Variant report

Variant	nsv881729
Chromosome Location	chr5:61719506-61857577
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:980)
CpG islands
(count:122)
Chromatin interactive
region (count:82)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:980 , 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	chr5:61739584-61739797	K562	blood:	n/a	n/a
2	ARID3A	chr5:61728417-61729030	K562	blood:	n/a	n/a
3	ARID3A	chr5:61739604-61739817	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:61834143-61834798	K562	blood:	n/a	n/a
5	ATF1	chr5:61728495-61728807	K562	blood:	n/a	n/a
6	ATF1	chr5:61782636-61782747	K562	blood:	n/a	n/a
7	ATF1	chr5:61834328-61834785	K562	blood:	n/a	n/a
8	ATF1	chr5:61773463-61773905	K562	blood:	n/a	n/a
9	ATF3	chr5:61728423-61728847	K562	blood:	n/a	n/a
10	BACH1	chr5:61847461-61847507	K562	blood:	n/a	n/a
11	BACH1	chr5:61833258-61833381	K562	blood:	n/a	n/a
12	BACH1	chr5:61834564-61834771	K562	blood:	n/a	n/a
13	BACH1	chr5:61792631-61793055	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr5:61739279-61739313	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr5:61823230-61823237	K562	blood:	n/a	n/a
16	BHLHE40	chr5:61739412-61739507	K562	blood:	n/a	n/a
17	BHLHE40	chr5:61834289-61834768	K562	blood:	n/a	n/a
18	BRCA1	chr5:61834474-61834740	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr5:61756334-61756594	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr5:61834280-61834852	K562	blood:	n/a	n/a
21	CCNT2	chr5:61834507-61834787	K562	blood:	n/a	n/a
22	CEBPB	chr5:61728481-61728804	Hela-S3	cervix:	n/a	chr5:61728654-61728665
23	CEBPB	chr5:61851781-61852057	H1-hESC	embryonic stem cell:	n/a	chr5:61851945-61851956
24	CEBPB	chr5:61720703-61720918	A549	lung:	n/a	chr5:61720791-61720808 chr5:61720792-61720805 chr5:61720793-61720804 chr5:61720792-61720805
25	CEBPB	chr5:61742831-61743028	K562	blood:	n/a	n/a
26	CEBPB	chr5:61845040-61845323	HepG2	liver:	n/a	n/a
27	CEBPB	chr5:61789789-61789989	K562	blood:	n/a	n/a
28	CEBPB	chr5:61851780-61852127	IMR90	lung:	n/a	chr5:61851945-61851956
29	CEBPB	chr5:61720640-61720974	HepG2	liver:	n/a	chr5:61720791-61720808 chr5:61720792-61720805 chr5:61720793-61720804 chr5:61720792-61720805
30	CEBPB	chr5:61834495-61834802	MCF-7	breast:	n/a	n/a
31	CEBPB	chr5:61773639-61774006	IMR90	lung:	n/a	n/a
32	CEBPB	chr5:61826186-61826369	HepG2	liver:	n/a	chr5:61826345-61826356 chr5:61826285-61826296 chr5:61826343-61826356
33	CEBPB	chr5:61845040-61845363	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr5:61834394-61834792	A549	lung:	n/a	n/a
35	CEBPB	chr5:61728246-61728869	K562	blood:	n/a	chr5:61728654-61728665
36	CEBPB	chr5:61728533-61728826	A549	lung:	n/a	chr5:61728654-61728665
37	CEBPB	chr5:61834195-61834842	K562	blood:	n/a	n/a
38	CEBPB	chr5:61720690-61720838	H1-hESC	embryonic stem cell:	n/a	chr5:61720791-61720808 chr5:61720792-61720805 chr5:61720793-61720804 chr5:61720792-61720805
39	CEBPB	chr5:61834383-61834832	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr5:61770862-61771320	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr5:61720617-61720978	K562	blood:	n/a	chr5:61720791-61720808 chr5:61720792-61720805 chr5:61720793-61720804 chr5:61720792-61720805
42	CEBPB	chr5:61751335-61751648	IMR90	lung:	n/a	chr5:61751510-61751519 chr5:61751510-61751519 chr5:61751509-61751520
43	CEBPB	chr5:61834390-61834854	IMR90	lung:	n/a	n/a
44	CEBPB	chr5:61773728-61773947	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr5:61851779-61852116	K562	blood:	n/a	chr5:61851945-61851956
46	CEBPB	chr5:61773671-61773930	HepG2	liver:	n/a	n/a
47	CEBPB	chr5:61724735-61725082	K562	blood:	n/a	chr5:61724926-61724937
48	CEBPB	chr5:61834005-61834821	K562	blood:	n/a	n/a
49	CEBPB	chr5:61751201-61751660	HepG2	liver:	n/a	chr5:61751510-61751519 chr5:61751510-61751519 chr5:61751509-61751520
50	CEBPB	chr5:61724746-61725084	HepG2	liver:	n/a	chr5:61724926-61724937

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:61818801-61818851	AG04449	skin:	fetal
2	chr5:61818801-61818851	HL-60	blood:	n/a
3	chr5:61818801-61818851	SK-N-MC	brain:	n/a
4	chr5:61844855-61844905	Jurkat	blood:	n/a
5	chr5:61844855-61844905	HIPEpiC	eye:	n/a
6	chr5:61844855-61844905	HRPEpiC	eye:	n/a
7	chr5:61844855-61844905	IMR90	lung:	fetal
8	chr5:61844855-61844905	HCT-116	colon:	n/a
9	chr5:61844855-61844905	HCPEpiC	choroid plexus:	n/a
10	chr5:61818801-61818851	HCPEpiC	choroid plexus:	n/a
11	chr5:61844855-61844905	SAEC	small airway:	n/a
12	chr5:61818801-61818851	HRPEpiC	eye:	n/a
13	chr5:61818801-61818851	K562	blood:	n/a
14	chr5:61844855-61844905	BE2_C	brain:	n/a
15	chr5:61844855-61844905	MCF10A-Er-Src	breast:	n/a
16	chr5:61818801-61818851	NH-A	brain:	n/a
17	chr5:61818801-61818851	Hepatocyte	liver:	n/a
18	chr5:61844855-61844905	HAEpiC	amniotic membrane:	n/a
19	chr5:61818801-61818851	HIPEpiC	eye:	n/a
20	chr5:61818801-61818851	NHBE	bronchial:	n/a
21	chr5:61844855-61844905	NT2-D1	testis:	n/a
22	chr5:61818801-61818851	NHDF-neo	bronchial:	n/a
23	chr5:61844855-61844905	AG04449	skin:	fetal
24	chr5:61818801-61818851	HEK293	kidney:	embryo
25	chr5:61844855-61844905	ProgFib	skin:	n/a
26	chr5:61818801-61818851	AoSMC	blood vessel:	n/a
27	chr5:61818801-61818851	ProgFib	skin:	n/a
28	chr5:61818801-61818851	SK-N-SH_RA	brain:	n/a
29	chr5:61844855-61844905	HEK293	kidney:	embryo
30	chr5:61818801-61818851	SAEC	small airway:	n/a
31	chr5:61818801-61818851	HCT-116	colon:	n/a
32	chr5:61818801-61818851	IMR90	lung:	fetal
33	chr5:61844855-61844905	AoSMC	blood vessel:	n/a
34	chr5:61818801-61818851	NT2-D1	testis:	n/a
35	chr5:61818801-61818851	PANC-1	pancreas:	n/a
36	chr5:61844855-61844905	HRCEpiC	kidney:	n/a
37	chr5:61818801-61818851	Caco-2	colon:	n/a
38	chr5:61844855-61844905	Caco-2	colon:	n/a
39	chr5:61818801-61818851	SK-N-SH	brain:	n/a
40	chr5:61818801-61818851	MCF-7	breast:	n/a
41	chr5:61844855-61844905	ECC-1	luminal epithelium:	n/a
42	chr5:61844855-61844905	NHDF-neo	bronchial:	n/a
43	chr5:61818801-61818851	HRE	kidney:	n/a
44	chr5:61844855-61844905	GM19239	blood:	n/a
45	chr5:61818801-61818851	HAEpiC	amniotic membrane:	n/a
46	chr5:61844855-61844905	PANC-1	pancreas:	n/a
47	chr5:61818801-61818851	U87	brain:	n/a
48	chr5:61818801-61818851	HEEpiC	esophagus:	n/a
49	chr5:61818801-61818851	PFSK-1	brain:	n/a
50	chr5:61844855-61844905	AG09309	skin:	n/a

(count:82 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:61708675..61710194-chr5:61723245..61724819,2	K562	blood:
2	chr5:61723264..61725509-chr5:61726691..61728458,2	K562	blood:
3	chr5:61772217..61774196-chr5:61781194..61783059,2	MCF-7	breast:
4	chr5:61717680..61720586-chr5:61720759..61724010,4	K562	blood:
5	chr5:61756163..61758151-chr5:61762840..61764652,2	K562	blood:
6	chr5:61833675..61836577-chr5:61862911..61865153,3	K562	blood:
7	chr5:61714025..61717535-chr5:61719136..61721817,3	K562	blood:
8	chr5:61696731..61700669-chr5:61725889..61729809,4	MCF-7	breast:
9	chr5:61781558..61784548-chr5:61790648..61794410,3	K562	blood:
10	chr5:61833268..61834812-chr5:61850872..61852954,2	K562	blood:
11	chr5:61821283..61823218-chr5:61824428..61826675,2	MCF-7	breast:
12	chr5:61793500..61795640-chr5:61797559..61799676,2	K562	blood:
13	chr5:61822169..61825461-chr5:61826034..61828796,3	K562	blood:
14	chr5:61697950..61699779-chr5:61731524..61733895,2	MCF-7	breast:
15	chr5:61695775..61698135-chr5:61722484..61724142,2	K562	blood:
16	chr5:61715203..61717539-chr5:61717631..61720268,2	K562	blood:
17	chr5:61741039..61743248-chr5:61746632..61748600,2	K562	blood:
18	chr5:61766130..61769204-chr5:61785246..61788034,3	K562	blood:
19	chr5:61795098..61797739-chr5:61799881..61802106,2	K562	blood:
20	chr5:61730501..61733292-chr5:61772580..61775158,2	K562	blood:
21	chr5:61701249..61703981-chr5:61732998..61735157,2	K562	blood:
22	chr5:61756022..61757748-chr5:62074424..62075807,9	MCF-7	breast:
23	chr5:61719601..61722587-chr5:61724504..61726966,2	MCF-7	breast:
24	chr5:61795098..61797739-chr5:61799881..61802106,2	K562	blood:
25	chr5:61833268..61834812-chr5:61850872..61852954,2	K562	blood:
26	chr5:61717104..61719301-chr5:61731721..61733854,2	K562	blood:
27	chr5:61712841..61714503-chr5:61724688..61726349,2	K562	blood:
28	chr5:61756074..61756595-chr5:61927958..61928492,2	MCF-7	breast:
29	chr5:61827589..61829469-chr5:61829575..61831772,2	MCF-7	breast:
30	chr5:61707104..61708632-chr5:61728133..61729715,2	K562	blood:
31	chr5:61756416..61757318-chr5:62074341..62075268,4	K562	blood:
32	chr5:61766130..61769204-chr5:61785246..61788034,3	K562	blood:
33	chr5:61781558..61784548-chr5:61790648..61794410,3	K562	blood:
34	chr5:61728041..61729756-chr5:61733512..61736451,2	K562	blood:
35	chr5:61829519..61831113-chr5:61834353..61836301,2	MCF-7	breast:
36	chr5:61708636..61711754-chr5:61726826..61730056,3	K562	blood:
37	chr5:61723264..61725509-chr5:61726691..61728458,2	K562	blood:
38	chr5:61697301..61700669-chr5:61729156..61732578,4	K562	blood:
39	chr5:61767541..61769044-chr5:62072655..62075082,2	MCF-7	breast:
40	chr5:61687643..61690637-chr5:61717431..61720022,2	K562	blood:
41	chr5:61826046..61828158-chr5:61830735..61833492,2	K562	blood:
42	chr5:61822169..61825461-chr5:61826034..61828796,3	K562	blood:
43	chr5:61782970..61785454-chr5:61790224..61793065,2	K562	blood:
44	chr5:61747217..61749290-chr5:61754763..61757506,2	K562	blood:
45	chr5:61833161..61835046-chr5:61842892..61845396,3	K562	blood:
46	chr5:61728041..61729756-chr5:61733512..61736451,2	K562	blood:
47	chr5:61716804..61719809-chr5:61726970..61730058,3	K562	blood:
48	chr5:61708475..61710224-chr5:61720231..61721917,3	MCF-7	breast:
49	chr5:61762888..61765015-chr5:61768126..61770339,2	K562	blood:
50	chr5:61717153..61720586-chr5:61722238..61726435,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC70-1	chr5:61856523-61856832	NONHSAT101713
2	lnc-LRRC70-1	chr5:61856963-61857084	NONHSAT101713

No data

Variant related genes	Relation type
ENSG00000268942	TF binding region
RNU6-661P	TF binding region
IPO11	TF binding region
ENSG00000268942	CpG island
RNU6-661P	CpG island
IPO11	CpG island
ENSG00000086200	chromatin interactions
ENSG00000217416	chromatin interactions
ENSG00000086189	chromatin interactions

Extended variants
information (count: 5544 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:5544 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs152186	chr5:61719506-61719507	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184356307	chr5:61719540-61719541	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs370376448	chr5:61719557-61719558	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs147651963	chr5:61719561-61719562	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs549698436	chr5:61719623-61719624	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs538230972	chr5:61719640-61719641	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs550612589	chr5:61719642-61719643	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs570679697	chr5:61719654-61719655	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs530756230	chr5:61719676-61719677	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs569365374	chr5:61719683-61719684	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs539279038	chr5:61719688-61719689	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs553098215	chr5:61719708-61719709	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs572686671	chr5:61719833-61719834	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs188831185	chr5:61719846-61719847	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs530113559	chr5:61719855-61719856	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs555040027	chr5:61719860-61719861	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs574934367	chr5:61719890-61719891	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs544154502	chr5:61719928-61719929	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs11428881	chr5:61719965-61719966	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs34205379	chr5:61719966-61719967	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs398108991	chr5:61719977-61719978	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs375041751	chr5:61719978-61719979	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs142271045	chr5:61720005-61720006	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs111342318	chr5:61720027-61720028	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs540484163	chr5:61720028-61720029	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs373569522	chr5:61720035-61720036	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs529509783	chr5:61720038-61720039	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs153865	chr5:61720065-61720066	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs186299763	chr5:61720067-61720068	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs531614689	chr5:61720076-61720077	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs548622059	chr5:61720091-61720092	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs59475513	chr5:61720115-61720116	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs570670969	chr5:61720123-61720124	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs566834329	chr5:61720128-61720129	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs533293682	chr5:61720182-61720183	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs534500903	chr5:61720208-61720209	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs546468179	chr5:61720212-61720213	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs566375894	chr5:61720213-61720214	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs149274951	chr5:61720245-61720246	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs191144139	chr5:61720250-61720251	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs568565486	chr5:61720257-61720258	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs112351724	chr5:61720258-61720259	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs58672047	chr5:61720264-61720265	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs570610458	chr5:61720287-61720288	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs537462997	chr5:61720326-61720327	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs11463637	chr5:61720349-61720350	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs397748376	chr5:61720350-61720351	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs143482171	chr5:61720363-61720364	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs577548164	chr5:61720371-61720372	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs540947590	chr5:61720520-61720521	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2167 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:61709200-61770800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:61709400-61727400	Weak transcription	Placenta	Placenta
3	chr5:61709400-61727400	Weak transcription	Pancreas	Pancrea
4	chr5:61709400-61763400	Weak transcription	Aorta	Aorta
5	chr5:61709600-61723000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr5:61709600-61724600	Weak transcription	Fetal Stomach	stomach
7	chr5:61709600-61726400	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr5:61709600-61728000	Weak transcription	Gastric	stomach
9	chr5:61709600-61738800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr5:61709600-61738800	Weak transcription	Fetal Muscle Trunk	muscle
11	chr5:61709600-61739800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr5:61709600-61744000	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr5:61709800-61727400	Weak transcription	HSMM	muscle
14	chr5:61709800-61728000	Weak transcription	Fetal Lung	lung
15	chr5:61709800-61728000	Weak transcription	Right Ventricle	heart
16	chr5:61709800-61728000	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr5:61709800-61728200	Weak transcription	Brain Hippocampus Middle	brain
18	chr5:61709800-61738800	Weak transcription	Fetal Kidney	kidney
19	chr5:61709800-61743800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr5:61709800-61746000	Weak transcription	Primary hematopoietic stem cells	blood
21	chr5:61709800-61746600	Weak transcription	Fetal Thymus	thymus
22	chr5:61709800-61769000	Weak transcription	NH-A	brain
23	chr5:61709800-61809200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr5:61710000-61721200	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr5:61710000-61721400	Weak transcription	Duodenum Mucosa	Duodenum
26	chr5:61710000-61727000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr5:61710000-61727200	Weak transcription	Fetal Muscle Leg	muscle
28	chr5:61710000-61727600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr5:61710000-61729000	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr5:61710000-61734200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr5:61710000-61734200	Weak transcription	Fetal Intestine Small	intestine
32	chr5:61710000-61737400	Weak transcription	Fetal Intestine Large	intestine
33	chr5:61710000-61739000	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr5:61710000-61746000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr5:61710200-61720400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr5:61710200-61728000	Weak transcription	Stomach Smooth Muscle	stomach
37	chr5:61710200-61733400	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr5:61710200-61738800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr5:61710200-61746000	Weak transcription	Primary B cells from cord blood	blood
40	chr5:61710400-61733600	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr5:61710400-61739000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr5:61710400-61746000	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr5:61710600-61738800	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr5:61710600-61739000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr5:61710600-61739200	Weak transcription	HMEC	breast
46	chr5:61710600-61739200	Weak transcription	NHEK	skin
47	chr5:61710600-61744000	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr5:61710600-61746000	Weak transcription	A549	lung
49	chr5:61710800-61723600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr5:61710800-61727200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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