Variant report

Variant	esv1802816
Chromosome Location	chr10:94232247-94294291
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	chr10:94246287-94246781	K562	blood:	n/a	n/a
2	ATF1	chr10:94246394-94246825	K562	blood:	n/a	n/a
3	BACH1	chr10:94268655-94268681	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr10:94276758-94277135	GM12878	blood:	n/a	chr10:94276906-94276915
5	BRCA1	chr10:94232207-94232470	Hela-S3	cervix:	n/a	chr10:94232389-94232396
6	CBX3	chr10:94246363-94246814	K562	blood:	n/a	n/a
7	CCNT2	chr10:94246422-94246680	K562	blood:	n/a	n/a
8	CEBPB	chr10:94252709-94253020	K562	blood:	n/a	n/a
9	CEBPB	chr10:94252709-94253032	IMR90	lung:	n/a	n/a
10	CEBPB	chr10:94232190-94232430	A549	lung:	n/a	n/a
11	CEBPB	chr10:94232119-94232515	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr10:94252698-94253023	A549	lung:	n/a	n/a
13	CEBPB	chr10:94261281-94261479	IMR90	lung:	n/a	n/a
14	CEBPB	chr10:94252717-94252977	HepG2	liver:	n/a	n/a
15	CEBPB	chr10:94238411-94238555	A549	lung:	n/a	n/a
16	CEBPB	chr10:94232201-94232464	HepG2	liver:	n/a	n/a
17	CEBPB	chr10:94246514-94246765	K562	blood:	n/a	chr10:94246674-94246686
18	CEBPB	chr10:94252727-94252973	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr10:94276880-94277030	AG09319	gingival:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
20	CTCF	chr10:94276880-94277030	MCF-7	breast:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
21	CTCF	chr10:94276865-94277055	GM19240	blood:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
22	CTCF	chr10:94246480-94246630	HVMF	connective:	n/a	n/a
23	CTCF	chr10:94276920-94277070	Hela-S3	cervix:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
24	CTCF	chr10:94246540-94246690	HFF	foreskin:	n/a	n/a
25	CTCF	chr10:94277229-94277273	GM12892	blood:	n/a	n/a
26	CTCF	chr10:94276900-94277050	HRE	kidney:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
27	CTCF	chr10:94276880-94277030	Caco-2	colon:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
28	CTCF	chr10:94276900-94277050	GM12872	blood:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
29	CTCF	chr10:94276840-94276990	BE2_C	brain:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
30	CTCF	chr10:94276880-94277030	HA-sp	spinal cord:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
31	CTCF	chr10:94276880-94277030	A549	lung:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
32	CTCF	chr10:94276860-94277010	AoAF	blood vessel:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
33	CTCF	chr10:94276880-94277030	GM12868	blood:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
34	CTCF	chr10:94276860-94277010	GM12864	blood:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
35	CTCF	chr10:94275943-94276014	Medullo	brain:	n/a	n/a
36	CTCF	chr10:94276900-94277050	Caco-2	colon:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
37	CTCF	chr10:94276846-94277164	HCT-116	colon:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
38	CTCF	chr10:94276900-94277050	AG09309	skin:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
39	CTCF	chr10:94290280-94290430	AG04449	skin:	n/a	n/a
40	CTCF	chr10:94276900-94277050	GM12866	blood:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
41	CTCF	chr10:94276880-94277030	RPTEC	kidney:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
42	CTCF	chr10:94276692-94277205	IMR90	lung:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
43	CTCF	chr10:94276860-94277010	HFF	foreskin:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
44	CTCF	chr10:94276841-94277096	K562	blood:	n/a	chr10:94276949-94276959 chr10:94276947-94276960 chr10:94276944-94276962 chr10:94276946-94276967 chr10:94276947-94276960 chr10:94276945-94276961
45	CTCF	chr10:94276840-94276990	GM06990	blood:	n/a	chr10:94276949-94276959 chr10:94276947-94276960 chr10:94276944-94276962 chr10:94276946-94276967 chr10:94276947-94276960 chr10:94276945-94276961
46	CTCF	chr10:94276900-94277050	GM12875	blood:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
47	CTCF	chr10:94276900-94277050	GM12874	blood:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
48	CTCF	chr10:94276740-94276890	WI-38	lung:	n/a	n/a
49	CTCF	chr10:94276840-94276990	HVMF	connective:	n/a	chr10:94276944-94276962 chr10:94276947-94276960 chr10:94276947-94276960 chr10:94276945-94276961 chr10:94276949-94276959 chr10:94276946-94276967
50	CTCF	chr10:94276960-94277110	WI-38	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:94250311-94250361	CMK	blood:	n/a
2	chr10:94250865-94250915	H1-hESC	embryonic stem cell:	embryo
3	chr10:94250311-94250361	HUVEC	blood vessel:	n/a
4	chr10:94250865-94250915	SK-N-MC	brain:	n/a
5	chr10:94250311-94250361	SK-N-MC	brain:	n/a
6	chr10:94250865-94250915	GM12878	blood:	n/a
7	chr10:94250865-94250915	ovcar-3	ovarian:	n/a
8	chr10:94250865-94250915	Hepatocyte	liver:	n/a
9	chr10:94250865-94250915	RPTEC	kidney:	n/a
10	chr10:94250311-94250361	Hela-S3	cervix:	n/a
11	chr10:94250311-94250361	MCF-7	breast:	n/a
12	chr10:94250311-94250361	HIPEpiC	eye:	n/a
13	chr10:94250311-94250361	PrEC	prostate:	n/a
14	chr10:94250865-94250915	AG04450	lung:	fetal
15	chr10:94250311-94250361	BE2_C	brain:	n/a
16	chr10:94250865-94250915	AoSMC	blood vessel:	n/a
17	chr10:94250311-94250361	HEEpiC	esophagus:	n/a
18	chr10:94250865-94250915	PrEC	prostate:	n/a
19	chr10:94250311-94250361	A549	lung:	n/a
20	chr10:94250311-94250361	HAEpiC	amniotic membrane:	n/a
21	chr10:94250865-94250915	T-47D	breast:	n/a
22	chr10:94250865-94250915	ProgFib	skin:	n/a
23	chr10:94250865-94250915	K562	blood:	n/a
24	chr10:94250865-94250915	NH-A	brain:	n/a
25	chr10:94250865-94250915	SKMC	muscle:	n/a
26	chr10:94250311-94250361	HCM	heart:	n/a
27	chr10:94250865-94250915	ECC-1	luminal epithelium:	n/a
28	chr10:94250311-94250361	NT2-D1	testis:	n/a
29	chr10:94250311-94250361	PFSK-1	brain:	n/a
30	chr10:94250865-94250915	GM12892	blood:	n/a
31	chr10:94250311-94250361	HRCEpiC	kidney:	n/a
32	chr10:94250865-94250915	BJ	skin:	n/a
33	chr10:94250311-94250361	NHBE	bronchial:	n/a
34	chr10:94250311-94250361	NB4	blood:	n/a
35	chr10:94250311-94250361	HCT-116	colon:	n/a
36	chr10:94250311-94250361	AG04450	lung:	fetal
37	chr10:94250311-94250361	RPTEC	kidney:	n/a
38	chr10:94250311-94250361	IMR90	lung:	fetal
39	chr10:94250311-94250361	SAEC	small airway:	n/a
40	chr10:94250311-94250361	HNPCEpiC	eye:	n/a
41	chr10:94250311-94250361	K562	blood:	n/a
42	chr10:94250865-94250915	HCF	heart:	n/a
43	chr10:94250865-94250915	LNCaP	prostate:	n/a
44	chr10:94250865-94250915	U87	brain:	n/a
45	chr10:94250865-94250915	Jurkat	blood:	n/a
46	chr10:94250311-94250361	HMEC	breast:	n/a
47	chr10:94250865-94250915	HNPCEpiC	eye:	n/a
48	chr10:94250311-94250361	SK-N-SH	brain:	n/a
49	chr10:94250311-94250361	MCF10A-Er-Src	breast:	n/a
50	chr10:94250311-94250361	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:94286791..94289447-chr10:94291789..94294504,3	K562	blood:
2	chr10:94231625..94235383-chr10:94350163..94352674,3	MCF-7	breast:
3	chr10:94286303..94289350-chr10:94289651..94292347,3	MCF-7	breast:
4	chr10:94274982..94277833-chr10:94333468..94335279,2	K562	blood:
5	chr10:94268762..94273996-chr10:94332420..94336141,6	MCF-7	breast:
6	chr10:94276477..94277687-chr10:94333813..94334950,12	MCF-7	breast:
7	chr10:94286303..94289350-chr10:94289651..94292347,3	MCF-7	breast:
8	chr10:94289161..94292138-chr10:94332581..94334284,2	MCF-7	breast:
9	chr10:94276434..94277468-chr10:94333831..94335118,8	K562	blood:
10	chr10:94286301..94289329-chr10:94351494..94353935,3	MCF-7	breast:
11	chr10:94290717..94292368-chr10:94351080..94353916,2	K562	blood:
12	chr10:94251458..94254176-chr10:94257823..94260134,2	MCF-7	breast:
13	chr10:94271122..94273311-chr10:94351140..94352702,2	MCF-7	breast:
14	chr10:94255617..94258093-chr10:94258100..94259635,2	MCF-7	breast:
15	chr10:94276451..94277382-chr10:94333873..94334623,6	MCF-7	breast:
16	chr10:94265816..94268647-chr10:94273130..94275681,2	K562	blood:
17	chr10:94252651..94255097-chr10:94255766..94258601,2	K562	blood:
18	chr10:94266903..94270472-chr10:94333012..94335202,3	K562	blood:
19	chr10:94265816..94268647-chr10:94273130..94275681,2	K562	blood:
20	chr10:94263991..94266958-chr10:94266997..94268631,2	MCF-7	breast:
21	chr10:94276542..94277057-chr15:77040784..77041284,2	MCF-7	breast:
22	chr10:94276555..94279204-chr10:94332379..94335098,3	MCF-7	breast:
23	chr10:94256381..94258076-chr10:94263936..94266038,2	MCF-7	breast:
24	chr10:94280636..94284278-chr10:94349670..94353388,3	K562	blood:
25	chr10:94239126..94239929-chr5:64858485..64859436,2	Hela-S3	cervix:
26	chr10:94276559..94277094-chr8:110249687..110250189,3	MCF-7	breast:
27	chr10:94251458..94254176-chr10:94257823..94260134,2	MCF-7	breast:
28	chr10:94263991..94266958-chr10:94266997..94268631,2	MCF-7	breast:
29	chr10:94286791..94289447-chr10:94291789..94294504,3	K562	blood:
30	chr10:94276333..94278626-chr10:94332355..94335279,2	K562	blood:
31	chr10:94274603..94278962-chr10:94330841..94335301,9	MCF-7	breast:

Variant related genes	Relation type
IDE	TF binding region
IDE	CpG island
ENSG00000138160	chromatin interactions
ENSG00000113593	chromatin interactions
ENSG00000123219	chromatin interactions
ENSG00000119912	chromatin interactions

Extended variants
information (count: 2277 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2277 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2149632	chr10:94232247-94232248	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs190909863	chr10:94232260-94232261	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs74479757	chr10:94232308-94232309	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs55968843	chr10:94232311-94232312	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs369609227	chr10:94232340-94232341	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs113179017	chr10:94232349-94232350	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs369457725	chr10:94232399-94232400	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568422949	chr10:94232400-94232401	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs35959170	chr10:94232418-94232419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188069837	chr10:94232420-94232421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs193018477	chr10:94232437-94232438	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568293737	chr10:94232464-94232465	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537249328	chr10:94232465-94232466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs377006965	chr10:94232499-94232500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184568420	chr10:94232583-94232584	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187663543	chr10:94232615-94232616	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576636529	chr10:94232635-94232636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531491786	chr10:94232636-94232637	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550595772	chr10:94232639-94232640	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369766027	chr10:94232661-94232662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535455118	chr10:94232699-94232700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376548262	chr10:94232744-94232745	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552673793	chr10:94232785-94232786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572472945	chr10:94232835-94232836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541497395	chr10:94232862-94232863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs35551274	chr10:94232880-94232881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs7087153	chr10:94232901-94232902	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs531147246	chr10:94232920-94232921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544895319	chr10:94232923-94232924	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564620326	chr10:94232938-94232939	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192516024	chr10:94232982-94232983	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185032166	chr10:94232983-94232984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12762802	chr10:94232984-94232985	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs371726393	chr10:94233018-94233019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567003748	chr10:94233030-94233031	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530243667	chr10:94233046-94233047	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189399922	chr10:94233050-94233051	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12763971	chr10:94233058-94233059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs376146451	chr10:94233079-94233080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568335345	chr10:94233089-94233090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs11187017	chr10:94233105-94233106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570070683	chr10:94233112-94233113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2249960	chr10:94233120-94233121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150243582	chr10:94233156-94233157	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs72809182	chr10:94233183-94233184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552839357	chr10:94233227-94233228	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12262931	chr10:94233295-94233296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs61875363	chr10:94233380-94233381	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539267455	chr10:94233382-94233383	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552636835	chr10:94233454-94233455	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Sezary syndrome	18413736	CNVD
Intracranial aneurysm	16715129	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1639 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:94208400-94276800	Weak transcription	Stomach Mucosa	stomach
2	chr10:94209800-94234400	Weak transcription	Fetal Heart	heart
3	chr10:94210000-94243000	Weak transcription	Fetal Brain Female	brain
4	chr10:94210400-94235600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr10:94210400-94239200	Weak transcription	Fetal Brain Male	brain
6	chr10:94210600-94250000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr10:94211000-94235600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr10:94211400-94235600	Strong transcription	Primary T helper cells fromperipheralblood	blood
9	chr10:94211400-94235800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr10:94211400-94253200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr10:94212000-94232400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr10:94212400-94233800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr10:94212800-94270400	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr10:94214400-94234200	Strong transcription	Fetal Stomach	stomach
15	chr10:94217200-94232400	Weak transcription	Small Intestine	intestine
16	chr10:94217400-94251800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr10:94217600-94270200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr10:94217800-94245600	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr10:94218000-94245400	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr10:94218200-94251800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr10:94218400-94237800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr10:94222600-94243200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr10:94222800-94250800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr10:94223200-94252600	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr10:94224600-94238800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr10:94225400-94248800	Weak transcription	Brain Germinal Matrix	brain
27	chr10:94225600-94238600	Weak transcription	NHEK	skin
28	chr10:94225600-94248400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr10:94225600-94252600	Weak transcription	Fetal Kidney	kidney
30	chr10:94225800-94239000	Weak transcription	Right Ventricle	heart
31	chr10:94225800-94239200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr10:94226000-94245000	Weak transcription	K562	blood
33	chr10:94226200-94234200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr10:94227400-94251200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr10:94227800-94243000	Weak transcription	Colonic Mucosa	Colon
36	chr10:94228000-94242800	Weak transcription	NHDF-Ad	bronchial
37	chr10:94228800-94238400	Weak transcription	Brain Cingulate Gyrus	brain
38	chr10:94229000-94235000	Weak transcription	HSMMtube	muscle
39	chr10:94229200-94238000	Weak transcription	Osteobl	bone
40	chr10:94229200-94246400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr10:94229600-94233400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr10:94229800-94238400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr10:94230000-94233000	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr10:94230000-94233200	Weak transcription	HMEC	breast
45	chr10:94230000-94233400	Weak transcription	Fetal Intestine Large	intestine
46	chr10:94230000-94233800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr10:94230000-94233800	Weak transcription	Thymus	Thymus
48	chr10:94230000-94234000	Weak transcription	Fetal Muscle Trunk	muscle
49	chr10:94230000-94235000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr10:94230000-94235000	Weak transcription	Colon Smooth Muscle	Colon

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