Variant report

Variant	nsv892624
Chromosome Location	chr9:15283761-15415461
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1564)
CpG islands
(count:489)
Chromatin interactive
region (count:41)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1564 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:15351035-15351548	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:15357028-15357575	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:15306129-15306386	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:15403256-15403512	K562	blood:	n/a	n/a
5	ARID3A	chr9:15307077-15307551	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:15350374-15350711	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:15333319-15333669	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:15403228-15403452	HepG2	liver:	n/a	n/a
9	ATF1	chr9:15299673-15299858	K562	blood:	n/a	n/a
10	ATF1	chr9:15287263-15287635	K562	blood:	n/a	n/a
11	ATF1	chr9:15386543-15386855	K562	blood:	n/a	n/a
12	ATF1	chr9:15293783-15294043	K562	blood:	n/a	n/a
13	BACH1	chr9:15306339-15306925	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr9:15370513-15370989	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr9:15328555-15328874	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr9:15328520-15328827	K562	blood:	n/a	n/a
17	BATF	chr9:15306084-15306387	GM12878	blood:	n/a	n/a
18	BATF	chr9:15299577-15299867	GM12878	blood:	n/a	chr9:15299785-15299794
19	BCL3	chr9:15331480-15331831	GM12878	blood:	n/a	n/a
20	BCL3	chr9:15331510-15331929	GM12878	blood:	n/a	n/a
21	BCL3	chr9:15293395-15293760	GM12878	blood:	n/a	n/a
22	BCLAF1	chr9:15299556-15300027	GM12878	blood:	n/a	chr9:15299645-15299654
23	BHLHE40	chr9:15318021-15318086	K562	blood:	n/a	n/a
24	BHLHE40	chr9:15306190-15306323	K562	blood:	n/a	n/a
25	BHLHE40	chr9:15351043-15351484	HepG2	liver:	n/a	n/a
26	BHLHE40	chr9:15357545-15357594	GM12878	blood:	n/a	n/a
27	BHLHE40	chr9:15386531-15386879	K562	blood:	n/a	n/a
28	BHLHE40	chr9:15315454-15315624	K562	blood:	n/a	n/a
29	BHLHE40	chr9:15403322-15403478	K562	blood:	n/a	n/a
30	BHLHE40	chr9:15307159-15307687	K562	blood:	n/a	n/a
31	BHLHE40	chr9:15307178-15307437	GM12878	blood:	n/a	n/a
32	BRCA1	chr9:15307498-15307506	HepG2	liver:	n/a	n/a
33	BRCA1	chr9:15295906-15296187	GM12878	blood:	n/a	n/a
34	BRCA1	chr9:15299127-15299177	GM12878	blood:	n/a	n/a
35	CBX3	chr9:15323298-15323578	K562	blood:	n/a	n/a
36	CCNT2	chr9:15307181-15307674	K562	blood:	n/a	n/a
37	CEBPB	chr9:15305868-15306420	MCF-7	breast:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
38	CEBPB	chr9:15357074-15357375	A549	lung:	n/a	chr9:15357245-15357256
39	CEBPB	chr9:15307255-15307554	HepG2	liver:	n/a	n/a
40	CEBPB	chr9:15364953-15365251	A549	lung:	n/a	n/a
41	CEBPB	chr9:15350243-15350844	A549	lung:	n/a	chr9:15350602-15350613
42	CEBPB	chr9:15350317-15350793	MCF-7	breast:	n/a	chr9:15350602-15350613
43	CEBPB	chr9:15364895-15365238	HepG2	liver:	n/a	n/a
44	CEBPB	chr9:15350328-15350801	A549	lung:	n/a	chr9:15350602-15350613
45	CEBPB	chr9:15300306-15300673	IMR90	lung:	n/a	n/a
46	CEBPB	chr9:15357133-15357334	IMR90	lung:	n/a	chr9:15357245-15357256
47	CEBPB	chr9:15305866-15306396	ECC-1	luminal epithelium:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
48	CEBPB	chr9:15361744-15362104	HepG2	liver:	n/a	chr9:15361911-15361922
49	CEBPB	chr9:15328968-15329287	HepG2	liver:	n/a	chr9:15329145-15329156
50	CEBPB	chr9:15296139-15296371	HepG2	liver:	n/a	chr9:15296245-15296258 chr9:15296246-15296257

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:15371248-15371298	GM06990	blood:	n/a
2	chr9:15371248-15371298	GM06990	blood:	n/a
3	chr9:15310979-15311029	IMR90	lung:	fetal
4	chr9:15307873-15307923	HEEpiC	esophagus:	n/a
5	chr9:15310979-15311029	HEEpiC	esophagus:	n/a
6	chr9:15310979-15311029	BE2_C	brain:	n/a
7	chr9:15306337-15306387	SK-N-MC	brain:	n/a
8	chr9:15371248-15371298	Hela-S3	cervix:	n/a
9	chr9:15307376-15307426	Caco-2	colon:	n/a
10	chr9:15307376-15307426	AG04449	skin:	fetal
11	chr9:15307873-15307923	AoSMC	blood vessel:	n/a
12	chr9:15306736-15306786	NT2-D1	testis:	n/a
13	chr9:15306337-15306387	K562	blood:	n/a
14	chr9:15401531-15401581	Jurkat	blood:	n/a
15	chr9:15371248-15371298	PANC-1	pancreas:	n/a
16	chr9:15306337-15306387	HepG2	liver:	n/a
17	chr9:15307376-15307426	HCT-116	colon:	n/a
18	chr9:15305873-15305923	GM19239	blood:	n/a
19	chr9:15306337-15306387	NB4	blood:	n/a
20	chr9:15401531-15401581	Caco-2	colon:	n/a
21	chr9:15305873-15305923	Caco-2	colon:	n/a
22	chr9:15401531-15401581	AG09309	skin:	n/a
23	chr9:15306337-15306387	HAEpiC	amniotic membrane:	n/a
24	chr9:15371248-15371298	ovcar-3	ovarian:	n/a
25	chr9:15306337-15306387	SKMC	muscle:	n/a
26	chr9:15305873-15305923	SK-N-SH	brain:	n/a
27	chr9:15310979-15311029	H1-hESC	embryonic stem cell:	embryo
28	chr9:15401531-15401581	SK-N-SH	brain:	n/a
29	chr9:15305873-15305923	Hela-S3	cervix:	n/a
30	chr9:15371248-15371298	AG10803	skin:	n/a
31	chr9:15310979-15311029	CMK	blood:	n/a
32	chr9:15307376-15307426	IMR90	lung:	fetal
33	chr9:15307873-15307923	AG09319	gingival:	n/a
34	chr9:15307873-15307923	MCF10A-Er-Src	breast:	n/a
35	chr9:15371248-15371298	HepG2	liver:	n/a
36	chr9:15401531-15401581	AG04450	lung:	fetal
37	chr9:15371248-15371298	H1-hESC	embryonic stem cell:	embryo
38	chr9:15306736-15306786	AoSMC	blood vessel:	n/a
39	chr9:15310979-15311029	GM19239	blood:	n/a
40	chr9:15401531-15401581	ProgFib	skin:	n/a
41	chr9:15305873-15305923	A549	lung:	n/a
42	chr9:15306736-15306786	HepG2	liver:	n/a
43	chr9:15306337-15306387	HCM	heart:	n/a
44	chr9:15310979-15311029	K562	blood:	n/a
45	chr9:15310979-15311029	HNPCEpiC	eye:	n/a
46	chr9:15307376-15307426	NHDF-neo	bronchial:	n/a
47	chr9:15305873-15305923	HRCEpiC	kidney:	n/a
48	chr9:15307873-15307923	BE2_C	brain:	n/a
49	chr9:15371248-15371298	NB4	blood:	n/a
50	chr9:15305873-15305923	T-47D	breast:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:15283111..15284924-chr9:15291453..15293765,2	MCF-7	breast:
2	chr9:15305818..15308791-chr9:15400718..15402980,2	MCF-7	breast:
3	chr9:15300090..15302521-chr9:15304681..15306725,2	MCF-7	breast:
4	chr9:15300090..15302521-chr9:15304681..15306725,2	MCF-7	breast:
5	chr9:15283042..15284645-chr9:15287369..15289731,2	K562	blood:
6	chr9:15393231..15396045-chr9:15401354..15402871,2	MCF-7	breast:
7	chr9:15393231..15396045-chr9:15401354..15402871,2	MCF-7	breast:
8	chr9:15306135..15309581-chr9:15420818..15425516,6	MCF-7	breast:
9	chr9:15277443..15278337-chr9:15356714..15357650,2	MCF-7	breast:
10	chr9:15352501..15354066-chr9:15419261..15422025,2	MCF-7	breast:
11	chr9:15357011..15359248-chr9:15422187..15424051,2	MCF-7	breast:
12	chr9:15290133..15292362-chr9:15306023..15308672,3	MCF-7	breast:
13	chr9:15305128..15307154-chr9:15417021..15419951,2	MCF-7	breast:
14	chr9:15298408..15301257-chr9:15344895..15347811,2	MCF-7	breast:
15	chr9:15332011..15334775-chr9:15347128..15349228,2	MCF-7	breast:
16	chr9:15385459..15387196-chr9:15436159..15438276,2	K562	blood:
17	chr9:15298408..15301257-chr9:15344895..15347811,2	MCF-7	breast:
18	chr9:15415166..15416789-chr9:15420978..15423004,2	MCF-7	breast:
19	chr9:15285917..15290029-chr9:15305142..15308889,4	MCF-7	breast:
20	chr9:15399457..15401521-chr9:15510230..15512381,2	MCF-7	breast:
21	chr9:15305088..15306661-chr9:15415103..15416933,2	MCF-7	breast:
22	chr9:15285882..15288246-chr9:15510557..15512091,2	K562	blood:
23	chr9:15372087..15374863-chr9:15401359..15403431,2	MCF-7	breast:
24	chr9:15306963..15308773-chr9:15314988..15318754,3	MCF-7	breast:
25	chr9:15305088..15306661-chr9:15415103..15416933,2	MCF-7	breast:
26	chr9:15283111..15284924-chr9:15291453..15293765,2	MCF-7	breast:
27	chr9:15303560..15305523-chr9:15350040..15352891,2	MCF-7	breast:
28	chr9:15414032..15416513-chr9:15421401..15423007,2	K562	blood:
29	chr9:15293831..15297894-chr9:15305171..15308300,4	MCF-7	breast:
30	chr9:15211338..15211919-chr9:15356761..15357369,2	MCF-7	breast:
31	chr9:15386697..15389614-chr9:15422790..15424352,2	K562	blood:
32	chr9:15303560..15305523-chr9:15350040..15352891,2	MCF-7	breast:
33	chr9:15305709..15307336-chr9:15348928..15350627,2	MCF-7	breast:
34	chr9:15273274..15274780-chr9:15289457..15291065,2	K562	blood:
35	chr9:15298942..15301605-chr9:15420446..15422025,2	MCF-7	breast:
36	chr9:15218010..15219971-chr9:15288500..15290967,2	MCF-7	breast:
37	chr9:15283042..15284645-chr9:15287369..15289731,2	K562	blood:
38	chr9:15380318..15382150-chr9:15422368..15424031,2	MCF-7	breast:
39	chr9:15414997..15416790-chr9:15421464..15423490,2	MCF-7	breast:
40	chr9:15356402..15356902-chr9:134721602..134722134,2	NB4	blood:
41	chr9:15372087..15374863-chr9:15401359..15403431,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNAPC3-2	chr9:15348166-15348453	NONHSAT130262

No data

Variant related genes	Relation type
RN7SL157P	TF binding region
TTC39B	TF binding region
RPL7P33	TF binding region
RN7SL157P	CpG island
TTC39B	CpG island
RPL7P33	CpG island
ENSG00000155158	chromatin interactions
ENSG00000164975	chromatin interactions
ENSG00000164985	chromatin interactions
ENSG00000263817	chromatin interactions

Extended variants
information (count: 5590 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:5590 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575442	chr9:15283761-15283762	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs577987132	chr9:15283781-15283782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs539003735	chr9:15283784-15283785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554182825	chr9:15283787-15283788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs111242665	chr9:15283789-15283790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs12346135	chr9:15283811-15283812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs185022190	chr9:15283836-15283837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142317904	chr9:15283847-15283848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs576707060	chr9:15283877-15283878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531993682	chr9:15283901-15283902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567219568	chr9:15283914-15283915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187876939	chr9:15283929-15283930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs73646030	chr9:15283948-15283949	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs149347092	chr9:15283964-15283965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551370622	chr9:15284007-15284008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs80257424	chr9:15284044-15284045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs641579	chr9:15284100-15284101	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs693223	chr9:15284120-15284121	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs551795765	chr9:15284166-15284167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs116340798	chr9:15284177-15284178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs139533147	chr9:15284187-15284188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs551696223	chr9:15284190-15284191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112039931	chr9:15284192-15284193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs571616414	chr9:15284193-15284194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149271168	chr9:15284237-15284238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572423897	chr9:15284245-15284246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369773034	chr9:15284305-15284306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536791064	chr9:15284328-15284329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs73646031	chr9:15284355-15284356	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs571947974	chr9:15284400-15284401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192313019	chr9:15284408-15284409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs72700670	chr9:15284420-15284421	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs184371773	chr9:15284428-15284429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148759582	chr9:15284437-15284438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs113637932	chr9:15284446-15284447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537200589	chr9:15284473-15284474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527279575	chr9:15284499-15284500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1215120	chr9:15284527-15284528	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs189577454	chr9:15284560-15284561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371102637	chr9:15284569-15284570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560630512	chr9:15284571-15284572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531280787	chr9:15284587-15284588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144929197	chr9:15284594-15284595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10961955	chr9:15284640-15284641	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs181165163	chr9:15284679-15284680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547711203	chr9:15284683-15284684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2890997	chr9:15284696-15284697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536625651	chr9:15284715-15284716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs78248115	chr9:15284724-15284725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570148316	chr9:15284726-15284727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	19835627	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1990 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15241200-15286200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr9:15243000-15293400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr9:15250200-15288200	Weak transcription	Fetal Stomach	stomach
4	chr9:15253800-15286400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr9:15254000-15293000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr9:15254200-15293000	Weak transcription	NHEK	skin
7	chr9:15254200-15295600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr9:15259200-15293400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr9:15264200-15285800	Weak transcription	Primary hematopoietic stem cells	blood
10	chr9:15273600-15286000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr9:15273600-15293400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr9:15274000-15286000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr9:15274000-15288400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr9:15274000-15288400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr9:15276800-15284800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr9:15277000-15292200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr9:15277000-15293000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr9:15277600-15288400	Weak transcription	Lung	lung
19	chr9:15277600-15296800	Weak transcription	Gastric	stomach
20	chr9:15278000-15286000	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr9:15278000-15286200	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr9:15278000-15295200	Weak transcription	Pancreas	Pancrea
23	chr9:15278200-15289400	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr9:15278600-15286200	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr9:15278600-15291200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr9:15279600-15287400	Weak transcription	Small Intestine	intestine
27	chr9:15279800-15293200	Weak transcription	Rectal Smooth Muscle	rectum
28	chr9:15280800-15288600	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr9:15281600-15289000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr9:15282400-15285600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr9:15282600-15284200	Enhancers	Fetal Intestine Small	intestine
32	chr9:15282800-15284200	Enhancers	Primary T cells from cord blood	blood
33	chr9:15283200-15284000	Weak transcription	Aorta	Aorta
34	chr9:15283400-15287200	Weak transcription	HepG2	liver
35	chr9:15283600-15284000	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr9:15283600-15286000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr9:15283600-15286000	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr9:15283600-15286000	Weak transcription	Stomach Mucosa	stomach
39	chr9:15283600-15286200	Weak transcription	Primary T helper cells PMA-I stimulated	--
40	chr9:15283600-15293800	Weak transcription	Duodenum Mucosa	Duodenum
41	chr9:15284000-15284200	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr9:15284200-15285800	Weak transcription	Fetal Intestine Small	intestine
43	chr9:15284200-15286000	Weak transcription	Primary T cells from cord blood	blood
44	chr9:15284200-15286000	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr9:15284800-15285000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr9:15284800-15287000	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr9:15285000-15287600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr9:15285200-15293800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr9:15285800-15286200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr9:15285800-15286800	Enhancers	Primary hematopoietic stem cells	blood

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