Variant report

Variant	esv1835096
Chromosome Location	chr5:74336883-74356857
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:949)
CpG islands
(count:1099)
Chromatin interactive
region (count:20)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:949 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:74344241-74344923	GM12878	blood:	n/a	n/a
2	ATF2	chr5:74349551-74350155	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr5:74351364-74352195	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr5:74345596-74346055	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr5:74346230-74346497	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr5:74348686-74350492	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr5:74344236-74344915	GM12878	blood:	n/a	n/a
8	BATF	chr5:74340153-74340494	GM12878	blood:	n/a	chr5:74340315-74340326
9	BATF	chr5:74344363-74344864	GM12878	blood:	n/a	n/a
10	BATF	chr5:74340186-74340495	GM12878	blood:	n/a	chr5:74340315-74340326
11	BHLHE40	chr5:74349196-74349715	HepG2	liver:	n/a	chr5:74349390-74349406 chr5:74349377-74349393 chr5:74349389-74349405
12	BHLHE40	chr5:74344153-74344917	GM12878	blood:	n/a	n/a
13	BRCA1	chr5:74348656-74348704	HepG2	liver:	n/a	n/a
14	BRCA1	chr5:74349979-74350422	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr5:74349319-74349422	HepG2	liver:	n/a	n/a
16	CBX3	chr5:74340035-74340699	HCT-116	colon:	n/a	n/a
17	CEBPB	chr5:74336777-74337168	IMR90	lung:	n/a	chr5:74336869-74336877 chr5:74336994-74337006
18	CEBPB	chr5:74351209-74352017	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr5:74345625-74345985	K562	blood:	n/a	chr5:74345780-74345791
20	CEBPB	chr5:74345604-74345984	IMR90	lung:	n/a	chr5:74345780-74345791
21	CEBPB	chr5:74342669-74342986	K562	blood:	n/a	n/a
22	CEBPB	chr5:74345636-74346047	H1-hESC	embryonic stem cell:	n/a	chr5:74345780-74345791
23	CEBPB	chr5:74356651-74356897	HepG2	liver:	n/a	chr5:74356752-74356763
24	CEBPB	chr5:74348623-74348748	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr5:74345612-74345943	ECC-1	luminal epithelium:	n/a	chr5:74345780-74345791
26	CEBPB	chr5:74345493-74346108	A549	lung:	n/a	chr5:74345780-74345791
27	CEBPB	chr5:74342627-74342857	HepG2	liver:	n/a	n/a
28	CEBPB	chr5:74345620-74345983	A549	lung:	n/a	chr5:74345780-74345791
29	CEBPB	chr5:74345627-74345992	HepG2	liver:	n/a	chr5:74345780-74345791
30	CEBPB	chr5:74342670-74342905	K562	blood:	n/a	n/a
31	CEBPB	chr5:74356648-74356887	IMR90	lung:	n/a	chr5:74356752-74356763
32	CEBPB	chr5:74336811-74337100	Hela-S3	cervix:	n/a	chr5:74336869-74336877 chr5:74336994-74337006
33	CEBPB	chr5:74345611-74346027	Hela-S3	cervix:	n/a	chr5:74345780-74345791
34	CEBPB	chr5:74345612-74345984	K562	blood:	n/a	chr5:74345780-74345791
35	CEBPB	chr5:74345544-74345965	A549	lung:	n/a	chr5:74345780-74345791
36	CEBPB	chr5:74345526-74346089	MCF-7	breast:	n/a	chr5:74345780-74345791
37	CEBPB	chr5:74351654-74351976	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr5:74345609-74346093	MCF-7	breast:	n/a	chr5:74345780-74345791
39	CEBPB	chr5:74348978-74349139	Hela-S3	cervix:	n/a	n/a
40	CHD1	chr5:74347519-74350428	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr5:74350645-74351820	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr5:74345576-74346508	H1-hESC	embryonic stem cell:	n/a	chr5:74346307-74346317
43	CHD2	chr5:74348665-74348815	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr5:74349147-74349199	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr5:74350149-74350361	HepG2	liver:	n/a	n/a
46	CHD2	chr5:74349347-74349703	HepG2	liver:	n/a	n/a
47	CHD2	chr5:74351422-74352020	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr5:74350013-74350679	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr5:74349249-74349726	A549	lung:	n/a	n/a
50	CREB1	chr5:74349380-74349941	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:74353010-74353060	SAEC	small airway:	n/a
2	chr5:74353010-74353060	SAEC	small airway:	n/a
3	chr5:74348373-74348423	AG04450	lung:	fetal
4	chr5:74349644-74349694	BE2_C	brain:	n/a
5	chr5:74350752-74350802	NT2-D1	testis:	n/a
6	chr5:74349644-74349694	PFSK-1	brain:	n/a
7	chr5:74346730-74346780	PANC-1	pancreas:	n/a
8	chr5:74350752-74350802	HCT-116	colon:	n/a
9	chr5:74353351-74353401	ECC-1	luminal epithelium:	n/a
10	chr5:74353010-74353060	T-47D	breast:	n/a
11	chr5:74349993-74350043	Hela-S3	cervix:	n/a
12	chr5:74346730-74346780	HRCEpiC	kidney:	n/a
13	chr5:74346260-74346310	SK-N-SH_RA	brain:	n/a
14	chr5:74349993-74350043	NHDF-neo	bronchial:	n/a
15	chr5:74353351-74353401	HCT-116	colon:	n/a
16	chr5:74347539-74347589	HepG2	liver:	n/a
17	chr5:74344779-74344829	NH-A	brain:	n/a
18	chr5:74346730-74346780	GM12878	blood:	n/a
19	chr5:74349644-74349694	GM12878	blood:	n/a
20	chr5:74348903-74348953	AG09309	skin:	n/a
21	chr5:74349993-74350043	SAEC	small airway:	n/a
22	chr5:74348373-74348423	ProgFib	skin:	n/a
23	chr5:74350752-74350802	SK-N-SH	brain:	n/a
24	chr5:74350815-74350865	MCF10A-Er-Src	breast:	n/a
25	chr5:74348373-74348423	HRPEpiC	eye:	n/a
26	chr5:74350815-74350865	T-47D	breast:	n/a
27	chr5:74353010-74353060	GM06990	blood:	n/a
28	chr5:74353010-74353060	AG04449	skin:	fetal
29	chr5:74353351-74353401	Caco-2	colon:	n/a
30	chr5:74350132-74350182	AG09309	skin:	n/a
31	chr5:74349804-74349854	AG09309	skin:	n/a
32	chr5:74344416-74344466	NB4	blood:	n/a
33	chr5:74348187-74348237	MCF10A-Er-Src	breast:	n/a
34	chr5:74350815-74350865	AoSMC	blood vessel:	n/a
35	chr5:74350214-74350264	LNCaP	prostate:	n/a
36	chr5:74353351-74353401	AG04450	lung:	fetal
37	chr5:74348187-74348237	AG09309	skin:	n/a
38	chr5:74353351-74353401	MCF-7	breast:	n/a
39	chr5:74354835-74354885	MCF-7	breast:	n/a
40	chr5:74344416-74344466	HCF	heart:	n/a
41	chr5:74347539-74347589	PFSK-1	brain:	n/a
42	chr5:74348373-74348423	HCPEpiC	choroid plexus:	n/a
43	chr5:74353010-74353060	AG09309	skin:	n/a
44	chr5:74350815-74350865	AG04449	skin:	fetal
45	chr5:74347539-74347589	HCF	heart:	n/a
46	chr5:74346730-74346780	MCF10A-Er-Src	breast:	n/a
47	chr5:74344779-74344829	A549	lung:	n/a
48	chr5:74348903-74348953	GM12878	blood:	n/a
49	chr5:74350752-74350802	HUVEC	blood vessel:	n/a
50	chr5:74350214-74350264	ovcar-3	ovarian:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:74341045..74343910-chr5:74344011..74347485,4	MCF-7	breast:
2	chr5:74343721..74346711-chr5:74348510..74350046,2	MCF-7	breast:
3	chr5:74331704..74333232-chr5:74343101..74344687,2	MCF-7	breast:
4	chr5:74334981..74336782-chr5:74342190..74344248,2	MCF-7	breast:
5	chr5:74341045..74343910-chr5:74344011..74347485,4	MCF-7	breast:
6	chr5:74346800..74348616-chr5:74350730..74353345,2	MCF-7	breast:
7	chr5:74220860..74221763-chr5:74345733..74346235,2	MCF-7	breast:
8	chr5:74330454..74335475-chr5:74336350..74340630,5	MCF-7	breast:
9	chr5:74349473..74351177-chr5:74531614..74533984,2	MCF-7	breast:
10	chr5:74338841..74341157-chr5:74343981..74347541,4	MCF-7	breast:
11	chr5:74338841..74341157-chr5:74343981..74347541,4	MCF-7	breast:
12	chr5:74343645..74345260-chr5:74345382..74347449,2	K562	blood:
13	chr5:74230526..74231383-chr5:74345361..74346008,2	MCF-7	breast:
14	chr5:74345325..74346339-chr5:74561197..74562160,5	MCF-7	breast:
15	chr5:74315578..74317119-chr5:74341476..74343130,2	MCF-7	breast:
16	chr5:74349068..74351249-chr5:74356524..74358401,2	MCF-7	breast:
17	chr5:74345728..74346291-chr5:74523458..74524224,2	MCF-7	breast:
18	chr5:74343645..74345260-chr5:74345382..74347449,2	K562	blood:
19	chr5:74332922..74335648-chr5:74338677..74341293,2	MCF-7	breast:
20	chr5:74349068..74351249-chr5:74356524..74358401,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GCNT4-2	chr5:74337995-74338722	NONHSAT102193
2	lnc-GCNT4-2	chr5:74339379-74339914	NONHSAT102193
3	lnc-ANKRD31-1	chr5:74343858-74343862	ENSG00000250889
4	lnc-ANKRD31-1	chr5:74347994-74348052	ENSG00000250889
5	lnc-ANKRD31-1	chr5:74349340-74349594	NONHSAT102195
6	lnc-ANKRD31-1	chr5:74347993-74348052	XLOC_004890
7	lnc-ANKRD31-1	chr5:74343722-74343862	NONHSAT102195
8	lnc-ANKRD31-1	chr5:74343858-74343862	XLOC_004890
9	lnc-ANKRD31-1	chr5:74348254-74348668	XLOC_004890
10	lnc-ANKRD31-1	chr5:74348254-74348668	ENSG00000250889
11	lnc-GCNT4-2	chr5:74340718-74341142	NONHSAT102193
12	lnc-GCNT4-2	chr5:74337140-74337513	NONHSAT102193

No data

Variant related genes	Relation type
ENSG00000250889	TF binding region
ENSG00000250889	CpG island
ENSG00000250889	chromatin interactions
ENSG00000145700	chromatin interactions

Extended variants
information (count: 780 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:780 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11955513	chr5:74336883-74336884	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs114712684	chr5:74336896-74336897	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566429217	chr5:74336900-74336901	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371664614	chr5:74336908-74336909	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532315883	chr5:74336924-74336925	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs7730062	chr5:74336943-74336944	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs562005797	chr5:74336948-74336949	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs73122599	chr5:74337078-74337079	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs77906488	chr5:74337079-74337080	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555004771	chr5:74337100-74337101	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568463629	chr5:74337101-74337102	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534400082	chr5:74337102-74337103	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554446610	chr5:74337104-74337105	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs527913044	chr5:74337133-74337134	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs7726378	chr5:74337139-74337140	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs373955029	chr5:74337174-74337175	Weak transcription Genic enhancers Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs187219947	chr5:74337237-74337238	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs556918668	chr5:74337241-74337242	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs189426831	chr5:74337269-74337270	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs543876530	chr5:74337324-74337325	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs375966352	chr5:74337374-74337375	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs570854280	chr5:74337376-74337377	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs560994136	chr5:74337378-74337379	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs182078061	chr5:74337392-74337393	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs369883966	chr5:74337398-74337399	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs539732398	chr5:74337414-74337415	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs529799833	chr5:74337435-74337436	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs540416204	chr5:74337468-74337469	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs559941394	chr5:74337472-74337473	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs532195084	chr5:74337473-74337474	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs185222329	chr5:74337480-74337481	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs200763320	chr5:74337527-74337528	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370525214	chr5:74337528-74337529	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs552016847	chr5:74337538-74337539	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs73765654	chr5:74337552-74337553	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs531683297	chr5:74337603-74337604	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548338909	chr5:74337663-74337664	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs147574486	chr5:74337664-74337665	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs376895380	chr5:74337711-74337712	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534067909	chr5:74337801-74337802	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554385389	chr5:74337828-74337829	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs75348645	chr5:74337846-74337847	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs540054903	chr5:74337851-74337852	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs541261643	chr5:74337876-74337877	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs113805016	chr5:74337885-74337886	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73765655	chr5:74337939-74337940	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs189978056	chr5:74337944-74337945	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs370271393	chr5:74337947-74337948	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs369259589	chr5:74337984-74337985	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs574462337	chr5:74338015-74338016	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Bladder cancer	21909424	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
Ovarian cancer	21720365	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
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD

Chromatin state (count:1258 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74313600-74341800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:74317600-74344200	Weak transcription	Ovary	ovary
3	chr5:74328000-74339400	Weak transcription	Fetal Stomach	stomach
4	chr5:74328600-74345600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:74329200-74346800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr5:74329600-74338000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr5:74329800-74344400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr5:74330000-74339800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr5:74330000-74344400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr5:74330400-74339400	Weak transcription	Gastric	stomach
11	chr5:74330400-74340400	Weak transcription	Stomach Smooth Muscle	stomach
12	chr5:74330400-74341800	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr5:74330400-74344200	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr5:74330600-74337200	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
15	chr5:74330600-74339400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr5:74330600-74339400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr5:74330600-74339600	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr5:74330600-74339600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr5:74330600-74341800	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr5:74330600-74342600	Weak transcription	Colon Smooth Muscle	Colon
21	chr5:74330600-74345400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr5:74330600-74348000	Weak transcription	Primary hematopoietic stem cells	blood
23	chr5:74331400-74345400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr5:74331400-74345600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr5:74331600-74339800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr5:74331600-74344000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr5:74331600-74347000	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr5:74332600-74340400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr5:74332600-74343200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr5:74332800-74338400	Weak transcription	Esophagus	oesophagus
31	chr5:74332800-74339600	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr5:74333200-74337000	Weak transcription	Fetal Intestine Large	intestine
33	chr5:74333200-74337000	Weak transcription	NHLF	lung
34	chr5:74333200-74337200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr5:74333200-74339800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr5:74333200-74339800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr5:74333200-74344000	Weak transcription	Osteobl	bone
38	chr5:74333200-74346000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr5:74333400-74337600	Weak transcription	NHDF-Ad	bronchial
40	chr5:74333400-74338200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr5:74333400-74339200	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr5:74333400-74343800	Weak transcription	NH-A	brain
43	chr5:74333400-74344000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr5:74333400-74344000	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr5:74333600-74337000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr5:74333600-74337000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr5:74333600-74337000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr5:74333600-74339600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr5:74333800-74337400	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr5:74334200-74340200	Strong transcription	Primary T cells from cord blood	blood

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