Variant report

Variant	nsv522850
Chromosome Location	chr14:21989841-21998108
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:454)
CpG islands
(count:244)
Chromatin interactive
region (count:21)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:454 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:21993728-21993871	K562	blood:	n/a	n/a
2	ARID3A	chr14:21994448-21994458	K562	blood:	n/a	n/a
3	ARID3A	chr14:21996539-21997519	K562	blood:	n/a	n/a
4	ARID3A	chr14:21994508-21994645	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:21996905-21997545	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:21994992-21995458	HepG2	liver:	n/a	n/a
7	ATF1	chr14:21997147-21997541	K562	blood:	n/a	n/a
8	ATF2	chr14:21995072-21995731	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr14:21994733-21995492	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr14:21997198-21997469	K562	blood:	n/a	n/a
11	ATF3	chr14:21993700-21993961	K562	blood:	n/a	n/a
12	BACH1	chr14:21993741-21993870	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr14:21994496-21994721	H1-hESC	embryonic stem cell:	n/a	n/a
14	BHLHE40	chr14:21994842-21994853	K562	blood:	n/a	n/a
15	BHLHE40	chr14:21994443-21994816	GM12878	blood:	n/a	chr14:21994617-21994633
16	BHLHE40	chr14:21994471-21994860	HepG2	liver:	n/a	chr14:21994617-21994633
17	BRCA1	chr14:21994408-21995376	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr14:21997347-21997515	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr14:21993685-21993772	H1-hESC	embryonic stem cell:	n/a	n/a
20	CCNT2	chr14:21994243-21994725	K562	blood:	n/a	n/a
21	CCNT2	chr14:21996629-21996886	K562	blood:	n/a	n/a
22	CEBPB	chr14:21997188-21997503	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:21996548-21996979	K562	blood:	n/a	chr14:21996758-21996771
24	CEBPB	chr14:21997107-21997470	HepG2	liver:	n/a	n/a
25	CEBPB	chr14:21997182-21997489	K562	blood:	n/a	n/a
26	CEBPB	chr14:21996607-21996843	K562	blood:	n/a	chr14:21996758-21996771
27	CEBPB	chr14:21989685-21990005	IMR90	lung:	n/a	n/a
28	CEBPB	chr14:21995136-21995324	K562	blood:	n/a	n/a
29	CEBPB	chr14:21995100-21995451	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr14:21997130-21997447	K562	blood:	n/a	n/a
31	CEBPB	chr14:21996594-21996953	IMR90	lung:	n/a	chr14:21996758-21996771
32	CEBPB	chr14:21996394-21996864	HepG2	liver:	n/a	chr14:21996758-21996771
33	CEBPB	chr14:21995185-21995252	HepG2	liver:	n/a	n/a
34	CEBPB	chr14:21994440-21994784	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr14:21996378-21996958	K562	blood:	n/a	chr14:21996758-21996771
36	CEBPD	chr14:21994177-21994608	HepG2	liver:	n/a	n/a
37	CEBPD	chr14:21997093-21997548	K562	blood:	n/a	n/a
38	CEBPD	chr14:21994112-21994840	HepG2	liver:	n/a	n/a
39	CEBPD	chr14:21996538-21997008	K562	blood:	n/a	n/a
40	CEBPD	chr14:21997214-21997402	HepG2	liver:	n/a	n/a
41	CEBPZ	chr14:21997226-21997351	HepG2	liver:	n/a	n/a
42	CHD1	chr14:21994217-21994697	H1-hESC	embryonic stem cell:	n/a	chr14:21994672-21994682
43	CHD1	chr14:21996453-21996650	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr14:21994941-21995687	H1-hESC	embryonic stem cell:	n/a	chr14:21995092-21995102 chr14:21995333-21995343
45	CHD2	chr14:21994922-21995415	GM12878	blood:	n/a	chr14:21995092-21995102 chr14:21995333-21995343
46	CHD2	chr14:21994219-21994668	GM12878	blood:	n/a	n/a
47	CHD2	chr14:21993801-21993833	K562	blood:	n/a	n/a
48	CHD2	chr14:21997252-21997358	HepG2	liver:	n/a	n/a
49	CHD2	chr14:21994879-21995355	HepG2	liver:	n/a	chr14:21995092-21995102 chr14:21995333-21995343
50	CHD2	chr14:21994157-21995528	H1-hESC	embryonic stem cell:	n/a	chr14:21995092-21995102 chr14:21995333-21995343 chr14:21994712-21994722 chr14:21994672-21994682

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21994785-21994835	HCM	heart:	n/a
2	chr14:21991414-21991464	HAEpiC	amniotic membrane:	n/a
3	chr14:21994644-21994694	HUVEC	blood vessel:	n/a
4	chr14:21991255-21991305	HAEpiC	amniotic membrane:	n/a
5	chr14:21994644-21994694	HRCEpiC	kidney:	n/a
6	chr14:21994785-21994835	Hela-S3	cervix:	n/a
7	chr14:21991255-21991305	HRCEpiC	kidney:	n/a
8	chr14:21991255-21991305	GM12892	blood:	n/a
9	chr14:21991414-21991464	MCF-7	breast:	n/a
10	chr14:21991414-21991464	HCM	heart:	n/a
11	chr14:21991414-21991464	K562	blood:	n/a
12	chr14:21991255-21991305	HEEpiC	esophagus:	n/a
13	chr14:21994785-21994835	PFSK-1	brain:	n/a
14	chr14:21994785-21994835	HRPEpiC	eye:	n/a
15	chr14:21994644-21994694	LNCaP	prostate:	n/a
16	chr14:21994644-21994694	SKMC	muscle:	n/a
17	chr14:21991255-21991305	AG04449	skin:	fetal
18	chr14:21994644-21994694	AG09309	skin:	n/a
19	chr14:21991414-21991464	ovcar-3	ovarian:	n/a
20	chr14:21994785-21994835	GM12892	blood:	n/a
21	chr14:21994785-21994835	HRCEpiC	kidney:	n/a
22	chr14:21991414-21991464	Hela-S3	cervix:	n/a
23	chr14:21994644-21994694	GM12892	blood:	n/a
24	chr14:21991414-21991464	MCF10A-Er-Src	breast:	n/a
25	chr14:21991255-21991305	Hepatocyte	liver:	n/a
26	chr14:21994785-21994835	T-47D	breast:	n/a
27	chr14:21994644-21994694	T-47D	breast:	n/a
28	chr14:21991255-21991305	ECC-1	luminal epithelium:	n/a
29	chr14:21994644-21994694	RPTEC	kidney:	n/a
30	chr14:21991255-21991305	ovcar-3	ovarian:	n/a
31	chr14:21991414-21991464	NHDF-neo	bronchial:	n/a
32	chr14:21991255-21991305	MCF10A-Er-Src	breast:	n/a
33	chr14:21994785-21994835	CMK	blood:	n/a
34	chr14:21991255-21991305	HIPEpiC	eye:	n/a
35	chr14:21994785-21994835	HepG2	liver:	n/a
36	chr14:21991255-21991305	GM12891	blood:	n/a
37	chr14:21991414-21991464	AoSMC	blood vessel:	n/a
38	chr14:21991255-21991305	HCM	heart:	n/a
39	chr14:21991255-21991305	A549	lung:	n/a
40	chr14:21994785-21994835	MCF10A-Er-Src	breast:	n/a
41	chr14:21991414-21991464	HEEpiC	esophagus:	n/a
42	chr14:21994644-21994694	HepG2	liver:	n/a
43	chr14:21994785-21994835	LNCaP	prostate:	n/a
44	chr14:21991414-21991464	AG04449	skin:	fetal
45	chr14:21994644-21994694	K562	blood:	n/a
46	chr14:21991414-21991464	SK-N-SH	brain:	n/a
47	chr14:21994644-21994694	SK-N-MC	brain:	n/a
48	chr14:21994785-21994835	Jurkat	blood:	n/a
49	chr14:21991255-21991305	BJ	skin:	n/a
50	chr14:21994644-21994694	HCF	heart:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:21970942..21973868-chr14:21992084..21994345,2	MCF-7	breast:
2	chr14:21996508..21998205-chr14:22004849..22006828,2	K562	blood:
3	chr14:21924995..21926631-chr14:21995228..21997322,2	K562	blood:
4	chr14:21993185..21995225-chr14:22004825..22007196,2	K562	blood:
5	chr14:21904269..21906743-chr14:21992458..21995215,2	K562	blood:
6	chr14:21976926..21983845-chr14:21991695..21998209,25	K562	blood:
7	chr14:21977974..21981747-chr14:21991693..21997000,9	MCF-7	breast:
8	chr1:149856183..149858038-chr14:21995590..21998397,2	K562	blood:
9	chr14:21905273..21907217-chr14:21995452..21997154,2	K562	blood:
10	chr14:21991104..21993583-chr14:21997557..21999607,2	MCF-7	breast:
11	chr14:21986110..21991599-chr14:21992205..21995667,7	MCF-7	breast:
12	chr14:21986110..21991599-chr14:21992205..21995667,7	MCF-7	breast:
13	chr14:21978865..21980479-chr14:21995684..21997193,2	MCF-7	breast:
14	chr14:21977943..21985344-chr14:21985568..21995608,22	MCF-7	breast:
15	chr14:21990799..21992419-chr14:22010466..22012179,2	K562	blood:
16	chr14:21983078..21988753-chr14:21989442..21992555,6	MCF-7	breast:
17	chr14:21966582..21968425-chr14:21990390..21992940,3	K562	blood:
18	chr14:21991104..21993583-chr14:21997557..21999607,2	MCF-7	breast:
19	chr14:21977163..21984004-chr14:21985497..21991656,11	K562	blood:
20	chr14:21997433..21999018-chr14:22000681..22002820,2	K562	blood:
21	chr14:21944743..21947528-chr14:21994092..21996767,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TOX4-1	chr14:21990540-21990794	ENSG00000257096.1

No data

Variant related genes	Relation type
SALL2	TF binding region
SALL2	CpG island
ENSG00000100888	chromatin interactions
ENSG00000092203	chromatin interactions
ENSG00000257096	chromatin interactions
ENSG00000165821	chromatin interactions
ENSG00000165819	chromatin interactions
ENSG00000129472	chromatin interactions

Extended variants
information (count: 361 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs712322	chr14:21989841-21989842	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
2	rs369198460	chr14:21989857-21989858	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs565182762	chr14:21989908-21989909	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs537004320	chr14:21989916-21989917	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs183330297	chr14:21989930-21989931	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs74034936	chr14:21989985-21989986	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs145980251	chr14:21990034-21990035	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs373507379	chr14:21990049-21990050	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs117696798	chr14:21990059-21990060	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs573064675	chr14:21990092-21990093	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs138405607	chr14:21990116-21990117	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs558781041	chr14:21990172-21990173	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs368459365	chr14:21990178-21990179	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs741707	chr14:21990181-21990182	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs576985829	chr14:21990204-21990205	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs541184864	chr14:21990206-21990207	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs368347412	chr14:21990212-21990213	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs543045059	chr14:21990237-21990238	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs563445167	chr14:21990240-21990241	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs371993969	chr14:21990250-21990251	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs143006178	chr14:21990252-21990253	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs139716556	chr14:21990315-21990316	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs200715579	chr14:21990342-21990343	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs3177952	chr14:21990349-21990350	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs547934925	chr14:21990381-21990382	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs117928550	chr14:21990408-21990409	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs113494865	chr14:21990420-21990421	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs528247190	chr14:21990488-21990489	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs551708959	chr14:21990503-21990504	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs71410281	chr14:21990532-21990533	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs1124981	chr14:21990537-21990538	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs72683986	chr14:21990555-21990556	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
33	rs550675986	chr14:21990662-21990663	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs371020038	chr14:21990693-21990694	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs188806798	chr14:21990695-21990696	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs146124568	chr14:21990708-21990709	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs139948513	chr14:21990723-21990724	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs367650822	chr14:21990773-21990774	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs563327913	chr14:21990783-21990784	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs45458492	chr14:21990796-21990797	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs144664350	chr14:21990797-21990798	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs575844953	chr14:21990801-21990802	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs202016107	chr14:21990827-21990828	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs556669432	chr14:21990865-21990866	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs148639100	chr14:21990883-21990884	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs376502263	chr14:21990884-21990885	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs142138768	chr14:21990897-21990898	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs151141071	chr14:21990901-21990902	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs372571091	chr14:21990902-21990903	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs200074438	chr14:21990912-21990913	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD
Mortal	21835882	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21858162	CNVD
Schizophrenia	20967226	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22102821	CNVD
Neuroblastoma	19536264	CNVD
Schizophrenia	23813976	CNVD
Ewing''s sarcoma	18628472	CNVD
Rheumatoid arthritis	23223014	CNVD
Ependymoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:698 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21980000-21990000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:21980000-21993600	Weak transcription	Aorta	Aorta
3	chr14:21980200-21990000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr14:21980200-21990000	Weak transcription	Ovary	ovary
5	chr14:21980200-21990200	Weak transcription	Primary T cells from cord blood	blood
6	chr14:21980200-21991400	Weak transcription	Fetal Kidney	kidney
7	chr14:21980200-21993400	Weak transcription	Right Atrium	heart
8	chr14:21980400-21990000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr14:21980400-21990000	Weak transcription	Stomach Smooth Muscle	stomach
10	chr14:21980400-21990200	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr14:21980400-21990400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr14:21980400-21991400	Weak transcription	Brain Hippocampus Middle	brain
13	chr14:21980600-21991800	Weak transcription	Fetal Lung	lung
14	chr14:21980600-21991800	Weak transcription	Dnd41	blood
15	chr14:21980600-21993400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr14:21982800-21992800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr14:21983600-21991800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr14:21986400-21990800	Weak transcription	Fetal Intestine Small	intestine
19	chr14:21986800-21991600	Weak transcription	Thymus	Thymus
20	chr14:21987200-21990000	Weak transcription	Fetal Stomach	stomach
21	chr14:21987200-21990400	Weak transcription	Fetal Intestine Large	intestine
22	chr14:21987200-21993600	Weak transcription	Rectal Smooth Muscle	rectum
23	chr14:21987600-21990000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr14:21987600-21990000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr14:21988000-21994200	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr14:21988200-21990000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr14:21988200-21990400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
28	chr14:21988400-21993000	Weak transcription	Fetal Thymus	thymus
29	chr14:21988600-21990000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
30	chr14:21988600-21990000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr14:21988600-21993600	Weak transcription	Right Ventricle	heart
32	chr14:21988800-21990000	Strong transcription	H9 Cell Line	embryonic stem cell
33	chr14:21988800-21992800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr14:21989000-21990000	Genic enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr14:21989000-21990200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr14:21989000-21992400	Strong transcription	Fetal Muscle Trunk	muscle
37	chr14:21989000-21992800	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr14:21989000-21992800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
39	chr14:21989200-21990200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr14:21989200-21990200	Enhancers	NH-A	brain
41	chr14:21989200-21990400	Enhancers	K562	blood
42	chr14:21989200-21990600	Enhancers	Fetal Brain Female	brain
43	chr14:21989200-21991200	Weak transcription	Brain Cingulate Gyrus	brain
44	chr14:21989200-21993400	Genic enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr14:21989200-21993400	Genic enhancers	HUES48 Cell Line	embryonic stem cell
46	chr14:21989400-21990000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr14:21989400-21990000	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr14:21989400-21990200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr14:21989400-21990400	Enhancers	Osteobl	bone
50	chr14:21989400-21993200	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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