Variant report

Variant	esv2422258
Chromosome Location	chr9:71234845-71663340
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5926)
CpG islands
(count:2017)
Chromatin interactive
region (count:319)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:5926 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:71634748-71635103	K562	blood:	n/a	n/a
2	ARID3A	chr9:71317436-71317732	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:71362885-71363286	K562	blood:	n/a	n/a
4	ARID3A	chr9:71642563-71642873	K562	blood:	n/a	n/a
5	ARID3A	chr9:71576402-71576900	K562	blood:	n/a	n/a
6	ARID3A	chr9:71374566-71374601	K562	blood:	n/a	n/a
7	ARID3A	chr9:71460000-71460212	K562	blood:	n/a	n/a
8	ARID3A	chr9:71354673-71355058	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:71394475-71395468	HepG2	liver:	n/a	n/a
10	ARID3A	chr9:71347230-71347977	HepG2	liver:	n/a	n/a
11	ARID3A	chr9:71321237-71321426	HepG2	liver:	n/a	n/a
12	ARID3A	chr9:71614594-71614886	HepG2	liver:	n/a	n/a
13	ARID3A	chr9:71300073-71301012	HepG2	liver:	n/a	n/a
14	ARID3A	chr9:71394661-71395015	K562	blood:	n/a	n/a
15	ARID3A	chr9:71313920-71314482	K562	blood:	n/a	n/a
16	ARID3A	chr9:71355349-71355811	HepG2	liver:	n/a	n/a
17	ARID3A	chr9:71598080-71598400	K562	blood:	n/a	n/a
18	ARID3A	chr9:71635426-71635919	K562	blood:	n/a	n/a
19	ARID3A	chr9:71651502-71651839	K562	blood:	n/a	n/a
20	ARID3A	chr9:71431767-71432536	HepG2	liver:	n/a	n/a
21	ARID3A	chr9:71258770-71259620	K562	blood:	n/a	n/a
22	ARID3A	chr9:71584464-71585376	K562	blood:	n/a	n/a
23	ARID3A	chr9:71319020-71319266	K562	blood:	n/a	n/a
24	ARID3A	chr9:71334977-71335149	HepG2	liver:	n/a	n/a
25	ARID3A	chr9:71542080-71542315	K562	blood:	n/a	n/a
26	ARID3A	chr9:71432365-71432517	K562	blood:	n/a	n/a
27	ARID3A	chr9:71319857-71320037	HepG2	liver:	n/a	n/a
28	ARID3A	chr9:71364814-71365867	K562	blood:	n/a	n/a
29	ARID3A	chr9:71631852-71631872	K562	blood:	n/a	n/a
30	ARID3A	chr9:71650444-71651128	HepG2	liver:	n/a	n/a
31	ARID3A	chr9:71320671-71320784	K562	blood:	n/a	n/a
32	ARID3A	chr9:71335807-71336197	K562	blood:	n/a	n/a
33	ARID3A	chr9:71584469-71584970	HepG2	liver:	n/a	n/a
34	ARID3A	chr9:71650526-71650743	K562	blood:	n/a	n/a
35	ARID3A	chr9:71393374-71393765	K562	blood:	n/a	n/a
36	ARID3A	chr9:71361914-71362649	K562	blood:	n/a	n/a
37	ATF1	chr9:71598096-71598406	K562	blood:	n/a	n/a
38	ATF1	chr9:71314125-71314344	K562	blood:	n/a	n/a
39	ATF1	chr9:71590616-71590989	K562	blood:	n/a	n/a
40	ATF1	chr9:71420516-71420729	K562	blood:	n/a	n/a
41	ATF1	chr9:71635543-71635967	K562	blood:	n/a	n/a
42	ATF1	chr9:71279328-71279493	K562	blood:	n/a	n/a
43	ATF1	chr9:71335758-71336174	K562	blood:	n/a	n/a
44	ATF1	chr9:71634756-71635094	K562	blood:	n/a	n/a
45	ATF1	chr9:71266214-71266489	K562	blood:	n/a	n/a
46	ATF1	chr9:71413396-71413615	K562	blood:	n/a	n/a
47	ATF1	chr9:71394632-71395101	K562	blood:	n/a	n/a
48	ATF1	chr9:71375298-71375690	K562	blood:	n/a	n/a
49	ATF1	chr9:71361951-71362362	K562	blood:	n/a	n/a
50	ATF1	chr9:71613777-71614153	K562	blood:	n/a	n/a

(count:2017 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:71393662-71393712	ovcar-3	ovarian:	n/a
2	chr9:71623401-71623451	NH-A	brain:	n/a
3	chr9:71397641-71397691	RPTEC	kidney:	n/a
4	chr9:71393662-71393712	HL-60	blood:	n/a
5	chr9:71393662-71393712	ovcar-3	ovarian:	n/a
6	chr9:71623401-71623451	NH-A	brain:	n/a
7	chr9:71397641-71397691	RPTEC	kidney:	n/a
8	chr9:71393662-71393712	HL-60	blood:	n/a
9	chr9:71623401-71623451	SKMC	muscle:	n/a
10	chr9:71589563-71589613	AG04449	skin:	fetal
11	chr9:71627667-71627717	HIPEpiC	eye:	n/a
12	chr9:71647192-71647242	HIPEpiC	eye:	n/a
13	chr9:71629130-71629180	SAEC	small airway:	n/a
14	chr9:71647192-71647242	HCM	heart:	n/a
15	chr9:71661107-71661157	HRPEpiC	eye:	n/a
16	chr9:71627524-71627574	HEK293	kidney:	embryo
17	chr9:71397641-71397691	Jurkat	blood:	n/a
18	chr9:71631514-71631564	SK-N-SH	brain:	n/a
19	chr9:71320601-71320651	NT2-D1	testis:	n/a
20	chr9:71393662-71393712	A549	lung:	n/a
21	chr9:71589563-71589613	SK-N-SH	brain:	n/a
22	chr9:71623401-71623451	GM12892	blood:	n/a
23	chr9:71395063-71395113	HEK293	kidney:	embryo
24	chr9:71652532-71652582	BE2_C	brain:	n/a
25	chr9:71628906-71628956	PrEC	prostate:	n/a
26	chr9:71316119-71316169	HCPEpiC	choroid plexus:	n/a
27	chr9:71393662-71393712	SK-N-SH	brain:	n/a
28	chr9:71651331-71651381	PANC-1	pancreas:	n/a
29	chr9:71623401-71623451	HRE	kidney:	n/a
30	chr9:71631514-71631564	LNCaP	prostate:	n/a
31	chr9:71395167-71395217	HAEpiC	amniotic membrane:	n/a
32	chr9:71319485-71319535	U87	brain:	n/a
33	chr9:71394810-71394860	Hepatocyte	liver:	n/a
34	chr9:71651331-71651381	Jurkat	blood:	n/a
35	chr9:71650331-71650381	HCPEpiC	choroid plexus:	n/a
36	chr9:71647192-71647242	MCF10A-Er-Src	breast:	n/a
37	chr9:71320693-71320743	HCF	heart:	n/a
38	chr9:71589563-71589613	HPAEpiC	pulmonary alveolar:	n/a
39	chr9:71320693-71320743	Caco-2	colon:	n/a
40	chr9:71395330-71395380	GM06990	blood:	n/a
41	chr9:71647192-71647242	AG09319	gingival:	n/a
42	chr9:71316119-71316169	GM06990	blood:	n/a
43	chr9:71397641-71397691	AG04450	lung:	fetal
44	chr9:71319485-71319535	NT2-D1	testis:	n/a
45	chr9:71651331-71651381	MCF10A-Er-Src	breast:	n/a
46	chr9:71628906-71628956	H1-hESC	embryonic stem cell:	embryo
47	chr9:71654823-71654873	PFSK-1	brain:	n/a
48	chr9:71316119-71316169	HIPEpiC	eye:	n/a
49	chr9:71651331-71651381	ProgFib	skin:	n/a
50	chr9:71623401-71623451	HIPEpiC	eye:	n/a

(count:319 , 50 per page) page: 1 2 3 4 5 6 7

No.	Distal block	Cell Line	Cell type
1	chr11:62608645..62609222-chr9:71420682..71421202,5	MCF-7	breast:
2	chr9:71314661..71316622-chr9:71318012..71320131,2	MCF-7	breast:
3	chr9:71357154..71359879-chr9:71394031..71396553,2	MCF-7	breast:
4	chr9:71392687..71396802-chr9:71403243..71407898,5	MCF-7	breast:
5	chr9:71287783..71290645-chr9:71299909..71302251,2	MCF-7	breast:
6	chr9:71360686..71364939-chr9:71391201..71394992,4	K562	blood:
7	chr9:71362860..71364586-chr9:71376737..71378891,2	K562	blood:
8	chr9:71627843..71630592-chr9:71632071..71633725,3	K562	blood:
9	chr9:71459672..71460600-chr9:71642433..71642935,2	K562	blood:
10	chr9:71577956..71581283-chr9:71582183..71585440,6	K562	blood:
11	chr9:71546260..71548319-chr9:71558934..71561181,2	K562	blood:
12	chr9:71316561..71319400-chr9:71390897..71393133,2	K562	blood:
13	chr9:71314661..71316622-chr9:71318012..71320131,2	MCF-7	breast:
14	chr9:71594449..71596709-chr9:71598735..71600800,2	K562	blood:
15	chr9:71317900..71319915-chr9:71391633..71393560,2	K562	blood:
16	chr9:71651712..71654573-chr9:71656499..71659593,3	K562	blood:
17	chr9:71400597..71404451-chr9:71406708..71409668,4	MCF-7	breast:
18	chr9:71379701..71382544-chr9:71392331..71394766,2	K562	blood:
19	chr9:71474756..71477086-chr9:71501374..71504122,2	K562	blood:
20	chr9:71649378..71651041-chr9:71654267..71655823,2	MCF-7	breast:
21	chr11:62607625..62610617-chr9:71419682..71421202,4	K562	blood:
22	chr9:71468331..71470715-chr9:71473638..71476429,2	K562	blood:
23	chr9:71397068..71400120-chr9:71405362..71406999,3	MCF-7	breast:
24	chr9:71255429..71258237-chr9:71267867..71269375,2	MCF-7	breast:
25	chr9:71318773..71321660-chr9:71357020..71360216,3	K562	blood:
26	chr9:71587606..71589215-chr9:71606682..71608603,2	MCF-7	breast:
27	chr9:71199122..71199719-chr9:71614348..71615097,4	MCF-7	breast:
28	chr9:71199104..71200136-chr9:71459624..71460607,5	MCF-7	breast:
29	chr9:71362860..71364586-chr9:71376737..71378891,2	K562	blood:
30	chr9:71612570..71616113-chr9:71618356..71621633,3	K562	blood:
31	chr9:71590575..71592087-chr9:71593583..71595166,2	K562	blood:
32	chr9:71361257..71364169-chr9:71367076..71369811,4	K562	blood:
33	chr9:71199061..71199763-chr9:71459847..71460712,3	MCF-7	breast:
34	chr9:71420662..71423189-chr9:71425741..71428511,3	K562	blood:
35	chr9:71388257..71390428-chr9:71458098..71459800,2	K562	blood:
36	chr9:71341357..71343787-chr9:71348342..71350761,2	K562	blood:
37	chr9:71398863..71402159-chr9:71407140..71410574,3	K562	blood:
38	chr9:71573438..71576022-chr9:71576543..71579524,3	K562	blood:
39	chr9:71465582..71467985-chr9:71469828..71471360,2	MCF-7	breast:
40	chr9:71491880..71494040-chr9:71553268..71555351,2	K562	blood:
41	chr9:71392572..71394227-chr9:71414871..71416644,2	K562	blood:
42	chr9:71199101..71200031-chr9:71292976..71293754,4	MCF-7	breast:
43	chr9:71366829..71368942-chr9:71393565..71396031,2	K562	blood:
44	chr9:71361634..71364182-chr9:71379350..71381885,2	K562	blood:
45	chr9:71354907..71358283-chr9:71360291..71362317,4	MCF-7	breast:
46	chr11:62608622..62609223-chr9:71420682..71421202,6	Hela-S3	cervix:
47	chr9:71320265..71322266-chr9:71464991..71467185,2	K562	blood:
48	chr9:71398048..71400496-chr9:71420484..71423422,2	K562	blood:
49	chr9:71319577..71321555-chr9:71393458..71395334,2	MCF-7	breast:
50	chr9:71333441..71335989-chr9:71487302..71489155,2	K562	blood:

(count:28 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PGM5-1	chr9:71258509-71259358	NONHSAT131748
2	lnc-PRKACG-1	chr9:71590580-71590757	ENSG00000249652
3	lnc-PGM5-1	chr9:71240557-71240763	ENSG00000226337.2
4	lnc-PGM5-1	chr9:71240557-71240763	NONHSAT131748
5	lnc-PGM5-1	chr9:71258509-71259358	ENSG00000226337.3
6	lnc-PRKACG-5	chr9:71563250-71563521	expReg_chr9_3063_-
7	lnc-FAM122A-1	chr9:71320902-71321138	NONHSAT131754
8	lnc-PGM5-1	chr9:71247955-71248176	ENSG00000226337.3
9	lnc-PRKACG-1	chr9:71590580-71590735	NONHSAT131759
10	lnc-FAM122A-1	chr9:71400999-71401076	NONHSAT131753
11	lnc-PRKACG-1	chr9:71570856-71572127	NONHSAT131759
12	lnc-PRKACG-4	chr9:71625289-71625403	ucscGeneNc_uc004ahk_2
13	lnc-PRKACG-1	chr9:71571942-71572127	ENSG00000249652
14	lnc-PRKACG-3	chr9:71439046-71439206	ENSG00000236733.1
15	lnc-FAM122A-1	chr9:71357417-71357573	NONHSAT131753
16	lnc-FAM122A-1	chr9:71343681-71343850	NONHSAT131753
17	lnc-PGM5-1	chr9:71247955-71248176	ENSG00000226337.2
18	lnc-FAM122A-1	chr9:71322519-71323057	NONHSAT131754
19	lnc-PGM5-1	chr9:71247945-71248176	NONHSAT131752
20	lnc-PGM5-1	chr9:71247955-71248176	NONHSAT131748
21	lnc-PRKACG-1	chr9:71568004-71569861	ENSG00000249652
22	lnc-PRKACG-3	chr9:71437319-71437564	ENSG00000236733.1
23	lnc-PRKACG-3	chr9:71458083-71458191	ENSG00000236733.1
24	lnc-PRKACG-4	chr9:71624143-71625000	ucscGeneNc_uc004ahk_2
25	lnc-PGM5-1	chr9:71240557-71240763	ENSG00000226337.3
26	lnc-PGM5-1	chr9:71258509-71259358	NONHSAT131752
27	lnc-FAM122A-1	chr9:71320901-71321138	NONHSAT131753
28	lnc-FAM122A-1	chr9:71342512-71342599	NONHSAT131753

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	FAM122A	hsa-miR-421	chr9:71396274-71396296
2	FAM122A	hsa-miR-16-5p	chr9:71396189-71396195
3	FAM122A	hsa-miR-425-5p	chr9:71397605-71397628
4	FAM122A	hsa-miR-421	chr9:71396259-71396281
5	FAM122A	hsa-miR-16-5p	chr9:71396176-71396195
6	FAM122A	hsa-miR-421	chr9:71396168-71396174

Variant related genes	Relation type
FAM122A	TF binding region
PIP5K1B	TF binding region
PRKACG	TF binding region
ENSG00000236733	TF binding region
FXN	TF binding region
ENSG00000236998	TF binding region
RNU6-820P	TF binding region
FAM122A	CpG island
PIP5K1B	CpG island
PRKACG	CpG island
ENSG00000236733	CpG island
FXN	CpG island
ENSG00000236998	CpG island
RNU6-820P	CpG island
ENSG00000133316	chromatin interactions
ENSG00000165059	chromatin interactions
ENSG00000165060	chromatin interactions
ENSG00000119139	chromatin interactions
ENSG00000236733	chromatin interactions
ENSG00000187866	chromatin interactions
ENSG00000107242	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000135736	chromatin interactions
ENSG00000236998	chromatin interactions
ENSG00000188825	chromatin interactions
TRIP12	miRNA target sites
NFIB	miRNA target sites
SMAD7	miRNA target sites

Extended variants
information (count: 14458 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:14458 , 50 per page) page: 1 2 3 4 5 6 7 ... 290

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535554481	chr9:71240604-71240605	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs146574111	chr9:71240620-71240621	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs191120046	chr9:71240621-71240622	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs544732918	chr9:71240643-71240644	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs141251632	chr9:71240654-71240655	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs10781094	chr9:71240672-71240673	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs144960128	chr9:71240686-71240687	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs115990644	chr9:71240698-71240699	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs375526962	chr9:71240702-71240703	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs567406537	chr9:71240705-71240706	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs571295595	chr9:71240770-71240771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571491746	chr9:71240839-71240840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533434075	chr9:71240867-71240868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs551919067	chr9:71240908-71240909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs183653314	chr9:71240927-71240928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs575712878	chr9:71240940-71240941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs10781095	chr9:71240969-71240970	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs139024902	chr9:71240986-71240987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567940091	chr9:71241010-71241011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs75504114	chr9:71241016-71241017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10781096	chr9:71241017-71241018	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs545432803	chr9:71241068-71241069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187433003	chr9:71241081-71241082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191056704	chr9:71241088-71241089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs944550	chr9:71241117-71241118	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs370230180	chr9:71241141-71241142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572091016	chr9:71241184-71241185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11789381	chr9:71241221-71241222	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs116173530	chr9:71241238-71241239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541527899	chr9:71241241-71241242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141554334	chr9:71241281-71241282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543760806	chr9:71241342-71241343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10869160	chr9:71241343-71241344	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs35443307	chr9:71241357-71241358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs11788138	chr9:71241366-71241367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545639976	chr9:71241397-71241398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150456927	chr9:71241414-71241415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs944551	chr9:71241448-71241449	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs560633062	chr9:71241487-71241488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs527824415	chr9:71241488-71241489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182883710	chr9:71241510-71241511	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs78083774	chr9:71241556-71241557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531228646	chr9:71241562-71241563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2183737	chr9:71241633-71241634	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs550080015	chr9:71241641-71241642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571469519	chr9:71241679-71241680	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138299436	chr9:71241714-71241715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187480545	chr9:71241768-71241769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550795099	chr9:71241779-71241780	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149612865	chr9:71241839-71241840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17899364	CNVD
Mantle cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Bipolar disorder	19214233	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:6942 , 50 per page) page: 1 2 3 4 5 6 7 ... 139

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71240600-71241000	Enhancers	Pancreas	Pancrea
2	chr9:71241000-71244200	Weak transcription	Pancreas	Pancrea
3	chr9:71241400-71243400	Enhancers	Fetal Heart	heart
4	chr9:71241600-71242000	Enhancers	K562	blood
5	chr9:71242000-71243200	Weak transcription	K562	blood
6	chr9:71242200-71244400	Enhancers	Duodenum Mucosa	Duodenum
7	chr9:71243200-71244400	Enhancers	K562	blood
8	chr9:71243400-71243800	Flanking Active TSS	Fetal Heart	heart
9	chr9:71243800-71247400	Enhancers	Fetal Heart	heart
10	chr9:71244000-71244800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr9:71244200-71244400	Enhancers	Pancreas	Pancrea
12	chr9:71246400-71247000	Enhancers	Left Ventricle	heart
13	chr9:71247400-71249000	Weak transcription	Fetal Heart	heart
14	chr9:71249000-71250200	Enhancers	Fetal Heart	heart
15	chr9:71249400-71255200	Enhancers	Primary B cells from peripheral blood	blood
16	chr9:71249600-71251400	Enhancers	Primary B cells from cord blood	blood
17	chr9:71250200-71250600	Weak transcription	Fetal Heart	heart
18	chr9:71250400-71250600	Enhancers	Adipose Nuclei	Adipose
19	chr9:71250600-71251800	Enhancers	Fetal Heart	heart
20	chr9:71250800-71251800	Weak transcription	Adipose Nuclei	Adipose
21	chr9:71251000-71251800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr9:71251400-71251800	Flanking Active TSS	Primary B cells from cord blood	blood
23	chr9:71251400-71251800	Enhancers	Rectal Mucosa Donor 29	rectum
24	chr9:71251600-71252200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
25	chr9:71251600-71252400	Enhancers	Stomach Mucosa	stomach
26	chr9:71251600-71254400	Enhancers	GM12878-XiMat	blood
27	chr9:71251800-71252200	Enhancers	Adipose Nuclei	Adipose
28	chr9:71251800-71252800	Active TSS	Rectal Mucosa Donor 29	rectum
29	chr9:71251800-71254200	Enhancers	Primary B cells from cord blood	blood
30	chr9:71252000-71253400	Enhancers	Duodenum Mucosa	Duodenum
31	chr9:71252200-71253200	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr9:71252800-71253000	Enhancers	Rectal Mucosa Donor 29	rectum
33	chr9:71253200-71253400	Enhancers	Primary hematopoietic stem cells	blood
34	chr9:71253200-71258600	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr9:71253400-71254800	Weak transcription	Primary hematopoietic stem cells	blood
36	chr9:71254200-71254400	Flanking Active TSS	Primary B cells from cord blood	blood
37	chr9:71254400-71254800	Enhancers	Primary B cells from cord blood	blood
38	chr9:71254400-71256200	Flanking Active TSS	GM12878-XiMat	blood
39	chr9:71254400-71256200	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr9:71254800-71255600	Enhancers	Right Ventricle	heart
41	chr9:71254800-71256000	Enhancers	Primary hematopoietic stem cells	blood
42	chr9:71254800-71256200	Enhancers	Fetal Heart	heart
43	chr9:71254800-71256400	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr9:71254800-71256600	Flanking Active TSS	Primary B cells from cord blood	blood
45	chr9:71255000-71255200	Enhancers	Left Ventricle	heart
46	chr9:71255000-71256000	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr9:71255000-71256000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr9:71255200-71255400	Flanking Active TSS	Primary B cells from peripheral blood	blood
49	chr9:71255200-71255600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr9:71255400-71255800	Enhancers	Primary B cells from peripheral blood	blood

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