Variant report

Variant	esv3407255
Chromosome Location	chr4:95677954-95680802
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:241)
CpG islands
(count:610)
Chromatin interactive
region (count:6)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:241 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:95679125-95679401	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr4:95680774-95681087	A549	lung:	n/a	chr4:95680962-95680973 chr4:95680962-95680975 chr4:95680964-95680973 chr4:95680963-95680974 chr4:95680964-95680973 chr4:95680964-95680973 chr4:95680964-95680973
3	CEBPB	chr4:95680674-95681370	A549	lung:	n/a	chr4:95680962-95680973 chr4:95680962-95680975 chr4:95680964-95680973 chr4:95680963-95680974 chr4:95680964-95680973 chr4:95680964-95680973 chr4:95680964-95680973
4	CEBPB	chr4:95680794-95681137	A549	lung:	n/a	chr4:95680962-95680973 chr4:95680962-95680975 chr4:95680964-95680973 chr4:95680963-95680974 chr4:95680964-95680973 chr4:95680964-95680973 chr4:95680964-95680973
5	CHD1	chr4:95677993-95680028	IMR90	lung:	n/a	chr4:95679126-95679136 chr4:95679131-95679141
6	CHD2	chr4:95679975-95680315	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr4:95678813-95679126	H1-hESC	embryonic stem cell:	n/a	n/a
8	CREB1	chr4:95678728-95679047	A549	lung:	n/a	n/a
9	CTBP2	chr4:95678812-95680327	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr4:95678900-95679050	AG09309	skin:	n/a	n/a
11	CTCF	chr4:95678860-95679010	HCPEpiC	choroid plexus:	n/a	n/a
12	CTCF	chr4:95678860-95679010	HEEpiC	esophagus:	n/a	n/a
13	CTCF	chr4:95678600-95678750	BJ	skin:	n/a	n/a
14	CTCF	chr4:95678814-95679007	Fibrobl	skin:	n/a	n/a
15	CTCF	chr4:95678791-95679131	IMR90	lung:	n/a	n/a
16	CTCF	chr4:95678940-95679090	NHDF-neo	bronchial:	n/a	n/a
17	CTCF	chr4:95678860-95679010	SAEC	small airway:	n/a	n/a
18	CTCF	chr4:95678900-95679050	SAEC	small airway:	n/a	n/a
19	CTCF	chr4:95678840-95678990	Caco-2	colon:	n/a	n/a
20	CTCF	chr4:95678913-95678994	Pancreas_OC	pancreas:	n/a	n/a
21	CTCF	chr4:95678840-95678990	HVMF	connective:	n/a	n/a
22	CTCF	chr4:95678860-95679010	AG04449	skin:	n/a	n/a
23	CTCF	chr4:95678860-95679010	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr4:95678872-95678993	NHEK	skin:	n/a	n/a
25	CTCF	chr4:95678880-95679030	HRPEpiC	eye:	n/a	n/a
26	CTCF	chr4:95678860-95679010	BJ	skin:	n/a	n/a
27	CTCF	chr4:95678920-95679070	HA-sp	spinal cord:	n/a	n/a
28	CTCF	chr4:95678850-95679013	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr4:95678885-95678981	MCF-7	breast:	n/a	n/a
30	CTCF	chr4:95678900-95679050	AG09319	gingival:	n/a	n/a
31	CTCF	chr4:95678880-95679030	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr4:95678880-95679030	MCF-7	breast:	n/a	n/a
33	CTCF	chr4:95678900-95679050	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr4:95678860-95679010	AoAF	blood vessel:	n/a	n/a
35	CTCF	chr4:95678840-95678990	NHEK	skin:	n/a	n/a
36	CTCF	chr4:95678900-95679050	HMEC	breast:	n/a	n/a
37	CTCF	chr4:95678900-95679050	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr4:95678840-95678990	MCF-7	breast:	n/a	n/a
39	CTCF	chr4:95678860-95679010	Caco-2	colon:	n/a	n/a
40	CTCF	chr4:95678860-95679010	HMEC	breast:	n/a	n/a
41	CTCF	chr4:95678920-95679070	HRE	kidney:	n/a	n/a
42	CTCF	chr4:95678860-95679010	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr4:95678900-95679050	NHLF	lung:	n/a	n/a
44	CTCF	chr4:95678820-95678970	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr4:95678860-95679010	HPF	lung:	n/a	n/a
46	CTCF	chr4:95678820-95678970	BJ	skin:	n/a	n/a
47	CTCF	chr4:95678860-95679010	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr4:95678900-95679050	RPTEC	kidney:	n/a	n/a
49	CTCF	chr4:95678875-95679031	Medullo	brain:	n/a	n/a
50	CTCF	chr4:95678640-95678790	HAc	cerebellar:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:95678898-95678948	HL-60	blood:	n/a
2	chr4:95678898-95678948	Hela-S3	cervix:	n/a
3	chr4:95678939-95678989	K562	blood:	n/a
4	chr4:95678918-95678968	HCPEpiC	choroid plexus:	n/a
5	chr4:95680102-95680152	AG10803	skin:	n/a
6	chr4:95680102-95680152	MCF-7	breast:	n/a
7	chr4:95680414-95680464	AG10803	skin:	n/a
8	chr4:95679705-95679755	MCF10A-Er-Src	breast:	n/a
9	chr4:95678898-95678948	SKMC	muscle:	n/a
10	chr4:95679705-95679755	AG09309	skin:	n/a
11	chr4:95678918-95678968	NHBE	bronchial:	n/a
12	chr4:95678918-95678968	HMEC	breast:	n/a
13	chr4:95679808-95679858	SK-N-SH	brain:	n/a
14	chr4:95679381-95679431	NT2-D1	testis:	n/a
15	chr4:95679381-95679431	U87	brain:	n/a
16	chr4:95678939-95678989	HNPCEpiC	eye:	n/a
17	chr4:95678939-95678989	HRCEpiC	kidney:	n/a
18	chr4:95678918-95678968	ProgFib	skin:	n/a
19	chr4:95678817-95678867	HCM	heart:	n/a
20	chr4:95680102-95680152	AG09319	gingival:	n/a
21	chr4:95678939-95678989	BE2_C	brain:	n/a
22	chr4:95678817-95678867	AG10803	skin:	n/a
23	chr4:95680414-95680464	CMK	blood:	n/a
24	chr4:95678918-95678968	T-47D	breast:	n/a
25	chr4:95678703-95678753	Hepatocyte	liver:	n/a
26	chr4:95680102-95680152	GM19239	blood:	n/a
27	chr4:95678817-95678867	HUVEC	blood vessel:	n/a
28	chr4:95679705-95679755	HNPCEpiC	eye:	n/a
29	chr4:95679808-95679858	Hepatocyte	liver:	n/a
30	chr4:95679808-95679858	GM06990	blood:	n/a
31	chr4:95679381-95679431	GM12891	blood:	n/a
32	chr4:95678898-95678948	SAEC	small airway:	n/a
33	chr4:95678898-95678948	HIPEpiC	eye:	n/a
34	chr4:95679381-95679431	ProgFib	skin:	n/a
35	chr4:95680102-95680152	NB4	blood:	n/a
36	chr4:95678817-95678867	A549	lung:	n/a
37	chr4:95679381-95679431	HL-60	blood:	n/a
38	chr4:95678703-95678753	PANC-1	pancreas:	n/a
39	chr4:95679705-95679755	HRE	kidney:	n/a
40	chr4:95678703-95678753	HMEC	breast:	n/a
41	chr4:95678918-95678968	CMK	blood:	n/a
42	chr4:95678898-95678948	K562	blood:	n/a
43	chr4:95679705-95679755	T-47D	breast:	n/a
44	chr4:95678703-95678753	NHDF-neo	bronchial:	n/a
45	chr4:95678898-95678948	T-47D	breast:	n/a
46	chr4:95678703-95678753	HCPEpiC	choroid plexus:	n/a
47	chr4:95678939-95678989	SAEC	small airway:	n/a
48	chr4:95678703-95678753	PFSK-1	brain:	n/a
49	chr4:95678898-95678948	AG09319	gingival:	n/a
50	chr4:95678703-95678753	HNPCEpiC	eye:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:95679956..95681773-chr4:96032755..96034458,2	MCF-7	breast:
2	chr4:95679588..95681847-chr4:96013272..96015095,2	MCF-7	breast:
3	chr4:95675993..95678993-chr6:26054520..26056880,3	K562	blood:
4	chr4:95679187..95680719-chr4:95971290..95974263,2	MCF-7	breast:
5	chr4:95679939..95682877-chr4:95683215..95684845,2	MCF-7	breast:
6	chr4:95678678..95680883-chr4:96023985..96026151,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC5C-1	chr4:95678545-95679036	NONHSAT097457
2	lnc-UNC5C-1	chr4:95678545-95678684	XLOC_004019
3	lnc-UNC5C-1	chr4:95678545-95679011	XLOC_004019

No data

Variant related genes	Relation type
ENSG00000249599	TF binding region
BMPR1B	TF binding region
ENSG00000249599	CpG island
BMPR1B	CpG island
ENSG00000187837	chromatin interactions
ENSG00000138696	chromatin interactions
KIF2A	miRNA target sites

Extended variants
information (count: 92 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:92 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575572017	chr4:95678017-95678018	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs374612455	chr4:95678018-95678019	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs113220850	chr4:95678047-95678048	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs368243520	chr4:95678052-95678053	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs190926025	chr4:95678074-95678075	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs536937284	chr4:95678121-95678122	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs573279782	chr4:95678138-95678139	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs576604866	chr4:95678162-95678163	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs182154488	chr4:95678172-95678173	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs113023902	chr4:95678173-95678174	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs115792847	chr4:95678190-95678191	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs373167201	chr4:95678194-95678195	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs541419224	chr4:95678269-95678270	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs561087894	chr4:95678324-95678325	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs530467997	chr4:95678393-95678394	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs543275796	chr4:95678414-95678415	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs4348103	chr4:95678443-95678444	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs370352625	chr4:95678444-95678445	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs114473839	chr4:95678500-95678501	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs144164558	chr4:95678506-95678507	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs552774549	chr4:95678518-95678519	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs146418441	chr4:95678529-95678530	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs186439226	chr4:95678631-95678632	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs190865632	chr4:95678639-95678640	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs548208503	chr4:95678649-95678650	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs567959621	chr4:95678708-95678709	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
27	rs536976061	chr4:95678804-95678805	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
28	rs72669023	chr4:95678822-95678823	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
29	rs370566699	chr4:95678832-95678833	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
30	rs539271583	chr4:95678835-95678836	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
31	rs552845907	chr4:95678844-95678845	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
32	rs572512093	chr4:95678848-95678849	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
33	rs374593668	chr4:95678850-95678851	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
34	rs534801894	chr4:95678864-95678865	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
35	rs554997222	chr4:95678894-95678895	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
36	rs115737709	chr4:95678931-95678932	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
37	rs374976274	chr4:95679070-95679071	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs544163908	chr4:95679078-95679079	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs202068629	chr4:95679090-95679091	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs563992994	chr4:95679173-95679174	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs149673144	chr4:95679320-95679321	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs546427396	chr4:95679423-95679424	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs370399814	chr4:95679488-95679489	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs559679402	chr4:95679489-95679490	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs539479910	chr4:95679570-95679571	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs111448434	chr4:95679602-95679603	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs143954594	chr4:95679622-95679623	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs368638988	chr4:95679631-95679632	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs561757048	chr4:95679639-95679640	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs533112035	chr4:95679673-95679674	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:95676000-95678200	Weak transcription	Aorta	Aorta
2	chr4:95677400-95678000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr4:95677400-95678000	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr4:95677600-95678000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr4:95677800-95678000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr4:95677800-95678000	Enhancers	HUVEC	blood vessel
7	chr4:95677800-95678200	Enhancers	Muscle Satellite Cultured Cells	--
8	chr4:95677800-95681800	Active TSS	A549	lung
9	chr4:95678000-95678200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr4:95678000-95678200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr4:95678000-95678200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr4:95678000-95678200	Active TSS	Rectal Smooth Muscle	rectum
13	chr4:95678000-95678400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:95678000-95678400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
15	chr4:95678000-95678800	Flanking Active TSS	HUVEC	blood vessel
16	chr4:95678000-95679000	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
17	chr4:95678000-95680000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr4:95678000-95680200	Active TSS	NH-A	brain
19	chr4:95678000-95682000	Active TSS	Stomach Smooth Muscle	stomach
20	chr4:95678200-95678400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr4:95678200-95678400	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr4:95678200-95678400	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr4:95678200-95678400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
24	chr4:95678200-95678400	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
25	chr4:95678200-95678400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr4:95678200-95678400	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr4:95678200-95678400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr4:95678200-95678400	Flanking Active TSS	NHEK	skin
29	chr4:95678200-95678600	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
30	chr4:95678200-95678600	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
31	chr4:95678200-95678600	Bivalent/Poised TSS	Fetal Kidney	kidney
32	chr4:95678200-95678600	Bivalent Enhancer	NHDF-Ad	bronchial
33	chr4:95678200-95678800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
34	chr4:95678200-95678800	Bivalent Enhancer	Fetal Brain Male	brain
35	chr4:95678200-95679000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
36	chr4:95678200-95679000	Flanking Bivalent TSS/Enh	Dnd41	blood
37	chr4:95678200-95679600	Bivalent/Poised TSS	Brain Germinal Matrix	brain
38	chr4:95678200-95680000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:95678200-95680400	Active TSS	Aorta	Aorta
40	chr4:95678200-95680400	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
41	chr4:95678200-95680400	Active TSS	HMEC	breast
42	chr4:95678400-95678600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr4:95678400-95678600	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
44	chr4:95678400-95678600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
45	chr4:95678400-95678600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr4:95678400-95678600	Active TSS	Cortex derived primary cultured neurospheres	brain
47	chr4:95678400-95678600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr4:95678400-95678600	Enhancers	Brain Anterior Caudate	brain
49	chr4:95678400-95678600	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
50	chr4:95678400-95678600	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland

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