Variant report

Variant	nsv1015514
Chromosome Location	chr5:37409579-37522074
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:698)
CpG islands
(count:62)
Chromatin interactive
region (count:32)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:698 , 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	chr5:37413045-37413386	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:37435813-37436000	K562	blood:	n/a	chr5:37435891-37435907
3	ARID3A	chr5:37424736-37424788	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:37412949-37413405	K562	blood:	n/a	n/a
5	ARID3A	chr5:37435399-37435833	HepG2	liver:	n/a	n/a
6	ATF1	chr5:37413139-37413402	K562	blood:	n/a	n/a
7	ATF3	chr5:37413096-37413476	K562	blood:	n/a	n/a
8	BACH1	chr5:37512136-37512171	K562	blood:	n/a	n/a
9	BATF	chr5:37413135-37413360	GM12878	blood:	n/a	n/a
10	BCL11A	chr5:37436356-37436593	GM12878	blood:	n/a	n/a
11	BRCA1	chr5:37413063-37413459	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr5:37471796-37472190	K562	blood:	n/a	n/a
13	CBX3	chr5:37481486-37481876	K562	blood:	n/a	n/a
14	CBX3	chr5:37488479-37488841	K562	blood:	n/a	n/a
15	CBX3	chr5:37480974-37481326	K562	blood:	n/a	n/a
16	CBX3	chr5:37481023-37481289	K562	blood:	n/a	n/a
17	CBX3	chr5:37453412-37453631	K562	blood:	n/a	n/a
18	CEBPB	chr5:37444819-37445115	HepG2	liver:	n/a	chr5:37444971-37444982 chr5:37445001-37445012
19	CEBPB	chr5:37481844-37481981	K562	blood:	n/a	chr5:37481876-37481887
20	CEBPB	chr5:37494846-37495179	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr5:37463538-37463865	HepG2	liver:	n/a	chr5:37463690-37463703 chr5:37463692-37463701 chr5:37463690-37463703 chr5:37463692-37463701 chr5:37463690-37463701 chr5:37463692-37463701 chr5:37463691-37463702 chr5:37463692-37463701
22	CEBPB	chr5:37413064-37413458	K562	blood:	n/a	n/a
23	CEBPB	chr5:37436676-37436947	A549	lung:	n/a	chr5:37436833-37436844 chr5:37436832-37436845
24	CEBPB	chr5:37413083-37413456	A549	lung:	n/a	n/a
25	CEBPB	chr5:37474447-37474554	HepG2	liver:	n/a	n/a
26	CEBPB	chr5:37444823-37445171	A549	lung:	n/a	chr5:37444971-37444982 chr5:37445001-37445012
27	CEBPB	chr5:37413145-37413394	HepG2	liver:	n/a	n/a
28	CEBPB	chr5:37463617-37463777	MCF-7	breast:	n/a	chr5:37463690-37463703 chr5:37463692-37463701 chr5:37463690-37463703 chr5:37463692-37463701 chr5:37463690-37463701 chr5:37463692-37463701 chr5:37463691-37463702 chr5:37463692-37463701
29	CEBPB	chr5:37412891-37413491	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr5:37413127-37413467	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr5:37413013-37413479	HCT-116	colon:	n/a	n/a
32	CEBPB	chr5:37413095-37413442	HepG2	liver:	n/a	n/a
33	CEBPB	chr5:37413086-37413440	MCF-7	breast:	n/a	n/a
34	CEBPB	chr5:37503418-37503494	A549	lung:	n/a	n/a
35	CEBPB	chr5:37413140-37413393	K562	blood:	n/a	n/a
36	CEBPB	chr5:37463652-37463834	IMR90	lung:	n/a	chr5:37463690-37463703 chr5:37463692-37463701 chr5:37463690-37463703 chr5:37463692-37463701 chr5:37463690-37463701 chr5:37463692-37463701 chr5:37463691-37463702 chr5:37463692-37463701
37	CEBPB	chr5:37444992-37445006	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr5:37480989-37481283	K562	blood:	n/a	n/a
39	CEBPB	chr5:37463551-37463849	K562	blood:	n/a	chr5:37463690-37463703 chr5:37463692-37463701 chr5:37463690-37463703 chr5:37463692-37463701 chr5:37463690-37463701 chr5:37463692-37463701 chr5:37463691-37463702 chr5:37463692-37463701
40	CEBPB	chr5:37412973-37413503	A549	lung:	n/a	n/a
41	CEBPB	chr5:37493291-37493471	A549	lung:	n/a	n/a
42	CEBPB	chr5:37413166-37413488	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr5:37480974-37481250	K562	blood:	n/a	n/a
44	CEBPB	chr5:37413101-37413470	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPB	chr5:37412995-37413530	MCF-7	breast:	n/a	n/a
46	CEBPB	chr5:37413105-37413436	HepG2	liver:	n/a	n/a
47	CEBPB	chr5:37444828-37445104	IMR90	lung:	n/a	chr5:37444971-37444982 chr5:37445001-37445012
48	CEBPB	chr5:37436665-37437176	IMR90	lung:	n/a	chr5:37436833-37436844 chr5:37436832-37436845
49	CEBPB	chr5:37413144-37413460	A549	lung:	n/a	n/a
50	CEBPB	chr5:37413155-37413362	HepG2	liver:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37484025-37484075	HEK293	kidney:	embryo
2	chr5:37484025-37484075	HEK293	kidney:	embryo
3	chr5:37484025-37484075	HCF	heart:	n/a
4	chr5:37484025-37484075	U87	brain:	n/a
5	chr5:37484025-37484075	HRPEpiC	eye:	n/a
6	chr5:37484025-37484075	GM06990	blood:	n/a
7	chr5:37484025-37484075	PrEC	prostate:	n/a
8	chr5:37484025-37484075	MCF10A-Er-Src	breast:	n/a
9	chr5:37484025-37484075	CMK	blood:	n/a
10	chr5:37484025-37484075	A549	lung:	n/a
11	chr5:37484025-37484075	AoSMC	blood vessel:	n/a
12	chr5:37484025-37484075	GM12892	blood:	n/a
13	chr5:37484025-37484075	Jurkat	blood:	n/a
14	chr5:37484025-37484075	T-47D	breast:	n/a
15	chr5:37484025-37484075	HUVEC	blood vessel:	n/a
16	chr5:37484025-37484075	HMEC	breast:	n/a
17	chr5:37484025-37484075	H1-hESC	embryonic stem cell:	embryo
18	chr5:37484025-37484075	BE2_C	brain:	n/a
19	chr5:37484025-37484075	HCT-116	colon:	n/a
20	chr5:37484025-37484075	NB4	blood:	n/a
21	chr5:37484025-37484075	K562	blood:	n/a
22	chr5:37484025-37484075	GM19239	blood:	n/a
23	chr5:37484025-37484075	ovcar-3	ovarian:	n/a
24	chr5:37484025-37484075	AG04450	lung:	fetal
25	chr5:37484025-37484075	HNPCEpiC	eye:	n/a
26	chr5:37484025-37484075	ProgFib	skin:	n/a
27	chr5:37484025-37484075	AG10803	skin:	n/a
28	chr5:37484025-37484075	HEEpiC	esophagus:	n/a
29	chr5:37484025-37484075	NT2-D1	testis:	n/a
30	chr5:37484025-37484075	PANC-1	pancreas:	n/a
31	chr5:37484025-37484075	ECC-1	luminal epithelium:	n/a
32	chr5:37484025-37484075	GM12891	blood:	n/a
33	chr5:37484025-37484075	GM12878	blood:	n/a
34	chr5:37484025-37484075	AG09319	gingival:	n/a
35	chr5:37484025-37484075	LNCaP	prostate:	n/a
36	chr5:37484025-37484075	Hela-S3	cervix:	n/a
37	chr5:37484025-37484075	BJ	skin:	n/a
38	chr5:37484025-37484075	NHDF-neo	bronchial:	n/a
39	chr5:37484025-37484075	HRE	kidney:	n/a
40	chr5:37484025-37484075	HIPEpiC	eye:	n/a
41	chr5:37484025-37484075	PFSK-1	brain:	n/a
42	chr5:37484025-37484075	SK-N-SH_RA	brain:	n/a
43	chr5:37484025-37484075	NH-A	brain:	n/a
44	chr5:37484025-37484075	Caco-2	colon:	n/a
45	chr5:37484025-37484075	SAEC	small airway:	n/a
46	chr5:37484025-37484075	HCM	heart:	n/a
47	chr5:37484025-37484075	SK-N-MC	brain:	n/a
48	chr5:37484025-37484075	SK-N-SH	brain:	n/a
49	chr5:37484025-37484075	HCPEpiC	choroid plexus:	n/a
50	chr5:37484025-37484075	AG09309	skin:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:37412800..37413850-chr5:37837177..37838175,5	MCF-7	breast:
2	chr5:37412738..37413377-chr5:38194610..38195311,2	MCF-7	breast:
3	chr5:37402668..37405027-chr5:37408741..37410429,2	K562	blood:
4	chr5:37413110..37413637-chr5:37840070..37840640,2	MCF-7	breast:
5	chr5:37438128..37441611-chr5:37451601..37454118,3	K562	blood:
6	chr5:37412783..37413436-chr5:37723453..37724202,2	K562	blood:
7	chr5:37412806..37413850-chr5:37900474..37901433,3	MCF-7	breast:
8	chr5:37423699..37426165-chr5:37428640..37431370,2	MCF-7	breast:
9	chr5:37412825..37413381-chr5:37926629..37927147,2	MCF-7	breast:
10	chr5:37412766..37413683-chr5:37757982..37759001,7	MCF-7	breast:
11	chr5:37423699..37426165-chr5:37428640..37431370,2	MCF-7	breast:
12	chr5:37503334..37505446-chr5:37509179..37510910,2	K562	blood:
13	chr5:37503334..37505446-chr5:37509179..37510910,2	K562	blood:
14	chr5:37412794..37413863-chr5:38192922..38193865,5	K562	blood:
15	chr5:37413098..37413750-chr5:37837537..37838115,2	MCF-7	breast:
16	chr5:37477675..37480288-chr5:37486843..37489829,2	K562	blood:
17	chr5:37412768..37413768-chr5:38192655..38193859,13	MCF-7	breast:
18	chr5:37440538..37443537-chr5:37502324..37504824,2	K562	blood:
19	chr17:61358570..61359089-chr5:37412803..37413392,2	MCF-7	breast:
20	chr5:37509914..37511896-chr5:37518755..37521412,2	K562	blood:
21	chr5:37496762..37498368-chr5:37500019..37501730,2	MCF-7	breast:
22	chr5:37438128..37441611-chr5:37451601..37454118,3	K562	blood:
23	chr5:37413185..37413702-chr5:37723532..37724165,2	MCF-7	breast:
24	chr5:37496762..37498368-chr5:37500019..37501730,2	MCF-7	breast:
25	chr5:37412788..37413557-chr5:38023669..38024455,2	MCF-7	breast:
26	chr5:37412852..37413708-chr5:37554717..37555628,3	MCF-7	breast:
27	chr5:37495029..37495917-chr5:37837475..37838072,2	MCF-7	breast:
28	chr5:37495049..37495731-chr5:37758036..37758591,2	MCF-7	breast:
29	chr5:37488881..37490858-chr5:37567347..37569058,2	K562	blood:
30	chr5:37395673..37397370-chr5:37410862..37413241,2	MCF-7	breast:
31	chr5:37509914..37511896-chr5:37518755..37521412,2	K562	blood:
32	chr5:37440538..37443537-chr5:37502324..37504824,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUP155-5	chr5:37505790-37506959	NONHSAT101066

No data

Variant related genes	Relation type
WDR70	TF binding region
ENSG00000248216	TF binding region
WDR70	CpG island
ENSG00000248216	CpG island
ENSG00000248587	chromatin interactions
ENSG00000082068	chromatin interactions

Extended variants
information (count: 4277 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:4277 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13178300	chr5:37409579-37409580	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs148394885	chr5:37409600-37409601	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs71604863	chr5:37409607-37409608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs70978811	chr5:37409622-37409623	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186488668	chr5:37409669-37409670	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs79114955	chr5:37409670-37409671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373186220	chr5:37409698-37409699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531145237	chr5:37409718-37409719	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572223005	chr5:37409795-37409796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541224910	chr5:37409796-37409797	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370692381	chr5:37409888-37409889	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561205874	chr5:37409903-37409904	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189429349	chr5:37409972-37409973	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181025178	chr5:37410076-37410077	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs116399344	chr5:37410108-37410109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141636144	chr5:37410117-37410118	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576169663	chr5:37410152-37410153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540994023	chr5:37410154-37410155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112303347	chr5:37410164-37410165	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536971740	chr5:37410187-37410188	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555630182	chr5:37410196-37410197	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574119946	chr5:37410257-37410258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs78410900	chr5:37410296-37410297	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186081210	chr5:37410307-37410308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201974668	chr5:37410311-37410312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375941917	chr5:37410317-37410318	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559758009	chr5:37410335-37410336	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs578156898	chr5:37410341-37410342	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375067947	chr5:37410391-37410392	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550146836	chr5:37410402-37410403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545471289	chr5:37410421-37410422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563759705	chr5:37410432-37410433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531132766	chr5:37410433-37410434	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549453130	chr5:37410449-37410450	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565785077	chr5:37410471-37410472	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78650033	chr5:37410499-37410500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs13165813	chr5:37410574-37410575	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs549537193	chr5:37410581-37410582	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs374375267	chr5:37410623-37410624	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375072271	chr5:37410628-37410629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs57985484	chr5:37410691-37410692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563265443	chr5:37410722-37410723	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535655926	chr5:37410866-37410867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539181441	chr5:37410871-37410872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551433796	chr5:37410988-37410989	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532121065	chr5:37411051-37411052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551812864	chr5:37411097-37411098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs79580514	chr5:37411141-37411142	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555227669	chr5:37411233-37411234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567567494	chr5:37411234-37411235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
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
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	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
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
Medulloblastoma	19270706	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
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	21346763	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD

Chromatin state (count:1734 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37379800-37434200	Weak transcription	Small Intestine	intestine
2	chr5:37379800-37444400	Weak transcription	Gastric	stomach
3	chr5:37380000-37427800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr5:37380000-37428200	Weak transcription	Stomach Mucosa	stomach
5	chr5:37380000-37443400	Weak transcription	Colonic Mucosa	Colon
6	chr5:37380200-37420400	Weak transcription	NHDF-Ad	bronchial
7	chr5:37380200-37432600	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr5:37380200-37435000	Weak transcription	Rectal Smooth Muscle	rectum
9	chr5:37380200-37446800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr5:37380200-37446800	Weak transcription	Fetal Brain Male	brain
11	chr5:37380200-37451200	Weak transcription	Right Ventricle	heart
12	chr5:37380400-37434800	Weak transcription	NHLF	lung
13	chr5:37389800-37420000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr5:37390200-37428600	Weak transcription	HMEC	breast
15	chr5:37391000-37411600	Strong transcription	Primary T helper cells fromperipheralblood	blood
16	chr5:37392200-37410600	Strong transcription	Adipose Nuclei	Adipose
17	chr5:37393200-37416800	Weak transcription	NHEK	skin
18	chr5:37393200-37419000	Weak transcription	HUVEC	blood vessel
19	chr5:37393200-37427200	Weak transcription	Esophagus	oesophagus
20	chr5:37393200-37451400	Weak transcription	Pancreas	Pancrea
21	chr5:37393400-37409600	Weak transcription	Aorta	Aorta
22	chr5:37394800-37431800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr5:37395000-37428800	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr5:37395400-37447000	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr5:37396200-37426000	Weak transcription	Primary hematopoietic stem cells	blood
26	chr5:37396200-37429000	Weak transcription	Brain Cingulate Gyrus	brain
27	chr5:37396400-37427200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr5:37396600-37424400	Weak transcription	Fetal Lung	lung
29	chr5:37396800-37454600	Weak transcription	A549	lung
30	chr5:37397000-37412600	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr5:37397200-37416800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr5:37397200-37417400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr5:37397200-37417400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr5:37397200-37419000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr5:37397200-37425200	Weak transcription	Spleen	Spleen
36	chr5:37397200-37446600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr5:37397400-37413000	Strong transcription	Monocytes-CD14+_RO01746	blood
38	chr5:37397600-37410400	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr5:37397600-37411600	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr5:37397600-37424200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr5:37397600-37426000	Weak transcription	Ovary	ovary
42	chr5:37398000-37424400	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr5:37398400-37417400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr5:37398600-37423800	Weak transcription	Lung	lung
45	chr5:37399800-37417000	Weak transcription	Brain Germinal Matrix	brain
46	chr5:37400800-37415400	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr5:37401000-37436200	Weak transcription	K562	blood
48	chr5:37401000-37454000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr5:37401200-37410400	Weak transcription	NH-A	brain
50	chr5:37401200-37410600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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