Variant report

Variant	nsv1023438
Chromosome Location	chr5:53722407-53788276
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:746)
CpG islands
(count:489)
Chromatin interactive
region (count:41)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:746 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:53785264-53785512	K562	blood:	n/a	n/a
2	ARID3A	chr5:53756340-53756670	K562	blood:	n/a	n/a
3	ARID3A	chr5:53752837-53753279	K562	blood:	n/a	n/a
4	ARID3A	chr5:53739263-53739417	K562	blood:	n/a	n/a
5	ATF1	chr5:53756037-53756711	K562	blood:	n/a	n/a
6	ATF1	chr5:53734402-53734741	K562	blood:	n/a	n/a
7	ATF2	chr5:53736228-53736792	GM12878	blood:	n/a	n/a
8	ATF2	chr5:53736217-53736820	GM12878	blood:	n/a	n/a
9	BACH1	chr5:53726222-53726291	K562	blood:	n/a	n/a
10	BACH1	chr5:53756277-53756862	K562	blood:	n/a	n/a
11	BACH1	chr5:53756533-53756562	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr5:53736320-53736624	GM12878	blood:	n/a	n/a
13	BCL11A	chr5:53765505-53765804	GM12878	blood:	n/a	chr5:53765638-53765646 chr5:53765598-53765607
14	BCL11A	chr5:53765506-53765707	GM12878	blood:	n/a	chr5:53765638-53765646 chr5:53765598-53765607
15	BCLAF1	chr5:53736158-53736816	GM12878	blood:	n/a	chr5:53736558-53736567
16	BCLAF1	chr5:53765390-53765945	GM12878	blood:	n/a	chr5:53765638-53765646 chr5:53765598-53765607
17	BHLHE40	chr5:53759655-53759854	K562	blood:	n/a	n/a
18	BHLHE40	chr5:53752981-53753216	K562	blood:	n/a	n/a
19	BHLHE40	chr5:53785252-53785498	K562	blood:	n/a	n/a
20	CBX3	chr5:53756397-53756649	K562	blood:	n/a	n/a
21	CCNT2	chr5:53734412-53734711	K562	blood:	n/a	n/a
22	CEBPB	chr5:53784932-53785496	A549	lung:	n/a	chr5:53785263-53785274
23	CEBPB	chr5:53785036-53785461	H1-hESC	embryonic stem cell:	n/a	chr5:53785263-53785274
24	CEBPB	chr5:53751305-53751505	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr5:53785004-53785509	Hela-S3	cervix:	n/a	chr5:53785263-53785274
26	CEBPB	chr5:53767265-53767636	K562	blood:	n/a	n/a
27	CEBPB	chr5:53736304-53736642	K562	blood:	n/a	n/a
28	CEBPB	chr5:53762370-53762470	A549	lung:	n/a	n/a
29	CEBPB	chr5:53785016-53785499	MCF-7	breast:	n/a	chr5:53785263-53785274
30	CEBPB	chr5:53777957-53777963	K562	blood:	n/a	n/a
31	CEBPB	chr5:53784934-53785454	IMR90	lung:	n/a	chr5:53785263-53785274
32	CEBPB	chr5:53753020-53753487	A549	lung:	n/a	n/a
33	CEBPB	chr5:53753011-53753467	A549	lung:	n/a	n/a
34	CEBPB	chr5:53753059-53753399	K562	blood:	n/a	n/a
35	CEBPB	chr5:53752998-53753456	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr5:53734372-53734560	K562	blood:	n/a	n/a
37	CEBPB	chr5:53767274-53767586	K562	blood:	n/a	n/a
38	CEBPB	chr5:53734401-53734651	K562	blood:	n/a	n/a
39	CEBPB	chr5:53736191-53736905	GM12878	blood:	n/a	n/a
40	CEBPB	chr5:53784910-53785452	HepG2	liver:	n/a	chr5:53785263-53785274
41	CEBPB	chr5:53752974-53753492	IMR90	lung:	n/a	n/a
42	CEBPB	chr5:53784989-53785443	K562	blood:	n/a	chr5:53785263-53785274
43	CEBPB	chr5:53767376-53767507	K562	blood:	n/a	n/a
44	CHD1	chr5:53784967-53785741	IMR90	lung:	n/a	n/a
45	CTCF	chr5:53739240-53739390	AG04449	skin:	n/a	chr5:53739275-53739288 chr5:53739274-53739295 chr5:53739275-53739284 chr5:53739272-53739290 chr5:53739277-53739287
46	CTCF	chr5:53739240-53739390	HCT-116	colon:	n/a	chr5:53739275-53739288 chr5:53739274-53739295 chr5:53739275-53739284 chr5:53739272-53739290 chr5:53739277-53739287
47	CTCF	chr5:53738900-53739050	GM06990	blood:	n/a	n/a
48	CTCF	chr5:53739220-53739370	BJ	skin:	n/a	chr5:53739275-53739288 chr5:53739274-53739295 chr5:53739275-53739284 chr5:53739272-53739290 chr5:53739277-53739287
49	CTCF	chr5:53739160-53739310	HUVEC	blood vessel:	n/a	chr5:53739275-53739288 chr5:53739274-53739295 chr5:53739275-53739284 chr5:53739272-53739290 chr5:53739277-53739287
50	CTCF	chr5:53739271-53739360	NHEK	skin:	n/a	chr5:53739275-53739288 chr5:53739274-53739295 chr5:53739275-53739284 chr5:53739272-53739290 chr5:53739277-53739287

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:53751045-53751095	ProgFib	skin:	n/a
2	chr5:53751045-53751095	ProgFib	skin:	n/a
3	chr5:53751411-53751461	AG04449	skin:	fetal
4	chr5:53751493-53751543	HCT-116	colon:	n/a
5	chr5:53751272-53751322	SK-N-SH	brain:	n/a
6	chr5:53751411-53751461	PrEC	prostate:	n/a
7	chr5:53751272-53751322	SKMC	muscle:	n/a
8	chr5:53765871-53765921	HEK293	kidney:	embryo
9	chr5:53750818-53750868	K562	blood:	n/a
10	chr5:53751493-53751543	LNCaP	prostate:	n/a
11	chr5:53752133-53752183	HCPEpiC	choroid plexus:	n/a
12	chr5:53765871-53765921	HRCEpiC	kidney:	n/a
13	chr5:53765871-53765921	HCPEpiC	choroid plexus:	n/a
14	chr5:53750818-53750868	T-47D	breast:	n/a
15	chr5:53751493-53751543	SK-N-SH_RA	brain:	n/a
16	chr5:53765871-53765921	ProgFib	skin:	n/a
17	chr5:53751045-53751095	HCM	heart:	n/a
18	chr5:53751411-53751461	NT2-D1	testis:	n/a
19	chr5:53751272-53751322	CMK	blood:	n/a
20	chr5:53751045-53751095	AG04449	skin:	fetal
21	chr5:53751272-53751322	GM12878	blood:	n/a
22	chr5:53751272-53751322	PANC-1	pancreas:	n/a
23	chr5:53751411-53751461	NB4	blood:	n/a
24	chr5:53751272-53751322	BE2_C	brain:	n/a
25	chr5:53752133-53752183	Hela-S3	cervix:	n/a
26	chr5:53751411-53751461	AG09309	skin:	n/a
27	chr5:53765871-53765921	HAEpiC	amniotic membrane:	n/a
28	chr5:53751919-53751969	PrEC	prostate:	n/a
29	chr5:53751411-53751461	GM12892	blood:	n/a
30	chr5:53765871-53765921	SKMC	muscle:	n/a
31	chr5:53765871-53765921	IMR90	lung:	fetal
32	chr5:53751272-53751322	LNCaP	prostate:	n/a
33	chr5:53752133-53752183	PFSK-1	brain:	n/a
34	chr5:53751272-53751322	Caco-2	colon:	n/a
35	chr5:53751919-53751969	T-47D	breast:	n/a
36	chr5:53751272-53751322	HEEpiC	esophagus:	n/a
37	chr5:53751272-53751322	PFSK-1	brain:	n/a
38	chr5:53750818-53750868	GM12892	blood:	n/a
39	chr5:53751272-53751322	GM12892	blood:	n/a
40	chr5:53751919-53751969	AoSMC	blood vessel:	n/a
41	chr5:53750818-53750868	PFSK-1	brain:	n/a
42	chr5:53751493-53751543	HL-60	blood:	n/a
43	chr5:53751919-53751969	HUVEC	blood vessel:	n/a
44	chr5:53751919-53751969	HPAEpiC	pulmonary alveolar:	n/a
45	chr5:53750818-53750868	AoSMC	blood vessel:	n/a
46	chr5:53751919-53751969	HL-60	blood:	n/a
47	chr5:53765871-53765921	MCF-7	breast:	n/a
48	chr5:53751493-53751543	HNPCEpiC	eye:	n/a
49	chr5:53751919-53751969	H1-hESC	embryonic stem cell:	embryo
50	chr5:53751919-53751969	PFSK-1	brain:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:53605333..53606958-chr5:53734217..53736904,2	MCF-7	breast:
2	chr5:53606403..53609001-chr5:53736027..53738147,2	K562	blood:
3	chr5:53741490..53743008-chr5:53744809..53747063,2	K562	blood:
4	chr5:53539002..53539903-chr5:53784949..53785932,7	MCF-7	breast:
5	chr5:53605672..53607647-chr5:53735222..53737387,2	MCF-7	breast:
6	chr5:53605136..53609214-chr5:53716413..53722690,8	K562	blood:
7	chr5:53607949..53610461-chr5:53730015..53732514,2	K562	blood:
8	chr5:53756519..53758534-chr5:53771321..53774318,2	K562	blood:
9	chr5:53605268..53607930-chr5:53720839..53723651,4	MCF-7	breast:
10	chr5:53718578..53720158-chr5:53723244..53724898,2	K562	blood:
11	chr5:53604852..53607754-chr5:53784774..53787952,4	MCF-7	breast:
12	chr5:53724915..53728261-chr5:53730572..53734606,4	K562	blood:
13	chr5:53743067..53745625-chr5:53748167..53749802,2	K562	blood:
14	chr5:53738808..53739784-chr5:53784919..53785489,3	K562	blood:
15	chr5:53761731..53763988-chr5:53766233..53767845,2	MCF-7	breast:
16	chr5:53766279..53767973-chr5:53769873..53772651,2	K562	blood:
17	chr5:53605229..53608006-chr5:53721190..53723549,2	K562	blood:
18	chr5:53539055..53540163-chr5:53784904..53785491,3	K562	blood:
19	chr5:53604953..53608001-chr5:53751983..53754674,3	K562	blood:
20	chr5:53724915..53728261-chr5:53730572..53734606,4	K562	blood:
21	chr5:53732856..53736640-chr5:53736817..53740008,4	MCF-7	breast:
22	chr5:53756519..53758534-chr5:53771321..53774318,2	K562	blood:
23	chr5:53766279..53767973-chr5:53769873..53772651,2	K562	blood:
24	chr5:53743027..53745076-chr5:53751823..53754476,2	K562	blood:
25	chr5:53607171..53608970-chr5:53724887..53727765,2	K562	blood:
26	chr5:53602939..53610771-chr5:53710247..53722415,26	MCF-7	breast:
27	chr5:53719508..53722499-chr5:54137600..54140313,3	K562	blood:
28	chr5:53761731..53763988-chr5:53766233..53767845,2	MCF-7	breast:
29	chr5:53749102..53750606-chr5:53752855..53755258,2	K562	blood:
30	chr5:53730275..53731921-chr5:54232110..54233824,2	K562	blood:
31	chr5:53743067..53745625-chr5:53748167..53749802,2	K562	blood:
32	chr5:53533228..53533986-chr5:53785485..53786082,2	MCF-7	breast:
33	chr5:53606138..53608273-chr5:53737949..53740240,2	K562	blood:
34	chr5:53741490..53743008-chr5:53744809..53747063,2	K562	blood:
35	chr5:53539249..53539895-chr5:53785104..53785871,2	MCF-7	breast:
36	chr5:53738808..53739784-chr5:53784919..53785489,3	K562	blood:
37	chr5:53538916..53540984-chr5:53784081..53786759,2	MCF-7	breast:
38	chr5:53743027..53745076-chr5:53751823..53754476,2	K562	blood:
39	chr5:53784259..53786947-chr5:53789451..53791011,2	K562	blood:
40	chr5:53732856..53736640-chr5:53736817..53740008,4	MCF-7	breast:
41	chr5:53749102..53750606-chr5:53752855..53755258,2	K562	blood:

No data

Variant related genes	Relation type
HSPB3	TF binding region
HSPB3	CpG island
ENSG00000185305	chromatin interactions

Extended variants
information (count: 2653 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2653 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187148506	chr5:53722482-53722483	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs555488725	chr5:53722509-53722510	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs375909010	chr5:53722515-53722516	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs192003775	chr5:53722556-53722557	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs376543982	chr5:53722590-53722591	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs139690667	chr5:53722616-53722617	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs530582182	chr5:53722618-53722619	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs12514912	chr5:53722659-53722660	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs182793951	chr5:53722663-53722664	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs570298674	chr5:53722665-53722666	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs149361195	chr5:53722686-53722687	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs187441342	chr5:53722765-53722766	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs76790019	chr5:53722766-53722767	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs375673905	chr5:53722785-53722786	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs536124407	chr5:53722794-53722795	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs568949898	chr5:53722809-53722810	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs193023981	chr5:53722827-53722828	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs114030430	chr5:53722837-53722838	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs146327771	chr5:53722929-53722930	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs534264624	chr5:53722930-53722931	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs555732785	chr5:53722936-53722937	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs139638954	chr5:53722998-53722999	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs144316547	chr5:53723014-53723015	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs556352288	chr5:53723025-53723026	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs578146042	chr5:53723039-53723040	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs185708130	chr5:53723047-53723048	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs189126866	chr5:53723062-53723063	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs528391045	chr5:53723088-53723089	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs567357333	chr5:53723099-53723100	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs79148144	chr5:53723102-53723103	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs567854360	chr5:53723105-53723106	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs4865824	chr5:53723124-53723125	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs75263359	chr5:53723172-53723173	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs192780697	chr5:53723181-53723182	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs550573003	chr5:53723239-53723240	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs7729424	chr5:53723254-53723255	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs532875240	chr5:53723270-53723271	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs535065577	chr5:53723301-53723302	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs566148136	chr5:53723326-53723327	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs148457196	chr5:53723332-53723333	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs553378904	chr5:53723355-53723356	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs4865825	chr5:53723362-53723363	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs549374065	chr5:53723363-53723364	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs567968635	chr5:53723384-53723385	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs537801934	chr5:53723417-53723418	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs77521250	chr5:53723427-53723428	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs184073383	chr5:53723447-53723448	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs539180820	chr5:53723467-53723468	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs542870845	chr5:53723497-53723498	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs558288585	chr5:53723500-53723501	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	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
Hepatocellular carcinoma	16750200	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
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Oral cancer	21386901	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:670 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:53709000-53724000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:53718200-53727800	Weak transcription	K562	blood
3	chr5:53723800-53724200	Enhancers	Fetal Intestine Large	intestine
4	chr5:53724000-53724200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:53725600-53726600	Weak transcription	Thymus	Thymus
6	chr5:53726600-53726800	Enhancers	Thymus	Thymus
7	chr5:53727800-53728200	Enhancers	K562	blood
8	chr5:53728200-53734000	Weak transcription	K562	blood
9	chr5:53730000-53730400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr5:53730200-53730600	Enhancers	Fetal Lung	lung
11	chr5:53733400-53734800	Enhancers	Placenta	Placenta
12	chr5:53733600-53738600	Enhancers	Fetal Intestine Large	intestine
13	chr5:53734000-53736800	Enhancers	K562	blood
14	chr5:53734200-53734800	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr5:53734200-53736800	Enhancers	Fetal Intestine Small	intestine
16	chr5:53734400-53734800	Enhancers	Primary B cells from peripheral blood	blood
17	chr5:53734400-53734800	Enhancers	GM12878-XiMat	blood
18	chr5:53734400-53735000	Enhancers	A549	lung
19	chr5:53734400-53735200	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr5:53734400-53736200	Enhancers	Primary T cells from cord blood	blood
21	chr5:53734600-53734800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr5:53734600-53734800	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr5:53734600-53734800	Enhancers	Primary B cells from cord blood	blood
24	chr5:53734600-53734800	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr5:53734600-53735000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
26	chr5:53734800-53735800	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr5:53734800-53735800	Weak transcription	Primary B cells from cord blood	blood
28	chr5:53734800-53735800	Weak transcription	Primary B cells from peripheral blood	blood
29	chr5:53734800-53735800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr5:53734800-53735800	Weak transcription	Placenta	Placenta
31	chr5:53734800-53735800	Weak transcription	GM12878-XiMat	blood
32	chr5:53734800-53736200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr5:53735000-53735400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr5:53735000-53736600	Weak transcription	A549	lung
35	chr5:53735000-53742600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr5:53735200-53735600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr5:53735400-53736000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr5:53735600-53736200	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr5:53735600-53737400	Enhancers	Dnd41	blood
40	chr5:53735600-53738000	Enhancers	Primary T helper cells fromperipheralblood	blood
41	chr5:53735800-53736200	Enhancers	GM12878-XiMat	blood
42	chr5:53735800-53736400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr5:53735800-53736800	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr5:53735800-53737000	Enhancers	Primary B cells from cord blood	blood
45	chr5:53735800-53737000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr5:53735800-53737200	Enhancers	Primary B cells from peripheral blood	blood
47	chr5:53735800-53737200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
48	chr5:53735800-53737200	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr5:53735800-53737200	Enhancers	Primary T killer memory cells from peripheral blood	blood
50	chr5:53735800-53738000	Enhancers	Fetal Thymus	thymus

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