Variant report

Variant	nsv1002823
Chromosome Location	chr3:23277838-23623083
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1630)
CpG islands
(count:793)
Chromatin interactive
region (count:73)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1630 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:23382835-23383365	GM12878	blood:	n/a	n/a
2	ATF2	chr3:23367108-23367548	GM12878	blood:	n/a	n/a
3	ATF2	chr3:23472393-23472877	GM12878	blood:	n/a	n/a
4	ATF2	chr3:23367105-23367549	GM12878	blood:	n/a	n/a
5	BACH1	chr3:23585155-23585177	K562	blood:	n/a	n/a
6	BACH1	chr3:23299743-23299785	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr3:23533686-23533737	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr3:23463964-23464237	GM12878	blood:	n/a	n/a
9	BATF	chr3:23480155-23480444	GM12878	blood:	n/a	n/a
10	BATF	chr3:23436607-23436931	GM12878	blood:	n/a	chr3:23436755-23436764
11	BATF	chr3:23367094-23367570	GM12878	blood:	n/a	n/a
12	BATF	chr3:23480171-23480448	GM12878	blood:	n/a	n/a
13	BATF	chr3:23313878-23314156	GM12878	blood:	n/a	n/a
14	BATF	chr3:23591928-23592183	GM12878	blood:	n/a	n/a
15	BATF	chr3:23367272-23367502	GM12878	blood:	n/a	n/a
16	BATF	chr3:23581038-23581276	GM12878	blood:	n/a	n/a
17	BATF	chr3:23298327-23298695	GM12878	blood:	n/a	n/a
18	BCL11A	chr3:23367192-23367517	GM12878	blood:	n/a	n/a
19	BCL3	chr3:23617886-23618518	A549	lung:	n/a	n/a
20	BCL3	chr3:23621629-23622436	A549	lung:	n/a	n/a
21	BCL3	chr3:23367262-23367545	GM12878	blood:	n/a	n/a
22	BCLAF1	chr3:23463910-23464435	GM12878	blood:	n/a	n/a
23	BCLAF1	chr3:23367134-23367570	GM12878	blood:	n/a	n/a
24	BCLAF1	chr3:23591798-23592336	GM12878	blood:	n/a	n/a
25	BHLHE40	chr3:23446575-23446933	GM12878	blood:	n/a	n/a
26	BHLHE40	chr3:23609332-23609762	GM12878	blood:	n/a	n/a
27	BHLHE40	chr3:23429181-23429214	GM12878	blood:	n/a	n/a
28	BRCA1	chr3:23621584-23622216	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr3:23445745-23446118	Hela-S3	cervix:	n/a	n/a
30	CCNT2	chr3:23537824-23537939	K562	blood:	n/a	n/a
31	CCNT2	chr3:23330795-23330876	K562	blood:	n/a	n/a
32	CEBPB	chr3:23466068-23466225	A549	lung:	n/a	n/a
33	CEBPB	chr3:23490782-23490938	K562	blood:	n/a	n/a
34	CEBPB	chr3:23617929-23618279	MCF-7	breast:	n/a	chr3:23618041-23618052
35	CEBPB	chr3:23556265-23556515	A549	lung:	n/a	n/a
36	CEBPB	chr3:23538554-23539070	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr3:23617878-23618227	HepG2	liver:	n/a	chr3:23618041-23618052
38	CEBPB	chr3:23438341-23438541	HepG2	liver:	n/a	chr3:23438451-23438464 chr3:23438451-23438464 chr3:23438451-23438462
39	CEBPB	chr3:23621793-23622357	A549	lung:	n/a	n/a
40	CEBPB	chr3:23586749-23587105	A549	lung:	n/a	chr3:23586919-23586930
41	CEBPB	chr3:23397764-23397950	HepG2	liver:	n/a	chr3:23397809-23397820
42	CEBPB	chr3:23438342-23438564	A549	lung:	n/a	chr3:23438451-23438464 chr3:23438451-23438464 chr3:23438451-23438462
43	CEBPB	chr3:23466027-23466260	HepG2	liver:	n/a	n/a
44	CEBPB	chr3:23617863-23618372	Hela-S3	cervix:	n/a	chr3:23618041-23618052
45	CEBPB	chr3:23572135-23572324	HepG2	liver:	n/a	n/a
46	CEBPB	chr3:23621747-23622376	HCT-116	colon:	n/a	n/a
47	CEBPB	chr3:23586737-23587115	HepG2	liver:	n/a	chr3:23586919-23586930
48	CEBPB	chr3:23617769-23618529	A549	lung:	n/a	chr3:23618041-23618052
49	CEBPB	chr3:23617870-23618219	IMR90	lung:	n/a	chr3:23618041-23618052
50	CEBPB	chr3:23404653-23405172	IMR90	lung:	n/a	chr3:23404763-23404774

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:23578676-23578726	MCF-7	breast:	n/a
2	chr3:23448023-23448073	U87	brain:	n/a
3	chr3:23522396-23522446	AG09319	gingival:	n/a
4	chr3:23331228-23331278	BE2_C	brain:	n/a
5	chr3:23567565-23567615	GM06990	blood:	n/a
6	chr3:23415040-23415090	NB4	blood:	n/a
7	chr3:23305946-23305996	H1-hESC	embryonic stem cell:	embryo
8	chr3:23305946-23305996	NHDF-neo	bronchial:	n/a
9	chr3:23415040-23415090	HL-60	blood:	n/a
10	chr3:23522396-23522446	HEK293	kidney:	embryo
11	chr3:23415040-23415090	U87	brain:	n/a
12	chr3:23590052-23590102	K562	blood:	n/a
13	chr3:23313729-23313779	BJ	skin:	n/a
14	chr3:23415040-23415090	HCM	heart:	n/a
15	chr3:23305946-23305996	PrEC	prostate:	n/a
16	chr3:23448023-23448073	NHBE	bronchial:	n/a
17	chr3:23567565-23567615	ECC-1	luminal epithelium:	n/a
18	chr3:23590052-23590102	ovcar-3	ovarian:	n/a
19	chr3:23478304-23478354	HIPEpiC	eye:	n/a
20	chr3:23578676-23578726	NB4	blood:	n/a
21	chr3:23567565-23567615	IMR90	lung:	fetal
22	chr3:23478304-23478354	GM12891	blood:	n/a
23	chr3:23496403-23496453	CMK	blood:	n/a
24	chr3:23415040-23415090	AG09309	skin:	n/a
25	chr3:23478304-23478354	AG09319	gingival:	n/a
26	chr3:23305946-23305996	K562	blood:	n/a
27	chr3:23478304-23478354	HL-60	blood:	n/a
28	chr3:23415040-23415090	AoSMC	blood vessel:	n/a
29	chr3:23504894-23504944	NHDF-neo	bronchial:	n/a
30	chr3:23415040-23415090	Caco-2	colon:	n/a
31	chr3:23448023-23448073	H1-hESC	embryonic stem cell:	embryo
32	chr3:23496403-23496453	HUVEC	blood vessel:	n/a
33	chr3:23478304-23478354	HCPEpiC	choroid plexus:	n/a
34	chr3:23496403-23496453	AG04449	skin:	fetal
35	chr3:23415040-23415090	HRE	kidney:	n/a
36	chr3:23305946-23305996	HUVEC	blood vessel:	n/a
37	chr3:23504894-23504944	ECC-1	luminal epithelium:	n/a
38	chr3:23331228-23331278	HCM	heart:	n/a
39	chr3:23313729-23313779	GM12878	blood:	n/a
40	chr3:23522396-23522446	HIPEpiC	eye:	n/a
41	chr3:23567565-23567615	SAEC	small airway:	n/a
42	chr3:23590052-23590102	GM12878	blood:	n/a
43	chr3:23331228-23331278	SK-N-MC	brain:	n/a
44	chr3:23331228-23331278	MCF-7	breast:	n/a
45	chr3:23448023-23448073	SK-N-MC	brain:	n/a
46	chr3:23522396-23522446	GM19239	blood:	n/a
47	chr3:23522396-23522446	HAEpiC	amniotic membrane:	n/a
48	chr3:23331228-23331278	HRPEpiC	eye:	n/a
49	chr3:23305946-23305996	GM06990	blood:	n/a
50	chr3:23415040-23415090	SK-N-SH_RA	brain:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:23505766..23508563-chr3:23511877..23514869,2	K562	blood:
2	chr3:23576275..23577975-chr3:23583689..23585549,2	K562	blood:
3	chr3:23566672..23568510-chr3:23579299..23582210,2	K562	blood:
4	chr3:23489983..23492292-chr3:23500438..23503341,2	MCF-7	breast:
5	chr3:23563683..23566443-chr3:23573278..23576217,2	MCF-7	breast:
6	chr3:23594511..23597259-chr3:23606854..23610185,3	MCF-7	breast:
7	chr3:23447289..23448831-chr3:23450533..23452284,2	K562	blood:
8	chr3:23360954..23362532-chr3:23363082..23365861,2	MCF-7	breast:
9	chr3:23443862..23447627-chr3:23449749..23452969,4	MCF-7	breast:
10	chr3:23543180..23548543-chr3:23549132..23552642,5	MCF-7	breast:
11	chr3:23557942..23560310-chr3:23562476..23565287,2	K562	blood:
12	chr3:23489870..23492697-chr3:23493234..23495139,2	MCF-7	breast:
13	chr3:23370714..23373096-chr3:23375354..23377337,2	K562	blood:
14	chr3:23398268..23400293-chr3:23402710..23405112,2	MCF-7	breast:
15	chr3:23489983..23492292-chr3:23500438..23503341,2	MCF-7	breast:
16	chr3:23370714..23373096-chr3:23375354..23377337,2	K562	blood:
17	chr3:23535866..23538759-chr3:23551729..23554341,2	MCF-7	breast:
18	chr3:23442881..23445228-chr3:23445484..23447259,2	K562	blood:
19	chr3:23466052..23468838-chr3:23474911..23476655,2	MCF-7	breast:
20	chr3:23505766..23508563-chr3:23511877..23514869,2	K562	blood:
21	chr3:23466052..23468838-chr3:23474911..23476655,2	MCF-7	breast:
22	chr3:23566672..23568510-chr3:23579299..23582210,2	K562	blood:
23	chr3:23284952..23287695-chr3:23289326..23291059,2	K562	blood:
24	chr3:23576275..23577975-chr3:23583689..23585549,2	K562	blood:
25	chr3:23375136..23376980-chr3:23383143..23385276,2	MCF-7	breast:
26	chr3:23563683..23566443-chr3:23573278..23576217,2	MCF-7	breast:
27	chr3:23483538..23485535-chr3:23501695..23503485,2	K562	blood:
28	chr3:23361011..23363823-chr3:23364424..23367156,3	MCF-7	breast:
29	chr3:23557942..23560310-chr3:23562476..23565287,2	K562	blood:
30	chr3:23361011..23363823-chr3:23364424..23367156,3	MCF-7	breast:
31	chr3:23429124..23431176-chr3:23435283..23438143,3	MCF-7	breast:
32	chr3:23535866..23538759-chr3:23551729..23554341,2	MCF-7	breast:
33	chr3:23489870..23492697-chr3:23493234..23495139,2	MCF-7	breast:
34	chr3:23429124..23431176-chr3:23435283..23438143,3	MCF-7	breast:
35	chr3:23551036..23552990-chr3:23555167..23556922,2	MCF-7	breast:
36	chr3:23477379..23479456-chr3:23479836..23482736,2	MCF-7	breast:
37	chr3:23245352..23245950-chr3:23374735..23375546,2	MCF-7	breast:
38	chr3:23543180..23548543-chr3:23549132..23552642,5	MCF-7	breast:
39	chr3:23413992..23416641-chr3:23420982..23423774,2	MCF-7	breast:
40	chr3:23398268..23400293-chr3:23402710..23405112,2	MCF-7	breast:
41	chr3:23436371..23438292-chr3:23438375..23440407,2	MCF-7	breast:
42	chr3:23533666..23536566-chr3:23556700..23559047,2	MCF-7	breast:
43	chr3:23333702..23336217-chr3:23346722..23349222,2	MCF-7	breast:
44	chr3:23375136..23376980-chr3:23383143..23385276,2	MCF-7	breast:
45	chr3:23443862..23447627-chr3:23449749..23452969,4	MCF-7	breast:
46	chr3:23447289..23448831-chr3:23450533..23452284,2	K562	blood:
47	chr3:23442881..23445228-chr3:23445484..23447259,2	K562	blood:
48	chr3:23413992..23416641-chr3:23420982..23423774,2	MCF-7	breast:
49	chr3:23442881..23445378-chr3:23445759..23448586,2	K562	blood:
50	chr3:23483538..23485535-chr3:23501695..23503485,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NKIRAS1-5	chr3:23431152-23431400	NONHSAT088668

No data

Variant related genes	Relation type
ENSG00000221506	TF binding region
ENSG00000265645	TF binding region
ENSG00000206728	TF binding region
ENSG00000228171	TF binding region
ENSG00000221506	CpG island
ENSG00000265645	CpG island
ENSG00000206728	CpG island
ENSG00000228171	CpG island

Extended variants
information (count: 14132 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:14132 , 50 per page) page: 1 2 3 4 5 6 7 ... 283

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17401815	chr3:23277838-23277839	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555139714	chr3:23277878-23277879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542411216	chr3:23277899-23277900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs191970145	chr3:23277953-23277954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs17401836	chr3:23277961-23277962	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs556546953	chr3:23277964-23277965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553333202	chr3:23277975-23277976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs370352784	chr3:23278008-23278009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562824001	chr3:23278096-23278097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs544911398	chr3:23278126-23278127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532436952	chr3:23278162-23278163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs560312674	chr3:23278165-23278166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs572119881	chr3:23278173-23278174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs35892300	chr3:23278174-23278175	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs559936285	chr3:23278239-23278240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368105199	chr3:23278244-23278245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374282742	chr3:23278266-23278267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs75886813	chr3:23278281-23278282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs530205272	chr3:23278290-23278291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544196971	chr3:23278449-23278450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs184800523	chr3:23278502-23278503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533428878	chr3:23278508-23278509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs139205323	chr3:23278540-23278541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs77892415	chr3:23278630-23278631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs144025687	chr3:23278657-23278658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187731123	chr3:23278681-23278682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192809215	chr3:23278684-23278685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs11715035	chr3:23278691-23278692	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs532393184	chr3:23278796-23278797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545308383	chr3:23278801-23278802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11707450	chr3:23278847-23278848	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs9836787	chr3:23278883-23278884	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs146489709	chr3:23278897-23278898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs11715107	chr3:23278900-23278901	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs542448064	chr3:23278903-23278904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555487472	chr3:23278916-23278917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573775133	chr3:23278922-23278923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs117208461	chr3:23278972-23278973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs562558085	chr3:23279078-23279079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533144448	chr3:23279085-23279086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs184368566	chr3:23279141-23279142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs9821101	chr3:23279169-23279170	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs9841123	chr3:23279182-23279183	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs549578661	chr3:23279237-23279238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs567406190	chr3:23279279-23279280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs9841308	chr3:23279307-23279308	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs140847468	chr3:23279331-23279332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs149712862	chr3:23279390-23279391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs13095887	chr3:23279441-23279442	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs59185768	chr3:23279449-23279450	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3139 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23261400-23278200	Weak transcription	Brain Angular Gyrus	brain
2	chr3:23265400-23282000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:23270600-23278200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr3:23270600-23278400	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr3:23271200-23278200	Weak transcription	Right Ventricle	heart
6	chr3:23272600-23283000	Weak transcription	HMEC	breast
7	chr3:23274400-23280800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr3:23274600-23278200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr3:23274600-23278200	Weak transcription	Left Ventricle	heart
10	chr3:23274600-23279800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr3:23274600-23281400	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr3:23274600-23283000	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr3:23274800-23278000	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr3:23274800-23278000	Weak transcription	Primary B cells from peripheral blood	blood
15	chr3:23274800-23278200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr3:23274800-23280200	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr3:23274800-23298200	Weak transcription	Aorta	Aorta
18	chr3:23275000-23278000	Weak transcription	Brain Cingulate Gyrus	brain
19	chr3:23275000-23280800	Weak transcription	Brain Anterior Caudate	brain
20	chr3:23276400-23279600	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr3:23276800-23281000	Weak transcription	Fetal Heart	heart
22	chr3:23277000-23279600	Weak transcription	Brain Hippocampus Middle	brain
23	chr3:23277400-23279800	Weak transcription	Psoas Muscle	Psoas
24	chr3:23277400-23280800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr3:23277800-23278400	Enhancers	Primary hematopoietic stem cells	blood
26	chr3:23277800-23278400	Enhancers	Brain Substantia Nigra	brain
27	chr3:23277800-23278400	Enhancers	Fetal Lung	lung
28	chr3:23277800-23278600	Enhancers	Fetal Thymus	thymus
29	chr3:23277800-23278800	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr3:23277800-23279200	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr3:23278000-23278400	Enhancers	Brain Cingulate Gyrus	brain
32	chr3:23278000-23278600	Enhancers	Primary B cells from peripheral blood	blood
33	chr3:23278000-23280200	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr3:23278200-23278400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr3:23278200-23278400	Enhancers	Right Ventricle	heart
36	chr3:23278200-23278600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr3:23278200-23278600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr3:23278200-23278600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr3:23278200-23278600	Enhancers	Adipose Nuclei	Adipose
40	chr3:23278200-23278600	Enhancers	Brain Angular Gyrus	brain
41	chr3:23278200-23278800	Enhancers	Left Ventricle	heart
42	chr3:23278200-23279000	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr3:23278200-23279200	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr3:23278400-23279800	Weak transcription	Brain Substantia Nigra	brain
45	chr3:23278400-23280000	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr3:23278400-23280000	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr3:23278400-23280800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr3:23278400-23280800	Weak transcription	Brain Cingulate Gyrus	brain
49	chr3:23278600-23279800	Weak transcription	Primary B cells from peripheral blood	blood
50	chr3:23278600-23279800	Weak transcription	Brain Angular Gyrus	brain

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