Variant report

Variant	nsv526333
Chromosome Location	chr5:126732427-126746277
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	CTCF	chr5:126732580-126732730	MCF-7	breast:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
2	CTCF	chr5:126732550-126732723	A549	lung:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
3	CTCF	chr5:126732566-126732717	K562	blood:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
4	CTCF	chr5:126732539-126732733	HepG2	liver:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
5	CTCF	chr5:126732520-126732670	GM12867	blood:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
6	CTCF	chr5:126732600-126732750	HCPEpiC	choroid plexus:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
7	CTCF	chr5:126732600-126732750	GM12865	blood:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
8	CTCF	chr5:126732560-126732710	HCT-116	colon:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
9	CTCF	chr5:126732560-126732710	GM12872	blood:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
10	CTCF	chr5:126732520-126732670	HRPEpiC	eye:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
11	CTCF	chr5:126732572-126732698	HepG2	liver:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
12	CTCF	chr5:126732521-126732735	MCF-7	breast:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
13	CTCF	chr5:126732540-126732690	GM12872	blood:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
14	CTCF	chr5:126732597-126732680	Pancreas_OC	pancreas:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
15	CTCF	chr5:126732620-126732770	GM12869	blood:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
16	CTCF	chr5:126732535-126732774	GM12878	blood:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
17	CTCF	chr5:126732600-126732750	RPTEC	kidney:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
18	CTCF	chr5:126732580-126732730	WERI-Rb-1	eye:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
19	CTCF	chr5:126732560-126732710	A549	lung:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
20	CTCF	chr5:126732571-126732695	GM12891	blood:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
21	CTCF	chr5:126732612-126732659	GM10266	blood:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
22	CTCF	chr5:126732580-126732730	HepG2	liver:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
23	CTCF	chr5:126732524-126732748	MCF-7	breast:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
24	CTCF	chr5:126732570-126732710	GM19240	blood:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
25	CTCF	chr5:126732517-126732739	MCF-7	breast:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
26	CTCF	chr5:126732592-126732675	GM10248	blood:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
27	CTCF	chr5:126732562-126732720	ProgFib	skin:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
28	CTCF	chr5:126745320-126745470	AG09319	gingival:	n/a	n/a
29	CTCF	chr5:126732580-126732730	GM12873	blood:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
30	CTCF	chr5:126732560-126732710	HMF	breast:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
31	CTCF	chr5:126732520-126732670	GM12878	blood:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
32	CTCF	chr5:126732500-126732650	HCPEpiC	choroid plexus:	n/a	chr5:126732632-126732639 chr5:126732631-126732644 chr5:126732628-126732646
33	CTCF	chr5:126732520-126732670	HA-sp	spinal cord:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
34	CTCF	chr5:126732560-126732710	SK-N-SH_RA	brain:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
35	CTCF	chr5:126732540-126732690	GM06990	blood:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
36	CTCF	chr5:126732540-126732690	HBMEC	blood vessel:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
37	CTCF	chr5:126732512-126732744	MCF-7	breast:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
38	CTCF	chr5:126732580-126732730	RPTEC	kidney:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
39	CTCF	chr5:126732560-126732710	NHEK	skin:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
40	CTCF	chr5:126732548-126732721	H1-hESC	embryonic stem cell:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
41	CTCF	chr5:126734391-126734465	ProgFib	skin:	n/a	n/a
42	CTCF	chr5:126732560-126732710	HEK293	kidney:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
43	CTCF	chr5:126732542-126732738	GM19238	blood:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
44	CTCF	chr5:126732620-126732770	AG09309	skin:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
45	CTCF	chr5:126732480-126732630	HRE	kidney:	n/a	n/a
46	CTCF	chr5:126732580-126732730	Caco-2	colon:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
47	CTCF	chr5:126732500-126732650	HBMEC	blood vessel:	n/a	chr5:126732632-126732639 chr5:126732631-126732644 chr5:126732628-126732646
48	CTCF	chr5:126732621-126732668	NHEK	skin:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
49	CTCF	chr5:126732553-126732796	K562	blood:	n/a	chr5:126732632-126732639 chr5:126732630-126732651 chr5:126732631-126732644 chr5:126732628-126732646
50	CTCF	chr5:126732660-126732810	HRPEpiC	eye:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:126742185-126742235	HRE	kidney:	n/a
2	chr5:126742185-126742235	HRCEpiC	kidney:	n/a
3	chr5:126742185-126742235	GM19239	blood:	n/a
4	chr5:126742185-126742235	SK-N-MC	brain:	n/a
5	chr5:126742185-126742235	HEEpiC	esophagus:	n/a
6	chr5:126742185-126742235	ovcar-3	ovarian:	n/a
7	chr5:126742185-126742235	Hepatocyte	liver:	n/a
8	chr5:126742185-126742235	MCF-7	breast:	n/a
9	chr5:126742185-126742235	NHDF-neo	bronchial:	n/a
10	chr5:126742185-126742235	GM12892	blood:	n/a
11	chr5:126742185-126742235	HEK293	kidney:	embryo
12	chr5:126742185-126742235	K562	blood:	n/a
13	chr5:126742185-126742235	MCF10A-Er-Src	breast:	n/a
14	chr5:126742185-126742235	AG04450	lung:	fetal
15	chr5:126742185-126742235	SK-N-SH	brain:	n/a
16	chr5:126742185-126742235	NB4	blood:	n/a
17	chr5:126742185-126742235	BE2_C	brain:	n/a
18	chr5:126742185-126742235	NT2-D1	testis:	n/a
19	chr5:126742185-126742235	H1-hESC	embryonic stem cell:	embryo
20	chr5:126742185-126742235	HRPEpiC	eye:	n/a
21	chr5:126742185-126742235	ProgFib	skin:	n/a
22	chr5:126742185-126742235	NHBE	bronchial:	n/a
23	chr5:126742185-126742235	PANC-1	pancreas:	n/a
24	chr5:126742185-126742235	HIPEpiC	eye:	n/a
25	chr5:126742185-126742235	AoSMC	blood vessel:	n/a
26	chr5:126742185-126742235	AG09309	skin:	n/a
27	chr5:126742185-126742235	LNCaP	prostate:	n/a
28	chr5:126742185-126742235	HNPCEpiC	eye:	n/a
29	chr5:126742185-126742235	HMEC	breast:	n/a
30	chr5:126742185-126742235	SK-N-SH_RA	brain:	n/a
31	chr5:126742185-126742235	NH-A	brain:	n/a
32	chr5:126742185-126742235	Caco-2	colon:	n/a
33	chr5:126742185-126742235	A549	lung:	n/a
34	chr5:126742185-126742235	RPTEC	kidney:	n/a
35	chr5:126742185-126742235	PFSK-1	brain:	n/a
36	chr5:126742185-126742235	T-47D	breast:	n/a
37	chr5:126742185-126742235	HL-60	blood:	n/a
38	chr5:126742185-126742235	HUVEC	blood vessel:	n/a
39	chr5:126742185-126742235	SKMC	muscle:	n/a
40	chr5:126742185-126742235	HCM	heart:	n/a
41	chr5:126742185-126742235	HCF	heart:	n/a
42	chr5:126742185-126742235	HCT-116	colon:	n/a
43	chr5:126742185-126742235	SAEC	small airway:	n/a
44	chr5:126742185-126742235	BJ	skin:	n/a
45	chr5:126742185-126742235	AG09319	gingival:	n/a
46	chr5:126742185-126742235	CMK	blood:	n/a
47	chr5:126742185-126742235	HCPEpiC	choroid plexus:	n/a
48	chr5:126742185-126742235	PrEC	prostate:	n/a
49	chr5:126742185-126742235	HAEpiC	amniotic membrane:	n/a
50	chr5:126742185-126742235	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr5:126732573..126736586-chr5:126737004..126738980,3	K562	blood:
2	chr5:126732573..126736586-chr5:126737004..126738980,3	K562	blood:
3	chr5:126732318..126732969-chr5:126828411..126828936,2	MCF-7	breast:

Variant related genes	Relation type
MEGF10	TF binding region
MEGF10	CpG island

Extended variants
information (count: 547 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:547 , 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	rs3812054	chr5:126732427-126732428	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574427804	chr5:126732431-126732432	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs200236385	chr5:126732442-126732443	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs377520032	chr5:126732443-126732444	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs144079313	chr5:126732459-126732460	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148663427	chr5:126732463-126732464	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532194218	chr5:126732480-126732481	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371350255	chr5:126732493-126732494	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs375189988	chr5:126732519-126732520	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs532329096	chr5:126732527-126732528	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150309123	chr5:126732623-126732624	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs191727880	chr5:126732624-126732625	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531778588	chr5:126732659-126732660	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548597408	chr5:126732728-126732729	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs116312116	chr5:126732735-126732736	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs72788599	chr5:126732772-126732773	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs56408687	chr5:126732777-126732778	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs570997251	chr5:126732779-126732780	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs149015365	chr5:126732787-126732788	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs373958151	chr5:126732794-126732795	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534934597	chr5:126732800-126732801	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs116816975	chr5:126732808-126732809	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs17839695	chr5:126732812-126732813	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs537452456	chr5:126732815-126732816	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183503357	chr5:126732828-126732829	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188104548	chr5:126732840-126732841	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs147117501	chr5:126732841-126732842	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs74435440	chr5:126732851-126732852	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs144004730	chr5:126732894-126732895	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs577145322	chr5:126733027-126733028	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs146749679	chr5:126733189-126733190	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs148337683	chr5:126733195-126733196	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531587282	chr5:126733217-126733218	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375523003	chr5:126733293-126733294	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs17604819	chr5:126733304-126733305	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs115032896	chr5:126733323-126733324	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs1363384	chr5:126733395-126733396	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs1363385	chr5:126733399-126733400	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs114461925	chr5:126733400-126733401	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs55851028	chr5:126733403-126733404	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs564251689	chr5:126733415-126733416	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs141457761	chr5:126733442-126733443	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576922461	chr5:126733445-126733446	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs570024352	chr5:126733446-126733447	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs150834114	chr5:126733466-126733467	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554292105	chr5:126733477-126733478	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs568078302	chr5:126733494-126733495	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs533539877	chr5:126733503-126733504	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs139262530	chr5:126733512-126733513	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs1363386	chr5:126733515-126733516	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Myelofibrosis	22110671	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	16397240	CNVD
Parathyroid adenoma	22454399	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:312 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:126691000-126746000	Weak transcription	Fetal Muscle Trunk	muscle
2	chr5:126710200-126741200	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr5:126712800-126734200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr5:126720000-126742000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr5:126722800-126736000	Weak transcription	HSMM	muscle
6	chr5:126729400-126732600	Weak transcription	Brain Angular Gyrus	brain
7	chr5:126730800-126734400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr5:126731000-126734400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr5:126731600-126732800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr5:126731600-126733800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr5:126731600-126735000	Enhancers	Brain Hippocampus Middle	brain
12	chr5:126731800-126733000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
13	chr5:126731800-126733000	Strong transcription	Fetal Muscle Leg	muscle
14	chr5:126731800-126735000	Genic enhancers	Brain Substantia Nigra	brain
15	chr5:126731800-126741800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr5:126731800-126742000	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr5:126732000-126734400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr5:126732000-126735200	Strong transcription	Cortex derived primary cultured neurospheres	brain
19	chr5:126732000-126741200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr5:126732200-126732800	Strong transcription	HSMMtube	muscle
21	chr5:126732400-126732600	Enhancers	H1 Cell Line	embryonic stem cell
22	chr5:126732400-126732800	Genic enhancers	Brain Anterior Caudate	brain
23	chr5:126732400-126734200	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr5:126732400-126734800	Enhancers	Brain Cingulate Gyrus	brain
25	chr5:126732400-126741600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr5:126732600-126732800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr5:126732600-126732800	Genic enhancers	Brain Angular Gyrus	brain
28	chr5:126732600-126741800	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr5:126732800-126734000	Weak transcription	Brain Anterior Caudate	brain
30	chr5:126732800-126734200	Weak transcription	Brain Angular Gyrus	brain
31	chr5:126732800-126734200	Weak transcription	HSMMtube	muscle
32	chr5:126732800-126737400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr5:126733000-126733400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr5:126733000-126734400	Weak transcription	Fetal Muscle Leg	muscle
35	chr5:126733200-126736800	Weak transcription	Fetal Brain Female	brain
36	chr5:126733200-126739400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr5:126733400-126733600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr5:126733600-126736600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr5:126733800-126734400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr5:126734000-126734800	Genic enhancers	Brain Anterior Caudate	brain
41	chr5:126734200-126734400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
42	chr5:126734200-126734600	Enhancers	Brain Angular Gyrus	brain
43	chr5:126734200-126735000	Strong transcription	HUES48 Cell Line	embryonic stem cell
44	chr5:126734200-126735600	Genic enhancers	HSMMtube	muscle
45	chr5:126734400-126734600	Genic enhancers	Brain Inferior Temporal Lobe	brain
46	chr5:126734400-126734800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr5:126734400-126735200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr5:126734400-126735800	Strong transcription	Fetal Muscle Leg	muscle
49	chr5:126734400-126736000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr5:126734400-126736200	Strong transcription	iPS-20b Cell Line	embryonic stem cell

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