Variant report

Variant	esv2763030
Chromosome Location	chr13:64545539-64719372
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:64647343-64648012	K562	blood:	n/a	n/a
2	ARID3A	chr13:64649942-64650348	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:64648424-64648624	K562	blood:	n/a	n/a
4	ARID3A	chr13:64647471-64647547	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:64649045-64649723	HepG2	liver:	n/a	n/a
6	ATF1	chr13:64649727-64650392	K562	blood:	n/a	n/a
7	ATF3	chr13:64649966-64650442	HepG2	liver:	n/a	n/a
8	ATF3	chr13:64649957-64650249	HepG2	liver:	n/a	n/a
9	ATF3	chr13:64650004-64650247	K562	blood:	n/a	n/a
10	BHLHE40	chr13:64649695-64650426	K562	blood:	n/a	n/a
11	BHLHE40	chr13:64649668-64650427	HepG2	liver:	n/a	n/a
12	BRCA1	chr13:64650041-64650270	HepG2	liver:	n/a	n/a
13	CBX3	chr13:64649553-64650322	K562	blood:	n/a	n/a
14	CCNT2	chr13:64649960-64650241	K562	blood:	n/a	n/a
15	CEBPB	chr13:64562560-64562797	HepG2	liver:	n/a	chr13:64562678-64562689 chr13:64562678-64562691
16	CEBPB	chr13:64704806-64705056	H1-hESC	embryonic stem cell:	n/a	chr13:64704897-64704908
17	CEBPB	chr13:64590178-64590414	K562	blood:	n/a	n/a
18	CEBPB	chr13:64675653-64675957	A549	lung:	n/a	chr13:64675800-64675813 chr13:64675800-64675813 chr13:64675802-64675811 chr13:64675802-64675811 chr13:64675800-64675813 chr13:64675802-64675811 chr13:64675802-64675811 chr13:64675802-64675813 chr13:64675800-64675811
19	CEBPB	chr13:64645645-64645840	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr13:64675622-64675994	IMR90	lung:	n/a	chr13:64675800-64675813 chr13:64675800-64675813 chr13:64675802-64675811 chr13:64675802-64675811 chr13:64675800-64675813 chr13:64675802-64675811 chr13:64675802-64675811 chr13:64675802-64675813 chr13:64675800-64675811
21	CEBPB	chr13:64704718-64705094	HepG2	liver:	n/a	chr13:64704897-64704908
22	CEBPB	chr13:64704853-64704978	K562	blood:	n/a	chr13:64704897-64704908
23	CEBPB	chr13:64646320-64646576	A549	lung:	n/a	chr13:64646454-64646467 chr13:64646455-64646466
24	CEBPB	chr13:64550843-64551208	HepG2	liver:	n/a	chr13:64551014-64551025 chr13:64551013-64551026
25	CEBPB	chr13:64675628-64675976	HepG2	liver:	n/a	chr13:64675800-64675813 chr13:64675800-64675813 chr13:64675802-64675811 chr13:64675802-64675811 chr13:64675800-64675813 chr13:64675802-64675811 chr13:64675802-64675811 chr13:64675802-64675813 chr13:64675800-64675811
26	CEBPB	chr13:64574784-64575086	HepG2	liver:	n/a	chr13:64574932-64574943
27	CEBPB	chr13:64631631-64631969	HepG2	liver:	n/a	chr13:64631808-64631819 chr13:64631809-64631820 chr13:64631808-64631821
28	CEBPB	chr13:64675737-64675975	H1-hESC	embryonic stem cell:	n/a	chr13:64675800-64675813 chr13:64675800-64675813 chr13:64675802-64675811 chr13:64675802-64675811 chr13:64675800-64675813 chr13:64675802-64675811 chr13:64675802-64675811 chr13:64675802-64675813 chr13:64675800-64675811
29	CEBPB	chr13:64645492-64645866	K562	blood:	n/a	n/a
30	CEBPB	chr13:64574892-64574972	H1-hESC	embryonic stem cell:	n/a	chr13:64574932-64574943
31	CEBPB	chr13:64631661-64631931	K562	blood:	n/a	chr13:64631808-64631819 chr13:64631809-64631820 chr13:64631808-64631821
32	CEBPB	chr13:64645538-64645794	HepG2	liver:	n/a	n/a
33	CEBPB	chr13:64550954-64551166	K562	blood:	n/a	chr13:64551014-64551025 chr13:64551013-64551026
34	CEBPB	chr13:64646287-64646619	HepG2	liver:	n/a	chr13:64646454-64646467 chr13:64646455-64646466
35	CEBPB	chr13:64704763-64705044	IMR90	lung:	n/a	chr13:64704897-64704908
36	CEBPB	chr13:64675687-64675952	K562	blood:	n/a	chr13:64675800-64675813 chr13:64675800-64675813 chr13:64675802-64675811 chr13:64675802-64675811 chr13:64675800-64675813 chr13:64675802-64675811 chr13:64675802-64675811 chr13:64675802-64675813 chr13:64675800-64675811
37	CEBPB	chr13:64631725-64631858	HepG2	liver:	n/a	chr13:64631808-64631819 chr13:64631809-64631820 chr13:64631808-64631821
38	CEBPB	chr13:64704673-64705102	HepG2	liver:	n/a	chr13:64704897-64704908
39	CEBPB	chr13:64646318-64646667	K562	blood:	n/a	chr13:64646454-64646467 chr13:64646617-64646630 chr13:64646455-64646466
40	CEBPB	chr13:64702066-64702266	HepG2	liver:	n/a	n/a
41	CEBPD	chr13:64626677-64626975	K562	blood:	n/a	n/a
42	CHD1	chr13:64665118-64665232	GM12878	blood:	n/a	n/a
43	CHD2	chr13:64649566-64650350	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr13:64652263-64652599	HepG2	liver:	n/a	n/a
45	CHD2	chr13:64649689-64650297	HepG2	liver:	n/a	n/a
46	CHD2	chr13:64649133-64649288	HepG2	liver:	n/a	n/a
47	CHD2	chr13:64630471-64630608	GM12878	blood:	n/a	n/a
48	CHD2	chr13:64649076-64649336	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr13:64649204-64649244	GM12878	blood:	n/a	n/a
50	CHD2	chr13:64649881-64650338	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:64650215-64650265	PFSK-1	brain:	n/a
2	chr13:64650183-64650233	AG09319	gingival:	n/a
3	chr13:64651269-64651319	AoSMC	blood vessel:	n/a
4	chr13:64651269-64651319	AG04449	skin:	fetal
5	chr13:64650215-64650265	HCF	heart:	n/a
6	chr13:64650183-64650233	NB4	blood:	n/a
7	chr13:64650183-64650233	HNPCEpiC	eye:	n/a
8	chr13:64650215-64650265	PrEC	prostate:	n/a
9	chr13:64650188-64650238	NT2-D1	testis:	n/a
10	chr13:64650183-64650233	NHDF-neo	bronchial:	n/a
11	chr13:64650215-64650265	GM12891	blood:	n/a
12	chr13:64650183-64650233	HMEC	breast:	n/a
13	chr13:64651269-64651319	GM06990	blood:	n/a
14	chr13:64650183-64650233	IMR90	lung:	fetal
15	chr13:64650183-64650233	A549	lung:	n/a
16	chr13:64651269-64651319	SKMC	muscle:	n/a
17	chr13:64650188-64650238	HRE	kidney:	n/a
18	chr13:64650188-64650238	PFSK-1	brain:	n/a
19	chr13:64650183-64650233	AoSMC	blood vessel:	n/a
20	chr13:64650188-64650238	Jurkat	blood:	n/a
21	chr13:64650188-64650238	SAEC	small airway:	n/a
22	chr13:64651269-64651319	GM12892	blood:	n/a
23	chr13:64650183-64650233	BJ	skin:	n/a
24	chr13:64650188-64650238	ProgFib	skin:	n/a
25	chr13:64650188-64650238	HepG2	liver:	n/a
26	chr13:64651269-64651319	T-47D	breast:	n/a
27	chr13:64650215-64650265	K562	blood:	n/a
28	chr13:64651269-64651319	HEK293	kidney:	embryo
29	chr13:64651269-64651319	HCF	heart:	n/a
30	chr13:64650183-64650233	HCM	heart:	n/a
31	chr13:64650215-64650265	HRCEpiC	kidney:	n/a
32	chr13:64651269-64651319	ECC-1	luminal epithelium:	n/a
33	chr13:64650215-64650265	GM12878	blood:	n/a
34	chr13:64651269-64651319	Jurkat	blood:	n/a
35	chr13:64651269-64651319	AG04450	lung:	fetal
36	chr13:64650188-64650238	GM12878	blood:	n/a
37	chr13:64650188-64650238	GM06990	blood:	n/a
38	chr13:64651269-64651319	NHDF-neo	bronchial:	n/a
39	chr13:64650215-64650265	BJ	skin:	n/a
40	chr13:64650188-64650238	H1-hESC	embryonic stem cell:	embryo
41	chr13:64650215-64650265	H1-hESC	embryonic stem cell:	embryo
42	chr13:64650183-64650233	HL-60	blood:	n/a
43	chr13:64650215-64650265	NT2-D1	testis:	n/a
44	chr13:64650188-64650238	HCT-116	colon:	n/a
45	chr13:64650188-64650238	GM19239	blood:	n/a
46	chr13:64651269-64651319	AG09309	skin:	n/a
47	chr13:64650183-64650233	AG09309	skin:	n/a
48	chr13:64651269-64651319	SAEC	small airway:	n/a
49	chr13:64650188-64650238	HCF	heart:	n/a
50	chr13:64651269-64651319	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:64663876..64666807-chr13:64668849..64670966,2	MCF-7	breast:
2	chr13:64569387..64571962-chr13:64582187..64583914,2	MCF-7	breast:
3	chr13:64663876..64666807-chr13:64668849..64670966,2	MCF-7	breast:
4	chr13:64553735..64556887-chr13:64557043..64560591,3	K562	blood:
5	chr13:64597503..64599019-chr13:64609269..64611005,2	K562	blood:
6	chr13:64570537..64572050-chr13:64574035..64576915,2	K562	blood:
7	chr13:64573569..64576340-chr13:64627433..64629862,2	K562	blood:
8	chr13:64637404..64639561-chr13:64642021..64643825,2	K562	blood:
9	chr13:64632651..64634373-chr13:64649799..64652213,2	K562	blood:
10	chr13:64600090..64601609-chr13:64604264..64606760,2	K562	blood:
11	chr13:64629925..64632065-chr13:64645172..64647089,2	K562	blood:
12	chr13:64642973..64645650-chr13:64650232..64651765,2	K562	blood:
13	chr13:64637718..64641008-chr13:64648657..64651427,4	K562	blood:
14	chr13:64642482..64644473-chr13:64648903..64651732,2	K562	blood:
15	chr13:64645390..64648132-chr13:64648675..64650217,2	K562	blood:
16	chr13:64652193..64655150-chr13:64666356..64668232,2	K562	blood:
17	chr13:64569387..64571962-chr13:64582187..64583914,2	MCF-7	breast:
18	chr13:64648914..64651680-chr13:64658514..64661246,2	K562	blood:
19	chr13:64587782..64590313-chr13:64593691..64596528,2	MCF-7	breast:
20	chr13:64611241..64613586-chr13:64615130..64617717,2	K562	blood:
21	chr13:64652193..64655150-chr13:64666356..64668232,2	K562	blood:
22	chr13:64611241..64613586-chr13:64615130..64617717,2	K562	blood:
23	chr13:64629925..64632065-chr13:64645172..64647089,2	K562	blood:
24	chr13:64589018..64592206-chr13:64593132..64595974,4	K562	blood:
25	chr13:64570537..64572050-chr13:64574035..64576915,2	K562	blood:
26	chr13:64625157..64626688-chr13:64631104..64632843,2	K562	blood:
27	chr13:64597503..64599019-chr13:64609269..64611005,2	K562	blood:
28	chr13:64651720..64653220-chr20:35806448..35807989,2	K562	blood:
29	chr13:64553735..64556887-chr13:64557043..64560591,3	K562	blood:
30	chr13:64573569..64576340-chr13:64627433..64629862,2	K562	blood:
31	chr13:64642973..64645650-chr13:64650232..64651765,2	K562	blood:
32	chr13:64625157..64626688-chr13:64631104..64632843,2	K562	blood:
33	chr13:64587782..64590313-chr13:64593691..64596528,2	MCF-7	breast:
34	chr13:64589018..64592206-chr13:64593132..64595974,4	K562	blood:
35	chr13:64580543..64583349-chr13:64585770..64588004,2	MCF-7	breast:
36	chr13:64580543..64583349-chr13:64585770..64588004,2	MCF-7	breast:
37	chr13:64637404..64639561-chr13:64642021..64643825,2	K562	blood:
38	chr13:64650229..64650817-chr15:52311651..52312545,2	Hela-S3	cervix:
39	chr13:64600090..64601609-chr13:64604264..64606760,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH9-4	chr13:64608480-64608670	NONHSAT034190
2	lnc-PCDH9-13	chr13:64549584-64550555	NONHSAT034188
3	lnc-PCDH9-4	chr13:64577481-64577601	NONHSAT034190
4	lnc-PCDH9-4	chr13:64576518-64576542	NONHSAT034190
5	lnc-PCDH9-4	chr13:64564229-64564333	NONHSAT034190

Variant related genes	Relation type
LINC00355	TF binding region
NFYAP1	TF binding region
LINC00355	CpG island
NFYAP1	CpG island
ENSG00000069956	chromatin interactions
ENSG00000118705	chromatin interactions
ENSG00000101353	chromatin interactions
ENSG00000227674	chromatin interactions

Extended variants
information (count: 2405 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:2405 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2875355	chr13:64549597-64549598	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs141768677	chr13:64549665-64549666	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs563761679	chr13:64549671-64549672	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs534048817	chr13:64549675-64549676	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs376242016	chr13:64549704-64549705	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs550118284	chr13:64549708-64549709	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs9592308	chr13:64549719-64549720	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs549519102	chr13:64549721-64549722	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs12872970	chr13:64549727-64549728	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs532508241	chr13:64549744-64549745	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs79521663	chr13:64549750-64549751	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs369116756	chr13:64549752-64549753	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs373153357	chr13:64549753-64549754	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs561217963	chr13:64549766-64549767	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs528506395	chr13:64549767-64549768	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs570197384	chr13:64549778-64549779	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs571517362	chr13:64549809-64549810	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs182378224	chr13:64549836-64549837	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs560880761	chr13:64549868-64549869	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs528294352	chr13:64549870-64549871	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs539158147	chr13:64549934-64549935	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs9598678	chr13:64549942-64549943	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs535916671	chr13:64549944-64549945	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs554251753	chr13:64549981-64549982	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs186651922	chr13:64550028-64550029	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs533779782	chr13:64550032-64550033	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs558296048	chr13:64550033-64550034	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs34525356	chr13:64550085-64550086	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs112816867	chr13:64550089-64550090	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs35828123	chr13:64550090-64550091	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs190269856	chr13:64550125-64550126	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs12584886	chr13:64550127-64550128	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs377222836	chr13:64550128-64550129	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs41382744	chr13:64550160-64550161	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs182498582	chr13:64550175-64550176	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs561360476	chr13:64550227-64550228	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs552403999	chr13:64550289-64550290	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs528627425	chr13:64550291-64550292	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs556836790	chr13:64550295-64550296	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs546953120	chr13:64550300-64550301	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs188835719	chr13:64550330-64550331	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs565170837	chr13:64550332-64550333	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs532402196	chr13:64550375-64550376	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs112204869	chr13:64550396-64550397	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs192882766	chr13:64550466-64550467	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs185817765	chr13:64550468-64550469	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs537307977	chr13:64550502-64550503	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs537697338	chr13:64550528-64550529	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs548027811	chr13:64550548-64550549	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs566208398	chr13:64550549-64550550	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:64550000-64550800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr13:64551800-64552000	Enhancers	HUVEC	blood vessel
3	chr13:64552000-64553400	Weak transcription	HUVEC	blood vessel
4	chr13:64553400-64558400	Enhancers	HUVEC	blood vessel
5	chr13:64554000-64554800	Enhancers	HepG2	liver
6	chr13:64569600-64571200	Enhancers	Fetal Lung	lung
7	chr13:64574200-64574800	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr13:64574800-64575200	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr13:64594600-64595200	Enhancers	Fetal Stomach	stomach
10	chr13:64594800-64595200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr13:64608200-64608600	Enhancers	Fetal Lung	lung
12	chr13:64608200-64608800	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr13:64608400-64608800	ZNF genes & repeats	Pancreas	Pancrea
14	chr13:64615400-64615800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr13:64621400-64622000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr13:64623400-64624000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr13:64624000-64624400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr13:64626600-64628800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr13:64626800-64627000	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr13:64627000-64627200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
21	chr13:64627200-64627400	Active TSS	Primary hematopoietic stem cells short term culture	blood
22	chr13:64627400-64627600	Enhancers	K562	blood
23	chr13:64627400-64627800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
24	chr13:64627600-64631400	Weak transcription	K562	blood
25	chr13:64627800-64629800	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr13:64627800-64630200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr13:64629800-64630000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
28	chr13:64630000-64630200	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr13:64630200-64630400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
30	chr13:64630400-64630600	Active TSS	Primary hematopoietic stem cells short term culture	blood
31	chr13:64630600-64631400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr13:64631400-64631800	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr13:64631400-64632000	Enhancers	HepG2	liver
34	chr13:64631400-64632800	Enhancers	K562	blood
35	chr13:64632000-64646200	Weak transcription	HepG2	liver
36	chr13:64634600-64635200	Enhancers	Brain Germinal Matrix	brain
37	chr13:64635800-64636200	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr13:64636200-64640600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr13:64640600-64641000	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr13:64640600-64642200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr13:64640800-64642000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr13:64641200-64641600	Enhancers	Primary hematopoietic stem cells	blood
43	chr13:64644800-64645200	Enhancers	K562	blood
44	chr13:64645200-64645400	Weak transcription	K562	blood
45	chr13:64645400-64645800	Enhancers	K562	blood
46	chr13:64645800-64646200	Weak transcription	K562	blood
47	chr13:64646200-64647400	Enhancers	HepG2	liver
48	chr13:64646200-64651400	Active TSS	K562	blood
49	chr13:64647400-64649000	Active TSS	HepG2	liver
50	chr13:64648200-64654200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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