Variant report

Variant	nsv829985
Chromosome Location	chr4:82199328-82353656
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:82326956-82327545	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:82332228-82332294	K562	blood:	n/a	n/a
3	ARID3A	chr4:82342499-82343466	K562	blood:	n/a	n/a
4	ARID3A	chr4:82326930-82327433	K562	blood:	n/a	n/a
5	ARID3A	chr4:82329631-82329784	K562	blood:	n/a	n/a
6	ATF1	chr4:82342595-82343231	K562	blood:	n/a	n/a
7	ATF2	chr4:82342484-82343053	GM12878	blood:	n/a	n/a
8	ATF3	chr4:82342472-82343073	K562	blood:	n/a	n/a
9	BACH1	chr4:82297050-82297250	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:82342648-82343445	K562	blood:	n/a	n/a
11	BACH1	chr4:82272960-82273187	K562	blood:	n/a	n/a
12	BACH1	chr4:82266883-82266911	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr4:82343802-82344096	GM12878	blood:	n/a	n/a
14	BATF	chr4:82343728-82344077	GM12878	blood:	n/a	n/a
15	BATF	chr4:82342610-82342946	GM12878	blood:	n/a	chr4:82342803-82342812 chr4:82342791-82342801 chr4:82342787-82342797 chr4:82342790-82342801
16	BATF	chr4:82342612-82342992	GM12878	blood:	n/a	chr4:82342803-82342812 chr4:82342791-82342801 chr4:82342787-82342797 chr4:82342790-82342801
17	BHLHE40	chr4:82235715-82236076	K562	blood:	n/a	n/a
18	BHLHE40	chr4:82327379-82327539	K562	blood:	n/a	n/a
19	BHLHE40	chr4:82343813-82343967	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:82312717-82312819	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:82235749-82236021	HepG2	liver:	n/a	n/a
22	BHLHE40	chr4:82272933-82273130	K562	blood:	n/a	n/a
23	BHLHE40	chr4:82342679-82342966	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:82329613-82329660	K562	blood:	n/a	n/a
25	BHLHE40	chr4:82342487-82343338	K562	blood:	n/a	n/a
26	BHLHE40	chr4:82235752-82235984	GM12878	blood:	n/a	n/a
27	CBX3	chr4:82342417-82343460	K562	blood:	n/a	n/a
28	CBX3	chr4:82342440-82343147	K562	blood:	n/a	n/a
29	CCNT2	chr4:82342603-82343344	K562	blood:	n/a	chr4:82343058-82343067
30	CEBPB	chr4:82326865-82327631	HCT-116	colon:	n/a	chr4:82327174-82327183 chr4:82327172-82327183 chr4:82327174-82327183 chr4:82327174-82327183 chr4:82327172-82327185 chr4:82327174-82327183
31	CEBPB	chr4:82326975-82327346	K562	blood:	n/a	chr4:82327174-82327183 chr4:82327172-82327183 chr4:82327174-82327183 chr4:82327174-82327183 chr4:82327172-82327185 chr4:82327174-82327183
32	CEBPB	chr4:82327028-82327250	HepG2	liver:	n/a	chr4:82327174-82327183 chr4:82327172-82327183 chr4:82327174-82327183 chr4:82327174-82327183 chr4:82327172-82327185 chr4:82327174-82327183
33	CEBPB	chr4:82326956-82327408	IMR90	lung:	n/a	chr4:82327174-82327183 chr4:82327172-82327183 chr4:82327174-82327183 chr4:82327174-82327183 chr4:82327172-82327185 chr4:82327174-82327183
34	CEBPB	chr4:82284117-82284338	IMR90	lung:	n/a	n/a
35	CEBPB	chr4:82254070-82254313	IMR90	lung:	n/a	chr4:82254167-82254178
36	CEBPB	chr4:82226143-82226425	IMR90	lung:	n/a	n/a
37	CEBPB	chr4:82286255-82286458	A549	lung:	n/a	chr4:82286331-82286344
38	CEBPB	chr4:82326898-82327427	ECC-1	luminal epithelium:	n/a	chr4:82327174-82327183 chr4:82327172-82327183 chr4:82327174-82327183 chr4:82327174-82327183 chr4:82327172-82327185 chr4:82327174-82327183
39	CEBPB	chr4:82326905-82327433	MCF-7	breast:	n/a	chr4:82327174-82327183 chr4:82327172-82327183 chr4:82327174-82327183 chr4:82327174-82327183 chr4:82327172-82327185 chr4:82327174-82327183
40	CEBPB	chr4:82311043-82311317	K562	blood:	n/a	chr4:82311179-82311190
41	CEBPB	chr4:82326947-82327512	H1-hESC	embryonic stem cell:	n/a	chr4:82327174-82327183 chr4:82327172-82327183 chr4:82327174-82327183 chr4:82327174-82327183 chr4:82327172-82327185 chr4:82327174-82327183
42	CEBPB	chr4:82282122-82282305	IMR90	lung:	n/a	n/a
43	CEBPB	chr4:82326852-82327490	HCT-116	colon:	n/a	chr4:82327174-82327183 chr4:82327172-82327183 chr4:82327174-82327183 chr4:82327174-82327183 chr4:82327172-82327185 chr4:82327174-82327183
44	CEBPB	chr4:82326843-82327465	A549	lung:	n/a	chr4:82327174-82327183 chr4:82327172-82327183 chr4:82327174-82327183 chr4:82327174-82327183 chr4:82327172-82327185 chr4:82327174-82327183
45	CEBPB	chr4:82286351-82286355	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr4:82331925-82332213	K562	blood:	n/a	n/a
47	CEBPB	chr4:82342538-82343133	K562	blood:	n/a	n/a
48	CEBPB	chr4:82311085-82311402	HepG2	liver:	n/a	chr4:82311179-82311190
49	CEBPB	chr4:82326797-82327611	K562	blood:	n/a	chr4:82327174-82327183 chr4:82327172-82327183 chr4:82327174-82327183 chr4:82327174-82327183 chr4:82327172-82327185 chr4:82327174-82327183
50	CEBPB	chr4:82311090-82311403	A549	lung:	n/a	chr4:82311179-82311190

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:82348507-82348557	HCF	heart:	n/a
2	chr4:82348507-82348557	HCF	heart:	n/a
3	chr4:82350883-82350933	HepG2	liver:	n/a
4	chr4:82340537-82340587	HL-60	blood:	n/a
5	chr4:82350883-82350933	SKMC	muscle:	n/a
6	chr4:82340537-82340587	GM19239	blood:	n/a
7	chr4:82348507-82348557	RPTEC	kidney:	n/a
8	chr4:82351016-82351066	ovcar-3	ovarian:	n/a
9	chr4:82226093-82226143	H1-hESC	embryonic stem cell:	embryo
10	chr4:82273176-82273226	GM12878	blood:	n/a
11	chr4:82273176-82273226	HIPEpiC	eye:	n/a
12	chr4:82273176-82273226	AG04450	lung:	fetal
13	chr4:82283507-82283557	H1-hESC	embryonic stem cell:	embryo
14	chr4:82346163-82346213	GM12878	blood:	n/a
15	chr4:82283507-82283557	HL-60	blood:	n/a
16	chr4:82256560-82256610	HEEpiC	esophagus:	n/a
17	chr4:82256560-82256610	ECC-1	luminal epithelium:	n/a
18	chr4:82283507-82283557	RPTEC	kidney:	n/a
19	chr4:82226093-82226143	Caco-2	colon:	n/a
20	chr4:82280241-82280291	Jurkat	blood:	n/a
21	chr4:82340537-82340587	HRCEpiC	kidney:	n/a
22	chr4:82256560-82256610	HCT-116	colon:	n/a
23	chr4:82280241-82280291	ProgFib	skin:	n/a
24	chr4:82256560-82256610	HCM	heart:	n/a
25	chr4:82350842-82350892	IMR90	lung:	fetal
26	chr4:82226093-82226143	HCPEpiC	choroid plexus:	n/a
27	chr4:82283507-82283557	T-47D	breast:	n/a
28	chr4:82350842-82350892	A549	lung:	n/a
29	chr4:82280241-82280291	AG04449	skin:	fetal
30	chr4:82350883-82350933	SAEC	small airway:	n/a
31	chr4:82256560-82256610	GM12878	blood:	n/a
32	chr4:82351016-82351066	AoSMC	blood vessel:	n/a
33	chr4:82351016-82351066	HPAEpiC	pulmonary alveolar:	n/a
34	chr4:82340537-82340587	NHBE	bronchial:	n/a
35	chr4:82348507-82348557	GM19239	blood:	n/a
36	chr4:82350883-82350933	LNCaP	prostate:	n/a
37	chr4:82350842-82350892	BE2_C	brain:	n/a
38	chr4:82351016-82351066	ECC-1	luminal epithelium:	n/a
39	chr4:82280241-82280291	Hepatocyte	liver:	n/a
40	chr4:82273176-82273226	AG04449	skin:	fetal
41	chr4:82273176-82273226	HMEC	breast:	n/a
42	chr4:82273176-82273226	GM19239	blood:	n/a
43	chr4:82273176-82273226	Jurkat	blood:	n/a
44	chr4:82226093-82226143	NHBE	bronchial:	n/a
45	chr4:82348507-82348557	GM06990	blood:	n/a
46	chr4:82256560-82256610	HepG2	liver:	n/a
47	chr4:82280241-82280291	AG09309	skin:	n/a
48	chr4:82283507-82283557	AG04450	lung:	fetal
49	chr4:82280241-82280291	HCT-116	colon:	n/a
50	chr4:82256560-82256610	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr4:82338718..82341149-chr4:82343228..82345190,2	K562	blood:
2	chr4:82330902..82334984-chr4:82339313..82344776,5	K562	blood:
3	chr4:82327000..82327810-chr4:82341931..82342605,2	K562	blood:
4	chr4:82317438..82320291-chr4:82320653..82322618,2	K562	blood:
5	chr4:82341740..82344236-chr4:82345813..82347931,2	MCF-7	breast:
6	chr4:82326953..82327888-chr4:82765613..82766496,6	MCF-7	breast:
7	chr4:82326952..82327640-chr4:83139246..83140172,3	MCF-7	breast:
8	chr4:82328359..82330272-chr4:82331686..82335008,3	K562	blood:
9	chr4:82191920..82194351-chr4:82199658..82201341,2	K562	blood:
10	chr4:82296919..82298708-chr4:82299908..82301828,2	MCF-7	breast:
11	chr4:81990998..81991602-chr4:82272501..82273357,5	MCF-7	breast:
12	chr4:82328359..82330272-chr4:82331686..82335008,3	K562	blood:
13	chr4:82342860..82344646-chr4:82347755..82350982,3	K562	blood:
14	chr4:82327015..82327603-chr4:83122849..83123538,2	MCF-7	breast:
15	chr4:82327129..82328804-chr4:82341208..82343737,2	K562	blood:
16	chr4:82330902..82334984-chr4:82339313..82344776,5	K562	blood:
17	chr4:82326836..82327578-chr4:82476960..82477646,2	K562	blood:
18	chr4:82327052..82327580-chr4:83189067..83189954,2	K562	blood:
19	chr4:82327020..82327704-chr4:83189488..83190807,3	MCF-7	breast:
20	chr4:81990624..81991565-chr4:82272517..82273470,4	MCF-7	breast:
21	chr4:82005004..82005857-chr4:82272588..82273446,6	MCF-7	breast:
22	chr4:82342653..82344315-chr4:82756584..82758105,2	K562	blood:
23	chr4:82342729..82344646-chr4:82349482..82351498,2	K562	blood:
24	chr4:82326946..82327647-chr4:83122824..83123511,5	K562	blood:
25	chr4:82276224..82278313-chr4:82278695..82280977,2	K562	blood:
26	chr4:82005126..82005787-chr4:82272560..82273161,2	MCF-7	breast:
27	chr4:82327008..82327570-chr4:82765988..82766495,2	K562	blood:
28	chr4:82337897..82339898-chr4:82380969..82382702,2	K562	blood:
29	chr4:82209550..82211788-chr4:82211978..82214225,2	K562	blood:
30	chr4:82326902..82327525-chr4:82765379..82766275,4	MCF-7	breast:
31	chr4:82263937..82264497-chr4:82272498..82273225,2	K562	blood:
32	chr4:82332819..82334854-chr4:82340131..82342446,3	K562	blood:
33	chr4:82276224..82278313-chr4:82278695..82280977,2	K562	blood:
34	chr4:82326927..82327852-chr4:82345884..82346881,4	K562	blood:
35	chr4:82343748..82345292-chr4:82377281..82379980,2	K562	blood:
36	chr4:82340135..82342826-chr4:82350602..82352367,3	K562	blood:
37	chr4:82338718..82341149-chr4:82343228..82345190,2	K562	blood:
38	chr4:82342729..82344646-chr4:82349482..82351498,2	K562	blood:
39	chr4:82326919..82327448-chr4:83206445..83206978,2	MCF-7	breast:
40	chr4:82209550..82211788-chr4:82211978..82214225,2	K562	blood:
41	chr4:82340135..82342826-chr4:82350602..82352367,3	K562	blood:
42	chr4:82296919..82298708-chr4:82299908..82301828,2	MCF-7	breast:
43	chr4:81990848..81991586-chr4:82272501..82273236,3	K562	blood:
44	chr4:82251203..82252769-chr4:82254492..82256214,2	K562	blood:
45	chr4:82327000..82327810-chr4:82341931..82342605,2	K562	blood:
46	chr4:82342860..82344646-chr4:82347755..82350982,3	K562	blood:
47	chr4:82341314..82344179-chr4:82360678..82363894,3	K562	blood:
48	chr4:82327037..82327640-chr4:83122910..83123879,5	MCF-7	breast:
49	chr4:82326881..82327563-chr4:82770505..82771402,2	MCF-7	breast:
50	chr4:82327129..82328804-chr4:82341208..82343737,2	K562	blood:

Variant related genes	Relation type
RNU5A-2P	TF binding region
RNU5A-2P	CpG island
ENSG00000207065	chromatin interactions
ENSG00000138670	chromatin interactions

Extended variants
information (count: 4040 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4040 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545927176	chr4:82199358-82199359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs377105695	chr4:82199359-82199360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542454497	chr4:82199400-82199401	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs78112556	chr4:82199437-82199438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548485701	chr4:82199438-82199439	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150795877	chr4:82199453-82199454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527905588	chr4:82199504-82199505	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1452365	chr4:82199568-82199569	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs570493933	chr4:82199575-82199576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539516306	chr4:82199682-82199683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556247054	chr4:82199718-82199719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569684757	chr4:82199728-82199729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12505180	chr4:82199771-82199772	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs139172168	chr4:82199805-82199806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185692599	chr4:82199862-82199863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201587402	chr4:82199880-82199881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563952198	chr4:82199891-82199892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs10011265	chr4:82199892-82199893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532961895	chr4:82199945-82199946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145987107	chr4:82199948-82199949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563251681	chr4:82199953-82199954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545905786	chr4:82199996-82199997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139873695	chr4:82200002-82200003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548811013	chr4:82200040-82200041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576048484	chr4:82200071-82200072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374997935	chr4:82200076-82200077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562278084	chr4:82200097-82200098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533087493	chr4:82200103-82200104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190965863	chr4:82200131-82200132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4463061	chr4:82200142-82200143	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs145474541	chr4:82200176-82200177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549923059	chr4:82200206-82200207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs370247376	chr4:82200230-82200231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535476708	chr4:82200233-82200234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6828846	chr4:82200237-82200238	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs565880276	chr4:82200243-82200244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534917948	chr4:82200248-82200249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183104242	chr4:82200275-82200276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577787413	chr4:82200301-82200302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185197421	chr4:82200308-82200309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547849479	chr4:82200343-82200344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556269054	chr4:82200351-82200352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576114598	chr4:82200358-82200359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190687800	chr4:82200369-82200370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6850833	chr4:82200371-82200372	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs572303687	chr4:82200378-82200379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541720652	chr4:82200404-82200405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs539858455	chr4:82200411-82200412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564596126	chr4:82200420-82200421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533593870	chr4:82200515-82200516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Myelodysplastic syndrome	18508791	CNVD
abnormal development	18461090	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:895 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:82193800-82203200	Weak transcription	Fetal Intestine Small	intestine
2	chr4:82199400-82199600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr4:82199600-82208200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr4:82202000-82202800	Enhancers	NHDF-Ad	bronchial
5	chr4:82202200-82202600	Enhancers	NHLF	lung
6	chr4:82203200-82204000	Enhancers	Fetal Intestine Large	intestine
7	chr4:82203200-82204200	Enhancers	Fetal Intestine Small	intestine
8	chr4:82204000-82210600	Weak transcription	Fetal Intestine Large	intestine
9	chr4:82204200-82205200	Weak transcription	Fetal Intestine Small	intestine
10	chr4:82205200-82205400	Enhancers	Fetal Intestine Small	intestine
11	chr4:82205200-82205400	Enhancers	Small Intestine	intestine
12	chr4:82206800-82209200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr4:82208200-82208600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr4:82208200-82209000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr4:82208800-82209600	Enhancers	Fetal Brain Male	brain
16	chr4:82209000-82209600	Enhancers	Fetal Heart	heart
17	chr4:82209200-82209600	Enhancers	Brain Germinal Matrix	brain
18	chr4:82210600-82214200	Enhancers	Fetal Intestine Large	intestine
19	chr4:82211000-82215000	Enhancers	Fetal Intestine Small	intestine
20	chr4:82211200-82211400	Enhancers	Fetal Kidney	kidney
21	chr4:82211600-82212600	Weak transcription	Fetal Kidney	kidney
22	chr4:82212400-82212800	Enhancers	Duodenum Mucosa	Duodenum
23	chr4:82212400-82213200	Enhancers	Small Intestine	intestine
24	chr4:82212600-82213200	Enhancers	Fetal Kidney	kidney
25	chr4:82212800-82213600	Enhancers	Fetal Lung	lung
26	chr4:82219000-82220200	ZNF genes & repeats	Fetal Intestine Small	intestine
27	chr4:82219000-82220600	Enhancers	Fetal Intestine Large	intestine
28	chr4:82219200-82219600	Enhancers	Small Intestine	intestine
29	chr4:82220200-82220600	Enhancers	Fetal Intestine Small	intestine
30	chr4:82220400-82221000	Enhancers	Primary hematopoietic stem cells	blood
31	chr4:82220400-82221000	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr4:82220400-82221200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr4:82220400-82221200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr4:82223200-82224000	Enhancers	Fetal Lung	lung
35	chr4:82223400-82224000	Enhancers	Fetal Brain Male	brain
36	chr4:82223400-82224200	Enhancers	Fetal Brain Female	brain
37	chr4:82224000-82224400	Weak transcription	Fetal Brain Male	brain
38	chr4:82224000-82224600	Weak transcription	Fetal Lung	lung
39	chr4:82224200-82224800	Weak transcription	Fetal Brain Female	brain
40	chr4:82224400-82224800	Enhancers	Fetal Brain Male	brain
41	chr4:82224600-82224800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr4:82224600-82224800	Enhancers	Fetal Lung	lung
43	chr4:82224800-82225400	Enhancers	Fetal Brain Female	brain
44	chr4:82224800-82225800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr4:82224800-82226000	Weak transcription	Fetal Lung	lung
46	chr4:82224800-82227800	Weak transcription	Fetal Brain Male	brain
47	chr4:82225400-82228600	Weak transcription	Fetal Brain Female	brain
48	chr4:82225800-82227000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr4:82226000-82226200	Enhancers	Fetal Lung	lung
50	chr4:82226200-82226600	Weak transcription	Fetal Lung	lung

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