Variant report

Variant	nsv1023537
Chromosome Location	chr5:179791679-179982822
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2374)
CpG islands
(count:2139)
Chromatin interactive
region (count:167)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2374 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:179942463-179942560	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:179975587-179975877	K562	blood:	n/a	n/a
3	ARID3A	chr5:179839178-179839187	K562	blood:	n/a	n/a
4	ARID3A	chr5:179920256-179920489	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:179978584-179978636	K562	blood:	n/a	n/a
6	ARID3A	chr5:179921098-179921441	K562	blood:	n/a	n/a
7	ARID3A	chr5:179982176-179983500	K562	blood:	n/a	n/a
8	ARID3A	chr5:179980269-179980947	K562	blood:	n/a	n/a
9	ARID3A	chr5:179921113-179921482	HepG2	liver:	n/a	n/a
10	ATF1	chr5:179982258-179982960	K562	blood:	n/a	n/a
11	ATF1	chr5:179980451-179980815	K562	blood:	n/a	n/a
12	ATF2	chr5:179921005-179921489	GM12878	blood:	n/a	n/a
13	ATF2	chr5:179966866-179967742	GM12878	blood:	n/a	n/a
14	BACH1	chr5:179897963-179898282	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr5:179975564-179975823	K562	blood:	n/a	n/a
16	BACH1	chr5:179921849-179922049	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr5:179928420-179928427	K562	blood:	n/a	n/a
18	BATF	chr5:179920672-179920856	GM12878	blood:	n/a	n/a
19	BATF	chr5:179967271-179967670	GM12878	blood:	n/a	chr5:179967376-179967387
20	BATF	chr5:179794267-179794718	GM12878	blood:	n/a	n/a
21	BATF	chr5:179794372-179794604	GM12878	blood:	n/a	n/a
22	BATF	chr5:179967060-179967643	GM12878	blood:	n/a	chr5:179967376-179967387
23	BCL11A	chr5:179794291-179794620	GM12878	blood:	n/a	n/a
24	BCL11A	chr5:179967329-179967703	GM12878	blood:	n/a	n/a
25	BCL11A	chr5:179967330-179967536	GM12878	blood:	n/a	n/a
26	BCL3	chr5:179954713-179954975	GM12878	blood:	n/a	n/a
27	BCL3	chr5:179920971-179921485	A549	lung:	n/a	chr5:179921385-179921398
28	BCL3	chr5:179954691-179955054	GM12878	blood:	n/a	n/a
29	BCL3	chr5:179792018-179792284	GM12878	blood:	n/a	n/a
30	BCL3	chr5:179920888-179921352	A549	lung:	n/a	n/a
31	BCL3	chr5:179896707-179896968	GM12878	blood:	n/a	n/a
32	BCL3	chr5:179894036-179894564	A549	lung:	n/a	chr5:179894213-179894222
33	BCL3	chr5:179868437-179868959	A549	lung:	n/a	n/a
34	BCLAF1	chr5:179920923-179921525	GM12878	blood:	n/a	chr5:179921385-179921398
35	BCLAF1	chr5:179967270-179967735	GM12878	blood:	n/a	n/a
36	BHLHE40	chr5:179971806-179971955	K562	blood:	n/a	n/a
37	BHLHE40	chr5:179817911-179818150	K562	blood:	n/a	n/a
38	BHLHE40	chr5:179921030-179921507	K562	blood:	n/a	chr5:179921201-179921217 chr5:179921352-179921368
39	BHLHE40	chr5:179975467-179975475	K562	blood:	n/a	n/a
40	BHLHE40	chr5:179921070-179921448	A549	lung:	n/a	chr5:179921201-179921217 chr5:179921352-179921368
41	BHLHE40	chr5:179891686-179891866	HepG2	liver:	n/a	n/a
42	BHLHE40	chr5:179967103-179967608	GM12878	blood:	n/a	n/a
43	BHLHE40	chr5:179921021-179921760	HepG2	liver:	n/a	chr5:179921201-179921217 chr5:179921352-179921368
44	BHLHE40	chr5:179898034-179898300	K562	blood:	n/a	n/a
45	BHLHE40	chr5:179921026-179921502	GM12878	blood:	n/a	chr5:179921201-179921217 chr5:179921352-179921368
46	BHLHE40	chr5:179975767-179975857	K562	blood:	n/a	n/a
47	BHLHE40	chr5:179982128-179982802	K562	blood:	n/a	n/a
48	BRCA1	chr5:179921108-179921449	HepG2	liver:	n/a	n/a
49	BRCA1	chr5:179921129-179921385	GM12878	blood:	n/a	n/a
50	BRCA1	chr5:179868488-179868947	Hela-S3	cervix:	n/a	n/a

(count:2139 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:179920971-179921021	AG04449	skin:	fetal
2	chr5:179958483-179958533	Hepatocyte	liver:	n/a
3	chr5:179921286-179921336	LNCaP	prostate:	n/a
4	chr5:179958313-179958363	AoSMC	blood vessel:	n/a
5	chr5:179920971-179921021	AG04449	skin:	fetal
6	chr5:179958483-179958533	Hepatocyte	liver:	n/a
7	chr5:179921286-179921336	LNCaP	prostate:	n/a
8	chr5:179958313-179958363	AoSMC	blood vessel:	n/a
9	chr5:179961652-179961702	AG09309	skin:	n/a
10	chr5:179920202-179920252	Caco-2	colon:	n/a
11	chr5:179886241-179886291	LNCaP	prostate:	n/a
12	chr5:179918462-179918512	PANC-1	pancreas:	n/a
13	chr5:179958483-179958533	SK-N-MC	brain:	n/a
14	chr5:179922339-179922389	Hela-S3	cervix:	n/a
15	chr5:179958313-179958363	NHBE	bronchial:	n/a
16	chr5:179921349-179921399	ovcar-3	ovarian:	n/a
17	chr5:179859344-179859394	PFSK-1	brain:	n/a
18	chr5:179921426-179921476	HEEpiC	esophagus:	n/a
19	chr5:179962105-179962155	HPAEpiC	pulmonary alveolar:	n/a
20	chr5:179921670-179921720	NB4	blood:	n/a
21	chr5:179922147-179922197	HCPEpiC	choroid plexus:	n/a
22	chr5:179958313-179958363	Hela-S3	cervix:	n/a
23	chr5:179806865-179806915	IMR90	lung:	fetal
24	chr5:179806747-179806797	HCT-116	colon:	n/a
25	chr5:179920202-179920252	MCF10A-Er-Src	breast:	n/a
26	chr5:179958313-179958363	PFSK-1	brain:	n/a
27	chr5:179886642-179886692	H1-hESC	embryonic stem cell:	embryo
28	chr5:179962105-179962155	NH-A	brain:	n/a
29	chr5:179816503-179816553	HCPEpiC	choroid plexus:	n/a
30	chr5:179921286-179921336	HCPEpiC	choroid plexus:	n/a
31	chr5:179813829-179813879	HMEC	breast:	n/a
32	chr5:179921670-179921720	H1-hESC	embryonic stem cell:	embryo
33	chr5:179921655-179921705	K562	blood:	n/a
34	chr5:179920971-179921021	Hepatocyte	liver:	n/a
35	chr5:179921670-179921720	HIPEpiC	eye:	n/a
36	chr5:179921286-179921336	H1-hESC	embryonic stem cell:	embryo
37	chr5:179868587-179868637	HCF	heart:	n/a
38	chr5:179859512-179859562	GM06990	blood:	n/a
39	chr5:179920582-179920632	HL-60	blood:	n/a
40	chr5:179815975-179816025	Hepatocyte	liver:	n/a
41	chr5:179806865-179806915	HepG2	liver:	n/a
42	chr5:179958313-179958363	NB4	blood:	n/a
43	chr5:179962105-179962155	A549	lung:	n/a
44	chr5:179922147-179922197	ovcar-3	ovarian:	n/a
45	chr5:179922147-179922197	GM12892	blood:	n/a
46	chr5:179921704-179921754	U87	brain:	n/a
47	chr5:179815975-179816025	MCF-7	breast:	n/a
48	chr5:179859344-179859394	HL-60	blood:	n/a
49	chr5:179886241-179886291	CMK	blood:	n/a
50	chr5:179918462-179918512	HIPEpiC	eye:	n/a

(count:167 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr12:120730813..120731447-chr5:179921399..179922129,2	Hela-S3	cervix:
2	chr5:179817994..179819684-chr5:179863109..179865015,2	MCF-7	breast:
3	chr5:179943961..179945573-chr5:179952586..179955313,2	MCF-7	breast:
4	chr5:179718174..179720847-chr5:179898001..179899613,2	MCF-7	breast:
5	chr5:179890341..179892861-chr5:179894283..179898100,3	MCF-7	breast:
6	chr5:179928152..179929958-chr6:152022823..152024616,2	MCF-7	breast:
7	chr5:179920138..179923580-chr5:179954774..179958751,3	MCF-7	breast:
8	chr5:179778666..179781236-chr5:179881517..179884187,2	MCF-7	breast:
9	chr5:179720197..179721174-chr5:179911166..179912161,9	MCF-7	breast:
10	chr5:179954302..179955834-chr5:179973302..179975583,2	K562	blood:
11	chr5:179776807..179778775-chr5:179896611..179898165,2	MCF-7	breast:
12	chr3:158973363..158973863-chr5:179971569..179972230,2	MCF-7	breast:
13	chr5:179892192..179893698-chr5:179898781..179900873,2	MCF-7	breast:
14	chr5:179909233..179911875-chr5:179913971..179916434,2	MCF-7	breast:
15	chr5:179850803..179853162-chr5:179854967..179857524,2	K562	blood:
16	chr5:179850450..179853162-chr5:179855103..179857524,2	K562	blood:
17	chr5:179719269..179721828-chr5:179910236..179912739,3	MCF-7	breast:
18	chr15:40226287..40226791-chr5:179921184..179922100,2	Hela-S3	cervix:
19	chr5:179720229..179721221-chr5:179897697..179898870,4	K562	blood:
20	chr5:179933515..179935509-chr5:179936709..179938826,2	K562	blood:
21	chr5:179887683..179889324-chr5:179889418..179891911,2	K562	blood:
22	chr5:179946293..179947943-chr5:179949478..179951199,2	MCF-7	breast:
23	chr5:179627973..179628851-chr5:179897510..179898199,3	K562	blood:
24	chr19:13263786..13264489-chr5:179894149..179895088,2	Hela-S3	cervix:
25	chr5:179850803..179853162-chr5:179854967..179857524,2	K562	blood:
26	chr5:179841196..179841781-chr5:179897664..179898357,3	MCF-7	breast:
27	chr5:179770572..179772662-chr5:179890635..179892698,2	MCF-7	breast:
28	chr5:179934009..179936437-chr5:179937326..179939535,2	K562	blood:
29	chr5:179909233..179911875-chr5:179913971..179916434,2	MCF-7	breast:
30	chr5:179744163..179746642-chr5:179892937..179895669,2	MCF-7	breast:
31	chr5:179932250..179934206-chr5:179936886..179939142,2	MCF-7	breast:
32	chr5:179923854..179927597-chr5:179974532..179977818,3	MCF-7	breast:
33	chr5:179946293..179947943-chr5:179949478..179951199,2	MCF-7	breast:
34	chr5:179773523..179775138-chr5:179800257..179803108,2	MCF-7	breast:
35	chr5:179795278..179797772-chr5:179803121..179806060,2	MCF-7	breast:
36	chr5:179742474..179743351-chr5:179897684..179898604,3	MCF-7	breast:
37	chr5:179922992..179929395-chr5:179931202..179936163,8	K562	blood:
38	chr5:179920260..179922999-chr5:180038598..180040134,2	MCF-7	breast:
39	chr5:179778332..179781251-chr5:179920436..179923318,3	MCF-7	breast:
40	chr5:179718171..179722134-chr5:179892968..179897954,8	MCF-7	breast:
41	chr5:179817994..179819684-chr5:179863109..179865015,2	MCF-7	breast:
42	chr5:179910027..179911879-chr5:179947833..179949549,2	MCF-7	breast:
43	chr5:179804942..179807127-chr5:179808323..179810526,2	K562	blood:
44	chr5:179805841..179808763-chr5:179880689..179883410,2	MCF-7	breast:
45	chr5:179896623..179899135-chr5:179900474..179902036,2	MCF-7	breast:
46	chr5:179933515..179935509-chr5:179936709..179938826,2	K562	blood:
47	chr5:179756438..179759576-chr5:179909239..179913349,3	MCF-7	breast:
48	chr5:179897206..179899731-chr5:179901883..179904757,4	K562	blood:
49	chr5:179803275..179805488-chr5:179810021..179812217,2	MCF-7	breast:
50	chr5:179951729..179953788-chr5:179957919..179959696,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNOT6-1	chr5:179910115-179910503	XLOC_004680
2	lnc-CNOT6-2	chr5:179868559-179868855	XLOC_004679
3	lnc-CNOT6-2	chr5:179869730-179870238	XLOC_004679
4	lnc-CNOT6-1	chr5:179894886-179895269	XLOC_004680

No data

Variant related genes	Relation type
CNOT6	TF binding region
ENSG00000250749	TF binding region
RNU6-525P	TF binding region
ENSG00000250509	TF binding region
CNOT6	CpG island
ENSG00000250749	CpG island
RNU6-525P	CpG island
ENSG00000250509	CpG island
ENSG00000042753	chromatin interactions
ENSG00000237310	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000050748	chromatin interactions
ENSG00000100084	chromatin interactions
ENSG00000185065	chromatin interactions
ENSG00000131459	chromatin interactions
ENSG00000248367	chromatin interactions
ENSG00000113300	chromatin interactions
ENSG00000128829	chromatin interactions
ENSG00000242259	chromatin interactions
ENSG00000250509	chromatin interactions
ENSG00000037280	chromatin interactions
ENSG00000223473	chromatin interactions
ATXN1L	miRNA target sites
ATXN7	miRNA target sites

Extended variants
information (count: 7603 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:7603 , 50 per page) page: 1 2 3 4 5 6 7 ... 153

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116129986	chr5:179791679-179791680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs138632176	chr5:179791682-179791683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185303226	chr5:179791702-179791703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551004407	chr5:179791731-179791732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568835247	chr5:179791788-179791789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568833932	chr5:179791803-179791804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs6880102	chr5:179791869-179791870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs56915030	chr5:179791894-179791895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs79074858	chr5:179791897-179791898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553544533	chr5:179791901-179791902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576628873	chr5:179791908-179791909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs142912876	chr5:179792037-179792038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537776138	chr5:179792073-179792074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562466391	chr5:179792103-179792104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554682422	chr5:179792118-179792119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576316520	chr5:179792150-179792151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574494215	chr5:179792164-179792165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs35352523	chr5:179792172-179792173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs33923889	chr5:179792173-179792174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs77917439	chr5:179792244-179792245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562153584	chr5:179792269-179792270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372937008	chr5:179792277-179792278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527780884	chr5:179792289-179792290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146999487	chr5:179792313-179792314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs564630622	chr5:179792350-179792351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533580841	chr5:179792356-179792357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs550466137	chr5:179792436-179792437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570342255	chr5:179792444-179792445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs76760530	chr5:179792477-179792478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547865305	chr5:179792523-179792524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568092312	chr5:179792551-179792552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368575491	chr5:179792578-179792579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533603014	chr5:179792583-179792584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553458436	chr5:179792586-179792587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570285672	chr5:179792599-179792600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557022904	chr5:179792617-179792618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs117821613	chr5:179792647-179792648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555977218	chr5:179792653-179792654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7721160	chr5:179792683-179792684	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs546055387	chr5:179792698-179792699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542154097	chr5:179792733-179792734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562877358	chr5:179792765-179792766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373102843	chr5:179792766-179792767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555429350	chr5:179792778-179792779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572414188	chr5:179792807-179792808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573897704	chr5:179792810-179792811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576006417	chr5:179792830-179792831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564592474	chr5:179792838-179792839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112742655	chr5:179792849-179792850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7704690	chr5:179792855-179792856	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
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
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
small cell lung cancer	20016488	CNVD
Autism	22543975	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:2866 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179790400-179793200	Weak transcription	Fetal Muscle Leg	muscle
2	chr5:179790400-179796400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr5:179790600-179799000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr5:179793000-179793200	Enhancers	Osteobl	bone
5	chr5:179793000-179793600	Enhancers	Brain Anterior Caudate	brain
6	chr5:179793000-179793800	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr5:179793000-179794200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr5:179793000-179794200	Enhancers	HSMMtube	muscle
9	chr5:179793000-179795400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr5:179793000-179795600	Enhancers	Brain Cingulate Gyrus	brain
11	chr5:179793000-179795600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
12	chr5:179793000-179795600	Enhancers	Brain Substantia Nigra	brain
13	chr5:179793200-179793400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr5:179793200-179793400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr5:179793200-179793400	Enhancers	Brain Angular Gyrus	brain
16	chr5:179793200-179793600	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr5:179793200-179793600	Enhancers	Muscle Satellite Cultured Cells	--
18	chr5:179793200-179793600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr5:179793200-179793600	Enhancers	Fetal Muscle Leg	muscle
20	chr5:179793200-179793600	Enhancers	Placenta	Placenta
21	chr5:179793200-179793600	Enhancers	HSMM	muscle
22	chr5:179793200-179793600	Flanking Active TSS	Osteobl	bone
23	chr5:179793200-179794000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr5:179793200-179794200	Enhancers	Fetal Muscle Trunk	muscle
25	chr5:179793200-179795000	Enhancers	Primary T cells fromperipheralblood	blood
26	chr5:179793200-179796200	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr5:179793200-179796400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr5:179793200-179796400	Enhancers	Brain Hippocampus Middle	brain
29	chr5:179793400-179793600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr5:179793400-179793600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr5:179793400-179793600	Flanking Active TSS	Stomach Smooth Muscle	stomach
32	chr5:179793400-179794600	Weak transcription	Brain Angular Gyrus	brain
33	chr5:179793600-179793800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr5:179793600-179793800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr5:179793600-179793800	Enhancers	Osteobl	bone
36	chr5:179793600-179794000	Weak transcription	Brain Anterior Caudate	brain
37	chr5:179793600-179794800	Weak transcription	Fetal Muscle Leg	muscle
38	chr5:179793600-179797400	Weak transcription	Placenta	Placenta
39	chr5:179793600-179797400	Weak transcription	HSMM	muscle
40	chr5:179793600-179797800	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr5:179793800-179795600	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr5:179794000-179794800	Enhancers	Brain Anterior Caudate	brain
43	chr5:179794000-179795000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr5:179794000-179795600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr5:179794200-179794600	Weak transcription	Fetal Muscle Trunk	muscle
46	chr5:179794200-179797400	Weak transcription	HSMMtube	muscle
47	chr5:179794600-179795600	Enhancers	Brain Angular Gyrus	brain
48	chr5:179794600-179796200	Enhancers	Fetal Muscle Trunk	muscle
49	chr5:179794800-179795200	Flanking Active TSS	Brain Anterior Caudate	brain
50	chr5:179794800-179795400	Enhancers	Fetal Muscle Leg	muscle

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