Variant report

Variant	nsv883238
Chromosome Location	chr5:178722356-178796142
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:603)
CpG islands
(count:2323)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:603 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:178729527-178729868	K562	blood:	n/a	n/a
2	ATF2	chr5:178753597-178754030	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr5:178763657-178763929	K562	blood:	n/a	n/a
4	BACH1	chr5:178770779-178771405	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr5:178782018-178782023	K562	blood:	n/a	n/a
6	BACH1	chr5:178753623-178753861	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr5:178746298-178746633	GM12878	blood:	n/a	n/a
8	BCL3	chr5:178746077-178746614	GM12878	blood:	n/a	n/a
9	BHLHE40	chr5:178722893-178723057	K562	blood:	n/a	chr5:178723031-178723040 chr5:178723031-178723040
10	BHLHE40	chr5:178763708-178763938	K562	blood:	n/a	n/a
11	BRCA1	chr5:178754565-178754676	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr5:178729517-178729803	K562	blood:	n/a	n/a
13	CCNT2	chr5:178772466-178772783	K562	blood:	n/a	n/a
14	CCNT2	chr5:178771882-178771973	K562	blood:	n/a	n/a
15	CEBPB	chr5:178789476-178789561	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr5:178780118-178780254	K562	blood:	n/a	n/a
17	CEBPB	chr5:178786162-178786480	Hela-S3	cervix:	n/a	chr5:178786328-178786339
18	CEBPB	chr5:178749384-178749670	IMR90	lung:	n/a	n/a
19	CEBPB	chr5:178783645-178783928	A549	lung:	n/a	chr5:178783766-178783775 chr5:178783815-178783826 chr5:178783813-178783824 chr5:178783865-178783878 chr5:178783765-178783776
20	CEBPB	chr5:178786289-178786460	HepG2	liver:	n/a	chr5:178786328-178786339
21	CEBPB	chr5:178783725-178783925	K562	blood:	n/a	chr5:178783766-178783775 chr5:178783815-178783826 chr5:178783813-178783824 chr5:178783865-178783878 chr5:178783765-178783776
22	CEBPB	chr5:178771987-178772057	IMR90	lung:	n/a	n/a
23	CEBPB	chr5:178734831-178734994	HepG2	liver:	n/a	n/a
24	CEBPB	chr5:178791997-178792197	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr5:178783625-178783949	HepG2	liver:	n/a	chr5:178783766-178783775 chr5:178783815-178783826 chr5:178783813-178783824 chr5:178783865-178783878 chr5:178783765-178783776
26	CEBPB	chr5:178786252-178786390	K562	blood:	n/a	chr5:178786328-178786339
27	CEBPB	chr5:178786316-178786363	A549	lung:	n/a	chr5:178786328-178786339
28	CEBPB	chr5:178780036-178780236	IMR90	lung:	n/a	n/a
29	CEBPB	chr5:178783581-178783974	IMR90	lung:	n/a	chr5:178783766-178783775 chr5:178783815-178783826 chr5:178783813-178783824 chr5:178783865-178783878 chr5:178783765-178783776
30	CEBPB	chr5:178783646-178783964	Hela-S3	cervix:	n/a	chr5:178783766-178783775 chr5:178783815-178783826 chr5:178783813-178783824 chr5:178783865-178783878 chr5:178783765-178783776
31	CEBPB	chr5:178731436-178731883	IMR90	lung:	n/a	n/a
32	CHD1	chr5:178769622-178773044	IMR90	lung:	n/a	chr5:178772444-178772454
33	CHD1	chr5:178771062-178771490	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chr5:178771804-178771970	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr5:178771048-178771541	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr5:178729729-178729764	K562	blood:	n/a	n/a
37	CHD2	chr5:178772523-178772566	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr5:178729457-178729948	K562	blood:	n/a	n/a
39	CTBP2	chr5:178772320-178773389	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTBP2	chr5:178770889-178772047	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr5:178770620-178770770	HPF	lung:	n/a	n/a
42	CTCF	chr5:178789480-178789630	SK-N-SH_RA	brain:	n/a	chr5:178789556-178789572
43	CTCF	chr5:178771080-178771230	HRE	kidney:	n/a	n/a
44	CTCF	chr5:178770980-178771130	HAc	cerebellar:	n/a	n/a
45	CTCF	chr5:178769740-178769890	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr5:178771029-178771207	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr5:178769800-178769950	HCPEpiC	choroid plexus:	n/a	chr5:178769882-178769895
48	CTCF	chr5:178771060-178771210	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr5:178741380-178741530	AG10803	skin:	n/a	n/a
50	CTCF	chr5:178771167-178771168	GM19238	blood:	n/a	n/a

(count:2323 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178767472-178767522	GM12891	blood:	n/a
2	chr5:178772390-178772440	BJ	skin:	n/a
3	chr5:178770998-178771048	PFSK-1	brain:	n/a
4	chr5:178772385-178772435	NH-A	brain:	n/a
5	chr5:178763419-178763469	CMK	blood:	n/a
6	chr5:178767472-178767522	GM12891	blood:	n/a
7	chr5:178772390-178772440	BJ	skin:	n/a
8	chr5:178770998-178771048	PFSK-1	brain:	n/a
9	chr5:178772385-178772435	NH-A	brain:	n/a
10	chr5:178763419-178763469	CMK	blood:	n/a
11	chr5:178736443-178736493	HRE	kidney:	n/a
12	chr5:178775192-178775242	A549	lung:	n/a
13	chr5:178772793-178772843	SAEC	small airway:	n/a
14	chr5:178748193-178748243	HepG2	liver:	n/a
15	chr5:178771781-178771831	HEK293	kidney:	embryo
16	chr5:178763771-178763821	H1-hESC	embryonic stem cell:	embryo
17	chr5:178735372-178735422	MCF10A-Er-Src	breast:	n/a
18	chr5:178772969-178773019	ProgFib	skin:	n/a
19	chr5:178772390-178772440	SKMC	muscle:	n/a
20	chr5:178772203-178772253	HNPCEpiC	eye:	n/a
21	chr5:178781563-178781613	HAEpiC	amniotic membrane:	n/a
22	chr5:178763419-178763469	HCF	heart:	n/a
23	chr5:178784097-178784147	Caco-2	colon:	n/a
24	chr5:178735372-178735422	U87	brain:	n/a
25	chr5:178772782-178772832	Caco-2	colon:	n/a
26	chr5:178772390-178772440	HEEpiC	esophagus:	n/a
27	chr5:178759017-178759067	NHBE	bronchial:	n/a
28	chr5:178781563-178781613	SK-N-SH	brain:	n/a
29	chr5:178775192-178775242	NH-A	brain:	n/a
30	chr5:178722726-178722776	HCPEpiC	choroid plexus:	n/a
31	chr5:178772782-178772832	PFSK-1	brain:	n/a
32	chr5:178771329-178771379	AG04450	lung:	fetal
33	chr5:178789651-178789701	HMEC	breast:	n/a
34	chr5:178741205-178741255	GM12891	blood:	n/a
35	chr5:178772203-178772253	H1-hESC	embryonic stem cell:	embryo
36	chr5:178776021-178776071	HCF	heart:	n/a
37	chr5:178781563-178781613	SKMC	muscle:	n/a
38	chr5:178789651-178789701	SKMC	muscle:	n/a
39	chr5:178771393-178771443	U87	brain:	n/a
40	chr5:178776021-178776071	AG10803	skin:	n/a
41	chr5:178784097-178784147	NT2-D1	testis:	n/a
42	chr5:178770998-178771048	HCPEpiC	choroid plexus:	n/a
43	chr5:178772385-178772435	AG04450	lung:	fetal
44	chr5:178773355-178773405	LNCaP	prostate:	n/a
45	chr5:178735241-178735291	HMEC	breast:	n/a
46	chr5:178771781-178771831	HMEC	breast:	n/a
47	chr5:178775192-178775242	NB4	blood:	n/a
48	chr5:178735241-178735291	HCT-116	colon:	n/a
49	chr5:178748193-178748243	ProgFib	skin:	n/a
50	chr5:178781563-178781613	HNPCEpiC	eye:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:178719721..178723694-chr5:178743933..178746463,3	K562	blood:
2	chr5:178793109..178796105-chr5:179125384..179128079,2	K562	blood:
3	chr5:178719721..178723694-chr5:178743933..178746463,3	K562	blood:
4	chr5:178748584..178750238-chr5:178758412..178760319,2	MCF-7	breast:
5	chr5:178770291..178772174-chr5:178775649..178777213,2	MCF-7	breast:
6	chr5:178763364..178765890-chr5:178804717..178806886,2	K562	blood:
7	chr5:178751231..178753197-chr5:178755873..178757949,2	MCF-7	breast:
8	chr5:178762053..178764261-chr5:178817559..178819340,2	K562	blood:
9	chr5:178751231..178753197-chr5:178755873..178757949,2	MCF-7	breast:
10	chr5:178780858..178782954-chr5:178784606..178786505,2	MCF-7	breast:
11	chr5:178774195..178776525-chr5:178779659..178783563,3	K562	blood:
12	chr5:178795348..178797290-chr5:178808669..178810729,2	K562	blood:
13	chr5:178774195..178776525-chr5:178779659..178783563,3	K562	blood:
14	chr5:178780858..178782954-chr5:178784606..178786505,2	MCF-7	breast:
15	chr5:178786828..178788661-chr5:178798258..178800552,2	K562	blood:
16	chr5:178748584..178750238-chr5:178758412..178760319,2	MCF-7	breast:
17	chr5:178770291..178772174-chr5:178775649..178777213,2	MCF-7	breast:

No data

Variant related genes	Relation type
ADAMTS2	TF binding region
ADAMTS2	CpG island
ENSG00000127022	chromatin interactions
ENSG00000253163	chromatin interactions

Extended variants
information (count: 3605 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:3605 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6874467	chr5:178722356-178722357	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs369378351	chr5:178722362-178722363	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs145931736	chr5:178722368-178722369	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs532903888	chr5:178722390-178722391	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs190383552	chr5:178722395-178722396	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs571025921	chr5:178722399-178722400	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs405302	chr5:178722432-178722433	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs138120182	chr5:178722495-178722496	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs568629755	chr5:178722531-178722532	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs536135665	chr5:178722532-178722533	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs554244468	chr5:178722536-178722537	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs145187935	chr5:178722584-178722585	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs546366317	chr5:178722585-178722586	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs557919444	chr5:178722610-178722611	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs115290436	chr5:178722637-178722638	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs543219156	chr5:178722638-178722639	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs561897244	chr5:178722661-178722662	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs529183233	chr5:178722666-178722667	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs540915753	chr5:178722689-178722690	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs467340	chr5:178722698-178722699	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs457659	chr5:178722700-178722701	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs532720373	chr5:178722724-178722725	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs76111681	chr5:178722727-178722728	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs182596897	chr5:178722736-178722737	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs531953862	chr5:178722778-178722779	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs168147	chr5:178722820-178722821	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs550136943	chr5:178722831-178722832	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs466617	chr5:178722833-178722834	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs186884766	chr5:178722852-178722853	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs377046059	chr5:178722856-178722857	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs458267	chr5:178722869-178722870	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs192595820	chr5:178722892-178722893	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs566085277	chr5:178722894-178722895	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs75848657	chr5:178722898-178722899	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs111916091	chr5:178722917-178722918	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs546836111	chr5:178722932-178722933	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs371445870	chr5:178722965-178722966	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs576433376	chr5:178722998-178722999	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs73808248	chr5:178723042-178723043	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs566648631	chr5:178723047-178723048	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs539168549	chr5:178723069-178723070	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs561991023	chr5:178723081-178723082	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs540926395	chr5:178723082-178723083	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs559181159	chr5:178723093-178723094	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs111945621	chr5:178723105-178723106	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs142179203	chr5:178723132-178723133	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs183930844	chr5:178723136-178723137	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs530555519	chr5:178723139-178723140	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs549053832	chr5:178723146-178723147	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs562316911	chr5:178723235-178723236	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
small cell lung cancer	20016488	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1681 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178713400-178727200	Weak transcription	NHLF	lung
2	chr5:178715800-178722400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr5:178716000-178722800	Weak transcription	Spleen	Spleen
4	chr5:178716200-178730800	Weak transcription	HSMM	muscle
5	chr5:178717200-178724400	Weak transcription	Ovary	ovary
6	chr5:178718200-178722400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr5:178718200-178725000	Weak transcription	Gastric	stomach
8	chr5:178718400-178722800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr5:178719800-178722400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr5:178719800-178722800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr5:178719800-178725200	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr5:178720000-178722400	Enhancers	NHDF-Ad	bronchial
13	chr5:178720000-178726000	Enhancers	Osteobl	bone
14	chr5:178720600-178724200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr5:178720600-178728000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr5:178721200-178722800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr5:178721200-178723400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr5:178721400-178722400	Enhancers	Fetal Brain Male	brain
19	chr5:178721400-178722800	Enhancers	Stomach Smooth Muscle	stomach
20	chr5:178721400-178723000	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr5:178721400-178723600	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr5:178721400-178725200	Enhancers	Fetal Stomach	stomach
23	chr5:178721600-178722800	Enhancers	Duodenum Smooth Muscle	Duodenum
24	chr5:178721600-178723000	Enhancers	Fetal Brain Female	brain
25	chr5:178721600-178723200	Enhancers	Colon Smooth Muscle	Colon
26	chr5:178721600-178723800	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr5:178721600-178724600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr5:178721800-178722400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr5:178721800-178722600	Enhancers	Fetal Muscle Leg	muscle
30	chr5:178721800-178723000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr5:178721800-178723000	Enhancers	Rectal Smooth Muscle	rectum
32	chr5:178721800-178725200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr5:178721800-178725400	Enhancers	Adipose Nuclei	Adipose
34	chr5:178722000-178722600	Weak transcription	Fetal Lung	lung
35	chr5:178722000-178722800	Enhancers	Right Atrium	heart
36	chr5:178722000-178722800	Enhancers	Right Ventricle	heart
37	chr5:178722000-178723000	Enhancers	Brain Germinal Matrix	brain
38	chr5:178722200-178722400	Enhancers	Fetal Intestine Small	intestine
39	chr5:178722200-178723000	Enhancers	Colonic Mucosa	Colon
40	chr5:178722200-178723600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr5:178722400-178723000	Enhancers	Placenta Amnion	Placenta Amnion
42	chr5:178722400-178723200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr5:178722400-178723600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr5:178722400-178723600	Weak transcription	Fetal Brain Male	brain
45	chr5:178722400-178724200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr5:178722400-178727200	Weak transcription	NHDF-Ad	bronchial
47	chr5:178722600-178723200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
48	chr5:178722600-178723200	Bivalent Enhancer	Fetal Muscle Leg	muscle
49	chr5:178722600-178725200	Enhancers	Fetal Lung	lung
50	chr5:178722800-178723200	Enhancers	Pancreas	Pancrea

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