Variant report

Variant	esv3378645
Chromosome Location	chr4:698602-700850
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:354)
CpG islands
(count:610)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:354 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr4:699601-699851	HepG2	liver:	n/a	n/a
2	BHLHE40	chr4:699172-699754	K562	blood:	n/a	n/a
3	BHLHE40	chr4:699146-699836	GM12878	blood:	n/a	n/a
4	BRCA1	chr4:699246-699395	HepG2	liver:	n/a	n/a
5	BRCA1	chr4:699438-699725	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr4:698708-699492	K562	blood:	n/a	n/a
7	CCNT2	chr4:699219-699986	K562	blood:	n/a	n/a
8	CEBPB	chr4:698750-699349	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPD	chr4:699428-699895	HepG2	liver:	n/a	n/a
10	CHD1	chr4:699022-699031	GM12878	blood:	n/a	n/a
11	CHD1	chr4:698766-700226	IMR90	lung:	n/a	n/a
12	CHD2	chr4:699329-699341	HepG2	liver:	n/a	n/a
13	CHD2	chr4:699024-699441	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr4:699122-699862	Hela-S3	cervix:	n/a	n/a
15	CHD2	chr4:699252-699802	GM12878	blood:	n/a	n/a
16	CHD2	chr4:699649-699755	K562	blood:	n/a	n/a
17	CHD2	chr4:699130-699449	K562	blood:	n/a	n/a
18	CREB1	chr4:699493-699883	A549	lung:	n/a	n/a
19	CREB1	chr4:699211-699489	A549	lung:	n/a	n/a
20	CTCF	chr4:699530-699649	Spleen_OC	spleen:	n/a	n/a
21	CTCF	chr4:700425-700439	Spleen_OC	spleen:	n/a	n/a
22	CTCF	chr4:699678-699781	K562	blood:	n/a	n/a
23	CTCF	chr4:699298-699359	GM12891	blood:	n/a	n/a
24	CTCF	chr4:699350-699496	Spleen_OC	spleen:	n/a	n/a
25	CTCF	chr4:699517-699520	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr4:699336-699337	GM19239	blood:	n/a	n/a
27	CTCF	chr4:699339-699430	GM19239	blood:	n/a	n/a
28	CTCF	chr4:700374-700398	Spleen_OC	spleen:	n/a	n/a
29	CUX1	chr4:698883-698886	K562	blood:	n/a	n/a
30	E2F4	chr4:699256-699657	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F6	chr4:699620-699950	K562	blood:	n/a	n/a
32	E2F6	chr4:699226-699595	K562	blood:	n/a	n/a
33	E2F6	chr4:699300-699616	A549	lung:	n/a	n/a
34	E2F6	chr4:699143-699600	A549	lung:	n/a	n/a
35	E2F6	chr4:699293-699550	K562	blood:	n/a	n/a
36	E2F6	chr4:699178-699874	K562	blood:	n/a	n/a
37	EGR1	chr4:699158-699815	HCT-116	colon:	n/a	chr4:699521-699535
38	EGR1	chr4:699326-699730	K562	blood:	n/a	chr4:699521-699535
39	EGR1	chr4:699344-699725	K562	blood:	n/a	chr4:699521-699535
40	EGR1	chr4:699428-699646	GM12878	blood:	n/a	chr4:699521-699535
41	EGR1	chr4:699420-699627	GM12878	blood:	n/a	chr4:699521-699535
42	ELF1	chr4:699287-700052	K562	blood:	n/a	chr4:699811-699823
43	ELF1	chr4:699528-699896	HepG2	liver:	n/a	chr4:699811-699823
44	ELF1	chr4:699089-700144	GM12878	blood:	n/a	chr4:699811-699823
45	ELF1	chr4:699497-699818	HepG2	liver:	n/a	n/a
46	ELF1	chr4:699363-700013	K562	blood:	n/a	chr4:699811-699823
47	ELK1	chr4:699127-699230	K562	blood:	n/a	n/a
48	ELK1	chr4:699167-699713	Hela-S3	cervix:	n/a	n/a
49	EP300	chr4:699214-699334	K562	blood:	n/a	n/a
50	EP300	chr4:699145-699319	HepG2	liver:	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	chr4:700219-700269	HCF	heart:	n/a
2	chr4:699386-699436	MCF10A-Er-Src	breast:	n/a
3	chr4:699950-700000	IMR90	lung:	fetal
4	chr4:699386-699436	Hepatocyte	liver:	n/a
5	chr4:700219-700269	HNPCEpiC	eye:	n/a
6	chr4:699691-699741	T-47D	breast:	n/a
7	chr4:699691-699741	HNPCEpiC	eye:	n/a
8	chr4:699691-699741	HCT-116	colon:	n/a
9	chr4:699691-699741	AG04450	lung:	fetal
10	chr4:699224-699274	PrEC	prostate:	n/a
11	chr4:699372-699422	HEEpiC	esophagus:	n/a
12	chr4:699950-700000	MCF10A-Er-Src	breast:	n/a
13	chr4:699691-699741	Jurkat	blood:	n/a
14	chr4:699401-699451	IMR90	lung:	fetal
15	chr4:699950-700000	HRE	kidney:	n/a
16	chr4:699288-699338	SK-N-SH	brain:	n/a
17	chr4:699435-699485	ProgFib	skin:	n/a
18	chr4:699401-699451	NT2-D1	testis:	n/a
19	chr4:699386-699436	ovcar-3	ovarian:	n/a
20	chr4:699372-699422	IMR90	lung:	fetal
21	chr4:698616-698666	IMR90	lung:	fetal
22	chr4:699372-699422	BE2_C	brain:	n/a
23	chr4:698616-698666	NHBE	bronchial:	n/a
24	chr4:700219-700269	HEEpiC	esophagus:	n/a
25	chr4:699386-699436	AG09309	skin:	n/a
26	chr4:699691-699741	HL-60	blood:	n/a
27	chr4:699372-699422	HRCEpiC	kidney:	n/a
28	chr4:699372-699422	BJ	skin:	n/a
29	chr4:699435-699485	HRCEpiC	kidney:	n/a
30	chr4:698616-698666	HL-60	blood:	n/a
31	chr4:699950-700000	GM12892	blood:	n/a
32	chr4:699950-700000	AG10803	skin:	n/a
33	chr4:699435-699485	HCPEpiC	choroid plexus:	n/a
34	chr4:699288-699338	NB4	blood:	n/a
35	chr4:699950-700000	AG09309	skin:	n/a
36	chr4:699288-699338	Hepatocyte	liver:	n/a
37	chr4:699372-699422	CMK	blood:	n/a
38	chr4:699224-699274	Hela-S3	cervix:	n/a
39	chr4:699224-699274	ECC-1	luminal epithelium:	n/a
40	chr4:699401-699451	ovcar-3	ovarian:	n/a
41	chr4:699435-699485	NT2-D1	testis:	n/a
42	chr4:698616-698666	BE2_C	brain:	n/a
43	chr4:699372-699422	HMEC	breast:	n/a
44	chr4:699386-699436	U87	brain:	n/a
45	chr4:699386-699436	HCM	heart:	n/a
46	chr4:700219-700269	AG09309	skin:	n/a
47	chr4:699691-699741	LNCaP	prostate:	n/a
48	chr4:699435-699485	IMR90	lung:	fetal
49	chr4:699950-700000	HIPEpiC	eye:	n/a
50	chr4:699950-700000	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr4:700678..704217-chr4:710705..714201,3	MCF-7	breast:
2	chr4:694824..697589-chr4:697861..699485,2	K562	blood:
3	chr4:672883..676399-chr4:697081..701106,5	MCF-7	breast:
4	chr4:666295..671517-chr4:698228..703248,8	MCF-7	breast:
5	chr4:679574..681875-chr4:700268..702006,2	K562	blood:
6	chr4:684700..687240-chr4:700658..702428,2	MCF-7	breast:
7	chr4:691381..694386-chr4:695506..698892,4	K562	blood:
8	chr4:699605..701232-chr4:847515..849852,2	K562	blood:
9	chr4:666011..668174-chr4:698640..701171,3	K562	blood:
10	chr4:700770..703438-chr4:730148..732108,2	K562	blood:
11	chr4:672428..678608-chr4:693605..699154,7	MCF-7	breast:
12	chr4:693289..694985-chr4:696803..698794,2	MCF-7	breast:
13	chr4:674123..676409-chr4:700716..703557,3	K562	blood:
14	chr4:696628..698929-chr4:713327..715075,2	MCF-7	breast:
15	chr4:680242..683670-chr4:697022..701034,8	MCF-7	breast:
16	chr17:73773135..73777353-chr4:698527..702357,3	MCF-7	breast:
17	chr4:679478..681319-chr4:699446..701129,2	K562	blood:
18	chr4:682326..684833-chr4:700614..702994,2	MCF-7	breast:
19	chr4:681383..683193-chr4:698223..700658,3	K562	blood:
20	chr4:681693..683683-chr4:698278..699853,2	K562	blood:
21	chr4:697549..703820-chr4:770860..775722,9	K562	blood:
22	chr4:666292..671732-chr4:694079..701503,8	MCF-7	breast:
23	chr4:673479..675144-chr4:696764..699498,2	K562	blood:

No data

Variant related genes	Relation type
PCGF3	TF binding region
PCGF3	CpG island
ENSG00000132475	chromatin interactions
ENSG00000178950	chromatin interactions
ENSG00000215375	chromatin interactions
ENSG00000169020	chromatin interactions
ENSG00000169026	chromatin interactions
ENSG00000249592	chromatin interactions

Extended variants
information (count: 116 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:116 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs578029555	chr4:698610-698611	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs374977801	chr4:698611-698612	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs545331644	chr4:698614-698615	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs60170002	chr4:698617-698618	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs575154539	chr4:698626-698627	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs187557924	chr4:698628-698629	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs560856100	chr4:698629-698630	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs111232186	chr4:698630-698631	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs577860122	chr4:698648-698649	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs559527277	chr4:698658-698659	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs192505500	chr4:698662-698663	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs551677607	chr4:698664-698665	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs373071608	chr4:698667-698668	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs28639727	chr4:698678-698679	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs530843994	chr4:698690-698691	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs549435589	chr4:698691-698692	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs567701436	chr4:698692-698693	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs6844082	chr4:698699-698700	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs553163290	chr4:698722-698723	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs571471216	chr4:698724-698725	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs538909553	chr4:698742-698743	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs371078500	chr4:698752-698753	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs545340308	chr4:698755-698756	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs556992471	chr4:698782-698783	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs575163312	chr4:698785-698786	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs112237461	chr4:698788-698789	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs111873435	chr4:698791-698792	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs184318732	chr4:698800-698801	Bivalent/Poised TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs189091737	chr4:698845-698846	Bivalent/Poised TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs147746823	chr4:698850-698851	Bivalent/Poised TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs140983184	chr4:698869-698870	Bivalent/Poised TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs554427596	chr4:698874-698875	Bivalent/Poised TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs547427519	chr4:698887-698888	Bivalent/Poised TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs539940447	chr4:698903-698904	Bivalent/Poised TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs373948669	chr4:698955-698956	Bivalent/Poised TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs572825684	chr4:698968-698969	Bivalent/Poised TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs144918426	chr4:698986-698987	Bivalent/Poised TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs111792032	chr4:699052-699053	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs192879234	chr4:699131-699132	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs540477310	chr4:699160-699161	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs117507244	chr4:699173-699174	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs74282736	chr4:699216-699217	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs79086820	chr4:699217-699218	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs547138502	chr4:699219-699220	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs571434266	chr4:699234-699235	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs538872076	chr4:699251-699252	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs557201174	chr4:699252-699253	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs112036919	chr4:699264-699265	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs370804338	chr4:699278-699279	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs569105970	chr4:699293-699294	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:480 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:683600-699000	Weak transcription	Right Atrium	heart
2	chr4:684200-699000	Weak transcription	Right Ventricle	heart
3	chr4:693400-698800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr4:693600-698800	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr4:693600-698800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr4:693600-698800	Weak transcription	Hela-S3	cervix
7	chr4:693800-698800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr4:693800-698800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr4:693800-698800	Weak transcription	Liver	Liver
10	chr4:694000-698800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:694000-698800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr4:694000-698800	Weak transcription	Primary B cells from cord blood	blood
13	chr4:694000-698800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr4:694000-698800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr4:694000-698800	Weak transcription	Fetal Thymus	thymus
16	chr4:694000-698800	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr4:694000-699000	Weak transcription	GM12878-XiMat	blood
18	chr4:694200-698800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr4:694200-699000	Weak transcription	Primary hematopoietic stem cells	blood
20	chr4:694600-698800	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr4:694800-698800	Weak transcription	Duodenum Mucosa	Duodenum
22	chr4:694800-699000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr4:695000-699000	Weak transcription	Brain Angular Gyrus	brain
24	chr4:696000-699000	Enhancers	Stomach Mucosa	stomach
25	chr4:697000-698800	Weak transcription	NHEK	skin
26	chr4:697000-699000	Weak transcription	Fetal Intestine Large	intestine
27	chr4:697000-699000	Enhancers	K562	blood
28	chr4:697200-699000	Enhancers	Spleen	Spleen
29	chr4:697400-698800	Weak transcription	Brain Anterior Caudate	brain
30	chr4:697400-699000	Weak transcription	Brain Hippocampus Middle	brain
31	chr4:697600-699000	Enhancers	Placenta	Placenta
32	chr4:697800-699000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr4:697800-699000	Enhancers	Gastric	stomach
34	chr4:698000-699000	Enhancers	Esophagus	oesophagus
35	chr4:698200-698800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr4:698200-699000	Enhancers	Primary T cells fromperipheralblood	blood
37	chr4:698200-699000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr4:698200-699000	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr4:698400-698800	Bivalent Enhancer	HepG2	liver
40	chr4:698400-699000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr4:698400-699000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr4:698400-699000	Active TSS	Brain Germinal Matrix	brain
43	chr4:698400-699000	Active TSS	Colonic Mucosa	Colon
44	chr4:698400-699000	Enhancers	Lung	lung
45	chr4:698400-699000	Enhancers	Pancreas	Pancrea
46	chr4:698600-698800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
47	chr4:698600-698800	Active TSS	Breast Myoepithelial Primary Cells	Breast
48	chr4:698600-698800	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr4:698600-698800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr4:698600-698800	Enhancers	Primary T helper cells fromperipheralblood	blood

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