Variant report

Variant	nsv901589
Chromosome Location	chr14:31768231-31944723
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2835)
CpG islands
(count:1527)
Chromatin interactive
region (count:121)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2835 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:31825017-31825479	K562	blood:	n/a	chr14:31825219-31825235
2	ARID3A	chr14:31824941-31825507	HepG2	liver:	n/a	chr14:31825219-31825235
3	ARID3A	chr14:31847057-31847719	HepG2	liver:	n/a	chr14:31847087-31847103
4	ARID3A	chr14:31805945-31806204	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:31902751-31902786	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:31889740-31890190	K562	blood:	n/a	n/a
7	ARID3A	chr14:31919193-31919618	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:31925760-31927934	HepG2	liver:	n/a	n/a
9	ARID3A	chr14:31820348-31820569	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:31926692-31926973	K562	blood:	n/a	n/a
11	ARID3A	chr14:31919242-31919576	K562	blood:	n/a	n/a
12	ARID3A	chr14:31888898-31891391	HepG2	liver:	n/a	n/a
13	ATF1	chr14:31875168-31875448	K562	blood:	n/a	n/a
14	ATF1	chr14:31926120-31926865	K562	blood:	n/a	n/a
15	ATF1	chr14:31919264-31919476	K562	blood:	n/a	n/a
16	ATF1	chr14:31847379-31847549	K562	blood:	n/a	n/a
17	ATF2	chr14:31889508-31890142	GM12878	blood:	n/a	n/a
18	ATF2	chr14:31889628-31890309	GM12878	blood:	n/a	n/a
19	ATF3	chr14:31875173-31875422	K562	blood:	n/a	n/a
20	ATF3	chr14:31889517-31890325	A549	lung:	n/a	n/a
21	BACH1	chr14:31825281-31825293	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr14:31889072-31890103	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr14:31893454-31893489	K562	blood:	n/a	n/a
24	BACH1	chr14:31926111-31926143	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr14:31857940-31858574	GM12878	blood:	n/a	chr14:31858232-31858243
26	BATF	chr14:31890090-31890408	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	chr14:31925991-31926652	A549	lung:	n/a	n/a
30	BCL3	chr14:31910564-31911423	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	chr14:31891044-31891269	HepG2	liver:	n/a	n/a
34	BHLHE40	chr14:31889290-31890317	K562	blood:	n/a	n/a
35	BHLHE40	chr14:31879528-31879697	GM12878	blood:	n/a	n/a
36	BHLHE40	chr14:31889581-31890436	GM12878	blood:	n/a	n/a
37	BHLHE40	chr14:31927411-31928024	HepG2	liver:	n/a	n/a
38	BHLHE40	chr14:31919407-31919421	GM12878	blood:	n/a	n/a
39	BHLHE40	chr14:31927568-31927695	K562	blood:	n/a	n/a
40	BHLHE40	chr14:31847246-31847664	HepG2	liver:	n/a	n/a
41	BHLHE40	chr14:31889153-31890737	HepG2	liver:	n/a	n/a
42	BHLHE40	chr14:31926028-31927013	HepG2	liver:	n/a	n/a
43	BHLHE40	chr14:31847243-31847640	HepG2	liver:	n/a	n/a
44	BHLHE40	chr14:31926041-31926306	GM12878	blood:	n/a	n/a
45	BHLHE40	chr14:31926519-31926988	GM12878	blood:	n/a	n/a
46	BHLHE40	chr14:31926046-31926988	K562	blood:	n/a	n/a
47	BHLHE40	chr14:31890651-31890764	K562	blood:	n/a	n/a
48	BRCA1	chr14:31926086-31926643	HepG2	liver:	n/a	n/a
49	BRCA1	chr14:31888868-31890285	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr14:31910692-31911392	Hela-S3	cervix:	n/a	n/a

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:31892296-31892346	RPTEC	kidney:	n/a
2	chr14:31859505-31859555	Caco-2	colon:	n/a
3	chr14:31892296-31892346	RPTEC	kidney:	n/a
4	chr14:31859505-31859555	Caco-2	colon:	n/a
5	chr14:31858067-31858117	Hela-S3	cervix:	n/a
6	chr14:31890001-31890051	HAEpiC	amniotic membrane:	n/a
7	chr14:31926776-31926826	K562	blood:	n/a
8	chr14:31859515-31859565	GM12892	blood:	n/a
9	chr14:31926216-31926266	T-47D	breast:	n/a
10	chr14:31858067-31858117	Caco-2	colon:	n/a
11	chr14:31889912-31889962	HL-60	blood:	n/a
12	chr14:31926299-31926349	AG09319	gingival:	n/a
13	chr14:31890052-31890102	PFSK-1	brain:	n/a
14	chr14:31926216-31926266	U87	brain:	n/a
15	chr14:31926862-31926912	HRCEpiC	kidney:	n/a
16	chr14:31907252-31907302	GM12891	blood:	n/a
17	chr14:31927974-31928024	MCF10A-Er-Src	breast:	n/a
18	chr14:31926216-31926266	AoSMC	blood vessel:	n/a
19	chr14:31889003-31889053	GM19239	blood:	n/a
20	chr14:31926483-31926533	HNPCEpiC	eye:	n/a
21	chr14:31890052-31890102	HAEpiC	amniotic membrane:	n/a
22	chr14:31929696-31929746	GM12891	blood:	n/a
23	chr14:31926792-31926842	SK-N-SH_RA	brain:	n/a
24	chr14:31859505-31859555	AG09319	gingival:	n/a
25	chr14:31915923-31915973	HMEC	breast:	n/a
26	chr14:31923667-31923717	AG10803	skin:	n/a
27	chr14:31926483-31926533	HRCEpiC	kidney:	n/a
28	chr14:31926483-31926533	NH-A	brain:	n/a
29	chr14:31889640-31889690	IMR90	lung:	fetal
30	chr14:31907252-31907302	AoSMC	blood vessel:	n/a
31	chr14:31889169-31889219	AG04450	lung:	fetal
32	chr14:31927974-31928024	GM12892	blood:	n/a
33	chr14:31890052-31890102	U87	brain:	n/a
34	chr14:31889003-31889053	HNPCEpiC	eye:	n/a
35	chr14:31889003-31889053	HPAEpiC	pulmonary alveolar:	n/a
36	chr14:31915923-31915973	AG09319	gingival:	n/a
37	chr14:31907252-31907302	HCF	heart:	n/a
38	chr14:31890052-31890102	MCF10A-Er-Src	breast:	n/a
39	chr14:31890001-31890051	MCF-7	breast:	n/a
40	chr14:31926792-31926842	HCM	heart:	n/a
41	chr14:31889169-31889219	PFSK-1	brain:	n/a
42	chr14:31926216-31926266	HIPEpiC	eye:	n/a
43	chr14:31889169-31889219	MCF10A-Er-Src	breast:	n/a
44	chr14:31926483-31926533	T-47D	breast:	n/a
45	chr14:31858202-31858252	NB4	blood:	n/a
46	chr14:31926564-31926614	HCPEpiC	choroid plexus:	n/a
47	chr14:31859505-31859555	U87	brain:	n/a
48	chr14:31926792-31926842	K562	blood:	n/a
49	chr14:31859515-31859565	NHDF-neo	bronchial:	n/a
50	chr14:31926299-31926349	MCF-7	breast:	n/a

(count:121 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:31676477..31678166-chr14:31816851..31818832,2	MCF-7	breast:
2	chr14:31878802..31880450-chr14:31888650..31890731,2	MCF-7	breast:
3	chr14:31880032..31886531-chr14:31888185..31891239,11	MCF-7	breast:
4	chr14:31854067..31858154-chr14:31887468..31890013,3	MCF-7	breast:
5	chr14:31805474..31807050-chr14:31809442..31811076,2	K562	blood:
6	chr14:31676619..31677277-chr14:31889333..31889964,2	K562	blood:
7	chr14:31907031..31909539-chr14:31909575..31912143,2	K562	blood:
8	chr14:31720575..31722092-chr14:31768141..31769654,2	MCF-7	breast:
9	chr14:31677123..31678687-chr14:31776671..31778228,2	MCF-7	breast:
10	chr14:31888413..31890616-chr14:31917360..31920011,3	MCF-7	breast:
11	chr14:31675912..31678861-chr14:31887661..31889789,2	K562	blood:
12	chr14:31906586..31908599-chr14:31913797..31916070,2	MCF-7	breast:
13	chr14:31675991..31678700-chr14:31818216..31819802,2	MCF-7	breast:
14	chr14:31782463..31784081-chr14:31788737..31791376,2	K562	blood:
15	chr14:31868409..31871104-chr14:31872239..31873925,2	K562	blood:
16	chr12:96591531..96592044-chr14:31831540..31832040,2	Hela-S3	cervix:
17	chr14:31833436..31835914-chr14:31836685..31838685,2	K562	blood:
18	chr14:31671940..31673668-chr14:31776880..31779409,2	MCF-7	breast:
19	chr14:31926509..31929146-chr14:31940368..31943663,3	MCF-7	breast:
20	chr14:31698046..31700432-chr14:31824994..31826810,2	K562	blood:
21	chr14:31899509..31901563-chr14:31901913..31904667,2	K562	blood:
22	chr14:31918485..31921453-chr14:31921609..31924237,3	MCF-7	breast:
23	chr14:31899509..31901563-chr14:31901913..31904667,2	K562	blood:
24	chr14:31909214..31911851-chr14:31915493..31917225,2	K562	blood:
25	chr14:31674936..31677888-chr14:31819206..31821782,3	MCF-7	breast:
26	chr14:31811249..31813398-chr14:31813760..31815314,2	MCF-7	breast:
27	chr14:31905050..31906638-chr14:31906776..31909651,2	K562	blood:
28	chr14:31909214..31911851-chr14:31915493..31917225,2	K562	blood:
29	chr14:31854067..31858154-chr14:31887468..31890013,3	MCF-7	breast:
30	chr14:31888336..31890825-chr14:31917653..31919383,2	MCF-7	breast:
31	chr14:31819147..31821275-chr14:31824530..31827299,2	K562	blood:
32	chr11:122932393..122933144-chr14:31926505..31927244,2	NB4	blood:
33	chr14:31676589..31678359-chr14:31823453..31827063,4	MCF-7	breast:
34	chr14:31888742..31889382-chr3:41241031..41241649,2	Hela-S3	cervix:
35	chr14:31914833..31916596-chr14:31919367..31920967,2	MCF-7	breast:
36	chr14:31890242..31892614-chr14:31901862..31904809,2	MCF-7	breast:
37	chr14:31906586..31908599-chr14:31913797..31916070,2	MCF-7	breast:
38	chr14:31864866..31867235-chr14:31869226..31871358,2	MCF-7	breast:
39	chr14:31861407..31863284-chr14:31887639..31889155,2	K562	blood:
40	chr14:31887818..31891601-chr14:31923594..31927929,15	K562	blood:
41	chr14:31675418..31678639-chr14:31811864..31816181,5	MCF-7	breast:
42	chr14:31925030..31927583-chr14:31933327..31936225,2	MCF-7	breast:
43	chr14:31872181..31874850-chr14:31924970..31926788,2	K562	blood:
44	chr14:31863925..31866635-chr14:31868935..31870560,2	K562	blood:
45	chr14:31914833..31916596-chr14:31919367..31920967,2	MCF-7	breast:
46	chr14:31874749..31876483-chr14:31879400..31881889,2	MCF-7	breast:
47	chr14:31913970..31917383-chr14:31917651..31919831,3	MCF-7	breast:
48	chr14:31887438..31889783-chr14:31913776..31915504,2	MCF-7	breast:
49	chr14:31676274..31678860-chr14:31889133..31891124,4	MCF-7	breast:
50	chr14:31889308..31890174-chr6:31795417..31795943,2	Hela-S3	cervix:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUBPL-1	chr14:31891050-31891174	ENSG00000250365
2	lnc-NUBPL-1	chr14:31889492-31889791	ENSG00000250365
3	lnc-NUBPL-1	chr14:31889964-31890183	ENSG00000250365
4	lnc-NUBPL-1	chr14:31891054-31891174	ENSG00000250365
5	lnc-NUBPL-1	chr14:31921313-31922089	ENSG00000250365
6	lnc-NUBPL-1	chr14:31891054-31891174	ENSG00000250365
7	lnc-NUBPL-1	chr14:31908878-31909151	ENSG00000250365
8	lnc-NUBPL-1	chr14:31908878-31909155	ENSG00000250365
9	lnc-NUBPL-1	chr14:31890150-31890183	ENSG00000250365
10	lnc-NUBPL-1	chr14:31914850-31914940	ENSG00000250365
11	lnc-C14orf126-7	chr14:31932001-31932577	NONHSAT036283

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
ENSG00000263784	TF binding region
ENSG00000203546	TF binding region
DTD2	TF binding region
HEATR5A	TF binding region
ENSG00000250365	TF binding region
ENSG00000239323	TF binding region
ENSG00000263784	CpG island
ENSG00000203546	CpG island
DTD2	CpG island
HEATR5A	CpG island
ENSG00000250365	CpG island
ENSG00000239323	CpG island
ENSG00000101361	chromatin interactions
ENSG00000257155	chromatin interactions
ENSG00000120533	chromatin interactions
ENSG00000187742	chromatin interactions
ENSG00000221062	chromatin interactions
ENSG00000250365	chromatin interactions
ENSG00000129493	chromatin interactions
ENSG00000204388	chromatin interactions
ENSG00000270820	chromatin interactions
ENSG00000109971	chromatin interactions
ENSG00000092148	chromatin interactions
ENSG00000120697	chromatin interactions
ENSG00000120699	chromatin interactions
ENSG00000196792	chromatin interactions
ENSG00000092108	chromatin interactions
ENSG00000129480	chromatin interactions
ENSG00000142188	chromatin interactions
ENSG00000120526	chromatin interactions
ENSG00000100478	chromatin interactions
ENSG00000168036	chromatin interactions
ENSG00000151413	chromatin interactions
ENSG00000200463	chromatin interactions
ENSG00000203546	chromatin interactions
ENSG00000245532	chromatin interactions
YTHDC1	miRNA target sites
CD274	miRNA target sites
SLC26A2	miRNA target sites
SERPINB5	miRNA target sites
ALG2	miRNA target sites
CCNG1	miRNA target sites

Extended variants
information (count: 6574 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:6574 , 50 per page) page: 1 2 3 4 5 6 7 ... 132

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10143519	chr14:31768231-31768232	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs530252908	chr14:31768232-31768233	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs4981837	chr14:31768253-31768254	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs570339323	chr14:31768268-31768269	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537300265	chr14:31768372-31768373	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs552190497	chr14:31768398-31768399	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570336522	chr14:31768420-31768421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534743651	chr14:31768421-31768422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553126063	chr14:31768525-31768526	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372308164	chr14:31768528-31768529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532369022	chr14:31768550-31768551	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561108212	chr14:31768575-31768576	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs142883617	chr14:31768601-31768602	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147263685	chr14:31768619-31768620	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550030939	chr14:31768641-31768642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12589270	chr14:31768642-31768643	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs191646793	chr14:31768653-31768654	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs77271170	chr14:31768654-31768655	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs373472797	chr14:31768684-31768685	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541001831	chr14:31768827-31768828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559437126	chr14:31768845-31768846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530094498	chr14:31768908-31768909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532523973	chr14:31768928-31768929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552493306	chr14:31768931-31768932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111614999	chr14:31768943-31768944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531268948	chr14:31768961-31768962	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559757404	chr14:31769022-31769023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183409251	chr14:31769044-31769045	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147929593	chr14:31769058-31769059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536807534	chr14:31769080-31769081	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547584184	chr14:31769089-31769090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113923837	chr14:31769101-31769102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs150057697	chr14:31769106-31769107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568161955	chr14:31769113-31769114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs59213341	chr14:31769196-31769197	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535539688	chr14:31769197-31769198	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187768156	chr14:31769200-31769201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565975334	chr14:31769204-31769205	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575332802	chr14:31769231-31769232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12888875	chr14:31769295-31769296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539751243	chr14:31769347-31769348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557791448	chr14:31769359-31769360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs75624002	chr14:31769364-31769365	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564197829	chr14:31769373-31769374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145475893	chr14:31769374-31769375	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528689475	chr14:31769376-31769377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370505620	chr14:31769380-31769381	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs548294442	chr14:31769431-31769432	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs367648392	chr14:31769501-31769502	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs191524202	chr14:31769534-31769535	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
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
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	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

Chromatin state (count:4550 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31749400-31789000	Weak transcription	Psoas Muscle	Psoas
2	chr14:31753200-31769400	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr14:31753200-31776600	Weak transcription	Aorta	Aorta
4	chr14:31753400-31769400	Weak transcription	Brain Anterior Caudate	brain
5	chr14:31753400-31769400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr14:31753400-31774000	Weak transcription	NHDF-Ad	bronchial
7	chr14:31753600-31772600	Weak transcription	Primary hematopoietic stem cells	blood
8	chr14:31755200-31769400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr14:31756200-31769800	Weak transcription	Liver	Liver
10	chr14:31756400-31769600	Weak transcription	Lung	lung
11	chr14:31756600-31769200	Weak transcription	Spleen	Spleen
12	chr14:31757200-31769200	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr14:31757200-31769400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr14:31757800-31769400	Weak transcription	Fetal Muscle Leg	muscle
15	chr14:31758000-31775600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr14:31759200-31769200	Weak transcription	Primary T cells from cord blood	blood
17	chr14:31759600-31769400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr14:31759800-31769400	Weak transcription	Fetal Brain Male	brain
19	chr14:31760200-31769200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr14:31760600-31779400	Weak transcription	Pancreas	Pancrea
21	chr14:31760800-31769200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr14:31760800-31769200	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr14:31760800-31771400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr14:31760800-31772800	Weak transcription	Primary B cells from peripheral blood	blood
25	chr14:31760800-31773200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr14:31760800-31774000	Weak transcription	Primary B cells from cord blood	blood
27	chr14:31760800-31776400	Weak transcription	Stomach Mucosa	stomach
28	chr14:31760800-31781000	Weak transcription	Fetal Kidney	kidney
29	chr14:31761000-31769200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr14:31761000-31769200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr14:31761000-31770600	Weak transcription	A549	lung
32	chr14:31761200-31771200	Weak transcription	Fetal Intestine Large	intestine
33	chr14:31761400-31769600	Weak transcription	Primary T cells fromperipheralblood	blood
34	chr14:31761400-31769600	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr14:31761400-31771200	Weak transcription	Primary T helper cells PMA-I stimulated	--
36	chr14:31761600-31769400	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr14:31761600-31770600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr14:31761600-31794400	Strong transcription	Primary neutrophils fromperipheralblood	blood
39	chr14:31761600-31794400	Strong transcription	Monocytes-CD14+_RO01746	blood
40	chr14:31762200-31780600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr14:31762200-31785200	Weak transcription	HMEC	breast
42	chr14:31762400-31769200	Weak transcription	Colon Smooth Muscle	Colon
43	chr14:31762400-31794800	Strong transcription	Primary monocytes fromperipheralblood	blood
44	chr14:31762600-31779800	Weak transcription	Esophagus	oesophagus
45	chr14:31762800-31769400	Weak transcription	Fetal Lung	lung
46	chr14:31762800-31771000	Weak transcription	Right Ventricle	heart
47	chr14:31762800-31783000	Weak transcription	Fetal Thymus	thymus
48	chr14:31762800-31811800	Weak transcription	Fetal Heart	heart
49	chr14:31763000-31769200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr14:31763000-31769400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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