Variant report

Variant	nsv537355
Chromosome Location	chr4:171982072-172496279
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:762)
CpG islands
(count:122)
Chromatin interactive
region (count:48)
LncRNA
region (count:15)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:762 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:172255667-172256054	GM12878	blood:	n/a	n/a
2	ATF2	chr4:172255624-172256043	GM12878	blood:	n/a	n/a
3	BACH1	chr4:172431444-172431445	K562	blood:	n/a	n/a
4	BATF	chr4:172482588-172482958	GM12878	blood:	n/a	n/a
5	BATF	chr4:172482626-172482847	GM12878	blood:	n/a	n/a
6	BATF	chr4:172437873-172438100	GM12878	blood:	n/a	n/a
7	BATF	chr4:172440668-172440899	GM12878	blood:	n/a	n/a
8	BATF	chr4:172200351-172200545	GM12878	blood:	n/a	chr4:172200493-172200503
9	BATF	chr4:172351661-172352035	GM12878	blood:	n/a	n/a
10	BATF	chr4:172255782-172256095	GM12878	blood:	n/a	n/a
11	BATF	chr4:172437862-172438152	GM12878	blood:	n/a	n/a
12	BATF	chr4:172442956-172443210	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:172255762-172256128	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:172442922-172443175	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:172290340-172290372	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:172394476-172394542	GM12878	blood:	n/a	n/a
17	CBX3	chr4:172022964-172023416	HCT-116	colon:	n/a	n/a
18	CCNT2	chr4:172417411-172417571	K562	blood:	n/a	n/a
19	CCNT2	chr4:172392140-172392340	K562	blood:	n/a	n/a
20	CEBPB	chr4:172203896-172204135	HepG2	liver:	n/a	chr4:172204045-172204056
21	CEBPB	chr4:172124641-172125050	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr4:172455392-172455592	K562	blood:	n/a	chr4:172455485-172455496 chr4:172455485-172455498
23	CEBPB	chr4:172360395-172360608	HepG2	liver:	n/a	chr4:172360473-172360490
24	CEBPB	chr4:172053522-172053763	A549	lung:	n/a	chr4:172053668-172053679
25	CEBPB	chr4:172495139-172495358	A549	lung:	n/a	n/a
26	CEBPB	chr4:172495068-172495402	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:172478592-172478766	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr4:172398667-172398910	HepG2	liver:	n/a	chr4:172398829-172398840
29	CEBPB	chr4:172369264-172369330	K562	blood:	n/a	chr4:172369274-172369283 chr4:172369274-172369283 chr4:172369274-172369283 chr4:172369272-172369283 chr4:172369274-172369283 chr4:172369274-172369285
30	CEBPB	chr4:172167014-172167195	A549	lung:	n/a	chr4:172167137-172167148 chr4:172167137-172167148 chr4:172167135-172167148 chr4:172167135-172167148
31	CEBPB	chr4:172369109-172369454	HepG2	liver:	n/a	chr4:172369274-172369283 chr4:172369274-172369283 chr4:172369274-172369283 chr4:172369272-172369283 chr4:172369274-172369283 chr4:172369274-172369285
32	CEBPB	chr4:172053577-172053717	K562	blood:	n/a	chr4:172053668-172053679
33	CEBPB	chr4:172166965-172167188	HepG2	liver:	n/a	chr4:172167137-172167148 chr4:172167137-172167148 chr4:172167135-172167148 chr4:172167135-172167148
34	CEBPB	chr4:172433261-172433503	HepG2	liver:	n/a	chr4:172433432-172433443
35	CEBPB	chr4:172459925-172460246	HepG2	liver:	n/a	chr4:172460071-172460082 chr4:172460070-172460083 chr4:172460070-172460081 chr4:172460070-172460083
36	CEBPB	chr4:172459975-172460213	A549	lung:	n/a	chr4:172460071-172460082 chr4:172460070-172460083 chr4:172460070-172460081 chr4:172460070-172460083
37	CEBPB	chr4:172362417-172362543	Hela-S3	cervix:	n/a	chr4:172362429-172362442 chr4:172362426-172362443 chr4:172362431-172362442 chr4:172362429-172362442 chr4:172362451-172362462 chr4:172362431-172362442
38	CEBPB	chr4:172166854-172167190	IMR90	lung:	n/a	chr4:172167137-172167148 chr4:172167137-172167148 chr4:172167135-172167148 chr4:172167135-172167148
39	CEBPB	chr4:172104756-172105053	HepG2	liver:	n/a	chr4:172104935-172104946
40	CEBPB	chr4:172369099-172369446	IMR90	lung:	n/a	chr4:172369274-172369283 chr4:172369274-172369283 chr4:172369274-172369283 chr4:172369272-172369283 chr4:172369274-172369283 chr4:172369274-172369285
41	CEBPB	chr4:172356271-172356397	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:172369158-172369405	H1-hESC	embryonic stem cell:	n/a	chr4:172369274-172369283 chr4:172369274-172369283 chr4:172369274-172369283 chr4:172369272-172369283 chr4:172369274-172369283 chr4:172369274-172369285
43	CEBPB	chr4:172053509-172053823	HepG2	liver:	n/a	chr4:172053668-172053679
44	CEBPB	chr4:172467371-172467590	K562	blood:	n/a	n/a
45	CEBPB	chr4:172104656-172104928	A549	lung:	n/a	chr4:172104694-172104707
46	CEBPB	chr4:172125836-172126036	HepG2	liver:	n/a	chr4:172125958-172125969
47	CEBPB	chr4:172459966-172460180	K562	blood:	n/a	chr4:172460071-172460082 chr4:172460070-172460083 chr4:172460070-172460081 chr4:172460070-172460083
48	CEBPB	chr4:172053629-172053681	H1-hESC	embryonic stem cell:	n/a	chr4:172053668-172053679
49	CEBPB	chr4:172455324-172455674	HepG2	liver:	n/a	chr4:172455485-172455496 chr4:172455485-172455498
50	CEBPB	chr4:172455391-172455591	A549	lung:	n/a	chr4:172455485-172455496 chr4:172455485-172455498

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:172032402-172032452	HepG2	liver:	n/a
2	chr4:172032402-172032452	HMEC	breast:	n/a
3	chr4:172219751-172219801	SK-N-SH	brain:	n/a
4	chr4:172219751-172219801	H1-hESC	embryonic stem cell:	embryo
5	chr4:172032402-172032452	PrEC	prostate:	n/a
6	chr4:172032402-172032452	BJ	skin:	n/a
7	chr4:172032402-172032452	AG09319	gingival:	n/a
8	chr4:172032402-172032452	NB4	blood:	n/a
9	chr4:172219751-172219801	HL-60	blood:	n/a
10	chr4:172032402-172032452	GM19239	blood:	n/a
11	chr4:172032402-172032452	ECC-1	luminal epithelium:	n/a
12	chr4:172219751-172219801	SK-N-SH_RA	brain:	n/a
13	chr4:172219751-172219801	Hela-S3	cervix:	n/a
14	chr4:172032402-172032452	Jurkat	blood:	n/a
15	chr4:172219751-172219801	Jurkat	blood:	n/a
16	chr4:172219751-172219801	GM12892	blood:	n/a
17	chr4:172032402-172032452	MCF-7	breast:	n/a
18	chr4:172032402-172032452	A549	lung:	n/a
19	chr4:172219751-172219801	Caco-2	colon:	n/a
20	chr4:172219751-172219801	PFSK-1	brain:	n/a
21	chr4:172219751-172219801	HepG2	liver:	n/a
22	chr4:172219751-172219801	HCM	heart:	n/a
23	chr4:172032402-172032452	Caco-2	colon:	n/a
24	chr4:172219751-172219801	NT2-D1	testis:	n/a
25	chr4:172219751-172219801	T-47D	breast:	n/a
26	chr4:172219751-172219801	BJ	skin:	n/a
27	chr4:172032402-172032452	HCF	heart:	n/a
28	chr4:172032402-172032452	K562	blood:	n/a
29	chr4:172032402-172032452	PANC-1	pancreas:	n/a
30	chr4:172032402-172032452	Hepatocyte	liver:	n/a
31	chr4:172219751-172219801	BE2_C	brain:	n/a
32	chr4:172219751-172219801	AG04450	lung:	fetal
33	chr4:172219751-172219801	HRCEpiC	kidney:	n/a
34	chr4:172032402-172032452	U87	brain:	n/a
35	chr4:172219751-172219801	MCF10A-Er-Src	breast:	n/a
36	chr4:172219751-172219801	IMR90	lung:	fetal
37	chr4:172032402-172032452	NH-A	brain:	n/a
38	chr4:172219751-172219801	GM12878	blood:	n/a
39	chr4:172032402-172032452	HRE	kidney:	n/a
40	chr4:172032402-172032452	HNPCEpiC	eye:	n/a
41	chr4:172032402-172032452	GM06990	blood:	n/a
42	chr4:172219751-172219801	CMK	blood:	n/a
43	chr4:172219751-172219801	SAEC	small airway:	n/a
44	chr4:172032402-172032452	RPTEC	kidney:	n/a
45	chr4:172219751-172219801	HMEC	breast:	n/a
46	chr4:172032402-172032452	AG04450	lung:	fetal
47	chr4:172032402-172032452	GM12892	blood:	n/a
48	chr4:172032402-172032452	NT2-D1	testis:	n/a
49	chr4:172219751-172219801	HEEpiC	esophagus:	n/a
50	chr4:172219751-172219801	MCF-7	breast:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:172177315..172180021-chr4:172192339..172193935,2	MCF-7	breast:
2	chr4:171912038..171912871-chr4:172107600..172108526,5	MCF-7	breast:
3	chr4:172215180..172217206-chr4:172338805..172340584,2	K562	blood:
4	chr4:172207640..172210235-chr4:172213745..172216390,2	K562	blood:
5	chr4:171988253..171989053-chr4:172107601..172108441,2	MCF-7	breast:
6	chr4:171988510..171989198-chr4:172107647..172108598,3	MCF-7	breast:
7	chr4:172430767..172434419-chr4:172434504..172437331,3	K562	blood:
8	chr4:172251016..172251858-chr8:105627743..105628264,2	MCF-7	breast:
9	chr4:172207640..172210235-chr4:172213745..172216390,2	K562	blood:
10	chr20:46012485..46013388-chr4:172055587..172056582,2	MCF-7	breast:
11	chr4:172406443..172409078-chr4:172410535..172412663,2	MCF-7	breast:
12	chr4:172410818..172412907-chr4:172427241..172429415,2	K562	blood:
13	chr4:171929252..171929804-chr4:172107612..172108208,2	MCF-7	breast:
14	chr4:172358064..172360029-chr4:172362493..172364651,2	MCF-7	breast:
15	chr4:172410818..172412907-chr4:172427241..172429415,2	K562	blood:
16	chr4:172039170..172041324-chr4:172052876..172055038,2	K562	blood:
17	chr4:172039170..172041324-chr4:172052876..172055038,2	K562	blood:
18	chr4:171796784..171797466-chr4:172107812..172108701,2	MCF-7	breast:
19	chr4:172177315..172180021-chr4:172192339..172193935,2	MCF-7	breast:
20	chr4:171180830..171181408-chr4:172107535..172108542,3	MCF-7	breast:
21	chr4:172176185..172177998-chr4:172184705..172186321,2	MCF-7	breast:
22	chr4:172107312..172109351-chr4:172113285..172116114,4	MCF-7	breast:
23	chr4:171510438..171511386-chr4:172107962..172108533,2	MCF-7	breast:
24	chr4:172164256..172166842-chr4:172197011..172199170,2	MCF-7	breast:
25	chr4:171988253..171989053-chr4:172107601..172108441,2	MCF-7	breast:
26	chr4:172176185..172177998-chr4:172184705..172186321,2	MCF-7	breast:
27	chr4:172406443..172409078-chr4:172410535..172412663,2	MCF-7	breast:
28	chr4:172430767..172434419-chr4:172434504..172437331,3	K562	blood:
29	chr4:172107475..172108527-chr4:172706281..172707121,4	MCF-7	breast:
30	chr4:172066871..172068537-chr4:172070530..172072386,2	K562	blood:
31	chr4:172215180..172217206-chr4:172338805..172340584,2	K562	blood:
32	chr4:172435507..172438081-chr4:172439461..172441174,2	MCF-7	breast:
33	chr4:172212656..172215279-chr4:172273980..172275669,2	K562	blood:
34	chr1:214429883..214430693-chr4:172382652..172383247,2	MCF-7	breast:
35	chr4:172190237..172191869-chr4:172194086..172195652,2	K562	blood:
36	chr4:172435507..172438081-chr4:172439461..172441174,2	MCF-7	breast:
37	chr4:172190237..172191869-chr4:172194086..172195652,2	K562	blood:
38	chr4:172066253..172068537-chr4:172070399..172072386,3	K562	blood:
39	chr4:172358064..172360029-chr4:172362493..172364651,2	MCF-7	breast:
40	chr4:172177030..172177816-chr8:102919199..102919846,2	MCF-7	breast:
41	chr4:172066253..172068537-chr4:172070399..172072386,3	K562	blood:
42	chr4:172164256..172166842-chr4:172197011..172199170,2	MCF-7	breast:
43	chr4:172212656..172215279-chr4:172273980..172275669,2	K562	blood:
44	chr4:172108195..172108993-chr4:173123571..173124091,2	MCF-7	breast:
45	chr4:172107312..172109351-chr4:172113285..172116114,4	MCF-7	breast:
46	chr4:172491997..172494693-chr4:173072561..173074152,2	K562	blood:
47	chr4:172066871..172068537-chr4:172070530..172072386,2	K562	blood:
48	chr4:171988510..171989198-chr4:172107647..172108598,3	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GALNTL6-3	chr4:172213931-172214064	ucscGeneNc_uc003isu_1
2	lnc-GALNTL6-3	chr4:172213554-172213624	ucscGeneNc_uc003isu_1
3	lnc-GALNTL6-3	chr4:172215603-172216886	ucscGeneNc_uc003isu_1
4	lnc-GALNTL6-3	chr4:172213081-172213143	ucscGeneNc_uc003isu_1
5	lnc-GALNTL6-5	chr4:172034940-172034963	NONHSAT099197
6	lnc-GALNTL6-1	chr4:172207154-172207173	XLOC_003778
7	lnc-AADAT-12	chr4:172090360-172091093	NONHSAT099198
8	lnc-AADAT-5	chr4:172474151-172474376	XLOC_004159
9	lnc-GALNTL6-3	chr4:172198334-172198560	ucscGeneNc_uc003isu_1
10	lnc-GALNTL6-1	chr4:172209255-172209571	XLOC_003778
11	lnc-GALNTL6-4	chr4:172151463-172152858	l_2776_chr4:172136918-172152369_testes
12	lnc-AADAT-5	chr4:172485115-172485236	XLOC_004159
13	lnc-AADAT-5	chr4:172485363-172485418	XLOC_004159
14	lnc-GALNTL6-4	chr4:172136919-172136961	l_2776_chr4:172136918-172152369_testes
15	lnc-GALNTL6-5	chr4:172035174-172035732	NONHSAT099197

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6082	chr4:172107340-172107358	MIMAT0023707

No data

Variant related genes	Relation type
ENSG00000248339	TF binding region
ENSG00000249525	TF binding region
ENSG00000251176	TF binding region
ENSG00000248755	TF binding region
ENSG00000248339	CpG island
ENSG00000249525	CpG island
ENSG00000251176	CpG island
ENSG00000248755	CpG island
LYSMD1	miRNA target sites
LYSMD3	miRNA target sites
GNA13	miRNA target sites

Extended variants
information (count: 3782 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:3782 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562803893	chr4:171986072-171986073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs531847904	chr4:171986101-171986102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs191551633	chr4:171986114-171986115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs114431659	chr4:171986162-171986163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs72706581	chr4:171986177-171986178	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs565457809	chr4:171986633-171986634	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs28896814	chr4:171986641-171986642	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs138710376	chr4:171986688-171986689	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs200846396	chr4:171986691-171986692	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs72706585	chr4:171986743-171986744	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs72706586	chr4:171986751-171986752	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs568544994	chr4:171986783-171986784	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs546373119	chr4:171986796-171986797	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs551031312	chr4:171986803-171986804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs571023102	chr4:171986804-171986805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs184115272	chr4:171986917-171986918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs553938545	chr4:171986918-171986919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567448006	chr4:171986942-171986943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs72706587	chr4:171986984-171986985	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs147973387	chr4:171987002-171987003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs576535583	chr4:171987030-171987031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs545441817	chr4:171987056-171987057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538815708	chr4:171987156-171987157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559365147	chr4:172007403-172007404	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs35913756	chr4:172007418-172007419	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs67589304	chr4:172007431-172007432	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs368210332	chr4:172007432-172007433	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs70937429	chr4:172007433-172007434	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs74281532	chr4:172007437-172007438	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs574353094	chr4:172007459-172007460	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs192770306	chr4:172007488-172007489	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs568103733	chr4:172007517-172007518	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs185542098	chr4:172007559-172007560	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs577185239	chr4:172007560-172007561	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs113756607	chr4:172007602-172007603	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs370816874	chr4:172007612-172007613	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs537247561	chr4:172007623-172007624	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs550390743	chr4:172007638-172007639	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs190672810	chr4:172007649-172007650	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs578042014	chr4:172007732-172007733	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs181482204	chr4:172007769-172007770	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs184143502	chr4:172031626-172031627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs28650805	chr4:172031650-172031651	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs76741083	chr4:172031653-172031654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs189612340	chr4:172031687-172031688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs28417378	chr4:172031703-172031704	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs28366750	chr4:172031710-172031711	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs531357403	chr4:172031723-172031724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs536114382	chr4:172031757-172031758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548524304	chr4:172031788-172031789	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
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
Acute lymphoblastic leukemia	20067559	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
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Neuroblastoma	16790693	CNVD
Developmental delay	22127048	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16774939	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Gastric adenocarcinoma	19115996	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:179 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:171986000-171986200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:171986600-171986800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr4:171986800-171987200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr4:172007400-172007800	Active TSS	Fetal Heart	heart
5	chr4:172031600-172032600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr4:172032000-172032400	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr4:172032000-172032400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr4:172032000-172032800	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr4:172032200-172032600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:172032200-172032600	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr4:172039000-172039400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:172051400-172051600	Enhancers	Fetal Kidney	kidney
13	chr4:172051600-172051800	Enhancers	Gastric	stomach
14	chr4:172051600-172052000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr4:172051600-172052000	Flanking Active TSS	Fetal Kidney	kidney
16	chr4:172052000-172052200	Enhancers	Fetal Kidney	kidney
17	chr4:172054000-172054200	Enhancers	Primary hematopoietic stem cells	blood
18	chr4:172054400-172056000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr4:172054800-172055000	Enhancers	Primary hematopoietic stem cells	blood
20	chr4:172055200-172055600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:172073400-172074000	Enhancers	Aorta	Aorta
22	chr4:172077600-172077800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr4:172077800-172079600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr4:172078000-172078800	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr4:172078400-172078800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr4:172078400-172079000	Enhancers	Fetal Intestine Small	intestine
27	chr4:172078400-172079200	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr4:172078400-172079200	Enhancers	Small Intestine	intestine
29	chr4:172078400-172079400	Enhancers	Fetal Intestine Large	intestine
30	chr4:172078600-172078800	Enhancers	Duodenum Mucosa	Duodenum
31	chr4:172078600-172079200	Enhancers	Pancreas	Pancrea
32	chr4:172078800-172080000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr4:172079000-172079400	Active TSS	Fetal Intestine Small	intestine
34	chr4:172079600-172080200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr4:172080000-172080200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr4:172080200-172082600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr4:172083200-172083400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr4:172088400-172089000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr4:172088800-172089200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr4:172102200-172102600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr4:172113600-172114000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr4:172123800-172124400	Enhancers	Pancreas	Pancrea
43	chr4:172123800-172124400	Enhancers	A549	lung
44	chr4:172124400-172125400	Weak transcription	A549	lung
45	chr4:172124600-172125000	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr4:172124600-172125000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr4:172124800-172125400	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr4:172125400-172125600	Enhancers	A549	lung
49	chr4:172142200-172142600	Enhancers	Pancreas	Pancrea
50	chr4:172153600-172154200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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