Variant report

Variant	nsv1057229
Chromosome Location	chr18:29335175-29514265
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1074)
CpG islands
(count:427)
Chromatin interactive
region (count:87)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1074 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:29410587-29411037	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:29399616-29400000	K562	blood:	n/a	n/a
3	ARID3A	chr18:29353089-29353218	HepG2	liver:	n/a	chr18:29353104-29353120 chr18:29353105-29353121
4	ARID3A	chr18:29354185-29354541	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:29353021-29353274	K562	blood:	n/a	chr18:29353104-29353120 chr18:29353105-29353121
6	ARID3A	chr18:29354946-29355261	HepG2	liver:	n/a	n/a
7	ATF1	chr18:29401606-29402106	K562	blood:	n/a	n/a
8	ATF1	chr18:29440689-29440984	K562	blood:	n/a	n/a
9	ATF1	chr18:29399629-29399927	K562	blood:	n/a	n/a
10	ATF2	chr18:29405727-29406206	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr18:29406652-29407178	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr18:29354318-29354709	GM12878	blood:	n/a	n/a
13	ATF2	chr18:29371602-29372544	GM12878	blood:	n/a	n/a
14	ATF2	chr18:29371699-29372406	GM12878	blood:	n/a	n/a
15	ATF2	chr18:29399490-29399948	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr18:29406502-29407104	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr18:29399592-29399986	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr18:29405635-29406183	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr18:29354133-29354876	GM12878	blood:	n/a	n/a
20	BACH1	chr18:29399184-29400109	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr18:29405473-29405587	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr18:29379832-29380106	GM12878	blood:	n/a	n/a
23	BATF	chr18:29371452-29372095	GM12878	blood:	n/a	n/a
24	BATF	chr18:29371486-29372130	GM12878	blood:	n/a	n/a
25	BATF	chr18:29372132-29372577	GM12878	blood:	n/a	n/a
26	BCL11A	chr18:29371641-29372573	GM12878	blood:	n/a	n/a
27	BCL11A	chr18:29371693-29372493	GM12878	blood:	n/a	n/a
28	BCLAF1	chr18:29371608-29372303	GM12878	blood:	n/a	n/a
29	BHLHE40	chr18:29371685-29372594	GM12878	blood:	n/a	n/a
30	BHLHE40	chr18:29401508-29402184	K562	blood:	n/a	n/a
31	BHLHE40	chr18:29369372-29369717	K562	blood:	n/a	n/a
32	BHLHE40	chr18:29399717-29399878	GM12878	blood:	n/a	n/a
33	BHLHE40	chr18:29405874-29406016	GM12878	blood:	n/a	n/a
34	BHLHE40	chr18:29354566-29354617	GM12878	blood:	n/a	n/a
35	BRCA1	chr18:29372509-29372526	GM12878	blood:	n/a	n/a
36	CBX3	chr18:29358270-29358801	HCT-116	colon:	n/a	n/a
37	CBX3	chr18:29358358-29358680	K562	blood:	n/a	n/a
38	CBX3	chr18:29358323-29358696	K562	blood:	n/a	n/a
39	CBX3	chr18:29401628-29402091	K562	blood:	n/a	n/a
40	CCNT2	chr18:29340804-29340984	K562	blood:	n/a	n/a
41	CCNT2	chr18:29401571-29402076	K562	blood:	n/a	n/a
42	CCNT2	chr18:29449383-29449518	K562	blood:	n/a	n/a
43	CCNT2	chr18:29451961-29452161	K562	blood:	n/a	n/a
44	CEBPB	chr18:29507035-29507251	HepG2	liver:	n/a	chr18:29507126-29507137
45	CEBPB	chr18:29443099-29443453	IMR90	lung:	n/a	chr18:29443277-29443288
46	CEBPB	chr18:29365429-29365739	Hela-S3	cervix:	n/a	chr18:29365576-29365587
47	CEBPB	chr18:29506931-29507389	MCF-7	breast:	n/a	chr18:29507126-29507137
48	CEBPB	chr18:29352704-29353014	A549	lung:	n/a	chr18:29352856-29352865 chr18:29352851-29352868 chr18:29352856-29352865 chr18:29352856-29352865
49	CEBPB	chr18:29506940-29507321	Hela-S3	cervix:	n/a	chr18:29507126-29507137
50	CEBPB	chr18:29506960-29507283	K562	blood:	n/a	chr18:29507126-29507137

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29340902-29340952	NHBE	bronchial:	n/a
2	chr18:29341842-29341892	NHDF-neo	bronchial:	n/a
3	chr18:29409612-29409662	HRE	kidney:	n/a
4	chr18:29340788-29340838	HCM	heart:	n/a
5	chr18:29340788-29340838	GM12891	blood:	n/a
6	chr18:29340902-29340952	IMR90	lung:	fetal
7	chr18:29409612-29409662	HRPEpiC	eye:	n/a
8	chr18:29340788-29340838	HAEpiC	amniotic membrane:	n/a
9	chr18:29341842-29341892	HPAEpiC	pulmonary alveolar:	n/a
10	chr18:29409612-29409662	Caco-2	colon:	n/a
11	chr18:29341865-29341915	GM06990	blood:	n/a
12	chr18:29340916-29340966	HIPEpiC	eye:	n/a
13	chr18:29409612-29409662	GM12891	blood:	n/a
14	chr18:29341842-29341892	NHBE	bronchial:	n/a
15	chr18:29409612-29409662	HMEC	breast:	n/a
16	chr18:29340916-29340966	GM06990	blood:	n/a
17	chr18:29340902-29340952	AG09319	gingival:	n/a
18	chr18:29341865-29341915	AG09319	gingival:	n/a
19	chr18:29340788-29340838	HEK293	kidney:	embryo
20	chr18:29341842-29341892	MCF-7	breast:	n/a
21	chr18:29340902-29340952	HIPEpiC	eye:	n/a
22	chr18:29341842-29341892	AG04450	lung:	fetal
23	chr18:29340788-29340838	ProgFib	skin:	n/a
24	chr18:29341842-29341892	AoSMC	blood vessel:	n/a
25	chr18:29409612-29409662	PFSK-1	brain:	n/a
26	chr18:29409612-29409662	AG10803	skin:	n/a
27	chr18:29341865-29341915	HL-60	blood:	n/a
28	chr18:29341842-29341892	HCPEpiC	choroid plexus:	n/a
29	chr18:29409612-29409662	MCF-7	breast:	n/a
30	chr18:29340788-29340838	HCPEpiC	choroid plexus:	n/a
31	chr18:29409612-29409662	IMR90	lung:	fetal
32	chr18:29341865-29341915	SK-N-MC	brain:	n/a
33	chr18:29340916-29340966	HEEpiC	esophagus:	n/a
34	chr18:29341865-29341915	ovcar-3	ovarian:	n/a
35	chr18:29340902-29340952	AG04449	skin:	fetal
36	chr18:29340916-29340966	HRCEpiC	kidney:	n/a
37	chr18:29409612-29409662	A549	lung:	n/a
38	chr18:29340919-29340969	GM06990	blood:	n/a
39	chr18:29341865-29341915	PFSK-1	brain:	n/a
40	chr18:29340788-29340838	HCF	heart:	n/a
41	chr18:29340916-29340966	SK-N-MC	brain:	n/a
42	chr18:29409612-29409662	SKMC	muscle:	n/a
43	chr18:29340788-29340838	SK-N-SH_RA	brain:	n/a
44	chr18:29409612-29409662	H1-hESC	embryonic stem cell:	embryo
45	chr18:29341842-29341892	LNCaP	prostate:	n/a
46	chr18:29340916-29340966	IMR90	lung:	fetal
47	chr18:29409612-29409662	MCF10A-Er-Src	breast:	n/a
48	chr18:29340902-29340952	HepG2	liver:	n/a
49	chr18:29341842-29341892	Caco-2	colon:	n/a
50	chr18:29340916-29340966	HPAEpiC	pulmonary alveolar:	n/a

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr18:29407667..29410510-chr18:29494386..29496036,2	K562	blood:
2	chr18:29487420..29490004-chr18:29496191..29498820,2	K562	blood:
3	chr18:29490307..29491921-chr18:29494473..29497276,2	K562	blood:
4	chr18:29401567..29403770-chr18:29418064..29420663,2	K562	blood:
5	chr18:29487420..29490004-chr18:29496191..29498820,2	K562	blood:
6	chr18:29359553..29362434-chr18:29368590..29370453,2	K562	blood:
7	chr18:29450239..29451940-chr18:29466117..29468159,2	K562	blood:
8	chr18:29493108..29495287-chr18:29497330..29499746,2	K562	blood:
9	chr18:29452756..29454913-chr18:29671972..29673873,2	MCF-7	breast:
10	chr18:29290630..29291464-chr18:29399315..29400108,2	MCF-7	breast:
11	chr18:29501674..29503497-chr18:29522527..29524041,2	MCF-7	breast:
12	chr18:29408804..29411024-chr18:29521543..29524021,2	K562	blood:
13	chr18:29511145..29516088-chr18:29521483..29523975,5	MCF-7	breast:
14	chr18:29473750..29476339-chr18:29521274..29523147,2	K562	blood:
15	chr18:29469486..29471321-chr18:29471990..29473993,2	MCF-7	breast:
16	chr18:29372571..29374604-chr18:29381332..29383402,2	MCF-7	breast:
17	chr18:29483369..29487458-chr18:29519948..29522209,3	K562	blood:
18	chr18:29503480..29505119-chr18:29513383..29515079,2	K562	blood:
19	chr18:29439841..29442303-chr18:29446126..29448884,2	K562	blood:
20	chr18:29320909..29321461-chr18:29399293..29400251,2	MCF-7	breast:
21	chr18:29474340..29476672-chr18:29479905..29482693,2	K562	blood:
22	chr18:29506087..29508444-chr18:29510343..29513453,3	MCF-7	breast:
23	chr18:29503480..29505119-chr18:29513383..29515079,2	K562	blood:
24	chr18:29493108..29495287-chr18:29497330..29499746,2	K562	blood:
25	chr18:29406625..29408228-chr18:29410273..29412352,2	K562	blood:
26	chr18:29364264..29367845-chr18:29371473..29373588,3	MCF-7	breast:
27	chr18:29490421..29492288-chr18:29494638..29497276,2	K562	blood:
28	chr18:29490577..29492633-chr18:29522032..29523871,2	MCF-7	breast:
29	chr18:29486555..29488641-chr18:29494297..29496316,2	K562	blood:
30	chr18:29457834..29460225-chr18:29482969..29485185,2	MCF-7	breast:
31	chr18:29494660..29496400-chr18:29519916..29522882,2	K562	blood:
32	chr18:29513029..29515925-chr18:29517093..29518613,2	K562	blood:
33	chr18:29340666..29342583-chr18:29343902..29345487,2	K562	blood:
34	chr18:29442434..29445260-chr18:29447631..29449836,2	K562	blood:
35	chr18:29503360..29505001-chr18:29640249..29641750,2	K562	blood:
36	chr18:29364264..29367845-chr18:29371473..29373588,3	MCF-7	breast:
37	chr18:29506087..29508444-chr18:29510343..29513453,3	MCF-7	breast:
38	chr18:29492718..29495244-chr18:29521543..29523372,2	MCF-7	breast:
39	chr18:29403964..29405650-chr18:29407581..29409258,2	K562	blood:
40	chr18:29407667..29410510-chr18:29494386..29496036,2	K562	blood:
41	chr18:29333142..29335826-chr3:113464597..113467025,2	MCF-7	breast:
42	chr18:29509835..29512655-chr18:29521511..29523719,2	MCF-7	breast:
43	chr18:29446087..29447957-chr18:29452902..29455366,2	K562	blood:
44	chr18:29477012..29478929-chr18:29485217..29488181,2	K562	blood:
45	chr18:29402476..29405464-chr18:29407548..29409258,2	K562	blood:
46	chr18:29439841..29442303-chr18:29446126..29448884,2	K562	blood:
47	chr18:29449762..29451943-chr18:29462101..29464168,2	K562	blood:
48	chr18:29503480..29506352-chr18:29513383..29515079,3	K562	blood:
49	chr18:29486555..29488641-chr18:29494297..29496316,2	K562	blood:
50	chr18:29359927..29362760-chr18:29363290..29365920,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF125-3	chr18:29424351-29424567	ENSG00000263924.1
2	lnc-RNF125-3	chr18:29425011-29425141	ENSG00000263924.1
3	lnc-RNF125-5	chr18:29464821-29465106	NONHSAT058841
4	lnc-TTR-4	chr18:29387008-29387182	NONHSAT058834
5	lnc-RNF125-6	chr18:29462583-29462865	NONHSAT058840
6	lnc-TTR-4	chr18:29386112-29386292	NONHSAT058834

No data

Variant related genes	Relation type
ENSG00000263924	TF binding region
SLC25A52	TF binding region
ENSG00000270879	TF binding region
TRAPPC8	TF binding region
ENSG00000270518	TF binding region
RNU6-1050P	TF binding region
ENSG00000263924	CpG island
SLC25A52	CpG island
ENSG00000270879	CpG island
TRAPPC8	CpG island
ENSG00000270518	CpG island
RNU6-1050P	CpG island
ENSG00000121579	chromatin interactions
ENSG00000265008	chromatin interactions
ENSG00000238982	chromatin interactions
ENSG00000114573	chromatin interactions
ENSG00000153339	chromatin interactions
ENSG00000265063	chromatin interactions
ENSG00000199753	chromatin interactions
ENSG00000266402	chromatin interactions
ENSG00000222320	chromatin interactions
ENSG00000270879	chromatin interactions
ENSG00000270518	chromatin interactions
ENSG00000263823	chromatin interactions
ENSG00000242659	chromatin interactions
ENSG00000141437	chromatin interactions
ENSG00000134758	chromatin interactions

Extended variants
information (count: 7058 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:7058 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4799602	chr18:29335201-29335202	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs562143389	chr18:29335228-29335229	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs34064741	chr18:29335271-29335272	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs574032045	chr18:29335311-29335312	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs541478458	chr18:29335375-29335376	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs72926712	chr18:29335388-29335389	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs11384411	chr18:29335389-29335390	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs533110604	chr18:29335391-29335392	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs397965582	chr18:29335401-29335402	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs113773024	chr18:29335422-29335423	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs545955123	chr18:29335441-29335442	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs563565027	chr18:29335507-29335508	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs34887419	chr18:29335515-29335516	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs567079591	chr18:29335531-29335532	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs534491057	chr18:29335543-29335544	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs530873176	chr18:29335571-29335572	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs548686769	chr18:29335614-29335615	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs371748753	chr18:29335623-29335624	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs567219270	chr18:29335624-29335625	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs558949338	chr18:29335666-29335667	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs140224661	chr18:29335670-29335671	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs576793232	chr18:29335672-29335673	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs150322830	chr18:29335701-29335702	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs571021069	chr18:29335731-29335732	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs539637663	chr18:29335746-29335747	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs557978952	chr18:29335798-29335799	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs61354894	chr18:29335863-29335864	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs58349569	chr18:29335868-29335869	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs138056688	chr18:29335917-29335918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574581304	chr18:29335941-29335942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374941286	chr18:29335966-29335967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189477507	chr18:29335968-29335969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541066933	chr18:29335976-29335977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542074790	chr18:29335978-29335979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559756909	chr18:29335984-29335985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142530043	chr18:29335991-29335992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs375251104	chr18:29335992-29335993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201886639	chr18:29336023-29336024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs59515361	chr18:29336025-29336026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs56033899	chr18:29336105-29336106	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs545220687	chr18:29336193-29336194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs56352737	chr18:29336213-29336214	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs530742279	chr18:29336239-29336240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542879345	chr18:29336255-29336256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546102100	chr18:29336279-29336280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561030562	chr18:29336303-29336304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115368181	chr18:29336424-29336425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115776489	chr18:29336428-29336429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571008671	chr18:29336445-29336446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532107670	chr18:29336465-29336466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Esophageal squamous carcinoma	18350619	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Glioblastoma multiforme	21922591	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21297112	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	17002787	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	16912164	CNVD
Renal cell carcinoma	19150565	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19150955	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	21811587	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:3136 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29321400-29353800	Weak transcription	Liver	Liver
2	chr18:29338200-29338400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr18:29338800-29339400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr18:29338800-29339800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr18:29339000-29339200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr18:29340400-29341200	Bivalent/Poised TSS	K562	blood
7	chr18:29342600-29343000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr18:29344600-29345000	Enhancers	Placenta Amnion	Placenta Amnion
9	chr18:29345800-29346200	Enhancers	HepG2	liver
10	chr18:29346000-29346200	Enhancers	Duodenum Mucosa	Duodenum
11	chr18:29347000-29348200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr18:29347200-29348400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr18:29347200-29348600	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr18:29348600-29353800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr18:29353600-29353800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr18:29353800-29354000	Active TSS	Liver	Liver
17	chr18:29353800-29354000	Enhancers	Duodenum Mucosa	Duodenum
18	chr18:29353800-29354000	Enhancers	Fetal Intestine Large	intestine
19	chr18:29353800-29354000	Enhancers	Fetal Intestine Small	intestine
20	chr18:29353800-29354200	Enhancers	GM12878-XiMat	blood
21	chr18:29353800-29354600	Active TSS	HepG2	liver
22	chr18:29353800-29354800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr18:29353800-29354800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr18:29353800-29355600	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr18:29354000-29354400	Active TSS	Fetal Intestine Large	intestine
26	chr18:29354000-29354400	Flanking Active TSS	Fetal Intestine Small	intestine
27	chr18:29354000-29354600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr18:29354000-29354600	Active TSS	Duodenum Mucosa	Duodenum
29	chr18:29354000-29354600	Active TSS	Osteobl	bone
30	chr18:29354000-29354800	Flanking Active TSS	Liver	Liver
31	chr18:29354000-29357600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr18:29354200-29354400	Active TSS	Rectal Mucosa Donor 29	rectum
33	chr18:29354200-29354400	Active TSS	Rectal Mucosa Donor 31	rectum
34	chr18:29354200-29354800	Flanking Active TSS	GM12878-XiMat	blood
35	chr18:29354200-29355400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr18:29354200-29357600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr18:29354400-29354600	Flanking Active TSS	Fetal Intestine Large	intestine
38	chr18:29354400-29354600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
39	chr18:29354400-29354600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
40	chr18:29354400-29355400	Enhancers	Fetal Intestine Small	intestine
41	chr18:29354600-29354800	Enhancers	Duodenum Mucosa	Duodenum
42	chr18:29354600-29354800	Flanking Active TSS	Osteobl	bone
43	chr18:29354600-29355400	Enhancers	Fetal Intestine Large	intestine
44	chr18:29354600-29355400	Flanking Active TSS	HepG2	liver
45	chr18:29354800-29355200	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr18:29354800-29355200	Enhancers	Liver	Liver
47	chr18:29354800-29355400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr18:29354800-29355400	Enhancers	GM12878-XiMat	blood
49	chr18:29354800-29355800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr18:29354800-29356600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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