Variant report

Variant	nsv542019
Chromosome Location	chr14:31844026-32003929
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2444)
CpG islands
(count:1709)
Chromatin interactive
region (count:92)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2444 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:31979345-31979767	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:31888898-31891391	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:31979285-31979597	K562	blood:	n/a	n/a
4	ARID3A	chr14:31919242-31919576	K562	blood:	n/a	n/a
5	ARID3A	chr14:31889740-31890190	K562	blood:	n/a	n/a
6	ARID3A	chr14:31919193-31919618	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:31925760-31927934	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:31926692-31926973	K562	blood:	n/a	n/a
9	ARID3A	chr14:31998310-31998539	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:31847057-31847719	HepG2	liver:	n/a	chr14:31847087-31847103
11	ARID3A	chr14:31902751-31902786	HepG2	liver:	n/a	n/a
12	ATF1	chr14:31847379-31847549	K562	blood:	n/a	n/a
13	ATF1	chr14:31919264-31919476	K562	blood:	n/a	n/a
14	ATF1	chr14:31875168-31875448	K562	blood:	n/a	n/a
15	ATF1	chr14:31926120-31926865	K562	blood:	n/a	n/a
16	ATF2	chr14:31889628-31890309	GM12878	blood:	n/a	n/a
17	ATF2	chr14:31958860-31959365	GM12878	blood:	n/a	n/a
18	ATF2	chr14:31889508-31890142	GM12878	blood:	n/a	n/a
19	ATF3	chr14:31889517-31890325	A549	lung:	n/a	n/a
20	ATF3	chr14:31875173-31875422	K562	blood:	n/a	n/a
21	BACH1	chr14:31893454-31893489	K562	blood:	n/a	n/a
22	BACH1	chr14:31926111-31926143	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr14:31889072-31890103	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr14:31890090-31890408	GM12878	blood:	n/a	n/a
25	BATF	chr14:31857940-31858574	GM12878	blood:	n/a	chr14:31858232-31858243
26	BCL11A	chr14:31969113-31969289	GM12878	blood:	n/a	n/a
27	BCL11A	chr14:31887740-31887953	GM12878	blood:	n/a	n/a
28	BCL3	chr14:31889359-31890148	A549	lung:	n/a	chr14:31889766-31889779
29	BCL3	chr14:31910564-31911423	A549	lung:	n/a	n/a
30	BCL3	chr14:31925991-31926652	A549	lung:	n/a	n/a
31	BCLAF1	chr14:31889496-31890203	GM12878	blood:	n/a	chr14:31889766-31889779
32	BCLAF1	chr14:31926271-31926791	GM12878	blood:	n/a	n/a
33	BHLHE40	chr14:31847246-31847664	HepG2	liver:	n/a	n/a
34	BHLHE40	chr14:31926041-31926306	GM12878	blood:	n/a	n/a
35	BHLHE40	chr14:31847243-31847640	HepG2	liver:	n/a	n/a
36	BHLHE40	chr14:31889290-31890317	K562	blood:	n/a	n/a
37	BHLHE40	chr14:31926046-31926988	K562	blood:	n/a	n/a
38	BHLHE40	chr14:31919407-31919421	GM12878	blood:	n/a	n/a
39	BHLHE40	chr14:31927411-31928024	HepG2	liver:	n/a	n/a
40	BHLHE40	chr14:31891044-31891269	HepG2	liver:	n/a	n/a
41	BHLHE40	chr14:31927568-31927695	K562	blood:	n/a	n/a
42	BHLHE40	chr14:31889581-31890436	GM12878	blood:	n/a	n/a
43	BHLHE40	chr14:31890651-31890764	K562	blood:	n/a	n/a
44	BHLHE40	chr14:31926519-31926988	GM12878	blood:	n/a	n/a
45	BHLHE40	chr14:31889153-31890737	HepG2	liver:	n/a	n/a
46	BHLHE40	chr14:31879528-31879697	GM12878	blood:	n/a	n/a
47	BHLHE40	chr14:31926028-31927013	HepG2	liver:	n/a	n/a
48	BRCA1	chr14:31889333-31890264	HepG2	liver:	n/a	n/a
49	BRCA1	chr14:31889790-31890122	GM12878	blood:	n/a	n/a
50	BRCA1	chr14:31910692-31911392	Hela-S3	cervix:	n/a	n/a

(count:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:31889912-31889962	HCPEpiC	choroid plexus:	n/a
2	chr14:31889912-31889962	HCPEpiC	choroid plexus:	n/a
3	chr14:31974893-31974943	ECC-1	luminal epithelium:	n/a
4	chr14:31926789-31926839	NH-A	brain:	n/a
5	chr14:31890052-31890102	H1-hESC	embryonic stem cell:	embryo
6	chr14:31926792-31926842	A549	lung:	n/a
7	chr14:31974893-31974943	Caco-2	colon:	n/a
8	chr14:31889169-31889219	GM19239	blood:	n/a
9	chr14:31889003-31889053	SK-N-SH_RA	brain:	n/a
10	chr14:31926216-31926266	RPTEC	kidney:	n/a
11	chr14:31926792-31926842	GM06990	blood:	n/a
12	chr14:31926776-31926826	MCF-7	breast:	n/a
13	chr14:31926776-31926826	ProgFib	skin:	n/a
14	chr14:31929696-31929746	NB4	blood:	n/a
15	chr14:31892296-31892346	PANC-1	pancreas:	n/a
16	chr14:31974893-31974943	HEK293	kidney:	embryo
17	chr14:31927974-31928024	NHDF-neo	bronchial:	n/a
18	chr14:31996486-31996536	K562	blood:	n/a
19	chr14:31889169-31889219	SAEC	small airway:	n/a
20	chr14:31926862-31926912	HRE	kidney:	n/a
21	chr14:31886488-31886538	SKMC	muscle:	n/a
22	chr14:31907252-31907302	NT2-D1	testis:	n/a
23	chr14:31926776-31926826	T-47D	breast:	n/a
24	chr14:31926216-31926266	NT2-D1	testis:	n/a
25	chr14:31926299-31926349	AG04450	lung:	fetal
26	chr14:31974893-31974943	NHDF-neo	bronchial:	n/a
27	chr14:31974893-31974943	SAEC	small airway:	n/a
28	chr14:31915923-31915973	IMR90	lung:	fetal
29	chr14:31859505-31859555	HEK293	kidney:	embryo
30	chr14:31923667-31923717	HEK293	kidney:	embryo
31	chr14:31929696-31929746	Caco-2	colon:	n/a
32	chr14:31892296-31892346	AG04450	lung:	fetal
33	chr14:31974893-31974943	HL-60	blood:	n/a
34	chr14:31889003-31889053	GM12892	blood:	n/a
35	chr14:31889169-31889219	BE2_C	brain:	n/a
36	chr14:31929696-31929746	HUVEC	blood vessel:	n/a
37	chr14:31859515-31859565	PrEC	prostate:	n/a
38	chr14:31926564-31926614	NB4	blood:	n/a
39	chr14:31927974-31928024	SKMC	muscle:	n/a
40	chr14:31926776-31926826	IMR90	lung:	fetal
41	chr14:31889640-31889690	GM12878	blood:	n/a
42	chr14:31859505-31859555	HEEpiC	esophagus:	n/a
43	chr14:31926862-31926912	Hepatocyte	liver:	n/a
44	chr14:31996632-31996682	H1-hESC	embryonic stem cell:	embryo
45	chr14:31892296-31892346	U87	brain:	n/a
46	chr14:31859505-31859555	H1-hESC	embryonic stem cell:	embryo
47	chr14:31926789-31926839	AG04449	skin:	fetal
48	chr14:31926862-31926912	HMEC	breast:	n/a
49	chr14:31858067-31858117	HL-60	blood:	n/a
50	chr14:31889912-31889962	Hela-S3	cervix:	n/a

(count:92 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:31907031..31909539-chr14:31909575..31912143,2	K562	blood:
2	chr14:31906586..31908599-chr14:31913797..31916070,2	MCF-7	breast:
3	chr14:31890242..31892614-chr14:31901862..31904809,2	MCF-7	breast:
4	chr14:31918485..31921453-chr14:31921609..31924237,3	MCF-7	breast:
5	chr14:31979147..31979905-chr14:32256388..32256891,2	MCF-7	breast:
6	chr14:31979520..31980020-chr14:32542725..32543442,2	MCF-7	breast:
7	chr14:31874749..31876483-chr14:31879400..31881889,2	MCF-7	breast:
8	chr14:31888742..31889382-chr3:41241031..41241649,2	Hela-S3	cervix:
9	chr14:31675912..31678861-chr14:31887650..31889789,3	K562	blood:
10	chr14:31856402..31859394-chr14:31860227..31863431,5	K562	blood:
11	chr14:31925030..31927583-chr14:31933327..31936225,2	MCF-7	breast:
12	chr14:31888413..31890616-chr14:31917360..31920011,3	MCF-7	breast:
13	chr14:31905050..31906707-chr14:31906776..31909428,2	K562	blood:
14	chr14:31923625..31927013-chr14:32030157..32032112,3	K562	blood:
15	chr14:31888444..31892446-chr14:31892724..31897271,5	K562	blood:
16	chr14:31872181..31874850-chr14:31924970..31926788,2	K562	blood:
17	chr14:31888418..31891014-chr14:31913687..31916039,2	K562	blood:
18	chr14:31926509..31929146-chr14:31940368..31943663,3	MCF-7	breast:
19	chr14:31887046..31892106-chr14:31923824..31928892,9	K562	blood:
20	chr14:31888318..31891005-chr14:31919529..31921805,3	MCF-7	breast:
21	chr14:31913970..31917383-chr14:31917651..31919831,3	MCF-7	breast:
22	chr11:122932393..122933144-chr14:31926505..31927244,2	NB4	blood:
23	chr14:31878802..31880450-chr14:31888650..31890731,2	MCF-7	breast:
24	chr14:31889397..31890218-chr9:91933424..91934086,2	Hela-S3	cervix:
25	chr14:31880032..31886531-chr14:31888185..31891239,11	MCF-7	breast:
26	chr14:31906586..31908599-chr14:31913797..31916070,2	MCF-7	breast:
27	chr14:31905050..31906707-chr14:31906776..31909428,2	K562	blood:
28	chr14:31868409..31871104-chr14:31872239..31873925,2	K562	blood:
29	chr14:31907031..31909539-chr14:31909575..31912143,2	K562	blood:
30	chr14:31881996..31884911-chr14:31918681..31921369,2	MCF-7	breast:
31	chr14:31926644..31929603-chr14:31946033..31947573,2	K562	blood:
32	chr14:31675912..31678861-chr14:31887661..31889789,2	K562	blood:
33	chr14:31881996..31884911-chr14:31918681..31921369,2	MCF-7	breast:
34	chr14:31905050..31906638-chr14:31906776..31909651,2	K562	blood:
35	chr14:31887438..31889783-chr14:31913776..31915504,2	MCF-7	breast:
36	chr14:31925687..31926473-chr17:8076447..8076967,2	Hela-S3	cervix:
37	chr14:31863925..31866635-chr14:31868935..31870560,2	K562	blood:
38	chr14:31854067..31858154-chr14:31887468..31890013,3	MCF-7	breast:
39	chr14:31890242..31892614-chr14:31901862..31904809,2	MCF-7	breast:
40	chr14:31899509..31901563-chr14:31901913..31904667,2	K562	blood:
41	chr14:31900629..31902248-chr14:31924546..31926804,2	MCF-7	breast:
42	chr14:31861407..31863284-chr14:31887639..31889155,2	K562	blood:
43	chr14:31090018..31093014-chr14:31887951..31890191,2	MCF-7	breast:
44	chr14:31854043..31856997-chr14:31862023..31864715,2	MCF-7	breast:
45	chr14:31676274..31678860-chr14:31889133..31891124,4	MCF-7	breast:
46	chr14:31861407..31863284-chr14:31887639..31889155,2	K562	blood:
47	chr14:31915577..31920525-chr14:31924298..31927871,6	MCF-7	breast:
48	chr14:31888336..31890825-chr14:31917653..31919383,2	MCF-7	breast:
49	chr14:31863925..31866635-chr14:31868935..31870560,2	K562	blood:
50	chr14:31676619..31677277-chr14:31889333..31889964,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUBPL-1	chr14:31891050-31891174	ENSG00000250365
2	lnc-AP4S1-2	chr14:31959233-31959309	XLOC_010789
3	lnc-NUBPL-1	chr14:31908878-31909151	ENSG00000250365
4	lnc-NUBPL-1	chr14:31889964-31890183	ENSG00000250365
5	lnc-NUBPL-1	chr14:31921313-31922089	ENSG00000250365
6	lnc-AP4S1-2	chr14:31995258-31995393	XLOC_010789
7	lnc-NUBPL-1	chr14:31890150-31890183	ENSG00000250365
8	lnc-NUBPL-1	chr14:31889492-31889791	ENSG00000250365
9	lnc-NUBPL-1	chr14:31914850-31914940	ENSG00000250365
10	lnc-C14orf126-7	chr14:31932001-31932577	NONHSAT036283
11	lnc-RP11-187E13.1.1-1	chr14:31995361-31995382	NONHSAT036285
12	lnc-NUBPL-1	chr14:31891054-31891174	ENSG00000250365
13	lnc-NUBPL-1	chr14:31891054-31891174	ENSG00000250365
14	lnc-NUBPL-1	chr14:31908878-31909155	ENSG00000250365

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C14orf126	hsa-miR-181b-5p	chr14:31915941-31915963

Variant related genes	Relation type
NUBPL	TF binding region
ENSG00000250365	TF binding region
ENSG00000239323	TF binding region
ENSG00000203546	TF binding region
DTD2	TF binding region
HEATR5A	TF binding region
GPR33	TF binding region
NUBPL	CpG island
ENSG00000250365	CpG island
ENSG00000239323	CpG island
ENSG00000203546	CpG island
DTD2	CpG island
HEATR5A	CpG island
GPR33	CpG island
ENSG00000129493	chromatin interactions
ENSG00000200463	chromatin interactions
ENSG00000245532	chromatin interactions
ENSG00000204388	chromatin interactions
ENSG00000101361	chromatin interactions
ENSG00000100478	chromatin interactions
ENSG00000214943	chromatin interactions
ENSG00000120699	chromatin interactions
ENSG00000120533	chromatin interactions
ENSG00000257155	chromatin interactions
ENSG00000109971	chromatin interactions
ENSG00000120697	chromatin interactions
ENSG00000168036	chromatin interactions
ENSG00000120526	chromatin interactions
ENSG00000270820	chromatin interactions
ENSG00000187742	chromatin interactions
ENSG00000092108	chromatin interactions
ENSG00000203546	chromatin interactions
ENSG00000129480	chromatin interactions
ENSG00000250365	chromatin interactions
ENSG00000142188	chromatin interactions
ENSG00000151413	chromatin interactions
ENSG00000092148	chromatin interactions
ENSG00000196792	chromatin interactions
ENSG00000221062	chromatin interactions
SERPINB5	miRNA target sites
CCNG1	miRNA target sites
CD274	miRNA target sites
ALG2	miRNA target sites
SLC26A2	miRNA target sites
YTHDC1	miRNA target sites

Extended variants
information (count: 5385 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:5385 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376522134	chr14:31844040-31844041	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs199501778	chr14:31844064-31844065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs374390961	chr14:31844069-31844070	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs370516053	chr14:31844078-31844079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374557944	chr14:31844110-31844111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557686804	chr14:31844144-31844145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200751288	chr14:31844163-31844164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370547366	chr14:31844217-31844218	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373682783	chr14:31844218-31844219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34843718	chr14:31844231-31844232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs12885363	chr14:31844285-31844286	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs573879827	chr14:31844308-31844309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544537899	chr14:31844335-31844336	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556194872	chr14:31844373-31844374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs10134212	chr14:31844402-31844403	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs190771227	chr14:31844455-31844456	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564106526	chr14:31844517-31844518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370531022	chr14:31844530-31844531	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540308174	chr14:31844552-31844553	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143132881	chr14:31844572-31844573	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561990183	chr14:31844583-31844584	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147474329	chr14:31844678-31844679	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551111801	chr14:31844784-31844785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183326218	chr14:31844805-31844806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs114021907	chr14:31844817-31844818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551126781	chr14:31844838-31844839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566456746	chr14:31844857-31844858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188491354	chr14:31844893-31844894	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs8011770	chr14:31844923-31844924	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs192900912	chr14:31844924-31844925	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537648673	chr14:31844964-31844965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556296341	chr14:31845145-31845146	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs577876413	chr14:31845173-31845174	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs538908374	chr14:31845200-31845201	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs185457753	chr14:31845314-31845315	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs564605229	chr14:31845315-31845316	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs540367933	chr14:31845327-31845328	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs138483182	chr14:31845329-31845330	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs117069545	chr14:31845357-31845358	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544498492	chr14:31845369-31845370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562097634	chr14:31845405-31845406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563062100	chr14:31845407-31845408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533487442	chr14:31845408-31845409	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552103167	chr14:31845412-31845413	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560232470	chr14:31845413-31845414	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527295585	chr14:31845421-31845422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548953915	chr14:31845423-31845424	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567392062	chr14:31845487-31845488	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs367677760	chr14:31845488-31845489	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs79036156	chr14:31845546-31845547	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
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
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
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21990379	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2849 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31771000-31888800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr14:31782200-31875200	Weak transcription	Gastric	stomach
3	chr14:31799800-31866800	Weak transcription	Esophagus	oesophagus
4	chr14:31801200-31883800	Weak transcription	Small Intestine	intestine
5	chr14:31801400-31862800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr14:31801400-31875600	Weak transcription	Brain Germinal Matrix	brain
7	chr14:31801600-31872400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr14:31801800-31862600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr14:31802800-31872000	Weak transcription	Fetal Brain Male	brain
10	chr14:31803600-31872600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr14:31803800-31852200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr14:31805600-31851800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr14:31806200-31850800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr14:31808000-31872600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr14:31809600-31872000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr14:31811800-31854600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr14:31812200-31857400	Weak transcription	Fetal Heart	heart
18	chr14:31812800-31852400	Weak transcription	Brain Angular Gyrus	brain
19	chr14:31813200-31872800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr14:31814600-31849200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr14:31816000-31888800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr14:31824600-31846000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr14:31825400-31847200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr14:31825600-31872800	Weak transcription	Fetal Kidney	kidney
25	chr14:31825600-31878600	Weak transcription	Pancreas	Pancrea
26	chr14:31825800-31860200	Weak transcription	Psoas Muscle	Psoas
27	chr14:31826600-31847000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr14:31827000-31847200	Strong transcription	Adipose Nuclei	Adipose
29	chr14:31827400-31847400	Weak transcription	NHLF	lung
30	chr14:31827400-31874400	Weak transcription	Spleen	Spleen
31	chr14:31827600-31846400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr14:31828000-31866800	Weak transcription	Colonic Mucosa	Colon
33	chr14:31828200-31852600	Weak transcription	Fetal Brain Female	brain
34	chr14:31828400-31849000	Weak transcription	Primary T cells fromperipheralblood	blood
35	chr14:31830600-31862000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr14:31832400-31844600	Weak transcription	Aorta	Aorta
37	chr14:31833800-31854400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr14:31836800-31847000	Strong transcription	Duodenum Mucosa	Duodenum
39	chr14:31837000-31853800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
40	chr14:31837000-31858400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr14:31837200-31846800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr14:31837200-31852800	Strong transcription	Placenta	Placenta
43	chr14:31837200-31871800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr14:31838000-31852400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr14:31838000-31857200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr14:31838000-31875000	Weak transcription	K562	blood
47	chr14:31838600-31845800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr14:31838600-31852600	Weak transcription	Brain Substantia Nigra	brain
49	chr14:31839000-31862400	Weak transcription	Ovary	ovary
50	chr14:31839200-31844800	Strong transcription	Brain Inferior Temporal Lobe	brain

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