Variant report

Variant	nsv881730
Chromosome Location	chr5:61750667-61883581
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:851)
CpG islands
(count:244)
Chromatin interactive
region (count:55)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:851 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:61881564-61882083	K562	blood:	n/a	n/a
2	ARID3A	chr5:61834143-61834798	K562	blood:	n/a	n/a
3	ATF1	chr5:61834328-61834785	K562	blood:	n/a	n/a
4	ATF1	chr5:61881568-61881851	K562	blood:	n/a	n/a
5	ATF1	chr5:61773463-61773905	K562	blood:	n/a	n/a
6	ATF1	chr5:61782636-61782747	K562	blood:	n/a	n/a
7	ATF2	chr5:61870304-61870858	GM12878	blood:	n/a	n/a
8	BACH1	chr5:61847461-61847507	K562	blood:	n/a	n/a
9	BACH1	chr5:61833258-61833381	K562	blood:	n/a	n/a
10	BACH1	chr5:61823230-61823237	K562	blood:	n/a	n/a
11	BACH1	chr5:61792631-61793055	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr5:61865990-61866018	K562	blood:	n/a	n/a
13	BACH1	chr5:61834564-61834771	K562	blood:	n/a	n/a
14	BATF	chr5:61865376-61865608	GM12878	blood:	n/a	chr5:61865577-61865585
15	BATF	chr5:61870477-61870741	GM12878	blood:	n/a	n/a
16	BATF	chr5:61870405-61870771	GM12878	blood:	n/a	n/a
17	BCLAF1	chr5:61870371-61870825	GM12878	blood:	n/a	n/a
18	BHLHE40	chr5:61872555-61872604	K562	blood:	n/a	n/a
19	BHLHE40	chr5:61834289-61834768	K562	blood:	n/a	n/a
20	BRCA1	chr5:61834474-61834740	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr5:61756334-61756594	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr5:61863976-61864361	K562	blood:	n/a	n/a
23	CBX3	chr5:61863983-61864320	K562	blood:	n/a	n/a
24	CBX3	chr5:61834280-61834852	K562	blood:	n/a	n/a
25	CCNT2	chr5:61881616-61881828	K562	blood:	n/a	n/a
26	CCNT2	chr5:61834507-61834787	K562	blood:	n/a	n/a
27	CCNT2	chr5:61876573-61876767	K562	blood:	n/a	n/a
28	CEBPB	chr5:61826186-61826369	HepG2	liver:	n/a	chr5:61826345-61826356 chr5:61826285-61826296 chr5:61826343-61826356
29	CEBPB	chr5:61789789-61789989	K562	blood:	n/a	n/a
30	CEBPB	chr5:61845071-61845358	A549	lung:	n/a	n/a
31	CEBPB	chr5:61834495-61834802	MCF-7	breast:	n/a	n/a
32	CEBPB	chr5:61834454-61834768	K562	blood:	n/a	n/a
33	CEBPB	chr5:61773649-61773972	K562	blood:	n/a	n/a
34	CEBPB	chr5:61838580-61838893	HepG2	liver:	n/a	chr5:61838755-61838764 chr5:61838673-61838686 chr5:61838754-61838765 chr5:61838753-61838764 chr5:61838673-61838686
35	CEBPB	chr5:61834346-61834856	A549	lung:	n/a	n/a
36	CEBPB	chr5:61824027-61824042	K562	blood:	n/a	n/a
37	CEBPB	chr5:61851767-61852130	HepG2	liver:	n/a	chr5:61851945-61851956
38	CEBPB	chr5:61834005-61834821	K562	blood:	n/a	n/a
39	CEBPB	chr5:61785474-61785537	K562	blood:	n/a	n/a
40	CEBPB	chr5:61773728-61773947	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr5:61851773-61852131	Hela-S3	cervix:	n/a	chr5:61851945-61851956
42	CEBPB	chr5:61845040-61845323	HepG2	liver:	n/a	n/a
43	CEBPB	chr5:61845040-61845363	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr5:61838622-61838854	A549	lung:	n/a	chr5:61838755-61838764 chr5:61838673-61838686 chr5:61838754-61838765 chr5:61838753-61838764 chr5:61838673-61838686
45	CEBPB	chr5:61785438-61785641	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr5:61834427-61834676	HepG2	liver:	n/a	n/a
47	CEBPB	chr5:61851780-61852127	IMR90	lung:	n/a	chr5:61851945-61851956
48	CEBPB	chr5:61861251-61861340	A549	lung:	n/a	chr5:61861263-61861274
49	CEBPB	chr5:61751201-61751660	HepG2	liver:	n/a	chr5:61751510-61751519 chr5:61751510-61751519 chr5:61751509-61751520
50	CEBPB	chr5:61770862-61771320	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:61844855-61844905	IMR90	lung:	fetal
2	chr5:61876634-61876684	HMEC	breast:	n/a
3	chr5:61818801-61818851	MCF10A-Er-Src	breast:	n/a
4	chr5:61818801-61818851	ECC-1	luminal epithelium:	n/a
5	chr5:61876634-61876684	NHBE	bronchial:	n/a
6	chr5:61876634-61876684	PrEC	prostate:	n/a
7	chr5:61818801-61818851	GM12878	blood:	n/a
8	chr5:61876634-61876684	NT2-D1	testis:	n/a
9	chr5:61874017-61874067	LNCaP	prostate:	n/a
10	chr5:61874017-61874067	HIPEpiC	eye:	n/a
11	chr5:61876634-61876684	AG09319	gingival:	n/a
12	chr5:61874017-61874067	SK-N-MC	brain:	n/a
13	chr5:61818801-61818851	PrEC	prostate:	n/a
14	chr5:61844855-61844905	SK-N-MC	brain:	n/a
15	chr5:61844855-61844905	H1-hESC	embryonic stem cell:	embryo
16	chr5:61874017-61874067	NH-A	brain:	n/a
17	chr5:61844855-61844905	NB4	blood:	n/a
18	chr5:61818801-61818851	SK-N-SH	brain:	n/a
19	chr5:61818801-61818851	ovcar-3	ovarian:	n/a
20	chr5:61876634-61876684	HUVEC	blood vessel:	n/a
21	chr5:61876634-61876684	HL-60	blood:	n/a
22	chr5:61876634-61876684	NHDF-neo	bronchial:	n/a
23	chr5:61876634-61876684	GM06990	blood:	n/a
24	chr5:61844855-61844905	ECC-1	luminal epithelium:	n/a
25	chr5:61876634-61876684	BE2_C	brain:	n/a
26	chr5:61876634-61876684	GM12892	blood:	n/a
27	chr5:61876634-61876684	HPAEpiC	pulmonary alveolar:	n/a
28	chr5:61876634-61876684	U87	brain:	n/a
29	chr5:61876634-61876684	K562	blood:	n/a
30	chr5:61876634-61876684	SK-N-SH	brain:	n/a
31	chr5:61874017-61874067	U87	brain:	n/a
32	chr5:61876634-61876684	IMR90	lung:	fetal
33	chr5:61844855-61844905	HRPEpiC	eye:	n/a
34	chr5:61874017-61874067	BE2_C	brain:	n/a
35	chr5:61874017-61874067	A549	lung:	n/a
36	chr5:61818801-61818851	HNPCEpiC	eye:	n/a
37	chr5:61876634-61876684	AG10803	skin:	n/a
38	chr5:61818801-61818851	ProgFib	skin:	n/a
39	chr5:61818801-61818851	AG10803	skin:	n/a
40	chr5:61844855-61844905	GM06990	blood:	n/a
41	chr5:61818801-61818851	NH-A	brain:	n/a
42	chr5:61818801-61818851	BE2_C	brain:	n/a
43	chr5:61874017-61874067	AG04450	lung:	fetal
44	chr5:61844855-61844905	GM12878	blood:	n/a
45	chr5:61818801-61818851	HL-60	blood:	n/a
46	chr5:61818801-61818851	GM12891	blood:	n/a
47	chr5:61874017-61874067	Hepatocyte	liver:	n/a
48	chr5:61844855-61844905	SK-N-SH	brain:	n/a
49	chr5:61874017-61874067	GM19239	blood:	n/a
50	chr5:61844855-61844905	HepG2	liver:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:61826046..61828158-chr5:61830735..61833492,2	K562	blood:
2	chr5:61881015..61883459-chr5:61884759..61886658,3	K562	blood:
3	chr5:61822169..61825461-chr5:61826034..61828796,3	K562	blood:
4	chr5:61865017..61866532-chr5:61879181..61880802,2	K562	blood:
5	chr5:61756416..61757318-chr5:62074341..62075268,4	K562	blood:
6	chr5:61875507..61877206-chr5:61878546..61880725,2	K562	blood:
7	chr5:61781558..61784548-chr5:61790648..61794410,3	K562	blood:
8	chr5:61829519..61831113-chr5:61834353..61836301,2	MCF-7	breast:
9	chr5:61833675..61836577-chr5:61862911..61865153,3	K562	blood:
10	chr5:61747217..61749290-chr5:61754763..61757506,2	K562	blood:
11	chr5:61753206..61755091-chr5:61766346..61768093,2	MCF-7	breast:
12	chr5:61833675..61836577-chr5:61862911..61865153,3	K562	blood:
13	chr5:61827589..61829469-chr5:61829575..61831772,2	MCF-7	breast:
14	chr5:61767541..61769044-chr5:62072655..62075082,2	MCF-7	breast:
15	chr5:61793500..61795640-chr5:61797559..61799676,2	K562	blood:
16	chr5:61833268..61834812-chr5:61850872..61852954,2	K562	blood:
17	chr5:61820977..61823095-chr5:61832322..61835003,2	MCF-7	breast:
18	chr5:61513831..61515618-chr5:61821739..61824122,2	K562	blood:
19	chr5:61782970..61785454-chr5:61790224..61793065,2	K562	blood:
20	chr5:61730501..61733292-chr5:61772580..61775158,2	K562	blood:
21	chr5:61826046..61828158-chr5:61830735..61833492,2	K562	blood:
22	chr5:61882277..61887456-chr5:61887734..61891517,4	K562	blood:
23	chr5:61772217..61774196-chr5:61781194..61783059,2	MCF-7	breast:
24	chr5:61821283..61823218-chr5:61824428..61826675,2	MCF-7	breast:
25	chr5:61829519..61831113-chr5:61834353..61836301,2	MCF-7	breast:
26	chr5:61782970..61785454-chr5:61790224..61793065,2	K562	blood:
27	chr5:61865017..61866532-chr5:61879181..61880802,2	K562	blood:
28	chr5:61833161..61835046-chr5:61842892..61845396,3	K562	blood:
29	chr5:61833161..61835046-chr5:61842892..61845396,3	K562	blood:
30	chr5:61820977..61823095-chr5:61832322..61835003,2	MCF-7	breast:
31	chr5:61875507..61877206-chr5:61878546..61880725,2	K562	blood:
32	chr5:61795098..61797739-chr5:61799881..61802106,2	K562	blood:
33	chr5:61770750..61773318-chr5:61799934..61802910,2	K562	blood:
34	chr5:61833268..61834812-chr5:61850872..61852954,2	K562	blood:
35	chr5:61875725..61878816-chr5:61880010..61882591,3	MCF-7	breast:
36	chr5:61779738..61781733-chr5:61782229..61785139,2	MCF-7	breast:
37	chr5:61766130..61769204-chr5:61785246..61788034,3	K562	blood:
38	chr5:61827589..61829469-chr5:61829575..61831772,2	MCF-7	breast:
39	chr5:61770750..61773318-chr5:61799934..61802910,2	K562	blood:
40	chr5:61781558..61784548-chr5:61790648..61794410,3	K562	blood:
41	chr5:61762888..61765015-chr5:61768126..61770339,2	K562	blood:
42	chr5:61875725..61878816-chr5:61880010..61882591,3	MCF-7	breast:
43	chr5:61821283..61823218-chr5:61824428..61826675,2	MCF-7	breast:
44	chr5:61779738..61781733-chr5:61782229..61785139,2	MCF-7	breast:
45	chr5:61766130..61769204-chr5:61785246..61788034,3	K562	blood:
46	chr5:61795098..61797739-chr5:61799881..61802106,2	K562	blood:
47	chr5:61753206..61755091-chr5:61766346..61768093,2	MCF-7	breast:
48	chr5:61878602..61881292-chr5:61887209..61889538,2	K562	blood:
49	chr5:61756074..61756595-chr5:61927958..61928492,2	MCF-7	breast:
50	chr5:61822169..61825461-chr5:61826034..61828796,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC70-1	chr5:61856963-61857084	NONHSAT101713
2	lnc-LRRC70-1	chr5:61876281-61877269	NONHSAT101716
3	lnc-LRRC70-1	chr5:61874664-61874762	NONHSAT101716
4	lnc-LRRC70-1	chr5:61875228-61875310	NONHSAT101716
5	lnc-DIMT1-1	chr5:61857686-61858043	NONHSAT101714
6	lnc-LRRC70-1	chr5:61856523-61856832	NONHSAT101713
7	lnc-DIMT1-2	chr5:61871778-61872098	NONHSAT101715

No data

Variant related genes	Relation type
ENSG00000241991	TF binding region
LRRC70	TF binding region
ENSG00000240436	TF binding region
ENSG00000268942	TF binding region
IPO11	TF binding region
ENSG00000241991	CpG island
LRRC70	CpG island
ENSG00000240436	CpG island
ENSG00000268942	CpG island
IPO11	CpG island
ENSG00000217416	chromatin interactions
ENSG00000086200	chromatin interactions

Extended variants
information (count: 5076 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:5076 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs247230	chr5:61750667-61750668	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529518764	chr5:61750678-61750679	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555800508	chr5:61750716-61750717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs173522	chr5:61750731-61750732	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs538272787	chr5:61750739-61750740	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557846327	chr5:61750832-61750833	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs372244947	chr5:61750842-61750843	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115813564	chr5:61750860-61750861	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs140083439	chr5:61750892-61750893	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs371992851	chr5:61751087-61751088	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559134240	chr5:61751089-61751090	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572656842	chr5:61751091-61751092	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs142312377	chr5:61751106-61751107	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546165635	chr5:61751113-61751114	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs112656085	chr5:61751166-61751167	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549519640	chr5:61751172-61751173	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs550595340	chr5:61751180-61751181	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564058356	chr5:61751192-61751193	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553858815	chr5:61751219-61751220	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533677048	chr5:61751281-61751282	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547267320	chr5:61751287-61751288	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567090925	chr5:61751290-61751291	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536011913	chr5:61751307-61751308	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs368589240	chr5:61751323-61751324	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140461899	chr5:61751340-61751341	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs150398684	chr5:61751365-61751366	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs34082638	chr5:61751402-61751403	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs115399926	chr5:61751405-61751406	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs147861275	chr5:61751471-61751472	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs571269399	chr5:61751514-61751515	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539354236	chr5:61751515-61751516	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs372911717	chr5:61751520-61751521	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs552822258	chr5:61751532-61751533	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs564657280	chr5:61751545-61751546	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs145494846	chr5:61751597-61751598	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572717709	chr5:61751606-61751607	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs531858477	chr5:61751609-61751610	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs141435899	chr5:61751631-61751632	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs555266452	chr5:61751700-61751701	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs575335367	chr5:61751705-61751706	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs549976306	chr5:61751733-61751734	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543929130	chr5:61751738-61751739	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs564074326	chr5:61751744-61751745	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs539584824	chr5:61751748-61751749	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs112336211	chr5:61751774-61751775	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs146984909	chr5:61751807-61751808	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs528956379	chr5:61751832-61751833	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs551124848	chr5:61751860-61751861	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs114558843	chr5:61751865-61751866	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs187556244	chr5:61751918-61751919	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2192 , 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	chr5:61709400-61763400	Weak transcription	Aorta	Aorta
3	chr5:61709800-61769000	Weak transcription	NH-A	brain
4	chr5:61709800-61809200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr5:61722800-61770600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr5:61728200-61752800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr5:61728400-61752800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr5:61728400-61763400	Weak transcription	Pancreas	Pancrea
9	chr5:61728400-61807600	Weak transcription	Psoas Muscle	Psoas
10	chr5:61728800-61763000	Weak transcription	Fetal Brain Female	brain
11	chr5:61728800-61838200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr5:61729600-61752800	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr5:61730000-61834200	Weak transcription	Gastric	stomach
14	chr5:61731800-61764000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr5:61732200-61753200	Weak transcription	NHLF	lung
16	chr5:61732800-61805200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr5:61733200-61756800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr5:61733600-61763000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr5:61738800-61763000	Weak transcription	Stomach Smooth Muscle	stomach
20	chr5:61739200-61763000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr5:61739200-61763400	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr5:61739200-61862800	Weak transcription	Brain Substantia Nigra	brain
23	chr5:61739600-61787800	Weak transcription	Brain Cingulate Gyrus	brain
24	chr5:61739800-61752600	Weak transcription	NHEK	skin
25	chr5:61739800-61752800	Weak transcription	HMEC	breast
26	chr5:61741600-61751200	Strong transcription	Primary B cells from peripheral blood	blood
27	chr5:61741600-61753400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr5:61742000-61751200	Weak transcription	Colon Smooth Muscle	Colon
29	chr5:61742200-61754400	Weak transcription	Stomach Mucosa	stomach
30	chr5:61743000-61752800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr5:61743000-61763400	Weak transcription	Brain Angular Gyrus	brain
32	chr5:61743600-61753400	Strong transcription	Primary T helper cells fromperipheralblood	blood
33	chr5:61743800-61750800	Weak transcription	Rectal Smooth Muscle	rectum
34	chr5:61744000-61751000	Strong transcription	HUES64 Cell Line	embryonic stem cell
35	chr5:61744000-61752600	Strong transcription	Primary T helper cells PMA-I stimulated	--
36	chr5:61744600-61752800	Weak transcription	Brain Germinal Matrix	brain
37	chr5:61744600-61764000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr5:61744800-61838600	Weak transcription	Colonic Mucosa	Colon
39	chr5:61745000-61751000	Strong transcription	Monocytes-CD14+_RO01746	blood
40	chr5:61745600-61751200	Strong transcription	Primary monocytes fromperipheralblood	blood
41	chr5:61745600-61753600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr5:61746000-61751000	Strong transcription	A549	lung
43	chr5:61746000-61751400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
44	chr5:61746000-61751600	Strong transcription	Primary B cells from cord blood	blood
45	chr5:61746000-61753400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
46	chr5:61746000-61755000	Strong transcription	Dnd41	blood
47	chr5:61746200-61783600	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr5:61747200-61754800	Strong transcription	Primary T cells from cord blood	blood
49	chr5:61747400-61753000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr5:61747800-61752800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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