Variant report

Variant	nsv999741
Chromosome Location	chr4:102009017-102454115
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4539)
CpG islands
(count:2139)
Chromatin interactive
region (count:154)
LncRNA
region (count:9)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:4539 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:102110166-102110436	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:102057151-102057201	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:102277128-102278568	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:102090041-102090740	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:102206748-102207057	HepG2	liver:	n/a	chr4:102206940-102206956
6	ARID3A	chr4:102035646-102036596	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:102192451-102192992	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:102118617-102118959	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:102184728-102184804	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:102186628-102186925	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:102097145-102097441	HepG2	liver:	n/a	n/a
12	ARID3A	chr4:102185528-102186188	HepG2	liver:	n/a	n/a
13	ARID3A	chr4:102113451-102113735	HepG2	liver:	n/a	n/a
14	ARID3A	chr4:102268870-102269129	HepG2	liver:	n/a	n/a
15	ARID3A	chr4:102270051-102270246	HepG2	liver:	n/a	n/a
16	ARID3A	chr4:102121858-102122138	HepG2	liver:	n/a	n/a
17	ARID3A	chr4:102266883-102267082	HepG2	liver:	n/a	n/a
18	ATF1	chr4:102127133-102127436	K562	blood:	n/a	n/a
19	ATF1	chr4:102090163-102090344	K562	blood:	n/a	n/a
20	ATF1	chr4:102024793-102025046	K562	blood:	n/a	n/a
21	ATF1	chr4:102200644-102201058	K562	blood:	n/a	n/a
22	ATF1	chr4:102121866-102122066	K562	blood:	n/a	n/a
23	ATF1	chr4:102165595-102165725	K562	blood:	n/a	n/a
24	ATF2	chr4:102276346-102276818	GM12878	blood:	n/a	n/a
25	ATF2	chr4:102024725-102025276	GM12878	blood:	n/a	n/a
26	ATF2	chr4:102448264-102448795	GM12878	blood:	n/a	n/a
27	ATF2	chr4:102448337-102448789	GM12878	blood:	n/a	n/a
28	ATF2	chr4:102339234-102339683	GM12878	blood:	n/a	n/a
29	ATF2	chr4:102249102-102249943	GM12878	blood:	n/a	n/a
30	ATF2	chr4:102276329-102276842	GM12878	blood:	n/a	n/a
31	ATF2	chr4:102200605-102201032	GM12878	blood:	n/a	n/a
32	ATF2	chr4:102339134-102339737	GM12878	blood:	n/a	n/a
33	ATF2	chr4:102340441-102340905	GM12878	blood:	n/a	n/a
34	ATF2	chr4:102249182-102249856	GM12878	blood:	n/a	n/a
35	ATF3	chr4:102159877-102160294	HCT-116	colon:	n/a	n/a
36	ATF3	chr4:102082206-102082688	A549	lung:	n/a	n/a
37	ATF3	chr4:102082178-102082689	A549	lung:	n/a	n/a
38	ATF3	chr4:102132174-102132682	A549	lung:	n/a	n/a
39	BACH1	chr4:102036212-102036498	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr4:102269007-102269398	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr4:102153463-102153466	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr4:102091038-102091072	K562	blood:	n/a	n/a
43	BACH1	chr4:102268296-102268651	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr4:102234818-102234843	K562	blood:	n/a	n/a
45	BACH1	chr4:102266603-102267217	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr4:102278170-102278287	H1-hESC	embryonic stem cell:	n/a	n/a
47	BATF	chr4:102256033-102256341	GM12878	blood:	n/a	n/a
48	BATF	chr4:102249224-102249502	GM12878	blood:	n/a	n/a
49	BATF	chr4:102339267-102339612	GM12878	blood:	n/a	n/a
50	BATF	chr4:102249135-102249874	GM12878	blood:	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	chr4:102154513-102154563	BE2_C	brain:	n/a
2	chr4:102268125-102268175	RPTEC	kidney:	n/a
3	chr4:102246975-102247025	NHDF-neo	bronchial:	n/a
4	chr4:102154513-102154563	LNCaP	prostate:	n/a
5	chr4:102154513-102154563	BE2_C	brain:	n/a
6	chr4:102268125-102268175	RPTEC	kidney:	n/a
7	chr4:102246975-102247025	NHDF-neo	bronchial:	n/a
8	chr4:102154513-102154563	LNCaP	prostate:	n/a
9	chr4:102207435-102207485	HRPEpiC	eye:	n/a
10	chr4:102341105-102341155	Caco-2	colon:	n/a
11	chr4:102340823-102340873	Hela-S3	cervix:	n/a
12	chr4:102268075-102268125	PFSK-1	brain:	n/a
13	chr4:102154513-102154563	NHDF-neo	bronchial:	n/a
14	chr4:102272871-102272921	HMEC	breast:	n/a
15	chr4:102160529-102160579	NHDF-neo	bronchial:	n/a
16	chr4:102340823-102340873	CMK	blood:	n/a
17	chr4:102258631-102258681	ECC-1	luminal epithelium:	n/a
18	chr4:102207435-102207485	NB4	blood:	n/a
19	chr4:102267366-102267416	H1-hESC	embryonic stem cell:	embryo
20	chr4:102277629-102277679	HEK293	kidney:	embryo
21	chr4:102087758-102087808	GM12892	blood:	n/a
22	chr4:102269425-102269475	HCM	heart:	n/a
23	chr4:102272871-102272921	HAEpiC	amniotic membrane:	n/a
24	chr4:102268622-102268672	GM12878	blood:	n/a
25	chr4:102112217-102112267	HIPEpiC	eye:	n/a
26	chr4:102341105-102341155	ovcar-3	ovarian:	n/a
27	chr4:102087758-102087808	NB4	blood:	n/a
28	chr4:102267974-102268024	RPTEC	kidney:	n/a
29	chr4:102132302-102132352	AG10803	skin:	n/a
30	chr4:102264326-102264376	SK-N-SH_RA	brain:	n/a
31	chr4:102268949-102268999	PANC-1	pancreas:	n/a
32	chr4:102268821-102268871	ProgFib	skin:	n/a
33	chr4:102268821-102268871	SAEC	small airway:	n/a
34	chr4:102272871-102272921	NHBE	bronchial:	n/a
35	chr4:102087758-102087808	K562	blood:	n/a
36	chr4:102269374-102269424	Hepatocyte	liver:	n/a
37	chr4:102097226-102097276	HCM	heart:	n/a
38	chr4:102268957-102269007	CMK	blood:	n/a
39	chr4:102264326-102264376	Hepatocyte	liver:	n/a
40	chr4:102340823-102340873	GM12878	blood:	n/a
41	chr4:102097226-102097276	ProgFib	skin:	n/a
42	chr4:102154513-102154563	Jurkat	blood:	n/a
43	chr4:102227740-102227790	T-47D	breast:	n/a
44	chr4:102340823-102340873	AG04449	skin:	fetal
45	chr4:102087758-102087808	ProgFib	skin:	n/a
46	chr4:102268957-102269007	HAEpiC	amniotic membrane:	n/a
47	chr4:102277629-102277679	NT2-D1	testis:	n/a
48	chr4:102269374-102269424	SK-N-SH_RA	brain:	n/a
49	chr4:102154513-102154563	RPTEC	kidney:	n/a
50	chr4:102340691-102340741	GM19239	blood:	n/a

(count:154 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr4:102022887..102025645-chr4:102079207..102081284,2	MCF-7	breast:
2	chr4:102091067..102093377-chr4:102267851..102271063,3	MCF-7	breast:
3	chr4:102232326..102233842-chr4:102235389..102237956,2	MCF-7	breast:
4	chr4:102206850..102209343-chr4:102209669..102211406,2	MCF-7	breast:
5	chr4:102205631..102207880-chr4:102239422..102240935,2	MCF-7	breast:
6	chr4:102121617..102124341-chr4:102190145..102192909,2	MCF-7	breast:
7	chr4:102131746..102133996-chr4:102142309..102145275,2	MCF-7	breast:
8	chr4:102229250..102230989-chr4:102267695..102270675,2	MCF-7	breast:
9	chr4:102160185..102162407-chr4:102162832..102166466,3	MCF-7	breast:
10	chr4:102248729..102250846-chr4:102268529..102271038,2	K562	blood:
11	chr4:102234738..102237332-chr4:102239450..102241192,2	MCF-7	breast:
12	chr4:102244312..102246286-chr4:102248183..102250301,2	K562	blood:
13	chr4:102114465..102117225-chr4:102221024..102223068,2	MCF-7	breast:
14	chr4:102171123..102173007-chr4:102176069..102177893,2	MCF-7	breast:
15	chr4:102130741..102132972-chr4:102224508..102226264,2	MCF-7	breast:
16	chr4:102048414..102050219-chr4:102262763..102264265,2	MCF-7	breast:
17	chr4:102228684..102230512-chr4:102715753..102717632,2	K562	blood:
18	chr4:102439215..102441659-chr4:102442690..102444241,2	MCF-7	breast:
19	chr4:102129139..102132021-chr4:102226843..102229507,2	MCF-7	breast:
20	chr4:102206153..102209881-chr4:102222002..102225867,4	MCF-7	breast:
21	chr4:102132632..102134649-chr4:102137778..102139733,2	MCF-7	breast:
22	chr4:102149127..102151835-chr4:102160270..102161845,2	MCF-7	breast:
23	chr4:102178495..102180212-chr4:102267850..102269476,2	MCF-7	breast:
24	chr4:102439215..102441659-chr4:102442690..102444241,2	MCF-7	breast:
25	chr4:102263328..102265199-chr4:102265515..102267436,2	K562	blood:
26	chr4:102088927..102090485-chr4:102267393..102270009,2	MCF-7	breast:
27	chr4:102072492..102076401-chr4:102080849..102083286,3	MCF-7	breast:
28	chr4:102086824..102091694-chr4:102266945..102270646,5	MCF-7	breast:
29	chr12:70082527..70083460-chr4:102029317..102030043,2	HCT-116	colon:
30	chr4:102242973..102245664-chr4:102246576..102249048,2	MCF-7	breast:
31	chr4:102116031..102123578-chr4:102130356..102136503,10	MCF-7	breast:
32	chr4:102058000..102061139-chr4:102062648..102064879,3	MCF-7	breast:
33	chr4:102064685..102066455-chr4:102068681..102071508,2	K562	blood:
34	chr4:102119014..102119905-chr4:102132461..102133442,2	MCF-7	breast:
35	chr4:102064685..102066455-chr4:102068681..102071508,2	K562	blood:
36	chr4:102432296..102434415-chr4:102447007..102448829,2	MCF-7	breast:
37	chr4:102234738..102237332-chr4:102239450..102241192,2	MCF-7	breast:
38	chr4:102195924..102197828-chr4:102197839..102200644,3	MCF-7	breast:
39	chr11:113966492..113967012-chr4:102236344..102236864,2	Hela-S3	cervix:
40	chr4:102219978..102222828-chr4:102224431..102227610,3	MCF-7	breast:
41	chr4:102208778..102209725-chr4:102317892..102318526,2	MCF-7	breast:
42	chr4:102238335..102240230-chr4:102246275..102248377,2	MCF-7	breast:
43	chr4:101039108..101041675-chr4:102229054..102231223,2	K562	blood:
44	chr4:102276355..102278194-chr4:102281593..102284291,2	MCF-7	breast:
45	chr4:102206153..102209881-chr4:102222002..102225867,4	MCF-7	breast:
46	chr4:102195298..102197332-chr4:102200967..102203266,2	MCF-7	breast:
47	chr4:102252145..102254033-chr4:102258356..102260817,2	MCF-7	breast:
48	chr4:102158963..102160563-chr4:102166791..102168872,2	MCF-7	breast:
49	chr4:102252145..102254033-chr4:102258356..102260817,2	MCF-7	breast:
50	chr4:102152625..102154984-chr4:102158702..102160771,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EMCN-2	chr4:102218141-102219108	NONHSAT097569
2	lnc-BANK1-1	chr4:102333336-102333506	NONHSAT097572
3	lnc-BANK1-1	chr4:102343790-102343815	NONHSAT097572
4	lnc-EMCN-3	chr4:102265025-102267178	NONHSAT097571
5	lnc-AP001816.1.1-1	chr4:102268934-102269166	NR_033874
6	lnc-BANK1-1	chr4:102332443-102332593	NONHSAT097572
7	lnc-BANK1-1	chr4:102348718-102348797	NONHSAT097572
8	lnc-AP001816.1.1-1	chr4:102269481-102270040	NR_033874
9	lnc-BANK1-1	chr4:102341171-102341254	NONHSAT097572

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1255a	chr4:102251522-102251544	MIMAT0005906
hsa-miR-8066	chr4:102161962-102161982	MIMAT0030993

No data

Variant related genes	Relation type
BANK1	TF binding region
MIR1255A	TF binding region
ENSG00000254531	TF binding region
PPP3CA	TF binding region
BANK1	CpG island
MIR1255A	CpG island
ENSG00000254531	CpG island
PPP3CA	CpG island
ENSG00000127325	chromatin interactions
ENSG00000254531	chromatin interactions
ENSG00000164032	chromatin interactions
ENSG00000221265	chromatin interactions
ENSG00000245322	chromatin interactions
ENSG00000138814	chromatin interactions

Extended variants
information (count: 13462 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:13462 , 50 per page) page: 1 2 3 4 5 6 7 ... 270

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138767359	chr4:102009025-102009026	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs551530899	chr4:102009051-102009052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569930374	chr4:102009094-102009095	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536708694	chr4:102009122-102009123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555172472	chr4:102009177-102009178	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs372935835	chr4:102009198-102009199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191594822	chr4:102009244-102009245	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs534359184	chr4:102009245-102009246	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs529385850	chr4:102009277-102009278	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181441860	chr4:102009302-102009303	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146544831	chr4:102009304-102009305	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs578018288	chr4:102009327-102009328	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558296688	chr4:102009337-102009338	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531997563	chr4:102009338-102009339	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs550515283	chr4:102009366-102009367	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142758093	chr4:102009369-102009370	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs150707237	chr4:102009392-102009393	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534459065	chr4:102009411-102009412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs114548884	chr4:102009441-102009442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529272337	chr4:102009514-102009515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541097121	chr4:102009524-102009525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555835164	chr4:102009563-102009564	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533410901	chr4:102009650-102009651	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186336708	chr4:102009660-102009661	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113159161	chr4:102009720-102009721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369141154	chr4:102009723-102009724	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs13125356	chr4:102009773-102009774	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs2732504	chr4:102009827-102009828	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs149420980	chr4:102009850-102009851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs567282836	chr4:102009866-102009867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376128802	chr4:102009872-102009873	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190835429	chr4:102009901-102009902	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552661889	chr4:102009906-102009907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571274465	chr4:102009946-102009947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182298678	chr4:102009974-102009975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs17232534	chr4:102009986-102009987	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs575501770	chr4:102010003-102010004	Weak transcription Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542491019	chr4:102010033-102010034	Weak transcription Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs17030741	chr4:102010038-102010039	Weak transcription Active TSS Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs574023116	chr4:102010062-102010063	Weak transcription Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541529637	chr4:102010073-102010074	Weak transcription Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144857090	chr4:102010096-102010097	Weak transcription Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186646607	chr4:102010244-102010245	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201703816	chr4:102010273-102010274	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568622311	chr4:102010289-102010290	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547556866	chr4:102010296-102010297	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563676866	chr4:102010297-102010298	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542903612	chr4:102010299-102010300	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542675884	chr4:102010304-102010305	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10026289	chr4:102010318-102010319	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:79)

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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	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
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:6363 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:101941200-102035600	Weak transcription	Fetal Intestine Small	intestine
2	chr4:101942600-102024400	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr4:101943800-102023400	Weak transcription	Fetal Lung	lung
4	chr4:101947800-102012600	Weak transcription	Fetal Muscle Leg	muscle
5	chr4:101953600-102015200	Weak transcription	Fetal Intestine Large	intestine
6	chr4:101959000-102023000	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr4:101960800-102019800	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr4:101961000-102024600	Weak transcription	NHEK	skin
9	chr4:101961200-102024600	Weak transcription	Small Intestine	intestine
10	chr4:101978000-102024600	Weak transcription	Left Ventricle	heart
11	chr4:101978400-102023000	Weak transcription	NHLF	lung
12	chr4:101980000-102023200	Weak transcription	NHDF-Ad	bronchial
13	chr4:101981600-102010600	Weak transcription	Aorta	Aorta
14	chr4:101981800-102025000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr4:101982000-102023000	Weak transcription	Osteobl	bone
16	chr4:101982400-102024400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr4:101986000-102010200	Weak transcription	Psoas Muscle	Psoas
18	chr4:101986200-102023000	Weak transcription	Fetal Brain Female	brain
19	chr4:101988000-102010800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr4:101988200-102024400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr4:101988400-102023800	Weak transcription	Fetal Kidney	kidney
22	chr4:101989400-102024600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr4:101990000-102014200	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr4:101991800-102015600	Weak transcription	Placenta	Placenta
25	chr4:101992400-102010000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr4:101992400-102010400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr4:101992400-102024600	Weak transcription	Pancreas	Pancrea
28	chr4:101992800-102023600	Weak transcription	NH-A	brain
29	chr4:101993000-102031600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr4:101993600-102010400	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr4:101994800-102029800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr4:101995800-102009200	Weak transcription	Fetal Brain Male	brain
33	chr4:101996600-102024600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr4:101997600-102023400	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr4:101997800-102012600	Weak transcription	Brain Hippocampus Middle	brain
36	chr4:101997800-102034600	Weak transcription	HepG2	liver
37	chr4:101998600-102010000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr4:101999600-102025200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr4:102000400-102010200	Weak transcription	Ovary	ovary
40	chr4:102000600-102018800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr4:102000800-102023600	Weak transcription	Fetal Stomach	stomach
42	chr4:102000800-102024600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr4:102000800-102032400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr4:102002600-102023200	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr4:102002800-102030600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
46	chr4:102003400-102019400	Weak transcription	Liver	Liver
47	chr4:102003400-102024400	Weak transcription	Duodenum Mucosa	Duodenum
48	chr4:102003600-102011800	Weak transcription	Rectal Smooth Muscle	rectum
49	chr4:102003600-102023400	Weak transcription	HMEC	breast
50	chr4:102004200-102023400	Weak transcription	HSMM	muscle

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