Variant report

Variant	esv3393424
Chromosome Location	chr5:76122720-76287744
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1286)
CpG islands
(count:1714)
Chromatin interactive
region (count:45)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1286 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:76145750-76146088	K562	blood:	n/a	n/a
2	ARID3A	chr5:76163911-76164256	K562	blood:	n/a	n/a
3	ARID3A	chr5:76165986-76166156	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:76242836-76243553	K562	blood:	n/a	n/a
5	ARID3A	chr5:76126576-76126776	K562	blood:	n/a	n/a
6	ARID3A	chr5:76169967-76170322	K562	blood:	n/a	n/a
7	ARID3A	chr5:76147455-76147464	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:76241220-76241321	K562	blood:	n/a	n/a
9	ARID3A	chr5:76163901-76164233	HepG2	liver:	n/a	n/a
10	ARID3A	chr5:76255264-76255705	K562	blood:	n/a	n/a
11	ATF1	chr5:76170064-76170385	K562	blood:	n/a	n/a
12	ATF1	chr5:76152591-76152875	K562	blood:	n/a	n/a
13	ATF2	chr5:76126912-76127331	GM12878	blood:	n/a	n/a
14	ATF2	chr5:76163943-76164306	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr5:76126950-76127363	GM12878	blood:	n/a	n/a
16	ATF3	chr5:76250169-76250473	H1-hESC	embryonic stem cell:	n/a	chr5:76250333-76250344
17	ATF3	chr5:76145745-76146124	K562	blood:	n/a	n/a
18	BACH1	chr5:76169930-76170265	K562	blood:	n/a	n/a
19	BACH1	chr5:76249241-76249615	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr5:76170008-76170259	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr5:76250317-76250517	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr5:76126596-76126774	K562	blood:	n/a	n/a
23	BATF	chr5:76274677-76274945	GM12878	blood:	n/a	n/a
24	BATF	chr5:76126956-76127325	GM12878	blood:	n/a	n/a
25	BATF	chr5:76233684-76233893	GM12878	blood:	n/a	n/a
26	BATF	chr5:76236874-76237087	GM12878	blood:	n/a	n/a
27	BATF	chr5:76233915-76234338	GM12878	blood:	n/a	n/a
28	BATF	chr5:76234063-76234276	GM12878	blood:	n/a	n/a
29	BCL11A	chr5:76126997-76127227	GM12878	blood:	n/a	chr5:76127105-76127114
30	BCL11A	chr5:76126931-76127279	GM12878	blood:	n/a	chr5:76127105-76127114
31	BCL3	chr5:76126926-76127294	GM12878	blood:	n/a	chr5:76127105-76127114
32	BCL3	chr5:76126983-76127322	GM12878	blood:	n/a	chr5:76127105-76127114
33	BCL3	chr5:76126569-76127455	A549	lung:	n/a	chr5:76127105-76127114
34	BCL3	chr5:76126827-76127402	A549	lung:	n/a	chr5:76127105-76127114
35	BCLAF1	chr5:76126973-76127278	GM12878	blood:	n/a	chr5:76127105-76127114
36	BHLHE40	chr5:76163936-76164249	GM12878	blood:	n/a	n/a
37	BHLHE40	chr5:76242986-76243264	K562	blood:	n/a	n/a
38	BHLHE40	chr5:76165863-76166236	HepG2	liver:	n/a	n/a
39	BHLHE40	chr5:76268534-76268844	K562	blood:	n/a	n/a
40	BHLHE40	chr5:76169996-76170347	K562	blood:	n/a	n/a
41	BHLHE40	chr5:76145340-76145346	K562	blood:	n/a	n/a
42	BHLHE40	chr5:76164044-76164139	K562	blood:	n/a	n/a
43	BHLHE40	chr5:76152823-76152904	K562	blood:	n/a	n/a
44	BHLHE40	chr5:76145717-76145893	GM12878	blood:	n/a	n/a
45	BHLHE40	chr5:76126954-76127367	GM12878	blood:	n/a	n/a
46	BHLHE40	chr5:76145594-76146150	K562	blood:	n/a	n/a
47	BHLHE40	chr5:76126969-76127195	A549	lung:	n/a	n/a
48	BHLHE40	chr5:76255195-76255603	K562	blood:	n/a	n/a
49	BRCA1	chr5:76163801-76164243	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr5:76142105-76142119	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1714 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:76245649-76245699	HIPEpiC	eye:	n/a
2	chr5:76251688-76251738	MCF10A-Er-Src	breast:	n/a
3	chr5:76245649-76245699	GM06990	blood:	n/a
4	chr5:76249776-76249826	SK-N-SH_RA	brain:	n/a
5	chr5:76250351-76250401	HMEC	breast:	n/a
6	chr5:76245649-76245699	GM19239	blood:	n/a
7	chr5:76245649-76245699	HIPEpiC	eye:	n/a
8	chr5:76251688-76251738	MCF10A-Er-Src	breast:	n/a
9	chr5:76245649-76245699	GM06990	blood:	n/a
10	chr5:76249776-76249826	SK-N-SH_RA	brain:	n/a
11	chr5:76250351-76250401	HMEC	breast:	n/a
12	chr5:76245649-76245699	GM19239	blood:	n/a
13	chr5:76264831-76264881	SKMC	muscle:	n/a
14	chr5:76264831-76264881	A549	lung:	n/a
15	chr5:76250351-76250401	AG04449	skin:	fetal
16	chr5:76170418-76170468	Hepatocyte	liver:	n/a
17	chr5:76247647-76247697	HIPEpiC	eye:	n/a
18	chr5:76245649-76245699	MCF10A-Er-Src	breast:	n/a
19	chr5:76238976-76239026	ProgFib	skin:	n/a
20	chr5:76145809-76145859	AG09319	gingival:	n/a
21	chr5:76210838-76210888	HCPEpiC	choroid plexus:	n/a
22	chr5:76250351-76250401	HRCEpiC	kidney:	n/a
23	chr5:76248637-76248687	SK-N-SH_RA	brain:	n/a
24	chr5:76248749-76248799	HL-60	blood:	n/a
25	chr5:76145903-76145953	HMEC	breast:	n/a
26	chr5:76134399-76134449	Hepatocyte	liver:	n/a
27	chr5:76132547-76132597	HCT-116	colon:	n/a
28	chr5:76210838-76210888	ProgFib	skin:	n/a
29	chr5:76247647-76247697	K562	blood:	n/a
30	chr5:76145903-76145953	T-47D	breast:	n/a
31	chr5:76252686-76252736	Jurkat	blood:	n/a
32	chr5:76252686-76252736	K562	blood:	n/a
33	chr5:76170418-76170468	SK-N-SH_RA	brain:	n/a
34	chr5:76245649-76245699	HepG2	liver:	n/a
35	chr5:76132547-76132597	AG09309	skin:	n/a
36	chr5:76250351-76250401	NH-A	brain:	n/a
37	chr5:76249502-76249552	AG04450	lung:	fetal
38	chr5:76247647-76247697	HRCEpiC	kidney:	n/a
39	chr5:76134399-76134449	SK-N-SH_RA	brain:	n/a
40	chr5:76171906-76171956	NB4	blood:	n/a
41	chr5:76145903-76145953	K562	blood:	n/a
42	chr5:76144940-76144990	HIPEpiC	eye:	n/a
43	chr5:76248923-76248973	K562	blood:	n/a
44	chr5:76238976-76239026	SK-N-SH	brain:	n/a
45	chr5:76144940-76144990	AG09309	skin:	n/a
46	chr5:76249502-76249552	HIPEpiC	eye:	n/a
47	chr5:76249502-76249552	GM12892	blood:	n/a
48	chr5:76132547-76132597	HCF	heart:	n/a
49	chr5:76248923-76248973	HL-60	blood:	n/a
50	chr5:76248131-76248181	AG04449	skin:	fetal

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:76251526..76253718-chr5:76253907..76256159,2	K562	blood:
2	chr5:76132665..76134749-chr5:76137165..76139299,2	K562	blood:
3	chr5:76272385..76275331-chr5:76277061..76279168,2	K562	blood:
4	chr5:76269267..76270809-chr5:76325921..76328545,2	MCF-7	breast:
5	chr5:76163632..76164571-chr5:76382049..76382765,2	MCF-7	breast:
6	chr5:76277492..76279372-chr5:76295469..76297110,2	K562	blood:
7	chr5:76201621..76204477-chr5:76206976..76209585,2	K562	blood:
8	chr5:76149093..76150688-chr5:76152808..76155326,2	K562	blood:
9	chr5:76163618..76164624-chr5:76373134..76374055,4	K562	blood:
10	chr5:76219477..76221427-chr5:76228225..76229868,2	K562	blood:
11	chr5:76241349..76243178-chr5:76245408..76247469,2	K562	blood:
12	chr5:76123012..76125302-chr5:76125595..76128318,2	MCF-7	breast:
13	chr5:76241349..76243178-chr5:76245408..76247469,2	K562	blood:
14	chr5:76201621..76204477-chr5:76206976..76209585,2	K562	blood:
15	chr5:76219477..76221427-chr5:76228225..76229868,2	K562	blood:
16	chr5:76127088..76128697-chr5:76136604..76139100,2	K562	blood:
17	chr5:76127088..76128697-chr5:76136604..76139100,2	K562	blood:
18	chr5:76163643..76164600-chr5:76311594..76312851,8	K562	blood:
19	chr5:76216275..76218652-chr5:76220966..76223336,2	K562	blood:
20	chr5:76150968..76153966-chr5:76157599..76160236,2	K562	blood:
21	chr5:76163903..76164537-chr5:76440482..76441271,2	MCF-7	breast:
22	chr5:76144979..76147946-chr5:76325039..76327688,2	K562	blood:
23	chr5:76149093..76150688-chr5:76152808..76155326,2	K562	blood:
24	chr5:76216275..76218652-chr5:76220966..76223336,2	K562	blood:
25	chr5:76272385..76275331-chr5:76277061..76279168,2	K562	blood:
26	chr5:76221898..76224119-chr5:76227208..76231002,3	K562	blood:
27	chr5:76145559..76148481-chr5:76149405..76151711,4	K562	blood:
28	chr5:76115175..76117196-chr5:76160540..76162682,2	MCF-7	breast:
29	chr5:76163515..76164197-chr5:76787927..76788778,2	K562	blood:
30	chr5:76221898..76224119-chr5:76227208..76231002,3	K562	blood:
31	chr5:76241349..76243990-chr5:76244502..76247469,2	K562	blood:
32	chr5:75973826..75975865-chr5:76141935..76143640,2	MCF-7	breast:
33	chr5:76162914..76165922-chr5:76372633..76374807,3	K562	blood:
34	chr5:76163711..76164616-chr5:76311702..76312587,6	MCF-7	breast:
35	chr5:76136037..76139434-chr5:76141594..76145921,5	K562	blood:
36	chr5:76135978..76138972-chr5:76140477..76142942,2	MCF-7	breast:
37	chr5:76135978..76138972-chr5:76140477..76142942,2	MCF-7	breast:
38	chr5:76113078..76116046-chr5:76145704..76148210,2	K562	blood:
39	chr5:76285886..76288601-chr5:76290916..76293465,2	K562	blood:
40	chr5:76163760..76164637-chr5:76311217..76312283,3	MCF-7	breast:
41	chr5:76276361..76277029-chr5:76463737..76464559,2	MCF-7	breast:
42	chr5:76150968..76153966-chr5:76157599..76160236,2	K562	blood:
43	chr5:76170197..76172032-chr5:76326129..76328554,2	MCF-7	breast:
44	chr5:76163387..76165111-chr5:76366962..76369589,2	K562	blood:
45	chr5:76123012..76125302-chr5:76125595..76128318,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AGGF1-2	chr5:76272216-76272345	XLOC_004433
2	lnc-CRHBP-1	chr5:76287641-76287694	XLOC_004434
3	lnc-AGGF1-2	chr5:76276786-76276874	XLOC_004433
4	lnc-F2RL2-4	chr5:76132727-76133020	NONHSAT102252

No data

Variant related genes	Relation type
RN7SL208P	TF binding region
CRHBP	TF binding region
S100Z	TF binding region
RNU6ATAC36P	TF binding region
RN7SL208P	CpG island
CRHBP	CpG island
S100Z	CpG island
RNU6ATAC36P	CpG island
ENSG00000164252	chromatin interactions
ENSG00000264391	chromatin interactions
ENSG00000145708	chromatin interactions
ENSG00000171643	chromatin interactions
ENSG00000250802	chromatin interactions
ENSG00000164253	chromatin interactions
ENSG00000252684	chromatin interactions
ENSG00000164251	chromatin interactions

Extended variants
information (count: 6699 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:6699 , 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	rs2243038	chr5:76122720-76122721	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550113593	chr5:76122756-76122757	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs35622075	chr5:76122770-76122771	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs370068720	chr5:76122772-76122773	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs557572273	chr5:76122872-76122873	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574246058	chr5:76122878-76122879	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542864461	chr5:76122882-76122883	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2243039	chr5:76122937-76122938	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs572865093	chr5:76122981-76122982	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs149460205	chr5:76122988-76122989	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545030709	chr5:76122990-76122991	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565221363	chr5:76123010-76123011	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531076586	chr5:76123033-76123034	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2243040	chr5:76123072-76123073	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs2243041	chr5:76123082-76123083	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529087836	chr5:76123084-76123085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs370345319	chr5:76123101-76123102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2243042	chr5:76123123-76123124	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs2243076	chr5:76123128-76123129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2243077	chr5:76123133-76123134	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10074011	chr5:76123149-76123150	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112858680	chr5:76123188-76123189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570205761	chr5:76123189-76123190	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186302768	chr5:76123193-76123194	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551428881	chr5:76123241-76123242	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374376742	chr5:76123249-76123250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs563326055	chr5:76123264-76123265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571245141	chr5:76123302-76123303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs536162130	chr5:76123303-76123304	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs549169239	chr5:76123305-76123306	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113522070	chr5:76123326-76123327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574134817	chr5:76123351-76123352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536461167	chr5:76123367-76123368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553231769	chr5:76123368-76123369	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372026443	chr5:76123426-76123427	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs70982643	chr5:76123447-76123448	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs13154623	chr5:76123450-76123451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573239070	chr5:76123453-76123454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs13175126	chr5:76123455-76123456	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555959489	chr5:76123511-76123512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572707960	chr5:76123549-76123550	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs3135471	chr5:76123570-76123571	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs565329872	chr5:76123604-76123605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531426634	chr5:76123635-76123636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553628287	chr5:76123654-76123655	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576772584	chr5:76123655-76123656	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575553558	chr5:76123676-76123677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs62365145	chr5:76123680-76123681	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545437051	chr5:76123702-76123703	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191542118	chr5:76123706-76123707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1623 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:76116000-76131600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr5:76116200-76126800	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr5:76116400-76131600	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr5:76116600-76128800	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr5:76116800-76134200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr5:76117000-76126600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr5:76117000-76128600	Weak transcription	NHLF	lung
8	chr5:76117200-76128400	Weak transcription	Duodenum Mucosa	Duodenum
9	chr5:76117200-76128600	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr5:76117200-76128800	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr5:76117400-76125800	Weak transcription	HUVEC	blood vessel
12	chr5:76117400-76125800	Weak transcription	NH-A	brain
13	chr5:76117400-76126400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr5:76117400-76126600	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr5:76117400-76128400	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr5:76117400-76130800	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr5:76117400-76134200	Weak transcription	Stomach Mucosa	stomach
18	chr5:76117400-76135200	Weak transcription	Colonic Mucosa	Colon
19	chr5:76117600-76128600	Weak transcription	Primary hematopoietic stem cells	blood
20	chr5:76117800-76126600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr5:76118800-76134600	Weak transcription	HepG2	liver
22	chr5:76119200-76123800	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr5:76119400-76123000	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr5:76119400-76128600	Weak transcription	Liver	Liver
25	chr5:76120400-76123000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr5:76121000-76123000	Genic enhancers	Fetal Intestine Large	intestine
27	chr5:76121200-76123000	Enhancers	NHEK	skin
28	chr5:76121400-76123000	Enhancers	HMEC	breast
29	chr5:76121600-76125800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr5:76121800-76128600	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr5:76122200-76122800	Enhancers	A549	lung
32	chr5:76122400-76122800	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr5:76122400-76123000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr5:76122400-76123000	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr5:76122400-76123000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr5:76122400-76126400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr5:76122600-76122800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr5:76122600-76122800	Genic enhancers	Fetal Intestine Small	intestine
39	chr5:76122600-76126600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr5:76122800-76123000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr5:76122800-76123600	Weak transcription	Fetal Intestine Small	intestine
42	chr5:76122800-76125200	Weak transcription	A549	lung
43	chr5:76122800-76125800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr5:76123000-76125200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr5:76123000-76125200	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr5:76123000-76125400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr5:76123000-76125800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr5:76123000-76125800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr5:76123000-76126400	Weak transcription	HMEC	breast
50	chr5:76123000-76126400	Weak transcription	NHEK	skin

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