Variant report

Variant	esv3401617
Chromosome Location	chr5:115205732-115238678
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	chr5:115209164-115209423	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:115223798-115224003	K562	blood:	n/a	n/a
3	ARID3A	chr5:115223854-115223991	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:115220750-115220987	HepG2	liver:	n/a	n/a
5	CEBPB	chr5:115223854-115224036	A549	lung:	n/a	n/a
6	CEBPB	chr5:115205274-115205767	K562	blood:	n/a	n/a
7	CEBPB	chr5:115229078-115229162	A549	lung:	n/a	n/a
8	CEBPB	chr5:115204972-115205823	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr5:115208948-115209417	IMR90	lung:	n/a	chr5:115209009-115209020 chr5:115209009-115209020 chr5:115209005-115209016
10	CEBPB	chr5:115223862-115224040	K562	blood:	n/a	n/a
11	CTCF	chr5:115211256-115211443	MCF-7	breast:	n/a	chr5:115211325-115211343
12	CTCF	chr5:115211240-115211390	AG09309	skin:	n/a	chr5:115211325-115211343
13	CTCF	chr5:115223878-115223945	Pancreas_OC	pancreas:	n/a	chr5:115223904-115223925 chr5:115223905-115223918
14	CTCF	chr5:115211300-115211450	HFF	foreskin:	n/a	chr5:115211325-115211343
15	CTCF	chr5:115223820-115223970	HPAF	blood vessel:	n/a	chr5:115223904-115223925 chr5:115223905-115223918
16	CTCF	chr5:115223844-115223962	Kidney_OC	kidney:	n/a	chr5:115223904-115223925 chr5:115223905-115223918
17	CTCF	chr5:115223820-115223970	AG04449	skin:	n/a	chr5:115223904-115223925 chr5:115223905-115223918
18	CTCF	chr5:115223880-115224030	HCT-116	colon:	n/a	chr5:115223904-115223925 chr5:115223905-115223918
19	CTCF	chr5:115211280-115211430	HRPEpiC	eye:	n/a	chr5:115211325-115211343
20	CTCF	chr5:115223626-115224330	HCT-116	colon:	n/a	chr5:115223904-115223925 chr5:115223905-115223918
21	CTCF	chr5:115223860-115224010	AG09309	skin:	n/a	chr5:115223904-115223925 chr5:115223905-115223918
22	CTCF	chr5:115211320-115211470	NHDF-neo	bronchial:	n/a	chr5:115211325-115211343
23	CTCF	chr5:115223860-115224010	BE2_C	brain:	n/a	chr5:115223904-115223925 chr5:115223905-115223918
24	CTCF	chr5:115211260-115211410	WERI-Rb-1	eye:	n/a	chr5:115211325-115211343
25	CTCF	chr5:115223840-115223990	AoAF	blood vessel:	n/a	chr5:115223904-115223925 chr5:115223905-115223918
26	CTCF	chr5:115223880-115224030	HMF	breast:	n/a	chr5:115223904-115223925 chr5:115223905-115223918
27	CTCF	chr5:115211260-115211410	HCM	heart:	n/a	chr5:115211325-115211343
28	CTCF	chr5:115211200-115211350	AG04450	lung:	n/a	chr5:115211325-115211343
29	CTCF	chr5:115223773-115224072	K562	blood:	n/a	chr5:115223904-115223925 chr5:115223905-115223918
30	CTCF	chr5:115223800-115223950	HA-sp	spinal cord:	n/a	chr5:115223904-115223925 chr5:115223905-115223918
31	CTCF	chr5:115211240-115211390	HPF	lung:	n/a	chr5:115211325-115211343
32	CTCF	chr5:115223860-115224010	NHDF-neo	bronchial:	n/a	chr5:115223904-115223925 chr5:115223905-115223918
33	CTCF	chr5:115223878-115223968	K562	blood:	n/a	chr5:115223904-115223925 chr5:115223905-115223918
34	CTCF	chr5:115211280-115211430	RPTEC	kidney:	n/a	chr5:115211325-115211343
35	CTCF	chr5:115224721-115224797	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr5:115223754-115224059	H1-hESC	embryonic stem cell:	n/a	chr5:115223904-115223925 chr5:115223905-115223918
37	CTCF	chr5:115211260-115211410	HepG2	liver:	n/a	chr5:115211325-115211343
38	CTCF	chr5:115211313-115211386	A549	lung:	n/a	chr5:115211325-115211343
39	CTCF	chr5:115224644-115224893	GM12878	blood:	n/a	n/a
40	CTCF	chr5:115211240-115211390	HFF-Myc	foreskin:	n/a	chr5:115211325-115211343
41	CTCF	chr5:115223833-115223981	Spleen_OC	spleen:	n/a	chr5:115223904-115223925 chr5:115223905-115223918
42	CTCF	chr5:115211260-115211410	HMEC	breast:	n/a	chr5:115211325-115211343
43	CTCF	chr5:115211240-115211390	MCF-7	breast:	n/a	chr5:115211325-115211343
44	CTCF	chr5:115223860-115224010	HRPEpiC	eye:	n/a	chr5:115223904-115223925 chr5:115223905-115223918
45	CTCF	chr5:115223900-115224050	HRPEpiC	eye:	n/a	chr5:115223904-115223925 chr5:115223905-115223918
46	CTCF	chr5:115211320-115211470	RPTEC	kidney:	n/a	chr5:115211325-115211343
47	CTCF	chr5:115223900-115224050	Hela-S3	cervix:	n/a	chr5:115223904-115223925 chr5:115223905-115223918
48	CTCF	chr5:115211240-115211390	HepG2	liver:	n/a	chr5:115211325-115211343
49	CTCF	chr5:115211220-115211370	HCT-116	colon:	n/a	chr5:115211325-115211343
50	CTCF	chr5:115211260-115211410	HUVEC	blood vessel:	n/a	chr5:115211325-115211343

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:115209107-115209157	AG10803	skin:	n/a
2	chr5:115209107-115209157	AG10803	skin:	n/a
3	chr5:115233711-115233761	GM12878	blood:	n/a
4	chr5:115233711-115233761	AG04450	lung:	fetal
5	chr5:115209107-115209157	Hela-S3	cervix:	n/a
6	chr5:115209107-115209157	MCF-7	breast:	n/a
7	chr5:115209107-115209157	HUVEC	blood vessel:	n/a
8	chr5:115233711-115233761	HRE	kidney:	n/a
9	chr5:115209107-115209157	SK-N-SH_RA	brain:	n/a
10	chr5:115209107-115209157	RPTEC	kidney:	n/a
11	chr5:115209107-115209157	BE2_C	brain:	n/a
12	chr5:115233711-115233761	Hepatocyte	liver:	n/a
13	chr5:115233711-115233761	K562	blood:	n/a
14	chr5:115209107-115209157	HCF	heart:	n/a
15	chr5:115209107-115209157	A549	lung:	n/a
16	chr5:115209107-115209157	AG09309	skin:	n/a
17	chr5:115233711-115233761	NHBE	bronchial:	n/a
18	chr5:115233711-115233761	NHDF-neo	bronchial:	n/a
19	chr5:115233711-115233761	IMR90	lung:	fetal
20	chr5:115233711-115233761	NB4	blood:	n/a
21	chr5:115209107-115209157	U87	brain:	n/a
22	chr5:115209107-115209157	HepG2	liver:	n/a
23	chr5:115233711-115233761	MCF-7	breast:	n/a
24	chr5:115209107-115209157	HEEpiC	esophagus:	n/a
25	chr5:115233711-115233761	NH-A	brain:	n/a
26	chr5:115233711-115233761	HepG2	liver:	n/a
27	chr5:115209107-115209157	AG04450	lung:	fetal
28	chr5:115233711-115233761	T-47D	breast:	n/a
29	chr5:115209107-115209157	HEK293	kidney:	embryo
30	chr5:115209107-115209157	AG09319	gingival:	n/a
31	chr5:115209107-115209157	NH-A	brain:	n/a
32	chr5:115209107-115209157	HCPEpiC	choroid plexus:	n/a
33	chr5:115209107-115209157	SAEC	small airway:	n/a
34	chr5:115233711-115233761	HRPEpiC	eye:	n/a
35	chr5:115233711-115233761	PANC-1	pancreas:	n/a
36	chr5:115209107-115209157	HIPEpiC	eye:	n/a
37	chr5:115233711-115233761	BJ	skin:	n/a
38	chr5:115233711-115233761	PrEC	prostate:	n/a
39	chr5:115209107-115209157	ProgFib	skin:	n/a
40	chr5:115209107-115209157	HPAEpiC	pulmonary alveolar:	n/a
41	chr5:115233711-115233761	LNCaP	prostate:	n/a
42	chr5:115209107-115209157	Jurkat	blood:	n/a
43	chr5:115209107-115209157	SKMC	muscle:	n/a
44	chr5:115209107-115209157	IMR90	lung:	fetal
45	chr5:115233711-115233761	Caco-2	colon:	n/a
46	chr5:115233711-115233761	SAEC	small airway:	n/a
47	chr5:115209107-115209157	NHDF-neo	bronchial:	n/a
48	chr5:115209107-115209157	AG04449	skin:	fetal
49	chr5:115233711-115233761	H1-hESC	embryonic stem cell:	embryo
50	chr5:115233711-115233761	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:115206874..115208478-chr5:115208697..115211517,2	MCF-7	breast:
2	chr5:115223474..115224422-chr5:115405380..115406073,2	MCF-7	breast:
3	chr5:115227371..115230053-chr5:115419222..115421109,2	MCF-7	breast:
4	chr5:115175467..115180084-chr5:115209900..115212973,5	MCF-7	breast:
5	chr16:71323238..71324801-chr5:115205748..115207250,2	K562	blood:
6	chr5:115204352..115206713-chr5:115207529..115209767,2	K562	blood:
7	chr5:115231047..115233033-chr5:115237062..115238617,2	MCF-7	breast:
8	chr5:115206874..115208478-chr5:115208697..115211517,2	MCF-7	breast:
9	chr5:115231047..115233033-chr5:115237062..115238617,2	MCF-7	breast:
10	chr5:115176895..115178900-chr5:115236267..115238084,2	MCF-7	breast:
11	chr5:115175680..115177440-chr5:115210427..115212730,2	MCF-7	breast:
12	chr5:115177088..115179006-chr5:115205990..115207526,2	MCF-7	breast:
13	chr5:115204790..115207353-chr5:115207860..115210489,2	MCF-7	breast:
14	chr5:115210792..115211545-chr5:115403396..115404332,2	MCF-7	breast:
15	chr5:115197705..115199807-chr5:115209028..115210592,2	MCF-7	breast:
16	chr5:115175801..115178780-chr5:115205651..115208608,2	K562	blood:
17	chr5:115223646..115224387-chr5:115397745..115398268,2	MCF-7	breast:
18	chr5:115183571..115185116-chr5:115205126..115206631,2	K562	blood:
19	chr5:115223617..115224331-chr5:115367917..115368436,2	MCF-7	breast:
20	chr5:115204790..115207353-chr5:115207860..115210489,2	MCF-7	breast:
21	chr19:49121390..49123356-chr5:115205123..115206693,2	MCF-7	breast:
22	chr5:115204352..115206713-chr5:115207529..115209767,2	K562	blood:
23	chr5:115220382..115222331-chr5:115228507..115231029,2	K562	blood:
24	chr5:115200336..115203007-chr5:115203929..115206460,2	K562	blood:
25	chr5:115232531..115235335-chr5:115239466..115241502,2	MCF-7	breast:
26	chr5:115175799..115178442-chr5:115221185..115223278,2	MCF-7	breast:
27	chr5:115169901..115171516-chr5:115224823..115226377,2	K562	blood:

Variant related genes	Relation type
AP3S1	TF binding region
AP3S1	CpG island
ENSG00000145781	chromatin interactions
ENSG00000177879	chromatin interactions
ENSG00000063176	chromatin interactions
ENSG00000145782	chromatin interactions
ENSG00000180917	chromatin interactions
ENSG00000063177	chromatin interactions

Extended variants
information (count: 1281 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1281 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528260526	chr5:115205891-115205892	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs1500270	chr5:115206006-115206007	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs544973129	chr5:115206039-115206040	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs537153247	chr5:115206047-115206048	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs191401076	chr5:115206051-115206052	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs116519935	chr5:115206078-115206079	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs540098609	chr5:115206111-115206112	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs553367727	chr5:115206129-115206130	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs147108040	chr5:115206158-115206159	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs75249068	chr5:115206262-115206263	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs556041187	chr5:115206268-115206269	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs574536205	chr5:115206282-115206283	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs36083750	chr5:115206348-115206349	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs537915601	chr5:115206363-115206364	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs138581904	chr5:115206380-115206381	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs368769387	chr5:115206394-115206395	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs549201431	chr5:115206437-115206438	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs182971807	chr5:115206443-115206444	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs567426401	chr5:115206460-115206461	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs559378107	chr5:115206498-115206499	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs528433616	chr5:115206511-115206512	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs548034952	chr5:115206512-115206513	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs561557562	chr5:115206519-115206520	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs373991041	chr5:115206532-115206533	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs144116047	chr5:115206537-115206538	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs550682478	chr5:115206543-115206544	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs187305385	chr5:115206579-115206580	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs539433682	chr5:115206588-115206589	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs547009668	chr5:115206614-115206615	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs567046779	chr5:115206645-115206646	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs536147030	chr5:115206655-115206656	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs192561015	chr5:115206679-115206680	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs557572140	chr5:115206698-115206699	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs183143496	chr5:115206700-115206701	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs550767139	chr5:115206708-115206709	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs533789271	chr5:115206814-115206815	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs557079559	chr5:115206819-115206820	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs386691416	chr5:115206865-115206866	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs78252365	chr5:115206867-115206868	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs252736	chr5:115206879-115206880	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs187873261	chr5:115206885-115206886	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs573014518	chr5:115206919-115206920	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs138894105	chr5:115206933-115206934	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs11241337	chr5:115206937-115206938	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs192168102	chr5:115206942-115206943	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs544035275	chr5:115206958-115206959	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs566873519	chr5:115206961-115206962	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs564411455	chr5:115206972-115206973	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs184467576	chr5:115206987-115206988	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs534178796	chr5:115206994-115206995	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD
Prostate cancer	22341455	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115185600-115218600	Weak transcription	Lung	lung
2	chr5:115187200-115206600	Weak transcription	Ovary	ovary
3	chr5:115187400-115206200	Weak transcription	Brain Hippocampus Middle	brain
4	chr5:115189800-115218600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr5:115189800-115235800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr5:115190400-115206000	Weak transcription	Primary B cells from cord blood	blood
7	chr5:115191000-115223000	Weak transcription	Right Ventricle	heart
8	chr5:115192400-115207600	Weak transcription	Pancreas	Pancrea
9	chr5:115192800-115206000	Weak transcription	Left Ventricle	heart
10	chr5:115193200-115207400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr5:115193200-115239000	Weak transcription	Gastric	stomach
12	chr5:115193600-115234600	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr5:115194000-115206000	Weak transcription	Fetal Lung	lung
14	chr5:115194000-115206000	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr5:115194000-115206200	Weak transcription	Fetal Kidney	kidney
16	chr5:115194000-115211000	Weak transcription	HepG2	liver
17	chr5:115194200-115206000	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr5:115194200-115206200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr5:115194200-115209000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr5:115194400-115206000	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr5:115194400-115218000	Weak transcription	Fetal Intestine Small	intestine
22	chr5:115194400-115220800	Weak transcription	Rectal Smooth Muscle	rectum
23	chr5:115195000-115206000	Weak transcription	Fetal Intestine Large	intestine
24	chr5:115195200-115206000	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr5:115195200-115206000	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr5:115195200-115206200	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr5:115195400-115209000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr5:115195400-115263200	Weak transcription	Aorta	Aorta
29	chr5:115195600-115205800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr5:115195600-115206000	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr5:115195600-115208600	Weak transcription	Osteobl	bone
32	chr5:115195600-115214600	Weak transcription	HSMMtube	muscle
33	chr5:115195800-115206000	Weak transcription	NHDF-Ad	bronchial
34	chr5:115196000-115206000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr5:115196000-115206000	Weak transcription	Placenta	Placenta
36	chr5:115196000-115211200	Weak transcription	Psoas Muscle	Psoas
37	chr5:115196000-115233600	Weak transcription	Esophagus	oesophagus
38	chr5:115200000-115206000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr5:115200200-115206000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr5:115200200-115209000	Weak transcription	K562	blood
41	chr5:115200400-115208600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr5:115200400-115218200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr5:115200600-115206000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr5:115200600-115209000	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr5:115200600-115209000	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr5:115200600-115213800	Weak transcription	Fetal Heart	heart
47	chr5:115200800-115206400	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr5:115200800-115209000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr5:115200800-115221000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr5:115201000-115218200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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