Variant report

Variant	esv3437706
Chromosome Location	chr11:10313476-10317774
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:484)
CpG islands
(count:977)
Chromatin interactive
region (count:23)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:484 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr11:10315471-10316500	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr11:10315845-10316722	A549	lung:	n/a	chr11:10316696-10316705 chr11:10316320-10316329
3	BHLHE40	chr11:10315574-10316601	HepG2	liver:	n/a	n/a
4	BHLHE40	chr11:10313506-10313530	K562	blood:	n/a	n/a
5	BHLHE40	chr11:10315601-10315801	K562	blood:	n/a	n/a
6	BHLHE40	chr11:10315548-10315745	GM12878	blood:	n/a	n/a
7	BHLHE40	chr11:10316135-10316212	K562	blood:	n/a	n/a
8	BRCA1	chr11:10315997-10316318	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr11:10314850-10315335	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr11:10315585-10315640	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr11:10314909-10315040	HepG2	liver:	n/a	n/a
12	CBX3	chr11:10314920-10315290	K562	blood:	n/a	n/a
13	CCNT2	chr11:10315172-10315954	K562	blood:	n/a	chr11:10315798-10315807
14	CEBPB	chr11:10316063-10316484	IMR90	lung:	n/a	n/a
15	CEBPB	chr11:10314944-10316615	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr11:10316120-10316330	HepG2	liver:	n/a	n/a
17	CEBPB	chr11:10316079-10316392	HepG2	liver:	n/a	n/a
18	CEBPB	chr11:10316137-10316371	K562	blood:	n/a	n/a
19	CEBPB	chr11:10316074-10316447	HepG2	liver:	n/a	n/a
20	CEBPB	chr11:10316067-10316445	A549	lung:	n/a	n/a
21	CEBPB	chr11:10315046-10315157	HepG2	liver:	n/a	n/a
22	CEBPB	chr11:10315127-10316474	HepG2	liver:	n/a	n/a
23	CEBPB	chr11:10316064-10316458	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr11:10315915-10316828	A549	lung:	n/a	n/a
25	CEBPB	chr11:10316029-10316469	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr11:10316064-10316450	MCF-7	breast:	n/a	n/a
27	CEBPB	chr11:10315969-10316535	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr11:10316018-10316414	A549	lung:	n/a	n/a
29	CEBPD	chr11:10316045-10316351	HepG2	liver:	n/a	n/a
30	CEBPD	chr11:10315198-10316026	HepG2	liver:	n/a	n/a
31	CHD1	chr11:10315871-10316765	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr11:10315052-10315260	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr11:10315019-10315379	HepG2	liver:	n/a	n/a
34	CHD2	chr11:10315653-10316325	HepG2	liver:	n/a	chr11:10315792-10315802
35	CHD2	chr11:10315650-10316533	H1-hESC	embryonic stem cell:	n/a	chr11:10315792-10315802
36	CHD2	chr11:10315616-10315995	GM12878	blood:	n/a	chr11:10315792-10315802
37	CHD2	chr11:10315478-10316000	K562	blood:	n/a	chr11:10315792-10315802
38	CHD2	chr11:10314893-10316604	Hela-S3	cervix:	n/a	chr11:10315792-10315802
39	CREB1	chr11:10314908-10315306	A549	lung:	n/a	n/a
40	CREB1	chr11:10314881-10316035	A549	lung:	n/a	n/a
41	CREB1	chr11:10314891-10316173	HepG2	liver:	n/a	n/a
42	CREB1	chr11:10314878-10315873	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr11:10314889-10315459	K562	blood:	n/a	n/a
44	CTCF	chr11:10315820-10315970	GM12871	blood:	n/a	chr11:10315931-10315944 chr11:10315935-10315944
45	CTCF	chr11:10316720-10316870	GM12873	blood:	n/a	n/a
46	CTCF	chr11:10316720-10316870	HRE	kidney:	n/a	n/a
47	CTCF	chr11:10314980-10315130	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr11:10315840-10315990	SK-N-SH_RA	brain:	n/a	chr11:10315931-10315944 chr11:10315935-10315944
49	CTCF	chr11:10315840-10315990	NHEK	skin:	n/a	chr11:10315931-10315944 chr11:10315935-10315944
50	CTCF	chr11:10315000-10315150	HCPEpiC	choroid plexus:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:10315732-10315782	CMK	blood:	n/a
2	chr11:10315732-10315782	CMK	blood:	n/a
3	chr11:10316358-10316408	GM06990	blood:	n/a
4	chr11:10316295-10316345	Hepatocyte	liver:	n/a
5	chr11:10315924-10315974	CMK	blood:	n/a
6	chr11:10314098-10314148	Hepatocyte	liver:	n/a
7	chr11:10316367-10316417	Hela-S3	cervix:	n/a
8	chr11:10316295-10316345	HL-60	blood:	n/a
9	chr11:10315759-10315809	K562	blood:	n/a
10	chr11:10316851-10316901	CMK	blood:	n/a
11	chr11:10315914-10315964	HRPEpiC	eye:	n/a
12	chr11:10315754-10315804	HMEC	breast:	n/a
13	chr11:10316367-10316417	HNPCEpiC	eye:	n/a
14	chr11:10315761-10315811	H1-hESC	embryonic stem cell:	embryo
15	chr11:10316295-10316345	HPAEpiC	pulmonary alveolar:	n/a
16	chr11:10316851-10316901	HCT-116	colon:	n/a
17	chr11:10315754-10315804	Hela-S3	cervix:	n/a
18	chr11:10315759-10315809	GM12878	blood:	n/a
19	chr11:10315434-10315484	HRE	kidney:	n/a
20	chr11:10314098-10314148	HRE	kidney:	n/a
21	chr11:10315754-10315804	HRCEpiC	kidney:	n/a
22	chr11:10316358-10316408	HRCEpiC	kidney:	n/a
23	chr11:10315761-10315811	HCPEpiC	choroid plexus:	n/a
24	chr11:10314098-10314148	K562	blood:	n/a
25	chr11:10315754-10315804	Hepatocyte	liver:	n/a
26	chr11:10316461-10316511	HRCEpiC	kidney:	n/a
27	chr11:10315434-10315484	NHDF-neo	bronchial:	n/a
28	chr11:10315932-10315982	AG10803	skin:	n/a
29	chr11:10315434-10315484	RPTEC	kidney:	n/a
30	chr11:10315732-10315782	HNPCEpiC	eye:	n/a
31	chr11:10315732-10315782	Hepatocyte	liver:	n/a
32	chr11:10315759-10315809	PANC-1	pancreas:	n/a
33	chr11:10315609-10315659	ProgFib	skin:	n/a
34	chr11:10315732-10315782	HCF	heart:	n/a
35	chr11:10315759-10315809	SK-N-SH	brain:	n/a
36	chr11:10315434-10315484	HRCEpiC	kidney:	n/a
37	chr11:10315434-10315484	SAEC	small airway:	n/a
38	chr11:10315732-10315782	SK-N-SH	brain:	n/a
39	chr11:10316851-10316901	GM12892	blood:	n/a
40	chr11:10315761-10315811	SAEC	small airway:	n/a
41	chr11:10316367-10316417	Jurkat	blood:	n/a
42	chr11:10315754-10315804	RPTEC	kidney:	n/a
43	chr11:10315434-10315484	MCF-7	breast:	n/a
44	chr11:10315924-10315974	HAEpiC	amniotic membrane:	n/a
45	chr11:10315914-10315964	T-47D	breast:	n/a
46	chr11:10315759-10315809	HPAEpiC	pulmonary alveolar:	n/a
47	chr11:10316555-10316605	LNCaP	prostate:	n/a
48	chr11:10316461-10316511	HIPEpiC	eye:	n/a
49	chr11:10315914-10315964	HIPEpiC	eye:	n/a
50	chr11:10316851-10316901	H1-hESC	embryonic stem cell:	embryo

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:10315011..10315557-chr11:10326617..10327541,2	Hela-S3	cervix:
2	chr11:10308479..10310637-chr11:10311551..10314059,2	K562	blood:
3	chr11:9683805..9685652-chr11:10315027..10316546,2	MCF-7	breast:
4	chr11:10315551..10316429-chr11:76155187..76155779,2	Hela-S3	cervix:
5	chr11:10314668..10317041-chr11:10325018..10327085,3	K562	blood:
6	chr11:9807438..9810264-chr11:10314419..10316538,2	MCF-7	breast:
7	chr10:90750116..90750832-chr11:10315037..10315557,2	Hela-S3	cervix:
8	chr11:10315206..10317508-chr11:10317757..10321006,5	K562	blood:
9	chr11:10315792..10316538-chr6:30524081..30524596,2	Hela-S3	cervix:
10	chr11:10309394..10313803-chr11:10314307..10318397,4	K562	blood:
11	chr11:10314888..10315583-chr16:2301167..2301673,2	Hela-S3	cervix:
12	chr11:10315128..10316131-chr5:158636153..158636928,3	Hela-S3	cervix:
13	chr1:110881866..110882489-chr11:10315671..10316498,2	Hela-S3	cervix:
14	chr11:10311957..10313803-chr11:10314378..10316867,2	K562	blood:
15	chr11:10314422..10317147-chr11:10327890..10331590,5	MCF-7	breast:
16	chr11:10315206..10317508-chr11:10317757..10320050,3	K562	blood:
17	chr11:10314963..10315757-chr16:57835571..57836779,3	Hela-S3	cervix:
18	chr11:10312910..10314444-chr11:10314747..10317022,2	MCF-7	breast:
19	chr11:10315975..10316678-chr16:2802548..2803211,2	Hela-S3	cervix:
20	chr11:10314677..10315524-chr5:126852926..126853898,2	Hela-S3	cervix:
21	chr11:10315805..10316653-chr8:56685830..56686481,2	Hela-S3	cervix:
22	chr11:10316317..10316870-chr19:16438000..16438938,2	Hela-S3	cervix:
23	chr11:10314893..10315882-chr3:156392156..156392695,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADM-1	chr11:10315852-10316615	XLOC_009060

No data

Variant related genes	Relation type
SBF2	TF binding region
SBF2	CpG island
ENSG00000137574	chromatin interactions
ENSG00000133812	chromatin interactions
ENSG00000163659	chromatin interactions
ENSG00000133789	chromatin interactions
ENSG00000162775	chromatin interactions
ENSG00000026103	chromatin interactions
ENSG00000167978	chromatin interactions
ENSG00000164244	chromatin interactions
ENSG00000148926	chromatin interactions
ENSG00000167969	chromatin interactions
ENSG00000205913	chromatin interactions
ENSG00000254554	chromatin interactions
ENSG00000243926	chromatin interactions
ENSG00000133805	chromatin interactions
ENSG00000145860	chromatin interactions
ENSG00000140859	chromatin interactions
ENSG00000167904	chromatin interactions
ENSG00000255135	chromatin interactions

Extended variants
information (count: 142 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:142 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567808530	chr11:10313488-10313489	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs191678260	chr11:10313494-10313495	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs572187072	chr11:10313583-10313584	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs532738660	chr11:10313592-10313593	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs548574856	chr11:10313603-10313604	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs570030477	chr11:10313617-10313618	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs538918938	chr11:10313657-10313658	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs558135986	chr11:10313673-10313674	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs139540196	chr11:10313688-10313689	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs71454403	chr11:10313693-10313694	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs7111631	chr11:10313694-10313695	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs547091862	chr11:10313712-10313713	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs574577967	chr11:10313730-10313731	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs149716120	chr11:10313742-10313743	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs10840387	chr11:10313750-10313751	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs187051818	chr11:10313752-10313753	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs370686935	chr11:10313784-10313785	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs546078465	chr11:10313831-10313832	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs148896810	chr11:10313856-10313857	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs191882388	chr11:10313860-10313861	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs564143678	chr11:10313875-10313876	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs147014642	chr11:10313920-10313921	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs567733711	chr11:10313950-10313951	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs533537298	chr11:10313952-10313953	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs185363887	chr11:10313966-10313967	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs549984762	chr11:10313994-10313995	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs569871091	chr11:10314018-10314019	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs538958223	chr11:10314099-10314100	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs558818702	chr11:10314138-10314139	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs565589473	chr11:10314192-10314193	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs190240233	chr11:10314197-10314198	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs193284572	chr11:10314203-10314204	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs554230564	chr11:10314214-10314215	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs563853048	chr11:10314224-10314225	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs370521976	chr11:10314226-10314227	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs5789633	chr11:10314245-10314246	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs376522916	chr11:10314264-10314265	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs548351866	chr11:10314322-10314323	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs574495739	chr11:10314343-10314344	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs543102288	chr11:10314347-10314348	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs557201906	chr11:10314381-10314382	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs577101844	chr11:10314393-10314394	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs569559828	chr11:10314407-10314408	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs551353294	chr11:10314468-10314469	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs546165996	chr11:10314499-10314500	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs559664452	chr11:10314525-10314526	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs527719901	chr11:10314530-10314531	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs184228330	chr11:10314587-10314588	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs370889098	chr11:10314598-10314599	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs142345328	chr11:10314611-10314612	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
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
Autism	22495311	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:713 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:10291200-10313600	Weak transcription	NHEK	skin
2	chr11:10291200-10314400	Weak transcription	HSMM	muscle
3	chr11:10299400-10314800	Weak transcription	Small Intestine	intestine
4	chr11:10299800-10314400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:10306400-10313800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr11:10306600-10314400	Weak transcription	Brain Germinal Matrix	brain
7	chr11:10306600-10314800	Weak transcription	Aorta	Aorta
8	chr11:10307000-10313800	Weak transcription	Psoas Muscle	Psoas
9	chr11:10307000-10314400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr11:10307200-10313800	Weak transcription	Colon Smooth Muscle	Colon
11	chr11:10307200-10314400	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr11:10307600-10314400	Weak transcription	Primary B cells from cord blood	blood
13	chr11:10307600-10314400	Weak transcription	Brain Angular Gyrus	brain
14	chr11:10307800-10313600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr11:10307800-10314400	Weak transcription	Liver	Liver
16	chr11:10308200-10314400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr11:10308400-10313800	Weak transcription	Fetal Thymus	thymus
18	chr11:10308400-10314400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr11:10308600-10314400	Weak transcription	NH-A	brain
20	chr11:10308800-10314600	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr11:10308800-10315000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr11:10309200-10314400	Weak transcription	Brain Substantia Nigra	brain
23	chr11:10309200-10314400	Weak transcription	HSMMtube	muscle
24	chr11:10309400-10314600	Weak transcription	Thymus	Thymus
25	chr11:10310000-10314800	Weak transcription	Left Ventricle	heart
26	chr11:10310200-10314400	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr11:10310400-10313600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr11:10310400-10313800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:10310400-10314400	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr11:10310600-10314000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr11:10310600-10314400	Weak transcription	Rectal Smooth Muscle	rectum
32	chr11:10310800-10314400	Weak transcription	Colonic Mucosa	Colon
33	chr11:10310800-10314400	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr11:10311200-10313600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr11:10311200-10314400	Enhancers	Adipose Nuclei	Adipose
36	chr11:10311200-10314400	Enhancers	Fetal Intestine Large	intestine
37	chr11:10311400-10313600	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr11:10311400-10313600	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr11:10311400-10313800	Weak transcription	Right Atrium	heart
40	chr11:10311400-10315000	Weak transcription	Lung	lung
41	chr11:10311400-10315200	Weak transcription	Spleen	Spleen
42	chr11:10311600-10313800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr11:10311600-10314400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr11:10311600-10314400	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr11:10311600-10314400	Enhancers	HepG2	liver
46	chr11:10311600-10314800	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr11:10311800-10313600	Genic enhancers	Fetal Lung	lung
48	chr11:10312000-10314000	Weak transcription	Fetal Muscle Trunk	muscle
49	chr11:10312000-10314200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr11:10312000-10314400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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