Variant report

Variant	nsv895090
Chromosome Location	chr10:44874867-44884959
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	chr10:44882107-44882307	HepG2	liver:	n/a	n/a
2	ATF3	chr10:44882112-44882269	K562	blood:	n/a	n/a
3	BACH1	chr10:44879399-44880089	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr10:44881774-44881807	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr10:44882052-44882506	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr10:44880796-44881429	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr10:44881995-44882274	GM12878	blood:	n/a	n/a
8	BHLHE40	chr10:44882094-44882278	K562	blood:	n/a	chr10:44882150-44882166
9	BRCA1	chr10:44882054-44882214	HepG2	liver:	n/a	n/a
10	CCNT2	chr10:44882111-44882345	K562	blood:	n/a	n/a
11	CEBPB	chr10:44882112-44882349	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr10:44882105-44882260	HepG2	liver:	n/a	n/a
13	CEBPB	chr10:44882134-44882409	K562	blood:	n/a	n/a
14	CEBPB	chr10:44876183-44876222	HepG2	liver:	n/a	n/a
15	CEBPB	chr10:44882081-44882254	HepG2	liver:	n/a	n/a
16	CHD2	chr10:44882077-44882239	HepG2	liver:	n/a	n/a
17	CREB1	chr10:44879975-44880721	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTBP2	chr10:44877649-44880413	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTBP2	chr10:44882086-44882642	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr10:44881749-44882554	GM12878	blood:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
21	CTCF	chr10:44882009-44882345	H1-hESC	embryonic stem cell:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
22	CTCF	chr10:44882449-44882537	GM10248	blood:	n/a	n/a
23	CTCF	chr10:44882140-44882290	AG09319	gingival:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
24	CTCF	chr10:44882121-44882271	Hela-S3	cervix:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
25	CTCF	chr10:44882120-44882270	GM12864	blood:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
26	CTCF	chr10:44882006-44882349	K562	blood:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
27	CTCF	chr10:44882120-44882270	HAc	cerebellar:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
28	CTCF	chr10:44882140-44882290	HEEpiC	esophagus:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
29	CTCF	chr10:44882050-44882367	MCF-7	breast:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
30	CTCF	chr10:44882120-44882270	NHDF-neo	bronchial:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
31	CTCF	chr10:44882360-44882510	Caco-2	colon:	n/a	n/a
32	CTCF	chr10:44882140-44882290	AoAF	blood vessel:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
33	CTCF	chr10:44882080-44882230	AG04450	lung:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
34	CTCF	chr10:44881720-44881870	AG04449	skin:	n/a	n/a
35	CTCF	chr10:44882100-44882250	GM12866	blood:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
36	CTCF	chr10:44882120-44882270	AG10803	skin:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
37	CTCF	chr10:44882140-44882290	BJ	skin:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
38	CTCF	chr10:44879740-44879890	BJ	skin:	n/a	n/a
39	CTCF	chr10:44882041-44882461	MCF-7	breast:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
40	CTCF	chr10:44882058-44882313	ProgFib	skin:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
41	CTCF	chr10:44882140-44882290	GM12878	blood:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
42	CTCF	chr10:44882120-44882270	GM12878	blood:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
43	CTCF	chr10:44882463-44882539	GM19240	blood:	n/a	n/a
44	CTCF	chr10:44882080-44882230	NHLF	lung:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
45	CTCF	chr10:44882100-44882250	HEK293	kidney:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
46	CTCF	chr10:44882140-44882290	NB4	blood:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
47	CTCF	chr10:44881937-44882374	HepG2	liver:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
48	CTCF	chr10:44882080-44882230	WERI-Rb-1	eye:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
49	CTCF	chr10:44882423-44882541	GM10266	blood:	n/a	n/a
50	CTCF	chr10:44882040-44882326	Pancreas_OC	pancreas:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:44880730-44880780	CMK	blood:	n/a
2	chr10:44880730-44880780	CMK	blood:	n/a
3	chr10:44880730-44880780	PFSK-1	brain:	n/a
4	chr10:44880562-44880612	GM06990	blood:	n/a
5	chr10:44880542-44880592	NT2-D1	testis:	n/a
6	chr10:44881551-44881601	AG04449	skin:	fetal
7	chr10:44882599-44882649	AG10803	skin:	n/a
8	chr10:44881054-44881104	GM12891	blood:	n/a
9	chr10:44878373-44878423	T-47D	breast:	n/a
10	chr10:44878373-44878423	Hela-S3	cervix:	n/a
11	chr10:44882599-44882649	HepG2	liver:	n/a
12	chr10:44880730-44880780	SAEC	small airway:	n/a
13	chr10:44880559-44880609	HEEpiC	esophagus:	n/a
14	chr10:44876162-44876212	ovcar-3	ovarian:	n/a
15	chr10:44881054-44881104	Caco-2	colon:	n/a
16	chr10:44880128-44880178	SK-N-SH_RA	brain:	n/a
17	chr10:44876292-44876342	IMR90	lung:	fetal
18	chr10:44880819-44880869	ProgFib	skin:	n/a
19	chr10:44878373-44878423	A549	lung:	n/a
20	chr10:44880128-44880178	HPAEpiC	pulmonary alveolar:	n/a
21	chr10:44880545-44880595	HRCEpiC	kidney:	n/a
22	chr10:44882135-44882185	NH-A	brain:	n/a
23	chr10:44880708-44880758	AG04450	lung:	fetal
24	chr10:44880236-44880286	A549	lung:	n/a
25	chr10:44880819-44880869	K562	blood:	n/a
26	chr10:44880819-44880869	GM12892	blood:	n/a
27	chr10:44880819-44880869	HIPEpiC	eye:	n/a
28	chr10:44880708-44880758	HEK293	kidney:	embryo
29	chr10:44876292-44876342	HEEpiC	esophagus:	n/a
30	chr10:44880708-44880758	MCF-7	breast:	n/a
31	chr10:44875989-44876039	BJ	skin:	n/a
32	chr10:44881750-44881800	BJ	skin:	n/a
33	chr10:44880545-44880595	U87	brain:	n/a
34	chr10:44880562-44880612	HNPCEpiC	eye:	n/a
35	chr10:44880559-44880609	ECC-1	luminal epithelium:	n/a
36	chr10:44882135-44882185	SAEC	small airway:	n/a
37	chr10:44879465-44879515	MCF10A-Er-Src	breast:	n/a
38	chr10:44880730-44880780	HCF	heart:	n/a
39	chr10:44880559-44880609	ProgFib	skin:	n/a
40	chr10:44880730-44880780	PANC-1	pancreas:	n/a
41	chr10:44875989-44876039	RPTEC	kidney:	n/a
42	chr10:44881054-44881104	PrEC	prostate:	n/a
43	chr10:44875989-44876039	SK-N-SH	brain:	n/a
44	chr10:44880236-44880286	HCPEpiC	choroid plexus:	n/a
45	chr10:44880128-44880178	HRPEpiC	eye:	n/a
46	chr10:44880730-44880780	AG09319	gingival:	n/a
47	chr10:44880545-44880595	HL-60	blood:	n/a
48	chr10:44875989-44876039	NH-A	brain:	n/a
49	chr10:44878373-44878423	PrEC	prostate:	n/a
50	chr10:44880236-44880286	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:44874626..44876126-chr10:44876143..44877664,2	MCF-7	breast:
2	chr10:44166808..44167608-chr10:44882043..44882606,2	MCF-7	breast:
3	chr10:44779480..44780239-chr10:44881943..44882604,2	K562	blood:
4	chr10:44882608..44885734-chr10:44887032..44891125,3	MCF-7	breast:
5	chr10:44874626..44876126-chr10:44876143..44877664,2	MCF-7	breast:

Variant related genes	Relation type
CXCL12	TF binding region
CXCL12	CpG island

Extended variants
information (count: 412 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2839692	chr10:44874867-44874868	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs369508618	chr10:44874869-44874870	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs543953465	chr10:44874886-44874887	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs1023265	chr10:44874888-44874889	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs574041093	chr10:44874944-44874945	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541310930	chr10:44874955-44874956	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs145564002	chr10:44874956-44874957	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs17885644	chr10:44874980-44874981	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532753950	chr10:44875016-44875017	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs11594377	chr10:44875040-44875041	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs369360866	chr10:44875056-44875057	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563763467	chr10:44875110-44875111	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538985110	chr10:44875138-44875139	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs2839691	chr10:44875144-44875145	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs398054319	chr10:44875149-44875150	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs2839690	chr10:44875166-44875167	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs376965553	chr10:44875187-44875188	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs4948879	chr10:44875205-44875206	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs568255302	chr10:44875212-44875213	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs55649793	chr10:44875229-44875230	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529235605	chr10:44875263-44875264	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs4948880	chr10:44875273-44875274	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs192045813	chr10:44875326-44875327	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376519384	chr10:44875361-44875362	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs371069602	chr10:44875372-44875373	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565699736	chr10:44875416-44875417	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs539382154	chr10:44875444-44875445	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546113700	chr10:44875454-44875455	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs2839689	chr10:44875459-44875460	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs554122247	chr10:44875469-44875470	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183214583	chr10:44875508-44875509	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs186807799	chr10:44875524-44875525	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs17884144	chr10:44875564-44875565	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs143281512	chr10:44875570-44875571	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541347884	chr10:44875596-44875597	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs57081172	chr10:44875620-44875621	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs77003353	chr10:44875635-44875636	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs183128491	chr10:44875646-44875647	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs182544125	chr10:44875718-44875719	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs563531433	chr10:44875721-44875722	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs566074500	chr10:44875731-44875732	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs113088049	chr10:44875775-44875776	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs17883825	chr10:44875839-44875840	Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs186907818	chr10:44875851-44875852	Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs561889952	chr10:44875871-44875872	Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs529068543	chr10:44875876-44875877	Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs2839688	chr10:44875882-44875883	Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs565924328	chr10:44875891-44875892	Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs532791694	chr10:44875943-44875944	Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs559690351	chr10:44875973-44875974	Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
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
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	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
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	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
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:669 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44850600-44877600	Weak transcription	Duodenum Mucosa	Duodenum
2	chr10:44860000-44879000	Weak transcription	Gastric	stomach
3	chr10:44864600-44876200	Weak transcription	Brain Anterior Caudate	brain
4	chr10:44864600-44876800	Strong transcription	Fetal Stomach	stomach
5	chr10:44864800-44877800	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr10:44865400-44876200	Weak transcription	Right Atrium	heart
7	chr10:44865600-44878000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr10:44866000-44876200	Strong transcription	Left Ventricle	heart
9	chr10:44866000-44877600	Weak transcription	Fetal Brain Female	brain
10	chr10:44866200-44876000	Strong transcription	Osteobl	bone
11	chr10:44866400-44875600	Weak transcription	Fetal Brain Male	brain
12	chr10:44866400-44878600	Weak transcription	Liver	Liver
13	chr10:44866600-44876200	Weak transcription	Brain Germinal Matrix	brain
14	chr10:44866600-44877600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr10:44866800-44875600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr10:44867000-44878200	Weak transcription	Brain Hippocampus Middle	brain
17	chr10:44867400-44875200	Strong transcription	Ovary	ovary
18	chr10:44867400-44876000	Strong transcription	Adipose Nuclei	Adipose
19	chr10:44867400-44876400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr10:44867400-44878000	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr10:44867600-44878600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr10:44867800-44875400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
23	chr10:44868000-44875600	Strong transcription	HUES64 Cell Line	embryonic stem cell
24	chr10:44869400-44875800	Genic enhancers	Skeletal Muscle Male	skeletal muscle
25	chr10:44869600-44878200	Weak transcription	Brain Substantia Nigra	brain
26	chr10:44869800-44876000	Strong transcription	H1 Cell Line	embryonic stem cell
27	chr10:44870200-44877600	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr10:44871000-44875000	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr10:44871000-44877600	Weak transcription	Rectal Smooth Muscle	rectum
30	chr10:44871200-44875000	Weak transcription	Colonic Mucosa	Colon
31	chr10:44871400-44875400	Strong transcription	HUES6 Cell Line	embryonic stem cell
32	chr10:44871600-44877000	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr10:44871800-44877000	Weak transcription	Stomach Smooth Muscle	stomach
34	chr10:44872000-44875600	Weak transcription	Colon Smooth Muscle	Colon
35	chr10:44872000-44875800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr10:44872400-44875600	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr10:44872400-44877400	Weak transcription	Fetal Kidney	kidney
38	chr10:44872600-44875200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr10:44873000-44875000	Strong transcription	Fetal Intestine Small	intestine
40	chr10:44873000-44875800	Strong transcription	NHLF	lung
41	chr10:44873200-44875200	Genic enhancers	Fetal Muscle Trunk	muscle
42	chr10:44873200-44875600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr10:44873200-44877600	Weak transcription	Lung	lung
44	chr10:44873400-44875200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
45	chr10:44873400-44875600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
46	chr10:44873400-44876200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr10:44873600-44876400	Strong transcription	NHDF-Ad	bronchial
48	chr10:44873600-44876600	Strong transcription	Fetal Lung	lung
49	chr10:44874200-44875000	Genic enhancers	Pancreas	Pancrea
50	chr10:44874200-44875400	Strong transcription	HUES48 Cell Line	embryonic stem cell

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