Variant report

Variant	esv3385008
Chromosome Location	chr4:128959396-128991050
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1288)
CpG islands
(count:855)
Chromatin interactive
region (count:56)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1288 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:128986727-128987315	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:128972329-128972573	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:128981543-128982598	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:128984105-128984249	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:128983400-128983649	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:128981911-128982070	K562	blood:	n/a	n/a
7	ATF2	chr4:128983220-128983669	GM12878	blood:	n/a	n/a
8	ATF2	chr4:128982074-128982372	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr4:128982261-128982629	GM12878	blood:	n/a	n/a
10	BACH1	chr4:128982219-128982529	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr4:128983464-128983885	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCLAF1	chr4:128983180-128983608	GM12878	blood:	n/a	chr4:128983286-128983295 chr4:128983261-128983274
13	BCLAF1	chr4:128981785-128982624	GM12878	blood:	n/a	chr4:128981987-128982000 chr4:128982154-128982167 chr4:128982206-128982215 chr4:128982534-128982543 chr4:128982538-128982551 chr4:128981979-128981992
14	BCLAF1	chr4:128982700-128983596	GM12878	blood:	n/a	chr4:128983023-128983036 chr4:128983286-128983295 chr4:128983261-128983274 chr4:128982948-128982961
15	BCLAF1	chr4:128981808-128982661	GM12878	blood:	n/a	chr4:128981987-128982000 chr4:128982154-128982167 chr4:128982206-128982215 chr4:128982534-128982543 chr4:128982538-128982551 chr4:128981979-128981992
16	BCLAF1	chr4:128981687-128982576	K562	blood:	n/a	chr4:128981987-128982000 chr4:128982154-128982167 chr4:128982206-128982215 chr4:128982534-128982543 chr4:128982538-128982551 chr4:128981979-128981992
17	BHLHE40	chr4:128983066-128983096	K562	blood:	n/a	n/a
18	BHLHE40	chr4:128981630-128982643	HepG2	liver:	n/a	chr4:128982345-128982361 chr4:128982410-128982426 chr4:128981962-128981978 chr4:128982321-128982337
19	BHLHE40	chr4:128984053-128984320	K562	blood:	n/a	n/a
20	BHLHE40	chr4:128983328-128983528	K562	blood:	n/a	n/a
21	BHLHE40	chr4:128981762-128982726	K562	blood:	n/a	chr4:128982345-128982361 chr4:128982410-128982426 chr4:128981962-128981978 chr4:128982321-128982337
22	BHLHE40	chr4:128982019-128983699	GM12878	blood:	n/a	chr4:128983261-128983277 chr4:128982951-128982967 chr4:128982345-128982361 chr4:128982410-128982426 chr4:128983045-128983061 chr4:128982321-128982337
23	BRCA1	chr4:128982927-128982934	HepG2	liver:	n/a	n/a
24	BRCA1	chr4:128982144-128982530	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr4:128982124-128982545	GM12878	blood:	n/a	n/a
26	BRCA1	chr4:128981582-128982559	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr4:128981937-128982575	HepG2	liver:	n/a	n/a
28	CBX3	chr4:128981716-128982568	K562	blood:	n/a	n/a
29	CBX3	chr4:128983157-128983733	K562	blood:	n/a	n/a
30	CBX3	chr4:128982070-128982300	K562	blood:	n/a	n/a
31	CCNT2	chr4:128981845-128983664	K562	blood:	n/a	n/a
32	CEBPB	chr4:128987002-128987347	ECC-1	luminal epithelium:	n/a	n/a
33	CEBPB	chr4:128960990-128961190	K562	blood:	n/a	n/a
34	CEBPB	chr4:128971717-128971924	HepG2	liver:	n/a	chr4:128971874-128971885
35	CEBPB	chr4:128981764-128982617	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr4:128981890-128982576	HepG2	liver:	n/a	n/a
37	CEBPB	chr4:128987322-128987482	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr4:128971720-128971927	Hela-S3	cervix:	n/a	chr4:128971874-128971885
39	CEBPB	chr4:128986958-128987539	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:128986915-128987537	HepG2	liver:	n/a	n/a
41	CEBPB	chr4:128983273-128983627	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr4:128971730-128971923	IMR90	lung:	n/a	chr4:128971874-128971885
43	CEBPB	chr4:128961019-128961299	IMR90	lung:	n/a	n/a
44	CEBPB	chr4:128982290-128982569	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr4:128981746-128981955	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr4:128971720-128972069	H1-hESC	embryonic stem cell:	n/a	chr4:128971874-128971885
47	CEBPB	chr4:128976570-128977013	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPD	chr4:128982361-128982731	HepG2	liver:	n/a	n/a
49	CEBPD	chr4:128982442-128982617	HepG2	liver:	n/a	n/a
50	CEBPD	chr4:128981823-128982353	HepG2	liver:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:128987117-128987167	HNPCEpiC	eye:	n/a
2	chr4:128987117-128987167	HNPCEpiC	eye:	n/a
3	chr4:128968151-128968201	ovcar-3	ovarian:	n/a
4	chr4:128987117-128987167	AG04449	skin:	fetal
5	chr4:128981486-128981536	NHDF-neo	bronchial:	n/a
6	chr4:128982446-128982496	H1-hESC	embryonic stem cell:	embryo
7	chr4:128979593-128979643	ProgFib	skin:	n/a
8	chr4:128983807-128983857	NB4	blood:	n/a
9	chr4:128983634-128983684	AG10803	skin:	n/a
10	chr4:128983634-128983684	Hepatocyte	liver:	n/a
11	chr4:128982446-128982496	HRE	kidney:	n/a
12	chr4:128982462-128982512	GM12891	blood:	n/a
13	chr4:128983441-128983491	HPAEpiC	pulmonary alveolar:	n/a
14	chr4:128987117-128987167	ECC-1	luminal epithelium:	n/a
15	chr4:128982454-128982504	HUVEC	blood vessel:	n/a
16	chr4:128983441-128983491	HNPCEpiC	eye:	n/a
17	chr4:128979593-128979643	AG09319	gingival:	n/a
18	chr4:128983807-128983857	AG10803	skin:	n/a
19	chr4:128983279-128983329	GM12892	blood:	n/a
20	chr4:128982446-128982496	IMR90	lung:	fetal
21	chr4:128979593-128979643	K562	blood:	n/a
22	chr4:128983441-128983491	HEEpiC	esophagus:	n/a
23	chr4:128983279-128983329	MCF-7	breast:	n/a
24	chr4:128983279-128983329	T-47D	breast:	n/a
25	chr4:128982454-128982504	Caco-2	colon:	n/a
26	chr4:128981486-128981536	ECC-1	luminal epithelium:	n/a
27	chr4:128981985-128982035	HPAEpiC	pulmonary alveolar:	n/a
28	chr4:128983807-128983857	GM19239	blood:	n/a
29	chr4:128981252-128981302	AG04449	skin:	fetal
30	chr4:128983279-128983329	ProgFib	skin:	n/a
31	chr4:128981985-128982035	SK-N-SH_RA	brain:	n/a
32	chr4:128983279-128983329	NB4	blood:	n/a
33	chr4:128981918-128981968	BJ	skin:	n/a
34	chr4:128983634-128983684	AG04450	lung:	fetal
35	chr4:128987117-128987167	HCM	heart:	n/a
36	chr4:128981486-128981536	HCPEpiC	choroid plexus:	n/a
37	chr4:128982454-128982504	SK-N-SH	brain:	n/a
38	chr4:128982462-128982512	AG10803	skin:	n/a
39	chr4:128968151-128968201	SAEC	small airway:	n/a
40	chr4:128983807-128983857	AG04449	skin:	fetal
41	chr4:128979593-128979643	GM06990	blood:	n/a
42	chr4:128982462-128982512	PANC-1	pancreas:	n/a
43	chr4:128968151-128968201	ProgFib	skin:	n/a
44	chr4:128987117-128987167	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:128981985-128982035	LNCaP	prostate:	n/a
46	chr4:128982446-128982496	SK-N-SH	brain:	n/a
47	chr4:128983807-128983857	ovcar-3	ovarian:	n/a
48	chr4:128983807-128983857	HCT-116	colon:	n/a
49	chr4:128979593-128979643	HCPEpiC	choroid plexus:	n/a
50	chr4:128982446-128982496	ovcar-3	ovarian:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:128884064..128888795-chr4:128980591..128984632,7	MCF-7	breast:
2	chr4:128981936..128982808-chrX:48754752..48755652,2	Hela-S3	cervix:
3	chr4:128951358..128954416-chr4:128957350..128961116,3	K562	blood:
4	chr4:128980667..128982380-chr4:129732444..129734327,2	MCF-7	breast:
5	chr4:128982778..128984793-chr4:129000011..129002155,2	K562	blood:
6	chr17:79478887..79479404-chr4:128982377..128982993,2	HCT-116	colon:
7	chr4:128980795..128984031-chr4:129730059..129735028,7	K562	blood:
8	chr4:128980866..128984600-chr4:128984636..128991176,13	K562	blood:
9	chr4:128885127..128890546-chr4:128980550..128983845,11	K562	blood:
10	chr4:128981378..128983346-chr4:128988931..128991317,2	MCF-7	breast:
11	chr4:128976139..128978653-chr4:128980606..128983915,3	K562	blood:
12	chr4:128978832..128981419-chr4:128985568..128987375,3	MCF-7	breast:
13	chr4:128980375..128984020-chr4:128989687..128993521,7	MCF-7	breast:
14	chr4:128701934..128705815-chr4:128979420..128984468,5	K562	blood:
15	chr4:128965043..128967324-chr4:128970165..128972854,2	K562	blood:
16	chr19:14229250..14230220-chr4:128982049..128982904,2	NB4	blood:
17	chr4:128884631..128886796-chr4:128984225..128985783,2	K562	blood:
18	chr4:128962288..128965016-chr4:128980229..128982720,2	MCF-7	breast:
19	chr4:128971956..128976061-chr4:128979961..128983242,4	MCF-7	breast:
20	chr4:128894792..128897559-chr4:128980082..128981594,2	K562	blood:
21	chr4:128704412..128707298-chr4:128961390..128962950,2	MCF-7	breast:
22	chr4:128965043..128967324-chr4:128970165..128972854,2	K562	blood:
23	chr4:128981725..128985397-chr4:129207989..129209697,3	K562	blood:
24	chr4:128884948..128891801-chr4:128980633..128984811,17	K562	blood:
25	chr4:128989561..128991603-chr4:128996891..128999505,2	K562	blood:
26	chr4:128986963..128989911-chr4:129006823..129010664,3	K562	blood:
27	chr4:128702147..128704685-chr4:128980177..128982661,2	MCF-7	breast:
28	chr4:128976139..128979526-chr4:128980143..128983915,6	K562	blood:
29	chr15:45003006..45003782-chr4:128982373..128982889,2	Hela-S3	cervix:
30	chr4:128959166..128961606-chr4:128981909..128983622,2	MCF-7	breast:
31	chr4:128981661..128982334-chr6:130031273..130031967,2	NB4	blood:
32	chr4:128980375..128984020-chr4:128989687..128993521,7	MCF-7	breast:
33	chr4:128869172..128871004-chr4:128982512..128984743,2	K562	blood:
34	chr4:128978832..128981419-chr4:128985568..128987375,3	MCF-7	breast:
35	chr4:128980866..128984600-chr4:128984636..128991176,13	K562	blood:
36	chr11:61129378..61130089-chr4:128981023..128981777,2	Hela-S3	cervix:
37	chr4:128553197..128555974-chr4:128981706..128984336,2	K562	blood:
38	chr1:110577159..110578119-chr4:128981949..128982607,2	Hela-S3	cervix:
39	chr4:128986963..128988724-chr4:129006823..129009589,2	K562	blood:
40	chr4:128980795..128982891-chr4:129730267..129732892,3	K562	blood:
41	chr4:128970942..128973743-chr4:128980742..128984354,4	K562	blood:
42	chr4:128974249..128979637-chr4:128979760..128983814,7	MCF-7	breast:
43	chr4:128981817..128983526-chr4:129043171..129045384,2	MCF-7	breast:
44	chr4:128884518..128888041-chr4:128980422..128985043,7	MCF-7	breast:
45	chr2:85132320..85133212-chr4:128982045..128982946,2	Hela-S3	cervix:
46	chr4:128869172..128872005-chr4:128982512..128984948,2	K562	blood:
47	chr16:67217539..67218173-chr4:128981980..128982888,2	Hela-S3	cervix:
48	chr4:128981698..128985397-chr4:129207989..129210555,4	K562	blood:
49	chr4:128986308..128988664-chr4:129730557..129733784,3	K562	blood:
50	chr4:128593863..128595593-chr4:128981619..128984198,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MFSD8-7	chr4:128981059-128981632	NONHSAT098254

No data

Variant related genes	Relation type
ENSG00000241651	TF binding region
LARP1B	TF binding region
ENSG00000241651	CpG island
LARP1B	CpG island
ENSG00000267783	chromatin interactions
ENSG00000102103	chromatin interactions
ENSG00000142731	chromatin interactions
ENSG00000166710	chromatin interactions
ENSG00000164070	chromatin interactions
ENSG00000164074	chromatin interactions
ENSG00000184009	chromatin interactions
ENSG00000149483	chromatin interactions
ENSG00000138709	chromatin interactions
ENSG00000229474	chromatin interactions
ENSG00000077684	chromatin interactions
ENSG00000265072	chromatin interactions
ENSG00000241651	chromatin interactions
ENSG00000164073	chromatin interactions
ENSG00000146376	chromatin interactions
ENSG00000166598	chromatin interactions
ENSG00000126768	chromatin interactions
ENSG00000034510	chromatin interactions
ENSG00000164066	chromatin interactions
ENSG00000143093	chromatin interactions
ENSG00000196123	chromatin interactions
ENSG00000162144	chromatin interactions
ENSG00000164040	chromatin interactions

Extended variants
information (count: 1227 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1227 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142950239	chr4:128959440-128959441	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs189525127	chr4:128959510-128959511	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs541768202	chr4:128959570-128959571	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs371183252	chr4:128959646-128959647	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs112793133	chr4:128959742-128959743	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs532797804	chr4:128959767-128959768	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs369053807	chr4:128959808-128959809	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs116109101	chr4:128959901-128959902	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs550641134	chr4:128960026-128960027	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs35443257	chr4:128960059-128960060	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs530546236	chr4:128960066-128960067	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs181379972	chr4:128960108-128960109	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs185998000	chr4:128960149-128960150	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs111520131	chr4:128960151-128960152	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs33997142	chr4:128960156-128960157	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs534484158	chr4:128960202-128960203	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs539717637	chr4:128960203-128960204	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs190525983	chr4:128960215-128960216	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs554223655	chr4:128960241-128960242	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs199621017	chr4:128960248-128960249	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs201395368	chr4:128960300-128960301	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs61578534	chr4:128960335-128960336	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs139524281	chr4:128960337-128960338	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs68181480	chr4:128960340-128960341	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs571480458	chr4:128960457-128960458	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs538548669	chr4:128960539-128960540	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs11098945	chr4:128960569-128960570	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs115661869	chr4:128960592-128960593	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs543969012	chr4:128960615-128960616	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs73847089	chr4:128960636-128960637	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs80185718	chr4:128960672-128960673	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs541572644	chr4:128960685-128960686	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs78319303	chr4:128960841-128960842	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs533727105	chr4:128960881-128960882	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs545352692	chr4:128960887-128960888	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs563328704	chr4:128960897-128960898	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs530387545	chr4:128960905-128960906	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs138685224	chr4:128960948-128960949	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs183087199	chr4:128961018-128961019	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs528281608	chr4:128961098-128961099	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs566038485	chr4:128961109-128961110	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs113733421	chr4:128961116-128961117	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs370751625	chr4:128961120-128961121	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs77829959	chr4:128961201-128961202	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs146961850	chr4:128961245-128961246	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs187009596	chr4:128961246-128961247	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs192301609	chr4:128961278-128961279	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs138019954	chr4:128961300-128961301	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs537395765	chr4:128961323-128961324	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs114032069	chr4:128961368-128961369	Weak transcription	Chromatin interactive region	1 gene(s)	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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	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
Breast cancer	17603634	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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Olfactory neuroblastoma	18408657	CNVD
Developmental delay	21147756	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myelofibrosis	22110671	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Gastric cancer	16891809	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:583 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:128887600-128981200	Weak transcription	Psoas Muscle	Psoas
2	chr4:128934400-128963000	Weak transcription	Brain Hippocampus Middle	brain
3	chr4:128935600-128962400	Weak transcription	HMEC	breast
4	chr4:128938800-128962000	Weak transcription	NH-A	brain
5	chr4:128941800-128962600	Weak transcription	Small Intestine	intestine
6	chr4:128941800-128963000	Weak transcription	Fetal Kidney	kidney
7	chr4:128945600-128961800	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr4:128947000-128963000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:128948000-128962800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr4:128950400-128960400	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr4:128950600-128959400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:128951200-128960200	Weak transcription	Fetal Stomach	stomach
13	chr4:128951200-128961400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr4:128951400-128960200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr4:128951400-128963800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr4:128951400-128981800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr4:128951800-128962200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr4:128952000-128962400	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr4:128952200-128962400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr4:128952200-128962600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr4:128952200-128962800	Weak transcription	Primary B cells from cord blood	blood
22	chr4:128952200-128962800	Weak transcription	HSMM	muscle
23	chr4:128953400-128963200	Weak transcription	Fetal Thymus	thymus
24	chr4:128953600-128959400	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr4:128953600-128962800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr4:128953800-128963600	Weak transcription	Fetal Muscle Leg	muscle
27	chr4:128954000-128959400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr4:128954200-128962800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr4:128954200-128963000	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr4:128954200-128963200	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr4:128956200-128960000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr4:128958000-128961400	Weak transcription	Fetal Intestine Small	intestine
33	chr4:128963800-128964000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
34	chr4:128967400-128967800	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr4:128968600-128968800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr4:128968800-128975400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr4:128970800-128971400	Enhancers	HSMMtube	muscle
38	chr4:128971000-128971400	Enhancers	A549	lung
39	chr4:128971400-128972000	Weak transcription	HSMMtube	muscle
40	chr4:128971800-128972600	Active TSS	HepG2	liver
41	chr4:128972000-128972200	Enhancers	HSMMtube	muscle
42	chr4:128974600-128976200	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr4:128975400-128976000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr4:128975600-128976800	Enhancers	H1 Cell Line	embryonic stem cell
45	chr4:128975800-128976200	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr4:128975800-128977000	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr4:128975800-128977000	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr4:128976000-128976200	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr4:128976000-128976600	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr4:128976000-128979400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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