Variant report

Variant	esv2755799
Chromosome Location	chr5:177390271-177488246
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:496)
CpG islands
(count:3053)
Chromatin interactive
region (count:17)
LncRNA
region (count:61)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:496 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:177397729-177397797	K562	blood:	n/a	n/a
2	ATF1	chr5:177488127-177488326	K562	blood:	n/a	n/a
3	BCL3	chr5:177407457-177407839	GM12878	blood:	n/a	n/a
4	BHLHE40	chr5:177473936-177474136	K562	blood:	n/a	n/a
5	BHLHE40	chr5:177424317-177424636	K562	blood:	n/a	n/a
6	BHLHE40	chr5:177473797-177474152	GM12878	blood:	n/a	n/a
7	BHLHE40	chr5:177409159-177409407	K562	blood:	n/a	n/a
8	BRCA1	chr5:177409151-177409466	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr5:177411778-177411808	H1-hESC	embryonic stem cell:	n/a	n/a
10	CBX3	chr5:177433880-177434330	K562	blood:	n/a	n/a
11	CBX3	chr5:177405853-177406665	K562	blood:	n/a	n/a
12	CBX3	chr5:177433930-177434263	K562	blood:	n/a	n/a
13	CEBPB	chr5:177423981-177424258	K562	blood:	n/a	chr5:177424111-177424122
14	CEBPB	chr5:177423938-177424282	H1-hESC	embryonic stem cell:	n/a	chr5:177424111-177424122
15	CEBPB	chr5:177430455-177430566	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr5:177423958-177424279	A549	lung:	n/a	chr5:177424111-177424122
17	CEBPB	chr5:177416951-177417052	K562	blood:	n/a	chr5:177417022-177417035 chr5:177417024-177417033
18	CEBPB	chr5:177426281-177426497	A549	lung:	n/a	chr5:177426363-177426374
19	CEBPB	chr5:177484353-177484391	HepG2	liver:	n/a	chr5:177484379-177484390
20	CEBPB	chr5:177426206-177426505	HepG2	liver:	n/a	chr5:177426363-177426374
21	CEBPB	chr5:177439336-177439525	Hela-S3	cervix:	n/a	chr5:177439419-177439432
22	CEBPB	chr5:177423969-177424295	Hela-S3	cervix:	n/a	chr5:177424111-177424122
23	CEBPB	chr5:177423948-177424287	IMR90	lung:	n/a	chr5:177424111-177424122
24	CEBPB	chr5:177423950-177424288	HepG2	liver:	n/a	chr5:177424111-177424122
25	CHD2	chr5:177409126-177409376	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr5:177473878-177474201	GM12878	blood:	n/a	n/a
27	CTCF	chr5:177409180-177409330	K562	blood:	n/a	chr5:177409269-177409282
28	CTCF	chr5:177409200-177409350	AoAF	blood vessel:	n/a	chr5:177409269-177409282
29	CTCF	chr5:177409084-177409480	A549	lung:	n/a	chr5:177409269-177409282
30	CTCF	chr5:177409180-177409330	NHEK	skin:	n/a	chr5:177409269-177409282
31	CTCF	chr5:177409160-177409310	HFF	foreskin:	n/a	chr5:177409269-177409282
32	CTCF	chr5:177441118-177441159	GM10248	blood:	n/a	n/a
33	CTCF	chr5:177421819-177421865	NHEK	skin:	n/a	n/a
34	CTCF	chr5:177409220-177409370	GM12870	blood:	n/a	chr5:177409269-177409282
35	CTCF	chr5:177409091-177409441	GM12878	blood:	n/a	chr5:177409269-177409282
36	CTCF	chr5:177409169-177409356	GM12892	blood:	n/a	chr5:177409269-177409282
37	CTCF	chr5:177409200-177409302	HUVEC	blood vessel:	n/a	chr5:177409269-177409282
38	CTCF	chr5:177409020-177409522	SK-N-SH	brain:	n/a	chr5:177409269-177409282
39	CTCF	chr5:177409220-177409510	BE2_C	brain:	n/a	chr5:177409269-177409282
40	CTCF	chr5:177409137-177409306	A549	lung:	n/a	chr5:177409269-177409282
41	CTCF	chr5:177409180-177409330	GM12864	blood:	n/a	chr5:177409269-177409282
42	CTCF	chr5:177409140-177409290	GM12866	blood:	n/a	chr5:177409269-177409282
43	CTCF	chr5:177409180-177409330	HCFaa	heart:	n/a	chr5:177409269-177409282
44	CTCF	chr5:177409160-177409310	GM12868	blood:	n/a	chr5:177409269-177409282
45	CTCF	chr5:177409200-177409350	NB4	blood:	n/a	chr5:177409269-177409282
46	CTCF	chr5:177407470-177407507	NHEK	skin:	n/a	n/a
47	CTCF	chr5:177409222-177409292	GM13976	blood:	n/a	chr5:177409269-177409282
48	CTCF	chr5:177407340-177407490	SAEC	small airway:	n/a	n/a
49	CTCF	chr5:177412879-177412887	NHEK	skin:	n/a	n/a
50	CTCF	chr5:177409108-177409357	HepG2	liver:	n/a	chr5:177409269-177409282

(count:3053 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:177423598-177423648	AG09319	gingival:	n/a
2	chr5:177396838-177396888	PrEC	prostate:	n/a
3	chr5:177436178-177436228	HMEC	breast:	n/a
4	chr5:177423598-177423648	AG09319	gingival:	n/a
5	chr5:177396838-177396888	PrEC	prostate:	n/a
6	chr5:177436178-177436228	HMEC	breast:	n/a
7	chr5:177409334-177409384	AG09319	gingival:	n/a
8	chr5:177391178-177391228	AoSMC	blood vessel:	n/a
9	chr5:177410766-177410816	HUVEC	blood vessel:	n/a
10	chr5:177482771-177482821	SK-N-MC	brain:	n/a
11	chr5:177411733-177411783	CMK	blood:	n/a
12	chr5:177481396-177481446	NT2-D1	testis:	n/a
13	chr5:177399722-177399772	MCF-7	breast:	n/a
14	chr5:177424291-177424341	AoSMC	blood vessel:	n/a
15	chr5:177474496-177474546	HEK293	kidney:	embryo
16	chr5:177399722-177399772	ECC-1	luminal epithelium:	n/a
17	chr5:177432811-177432861	BJ	skin:	n/a
18	chr5:177412636-177412686	AG04449	skin:	fetal
19	chr5:177471165-177471215	AG10803	skin:	n/a
20	chr5:177432923-177432973	BE2_C	brain:	n/a
21	chr5:177391178-177391228	GM12878	blood:	n/a
22	chr5:177423311-177423361	ovcar-3	ovarian:	n/a
23	chr5:177431038-177431088	NH-A	brain:	n/a
24	chr5:177432811-177432861	NHBE	bronchial:	n/a
25	chr5:177409992-177410042	Hela-S3	cervix:	n/a
26	chr5:177436178-177436228	U87	brain:	n/a
27	chr5:177481396-177481446	CMK	blood:	n/a
28	chr5:177413557-177413607	HAEpiC	amniotic membrane:	n/a
29	chr5:177395755-177395805	IMR90	lung:	fetal
30	chr5:177432923-177432973	GM06990	blood:	n/a
31	chr5:177434438-177434488	AG09309	skin:	n/a
32	chr5:177474496-177474546	ECC-1	luminal epithelium:	n/a
33	chr5:177434336-177434386	GM06990	blood:	n/a
34	chr5:177413021-177413071	AG09319	gingival:	n/a
35	chr5:177396838-177396888	HCM	heart:	n/a
36	chr5:177481396-177481446	GM12878	blood:	n/a
37	chr5:177486005-177486055	NHBE	bronchial:	n/a
38	chr5:177411528-177411578	PFSK-1	brain:	n/a
39	chr5:177431038-177431088	GM12891	blood:	n/a
40	chr5:177399722-177399772	SKMC	muscle:	n/a
41	chr5:177423379-177423429	Caco-2	colon:	n/a
42	chr5:177423236-177423286	Caco-2	colon:	n/a
43	chr5:177424343-177424393	GM12891	blood:	n/a
44	chr5:177484324-177484374	GM12892	blood:	n/a
45	chr5:177482458-177482508	LNCaP	prostate:	n/a
46	chr5:177412586-177412636	HRCEpiC	kidney:	n/a
47	chr5:177432811-177432861	HIPEpiC	eye:	n/a
48	chr5:177423598-177423648	HepG2	liver:	n/a
49	chr5:177424291-177424341	T-47D	breast:	n/a
50	chr5:177411733-177411783	AG04449	skin:	fetal

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:177484844..177487302-chr5:177630950..177633253,2	MCF-7	breast:
2	chr5:177487426..177490684-chr5:177499870..177503540,6	MCF-7	breast:
3	chr5:177408911..177409847-chr5:177488224..177489587,7	MCF-7	breast:
4	chr5:177415478..177418787-chr5:177421385..177423708,4	MCF-7	breast:
5	chr5:177389362..177391423-chr5:177551819..177554278,2	MCF-7	breast:
6	chr5:177410800..177413779-chr5:177425270..177427060,2	MCF-7	breast:
7	chr5:177407733..177409330-chr5:177502018..177504540,2	MCF-7	breast:
8	chr5:177419524..177421391-chr5:177640388..177643109,2	K562	blood:
9	chr5:177406767..177409491-chr5:177412491..177414638,2	MCF-7	breast:
10	chr5:177487397..177490398-chr5:177500448..177504603,3	MCF-7	breast:
11	chr5:177487221..177488985-chr5:177489286..177490868,2	MCF-7	breast:
12	chr5:177399899..177402240-chr5:177658876..177660987,2	K562	blood:
13	chr5:177408911..177409847-chr5:177488224..177489587,7	MCF-7	breast:
14	chr5:177484315..177487121-chr5:177489310..177491677,2	MCF-7	breast:
15	chr5:177410800..177413779-chr5:177425270..177427060,2	MCF-7	breast:
16	chr5:177409168..177409692-chr5:177488717..177489218,2	K562	blood:
17	chr5:177406767..177409491-chr5:177412491..177414638,2	MCF-7	breast:

(count:61 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM153C-1	chr5:177468694-177468764	NR_038353
2	lnc-FAM153C-1	chr5:177476298-177476322	NONHSAT105506
3	lnc-FAM153C-1	chr5:177473873-177473940	NR_038353
4	lnc-FAM153C-1	chr5:177479557-177479688	NONHSAT147373
5	lnc-FAM153C-1	chr5:177480841-177480974	NONHSAT105509
6	lnc-FAM153C-1	chr5:177480841-177480974	NONHSAT105504
7	lnc-FAM153C-1	chr5:177465839-177465918	NR_038353
8	lnc-FAM153C-1	chr5:177481739-177481780	NONHSAT105509
9	lnc-FAM153C-1	chr5:177479420-177479688	NONHSAT105509
10	lnc-FAM153C-1	chr5:177474029-177474134	NR_038353
11	lnc-PROP1-1	chr5:177446441-177446907	ENSG00000255684
12	lnc-FAM153C-1	chr5:177484650-177484770	NONHSAT105504
13	lnc-FAM153C-1	chr5:177475666-177476088	NR_038353
14	lnc-PROP1-1	chr5:177433441-177433466	ENSG00000255684
15	lnc-FAM153C-1	chr5:177476289-177476322	NONHSAT105505
16	lnc-FAM153C-1	chr5:177480841-177480974	NONHSAT105503
17	lnc-FAM153C-1	chr5:177463013-177463037	NR_038353
18	lnc-PROP1-3	chr5:177479808-177479818	XLOC_005101
19	lnc-FAM153C-1	chr5:177466388-177466412	NR_038353
20	lnc-FAM153C-1	chr5:177485553-177486069	NONHSAT105513
21	lnc-FAM153C-1	chr5:177479627-177479688	NONHSAT105510
22	lnc-FAM153C-1	chr5:177481739-177481799	NONHSAT147373
23	lnc-FAM153C-1	chr5:177473415-177473452	NR_038353
24	lnc-FAM153C-1	chr5:177475777-177476322	NONHSAT105503
25	lnc-FAM153C-1	chr5:177476416-177476911	NONHSAT105507
26	lnc-FAM153C-1	chr5:177485726-177485981	XLOC_004671
27	lnc-FAM153C-1	chr5:177436327-177436382	NONHSAT105499
28	lnc-FAM153C-1	chr5:177482370-177482560	NONHSAT105510
29	lnc-FAM153C-1	chr5:177479534-177479688	NONHSAT105503
30	lnc-FAM153C-1	chr5:177476266-177476322	NONHSAT105504
31	lnc-FAM153C-1	chr5:177481717-177481808	NONHSAT105511
32	lnc-FAM153C-1	chr5:177479534-177479688	NONHSAT105505
33	lnc-FAM153C-1	chr5:177480841-177480974	NONHSAT105507
34	lnc-FAM153C-1	chr5:177482370-177482560	NONHSAT105511
35	lnc-FAM153C-7	chr5:177425135-177425904	NONHSAT105495
36	lnc-FAM153C-1	chr5:177436327-177436382	NONHSAT105500
37	lnc-FAM153C-7	chr5:177426025-177426828	NONHSAT105495
38	lnc-FAM153C-1	chr5:177480841-177480974	NONHSAT105505
39	lnc-FAM153C-1	chr5:177481059-177481134	NONHSAT105503
40	lnc-FAM153C-1	chr5:177480873-177480974	NONHSAT105511
41	lnc-FAM153C-1	chr5:177433991-177434061	NONHSAT105499
42	lnc-FAM153C-1	chr5:177435154-177435253	NONHSAT105500
43	lnc-FAM153C-1	chr5:177433967-177434061	NR_038353
44	lnc-FAM153C-1	chr5:177469196-177469226	NR_038353
45	lnc-FAM153C-1	chr5:177479804-177479990	NONHSAT105503
46	lnc-FAM153C-1	chr5:177481739-177481808	NONHSAT105510
47	lnc-FAM153C-1	chr5:177480841-177480974	NONHSAT147373
48	lnc-FAM153C-1	chr5:177480841-177480974	NONHSAT105510
49	lnc-FAM153C-1	chr5:177480841-177480974	NONHSAT105506
50	lnc-FAM153C-1	chr5:177479804-177479990	NONHSAT105509

No data

Variant related genes	Relation type
PROP1	TF binding region
FAM153C	TF binding region
SUDS3P1	TF binding region
ENSG00000218227	TF binding region
PROP1	CpG island
FAM153C	CpG island
SUDS3P1	CpG island
ENSG00000218227	CpG island
ENSG00000175309	chromatin interactions
ENSG00000175325	chromatin interactions
ENSG00000197451	chromatin interactions

Extended variants
information (count: 2422 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:2422 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4580789	chr5:177390271-177390272	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs117243247	chr5:177390300-177390301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs543877540	chr5:177390337-177390338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs201497841	chr5:177390340-177390341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562072880	chr5:177390352-177390353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555206880	chr5:177390380-177390381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529254105	chr5:177390409-177390410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536873993	chr5:177390414-177390415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547931765	chr5:177390415-177390416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559579841	chr5:177390444-177390445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557403283	chr5:177390479-177390480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181478704	chr5:177390481-177390482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6601190	chr5:177390482-177390483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369231687	chr5:177390495-177390496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs186116198	chr5:177390507-177390508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537358465	chr5:177390508-177390509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549220201	chr5:177390511-177390512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190239188	chr5:177390527-177390528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs6874403	chr5:177390533-177390534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs373481333	chr5:177390555-177390556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537013823	chr5:177390597-177390598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577642618	chr5:177390599-177390600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553448706	chr5:177390607-177390608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112705628	chr5:177390625-177390626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs147781642	chr5:177390629-177390630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575467808	chr5:177390633-177390634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182822762	chr5:177390647-177390648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573277326	chr5:177390661-177390662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542943829	chr5:177390671-177390672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561136062	chr5:177390672-177390673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545674892	chr5:177390673-177390674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541418104	chr5:177390674-177390675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs6601191	chr5:177390678-177390679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187550808	chr5:177390690-177390691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531105213	chr5:177390720-177390721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78693149	chr5:177390724-177390725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs377696329	chr5:177390749-177390750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73807316	chr5:177390777-177390778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563735060	chr5:177390803-177390804	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530982601	chr5:177390813-177390814	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148477325	chr5:177390853-177390854	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs373233410	chr5:177390865-177390866	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs567604793	chr5:177390874-177390875	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs114104337	chr5:177390880-177390881	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs546274967	chr5:177390882-177390883	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs557860923	chr5:177390888-177390889	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs529027545	chr5:177390900-177390901	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs142718545	chr5:177390907-177390908	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs538363970	chr5:177390914-177390915	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs151015676	chr5:177390937-177390938	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
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
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	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
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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:404 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177368200-177396400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr5:177371000-177393000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr5:177371800-177390800	Weak transcription	Ovary	ovary
4	chr5:177371800-177392800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr5:177371800-177394200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr5:177371800-177394200	Weak transcription	Right Ventricle	heart
7	chr5:177379200-177392400	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr5:177383800-177393600	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr5:177386400-177393600	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr5:177386400-177394400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr5:177386600-177395600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr5:177386800-177395800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr5:177388400-177391200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr5:177388400-177397400	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr5:177388400-177411400	Weak transcription	Gastric	stomach
16	chr5:177388600-177393200	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr5:177388800-177390800	Weak transcription	Esophagus	oesophagus
18	chr5:177390200-177390800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr5:177390800-177391000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr5:177390800-177391600	Strong transcription	Esophagus	oesophagus
21	chr5:177391000-177391200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr5:177391000-177391600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
23	chr5:177391200-177391800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr5:177391200-177402400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr5:177391600-177392000	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr5:177391600-177393200	Weak transcription	Esophagus	oesophagus
27	chr5:177391800-177395600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr5:177393000-177393200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr5:177393000-177394200	Enhancers	Fetal Brain Male	brain
30	chr5:177393200-177393400	Enhancers	Esophagus	oesophagus
31	chr5:177393200-177393800	Enhancers	Pancreas	Pancrea
32	chr5:177393600-177395200	Enhancers	HUVEC	blood vessel
33	chr5:177393800-177394800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr5:177394000-177394800	Enhancers	NHEK	skin
35	chr5:177394200-177394600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr5:177394200-177394800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr5:177394600-177394800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr5:177395600-177396000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr5:177395600-177396000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
40	chr5:177395600-177396200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr5:177395800-177396000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr5:177396200-177397800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr5:177397400-177398600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
44	chr5:177397800-177398400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr5:177398000-177398200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr5:177398000-177398600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr5:177398200-177398600	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
48	chr5:177398200-177398600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr5:177398200-177398600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr5:177398400-177407200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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