Variant report

Variant	nsv1033907
Chromosome Location	chr5:147109014-147309076
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1891)
CpG islands
(count:2018)
Chromatin interactive
region (count:37)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1891 , 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	chr5:147202273-147202629	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:147215845-147216145	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:147217609-147218096	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:147286007-147286246	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:147214584-147215634	HepG2	liver:	n/a	n/a
6	ATF1	chr5:147275521-147275631	K562	blood:	n/a	n/a
7	ATF1	chr5:147262570-147262757	K562	blood:	n/a	n/a
8	ATF2	chr5:147252333-147252635	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr5:147240926-147241670	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr5:147253932-147255056	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr5:147230878-147238649	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr5:147239669-147240197	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr5:147235141-147235632	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr5:147248491-147249068	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr5:147248499-147249707	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr5:147252669-147253100	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr5:147237018-147237506	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr5:147253743-147255142	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr5:147129626-147130078	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr5:147233864-147234303	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr5:147251599-147251998	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr5:147242872-147243242	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF3	chr5:147214831-147215360	A549	lung:	n/a	n/a
24	ATF3	chr5:147214855-147215336	A549	lung:	n/a	n/a
25	BACH1	chr5:147248613-147249016	H1-hESC	embryonic stem cell:	n/a	n/a
26	BCL11A	chr5:147248729-147248902	H1-hESC	embryonic stem cell:	n/a	n/a
27	BCL3	chr5:147214786-147215457	A549	lung:	n/a	n/a
28	BCL3	chr5:147214694-147215505	A549	lung:	n/a	n/a
29	BCL3	chr5:147217625-147218039	A549	lung:	n/a	n/a
30	BHLHE40	chr5:147214868-147215369	HepG2	liver:	n/a	n/a
31	BHLHE40	chr5:147214873-147215307	HepG2	liver:	n/a	n/a
32	BHLHE40	chr5:147214970-147215279	HepG2	liver:	n/a	n/a
33	BHLHE40	chr5:147237153-147237443	GM12878	blood:	n/a	n/a
34	BHLHE40	chr5:147217615-147217941	HepG2	liver:	n/a	n/a
35	BRCA1	chr5:147234021-147234316	H1-hESC	embryonic stem cell:	n/a	n/a
36	BRCA1	chr5:147236963-147237464	H1-hESC	embryonic stem cell:	n/a	n/a
37	BRCA1	chr5:147143509-147143604	H1-hESC	embryonic stem cell:	n/a	n/a
38	BRCA1	chr5:147231606-147231957	H1-hESC	embryonic stem cell:	n/a	n/a
39	BRCA1	chr5:147248624-147249087	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr5:147159567-147159607	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr5:147237189-147237534	Hela-S3	cervix:	n/a	n/a
42	CCNT2	chr5:147243867-147243998	K562	blood:	n/a	n/a
43	CEBPB	chr5:147115878-147116059	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr5:147282239-147282533	Hela-S3	cervix:	n/a	chr5:147282307-147282318 chr5:147282307-147282320 chr5:147282307-147282318 chr5:147282307-147282320
45	CEBPB	chr5:147214782-147215401	A549	lung:	n/a	chr5:147215060-147215073 chr5:147215060-147215071 chr5:147214838-147214849
46	CEBPB	chr5:147184483-147184851	A549	lung:	n/a	chr5:147184614-147184625
47	CEBPB	chr5:147188247-147188468	HepG2	liver:	n/a	chr5:147188351-147188362
48	CEBPB	chr5:147181038-147181291	HepG2	liver:	n/a	chr5:147181165-147181176
49	CEBPB	chr5:147237141-147237375	A549	lung:	n/a	n/a
50	CEBPB	chr5:147209693-147209946	A549	lung:	n/a	chr5:147209785-147209796

(count:2018 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:147163101-147163151	HCPEpiC	choroid plexus:	n/a
2	chr5:147211181-147211231	HIPEpiC	eye:	n/a
3	chr5:147260582-147260632	RPTEC	kidney:	n/a
4	chr5:147255652-147255702	K562	blood:	n/a
5	chr5:147160551-147160601	NHDF-neo	bronchial:	n/a
6	chr5:147163101-147163151	HCPEpiC	choroid plexus:	n/a
7	chr5:147211181-147211231	HIPEpiC	eye:	n/a
8	chr5:147260582-147260632	RPTEC	kidney:	n/a
9	chr5:147255652-147255702	K562	blood:	n/a
10	chr5:147160551-147160601	NHDF-neo	bronchial:	n/a
11	chr5:147204189-147204239	Hepatocyte	liver:	n/a
12	chr5:147212728-147212778	U87	brain:	n/a
13	chr5:147272300-147272350	HMEC	breast:	n/a
14	chr5:147205668-147205718	HAEpiC	amniotic membrane:	n/a
15	chr5:147130913-147130963	AG09319	gingival:	n/a
16	chr5:147211181-147211231	NH-A	brain:	n/a
17	chr5:147260582-147260632	HRPEpiC	eye:	n/a
18	chr5:147281313-147281363	GM19239	blood:	n/a
19	chr5:147281313-147281363	GM12892	blood:	n/a
20	chr5:147212748-147212798	K562	blood:	n/a
21	chr5:147261629-147261679	SK-N-SH_RA	brain:	n/a
22	chr5:147211181-147211231	AG09309	skin:	n/a
23	chr5:147154246-147154296	GM12891	blood:	n/a
24	chr5:147130913-147130963	MCF-7	breast:	n/a
25	chr5:147281313-147281363	NHBE	bronchial:	n/a
26	chr5:147162461-147162511	HCT-116	colon:	n/a
27	chr5:147257325-147257375	HepG2	liver:	n/a
28	chr5:147281313-147281363	HRCEpiC	kidney:	n/a
29	chr5:147257325-147257375	GM12891	blood:	n/a
30	chr5:147258132-147258182	A549	lung:	n/a
31	chr5:147260582-147260632	SK-N-MC	brain:	n/a
32	chr5:147286717-147286767	AG09319	gingival:	n/a
33	chr5:147162169-147162219	HAEpiC	amniotic membrane:	n/a
34	chr5:147260582-147260632	ECC-1	luminal epithelium:	n/a
35	chr5:147162161-147162211	IMR90	lung:	fetal
36	chr5:147286717-147286767	SK-N-MC	brain:	n/a
37	chr5:147162223-147162273	AoSMC	blood vessel:	n/a
38	chr5:147205668-147205718	HIPEpiC	eye:	n/a
39	chr5:147130913-147130963	NHBE	bronchial:	n/a
40	chr5:147160551-147160601	HRE	kidney:	n/a
41	chr5:147286719-147286769	PFSK-1	brain:	n/a
42	chr5:147255652-147255702	AG04449	skin:	fetal
43	chr5:147162432-147162482	HEEpiC	esophagus:	n/a
44	chr5:147162432-147162482	SKMC	muscle:	n/a
45	chr5:147161924-147161974	GM12878	blood:	n/a
46	chr5:147162461-147162511	SAEC	small airway:	n/a
47	chr5:147286717-147286767	HPAEpiC	pulmonary alveolar:	n/a
48	chr5:147205668-147205718	HCT-116	colon:	n/a
49	chr5:147162375-147162425	Jurkat	blood:	n/a
50	chr5:147257325-147257375	AG09319	gingival:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:147209006..147210576-chr5:147213475..147215044,2	MCF-7	breast:
2	chr5:147193050..147195321-chr5:147199717..147201347,2	MCF-7	breast:
3	chr5:147165883..147167877-chr5:147170991..147173910,2	K562	blood:
4	chr5:147164514..147166158-chr5:147166561..147168464,2	K562	blood:
5	chr5:147272144..147273653-chr5:147300672..147302249,2	MCF-7	breast:
6	chr5:146956209..146957226-chr5:147202038..147202593,3	MCF-7	breast:
7	chr5:147165883..147167877-chr5:147170991..147173910,2	K562	blood:
8	chr5:147236815..147237790-chr5:147266317..147266844,2	K562	blood:
9	chr2:88315772..88316335-chr5:147121532..147122052,3	HCT-116	colon:
10	chr5:147007364..147008316-chr5:147236786..147237763,3	MCF-7	breast:
11	chr5:147265148..147267409-chr5:147270950..147272492,2	MCF-7	breast:
12	chr5:147186734..147187415-chr7:5632329..5632946,2	NB4	blood:
13	chr5:147007357..147008291-chr5:147201975..147203349,14	MCF-7	breast:
14	chr5:147236987..147237740-chr5:147312978..147314003,3	MCF-7	breast:
15	chr5:147237167..147237749-chr5:148414576..148415153,2	K562	blood:
16	chr5:147206267..147209049-chr5:147212352..147214745,2	MCF-7	breast:
17	chr11:45877056..45879214-chr5:147116551..147119032,2	MCF-7	breast:
18	chr5:147164514..147166158-chr5:147166561..147168464,2	K562	blood:
19	chr5:147184794..147187475-chr5:147189094..147190857,2	MCF-7	breast:
20	chr5:147236854..147237741-chr5:147314334..147315282,8	MCF-7	breast:
21	chr5:147158425..147160468-chr5:147160831..147162494,2	MCF-7	breast:
22	chr5:147189801..147192086-chr5:147194141..147197431,4	MCF-7	breast:
23	chr5:147236958..147237672-chr5:147259068..147259579,2	MCF-7	breast:
24	chr5:147255398..147258341-chr5:147264911..147267895,3	MCF-7	breast:
25	chr5:147103170..147104982-chr5:147106913..147109194,2	K562	blood:
26	chr5:147226622..147229512-chr5:147232113..147233933,2	K562	blood:
27	chr5:147274656..147275267-chr9:127623855..127624555,2	Hela-S3	cervix:
28	chr5:147184794..147187475-chr5:147189094..147190857,2	MCF-7	breast:
29	chr5:147274175..147276959-chr5:147278370..147280406,2	MCF-7	breast:
30	chr5:147189801..147192086-chr5:147194141..147197431,4	MCF-7	breast:
31	chr5:147236518..147237633-chr5:147314355..147315282,3	MCF-7	breast:
32	chr5:147255398..147258341-chr5:147264911..147267895,3	MCF-7	breast:
33	chr5:147209006..147210576-chr5:147213475..147215044,2	MCF-7	breast:
34	chr5:147274175..147276959-chr5:147278370..147280406,2	MCF-7	breast:
35	chr5:147236958..147237672-chr5:147259068..147259579,2	MCF-7	breast:
36	chr5:147193050..147195321-chr5:147199717..147201347,2	MCF-7	breast:
37	chr5:147262805..147266093-chr5:147266242..147268509,3	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-JAKMIP2-1	chr5:147207585-147207693	NONHSAT104429
2	lnc-SPINK1-1	chr5:147265649-147266441	ENSG00000248362.1
3	lnc-SCGB3A2-2	chr5:147242868-147244700	NONHSAT104430
4	lnc-SCGB3A2-2	chr5:147245565-147246269	NONHSAT104430
5	lnc-JAKMIP2-1	chr5:147204135-147204269	NONHSAT104429
6	lnc-SCGB3A2-1	chr5:147266675-147267267	ENSG00000251320.1

No data

Variant related genes	Relation type
C5orf46	TF binding region
ENSG00000249518	TF binding region
SCGB3A2	TF binding region
EEF1GP2	TF binding region
ENSG00000248362	TF binding region
JAKMIP2	TF binding region
ENSG00000251320	TF binding region
SPINK1	TF binding region
C5orf46	CpG island
ENSG00000249518	CpG island
SCGB3A2	CpG island
EEF1GP2	CpG island
ENSG00000248362	CpG island
JAKMIP2	CpG island
ENSG00000251320	CpG island
SPINK1	CpG island
ENSG00000222724	chromatin interactions
ENSG00000136950	chromatin interactions
ENSG00000248362	chromatin interactions
ENSG00000251320	chromatin interactions
ENSG00000176049	chromatin interactions
ENSG00000164265	chromatin interactions
ENSG00000164266	chromatin interactions
ENSG00000249518	chromatin interactions
ENSG00000250346	chromatin interactions
ENSG00000075618	chromatin interactions
ENSG00000136942	chromatin interactions

Extended variants
information (count: 7445 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:7445 , 50 per page) page: 1 2 3 4 5 6 7 ... 149

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188426586	chr5:147109018-147109019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs139352227	chr5:147109056-147109057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs190764039	chr5:147109075-147109076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs182859851	chr5:147109090-147109091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs35928499	chr5:147109094-147109095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528079385	chr5:147109163-147109164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539940767	chr5:147109166-147109167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs370638799	chr5:147109193-147109194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs371530599	chr5:147109197-147109198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs546247382	chr5:147109210-147109211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs374902486	chr5:147109227-147109228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs113770769	chr5:147109263-147109264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533357418	chr5:147109291-147109292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556863722	chr5:147109292-147109293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs550059593	chr5:147109293-147109294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368040956	chr5:147109336-147109337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564811840	chr5:147109337-147109338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs79967389	chr5:147109429-147109430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554908055	chr5:147109445-147109446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187728625	chr5:147109456-147109457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540644899	chr5:147109464-147109465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192570598	chr5:147109514-147109515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs150526255	chr5:147109555-147109556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs374147527	chr5:147109570-147109571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553460788	chr5:147109679-147109680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544724122	chr5:147109731-147109732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562929982	chr5:147109773-147109774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs530363944	chr5:147109777-147109778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs139524768	chr5:147109780-147109781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556601370	chr5:147109797-147109798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs373460862	chr5:147109814-147109815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs6871771	chr5:147109819-147109820	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs373669383	chr5:147109856-147109857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371609652	chr5:147109865-147109866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs182936903	chr5:147109893-147109894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555660879	chr5:147109932-147109933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs367574963	chr5:147109983-147109984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs372771069	chr5:147109996-147109997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs564573946	chr5:147110005-147110006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201334200	chr5:147110011-147110012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200344018	chr5:147110012-147110013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs397999541	chr5:147110023-147110024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs13180561	chr5:147110025-147110026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187447387	chr5:147110036-147110037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192303513	chr5:147110051-147110052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs547024653	chr5:147110063-147110064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs568914626	chr5:147110075-147110076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs544468425	chr5:147110083-147110084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs13160882	chr5:147110094-147110095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs548472560	chr5:147110113-147110114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	16864856	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	20864512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatitis	16823394	CNVD
Pancreatic cancer	17952125	CNVD
Hyperekplexia	16941485	CNVD
Crohn''s disease	20877625	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1882 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:147078600-147146000	Weak transcription	Primary T cells from cord blood	blood
2	chr5:147101600-147114400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr5:147101800-147109800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr5:147102000-147109400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr5:147102000-147109600	Weak transcription	Brain Germinal Matrix	brain
6	chr5:147102000-147111600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr5:147102000-147112000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr5:147102200-147114400	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr5:147102600-147111600	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr5:147103600-147110400	Weak transcription	Brain Angular Gyrus	brain
11	chr5:147103600-147110400	Weak transcription	Brain Hippocampus Middle	brain
12	chr5:147103600-147111600	Weak transcription	Fetal Brain Female	brain
13	chr5:147103600-147121800	Weak transcription	Fetal Brain Male	brain
14	chr5:147105600-147109600	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr5:147105600-147114200	Weak transcription	Primary hematopoietic stem cells	blood
16	chr5:147105800-147110400	Weak transcription	Brain Anterior Caudate	brain
17	chr5:147105800-147114400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr5:147106000-147110400	Weak transcription	Brain Substantia Nigra	brain
19	chr5:147106400-147110400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr5:147106600-147111200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr5:147107200-147112800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr5:147108400-147110600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr5:147108600-147111200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr5:147108800-147110600	Weak transcription	Brain Cingulate Gyrus	brain
25	chr5:147109400-147110400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr5:147109600-147110800	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr5:147109600-147111000	Enhancers	Brain Germinal Matrix	brain
28	chr5:147109800-147113400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr5:147110400-147111000	Enhancers	Brain Hippocampus Middle	brain
30	chr5:147110400-147111200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr5:147110400-147111200	Enhancers	Brain Anterior Caudate	brain
32	chr5:147110400-147111400	Enhancers	Brain Angular Gyrus	brain
33	chr5:147110400-147113000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr5:147110400-147113000	Enhancers	Brain Substantia Nigra	brain
35	chr5:147110600-147111200	Enhancers	Brain Cingulate Gyrus	brain
36	chr5:147110600-147111200	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr5:147110600-147111200	Enhancers	Stomach Mucosa	stomach
38	chr5:147110600-147112000	Enhancers	Fetal Intestine Small	intestine
39	chr5:147110600-147112200	Enhancers	Duodenum Mucosa	Duodenum
40	chr5:147110800-147111200	Enhancers	Fetal Intestine Large	intestine
41	chr5:147110800-147111400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
42	chr5:147110800-147112200	Enhancers	Fetal Lung	lung
43	chr5:147111000-147111400	Flanking Active TSS	Brain Germinal Matrix	brain
44	chr5:147111000-147111600	Flanking Active TSS	Brain Hippocampus Middle	brain
45	chr5:147111200-147111400	Flanking Active TSS	Brain Anterior Caudate	brain
46	chr5:147111200-147111800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr5:147111200-147111800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
48	chr5:147111200-147112000	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr5:147111200-147112000	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr5:147111200-147112200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain

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