Variant report

Variant	nsv1018859
Chromosome Location	chr4:147055618-147138397
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:857)
CpG islands
(count:977)
Chromatin interactive
region (count:43)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:147096402-147097073	HepG2	liver:	n/a	n/a
2	ATF2	chr4:147096494-147096898	GM12878	blood:	n/a	n/a
3	ATF2	chr4:147096617-147097074	GM12878	blood:	n/a	n/a
4	BACH1	chr4:147096449-147096574	K562	blood:	n/a	n/a
5	BATF	chr4:147076538-147076733	GM12878	blood:	n/a	n/a
6	BATF	chr4:147080580-147081116	GM12878	blood:	n/a	chr4:147080606-147080615
7	BATF	chr4:147080620-147081059	GM12878	blood:	n/a	n/a
8	BATF	chr4:147096706-147096983	GM12878	blood:	n/a	n/a
9	BATF	chr4:147076449-147076795	GM12878	blood:	n/a	n/a
10	BCL3	chr4:147068118-147068485	GM12878	blood:	n/a	n/a
11	BCLAF1	chr4:147096677-147097175	GM12878	blood:	n/a	chr4:147096971-147096984
12	BCLAF1	chr4:147096628-147097235	GM12878	blood:	n/a	chr4:147096971-147096984
13	BHLHE40	chr4:147106486-147106729	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:147080804-147081186	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:147096725-147097191	K562	blood:	n/a	n/a
16	BRCA1	chr4:147080844-147080955	GM12878	blood:	n/a	n/a
17	BRCA1	chr4:147066139-147066151	HepG2	liver:	n/a	n/a
18	BRCA1	chr4:147096635-147097107	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr4:147096523-147097139	HCT-116	colon:	n/a	n/a
20	CBX3	chr4:147096596-147097146	K562	blood:	n/a	n/a
21	CCNT2	chr4:147096722-147097276	K562	blood:	n/a	n/a
22	CEBPB	chr4:147067412-147067608	HepG2	liver:	n/a	chr4:147067526-147067537
23	CEBPB	chr4:147099300-147099608	K562	blood:	n/a	n/a
24	CEBPB	chr4:147068074-147068456	HepG2	liver:	n/a	chr4:147068267-147068278 chr4:147068246-147068257
25	CEBPB	chr4:147072906-147073185	IMR90	lung:	n/a	chr4:147073012-147073023 chr4:147073014-147073023 chr4:147073014-147073023 chr4:147073014-147073023 chr4:147073013-147073024 chr4:147073014-147073023
26	CEBPB	chr4:147099279-147099596	K562	blood:	n/a	n/a
27	CEBPB	chr4:147087043-147087282	A549	lung:	n/a	chr4:147087135-147087146
28	CEBPB	chr4:147085939-147086011	HepG2	liver:	n/a	n/a
29	CEBPB	chr4:147072850-147073187	HepG2	liver:	n/a	chr4:147073012-147073023 chr4:147073014-147073023 chr4:147073014-147073023 chr4:147073014-147073023 chr4:147073013-147073024 chr4:147073014-147073023
30	CEBPB	chr4:147068087-147068405	Hela-S3	cervix:	n/a	chr4:147068267-147068278 chr4:147068246-147068257
31	CEBPB	chr4:147086986-147087379	IMR90	lung:	n/a	chr4:147087135-147087146
32	CEBPB	chr4:147065116-147065308	HepG2	liver:	n/a	n/a
33	CEBPB	chr4:147068149-147068409	MCF-7	breast:	n/a	chr4:147068267-147068278 chr4:147068246-147068257
34	CEBPB	chr4:147072865-147073105	A549	lung:	n/a	chr4:147073012-147073023 chr4:147073014-147073023 chr4:147073014-147073023 chr4:147073014-147073023 chr4:147073013-147073024 chr4:147073014-147073023
35	CEBPB	chr4:147085824-147086136	IMR90	lung:	n/a	n/a
36	CEBPB	chr4:147068134-147068329	HepG2	liver:	n/a	chr4:147068267-147068278 chr4:147068246-147068257
37	CEBPB	chr4:147087058-147087303	HepG2	liver:	n/a	chr4:147087135-147087146
38	CEBPB	chr4:147086944-147087334	A549	lung:	n/a	chr4:147087135-147087146
39	CEBPB	chr4:147087046-147087319	ECC-1	luminal epithelium:	n/a	chr4:147087135-147087146
40	CEBPB	chr4:147110086-147110323	IMR90	lung:	n/a	chr4:147110197-147110208
41	CEBPB	chr4:147110096-147110307	HepG2	liver:	n/a	chr4:147110197-147110208
42	CEBPB	chr4:147099288-147099598	HepG2	liver:	n/a	n/a
43	CEBPB	chr4:147086984-147087347	Hela-S3	cervix:	n/a	chr4:147087135-147087146
44	CEBPB	chr4:147110114-147110268	K562	blood:	n/a	chr4:147110197-147110208
45	CEBPB	chr4:147068103-147068404	A549	lung:	n/a	chr4:147068267-147068278 chr4:147068246-147068257
46	CEBPB	chr4:147114678-147114836	A549	lung:	n/a	chr4:147114704-147114717 chr4:147114703-147114720 chr4:147114704-147114715 chr4:147114704-147114717
47	CHD1	chr4:147096650-147097530	GM12878	blood:	n/a	n/a
48	CHD1	chr4:147097010-147097660	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr4:147096795-147096995	K562	blood:	n/a	n/a
50	CHD2	chr4:147096808-147097285	HepG2	liver:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:147075042-147075092	GM06990	blood:	n/a
2	chr4:147075042-147075092	GM06990	blood:	n/a
3	chr4:147095635-147095685	BJ	skin:	n/a
4	chr4:147096787-147096837	NB4	blood:	n/a
5	chr4:147096785-147096835	GM19239	blood:	n/a
6	chr4:147097364-147097414	SK-N-MC	brain:	n/a
7	chr4:147096787-147096837	HRE	kidney:	n/a
8	chr4:147097443-147097493	ECC-1	luminal epithelium:	n/a
9	chr4:147097364-147097414	AoSMC	blood vessel:	n/a
10	chr4:147097364-147097414	GM12878	blood:	n/a
11	chr4:147096785-147096835	BJ	skin:	n/a
12	chr4:147096828-147096878	HCF	heart:	n/a
13	chr4:147096820-147096870	RPTEC	kidney:	n/a
14	chr4:147097886-147097936	GM12892	blood:	n/a
15	chr4:147095396-147095446	GM19239	blood:	n/a
16	chr4:147096909-147096959	HAEpiC	amniotic membrane:	n/a
17	chr4:147138044-147138094	SK-N-MC	brain:	n/a
18	chr4:147096787-147096837	GM12892	blood:	n/a
19	chr4:147095635-147095685	NH-A	brain:	n/a
20	chr4:147056211-147056261	U87	brain:	n/a
21	chr4:147097443-147097493	HRE	kidney:	n/a
22	chr4:147097886-147097936	HCT-116	colon:	n/a
23	chr4:147096828-147096878	ProgFib	skin:	n/a
24	chr4:147097443-147097493	MCF10A-Er-Src	breast:	n/a
25	chr4:147075042-147075092	HRE	kidney:	n/a
26	chr4:147106103-147106153	GM12878	blood:	n/a
27	chr4:147097209-147097259	BJ	skin:	n/a
28	chr4:147096785-147096835	PrEC	prostate:	n/a
29	chr4:147138044-147138094	Hela-S3	cervix:	n/a
30	chr4:147106103-147106153	ECC-1	luminal epithelium:	n/a
31	chr4:147097443-147097493	ovcar-3	ovarian:	n/a
32	chr4:147075042-147075092	GM12892	blood:	n/a
33	chr4:147097364-147097414	NT2-D1	testis:	n/a
34	chr4:147096909-147096959	GM12891	blood:	n/a
35	chr4:147097886-147097936	HUVEC	blood vessel:	n/a
36	chr4:147097443-147097493	HEEpiC	esophagus:	n/a
37	chr4:147097886-147097936	AG09319	gingival:	n/a
38	chr4:147096828-147096878	H1-hESC	embryonic stem cell:	embryo
39	chr4:147075042-147075092	MCF10A-Er-Src	breast:	n/a
40	chr4:147095396-147095446	AG04450	lung:	fetal
41	chr4:147095635-147095685	K562	blood:	n/a
42	chr4:147096909-147096959	Jurkat	blood:	n/a
43	chr4:147095396-147095446	ECC-1	luminal epithelium:	n/a
44	chr4:147095396-147095446	Hepatocyte	liver:	n/a
45	chr4:147106103-147106153	AG10803	skin:	n/a
46	chr4:147097886-147097936	SK-N-SH	brain:	n/a
47	chr4:147096787-147096837	HCM	heart:	n/a
48	chr4:147138044-147138094	GM12892	blood:	n/a
49	chr4:147138044-147138094	AG10803	skin:	n/a
50	chr4:147097364-147097414	NH-A	brain:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:147096691..147098879-chr4:147107983..147110600,2	MCF-7	breast:
2	chr4:147099369..147101389-chr4:147104400..147106028,2	MCF-7	breast:
3	chr4:147055908..147058873-chr4:147059749..147061908,2	K562	blood:
4	chr4:147095588..147099041-chr4:147101501..147104102,4	MCF-7	breast:
5	chr4:147055908..147058873-chr4:147059749..147061908,2	K562	blood:
6	chr4:147098952..147101592-chr4:147130358..147132148,2	K562	blood:
7	chr4:147103613..147105948-chr4:147107918..147110388,3	K562	blood:
8	chr4:147111066..147113405-chr4:147115907..147118837,2	K562	blood:
9	chr4:147094825..147098572-chr4:147107210..147109613,3	MCF-7	breast:
10	chr4:147086830..147091007-chr4:147091903..147096779,4	K562	blood:
11	chr4:147103613..147105948-chr4:147107918..147110388,2	K562	blood:
12	chr4:147055512..147057408-chr4:147060408..147062142,2	K562	blood:
13	chr4:147131915..147134397-chr4:147145047..147146932,2	MCF-7	breast:
14	chr4:147059542..147061750-chr4:147066448..147068340,2	K562	blood:
15	chr4:147088096..147091007-chr4:147093172..147095753,2	K562	blood:
16	chr4:147116335..147119084-chr4:147119994..147121504,2	MCF-7	breast:
17	chr4:147049621..147051937-chr4:147059777..147061735,2	K562	blood:
18	chr4:147100998..147102686-chr4:147106253..147108281,2	K562	blood:
19	chr4:147086830..147091007-chr4:147091903..147096779,4	K562	blood:
20	chr4:147099369..147101389-chr4:147104400..147106028,2	MCF-7	breast:
21	chr4:147106019..147107613-chr4:147111595..147114491,2	K562	blood:
22	chr4:147096162..147099903-chr4:147161380..147165203,4	MCF-7	breast:
23	chr4:147055512..147057408-chr4:147060408..147062142,2	K562	blood:
24	chr4:147113098..147115033-chr4:147118947..147121819,2	K562	blood:
25	chr4:147116009..147117870-chr4:147118795..147120333,2	MCF-7	breast:
26	chr4:147095588..147099041-chr4:147101501..147104102,4	MCF-7	breast:
27	chr4:147116335..147119084-chr4:147119994..147121504,2	MCF-7	breast:
28	chr4:147076257..147079097-chr4:147084297..147086831,2	MCF-7	breast:
29	chr4:147100998..147102686-chr4:147106253..147108281,2	K562	blood:
30	chr4:147059542..147061750-chr4:147066448..147068340,2	K562	blood:
31	chr4:147111066..147113405-chr4:147115907..147118837,2	K562	blood:
32	chr4:146538731..146541596-chr4:147058799..147061667,2	MCF-7	breast:
33	chr4:147088096..147091007-chr4:147093172..147095753,2	K562	blood:
34	chr4:147116009..147117870-chr4:147118795..147120333,2	MCF-7	breast:
35	chr4:147096699..147098795-chr4:147099511..147101268,2	MCF-7	breast:
36	chr4:147076257..147079097-chr4:147084297..147086831,2	MCF-7	breast:
37	chr4:147090038..147091690-chr4:147095340..147097162,2	MCF-7	breast:
38	chr4:147103019..147105139-chr4:147110887..147113160,2	K562	blood:
39	chr4:147111066..147113636-chr4:147115907..147120334,4	K562	blood:
40	chr4:147106019..147107613-chr4:147111595..147114491,2	K562	blood:
41	chr4:147098952..147101592-chr4:147130358..147132148,2	K562	blood:
42	chr4:147111066..147113636-chr4:147115907..147120334,4	K562	blood:
43	chr4:147113098..147115033-chr4:147118947..147121819,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-6L6.2.1-3	chr4:147096922-147096963	NONHSAT098665
2	lnc-RP11-6L6.2.1-2	chr4:147111638-147114339	NONHSAT098666
3	lnc-SLC10A7-2	chr4:147079257-147079602	expReg_chr4_6941_-
4	lnc-RP11-6L6.2.1-3	chr4:147097320-147097838	NONHSAT098665

No data

Variant related genes	Relation type
LSM6	TF binding region
LSM6	CpG island
ENSG00000164167	chromatin interactions
ENSG00000151611	chromatin interactions
ENSG00000251010	chromatin interactions
ENSG00000250673	chromatin interactions

Extended variants
information (count: 3154 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:3154 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17021106	chr4:147055618-147055619	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544942680	chr4:147055642-147055643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564751903	chr4:147055668-147055669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs527348323	chr4:147055708-147055709	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547211595	chr4:147055716-147055717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567828424	chr4:147055751-147055752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183742694	chr4:147055868-147055869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140346196	chr4:147055888-147055889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370500081	chr4:147055896-147055897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34418017	chr4:147055924-147055925	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs538966551	chr4:147055984-147055985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558874230	chr4:147056063-147056064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs116412536	chr4:147056064-147056065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145297601	chr4:147056078-147056079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs6826901	chr4:147056144-147056145	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs74534264	chr4:147056156-147056157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs72727925	chr4:147056186-147056187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs72727926	chr4:147056199-147056200	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs556397454	chr4:147056209-147056210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544872430	chr4:147056211-147056212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs7695415	chr4:147056235-147056236	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs370089422	chr4:147056247-147056248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374726085	chr4:147056250-147056251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs527319057	chr4:147056347-147056348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs140761922	chr4:147056356-147056357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs386680512	chr4:147056381-147056382	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs17021111	chr4:147056382-147056383	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs144622662	chr4:147056396-147056397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549931526	chr4:147056397-147056398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181192976	chr4:147056424-147056425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569928583	chr4:147056453-147056454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148160353	chr4:147056454-147056455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs377382037	chr4:147056473-147056474	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185844186	chr4:147056494-147056495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191707593	chr4:147056510-147056511	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548572407	chr4:147056518-147056519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6832576	chr4:147056551-147056552	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs142031400	chr4:147056554-147056555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556361284	chr4:147056610-147056611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576340503	chr4:147056673-147056674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560530493	chr4:147056691-147056692	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs6537400	chr4:147056715-147056716	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs57655663	chr4:147056720-147056721	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs540684993	chr4:147056737-147056738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572001094	chr4:147056738-147056739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181808302	chr4:147056740-147056741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187202528	chr4:147056748-147056749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574158216	chr4:147056749-147056750	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532321153	chr4:147056751-147056752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368266440	chr4:147056802-147056803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
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
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
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	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
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21633010	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1366 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:147052600-147056000	Weak transcription	Right Atrium	heart
2	chr4:147054600-147055800	Weak transcription	Osteobl	bone
3	chr4:147054600-147056600	Enhancers	Fetal Brain Male	brain
4	chr4:147055200-147056600	Enhancers	Fetal Brain Female	brain
5	chr4:147055200-147057400	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr4:147055200-147057400	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr4:147055400-147055800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr4:147055400-147056200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:147055400-147056200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr4:147055400-147056600	Enhancers	HMEC	breast
11	chr4:147055400-147056800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr4:147055600-147056600	Enhancers	Esophagus	oesophagus
13	chr4:147055600-147056800	Enhancers	Brain Germinal Matrix	brain
14	chr4:147055600-147057200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr4:147055800-147056200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr4:147055800-147056200	Enhancers	NHEK	skin
17	chr4:147055800-147056400	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr4:147055800-147056600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr4:147055800-147056600	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr4:147055800-147056600	Enhancers	Osteobl	bone
21	chr4:147055800-147057400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr4:147055800-147057400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr4:147055800-147057600	Enhancers	Fetal Muscle Leg	muscle
24	chr4:147055800-147058000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr4:147055800-147058400	Enhancers	Adipose Nuclei	Adipose
26	chr4:147056000-147056200	Enhancers	Muscle Satellite Cultured Cells	--
27	chr4:147056000-147056600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:147056000-147056600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:147056000-147056600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr4:147056000-147056600	Enhancers	Right Atrium	heart
31	chr4:147056000-147056800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr4:147056000-147057200	Enhancers	Brain Cingulate Gyrus	brain
33	chr4:147056200-147056600	Enhancers	Brain Anterior Caudate	brain
34	chr4:147056200-147057600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr4:147056600-147058000	Weak transcription	Right Atrium	heart
36	chr4:147056600-147064000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:147057200-147057400	Enhancers	Brain Hippocampus Middle	brain
38	chr4:147058000-147058200	Enhancers	Right Atrium	heart
39	chr4:147058400-147062400	Weak transcription	Adipose Nuclei	Adipose
40	chr4:147062400-147062800	Enhancers	Adipose Nuclei	Adipose
41	chr4:147063600-147065400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr4:147063800-147064400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr4:147063800-147065600	Enhancers	HMEC	breast
44	chr4:147064000-147064400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr4:147064000-147064400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr4:147064000-147064600	Enhancers	NHEK	skin
47	chr4:147064000-147065800	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr4:147064400-147064800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr4:147064400-147065600	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr4:147064600-147065400	Weak transcription	NHEK	skin

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