Variant report

Variant	nsv882233
Chromosome Location	chr5:80849084-81049187
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1593)
CpG islands
(count:1100)
Chromatin interactive
region (count:107)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1593 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:80922388-80922581	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:80922360-80922638	K562	blood:	n/a	n/a
3	ARID3A	chr5:80849397-80849518	K562	blood:	n/a	n/a
4	ARID3A	chr5:80875360-80875795	K562	blood:	n/a	chr5:80875651-80875667 chr5:80875650-80875666
5	ARID3A	chr5:80849720-80849942	K562	blood:	n/a	n/a
6	ARID3A	chr5:81048263-81048618	K562	blood:	n/a	n/a
7	ARID3A	chr5:80992633-80992831	K562	blood:	n/a	n/a
8	ARID3A	chr5:81047152-81047393	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:81047100-81047417	K562	blood:	n/a	n/a
10	ATF1	chr5:80875425-80875669	K562	blood:	n/a	n/a
11	ATF1	chr5:81003103-81003284	K562	blood:	n/a	n/a
12	ATF1	chr5:81046732-81047309	K562	blood:	n/a	n/a
13	ATF2	chr5:81047037-81047445	GM12878	blood:	n/a	n/a
14	ATF2	chr5:81046902-81047549	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr5:80926794-80927286	GM12878	blood:	n/a	n/a
16	ATF2	chr5:81046961-81047462	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr5:81045187-81045739	GM12878	blood:	n/a	n/a
18	ATF2	chr5:81045141-81045881	GM12878	blood:	n/a	n/a
19	ATF2	chr5:81046629-81047509	GM12878	blood:	n/a	n/a
20	ATF3	chr5:81047029-81047461	A549	lung:	n/a	chr5:81047261-81047270
21	ATF3	chr5:81047089-81047411	K562	blood:	n/a	chr5:81047261-81047270
22	ATF3	chr5:81046976-81047516	A549	lung:	n/a	chr5:81047469-81047478 chr5:81047261-81047270
23	BACH1	chr5:81045559-81045802	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr5:81046756-81046995	K562	blood:	n/a	n/a
25	BACH1	chr5:81047249-81047453	K562	blood:	n/a	n/a
26	BACH1	chr5:81046703-81047547	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr5:80902101-80902295	H1-hESC	embryonic stem cell:	n/a	n/a
28	BATF	chr5:81045268-81045772	GM12878	blood:	n/a	n/a
29	BATF	chr5:81045329-81045704	GM12878	blood:	n/a	n/a
30	BATF	chr5:80992222-80992515	GM12878	blood:	n/a	n/a
31	BCL11A	chr5:81046689-81046983	GM12878	blood:	n/a	n/a
32	BCL11A	chr5:81047114-81047360	GM12878	blood:	n/a	n/a
33	BCL11A	chr5:81047062-81047309	H1-hESC	embryonic stem cell:	n/a	n/a
34	BCL11A	chr5:81045363-81045810	GM12878	blood:	n/a	n/a
35	BCL3	chr5:81046876-81047552	A549	lung:	n/a	chr5:81046985-81046994
36	BCL3	chr5:81046899-81047536	A549	lung:	n/a	chr5:81046985-81046994
37	BCL3	chr5:81046691-81047677	GM12878	blood:	n/a	chr5:81046985-81046994
38	BCL3	chr5:81045244-81045847	GM12878	blood:	n/a	n/a
39	BCLAF1	chr5:81045100-81045822	GM12878	blood:	n/a	n/a
40	BCLAF1	chr5:81046631-81047845	GM12878	blood:	n/a	chr5:81046985-81046994 chr5:81047770-81047783
41	BCLAF1	chr5:81045131-81045806	GM12878	blood:	n/a	n/a
42	BCLAF1	chr5:80926895-80927254	GM12878	blood:	n/a	chr5:80927071-80927080
43	BCLAF1	chr5:81047006-81047548	K562	blood:	n/a	n/a
44	BCLAF1	chr5:81046616-81047549	GM12878	blood:	n/a	chr5:81046985-81046994
45	BHLHE40	chr5:81015177-81015185	K562	blood:	n/a	n/a
46	BHLHE40	chr5:81045521-81045682	K562	blood:	n/a	n/a
47	BHLHE40	chr5:81014175-81014553	GM12878	blood:	n/a	n/a
48	BHLHE40	chr5:81046589-81047662	GM12878	blood:	n/a	chr5:81047331-81047347
49	BHLHE40	chr5:81046674-81047690	K562	blood:	n/a	chr5:81047331-81047347
50	BHLHE40	chr5:81022463-81022471	GM12878	blood:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:81043172-81043222	H1-hESC	embryonic stem cell:	embryo
2	chr5:81046408-81046458	CMK	blood:	n/a
3	chr5:81043172-81043222	H1-hESC	embryonic stem cell:	embryo
4	chr5:81046408-81046458	CMK	blood:	n/a
5	chr5:80885936-80885986	HNPCEpiC	eye:	n/a
6	chr5:81047246-81047296	ProgFib	skin:	n/a
7	chr5:81045966-81046016	HNPCEpiC	eye:	n/a
8	chr5:81048305-81048355	MCF-7	breast:	n/a
9	chr5:81045418-81045468	Hepatocyte	liver:	n/a
10	chr5:81046758-81046808	H1-hESC	embryonic stem cell:	embryo
11	chr5:81047184-81047234	T-47D	breast:	n/a
12	chr5:81047246-81047296	HCPEpiC	choroid plexus:	n/a
13	chr5:80901358-80901408	NT2-D1	testis:	n/a
14	chr5:80885936-80885986	MCF-7	breast:	n/a
15	chr5:81047184-81047234	LNCaP	prostate:	n/a
16	chr5:81047249-81047299	Hela-S3	cervix:	n/a
17	chr5:81047188-81047238	PFSK-1	brain:	n/a
18	chr5:81047184-81047234	SK-N-SH_RA	brain:	n/a
19	chr5:81046758-81046808	K562	blood:	n/a
20	chr5:81047184-81047234	PANC-1	pancreas:	n/a
21	chr5:81047188-81047238	PANC-1	pancreas:	n/a
22	chr5:81046408-81046458	ProgFib	skin:	n/a
23	chr5:81047184-81047234	PFSK-1	brain:	n/a
24	chr5:81047188-81047238	IMR90	lung:	fetal
25	chr5:81048305-81048355	HepG2	liver:	n/a
26	chr5:81046408-81046458	AG09309	skin:	n/a
27	chr5:81048305-81048355	H1-hESC	embryonic stem cell:	embryo
28	chr5:81047184-81047234	HNPCEpiC	eye:	n/a
29	chr5:81045418-81045468	K562	blood:	n/a
30	chr5:81047184-81047234	GM06990	blood:	n/a
31	chr5:81017303-81017353	NHBE	bronchial:	n/a
32	chr5:80992249-80992299	NT2-D1	testis:	n/a
33	chr5:81043172-81043222	NHBE	bronchial:	n/a
34	chr5:81047848-81047898	HRE	kidney:	n/a
35	chr5:81045418-81045468	ovcar-3	ovarian:	n/a
36	chr5:81043172-81043222	BE2_C	brain:	n/a
37	chr5:80922537-80922587	HPAEpiC	pulmonary alveolar:	n/a
38	chr5:81043172-81043222	SK-N-SH	brain:	n/a
39	chr5:81047249-81047299	T-47D	breast:	n/a
40	chr5:81047188-81047238	Jurkat	blood:	n/a
41	chr5:80901358-80901408	AG10803	skin:	n/a
42	chr5:81045418-81045468	SAEC	small airway:	n/a
43	chr5:80992249-80992299	SK-N-SH	brain:	n/a
44	chr5:81047188-81047238	SK-N-SH	brain:	n/a
45	chr5:81047188-81047238	HPAEpiC	pulmonary alveolar:	n/a
46	chr5:81045966-81046016	AG09319	gingival:	n/a
47	chr5:80885936-80885986	HCM	heart:	n/a
48	chr5:80885936-80885986	HIPEpiC	eye:	n/a
49	chr5:81046408-81046458	A549	lung:	n/a
50	chr5:81045418-81045468	LNCaP	prostate:	n/a

(count:107 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:81047531..81050440-chr5:81268054..81269557,2	K562	blood:
2	chr5:81013446..81015867-chr5:81016678..81018920,2	K562	blood:
3	chr5:80996121..80997838-chr5:81001876..81003774,2	K562	blood:
4	chr5:80934108..80935930-chr5:80938567..80940586,2	K562	blood:
5	chr5:81036698..81038199-chr5:81047468..81049173,2	K562	blood:
6	chr5:80931139..80933943-chr5:80935605..80937292,2	K562	blood:
7	chr5:80946322..80948172-chr5:80949841..80952303,2	K562	blood:
8	chr5:80959308..80961024-chr5:81090290..81092398,2	K562	blood:
9	chr5:81037454..81039351-chr5:81039497..81041595,2	K562	blood:
10	chr5:81045699..81050245-chr5:81142897..81150556,22	MCF-7	breast:
11	chr5:81044026..81052051-chr5:81142054..81153115,35	K562	blood:
12	chr5:81044752..81060050-chr5:81140268..81152732,43	K562	blood:
13	chr5:81025124..81028928-chr5:81046978..81048834,3	K562	blood:
14	chr5:80971757..80974379-chr5:80975193..80977880,3	K562	blood:
15	chr5:80965614..80968004-chr5:80970828..80973570,3	K562	blood:
16	chr5:80961823..80964261-chr5:80965222..80967772,3	K562	blood:
17	chr5:81017452..81019959-chr5:81020706..81023744,3	K562	blood:
18	chr5:81004548..81007464-chr5:81143257..81145481,2	K562	blood:
19	chr5:80970290..80973257-chr5:80975148..80979422,4	K562	blood:
20	chr5:80983475..80985751-chr5:80991739..80993703,2	MCF-7	breast:
21	chr5:80987236..80988906-chr5:80991479..80993705,2	K562	blood:
22	chr5:80991735..80994087-chr5:80998688..81001325,2	K562	blood:
23	chr5:80895098..80897934-chr5:80899967..80903607,4	K562	blood:
24	chr5:80931139..80933943-chr5:80935605..80937292,2	K562	blood:
25	chr5:81029893..81032355-chr5:81038922..81041227,2	K562	blood:
26	chr5:80897320..80900374-chr5:80908175..80911251,3	K562	blood:
27	chr5:80895098..80897934-chr5:80899967..80903607,4	K562	blood:
28	chr5:81018633..81021063-chr5:81032875..81035374,3	K562	blood:
29	chr5:81034741..81036819-chr5:81039221..81041707,2	K562	blood:
30	chr5:80991735..80993822-chr5:80998688..81000196,2	K562	blood:
31	chr5:81002134..81004521-chr5:81007917..81010002,2	K562	blood:
32	chr5:80991735..80993822-chr5:80998688..81000196,2	K562	blood:
33	chr5:80998159..81001011-chr5:81003180..81006000,3	K562	blood:
34	chr5:81029893..81032355-chr5:81038922..81041227,2	K562	blood:
35	chr5:80802774..80803458-chr5:81044304..81045045,2	MCF-7	breast:
36	chr5:80991735..80994087-chr5:80998688..81001325,2	K562	blood:
37	chr5:81011299..81014307-chr5:81021484..81024524,3	K562	blood:
38	chr5:80874625..80877374-chr5:81570400..81571959,2	K562	blood:
39	chr5:81047664..81050586-chr5:81054821..81057159,3	MCF-7	breast:
40	chr5:80983475..80985751-chr5:80991739..80993703,2	MCF-7	breast:
41	chr5:81017452..81019271-chr5:81022244..81024065,2	K562	blood:
42	chr5:80931196..80933943-chr5:80935625..80937292,2	K562	blood:
43	chr5:80853359..80856106-chr5:80858395..80860848,2	K562	blood:
44	chr5:80846060..80848703-chr5:80848977..80851148,2	MCF-7	breast:
45	chr5:81045316..81049074-chr5:81266561..81269658,5	K562	blood:
46	chr5:80961632..80964415-chr5:80970591..80972149,2	MCF-7	breast:
47	chr5:80946322..80948172-chr5:80949841..80952303,2	K562	blood:
48	chr5:81022356..81025954-chr5:81027509..81030484,4	K562	blood:
49	chr5:80870794..80873300-chr5:80875722..80877575,2	K562	blood:
50	chr5:80998159..81001011-chr5:81003180..81006000,3	K562	blood:

No data

Variant related genes	Relation type
SSBP2	TF binding region
SSBP2	CpG island
ENSG00000152348	chromatin interactions
ENSG00000249483	chromatin interactions
ENSG00000145687	chromatin interactions

Extended variants
information (count: 6673 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:6673 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2972229	chr5:80849084-80849085	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs6891181	chr5:80849101-80849102	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs183820203	chr5:80849153-80849154	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs548973137	chr5:80849154-80849155	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs565491088	chr5:80849168-80849169	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs528012328	chr5:80849193-80849194	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs548076590	chr5:80849252-80849253	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs562928087	chr5:80849343-80849344	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs571092815	chr5:80849362-80849363	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs540017882	chr5:80849387-80849388	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs141473374	chr5:80849476-80849477	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs145165250	chr5:80849500-80849501	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs2972228	chr5:80849555-80849556	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs555737139	chr5:80849569-80849570	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs201021630	chr5:80849586-80849587	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs138924535	chr5:80849618-80849619	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs10474032	chr5:80849728-80849729	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs189244351	chr5:80849758-80849759	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs192858418	chr5:80849775-80849776	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs534581519	chr5:80849795-80849796	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs543201620	chr5:80849833-80849834	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs560898621	chr5:80849844-80849845	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs563297853	chr5:80849872-80849873	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs528986707	chr5:80850026-80850027	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs149355146	chr5:80850082-80850083	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs184656922	chr5:80850087-80850088	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs11954000	chr5:80850092-80850093	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs10474033	chr5:80850107-80850108	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs114335134	chr5:80850108-80850109	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs533610096	chr5:80850111-80850112	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs35340025	chr5:80850166-80850167	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs570104893	chr5:80850232-80850233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs143642128	chr5:80850333-80850334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs555562034	chr5:80850440-80850441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551700436	chr5:80850458-80850459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs201918758	chr5:80850489-80850490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565762464	chr5:80850501-80850502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534691488	chr5:80850515-80850516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557667768	chr5:80850642-80850643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs10057707	chr5:80850664-80850665	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs543304994	chr5:80850787-80850788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs148121329	chr5:80850793-80850794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs368766287	chr5:80850798-80850799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537958291	chr5:80850808-80850809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs537303186	chr5:80850810-80850811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs10064862	chr5:80850815-80850816	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs573652102	chr5:80850839-80850840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs376280781	chr5:80850880-80850881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs386689540	chr5:80850881-80850882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs187552996	chr5:80850888-80850889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	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
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
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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
lymphocytic leukemia	21291569	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Tetralogy of Fallot	22912587	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3402 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:80803600-80875200	Weak transcription	Fetal Brain Female	brain
2	chr5:80820200-80851800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:80825200-80865200	Weak transcription	Fetal Brain Male	brain
4	chr5:80828800-80863400	Weak transcription	Fetal Lung	lung
5	chr5:80830000-80853800	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr5:80830800-80849600	Weak transcription	Adipose Nuclei	Adipose
7	chr5:80830800-80850000	Weak transcription	Colon Smooth Muscle	Colon
8	chr5:80834000-80849600	Weak transcription	Brain Angular Gyrus	brain
9	chr5:80834000-80851600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr5:80834400-80867000	Weak transcription	Stomach Smooth Muscle	stomach
11	chr5:80834800-80866400	Weak transcription	Primary B cells from peripheral blood	blood
12	chr5:80834800-80870000	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr5:80835000-80852000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr5:80835200-80850400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr5:80835200-80863000	Weak transcription	Fetal Muscle Leg	muscle
16	chr5:80835200-80872800	Weak transcription	Fetal Kidney	kidney
17	chr5:80835200-80875200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr5:80835600-80876000	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr5:80840800-80883400	Weak transcription	HSMM	muscle
20	chr5:80840800-80884600	Weak transcription	Ovary	ovary
21	chr5:80841600-80849200	Weak transcription	Brain Anterior Caudate	brain
22	chr5:80844200-80884600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr5:80844600-80849600	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr5:80845800-80862000	Weak transcription	Thymus	Thymus
25	chr5:80845800-80863000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr5:80846000-80849600	Weak transcription	Primary B cells from cord blood	blood
27	chr5:80846200-80850600	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr5:80846200-80880600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr5:80846600-80849400	Weak transcription	Primary T cells from cord blood	blood
30	chr5:80846600-80849400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr5:80846600-80860000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr5:80846800-80851800	Weak transcription	Fetal Thymus	thymus
33	chr5:80848000-80856400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr5:80848600-80849200	Enhancers	HMEC	breast
35	chr5:80848600-80850200	Enhancers	Stomach Mucosa	stomach
36	chr5:80848600-80850200	Flanking Active TSS	HUVEC	blood vessel
37	chr5:80848600-80851400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr5:80848800-80849400	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr5:80848800-80849400	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr5:80848800-80849600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr5:80848800-80849800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr5:80848800-80850000	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr5:80848800-80850800	Enhancers	Primary hematopoietic stem cells	blood
44	chr5:80849000-80849200	Enhancers	K562	blood
45	chr5:80849000-80849600	Weak transcription	Dnd41	blood
46	chr5:80849000-80849800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr5:80849000-80885600	Weak transcription	Left Ventricle	heart
48	chr5:80849200-80849400	Enhancers	Brain Anterior Caudate	brain
49	chr5:80849400-80849600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr5:80849400-80849800	Enhancers	Pancreatic Islets	Pancreatic Islet

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