Variant report

Variant	nsv895092
Chromosome Location	chr10:44875166-44884959
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	chr10:44880796-44881429	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	chr10:44879399-44880089	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr10:44882052-44882506	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	chr10:44882081-44882254	HepG2	liver:	n/a	n/a
12	CEBPB	chr10:44882112-44882349	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr10:44882134-44882409	K562	blood:	n/a	n/a
14	CEBPB	chr10:44882105-44882260	HepG2	liver:	n/a	n/a
15	CEBPB	chr10:44876183-44876222	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	chr10:44882086-44882642	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTBP2	chr10:44877649-44880413	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr10:44882083-44882285	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
21	CTCF	chr10:44882080-44882230	HVMF	connective:	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	chr10:44882039-44882268	SK-N-SH_RA	brain:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
23	CTCF	chr10:44882140-44882290	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
24	CTCF	chr10:44882079-44882292	GM20000	blood:	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	chr10:44882059-44882327	SK-N-SH_RA	brain:	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	chr10:44882580-44882730	AG04450	lung:	n/a	n/a
27	CTCF	chr10:44882049-44882323	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
28	CTCF	chr10:44882047-44882329	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
29	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
30	CTCF	chr10:44879780-44879879	ProgFib	skin:	n/a	n/a
31	CTCF	chr10:44882100-44882250	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
32	CTCF	chr10:44881999-44882315	ECC-1	luminal epithelium:	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	chr10:44882445-44882447	GM10248	blood:	n/a	n/a
34	CTCF	chr10:44877840-44877990	AG04449	skin:	n/a	n/a
35	CTCF	chr10:44882140-44882290	GM06990	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	chr10:44882140-44882290	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
37	CTCF	chr10:44882056-44882320	Gliobla	brain:	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	chr10:44882100-44882250	GM12865	blood:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
39	CTCF	chr10:44882020-44882170	WI-38	lung:	n/a	n/a
40	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
41	CTCF	chr10:44882140-44882290	BE2_C	brain:	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	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
43	CTCF	chr10:44882051-44882342	Spleen_OC	spleen:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
44	CTCF	chr10:44882120-44882270	GM12873	blood:	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	chr10:44881749-44882554	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
46	CTCF	chr10:44879800-44879950	AG04449	skin:	n/a	n/a
47	CTCF	chr10:44882120-44882270	Caco-2	colon:	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	chr10:44882423-44882541	GM10266	blood:	n/a	n/a
49	CTCF	chr10:44882120-44882270	GM12865	blood:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
50	CTCF	chr10:44882064-44882328	Kidney_OC	kidney:	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	chr10:44878373-44878423	GM12878	blood:	n/a
2	chr10:44878373-44878423	GM12878	blood:	n/a
3	chr10:44880559-44880609	HL-60	blood:	n/a
4	chr10:44882135-44882185	HMEC	breast:	n/a
5	chr10:44880236-44880286	HCPEpiC	choroid plexus:	n/a
6	chr10:44882135-44882185	NT2-D1	testis:	n/a
7	chr10:44881750-44881800	HRE	kidney:	n/a
8	chr10:44882599-44882649	HPAEpiC	pulmonary alveolar:	n/a
9	chr10:44881054-44881104	PFSK-1	brain:	n/a
10	chr10:44880545-44880595	HIPEpiC	eye:	n/a
11	chr10:44880236-44880286	HUVEC	blood vessel:	n/a
12	chr10:44882135-44882185	GM12878	blood:	n/a
13	chr10:44876162-44876212	HCT-116	colon:	n/a
14	chr10:44880730-44880780	A549	lung:	n/a
15	chr10:44880562-44880612	HRPEpiC	eye:	n/a
16	chr10:44880128-44880178	RPTEC	kidney:	n/a
17	chr10:44880128-44880178	Hela-S3	cervix:	n/a
18	chr10:44880559-44880609	K562	blood:	n/a
19	chr10:44879465-44879515	HCF	heart:	n/a
20	chr10:44880236-44880286	HIPEpiC	eye:	n/a
21	chr10:44878373-44878423	HCT-116	colon:	n/a
22	chr10:44878373-44878423	HNPCEpiC	eye:	n/a
23	chr10:44880128-44880178	AG04449	skin:	fetal
24	chr10:44882135-44882185	CMK	blood:	n/a
25	chr10:44878373-44878423	NT2-D1	testis:	n/a
26	chr10:44880730-44880780	AG09319	gingival:	n/a
27	chr10:44880730-44880780	MCF-7	breast:	n/a
28	chr10:44881750-44881800	NH-A	brain:	n/a
29	chr10:44880559-44880609	AG09309	skin:	n/a
30	chr10:44876162-44876212	SK-N-SH	brain:	n/a
31	chr10:44880559-44880609	U87	brain:	n/a
32	chr10:44880559-44880609	H1-hESC	embryonic stem cell:	embryo
33	chr10:44880559-44880609	Jurkat	blood:	n/a
34	chr10:44879465-44879515	Hepatocyte	liver:	n/a
35	chr10:44882135-44882185	GM12891	blood:	n/a
36	chr10:44882340-44882390	HCM	heart:	n/a
37	chr10:44880819-44880869	ovcar-3	ovarian:	n/a
38	chr10:44880730-44880780	HRCEpiC	kidney:	n/a
39	chr10:44876292-44876342	T-47D	breast:	n/a
40	chr10:44876292-44876342	HRPEpiC	eye:	n/a
41	chr10:44880236-44880286	CMK	blood:	n/a
42	chr10:44876162-44876212	U87	brain:	n/a
43	chr10:44880708-44880758	PFSK-1	brain:	n/a
44	chr10:44880730-44880780	AG04449	skin:	fetal
45	chr10:44882135-44882185	HCF	heart:	n/a
46	chr10:44881934-44881984	HRE	kidney:	n/a
47	chr10:44878373-44878423	Hepatocyte	liver:	n/a
48	chr10:44881750-44881800	HRPEpiC	eye:	n/a
49	chr10:44879465-44879515	NT2-D1	testis:	n/a
50	chr10:44882599-44882649	ProgFib	skin:	n/a

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

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

Extended variants
information (count: 397 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:397 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2839690	chr10:44875166-44875167	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs376965553	chr10:44875187-44875188	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs4948879	chr10:44875205-44875206	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs568255302	chr10:44875212-44875213	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs55649793	chr10:44875229-44875230	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529235605	chr10:44875263-44875264	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs4948880	chr10:44875273-44875274	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs192045813	chr10:44875326-44875327	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs376519384	chr10:44875361-44875362	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs371069602	chr10:44875372-44875373	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs565699736	chr10:44875416-44875417	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs539382154	chr10:44875444-44875445	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs546113700	chr10:44875454-44875455	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs2839689	chr10:44875459-44875460	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs554122247	chr10:44875469-44875470	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183214583	chr10:44875508-44875509	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs186807799	chr10:44875524-44875525	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs17884144	chr10:44875564-44875565	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143281512	chr10:44875570-44875571	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs541347884	chr10:44875596-44875597	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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
31	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
32	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
33	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
34	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
35	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
36	rs551403073	chr10:44875978-44875979	Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs193171525	chr10:44876003-44876004	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs141494178	chr10:44876019-44876020	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs373669617	chr10:44876061-44876062	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs74960776	chr10:44876092-44876093	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs534850377	chr10:44876126-44876127	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs147038711	chr10:44876141-44876142	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs578230105	chr10:44876143-44876144	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs76416040	chr10:44876157-44876158	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs200632037	chr10:44876162-44876163	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs371480399	chr10:44876163-44876164	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs374406686	chr10:44876169-44876170	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs375557870	chr10:44876172-44876173	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs185309544	chr10:44876182-44876183	Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs529109096	chr10:44876208-44876209	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	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:664 , 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	chr10:44871000-44877600	Weak transcription	Rectal Smooth Muscle	rectum
29	chr10:44871400-44875400	Strong transcription	HUES6 Cell Line	embryonic stem cell
30	chr10:44871600-44877000	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr10:44871800-44877000	Weak transcription	Stomach Smooth Muscle	stomach
32	chr10:44872000-44875600	Weak transcription	Colon Smooth Muscle	Colon
33	chr10:44872000-44875800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr10:44872400-44875600	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr10:44872400-44877400	Weak transcription	Fetal Kidney	kidney
36	chr10:44872600-44875200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr10:44873000-44875800	Strong transcription	NHLF	lung
38	chr10:44873200-44875200	Genic enhancers	Fetal Muscle Trunk	muscle
39	chr10:44873200-44875600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr10:44873200-44877600	Weak transcription	Lung	lung
41	chr10:44873400-44875200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
42	chr10:44873400-44875600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
43	chr10:44873400-44876200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr10:44873600-44876400	Strong transcription	NHDF-Ad	bronchial
45	chr10:44873600-44876600	Strong transcription	Fetal Lung	lung
46	chr10:44874200-44875400	Strong transcription	HUES48 Cell Line	embryonic stem cell
47	chr10:44874200-44875600	Genic enhancers	Skeletal Muscle Female	skeletal muscle
48	chr10:44874400-44875200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr10:44874400-44877800	Weak transcription	Right Ventricle	heart
50	chr10:44874600-44875600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell

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