Variant report

Variant	esv1847722
Chromosome Location	chr1:169782006-169885186
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1324)
CpG islands
(count:1403)
Chromatin interactive
region (count:145)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1324 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:169829990-169830266	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:169863072-169863727	K562	blood:	n/a	chr1:169863350-169863365
3	ARID3A	chr1:169862953-169863623	HepG2	liver:	n/a	chr1:169863350-169863365
4	ARID3A	chr1:169860875-169860966	K562	blood:	n/a	n/a
5	ATF1	chr1:169865206-169865592	K562	blood:	n/a	n/a
6	ATF1	chr1:169862930-169863924	K562	blood:	n/a	n/a
7	ATF1	chr1:169875679-169875771	K562	blood:	n/a	n/a
8	ATF2	chr1:169884641-169885463	GM12878	blood:	n/a	n/a
9	ATF2	chr1:169862846-169863677	H1-hESC	embryonic stem cell:	n/a	chr1:169863454-169863465
10	ATF2	chr1:169884728-169885478	GM12878	blood:	n/a	n/a
11	ATF2	chr1:169862830-169863705	GM12878	blood:	n/a	chr1:169863454-169863465
12	ATF2	chr1:169877793-169878291	GM12878	blood:	n/a	n/a
13	ATF2	chr1:169862853-169863669	H1-hESC	embryonic stem cell:	n/a	chr1:169863454-169863465
14	ATF2	chr1:169862698-169863773	GM12878	blood:	n/a	chr1:169863454-169863465
15	ATF3	chr1:169863084-169863541	A549	lung:	n/a	chr1:169863455-169863463 chr1:169863453-169863464 chr1:169863456-169863463 chr1:169863452-169863467 chr1:169863456-169863464 chr1:169863455-169863466
16	ATF3	chr1:169862875-169863699	A549	lung:	n/a	chr1:169863455-169863463 chr1:169863453-169863464 chr1:169863456-169863463 chr1:169863452-169863467 chr1:169863456-169863464 chr1:169863455-169863466
17	BACH1	chr1:169862827-169863255	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr1:169884881-169885145	GM12878	blood:	n/a	n/a
19	BATF	chr1:169863287-169863594	GM12878	blood:	n/a	n/a
20	BATF	chr1:169877905-169878096	GM12878	blood:	n/a	chr1:169878018-169878028 chr1:169878013-169878024
21	BATF	chr1:169862856-169863286	GM12878	blood:	n/a	n/a
22	BATF	chr1:169860249-169860769	GM12878	blood:	n/a	n/a
23	BATF	chr1:169884831-169885139	GM12878	blood:	n/a	n/a
24	BATF	chr1:169864809-169865538	GM12878	blood:	n/a	n/a
25	BATF	chr1:169874031-169874305	GM12878	blood:	n/a	chr1:169874171-169874182
26	BATF	chr1:169877820-169878170	GM12878	blood:	n/a	chr1:169878018-169878028 chr1:169878013-169878024
27	BCL11A	chr1:169884823-169885239	GM12878	blood:	n/a	n/a
28	BCL11A	chr1:169884782-169885191	GM12878	blood:	n/a	n/a
29	BCL3	chr1:169862816-169863742	A549	lung:	n/a	chr1:169863349-169863358
30	BCL3	chr1:169884855-169885429	GM12878	blood:	n/a	n/a
31	BCL3	chr1:169862802-169863712	A549	lung:	n/a	chr1:169863349-169863358
32	BCL3	chr1:169884753-169885434	GM12878	blood:	n/a	n/a
33	BCLAF1	chr1:169884749-169885490	GM12878	blood:	n/a	n/a
34	BCLAF1	chr1:169862426-169863510	GM12878	blood:	n/a	chr1:169863349-169863358
35	BCLAF1	chr1:169862490-169863548	GM12878	blood:	n/a	chr1:169863349-169863358
36	BCLAF1	chr1:169884787-169885510	GM12878	blood:	n/a	n/a
37	BHLHE40	chr1:169862858-169863846	K562	blood:	n/a	n/a
38	BHLHE40	chr1:169865220-169865548	GM12878	blood:	n/a	n/a
39	BHLHE40	chr1:169862703-169863638	GM12878	blood:	n/a	n/a
40	BHLHE40	chr1:169874113-169874231	GM12878	blood:	n/a	n/a
41	BHLHE40	chr1:169884680-169885636	GM12878	blood:	n/a	n/a
42	BRCA1	chr1:169863065-169863587	H1-hESC	embryonic stem cell:	n/a	n/a
43	BRCA1	chr1:169862944-169863597	HepG2	liver:	n/a	n/a
44	BRCA1	chr1:169862601-169863890	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr1:169877627-169877714	GM12878	blood:	n/a	n/a
46	BRCA1	chr1:169867310-169867364	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr1:169862959-169863575	GM12878	blood:	n/a	n/a
48	CBX3	chr1:169862848-169863596	K562	blood:	n/a	n/a
49	CBX3	chr1:169862685-169864290	K562	blood:	n/a	n/a
50	CCNT2	chr1:169862301-169863336	K562	blood:	n/a	n/a

(count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:169860805-169860855	HCPEpiC	choroid plexus:	n/a
2	chr1:169854522-169854572	HUVEC	blood vessel:	n/a
3	chr1:169859761-169859811	HAEpiC	amniotic membrane:	n/a
4	chr1:169863082-169863132	SK-N-MC	brain:	n/a
5	chr1:169847977-169848027	HEEpiC	esophagus:	n/a
6	chr1:169847977-169848027	HRE	kidney:	n/a
7	chr1:169863438-169863488	SK-N-MC	brain:	n/a
8	chr1:169859761-169859811	SK-N-SH_RA	brain:	n/a
9	chr1:169862509-169862559	HEK293	kidney:	embryo
10	chr1:169863169-169863219	HCM	heart:	n/a
11	chr1:169863532-169863582	RPTEC	kidney:	n/a
12	chr1:169878927-169878977	H1-hESC	embryonic stem cell:	embryo
13	chr1:169860805-169860855	AG04450	lung:	fetal
14	chr1:169854522-169854572	HEEpiC	esophagus:	n/a
15	chr1:169822076-169822126	Hela-S3	cervix:	n/a
16	chr1:169866315-169866365	NT2-D1	testis:	n/a
17	chr1:169878852-169878902	BE2_C	brain:	n/a
18	chr1:169863088-169863138	SKMC	muscle:	n/a
19	chr1:169878927-169878977	SAEC	small airway:	n/a
20	chr1:169863082-169863132	HRE	kidney:	n/a
21	chr1:169863169-169863219	HIPEpiC	eye:	n/a
22	chr1:169863516-169863566	HEEpiC	esophagus:	n/a
23	chr1:169852241-169852291	HL-60	blood:	n/a
24	chr1:169847977-169848027	GM12878	blood:	n/a
25	chr1:169863532-169863582	GM19239	blood:	n/a
26	chr1:169878814-169878864	U87	brain:	n/a
27	chr1:169863189-169863239	GM06990	blood:	n/a
28	chr1:169866315-169866365	HEK293	kidney:	embryo
29	chr1:169822076-169822126	IMR90	lung:	fetal
30	chr1:169878927-169878977	GM12878	blood:	n/a
31	chr1:169847977-169848027	PFSK-1	brain:	n/a
32	chr1:169863516-169863566	CMK	blood:	n/a
33	chr1:169863494-169863544	A549	lung:	n/a
34	chr1:169863516-169863566	HCPEpiC	choroid plexus:	n/a
35	chr1:169847977-169848027	MCF-7	breast:	n/a
36	chr1:169859761-169859811	U87	brain:	n/a
37	chr1:169863516-169863566	U87	brain:	n/a
38	chr1:169878852-169878902	A549	lung:	n/a
39	chr1:169863516-169863566	SK-N-SH_RA	brain:	n/a
40	chr1:169863088-169863138	ECC-1	luminal epithelium:	n/a
41	chr1:169863189-169863239	HPAEpiC	pulmonary alveolar:	n/a
42	chr1:169863516-169863566	AoSMC	blood vessel:	n/a
43	chr1:169863169-169863219	SK-N-SH	brain:	n/a
44	chr1:169854522-169854572	A549	lung:	n/a
45	chr1:169863532-169863582	GM06990	blood:	n/a
46	chr1:169863210-169863260	NH-A	brain:	n/a
47	chr1:169863169-169863219	LNCaP	prostate:	n/a
48	chr1:169862883-169862933	GM12891	blood:	n/a
49	chr1:169862509-169862559	AG10803	skin:	n/a
50	chr1:169862707-169862757	HRPEpiC	eye:	n/a

(count:145 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:169770689..169773107-chr1:169861267..169863060,2	K562	blood:
2	chr1:169810204..169812691-chr1:169819466..169821386,2	MCF-7	breast:
3	chr1:169810189..169813776-chr1:169821630..169824014,3	K562	blood:
4	chr1:169812533..169814235-chr1:169854142..169856140,2	MCF-7	breast:
5	chr1:169847953..169852057-chr1:169858381..169863040,5	MCF-7	breast:
6	chr1:169862695..169863202-chr11:76155222..76156123,2	Hela-S3	cervix:
7	chr1:169811782..169814022-chr1:169814299..169816027,2	MCF-7	breast:
8	chr1:169836590..169839885-chr1:169857998..169860650,3	MCF-7	breast:
9	chr1:169857692..169860981-chr1:169868132..169871394,3	K562	blood:
10	chr1:169764521..169766056-chr1:169860447..169863119,2	MCF-7	breast:
11	chr1:169825649..169828863-chr1:169858551..169863079,4	K562	blood:
12	chr1:169862704..169863379-chr17:42580368..42581030,2	Hela-S3	cervix:
13	chr1:169763673..169765585-chr1:169787149..169789701,2	MCF-7	breast:
14	chr1:169862774..169863319-chr2:102314198..102314758,2	Hela-S3	cervix:
15	chr1:169836372..169839147-chr1:169853972..169856036,2	K562	blood:
16	chr1:169862763..169864506-chr1:170500944..170502450,2	K562	blood:
17	chr1:169867701..169870686-chr1:169875443..169877977,2	K562	blood:
18	chr1:169862288..169862861-chr17:7738385..7739270,2	Hela-S3	cervix:
19	chr1:169836372..169839147-chr1:169853972..169856036,2	K562	blood:
20	chr1:169875733..169878335-chr1:170499104..170501946,2	MCF-7	breast:
21	chr1:169812533..169814235-chr1:169854142..169856140,2	MCF-7	breast:
22	chr1:169815997..169818292-chr1:169837214..169839882,2	K562	blood:
23	chr1:169751559..169753241-chr1:169780241..169782649,2	MCF-7	breast:
24	chr1:169806621..169807436-chr17:35409246..35410122,2	NB4	blood:
25	chr1:169837054..169838824-chr1:169842629..169844274,2	K562	blood:
26	chr1:169862684..169863338-chr4:146101247..146102153,2	Hela-S3	cervix:
27	chr1:169818623..169820125-chr1:169861453..169863170,2	MCF-7	breast:
28	chr1:169862694..169863202-chr5:86563268..86564128,2	Hela-S3	cervix:
29	chr1:169827363..169830253-chr1:169858202..169860051,2	K562	blood:
30	chr1:169847146..169850317-chr1:169850331..169854277,4	K562	blood:
31	chr1:169863583..169866323-chr1:169872602..169875354,3	MCF-7	breast:
32	chr1:169837435..169839435-chr1:169862331..169864097,2	MCF-7	breast:
33	chr1:169819515..169822344-chr1:169896401..169898488,2	MCF-7	breast:
34	chr1:169812131..169813776-chr1:169822514..169824878,2	K562	blood:
35	chr1:169862283..169862808-chr15:41098940..41099495,2	Hela-S3	cervix:
36	chr1:169826041..169827646-chr1:169861241..169863079,2	K562	blood:
37	chr1:169866713..169870686-chr1:169874035..169877977,4	K562	blood:
38	chr1:169763198..169765886-chr1:169860155..169862900,4	K562	blood:
39	chr1:169820262..169822965-chr1:169860933..169863920,2	MCF-7	breast:
40	chr1:169862195..169863184-chr2:70528826..70529358,2	Hela-S3	cervix:
41	chr1:169861326..169864449-chr1:170043806..170046469,4	K562	blood:
42	chr1:169881052..169883977-chr1:169885843..169888269,2	MCF-7	breast:
43	chr1:169863583..169866323-chr1:169872602..169875354,3	MCF-7	breast:
44	chr1:169837054..169838824-chr1:169842629..169844274,2	K562	blood:
45	chr1:169866713..169870686-chr1:169874035..169877977,4	K562	blood:
46	chr1:169798250..169800377-chr1:169845673..169848267,2	K562	blood:
47	chr1:169826425..169828479-chr1:169831022..169833757,2	K562	blood:
48	chr1:169789201..169792181-chr1:169792666..169794813,2	K562	blood:
49	chr1:169821793..169826224-chr1:169827537..169831257,5	K562	blood:
50	chr1:169823925..169827148-chr1:169828128..169831257,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C1orf112-3	chr1:169831703-169831902	NONHSAT007480
2	lnc-C1orf112-3	chr1:169840540-169842473	NONHSAT007480
3	lnc-C1orf112-3	chr1:169831686-169831902	NONHSAT007482
4	lnc-C1orf112-2	chr1:169828897-169829193	NONHSAT007481
5	lnc-C1orf112-3	chr1:169840540-169842471	NONHSAT007482
6	lnc-C1orf112-3	chr1:169824995-169825104	NONHSAT007480

No data

Variant related genes	Relation type
RN7SL333P	TF binding region
SCYL3	TF binding region
RN7SL333P	CpG island
SCYL3	CpG island
ENSG00000164164	chromatin interactions
ENSG00000000460	chromatin interactions
ENSG00000120370	chromatin interactions
ENSG00000171806	chromatin interactions
ENSG00000145715	chromatin interactions
ENSG00000224738	chromatin interactions
ENSG00000166140	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000158636	chromatin interactions
ENSG00000169241	chromatin interactions
ENSG00000122644	chromatin interactions
ENSG00000231407	chromatin interactions
ENSG00000186566	chromatin interactions
ENSG00000255135	chromatin interactions
ENSG00000075945	chromatin interactions
ENSG00000204859	chromatin interactions
ENSG00000071054	chromatin interactions
ENSG00000000457	chromatin interactions
ENSG00000108395	chromatin interactions
ENSG00000170374	chromatin interactions
ENSG00000266895	chromatin interactions
ENSG00000239494	chromatin interactions
ENSG00000035141	chromatin interactions

Extended variants
information (count: 3816 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:3816 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56280741	chr1:169782011-169782012	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs557020146	chr1:169782044-169782045	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs34910388	chr1:169782047-169782048	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs574443978	chr1:169782089-169782090	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs535094622	chr1:169782106-169782107	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs11576078	chr1:169782109-169782110	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs78136146	chr1:169782113-169782114	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	mRNA abundance
8	rs182354515	chr1:169782162-169782163	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs4614317	chr1:169782189-169782190	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs573365704	chr1:169782233-169782234	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs80225972	chr1:169782243-169782244	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs545190953	chr1:169782366-169782367	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs140583140	chr1:169782391-169782392	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs529424139	chr1:169782406-169782407	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs74122412	chr1:169782409-169782410	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs186624534	chr1:169782474-169782475	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs533264402	chr1:169782496-169782497	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs145684119	chr1:169782565-169782566	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs542418030	chr1:169782570-169782571	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs11581878	chr1:169782592-169782593	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs560972627	chr1:169782606-169782607	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs531626496	chr1:169782627-169782628	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs139321648	chr1:169782643-169782644	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs543386833	chr1:169782669-169782670	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs549362389	chr1:169782766-169782767	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs535199949	chr1:169782795-169782796	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs556633368	chr1:169782798-169782799	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs149583866	chr1:169782805-169782806	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs558189664	chr1:169782820-169782821	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs573448943	chr1:169782836-169782837	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs149562510	chr1:169782843-169782844	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs190250288	chr1:169782847-169782848	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs182463038	chr1:169782876-169782877	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs544756941	chr1:169782949-169782950	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs562926900	chr1:169782979-169782980	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs116457393	chr1:169783020-169783021	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs144256700	chr1:169783058-169783059	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs564241210	chr1:169783084-169783085	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs11581959	chr1:169783100-169783101	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs373336171	chr1:169783138-169783139	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs546558806	chr1:169783167-169783168	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs568293418	chr1:169783226-169783227	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs148262407	chr1:169783228-169783229	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs12120114	chr1:169783246-169783247	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs566367148	chr1:169783256-169783257	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs568565721	chr1:169783310-169783311	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs370359076	chr1:169783315-169783316	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539062404	chr1:169783350-169783351	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs532574366	chr1:169783455-169783456	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs566320971	chr1:169783462-169783463	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:3039 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169764600-169782400	Weak transcription	Pancreas	Pancrea
2	chr1:169764800-169793200	Weak transcription	Aorta	Aorta
3	chr1:169764800-169793200	Weak transcription	Brain Hippocampus Middle	brain
4	chr1:169764800-169793400	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr1:169764800-169795200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr1:169764800-169796200	Weak transcription	Spleen	Spleen
7	chr1:169764800-169818200	Weak transcription	Esophagus	oesophagus
8	chr1:169764800-169818200	Weak transcription	Lung	lung
9	chr1:169764800-169823600	Weak transcription	Gastric	stomach
10	chr1:169765000-169786000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr1:169765000-169793200	Weak transcription	Fetal Brain Male	brain
12	chr1:169765000-169808000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr1:169765000-169821800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr1:169765200-169783200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr1:169765200-169793200	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr1:169765200-169793200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr1:169765200-169793400	Weak transcription	Fetal Kidney	kidney
18	chr1:169765200-169797400	Weak transcription	HSMMtube	muscle
19	chr1:169765200-169802000	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr1:169765200-169807800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr1:169765200-169808000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr1:169765200-169809000	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr1:169765200-169814800	Weak transcription	Brain Anterior Caudate	brain
24	chr1:169765200-169815200	Weak transcription	Rectal Smooth Muscle	rectum
25	chr1:169765200-169818800	Weak transcription	Brain Angular Gyrus	brain
26	chr1:169765200-169820600	Weak transcription	Psoas Muscle	Psoas
27	chr1:169765200-169823400	Weak transcription	Right Ventricle	heart
28	chr1:169765400-169788200	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr1:169765400-169796800	Weak transcription	Colon Smooth Muscle	Colon
30	chr1:169765400-169798400	Weak transcription	Brain Germinal Matrix	brain
31	chr1:169765400-169798400	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr1:169765400-169808000	Weak transcription	Fetal Heart	heart
33	chr1:169765400-169822600	Weak transcription	Colonic Mucosa	Colon
34	chr1:169765600-169783800	Weak transcription	Fetal Intestine Small	intestine
35	chr1:169765600-169808000	Weak transcription	Small Intestine	intestine
36	chr1:169765600-169818200	Weak transcription	NHLF	lung
37	chr1:169765800-169793200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr1:169765800-169808000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr1:169765800-169815200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr1:169765800-169818400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr1:169766000-169796800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr1:169766000-169797000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr1:169766000-169797400	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr1:169769400-169785800	Strong transcription	HUES64 Cell Line	embryonic stem cell
45	chr1:169770400-169785000	Strong transcription	Dnd41	blood
46	chr1:169771200-169785800	Strong transcription	Fetal Thymus	thymus
47	chr1:169771800-169784600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr1:169772400-169784600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr1:169773400-169796200	Weak transcription	HMEC	breast
50	chr1:169773400-169798400	Weak transcription	Primary B cells from peripheral blood	blood

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