Variant report

Variant	nsv872161
Chromosome Location	chr1:114162194-114280135
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:992)
CpG islands
(count:244)
Chromatin interactive
region (count:100)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:992 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:114219158-114219547	K562	blood:	n/a	n/a
2	ARID3A	chr1:114233895-114234177	K562	blood:	n/a	n/a
3	ARID3A	chr1:114219950-114220876	K562	blood:	n/a	n/a
4	ARID3A	chr1:114201491-114201911	K562	blood:	n/a	n/a
5	ARID3A	chr1:114217182-114217592	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:114220522-114220865	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:114235641-114235919	K562	blood:	n/a	n/a
8	ATF1	chr1:114219861-114220243	K562	blood:	n/a	n/a
9	ATF1	chr1:114230027-114230144	K562	blood:	n/a	n/a
10	ATF1	chr1:114201436-114202016	K562	blood:	n/a	n/a
11	ATF1	chr1:114219236-114219478	K562	blood:	n/a	n/a
12	ATF3	chr1:114220497-114220758	K562	blood:	n/a	n/a
13	BACH1	chr1:114201703-114201852	K562	blood:	n/a	n/a
14	BACH1	chr1:114224275-114224574	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr1:114217218-114217540	GM12878	blood:	n/a	chr1:114217410-114217421 chr1:114217333-114217344
16	BCL3	chr1:114217115-114217652	A549	lung:	n/a	n/a
17	BHLHE40	chr1:114217389-114217619	HepG2	liver:	n/a	n/a
18	BHLHE40	chr1:114219311-114219476	K562	blood:	n/a	n/a
19	BHLHE40	chr1:114201621-114202077	K562	blood:	n/a	n/a
20	BHLHE40	chr1:114219929-114220240	K562	blood:	n/a	n/a
21	BRCA1	chr1:114163843-114163864	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr1:114261208-114261596	K562	blood:	n/a	n/a
23	CBX3	chr1:114171647-114171911	K562	blood:	n/a	n/a
24	CBX3	chr1:114237579-114237926	K562	blood:	n/a	n/a
25	CBX3	chr1:114263604-114263990	K562	blood:	n/a	n/a
26	CBX3	chr1:114219807-114220278	K562	blood:	n/a	n/a
27	CBX3	chr1:114171599-114171987	K562	blood:	n/a	n/a
28	CBX3	chr1:114261254-114261605	K562	blood:	n/a	n/a
29	CBX3	chr1:114237499-114237932	K562	blood:	n/a	n/a
30	CBX3	chr1:114260074-114260483	K562	blood:	n/a	n/a
31	CCNT2	chr1:114233924-114234178	K562	blood:	n/a	n/a
32	CCNT2	chr1:114245042-114245102	K562	blood:	n/a	n/a
33	CCNT2	chr1:114219965-114220280	K562	blood:	n/a	n/a
34	CCNT2	chr1:114201276-114201980	K562	blood:	n/a	n/a
35	CCNT2	chr1:114219226-114219488	K562	blood:	n/a	n/a
36	CEBPB	chr1:114213356-114213594	K562	blood:	n/a	chr1:114213467-114213478
37	CEBPB	chr1:114217828-114218403	A549	lung:	n/a	chr1:114218180-114218193 chr1:114218180-114218191
38	CEBPB	chr1:114213309-114213621	IMR90	lung:	n/a	chr1:114213467-114213478
39	CEBPB	chr1:114205025-114205382	K562	blood:	n/a	chr1:114205182-114205193
40	CEBPB	chr1:114217829-114218413	MCF-7	breast:	n/a	chr1:114218180-114218193 chr1:114218180-114218191
41	CEBPB	chr1:114229922-114230239	IMR90	lung:	n/a	n/a
42	CEBPB	chr1:114205041-114205349	Hela-S3	cervix:	n/a	chr1:114205182-114205193
43	CEBPB	chr1:114217977-114218380	K562	blood:	n/a	chr1:114218180-114218193 chr1:114218180-114218191
44	CEBPB	chr1:114219843-114220327	K562	blood:	n/a	n/a
45	CEBPB	chr1:114217125-114217611	A549	lung:	n/a	n/a
46	CEBPB	chr1:114218021-114218347	HepG2	liver:	n/a	chr1:114218180-114218193 chr1:114218180-114218191
47	CEBPB	chr1:114217230-114217518	A549	lung:	n/a	n/a
48	CEBPB	chr1:114205797-114205997	IMR90	lung:	n/a	n/a
49	CEBPB	chr1:114231152-114231340	HepG2	liver:	n/a	chr1:114231245-114231256 chr1:114231246-114231257 chr1:114231245-114231258 chr1:114231245-114231256
50	CEBPB	chr1:114217941-114218380	K562	blood:	n/a	chr1:114218180-114218193 chr1:114218180-114218191

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:114240177-114240227	MCF10A-Er-Src	breast:	n/a
2	chr1:114218186-114218236	ProgFib	skin:	n/a
3	chr1:114227391-114227441	AoSMC	blood vessel:	n/a
4	chr1:114227391-114227441	HIPEpiC	eye:	n/a
5	chr1:114244058-114244108	SK-N-MC	brain:	n/a
6	chr1:114227391-114227441	SK-N-SH	brain:	n/a
7	chr1:114244058-114244108	PFSK-1	brain:	n/a
8	chr1:114218186-114218236	Caco-2	colon:	n/a
9	chr1:114218186-114218236	PANC-1	pancreas:	n/a
10	chr1:114218186-114218236	SAEC	small airway:	n/a
11	chr1:114240177-114240227	ovcar-3	ovarian:	n/a
12	chr1:114240177-114240227	GM12891	blood:	n/a
13	chr1:114240177-114240227	CMK	blood:	n/a
14	chr1:114218186-114218236	PFSK-1	brain:	n/a
15	chr1:114227391-114227441	PFSK-1	brain:	n/a
16	chr1:114240177-114240227	BE2_C	brain:	n/a
17	chr1:114218186-114218236	LNCaP	prostate:	n/a
18	chr1:114244058-114244108	HUVEC	blood vessel:	n/a
19	chr1:114218186-114218236	HL-60	blood:	n/a
20	chr1:114227391-114227441	H1-hESC	embryonic stem cell:	embryo
21	chr1:114244058-114244108	SKMC	muscle:	n/a
22	chr1:114227391-114227441	HCT-116	colon:	n/a
23	chr1:114244058-114244108	ovcar-3	ovarian:	n/a
24	chr1:114244058-114244108	HEEpiC	esophagus:	n/a
25	chr1:114218186-114218236	SK-N-SH	brain:	n/a
26	chr1:114227391-114227441	HL-60	blood:	n/a
27	chr1:114227391-114227441	SAEC	small airway:	n/a
28	chr1:114244058-114244108	GM19239	blood:	n/a
29	chr1:114218186-114218236	HRE	kidney:	n/a
30	chr1:114240177-114240227	HCM	heart:	n/a
31	chr1:114244058-114244108	GM12892	blood:	n/a
32	chr1:114240177-114240227	H1-hESC	embryonic stem cell:	embryo
33	chr1:114218186-114218236	HNPCEpiC	eye:	n/a
34	chr1:114218186-114218236	HEK293	kidney:	embryo
35	chr1:114244058-114244108	NB4	blood:	n/a
36	chr1:114244058-114244108	HCF	heart:	n/a
37	chr1:114240177-114240227	HCT-116	colon:	n/a
38	chr1:114227391-114227441	GM06990	blood:	n/a
39	chr1:114244058-114244108	ProgFib	skin:	n/a
40	chr1:114244058-114244108	U87	brain:	n/a
41	chr1:114244058-114244108	ECC-1	luminal epithelium:	n/a
42	chr1:114227391-114227441	GM12878	blood:	n/a
43	chr1:114240177-114240227	LNCaP	prostate:	n/a
44	chr1:114218186-114218236	HCT-116	colon:	n/a
45	chr1:114240177-114240227	HNPCEpiC	eye:	n/a
46	chr1:114240177-114240227	ProgFib	skin:	n/a
47	chr1:114218186-114218236	Hela-S3	cervix:	n/a
48	chr1:114240177-114240227	RPTEC	kidney:	n/a
49	chr1:114244058-114244108	K562	blood:	n/a
50	chr1:114240177-114240227	PrEC	prostate:	n/a

(count:100 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:114189711..114191330-chr1:114193397..114195766,2	MCF-7	breast:
2	chr1:113932659..113933643-chr1:114220188..114220916,2	MCF-7	breast:
3	chr1:114185208..114187215-chr1:114207813..114209339,2	K562	blood:
4	chr1:114234213..114236174-chr1:114237098..114240028,2	MCF-7	breast:
5	chr1:113635215..113637983-chr1:114201241..114204129,2	K562	blood:
6	chr1:114197750..114199827-chr1:114202286..114204073,2	K562	blood:
7	chr1:114255171..114257504-chr1:114268146..114270647,2	K562	blood:
8	chr1:114192533..114195084-chr1:114195478..114197038,2	K562	blood:
9	chr1:114186716..114188262-chr1:114191600..114194124,2	MCF-7	breast:
10	chr1:113682884..113683782-chr1:114220579..114221082,2	K562	blood:
11	chr1:114212026..114215527-chr1:114217715..114221049,6	K562	blood:
12	chr1:114244773..114247949-chr1:114249396..114252408,3	MCF-7	breast:
13	chr1:114273951..114275482-chr1:114286454..114288640,2	K562	blood:
14	chr1:114223956..114226285-chr1:114471378..114474158,2	K562	blood:
15	chr1:114225725..114228259-chr1:114231817..114234548,2	MCF-7	breast:
16	chr1:114157193..114159777-chr1:114161576..114164133,2	K562	blood:
17	chr1:113995191..113995964-chr1:114220394..114221133,3	MCF-7	breast:
18	chr1:113933524..113935646-chr1:114221508..114224251,2	MCF-7	breast:
19	chr1:114196620..114199444-chr1:114200483..114202239,2	K562	blood:
20	chr1:114191701..114193455-chr1:114196104..114197721,2	MCF-7	breast:
21	chr1:114272431..114274896-chr1:114354448..114356333,2	MCF-7	breast:
22	chr1:114220350..114221100-chr17:62398423..62399162,2	MCF-7	breast:
23	chr1:114185827..114187693-chr17:4268175..4270589,2	MCF-7	breast:
24	chr1:114234213..114236174-chr1:114237098..114240028,2	MCF-7	breast:
25	chr1:114191701..114193455-chr1:114196104..114197721,2	MCF-7	breast:
26	chr1:114228136..114230531-chr1:114234621..114236141,2	K562	blood:
27	chr1:114248976..114251078-chr1:114251119..114252692,3	MCF-7	breast:
28	chr1:114187353..114189449-chr1:114189672..114191281,2	MCF-7	breast:
29	chr1:114210224..114212923-chr1:114219476..114221721,2	MCF-7	breast:
30	chr1:114225092..114226797-chr1:114232767..114235270,2	MCF-7	breast:
31	chr1:114223041..114225984-chr1:114230466..114232583,2	MCF-7	breast:
32	chr1:114276599..114278917-chr1:114301023..114303287,2	MCF-7	breast:
33	chr1:114272866..114275346-chr1:114279031..114281633,2	K562	blood:
34	chr1:114212058..114214688-chr1:114217824..114221724,4	K562	blood:
35	chr1:114212058..114214688-chr1:114217824..114221724,4	K562	blood:
36	chr1:114183983..114185528-chr1:114194793..114196565,2	MCF-7	breast:
37	chr1:114240657..114244104-chr1:114245278..114249575,4	MCF-7	breast:
38	chr1:113932839..113934722-chr1:114187354..114190196,2	MCF-7	breast:
39	chr1:114156923..114159777-chr1:114160586..114163076,2	K562	blood:
40	chr1:114225154..114227023-chr1:114236364..114238546,2	MCF-7	breast:
41	chr1:114186046..114188816-chr1:114192338..114195071,2	MCF-7	breast:
42	chr1:114244773..114247949-chr1:114249396..114252408,3	MCF-7	breast:
43	chr1:114212026..114215527-chr1:114217715..114221049,6	K562	blood:
44	chr1:114194523..114197911-chr1:114198408..114201889,3	K562	blood:
45	chr1:114222809..114226325-chr1:114228244..114229950,3	K562	blood:
46	chr1:114276830..114279009-chr1:114472031..114474564,2	MCF-7	breast:
47	chr1:114192533..114195084-chr1:114195478..114197038,2	K562	blood:
48	chr1:114228136..114230531-chr1:114234621..114236141,2	K562	blood:
49	chr1:114225154..114227023-chr1:114236364..114238546,2	MCF-7	breast:
50	chr1:114236180..114238815-chr22:28319168..28321227,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RSBN1-5	chr1:114241506-114242253	NONHSAT005327
2	lnc-RSBN1-3	chr1:114272848-114273403	ucscGeneNc_uc001eek_2
3	lnc-RSBN1-3	chr1:114272389-114272533	ucscGeneNc_uc001eek_2
4	lnc-RSBN1-3	chr1:114270773-114270886	ucscGeneNc_uc001eek_2
5	lnc-RSBN1-3	chr1:114268147-114268477	ucscGeneNc_uc001eek_2
6	lnc-RSBN1-3	chr1:114270998-114271967	ucscGeneNc_uc001eek_2

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PHTF1	hsa-miR-215-5p	chr1:114246625-114246646
2	PHTF1	hsa-miR-192-5p	chr1:114239856-114239875
3	PHTF1	hsa-miR-25-3p	chr1:114268082-114268103
4	PHTF1	hsa-miR-215-5p	chr1:114239856-114239875
5	PHTF1	hsa-miR-192-5p	chr1:114246625-114246646

Variant related genes	Relation type
ENSG00000232450	TF binding region
PHTF1	TF binding region
ENSG00000232450	CpG island
PHTF1	CpG island
ENSG00000238198	chromatin interactions
ENSG00000134262	chromatin interactions
ENSG00000163349	chromatin interactions
ENSG00000132388	chromatin interactions
ENSG00000226419	chromatin interactions
ENSG00000081026	chromatin interactions
ENSG00000198799	chromatin interactions
ENSG00000232450	chromatin interactions
ENSG00000155380	chromatin interactions
ENSG00000081019	chromatin interactions
ENSG00000116793	chromatin interactions
ENSG00000235527	chromatin interactions
ENSG00000118655	chromatin interactions
ENSG00000231128	chromatin interactions

Extended variants
information (count: 3934 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:3934 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1217192	chr1:114162194-114162195	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142600454	chr1:114162219-114162220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192795062	chr1:114162231-114162232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185494595	chr1:114162261-114162262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370056115	chr1:114162438-114162439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374433209	chr1:114162469-114162470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539487902	chr1:114162470-114162471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113408933	chr1:114162525-114162526	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs78351958	chr1:114162551-114162552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190724690	chr1:114162565-114162566	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112542389	chr1:114162582-114162583	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs1217193	chr1:114162619-114162620	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs544796018	chr1:114162662-114162663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564789644	chr1:114162689-114162690	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561341706	chr1:114162706-114162707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574838396	chr1:114162804-114162805	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540379085	chr1:114162852-114162853	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192021118	chr1:114162871-114162872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531943488	chr1:114162901-114162902	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560450824	chr1:114162940-114162941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200717891	chr1:114162947-114162948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184572585	chr1:114162952-114162953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188498824	chr1:114162953-114162954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562421432	chr1:114162960-114162961	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567934915	chr1:114162970-114162971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371012082	chr1:114162971-114162972	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs181276950	chr1:114163026-114163027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548331252	chr1:114163035-114163036	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568174513	chr1:114163074-114163075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs117658524	chr1:114163085-114163086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369309684	chr1:114163090-114163091	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547174284	chr1:114163116-114163117	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570569703	chr1:114163121-114163122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146900614	chr1:114163166-114163167	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186734588	chr1:114163250-114163251	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11589796	chr1:114163263-114163264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569540726	chr1:114163309-114163310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs189121238	chr1:114163333-114163334	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555103590	chr1:114163371-114163372	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574937287	chr1:114163418-114163419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540867857	chr1:114163489-114163490	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1217194	chr1:114163501-114163502	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs576953666	chr1:114163506-114163507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545766215	chr1:114163558-114163559	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6693766	chr1:114163583-114163584	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs371637485	chr1:114163585-114163586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181019983	chr1:114163602-114163603	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs77892281	chr1:114163617-114163618	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs562064775	chr1:114163621-114163622	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs527487700	chr1:114163658-114163659	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Asthma	20841430	CNVD
Aetanephric adenomas	20802469	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	21956041	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	16573809	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Breast cancer	17899364	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Melanoma	19671679	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:2137 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:114100600-114173400	Weak transcription	Gastric	stomach
2	chr1:114119200-114172400	Weak transcription	Pancreas	Pancrea
3	chr1:114119200-114173000	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr1:114124400-114172400	Weak transcription	Aorta	Aorta
5	chr1:114134600-114166400	Weak transcription	Hela-S3	cervix
6	chr1:114140600-114162200	Weak transcription	NHDF-Ad	bronchial
7	chr1:114140600-114172800	Weak transcription	Colonic Mucosa	Colon
8	chr1:114140800-114162600	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr1:114141000-114162600	Weak transcription	Fetal Intestine Large	intestine
10	chr1:114141200-114162200	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr1:114141400-114162400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr1:114146200-114163200	Weak transcription	Fetal Lung	lung
13	chr1:114147200-114163400	Weak transcription	Duodenum Mucosa	Duodenum
14	chr1:114151400-114172600	Weak transcription	Ovary	ovary
15	chr1:114151800-114166400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr1:114153000-114163600	Weak transcription	Fetal Kidney	kidney
17	chr1:114153600-114168400	Weak transcription	Fetal Muscle Trunk	muscle
18	chr1:114154000-114172400	Weak transcription	Fetal Stomach	stomach
19	chr1:114156200-114170000	Weak transcription	Small Intestine	intestine
20	chr1:114157400-114166400	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr1:114157600-114163800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:114158600-114166400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr1:114158800-114163200	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr1:114158800-114168600	Weak transcription	HUVEC	blood vessel
25	chr1:114159000-114168600	Weak transcription	Brain Hippocampus Middle	brain
26	chr1:114159000-114172200	Weak transcription	NH-A	brain
27	chr1:114159000-114173200	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr1:114159000-114195000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr1:114159200-114162200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr1:114159200-114165200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr1:114159200-114194800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr1:114160200-114162800	Weak transcription	Adipose Nuclei	Adipose
33	chr1:114160400-114169800	Weak transcription	Rectal Smooth Muscle	rectum
34	chr1:114160600-114165400	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr1:114160600-114165600	Weak transcription	Osteobl	bone
36	chr1:114160600-114168600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr1:114160600-114169000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr1:114160800-114168200	Weak transcription	Primary hematopoietic stem cells	blood
39	chr1:114161000-114166400	Weak transcription	Fetal Brain Male	brain
40	chr1:114161200-114168000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr1:114161400-114168600	Weak transcription	Fetal Intestine Small	intestine
42	chr1:114161600-114163200	Weak transcription	Primary T cells from cord blood	blood
43	chr1:114161600-114163600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr1:114161600-114164600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr1:114161600-114172400	Weak transcription	Placenta	Placenta
46	chr1:114161600-114184600	Weak transcription	Colon Smooth Muscle	Colon
47	chr1:114161600-114184600	Weak transcription	HepG2	liver
48	chr1:114161800-114164200	Weak transcription	Primary T helper cells fromperipheralblood	blood
49	chr1:114161800-114167000	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr1:114161800-114168600	Weak transcription	Fetal Muscle Leg	muscle

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