Variant report

Variant	esv2763368
Chromosome Location	chr4:76190070-76387413
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	chr4:76374262-76374511	HepG2	liver:	n/a	chr4:76374365-76374376
7	CEBPB	chr4:76319825-76319934	IMR90	lung:	n/a	n/a
8	CEBPB	chr4:76339442-76339558	K562	blood:	n/a	chr4:76339500-76339513 chr4:76339500-76339511 chr4:76339500-76339513 chr4:76339502-76339513
9	CEBPB	chr4:76339348-76339649	HepG2	liver:	n/a	chr4:76339500-76339513 chr4:76339500-76339511 chr4:76339500-76339513 chr4:76339502-76339513
10	CEBPB	chr4:76374340-76374490	H1-hESC	embryonic stem cell:	n/a	chr4:76374365-76374376
11	CEBPB	chr4:76321097-76321297	IMR90	lung:	n/a	chr4:76321162-76321173 chr4:76321164-76321173 chr4:76321163-76321174
12	CEBPB	chr4:76357985-76358149	K562	blood:	n/a	n/a
13	CEBPB	chr4:76319796-76319943	K562	blood:	n/a	n/a
14	CEBPB	chr4:76264522-76264645	HepG2	liver:	n/a	chr4:76264549-76264560
15	CEBPB	chr4:76321013-76321304	HepG2	liver:	n/a	chr4:76321162-76321173 chr4:76321164-76321173 chr4:76321163-76321174
16	CEBPB	chr4:76321118-76321291	K562	blood:	n/a	chr4:76321162-76321173 chr4:76321164-76321173 chr4:76321163-76321174
17	CEBPB	chr4:76379752-76380285	MCF-7	breast:	n/a	chr4:76379852-76379863 chr4:76379850-76379863
18	CEBPB	chr4:76321079-76321193	A549	lung:	n/a	chr4:76321162-76321173 chr4:76321164-76321173 chr4:76321163-76321174
19	CEBPB	chr4:76379920-76380120	IMR90	lung:	n/a	n/a
20	CTCF	chr4:76215081-76215347	MCF-7	breast:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
21	CTCF	chr4:76215160-76215310	HCPEpiC	choroid plexus:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
22	CTCF	chr4:76215240-76215390	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr4:76215123-76215286	Hela-S3	cervix:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
24	CTCF	chr4:76358020-76358170	AG10803	skin:	n/a	n/a
25	CTCF	chr4:76358000-76358150	GM12874	blood:	n/a	n/a
26	CTCF	chr4:76215120-76215270	GM12870	blood:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
27	CTCF	chr4:76358040-76358190	Caco-2	colon:	n/a	n/a
28	CTCF	chr4:76357943-76358164	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr4:76358040-76358190	HUVEC	blood vessel:	n/a	n/a
30	CTCF	chr4:76215100-76215250	BJ	skin:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
31	CTCF	chr4:76215080-76215230	Caco-2	colon:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
32	CTCF	chr4:76215140-76215290	GM06990	blood:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
33	CTCF	chr4:76214807-76215508	HCT-116	colon:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
34	CTCF	chr4:76215100-76215250	HCM	heart:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
35	CTCF	chr4:76357895-76358296	K562	blood:	n/a	n/a
36	CTCF	chr4:76215086-76215280	ECC-1	luminal epithelium:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
37	CTCF	chr4:76353040-76353190	BE2_C	brain:	n/a	n/a
38	CTCF	chr4:76358020-76358170	NHEK	skin:	n/a	n/a
39	CTCF	chr4:76215140-76215290	GM12867	blood:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
40	CTCF	chr4:76340700-76340850	GM12869	blood:	n/a	n/a
41	CTCF	chr4:76215120-76215270	MCF-7	breast:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
42	CTCF	chr4:76358018-76358177	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr4:76358020-76358170	AoAF	blood vessel:	n/a	n/a
44	CTCF	chr4:76214875-76215479	SK-N-SH	brain:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
45	CTCF	chr4:76358054-76358185	MCF-7	breast:	n/a	n/a
46	CTCF	chr4:76215240-76215390	NHEK	skin:	n/a	n/a
47	CTCF	chr4:76357920-76358070	HMEC	breast:	n/a	n/a
48	CTCF	chr4:76358020-76358170	GM12873	blood:	n/a	n/a
49	CTCF	chr4:76358000-76358150	GM12865	blood:	n/a	n/a
50	CTCF	chr4:76358000-76358150	GM12868	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:76264560-76264610	HPAEpiC	pulmonary alveolar:	n/a
2	chr4:76264560-76264610	HPAEpiC	pulmonary alveolar:	n/a
3	chr4:76264560-76264610	BJ	skin:	n/a
4	chr4:76373607-76373657	HCF	heart:	n/a
5	chr4:76373607-76373657	HCT-116	colon:	n/a
6	chr4:76201532-76201582	GM12892	blood:	n/a
7	chr4:76201532-76201582	K562	blood:	n/a
8	chr4:76317967-76318017	AoSMC	blood vessel:	n/a
9	chr4:76317967-76318017	ECC-1	luminal epithelium:	n/a
10	chr4:76201532-76201582	GM06990	blood:	n/a
11	chr4:76373607-76373657	IMR90	lung:	fetal
12	chr4:76201532-76201582	IMR90	lung:	fetal
13	chr4:76264560-76264610	K562	blood:	n/a
14	chr4:76201532-76201582	HCT-116	colon:	n/a
15	chr4:76373607-76373657	HRE	kidney:	n/a
16	chr4:76264560-76264610	HAEpiC	amniotic membrane:	n/a
17	chr4:76264560-76264610	HIPEpiC	eye:	n/a
18	chr4:76373607-76373657	SK-N-SH_RA	brain:	n/a
19	chr4:76317967-76318017	GM12891	blood:	n/a
20	chr4:76264560-76264610	SKMC	muscle:	n/a
21	chr4:76201532-76201582	CMK	blood:	n/a
22	chr4:76317967-76318017	CMK	blood:	n/a
23	chr4:76317967-76318017	HL-60	blood:	n/a
24	chr4:76201532-76201582	NH-A	brain:	n/a
25	chr4:76201532-76201582	NB4	blood:	n/a
26	chr4:76201532-76201582	PFSK-1	brain:	n/a
27	chr4:76201532-76201582	HRE	kidney:	n/a
28	chr4:76373607-76373657	HEK293	kidney:	embryo
29	chr4:76264560-76264610	CMK	blood:	n/a
30	chr4:76317967-76318017	PANC-1	pancreas:	n/a
31	chr4:76201532-76201582	SAEC	small airway:	n/a
32	chr4:76264560-76264610	AG09309	skin:	n/a
33	chr4:76264560-76264610	NH-A	brain:	n/a
34	chr4:76317967-76318017	GM12892	blood:	n/a
35	chr4:76201532-76201582	HCPEpiC	choroid plexus:	n/a
36	chr4:76264560-76264610	HepG2	liver:	n/a
37	chr4:76373607-76373657	RPTEC	kidney:	n/a
38	chr4:76264560-76264610	SAEC	small airway:	n/a
39	chr4:76373607-76373657	HL-60	blood:	n/a
40	chr4:76264560-76264610	AG10803	skin:	n/a
41	chr4:76201532-76201582	NHBE	bronchial:	n/a
42	chr4:76264560-76264610	PFSK-1	brain:	n/a
43	chr4:76373607-76373657	GM06990	blood:	n/a
44	chr4:76317967-76318017	GM06990	blood:	n/a
45	chr4:76264560-76264610	GM12891	blood:	n/a
46	chr4:76201532-76201582	BJ	skin:	n/a
47	chr4:76201532-76201582	HPAEpiC	pulmonary alveolar:	n/a
48	chr4:76373607-76373657	NH-A	brain:	n/a
49	chr4:76317967-76318017	AG04449	skin:	fetal
50	chr4:76373607-76373657	K562	blood:	n/a

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

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

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
SPTY2D1	miRNA target sites
ESRRA	miRNA target sites
ESYT1	miRNA target sites
AP1G1	miRNA target sites
SIX4	miRNA target sites
SMARCA2	miRNA target sites
ANXA5	miRNA target sites
IL6R	miRNA target sites
SMARCA4	miRNA target sites
SMAP2	miRNA target sites

Extended variants
information (count: 3355 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3355 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531805685	chr4:76191825-76191826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs550598744	chr4:76191857-76191858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568843434	chr4:76191866-76191867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs78748999	chr4:76191926-76191927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs75384043	chr4:76191927-76191928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs77893032	chr4:76191930-76191931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs11099473	chr4:76191931-76191932	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs78614084	chr4:76191936-76191937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs74551050	chr4:76191947-76191948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531177952	chr4:76191963-76191964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534895053	chr4:76191966-76191967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187336982	chr4:76191991-76191992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs147940064	chr4:76191992-76191993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs140102174	chr4:76191996-76191997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs150028998	chr4:76192022-76192023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs113378858	chr4:76192049-76192050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs6835428	chr4:76192050-76192051	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs554765421	chr4:76192052-76192053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573034537	chr4:76192066-76192067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs540064620	chr4:76192068-76192069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs565044404	chr4:76192090-76192091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532470370	chr4:76192115-76192116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs386676152	chr4:76192170-76192171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs13134069	chr4:76192171-76192172	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs35090341	chr4:76192278-76192279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs35380097	chr4:76192285-76192286	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs548344413	chr4:76192307-76192308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs200235497	chr4:76192333-76192334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs113600814	chr4:76192355-76192356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369867503	chr4:76192408-76192409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs72662501	chr4:76192420-76192421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs527331829	chr4:76192445-76192446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs546896404	chr4:76192470-76192471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571774907	chr4:76192483-76192484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs7665085	chr4:76192485-76192486	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs557213632	chr4:76192501-76192502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs17000419	chr4:76192571-76192572	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs192819330	chr4:76192580-76192581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs546501159	chr4:76194292-76194293	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs572406421	chr4:76194296-76194297	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs140013769	chr4:76194303-76194304	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs531731893	chr4:76194304-76194305	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs55914143	chr4:76194307-76194308	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs568551854	chr4:76194327-76194328	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs7664815	chr4:76194334-76194335	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs182488452	chr4:76194344-76194345	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs7664835	chr4:76194358-76194359	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs375308187	chr4:76194360-76194361	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs539383168	chr4:76194376-76194377	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs149846729	chr4:76194379-76194380	Inactive region	lncRNA	n/a	Overlapped CNVs	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:209 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:76191800-76192200	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr4:76191800-76192200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr4:76191800-76192400	Enhancers	H1 Cell Line	embryonic stem cell
4	chr4:76191800-76192400	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr4:76191800-76192600	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr4:76192000-76192600	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr4:76201400-76201600	Enhancers	H1 Cell Line	embryonic stem cell
8	chr4:76201400-76202000	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr4:76202000-76202200	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr4:76211200-76213400	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr4:76211800-76213600	Enhancers	Fetal Intestine Large	intestine
12	chr4:76211800-76213600	Enhancers	Fetal Intestine Small	intestine
13	chr4:76212800-76213600	Enhancers	Rectal Mucosa Donor 29	rectum
14	chr4:76213400-76213600	Enhancers	Fetal Muscle Trunk	muscle
15	chr4:76213400-76215800	Enhancers	Fetal Muscle Leg	muscle
16	chr4:76213600-76215200	Weak transcription	Fetal Muscle Trunk	muscle
17	chr4:76214200-76215400	Enhancers	Colon Smooth Muscle	Colon
18	chr4:76214800-76216200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr4:76215000-76216200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr4:76215200-76215400	Enhancers	Rectal Mucosa Donor 31	rectum
21	chr4:76215200-76215600	Enhancers	Fetal Muscle Trunk	muscle
22	chr4:76215200-76215600	Enhancers	HSMM	muscle
23	chr4:76215200-76215800	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr4:76215200-76215800	Enhancers	Psoas Muscle	Psoas
25	chr4:76215200-76216000	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr4:76215200-76216000	Enhancers	NHEK	skin
27	chr4:76215400-76216000	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr4:76215400-76216000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
29	chr4:76215400-76216000	Enhancers	H1 Cell Line	embryonic stem cell
30	chr4:76215400-76216000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr4:76225800-76227000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:76226800-76227000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
33	chr4:76227000-76232800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr4:76231400-76232200	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr4:76231800-76234800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr4:76232000-76232400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:76232800-76233600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr4:76233200-76233600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:76233600-76235000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr4:76235000-76235200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr4:76249000-76251400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr4:76249600-76254400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr4:76249600-76255000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr4:76249800-76250000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr4:76249800-76250400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr4:76250000-76250600	Enhancers	Colon Smooth Muscle	Colon
47	chr4:76250000-76250600	Enhancers	Fetal Brain Male	brain
48	chr4:76250000-76250600	Enhancers	Fetal Muscle Leg	muscle
49	chr4:76250000-76251200	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr4:76250200-76250400	Enhancers	Right Atrium	heart

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