Variant report

Variant	esv3413144
Chromosome Location	chr11:17755501-17757724
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	BACH1	chr11:17756192-17756315	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr11:17756580-17756727	K562	blood:	n/a	chr11:17756644-17756660
3	BHLHE40	chr11:17756573-17756763	GM12878	blood:	n/a	chr11:17756644-17756660
4	BHLHE40	chr11:17756560-17756818	HepG2	liver:	n/a	chr11:17756644-17756660
5	CEBPB	chr11:17756623-17756736	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD1	chr11:17756611-17756687	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr11:17756640-17756806	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr11:17757402-17757762	H1-hESC	embryonic stem cell:	n/a	chr11:17757442-17757452
9	CTCF	chr11:17757400-17757550	HUVEC	blood vessel:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
10	CTCF	chr11:17757400-17757550	GM12868	blood:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
11	CTCF	chr11:17756600-17756750	SK-N-SH_RA	brain:	n/a	n/a
12	CTCF	chr11:17757420-17757570	BE2_C	brain:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
13	CTCF	chr11:17757463-17757572	GM13977	blood:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
14	CTCF	chr11:17756120-17756270	HUVEC	blood vessel:	n/a	chr11:17756255-17756268
15	CTCF	chr11:17756078-17756246	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr11:17756120-17756270	SK-N-SH_RA	brain:	n/a	chr11:17756255-17756268
17	CTCF	chr11:17757420-17757570	RPTEC	kidney:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
18	CTCF	chr11:17757400-17757550	HAc	cerebellar:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
19	CTCF	chr11:17757440-17757590	BE2_C	brain:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
20	CTCF	chr11:17757477-17757501	GM12878	blood:	n/a	chr11:17757490-17757499 chr11:17757485-17757501
21	CTCF	chr11:17756080-17756230	HEK293	kidney:	n/a	n/a
22	CTCF	chr11:17757437-17757602	A549	lung:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
23	CTCF	chr11:17757380-17757530	HA-sp	spinal cord:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
24	CTCF	chr11:17757420-17757570	SAEC	small airway:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
25	CTCF	chr11:17757272-17757628	H1-hESC	embryonic stem cell:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
26	CTCF	chr11:17757460-17757610	A549	lung:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
27	CTCF	chr11:17756840-17756990	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr11:17757440-17757590	NHDF-neo	bronchial:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
29	CTCF	chr11:17757380-17757530	HVMF	connective:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
30	CTCF	chr11:17757380-17757530	HCPEpiC	choroid plexus:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
31	CTCF	chr11:17757460-17757730	GM12869	blood:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
32	CTCF	chr11:17757380-17757530	HMEC	breast:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
33	CTCF	chr11:17757254-17757873	SK-N-SH	brain:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
34	CTCF	chr11:17757600-17757750	WI-38	lung:	n/a	n/a
35	CTCF	chr11:17757420-17757570	HEK293	kidney:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
36	CTCF	chr11:17756740-17756890	GM12875	blood:	n/a	chr11:17756801-17756819 chr11:17756804-17756817
37	CTCF	chr11:17756100-17756250	GM12874	blood:	n/a	n/a
38	CTCF	chr11:17757460-17757610	HFF	foreskin:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
39	CTCF	chr11:17757440-17757590	GM12864	blood:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
40	CTCF	chr11:17757420-17757570	AG04450	lung:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
41	CTCF	chr11:17756820-17756970	HEK293	kidney:	n/a	n/a
42	CTCF	chr11:17757313-17757675	A549	lung:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
43	CTCF	chr11:17757400-17757550	GM12873	blood:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
44	CTCF	chr11:17757420-17757570	HBMEC	blood vessel:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
45	CTCF	chr11:17757536-17757617	ProgFib	skin:	n/a	n/a
46	CTCF	chr11:17757449-17757635	GM12891	blood:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
47	CTCF	chr11:17757400-17757550	HepG2	liver:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
48	CTCF	chr11:17757500-17757650	AG09319	gingival:	n/a	n/a
49	CTCF	chr11:17757400-17757550	AG09319	gingival:	n/a	chr11:17757484-17757502 chr11:17757490-17757499 chr11:17757485-17757501
50	CTCF	chr11:17757320-17757470	GM06990	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:17756761-17756811	PANC-1	pancreas:	n/a
2	chr11:17756750-17756800	IMR90	lung:	fetal
3	chr11:17756761-17756811	PANC-1	pancreas:	n/a
4	chr11:17756750-17756800	IMR90	lung:	fetal
5	chr11:17756435-17756485	GM19239	blood:	n/a
6	chr11:17755937-17755987	Caco-2	colon:	n/a
7	chr11:17756986-17757036	IMR90	lung:	fetal
8	chr11:17756750-17756800	HRE	kidney:	n/a
9	chr11:17756986-17757036	HAEpiC	amniotic membrane:	n/a
10	chr11:17755937-17755987	Hela-S3	cervix:	n/a
11	chr11:17756479-17756529	A549	lung:	n/a
12	chr11:17756435-17756485	SK-N-MC	brain:	n/a
13	chr11:17756986-17757036	MCF10A-Er-Src	breast:	n/a
14	chr11:17757129-17757179	A549	lung:	n/a
15	chr11:17757342-17757392	NHBE	bronchial:	n/a
16	chr11:17756750-17756800	HCM	heart:	n/a
17	chr11:17756986-17757036	PrEC	prostate:	n/a
18	chr11:17756750-17756800	NHDF-neo	bronchial:	n/a
19	chr11:17755937-17755987	NH-A	brain:	n/a
20	chr11:17757129-17757179	NH-A	brain:	n/a
21	chr11:17756479-17756529	MCF10A-Er-Src	breast:	n/a
22	chr11:17756986-17757036	ovcar-3	ovarian:	n/a
23	chr11:17756750-17756800	AG04449	skin:	fetal
24	chr11:17756761-17756811	SK-N-MC	brain:	n/a
25	chr11:17756986-17757036	GM12892	blood:	n/a
26	chr11:17756479-17756529	NT2-D1	testis:	n/a
27	chr11:17757129-17757179	HCT-116	colon:	n/a
28	chr11:17757415-17757465	U87	brain:	n/a
29	chr11:17756435-17756485	SAEC	small airway:	n/a
30	chr11:17756479-17756529	ovcar-3	ovarian:	n/a
31	chr11:17756750-17756800	HCPEpiC	choroid plexus:	n/a
32	chr11:17757415-17757465	GM12878	blood:	n/a
33	chr11:17757129-17757179	Hela-S3	cervix:	n/a
34	chr11:17756750-17756800	GM12878	blood:	n/a
35	chr11:17757342-17757392	HNPCEpiC	eye:	n/a
36	chr11:17757129-17757179	MCF-7	breast:	n/a
37	chr11:17756761-17756811	K562	blood:	n/a
38	chr11:17756750-17756800	GM12892	blood:	n/a
39	chr11:17756750-17756800	ECC-1	luminal epithelium:	n/a
40	chr11:17756986-17757036	SK-N-SH	brain:	n/a
41	chr11:17756761-17756811	LNCaP	prostate:	n/a
42	chr11:17757342-17757392	GM12878	blood:	n/a
43	chr11:17756750-17756800	ovcar-3	ovarian:	n/a
44	chr11:17756435-17756485	Caco-2	colon:	n/a
45	chr11:17756761-17756811	HAEpiC	amniotic membrane:	n/a
46	chr11:17756761-17756811	MCF10A-Er-Src	breast:	n/a
47	chr11:17757415-17757465	AG04449	skin:	fetal
48	chr11:17756750-17756800	AG09309	skin:	n/a
49	chr11:17756986-17757036	U87	brain:	n/a
50	chr11:17756479-17756529	GM19239	blood:	n/a

Variant related genes	Relation type
KCNC1	TF binding region
KCNC1	CpG island

Extended variants
information (count: 68 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:68 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531061298	chr11:17755511-17755512	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs4757586	chr11:17755517-17755518	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs3858514	chr11:17755532-17755533	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs141457426	chr11:17755547-17755548	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs546261622	chr11:17755550-17755551	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs571170875	chr11:17755583-17755584	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs145101747	chr11:17755648-17755649	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs114185822	chr11:17755677-17755678	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs114593486	chr11:17755696-17755697	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs536490655	chr11:17755732-17755733	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs563697218	chr11:17755738-17755739	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs554811280	chr11:17755742-17755743	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs573025334	chr11:17755750-17755751	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs541557352	chr11:17755777-17755778	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs59005803	chr11:17755807-17755808	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs139555436	chr11:17755810-17755811	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs373219588	chr11:17755811-17755812	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs3223030	chr11:17755812-17755813	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs56771220	chr11:17755834-17755835	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs78818838	chr11:17755835-17755836	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs577983804	chr11:17755875-17755876	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs78484863	chr11:17755923-17755924	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs563869226	chr11:17756065-17756066	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs531120704	chr11:17756069-17756070	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs542868347	chr11:17756070-17756071	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs561169699	chr11:17756161-17756162	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs549582146	chr11:17756193-17756194	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs528628427	chr11:17756198-17756199	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs549770393	chr11:17756202-17756203	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs28724581	chr11:17756213-17756214	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs201701706	chr11:17756216-17756217	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs571298851	chr11:17756235-17756236	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs568065999	chr11:17756273-17756274	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs550540137	chr11:17756288-17756289	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs568717514	chr11:17756299-17756300	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs140665086	chr11:17756347-17756348	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs150102860	chr11:17756351-17756352	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs28526619	chr11:17756354-17756355	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs533956369	chr11:17756517-17756518	Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs376304900	chr11:17756602-17756603	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs553240464	chr11:17756609-17756610	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs578044345	chr11:17756619-17756620	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs55974459	chr11:17756664-17756665	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs545133320	chr11:17756696-17756697	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs143460354	chr11:17756788-17756789	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs527871333	chr11:17756861-17756862	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs370603364	chr11:17756862-17756863	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs528682928	chr11:17756912-17756913	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs113618027	chr11:17756939-17756940	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs575207358	chr11:17757000-17757001	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
Breast cancer	22522925	CNVD

Chromatin state (count:337 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17752800-17755800	Weak transcription	HSMM	muscle
2	chr11:17754200-17755800	Bivalent Enhancer	Fetal Muscle Leg	muscle
3	chr11:17754600-17755600	Weak transcription	Fetal Brain Male	brain
4	chr11:17754600-17755800	Enhancers	HSMMtube	muscle
5	chr11:17754600-17756000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
6	chr11:17755000-17755800	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr11:17755000-17756200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr11:17755200-17755800	Bivalent Enhancer	Duodenum Mucosa	Duodenum
9	chr11:17755200-17755800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
10	chr11:17755400-17755600	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr11:17755400-17755600	Enhancers	Fetal Brain Female	brain
12	chr11:17755400-17755600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
13	chr11:17755400-17755800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr11:17755400-17755800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr11:17755400-17755800	Enhancers	Right Ventricle	heart
16	chr11:17755400-17756000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr11:17755400-17756000	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr11:17755400-17756000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr11:17755400-17756000	Bivalent Enhancer	Fetal Intestine Large	intestine
20	chr11:17755400-17756000	Enhancers	Psoas Muscle	Psoas
21	chr11:17755400-17756200	Bivalent Enhancer	Placenta	Placenta
22	chr11:17755400-17756200	Bivalent Enhancer	Stomach Mucosa	stomach
23	chr11:17755600-17755800	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr11:17755600-17755800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr11:17755600-17755800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr11:17755600-17755800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr11:17755600-17755800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr11:17755600-17755800	Bivalent Enhancer	Liver	Liver
29	chr11:17755600-17755800	Bivalent Enhancer	Colon Smooth Muscle	Colon
30	chr11:17755600-17755800	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
31	chr11:17755600-17755800	Flanking Active TSS	Fetal Brain Female	brain
32	chr11:17755600-17755800	Bivalent Enhancer	Fetal Kidney	kidney
33	chr11:17755600-17755800	Enhancers	Lung	lung
34	chr11:17755600-17755800	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
35	chr11:17755600-17755800	Bivalent Enhancer	HUVEC	blood vessel
36	chr11:17755600-17756000	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr11:17755600-17756000	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr11:17755600-17756000	Bivalent Enhancer	Fetal Intestine Small	intestine
39	chr11:17755600-17756000	Bivalent Enhancer	Fetal Stomach	stomach
40	chr11:17755600-17756000	Enhancers	Ovary	ovary
41	chr11:17755600-17756000	Enhancers	Pancreas	Pancrea
42	chr11:17755600-17756000	Enhancers	Right Atrium	heart
43	chr11:17755600-17756200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
44	chr11:17755600-17756400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
45	chr11:17755600-17756400	Enhancers	Fetal Brain Male	brain
46	chr11:17755600-17757600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
47	chr11:17755600-17757800	Enhancers	Fetal Heart	heart
48	chr11:17755800-17756000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr11:17755800-17756000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
50	chr11:17755800-17756000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung

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