Variant report

Variant	nsv1013260
Chromosome Location	chr4:75013441-75121643
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1852)
CpG islands
(count:854)
Chromatin interactive
region (count:136)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1852 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:75023522-75023797	K562	blood:	n/a	n/a
2	ARID3A	chr4:75067522-75068289	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:75023113-75023972	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:75071960-75072316	K562	blood:	n/a	n/a
5	ARID3A	chr4:75040243-75040439	K562	blood:	n/a	n/a
6	ARID3A	chr4:75021212-75021262	K562	blood:	n/a	n/a
7	ARID3A	chr4:75056779-75057213	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:75054958-75055346	K562	blood:	n/a	n/a
9	ARID3A	chr4:75020661-75020892	K562	blood:	n/a	n/a
10	ARID3A	chr4:75073507-75073514	K562	blood:	n/a	n/a
11	ARID3A	chr4:75054987-75055584	HepG2	liver:	n/a	n/a
12	ARID3A	chr4:75096789-75096882	K562	blood:	n/a	n/a
13	ATF1	chr4:75071874-75072276	K562	blood:	n/a	n/a
14	ATF2	chr4:75023507-75023908	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr4:75071823-75072691	GM12878	blood:	n/a	n/a
16	ATF2	chr4:75071810-75072598	GM12878	blood:	n/a	n/a
17	ATF2	chr4:75062780-75063229	GM12878	blood:	n/a	n/a
18	ATF2	chr4:75023487-75023984	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr4:75094472-75094740	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF3	chr4:75071934-75072120	K562	blood:	n/a	n/a
21	ATF3	chr4:75103285-75103754	HCT-116	colon:	n/a	n/a
22	ATF3	chr4:75023411-75023934	A549	lung:	n/a	chr4:75023646-75023655
23	ATF3	chr4:75071871-75072182	K562	blood:	n/a	n/a
24	BACH1	chr4:75023391-75024314	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr4:75073601-75073728	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr4:75096679-75096780	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr4:75024015-75024094	K562	blood:	n/a	n/a
28	BACH1	chr4:75096739-75096863	K562	blood:	n/a	n/a
29	BACH1	chr4:75023754-75023768	K562	blood:	n/a	n/a
30	BACH1	chr4:75083263-75083307	H1-hESC	embryonic stem cell:	n/a	n/a
31	BATF	chr4:75033917-75034237	GM12878	blood:	n/a	chr4:75034110-75034121
32	BCL11A	chr4:75023629-75024004	GM12878	blood:	n/a	n/a
33	BCL3	chr4:75023426-75024022	A549	lung:	n/a	chr4:75024006-75024019
34	BCL3	chr4:75023580-75024083	GM12878	blood:	n/a	chr4:75024006-75024019 chr4:75024013-75024026
35	BCL3	chr4:75067689-75068196	A549	lung:	n/a	n/a
36	BCLAF1	chr4:75023379-75024367	GM12878	blood:	n/a	chr4:75024006-75024019 chr4:75024013-75024026
37	BCLAF1	chr4:75023212-75023918	K562	blood:	n/a	n/a
38	BCLAF1	chr4:75071883-75072576	GM12878	blood:	n/a	chr4:75072403-75072412
39	BCLAF1	chr4:75094377-75094758	GM12878	blood:	n/a	n/a
40	BCLAF1	chr4:75023311-75024008	K562	blood:	n/a	n/a
41	BHLHE40	chr4:75056850-75057158	HepG2	liver:	n/a	n/a
42	BHLHE40	chr4:75054991-75055336	GM12878	blood:	n/a	n/a
43	BHLHE40	chr4:75023054-75024314	K562	blood:	n/a	chr4:75023644-75023660 chr4:75024010-75024026 chr4:75024026-75024042 chr4:75024005-75024021
44	BHLHE40	chr4:75023367-75024606	GM12878	blood:	n/a	chr4:75023644-75023660 chr4:75024010-75024026 chr4:75024026-75024042 chr4:75024005-75024021
45	BHLHE40	chr4:75046503-75046529	K562	blood:	n/a	n/a
46	BHLHE40	chr4:75067754-75068280	HepG2	liver:	n/a	n/a
47	BHLHE40	chr4:75073753-75073963	GM12878	blood:	n/a	n/a
48	BHLHE40	chr4:75071969-75072571	GM12878	blood:	n/a	n/a
49	BHLHE40	chr4:75071760-75072313	K562	blood:	n/a	n/a
50	BHLHE40	chr4:75023059-75024321	HepG2	liver:	n/a	chr4:75023644-75023660 chr4:75024010-75024026 chr4:75024026-75024042 chr4:75024005-75024021

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:75024153-75024203	NH-A	brain:	n/a
2	chr4:75024153-75024203	HepG2	liver:	n/a
3	chr4:75023849-75023899	GM06990	blood:	n/a
4	chr4:75023649-75023699	NT2-D1	testis:	n/a
5	chr4:75023658-75023708	HCPEpiC	choroid plexus:	n/a
6	chr4:75020915-75020965	HUVEC	blood vessel:	n/a
7	chr4:75026843-75026893	NH-A	brain:	n/a
8	chr4:75023664-75023714	SK-N-MC	brain:	n/a
9	chr4:75023606-75023656	NB4	blood:	n/a
10	chr4:75023540-75023590	GM12878	blood:	n/a
11	chr4:75023664-75023714	HRPEpiC	eye:	n/a
12	chr4:75023849-75023899	HNPCEpiC	eye:	n/a
13	chr4:75023849-75023899	IMR90	lung:	fetal
14	chr4:75023664-75023714	GM06990	blood:	n/a
15	chr4:75023746-75023796	NHDF-neo	bronchial:	n/a
16	chr4:75023719-75023769	HNPCEpiC	eye:	n/a
17	chr4:75023606-75023656	HPAEpiC	pulmonary alveolar:	n/a
18	chr4:75023649-75023699	PrEC	prostate:	n/a
19	chr4:75023719-75023769	ovcar-3	ovarian:	n/a
20	chr4:75026843-75026893	Hepatocyte	liver:	n/a
21	chr4:75020915-75020965	GM12878	blood:	n/a
22	chr4:75023719-75023769	HRCEpiC	kidney:	n/a
23	chr4:75023219-75023269	HCPEpiC	choroid plexus:	n/a
24	chr4:75023664-75023714	HRE	kidney:	n/a
25	chr4:75023851-75023901	SK-N-MC	brain:	n/a
26	chr4:75023219-75023269	RPTEC	kidney:	n/a
27	chr4:75023649-75023699	AG09309	skin:	n/a
28	chr4:75023219-75023269	PANC-1	pancreas:	n/a
29	chr4:75023746-75023796	HEEpiC	esophagus:	n/a
30	chr4:75023649-75023699	A549	lung:	n/a
31	chr4:75023719-75023769	SKMC	muscle:	n/a
32	chr4:75023849-75023899	HUVEC	blood vessel:	n/a
33	chr4:75023540-75023590	GM19239	blood:	n/a
34	chr4:75023219-75023269	HRPEpiC	eye:	n/a
35	chr4:75023540-75023590	A549	lung:	n/a
36	chr4:75023629-75023679	SAEC	small airway:	n/a
37	chr4:75020915-75020965	ovcar-3	ovarian:	n/a
38	chr4:75023664-75023714	PFSK-1	brain:	n/a
39	chr4:75023540-75023590	HCPEpiC	choroid plexus:	n/a
40	chr4:75020915-75020965	GM06990	blood:	n/a
41	chr4:75024153-75024203	NB4	blood:	n/a
42	chr4:75023629-75023679	NHDF-neo	bronchial:	n/a
43	chr4:75023849-75023899	AG10803	skin:	n/a
44	chr4:75023629-75023679	AoSMC	blood vessel:	n/a
45	chr4:75024153-75024203	SK-N-SH_RA	brain:	n/a
46	chr4:75023219-75023269	BE2_C	brain:	n/a
47	chr4:75023540-75023590	MCF-7	breast:	n/a
48	chr4:75023746-75023796	Hela-S3	cervix:	n/a
49	chr4:75023540-75023590	GM12892	blood:	n/a
50	chr4:75023219-75023269	HRCEpiC	kidney:	n/a

(count:136 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:75065926..75067463-chr4:75070226..75071957,2	K562	blood:
2	chr11:45943916..45944612-chr4:75023138..75023638,2	HCT-116	colon:
3	chr4:74956787..74958516-chr4:75030350..75032737,2	K562	blood:
4	chr4:75030845..75032521-chr4:75038666..75041397,2	MCF-7	breast:
5	chr4:75041824..75043889-chr4:75228570..75230405,2	K562	blood:
6	chr4:74513203..74514864-chr4:75031720..75034502,2	K562	blood:
7	chr4:75030705..75032456-chr4:75033958..75036294,2	MCF-7	breast:
8	chr4:75093827..75095059-chr4:75177130..75178054,11	MCF-7	breast:
9	chr4:75055132..75055639-chr4:75614656..75615248,2	K562	blood:
10	chr4:75013764..75016584-chr4:75022049..75024231,2	MCF-7	breast:
11	chr4:75028000..75030668-chr4:75031442..75033767,3	MCF-7	breast:
12	chr4:75085650..75087545-chr4:75089867..75092462,3	K562	blood:
13	chr4:75093762..75095528-chr4:75175394..75177161,2	MCF-7	breast:
14	chr4:75094355..75095090-chr4:75547966..75548494,2	K562	blood:
15	chr4:75018655..75021289-chr4:75023791..75025452,2	MCF-7	breast:
16	chr4:75071138..75073600-chr4:75079457..75081137,2	MCF-7	breast:
17	chr4:75015320..75016851-chr4:75026469..75028278,2	K562	blood:
18	chr4:75023679..75024199-chr6:117923622..117924531,2	NB4	blood:
19	chr4:75081253..75083346-chr4:75120623..75122127,2	K562	blood:
20	chr4:75023760..75025591-chr4:75092315..75094784,2	K562	blood:
21	chr4:75024221..75026156-chr4:75163622..75165985,2	K562	blood:
22	chr4:75023931..75025706-chr4:75026268..75029648,3	MCF-7	breast:
23	chr4:75029092..75030638-chr4:75098304..75099912,2	K562	blood:
24	chr4:75022859..75024733-chr4:75099700..75101269,2	MCF-7	breast:
25	chr4:75039914..75042879-chr4:75059516..75061047,2	K562	blood:
26	chr4:75031722..75034011-chr4:75130972..75132629,2	MCF-7	breast:
27	chr20:277413..278096-chr4:75023404..75023960,2	NB4	blood:
28	chr4:75093661..75096004-chr4:75147885..75149545,2	K562	blood:
29	chr4:75052779..75055705-chr4:75168128..75170187,2	MCF-7	breast:
30	chr4:75024505..75027399-chr4:75144223..75145811,2	K562	blood:
31	chr4:75055610..75058145-chr4:75064035..75065745,2	K562	blood:
32	chr4:74964506..74968474-chr4:75022087..75025768,6	K562	blood:
33	chr4:75054854..75055674-chr4:75177116..75178350,7	MCF-7	breast:
34	chr4:75022870..75024459-chr4:75044858..75046610,2	MCF-7	breast:
35	chr4:75018443..75019977-chr4:75023297..75025270,2	MCF-7	breast:
36	chr4:75032536..75034809-chr4:75036870..75039307,2	MCF-7	breast:
37	chr4:75025200..75026058-chr5:28474351..28475312,2	Hela-S3	cervix:
38	chr4:75023499..75025641-chr4:75097703..75100691,2	K562	blood:
39	chr4:75091219..75093823-chr4:75093870..75096715,2	MCF-7	breast:
40	chr4:74917982..74919932-chr4:75041196..75043826,2	K562	blood:
41	chr4:75026936..75029499-chr4:75048728..75050927,2	K562	blood:
42	chr4:74563928..74566862-chr4:75033357..75036869,3	K562	blood:
43	chr4:75030705..75032456-chr4:75033958..75036294,2	MCF-7	breast:
44	chr4:75049836..75051355-chr4:75053800..75056077,2	K562	blood:
45	chr4:75054653..75055732-chr4:75177181..75178135,3	K562	blood:
46	chr4:75011899..75013611-chr4:75013852..75015678,2	K562	blood:
47	chr4:75011899..75013611-chr4:75013852..75015678,2	K562	blood:
48	chr4:75023724..75025558-chr4:75028455..75031389,3	MCF-7	breast:
49	chr4:74976042..74977879-chr4:75018790..75020773,2	K562	blood:
50	chr4:75010641..75013526-chr4:75028499..75030027,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPGN-4	chr4:75023892-75023998	NONHSAT096886
2	lnc-EPGN-4	chr4:75025772-75027969	NONHSAT096885
3	lnc-EPGN-4	chr4:75027497-75027823	NONHSAT096886
4	lnc-EPGN-4	chr4:75025772-75026231	NONHSAT096883
5	lnc-EPGN-4	chr4:75025772-75026487	NONHSAT096884
6	lnc-EPGN-4	chr4:75025772-75025805	NONHSAT096886
7	lnc-EPGN-4	chr4:75023829-75023998	NONHSAT096885

No data

Variant related genes	Relation type
ENSG00000269559	TF binding region
MTHFD2L	TF binding region
ENSG00000269559	CpG island
MTHFD2L	CpG island
ENSG00000248848	chromatin interactions
ENSG00000081041	chromatin interactions
ENSG00000269559	chromatin interactions
ENSG00000182585	chromatin interactions
ENSG00000165905	chromatin interactions
ENSG00000163738	chromatin interactions
ENSG00000132466	chromatin interactions
ENSG00000124882	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000196787	chromatin interactions
ENSG00000124635	chromatin interactions
ENSG00000135269	chromatin interactions
ENSG00000047932	chromatin interactions
ENSG00000177764	chromatin interactions

Extended variants
information (count: 3916 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3916 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538775	chr4:75013441-75013442	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182576077	chr4:75013464-75013465	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187284045	chr4:75013465-75013466	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs522698	chr4:75013466-75013467	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs551056454	chr4:75013497-75013498	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs144250992	chr4:75013539-75013540	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530083794	chr4:75013559-75013560	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548551362	chr4:75013568-75013569	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577421879	chr4:75013645-75013646	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs567083891	chr4:75013666-75013667	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534483038	chr4:75013689-75013690	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558746436	chr4:75013690-75013691	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs151140925	chr4:75013702-75013703	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs139098597	chr4:75013707-75013708	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs546179126	chr4:75013767-75013768	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs149892904	chr4:75013784-75013785	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs145365719	chr4:75013785-75013786	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs541495635	chr4:75013841-75013842	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs553708658	chr4:75013976-75013977	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs544251604	chr4:75014021-75014022	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs572274857	chr4:75014024-75014025	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs147385523	chr4:75014032-75014033	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs386400497	chr4:75014033-75014034	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs59508344	chr4:75014039-75014040	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs113405355	chr4:75014040-75014041	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs116803815	chr4:75014046-75014047	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs564284682	chr4:75014100-75014101	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs199901253	chr4:75014107-75014108	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs35766294	chr4:75014109-75014110	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs540452176	chr4:75014110-75014111	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs376248086	chr4:75014112-75014113	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs375494400	chr4:75014114-75014115	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs374338193	chr4:75014137-75014138	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs576261606	chr4:75014185-75014186	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs543635666	chr4:75014202-75014203	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs75451741	chr4:75014376-75014377	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs368599571	chr4:75014396-75014397	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs562879230	chr4:75014402-75014403	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs370604089	chr4:75014421-75014422	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs183029291	chr4:75014435-75014436	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs560509562	chr4:75014476-75014477	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs113510205	chr4:75014506-75014507	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs60452831	chr4:75014512-75014513	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs78918649	chr4:75014589-75014590	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs527698104	chr4:75014600-75014601	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs193213197	chr4:75014608-75014609	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs538091057	chr4:75014634-75014635	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs549947792	chr4:75014655-75014656	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs568091603	chr4:75014681-75014682	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs506678	chr4:75014690-75014691	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Abnormal phenotypes	18644119	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Renal cell carcinoma	20952505	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1602 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:75004400-75013800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:75011800-75022000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr4:75013200-75014000	Strong transcription	HMEC	breast
4	chr4:75013200-75023200	Weak transcription	Psoas Muscle	Psoas
5	chr4:75013400-75013600	Strong transcription	NHEK	skin
6	chr4:75013600-75014200	Weak transcription	NHEK	skin
7	chr4:75013800-75014800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:75014000-75022000	Weak transcription	HMEC	breast
9	chr4:75014200-75014400	Strong transcription	NHEK	skin
10	chr4:75014400-75022200	Weak transcription	NHEK	skin
11	chr4:75014800-75016000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:75015400-75015800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr4:75015800-75022600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr4:75016000-75016600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr4:75016600-75016800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr4:75016800-75018200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr4:75018200-75018400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr4:75018200-75019000	Enhancers	Fetal Brain Male	brain
19	chr4:75018200-75019200	Enhancers	Fetal Lung	lung
20	chr4:75018400-75018800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr4:75018400-75019000	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr4:75018400-75019000	Enhancers	Colon Smooth Muscle	Colon
23	chr4:75018600-75019000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr4:75018800-75019000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr4:75018800-75019000	Enhancers	NHDF-Ad	bronchial
26	chr4:75019000-75019400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr4:75019000-75022600	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr4:75019000-75022800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr4:75019000-75023000	Weak transcription	Colon Smooth Muscle	Colon
30	chr4:75019000-75023000	Weak transcription	Fetal Brain Male	brain
31	chr4:75019400-75021200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr4:75020400-75021400	Enhancers	K562	blood
33	chr4:75021200-75022200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:75021400-75021800	Weak transcription	K562	blood
35	chr4:75021800-75022000	Enhancers	K562	blood
36	chr4:75021800-75022600	Enhancers	HUVEC	blood vessel
37	chr4:75021800-75023000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr4:75021800-75023000	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr4:75022000-75022200	Enhancers	Colonic Mucosa	Colon
40	chr4:75022000-75022600	Flanking Active TSS	K562	blood
41	chr4:75022000-75022600	Enhancers	NHLF	lung
42	chr4:75022000-75022800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr4:75022000-75022800	Enhancers	Muscle Satellite Cultured Cells	--
44	chr4:75022000-75022800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr4:75022000-75022800	Enhancers	Rectal Mucosa Donor 29	rectum
46	chr4:75022000-75022800	Enhancers	Hela-S3	cervix
47	chr4:75022000-75022800	Enhancers	HMEC	breast
48	chr4:75022000-75022800	Enhancers	NHDF-Ad	bronchial
49	chr4:75022200-75022400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr4:75022200-75022400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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