Variant report

Variant	esv2752948
Chromosome Location	chr1:114658958-114751958
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:698)
CpG islands
(count:1772)
Chromatin interactive
region (count:102)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:698 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:114661221-114661618	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr1:114707686-114708183	GM12878	blood:	n/a	n/a
3	BACH1	chr1:114696275-114696355	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:114693772-114694049	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:114697781-114698040	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr1:114707806-114708109	GM12878	blood:	n/a	n/a
7	BATF	chr1:114692734-114693008	GM12878	blood:	n/a	n/a
8	BATF	chr1:114707698-114708139	GM12878	blood:	n/a	n/a
9	BCL11A	chr1:114688187-114688378	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr1:114707712-114708106	GM12878	blood:	n/a	n/a
11	BHLHE40	chr1:114707497-114707662	HepG2	liver:	n/a	n/a
12	BRCA1	chr1:114695680-114695898	H1-hESC	embryonic stem cell:	n/a	n/a
13	CCNT2	chr1:114661185-114661385	K562	blood:	n/a	n/a
14	CEBPB	chr1:114717528-114717687	H1-hESC	embryonic stem cell:	n/a	chr1:114717603-114717616
15	CEBPB	chr1:114751497-114751811	IMR90	lung:	n/a	chr1:114751639-114751650
16	CEBPB	chr1:114667360-114667648	HepG2	liver:	n/a	n/a
17	CEBPB	chr1:114689956-114690104	A549	lung:	n/a	chr1:114690013-114690024
18	CEBPB	chr1:114702710-114702910	K562	blood:	n/a	chr1:114702791-114702800 chr1:114702789-114702800
19	CEBPB	chr1:114709744-114710258	MCF-7	breast:	n/a	chr1:114709994-114710005 chr1:114709993-114710006
20	CEBPB	chr1:114751490-114751785	H1-hESC	embryonic stem cell:	n/a	chr1:114751639-114751650
21	CEBPB	chr1:114751465-114751793	K562	blood:	n/a	chr1:114751639-114751650
22	CEBPB	chr1:114689945-114690160	K562	blood:	n/a	chr1:114690013-114690024
23	CEBPB	chr1:114690011-114690127	Hela-S3	cervix:	n/a	chr1:114690013-114690024
24	CEBPB	chr1:114709928-114710109	K562	blood:	n/a	chr1:114709994-114710005 chr1:114709993-114710006
25	CEBPB	chr1:114751487-114751791	A549	lung:	n/a	chr1:114751639-114751650
26	CEBPB	chr1:114695396-114695405	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr1:114709943-114710038	Hela-S3	cervix:	n/a	chr1:114709994-114710005 chr1:114709993-114710006
28	CEBPB	chr1:114722231-114722352	IMR90	lung:	n/a	n/a
29	CEBPB	chr1:114702629-114703093	HepG2	liver:	n/a	chr1:114702791-114702800 chr1:114702789-114702800
30	CEBPB	chr1:114751381-114751995	MCF-7	breast:	n/a	chr1:114751639-114751650
31	CEBPB	chr1:114659341-114659637	HepG2	liver:	n/a	chr1:114659478-114659489
32	CEBPB	chr1:114751470-114751818	HepG2	liver:	n/a	chr1:114751639-114751650
33	CEBPB	chr1:114709832-114710151	HepG2	liver:	n/a	chr1:114709994-114710005 chr1:114709993-114710006
34	CEBPB	chr1:114751358-114751930	MCF-7	breast:	n/a	chr1:114751639-114751650
35	CEBPB	chr1:114689887-114690122	HepG2	liver:	n/a	chr1:114690013-114690024
36	CEBPB	chr1:114659298-114659582	A549	lung:	n/a	chr1:114659478-114659489
37	CEBPB	chr1:114751489-114751785	Hela-S3	cervix:	n/a	chr1:114751639-114751650
38	CEBPD	chr1:114749006-114749485	K562	blood:	n/a	n/a
39	CHD1	chr1:114694774-114694939	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD1	chr1:114695300-114695667	IMR90	lung:	n/a	chr1:114695628-114695638
41	CHD1	chr1:114695305-114695559	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr1:114661238-114661480	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr1:114694971-114695915	H1-hESC	embryonic stem cell:	n/a	chr1:114695628-114695638
44	CHD2	chr1:114697647-114698055	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTBP2	chr1:114694759-114695509	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTBP2	chr1:114695808-114698181	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr1:114674621-114674648	GM10266	blood:	n/a	n/a
48	CTCF	chr1:114696149-114696463	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr1:114696200-114696350	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr1:114674520-114674670	AG09309	skin:	n/a	chr1:114674600-114674621 chr1:114674605-114674623

(count:1772 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:114696698-114696748	AoSMC	blood vessel:	n/a
2	chr1:114698730-114698780	HRCEpiC	kidney:	n/a
3	chr1:114697523-114697573	HPAEpiC	pulmonary alveolar:	n/a
4	chr1:114696698-114696748	AoSMC	blood vessel:	n/a
5	chr1:114698730-114698780	HRCEpiC	kidney:	n/a
6	chr1:114697523-114697573	HPAEpiC	pulmonary alveolar:	n/a
7	chr1:114696946-114696996	HUVEC	blood vessel:	n/a
8	chr1:114696698-114696748	HRCEpiC	kidney:	n/a
9	chr1:114695527-114695577	NHBE	bronchial:	n/a
10	chr1:114697582-114697632	NT2-D1	testis:	n/a
11	chr1:114698730-114698780	ProgFib	skin:	n/a
12	chr1:114665617-114665667	IMR90	lung:	fetal
13	chr1:114696350-114696400	A549	lung:	n/a
14	chr1:114696465-114696515	HRPEpiC	eye:	n/a
15	chr1:114695695-114695745	SAEC	small airway:	n/a
16	chr1:114698322-114698372	ProgFib	skin:	n/a
17	chr1:114696671-114696721	HEEpiC	esophagus:	n/a
18	chr1:114696822-114696872	T-47D	breast:	n/a
19	chr1:114697523-114697573	AG04449	skin:	fetal
20	chr1:114697095-114697145	AG04450	lung:	fetal
21	chr1:114696698-114696748	GM12878	blood:	n/a
22	chr1:114696822-114696872	HepG2	liver:	n/a
23	chr1:114698448-114698498	HCPEpiC	choroid plexus:	n/a
24	chr1:114696946-114696996	HL-60	blood:	n/a
25	chr1:114699963-114700013	HCF	heart:	n/a
26	chr1:114697095-114697145	GM12891	blood:	n/a
27	chr1:114696465-114696515	SK-N-SH_RA	brain:	n/a
28	chr1:114661683-114661733	MCF10A-Er-Src	breast:	n/a
29	chr1:114695261-114695311	HCT-116	colon:	n/a
30	chr1:114696465-114696515	T-47D	breast:	n/a
31	chr1:114694766-114694816	PANC-1	pancreas:	n/a
32	chr1:114695695-114695745	HAEpiC	amniotic membrane:	n/a
33	chr1:114697032-114697082	HRPEpiC	eye:	n/a
34	chr1:114697095-114697145	PFSK-1	brain:	n/a
35	chr1:114696641-114696691	IMR90	lung:	fetal
36	chr1:114695527-114695577	SK-N-SH	brain:	n/a
37	chr1:114696465-114696515	PANC-1	pancreas:	n/a
38	chr1:114696798-114696848	AG09309	skin:	n/a
39	chr1:114696946-114696996	Jurkat	blood:	n/a
40	chr1:114697032-114697082	BE2_C	brain:	n/a
41	chr1:114688688-114688738	AG04449	skin:	fetal
42	chr1:114696698-114696748	T-47D	breast:	n/a
43	chr1:114697523-114697573	Jurkat	blood:	n/a
44	chr1:114696698-114696748	Jurkat	blood:	n/a
45	chr1:114695261-114695311	PANC-1	pancreas:	n/a
46	chr1:114697523-114697573	SK-N-MC	brain:	n/a
47	chr1:114696462-114696512	ovcar-3	ovarian:	n/a
48	chr1:114696822-114696872	AG10803	skin:	n/a
49	chr1:114696698-114696748	NT2-D1	testis:	n/a
50	chr1:114696465-114696515	GM12891	blood:	n/a

(count:102 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:114657959..114660485-chr1:114662733..114665313,2	K562	blood:
2	chr1:114677849..114679630-chr1:114688942..114690524,2	MCF-7	breast:
3	chr1:114751604..114753631-chr1:115123647..115125171,2	MCF-7	breast:
4	chr1:114723148..114725642-chr1:114742907..114746376,3	MCF-7	breast:
5	chr1:114744417..114746434-chr1:114750098..114751784,3	MCF-7	breast:
6	chr1:114750777..114752318-chr1:114754429..114757059,2	MCF-7	breast:
7	chr1:114669510..114672116-chr1:114711936..114714457,2	MCF-7	breast:
8	chr1:114615330..114616862-chr1:114667170..114669272,2	MCF-7	breast:
9	chr1:114716114..114718689-chr1:114719767..114721760,2	MCF-7	breast:
10	chr1:114521070..114522208-chr1:114674217..114675146,6	MCF-7	breast:
11	chr1:114684881..114688842-chr1:114690829..114695857,6	MCF-7	breast:
12	chr1:114723148..114725642-chr1:114742907..114746376,3	MCF-7	breast:
13	chr1:114698663..114702320-chr1:114718252..114722488,4	MCF-7	breast:
14	chr1:114733258..114735480-chr1:114752470..114755080,2	MCF-7	breast:
15	chr1:114732259..114734527-chr1:114740706..114742384,2	K562	blood:
16	chr1:114684518..114686701-chr1:114698316..114700716,2	MCF-7	breast:
17	chr1:114705401..114708215-chr1:114716199..114718820,2	MCF-7	breast:
18	chr1:114520969..114522226-chr1:114673733..114674829,5	K562	blood:
19	chr1:114732606..114735372-chr1:114738856..114740885,2	MCF-7	breast:
20	chr1:114687115..114689440-chr1:114797827..114800190,2	K562	blood:
21	chr1:114661550..114663719-chr20:45985524..45987686,2	MCF-7	breast:
22	chr1:114732606..114735372-chr1:114738856..114740885,2	MCF-7	breast:
23	chr1:114710365..114712206-chr1:114714931..114717792,2	K562	blood:
24	chr1:114675134..114676800-chr1:114678767..114680633,2	K562	blood:
25	chr1:114698663..114702320-chr1:114718252..114722488,4	MCF-7	breast:
26	chr1:114657401..114660243-chr1:114668370..114670843,2	MCF-7	breast:
27	chr1:114699028..114701153-chr1:114701170..114706455,4	MCF-7	breast:
28	chr1:114665325..114672766-chr1:114673434..114676917,9	MCF-7	breast:
29	chr1:114677250..114677947-chr1:114825280..114825933,3	MCF-7	breast:
30	chr1:114681745..114684788-chr1:114694658..114697586,3	MCF-7	breast:
31	chr1:114669510..114672116-chr1:114711936..114714457,2	MCF-7	breast:
32	chr1:114635427..114637656-chr1:114664752..114666679,2	MCF-7	breast:
33	chr1:114705401..114708215-chr1:114716199..114718820,2	MCF-7	breast:
34	chr1:114696093..114698234-chr1:114705284..114707767,2	MCF-7	breast:
35	chr1:114717647..114719865-chr1:114722703..114725044,2	MCF-7	breast:
36	chr1:114665567..114667964-chr1:114670324..114672192,2	MCF-7	breast:
37	chr1:114717647..114719865-chr1:114722703..114725044,2	MCF-7	breast:
38	chr1:114672992..114678074-chr1:114678214..114684542,12	MCF-7	breast:
39	chr1:114699028..114701153-chr1:114701170..114706455,4	MCF-7	breast:
40	chr1:114710835..114713716-chr1:114715514..114717991,2	MCF-7	breast:
41	chr1:114710132..114712123-chr1:114732597..114734287,2	MCF-7	breast:
42	chr1:114692056..114693583-chr1:114718033..114720675,2	MCF-7	breast:
43	chr1:114732259..114734527-chr1:114740706..114742384,2	K562	blood:
44	chr1:114710835..114713716-chr1:114715514..114717991,2	MCF-7	breast:
45	chr1:114742748..114744849-chr1:114744878..114746575,2	MCF-7	breast:
46	chr1:114672158..114674852-chr1:114696513..114699491,2	K562	blood:
47	chr1:114659207..114660324-chr1:114825081..114825855,3	MCF-7	breast:
48	chr1:114682690..114683203-chr1:114757760..114758622,2	MCF-7	breast:
49	chr1:114517042..114518719-chr1:114677287..114679478,2	MCF-7	breast:
50	chr1:114692056..114693583-chr1:114718033..114720675,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OLFML3-1	chr1:114749049-114749307	XLOC_000352
2	lnc-SYT6-3	chr1:114749049-114749307	ENSG00000232895.2

No data

Variant related genes	Relation type
SYT6	TF binding region
SYT6	CpG island
ENSG00000134207	chromatin interactions
ENSG00000214252	chromatin interactions
ENSG00000116752	chromatin interactions
ENSG00000116774	chromatin interactions
ENSG00000101040	chromatin interactions
ZNF280B	miRNA target sites

Extended variants
information (count: 3179 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:3179 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79821840	chr1:114658961-114658962	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs553322429	chr1:114658962-114658963	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs78928139	chr1:114658963-114658964	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545193148	chr1:114658964-114658965	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs564982423	chr1:114658972-114658973	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575387654	chr1:114658983-114658984	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560443529	chr1:114659012-114659013	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs149521445	chr1:114659097-114659098	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs369102156	chr1:114659106-114659107	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs187037088	chr1:114659111-114659112	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs527581247	chr1:114659152-114659153	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs192377254	chr1:114659159-114659160	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs183237100	chr1:114659191-114659192	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546147955	chr1:114659203-114659204	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs76836138	chr1:114659245-114659246	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187401378	chr1:114659257-114659258	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs114134789	chr1:114659300-114659301	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552581	chr1:114659327-114659328	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs550815862	chr1:114659333-114659334	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs114468476	chr1:114659354-114659355	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536657701	chr1:114659394-114659395	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs588983	chr1:114659419-114659420	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs190659269	chr1:114659449-114659450	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs12045868	chr1:114659451-114659452	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12048377	chr1:114659605-114659606	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs139093131	chr1:114659611-114659612	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182514558	chr1:114659642-114659643	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1872477	chr1:114659681-114659682	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs34542322	chr1:114659698-114659699	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560407449	chr1:114659707-114659708	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs560658854	chr1:114659708-114659709	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574147845	chr1:114659741-114659742	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs149932658	chr1:114659866-114659867	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs143995586	chr1:114659875-114659876	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs532115979	chr1:114659880-114659881	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs12563387	chr1:114659908-114659909	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs551813995	chr1:114659928-114659929	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs148694921	chr1:114659978-114659979	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs531024703	chr1:114660030-114660031	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs111396445	chr1:114660188-114660189	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs547693190	chr1:114660247-114660248	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs551156454	chr1:114660263-114660264	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs547717195	chr1:114660281-114660282	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs536793111	chr1:114660386-114660387	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs187114155	chr1:114660414-114660415	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs877789	chr1:114660493-114660494	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs143455576	chr1:114660516-114660517	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs17032358	chr1:114660549-114660550	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs558601226	chr1:114660550-114660551	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs575454823	chr1:114660578-114660579	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Asthma	20841430	CNVD
Aetanephric adenomas	20802469	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	21956041	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	16573809	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Breast cancer	17899364	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Melanoma	19671679	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bipolar disorder	19114987	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1070 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:114630400-114675800	Weak transcription	Pancreas	Pancrea
2	chr1:114632200-114661000	Weak transcription	Brain Germinal Matrix	brain
3	chr1:114648800-114661600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:114649400-114661000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr1:114650800-114666000	Weak transcription	Brain Hippocampus Middle	brain
6	chr1:114652000-114660600	Weak transcription	Fetal Lung	lung
7	chr1:114654800-114661600	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr1:114655600-114659200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr1:114655600-114660600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr1:114655800-114659800	Weak transcription	Fetal Muscle Leg	muscle
11	chr1:114655800-114660000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr1:114655800-114662200	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr1:114655800-114683800	Weak transcription	Right Atrium	heart
14	chr1:114656600-114661200	Strong transcription	HUES48 Cell Line	embryonic stem cell
15	chr1:114656800-114660600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr1:114656800-114660800	Strong transcription	H9 Cell Line	embryonic stem cell
17	chr1:114657000-114659800	Strong transcription	H1 Cell Line	embryonic stem cell
18	chr1:114657200-114659000	Enhancers	NHEK	skin
19	chr1:114657200-114659400	Strong transcription	HUES64 Cell Line	embryonic stem cell
20	chr1:114657200-114659800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr1:114657200-114660600	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr1:114657200-114660800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr1:114657200-114661000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr1:114657200-114661600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr1:114657200-114661800	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr1:114657400-114659400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
27	chr1:114657400-114660600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
28	chr1:114657600-114665600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr1:114657600-114665800	Weak transcription	Brain Anterior Caudate	brain
30	chr1:114657800-114660000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr1:114657800-114661600	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr1:114658200-114666200	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr1:114658600-114661600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr1:114658800-114659400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr1:114658800-114660200	Strong transcription	Fetal Brain Female	brain
36	chr1:114658800-114660600	Weak transcription	Primary hematopoietic stem cells	blood
37	chr1:114658800-114661200	Genic enhancers	HUES6 Cell Line	embryonic stem cell
38	chr1:114659400-114660400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr1:114659400-114660400	Genic enhancers	HUES64 Cell Line	embryonic stem cell
40	chr1:114659400-114662200	Genic enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr1:114659800-114660400	Genic enhancers	H1 Cell Line	embryonic stem cell
42	chr1:114659800-114661200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr1:114659800-114661400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
44	chr1:114659800-114661600	Enhancers	Fetal Muscle Leg	muscle
45	chr1:114660000-114660800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr1:114660000-114661400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
47	chr1:114660200-114677200	Weak transcription	Fetal Brain Female	brain
48	chr1:114660400-114660600	Strong transcription	HUES64 Cell Line	embryonic stem cell
49	chr1:114660400-114661200	Enhancers	Fetal Stomach	stomach
50	chr1:114660400-114662000	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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