Variant report

Variant	nsv1026351
Chromosome Location	chr5:178429975-178535309
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:651)
CpG islands
(count:2262)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:651 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:178435793-178435958	K562	blood:	n/a	n/a
2	ARID3A	chr5:178450529-178450765	HepG2	liver:	n/a	n/a
3	ATF1	chr5:178516546-178516874	K562	blood:	n/a	n/a
4	ATF3	chr5:178516536-178516788	K562	blood:	n/a	chr5:178516689-178516699 chr5:178516688-178516703 chr5:178516689-178516702 chr5:178516691-178516711 chr5:178516692-178516702 chr5:178516688-178516701 chr5:178516690-178516701 chr5:178516692-178516700 chr5:178516692-178516699 chr5:178516690-178516701
5	BACH1	chr5:178481413-178481714	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr5:178481513-178481613	K562	blood:	n/a	n/a
7	BATF	chr5:178475729-178476166	GM12878	blood:	n/a	n/a
8	BATF	chr5:178475617-178476112	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:178475632-178476123	GM12878	blood:	n/a	n/a
10	BCL11A	chr5:178475718-178476032	GM12878	blood:	n/a	n/a
11	BHLHE40	chr5:178496356-178496412	K562	blood:	n/a	n/a
12	BHLHE40	chr5:178450583-178450973	K562	blood:	n/a	n/a
13	BRCA1	chr5:178487152-178487471	H1-hESC	embryonic stem cell:	n/a	n/a
14	CCNT2	chr5:178450829-178451180	K562	blood:	n/a	n/a
15	CCNT2	chr5:178516589-178516784	K562	blood:	n/a	n/a
16	CEBPB	chr5:178475566-178475775	HepG2	liver:	n/a	chr5:178475696-178475707
17	CEBPB	chr5:178475745-178475761	A549	lung:	n/a	n/a
18	CEBPB	chr5:178438682-178438878	HepG2	liver:	n/a	chr5:178438753-178438764
19	CEBPB	chr5:178519193-178519255	HepG2	liver:	n/a	chr5:178519229-178519240
20	CEBPB	chr5:178450536-178450937	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr5:178491913-178492012	HepG2	liver:	n/a	chr5:178491980-178491991
22	CHD2	chr5:178450585-178450833	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr5:178450589-178450864	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr5:178487228-178487321	GM12878	blood:	n/a	n/a
25	CHD2	chr5:178487037-178487551	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr5:178471927-178472081	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr5:178450606-178450764	HepG2	liver:	n/a	n/a
28	CREB1	chr5:178450590-178450977	A549	lung:	n/a	n/a
29	CREB1	chr5:178450452-178450978	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr5:178487093-178487507	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr5:178450607-178450769	A549	lung:	n/a	n/a
32	CREB1	chr5:178487134-178487475	H1-hESC	embryonic stem cell:	n/a	n/a
33	CREB1	chr5:178487083-178487670	A549	lung:	n/a	n/a
34	CTCF	chr5:178450563-178450792	Lung_OC	lung:	n/a	n/a
35	CTCF	chr5:178435780-178435930	HEK293	kidney:	n/a	n/a
36	CTCF	chr5:178492866-178492932	GM12878	blood:	n/a	n/a
37	CTCF	chr5:178435780-178435930	HRE	kidney:	n/a	n/a
38	CTCF	chr5:178435759-178435938	K562	blood:	n/a	n/a
39	CTCF	chr5:178504967-178505019	LNCaP	prostate:	n/a	n/a
40	CTCF	chr5:178435752-178435951	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr5:178435800-178435950	HCT-116	colon:	n/a	n/a
42	CTCF	chr5:178435800-178435950	BJ	skin:	n/a	n/a
43	CTCF	chr5:178492740-178492890	HEK293	kidney:	n/a	n/a
44	CTCF	chr5:178435760-178435910	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr5:178487216-178487223	Fibrobl	skin:	n/a	n/a
46	CTCF	chr5:178492819-178492940	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr5:178492859-178492931	MCF-7	breast:	n/a	n/a
48	CTCF	chr5:178523600-178523750	K562	blood:	n/a	n/a
49	CTCF	chr5:178487080-178487230	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr5:178450934-178450999	Spleen_OC	spleen:	n/a	n/a

(count:2262 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178447119-178447169	SK-N-SH_RA	brain:	n/a
2	chr5:178447119-178447169	HEEpiC	esophagus:	n/a
3	chr5:178488100-178488150	SK-N-MC	brain:	n/a
4	chr5:178487382-178487432	H1-hESC	embryonic stem cell:	embryo
5	chr5:178487310-178487360	HCPEpiC	choroid plexus:	n/a
6	chr5:178447119-178447169	SK-N-SH_RA	brain:	n/a
7	chr5:178447119-178447169	HEEpiC	esophagus:	n/a
8	chr5:178488100-178488150	SK-N-MC	brain:	n/a
9	chr5:178487382-178487432	H1-hESC	embryonic stem cell:	embryo
10	chr5:178487310-178487360	HCPEpiC	choroid plexus:	n/a
11	chr5:178489201-178489251	Jurkat	blood:	n/a
12	chr5:178488025-178488075	HUVEC	blood vessel:	n/a
13	chr5:178488100-178488150	AG09309	skin:	n/a
14	chr5:178487716-178487766	T-47D	breast:	n/a
15	chr5:178451176-178451226	AG10803	skin:	n/a
16	chr5:178489201-178489251	AG09309	skin:	n/a
17	chr5:178489201-178489251	GM19239	blood:	n/a
18	chr5:178478137-178478187	BJ	skin:	n/a
19	chr5:178451078-178451128	HAEpiC	amniotic membrane:	n/a
20	chr5:178487384-178487434	Hela-S3	cervix:	n/a
21	chr5:178487123-178487173	HRE	kidney:	n/a
22	chr5:178478236-178478286	RPTEC	kidney:	n/a
23	chr5:178452979-178453029	K562	blood:	n/a
24	chr5:178479627-178479677	MCF10A-Er-Src	breast:	n/a
25	chr5:178487826-178487876	HMEC	breast:	n/a
26	chr5:178487826-178487876	A549	lung:	n/a
27	chr5:178478236-178478286	Hepatocyte	liver:	n/a
28	chr5:178487465-178487515	HRPEpiC	eye:	n/a
29	chr5:178450763-178450813	AG09309	skin:	n/a
30	chr5:178487410-178487460	RPTEC	kidney:	n/a
31	chr5:178451078-178451128	HepG2	liver:	n/a
32	chr5:178487382-178487432	SK-N-SH	brain:	n/a
33	chr5:178450457-178450507	HCPEpiC	choroid plexus:	n/a
34	chr5:178450595-178450645	T-47D	breast:	n/a
35	chr5:178487485-178487535	HUVEC	blood vessel:	n/a
36	chr5:178488025-178488075	HNPCEpiC	eye:	n/a
37	chr5:178447119-178447169	MCF10A-Er-Src	breast:	n/a
38	chr5:178450506-178450556	Hela-S3	cervix:	n/a
39	chr5:178487465-178487515	HPAEpiC	pulmonary alveolar:	n/a
40	chr5:178479627-178479677	U87	brain:	n/a
41	chr5:178479627-178479677	GM06990	blood:	n/a
42	chr5:178478236-178478286	ECC-1	luminal epithelium:	n/a
43	chr5:178487123-178487173	HIPEpiC	eye:	n/a
44	chr5:178450506-178450556	GM12891	blood:	n/a
45	chr5:178487382-178487432	HCT-116	colon:	n/a
46	chr5:178487716-178487766	SKMC	muscle:	n/a
47	chr5:178487465-178487515	A549	lung:	n/a
48	chr5:178461226-178461276	AG10803	skin:	n/a
49	chr5:178489987-178490037	HPAEpiC	pulmonary alveolar:	n/a
50	chr5:178487826-178487876	AG10803	skin:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:178433803..178435714-chr5:178438411..178439911,2	MCF-7	breast:
2	chr5:178433803..178435714-chr5:178438411..178439911,2	MCF-7	breast:
3	chr5:178449642..178452190-chr5:178454798..178457420,2	MCF-7	breast:
4	chr5:178487018..178488525-chr5:178506434..178508036,2	MCF-7	breast:
5	chr5:178483088..178485401-chr5:178485853..178487367,2	MCF-7	breast:
6	chr5:178482671..178485018-chr5:178485499..178487463,2	MCF-7	breast:
7	chr5:178460496..178462361-chr5:178485766..178487782,2	MCF-7	breast:
8	chr5:178483141..178486203-chr5:178488375..178491712,3	MCF-7	breast:
9	chr5:178450567..178452511-chr5:178457855..178459672,2	MCF-7	breast:
10	chr5:178488576..178490984-chr5:178494204..178495758,2	MCF-7	breast:
11	chr5:178490747..178493004-chr5:178499608..178501771,2	K562	blood:
12	chr5:178508305..178510572-chr5:178515516..178518368,2	K562	blood:
13	chr5:178464139..178466564-chr5:178484015..178485914,2	K562	blood:
14	chr5:178451565..178453293-chr5:178455866..178457677,2	MCF-7	breast:
15	chr5:178483088..178485401-chr5:178485853..178487367,2	MCF-7	breast:
16	chr5:178286798..178288918-chr5:178487242..178488938,2	MCF-7	breast:
17	chr5:178487796..178490140-chr5:178490313..178493225,2	MCF-7	breast:
18	chr5:178427434..178429147-chr5:178457164..178458750,2	K562	blood:
19	chr5:178488576..178490984-chr5:178494204..178495758,2	MCF-7	breast:
20	chr5:178464139..178466564-chr5:178484015..178485914,2	K562	blood:
21	chr5:178483751..178486234-chr5:178558590..178560353,2	MCF-7	breast:
22	chr5:178451565..178453293-chr5:178455866..178457677,2	MCF-7	breast:
23	chr5:178488531..178490916-chr5:178493267..178496128,2	MCF-7	breast:
24	chr5:178490747..178493004-chr5:178499608..178501771,2	K562	blood:
25	chr5:178486677..178489431-chr5:178490895..178493650,2	MCF-7	breast:
26	chr5:178483141..178486203-chr5:178488375..178491712,3	MCF-7	breast:
27	chr5:178488531..178490916-chr5:178493267..178496128,2	MCF-7	breast:
28	chr5:178445660..178448153-chr5:178448435..178450460,2	MCF-7	breast:
29	chr5:178450308..178453089-chr5:178453235..178455700,3	MCF-7	breast:
30	chr5:178487796..178490140-chr5:178490313..178493225,2	MCF-7	breast:
31	chr5:178445660..178448153-chr5:178448435..178450460,2	MCF-7	breast:
32	chr5:178256899..178257517-chr5:178489612..178490272,2	K562	blood:
33	chr5:178413020..178415263-chr5:178437852..178440591,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000253144	TF binding region
ENSG00000254158	TF binding region
ZNF879	TF binding region
ZNF354C	TF binding region
ENSG00000253144	CpG island
ENSG00000254158	CpG island
ZNF879	CpG island
ZNF354C	CpG island
ENSG00000253144	chromatin interactions
ENSG00000113262	chromatin interactions
ENSG00000178338	chromatin interactions
ENSG00000177932	chromatin interactions
ENSG00000234284	chromatin interactions

Extended variants
information (count: 3097 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:3097 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553720193	chr5:178436215-178436216	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs569343087	chr5:178436240-178436241	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs565879978	chr5:178436245-178436246	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs539324162	chr5:178436330-178436331	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs113132927	chr5:178436357-178436358	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs575588929	chr5:178436371-178436372	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs151309114	chr5:178437885-178437886	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs563097318	chr5:178437958-178437959	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs7710552	chr5:178437979-178437980	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs548857856	chr5:178438029-178438030	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs567599209	chr5:178438042-178438043	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs7711801	chr5:178438044-178438045	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs116089462	chr5:178438066-178438067	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs113507219	chr5:178438077-178438078	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs538711517	chr5:178438078-178438079	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs552352644	chr5:178438165-178438166	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs570219351	chr5:178438166-178438167	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs144326070	chr5:178438175-178438176	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs183364507	chr5:178438179-178438180	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs574302669	chr5:178438217-178438218	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs112035485	chr5:178438251-178438252	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs116329556	chr5:178438301-178438302	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs577636847	chr5:178438303-178438304	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs199687400	chr5:178438304-178438305	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs374012658	chr5:178438305-178438306	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs149649292	chr5:178438312-178438313	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs57893042	chr5:178438322-178438323	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs545059320	chr5:178438355-178438356	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs563481380	chr5:178438439-178438440	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs530616923	chr5:178438484-178438485	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs377616555	chr5:178438496-178438497	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs542442749	chr5:178438505-178438506	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs561011129	chr5:178438506-178438507	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs528355500	chr5:178438542-178438543	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs546603628	chr5:178438568-178438569	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs571179219	chr5:178438569-178438570	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs188823145	chr5:178438597-178438598	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs550685123	chr5:178438611-178438612	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs192701816	chr5:178438640-178438641	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs35205217	chr5:178438643-178438644	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs537619000	chr5:178438646-178438647	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs397765329	chr5:178438649-178438650	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs73805393	chr5:178438650-178438651	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs568142599	chr5:178438654-178438655	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs77436322	chr5:178438656-178438657	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs187051659	chr5:178438660-178438661	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs530640732	chr5:178438691-178438692	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs577605805	chr5:178438767-178438768	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs545048838	chr5:178438778-178438779	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs557015295	chr5:178438809-178438810	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	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
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
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1899 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178436200-178436400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr5:178439600-178440000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
3	chr5:178442200-178443200	ZNF genes & repeats	Liver	Liver
4	chr5:178448400-178450200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:178449600-178449800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr5:178449600-178451600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr5:178449800-178450000	ZNF genes & repeats	Liver	Liver
8	chr5:178449800-178450200	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr5:178449800-178450200	Enhancers	HUVEC	blood vessel
10	chr5:178449800-178451000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
11	chr5:178449800-178451200	Active TSS	Brain Anterior Caudate	brain
12	chr5:178449800-178451200	Active TSS	Skeletal Muscle Male	skeletal muscle
13	chr5:178449800-178451400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr5:178449800-178451400	Active TSS	Skeletal Muscle Female	skeletal muscle
15	chr5:178449800-178451600	Active TSS	ES-I3 Cell Line	embryonic stem cell
16	chr5:178449800-178451600	Active TSS	H1 Cell Line	embryonic stem cell
17	chr5:178449800-178451600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr5:178449800-178451600	Active TSS	Duodenum Smooth Muscle	Duodenum
19	chr5:178449800-178451800	Active TSS	HMEC	breast
20	chr5:178449800-178452000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr5:178449800-178452000	Active TSS	Psoas Muscle	Psoas
22	chr5:178450000-178450200	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr5:178450000-178450200	Bivalent/Poised TSS	Primary B cells from cord blood	blood
24	chr5:178450000-178450200	Enhancers	Primary B cells from peripheral blood	blood
25	chr5:178450000-178450200	Active TSS	Primary T cells fromperipheralblood	blood
26	chr5:178450000-178450200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr5:178450000-178450200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr5:178450000-178450200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr5:178450000-178450200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
30	chr5:178450000-178450200	Active TSS	Fetal Muscle Trunk	muscle
31	chr5:178450000-178451000	Active TSS	Cortex derived primary cultured neurospheres	brain
32	chr5:178450000-178451200	Active TSS	HUES64 Cell Line	embryonic stem cell
33	chr5:178450000-178451200	Active TSS	Adipose Nuclei	Adipose
34	chr5:178450000-178451200	Active TSS	Fetal Brain Female	brain
35	chr5:178450000-178451400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr5:178450000-178451600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr5:178450000-178451600	Active TSS	Pancreatic Islets	Pancreatic Islet
38	chr5:178450000-178451600	Active TSS	Fetal Stomach	stomach
39	chr5:178450000-178451600	Active TSS	Right Atrium	heart
40	chr5:178450000-178451800	Active TSS	H9 Cell Line	embryonic stem cell
41	chr5:178450000-178452200	Active TSS	Duodenum Mucosa	Duodenum
42	chr5:178450000-178452200	Active TSS	Fetal Kidney	kidney
43	chr5:178450200-178450400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr5:178450200-178450400	Active TSS	Primary T helper cells fromperipheralblood	blood
45	chr5:178450200-178450400	Flanking Active TSS	Brain Germinal Matrix	brain
46	chr5:178450200-178450400	Flanking Active TSS	Esophagus	oesophagus
47	chr5:178450200-178450400	Flanking Active TSS	Fetal Muscle Leg	muscle
48	chr5:178450200-178450400	Flanking Active TSS	Ovary	ovary
49	chr5:178450200-178450600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
50	chr5:178450200-178450600	Flanking Active TSS	Primary B cells from peripheral blood	blood

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