Variant report

Variant	esv1811231
Chromosome Location	chr17:45520374-45764956
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5405)
CpG islands
(count:2076)
Chromatin interactive
region (count:140)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:11)

(count:5405 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:45764299-45764352	K562	blood:	n/a	n/a
2	ARID3A	chr17:45570956-45571035	HepG2	liver:	n/a	n/a
3	ARID3A	chr17:45726147-45727406	K562	blood:	n/a	chr17:45726715-45726723
4	ARID3A	chr17:45764133-45764847	HepG2	liver:	n/a	n/a
5	ARID3A	chr17:45726430-45727425	HepG2	liver:	n/a	chr17:45726715-45726723
6	ARID3A	chr17:45693174-45693540	K562	blood:	n/a	n/a
7	ARID3A	chr17:45741772-45742038	K562	blood:	n/a	n/a
8	ARID3A	chr17:45697829-45698241	HepG2	liver:	n/a	n/a
9	ARID3A	chr17:45569946-45569952	K562	blood:	n/a	n/a
10	ARID3A	chr17:45741727-45742046	HepG2	liver:	n/a	n/a
11	ARID3A	chr17:45569945-45570183	HepG2	liver:	n/a	n/a
12	ARID3A	chr17:45728051-45728218	K562	blood:	n/a	n/a
13	ATF1	chr17:45726594-45727381	K562	blood:	n/a	n/a
14	ATF1	chr17:45569891-45570104	K562	blood:	n/a	n/a
15	ATF2	chr17:45761715-45762265	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr17:45569649-45570147	GM12878	blood:	n/a	n/a
17	ATF2	chr17:45727926-45728447	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr17:45726910-45727484	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr17:45726982-45727451	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr17:45702182-45702433	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr17:45726478-45727487	GM12878	blood:	n/a	n/a
22	ATF2	chr17:45726190-45726921	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF3	chr17:45726893-45727331	K562	blood:	n/a	n/a
24	ATF3	chr17:45727109-45727454	K562	blood:	n/a	n/a
25	ATF3	chr17:45726097-45727536	A549	lung:	n/a	chr17:45726822-45726831 chr17:45726671-45726680
26	ATF3	chr17:45569734-45570294	A549	lung:	n/a	n/a
27	ATF3	chr17:45727015-45727178	GM12878	blood:	n/a	n/a
28	ATF3	chr17:45569636-45570283	A549	lung:	n/a	n/a
29	ATF3	chr17:45569908-45570164	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF3	chr17:45726845-45727478	A549	lung:	n/a	n/a
31	ATF3	chr17:45569872-45570174	K562	blood:	n/a	n/a
32	BACH1	chr17:45688008-45688377	K562	blood:	n/a	n/a
33	BACH1	chr17:45727020-45727417	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr17:45569861-45570142	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr17:45726533-45726750	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr17:45688020-45688343	H1-hESC	embryonic stem cell:	n/a	n/a
37	BATF	chr17:45579872-45580148	GM12878	blood:	n/a	chr17:45580000-45580010
38	BATF	chr17:45688037-45688336	GM12878	blood:	n/a	chr17:45688193-45688204
39	BATF	chr17:45579678-45580209	GM12878	blood:	n/a	chr17:45580000-45580010
40	BATF	chr17:45578032-45578241	GM12878	blood:	n/a	n/a
41	BATF	chr17:45569645-45570111	GM12878	blood:	n/a	n/a
42	BATF	chr17:45688022-45688356	GM12878	blood:	n/a	chr17:45688193-45688204
43	BCL11A	chr17:45579668-45580125	GM12878	blood:	n/a	chr17:45579999-45580008
44	BCL11A	chr17:45609110-45609438	GM12878	blood:	n/a	chr17:45609227-45609236 chr17:45609179-45609192 chr17:45609236-45609245
45	BCL11A	chr17:45579757-45579928	GM12878	blood:	n/a	n/a
46	BCL3	chr17:45726259-45727531	A549	lung:	n/a	chr17:45727383-45727392 chr17:45726766-45726779
47	BCL3	chr17:45761376-45762530	A549	lung:	n/a	chr17:45762320-45762329 chr17:45761498-45761507
48	BCL3	chr17:45764154-45765730	A549	lung:	n/a	n/a
49	BCL3	chr17:45726062-45727833	A549	lung:	n/a	chr17:45727383-45727392 chr17:45726766-45726779 chr17:45727591-45727600 chr17:45726149-45726158
50	BCL3	chr17:45727842-45729046	A549	lung:	n/a	chr17:45727864-45727873 chr17:45728192-45728205 chr17:45728149-45728158

(count:2076 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45726922-45726972	AG10803	skin:	n/a
2	chr17:45726674-45726724	NHBE	bronchial:	n/a
3	chr17:45726922-45726972	AG10803	skin:	n/a
4	chr17:45726674-45726724	NHBE	bronchial:	n/a
5	chr17:45566670-45566720	PFSK-1	brain:	n/a
6	chr17:45730222-45730272	AoSMC	blood vessel:	n/a
7	chr17:45728198-45728248	HNPCEpiC	eye:	n/a
8	chr17:45569959-45570009	GM12892	blood:	n/a
9	chr17:45726993-45727043	AoSMC	blood vessel:	n/a
10	chr17:45570168-45570218	SAEC	small airway:	n/a
11	chr17:45608114-45608164	ECC-1	luminal epithelium:	n/a
12	chr17:45727790-45727840	SK-N-SH	brain:	n/a
13	chr17:45728198-45728248	HepG2	liver:	n/a
14	chr17:45612338-45612388	Caco-2	colon:	n/a
15	chr17:45764416-45764466	K562	blood:	n/a
16	chr17:45608823-45608873	NHBE	bronchial:	n/a
17	chr17:45570168-45570218	A549	lung:	n/a
18	chr17:45730222-45730272	SK-N-SH	brain:	n/a
19	chr17:45727598-45727648	ovcar-3	ovarian:	n/a
20	chr17:45608315-45608365	HCF	heart:	n/a
21	chr17:45729462-45729512	HCM	heart:	n/a
22	chr17:45723587-45723637	ovcar-3	ovarian:	n/a
23	chr17:45609121-45609171	ProgFib	skin:	n/a
24	chr17:45608315-45608365	HRCEpiC	kidney:	n/a
25	chr17:45727224-45727274	BE2_C	brain:	n/a
26	chr17:45764416-45764466	Caco-2	colon:	n/a
27	chr17:45742350-45742400	Hela-S3	cervix:	n/a
28	chr17:45726624-45726674	HEK293	kidney:	embryo
29	chr17:45570133-45570183	HNPCEpiC	eye:	n/a
30	chr17:45608315-45608365	HRE	kidney:	n/a
31	chr17:45573695-45573745	HL-60	blood:	n/a
32	chr17:45729462-45729512	AG09309	skin:	n/a
33	chr17:45604514-45604564	AG04450	lung:	fetal
34	chr17:45608114-45608164	ovcar-3	ovarian:	n/a
35	chr17:45727082-45727132	Caco-2	colon:	n/a
36	chr17:45608114-45608164	HEEpiC	esophagus:	n/a
37	chr17:45570133-45570183	HRPEpiC	eye:	n/a
38	chr17:45681383-45681433	T-47D	breast:	n/a
39	chr17:45608315-45608365	HEK293	kidney:	embryo
40	chr17:45727082-45727132	ovcar-3	ovarian:	n/a
41	chr17:45699322-45699372	HCM	heart:	n/a
42	chr17:45690396-45690446	AG09309	skin:	n/a
43	chr17:45727224-45727274	ovcar-3	ovarian:	n/a
44	chr17:45727790-45727840	GM06990	blood:	n/a
45	chr17:45729462-45729512	HRPEpiC	eye:	n/a
46	chr17:45681383-45681433	AG09319	gingival:	n/a
47	chr17:45730222-45730272	PrEC	prostate:	n/a
48	chr17:45730222-45730272	Hela-S3	cervix:	n/a
49	chr17:45727790-45727840	GM19239	blood:	n/a
50	chr17:45727226-45727276	SK-N-SH_RA	brain:	n/a

(count:140 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr17:45730303..45731847-chr17:45769244..45772062,2	K562	blood:
2	chr17:45694884..45697521-chr17:45701270..45704059,2	MCF-7	breast:
3	chr17:45727442..45729892-chr17:45739351..45741247,2	MCF-7	breast:
4	chr17:45725427..45729938-chr17:45759883..45763405,4	K562	blood:
5	chr17:45697869..45699408-chr17:45722972..45724595,2	K562	blood:
6	chr17:45727061..45727672-chr19:32896650..32897193,2	Hela-S3	cervix:
7	chr17:45749460..45751951-chr17:45753751..45757866,4	MCF-7	breast:
8	chr17:45750672..45751212-chr17:45764128..45764905,2	MCF-7	breast:
9	chr17:45751990..45754304-chr17:45764467..45767340,2	K562	blood:
10	chr17:45729521..45732354-chr17:45842842..45844447,2	MCF-7	breast:
11	chr17:45752623..45755412-chr17:45757645..45762048,4	K562	blood:
12	chr17:45717280..45719877-chr17:45720528..45723492,3	K562	blood:
13	chr17:45730053..45732033-chr17:45770907..45773039,2	K562	blood:
14	chr17:45718911..45722559-chr17:45723248..45729310,6	MCF-7	breast:
15	chr17:45747731..45749258-chr17:45753796..45755965,2	K562	blood:
16	chr17:45608528..45610827-chr17:45614421..45616919,2	MCF-7	breast:
17	chr17:45726655..45728758-chr17:45764709..45766556,3	K562	blood:
18	chr17:45749677..45752105-chr17:45758082..45761229,3	MCF-7	breast:
19	chr17:45747412..45755395-chr17:49020513..49031227,19	MCF-7	breast:
20	chr17:45399473..45401724-chr17:45692079..45694320,2	K562	blood:
21	chr17:45694079..45700174-chr17:45702807..45705612,6	K562	blood:
22	chr17:45751758..45755455-chr17:45769353..45774872,5	MCF-7	breast:
23	chr17:45698425..45699322-chr17:45867182..45867731,2	MCF-7	breast:
24	chr17:45748954..45758231-chr17:45766475..45774270,24	MCF-7	breast:
25	chr17:45728622..45731157-chr17:45764804..45766776,2	MCF-7	breast:
26	chr17:45728509..45729299-chr3:169482236..169483194,2	Hela-S3	cervix:
27	chr17:45750672..45751212-chr17:45764128..45764905,2	MCF-7	breast:
28	chr17:45741427..45742405-chr17:45867146..45867910,3	MCF-7	breast:
29	chr17:45743966..45745807-chr17:45749328..45753090,3	K562	blood:
30	chr17:45739359..45743830-chr17:45751715..45754078,4	K562	blood:
31	chr17:45569553..45571642-chr17:45608535..45610078,2	MCF-7	breast:
32	chr17:45747430..45749206-chr17:45749942..45752288,2	MCF-7	breast:
33	chr17:45700634..45703555-chr17:45708176..45711349,3	MCF-7	breast:
34	chr12:49658462..49659340-chr17:45727327..45727843,2	HCT-116	colon:
35	chr17:45726968..45727634-chr2:128145066..128146033,2	HCT-116	colon:
36	chr17:45731399..45733307-chr17:45733395..45735702,2	MCF-7	breast:
37	chr17:45738206..45745873-chr17:45748268..45754078,8	K562	blood:
38	chr17:45751990..45754304-chr17:45764467..45767340,2	K562	blood:
39	chr17:45700978..45703641-chr17:45726585..45728583,2	K562	blood:
40	chr17:45758194..45759902-chr17:45762797..45765497,2	K562	blood:
41	chr17:45752325..45755092-chr17:45763938..45765718,2	K562	blood:
42	chr17:45744847..45747701-chr17:45770377..45772396,2	MCF-7	breast:
43	chr17:45750858..45751981-chr17:45764122..45765029,9	MCF-7	breast:
44	chr17:45750780..45752037-chr17:45770257..45771137,11	MCF-7	breast:
45	chr17:45681295..45682836-chr17:45684602..45686967,2	MCF-7	breast:
46	chr17:45727256..45728937-chr17:46047807..46049675,2	K562	blood:
47	chr17:45750793..45752075-chr17:45770216..45771134,22	MCF-7	breast:
48	chr17:45695726..45697562-chr17:45698247..45700833,3	K562	blood:
49	chr17:45736747..45739364-chr17:45750041..45751842,2	MCF-7	breast:
50	chr17:45749460..45751951-chr17:45753751..45757866,4	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC040934.1-3	chr17:45703372-45703993	ENSG00000263766.1
2	lnc-AC040934.1-3	chr17:45726762-45726786	ENSG00000263766.1
3	lnc-AC040934.1-3	chr17:45713878-45713967	ENSG00000263766.1
4	lnc-NPEPPS-1	chr17:45714104-45714793	NONHSAT054321
5	lnc-AC040934.1-3	chr17:45703913-45703993	ENSG00000263766.1
6	lnc-AC040934.1-3	chr17:45699208-45699453	ENSG00000263766.1
7	lnc-NPEPPS-1	chr17:45711118-45713021	NONHSAT054319
8	lnc-AC040934.1-3	chr17:45726762-45726782	ENSG00000263766.1
9	lnc-AC040934.1-3	chr17:45724887-45727274	NONHSAT054322
10	lnc-AC040934.1-3	chr17:45713878-45713967	ENSG00000263766.1
11	lnc-C17orf57-1	chr17:45522601-45522883	NONHSAT054305
12	lnc-NPEPPS-1	chr17:45712863-45714258	NONHSAT054320
13	lnc-OSBPL7-1	chr17:45759783-45760049	ENSG00000264558.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	NPEPPS	hsa-miR-27b-3p	chr17:45699528-45699550
2	KPNB1	hsa-miR-181b-5p	chr17:45760646-45760653
3	KPNB1	hsa-miR-181b-5p	chr17:45760631-45760653
4	NPEPPS	hsa-miR-122-5p	chr17:45699574-45699594
5	NPEPPS	hsa-miR-122-5p	chr17:45699436-45699443
6	KPNB1	hsa-miR-181b-5p	chr17:45759861-45759867
7	KPNB1	hsa-miR-128-3p	chr17:45760627-45760648
8	KPNB1	hsa-miR-181b-5p	chr17:45759849-45759868
9	NPEPPS	hsa-miR-27b-3p	chr17:45699543-45699550
10	KPNB1	hsa-miR-128-3p	chr17:45760146-45760168
11	NPEPPS	hsa-miR-122-5p	chr17:45699422-45699443

Variant related genes	Relation type
ENSG00000264558	TF binding region
KPNB1	TF binding region
NPEPPS	TF binding region
MRPL45P2	TF binding region
ENSG00000263766	TF binding region
ENSG00000206734	TF binding region
ENSG00000264558	CpG island
KPNB1	CpG island
NPEPPS	CpG island
MRPL45P2	CpG island
ENSG00000263766	CpG island
ENSG00000206734	CpG island
ENSG00000251665	chromatin interactions
ENSG00000263766	chromatin interactions
ENSG00000178904	chromatin interactions
ENSG00000141232	chromatin interactions
ENSG00000108424	chromatin interactions
ENSG00000258101	chromatin interactions
ENSG00000270141	chromatin interactions
ENSG00000073861	chromatin interactions
ENSG00000129514	chromatin interactions
ENSG00000264558	chromatin interactions
ENSG00000141279	chromatin interactions
ENSG00000159111	chromatin interactions
ENSG00000228782	chromatin interactions
ENSG00000141294	chromatin interactions
ENSG00000247011	chromatin interactions
ENSG00000167553	chromatin interactions
ENSG00000178852	chromatin interactions
ENSG00000107077	chromatin interactions
ENSG00000180198	chromatin interactions
ENSG00000117360	chromatin interactions
ENSG00000108465	chromatin interactions
ENSG00000201524	chromatin interactions
ENSG00000229980	chromatin interactions
ENSG00000198933	chromatin interactions
ENSG00000006025	chromatin interactions
ENSG00000263293	chromatin interactions
ENSG00000242125	chromatin interactions
ENSG00000007392	chromatin interactions
ENSG00000169967	chromatin interactions
ITM2B	miRNA target sites

Extended variants
information (count: 8341 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:8341 , 50 per page) page: 1 2 3 4 5 6 7 ... 167

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201403133	chr17:45520428-45520429	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs370297134	chr17:45520494-45520495	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554141101	chr17:45520511-45520512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192013832	chr17:45520593-45520594	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370399483	chr17:45520658-45520659	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182459473	chr17:45520712-45520713	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563160259	chr17:45520755-45520756	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532304182	chr17:45520761-45520762	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs74872857	chr17:45520833-45520834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554763668	chr17:45520914-45520915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559755014	chr17:45520927-45520928	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576751828	chr17:45520930-45520931	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140244041	chr17:45520935-45520936	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548648547	chr17:45520943-45520944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544018008	chr17:45520957-45520958	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs80216744	chr17:45520958-45520959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371623180	chr17:45520985-45520986	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185666751	chr17:45521026-45521027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189689081	chr17:45521042-45521043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570961997	chr17:45521110-45521111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2125872	chr17:45521120-45521121	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs541331681	chr17:45521132-45521133	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531617530	chr17:45521134-45521135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553282991	chr17:45521152-45521153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560100156	chr17:45521191-45521192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565814924	chr17:45521202-45521203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs56311726	chr17:45521216-45521217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554180166	chr17:45521367-45521368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11867373	chr17:45521373-45521374	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs145546893	chr17:45521433-45521434	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556788703	chr17:45521449-45521450	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs576971700	chr17:45521552-45521553	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182081483	chr17:45521553-45521554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368744409	chr17:45521596-45521597	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187879707	chr17:45521610-45521611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559277219	chr17:45521629-45521630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573314045	chr17:45521642-45521643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs28692901	chr17:45521644-45521645	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs562079070	chr17:45521675-45521676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2446754	chr17:45521693-45521694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530898210	chr17:45521766-45521767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144318291	chr17:45521773-45521774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564840612	chr17:45521787-45521788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs59851684	chr17:45521788-45521789	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs35146451	chr17:45521791-45521792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547200610	chr17:45521831-45521832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566939106	chr17:45522110-45522111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534430716	chr17:45522129-45522130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547854813	chr17:45522208-45522209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34213797	chr17:45522293-45522294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	21163964	CNVD
Epithelial cancer	20478067	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:5099 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45501400-45554200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr17:45501400-45554400	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr17:45501600-45555400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr17:45501600-45556400	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr17:45501800-45533400	Weak transcription	Gastric	stomach
6	chr17:45501800-45547400	Weak transcription	Fetal Muscle Trunk	muscle
7	chr17:45501800-45550200	Weak transcription	Ovary	ovary
8	chr17:45502200-45548000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr17:45502800-45548600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr17:45503200-45545400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr17:45505200-45550200	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr17:45506400-45523000	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr17:45507200-45555000	Weak transcription	Fetal Thymus	thymus
14	chr17:45507600-45554200	Weak transcription	Left Ventricle	heart
15	chr17:45508000-45521000	Weak transcription	Fetal Intestine Small	intestine
16	chr17:45509400-45527800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr17:45509600-45527800	Weak transcription	Fetal Stomach	stomach
18	chr17:45512200-45530400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr17:45512200-45530800	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr17:45512200-45550200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr17:45513000-45544000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr17:45513400-45545400	Weak transcription	Liver	Liver
23	chr17:45514000-45530200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr17:45515400-45551600	Weak transcription	Fetal Intestine Large	intestine
25	chr17:45515600-45554200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr17:45515800-45531800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr17:45516000-45556400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr17:45516200-45531800	Weak transcription	Esophagus	oesophagus
29	chr17:45516800-45553200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr17:45517000-45550600	Weak transcription	Adipose Nuclei	Adipose
31	chr17:45517200-45547600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr17:45517400-45547400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr17:45517600-45530200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr17:45517600-45550200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr17:45518000-45568800	Weak transcription	K562	blood
36	chr17:45518200-45554200	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr17:45518400-45520400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr17:45518400-45521400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr17:45518400-45545800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr17:45518400-45550200	Weak transcription	Lung	lung
41	chr17:45518600-45520400	Weak transcription	Hela-S3	cervix
42	chr17:45518600-45569200	Weak transcription	Brain Anterior Caudate	brain
43	chr17:45518800-45530200	Weak transcription	Fetal Muscle Leg	muscle
44	chr17:45519000-45545400	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr17:45519000-45551600	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr17:45519400-45569400	Weak transcription	Primary B cells from peripheral blood	blood
47	chr17:45519600-45520400	Weak transcription	Primary hematopoietic stem cells	blood
48	chr17:45519600-45550200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr17:45519800-45555000	Weak transcription	Thymus	Thymus
50	chr17:45520000-45542400	Weak transcription	Fetal Lung	lung

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