Variant report

Variant	nsv1059078
Chromosome Location	chr18:29225522-29454980
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3378)
CpG islands
(count:1468)
Chromatin interactive
region (count:71)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3378 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:29318770-29318953	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:29353089-29353218	HepG2	liver:	n/a	chr18:29353104-29353120 chr18:29353105-29353121
3	ARID3A	chr18:29291047-29291169	K562	blood:	n/a	n/a
4	ARID3A	chr18:29354946-29355261	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:29399616-29400000	K562	blood:	n/a	n/a
6	ARID3A	chr18:29410587-29411037	HepG2	liver:	n/a	n/a
7	ARID3A	chr18:29321162-29321484	HepG2	liver:	n/a	n/a
8	ARID3A	chr18:29353021-29353274	K562	blood:	n/a	chr18:29353104-29353120 chr18:29353105-29353121
9	ARID3A	chr18:29321149-29321432	K562	blood:	n/a	n/a
10	ARID3A	chr18:29354185-29354541	HepG2	liver:	n/a	n/a
11	ARID3A	chr18:29227351-29227651	HepG2	liver:	n/a	n/a
12	ATF1	chr18:29263987-29264156	K562	blood:	n/a	n/a
13	ATF1	chr18:29399629-29399927	K562	blood:	n/a	n/a
14	ATF1	chr18:29238852-29239148	K562	blood:	n/a	n/a
15	ATF1	chr18:29228931-29229286	K562	blood:	n/a	n/a
16	ATF1	chr18:29238101-29238424	K562	blood:	n/a	n/a
17	ATF1	chr18:29282382-29282993	K562	blood:	n/a	n/a
18	ATF1	chr18:29281125-29281211	K562	blood:	n/a	n/a
19	ATF1	chr18:29401606-29402106	K562	blood:	n/a	n/a
20	ATF1	chr18:29318878-29319223	K562	blood:	n/a	n/a
21	ATF1	chr18:29440689-29440984	K562	blood:	n/a	n/a
22	ATF2	chr18:29405635-29406183	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr18:29265483-29266189	GM12878	blood:	n/a	n/a
24	ATF2	chr18:29371602-29372544	GM12878	blood:	n/a	n/a
25	ATF2	chr18:29354318-29354709	GM12878	blood:	n/a	n/a
26	ATF2	chr18:29237893-29239453	GM12878	blood:	n/a	n/a
27	ATF2	chr18:29226017-29227024	GM12878	blood:	n/a	n/a
28	ATF2	chr18:29406502-29407104	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr18:29371699-29372406	GM12878	blood:	n/a	n/a
30	ATF2	chr18:29237694-29239617	GM12878	blood:	n/a	n/a
31	ATF2	chr18:29399490-29399948	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr18:29405727-29406206	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF2	chr18:29228784-29229366	GM12878	blood:	n/a	n/a
34	ATF2	chr18:29232002-29232796	GM12878	blood:	n/a	n/a
35	ATF2	chr18:29354133-29354876	GM12878	blood:	n/a	n/a
36	ATF2	chr18:29228730-29229349	GM12878	blood:	n/a	n/a
37	ATF2	chr18:29226069-29226812	GM12878	blood:	n/a	n/a
38	ATF2	chr18:29399592-29399986	H1-hESC	embryonic stem cell:	n/a	n/a
39	ATF2	chr18:29229695-29230492	GM12878	blood:	n/a	n/a
40	ATF2	chr18:29233146-29233882	GM12878	blood:	n/a	n/a
41	ATF2	chr18:29406652-29407178	H1-hESC	embryonic stem cell:	n/a	n/a
42	ATF3	chr18:29228930-29229196	K562	blood:	n/a	n/a
43	ATF3	chr18:29318872-29319267	K562	blood:	n/a	n/a
44	ATF3	chr18:29318916-29319149	K562	blood:	n/a	n/a
45	ATF3	chr18:29291367-29291679	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	chr18:29253684-29253730	H1-hESC	embryonic stem cell:	n/a	n/a
49	BACH1	chr18:29399184-29400109	H1-hESC	embryonic stem cell:	n/a	n/a
50	BACH1	chr18:29264840-29264850	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1468 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29258797-29258847	HCPEpiC	choroid plexus:	n/a
2	chr18:29300658-29300708	Hepatocyte	liver:	n/a
3	chr18:29340902-29340952	SKMC	muscle:	n/a
4	chr18:29340788-29340838	HRE	kidney:	n/a
5	chr18:29258797-29258847	HCPEpiC	choroid plexus:	n/a
6	chr18:29300658-29300708	Hepatocyte	liver:	n/a
7	chr18:29340902-29340952	SKMC	muscle:	n/a
8	chr18:29340788-29340838	HRE	kidney:	n/a
9	chr18:29340788-29340838	AG09309	skin:	n/a
10	chr18:29264051-29264101	GM06990	blood:	n/a
11	chr18:29300658-29300708	H1-hESC	embryonic stem cell:	embryo
12	chr18:29268737-29268787	RPTEC	kidney:	n/a
13	chr18:29340902-29340952	HMEC	breast:	n/a
14	chr18:29304253-29304303	LNCaP	prostate:	n/a
15	chr18:29262121-29262171	GM12892	blood:	n/a
16	chr18:29341865-29341915	AG10803	skin:	n/a
17	chr18:29263741-29263791	CMK	blood:	n/a
18	chr18:29265487-29265537	GM12891	blood:	n/a
19	chr18:29265842-29265892	Jurkat	blood:	n/a
20	chr18:29304482-29304532	HCF	heart:	n/a
21	chr18:29340902-29340952	GM12878	blood:	n/a
22	chr18:29340919-29340969	AG10803	skin:	n/a
23	chr18:29340916-29340966	AG09309	skin:	n/a
24	chr18:29340919-29340969	NHDF-neo	bronchial:	n/a
25	chr18:29258797-29258847	BE2_C	brain:	n/a
26	chr18:29263741-29263791	AG04449	skin:	fetal
27	chr18:29304111-29304161	SK-N-MC	brain:	n/a
28	chr18:29302528-29302578	GM12892	blood:	n/a
29	chr18:29262121-29262171	SK-N-MC	brain:	n/a
30	chr18:29340916-29340966	HL-60	blood:	n/a
31	chr18:29340919-29340969	SK-N-SH_RA	brain:	n/a
32	chr18:29340916-29340966	HCF	heart:	n/a
33	chr18:29409612-29409662	Jurkat	blood:	n/a
34	chr18:29264252-29264302	HAEpiC	amniotic membrane:	n/a
35	chr18:29265842-29265892	GM12891	blood:	n/a
36	chr18:29340916-29340966	Caco-2	colon:	n/a
37	chr18:29264252-29264302	ovcar-3	ovarian:	n/a
38	chr18:29340902-29340952	Hela-S3	cervix:	n/a
39	chr18:29268737-29268787	A549	lung:	n/a
40	chr18:29340916-29340966	GM19239	blood:	n/a
41	chr18:29268737-29268787	U87	brain:	n/a
42	chr18:29265840-29265890	MCF10A-Er-Src	breast:	n/a
43	chr18:29304111-29304161	HEK293	kidney:	embryo
44	chr18:29307959-29308009	HIPEpiC	eye:	n/a
45	chr18:29341842-29341892	SK-N-SH	brain:	n/a
46	chr18:29264252-29264302	HRE	kidney:	n/a
47	chr18:29340788-29340838	U87	brain:	n/a
48	chr18:29340788-29340838	Hepatocyte	liver:	n/a
49	chr18:29263741-29263791	HRCEpiC	kidney:	n/a
50	chr18:29264252-29264302	SK-N-MC	brain:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr18:29415005..29417838-chr18:29671668..29674584,2	K562	blood:
2	chr11:369439..370438-chr18:29265185..29265845,2	MCF-7	breast:
3	chr18:29408804..29411024-chr18:29521543..29524021,2	K562	blood:
4	chr18:29360934..29363033-chr18:29367742..29370453,2	K562	blood:
5	chr18:29449762..29451943-chr18:29462101..29464168,2	K562	blood:
6	chr18:29402476..29405464-chr18:29407548..29409258,2	K562	blood:
7	chr18:29442434..29445260-chr18:29447631..29449836,2	K562	blood:
8	chr18:29225539..29227273-chr18:29351127..29353466,2	K562	blood:
9	chr18:29251332..29253649-chr18:29260084..29261711,2	K562	blood:
10	chr18:29264481..29265444-chr18:29302123..29302943,2	MCF-7	breast:
11	chr18:29417534..29419307-chr18:29421565..29423101,2	K562	blood:
12	chr18:29004133..29005005-chr18:29399717..29400321,2	K562	blood:
13	chr18:29417534..29419307-chr18:29421565..29423101,2	K562	blood:
14	chr18:29320909..29321461-chr18:29399293..29400251,2	MCF-7	breast:
15	chr18:29439841..29442303-chr18:29446126..29448884,2	K562	blood:
16	chr18:29321255..29322089-chr18:29396487..29397335,2	MCF-7	breast:
17	chr18:29407667..29410510-chr18:29494386..29496036,2	K562	blood:
18	chr18:29403964..29405650-chr18:29407581..29409258,2	K562	blood:
19	chr18:29372571..29374604-chr18:29381332..29383402,2	MCF-7	breast:
20	chr18:29259339..29260872-chr18:29261230..29264110,2	K562	blood:
21	chr18:29442434..29445260-chr18:29447631..29449836,2	K562	blood:
22	chr18:29135564..29136362-chr18:29399476..29400304,3	MCF-7	breast:
23	chr18:29251332..29253649-chr18:29260084..29261711,2	K562	blood:
24	chr18:29266991..29268512-chr18:29271793..29273586,2	K562	blood:
25	chr18:29402476..29405464-chr18:29407548..29409258,2	K562	blood:
26	chr18:29259339..29260872-chr18:29261230..29264110,2	K562	blood:
27	chr18:29275310..29278274-chr18:29291077..29293888,2	MCF-7	breast:
28	chr18:29290630..29291464-chr18:29399315..29400108,2	MCF-7	breast:
29	chr18:29446087..29447957-chr18:29452902..29455366,2	K562	blood:
30	chr18:29275310..29278274-chr18:29291077..29293888,2	MCF-7	breast:
31	chr18:29321255..29322089-chr18:29396487..29397335,2	MCF-7	breast:
32	chr18:29406625..29408228-chr18:29410273..29412352,2	K562	blood:
33	chr18:29447981..29450768-chr18:29467717..29470542,2	K562	blood:
34	chr18:29340666..29342583-chr18:29343902..29345487,2	K562	blood:
35	chr18:29235060..29236900-chr18:29250262..29252488,2	MCF-7	breast:
36	chr18:29364264..29367845-chr18:29371473..29373588,3	MCF-7	breast:
37	chr18:29135071..29136376-chr18:29302039..29303290,3	MCF-7	breast:
38	chr18:29259001..29261313-chr18:29272206..29274958,2	MCF-7	breast:
39	chr18:29219249..29221553-chr18:29225572..29227383,2	MCF-7	breast:
40	chr18:29235239..29238459-chr18:29263541..29266170,4	MCF-7	breast:
41	chr18:29290630..29291464-chr18:29399315..29400108,2	MCF-7	breast:
42	chr18:29225539..29227273-chr18:29351127..29353466,2	K562	blood:
43	chr18:29359553..29362434-chr18:29368590..29370453,2	K562	blood:
44	chr18:29333142..29335826-chr3:113464597..113467025,2	MCF-7	breast:
45	chr18:29235239..29238459-chr18:29263541..29266170,4	MCF-7	breast:
46	chr18:29078002..29079523-chr18:29301802..29303631,2	K562	blood:
47	chr18:29359927..29362760-chr18:29363290..29365920,2	MCF-7	breast:
48	chr18:29266991..29268512-chr18:29271793..29273586,2	K562	blood:
49	chr18:29264959..29265684-chr18:29302461..29303010,2	MCF-7	breast:
50	chr18:29401567..29403770-chr18:29418064..29420663,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTR-1	chr18:29264688-29267822	NONHSAT058829
2	lnc-TTR-1	chr18:29265618-29266786	ENSG00000259985.1
3	lnc-TTR-3	chr18:29304191-29304638	NONHSAT058833
4	lnc-TTR-2	chr18:29298856-29299171	NONHSAT058831
5	lnc-TTR-4	chr18:29387008-29387182	NONHSAT058834
6	lnc-TTR-3	chr18:29304161-29306919	NONHSAT058832
7	lnc-TTR-4	chr18:29386112-29386292	NONHSAT058834
8	lnc-RNF125-3	chr18:29424351-29424567	ENSG00000263924.1
9	lnc-TTR-3	chr18:29304782-29305727	NONHSAT058833
10	lnc-RNF125-3	chr18:29425011-29425141	ENSG00000263924.1

No data

Variant related genes	Relation type
LRRC37A7P	TF binding region
B4GALT6	TF binding region
ENSG00000263924	TF binding region
RNU6-1002P	TF binding region
SLC25A52	TF binding region
RN7SKP44	TF binding region
TRAPPC8	TF binding region
ENSG00000259985	TF binding region
ENSG00000263772	TF binding region
LRRC37A7P	CpG island
B4GALT6	CpG island
ENSG00000263924	CpG island
RNU6-1002P	CpG island
SLC25A52	CpG island
RN7SKP44	CpG island
TRAPPC8	CpG island
ENSG00000259985	CpG island
ENSG00000263772	CpG island
ENSG00000121579	chromatin interactions
ENSG00000259985	chromatin interactions
ENSG00000265008	chromatin interactions
ENSG00000242659	chromatin interactions
ENSG00000263823	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000265158	chromatin interactions
ENSG00000046604	chromatin interactions
ENSG00000266402	chromatin interactions
ENSG00000238982	chromatin interactions
ENSG00000118276	chromatin interactions
ENSG00000199753	chromatin interactions
ENSG00000182272	chromatin interactions
ENSG00000270518	chromatin interactions
ENSG00000141437	chromatin interactions
ENSG00000153339	chromatin interactions
ENSG00000114573	chromatin interactions
ENSG00000134758	chromatin interactions

Extended variants
information (count: 8444 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:8444 , 50 per page) page: 1 2 3 4 5 6 7 ... 169

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117060609	chr18:29225583-29225584	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs547780069	chr18:29225590-29225591	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141485306	chr18:29225613-29225614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535745238	chr18:29225624-29225625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555044415	chr18:29225706-29225707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs573177125	chr18:29225730-29225731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs78410284	chr18:29225764-29225765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs540402565	chr18:29225820-29225821	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs8090252	chr18:29225873-29225874	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs539221286	chr18:29225896-29225897	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs186842837	chr18:29225899-29225900	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs575587005	chr18:29225933-29225934	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs190594818	chr18:29225954-29225955	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs536952429	chr18:29225981-29225982	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs554911691	chr18:29225983-29225984	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs368594567	chr18:29226003-29226004	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs573168431	chr18:29226020-29226021	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs540691152	chr18:29226021-29226022	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs565210978	chr18:29226085-29226086	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs117246633	chr18:29226090-29226091	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs543992618	chr18:29226123-29226124	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs182768331	chr18:29226140-29226141	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs138299385	chr18:29226181-29226182	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs1667284	chr18:29226208-29226209	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs562737482	chr18:29226264-29226265	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs115761440	chr18:29226375-29226376	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs4799311	chr18:29226444-29226445	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs552186354	chr18:29226519-29226520	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs187897032	chr18:29226530-29226531	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs149613009	chr18:29226536-29226537	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs551152073	chr18:29226538-29226539	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs569485723	chr18:29226592-29226593	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs538503513	chr18:29226605-29226606	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs559743930	chr18:29226612-29226613	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs554981944	chr18:29226623-29226624	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs28678782	chr18:29226686-29226687	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs551852789	chr18:29226693-29226694	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs533922911	chr18:29226697-29226698	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs558949608	chr18:29226704-29226705	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs576921177	chr18:29226722-29226723	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs544303194	chr18:29226738-29226739	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs555899372	chr18:29226758-29226759	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs193232114	chr18:29226813-29226814	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs112897734	chr18:29226893-29226894	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs116587544	chr18:29226900-29226901	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs527626632	chr18:29226909-29226910	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs16962246	chr18:29226954-29226955	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs184539061	chr18:29226998-29226999	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs550047069	chr18:29227015-29227016	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs564113889	chr18:29227021-29227022	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3485 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29194800-29226800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr18:29202800-29235000	Weak transcription	Pancreas	Pancrea
3	chr18:29202800-29240200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr18:29203800-29226000	Weak transcription	Fetal Lung	lung
5	chr18:29203800-29227400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr18:29204000-29228400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr18:29204400-29228400	Weak transcription	Psoas Muscle	Psoas
8	chr18:29204600-29238600	Weak transcription	Gastric	stomach
9	chr18:29205000-29227400	Weak transcription	A549	lung
10	chr18:29206800-29225800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr18:29208000-29227400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr18:29208400-29227000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr18:29208400-29229000	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr18:29209000-29226000	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr18:29209000-29228400	Weak transcription	Brain Angular Gyrus	brain
16	chr18:29211000-29227400	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr18:29211200-29225800	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr18:29211200-29226000	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr18:29211200-29227400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr18:29213800-29229000	Weak transcription	HUVEC	blood vessel
21	chr18:29214400-29226000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr18:29214600-29225800	Weak transcription	Fetal Thymus	thymus
23	chr18:29214800-29228800	Weak transcription	NH-A	brain
24	chr18:29216000-29229000	Weak transcription	Placenta	Placenta
25	chr18:29218800-29232200	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr18:29219200-29226600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr18:29219200-29227400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr18:29219200-29240000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr18:29219200-29252000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr18:29219200-29252000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr18:29220200-29227600	Weak transcription	Small Intestine	intestine
32	chr18:29222000-29226000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr18:29223200-29236400	Weak transcription	Esophagus	oesophagus
34	chr18:29223600-29228400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr18:29223600-29228800	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr18:29223800-29228800	Weak transcription	Osteobl	bone
37	chr18:29224000-29226200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr18:29224000-29226400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr18:29224000-29226400	Weak transcription	HMEC	breast
40	chr18:29224000-29228400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr18:29224000-29228400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr18:29224400-29228400	Weak transcription	NHEK	skin
43	chr18:29224600-29225600	Enhancers	Fetal Intestine Small	intestine
44	chr18:29224600-29225600	Genic enhancers	GM12878-XiMat	blood
45	chr18:29224600-29225800	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr18:29224600-29230800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr18:29224800-29226200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr18:29224800-29227000	Enhancers	Brain Anterior Caudate	brain
49	chr18:29224800-29228600	Enhancers	Brain Germinal Matrix	brain
50	chr18:29224800-29229200	Enhancers	HUES48 Cell Line	embryonic stem cell

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