Variant report

Variant	nsv1054013
Chromosome Location	chr14:21868964-21992109
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3624)
CpG islands
(count:3484)
Chromatin interactive
region (count:208)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:3624 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:21944173-21945505	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:21945763-21945767	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:21943952-21944111	K562	blood:	n/a	n/a
4	ARID3A	chr14:21905341-21905986	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:21944489-21944740	K562	blood:	n/a	n/a
6	ARID3A	chr14:21923992-21924994	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:21923518-21923683	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:21905416-21905636	K562	blood:	n/a	n/a
9	ARID3A	chr14:21979291-21979782	HepG2	liver:	n/a	chr14:21979443-21979458
10	ARID3A	chr14:21966738-21967030	K562	blood:	n/a	n/a
11	ARID3A	chr14:21945015-21945422	K562	blood:	n/a	n/a
12	ARID3A	chr14:21966671-21967139	HepG2	liver:	n/a	n/a
13	ATF1	chr14:21909009-21909364	K562	blood:	n/a	n/a
14	ATF1	chr14:21945060-21945516	K562	blood:	n/a	n/a
15	ATF1	chr14:21979341-21979788	K562	blood:	n/a	n/a
16	ATF1	chr14:21905327-21905918	K562	blood:	n/a	n/a
17	ATF1	chr14:21924142-21924679	K562	blood:	n/a	n/a
18	ATF2	chr14:21944895-21945496	GM12878	blood:	n/a	n/a
19	ATF2	chr14:21979113-21979851	GM12878	blood:	n/a	n/a
20	ATF2	chr14:21945128-21945466	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr14:21944987-21945661	GM12878	blood:	n/a	n/a
22	ATF2	chr14:21905255-21905759	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr14:21905204-21905788	GM12878	blood:	n/a	n/a
24	ATF2	chr14:21973180-21973706	GM12878	blood:	n/a	n/a
25	ATF2	chr14:21979242-21979799	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr14:21924321-21925038	GM12878	blood:	n/a	n/a
27	ATF2	chr14:21905255-21905664	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr14:21882106-21882854	GM12878	blood:	n/a	n/a
29	ATF2	chr14:21924081-21924931	GM12878	blood:	n/a	n/a
30	ATF2	chr14:21905270-21905749	GM12878	blood:	n/a	n/a
31	ATF2	chr14:21979271-21979788	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr14:21924544-21924861	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF2	chr14:21882139-21882796	GM12878	blood:	n/a	n/a
34	ATF2	chr14:21924316-21924827	H1-hESC	embryonic stem cell:	n/a	n/a
35	ATF3	chr14:21979193-21979791	A549	lung:	n/a	n/a
36	ATF3	chr14:21924290-21924804	A549	lung:	n/a	chr14:21924500-21924510
37	ATF3	chr14:21979380-21979699	K562	blood:	n/a	n/a
38	ATF3	chr14:21945064-21945537	A549	lung:	n/a	n/a
39	ATF3	chr14:21905296-21905785	A549	lung:	n/a	chr14:21905444-21905453
40	BACH1	chr14:21871511-21871605	K562	blood:	n/a	n/a
41	BACH1	chr14:21945348-21945422	K562	blood:	n/a	n/a
42	BACH1	chr14:21945179-21945506	H1-hESC	embryonic stem cell:	n/a	n/a
43	BATF	chr14:21882235-21882762	GM12878	blood:	n/a	chr14:21882430-21882439
44	BATF	chr14:21917516-21918064	GM12878	blood:	n/a	chr14:21917682-21917690
45	BATF	chr14:21917771-21918058	GM12878	blood:	n/a	n/a
46	BATF	chr14:21882185-21882522	GM12878	blood:	n/a	chr14:21882430-21882439
47	BCL11A	chr14:21895418-21895840	GM12878	blood:	n/a	n/a
48	BCL11A	chr14:21882211-21882615	GM12878	blood:	n/a	n/a
49	BCL11A	chr14:21882264-21882540	GM12878	blood:	n/a	n/a
50	BCL3	chr14:21895251-21896148	GM12878	blood:	n/a	n/a

(count:3484 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21991255-21991305	Jurkat	blood:	n/a
2	chr14:21942464-21942514	Jurkat	blood:	n/a
3	chr14:21901071-21901121	SK-N-SH_RA	brain:	n/a
4	chr14:21944873-21944923	AG09309	skin:	n/a
5	chr14:21924628-21924678	GM12892	blood:	n/a
6	chr14:21942464-21942514	HepG2	liver:	n/a
7	chr14:21905501-21905551	SK-N-SH	brain:	n/a
8	chr14:21991255-21991305	Jurkat	blood:	n/a
9	chr14:21942464-21942514	Jurkat	blood:	n/a
10	chr14:21901071-21901121	SK-N-SH_RA	brain:	n/a
11	chr14:21944873-21944923	AG09309	skin:	n/a
12	chr14:21924628-21924678	GM12892	blood:	n/a
13	chr14:21942464-21942514	HepG2	liver:	n/a
14	chr14:21905501-21905551	SK-N-SH	brain:	n/a
15	chr14:21945175-21945225	CMK	blood:	n/a
16	chr14:21945400-21945450	HCPEpiC	choroid plexus:	n/a
17	chr14:21944788-21944838	HNPCEpiC	eye:	n/a
18	chr14:21944788-21944838	GM19239	blood:	n/a
19	chr14:21924393-21924443	GM19239	blood:	n/a
20	chr14:21901071-21901121	PFSK-1	brain:	n/a
21	chr14:21924005-21924055	Caco-2	colon:	n/a
22	chr14:21945053-21945103	HCF	heart:	n/a
23	chr14:21905945-21905995	HCPEpiC	choroid plexus:	n/a
24	chr14:21979654-21979704	HCM	heart:	n/a
25	chr14:21900916-21900966	T-47D	breast:	n/a
26	chr14:21944853-21944903	T-47D	breast:	n/a
27	chr14:21949306-21949356	U87	brain:	n/a
28	chr14:21966454-21966504	SKMC	muscle:	n/a
29	chr14:21979464-21979514	AG04450	lung:	fetal
30	chr14:21979673-21979723	HAEpiC	amniotic membrane:	n/a
31	chr14:21979675-21979725	SKMC	muscle:	n/a
32	chr14:21945210-21945260	K562	blood:	n/a
33	chr14:21904906-21904956	GM12878	blood:	n/a
34	chr14:21924005-21924055	HCM	heart:	n/a
35	chr14:21901071-21901121	GM12891	blood:	n/a
36	chr14:21924489-21924539	PFSK-1	brain:	n/a
37	chr14:21944967-21945017	HCT-116	colon:	n/a
38	chr14:21905501-21905551	HEK293	kidney:	embryo
39	chr14:21979675-21979725	AG09319	gingival:	n/a
40	chr14:21924628-21924678	HCT-116	colon:	n/a
41	chr14:21979554-21979604	PFSK-1	brain:	n/a
42	chr14:21942464-21942514	HUVEC	blood vessel:	n/a
43	chr14:21979464-21979514	HAEpiC	amniotic membrane:	n/a
44	chr14:21944853-21944903	SKMC	muscle:	n/a
45	chr14:21924628-21924678	HEEpiC	esophagus:	n/a
46	chr14:21945285-21945335	GM12878	blood:	n/a
47	chr14:21905552-21905602	SK-N-SH_RA	brain:	n/a
48	chr14:21900916-21900966	Hepatocyte	liver:	n/a
49	chr14:21945210-21945260	SKMC	muscle:	n/a
50	chr14:21979594-21979644	IMR90	lung:	fetal

(count:208 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr14:21964090..21967088-chr14:22024145..22025808,2	K562	blood:
2	chr14:21959862..21960636-chr5:114825215..114825885,2	MCF-7	breast:
3	chr14:21927790..21931604-chr14:21933413..21935482,4	K562	blood:
4	chr14:21943699..21946735-chr14:21977733..21982256,4	MCF-7	breast:
5	chr14:21969916..21972018-chr14:21978032..21980758,3	K562	blood:
6	chr14:21895886..21898457-chr14:21923417..21926008,3	MCF-7	breast:
7	chr14:21974369..21977190-chr14:22017356..22019662,2	MCF-7	breast:
8	chr14:21972318..21975113-chr14:21978008..21980143,3	K562	blood:
9	chr14:21896024..21898915-chr14:21922681..21926768,3	MCF-7	breast:
10	chr14:21977974..21981747-chr14:21991693..21997000,9	MCF-7	breast:
11	chr14:21874917..21880880-chr14:21901855..21906138,6	MCF-7	breast:
12	chr14:21966582..21968425-chr14:21990390..21992940,3	K562	blood:
13	chr14:21904676..21909671-chr14:21916010..21919638,5	MCF-7	breast:
14	chr14:21966391..21966954-chr14:21994368..21995242,2	K562	blood:
15	chr14:21944239..21947571-chr14:21970430..21973821,4	MCF-7	breast:
16	chr14:21968819..21970753-chr14:21994142..21996626,2	K562	blood:
17	chr14:21931960..21934120-chr14:21934946..21937150,2	K562	blood:
18	chr14:21978397..21980476-chr14:21982589..21985443,4	K562	blood:
19	chr14:21927154..21929240-chr14:21977185..21979577,2	MCF-7	breast:
20	chr14:21958167..21960481-chr14:21978207..21981018,2	MCF-7	breast:
21	chr14:21876017..21878615-chr14:21922957..21924829,2	MCF-7	breast:
22	chr14:21904269..21906743-chr14:21992458..21995215,2	K562	blood:
23	chr14:21908719..21910349-chr14:21917450..21919306,2	K562	blood:
24	chr14:21977943..21985344-chr14:21985568..21995608,22	MCF-7	breast:
25	chr14:21943958..21946610-chr14:21966325..21968366,2	MCF-7	breast:
26	chr14:21977989..21980901-chr14:22001631..22005636,4	K562	blood:
27	chr14:21926286..21927863-chr14:21941529..21943943,2	K562	blood:
28	chr14:21903784..21905572-chr14:21943555..21945925,2	MCF-7	breast:
29	chr14:21908706..21910690-chr14:21978697..21980987,2	MCF-7	breast:
30	chr14:21922971..21924665-chr14:21973742..21975845,3	MCF-7	breast:
31	chr14:21948837..21951421-chr14:21953212..21956640,4	MCF-7	breast:
32	chr14:21922608..21930261-chr14:21941288..21947915,21	MCF-7	breast:
33	chr14:21924893..21927310-chr14:22025908..22027691,2	MCF-7	breast:
34	chr14:21737007..21739696-chr14:21870070..21871764,2	MCF-7	breast:
35	chr14:21904171..21908174-chr14:21922677..21925847,6	K562	blood:
36	chr14:21850845..21853690-chr14:21904139..21906102,2	K562	blood:
37	chr14:21898735..21900936-chr14:21901002..21903454,2	MCF-7	breast:
38	chr14:21941797..21947093-chr14:21954513..21961521,11	MCF-7	breast:
39	chr14:21932869..21935832-chr14:21936427..21939516,4	K562	blood:
40	chr14:21923462..21925701-chr14:21977921..21979566,3	MCF-7	breast:
41	chr14:21977974..21981747-chr14:21991693..21997000,9	MCF-7	breast:
42	chr14:21902087..21907117-chr14:21919849..21925728,16	MCF-7	breast:
43	chr14:21904171..21908174-chr14:21922677..21925847,6	K562	blood:
44	chr14:21933234..21935173-chr14:21944414..21946874,3	MCF-7	breast:
45	chr14:21979626..21980207-chr14:35451381..35451961,2	Hela-S3	cervix:
46	chr14:21924456..21927951-chr14:21928618..21932822,6	K562	blood:
47	chr14:21929955..21932056-chr14:21939536..21941971,2	MCF-7	breast:
48	chr14:21966153..21966705-chr20:52556158..52557026,2	MCF-7	breast:
49	chr14:21907278..21910254-chr14:21912129..21914781,3	K562	blood:
50	chr14:21923806..21924454-chr6:30584518..30585192,2	Hela-S3	cervix:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TOX4-1	chr14:21989234-21989450	ENSG00000257096.1
2	lnc-CHD8-1	chr14:21920031-21920326	NONHSAT035689
3	lnc-CHD8-1	chr14:21920436-21920463	NONHSAT035689
4	lnc-SALL2-1	chr14:21978797-21979122	NONHSAT035696
5	lnc-TOX4-2	chr14:21887779-21888119	NONHSAT035685
6	lnc-CHD8-1	chr14:21923108-21923302	NONHSAT035687
7	lnc-CHD8-1	chr14:21915532-21916694	NONHSAT035689
8	lnc-CHD8-1	chr14:21918923-21920648	ucscGeneNc_uc001wds_1
9	lnc-CHD8-1	chr14:21924191-21924285	NONHSAT035687
10	lnc-CHD8-1	chr14:21911321-21911699	NONHSAT035689
11	lnc-CHD8-1	chr14:21905353-21905457	NONHSAT035688
12	lnc-RAB2B-1	chr14:21897669-21897965	NONHSAT035686
13	lnc-CHD8-1	chr14:21899897-21900017	NONHSAT035688
14	lnc-CHD8-1	chr14:21905060-21905124	NONHSAT035688
15	lnc-CHD8-1	chr14:21924191-21924249	NONHSAT035689
16	lnc-CHD8-1	chr14:21899892-21900017	NONHSAT035687
17	lnc-SALL2-1	chr14:21979266-21979482	NONHSAT035695
18	lnc-SALL2-1	chr14:21976035-21976377	NONHSAT035694
19	lnc-SALL2-1	chr14:21979266-21979482	NONHSAT035694
20	lnc-TOX4-1	chr14:21990540-21990794	ENSG00000257096.1
21	lnc-CHD8-1	chr14:21921422-21921753	NONHSAT035689
22	lnc-SALL2-1	chr14:21978710-21979055	NONHSAT035695
23	lnc-SALL2-1	chr14:21979266-21979484	NONHSAT035696

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RAB2B	hsa-miR-421	chr14:21927219-21927240

Variant related genes	Relation type
SNORD8	TF binding region
ENSG00000257096	TF binding region
TOX4	TF binding region
EIF4EBP1P1	TF binding region
RAB2B	TF binding region
RN7SL650P	TF binding region
METTL3	TF binding region
CHD8	TF binding region
SNORD8	CpG island
ENSG00000257096	CpG island
TOX4	CpG island
EIF4EBP1P1	CpG island
RAB2B	CpG island
RN7SL650P	CpG island
METTL3	CpG island
CHD8	CpG island
ENSG00000092199	chromatin interactions
ENSG00000249944	chromatin interactions
ENSG00000233224	chromatin interactions
ENSG00000112701	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000129472	chromatin interactions
ENSG00000165821	chromatin interactions
ENSG00000257096	chromatin interactions
ENSG00000258704	chromatin interactions
ENSG00000260830	chromatin interactions
ENSG00000236352	chromatin interactions
ENSG00000172809	chromatin interactions
ENSG00000199436	chromatin interactions
ENSG00000141232	chromatin interactions
ENSG00000100883	chromatin interactions
ENSG00000204569	chromatin interactions
ENSG00000166295	chromatin interactions
ENSG00000184270	chromatin interactions
ENSG00000196331	chromatin interactions
ENSG00000263621	chromatin interactions
ENSG00000100888	chromatin interactions
ENSG00000092203	chromatin interactions
ENSG00000196262	chromatin interactions
ENSG00000092201	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000165819	chromatin interactions
ENSG00000178096	chromatin interactions
ENSG00000138303	chromatin interactions
ENSG00000165476	chromatin interactions

Extended variants
information (count: 4734 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:4734 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573166520	chr14:21868980-21868981	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs180736864	chr14:21868995-21868996	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs376085268	chr14:21869022-21869023	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs202038154	chr14:21869039-21869040	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs114613223	chr14:21869096-21869097	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs199879706	chr14:21869100-21869101	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs184431500	chr14:21869118-21869119	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs372249897	chr14:21869166-21869167	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs200990367	chr14:21869170-21869171	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs550810496	chr14:21869243-21869244	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561100431	chr14:21869248-21869249	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs377106104	chr14:21869251-21869252	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs114296736	chr14:21869276-21869277	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs553979887	chr14:21869283-21869284	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567031220	chr14:21869302-21869303	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532520194	chr14:21869309-21869310	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189276717	chr14:21869318-21869319	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573708536	chr14:21869322-21869323	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542962997	chr14:21869349-21869350	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs116406114	chr14:21869358-21869359	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537093907	chr14:21869442-21869443	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs557200117	chr14:21869472-21869473	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148945209	chr14:21869497-21869498	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536569745	chr14:21869510-21869511	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371635478	chr14:21869522-21869523	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181953883	chr14:21869539-21869540	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143716456	chr14:21869551-21869552	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565133430	chr14:21869577-21869578	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576454823	chr14:21869622-21869623	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201280690	chr14:21869650-21869651	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200532423	chr14:21869688-21869689	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113076568	chr14:21869705-21869706	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs199499304	chr14:21869708-21869709	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs386380840	chr14:21869709-21869710	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377491158	chr14:21869714-21869715	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs34206530	chr14:21869715-21869716	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs77328066	chr14:21869716-21869717	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs202081921	chr14:21869744-21869745	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375753246	chr14:21869751-21869752	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544260380	chr14:21869761-21869762	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561161811	chr14:21869769-21869770	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138082808	chr14:21869814-21869815	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186567579	chr14:21869820-21869821	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543869633	chr14:21869832-21869833	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76398661	chr14:21869835-21869836	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143655868	chr14:21869878-21869879	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs529286755	chr14:21869910-21869911	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375247980	chr14:21869991-21869992	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147214337	chr14:21870011-21870012	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571114390	chr14:21870042-21870043	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Ewing''s sarcoma	18628472	CNVD
Rheumatoid arthritis	23223014	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ependymoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:4897 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21853200-21884400	Strong transcription	NH-A	brain
2	chr14:21853200-21904000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr14:21853400-21875800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr14:21853400-21876000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr14:21853400-21876200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr14:21853400-21876200	Strong transcription	Osteobl	bone
7	chr14:21853400-21876400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr14:21853400-21877800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr14:21853400-21879800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr14:21853400-21884200	Strong transcription	Colon Smooth Muscle	Colon
11	chr14:21853400-21884400	Strong transcription	Fetal Muscle Leg	muscle
12	chr14:21853400-21884800	Strong transcription	Fetal Brain Female	brain
13	chr14:21853400-21900000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr14:21853400-21900000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr14:21853400-21900000	Strong transcription	Adipose Nuclei	Adipose
16	chr14:21853400-21900000	Strong transcription	Placenta	Placenta
17	chr14:21853400-21900200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr14:21853400-21901800	Strong transcription	HUES64 Cell Line	embryonic stem cell
19	chr14:21853600-21876800	Strong transcription	Fetal Stomach	stomach
20	chr14:21853600-21884000	Strong transcription	Brain Substantia Nigra	brain
21	chr14:21853600-21884400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr14:21853600-21884400	Strong transcription	HSMM	muscle
23	chr14:21853600-21885000	Strong transcription	Stomach Smooth Muscle	stomach
24	chr14:21853600-21885800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr14:21853600-21886800	Strong transcription	Duodenum Smooth Muscle	Duodenum
26	chr14:21853600-21888800	Strong transcription	Fetal Intestine Large	intestine
27	chr14:21853600-21897200	Strong transcription	Fetal Muscle Trunk	muscle
28	chr14:21853600-21900000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr14:21853600-21900200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr14:21853600-21900200	Strong transcription	Primary neutrophils fromperipheralblood	blood
31	chr14:21853600-21901400	Strong transcription	HUES6 Cell Line	embryonic stem cell
32	chr14:21853600-21902000	Strong transcription	HUES48 Cell Line	embryonic stem cell
33	chr14:21853600-21903400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr14:21853800-21884400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
35	chr14:21853800-21900000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr14:21853800-21900000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr14:21853800-21900200	Strong transcription	Fetal Thymus	thymus
38	chr14:21853800-21901400	Strong transcription	Primary T cells fromperipheralblood	blood
39	chr14:21854000-21873400	Strong transcription	Fetal Intestine Small	intestine
40	chr14:21854000-21885800	Strong transcription	HepG2	liver
41	chr14:21854000-21900200	Strong transcription	Monocytes-CD14+_RO01746	blood
42	chr14:21854000-21904000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr14:21854200-21884400	Strong transcription	H9 Cell Line	embryonic stem cell
44	chr14:21854200-21885400	Strong transcription	H1 Cell Line	embryonic stem cell
45	chr14:21854400-21886400	Strong transcription	Dnd41	blood
46	chr14:21854400-21900000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr14:21854400-21900200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
48	chr14:21855200-21900200	Strong transcription	Primary T helper cells fromperipheralblood	blood
49	chr14:21855600-21884400	Strong transcription	Brain Inferior Temporal Lobe	brain
50	chr14:21855600-21897000	Strong transcription	Skeletal Muscle Female	skeletal muscle

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