Variant report

Variant	nsv948613
Chromosome Location	chr5:119861955-119999008
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:820)
CpG islands
(count:244)
Chromatin interactive
region (count:40)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:820 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:119899838-119899993	K562	blood:	n/a	n/a
2	BACH1	chr5:119959300-119959328	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr5:119991637-119991644	K562	blood:	n/a	n/a
4	BRCA1	chr5:119974391-119974481	GM12878	blood:	n/a	n/a
5	BRCA1	chr5:119940521-119941137	Hela-S3	cervix:	n/a	n/a
6	CCNT2	chr5:119868130-119868256	K562	blood:	n/a	n/a
7	CCNT2	chr5:119927724-119927859	K562	blood:	n/a	n/a
8	CCNT2	chr5:119891204-119891275	K562	blood:	n/a	n/a
9	CEBPB	chr5:119935306-119935685	IMR90	lung:	n/a	n/a
10	CEBPB	chr5:119977079-119977372	H1-hESC	embryonic stem cell:	n/a	chr5:119977215-119977226
11	CEBPB	chr5:119935239-119935784	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr5:119993776-119994043	HepG2	liver:	n/a	chr5:119993879-119993890
13	CEBPB	chr5:119940538-119941604	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr5:119931729-119931789	A549	lung:	n/a	n/a
15	CEBPB	chr5:119937773-119938120	IMR90	lung:	n/a	chr5:119937940-119937951
16	CEBPB	chr5:119951672-119952058	Hela-S3	cervix:	n/a	chr5:119951865-119951878
17	CEBPB	chr5:119977083-119977356	IMR90	lung:	n/a	chr5:119977215-119977226
18	CEBPB	chr5:119977093-119977344	A549	lung:	n/a	chr5:119977215-119977226
19	CEBPB	chr5:119955906-119956141	HepG2	liver:	n/a	chr5:119956004-119956015
20	CEBPB	chr5:119864238-119864636	IMR90	lung:	n/a	chr5:119864549-119864562 chr5:119864549-119864562
21	CEBPB	chr5:119981493-119981734	HepG2	liver:	n/a	chr5:119981633-119981644
22	CEBPB	chr5:119908492-119908611	IMR90	lung:	n/a	n/a
23	CEBPB	chr5:119864268-119864570	K562	blood:	n/a	chr5:119864549-119864562 chr5:119864549-119864562
24	CEBPB	chr5:119937909-119937973	A549	lung:	n/a	chr5:119937940-119937951
25	CEBPB	chr5:119977083-119977287	K562	blood:	n/a	chr5:119977215-119977226
26	CEBPB	chr5:119984469-119984716	HepG2	liver:	n/a	n/a
27	CEBPB	chr5:119959582-119960151	IMR90	lung:	n/a	chr5:119959754-119959765 chr5:119959754-119959767 chr5:119959754-119959767
28	CEBPB	chr5:119936349-119936589	HepG2	liver:	n/a	n/a
29	CEBPB	chr5:119977038-119977401	Hela-S3	cervix:	n/a	chr5:119977215-119977226
30	CEBPB	chr5:119940627-119940974	IMR90	lung:	n/a	n/a
31	CEBPB	chr5:119918081-119918135	HepG2	liver:	n/a	chr5:119918093-119918104
32	CEBPB	chr5:119937786-119938093	HepG2	liver:	n/a	chr5:119937940-119937951
33	CEBPB	chr5:119959643-119959893	Hela-S3	cervix:	n/a	chr5:119959754-119959765 chr5:119959754-119959767 chr5:119959754-119959767
34	CEBPB	chr5:119873912-119874713	IMR90	lung:	n/a	n/a
35	CEBPB	chr5:119945256-119945647	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr5:119955880-119956197	K562	blood:	n/a	chr5:119956004-119956015
37	CEBPB	chr5:119984458-119984709	IMR90	lung:	n/a	n/a
38	CEBPB	chr5:119937714-119938123	Hela-S3	cervix:	n/a	chr5:119937940-119937951
39	CEBPB	chr5:119936395-119936681	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr5:119951673-119952096	IMR90	lung:	n/a	chr5:119951865-119951878
41	CEBPB	chr5:119950210-119950705	IMR90	lung:	n/a	n/a
42	CEBPB	chr5:119937761-119938116	K562	blood:	n/a	chr5:119937940-119937951
43	CEBPB	chr5:119980295-119980384	HepG2	liver:	n/a	chr5:119980319-119980332 chr5:119980319-119980330
44	CEBPB	chr5:119977078-119977396	HepG2	liver:	n/a	chr5:119977215-119977226
45	CHD2	chr5:119940555-119940962	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr5:119991660-119991810	GM12873	blood:	n/a	chr5:119991711-119991729 chr5:119991714-119991723 chr5:119991714-119991727 chr5:119991713-119991734 chr5:119991712-119991728
47	CTCF	chr5:119991680-119991830	AoAF	blood vessel:	n/a	chr5:119991711-119991729 chr5:119991714-119991723 chr5:119991714-119991727 chr5:119991713-119991734 chr5:119991712-119991728
48	CTCF	chr5:119991660-119991810	HPAF	blood vessel:	n/a	chr5:119991711-119991729 chr5:119991714-119991723 chr5:119991714-119991727 chr5:119991713-119991734 chr5:119991712-119991728
49	CTCF	chr5:119912440-119912590	Caco-2	colon:	n/a	n/a
50	CTCF	chr5:119991594-119991854	K562	blood:	n/a	chr5:119991711-119991729 chr5:119991714-119991723 chr5:119991714-119991727 chr5:119991713-119991734 chr5:119991712-119991728

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:119942454-119942504	HEK293	kidney:	embryo
2	chr5:119942454-119942504	ECC-1	luminal epithelium:	n/a
3	chr5:119951527-119951577	BE2_C	brain:	n/a
4	chr5:119942454-119942504	HRE	kidney:	n/a
5	chr5:119864497-119864547	HEK293	kidney:	embryo
6	chr5:119864497-119864547	CMK	blood:	n/a
7	chr5:119951527-119951577	Hela-S3	cervix:	n/a
8	chr5:119952679-119952729	U87	brain:	n/a
9	chr5:119942454-119942504	HPAEpiC	pulmonary alveolar:	n/a
10	chr5:119942454-119942504	AoSMC	blood vessel:	n/a
11	chr5:119942454-119942504	NH-A	brain:	n/a
12	chr5:119864497-119864547	HEEpiC	esophagus:	n/a
13	chr5:119864497-119864547	HCM	heart:	n/a
14	chr5:119942454-119942504	Jurkat	blood:	n/a
15	chr5:119942454-119942504	GM12891	blood:	n/a
16	chr5:119952679-119952729	PFSK-1	brain:	n/a
17	chr5:119864497-119864547	AG10803	skin:	n/a
18	chr5:119952679-119952729	HCPEpiC	choroid plexus:	n/a
19	chr5:119864497-119864547	Hepatocyte	liver:	n/a
20	chr5:119952679-119952729	Hela-S3	cervix:	n/a
21	chr5:119952679-119952729	HEEpiC	esophagus:	n/a
22	chr5:119942454-119942504	PrEC	prostate:	n/a
23	chr5:119942454-119942504	HIPEpiC	eye:	n/a
24	chr5:119864497-119864547	AoSMC	blood vessel:	n/a
25	chr5:119951527-119951577	AG10803	skin:	n/a
26	chr5:119864497-119864547	MCF10A-Er-Src	breast:	n/a
27	chr5:119951527-119951577	GM12878	blood:	n/a
28	chr5:119864497-119864547	GM06990	blood:	n/a
29	chr5:119942454-119942504	HCF	heart:	n/a
30	chr5:119951527-119951577	Hepatocyte	liver:	n/a
31	chr5:119951527-119951577	HCM	heart:	n/a
32	chr5:119864497-119864547	RPTEC	kidney:	n/a
33	chr5:119951527-119951577	HL-60	blood:	n/a
34	chr5:119951527-119951577	NHBE	bronchial:	n/a
35	chr5:119864497-119864547	SAEC	small airway:	n/a
36	chr5:119951527-119951577	HCT-116	colon:	n/a
37	chr5:119864497-119864547	NHDF-neo	bronchial:	n/a
38	chr5:119952679-119952729	LNCaP	prostate:	n/a
39	chr5:119942454-119942504	MCF-7	breast:	n/a
40	chr5:119864497-119864547	HRCEpiC	kidney:	n/a
41	chr5:119951527-119951577	A549	lung:	n/a
42	chr5:119952679-119952729	HUVEC	blood vessel:	n/a
43	chr5:119952679-119952729	GM12878	blood:	n/a
44	chr5:119864497-119864547	HNPCEpiC	eye:	n/a
45	chr5:119952679-119952729	K562	blood:	n/a
46	chr5:119864497-119864547	Caco-2	colon:	n/a
47	chr5:119864497-119864547	GM12891	blood:	n/a
48	chr5:119952679-119952729	HCT-116	colon:	n/a
49	chr5:119952679-119952729	HL-60	blood:	n/a
50	chr5:119951527-119951577	Jurkat	blood:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:119991257..119992549-chr5:121285272..121286241,6	MCF-7	breast:
2	chr5:119877678..119879721-chr5:119882058..119884163,2	K562	blood:
3	chr5:119991277..119991777-chr5:120137719..120138239,2	MCF-7	breast:
4	chr5:119906837..119908623-chr5:119910419..119912812,2	K562	blood:
5	chr5:119990484..119993004-chr5:119995293..119997349,2	K562	blood:
6	chr5:119901221..119903356-chr5:119911285..119913616,2	K562	blood:
7	chr5:119899537..119902283-chr5:119906756..119908959,2	K562	blood:
8	chr5:119858416..119860878-chr5:119871767..119873808,2	K562	blood:
9	chr5:119875090..119877798-chr5:119880363..119881947,2	K562	blood:
10	chr5:119926337..119929229-chr5:119929732..119932370,2	K562	blood:
11	chr5:119877678..119879721-chr5:119882058..119884163,2	K562	blood:
12	chr5:119891736..119894093-chr5:119898854..119902222,3	K562	blood:
13	chr5:119875090..119877798-chr5:119880363..119881947,2	K562	blood:
14	chr5:119980670..119983266-chr5:119989740..119991907,2	K562	blood:
15	chr5:119870688..119872446-chr5:119874411..119876714,2	K562	blood:
16	chr5:119847102..119848643-chr5:119877942..119880653,2	K562	blood:
17	chr5:119866722..119869345-chr5:119872405..119873933,2	K562	blood:
18	chr5:119901221..119903356-chr5:119911285..119913616,2	K562	blood:
19	chr5:119851956..119853481-chr5:119862285..119864209,2	K562	blood:
20	chr5:119991478..119992421-chr5:120138412..120139232,3	MCF-7	breast:
21	chr5:119859163..119862505-chr5:119863189..119865594,3	K562	blood:
22	chr5:119906837..119908623-chr5:119910419..119912812,2	K562	blood:
23	chr5:119933357..119934903-chr5:119957823..119959697,2	K562	blood:
24	chr5:119889111..119891337-chr5:119901156..119903856,2	K562	blood:
25	chr5:119886756..119889709-chr5:119891670..119893322,2	K562	blood:
26	chr5:119851956..119854339-chr5:119862015..119863785,2	K562	blood:
27	chr5:119889111..119891337-chr5:119901156..119903856,2	K562	blood:
28	chr5:119859163..119862505-chr5:119863189..119865594,3	K562	blood:
29	chr5:119980670..119983266-chr5:119989740..119991907,2	K562	blood:
30	chr5:119991420..119991957-chr5:121285300..121286207,2	MCF-7	breast:
31	chr5:119926337..119929229-chr5:119929732..119932370,2	K562	blood:
32	chr5:119990484..119993004-chr5:119995293..119997349,2	K562	blood:
33	chr5:119848883..119851465-chr5:119858913..119862355,3	K562	blood:
34	chr5:119886756..119889709-chr5:119891670..119893322,2	K562	blood:
35	chr5:119870688..119872446-chr5:119874411..119876714,2	K562	blood:
36	chr5:119799492..119801330-chr5:119860595..119862492,2	K562	blood:
37	chr5:119891736..119894093-chr5:119898854..119902222,3	K562	blood:
38	chr5:119849515..119851535-chr5:119903167..119905944,2	K562	blood:
39	chr5:119933357..119934903-chr5:119957823..119959697,2	K562	blood:
40	chr5:119899537..119902283-chr5:119906756..119908959,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LOX-9	chr5:119993772-119994066	NONHSAT103445

No data

Variant related genes	Relation type
PRR16	TF binding region
ENSG00000270741	TF binding region
PRR16	CpG island
ENSG00000270741	CpG island
ENSG00000184838	chromatin interactions

Extended variants
information (count: 5677 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:5677 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs41357149	chr5:119861955-119861956	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs566566276	chr5:119861956-119861957	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs535503506	chr5:119861981-119861982	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs375471514	chr5:119862018-119862019	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150942370	chr5:119862020-119862021	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs553391803	chr5:119862052-119862053	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs10079863	chr5:119862068-119862069	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs10057769	chr5:119862080-119862081	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs557649981	chr5:119862125-119862126	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs6881309	chr5:119862127-119862128	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs546379619	chr5:119862154-119862155	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs532163248	chr5:119862169-119862170	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs528602150	chr5:119862179-119862180	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs575886871	chr5:119862200-119862201	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs189540451	chr5:119862213-119862214	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs73784575	chr5:119862219-119862220	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs530801240	chr5:119862221-119862222	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs114850006	chr5:119862230-119862231	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs570748126	chr5:119862240-119862241	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs533034085	chr5:119862250-119862251	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs140718421	chr5:119862252-119862253	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs182005294	chr5:119862260-119862261	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs113524901	chr5:119862290-119862291	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs184851435	chr5:119862341-119862342	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs535591988	chr5:119862368-119862369	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs75934287	chr5:119862371-119862372	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs558249888	chr5:119862411-119862412	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs150102092	chr5:119862426-119862427	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs546106949	chr5:119862438-119862439	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs558519088	chr5:119862445-119862446	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs138605451	chr5:119862456-119862457	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs557421088	chr5:119862472-119862473	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs577474200	chr5:119862494-119862495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs189226069	chr5:119862499-119862500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540677666	chr5:119862509-119862510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553576234	chr5:119862522-119862523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562813307	chr5:119862538-119862539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541957305	chr5:119862541-119862542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs61393093	chr5:119862596-119862597	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs181853224	chr5:119862624-119862625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs10065202	chr5:119862626-119862627	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs186364836	chr5:119862687-119862688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs112703720	chr5:119862693-119862694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191267700	chr5:119862718-119862719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs566701452	chr5:119862725-119862726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529117214	chr5:119862769-119862770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs35646921	chr5:119862819-119862820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs375677501	chr5:119862845-119862846	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs180923227	chr5:119862882-119862883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs568975530	chr5:119862885-119862886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	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
Breast cancer	21858162	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
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:835 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:119839800-119879800	Weak transcription	Psoas Muscle	Psoas
2	chr5:119844200-119864200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr5:119853200-119863000	Weak transcription	HSMM	muscle
4	chr5:119853400-119864000	Weak transcription	NHDF-Ad	bronchial
5	chr5:119853800-119862800	Weak transcription	HSMMtube	muscle
6	chr5:119854000-119868800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr5:119854600-119864000	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr5:119854600-119864200	Weak transcription	Osteobl	bone
9	chr5:119857400-119864400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr5:119862400-119864600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr5:119862800-119865400	Enhancers	HSMMtube	muscle
12	chr5:119863000-119863200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr5:119863000-119863600	Enhancers	HSMM	muscle
14	chr5:119863200-119864000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr5:119863600-119864200	Weak transcription	HSMM	muscle
16	chr5:119864000-119864600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr5:119864000-119864600	Enhancers	Aorta	Aorta
18	chr5:119864000-119864600	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr5:119864000-119865200	Enhancers	NHDF-Ad	bronchial
20	chr5:119864000-119865400	Enhancers	Muscle Satellite Cultured Cells	--
21	chr5:119864200-119864600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr5:119864200-119865200	Enhancers	HSMM	muscle
23	chr5:119864200-119865400	Enhancers	Osteobl	bone
24	chr5:119864400-119867200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr5:119864600-119866400	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr5:119864600-119871400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr5:119864600-119874200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr5:119864600-119874400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr5:119865200-119865600	Weak transcription	HSMM	muscle
30	chr5:119865200-119867000	Weak transcription	NHDF-Ad	bronchial
31	chr5:119865400-119866400	Weak transcription	HSMMtube	muscle
32	chr5:119865400-119868600	Weak transcription	Osteobl	bone
33	chr5:119865400-119869600	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr5:119865600-119865800	Enhancers	HSMM	muscle
35	chr5:119865800-119874000	Weak transcription	HSMM	muscle
36	chr5:119866200-119867400	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr5:119866400-119867200	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr5:119866400-119867200	Enhancers	HSMMtube	muscle
39	chr5:119866800-119867400	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr5:119867000-119867200	Flanking Bivalent TSS/Enh	Gastric	stomach
41	chr5:119867000-119867200	Enhancers	Left Ventricle	heart
42	chr5:119867000-119867400	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr5:119867000-119867400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr5:119867000-119867400	Enhancers	H1 Cell Line	embryonic stem cell
45	chr5:119867000-119867400	Enhancers	K562	blood
46	chr5:119867000-119867400	Enhancers	NHDF-Ad	bronchial
47	chr5:119867000-119869000	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr5:119867200-119867400	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr5:119867200-119867600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr5:119867200-119879800	Weak transcription	Left Ventricle	heart

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