Variant report

Variant	esv3357417
Chromosome Location	chr14:67980624-67983572
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:140)
CpG islands
(count:734)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:140 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr14:67982506-67982510	K562	blood:	n/a	n/a
2	BRCA1	chr14:67981672-67981768	Hela-S3	cervix:	n/a	n/a
3	BRCA1	chr14:67980900-67981007	H1-hESC	embryonic stem cell:	n/a	n/a
4	CCNT2	chr14:67981433-67981901	K562	blood:	n/a	chr14:67981809-67981818
5	CHD2	chr14:67981380-67982108	Hela-S3	cervix:	n/a	chr14:67981903-67981913 chr14:67981946-67981956
6	CHD2	chr14:67981488-67981752	GM12878	blood:	n/a	n/a
7	CHD2	chr14:67982200-67982334	GM12878	blood:	n/a	n/a
8	CTCF	chr14:67982337-67982387	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr14:67982314-67982393	GM19238	blood:	n/a	n/a
10	CTCF	chr14:67981850-67981911	MCF-7	breast:	n/a	n/a
11	CTCF	chr14:67982200-67982350	GM12871	blood:	n/a	n/a
12	CTCF	chr14:67982220-67982370	SK-N-SH_RA	brain:	n/a	n/a
13	CTCF	chr14:67981760-67981910	SK-N-SH_RA	brain:	n/a	n/a
14	CTCF	chr14:67982313-67982389	Spleen_OC	spleen:	n/a	n/a
15	CTCF	chr14:67981740-67981890	SAEC	small airway:	n/a	n/a
16	CTCF	chr14:67981871-67981967	MCF-7	breast:	n/a	n/a
17	CTCF	chr14:67982220-67982370	HMEC	breast:	n/a	n/a
18	CTCF	chr14:67982333-67982413	GM12891	blood:	n/a	n/a
19	CTCF	chr14:67981040-67981190	BJ	skin:	n/a	n/a
20	CTCF	chr14:67981785-67981859	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr14:67981060-67981210	HMEC	breast:	n/a	n/a
22	CTCF	chr14:67982180-67982330	GM12868	blood:	n/a	n/a
23	CTCF	chr14:67982180-67982330	GM12871	blood:	n/a	n/a
24	CTCF	chr14:67982540-67982690	GM12872	blood:	n/a	n/a
25	CTCF	chr14:67982280-67982430	GM12874	blood:	n/a	n/a
26	CTCF	chr14:67981998-67982009	GM12892	blood:	n/a	n/a
27	CTCF	chr14:67982320-67982470	GM12867	blood:	n/a	n/a
28	CTCF	chr14:67982326-67982331	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr14:67982348-67982383	GM19239	blood:	n/a	n/a
30	CTCF	chr14:67981760-67981910	GM12874	blood:	n/a	n/a
31	CTCF	chr14:67982394-67982397	Spleen_OC	spleen:	n/a	n/a
32	CTCF	chr14:67981872-67981929	MCF-7	breast:	n/a	n/a
33	CTCF	chr14:67982273-67982378	GM19240	blood:	n/a	n/a
34	CTCF	chr14:67982040-67982190	GM12873	blood:	n/a	n/a
35	CTCF	chr14:67982240-67982390	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr14:67982280-67982430	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr14:67982260-67982410	GM12874	blood:	n/a	n/a
38	CTCF	chr14:67981040-67981190	HRE	kidney:	n/a	n/a
39	CTCF	chr14:67981760-67981910	GM12869	blood:	n/a	n/a
40	CTCF	chr14:67982180-67982330	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr14:67982260-67982410	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr14:67982388-67982444	GM19239	blood:	n/a	n/a
43	CTCF	chr14:67981900-67982050	GM12865	blood:	n/a	n/a
44	CTCF	chr14:67982010-67982035	GM12892	blood:	n/a	n/a
45	CTCF	chr14:67981820-67981970	GM12869	blood:	n/a	n/a
46	CTCF	chr14:67982260-67982410	GM12866	blood:	n/a	n/a
47	CTCF	chr14:67982306-67982396	MCF-7	breast:	n/a	n/a
48	CTCF	chr14:67982446-67982451	GM19239	blood:	n/a	n/a
49	E2F6	chr14:67982134-67982249	K562	blood:	n/a	n/a
50	E2F6	chr14:67981799-67982042	K562	blood:	n/a	chr14:67981945-67981957 chr14:67981948-67981957

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:67982149-67982199	A549	lung:	n/a
2	chr14:67983484-67983534	HUVEC	blood vessel:	n/a
3	chr14:67982149-67982199	A549	lung:	n/a
4	chr14:67983484-67983534	HUVEC	blood vessel:	n/a
5	chr14:67981876-67981926	NH-A	brain:	n/a
6	chr14:67981637-67981687	Caco-2	colon:	n/a
7	chr14:67982170-67982220	HRPEpiC	eye:	n/a
8	chr14:67982430-67982480	PrEC	prostate:	n/a
9	chr14:67982430-67982480	RPTEC	kidney:	n/a
10	chr14:67982149-67982199	SKMC	muscle:	n/a
11	chr14:67982149-67982199	SK-N-SH	brain:	n/a
12	chr14:67981637-67981687	BE2_C	brain:	n/a
13	chr14:67981637-67981687	HMEC	breast:	n/a
14	chr14:67981876-67981926	BJ	skin:	n/a
15	chr14:67982430-67982480	HIPEpiC	eye:	n/a
16	chr14:67982149-67982199	AG09309	skin:	n/a
17	chr14:67982176-67982226	U87	brain:	n/a
18	chr14:67981515-67981565	ECC-1	luminal epithelium:	n/a
19	chr14:67982149-67982199	GM12892	blood:	n/a
20	chr14:67982176-67982226	ECC-1	luminal epithelium:	n/a
21	chr14:67982176-67982226	NH-A	brain:	n/a
22	chr14:67982430-67982480	Hela-S3	cervix:	n/a
23	chr14:67982430-67982480	GM12891	blood:	n/a
24	chr14:67981637-67981687	HEEpiC	esophagus:	n/a
25	chr14:67982198-67982248	HCF	heart:	n/a
26	chr14:67981637-67981687	IMR90	lung:	fetal
27	chr14:67981876-67981926	HCM	heart:	n/a
28	chr14:67982170-67982220	MCF10A-Er-Src	breast:	n/a
29	chr14:67982176-67982226	HMEC	breast:	n/a
30	chr14:67982149-67982199	SK-N-SH_RA	brain:	n/a
31	chr14:67981876-67981926	HRCEpiC	kidney:	n/a
32	chr14:67981515-67981565	Caco-2	colon:	n/a
33	chr14:67982456-67982506	BJ	skin:	n/a
34	chr14:67981876-67981926	GM12878	blood:	n/a
35	chr14:67981637-67981687	HRCEpiC	kidney:	n/a
36	chr14:67982170-67982220	HUVEC	blood vessel:	n/a
37	chr14:67981515-67981565	HMEC	breast:	n/a
38	chr14:67982456-67982506	NHBE	bronchial:	n/a
39	chr14:67983484-67983534	IMR90	lung:	fetal
40	chr14:67983484-67983534	HIPEpiC	eye:	n/a
41	chr14:67981637-67981687	HCPEpiC	choroid plexus:	n/a
42	chr14:67981637-67981687	NHBE	bronchial:	n/a
43	chr14:67981876-67981926	U87	brain:	n/a
44	chr14:67982170-67982220	HNPCEpiC	eye:	n/a
45	chr14:67982146-67982196	ECC-1	luminal epithelium:	n/a
46	chr14:67982176-67982226	Jurkat	blood:	n/a
47	chr14:67982149-67982199	HEEpiC	esophagus:	n/a
48	chr14:67981637-67981687	SK-N-MC	brain:	n/a
49	chr14:67982430-67982480	HMEC	breast:	n/a
50	chr14:67982198-67982248	PANC-1	pancreas:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:67946481..67947300-chr14:67979982..67980806,3	MCF-7	breast:
2	chr14:67953824..67955734-chr14:67983233..67985363,2	MCF-7	breast:
3	chr14:67954053..67956925-chr14:67980005..67982672,2	MCF-7	breast:
4	chr14:67982264..67984804-chr14:68036407..68038355,2	MCF-7	breast:
5	chr14:67981257..67983579-chr14:67998739..68001743,3	MCF-7	breast:
6	chr14:67981445..67983281-chr15:99192294..99193975,2	MCF-7	breast:
7	chr14:67980933..67983898-chr14:67998089..68001326,3	MCF-7	breast:

No data

Variant related genes	Relation type
TMEM229B	TF binding region
TMEM229B	CpG island
ENSG00000198133	chromatin interactions
ENSG00000054690	chromatin interactions
ENSG00000140443	chromatin interactions

Extended variants
information (count: 105 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:105 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567429408	chr14:67980631-67980632	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs530519372	chr14:67980704-67980705	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs116955605	chr14:67980708-67980709	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs553334399	chr14:67980770-67980771	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs374007804	chr14:67980804-67980805	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs192065946	chr14:67980831-67980832	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs557648154	chr14:67980880-67980881	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs575802111	chr14:67980897-67980898	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs543453167	chr14:67980932-67980933	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs555395946	chr14:67981010-67981011	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs367546948	chr14:67981058-67981059	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs573830803	chr14:67981111-67981112	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs548855170	chr14:67981175-67981176	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs36091275	chr14:67981177-67981178	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs560993975	chr14:67981179-67981180	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs528285243	chr14:67981181-67981182	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs34550031	chr14:67981243-67981244	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs531226827	chr14:67981271-67981272	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs533169952	chr14:67981334-67981335	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs544847036	chr14:67981357-67981358	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs546355630	chr14:67981374-67981375	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs182889327	chr14:67981382-67981383	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs10133618	chr14:67981403-67981404	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs549007390	chr14:67981418-67981419	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs538574143	chr14:67981419-67981420	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs572908714	chr14:67981479-67981480	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs34799486	chr14:67981484-67981485	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs34471029	chr14:67981521-67981522	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs2273598	chr14:67981588-67981589	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs368758503	chr14:67981618-67981619	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs371862820	chr14:67981626-67981627	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs7148937	chr14:67981662-67981663	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs547053906	chr14:67981669-67981670	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs571615123	chr14:67981670-67981671	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs2273597	chr14:67981679-67981680	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs550856974	chr14:67981691-67981692	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs11395680	chr14:67981696-67981697	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs67772555	chr14:67981697-67981698	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs569614194	chr14:67981795-67981796	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs2273596	chr14:67981870-67981871	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs555430816	chr14:67981879-67981880	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs573664469	chr14:67981890-67981891	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs534566375	chr14:67981922-67981923	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs375330711	chr14:67981924-67981925	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs577618298	chr14:67981987-67981988	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs545197057	chr14:67982013-67982014	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs563328413	chr14:67982027-67982028	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs575192542	chr14:67982060-67982061	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs552146261	chr14:67982124-67982125	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs372704225	chr14:67982125-67982126	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Acute myeloid leukemia	21251322	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21611746	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD

Chromatin state (count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:67956200-67981000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr14:67964200-67980800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr14:67965400-67980800	Weak transcription	Primary T cells from cord blood	blood
4	chr14:67970200-67980800	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr14:67975800-67981000	Weak transcription	Primary hematopoietic stem cells	blood
6	chr14:67977600-67980800	Weak transcription	NHEK	skin
7	chr14:67977800-67980800	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr14:67977800-67981000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr14:67977800-67981000	Weak transcription	HMEC	breast
10	chr14:67978000-67981000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr14:67978200-67980800	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr14:67978200-67981200	Weak transcription	Hela-S3	cervix
13	chr14:67978600-67980800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr14:67979000-67981200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr14:67979200-67980800	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr14:67979200-67981000	Enhancers	Pancreas	Pancrea
17	chr14:67979400-67980800	Enhancers	Primary B cells from peripheral blood	blood
18	chr14:67979400-67981000	Enhancers	Primary B cells from cord blood	blood
19	chr14:67979400-67981000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr14:67979400-67981200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr14:67979400-67981400	Enhancers	Spleen	Spleen
22	chr14:67979400-67981400	Enhancers	GM12878-XiMat	blood
23	chr14:67979600-67981200	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr14:67979800-67981200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr14:67979800-67982600	Enhancers	Fetal Brain Male	brain
26	chr14:67980000-67981200	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr14:67980200-67980800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr14:67980200-67980800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
29	chr14:67980200-67980800	Enhancers	Placenta	Placenta
30	chr14:67980200-67981000	Enhancers	Primary T cells fromperipheralblood	blood
31	chr14:67980200-67981000	Flanking Active TSS	Fetal Intestine Large	intestine
32	chr14:67980200-67981400	Flanking Active TSS	Fetal Intestine Small	intestine
33	chr14:67980200-67981400	Enhancers	Small Intestine	intestine
34	chr14:67980200-67981600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr14:67980400-67980800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr14:67980400-67980800	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr14:67980400-67980800	Enhancers	Brain Germinal Matrix	brain
38	chr14:67980400-67980800	Enhancers	Brain Hippocampus Middle	brain
39	chr14:67980400-67980800	Weak transcription	Brain Substantia Nigra	brain
40	chr14:67980400-67980800	Enhancers	Duodenum Smooth Muscle	Duodenum
41	chr14:67980400-67980800	Enhancers	Stomach Mucosa	stomach
42	chr14:67980400-67981000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
43	chr14:67980400-67981000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr14:67980400-67981200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr14:67980400-67981200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr14:67980400-67981400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr14:67980400-67981400	Flanking Active TSS	Brain Angular Gyrus	brain
48	chr14:67980400-67981400	Flanking Active TSS	Brain Cingulate Gyrus	brain
49	chr14:67980400-67981400	Flanking Active TSS	Duodenum Mucosa	Duodenum
50	chr14:67980400-67981400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum

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