Variant report

Variant	nsv880627
Chromosome Location	chr5:41966551-42087954
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	chr5:42074423-42074897	HepG2	liver:	n/a	n/a
2	ATF1	chr5:41998998-41999157	K562	blood:	n/a	n/a
3	ATF1	chr5:41974136-41974295	K562	blood:	n/a	n/a
4	ATF2	chr5:42021889-42022441	GM12878	blood:	n/a	n/a
5	ATF2	chr5:42021932-42022393	GM12878	blood:	n/a	n/a
6	BACH1	chr5:42037569-42038065	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr5:41981051-41981251	K562	blood:	n/a	n/a
8	BATF	chr5:42022041-42022338	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:42021998-42022324	GM12878	blood:	n/a	n/a
10	CCNT2	chr5:42035889-42036029	K562	blood:	n/a	n/a
11	CEBPB	chr5:42017455-42017724	HepG2	liver:	n/a	chr5:42017600-42017611
12	CEBPB	chr5:41986086-41986341	K562	blood:	n/a	chr5:41986226-41986235 chr5:41986226-41986235 chr5:41986226-41986235 chr5:41986224-41986237
13	CEBPB	chr5:42076484-42076847	HepG2	liver:	n/a	chr5:42076669-42076680
14	CEBPB	chr5:42065561-42065755	K562	blood:	n/a	chr5:42065646-42065657
15	CEBPB	chr5:42065575-42065745	HepG2	liver:	n/a	chr5:42065646-42065657
16	CEBPB	chr5:42074366-42074840	HepG2	liver:	n/a	n/a
17	CEBPB	chr5:41967596-41967796	HepG2	liver:	n/a	n/a
18	CEBPB	chr5:42065595-42065744	H1-hESC	embryonic stem cell:	n/a	chr5:42065646-42065657
19	CEBPB	chr5:42073436-42073703	HepG2	liver:	n/a	n/a
20	CEBPB	chr5:41974102-41974329	K562	blood:	n/a	n/a
21	CEBPB	chr5:42063248-42063513	IMR90	lung:	n/a	n/a
22	CEBPB	chr5:41986051-41986410	IMR90	lung:	n/a	chr5:41986226-41986235 chr5:41986226-41986235 chr5:41986226-41986235 chr5:41986224-41986237
23	CEBPB	chr5:41981286-41981511	HepG2	liver:	n/a	chr5:41981401-41981412
24	CEBPB	chr5:42017466-42017794	K562	blood:	n/a	chr5:42017600-42017611
25	CEBPB	chr5:42049998-42050125	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr5:41986078-41986410	A549	lung:	n/a	chr5:41986226-41986235 chr5:41986226-41986235 chr5:41986226-41986235 chr5:41986224-41986237
27	CEBPB	chr5:41985866-41986431	K562	blood:	n/a	chr5:41986226-41986235 chr5:41986226-41986235 chr5:41986226-41986235 chr5:41986224-41986237
28	CEBPB	chr5:42076630-42076722	K562	blood:	n/a	chr5:42076669-42076680
29	CEBPB	chr5:41986083-41986403	Hela-S3	cervix:	n/a	chr5:41986226-41986235 chr5:41986226-41986235 chr5:41986226-41986235 chr5:41986224-41986237
30	CEBPB	chr5:42017607-42017805	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr5:41986104-41986414	H1-hESC	embryonic stem cell:	n/a	chr5:41986226-41986235 chr5:41986226-41986235 chr5:41986226-41986235 chr5:41986224-41986237
32	CEBPB	chr5:41986067-41986411	HepG2	liver:	n/a	chr5:41986226-41986235 chr5:41986226-41986235 chr5:41986226-41986235 chr5:41986224-41986237
33	CEBPB	chr5:42076651-42076774	Hela-S3	cervix:	n/a	chr5:42076669-42076680
34	CEBPB	chr5:41986037-41986400	K562	blood:	n/a	chr5:41986226-41986235 chr5:41986226-41986235 chr5:41986226-41986235 chr5:41986224-41986237
35	CEBPB	chr5:42076505-42076846	A549	lung:	n/a	chr5:42076669-42076680
36	CREB1	chr5:42021941-42022354	GM12878	blood:	n/a	n/a
37	CREB1	chr5:42021988-42022418	GM12878	blood:	n/a	n/a
38	CTCF	chr5:42005780-42005930	GM12864	blood:	n/a	chr5:42005837-42005858 chr5:42005836-42005852 chr5:42005835-42005853
39	CTCF	chr5:42005780-42005930	SAEC	small airway:	n/a	chr5:42005837-42005858 chr5:42005836-42005852 chr5:42005835-42005853
40	CTCF	chr5:42005685-42005977	Spleen_OC	spleen:	n/a	chr5:42005837-42005858 chr5:42005836-42005852 chr5:42005835-42005853
41	CTCF	chr5:42057398-42057697	GM19239	blood:	n/a	chr5:42057463-42057471 chr5:42057526-42057542 chr5:42057527-42057540 chr5:42057520-42057541 chr5:42057525-42057543
42	CTCF	chr5:42005760-42005910	HEK293	kidney:	n/a	chr5:42005837-42005858 chr5:42005836-42005852 chr5:42005835-42005853
43	CTCF	chr5:42057460-42057610	HPF	lung:	n/a	chr5:42057463-42057471 chr5:42057526-42057542 chr5:42057527-42057540 chr5:42057520-42057541 chr5:42057525-42057543
44	CTCF	chr5:41968540-41968690	HMF	breast:	n/a	chr5:41968629-41968638 chr5:41968626-41968644
45	CTCF	chr5:42047980-42048130	K562	blood:	n/a	n/a
46	CTCF	chr5:41968619-41968672	Gliobla	brain:	n/a	chr5:41968629-41968638 chr5:41968626-41968644
47	CTCF	chr5:42005720-42005870	RPTEC	kidney:	n/a	chr5:42005837-42005858 chr5:42005836-42005852 chr5:42005835-42005853
48	CTCF	chr5:42005720-42006010	GM12870	blood:	n/a	chr5:42005837-42005858 chr5:42005836-42005852 chr5:42005835-42005853
49	CTCF	chr5:41968500-41968650	Hela-S3	cervix:	n/a	chr5:41968629-41968638 chr5:41968626-41968644
50	CTCF	chr5:42057480-42057630	GM12874	blood:	n/a	chr5:42057526-42057542 chr5:42057527-42057540 chr5:42057520-42057541 chr5:42057525-42057543

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:41968459-41968509	HCF	heart:	n/a
2	chr5:41968441-41968491	CMK	blood:	n/a
3	chr5:41968459-41968509	AG04449	skin:	fetal
4	chr5:41968376-41968426	SAEC	small airway:	n/a
5	chr5:41968459-41968509	AoSMC	blood vessel:	n/a
6	chr5:41968376-41968426	GM12892	blood:	n/a
7	chr5:41968459-41968509	HPAEpiC	pulmonary alveolar:	n/a
8	chr5:41968441-41968491	AG09309	skin:	n/a
9	chr5:41968376-41968426	NH-A	brain:	n/a
10	chr5:41968441-41968491	HAEpiC	amniotic membrane:	n/a
11	chr5:41968459-41968509	MCF10A-Er-Src	breast:	n/a
12	chr5:41968376-41968426	HCM	heart:	n/a
13	chr5:41968441-41968491	PANC-1	pancreas:	n/a
14	chr5:41968376-41968426	K562	blood:	n/a
15	chr5:41968376-41968426	T-47D	breast:	n/a
16	chr5:41968459-41968509	NH-A	brain:	n/a
17	chr5:41968441-41968491	Hepatocyte	liver:	n/a
18	chr5:41968441-41968491	LNCaP	prostate:	n/a
19	chr5:41968459-41968509	IMR90	lung:	fetal
20	chr5:41968376-41968426	BJ	skin:	n/a
21	chr5:41968459-41968509	A549	lung:	n/a
22	chr5:41968441-41968491	AG04449	skin:	fetal
23	chr5:41968459-41968509	BJ	skin:	n/a
24	chr5:41968376-41968426	BE2_C	brain:	n/a
25	chr5:41968459-41968509	GM06990	blood:	n/a
26	chr5:41968459-41968509	SK-N-SH	brain:	n/a
27	chr5:41968459-41968509	K562	blood:	n/a
28	chr5:41968459-41968509	LNCaP	prostate:	n/a
29	chr5:41968441-41968491	T-47D	breast:	n/a
30	chr5:41968459-41968509	GM19239	blood:	n/a
31	chr5:41968376-41968426	AG04450	lung:	fetal
32	chr5:41968376-41968426	IMR90	lung:	fetal
33	chr5:41968376-41968426	A549	lung:	n/a
34	chr5:41968459-41968509	AG09319	gingival:	n/a
35	chr5:41968376-41968426	NHDF-neo	bronchial:	n/a
36	chr5:41968441-41968491	GM12892	blood:	n/a
37	chr5:41968441-41968491	U87	brain:	n/a
38	chr5:41968459-41968509	PFSK-1	brain:	n/a
39	chr5:41968376-41968426	PFSK-1	brain:	n/a
40	chr5:41968459-41968509	Caco-2	colon:	n/a
41	chr5:41968376-41968426	HNPCEpiC	eye:	n/a
42	chr5:41968376-41968426	PrEC	prostate:	n/a
43	chr5:41968376-41968426	MCF-7	breast:	n/a
44	chr5:41968459-41968509	ECC-1	luminal epithelium:	n/a
45	chr5:41968376-41968426	U87	brain:	n/a
46	chr5:41968376-41968426	AG04449	skin:	fetal
47	chr5:41968441-41968491	BJ	skin:	n/a
48	chr5:41968376-41968426	PANC-1	pancreas:	n/a
49	chr5:41968459-41968509	SAEC	small airway:	n/a
50	chr5:41968459-41968509	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:41978267..41980483-chr5:41985241..41987652,2	K562	blood:
2	chr5:42005693..42007368-chr5:42011421..42013927,2	MCF-7	breast:
3	chr5:41978267..41980483-chr5:41985241..41987652,2	K562	blood:
4	chr5:42051426..42053654-chr5:42055217..42057669,2	K562	blood:
5	chr5:41843846..41845908-chr5:42054612..42056725,2	K562	blood:
6	chr5:41925201..41926819-chr5:41999709..42001806,2	K562	blood:
7	chr5:41924690..41926858-chr5:42021925..42024916,2	K562	blood:
8	chr5:41924904..41925767-chr5:42005339..42006286,4	MCF-7	breast:
9	chr5:41964165..41967064-chr5:41969596..41972002,2	K562	blood:
10	chr5:41924384..41927117-chr5:42005549..42007741,2	K562	blood:
11	chr5:42011659..42014498-chr5:42016092..42018930,3	K562	blood:
12	chr5:41862125..41865078-chr5:42002913..42005308,2	K562	blood:
13	chr5:42037141..42039596-chr5:42040271..42043042,2	MCF-7	breast:
14	chr5:42051426..42053654-chr5:42055217..42057669,2	K562	blood:
15	chr5:42057339..42057915-chr5:42889168..42890099,2	K562	blood:
16	chr5:41856847..41857569-chr5:42057071..42057972,2	MCF-7	breast:
17	chr5:41859110..41859726-chr5:42056831..42057996,3	K562	blood:
18	chr5:42010842..42015595-chr5:42016092..42019954,4	K562	blood:
19	chr5:41902588..41905209-chr5:42048616..42051351,2	K562	blood:
20	chr5:41966817..41969777-chr5:41986218..41988473,2	K562	blood:
21	chr5:42058478..42060752-chr5:42063665..42066653,2	K562	blood:
22	chr5:42058478..42060752-chr5:42063665..42066653,2	K562	blood:
23	chr5:42010842..42015595-chr5:42016092..42019954,4	K562	blood:
24	chr5:41964165..41967064-chr5:41969596..41972002,2	K562	blood:
25	chr5:41856393..41857351-chr5:42005402..42006192,2	MCF-7	breast:
26	chr5:42005538..42006287-chr5:42057068..42058036,3	MCF-7	breast:
27	chr5:41856094..41857973-chr5:42056939..42058102,22	K562	blood:
28	chr5:42011659..42014498-chr5:42016092..42018930,3	K562	blood:
29	chr5:42005538..42006287-chr5:42057068..42058036,3	MCF-7	breast:
30	chr5:42037141..42039596-chr5:42040271..42043042,2	MCF-7	breast:
31	chr5:42005693..42007368-chr5:42011421..42013927,2	MCF-7	breast:
32	chr14:39638324..39641258-chr5:42070731..42072523,2	MCF-7	breast:

Variant related genes	Relation type
MTHFD2P6	TF binding region
ENSG00000199487	TF binding region
MTHFD2P6	CpG island
ENSG00000199487	CpG island
ENSG00000151876	chromatin interactions
ENSG00000205765	chromatin interactions
ENSG00000249266	chromatin interactions
ENSG00000182400	chromatin interactions

Extended variants
information (count: 2316 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:2316 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535613471	chr5:41967453-41967454	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs554221407	chr5:41967459-41967460	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs115960868	chr5:41967479-41967480	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs532827358	chr5:41967496-41967497	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs376313191	chr5:41967498-41967499	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs185076622	chr5:41967567-41967568	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs372804157	chr5:41967617-41967618	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs147138047	chr5:41967672-41967673	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs148203251	chr5:41967690-41967691	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs371741345	chr5:41967693-41967694	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs117933486	chr5:41967702-41967703	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs536458337	chr5:41967704-41967705	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs568394521	chr5:41968097-41968098	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs139102563	chr5:41968101-41968102	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs547598025	chr5:41968131-41968132	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs573576903	chr5:41968155-41968156	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs374917555	chr5:41968157-41968158	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs114698992	chr5:41968177-41968178	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs539261298	chr5:41968194-41968195	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs557484110	chr5:41968197-41968198	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs569512405	chr5:41968260-41968261	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs536987857	chr5:41968378-41968379	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs9885123	chr5:41968392-41968393	Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs187665104	chr5:41968414-41968415	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs35066804	chr5:41968429-41968430	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs144077414	chr5:41968431-41968432	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs192482567	chr5:41968432-41968433	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs577765674	chr5:41968448-41968449	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs545120195	chr5:41968478-41968479	Inactive region	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
30	rs146001491	chr5:41968544-41968545	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs201804786	chr5:41968598-41968599	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs377416350	chr5:41968751-41968752	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs184949499	chr5:41968780-41968781	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs531916715	chr5:41968795-41968796	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs200306157	chr5:41968811-41968812	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs552987131	chr5:41968815-41968816	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs74360444	chr5:41972387-41972388	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs548288694	chr5:41972425-41972426	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs566197986	chr5:41972437-41972438	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs186274432	chr5:41972457-41972458	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs75687258	chr5:41978667-41978668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191787333	chr5:41978708-41978709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs140743402	chr5:41978792-41978793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs554198200	chr5:41978804-41978805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531986073	chr5:41978864-41978865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs550666436	chr5:41979067-41979068	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs200749726	chr5:41979082-41979083	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs549201936	chr5:41979083-41979084	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs568818780	chr5:41979086-41979087	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs10076789	chr5:41979105-41979106	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Hepatocellular carcinoma	18929564	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:41968000-41968400	Enhancers	Placenta	Placenta
2	chr5:41978600-41979000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr5:41978800-41979800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr5:41979000-41979400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr5:41979000-41979600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr5:41979000-41979600	Enhancers	HSMM	muscle
7	chr5:41979000-41979800	Enhancers	HSMMtube	muscle
8	chr5:41979400-41979800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr5:41979600-41980000	Enhancers	Aorta	Aorta
10	chr5:41984600-41985000	Enhancers	Aorta	Aorta
11	chr5:41986600-41986800	Bivalent Enhancer	HSMMtube	muscle
12	chr5:41990400-41991200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr5:41990400-41991600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr5:41991000-41991200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr5:41991600-41995000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr5:41995000-41995600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr5:41995000-41996000	Enhancers	Liver	Liver
18	chr5:42005800-42006600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr5:42006600-42007600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr5:42007600-42008800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr5:42008800-42014400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr5:42013400-42015600	Enhancers	Liver	Liver
23	chr5:42013600-42014000	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr5:42014400-42016400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr5:42014800-42016600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr5:42015200-42016400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr5:42015200-42016600	Enhancers	HSMM	muscle
28	chr5:42015200-42016600	Enhancers	HSMMtube	muscle
29	chr5:42015400-42015800	Enhancers	NHLF	lung
30	chr5:42015400-42016200	Enhancers	NH-A	brain
31	chr5:42015400-42016400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr5:42015400-42016600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr5:42015400-42016600	Enhancers	NHDF-Ad	bronchial
34	chr5:42015600-42016000	Bivalent Enhancer	Liver	Liver
35	chr5:42015600-42016400	Enhancers	Muscle Satellite Cultured Cells	--
36	chr5:42016000-42016200	Enhancers	Liver	Liver
37	chr5:42016200-42022200	Weak transcription	NH-A	brain
38	chr5:42016400-42020400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr5:42016400-42021000	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr5:42016600-42020600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr5:42016600-42020600	Weak transcription	HSMMtube	muscle
42	chr5:42016600-42020800	Weak transcription	HSMM	muscle
43	chr5:42016600-42021000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr5:42020400-42023800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr5:42020600-42022200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr5:42020600-42022400	Enhancers	HSMMtube	muscle
47	chr5:42020800-42021200	Enhancers	H1 Cell Line	embryonic stem cell
48	chr5:42020800-42021200	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr5:42020800-42021400	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr5:42020800-42021400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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