Variant report

Variant	nsv542126
Chromosome Location	chr14:71212882-71623271
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5911)
CpG islands
(count:3540)
Chromatin interactive
region (count:207)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5911 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:71351840-71352115	K562	blood:	n/a	n/a
2	ARID3A	chr14:71284443-71284772	K562	blood:	n/a	n/a
3	ARID3A	chr14:71340419-71340591	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:71584599-71585049	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:71439131-71439396	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:71583321-71583963	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:71373929-71374421	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:71276464-71276848	HepG2	liver:	n/a	n/a
9	ARID3A	chr14:71375376-71375583	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:71453850-71454159	K562	blood:	n/a	n/a
11	ARID3A	chr14:71596906-71597822	K562	blood:	n/a	n/a
12	ARID3A	chr14:71610207-71610661	HepG2	liver:	n/a	n/a
13	ARID3A	chr14:71220371-71220825	HepG2	liver:	n/a	n/a
14	ARID3A	chr14:71361461-71362018	HepG2	liver:	n/a	n/a
15	ARID3A	chr14:71284372-71284814	HepG2	liver:	n/a	n/a
16	ATF1	chr14:71597363-71597860	K562	blood:	n/a	n/a
17	ATF1	chr14:71609002-71609339	K562	blood:	n/a	n/a
18	ATF1	chr14:71351546-71352024	K562	blood:	n/a	n/a
19	ATF1	chr14:71353461-71353701	K562	blood:	n/a	n/a
20	ATF1	chr14:71610189-71610768	K562	blood:	n/a	n/a
21	ATF1	chr14:71284404-71284743	K562	blood:	n/a	n/a
22	ATF1	chr14:71455163-71455464	K562	blood:	n/a	n/a
23	ATF1	chr14:71349878-71350140	K562	blood:	n/a	n/a
24	ATF2	chr14:71284266-71284837	GM12878	blood:	n/a	n/a
25	ATF2	chr14:71349705-71350296	GM12878	blood:	n/a	n/a
26	ATF2	chr14:71276357-71276899	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr14:71353081-71354548	GM12878	blood:	n/a	n/a
28	ATF2	chr14:71360585-71361103	GM12878	blood:	n/a	n/a
29	ATF2	chr14:71349760-71350288	GM12878	blood:	n/a	n/a
30	ATF2	chr14:71284376-71284776	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr14:71269918-71270409	GM12878	blood:	n/a	n/a
32	ATF2	chr14:71284309-71284784	GM12878	blood:	n/a	n/a
33	ATF2	chr14:71269885-71270492	GM12878	blood:	n/a	n/a
34	ATF2	chr14:71247208-71247665	GM12878	blood:	n/a	n/a
35	ATF2	chr14:71348200-71349213	GM12878	blood:	n/a	n/a
36	ATF2	chr14:71247054-71247788	GM12878	blood:	n/a	n/a
37	ATF2	chr14:71353074-71354442	GM12878	blood:	n/a	n/a
38	ATF2	chr14:71348210-71348994	GM12878	blood:	n/a	n/a
39	ATF2	chr14:71284315-71284822	H1-hESC	embryonic stem cell:	n/a	n/a
40	ATF3	chr14:71373936-71374105	K562	blood:	n/a	n/a
41	ATF3	chr14:71462500-71462644	K562	blood:	n/a	n/a
42	ATF3	chr14:71237208-71237637	HCT-116	colon:	n/a	n/a
43	ATF3	chr14:71610318-71610639	K562	blood:	n/a	n/a
44	ATF3	chr14:71488349-71488985	HCT-116	colon:	n/a	n/a
45	ATF3	chr14:71315650-71315906	K562	blood:	n/a	n/a
46	BACH1	chr14:71238595-71239093	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr14:71288671-71289319	H1-hESC	embryonic stem cell:	n/a	n/a
48	BACH1	chr14:71374691-71375583	H1-hESC	embryonic stem cell:	n/a	n/a
49	BATF	chr14:71284394-71284754	GM12878	blood:	n/a	n/a
50	BATF	chr14:71489604-71489981	GM12878	blood:	n/a	n/a

(count:3540 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:71472713-71472763	CMK	blood:	n/a
2	chr14:71606274-71606324	HIPEpiC	eye:	n/a
3	chr14:71472713-71472763	CMK	blood:	n/a
4	chr14:71606274-71606324	HIPEpiC	eye:	n/a
5	chr14:71375319-71375369	AG04450	lung:	fetal
6	chr14:71373858-71373908	AG09309	skin:	n/a
7	chr14:71288210-71288260	NT2-D1	testis:	n/a
8	chr14:71279803-71279853	NHBE	bronchial:	n/a
9	chr14:71276874-71276924	NHBE	bronchial:	n/a
10	chr14:71472713-71472763	PANC-1	pancreas:	n/a
11	chr14:71276874-71276924	CMK	blood:	n/a
12	chr14:71373980-71374030	SKMC	muscle:	n/a
13	chr14:71374612-71374662	AG09319	gingival:	n/a
14	chr14:71288210-71288260	T-47D	breast:	n/a
15	chr14:71375319-71375369	HL-60	blood:	n/a
16	chr14:71585510-71585560	NHDF-neo	bronchial:	n/a
17	chr14:71472713-71472763	HUVEC	blood vessel:	n/a
18	chr14:71555837-71555887	AoSMC	blood vessel:	n/a
19	chr14:71250264-71250314	HIPEpiC	eye:	n/a
20	chr14:71289843-71289893	HMEC	breast:	n/a
21	chr14:71250264-71250314	GM12892	blood:	n/a
22	chr14:71239883-71239933	Hepatocyte	liver:	n/a
23	chr14:71272941-71272991	AG10803	skin:	n/a
24	chr14:71323515-71323565	HUVEC	blood vessel:	n/a
25	chr14:71370423-71370473	AG04450	lung:	fetal
26	chr14:71277192-71277242	NT2-D1	testis:	n/a
27	chr14:71374784-71374834	U87	brain:	n/a
28	chr14:71272941-71272991	HNPCEpiC	eye:	n/a
29	chr14:71598219-71598269	GM12892	blood:	n/a
30	chr14:71373978-71374028	HRPEpiC	eye:	n/a
31	chr14:71581031-71581081	HPAEpiC	pulmonary alveolar:	n/a
32	chr14:71373978-71374028	HEEpiC	esophagus:	n/a
33	chr14:71374302-71374352	A549	lung:	n/a
34	chr14:71284925-71284975	GM12891	blood:	n/a
35	chr14:71288954-71289004	NH-A	brain:	n/a
36	chr14:71472713-71472763	MCF10A-Er-Src	breast:	n/a
37	chr14:71250277-71250327	HPAEpiC	pulmonary alveolar:	n/a
38	chr14:71279803-71279853	HIPEpiC	eye:	n/a
39	chr14:71605994-71606044	PFSK-1	brain:	n/a
40	chr14:71374299-71374349	Hela-S3	cervix:	n/a
41	chr14:71370423-71370473	SAEC	small airway:	n/a
42	chr14:71323515-71323565	H1-hESC	embryonic stem cell:	embryo
43	chr14:71290144-71290194	AG10803	skin:	n/a
44	chr14:71354913-71354963	ovcar-3	ovarian:	n/a
45	chr14:71275300-71275350	CMK	blood:	n/a
46	chr14:71606274-71606324	HRE	kidney:	n/a
47	chr14:71598219-71598269	NT2-D1	testis:	n/a
48	chr14:71606506-71606556	AG04450	lung:	fetal
49	chr14:71277141-71277191	HCF	heart:	n/a
50	chr14:71527576-71527626	CMK	blood:	n/a

(count:207 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr14:71299359..71302044-chr14:71302641..71304763,2	MCF-7	breast:
2	chr14:71237788..71240582-chr14:71241825..71244076,2	MCF-7	breast:
3	chr14:71283754..71285089-chr14:71421790..71423652,9	MCF-7	breast:
4	chr14:71605537..71606405-chr14:72219506..72220423,5	K562	blood:
5	chr14:71608562..71610263-chr14:71786915..71789760,2	MCF-7	breast:
6	chr14:71580577..71583944-chr14:71584359..71586589,3	K562	blood:
7	chr14:71274346..71277930-chr14:71282688..71286374,5	MCF-7	breast:
8	chr14:71370886..71377633-chr14:71420060..71424849,9	MCF-7	breast:
9	chr14:71214804..71217337-chr14:71274832..71276743,2	MCF-7	breast:
10	chr14:71441488..71443872-chr14:71448426..71449969,2	MCF-7	breast:
11	chr14:71189314..71191908-chr14:71220289..71222021,3	MCF-7	breast:
12	chr14:71340301..71340951-chr14:71422324..71423179,2	MCF-7	breast:
13	chr14:71212723..71214667-chr14:71236445..71239410,2	MCF-7	breast:
14	chr14:71414782..71415566-chr17:56717102..56717602,2	MCF-7	breast:
15	chr14:71362952..71365427-chr14:71368027..71370762,2	MCF-7	breast:
16	chr14:71372585..71374647-chr14:71376260..71377778,2	K562	blood:
17	chr14:71359505..71362289-chr14:71363900..71365887,4	MCF-7	breast:
18	chr14:71428566..71431049-chr14:71438511..71440761,2	MCF-7	breast:
19	chr14:71304429..71307285-chr14:71311780..71314188,2	K562	blood:
20	chr14:71212723..71214667-chr14:71236445..71239410,2	MCF-7	breast:
21	chr14:71373840..71374362-chr8:136469426..136469930,2	MCF-7	breast:
22	chr14:71284322..71285012-chr14:71422205..71423224,4	MCF-7	breast:
23	chr14:71605408..71606120-chr14:72322432..72323318,2	K562	blood:
24	chr14:71102508..71105172-chr14:71277207..71278775,2	MCF-7	breast:
25	chr14:71294085..71294861-chr14:71422503..71423266,2	MCF-7	breast:
26	chr14:71225781..71229364-chr14:71273423..71276710,3	MCF-7	breast:
27	chr14:71367722..71371068-chr14:71372863..71375706,4	MCF-7	breast:
28	chr14:71381579..71383875-chr14:71386950..71389719,2	MCF-7	breast:
29	chr14:71607200..71607876-chr14:72219653..72220319,2	MCF-7	breast:
30	chr14:71218602..71225147-chr14:71276029..71280278,8	MCF-7	breast:
31	chr14:71372532..71376222-chr14:71415679..71419226,4	MCF-7	breast:
32	chr14:71221857..71224156-chr14:71229104..71232104,3	MCF-7	breast:
33	chr14:71232260..71234567-chr14:71236816..71239226,2	MCF-7	breast:
34	chr14:71283754..71285089-chr14:71421790..71423652,9	MCF-7	breast:
35	chr14:71381579..71383875-chr14:71386950..71389719,2	MCF-7	breast:
36	chr14:71287734..71288653-chr14:71422559..71423263,2	MCF-7	breast:
37	chr14:71379419..71381346-chr14:71385671..71388258,2	MCF-7	breast:
38	chr14:71378921..71381459-chr14:71390825..71392481,2	MCF-7	breast:
39	chr14:71297374..71298989-chr14:71299419..71302162,2	MCF-7	breast:
40	chr14:71216108..71217908-chr14:71219307..71221968,2	MCF-7	breast:
41	chr14:71371849..71374730-chr14:71399686..71402743,4	MCF-7	breast:
42	chr14:71221751..71222316-chr14:71284453..71284972,2	MCF-7	breast:
43	chr14:71284164..71285160-chr14:71438670..71439594,2	MCF-7	breast:
44	chr14:71372925..71376620-chr14:71377787..71383660,12	MCF-7	breast:
45	chr14:71373112..71375503-chr14:71384629..71386969,3	MCF-7	breast:
46	chr14:71487162..71488929-chr14:71491873..71493814,2	MCF-7	breast:
47	chr14:71373548..71375387-chr14:71412068..71413840,2	MCF-7	breast:
48	chr14:71605729..71607505-chr14:71785859..71787973,2	MCF-7	breast:
49	chr14:71355468..71357237-chr14:71359840..71362416,2	MCF-7	breast:
50	chr14:71284204..71285103-chr14:72219527..72220049,2	K562	blood:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCNX-2	chr14:71277047-71277382	ENSG00000259153.1
2	lnc-PCNX-2	chr14:71281828-71282108	ENSG00000259153.1
3	lnc-MAP3K9-5	chr14:71337707-71338125	NONHSAT037596
4	lnc-MAP3K9-9	chr14:71552199-71552550	NONHSAT037605
5	lnc-PCNX-2	chr14:71276612-71277382	NONHSAT037591
6	lnc-MAP3K9-5	chr14:71339077-71339304	NONHSAT037596
7	lnc-MAP3K9-6	chr14:71416315-71416475	NONHSAT037599
8	lnc-PCNX-2	chr14:71281828-71282120	ENSG00000259153.1
9	lnc-SIPA1L1-5	chr14:71581486-71582098	NONHSAT037606
10	lnc-MAP3K9-8	chr14:71511092-71511357	NONHSAT037604
11	lnc-MAP3K9-10	chr14:71607842-71609970	ENSG00000269927.1
12	lnc-MAP3K9-4	chr14:71325561-71326146	NONHSAT037595
13	lnc-MAP3K9-5	chr14:71337707-71338125	FPKM1_group_9264_transcript_1
14	lnc-MAP3K9-7	chr14:71498403-71498687	NONHSAT037603
15	lnc-PCNX-2	chr14:71276922-71277008	ENSG00000259153.1
16	lnc-PCNX-2	chr14:71281828-71282021	NONHSAT037591
17	lnc-PCNX-2	chr14:71276648-71277391	NONHSAT037592
18	lnc-PCNX-4	chr14:71288641-71288839	NONHSAT037594
19	lnc-MAP3K9-5	chr14:71337844-71338071	FPKM1_group_9264_transcript_1
20	lnc-PCNX-2	chr14:71281828-71283587	NONHSAT037592
21	lnc-MAP3K9-6	chr14:71425183-71425396	NONHSAT037599
22	lnc-PCNX-4	chr14:71290537-71290888	NONHSAT037594

No data

Variant related genes	Relation type
ENSG00000258431	TF binding region
ENSG00000269927	TF binding region
ENSG00000259153	TF binding region
PCNX	TF binding region
ENSG00000258930	TF binding region
MAP3K9	TF binding region
PTTG4P	TF binding region
ENSG00000258966	TF binding region
ENSG00000258431	CpG island
ENSG00000269927	CpG island
ENSG00000259153	CpG island
PCNX	CpG island
ENSG00000258930	CpG island
MAP3K9	CpG island
PTTG4P	CpG island
ENSG00000258966	CpG island
ENSG00000164924	chromatin interactions
ENSG00000258930	chromatin interactions
ENSG00000133985	chromatin interactions
ENSG00000259153	chromatin interactions
ENSG00000240837	chromatin interactions
ENSG00000137274	chromatin interactions
ENSG00000266411	chromatin interactions
ENSG00000245466	chromatin interactions
ENSG00000006432	chromatin interactions
ENSG00000131773	chromatin interactions
ENSG00000100650	chromatin interactions
ENSG00000259115	chromatin interactions
ENSG00000080815	chromatin interactions
ENSG00000259146	chromatin interactions
ENSG00000258951	chromatin interactions
ENSG00000100731	chromatin interactions
ENSG00000063046	chromatin interactions
ENSG00000187742	chromatin interactions
ENSG00000197555	chromatin interactions
ENSG00000119787	chromatin interactions

Extended variants
information (count: 15623 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:15623 , 50 per page) page: 1 2 3 4 5 6 7 ... 313

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574426798	chr14:71212946-71212947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs534694768	chr14:71212991-71212992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553659518	chr14:71213023-71213024	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541687344	chr14:71213051-71213052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs34139058	chr14:71213071-71213072	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182945714	chr14:71213073-71213074	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs8011507	chr14:71213086-71213087	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs61988426	chr14:71213115-71213116	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs565417321	chr14:71213120-71213121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs61988427	chr14:71213190-71213191	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs61988428	chr14:71213214-71213215	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543160055	chr14:71213282-71213283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561618660	chr14:71213298-71213299	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141272854	chr14:71213332-71213333	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530429371	chr14:71213341-71213342	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs114935771	chr14:71213494-71213495	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs150345423	chr14:71213507-71213508	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528916120	chr14:71213561-71213562	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs187490522	chr14:71213574-71213575	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561678873	chr14:71213601-71213602	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570557980	chr14:71213653-71213654	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192933601	chr14:71213659-71213660	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138094881	chr14:71213686-71213687	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs574265567	chr14:71213723-71213724	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs184565519	chr14:71213726-71213727	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs541226338	chr14:71213763-71213764	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553609436	chr14:71213797-71213798	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187143854	chr14:71213856-71213857	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs2332455	chr14:71213871-71213872	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs36026675	chr14:71213885-71213886	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551659074	chr14:71213927-71213928	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs565112627	chr14:71213996-71213997	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs143700475	chr14:71214059-71214060	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs544343066	chr14:71214074-71214075	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563116562	chr14:71214141-71214142	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530268342	chr14:71214156-71214157	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548793025	chr14:71214186-71214187	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs147245521	chr14:71214196-71214197	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs527971174	chr14:71214210-71214211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552186783	chr14:71214221-71214222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs8018294	chr14:71214238-71214239	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs75324714	chr14:71214245-71214246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192316019	chr14:71214252-71214253	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113335018	chr14:71214267-71214268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535304884	chr14:71214307-71214308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553546370	chr14:71214379-71214380	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs572037291	chr14:71214391-71214392	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs564698316	chr14:71214420-71214421	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs34982178	chr14:71214459-71214460	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs140756803	chr14:71214489-71214490	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
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
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Epilepsy	20502679	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:11178 , 50 per page) page: 1 2 3 4 5 6 7 ... 224

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71185800-71219200	Weak transcription	Stomach Mucosa	stomach
2	chr14:71186000-71221600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr14:71186000-71221600	Weak transcription	Hela-S3	cervix
4	chr14:71190000-71214400	Weak transcription	Rectal Smooth Muscle	rectum
5	chr14:71191400-71220000	Weak transcription	Fetal Brain Male	brain
6	chr14:71191600-71220200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr14:71192400-71220200	Weak transcription	Fetal Kidney	kidney
8	chr14:71192600-71221800	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr14:71194000-71222000	Weak transcription	HSMMtube	muscle
10	chr14:71194400-71213400	Weak transcription	Psoas Muscle	Psoas
11	chr14:71194400-71221600	Weak transcription	Left Ventricle	heart
12	chr14:71194600-71218600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr14:71194600-71221600	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr14:71196200-71217000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr14:71197000-71228800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr14:71197600-71217000	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr14:71198400-71223400	Weak transcription	Primary hematopoietic stem cells	blood
18	chr14:71199600-71219600	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr14:71200200-71216400	Weak transcription	Brain Hippocampus Middle	brain
20	chr14:71200400-71215400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr14:71200600-71224200	Weak transcription	Spleen	Spleen
22	chr14:71200800-71213000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr14:71201200-71215200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr14:71201200-71228000	Weak transcription	Colonic Mucosa	Colon
25	chr14:71201600-71219000	Weak transcription	Lung	lung
26	chr14:71201600-71220600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr14:71204800-71229400	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr14:71205000-71219000	Weak transcription	Brain Angular Gyrus	brain
29	chr14:71205400-71220400	Weak transcription	Small Intestine	intestine
30	chr14:71206000-71218200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr14:71206800-71215000	Weak transcription	Aorta	Aorta
32	chr14:71206800-71221000	Weak transcription	Stomach Smooth Muscle	stomach
33	chr14:71206800-71231600	Weak transcription	Brain Anterior Caudate	brain
34	chr14:71207000-71215200	Weak transcription	HepG2	liver
35	chr14:71207000-71215400	Weak transcription	GM12878-XiMat	blood
36	chr14:71207000-71221800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr14:71207000-71221800	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr14:71207200-71214000	Weak transcription	Primary T cells from cord blood	blood
39	chr14:71207600-71214600	Weak transcription	Dnd41	blood
40	chr14:71207800-71213000	Weak transcription	Primary B cells from cord blood	blood
41	chr14:71207800-71215200	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr14:71208600-71215000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr14:71209000-71215400	Weak transcription	Liver	Liver
44	chr14:71209200-71215400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr14:71209200-71229400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr14:71209400-71213000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr14:71209400-71213800	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr14:71209400-71214400	Weak transcription	Primary T helper cells fromperipheralblood	blood
49	chr14:71209400-71215000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr14:71209400-71215000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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