chr11:17752680-17752830	HCPEpiC	choroid plexus:	n/a	chr11:17752746-17752764 chr11:17752747-17752763 chr11:17752748-17752769 chr11:17752769-17752778
44	CTCF	chr11:17757523-17757527	GM10266	blood:	n/a	n/a
45	CTCF	chr11:17752589-17752875	Lung_OC	lung:	n/a	chr11:17752746-17752764 chr11:17752747-17752763 chr11:17752748-17752769 chr11:17752769-17752778
46	CTCF	chr11:17752618-17752858	HepG2	liver:	n/a	chr11:17752746-17752764 chr11:17752747-17752763 chr11:17752748-17752769 chr11:17752769-17752778
47	CTCF	chr11:17752680-17752830	GM12870	blood:	n/a	chr11:17752746-17752764 chr11:17752747-17752763 chr11:17752748-17752769 chr11:17752769-17752778
48	CTCF	chr11:17753380-17753530	GM12864	blood:	n/a	n/a
49	CTCF	chr11:17752680-17752830	GM12867	blood:	n/a	chr11:17752746-17752764 chr11:17752747-17752763 chr11:17752748-17752769 chr11:17752769-17752778
50	CTCF	chr11:17752180-17752330	AG09309	skin:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:17757342-17757392	SK-N-SH_RA	brain:	n/a
2	chr11:17757342-17757392	SK-N-SH_RA	brain:	n/a
3	chr11:17757342-17757392	HMEC	breast:	n/a
4	chr11:17760956-17761006	BE2_C	brain:	n/a
5	chr11:17752634-17752684	GM19239	blood:	n/a
6	chr11:17758537-17758587	PrEC	prostate:	n/a
7	chr11:17765568-17765618	LNCaP	prostate:	n/a
8	chr11:17752634-17752684	HRCEpiC	kidney:	n/a
9	chr11:17758537-17758587	GM12891	blood:	n/a
10	chr11:17755937-17755987	BE2_C	brain:	n/a
11	chr11:17757129-17757179	NHBE	bronchial:	n/a
12	chr11:17758285-17758335	H1-hESC	embryonic stem cell:	embryo
13	chr11:17758285-17758335	HEK293	kidney:	embryo
14	chr11:17756435-17756485	Hepatocyte	liver:	n/a
15	chr11:17761718-17761768	HCT-116	colon:	n/a
16	chr11:17765568-17765618	SKMC	muscle:	n/a
17	chr11:17760956-17761006	AG10803	skin:	n/a
18	chr11:17765568-17765618	Caco-2	colon:	n/a
19	chr11:17752634-17752684	Hepatocyte	liver:	n/a
20	chr11:17756435-17756485	SK-N-SH	brain:	n/a
21	chr11:17760602-17760652	Hela-S3	cervix:	n/a
22	chr11:17761718-17761768	HEK293	kidney:	embryo
23	chr11:17760956-17761006	ovcar-3	ovarian:	n/a
24	chr11:17757129-17757179	PANC-1	pancreas:	n/a
25	chr11:17760602-17760652	HRPEpiC	eye:	n/a
26	chr11:17758285-17758335	SAEC	small airway:	n/a
27	chr11:17755937-17755987	PFSK-1	brain:	n/a
28	chr11:17752634-17752684	LNCaP	prostate:	n/a
29	chr11:17760574-17760624	Hela-S3	cervix:	n/a
30	chr11:17756750-17756800	K562	blood:	n/a
31	chr11:17756750-17756800	HPAEpiC	pulmonary alveolar:	n/a
32	chr11:17761718-17761768	ECC-1	luminal epithelium:	n/a
33	chr11:17756761-17756811	SK-N-SH	brain:	n/a
34	chr11:17757129-17757179	HEK293	kidney:	embryo
35	chr11:17758285-17758335	ECC-1	luminal epithelium:	n/a
36	chr11:17756761-17756811	NHBE	bronchial:	n/a
37	chr11:17758537-17758587	GM06990	blood:	n/a
38	chr11:17760956-17761006	RPTEC	kidney:	n/a
39	chr11:17757342-17757392	GM19239	blood:	n/a
40	chr11:17755937-17755987	RPTEC	kidney:	n/a
41	chr11:17761718-17761768	PFSK-1	brain:	n/a
42	chr11:17756435-17756485	AoSMC	blood vessel:	n/a
43	chr11:17757342-17757392	AG04449	skin:	fetal
44	chr11:17759573-17759623	HMEC	breast:	n/a
45	chr11:17756761-17756811	Jurkat	blood:	n/a
46	chr11:17755937-17755987	SKMC	muscle:	n/a
47	chr11:17758537-17758587	A549	lung:	n/a
48	chr11:17757129-17757179	BE2_C	brain:	n/a
49	chr11:17757415-17757465	HUVEC	blood vessel:	n/a
50	chr11:17761718-17761768	AG04449	skin:	fetal

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:17752308..17752866-chr11:17774705..17775593,2	MCF-7	breast:
2	chr11:17620215..17621250-chr11:17751773..17752935,12	MCF-7	breast:
3	chr11:17622618..17623441-chr11:17752027..17752742,2	K562	blood:
4	chr11:17752064..17753282-chr11:17994336..17995305,5	MCF-7	breast:
5	chr11:17614764..17616023-chr11:17751704..17752684,3	MCF-7	breast:
6	chr11:17755705..17757483-chr11:17762543..17764877,2	K562	blood:
7	chr11:17622422..17624117-chr11:17750393..17752396,2	MCF-7	breast:
8	chr11:17752436..17753246-chr11:17868432..17868961,2	MCF-7	breast:
9	chr11:17764908..17766462-chr11:17767114..17769351,2	K562	blood:
10	chr11:17622892..17623600-chr11:17752018..17752807,2	MCF-7	breast:
11	chr11:17751921..17752763-chr19:36040271..36040795,2	MCF-7	breast:
12	chr11:17753668..17754453-chr6:57615850..57616702,2	MCF-7	breast:
13	chr11:17751864..17753212-chr11:17999973..18001949,7	MCF-7	breast:
14	chr11:17768773..17771131-chr11:17771902..17774873,3	K562	blood:
15	chr11:17620168..17621149-chr11:17752060..17752755,3	K562	blood:
16	chr11:17752076..17753447-chr11:17867688..17868717,4	MCF-7	breast:
17	chr11:17762630..17764298-chr11:17768234..17770289,2	MCF-7	breast:
18	chr11:17752308..17753219-chr11:18785582..18786221,2	K562	blood:
19	chr11:17620244..17621142-chr11:17752157..17753016,5	MCF-7	breast:
20	chr11:17752210..17753037-chr11:17762564..17763159,2	K562	blood:
21	chr11:17762630..17764298-chr11:17768234..17770289,2	MCF-7	breast:
22	chr11:17768263..17770539-chr11:17771638..17773890,2	MCF-7	breast:
23	chr11:17752325..17753223-chr11:18001001..18001982,6	K562	blood:
24	chr11:17752210..17753037-chr11:17762564..17763159,2	K562	blood:
25	chr11:17757117..17759964-chr11:17765393..17768099,2	MCF-7	breast:
26	chr11:17769238..17771607-chr11:17779598..17782123,2	K562	blood:
27	chr11:17764908..17766462-chr11:17767114..17769351,2	K562	blood:
28	chr11:17588922..17590478-chr11:17766034..17768818,2	K562	blood:
29	chr11:17751795..17753232-chr11:17999934..18001786,19	MCF-7	breast:
30	chr11:17752483..17753383-chr11:17994354..17995164,3	MCF-7	breast:
31	chr11:17752292..17753246-chr11:17999986..18000903,4	K562	blood:

No data

Variant related genes	Relation type
KCNC1	TF binding region
KCNC1	CpG island
ENSG00000129159	chromatin interactions

Extended variants
information (count: 862 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:862 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12418323	chr11:17749028-17749029	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs7479607	chr11:17749045-17749046	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs112348302	chr11:17749112-17749113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541542931	chr11:17749144-17749145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559846070	chr11:17749145-17749146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188298240	chr11:17749146-17749147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551798346	chr11:17749160-17749161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs76943901	chr11:17749190-17749191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs34989524	chr11:17749191-17749192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs78572504	chr11:17749206-17749207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs61880602	chr11:17749208-17749209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564040891	chr11:17749212-17749213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531123959	chr11:17749243-17749244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147692648	chr11:17749336-17749337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553869478	chr11:17749340-17749341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs180704467	chr11:17749346-17749347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534848202	chr11:17749349-17749350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185720574	chr11:17749435-17749436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564685321	chr11:17749441-17749442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs55789309	chr11:17749478-17749479	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs371394459	chr11:17749484-17749485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538275371	chr11:17749511-17749512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556667744	chr11:17749512-17749513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575142818	chr11:17749513-17749514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190630709	chr11:17749549-17749550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554803675	chr11:17749555-17749556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573086304	chr11:17749574-17749575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181830524	chr11:17749597-17749598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559936330	chr11:17749615-17749616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs578130931	chr11:17749626-17749627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs34483340	chr11:17749648-17749649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545447031	chr11:17749651-17749652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186898885	chr11:17749698-17749699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530885089	chr11:17749775-17749776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549420867	chr11:17749785-17749786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561615138	chr11:17749810-17749811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546340318	chr11:17749849-17749850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs55715851	chr11:17749877-17749878	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs56335097	chr11:17749885-17749886	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs377441153	chr11:17749942-17749943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538361671	chr11:17749957-17749958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142462308	chr11:17749991-17749992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529554166	chr11:17750062-17750063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536206512	chr11:17750094-17750095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554610585	chr11:17750123-17750124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190362044	chr11:17750180-17750181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534009062	chr11:17750311-17750312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144601479	chr11:17750312-17750313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577081427	chr11:17750442-17750443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545173909	chr11:17750550-17750551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
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
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:562 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17741800-17750200	Weak transcription	Right Atrium	heart
2	chr11:17744200-17755400	Weak transcription	Psoas Muscle	Psoas
3	chr11:17744800-17752400	Weak transcription	HSMM	muscle
4	chr11:17745000-17751600	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr11:17746000-17751600	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr11:17746600-17751800	Weak transcription	Fetal Muscle Trunk	muscle
7	chr11:17747200-17752400	Weak transcription	Fetal Muscle Leg	muscle
8	chr11:17751600-17752000	Genic enhancers	Skeletal Muscle Male	skeletal muscle
9	chr11:17751600-17753800	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr11:17751800-17752000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
11	chr11:17751800-17752000	Genic enhancers	Fetal Muscle Trunk	muscle
12	chr11:17752000-17752200	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr11:17752000-17752400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
14	chr11:17752000-17752400	Enhancers	Hela-S3	cervix
15	chr11:17752000-17752800	Enhancers	Fetal Muscle Trunk	muscle
16	chr11:17752000-17753200	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr11:17752200-17752400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
18	chr11:17752400-17752600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
19	chr11:17752400-17752600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
20	chr11:17752400-17752600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
21	chr11:17752400-17752600	Bivalent Enhancer	Fetal Intestine Large	intestine
22	chr11:17752400-17752600	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
23	chr11:17752400-17752600	Flanking Active TSS	Hela-S3	cervix
24	chr11:17752400-17752600	Enhancers	HSMMtube	muscle
25	chr11:17752400-17752800	Enhancers	HSMM	muscle
26	chr11:17752400-17753000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr11:17752400-17753200	Enhancers	Fetal Muscle Leg	muscle
28	chr11:17752400-17753400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
29	chr11:17752600-17752800	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
30	chr11:17752600-17752800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
31	chr11:17752600-17752800	Active TSS	Hela-S3	cervix
32	chr11:17752600-17754600	Weak transcription	HSMMtube	muscle
33	chr11:17752800-17753000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr11:17752800-17753000	Bivalent Enhancer	Fetal Stomach	stomach
35	chr11:17752800-17753200	Enhancers	Liver	Liver
36	chr11:17752800-17753400	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr11:17752800-17753400	Enhancers	Fetal Brain Male	brain
38	chr11:17752800-17753400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
39	chr11:17752800-17753600	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr11:17752800-17755800	Weak transcription	HSMM	muscle
41	chr11:17753000-17753200	Enhancers	Fetal Brain Female	brain
42	chr11:17753200-17753400	Bivalent Enhancer	Fetal Muscle Leg	muscle
43	chr11:17753200-17753600	Bivalent Enhancer	Liver	Liver
44	chr11:17753400-17754400	Weak transcription	Fetal Brain Male	brain
45	chr11:17753400-17755400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr11:17753400-17755400	Weak transcription	Fetal Brain Female	brain
47	chr11:17753800-17755000	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr11:17754200-17755800	Bivalent Enhancer	Fetal Muscle Leg	muscle
49	chr11:17754400-17754600	Enhancers	Fetal Brain Male	brain
50	chr11:17754600-17755600	Weak transcription	Fetal Brain Male	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links