Variant report

Variant	nsv998511
Chromosome Location	chr4:76184807-76398377
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:76357925-76358217	K562	blood:	n/a	n/a
2	ATF1	chr4:76294711-76294852	K562	blood:	n/a	n/a
3	BACH1	chr4:76282966-76282978	K562	blood:	n/a	n/a
4	BCL3	chr4:76215762-76216089	GM12878	blood:	n/a	n/a
5	BCLAF1	chr4:76214975-76215350	GM12878	blood:	n/a	chr4:76215329-76215338
6	CEBPB	chr4:76379920-76380120	IMR90	lung:	n/a	n/a
7	CEBPB	chr4:76395124-76395494	IMR90	lung:	n/a	chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395301-76395314
8	CEBPB	chr4:76395099-76395509	A549	lung:	n/a	chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395301-76395314
9	CEBPB	chr4:76395203-76395510	MCF-7	breast:	n/a	chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395301-76395314
10	CEBPB	chr4:76321118-76321291	K562	blood:	n/a	chr4:76321162-76321173 chr4:76321164-76321173 chr4:76321163-76321174
11	CEBPB	chr4:76395126-76395486	K562	blood:	n/a	chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395301-76395314
12	CEBPB	chr4:76395143-76395496	HepG2	liver:	n/a	chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395301-76395314
13	CEBPB	chr4:76379752-76380285	MCF-7	breast:	n/a	chr4:76379852-76379863 chr4:76379850-76379863
14	CEBPB	chr4:76357985-76358149	K562	blood:	n/a	n/a
15	CEBPB	chr4:76395141-76395487	A549	lung:	n/a	chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395301-76395314
16	CEBPB	chr4:76321013-76321304	HepG2	liver:	n/a	chr4:76321162-76321173 chr4:76321164-76321173 chr4:76321163-76321174
17	CEBPB	chr4:76374340-76374490	H1-hESC	embryonic stem cell:	n/a	chr4:76374365-76374376
18	CEBPB	chr4:76264522-76264645	HepG2	liver:	n/a	chr4:76264549-76264560
19	CEBPB	chr4:76321079-76321193	A549	lung:	n/a	chr4:76321162-76321173 chr4:76321164-76321173 chr4:76321163-76321174
20	CEBPB	chr4:76395106-76395523	A549	lung:	n/a	chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395301-76395314
21	CEBPB	chr4:76395137-76395498	Hela-S3	cervix:	n/a	chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395301-76395314
22	CEBPB	chr4:76339348-76339649	HepG2	liver:	n/a	chr4:76339500-76339513 chr4:76339500-76339511 chr4:76339500-76339513 chr4:76339502-76339513
23	CEBPB	chr4:76395146-76395487	ECC-1	luminal epithelium:	n/a	chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395301-76395314
24	CEBPB	chr4:76395123-76395535	ECC-1	luminal epithelium:	n/a	chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395301-76395314
25	CEBPB	chr4:76374262-76374511	HepG2	liver:	n/a	chr4:76374365-76374376
26	CEBPB	chr4:76319796-76319943	K562	blood:	n/a	n/a
27	CEBPB	chr4:76395148-76395541	MCF-7	breast:	n/a	chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395301-76395314
28	CEBPB	chr4:76395141-76395464	H1-hESC	embryonic stem cell:	n/a	chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395301-76395314
29	CEBPB	chr4:76339442-76339558	K562	blood:	n/a	chr4:76339500-76339513 chr4:76339500-76339511 chr4:76339500-76339513 chr4:76339502-76339513
30	CEBPB	chr4:76319825-76319934	IMR90	lung:	n/a	n/a
31	CEBPB	chr4:76395231-76395353	HepG2	liver:	n/a	chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395303-76395312 chr4:76395301-76395314
32	CEBPB	chr4:76321097-76321297	IMR90	lung:	n/a	chr4:76321162-76321173 chr4:76321164-76321173 chr4:76321163-76321174
33	CTCF	chr4:76215160-76215310	HCT-116	colon:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
34	CTCF	chr4:76353040-76353190	BE2_C	brain:	n/a	n/a
35	CTCF	chr4:76358060-76358210	GM12864	blood:	n/a	n/a
36	CTCF	chr4:76215140-76215290	A549	lung:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
37	CTCF	chr4:76358000-76358150	GM06990	blood:	n/a	n/a
38	CTCF	chr4:76394021-76394327	GM12878	blood:	n/a	chr4:76394177-76394195 chr4:76394172-76394193
39	CTCF	chr4:76394152-76394264	A549	lung:	n/a	chr4:76394177-76394195 chr4:76394172-76394193
40	CTCF	chr4:76394100-76394250	Caco-2	colon:	n/a	chr4:76394177-76394195 chr4:76394172-76394193
41	CTCF	chr4:76358060-76358210	GM12868	blood:	n/a	n/a
42	CTCF	chr4:76215100-76215250	GM06990	blood:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
43	CTCF	chr4:76215100-76215250	BJ	skin:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
44	CTCF	chr4:76358018-76358177	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr4:76357980-76358130	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr4:76358000-76358191	GM19238	blood:	n/a	n/a
47	CTCF	chr4:76358020-76358170	HMF	breast:	n/a	n/a
48	CTCF	chr4:76397740-76397890	GM12872	blood:	n/a	n/a
49	CTCF	chr4:76215060-76215210	HCT-116	colon:	n/a	chr4:76215189-76215210 chr4:76215196-76215209
50	CTCF	chr4:76358020-76358170	AoAF	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:76201532-76201582	HCPEpiC	choroid plexus:	n/a
2	chr4:76317967-76318017	ProgFib	skin:	n/a
3	chr4:76201532-76201582	HCPEpiC	choroid plexus:	n/a
4	chr4:76317967-76318017	ProgFib	skin:	n/a
5	chr4:76317967-76318017	MCF10A-Er-Src	breast:	n/a
6	chr4:76264560-76264610	Caco-2	colon:	n/a
7	chr4:76373607-76373657	HRE	kidney:	n/a
8	chr4:76201532-76201582	SK-N-SH	brain:	n/a
9	chr4:76317967-76318017	AoSMC	blood vessel:	n/a
10	chr4:76201532-76201582	HPAEpiC	pulmonary alveolar:	n/a
11	chr4:76317967-76318017	Hepatocyte	liver:	n/a
12	chr4:76201532-76201582	A549	lung:	n/a
13	chr4:76264560-76264610	HAEpiC	amniotic membrane:	n/a
14	chr4:76373607-76373657	AG09309	skin:	n/a
15	chr4:76373607-76373657	Hela-S3	cervix:	n/a
16	chr4:76373607-76373657	ECC-1	luminal epithelium:	n/a
17	chr4:76373607-76373657	NHBE	bronchial:	n/a
18	chr4:76264560-76264610	SK-N-MC	brain:	n/a
19	chr4:76317967-76318017	HIPEpiC	eye:	n/a
20	chr4:76201532-76201582	AG10803	skin:	n/a
21	chr4:76201532-76201582	Jurkat	blood:	n/a
22	chr4:76264560-76264610	ovcar-3	ovarian:	n/a
23	chr4:76317967-76318017	HNPCEpiC	eye:	n/a
24	chr4:76264560-76264610	GM12891	blood:	n/a
25	chr4:76373607-76373657	T-47D	breast:	n/a
26	chr4:76201532-76201582	ovcar-3	ovarian:	n/a
27	chr4:76201532-76201582	HRE	kidney:	n/a
28	chr4:76201532-76201582	AoSMC	blood vessel:	n/a
29	chr4:76201532-76201582	RPTEC	kidney:	n/a
30	chr4:76264560-76264610	HepG2	liver:	n/a
31	chr4:76201532-76201582	BE2_C	brain:	n/a
32	chr4:76264560-76264610	GM19239	blood:	n/a
33	chr4:76317967-76318017	IMR90	lung:	fetal
34	chr4:76264560-76264610	Jurkat	blood:	n/a
35	chr4:76201532-76201582	T-47D	breast:	n/a
36	chr4:76201532-76201582	HAEpiC	amniotic membrane:	n/a
37	chr4:76264560-76264610	HRPEpiC	eye:	n/a
38	chr4:76317967-76318017	PANC-1	pancreas:	n/a
39	chr4:76373607-76373657	RPTEC	kidney:	n/a
40	chr4:76317967-76318017	U87	brain:	n/a
41	chr4:76201532-76201582	PANC-1	pancreas:	n/a
42	chr4:76373607-76373657	HCT-116	colon:	n/a
43	chr4:76317967-76318017	HRCEpiC	kidney:	n/a
44	chr4:76201532-76201582	SK-N-MC	brain:	n/a
45	chr4:76373607-76373657	NHDF-neo	bronchial:	n/a
46	chr4:76373607-76373657	GM12878	blood:	n/a
47	chr4:76264560-76264610	U87	brain:	n/a
48	chr4:76317967-76318017	HAEpiC	amniotic membrane:	n/a
49	chr4:76317967-76318017	Jurkat	blood:	n/a
50	chr4:76317967-76318017	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr4:76277770..76280636-chr4:76287963..76290651,3	K562	blood:
2	chr4:76358069..76359586-chr4:76396767..76398904,2	K562	blood:
3	chr4:76349656..76352296-chr4:76353820..76356620,3	K562	blood:
4	chr4:75973274..75973936-chr4:76393915..76394737,2	MCF-7	breast:
5	chr4:75857716..75858592-chr4:76214836..76215509,3	MCF-7	breast:
6	chr4:76210768..76213178-chr4:76214495..76216137,2	K562	blood:
7	chr4:75857312..75858654-chr4:76214491..76215648,6	MCF-7	breast:
8	chr4:76229171..76231861-chr4:76436993..76438920,2	MCF-7	breast:
9	chr4:75799924..75800563-chr4:76214703..76215703,2	MCF-7	breast:
10	chr4:76357680..76358190-chr4:76498602..76499548,2	MCF-7	breast:
11	chr4:75799685..75800426-chr4:76215952..76216615,2	MCF-7	breast:
12	chr4:76214761..76215324-chr4:76498679..76499192,2	MCF-7	breast:
13	chr4:76349656..76352296-chr4:76353820..76356620,3	K562	blood:
14	chr4:75718643..75719283-chr4:76213272..76214122,2	MCF-7	breast:
15	chr4:75185612..75186157-chr4:76214776..76215513,2	MCF-7	breast:
16	chr4:75948889..75950476-chr4:76335747..76337951,2	MCF-7	breast:
17	chr4:76210768..76213178-chr4:76214495..76216137,2	K562	blood:
18	chr4:76358069..76359586-chr4:76396767..76398904,2	K562	blood:
19	chr4:76278035..76280636-chr4:76286764..76289463,2	K562	blood:
20	chr4:76178186..76180045-chr4:76183353..76185602,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RCHY1-3	chr4:76286352-76286392	XLOC_003986
2	lnc-THAP6-2	chr4:76283191-76283545	XLOC_003576
3	lnc-THAP6-2	chr4:76280528-76280597	ENSG00000251383
4	lnc-THAP6-1	chr4:76326405-76326502	XLOC_003577
5	lnc-RCHY1-2	chr4:76272507-76272663	XLOC_003987
6	lnc-RCHY1-2	chr4:76266489-76266522	XLOC_003987
7	lnc-RCHY1-3	chr4:76194278-76194705	XLOC_003986
8	lnc-THAP6-1	chr4:76347789-76348233	XLOC_003577
9	lnc-RCHY1-1	chr4:76286417-76286557	XLOC_003988
10	lnc-THAP6-2	chr4:76279286-76279325	ENSG00000251383
11	lnc-THAP6-2	chr4:76286934-76287774	XLOC_003576
12	lnc-THAP6-1	chr4:76347789-76348232	XLOC_003577
13	lnc-THAP6-1	chr4:76347264-76347402	XLOC_003577
14	lnc-THAP6-2	chr4:76283191-76283380	XLOC_003576
15	lnc-THAP6-2	chr4:76279286-76279325	XLOC_003576
16	lnc-THAP6-2	chr4:76283191-76283380	ENSG00000251383
17	lnc-THAP6-1	chr4:76333105-76333222	XLOC_003577
18	lnc-THAP6-1	chr4:76326428-76326502	XLOC_003577
19	lnc-RCHY1-1	chr4:76359328-76359659	XLOC_003988
20	lnc-THAP6-2	chr4:76280531-76280597	XLOC_003576
21	lnc-THAP6-1	chr4:76347264-76347402	XLOC_003577
22	lnc-RCHY1-2	chr4:76266672-76266847	XLOC_003987
23	lnc-RCHY1-6	chr4:76324645-76324689	l_2668_chr4:76322897-76324689_adipose
24	lnc-RCHY1-6	chr4:76322898-76323124	l_2668_chr4:76322897-76324689_adipose
25	lnc-THAP6-2	chr4:76280528-76280597	XLOC_003576
26	lnc-RCHY1-2	chr4:76284180-76284234	XLOC_003987
27	lnc-THAP6-2	chr4:76286934-76287776	ENSG00000251383

Variant related genes	Relation type
ENSG00000250735	TF binding region
ENSG00000248646	TF binding region
ENSG00000251383	TF binding region
ENSG00000251185	TF binding region
ENSG00000251454	TF binding region
ENSG00000250735	CpG island
ENSG00000248646	CpG island
ENSG00000251383	CpG island
ENSG00000251185	CpG island
ENSG00000251454	CpG island
ENSG00000169116	chromatin interactions
ENSG00000251383	chromatin interactions
IL6R	miRNA target sites
SPTY2D1	miRNA target sites
ESRRA	miRNA target sites
SMARCA2	miRNA target sites
ESYT1	miRNA target sites
SIX4	miRNA target sites
SMARCA4	miRNA target sites
SMAP2	miRNA target sites
AP1G1	miRNA target sites
ANXA5	miRNA target sites

Extended variants
information (count: 3659 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3659 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2867289	chr4:76184807-76184808	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs6852782	chr4:76184837-76184838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2131690	chr4:76184846-76184847	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs145560182	chr4:76184897-76184898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566697526	chr4:76184916-76184917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs72604221	chr4:76184921-76184922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs5859455	chr4:76184922-76184923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200089581	chr4:76184923-76184924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs113827464	chr4:76184933-76184934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112757423	chr4:76184939-76184940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570855003	chr4:76184952-76184953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537850809	chr4:76184977-76184978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556662197	chr4:76184990-76184991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2867290	chr4:76184993-76184994	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs542294939	chr4:76184997-76184998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs6853162	chr4:76185007-76185008	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs201656410	chr4:76185008-76185009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572235173	chr4:76185009-76185010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs116732623	chr4:76185058-76185059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs144139176	chr4:76185151-76185152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146434646	chr4:76185160-76185161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543041257	chr4:76185167-76185168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs561683695	chr4:76185211-76185212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs528978260	chr4:76185214-76185215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140818556	chr4:76185232-76185233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544122846	chr4:76185247-76185248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182830818	chr4:76185248-76185249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs527858042	chr4:76185287-76185288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs188175906	chr4:76185291-76185292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552881765	chr4:76185330-76185331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571049488	chr4:76185373-76185374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs538494152	chr4:76185380-76185381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs67227453	chr4:76185397-76185398	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs568412637	chr4:76185398-76185399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs535966319	chr4:76185414-76185415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs144563415	chr4:76185420-76185421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191416443	chr4:76185428-76185429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs151171281	chr4:76185435-76185436	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534666784	chr4:76185467-76185468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543218293	chr4:76185494-76185495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576266988	chr4:76185546-76185547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543675198	chr4:76185548-76185549	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150467900	chr4:76185560-76185561	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528844172	chr4:76185565-76185566	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540756440	chr4:76185566-76185567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528572027	chr4:76185577-76185578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112210578	chr4:76185606-76185607	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs527923139	chr4:76185620-76185621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375364406	chr4:76185670-76185671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12648574	chr4:76185683-76185684	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Abnormal phenotypes	18644119	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20932292	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21364760	CNVD
Autism	18414403	CNVD

Chromatin state (count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:76174000-76185200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr4:76174800-76185200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr4:76180200-76185200	Weak transcription	Fetal Muscle Trunk	muscle
4	chr4:76180800-76185000	Weak transcription	Fetal Muscle Leg	muscle
5	chr4:76180800-76185200	Weak transcription	Placenta	Placenta
6	chr4:76185000-76185600	Enhancers	Fetal Muscle Leg	muscle
7	chr4:76185000-76185800	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr4:76185200-76185400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:76185200-76185400	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr4:76185200-76185400	Enhancers	Placenta	Placenta
11	chr4:76185200-76185600	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr4:76185200-76186000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr4:76185200-76186000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr4:76185400-76185800	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr4:76185400-76186200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr4:76185400-76186400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:76185800-76186000	Enhancers	Fetal Muscle Trunk	muscle
18	chr4:76186200-76186800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr4:76186400-76186600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr4:76186800-76187000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr4:76191800-76192200	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr4:76191800-76192200	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr4:76191800-76192400	Enhancers	H1 Cell Line	embryonic stem cell
24	chr4:76191800-76192400	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr4:76191800-76192600	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr4:76192000-76192600	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr4:76201400-76201600	Enhancers	H1 Cell Line	embryonic stem cell
28	chr4:76201400-76202000	Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr4:76202000-76202200	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr4:76211200-76213400	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr4:76211800-76213600	Enhancers	Fetal Intestine Large	intestine
32	chr4:76211800-76213600	Enhancers	Fetal Intestine Small	intestine
33	chr4:76212800-76213600	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr4:76213400-76213600	Enhancers	Fetal Muscle Trunk	muscle
35	chr4:76213400-76215800	Enhancers	Fetal Muscle Leg	muscle
36	chr4:76213600-76215200	Weak transcription	Fetal Muscle Trunk	muscle
37	chr4:76214200-76215400	Enhancers	Colon Smooth Muscle	Colon
38	chr4:76214800-76216200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr4:76215000-76216200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr4:76215200-76215400	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr4:76215200-76215600	Enhancers	Fetal Muscle Trunk	muscle
42	chr4:76215200-76215600	Enhancers	HSMM	muscle
43	chr4:76215200-76215800	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr4:76215200-76215800	Enhancers	Psoas Muscle	Psoas
45	chr4:76215200-76216000	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr4:76215200-76216000	Enhancers	NHEK	skin
47	chr4:76215400-76216000	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr4:76215400-76216000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
49	chr4:76215400-76216000	Enhancers	H1 Cell Line	embryonic stem cell
50	chr4:76215400-76216000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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