Variant report

Variant	nsv431975
Chromosome Location	chr18:29311034-29527902
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2374)
CpG islands
(count:1344)
Chromatin interactive
region (count:113)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2374 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:29524025-29524906	K562	blood:	n/a	n/a
2	ARID3A	chr18:29523487-29524214	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:29354185-29354541	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:29522908-29523247	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:29321162-29321484	HepG2	liver:	n/a	n/a
6	ARID3A	chr18:29318770-29318953	HepG2	liver:	n/a	n/a
7	ARID3A	chr18:29410587-29411037	HepG2	liver:	n/a	n/a
8	ARID3A	chr18:29353021-29353274	K562	blood:	n/a	chr18:29353104-29353120 chr18:29353105-29353121
9	ARID3A	chr18:29353089-29353218	HepG2	liver:	n/a	chr18:29353104-29353120 chr18:29353105-29353121
10	ARID3A	chr18:29523384-29523668	K562	blood:	n/a	n/a
11	ARID3A	chr18:29399616-29400000	K562	blood:	n/a	n/a
12	ARID3A	chr18:29321149-29321432	K562	blood:	n/a	n/a
13	ARID3A	chr18:29354946-29355261	HepG2	liver:	n/a	n/a
14	ATF1	chr18:29399629-29399927	K562	blood:	n/a	n/a
15	ATF1	chr18:29524097-29524682	K562	blood:	n/a	n/a
16	ATF1	chr18:29318878-29319223	K562	blood:	n/a	n/a
17	ATF1	chr18:29401606-29402106	K562	blood:	n/a	n/a
18	ATF1	chr18:29440689-29440984	K562	blood:	n/a	n/a
19	ATF2	chr18:29526686-29527108	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr18:29405635-29406183	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr18:29399490-29399948	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr18:29405727-29406206	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr18:29522911-29523275	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr18:29406652-29407178	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr18:29406502-29407104	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr18:29354318-29354709	GM12878	blood:	n/a	n/a
27	ATF2	chr18:29399592-29399986	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr18:29522789-29523752	GM12878	blood:	n/a	n/a
29	ATF2	chr18:29522071-29522586	GM12878	blood:	n/a	n/a
30	ATF2	chr18:29354133-29354876	GM12878	blood:	n/a	n/a
31	ATF2	chr18:29522854-29523220	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr18:29371699-29372406	GM12878	blood:	n/a	n/a
33	ATF2	chr18:29371602-29372544	GM12878	blood:	n/a	n/a
34	ATF2	chr18:29523281-29523810	H1-hESC	embryonic stem cell:	n/a	n/a
35	ATF3	chr18:29318916-29319149	K562	blood:	n/a	n/a
36	ATF3	chr18:29522915-29523195	HepG2	liver:	n/a	chr18:29523114-29523123 chr18:29523103-29523123
37	ATF3	chr18:29318872-29319267	K562	blood:	n/a	n/a
38	ATF3	chr18:29523004-29523182	GM12878	blood:	n/a	chr18:29523114-29523123 chr18:29523103-29523123
39	ATF3	chr18:29522818-29523234	H1-hESC	embryonic stem cell:	n/a	chr18:29523114-29523123 chr18:29523103-29523123
40	ATF3	chr18:29522864-29523406	HepG2	liver:	n/a	chr18:29523114-29523123 chr18:29523103-29523123 chr18:29523311-29523319 chr18:29523239-29523248
41	ATF3	chr18:29522931-29523228	K562	blood:	n/a	chr18:29523114-29523123 chr18:29523103-29523123
42	ATF3	chr18:29522850-29523231	GM12878	blood:	n/a	chr18:29523114-29523123 chr18:29523103-29523123
43	ATF3	chr18:29522919-29523241	H1-hESC	embryonic stem cell:	n/a	chr18:29523114-29523123 chr18:29523103-29523123
44	BACH1	chr18:29522805-29523692	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr18:29523016-29523134	K562	blood:	n/a	n/a
46	BACH1	chr18:29405473-29405587	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr18:29318876-29319232	H1-hESC	embryonic stem cell:	n/a	n/a
48	BACH1	chr18:29521754-29521776	K562	blood:	n/a	n/a
49	BACH1	chr18:29399184-29400109	H1-hESC	embryonic stem cell:	n/a	n/a
50	BATF	chr18:29371452-29372095	GM12878	blood:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29523417-29523467	PANC-1	pancreas:	n/a
2	chr18:29525892-29525942	HepG2	liver:	n/a
3	chr18:29523417-29523467	PANC-1	pancreas:	n/a
4	chr18:29525892-29525942	HepG2	liver:	n/a
5	chr18:29522728-29522778	HCT-116	colon:	n/a
6	chr18:29340902-29340952	ECC-1	luminal epithelium:	n/a
7	chr18:29522434-29522484	HEEpiC	esophagus:	n/a
8	chr18:29522728-29522778	NH-A	brain:	n/a
9	chr18:29523426-29523476	HPAEpiC	pulmonary alveolar:	n/a
10	chr18:29340902-29340952	HAEpiC	amniotic membrane:	n/a
11	chr18:29523078-29523128	AG09319	gingival:	n/a
12	chr18:29523289-29523339	HAEpiC	amniotic membrane:	n/a
13	chr18:29522957-29523007	HRCEpiC	kidney:	n/a
14	chr18:29523289-29523339	HRPEpiC	eye:	n/a
15	chr18:29522728-29522778	SK-N-SH_RA	brain:	n/a
16	chr18:29523277-29523327	HCPEpiC	choroid plexus:	n/a
17	chr18:29523271-29523321	IMR90	lung:	fetal
18	chr18:29340916-29340966	AG09309	skin:	n/a
19	chr18:29522262-29522312	ECC-1	luminal epithelium:	n/a
20	chr18:29523728-29523778	HL-60	blood:	n/a
21	chr18:29523417-29523467	ProgFib	skin:	n/a
22	chr18:29523078-29523128	SKMC	muscle:	n/a
23	chr18:29523728-29523778	HEEpiC	esophagus:	n/a
24	chr18:29523380-29523430	HIPEpiC	eye:	n/a
25	chr18:29341842-29341892	AG10803	skin:	n/a
26	chr18:29340919-29340969	HL-60	blood:	n/a
27	chr18:29409612-29409662	GM12891	blood:	n/a
28	chr18:29340919-29340969	HMEC	breast:	n/a
29	chr18:29523277-29523327	HCM	heart:	n/a
30	chr18:29523426-29523476	AoSMC	blood vessel:	n/a
31	chr18:29519807-29519857	Jurkat	blood:	n/a
32	chr18:29340788-29340838	Jurkat	blood:	n/a
33	chr18:29340916-29340966	PFSK-1	brain:	n/a
34	chr18:29341865-29341915	Hepatocyte	liver:	n/a
35	chr18:29523271-29523321	SK-N-MC	brain:	n/a
36	chr18:29523078-29523128	PFSK-1	brain:	n/a
37	chr18:29340902-29340952	H1-hESC	embryonic stem cell:	embryo
38	chr18:29523426-29523476	NH-A	brain:	n/a
39	chr18:29523271-29523321	AG04449	skin:	fetal
40	chr18:29523078-29523128	GM12878	blood:	n/a
41	chr18:29340788-29340838	Caco-2	colon:	n/a
42	chr18:29522728-29522778	HEEpiC	esophagus:	n/a
43	chr18:29340919-29340969	U87	brain:	n/a
44	chr18:29340916-29340966	NB4	blood:	n/a
45	chr18:29340916-29340966	HEK293	kidney:	embryo
46	chr18:29523063-29523113	HEK293	kidney:	embryo
47	chr18:29523271-29523321	HRCEpiC	kidney:	n/a
48	chr18:29522434-29522484	HRE	kidney:	n/a
49	chr18:29523380-29523430	HUVEC	blood vessel:	n/a
50	chr18:29523078-29523128	AG09309	skin:	n/a

(count:113 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr18:29225539..29227273-chr18:29351127..29353466,2	K562	blood:
2	chr18:29372571..29374604-chr18:29381332..29383402,2	MCF-7	breast:
3	chr18:29402476..29405464-chr18:29407548..29409258,2	K562	blood:
4	chr18:29450429..29452203-chr18:29521687..29523259,2	MCF-7	breast:
5	chr18:29450239..29451940-chr18:29466117..29468159,2	K562	blood:
6	chr18:29468408..29471507-chr18:29523062..29524905,3	K562	blood:
7	chr18:29509835..29512655-chr18:29521511..29523719,2	MCF-7	breast:
8	chr18:29321255..29322089-chr18:29396487..29397335,2	MCF-7	breast:
9	chr18:29501674..29503497-chr18:29522527..29524041,2	MCF-7	breast:
10	chr18:29522249..29524505-chr18:29596603..29599089,2	MCF-7	breast:
11	chr18:29517111..29520943-chr18:29521139..29523956,5	MCF-7	breast:
12	chr18:29486555..29488641-chr18:29494297..29496316,2	K562	blood:
13	chr18:29523882..29525586-chr18:29646566..29649385,2	K562	blood:
14	chr18:29364264..29367845-chr18:29371473..29373588,3	MCF-7	breast:
15	chr18:29457834..29460225-chr18:29482969..29485185,2	MCF-7	breast:
16	chr18:29321255..29322089-chr18:29396487..29397335,2	MCF-7	breast:
17	chr18:29521522..29523729-chr18:29672844..29674625,2	MCF-7	breast:
18	chr18:29403964..29405650-chr18:29407581..29409258,2	K562	blood:
19	chr18:29473750..29476339-chr18:29521274..29523147,2	K562	blood:
20	chr18:29518719..29521005-chr18:29521192..29525426,5	MCF-7	breast:
21	chr18:29320909..29321461-chr18:29399293..29400251,2	MCF-7	breast:
22	chr18:29446087..29447957-chr18:29452902..29455366,2	K562	blood:
23	chr18:29469874..29472927-chr18:29473896..29477156,4	K562	blood:
24	chr18:29463505..29465182-chr18:29472217..29474656,2	MCF-7	breast:
25	chr18:29475912..29478004-chr18:29521825..29524429,2	MCF-7	breast:
26	chr18:29490421..29492288-chr18:29494638..29497276,2	K562	blood:
27	chr18:29521537..29525393-chr18:29670839..29674328,7	K562	blood:
28	chr18:29359927..29362760-chr18:29363290..29365920,2	MCF-7	breast:
29	chr18:29333142..29335826-chr3:113464597..113467025,2	MCF-7	breast:
30	chr18:29447981..29450768-chr18:29467717..29470542,2	K562	blood:
31	chr18:29407667..29410510-chr18:29494386..29496036,2	K562	blood:
32	chr18:29485958..29488048-chr18:29520164..29521790,2	K562	blood:
33	chr18:29450429..29452203-chr18:29521687..29523259,2	MCF-7	breast:
34	chr18:29135564..29136362-chr18:29399476..29400304,3	MCF-7	breast:
35	chr18:29359553..29362434-chr18:29368590..29370453,2	K562	blood:
36	chr18:29485958..29488048-chr18:29520164..29521790,2	K562	blood:
37	chr18:29503480..29505119-chr18:29513383..29515079,2	K562	blood:
38	chr18:29494660..29496304-chr18:29519916..29522258,2	K562	blood:
39	chr18:29521939..29525237-chr18:29670716..29673913,4	MCF-7	breast:
40	chr18:29503360..29505001-chr18:29640249..29641750,2	K562	blood:
41	chr18:29487420..29490004-chr18:29496191..29498820,2	K562	blood:
42	chr18:29477012..29478929-chr18:29485217..29488181,2	K562	blood:
43	chr18:29004133..29005005-chr18:29399717..29400321,2	K562	blood:
44	chr18:29417534..29419307-chr18:29421565..29423101,2	K562	blood:
45	chr18:29452756..29454913-chr18:29671972..29673873,2	MCF-7	breast:
46	chr18:29340666..29342583-chr18:29343902..29345487,2	K562	blood:
47	chr18:29449762..29451943-chr18:29462101..29464168,2	K562	blood:
48	chr18:29359553..29362434-chr18:29368590..29370453,2	K562	blood:
49	chr18:29407667..29410510-chr18:29494386..29496036,2	K562	blood:
50	chr18:29503480..29506352-chr18:29513383..29515079,3	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF125-3	chr18:29425011-29425141	ENSG00000263924.1
2	lnc-RNF125-6	chr18:29462583-29462865	NONHSAT058840
3	lnc-TRAPPC8-3	chr18:29519358-29519707	NONHSAT058843
4	lnc-RNF125-3	chr18:29424351-29424567	ENSG00000263924.1
5	lnc-TTR-4	chr18:29387008-29387182	NONHSAT058834
6	lnc-TTR-4	chr18:29386112-29386292	NONHSAT058834
7	lnc-RNF125-5	chr18:29464821-29465106	NONHSAT058841

No data

Variant related genes	Relation type
ENSG00000263924	TF binding region
ENSG00000263823	TF binding region
SLC25A52	TF binding region
ENSG00000270879	TF binding region
TRAPPC8	TF binding region
ENSG00000270518	TF binding region
ENSG00000263772	TF binding region
RNU6-1050P	TF binding region
ENSG00000263924	CpG island
ENSG00000263823	CpG island
SLC25A52	CpG island
ENSG00000270879	CpG island
TRAPPC8	CpG island
ENSG00000270518	CpG island
ENSG00000263772	CpG island
RNU6-1050P	CpG island
ENSG00000238982	chromatin interactions
ENSG00000265063	chromatin interactions
ENSG00000263917	chromatin interactions
ENSG00000242659	chromatin interactions
ENSG00000141437	chromatin interactions
ENSG00000143641	chromatin interactions
ENSG00000229980	chromatin interactions
ENSG00000265008	chromatin interactions
ENSG00000263823	chromatin interactions
ENSG00000121579	chromatin interactions
ENSG00000153339	chromatin interactions
ENSG00000222320	chromatin interactions
ENSG00000266402	chromatin interactions
ENSG00000134759	chromatin interactions
ENSG00000141232	chromatin interactions
ENSG00000134758	chromatin interactions
ENSG00000114573	chromatin interactions
ENSG00000270518	chromatin interactions
ENSG00000266105	chromatin interactions
ENSG00000270879	chromatin interactions
ENSG00000101695	chromatin interactions
ENSG00000141424	chromatin interactions
ENSG00000143549	chromatin interactions
ENSG00000199753	chromatin interactions

Extended variants
information (count: 8472 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:8472 , 50 per page) page: 1 2 3 4 5 6 7 ... 170

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs985492	chr18:29311034-29311035	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs183613018	chr18:29311123-29311124	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs543920544	chr18:29311183-29311184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556104070	chr18:29311222-29311223	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558984379	chr18:29311223-29311224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370169930	chr18:29311253-29311254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188709213	chr18:29311265-29311266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs9965759	chr18:29311266-29311267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
9	rs562816345	chr18:29311303-29311304	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs141537340	chr18:29311338-29311339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs9965684	chr18:29311342-29311343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574622028	chr18:29311350-29311351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560340368	chr18:29311361-29311362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs985491	chr18:29311365-29311366	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs147065172	chr18:29311378-29311379	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570091847	chr18:29311383-29311384	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs75359680	chr18:29311479-29311480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549381137	chr18:29311513-29311514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568024751	chr18:29311527-29311528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs75032918	chr18:29311562-29311563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548496455	chr18:29311598-29311599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559936009	chr18:29311641-29311642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567096467	chr18:29311642-29311643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs77137848	chr18:29311704-29311705	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535661024	chr18:29311761-29311762	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577637687	chr18:29311763-29311764	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148105608	chr18:29311766-29311767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs556521529	chr18:29311791-29311792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574832805	chr18:29311793-29311794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545943324	chr18:29311794-29311795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371228075	chr18:29311942-29311943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs17661827	chr18:29311943-29311944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
33	rs7227940	chr18:29311945-29311946	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs192731435	chr18:29311955-29311956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141952372	chr18:29311974-29311975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531511434	chr18:29312073-29312074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549465481	chr18:29312125-29312126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12051918	chr18:29312126-29312127	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs528973205	chr18:29312204-29312205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547505883	chr18:29312236-29312237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77656826	chr18:29312341-29312342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534364612	chr18:29312345-29312346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552823562	chr18:29312351-29312352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs35368701	chr18:29312366-29312367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574302276	chr18:29312376-29312377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571108652	chr18:29312423-29312424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557719870	chr18:29312424-29312425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538583598	chr18:29312480-29312481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556272466	chr18:29312559-29312560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574809347	chr18:29312594-29312595	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:3905 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29306200-29323600	Weak transcription	Psoas Muscle	Psoas
2	chr18:29307600-29316800	Weak transcription	Liver	Liver
3	chr18:29310800-29311400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr18:29311400-29312000	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr18:29316400-29317200	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr18:29316600-29317000	Enhancers	GM12878-XiMat	blood
7	chr18:29316800-29317000	Enhancers	Duodenum Smooth Muscle	Duodenum
8	chr18:29316800-29317200	Enhancers	Liver	Liver
9	chr18:29317200-29318200	Weak transcription	Liver	Liver
10	chr18:29318200-29318400	Enhancers	Liver	Liver
11	chr18:29318200-29319000	Enhancers	HepG2	liver
12	chr18:29318400-29318800	Flanking Active TSS	Liver	Liver
13	chr18:29318400-29319400	Enhancers	Placenta	Placenta
14	chr18:29318400-29319400	Enhancers	K562	blood
15	chr18:29318800-29320000	Weak transcription	Liver	Liver
16	chr18:29320000-29321400	Enhancers	Liver	Liver
17	chr18:29320800-29321200	Enhancers	H9 Cell Line	embryonic stem cell
18	chr18:29321400-29353800	Weak transcription	Liver	Liver
19	chr18:29323400-29324000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr18:29323600-29324600	Enhancers	Psoas Muscle	Psoas
21	chr18:29324000-29324600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr18:29324000-29324600	Enhancers	Esophagus	oesophagus
23	chr18:29324200-29325000	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr18:29324400-29324600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr18:29324400-29325000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr18:29324400-29325400	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr18:29324400-29325600	Enhancers	H9 Cell Line	embryonic stem cell
28	chr18:29324400-29325800	Enhancers	H1 Cell Line	embryonic stem cell
29	chr18:29324600-29325000	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr18:29324600-29325000	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr18:29324600-29325400	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr18:29324600-29325400	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr18:29324600-29327400	Weak transcription	Esophagus	oesophagus
34	chr18:29324600-29331400	Weak transcription	Psoas Muscle	Psoas
35	chr18:29327400-29327800	Enhancers	Esophagus	oesophagus
36	chr18:29331400-29331800	Enhancers	Psoas Muscle	Psoas
37	chr18:29334600-29334800	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr18:29338200-29338400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr18:29338800-29339400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr18:29338800-29339800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr18:29339000-29339200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr18:29340400-29341200	Bivalent/Poised TSS	K562	blood
43	chr18:29342600-29343000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr18:29344600-29345000	Enhancers	Placenta Amnion	Placenta Amnion
45	chr18:29345800-29346200	Enhancers	HepG2	liver
46	chr18:29346000-29346200	Enhancers	Duodenum Mucosa	Duodenum
47	chr18:29347000-29348200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr18:29347200-29348400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr18:29347200-29348600	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr18:29348600-29353800	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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