Variant report

Variant	esv3357131
Chromosome Location	chr14:105713857-105716805
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:306)
CpG islands
(count:917)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr14:105714406-105715709	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCLAF1	chr14:105714554-105714894	GM12878	blood:	n/a	chr14:105714818-105714831
3	BHLHE40	chr14:105714708-105714897	GM12878	blood:	n/a	chr14:105714722-105714738
4	BRCA1	chr14:105714576-105714669	GM12878	blood:	n/a	n/a
5	BRCA1	chr14:105714311-105714507	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD1	chr14:105714496-105714696	GM12878	blood:	n/a	n/a
7	CHD2	chr14:105714688-105714896	Hela-S3	cervix:	n/a	chr14:105714767-105714777
8	CHD2	chr14:105714441-105714842	H1-hESC	embryonic stem cell:	n/a	chr14:105714767-105714777
9	CREB1	chr14:105714545-105715112	H1-hESC	embryonic stem cell:	n/a	n/a
10	CREB1	chr14:105714633-105714984	A549	lung:	n/a	n/a
11	CREB1	chr14:105714614-105715071	ECC-1	luminal epithelium:	n/a	n/a
12	CREB1	chr14:105714484-105715182	GM12878	blood:	n/a	n/a
13	CREB1	chr14:105714486-105715078	H1-hESC	embryonic stem cell:	n/a	n/a
14	CREB1	chr14:105714431-105715408	A549	lung:	n/a	n/a
15	CTCF	chr14:105715520-105715670	HUVEC	blood vessel:	n/a	n/a
16	CTCF	chr14:105714420-105714570	GM12873	blood:	n/a	n/a
17	CTCF	chr14:105714900-105715050	GM12866	blood:	n/a	n/a
18	CTCF	chr14:105714967-105715020	Lung_OC	lung:	n/a	n/a
19	CTCF	chr14:105714786-105714841	MCF-7	breast:	n/a	n/a
20	CTCF	chr14:105714960-105715110	GM12874	blood:	n/a	n/a
21	CTCF	chr14:105714880-105715030	GM12869	blood:	n/a	n/a
22	CTCF	chr14:105714860-105715010	HMEC	breast:	n/a	n/a
23	CTCF	chr14:105714940-105715090	HA-sp	spinal cord:	n/a	n/a
24	CTCF	chr14:105715480-105715630	GM12875	blood:	n/a	n/a
25	CTCF	chr14:105714940-105715090	AG04449	skin:	n/a	n/a
26	CTCF	chr14:105714600-105714750	GM12874	blood:	n/a	n/a
27	CTCF	chr14:105714920-105715070	GM12874	blood:	n/a	n/a
28	CTCF	chr14:105714860-105715010	GM12872	blood:	n/a	n/a
29	CTCF	chr14:105715520-105715670	AG04449	skin:	n/a	n/a
30	CTCF	chr14:105714900-105715050	AG09319	gingival:	n/a	n/a
31	CTCF	chr14:105714940-105715090	HEK293	kidney:	n/a	n/a
32	CTCF	chr14:105715380-105715530	GM12864	blood:	n/a	n/a
33	CTCF	chr14:105714940-105715090	NHEK	skin:	n/a	n/a
34	CTCF	chr14:105714782-105714866	LNCaP	prostate:	n/a	n/a
35	CTCF	chr14:105714928-105715101	GM12891	blood:	n/a	n/a
36	CTCF	chr14:105714746-105714889	Spleen_OC	spleen:	n/a	n/a
37	CTCF	chr14:105714974-105715078	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr14:105714900-105715050	GM12867	blood:	n/a	n/a
39	CTCF	chr14:105714956-105715086	GM19239	blood:	n/a	n/a
40	CTCF	chr14:105715360-105715510	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr14:105714820-105714970	GM12875	blood:	n/a	n/a
42	CTCF	chr14:105714820-105714970	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr14:105714776-105715121	GM12878	blood:	n/a	n/a
44	CTCF	chr14:105715860-105716010	SAEC	small airway:	n/a	n/a
45	CTCF	chr14:105715392-105715423	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr14:105715320-105715470	GM12867	blood:	n/a	n/a
47	CTCF	chr14:105714950-105715007	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr14:105714580-105714730	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr14:105714940-105715090	GM12873	blood:	n/a	n/a
50	CTCF	chr14:105715062-105715065	GM10266	blood:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105714274-105714324	Caco-2	colon:	n/a
2	chr14:105715926-105715976	ECC-1	luminal epithelium:	n/a
3	chr14:105714274-105714324	Caco-2	colon:	n/a
4	chr14:105715926-105715976	ECC-1	luminal epithelium:	n/a
5	chr14:105714153-105714203	AG09319	gingival:	n/a
6	chr14:105714400-105714450	HRPEpiC	eye:	n/a
7	chr14:105715926-105715976	HRCEpiC	kidney:	n/a
8	chr14:105715464-105715514	MCF10A-Er-Src	breast:	n/a
9	chr14:105714833-105714883	IMR90	lung:	fetal
10	chr14:105714379-105714429	MCF10A-Er-Src	breast:	n/a
11	chr14:105714379-105714429	NH-A	brain:	n/a
12	chr14:105714274-105714324	ECC-1	luminal epithelium:	n/a
13	chr14:105716052-105716102	ovcar-3	ovarian:	n/a
14	chr14:105714589-105714639	HRPEpiC	eye:	n/a
15	chr14:105714589-105714639	H1-hESC	embryonic stem cell:	embryo
16	chr14:105714274-105714324	NT2-D1	testis:	n/a
17	chr14:105714379-105714429	ProgFib	skin:	n/a
18	chr14:105714274-105714324	HRCEpiC	kidney:	n/a
19	chr14:105714274-105714324	HCT-116	colon:	n/a
20	chr14:105715464-105715514	LNCaP	prostate:	n/a
21	chr14:105715025-105715075	AoSMC	blood vessel:	n/a
22	chr14:105715926-105715976	HEEpiC	esophagus:	n/a
23	chr14:105715464-105715514	BE2_C	brain:	n/a
24	chr14:105715926-105715976	SK-N-SH_RA	brain:	n/a
25	chr14:105714833-105714883	MCF10A-Er-Src	breast:	n/a
26	chr14:105714400-105714450	RPTEC	kidney:	n/a
27	chr14:105714589-105714639	LNCaP	prostate:	n/a
28	chr14:105715025-105715075	H1-hESC	embryonic stem cell:	embryo
29	chr14:105713866-105713916	Caco-2	colon:	n/a
30	chr14:105714833-105714883	PFSK-1	brain:	n/a
31	chr14:105714379-105714429	HRCEpiC	kidney:	n/a
32	chr14:105715926-105715976	Hepatocyte	liver:	n/a
33	chr14:105715926-105715976	GM12891	blood:	n/a
34	chr14:105714833-105714883	Jurkat	blood:	n/a
35	chr14:105714274-105714324	PFSK-1	brain:	n/a
36	chr14:105716052-105716102	AG04449	skin:	fetal
37	chr14:105714843-105714893	HepG2	liver:	n/a
38	chr14:105714846-105714896	HMEC	breast:	n/a
39	chr14:105714589-105714639	HCPEpiC	choroid plexus:	n/a
40	chr14:105714274-105714324	SK-N-MC	brain:	n/a
41	chr14:105714833-105714883	HMEC	breast:	n/a
42	chr14:105716052-105716102	U87	brain:	n/a
43	chr14:105715464-105715514	T-47D	breast:	n/a
44	chr14:105715464-105715514	HMEC	breast:	n/a
45	chr14:105715926-105715976	BJ	skin:	n/a
46	chr14:105714153-105714203	HCT-116	colon:	n/a
47	chr14:105714379-105714429	SAEC	small airway:	n/a
48	chr14:105714843-105714893	A549	lung:	n/a
49	chr14:105715464-105715514	MCF-7	breast:	n/a
50	chr14:105714404-105714454	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:105713833..105716142-chr14:105716723..105718932,2	K562	blood:
2	chr14:105633069..105635536-chr14:105714407..105716304,2	MCF-7	breast:
3	chr11:62358871..62359665-chr14:105714579..105715245,2	Hela-S3	cervix:
4	chr14:105706521..105709177-chr14:105712711..105714374,2	MCF-7	breast:
5	chr14:105713379..105716522-chr14:105764463..105769159,4	MCF-7	breast:
6	chr14:105687326..105689962-chr14:105713390..105716265,3	MCF-7	breast:

No data

Variant related genes	Relation type
BRF1	TF binding region
BTBD6	TF binding region
BRF1	CpG island
BTBD6	CpG island
ENSG00000149016	chromatin interactions
ENSG00000184887	chromatin interactions
ENSG00000255508	chromatin interactions
ENSG00000179364	chromatin interactions
ENSG00000185024	chromatin interactions
ENSG00000184916	chromatin interactions

Extended variants
information (count: 152 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:152 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185478855	chr14:105713879-105713880	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs373572870	chr14:105713929-105713930	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs587640755	chr14:105713935-105713936	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs2816653	chr14:105713973-105713974	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs587595801	chr14:105713995-105713996	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs370197383	chr14:105714026-105714027	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs587672317	chr14:105714042-105714043	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs587699605	chr14:105714053-105714054	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs117319993	chr14:105714060-105714061	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs587674548	chr14:105714140-105714141	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs587758221	chr14:105714176-105714177	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs587631487	chr14:105714180-105714181	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs587686968	chr14:105714183-105714184	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs587766682	chr14:105714192-105714193	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs73353719	chr14:105714222-105714223	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs115383169	chr14:105714255-105714256	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs376441660	chr14:105714312-105714313	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs587728014	chr14:105714321-105714322	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs587630025	chr14:105714373-105714374	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs146908013	chr14:105714379-105714380	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs587766079	chr14:105714380-105714381	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs139330909	chr14:105714457-105714458	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs587695913	chr14:105714479-105714480	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs189408651	chr14:105714532-105714533	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs587641365	chr14:105714555-105714556	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs587702693	chr14:105714564-105714565	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs587600404	chr14:105714572-105714573	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs72709738	chr14:105714588-105714589	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs370883156	chr14:105714601-105714602	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs182011505	chr14:105714656-105714657	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs587733929	chr14:105714712-105714713	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs587631312	chr14:105714740-105714741	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs587686855	chr14:105714748-105714749	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs2735818	chr14:105714751-105714752	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs587669696	chr14:105714772-105714773	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs372844536	chr14:105714773-105714774	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs2816654	chr14:105714775-105714776	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs587622684	chr14:105714812-105714813	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs587685764	chr14:105714847-105714848	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs587742730	chr14:105714848-105714849	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs587616123	chr14:105714863-105714864	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs587727144	chr14:105714865-105714866	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs150454083	chr14:105714887-105714888	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs587760631	chr14:105714907-105714908	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs587744685	chr14:105714911-105714912	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs587646414	chr14:105714945-105714946	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs113720774	chr14:105715036-105715037	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs587697366	chr14:105715045-105715046	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs186857534	chr14:105715170-105715171	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs587676941	chr14:105715237-105715238	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	20369283	CNVD

Chromatin state (count:697 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105668600-105714200	Weak transcription	HUVEC	blood vessel
2	chr14:105679800-105714000	Weak transcription	NHDF-Ad	bronchial
3	chr14:105680600-105714000	Weak transcription	Psoas Muscle	Psoas
4	chr14:105681400-105714000	Weak transcription	HSMMtube	muscle
5	chr14:105681400-105714200	Weak transcription	HSMM	muscle
6	chr14:105687200-105714000	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr14:105687400-105714200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr14:105689800-105714000	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr14:105690400-105714000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr14:105690400-105721400	Weak transcription	K562	blood
11	chr14:105691600-105714000	Weak transcription	Primary hematopoietic stem cells	blood
12	chr14:105693200-105714000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr14:105693400-105714000	Weak transcription	Primary neutrophils fromperipheralblood	blood
14	chr14:105694000-105714200	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr14:105694200-105714200	Weak transcription	Primary T cells from cord blood	blood
16	chr14:105703800-105714200	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr14:105707200-105714000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
18	chr14:105707600-105714000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr14:105707800-105714000	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr14:105708200-105714000	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr14:105708400-105714000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr14:105708400-105714000	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr14:105708600-105714000	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr14:105708600-105714000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr14:105708600-105714000	Weak transcription	Brain Substantia Nigra	brain
26	chr14:105708600-105714000	Weak transcription	Esophagus	oesophagus
27	chr14:105708600-105714000	Weak transcription	Gastric	stomach
28	chr14:105708600-105714000	Weak transcription	Ovary	ovary
29	chr14:105708600-105714200	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr14:105708600-105714200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr14:105708600-105714400	Weak transcription	Aorta	Aorta
32	chr14:105710800-105714000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr14:105711000-105714000	Weak transcription	HMEC	breast
34	chr14:105711400-105714000	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr14:105711600-105714200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr14:105711800-105714000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr14:105711800-105717000	Enhancers	Fetal Brain Male	brain
38	chr14:105712000-105714000	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr14:105712000-105714000	Strong transcription	A549	lung
40	chr14:105712000-105714200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr14:105712200-105714000	Genic enhancers	Fetal Muscle Leg	muscle
42	chr14:105712800-105714000	Weak transcription	Liver	Liver
43	chr14:105712800-105714200	Genic enhancers	Primary T cells fromperipheralblood	blood
44	chr14:105713000-105714000	Strong transcription	Fetal Intestine Small	intestine
45	chr14:105713000-105714000	Genic enhancers	Fetal Muscle Trunk	muscle
46	chr14:105713200-105714000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr14:105713200-105714000	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr14:105713200-105714000	Genic enhancers	Adipose Nuclei	Adipose
49	chr14:105713200-105714000	Strong transcription	NHLF	lung
50	chr14:105713200-105714000	Strong transcription	Osteobl	bone

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