Variant report

Variant	nsv1047491
Chromosome Location	chr12:58603291-58643219
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	chr12:58618926-58619769	HepG2	liver:	n/a	n/a
2	CEBPB	chr12:58638743-58638950	A549	lung:	n/a	chr12:58638835-58638844 chr12:58638833-58638846 chr12:58638833-58638844
3	CTCF	chr12:58641500-58641650	BE2_C	brain:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
4	CTCF	chr12:58641560-58641710	Caco-2	colon:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
5	CTCF	chr12:58641485-58641731	MCF-7	breast:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
6	CTCF	chr12:58641480-58641630	SAEC	small airway:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641614-58641627 chr12:58641612-58641628
7	CTCF	chr12:58641600-58641750	HMEC	breast:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
8	CTCF	chr12:58641540-58641690	GM12864	blood:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
9	CTCF	chr12:58641528-58641696	NHEK	skin:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
10	CTCF	chr12:58641520-58641670	HMF	breast:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
11	CTCF	chr12:58641532-58641695	A549	lung:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
12	CTCF	chr12:58641480-58641630	HAc	cerebellar:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641614-58641627 chr12:58641612-58641628
13	CTCF	chr12:58641500-58641650	HEK293	kidney:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
14	CTCF	chr12:58641539-58641727	SK-N-SH_RA	brain:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
15	CTCF	chr12:58641580-58641730	GM06990	blood:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
16	CTCF	chr12:58641520-58641670	Hela-S3	cervix:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
17	CTCF	chr12:58641460-58641610	HMEC	breast:	n/a	n/a
18	CTCF	chr12:58641260-58641410	HFF-Myc	foreskin:	n/a	n/a
19	CTCF	chr12:58641520-58641670	HEK293	kidney:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
20	CTCF	chr12:58641401-58641871	MCF-7	breast:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
21	CTCF	chr12:58641500-58641650	K562	blood:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
22	CTCF	chr12:58641582-58641646	GM19238	blood:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
23	CTCF	chr12:58641518-58641676	SK-N-SH_RA	brain:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
24	CTCF	chr12:58641520-58641670	RPTEC	kidney:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
25	CTCF	chr12:58641560-58641710	GM06990	blood:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
26	CTCF	chr12:58641508-58641705	MCF-7	breast:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
27	CTCF	chr12:58628040-58628054	GM10248	blood:	n/a	n/a
28	CTCF	chr12:58641500-58641711	Gliobla	brain:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
29	CTCF	chr12:58641620-58641770	BE2_C	brain:	n/a	n/a
30	CTCF	chr12:58641570-58641670	A549	lung:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
31	CTCF	chr12:58641480-58641630	HCFaa	heart:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641614-58641627 chr12:58641612-58641628
32	CTCF	chr12:58641514-58641708	HepG2	liver:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
33	CTCF	chr12:58641498-58641756	GM12878	blood:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
34	CTCF	chr12:58641480-58641630	NHEK	skin:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641614-58641627 chr12:58641612-58641628
35	CTCF	chr12:58641563-58641676	H1-hESC	embryonic stem cell:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
36	CTCF	chr12:58641500-58641650	A549	lung:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
37	CTCF	chr12:58641473-58641758	H1-hESC	embryonic stem cell:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
38	CTCF	chr12:58641560-58641710	HCPEpiC	choroid plexus:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
39	CTCF	chr12:58641540-58641690	HVMF	connective:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
40	CTCF	chr12:58641578-58641656	GM19240	blood:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
41	CTCF	chr12:58641580-58641730	NB4	blood:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
42	CTCF	chr12:58640184-58640251	GM13976	blood:	n/a	n/a
43	CTCF	chr12:58641520-58641670	GM12874	blood:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
44	CTCF	chr12:58641553-58641681	GM12878	blood:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
45	CTCF	chr12:58641513-58641702	MCF-7	breast:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
46	CTCF	chr12:58641483-58641783	A549	lung:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
47	CTCF	chr12:58641353-58641953	A549	lung:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
48	CTCF	chr12:58641560-58641710	HBMEC	blood vessel:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
49	CTCF	chr12:58641560-58641710	BJ	skin:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628
50	CTCF	chr12:58641540-58641690	WERI-Rb-1	eye:	n/a	chr12:58641611-58641629 chr12:58641614-58641627 chr12:58641616-58641626 chr12:58641613-58641634 chr12:58641614-58641627 chr12:58641612-58641628

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:58637434-58637484	AG09319	gingival:	n/a
2	chr12:58637434-58637484	HIPEpiC	eye:	n/a
3	chr12:58637434-58637484	HUVEC	blood vessel:	n/a
4	chr12:58637434-58637484	SK-N-SH	brain:	n/a
5	chr12:58637434-58637484	IMR90	lung:	fetal
6	chr12:58637434-58637484	ovcar-3	ovarian:	n/a
7	chr12:58637434-58637484	HAEpiC	amniotic membrane:	n/a
8	chr12:58637434-58637484	NB4	blood:	n/a
9	chr12:58637434-58637484	AoSMC	blood vessel:	n/a
10	chr12:58637434-58637484	HCT-116	colon:	n/a
11	chr12:58637434-58637484	MCF-7	breast:	n/a
12	chr12:58637434-58637484	BJ	skin:	n/a
13	chr12:58637434-58637484	HMEC	breast:	n/a
14	chr12:58637434-58637484	HRCEpiC	kidney:	n/a
15	chr12:58637434-58637484	RPTEC	kidney:	n/a
16	chr12:58637434-58637484	GM12878	blood:	n/a
17	chr12:58637434-58637484	Caco-2	colon:	n/a
18	chr12:58637434-58637484	AG10803	skin:	n/a
19	chr12:58637434-58637484	HCF	heart:	n/a
20	chr12:58637434-58637484	AG04449	skin:	fetal
21	chr12:58637434-58637484	HCM	heart:	n/a
22	chr12:58637434-58637484	Hela-S3	cervix:	n/a
23	chr12:58637434-58637484	HEEpiC	esophagus:	n/a
24	chr12:58637434-58637484	GM12892	blood:	n/a
25	chr12:58637434-58637484	T-47D	breast:	n/a
26	chr12:58637434-58637484	NHDF-neo	bronchial:	n/a
27	chr12:58637434-58637484	PFSK-1	brain:	n/a
28	chr12:58637434-58637484	BE2_C	brain:	n/a
29	chr12:58637434-58637484	PANC-1	pancreas:	n/a
30	chr12:58637434-58637484	HCPEpiC	choroid plexus:	n/a
31	chr12:58637434-58637484	NH-A	brain:	n/a
32	chr12:58637434-58637484	LNCaP	prostate:	n/a
33	chr12:58637434-58637484	H1-hESC	embryonic stem cell:	embryo
34	chr12:58637434-58637484	AG09309	skin:	n/a
35	chr12:58637434-58637484	HL-60	blood:	n/a
36	chr12:58637434-58637484	Hepatocyte	liver:	n/a
37	chr12:58637434-58637484	CMK	blood:	n/a
38	chr12:58637434-58637484	HNPCEpiC	eye:	n/a
39	chr12:58637434-58637484	HRE	kidney:	n/a
40	chr12:58637434-58637484	NT2-D1	testis:	n/a
41	chr12:58637434-58637484	MCF10A-Er-Src	breast:	n/a
42	chr12:58637434-58637484	GM06990	blood:	n/a
43	chr12:58637434-58637484	A549	lung:	n/a
44	chr12:58637434-58637484	ProgFib	skin:	n/a
45	chr12:58637434-58637484	ECC-1	luminal epithelium:	n/a
46	chr12:58637434-58637484	Jurkat	blood:	n/a
47	chr12:58637434-58637484	PrEC	prostate:	n/a
48	chr12:58637434-58637484	HEK293	kidney:	embryo
49	chr12:58637434-58637484	SAEC	small airway:	n/a
50	chr12:58637434-58637484	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:58630860..58633144-chr12:58634673..58636687,3	K562	blood:
2	chr12:58615914..58618113-chr12:58633872..58636755,2	MCF-7	breast:
3	chr12:58630860..58633144-chr12:58634673..58636687,3	K562	blood:
4	chr12:58635246..58637167-chr12:58640268..58641799,2	K562	blood:
5	chr12:58641625..58645045-chr12:58645978..58649006,3	K562	blood:
6	chr12:58605234..58607787-chr12:58609232..58610950,2	MCF-7	breast:
7	chr12:58605234..58607787-chr12:58609232..58610950,2	MCF-7	breast:
8	chr12:58630980..58633788-chr12:58634242..58636754,3	K562	blood:
9	chr12:58635246..58637167-chr12:58640268..58641799,2	K562	blood:
10	chr12:58630980..58633788-chr12:58634242..58636754,3	K562	blood:
11	chr12:58615914..58618113-chr12:58633872..58636755,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-XRCC6BP1-7	chr12:58638161-58638648	NONHSAT029022

Variant related genes	Relation type
RPL21P103	TF binding region
RPL21P103	CpG island

Extended variants
information (count: 544 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:544 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570957063	chr12:58603338-58603339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs535152021	chr12:58603349-58603350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547130129	chr12:58603364-58603365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs111528336	chr12:58603370-58603371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs35903269	chr12:58603393-58603394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373614799	chr12:58603489-58603490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs145342660	chr12:58603518-58603519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571864040	chr12:58603528-58603529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs80232905	chr12:58603572-58603573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs182889080	chr12:58603589-58603590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572060786	chr12:58610641-58610642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs7488679	chr12:58610729-58610730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113007801	chr12:58610738-58610739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs375621760	chr12:58610739-58610740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs71448553	chr12:58610761-58610762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs60637392	chr12:58610765-58610766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs59488751	chr12:58610766-58610767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs74531312	chr12:58610798-58610799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148102502	chr12:58610819-58610820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs1553380	chr12:58610873-58610874	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs551518118	chr12:58610913-58610914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571400714	chr12:58610949-58610950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570633906	chr12:58611015-58611016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541178514	chr12:58611126-58611127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534816646	chr12:58611147-58611148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs553194390	chr12:58611176-58611177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192978843	chr12:58611186-58611187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs34387577	chr12:58616006-58616007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs150443278	chr12:58616104-58616105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs532552471	chr12:58616105-58616106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs79072049	chr12:58616159-58616160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs189972357	chr12:58616175-58616176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs58475396	chr12:58616224-58616225	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs549613614	chr12:58616250-58616251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567907262	chr12:58616286-58616287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs537848210	chr12:58616302-58616303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140902187	chr12:58616310-58616311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532841381	chr12:58616337-58616338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs549792755	chr12:58616340-58616341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs571394038	chr12:58616370-58616371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552857550	chr12:58616410-58616411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551424705	chr12:58616429-58616430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs553974555	chr12:58616449-58616450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs572162224	chr12:58616452-58616453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536096181	chr12:58616453-58616454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559586185	chr12:58616464-58616465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571262264	chr12:58616516-58616517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs138266685	chr12:58616589-58616590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs576432316	chr12:58616595-58616596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs543426373	chr12:58616596-58616597	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Autism	20531469	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21138945	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21364760	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:58603200-58603400	Enhancers	Fetal Brain Male	brain
2	chr12:58603200-58603600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr12:58610600-58611000	Enhancers	Fetal Brain Male	brain
4	chr12:58611000-58611200	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr12:58616000-58616600	Enhancers	Fetal Stomach	stomach
6	chr12:58616200-58616400	Enhancers	HepG2	liver
7	chr12:58616200-58616800	Enhancers	Fetal Lung	lung
8	chr12:58616600-58619400	Weak transcription	Fetal Stomach	stomach
9	chr12:58616800-58617800	Weak transcription	Fetal Lung	lung
10	chr12:58617400-58617600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr12:58617600-58618000	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr12:58617600-58618200	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr12:58617600-58618200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr12:58617600-58618400	Enhancers	Fetal Brain Male	brain
15	chr12:58617600-58618800	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr12:58617800-58618800	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr12:58617800-58619200	Enhancers	HepG2	liver
18	chr12:58617800-58620600	Enhancers	Fetal Lung	lung
19	chr12:58618200-58618800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr12:58618400-58618800	Flanking Active TSS	Fetal Brain Male	brain
21	chr12:58618800-58619000	Enhancers	Fetal Brain Male	brain
22	chr12:58618800-58619000	Bivalent Enhancer	HUVEC	blood vessel
23	chr12:58619000-58620200	Enhancers	Adipose Nuclei	Adipose
24	chr12:58619200-58619600	Flanking Active TSS	HepG2	liver
25	chr12:58619400-58620000	Enhancers	Duodenum Smooth Muscle	Duodenum
26	chr12:58619400-58620200	Enhancers	Fetal Stomach	stomach
27	chr12:58619600-58620600	Enhancers	HepG2	liver
28	chr12:58620000-58620200	Enhancers	Left Ventricle	heart
29	chr12:58626200-58626600	Active TSS	ES-I3 Cell Line	embryonic stem cell
30	chr12:58626400-58628000	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr12:58626600-58626800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr12:58626800-58627000	Enhancers	Left Ventricle	heart
33	chr12:58626800-58627800	Enhancers	Fetal Intestine Large	intestine
34	chr12:58627000-58627600	Enhancers	Fetal Intestine Small	intestine
35	chr12:58627000-58627600	Weak transcription	Left Ventricle	heart
36	chr12:58627600-58627800	Enhancers	Left Ventricle	heart
37	chr12:58627800-58630400	Weak transcription	Left Ventricle	heart
38	chr12:58628000-58630000	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr12:58628600-58628800	Enhancers	Fetal Stomach	stomach
40	chr12:58628800-58630000	Weak transcription	Fetal Stomach	stomach
41	chr12:58630000-58630800	Enhancers	Fetal Stomach	stomach
42	chr12:58630400-58630600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr12:58630400-58630800	Enhancers	H9 Cell Line	embryonic stem cell
44	chr12:58630400-58630800	Enhancers	Left Ventricle	heart
45	chr12:58633000-58633600	Active TSS	Gastric	stomach
46	chr12:58636400-58636800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr12:58636400-58636800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr12:58636600-58637400	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr12:58636600-58637400	Enhancers	Adipose Nuclei	Adipose
50	chr12:58636600-58637400	Enhancers	Fetal Stomach	stomach

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