Variant report

Variant	nsv594120
Chromosome Location	chr4:48251916-48274152
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:909)
CpG islands
(count:1221)
Chromatin interactive
region (count:53)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:909 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:48271156-48271462	K562	blood:	n/a	n/a
2	ARID3A	chr4:48271978-48272494	K562	blood:	n/a	n/a
3	ARID3A	chr4:48260893-48260896	K562	blood:	n/a	n/a
4	ATF1	chr4:48257322-48257741	K562	blood:	n/a	n/a
5	ATF1	chr4:48272999-48273508	K562	blood:	n/a	n/a
6	ATF1	chr4:48254522-48254801	K562	blood:	n/a	n/a
7	ATF2	chr4:48271888-48272435	GM12878	blood:	n/a	n/a
8	ATF2	chr4:48272043-48272668	GM12878	blood:	n/a	n/a
9	ATF2	chr4:48271260-48271747	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr4:48271289-48271867	GM12878	blood:	n/a	n/a
11	ATF3	chr4:48257249-48257555	K562	blood:	n/a	n/a
12	BACH1	chr4:48271610-48271743	K562	blood:	n/a	n/a
13	BACH1	chr4:48253636-48253639	K562	blood:	n/a	n/a
14	BACH1	chr4:48271474-48271674	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr4:48272139-48272826	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr4:48272285-48272805	K562	blood:	n/a	n/a
17	BATF	chr4:48273182-48273516	GM12878	blood:	n/a	n/a
18	BCL3	chr4:48254027-48254418	GM12878	blood:	n/a	n/a
19	BCL3	chr4:48271926-48272500	GM12878	blood:	n/a	chr4:48272028-48272041
20	BCL3	chr4:48252364-48252729	GM12878	blood:	n/a	n/a
21	BCL3	chr4:48252361-48252701	GM12878	blood:	n/a	n/a
22	BCLAF1	chr4:48272931-48273514	GM12878	blood:	n/a	n/a
23	BCLAF1	chr4:48271899-48272596	GM12878	blood:	n/a	chr4:48272028-48272041
24	BCLAF1	chr4:48271929-48272686	GM12878	blood:	n/a	chr4:48272028-48272041
25	BHLHE40	chr4:48257006-48257710	K562	blood:	n/a	n/a
26	BHLHE40	chr4:48271031-48271331	A549	lung:	n/a	chr4:48271167-48271176 chr4:48271162-48271183
27	BHLHE40	chr4:48270826-48272646	GM12878	blood:	n/a	chr4:48272386-48272407 chr4:48272391-48272400 chr4:48271167-48271176 chr4:48271162-48271183
28	BHLHE40	chr4:48269776-48272702	K562	blood:	n/a	chr4:48272386-48272407 chr4:48272391-48272400 chr4:48271167-48271176 chr4:48271162-48271183
29	BHLHE40	chr4:48271106-48272528	HepG2	liver:	n/a	chr4:48272386-48272407 chr4:48272391-48272400 chr4:48271167-48271176 chr4:48271162-48271183
30	BHLHE40	chr4:48273012-48273470	GM12878	blood:	n/a	n/a
31	BRCA1	chr4:48272079-48272126	GM12878	blood:	n/a	n/a
32	BRCA1	chr4:48271992-48272307	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr4:48271475-48271779	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr4:48257117-48257708	K562	blood:	n/a	n/a
35	CBX3	chr4:48273536-48274046	K562	blood:	n/a	n/a
36	CBX3	chr4:48271080-48271811	K562	blood:	n/a	n/a
37	CBX3	chr4:48257024-48257830	K562	blood:	n/a	n/a
38	CBX3	chr4:48271849-48272872	K562	blood:	n/a	n/a
39	CCNT2	chr4:48257456-48257726	K562	blood:	n/a	n/a
40	CCNT2	chr4:48271298-48272389	K562	blood:	n/a	n/a
41	CEBPB	chr4:48264951-48265244	IMR90	lung:	n/a	n/a
42	CEBPB	chr4:48268086-48268114	K562	blood:	n/a	n/a
43	CEBPB	chr4:48271928-48272438	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr4:48272017-48272162	K562	blood:	n/a	n/a
45	CEBPB	chr4:48271922-48272679	GM12878	blood:	n/a	n/a
46	CEBPB	chr4:48257258-48257772	K562	blood:	n/a	n/a
47	CEBPD	chr4:48272801-48273345	K562	blood:	n/a	n/a
48	CEBPD	chr4:48257294-48257844	K562	blood:	n/a	n/a
49	CEBPD	chr4:48257278-48257834	K562	blood:	n/a	n/a
50	CHD1	chr4:48271365-48271860	GM12878	blood:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:48272077-48272127	AG09309	skin:	n/a
2	chr4:48272077-48272127	AG09309	skin:	n/a
3	chr4:48271121-48271171	HRPEpiC	eye:	n/a
4	chr4:48272059-48272109	HEK293	kidney:	embryo
5	chr4:48271942-48271992	HRE	kidney:	n/a
6	chr4:48271107-48271157	SK-N-MC	brain:	n/a
7	chr4:48273240-48273290	HNPCEpiC	eye:	n/a
8	chr4:48269743-48269793	SKMC	muscle:	n/a
9	chr4:48272266-48272316	SAEC	small airway:	n/a
10	chr4:48272297-48272347	AG09319	gingival:	n/a
11	chr4:48271107-48271157	NHDF-neo	bronchial:	n/a
12	chr4:48271942-48271992	HCM	heart:	n/a
13	chr4:48271942-48271992	NHBE	bronchial:	n/a
14	chr4:48271826-48271876	AG09319	gingival:	n/a
15	chr4:48271893-48271943	SAEC	small airway:	n/a
16	chr4:48271893-48271943	MCF-7	breast:	n/a
17	chr4:48271149-48271199	SK-N-SH_RA	brain:	n/a
18	chr4:48271826-48271876	HAEpiC	amniotic membrane:	n/a
19	chr4:48273240-48273290	GM06990	blood:	n/a
20	chr4:48271072-48271122	GM12878	blood:	n/a
21	chr4:48257144-48257194	Caco-2	colon:	n/a
22	chr4:48272082-48272132	IMR90	lung:	fetal
23	chr4:48271918-48271968	SKMC	muscle:	n/a
24	chr4:48269743-48269793	Hepatocyte	liver:	n/a
25	chr4:48272082-48272132	HCF	heart:	n/a
26	chr4:48271942-48271992	LNCaP	prostate:	n/a
27	chr4:48269743-48269793	MCF10A-Er-Src	breast:	n/a
28	chr4:48272077-48272127	HCM	heart:	n/a
29	chr4:48271121-48271171	AG10803	skin:	n/a
30	chr4:48272513-48272563	PANC-1	pancreas:	n/a
31	chr4:48271121-48271171	HCPEpiC	choroid plexus:	n/a
32	chr4:48271107-48271157	GM19239	blood:	n/a
33	chr4:48273240-48273290	GM19239	blood:	n/a
34	chr4:48272082-48272132	ProgFib	skin:	n/a
35	chr4:48271918-48271968	Hela-S3	cervix:	n/a
36	chr4:48271072-48271122	NH-A	brain:	n/a
37	chr4:48272059-48272109	HCPEpiC	choroid plexus:	n/a
38	chr4:48271121-48271171	RPTEC	kidney:	n/a
39	chr4:48272082-48272132	LNCaP	prostate:	n/a
40	chr4:48272513-48272563	HEK293	kidney:	embryo
41	chr4:48269743-48269793	HUVEC	blood vessel:	n/a
42	chr4:48272077-48272127	SAEC	small airway:	n/a
43	chr4:48271149-48271199	CMK	blood:	n/a
44	chr4:48271893-48271943	K562	blood:	n/a
45	chr4:48271923-48271973	SKMC	muscle:	n/a
46	chr4:48272082-48272132	Hepatocyte	liver:	n/a
47	chr4:48271072-48271122	AG09319	gingival:	n/a
48	chr4:48271835-48271885	HCPEpiC	choroid plexus:	n/a
49	chr4:48271942-48271992	HepG2	liver:	n/a
50	chr4:48269743-48269793	HRPEpiC	eye:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:48269261..48273807-chr4:48342628..48344865,6	K562	blood:
2	chr4:48253065..48255231-chr4:48264308..48266240,2	K562	blood:
3	chr4:48257479..48259057-chr4:48261577..48263259,2	MCF-7	breast:
4	chr1:36234965..36235557-chr4:48271368..48271893,2	Hela-S3	cervix:
5	chr4:48270358..48273390-chr4:48340605..48344777,4	MCF-7	breast:
6	chr4:48260906..48263782-chr4:48270701..48273043,3	K562	blood:
7	chr4:48255521..48259627-chr4:48261501..48267509,10	K562	blood:
8	chr1:110090966..110091798-chr4:48271404..48272367,2	Hela-S3	cervix:
9	chr17:74448509..74449477-chr4:48271558..48272150,2	Hela-S3	cervix:
10	chr4:48255711..48257883-chr4:48270489..48272038,2	MCF-7	breast:
11	chr4:48271855..48272497-chr7:75544014..75544536,2	NB4	blood:
12	chr17:42297784..42298646-chr4:48271426..48272068,2	Hela-S3	cervix:
13	chr4:48265765..48268538-chr4:48269206..48271993,2	MCF-7	breast:
14	chr4:48253624..48256243-chr4:48267800..48270613,3	MCF-7	breast:
15	chr4:48248411..48250691-chr4:48255149..48257827,3	K562	blood:
16	chr4:48260906..48263782-chr4:48270701..48272361,2	K562	blood:
17	chr4:48272391..48273974-chr4:48279554..48281442,2	MCF-7	breast:
18	chr4:48255521..48259627-chr4:48261501..48267509,10	K562	blood:
19	chr16:30388892..30389437-chr4:48271312..48272199,2	Hela-S3	cervix:
20	chr12:120729424..120730098-chr4:48271378..48272195,2	Hela-S3	cervix:
21	chr4:48214281..48216760-chr4:48261228..48263562,2	K562	blood:
22	chr4:48204514..48206447-chr4:48263037..48265705,2	K562	blood:
23	chr12:56511687..56512571-chr4:48271561..48272061,2	Hela-S3	cervix:
24	chr4:48257479..48259057-chr4:48261577..48263259,2	MCF-7	breast:
25	chr4:48250701..48254731-chr4:48255352..48259390,5	K562	blood:
26	chr4:48253065..48255231-chr4:48264308..48266240,2	K562	blood:
27	chr4:48175041..48176757-chr4:48255815..48257585,2	K562	blood:
28	chr4:48259486..48261205-chr4:48485167..48487157,2	K562	blood:
29	chr19:40931605..40932510-chr4:48271137..48271845,2	Hela-S3	cervix:
30	chr4:48251827..48254565-chr4:48270153..48272053,2	K562	blood:
31	chr4:48191298..48193401-chr4:48269923..48271820,2	K562	blood:
32	chr4:48255045..48260439-chr4:48268334..48274456,6	K562	blood:
33	chr4:48264879..48267835-chr4:48269527..48271829,4	K562	blood:
34	chr4:48200101..48201896-chr4:48269773..48271789,2	K562	blood:
35	chr4:48248891..48252665-chr4:48270333..48273467,3	MCF-7	breast:
36	chr4:48250701..48254731-chr4:48255352..48259390,5	K562	blood:
37	chr3:156392017..156392697-chr4:48272003..48272899,2	NB4	blood:
38	chr4:48253624..48256243-chr4:48267800..48270613,3	MCF-7	breast:
39	chr4:48264879..48267835-chr4:48269527..48271829,4	K562	blood:
40	chr4:48264189..48268843-chr4:48269527..48273164,9	K562	blood:
41	chr4:48270141..48273598-chr4:48341900..48344865,7	K562	blood:
42	chr4:48256167..48259627-chr4:48260322..48264297,6	K562	blood:
43	chr16:9185283..9185902-chr4:48271309..48272302,2	Hela-S3	cervix:
44	chr4:48258706..48261232-chr4:48269979..48272552,2	MCF-7	breast:
45	chr4:48255487..48257034-chr4:48270351..48271892,2	K562	blood:
46	chr4:48262092..48265166-chr4:48265573..48268015,3	K562	blood:
47	chr2:96873932..96874574-chr4:48271406..48272081,2	Hela-S3	cervix:
48	chr4:48251770..48253352-chr4:48260141..48262130,2	K562	blood:
49	chr4:48256167..48259627-chr4:48260322..48264297,6	K562	blood:
50	chr4:48167349..48169980-chr4:48272046..48273556,2	K562	blood:

No data

Variant related genes	Relation type
TEC	TF binding region
TEC	CpG island
ENSG00000065135	chromatin interactions
ENSG00000243926	chromatin interactions
ENSG00000139641	chromatin interactions
ENSG00000109171	chromatin interactions
ENSG00000092853	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000204685	chromatin interactions
ENSG00000135482	chromatin interactions
ENSG00000127948	chromatin interactions
ENSG00000197019	chromatin interactions
ENSG00000129673	chromatin interactions
ENSG00000084090	chromatin interactions
ENSG00000135605	chromatin interactions
ENSG00000108312	chromatin interactions
ENSG00000180035	chromatin interactions
ENSG00000145248	chromatin interactions
ENSG00000163659	chromatin interactions
ENSG00000175931	chromatin interactions
ENSG00000265020	chromatin interactions
ENSG00000182831	chromatin interactions

Extended variants
information (count: 762 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:762 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1157532	chr4:48251916-48251917	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529901150	chr4:48251999-48252000	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs542085851	chr4:48252022-48252023	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs79407376	chr4:48252054-48252055	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs560632801	chr4:48252069-48252070	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs559766021	chr4:48252126-48252127	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs112871626	chr4:48252135-48252136	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs147930765	chr4:48252212-48252213	Weak transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs1355218	chr4:48252224-48252225	Weak transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs539240456	chr4:48252263-48252264	Weak transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs189807749	chr4:48252305-48252306	Weak transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs569543534	chr4:48252318-48252319	Weak transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs536898074	chr4:48252321-48252322	Weak transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs182477267	chr4:48252325-48252326	Weak transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs555297924	chr4:48252391-48252392	Weak transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs77357489	chr4:48252417-48252418	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs545903723	chr4:48252520-48252521	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs187073583	chr4:48252560-48252561	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs191883440	chr4:48252566-48252567	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs559031631	chr4:48252577-48252578	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs577233628	chr4:48252597-48252598	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs546599353	chr4:48252598-48252599	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs12507853	chr4:48252605-48252606	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs148970250	chr4:48252655-48252656	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs183293747	chr4:48252656-48252657	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs2352595	chr4:48252696-48252697	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs559997986	chr4:48252727-48252728	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs13117386	chr4:48252763-48252764	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs142918577	chr4:48252779-48252780	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs564220698	chr4:48252824-48252825	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs531267333	chr4:48252836-48252837	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs150969850	chr4:48252936-48252937	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs188739979	chr4:48252939-48252940	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs115691402	chr4:48252971-48252972	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs376542928	chr4:48252984-48252985	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs548929258	chr4:48252985-48252986	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs185659066	chr4:48252987-48252988	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs189519221	chr4:48253012-48253013	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs558641892	chr4:48253019-48253020	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs191204768	chr4:48253164-48253165	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs538003981	chr4:48253184-48253185	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs140769213	chr4:48253199-48253200	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs574324103	chr4:48253211-48253212	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs541600450	chr4:48253320-48253321	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs11732863	chr4:48253322-48253323	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs7674061	chr4:48253341-48253342	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs566680452	chr4:48253346-48253347	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs11724904	chr4:48253377-48253378	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs144613391	chr4:48253423-48253424	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs559465485	chr4:48253464-48253465	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	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
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	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
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:636 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:48242600-48252600	Weak transcription	Aorta	Aorta
2	chr4:48248800-48255200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr4:48248800-48270600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr4:48249600-48252600	Weak transcription	Primary B cells from cord blood	blood
5	chr4:48249600-48261600	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr4:48249800-48254200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr4:48249800-48255800	Weak transcription	NHDF-Ad	bronchial
8	chr4:48250000-48252600	Enhancers	Fetal Lung	lung
9	chr4:48250200-48254600	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr4:48250400-48254400	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr4:48250600-48252400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr4:48250600-48252400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr4:48250600-48255800	Weak transcription	Left Ventricle	heart
14	chr4:48250600-48259400	Weak transcription	Small Intestine	intestine
15	chr4:48251000-48252200	Enhancers	Primary hematopoietic stem cells	blood
16	chr4:48251000-48252200	Enhancers	GM12878-XiMat	blood
17	chr4:48251000-48256000	Weak transcription	Liver	Liver
18	chr4:48251400-48252000	Enhancers	K562	blood
19	chr4:48251400-48270000	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr4:48251600-48252400	Enhancers	Fetal Heart	heart
21	chr4:48251800-48270200	Weak transcription	Fetal Intestine Large	intestine
22	chr4:48252000-48253400	Weak transcription	K562	blood
23	chr4:48252200-48252600	Weak transcription	Primary hematopoietic stem cells	blood
24	chr4:48252200-48253600	ZNF genes & repeats	GM12878-XiMat	blood
25	chr4:48252400-48252600	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr4:48252400-48252600	Flanking Active TSS	Fetal Heart	heart
27	chr4:48252400-48252800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
28	chr4:48252600-48252800	ZNF genes & repeats	Aorta	Aorta
29	chr4:48252600-48253000	ZNF genes & repeats	Primary B cells from cord blood	blood
30	chr4:48252600-48253000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr4:48252600-48253200	Strong transcription	Primary hematopoietic stem cells	blood
32	chr4:48252600-48255200	Weak transcription	Fetal Lung	lung
33	chr4:48252600-48258200	Enhancers	Fetal Heart	heart
34	chr4:48252800-48253000	Weak transcription	Aorta	Aorta
35	chr4:48252800-48253600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
36	chr4:48253000-48253400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr4:48253000-48263000	Weak transcription	Primary B cells from cord blood	blood
38	chr4:48253200-48257400	Weak transcription	Primary hematopoietic stem cells	blood
39	chr4:48253400-48254800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr4:48253400-48255000	Enhancers	K562	blood
41	chr4:48253600-48254000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr4:48253600-48254000	Weak transcription	GM12878-XiMat	blood
43	chr4:48254000-48254600	Enhancers	GM12878-XiMat	blood
44	chr4:48254000-48254800	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr4:48254200-48254400	Enhancers	Brain Germinal Matrix	brain
46	chr4:48254200-48255200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr4:48254400-48254600	Enhancers	Lung	lung
48	chr4:48254400-48255400	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr4:48254400-48255400	Weak transcription	Brain Germinal Matrix	brain
50	chr4:48254600-48255000	Enhancers	Monocytes-CD14+_RO01746	blood

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