Variant report

Variant	nsv882204
Chromosome Location	chr5:74811497-74856142
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:273)
CpG islands
(count:61)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:273 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:74819121-74819443	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:74812604-74812638	K562	blood:	n/a	n/a
3	ARID3A	chr5:74814259-74814285	K562	blood:	n/a	n/a
4	ATF2	chr5:74819795-74820370	GM12878	blood:	n/a	n/a
5	ATF2	chr5:74819875-74820317	GM12878	blood:	n/a	n/a
6	BATF	chr5:74819848-74820276	GM12878	blood:	n/a	chr5:74820117-74820127 chr5:74820113-74820123
7	BATF	chr5:74819890-74820272	GM12878	blood:	n/a	chr5:74820117-74820127 chr5:74820113-74820123
8	BATF	chr5:74822009-74822205	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:74819918-74820233	GM12878	blood:	n/a	n/a
10	BCLAF1	chr5:74819810-74820284	GM12878	blood:	n/a	n/a
11	BCLAF1	chr5:74819857-74820282	GM12878	blood:	n/a	n/a
12	BRCA1	chr5:74818279-74818351	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr5:74817027-74817318	K562	blood:	n/a	n/a
14	CBX3	chr5:74816956-74817762	K562	blood:	n/a	n/a
15	CBX3	chr5:74817009-74817397	HCT-116	colon:	n/a	n/a
16	CEBPB	chr5:74818420-74818788	A549	lung:	n/a	chr5:74818555-74818566
17	CEBPB	chr5:74848312-74848409	K562	blood:	n/a	n/a
18	CEBPB	chr5:74819823-74820008	K562	blood:	n/a	n/a
19	CEBPB	chr5:74831987-74832299	K562	blood:	n/a	n/a
20	CEBPB	chr5:74832035-74832295	HepG2	liver:	n/a	n/a
21	CEBPB	chr5:74819770-74820410	GM12878	blood:	n/a	n/a
22	CEBPB	chr5:74848200-74848508	IMR90	lung:	n/a	n/a
23	CEBPB	chr5:74818399-74818725	Hela-S3	cervix:	n/a	chr5:74818555-74818566
24	CEBPB	chr5:74819136-74819467	HepG2	liver:	n/a	n/a
25	CEBPB	chr5:74819947-74820171	GM12878	blood:	n/a	n/a
26	CEBPB	chr5:74818388-74818744	IMR90	lung:	n/a	chr5:74818555-74818566
27	CEBPB	chr5:74841366-74841566	K562	blood:	n/a	n/a
28	CEBPB	chr5:74819145-74819534	MCF-7	breast:	n/a	n/a
29	CEBPB	chr5:74834257-74834302	A549	lung:	n/a	chr5:74834262-74834275 chr5:74834262-74834273
30	CEBPB	chr5:74854752-74854867	HepG2	liver:	n/a	n/a
31	CEBPB	chr5:74834106-74834416	IMR90	lung:	n/a	chr5:74834262-74834275 chr5:74834262-74834273
32	CEBPB	chr5:74818376-74818746	K562	blood:	n/a	chr5:74818555-74818566
33	CEBPB	chr5:74854768-74854933	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr5:74818413-74818736	HepG2	liver:	n/a	chr5:74818555-74818566
35	CEBPB	chr5:74818466-74818684	A549	lung:	n/a	chr5:74818555-74818566
36	CEBPB	chr5:74818438-74818707	H1-hESC	embryonic stem cell:	n/a	chr5:74818555-74818566
37	CEBPB	chr5:74848219-74848461	A549	lung:	n/a	n/a
38	CREB1	chr5:74819891-74820498	GM12878	blood:	n/a	n/a
39	CTCF	chr5:74832982-74833014	GM12878	blood:	n/a	n/a
40	CTCF	chr5:74832916-74833027	MCF-7	breast:	n/a	n/a
41	CTCF	chr5:74832939-74832983	NHEK	skin:	n/a	n/a
42	CTCF	chr5:74832910-74833001	MCF-7	breast:	n/a	n/a
43	CTCF	chr5:74824900-74825050	GM12870	blood:	n/a	n/a
44	CTCF	chr5:74853260-74853410	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr5:74832951-74832992	Fibrobl	skin:	n/a	n/a
46	CTCF	chr5:74832928-74833029	MCF-7	breast:	n/a	n/a
47	CTCF	chr5:74832916-74833013	MCF-7	breast:	n/a	n/a
48	CTCF	chr5:74832925-74833035	MCF-7	breast:	n/a	n/a
49	CTCF	chr5:74824480-74824630	GM12870	blood:	n/a	n/a
50	CTCF	chr5:74832935-74833014	A549	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:74833385-74833435	SAEC	small airway:	n/a
2	chr5:74833385-74833435	AG09319	gingival:	n/a
3	chr5:74833385-74833435	HRPEpiC	eye:	n/a
4	chr5:74833385-74833435	AG10803	skin:	n/a
5	chr5:74833385-74833435	HMEC	breast:	n/a
6	chr5:74833385-74833435	MCF-7	breast:	n/a
7	chr5:74833385-74833435	GM19239	blood:	n/a
8	chr5:74833385-74833435	HL-60	blood:	n/a
9	chr5:74833385-74833435	AG09309	skin:	n/a
10	chr5:74833385-74833435	Caco-2	colon:	n/a
11	chr5:74833385-74833435	GM12892	blood:	n/a
12	chr5:74833385-74833435	GM06990	blood:	n/a
13	chr5:74833385-74833435	AG04450	lung:	fetal
14	chr5:74833385-74833435	SK-N-SH_RA	brain:	n/a
15	chr5:74833385-74833435	Hela-S3	cervix:	n/a
16	chr5:74833385-74833435	T-47D	breast:	n/a
17	chr5:74833385-74833435	HEK293	kidney:	embryo
18	chr5:74833385-74833435	HAEpiC	amniotic membrane:	n/a
19	chr5:74833385-74833435	HCM	heart:	n/a
20	chr5:74833385-74833435	ovcar-3	ovarian:	n/a
21	chr5:74833385-74833435	RPTEC	kidney:	n/a
22	chr5:74833385-74833435	BJ	skin:	n/a
23	chr5:74833385-74833435	PFSK-1	brain:	n/a
24	chr5:74833385-74833435	GM12891	blood:	n/a
25	chr5:74833385-74833435	Hepatocyte	liver:	n/a
26	chr5:74833385-74833435	LNCaP	prostate:	n/a
27	chr5:74833385-74833435	HUVEC	blood vessel:	n/a
28	chr5:74833385-74833435	AG04449	skin:	fetal
29	chr5:74833385-74833435	K562	blood:	n/a
30	chr5:74833385-74833435	NH-A	brain:	n/a
31	chr5:74833385-74833435	NHDF-neo	bronchial:	n/a
32	chr5:74833385-74833435	U87	brain:	n/a
33	chr5:74833385-74833435	ProgFib	skin:	n/a
34	chr5:74833385-74833435	ECC-1	luminal epithelium:	n/a
35	chr5:74833385-74833435	H1-hESC	embryonic stem cell:	embryo
36	chr5:74833385-74833435	HPAEpiC	pulmonary alveolar:	n/a
37	chr5:74833385-74833435	NB4	blood:	n/a
38	chr5:74833385-74833435	NT2-D1	testis:	n/a
39	chr5:74833385-74833435	GM12878	blood:	n/a
40	chr5:74833385-74833435	NHBE	bronchial:	n/a
41	chr5:74833385-74833435	IMR90	lung:	fetal
42	chr5:74833385-74833435	HCF	heart:	n/a
43	chr5:74833385-74833435	PANC-1	pancreas:	n/a
44	chr5:74833385-74833435	HCPEpiC	choroid plexus:	n/a
45	chr5:74833385-74833435	HNPCEpiC	eye:	n/a
46	chr5:74833385-74833435	HIPEpiC	eye:	n/a
47	chr5:74833385-74833435	PrEC	prostate:	n/a
48	chr5:74833385-74833435	SK-N-SH	brain:	n/a
49	chr5:74833385-74833435	CMK	blood:	n/a
50	chr5:74833385-74833435	HRE	kidney:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:74820287..74822535-chr5:74827846..74830107,2	K562	blood:
2	chr5:74845037..74847535-chr5:74848930..74850561,2	K562	blood:
3	chr5:74820287..74822535-chr5:74827846..74830107,2	K562	blood:
4	chr5:74839175..74841677-chr5:74843205..74845206,2	K562	blood:
5	chr5:74806414..74809041-chr5:74824381..74827349,2	K562	blood:
6	chr5:74828971..74830534-chr5:74850595..74852572,2	K562	blood:
7	chr5:74852680..74855218-chr5:74864113..74866476,2	K562	blood:
8	chr5:74840733..74842326-chr5:74845611..74848333,2	K562	blood:
9	chr5:74845037..74847535-chr5:74848930..74850561,2	K562	blood:
10	chr5:74808667..74810597-chr5:74818060..74820048,3	K562	blood:
11	chr5:74805731..74808646-chr5:74817149..74819644,4	MCF-7	breast:
12	chr5:74811101..74813110-chr5:74815287..74817345,2	K562	blood:
13	chr5:74818089..74820423-chr5:74844136..74846157,2	MCF-7	breast:
14	chr5:74818089..74820423-chr5:74844136..74846157,2	MCF-7	breast:
15	chr5:74839175..74841677-chr5:74843205..74845206,2	K562	blood:
16	chr5:74819271..74821743-chr5:74831867..74834038,2	MCF-7	breast:
17	chr5:74805305..74807843-chr5:74822655..74824255,2	MCF-7	breast:
18	chr5:74808217..74810593-chr5:74816041..74817596,2	K562	blood:
19	chr5:74815294..74818982-chr5:74820247..74823584,4	K562	blood:
20	chr5:74811981..74814673-chr5:74874113..74876597,2	K562	blood:
21	chr5:74828971..74830534-chr5:74850595..74852572,2	K562	blood:
22	chr5:74835008..74837584-chr5:74853567..74856265,2	K562	blood:
23	chr5:74815294..74818982-chr5:74820247..74823584,4	K562	blood:
24	chr5:74811101..74813110-chr5:74815287..74817345,2	K562	blood:
25	chr5:74819271..74821743-chr5:74831867..74834038,2	MCF-7	breast:
26	chr5:74835008..74837584-chr5:74853567..74856265,2	K562	blood:
27	chr5:74793165..74795664-chr5:74814824..74817209,2	K562	blood:

No data

Variant related genes	Relation type
POLK	TF binding region
COL4A3BP	TF binding region
RNU7-175P	TF binding region
POLK	CpG island
COL4A3BP	CpG island
RNU7-175P	CpG island
ENSG00000122008	chromatin interactions
ENSG00000113163	chromatin interactions

Extended variants
information (count: 1541 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1541 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9293653	chr5:74811497-74811498	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs377145881	chr5:74811501-74811502	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs549633383	chr5:74811506-74811507	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs537106123	chr5:74811631-74811632	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs187248500	chr5:74811688-74811689	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs75376232	chr5:74811689-74811690	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs80180254	chr5:74811697-74811698	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs553222807	chr5:74811699-74811700	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs573203042	chr5:74811708-74811709	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs560232704	chr5:74811711-74811712	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs544978114	chr5:74811719-74811720	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs149896133	chr5:74811720-74811721	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs190492830	chr5:74811732-74811733	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs183351133	chr5:74811733-74811734	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs561155701	chr5:74811740-74811741	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs574968429	chr5:74811746-74811747	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs532124852	chr5:74811754-74811755	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs540620381	chr5:74811774-74811775	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs560820440	chr5:74811797-74811798	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs373709776	chr5:74811861-74811862	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs367577480	chr5:74811914-74811915	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs528110726	chr5:74811952-74811953	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs545838111	chr5:74811962-74811963	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs144898879	chr5:74811987-74811988	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs554413345	chr5:74812010-74812011	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs564844952	chr5:74812049-74812050	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs530624188	chr5:74812062-74812063	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs188760614	chr5:74812164-74812165	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs193096423	chr5:74812212-74812213	Weak transcription Enhancers Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs536443184	chr5:74812225-74812226	Weak transcription Enhancers Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs546604083	chr5:74812227-74812228	Weak transcription Enhancers Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs76018982	chr5:74812240-74812241	Weak transcription Enhancers Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs538518323	chr5:74812258-74812259	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs75500390	chr5:74812264-74812265	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs554117061	chr5:74812310-74812311	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs371382231	chr5:74812363-74812364	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs141916198	chr5:74812370-74812371	Weak transcription Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs201065884	chr5:74812427-74812428	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs372607582	chr5:74812428-74812429	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs555045826	chr5:74812435-74812436	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs146268289	chr5:74812469-74812470	Weak transcription Enhancers ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs574964043	chr5:74812507-74812508	Weak transcription Enhancers ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs566077538	chr5:74812565-74812566	Weak transcription Enhancers ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs138922946	chr5:74812644-74812645	Weak transcription Enhancers ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs560448588	chr5:74812683-74812684	Weak transcription Enhancers ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs185860911	chr5:74812726-74812727	Weak transcription Enhancers ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs546470363	chr5:74812744-74812745	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs186509429	chr5:74812784-74812785	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs77972878	chr5:74812804-74812805	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs564881377	chr5:74812845-74812846	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	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
Hepatocellular carcinoma	16750200	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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	22355333	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD

Chromatin state (count:1210 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74808000-74814600	Weak transcription	Gastric	stomach
2	chr5:74808200-74814600	Weak transcription	Left Ventricle	heart
3	chr5:74808200-74814600	Weak transcription	Pancreas	Pancrea
4	chr5:74808200-74814800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr5:74808200-74817600	Weak transcription	Esophagus	oesophagus
6	chr5:74808400-74812000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr5:74808400-74812000	Enhancers	Primary B cells from cord blood	blood
8	chr5:74808400-74812400	Enhancers	Primary B cells from peripheral blood	blood
9	chr5:74808600-74814600	Weak transcription	Right Ventricle	heart
10	chr5:74808600-74817600	Weak transcription	Thymus	Thymus
11	chr5:74808600-74819000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr5:74808800-74814400	Weak transcription	Fetal Muscle Trunk	muscle
13	chr5:74808800-74814600	Weak transcription	Lung	lung
14	chr5:74808800-74816200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr5:74808800-74816200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr5:74808800-74817600	Weak transcription	Aorta	Aorta
17	chr5:74808800-74817600	Weak transcription	Fetal Thymus	thymus
18	chr5:74808800-74817800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr5:74808800-74849600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr5:74809000-74811600	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr5:74809000-74812000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr5:74809000-74813000	Weak transcription	Fetal Brain Male	brain
23	chr5:74809000-74815600	Weak transcription	Fetal Intestine Large	intestine
24	chr5:74809000-74816200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr5:74809000-74816200	Weak transcription	Small Intestine	intestine
26	chr5:74809000-74819600	Weak transcription	Placenta	Placenta
27	chr5:74809000-74820000	Weak transcription	Colonic Mucosa	Colon
28	chr5:74809400-74814600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr5:74809400-74814600	Weak transcription	Fetal Intestine Small	intestine
30	chr5:74809400-74814600	Weak transcription	Right Atrium	heart
31	chr5:74809400-74814800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr5:74809400-74815200	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr5:74809400-74815800	Weak transcription	Primary T cells from cord blood	blood
34	chr5:74809400-74816200	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr5:74809400-74816200	Weak transcription	Ovary	ovary
36	chr5:74809400-74816400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr5:74809400-74816400	Weak transcription	Osteobl	bone
38	chr5:74809400-74817600	Weak transcription	HSMM	muscle
39	chr5:74809400-74817800	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr5:74809400-74830600	Weak transcription	Fetal Kidney	kidney
41	chr5:74809600-74812000	Weak transcription	Primary hematopoietic stem cells	blood
42	chr5:74809600-74814800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr5:74809600-74814800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr5:74809600-74816200	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr5:74809600-74816200	Weak transcription	Liver	Liver
46	chr5:74809600-74816600	Weak transcription	NHDF-Ad	bronchial
47	chr5:74809600-74817600	Weak transcription	HMEC	breast
48	chr5:74809600-74820600	Weak transcription	Brain Angular Gyrus	brain
49	chr5:74809600-74830200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr5:74809600-74839400	Weak transcription	Rectal Mucosa Donor 29	rectum

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