Variant report

Variant	nsv461557
Chromosome Location	chr4:76212995-76363477
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	chr4:76321013-76321304	HepG2	liver:	n/a	chr4:76321162-76321173 chr4:76321164-76321173 chr4:76321163-76321174
7	CEBPB	chr4:76339442-76339558	K562	blood:	n/a	chr4:76339500-76339513 chr4:76339500-76339511 chr4:76339500-76339513 chr4:76339502-76339513
8	CEBPB	chr4:76321097-76321297	IMR90	lung:	n/a	chr4:76321162-76321173 chr4:76321164-76321173 chr4:76321163-76321174
9	CEBPB	chr4:76321079-76321193	A549	lung:	n/a	chr4:76321162-76321173 chr4:76321164-76321173 chr4:76321163-76321174
10	CEBPB	chr4:76321118-76321291	K562	blood:	n/a	chr4:76321162-76321173 chr4:76321164-76321173 chr4:76321163-76321174
11	CEBPB	chr4:76319796-76319943	K562	blood:	n/a	n/a
12	CEBPB	chr4:76319825-76319934	IMR90	lung:	n/a	n/a
13	CEBPB	chr4:76339348-76339649	HepG2	liver:	n/a	chr4:76339500-76339513 chr4:76339500-76339511 chr4:76339500-76339513 chr4:76339502-76339513
14	CEBPB	chr4:76357985-76358149	K562	blood:	n/a	n/a
15	CEBPB	chr4:76264522-76264645	HepG2	liver:	n/a	chr4:76264549-76264560
16	CTCF	chr4:76215080-76215338	Spleen_OC	spleen:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
17	CTCF	chr4:76215158-76215352	GM12891	blood:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
18	CTCF	chr4:76215140-76215290	GM12872	blood:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
19	CTCF	chr4:76358040-76358190	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr4:76358020-76358170	GM12875	blood:	n/a	n/a
21	CTCF	chr4:76215063-76215335	H1-hESC	embryonic stem cell:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
22	CTCF	chr4:76358029-76358111	GM10266	blood:	n/a	n/a
23	CTCF	chr4:76357810-76358468	A549	lung:	n/a	n/a
24	CTCF	chr4:76357986-76358202	HepG2	liver:	n/a	n/a
25	CTCF	chr4:76215140-76215290	A549	lung:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
26	CTCF	chr4:76358000-76358150	HFF-Myc	foreskin:	n/a	n/a
27	CTCF	chr4:76357970-76358121	LNCaP	prostate:	n/a	n/a
28	CTCF	chr4:76215160-76215310	BE2_C	brain:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
29	CTCF	chr4:76215120-76215270	HEK293	kidney:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
30	CTCF	chr4:76358051-76358152	GM12891	blood:	n/a	n/a
31	CTCF	chr4:76358011-76358193	NHEK	skin:	n/a	n/a
32	CTCF	chr4:76357922-76358236	MCF-7	breast:	n/a	n/a
33	CTCF	chr4:76358060-76358210	HCM	heart:	n/a	n/a
34	CTCF	chr4:76296510-76296576	Lung_OC	lung:	n/a	n/a
35	CTCF	chr4:76215420-76215570	SAEC	small airway:	n/a	n/a
36	CTCF	chr4:76214904-76215469	HCT-116	colon:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
37	CTCF	chr4:76215100-76215250	HCFaa	heart:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
38	CTCF	chr4:76358040-76358190	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr4:76215100-76215250	GM12875	blood:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
40	CTCF	chr4:76357980-76358130	HPF	lung:	n/a	n/a
41	CTCF	chr4:76215100-76215250	GM06990	blood:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
42	CTCF	chr4:76358020-76358170	AG10803	skin:	n/a	n/a
43	CTCF	chr4:76358100-76358250	HVMF	connective:	n/a	n/a
44	CTCF	chr4:76215080-76215230	GM12867	blood:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
45	CTCF	chr4:76358000-76358150	GM12864	blood:	n/a	n/a
46	CTCF	chr4:76215060-76215210	AoAF	blood vessel:	n/a	chr4:76215189-76215210 chr4:76215196-76215209
47	CTCF	chr4:76215140-76215290	HCM	heart:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
48	CTCF	chr4:76215086-76215280	ECC-1	luminal epithelium:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
49	CTCF	chr4:76215074-76215333	T-47D	breast:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212
50	CTCF	chr4:76215118-76215346	GM19240	blood:	n/a	chr4:76215189-76215210 chr4:76215196-76215209 chr4:76215194-76215212

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:76317967-76318017	MCF-7	breast:	n/a
2	chr4:76317967-76318017	HNPCEpiC	eye:	n/a
3	chr4:76264560-76264610	HL-60	blood:	n/a
4	chr4:76264560-76264610	NHBE	bronchial:	n/a
5	chr4:76264560-76264610	SAEC	small airway:	n/a
6	chr4:76264560-76264610	HepG2	liver:	n/a
7	chr4:76317967-76318017	SK-N-SH_RA	brain:	n/a
8	chr4:76317967-76318017	PFSK-1	brain:	n/a
9	chr4:76264560-76264610	HCF	heart:	n/a
10	chr4:76317967-76318017	LNCaP	prostate:	n/a
11	chr4:76264560-76264610	ECC-1	luminal epithelium:	n/a
12	chr4:76317967-76318017	IMR90	lung:	fetal
13	chr4:76264560-76264610	MCF10A-Er-Src	breast:	n/a
14	chr4:76317967-76318017	Hela-S3	cervix:	n/a
15	chr4:76317967-76318017	HRCEpiC	kidney:	n/a
16	chr4:76317967-76318017	HCPEpiC	choroid plexus:	n/a
17	chr4:76317967-76318017	HUVEC	blood vessel:	n/a
18	chr4:76317967-76318017	HEEpiC	esophagus:	n/a
19	chr4:76317967-76318017	AG04449	skin:	fetal
20	chr4:76317967-76318017	U87	brain:	n/a
21	chr4:76264560-76264610	SK-N-MC	brain:	n/a
22	chr4:76317967-76318017	HRE	kidney:	n/a
23	chr4:76264560-76264610	HNPCEpiC	eye:	n/a
24	chr4:76264560-76264610	GM19239	blood:	n/a
25	chr4:76317967-76318017	Caco-2	colon:	n/a
26	chr4:76264560-76264610	HIPEpiC	eye:	n/a
27	chr4:76264560-76264610	Jurkat	blood:	n/a
28	chr4:76264560-76264610	AG04449	skin:	fetal
29	chr4:76317967-76318017	MCF10A-Er-Src	breast:	n/a
30	chr4:76317967-76318017	BE2_C	brain:	n/a
31	chr4:76264560-76264610	ProgFib	skin:	n/a
32	chr4:76317967-76318017	HMEC	breast:	n/a
33	chr4:76264560-76264610	NH-A	brain:	n/a
34	chr4:76317967-76318017	CMK	blood:	n/a
35	chr4:76317967-76318017	NB4	blood:	n/a
36	chr4:76264560-76264610	HCM	heart:	n/a
37	chr4:76317967-76318017	ProgFib	skin:	n/a
38	chr4:76317967-76318017	HCM	heart:	n/a
39	chr4:76317967-76318017	NHDF-neo	bronchial:	n/a
40	chr4:76264560-76264610	GM12891	blood:	n/a
41	chr4:76264560-76264610	GM06990	blood:	n/a
42	chr4:76317967-76318017	NT2-D1	testis:	n/a
43	chr4:76317967-76318017	K562	blood:	n/a
44	chr4:76264560-76264610	GM12878	blood:	n/a
45	chr4:76317967-76318017	SK-N-MC	brain:	n/a
46	chr4:76264560-76264610	BE2_C	brain:	n/a
47	chr4:76317967-76318017	T-47D	breast:	n/a
48	chr4:76317967-76318017	GM12892	blood:	n/a
49	chr4:76317967-76318017	BJ	skin:	n/a
50	chr4:76264560-76264610	AG10803	skin:	n/a

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

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

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

Extended variants
information (count: 3090 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:3090 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6535270	chr4:76212995-76212996	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565733840	chr4:76212999-76213000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs372633352	chr4:76213004-76213005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs10715009	chr4:76213005-76213006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs11727857	chr4:76213009-76213010	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs557837385	chr4:76213010-76213011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs569780571	chr4:76213013-76213014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537272496	chr4:76213046-76213047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs547230813	chr4:76213070-76213071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs188950951	chr4:76213071-76213072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs540956267	chr4:76213085-76213086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs7682487	chr4:76213086-76213087	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs544619159	chr4:76213097-76213098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs193205638	chr4:76213113-76213114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs72665305	chr4:76213128-76213129	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs7682650	chr4:76213130-76213131	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs575392043	chr4:76213181-76213182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs145516638	chr4:76213198-76213199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs562134516	chr4:76213202-76213203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs78546711	chr4:76213203-76213204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs7667892	chr4:76213223-76213224	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs183461424	chr4:76213253-76213254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371568842	chr4:76213254-76213255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs116116225	chr4:76213274-76213275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs76247438	chr4:76213300-76213301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569842231	chr4:76213301-76213302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs148426144	chr4:76213321-76213322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188534517	chr4:76213365-76213366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs116945866	chr4:76213375-76213376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs7672760	chr4:76213383-76213384	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs570155490	chr4:76213395-76213396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566420034	chr4:76213407-76213408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs553320634	chr4:76213411-76213412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577980160	chr4:76213471-76213472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538668860	chr4:76213477-76213478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs535325628	chr4:76213492-76213493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556983283	chr4:76213495-76213496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575339321	chr4:76213497-76213498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542355954	chr4:76213499-76213500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs75948771	chr4:76213508-76213509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs1353605	chr4:76213513-76213514	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs541047522	chr4:76213515-76213516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541578692	chr4:76213544-76213545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs12642778	chr4:76213552-76213553	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs533424573	chr4:76213572-76213573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs551393381	chr4:76213581-76213582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191858976	chr4:76213582-76213583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs75108528	chr4:76213587-76213588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs374465421	chr4:76213611-76213612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs549210698	chr4:76213711-76213712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21364760	CNVD
Autism	18414403	CNVD

Chromatin state (count:199 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:76211200-76213400	Enhancers	Rectal Mucosa Donor 31	rectum
2	chr4:76211800-76213600	Enhancers	Fetal Intestine Large	intestine
3	chr4:76211800-76213600	Enhancers	Fetal Intestine Small	intestine
4	chr4:76212800-76213600	Enhancers	Rectal Mucosa Donor 29	rectum
5	chr4:76213400-76213600	Enhancers	Fetal Muscle Trunk	muscle
6	chr4:76213400-76215800	Enhancers	Fetal Muscle Leg	muscle
7	chr4:76213600-76215200	Weak transcription	Fetal Muscle Trunk	muscle
8	chr4:76214200-76215400	Enhancers	Colon Smooth Muscle	Colon
9	chr4:76214800-76216200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr4:76215000-76216200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:76215200-76215400	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr4:76215200-76215600	Enhancers	Fetal Muscle Trunk	muscle
13	chr4:76215200-76215600	Enhancers	HSMM	muscle
14	chr4:76215200-76215800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr4:76215200-76215800	Enhancers	Psoas Muscle	Psoas
16	chr4:76215200-76216000	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr4:76215200-76216000	Enhancers	NHEK	skin
18	chr4:76215400-76216000	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr4:76215400-76216000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
20	chr4:76215400-76216000	Enhancers	H1 Cell Line	embryonic stem cell
21	chr4:76215400-76216000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr4:76225800-76227000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
23	chr4:76226800-76227000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
24	chr4:76227000-76232800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr4:76231400-76232200	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr4:76231800-76234800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr4:76232000-76232400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:76232800-76233600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr4:76233200-76233600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr4:76233600-76235000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr4:76235000-76235200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr4:76249000-76251400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr4:76249600-76254400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr4:76249600-76255000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr4:76249800-76250000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:76249800-76250400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr4:76250000-76250600	Enhancers	Colon Smooth Muscle	Colon
38	chr4:76250000-76250600	Enhancers	Fetal Brain Male	brain
39	chr4:76250000-76250600	Enhancers	Fetal Muscle Leg	muscle
40	chr4:76250000-76251200	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr4:76250200-76250400	Enhancers	Right Atrium	heart
42	chr4:76250200-76251000	Enhancers	Aorta	Aorta
43	chr4:76250200-76251200	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr4:76250200-76251400	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr4:76250400-76251200	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr4:76250400-76251200	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr4:76250400-76251600	Weak transcription	Right Atrium	heart
48	chr4:76250400-76252000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr4:76250600-76250800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr4:76250600-76251000	Enhancers	HUES48 Cell Line	embryonic stem cell

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