Variant report

Variant	nsv901635
Chromosome Location	chr14:37623177-37782273
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2246)
CpG islands
(count:1588)
Chromatin interactive
region (count:148)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2246 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:37640439-37641338	K562	blood:	n/a	n/a
2	ARID3A	chr14:37666578-37667618	K562	blood:	n/a	n/a
3	ARID3A	chr14:37642484-37642976	K562	blood:	n/a	n/a
4	ARID3A	chr14:37665962-37666204	K562	blood:	n/a	n/a
5	ARID3A	chr14:37636859-37637271	K562	blood:	n/a	n/a
6	ARID3A	chr14:37643767-37644084	K562	blood:	n/a	n/a
7	ARID3A	chr14:37699763-37700208	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:37699852-37700129	K562	blood:	n/a	n/a
9	ARID3A	chr14:37636253-37636339	K562	blood:	n/a	n/a
10	ARID3A	chr14:37707129-37707415	HepG2	liver:	n/a	n/a
11	ARID3A	chr14:37739891-37740124	HepG2	liver:	n/a	n/a
12	ARID3A	chr14:37640896-37641730	HepG2	liver:	n/a	n/a
13	ARID3A	chr14:37667012-37667537	HepG2	liver:	n/a	n/a
14	ARID3A	chr14:37641543-37641674	K562	blood:	n/a	n/a
15	ARID3A	chr14:37702174-37702457	K562	blood:	n/a	n/a
16	ARID3A	chr14:37637980-37638323	K562	blood:	n/a	n/a
17	ARID3A	chr14:37638798-37638998	K562	blood:	n/a	chr14:37638878-37638894 chr14:37638877-37638893
18	ARID3A	chr14:37715436-37716157	HepG2	liver:	n/a	n/a
19	ARID3A	chr14:37720992-37722152	HepG2	liver:	n/a	n/a
20	ARID3A	chr14:37747860-37748994	HepG2	liver:	n/a	n/a
21	ARID3A	chr14:37664464-37664897	HepG2	liver:	n/a	n/a
22	ARID3A	chr14:37702064-37702476	HepG2	liver:	n/a	n/a
23	ARID3A	chr14:37668114-37668178	HepG2	liver:	n/a	n/a
24	ATF1	chr14:37636855-37637252	K562	blood:	n/a	n/a
25	ATF1	chr14:37637957-37638275	K562	blood:	n/a	n/a
26	ATF2	chr14:37636807-37637410	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr14:37636749-37637333	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr14:37641468-37642010	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr14:37641089-37641818	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF3	chr14:37666986-37667277	K562	blood:	n/a	n/a
31	ATF3	chr14:37641048-37641567	A549	lung:	n/a	n/a
32	ATF3	chr14:37639465-37639767	K562	blood:	n/a	n/a
33	ATF3	chr14:37650651-37650943	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr14:37636967-37637160	K562	blood:	n/a	n/a
35	BACH1	chr14:37666966-37667533	K562	blood:	n/a	n/a
36	BACH1	chr14:37667015-37667867	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr14:37641174-37642006	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr14:37636808-37637367	H1-hESC	embryonic stem cell:	n/a	n/a
39	BCL3	chr14:37640978-37641543	A549	lung:	n/a	n/a
40	BCL3	chr14:37641013-37641625	A549	lung:	n/a	n/a
41	BCLAF1	chr14:37640954-37641540	K562	blood:	n/a	n/a
42	BHLHE40	chr14:37641028-37642076	K562	blood:	n/a	n/a
43	BHLHE40	chr14:37702192-37702420	HepG2	liver:	n/a	n/a
44	BHLHE40	chr14:37715661-37715909	HepG2	liver:	n/a	n/a
45	BHLHE40	chr14:37637932-37638567	K562	blood:	n/a	n/a
46	BHLHE40	chr14:37702149-37702324	K562	blood:	n/a	n/a
47	BHLHE40	chr14:37666734-37667614	K562	blood:	n/a	n/a
48	BRCA1	chr14:37666826-37667336	HepG2	liver:	n/a	n/a
49	BRCA1	chr14:37641083-37642134	H1-hESC	embryonic stem cell:	n/a	n/a
50	BRCA1	chr14:37641014-37641539	Hela-S3	cervix:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:37638478-37638528	GM12892	blood:	n/a
2	chr14:37640455-37640505	MCF-7	breast:	n/a
3	chr14:37638478-37638528	GM12892	blood:	n/a
4	chr14:37640455-37640505	MCF-7	breast:	n/a
5	chr14:37638478-37638528	SAEC	small airway:	n/a
6	chr14:37644675-37644725	LNCaP	prostate:	n/a
7	chr14:37667689-37667739	Caco-2	colon:	n/a
8	chr14:37773865-37773915	GM12878	blood:	n/a
9	chr14:37641964-37642014	HL-60	blood:	n/a
10	chr14:37666920-37666970	U87	brain:	n/a
11	chr14:37666994-37667044	GM12892	blood:	n/a
12	chr14:37667689-37667739	HRPEpiC	eye:	n/a
13	chr14:37644675-37644725	U87	brain:	n/a
14	chr14:37641660-37641710	NB4	blood:	n/a
15	chr14:37666994-37667044	HepG2	liver:	n/a
16	chr14:37667230-37667280	GM12892	blood:	n/a
17	chr14:37639757-37639807	GM06990	blood:	n/a
18	chr14:37644675-37644725	T-47D	breast:	n/a
19	chr14:37666931-37666981	AG04450	lung:	fetal
20	chr14:37641134-37641184	HNPCEpiC	eye:	n/a
21	chr14:37666893-37666943	AG09309	skin:	n/a
22	chr14:37641261-37641311	HPAEpiC	pulmonary alveolar:	n/a
23	chr14:37666893-37666943	HNPCEpiC	eye:	n/a
24	chr14:37638478-37638528	AG04449	skin:	fetal
25	chr14:37638478-37638528	HEK293	kidney:	embryo
26	chr14:37667230-37667280	RPTEC	kidney:	n/a
27	chr14:37641191-37641241	IMR90	lung:	fetal
28	chr14:37666931-37666981	Hepatocyte	liver:	n/a
29	chr14:37666931-37666981	HRPEpiC	eye:	n/a
30	chr14:37641261-37641311	SK-N-SH_RA	brain:	n/a
31	chr14:37667230-37667280	HCT-116	colon:	n/a
32	chr14:37664088-37664138	GM19239	blood:	n/a
33	chr14:37641726-37641776	HPAEpiC	pulmonary alveolar:	n/a
34	chr14:37640455-37640505	AoSMC	blood vessel:	n/a
35	chr14:37644675-37644725	HEK293	kidney:	embryo
36	chr14:37641191-37641241	GM19239	blood:	n/a
37	chr14:37640247-37640297	SAEC	small airway:	n/a
38	chr14:37670820-37670870	MCF10A-Er-Src	breast:	n/a
39	chr14:37667261-37667311	SK-N-SH_RA	brain:	n/a
40	chr14:37641600-37641650	GM12878	blood:	n/a
41	chr14:37641261-37641311	AoSMC	blood vessel:	n/a
42	chr14:37667261-37667311	MCF-7	breast:	n/a
43	chr14:37641436-37641486	CMK	blood:	n/a
44	chr14:37667230-37667280	MCF-7	breast:	n/a
45	chr14:37641436-37641486	HPAEpiC	pulmonary alveolar:	n/a
46	chr14:37666931-37666981	HEEpiC	esophagus:	n/a
47	chr14:37641726-37641776	NT2-D1	testis:	n/a
48	chr14:37667833-37667883	PrEC	prostate:	n/a
49	chr14:37666810-37666860	HUVEC	blood vessel:	n/a
50	chr14:37640455-37640505	PFSK-1	brain:	n/a

(count:148 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:37668579..37671562-chr14:37686406..37688160,2	MCF-7	breast:
2	chr14:37666297..37668856-chr14:38035873..38037389,2	MCF-7	breast:
3	chr14:37619842..37620362-chr14:37699681..37700515,2	K562	blood:
4	chr14:37723534..37725938-chr14:37730959..37732560,2	K562	blood:
5	chr14:37710312..37712829-chr14:37714356..37716232,3	MCF-7	breast:
6	chr14:37704955..37707594-chr14:37708330..37711962,3	K562	blood:
7	chr14:37723949..37726058-chr14:37737860..37739770,2	MCF-7	breast:
8	chr14:37723534..37725938-chr14:37730959..37732560,2	K562	blood:
9	chr14:37669239..37670769-chr14:37675458..37677421,2	K562	blood:
10	chr14:37559384..37561307-chr14:37642361..37644125,2	K562	blood:
11	chr14:37691512..37693036-chr14:38063542..38065340,2	MCF-7	breast:
12	chr14:37640829..37643687-chr14:37650994..37653256,2	K562	blood:
13	chr14:37699430..37701952-chr14:37706278..37708031,2	MCF-7	breast:
14	chr14:37664939..37667912-chr14:38062947..38065316,3	MCF-7	breast:
15	chr14:37697987..37700834-chr14:38057234..38059879,2	MCF-7	breast:
16	chr14:37696817..37699280-chr14:37707291..37710248,2	MCF-7	breast:
17	chr14:37698096..37705480-chr14:38061309..38066013,13	MCF-7	breast:
18	chr14:37667088..37669471-chr14:37678201..37679725,2	K562	blood:
19	chr14:37738574..37741001-chr14:37743646..37745651,2	MCF-7	breast:
20	chr14:37700806..37703619-chr14:37711035..37714311,4	MCF-7	breast:
21	chr14:37635891..37637422-chr14:37666864..37668416,2	MCF-7	breast:
22	chr14:37723784..37725511-chr14:37726243..37728327,2	MCF-7	breast:
23	chr14:37632758..37634640-chr14:37640795..37642566,2	MCF-7	breast:
24	chr14:37731472..37733246-chr14:38060600..38063260,2	MCF-7	breast:
25	chr14:37729939..37731852-chr14:37742042..37744319,2	K562	blood:
26	chr1:45187178..45188919-chr14:37715615..37718367,2	MCF-7	breast:
27	chr14:37773087..37774613-chr14:38035112..38036997,2	MCF-7	breast:
28	chr14:37715456..37719212-chr14:38032266..38035206,4	MCF-7	breast:
29	chr14:37639617..37644848-chr14:37662875..37669924,15	K562	blood:
30	chr14:37715577..37716109-chr14:38062848..38063529,2	MCF-7	breast:
31	chr14:37747627..37749985-chr14:38051291..38052830,2	MCF-7	breast:
32	chr14:37639697..37645467-chr14:37664720..37672395,14	K562	blood:
33	chr14:37131202..37132825-chr14:37638068..37640984,2	K562	blood:
34	chr14:37645255..37646966-chr14:37650853..37653735,2	MCF-7	breast:
35	chr13:21961882..21963808-chr14:37714535..37717476,2	MCF-7	breast:
36	chr14:37723949..37726058-chr14:37737860..37739770,2	MCF-7	breast:
37	chr14:37688211..37691178-chr9:38067581..38070359,2	MCF-7	breast:
38	chr14:37619444..37620212-chr14:37699781..37700486,2	MCF-7	breast:
39	chr14:37645255..37646966-chr14:37650853..37653735,2	MCF-7	breast:
40	chr14:37641298..37642813-chr14:37662827..37664578,2	MCF-7	breast:
41	chr14:37714570..37718771-chr14:37719606..37724141,5	MCF-7	breast:
42	chr14:37680569..37683226-chr14:37683414..37685864,2	MCF-7	breast:
43	chr14:37639865..37642120-chr14:37651580..37653237,2	MCF-7	breast:
44	chr14:37720748..37721511-chr14:38034504..38035461,3	MCF-7	breast:
45	chr14:37714570..37718771-chr14:37719606..37724141,5	MCF-7	breast:
46	chr14:37642507..37644578-chr14:38042317..38044678,2	MCF-7	breast:
47	chr14:37715306..37715938-chr14:38034662..38035728,3	MCF-7	breast:
48	chr14:37735920..37738317-chr14:37741909..37743974,2	MCF-7	breast:
49	chr14:37734748..37736405-chr14:37736490..37738328,2	MCF-7	breast:
50	chr14:37720959..37721697-chr14:38343187..38344314,3	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-537P22.1.1-1	chr14:37727929-37730334	NONHSAT036457
2	lnc-RP11-537P22.1.1-1	chr14:37737668-37742505	l_969_chr14:37729807-37741737_76bGuttman_hES
3	lnc-MIPOL1-5	chr14:37641231-37642998	NR_033240
4	lnc-RP11-537P22.1.1-1	chr14:37732158-37732474	l_969_chr14:37729807-37741737_76bGuttman_hES
5	lnc-RP11-537P22.1.1-1	chr14:37716308-37716445	NONHSAT036456
6	lnc-RP11-537P22.1.1-1	chr14:37729808-37730221	l_969_chr14:37729807-37741737_76bGuttman_hES
7	lnc-RP11-537P22.1.1-1	chr14:37734270-37737659	l_969_chr14:37729807-37741737_76bGuttman_hES
8	lnc-RP11-537P22.1.1-1	chr14:37736143-37736374	NONHSAT036456
9	lnc-RP11-537P22.1.1-1	chr14:37717034-37717112	NONHSAT036456
10	lnc-RP11-537P22.1.1-1	chr14:37709629-37709774	NONHSAT036456

No data

Variant related genes	Relation type
MIPOL1	TF binding region
SLC25A21-AS1	TF binding region
SLC25A21	TF binding region
RNU6-273P	TF binding region
MIPOL1	CpG island
SLC25A21-AS1	CpG island
SLC25A21	CpG island
RNU6-273P	CpG island
ENSG00000258414	chromatin interactions
ENSG00000129514	chromatin interactions
ENSG00000258708	chromatin interactions
ENSG00000255872	chromatin interactions
ENSG00000259087	chromatin interactions
ENSG00000198807	chromatin interactions
ENSG00000183032	chromatin interactions
ENSG00000151338	chromatin interactions
ENSG00000139865	chromatin interactions
ENSG00000199377	chromatin interactions
ENSG00000107338	chromatin interactions
ENSG00000124216	chromatin interactions
ENSG00000136327	chromatin interactions

Extended variants
information (count: 5679 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:5679 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6571791	chr14:37623177-37623178	Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs528935865	chr14:37623181-37623182	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs548604392	chr14:37623191-37623192	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs568528911	chr14:37623289-37623290	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs537821116	chr14:37623307-37623308	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs188818619	chr14:37623390-37623391	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs571868415	chr14:37623412-37623413	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs534167647	chr14:37623462-37623463	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs554339822	chr14:37623493-37623494	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs7157361	chr14:37623501-37623502	Inactive region	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs181567232	chr14:37623537-37623538	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs184561563	chr14:37623547-37623548	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs556658616	chr14:37623592-37623593	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs79772389	chr14:37623615-37623616	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs189293545	chr14:37623651-37623652	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs545348840	chr14:37623659-37623660	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs200879163	chr14:37623665-37623666	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs564267440	chr14:37623666-37623667	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs201310556	chr14:37623673-37623674	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs200378912	chr14:37623674-37623675	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs199855416	chr14:37623675-37623676	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs200479311	chr14:37623676-37623677	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs182334201	chr14:37623691-37623692	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs559902412	chr14:37623720-37623721	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs35213391	chr14:37623737-37623738	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs529021051	chr14:37623788-37623789	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs534458919	chr14:37623812-37623813	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs548690036	chr14:37623844-37623845	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs35417690	chr14:37623849-37623850	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs76430976	chr14:37623850-37623851	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs201420052	chr14:37623863-37623864	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs397853387	chr14:37623864-37623865	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs185999740	chr14:37623869-37623870	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs34360521	chr14:37623917-37623918	Inactive region	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs372993017	chr14:37623925-37623926	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs34123291	chr14:37623930-37623931	Inactive region	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs571891472	chr14:37623951-37623952	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs150950636	chr14:37623987-37623988	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs369422301	chr14:37624101-37624102	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs543731013	chr14:37624111-37624112	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs139505744	chr14:37624138-37624139	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs190921816	chr14:37624142-37624143	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs149676185	chr14:37624147-37624148	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs181149209	chr14:37624158-37624159	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs556707672	chr14:37624173-37624174	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs576604248	chr14:37624216-37624217	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs79950649	chr14:37624280-37624281	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs528801358	chr14:37624281-37624282	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs116396734	chr14:37624288-37624289	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs147769168	chr14:37624324-37624325	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Lung cancer	20031968	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Prostate cancer	21147910	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1265 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37622200-37623400	Enhancers	K562	blood
2	chr14:37622800-37623200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr14:37629800-37630000	Enhancers	Pancreas	Pancrea
4	chr14:37630000-37638000	Weak transcription	Pancreas	Pancrea
5	chr14:37631000-37631200	Enhancers	K562	blood
6	chr14:37631200-37635000	Weak transcription	K562	blood
7	chr14:37631600-37636200	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr14:37634800-37635600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr14:37635000-37635200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr14:37635000-37636800	Enhancers	K562	blood
11	chr14:37635200-37635400	Enhancers	H1 Cell Line	embryonic stem cell
12	chr14:37635200-37636200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr14:37635200-37636800	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr14:37635400-37636400	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr14:37635600-37636000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr14:37636000-37636800	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr14:37636000-37638600	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr14:37636200-37637200	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr14:37636200-37637200	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr14:37636400-37638600	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr14:37636400-37638600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr14:37636400-37638800	Enhancers	H1 Cell Line	embryonic stem cell
23	chr14:37636400-37638800	Enhancers	H9 Cell Line	embryonic stem cell
24	chr14:37636600-37637200	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr14:37636800-37637000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
26	chr14:37636800-37637000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr14:37636800-37637000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr14:37636800-37639000	Flanking Active TSS	K562	blood
29	chr14:37637000-37637200	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr14:37637000-37637200	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr14:37637200-37637400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr14:37637200-37637600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr14:37637200-37637600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
34	chr14:37637200-37637600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
35	chr14:37637200-37637600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr14:37637200-37638000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
37	chr14:37637200-37638200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr14:37637400-37638200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr14:37637600-37638400	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr14:37637600-37638600	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr14:37637600-37638600	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr14:37637600-37639000	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr14:37637800-37638000	Enhancers	Fetal Heart	heart
44	chr14:37637800-37638400	Enhancers	Duodenum Mucosa	Duodenum
45	chr14:37638000-37638600	Enhancers	Pancreas	Pancrea
46	chr14:37638000-37638800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr14:37638000-37639000	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr14:37638200-37638400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr14:37638200-37638400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr14:37638200-37638600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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