Variant report

Variant	esv3344706
Chromosome Location	chr18:29263704-29266352
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	ATF1	chr18:29263987-29264156	K562	blood:	n/a	n/a
2	ATF2	chr18:29265483-29266189	GM12878	blood:	n/a	n/a
3	BACH1	chr18:29265299-29265942	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr18:29264840-29264850	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr18:29265013-29265618	GM12878	blood:	n/a	chr18:29265139-29265152 chr18:29265437-29265450 chr18:29265359-29265368 chr18:29265348-29265357
6	BCLAF1	chr18:29265012-29266201	GM12878	blood:	n/a	chr18:29265139-29265152 chr18:29265437-29265450 chr18:29265359-29265368 chr18:29265809-29265818 chr18:29265348-29265357 chr18:29266138-29266147
7	BCLAF1	chr18:29264660-29265486	GM12878	blood:	n/a	chr18:29265139-29265152 chr18:29264714-29264727 chr18:29265437-29265450 chr18:29265359-29265368 chr18:29264766-29264779 chr18:29265348-29265357
8	BCLAF1	chr18:29264202-29264992	GM12878	blood:	n/a	chr18:29264714-29264727 chr18:29264766-29264779
9	BHLHE40	chr18:29264735-29265593	GM12878	blood:	n/a	chr18:29265261-29265277 chr18:29265141-29265157 chr18:29265431-29265447
10	BRCA1	chr18:29263818-29263857	GM12878	blood:	n/a	n/a
11	BRCA1	chr18:29265270-29265271	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr18:29265065-29265373	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr18:29266024-29266050	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPD	chr18:29265289-29265549	HepG2	liver:	n/a	n/a
15	CHD1	chr18:29265709-29266202	GM12878	blood:	n/a	n/a
16	CHD1	chr18:29263327-29264447	GM12878	blood:	n/a	n/a
17	CHD1	chr18:29265184-29265390	H1-hESC	embryonic stem cell:	n/a	chr18:29265352-29265362
18	CHD1	chr18:29265094-29265378	GM12878	blood:	n/a	chr18:29265352-29265362
19	CHD1	chr18:29263679-29264362	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD1	chr18:29265619-29266166	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr18:29265095-29266137	GM12878	blood:	n/a	chr18:29265480-29265490 chr18:29265352-29265362
22	CHD2	chr18:29265744-29266174	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr18:29265330-29265416	HepG2	liver:	n/a	chr18:29265352-29265362
24	CHD2	chr18:29264220-29264858	GM12878	blood:	n/a	chr18:29264724-29264734
25	CHD2	chr18:29265746-29265832	HepG2	liver:	n/a	n/a
26	CHD2	chr18:29264393-29264845	Hela-S3	cervix:	n/a	chr18:29264724-29264734
27	CHD2	chr18:29264604-29264717	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr18:29265049-29265549	Hela-S3	cervix:	n/a	chr18:29265480-29265490 chr18:29265352-29265362
29	CHD2	chr18:29265497-29265519	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr18:29265169-29266087	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr18:29264957-29266094	HepG2	liver:	n/a	n/a
32	CREB1	chr18:29265054-29265694	A549	lung:	n/a	n/a
33	CREB1	chr18:29265133-29266092	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr18:29265118-29266116	GM12878	blood:	n/a	n/a
35	CTCF	chr18:29265337-29265541	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr18:29264712-29264803	GM20000	blood:	n/a	n/a
37	CTCF	chr18:29265080-29265230	GM12867	blood:	n/a	chr18:29265145-29265158
38	CTCF	chr18:29265120-29265270	HCFaa	heart:	n/a	chr18:29265145-29265158
39	CTCF	chr18:29264673-29264883	GM19239	blood:	n/a	n/a
40	CTCF	chr18:29264300-29264450	GM12875	blood:	n/a	n/a
41	CTCF	chr18:29265140-29265290	RPTEC	kidney:	n/a	chr18:29265145-29265158
42	CTCF	chr18:29265400-29265550	GM12867	blood:	n/a	n/a
43	CTCF	chr18:29264640-29264790	AoAF	blood vessel:	n/a	n/a
44	CTCF	chr18:29265140-29265290	HCM	heart:	n/a	chr18:29265145-29265158
45	CTCF	chr18:29265140-29265290	GM12874	blood:	n/a	chr18:29265145-29265158
46	CTCF	chr18:29265160-29265310	GM12874	blood:	n/a	n/a
47	CTCF	chr18:29264680-29264830	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr18:29265180-29265330	GM12865	blood:	n/a	n/a
49	CTCF	chr18:29265180-29265330	HAc	cerebellar:	n/a	n/a
50	CTCF	chr18:29265300-29265450	BJ	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29265487-29265537	SK-N-SH_RA	brain:	n/a
2	chr18:29263741-29263791	GM12891	blood:	n/a
3	chr18:29264051-29264101	AG04449	skin:	fetal
4	chr18:29265487-29265537	SK-N-MC	brain:	n/a
5	chr18:29264051-29264101	ECC-1	luminal epithelium:	n/a
6	chr18:29265840-29265890	AG09319	gingival:	n/a
7	chr18:29264431-29264481	H1-hESC	embryonic stem cell:	embryo
8	chr18:29264252-29264302	HCT-116	colon:	n/a
9	chr18:29265842-29265892	HCPEpiC	choroid plexus:	n/a
10	chr18:29264051-29264101	Jurkat	blood:	n/a
11	chr18:29265842-29265892	SK-N-SH	brain:	n/a
12	chr18:29265840-29265890	HEEpiC	esophagus:	n/a
13	chr18:29265842-29265892	PANC-1	pancreas:	n/a
14	chr18:29265840-29265890	T-47D	breast:	n/a
15	chr18:29263741-29263791	MCF10A-Er-Src	breast:	n/a
16	chr18:29264051-29264101	HCPEpiC	choroid plexus:	n/a
17	chr18:29264252-29264302	MCF10A-Er-Src	breast:	n/a
18	chr18:29265487-29265537	IMR90	lung:	fetal
19	chr18:29265840-29265890	IMR90	lung:	fetal
20	chr18:29264051-29264101	ovcar-3	ovarian:	n/a
21	chr18:29264431-29264481	AoSMC	blood vessel:	n/a
22	chr18:29264252-29264302	HEK293	kidney:	embryo
23	chr18:29265840-29265890	HAEpiC	amniotic membrane:	n/a
24	chr18:29265840-29265890	PFSK-1	brain:	n/a
25	chr18:29265487-29265537	MCF-7	breast:	n/a
26	chr18:29264431-29264481	Jurkat	blood:	n/a
27	chr18:29264431-29264481	PFSK-1	brain:	n/a
28	chr18:29264051-29264101	AG04450	lung:	fetal
29	chr18:29265840-29265890	K562	blood:	n/a
30	chr18:29265840-29265890	Jurkat	blood:	n/a
31	chr18:29263741-29263791	A549	lung:	n/a
32	chr18:29264252-29264302	BJ	skin:	n/a
33	chr18:29263741-29263791	HUVEC	blood vessel:	n/a
34	chr18:29265840-29265890	HCF	heart:	n/a
35	chr18:29263741-29263791	BE2_C	brain:	n/a
36	chr18:29264252-29264302	T-47D	breast:	n/a
37	chr18:29265842-29265892	K562	blood:	n/a
38	chr18:29264051-29264101	PANC-1	pancreas:	n/a
39	chr18:29265840-29265890	AG04450	lung:	fetal
40	chr18:29263741-29263791	HCPEpiC	choroid plexus:	n/a
41	chr18:29264051-29264101	BE2_C	brain:	n/a
42	chr18:29265842-29265892	GM19239	blood:	n/a
43	chr18:29264051-29264101	Caco-2	colon:	n/a
44	chr18:29264252-29264302	AG04449	skin:	fetal
45	chr18:29265842-29265892	NHBE	bronchial:	n/a
46	chr18:29264431-29264481	PANC-1	pancreas:	n/a
47	chr18:29264051-29264101	T-47D	breast:	n/a
48	chr18:29264252-29264302	AG09309	skin:	n/a
49	chr18:29265840-29265890	RPTEC	kidney:	n/a
50	chr18:29264051-29264101	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:56708485..56709372-chr18:29264759..29265403,2	Hela-S3	cervix:
2	chr18:29259339..29260872-chr18:29261230..29264110,2	K562	blood:
3	chr11:369439..370438-chr18:29265185..29265845,2	MCF-7	breast:
4	chr18:29235239..29238459-chr18:29263541..29266170,4	MCF-7	breast:
5	chr18:29257336..29259422-chr18:29266158..29267928,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTR-1	chr18:29264688-29267822	NONHSAT058829
2	lnc-TTR-1	chr18:29265618-29266786	ENSG00000259985.1

Variant related genes	Relation type
B4GALT6	TF binding region
ENSG00000259985	TF binding region
B4GALT6	CpG island
ENSG00000259985	CpG island
ENSG00000182272	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000118276	chromatin interactions

Extended variants
information (count: 100 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:100 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542466348	chr18:29263749-29263750	Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs144016824	chr18:29263787-29263788	Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs562540859	chr18:29263791-29263792	Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs543971671	chr18:29263855-29263856	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs577989747	chr18:29263863-29263864	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs574427228	chr18:29263903-29263904	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs562110143	chr18:29263906-29263907	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs111929456	chr18:29263918-29263919	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs12607126	chr18:29263925-29263926	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs377404178	chr18:29263959-29263960	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs548064897	chr18:29263974-29263975	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs560138756	chr18:29263982-29263983	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs8089728	chr18:29264005-29264006	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs1449082	chr18:29264028-29264029	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs148764289	chr18:29264029-29264030	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs570113857	chr18:29264047-29264048	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs77428875	chr18:29264089-29264090	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs74642195	chr18:29264090-29264091	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs78176510	chr18:29264091-29264092	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs570334050	chr18:29264108-29264109	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs368692452	chr18:29264159-29264160	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs1449081	chr18:29264182-29264183	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs200653957	chr18:29264243-29264244	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs368631936	chr18:29264245-29264246	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs534512099	chr18:29264248-29264249	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs372732035	chr18:29264252-29264253	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs368863791	chr18:29264257-29264258	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs35210437	chr18:29264296-29264297	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs577554431	chr18:29264308-29264309	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs139096016	chr18:29264332-29264333	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs538228628	chr18:29264347-29264348	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs371323148	chr18:29264355-29264356	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs143211727	chr18:29264380-29264381	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs575214468	chr18:29264403-29264404	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs142482296	chr18:29264408-29264409	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs375350444	chr18:29264432-29264433	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs561043155	chr18:29264458-29264459	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs555336195	chr18:29264461-29264462	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs574284637	chr18:29264467-29264468	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs368124348	chr18:29264498-29264499	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs560072520	chr18:29264503-29264504	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs367905480	chr18:29264524-29264525	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs192748886	chr18:29264526-29264527	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs541100959	chr18:29264532-29264533	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs139043653	chr18:29264535-29264536	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs563499609	chr18:29264550-29264551	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs374654856	chr18:29264583-29264584	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs182517788	chr18:29264600-29264601	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs549161581	chr18:29264611-29264612	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs567467376	chr18:29264647-29264648	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Esophageal squamous carcinoma	18350619	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Glioblastoma multiforme	21922591	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21297112	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	17002787	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	16912164	CNVD
Renal cell carcinoma	19150565	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19150955	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:452 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29253600-29264200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr18:29258000-29263800	Weak transcription	Thymus	Thymus
3	chr18:29258200-29263800	Weak transcription	Small Intestine	intestine
4	chr18:29259000-29264000	Weak transcription	Esophagus	oesophagus
5	chr18:29259000-29264400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr18:29259400-29263800	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr18:29259600-29263800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr18:29259600-29264000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr18:29259800-29263800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr18:29259800-29263800	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr18:29259800-29263800	Weak transcription	NHDF-Ad	bronchial
12	chr18:29260000-29263800	Weak transcription	Osteobl	bone
13	chr18:29260200-29263800	Weak transcription	Adipose Nuclei	Adipose
14	chr18:29260400-29263800	Weak transcription	Liver	Liver
15	chr18:29260400-29264200	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr18:29260600-29263800	Weak transcription	Colonic Mucosa	Colon
17	chr18:29260600-29264200	Weak transcription	Left Ventricle	heart
18	chr18:29260600-29264200	Weak transcription	Lung	lung
19	chr18:29260600-29264200	Weak transcription	Pancreas	Pancrea
20	chr18:29260800-29264000	Weak transcription	Right Ventricle	heart
21	chr18:29261000-29263800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr18:29261000-29264000	Weak transcription	Stomach Mucosa	stomach
23	chr18:29261000-29264200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr18:29261000-29264200	Weak transcription	Gastric	stomach
25	chr18:29261600-29263800	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr18:29261600-29265600	Active TSS	GM12878-XiMat	blood
27	chr18:29262000-29266200	Active TSS	ES-I3 Cell Line	embryonic stem cell
28	chr18:29262400-29265800	Active TSS	HUES48 Cell Line	embryonic stem cell
29	chr18:29262600-29264400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
30	chr18:29262600-29266400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
31	chr18:29262800-29264400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr18:29262800-29265800	Active TSS	H1 Cell Line	embryonic stem cell
33	chr18:29262800-29265800	Active TSS	H9 Cell Line	embryonic stem cell
34	chr18:29262800-29265800	Active TSS	HUES6 Cell Line	embryonic stem cell
35	chr18:29263000-29264600	Flanking Active TSS	Dnd41	blood
36	chr18:29263000-29265600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr18:29263000-29265800	Active TSS	Psoas Muscle	Psoas
38	chr18:29263000-29266000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr18:29263000-29266400	Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr18:29263200-29263800	Active TSS	Duodenum Smooth Muscle	Duodenum
41	chr18:29263200-29263800	Enhancers	Fetal Heart	heart
42	chr18:29263200-29263800	Enhancers	Fetal Lung	lung
43	chr18:29263200-29263800	Flanking Active TSS	A549	lung
44	chr18:29263200-29263800	Flanking Active TSS	HMEC	breast
45	chr18:29263200-29264000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr18:29263200-29264000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr18:29263200-29264000	Flanking Active TSS	Fetal Brain Female	brain
48	chr18:29263200-29264000	Flanking Active TSS	NHEK	skin
49	chr18:29263200-29264400	Flanking Active TSS	HUVEC	blood vessel
50	chr18:29263200-29265600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell

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