Variant report

Variant	nsv1044554
Chromosome Location	chr14:21334087-21456092
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1867)
CpG islands
(count:1526)
Chromatin interactive
region (count:62)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1867 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:21443218-21443442	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:21439621-21439813	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:21423410-21423550	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:21439601-21439791	K562	blood:	n/a	n/a
5	ATF1	chr14:21455033-21455323	K562	blood:	n/a	n/a
6	ATF1	chr14:21349520-21349644	K562	blood:	n/a	n/a
7	ATF3	chr14:21439169-21439309	K562	blood:	n/a	n/a
8	BCL3	chr14:21439136-21439915	A549	lung:	n/a	chr14:21439850-21439863 chr14:21439838-21439847
9	BCLAF1	chr14:21341829-21342279	GM12878	blood:	n/a	chr14:21341956-21341969
10	BCLAF1	chr14:21341818-21342245	GM12878	blood:	n/a	chr14:21341956-21341969
11	BCLAF1	chr14:21439508-21439937	GM12878	blood:	n/a	chr14:21439850-21439863 chr14:21439838-21439847
12	BHLHE40	chr14:21439536-21439906	GM12878	blood:	n/a	n/a
13	BHLHE40	chr14:21439108-21439347	HepG2	liver:	n/a	chr14:21439238-21439254
14	BHLHE40	chr14:21341894-21342031	K562	blood:	n/a	chr14:21341954-21341970
15	BHLHE40	chr14:21439127-21440056	K562	blood:	n/a	chr14:21439238-21439254
16	BRCA1	chr14:21439020-21439308	HepG2	liver:	n/a	n/a
17	BRCA1	chr14:21439089-21439903	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr14:21439572-21439879	HepG2	liver:	n/a	n/a
19	BRCA1	chr14:21439088-21439855	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr14:21341821-21342185	K562	blood:	n/a	n/a
21	CCNT2	chr14:21438990-21439837	K562	blood:	n/a	chr14:21439604-21439613
22	CEBPB	chr14:21362201-21362274	K562	blood:	n/a	chr14:21362250-21362261
23	CEBPB	chr14:21455002-21455372	IMR90	lung:	n/a	n/a
24	CEBPB	chr14:21439166-21439394	K562	blood:	n/a	n/a
25	CEBPB	chr14:21404946-21405126	K562	blood:	n/a	n/a
26	CEBPB	chr14:21387183-21387567	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
27	CEBPB	chr14:21404892-21405089	MCF-7	breast:	n/a	n/a
28	CEBPB	chr14:21387189-21387569	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
29	CEBPB	chr14:21432342-21432666	HepG2	liver:	n/a	n/a
30	CEBPB	chr14:21439158-21439943	HepG2	liver:	n/a	n/a
31	CEBPB	chr14:21390806-21390847	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr14:21404959-21405123	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr14:21390712-21390883	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr14:21454989-21455384	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr14:21438802-21439886	IMR90	lung:	n/a	n/a
36	CEBPB	chr14:21341854-21342226	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr14:21341852-21342195	K562	blood:	n/a	n/a
38	CEBPB	chr14:21341851-21342133	K562	blood:	n/a	n/a
39	CEBPB	chr14:21387199-21387544	A549	lung:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
40	CEBPB	chr14:21439146-21439875	HepG2	liver:	n/a	n/a
41	CEBPB	chr14:21373948-21374221	HepG2	liver:	n/a	chr14:21374057-21374070
42	CEBPB	chr14:21341785-21342305	A549	lung:	n/a	n/a
43	CEBPB	chr14:21372661-21372946	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr14:21439122-21439919	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr14:21362247-21362271	H1-hESC	embryonic stem cell:	n/a	chr14:21362250-21362261
46	CEBPB	chr14:21390675-21390974	A549	lung:	n/a	n/a
47	CEBPB	chr14:21432359-21432575	K562	blood:	n/a	n/a
48	CEBPB	chr14:21423393-21423620	HepG2	liver:	n/a	chr14:21423498-21423509 chr14:21423498-21423511
49	CEBPB	chr14:21387184-21387565	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
50	CEBPB	chr14:21362153-21362361	IMR90	lung:	n/a	chr14:21362250-21362261

(count:1526 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21439883-21439933	GM19239	blood:	n/a
2	chr14:21439883-21439933	GM19239	blood:	n/a
3	chr14:21423837-21423887	HCM	heart:	n/a
4	chr14:21439883-21439933	AG04449	skin:	fetal
5	chr14:21439243-21439293	Hepatocyte	liver:	n/a
6	chr14:21422605-21422655	AG04450	lung:	fetal
7	chr14:21439440-21439490	HMEC	breast:	n/a
8	chr14:21436271-21436321	Jurkat	blood:	n/a
9	chr14:21446087-21446137	Caco-2	colon:	n/a
10	chr14:21439907-21439957	NHDF-neo	bronchial:	n/a
11	chr14:21439301-21439351	ECC-1	luminal epithelium:	n/a
12	chr14:21342066-21342116	HRCEpiC	kidney:	n/a
13	chr14:21342066-21342116	AG10803	skin:	n/a
14	chr14:21436271-21436321	T-47D	breast:	n/a
15	chr14:21439243-21439293	SK-N-SH_RA	brain:	n/a
16	chr14:21358233-21358283	NH-A	brain:	n/a
17	chr14:21342066-21342116	PrEC	prostate:	n/a
18	chr14:21423837-21423887	HAEpiC	amniotic membrane:	n/a
19	chr14:21359737-21359787	HCM	heart:	n/a
20	chr14:21341871-21341921	AG10803	skin:	n/a
21	chr14:21439301-21439351	HUVEC	blood vessel:	n/a
22	chr14:21341871-21341921	HCT-116	colon:	n/a
23	chr14:21423837-21423887	GM12878	blood:	n/a
24	chr14:21454954-21455004	NB4	blood:	n/a
25	chr14:21359295-21359345	GM12891	blood:	n/a
26	chr14:21439907-21439957	AG04450	lung:	fetal
27	chr14:21359737-21359787	AG09319	gingival:	n/a
28	chr14:21422205-21422255	HPAEpiC	pulmonary alveolar:	n/a
29	chr14:21386453-21386503	U87	brain:	n/a
30	chr14:21422605-21422655	NHBE	bronchial:	n/a
31	chr14:21358233-21358283	GM06990	blood:	n/a
32	chr14:21424117-21424167	ovcar-3	ovarian:	n/a
33	chr14:21439700-21439750	HCF	heart:	n/a
34	chr14:21358233-21358283	RPTEC	kidney:	n/a
35	chr14:21423684-21423734	NH-A	brain:	n/a
36	chr14:21423837-21423887	ProgFib	skin:	n/a
37	chr14:21341871-21341921	NHDF-neo	bronchial:	n/a
38	chr14:21446087-21446137	BJ	skin:	n/a
39	chr14:21424117-21424167	PANC-1	pancreas:	n/a
40	chr14:21386453-21386503	HCF	heart:	n/a
41	chr14:21436271-21436321	U87	brain:	n/a
42	chr14:21422605-21422655	SK-N-SH_RA	brain:	n/a
43	chr14:21422205-21422255	BE2_C	brain:	n/a
44	chr14:21359943-21359993	SK-N-SH	brain:	n/a
45	chr14:21386453-21386503	Jurkat	blood:	n/a
46	chr14:21439243-21439293	SAEC	small airway:	n/a
47	chr14:21439700-21439750	IMR90	lung:	fetal
48	chr14:21446087-21446137	HL-60	blood:	n/a
49	chr14:21422605-21422655	SK-N-SH	brain:	n/a
50	chr14:21439301-21439351	BJ	skin:	n/a

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:21429229..21430249-chr14:21438962..21439710,3	MCF-7	breast:
2	chr14:21452633..21454134-chr14:21456113..21458171,2	K562	blood:
3	chr14:21439178..21439847-chr9:129452391..129453279,2	MCF-7	breast:
4	chr14:21333855..21335979-chr14:21338238..21341618,3	K562	blood:
5	chr14:21438410..21440043-chr14:21441978..21444200,2	MCF-7	breast:
6	chr14:21333855..21336540-chr14:21338218..21341618,4	K562	blood:
7	chr14:21341929..21342586-chr14:21439203..21440051,2	K562	blood:
8	chr14:21446686..21449262-chr14:21451337..21453135,2	MCF-7	breast:
9	chr14:21345187..21348103-chr14:21455224..21457829,2	K562	blood:
10	chr14:21341929..21342586-chr14:21439203..21440051,2	K562	blood:
11	chr14:21439828..21441685-chr14:21441770..21443275,2	K562	blood:
12	chr14:21454547..21456911-chr14:21472680..21474390,2	MCF-7	breast:
13	chr14:20921981..20924966-chr14:21455832..21458950,3	MCF-7	breast:
14	chr14:21441200..21445003-chr14:21451754..21456149,6	MCF-7	breast:
15	chr14:21304584..21305497-chr14:21335137..21335696,2	MCF-7	breast:
16	chr14:21077613..21078284-chr14:21334820..21335746,2	K562	blood:
17	chr14:21325580..21326139-chr14:21341851..21342353,2	MCF-7	breast:
18	chr14:21450582..21454134-chr14:21456083..21458920,5	K562	blood:
19	chr14:21325535..21326543-chr14:21438744..21440024,15	MCF-7	breast:
20	chr14:21429613..21431283-chr14:21433107..21435716,2	MCF-7	breast:
21	chr14:21325871..21326463-chr14:21334726..21335414,2	K562	blood:
22	chr14:21439378..21440166-chr14:21507981..21508704,3	K562	blood:
23	chr14:21417758..21420748-chr14:21423705..21426897,3	MCF-7	breast:
24	chr14:21325537..21326206-chr14:21438780..21439731,4	MCF-7	breast:
25	chr14:21438254..21441187-chr14:21454392..21458605,4	MCF-7	breast:
26	chr14:20920787..20923218-chr14:21454532..21456112,2	MCF-7	breast:
27	chr14:21325949..21326651-chr14:21439270..21440179,3	K562	blood:
28	chr14:21438410..21440043-chr14:21441978..21444200,2	MCF-7	breast:
29	chr14:21165816..21166697-chr14:21334782..21335644,3	MCF-7	breast:
30	chr14:21326118..21326960-chr14:21336756..21337360,2	K562	blood:
31	chr14:21432822..21434534-chr14:21436325..21439304,2	K562	blood:
32	chr14:21441390..21444157-chr14:21460821..21462401,2	MCF-7	breast:
33	chr14:21439409..21441404-chr14:21464619..21467920,3	MCF-7	breast:
34	chr14:21450582..21454134-chr14:21456083..21458920,5	K562	blood:
35	chr14:21417758..21420748-chr14:21423705..21426897,3	MCF-7	breast:
36	chr14:21429229..21430249-chr14:21438962..21439710,3	MCF-7	breast:
37	chr14:21444710..21446595-chr14:21492523..21495132,2	MCF-7	breast:
38	chr14:21438667..21439824-chr14:21560356..21561352,5	K562	blood:
39	chr14:21341564..21342405-chr14:21439163..21439679,2	MCF-7	breast:
40	chr14:20937597..20940433-chr14:21438426..21440777,2	MCF-7	breast:
41	chr14:21439828..21441685-chr14:21441770..21443275,2	K562	blood:
42	chr14:21449771..21451295-chr14:21452559..21454888,2	MCF-7	breast:
43	chr14:21339048..21339766-chr3:63998651..63999205,2	MCF-7	breast:
44	chr14:21437415..21439351-chr14:21449337..21451535,2	K562	blood:
45	chr14:21432822..21434534-chr14:21436325..21439304,2	K562	blood:
46	chr14:21437415..21439351-chr14:21449337..21451535,2	K562	blood:
47	chr14:21446686..21449262-chr14:21451337..21453135,2	MCF-7	breast:
48	chr14:21164524..21167490-chr14:21438103..21441098,2	MCF-7	breast:
49	chr14:21440683..21443380-chr14:21445496..21447628,2	K562	blood:
50	chr14:21452044..21453634-chr14:21457203..21461213,3	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNASE3-1	chr14:21387500-21387563	ENSG00000136315
2	lnc-NDRG2-3	chr14:21404261-21404414	ENSG00000258918
3	lnc-RNASE1-1	chr14:21343696-21343904	XLOC_010966
4	lnc-NDRG2-2	chr14:21396396-21396739	ENSG00000258772
5	lnc-RNASE1-1	chr14:21338438-21338615	ENSG00000259130
6	lnc-RNASE3-1	chr14:21387795-21388335	ENSG00000136315
7	lnc-RNASE1-1	chr14:21343696-21343927	ENSG00000258642.1
8	lnc-RNASE2-2	chr14:21431738-21432024	NONHSAT035619
9	lnc-RNASE1-1	chr14:21341718-21341751	ENSG00000259130
10	lnc-RNASE1-1	chr14:21338437-21338615	ENSG00000259130
11	lnc-NDRG2-3	chr14:21366144-21366340	ENSG00000258918
12	lnc-RNASE1-1	chr14:21342464-21342995	ENSG00000258642.1
13	lnc-RNASE1-1	chr14:21341350-21341529	ENSG00000259130
14	lnc-RNASE1-1	chr14:21341079-21342995	XLOC_010966
15	lnc-RNASE2-1	chr14:21419045-21419476	NONHSAT035618
16	lnc-METTL17-2	chr14:21453987-21455430	NONHSAT035621
17	lnc-RNASE1-1	chr14:21340531-21340720	ENSG00000259130
18	lnc-NDRG2-2	chr14:21384925-21385029	ENSG00000258772
19	lnc-METTL17-2	chr14:21453058-21453674	NONHSAT035621
20	lnc-RNASE2-1	chr14:21418698-21418708	NONHSAT035618

No data

Variant related genes	Relation type
ENSG00000258772	TF binding region
ENSG00000136315	TF binding region
ENSG00000258642	TF binding region
RN7SL189P	TF binding region
ENSG00000258599	TF binding region
RNASE3	TF binding region
ENSG00000258918	TF binding region
ENSG00000259130	TF binding region
RNASE2	TF binding region
METTL17	TF binding region
ENSG00000258772	CpG island
ENSG00000136315	CpG island
ENSG00000258642	CpG island
RN7SL189P	CpG island
ENSG00000258599	CpG island
RNASE3	CpG island
ENSG00000258918	CpG island
ENSG00000259130	CpG island
RNASE2	CpG island
METTL17	CpG island
ENSG00000165804	chromatin interactions
ENSG00000100823	chromatin interactions
ENSG00000173464	chromatin interactions
ENSG00000165795	chromatin interactions
ENSG00000258599	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000259130	chromatin interactions
ENSG00000165794	chromatin interactions
ENSG00000198805	chromatin interactions
ENSG00000258471	chromatin interactions
ENSG00000165792	chromatin interactions
ENSG00000092094	chromatin interactions
ENSG00000259060	chromatin interactions

Extended variants
information (count: 4204 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:4204 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181016853	chr14:21334109-21334110	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs534620028	chr14:21334121-21334122	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs568055469	chr14:21334148-21334149	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs368493056	chr14:21334189-21334190	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs553827193	chr14:21334208-21334209	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs576908085	chr14:21334211-21334212	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs545580282	chr14:21334249-21334250	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs142354443	chr14:21334270-21334271	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs575906571	chr14:21334278-21334279	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs541736818	chr14:21334315-21334316	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs561894431	chr14:21334348-21334349	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs553183992	chr14:21334359-21334360	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs577007933	chr14:21334368-21334369	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs527690033	chr14:21334397-21334398	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs117014254	chr14:21334472-21334473	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs186383970	chr14:21334482-21334483	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs201359026	chr14:21334490-21334491	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs142616623	chr14:21334491-21334492	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs200940996	chr14:21334492-21334493	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs370304169	chr14:21334494-21334495	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs57652755	chr14:21334501-21334502	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs181696462	chr14:21334504-21334505	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs146468034	chr14:21334507-21334508	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs541201138	chr14:21334512-21334513	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs372756264	chr14:21334618-21334619	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs143909835	chr14:21334624-21334625	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs77996011	chr14:21334635-21334636	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs570278622	chr14:21334636-21334637	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs139151934	chr14:21334697-21334698	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs114966415	chr14:21334704-21334705	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs557177310	chr14:21334730-21334731	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs144562941	chr14:21334746-21334747	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs375368215	chr14:21334774-21334775	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs575836147	chr14:21334776-21334777	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs375685433	chr14:21334797-21334798	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs546290882	chr14:21334867-21334868	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs10139443	chr14:21334871-21334872	Inactive region	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs371803330	chr14:21335064-21335065	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs561429996	chr14:21335071-21335072	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs186804066	chr14:21335085-21335086	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs376751661	chr14:21335099-21335100	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs377471974	chr14:21335179-21335180	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs11844872	chr14:21335191-21335192	Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs11848869	chr14:21335266-21335267	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs115754963	chr14:21335267-21335268	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs148056275	chr14:21335268-21335269	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs533430015	chr14:21335286-21335287	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs543940524	chr14:21335323-21335324	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs10872858	chr14:21335354-21335355	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs191255351	chr14:21335389-21335390	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Breast cancer	22522925	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	21858162	CNVD

Chromatin state (count:1027 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21335000-21335200	Enhancers	Brain Substantia Nigra	brain
2	chr14:21335000-21335600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr14:21335200-21335600	Enhancers	Fetal Heart	heart
4	chr14:21335200-21337000	Weak transcription	Brain Substantia Nigra	brain
5	chr14:21335600-21338800	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr14:21337000-21337200	Enhancers	Brain Substantia Nigra	brain
7	chr14:21337000-21337600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr14:21337200-21337600	Enhancers	Brain Cingulate Gyrus	brain
9	chr14:21337200-21337800	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr14:21337200-21341600	Weak transcription	Brain Substantia Nigra	brain
11	chr14:21337600-21341600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr14:21337800-21338000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
13	chr14:21338800-21341600	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr14:21339200-21340200	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr14:21340200-21341200	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr14:21341200-21341400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr14:21341200-21341400	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr14:21341200-21341600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
19	chr14:21341200-21342200	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr14:21341200-21342200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chr14:21341200-21342200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr14:21341200-21342600	Active TSS	ES-I3 Cell Line	embryonic stem cell
23	chr14:21341200-21342600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr14:21341200-21343200	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr14:21341400-21341600	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr14:21341400-21341600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
27	chr14:21341400-21341600	Enhancers	Brain Cingulate Gyrus	brain
28	chr14:21341400-21341600	Enhancers	Dnd41	blood
29	chr14:21341400-21341800	Enhancers	Primary T cells from cord blood	blood
30	chr14:21341400-21342200	Active TSS	H1 Cell Line	embryonic stem cell
31	chr14:21341400-21342200	Enhancers	Primary B cells from peripheral blood	blood
32	chr14:21341400-21342200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
33	chr14:21341400-21342200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
34	chr14:21341400-21342200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr14:21341400-21342400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
36	chr14:21341400-21342400	Enhancers	Primary hematopoietic stem cells	blood
37	chr14:21341400-21342400	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr14:21341400-21342400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr14:21341400-21342400	Enhancers	Brain Anterior Caudate	brain
40	chr14:21341400-21342600	Enhancers	Primary B cells from cord blood	blood
41	chr14:21341400-21342600	Enhancers	Spleen	Spleen
42	chr14:21341400-21342600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
43	chr14:21341600-21341800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
44	chr14:21341600-21341800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr14:21341600-21341800	Flanking Active TSS	Brain Cingulate Gyrus	brain
46	chr14:21341600-21342000	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr14:21341600-21342000	Flanking Active TSS	Brain Substantia Nigra	brain
48	chr14:21341600-21342000	Enhancers	Colon Smooth Muscle	Colon
49	chr14:21341600-21342000	Active TSS	GM12878-XiMat	blood
50	chr14:21341600-21342000	Enhancers	HUVEC	blood vessel

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