Variant report

Variant	esv3341035
Chromosome Location	chr14:77964024-77966572
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:161)
CpG islands
(count:612)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:161 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:77965496-77965500	HepG2	liver:	n/a	n/a
2	BACH1	chr14:77965341-77965392	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr14:77964532-77965066	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr14:77964938-77965566	HepG2	liver:	n/a	n/a
5	CEBPD	chr14:77965258-77965545	HepG2	liver:	n/a	n/a
6	CHD2	chr14:77964996-77965009	HepG2	liver:	n/a	n/a
7	CHD2	chr14:77966274-77966671	HepG2	liver:	n/a	n/a
8	CTCF	chr14:77965040-77965090	GM19240	blood:	n/a	n/a
9	CTCF	chr14:77964420-77964570	HepG2	liver:	n/a	n/a
10	CTCF	chr14:77965058-77965112	GM10248	blood:	n/a	n/a
11	CTCF	chr14:77965023-77965170	MCF-7	breast:	n/a	n/a
12	CTCF	chr14:77965018-77965221	K562	blood:	n/a	n/a
13	CTCF	chr14:77965460-77965610	AG04449	skin:	n/a	n/a
14	CTCF	chr14:77965000-77965150	AG04449	skin:	n/a	n/a
15	CTCF	chr14:77965058-77965093	MCF-7	breast:	n/a	n/a
16	CTCF	chr14:77965000-77965150	GM12865	blood:	n/a	n/a
17	CTCF	chr14:77965049-77965141	GM19238	blood:	n/a	n/a
18	CTCF	chr14:77965000-77965150	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr14:77965000-77965150	GM12864	blood:	n/a	n/a
20	CTCF	chr14:77965071-77965121	NHEK	skin:	n/a	n/a
21	CTCF	chr14:77965024-77965142	MCF-7	breast:	n/a	n/a
22	CTCF	chr14:77965052-77965148	GM12891	blood:	n/a	n/a
23	CTCF	chr14:77965010-77965179	MCF-7	breast:	n/a	n/a
24	CTCF	chr14:77965060-77965210	HCM	heart:	n/a	n/a
25	CTCF	chr14:77965054-77965194	GM19239	blood:	n/a	n/a
26	CTCF	chr14:77964899-77965256	K562	blood:	n/a	n/a
27	CTCF	chr14:77966086-77966159	GM20000	blood:	n/a	n/a
28	CTCF	chr14:77965080-77965230	GM12874	blood:	n/a	n/a
29	E2F6	chr14:77964874-77965258	K562	blood:	n/a	n/a
30	E2F6	chr14:77964526-77965842	H1-hESC	embryonic stem cell:	n/a	chr14:77965434-77965446
31	E2F6	chr14:77964730-77965409	A549	lung:	n/a	n/a
32	E2F6	chr14:77964887-77965273	K562	blood:	n/a	n/a
33	E2F6	chr14:77964833-77965346	A549	lung:	n/a	n/a
34	E2F6	chr14:77965430-77965563	K562	blood:	n/a	chr14:77965434-77965446
35	E2F6	chr14:77964415-77965951	H1-hESC	embryonic stem cell:	n/a	chr14:77964513-77964523 chr14:77965434-77965446
36	EBF1	chr14:77966396-77966624	GM12878	blood:	n/a	n/a
37	EGR1	chr14:77965069-77965282	K562	blood:	n/a	chr14:77965210-77965223
38	ELF1	chr14:77964675-77965824	GM12878	blood:	n/a	n/a
39	EP300	chr14:77965272-77965602	HepG2	liver:	n/a	chr14:77965482-77965491
40	EP300	chr14:77964422-77964536	HepG2	liver:	n/a	chr14:77964507-77964523
41	EP300	chr14:77965489-77965680	HepG2	liver:	n/a	n/a
42	FOSL2	chr14:77966226-77966753	HepG2	liver:	n/a	chr14:77966540-77966548 chr14:77966540-77966547 chr14:77966541-77966552
43	FOXA1	chr14:77965090-77965643	HepG2	liver:	n/a	n/a
44	GABPA	chr14:77964619-77965205	H1-hESC	embryonic stem cell:	n/a	n/a
45	GTF2F1	chr14:77965112-77965138	H1-hESC	embryonic stem cell:	n/a	n/a
46	HDAC2	chr14:77964455-77965573	HepG2	liver:	n/a	chr14:77965311-77965320
47	HDAC2	chr14:77964842-77965901	MCF-7	breast:	n/a	chr14:77965614-77965623 chr14:77965311-77965320
48	HEY1	chr14:77964808-77965870	HepG2	liver:	n/a	n/a
49	HEY1	chr14:77966024-77967040	HepG2	liver:	n/a	n/a
50	HEY1	chr14:77964876-77965218	HepG2	liver:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:77965757-77965807	HL-60	blood:	n/a
2	chr14:77964542-77964592	GM12891	blood:	n/a
3	chr14:77965757-77965807	HL-60	blood:	n/a
4	chr14:77964542-77964592	GM12891	blood:	n/a
5	chr14:77965757-77965807	AG10803	skin:	n/a
6	chr14:77965284-77965334	HUVEC	blood vessel:	n/a
7	chr14:77965123-77965173	AoSMC	blood vessel:	n/a
8	chr14:77964712-77964762	HEEpiC	esophagus:	n/a
9	chr14:77964712-77964762	PANC-1	pancreas:	n/a
10	chr14:77964712-77964762	LNCaP	prostate:	n/a
11	chr14:77965313-77965363	NHBE	bronchial:	n/a
12	chr14:77965284-77965334	GM06990	blood:	n/a
13	chr14:77965284-77965334	T-47D	breast:	n/a
14	chr14:77964542-77964592	SK-N-SH_RA	brain:	n/a
15	chr14:77965859-77965909	MCF10A-Er-Src	breast:	n/a
16	chr14:77965284-77965334	HL-60	blood:	n/a
17	chr14:77966530-77966580	HEEpiC	esophagus:	n/a
18	chr14:77964712-77964762	NHBE	bronchial:	n/a
19	chr14:77965869-77965919	GM19239	blood:	n/a
20	chr14:77964542-77964592	AG04450	lung:	fetal
21	chr14:77965313-77965363	K562	blood:	n/a
22	chr14:77965859-77965909	GM12891	blood:	n/a
23	chr14:77966530-77966580	HCPEpiC	choroid plexus:	n/a
24	chr14:77964712-77964762	HRPEpiC	eye:	n/a
25	chr14:77965869-77965919	HCPEpiC	choroid plexus:	n/a
26	chr14:77965284-77965334	LNCaP	prostate:	n/a
27	chr14:77965859-77965909	HRPEpiC	eye:	n/a
28	chr14:77965313-77965363	GM19239	blood:	n/a
29	chr14:77965284-77965334	HMEC	breast:	n/a
30	chr14:77965859-77965909	NHDF-neo	bronchial:	n/a
31	chr14:77965757-77965807	ProgFib	skin:	n/a
32	chr14:77966530-77966580	IMR90	lung:	fetal
33	chr14:77965859-77965909	HIPEpiC	eye:	n/a
34	chr14:77965123-77965173	AG09309	skin:	n/a
35	chr14:77964712-77964762	SAEC	small airway:	n/a
36	chr14:77965757-77965807	GM06990	blood:	n/a
37	chr14:77965391-77965441	BJ	skin:	n/a
38	chr14:77965859-77965909	SKMC	muscle:	n/a
39	chr14:77964542-77964592	ECC-1	luminal epithelium:	n/a
40	chr14:77965859-77965909	AG10803	skin:	n/a
41	chr14:77965313-77965363	HIPEpiC	eye:	n/a
42	chr14:77965391-77965441	Jurkat	blood:	n/a
43	chr14:77965869-77965919	PrEC	prostate:	n/a
44	chr14:77964712-77964762	U87	brain:	n/a
45	chr14:77965284-77965334	PANC-1	pancreas:	n/a
46	chr14:77965757-77965807	CMK	blood:	n/a
47	chr14:77965391-77965441	HepG2	liver:	n/a
48	chr14:77965123-77965173	AG04449	skin:	fetal
49	chr14:77966530-77966580	ECC-1	luminal epithelium:	n/a
50	chr14:77965391-77965441	SAEC	small airway:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:77786622..77788558-chr14:77966272..77968373,2	MCF-7	breast:
2	chr14:77924153..77926705-chr14:77962100..77964578,3	MCF-7	breast:
3	chr14:77924491..77927029-chr14:77963244..77966693,3	MCF-7	breast:
4	chr14:77929404..77931486-chr14:77963841..77966397,2	MCF-7	breast:
5	chr14:77955188..77957338-chr14:77963090..77964747,2	MCF-7	breast:

No data

Variant related genes	Relation type
ISM2	TF binding region
ISM2	CpG island
ENSG00000100591	chromatin interactions
ENSG00000009830	chromatin interactions
ENSG00000100577	chromatin interactions
ENSG00000151445	chromatin interactions

Extended variants
information (count: 93 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:93 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576754844	chr14:77964032-77964033	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs545885845	chr14:77964054-77964055	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs7159348	chr14:77964082-77964083	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs8020952	chr14:77964088-77964089	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs189473046	chr14:77964096-77964097	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs576200634	chr14:77964098-77964099	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs181796846	chr14:77964100-77964101	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs375618963	chr14:77964104-77964105	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs369357689	chr14:77964112-77964113	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs6574377	chr14:77964116-77964117	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs377364550	chr14:77964120-77964121	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs370464824	chr14:77964124-77964125	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs542079083	chr14:77964133-77964134	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs187028051	chr14:77964137-77964138	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs191468581	chr14:77964148-77964149	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs181773287	chr14:77964152-77964153	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs146056177	chr14:77964171-77964172	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs144616672	chr14:77964182-77964183	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs547703030	chr14:77964214-77964215	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs12895900	chr14:77964248-77964249	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs114136549	chr14:77964316-77964317	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs374426443	chr14:77964341-77964342	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs532358263	chr14:77964347-77964348	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs377695231	chr14:77964429-77964430	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs3742727	chr14:77964460-77964461	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs569221347	chr14:77964468-77964469	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs11851856	chr14:77964500-77964501	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs548402978	chr14:77964602-77964603	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs568314200	chr14:77964648-77964649	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs12434449	chr14:77964661-77964662	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs80142751	chr14:77964666-77964667	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs368399977	chr14:77964679-77964680	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs576793126	chr14:77964705-77964706	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs528894071	chr14:77964710-77964711	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs142628021	chr14:77964764-77964765	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs556108016	chr14:77964824-77964825	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs370688761	chr14:77964869-77964870	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs541939979	chr14:77964954-77964955	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs114330715	chr14:77964957-77964958	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs572228822	chr14:77965032-77965033	Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs541322899	chr14:77965035-77965036	Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs12431905	chr14:77965094-77965095	Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs532557527	chr14:77965098-77965099	Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs373560078	chr14:77965101-77965102	Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs562878967	chr14:77965220-77965221	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs8006951	chr14:77965304-77965305	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs548269575	chr14:77965322-77965323	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' 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
48	rs568326542	chr14:77965337-77965338	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' 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
49	rs12431925	chr14:77965339-77965340	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs548083852	chr14:77965362-77965363	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' 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

Variant related diseases (count:74)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Hepatocellular carcinoma	16750200	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Biliary cancer	19435499	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Intracranial aneurysm	16715129	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	22209245	CNVD
Prostate cancer	22553170	CNVD
Cancer	20164919	CNVD

Chromatin state (count:408 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:77953400-77964200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:77962200-77964400	Weak transcription	Right Atrium	heart
3	chr14:77963200-77964200	Active TSS	HepG2	liver
4	chr14:77964000-77964200	Enhancers	Brain Anterior Caudate	brain
5	chr14:77964000-77964200	Active TSS	Placenta	Placenta
6	chr14:77964200-77964400	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr14:77964200-77964400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr14:77964200-77964400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr14:77964200-77964400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
10	chr14:77964200-77964400	Bivalent Enhancer	Primary B cells from cord blood	blood
11	chr14:77964200-77964400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
12	chr14:77964200-77964400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
13	chr14:77964200-77964400	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
14	chr14:77964200-77964400	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr14:77964200-77964400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
16	chr14:77964200-77964400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr14:77964200-77964400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr14:77964200-77964400	Flanking Bivalent TSS/Enh	Muscle Satellite Cultured Cells	--
19	chr14:77964200-77964400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
20	chr14:77964200-77964400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr14:77964200-77964400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr14:77964200-77964400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr14:77964200-77964400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr14:77964200-77964400	Bivalent Enhancer	Adipose Nuclei	Adipose
25	chr14:77964200-77964400	Enhancers	Brain Angular Gyrus	brain
26	chr14:77964200-77964400	Bivalent Enhancer	Brain Hippocampus Middle	brain
27	chr14:77964200-77964400	Bivalent/Poised TSS	Colonic Mucosa	Colon
28	chr14:77964200-77964400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
29	chr14:77964200-77964400	Bivalent Enhancer	Fetal Intestine Large	intestine
30	chr14:77964200-77964400	Bivalent Enhancer	Fetal Intestine Small	intestine
31	chr14:77964200-77964400	Flanking Active TSS	Placenta	Placenta
32	chr14:77964200-77964400	Bivalent Enhancer	Fetal Thymus	thymus
33	chr14:77964200-77964400	Enhancers	Lung	lung
34	chr14:77964200-77964400	Enhancers	Placenta Amnion	Placenta Amnion
35	chr14:77964200-77964400	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
36	chr14:77964200-77964400	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
37	chr14:77964200-77964400	Enhancers	Right Ventricle	heart
38	chr14:77964200-77964400	Bivalent Enhancer	Thymus	Thymus
39	chr14:77964200-77964600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
40	chr14:77964200-77964600	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
41	chr14:77964200-77964600	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
42	chr14:77964200-77964600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
43	chr14:77964200-77964600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
44	chr14:77964200-77964600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
45	chr14:77964200-77964600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr14:77964200-77964600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr14:77964200-77964600	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
48	chr14:77964200-77964600	Bivalent/Poised TSS	Fetal Kidney	kidney
49	chr14:77964200-77964600	Bivalent Enhancer	Fetal Muscle Leg	muscle
50	chr14:77964200-77964600	Bivalent Enhancer	Fetal Stomach	stomach

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