Variant report

Variant	nsv882364
Chromosome Location	chr5:89748142-89808531
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1144)
CpG islands
(count:1283)
Chromatin interactive
region (count:100)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:1144 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:89772341-89772608	K562	blood:	n/a	n/a
2	ARID3A	chr5:89770098-89770852	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:89770187-89770810	K562	blood:	n/a	n/a
4	ATF1	chr5:89770117-89770979	K562	blood:	n/a	n/a
5	ATF2	chr5:89769870-89770838	GM12878	blood:	n/a	n/a
6	ATF2	chr5:89772782-89773327	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr5:89770326-89770901	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr5:89775665-89775738	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr5:89806429-89806463	K562	blood:	n/a	n/a
10	BACH1	chr5:89776575-89776866	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr5:89776556-89776891	K562	blood:	n/a	n/a
12	BACH1	chr5:89772909-89773226	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr5:89769103-89771002	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL3	chr5:89769785-89770955	A549	lung:	n/a	n/a
15	BCL3	chr5:89770173-89770820	GM12878	blood:	n/a	n/a
16	BCL3	chr5:89770125-89770711	A549	lung:	n/a	n/a
17	BCLAF1	chr5:89769921-89770940	GM12878	blood:	n/a	n/a
18	BCLAF1	chr5:89770280-89770861	K562	blood:	n/a	n/a
19	BCLAF1	chr5:89769734-89770961	GM12878	blood:	n/a	n/a
20	BHLHE40	chr5:89769351-89769377	GM12878	blood:	n/a	n/a
21	BHLHE40	chr5:89769455-89770911	HepG2	liver:	n/a	chr5:89770378-89770394
22	BHLHE40	chr5:89769719-89770980	GM12878	blood:	n/a	chr5:89770378-89770394
23	BHLHE40	chr5:89769155-89771109	K562	blood:	n/a	chr5:89770378-89770394
24	BRCA1	chr5:89770412-89770861	GM12878	blood:	n/a	n/a
25	BRCA1	chr5:89768969-89769720	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr5:89770084-89770921	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr5:89784652-89784955	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr5:89770176-89770725	HepG2	liver:	n/a	n/a
29	BRCA1	chr5:89770047-89770330	H1-hESC	embryonic stem cell:	n/a	n/a
30	BRCA1	chr5:89770020-89770128	GM12878	blood:	n/a	n/a
31	BRCA1	chr5:89769666-89769715	GM12878	blood:	n/a	n/a
32	CBX3	chr5:89770155-89770747	K562	blood:	n/a	n/a
33	CBX3	chr5:89769576-89771126	K562	blood:	n/a	n/a
34	CBX3	chr5:89769768-89771020	HCT-116	colon:	n/a	n/a
35	CCNT2	chr5:89806758-89806958	K562	blood:	n/a	n/a
36	CCNT2	chr5:89769405-89770914	K562	blood:	n/a	chr5:89770633-89770642
37	CEBPB	chr5:89779790-89780034	K562	blood:	n/a	n/a
38	CEBPB	chr5:89758829-89759125	Hela-S3	cervix:	n/a	chr5:89758956-89758967
39	CEBPB	chr5:89769898-89770833	HepG2	liver:	n/a	n/a
40	CEBPB	chr5:89770191-89770809	ECC-1	luminal epithelium:	n/a	n/a
41	CEBPB	chr5:89758828-89759065	HepG2	liver:	n/a	chr5:89758956-89758967
42	CEBPB	chr5:89769008-89769474	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr5:89784762-89784962	IMR90	lung:	n/a	n/a
44	CEBPB	chr5:89789347-89789612	H1-hESC	embryonic stem cell:	n/a	chr5:89789467-89789478
45	CEBPB	chr5:89775411-89776129	IMR90	lung:	n/a	n/a
46	CEBPB	chr5:89807763-89808119	IMR90	lung:	n/a	n/a
47	CEBPB	chr5:89784600-89785080	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr5:89787558-89787854	HepG2	liver:	n/a	chr5:89787655-89787666
49	CEBPB	chr5:89758845-89759159	ECC-1	luminal epithelium:	n/a	chr5:89758956-89758967
50	CEBPB	chr5:89770326-89770622	K562	blood:	n/a	n/a

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:89755537-89755587	HUVEC	blood vessel:	n/a
2	chr5:89769642-89769692	AG04450	lung:	fetal
3	chr5:89755537-89755587	HUVEC	blood vessel:	n/a
4	chr5:89769642-89769692	AG04450	lung:	fetal
5	chr5:89769642-89769692	GM12878	blood:	n/a
6	chr5:89770699-89770749	GM12892	blood:	n/a
7	chr5:89770577-89770627	HIPEpiC	eye:	n/a
8	chr5:89771460-89771510	GM06990	blood:	n/a
9	chr5:89770455-89770505	HMEC	breast:	n/a
10	chr5:89770393-89770443	HL-60	blood:	n/a
11	chr5:89767709-89767759	AG09319	gingival:	n/a
12	chr5:89769860-89769910	HMEC	breast:	n/a
13	chr5:89770577-89770627	PrEC	prostate:	n/a
14	chr5:89770393-89770443	HAEpiC	amniotic membrane:	n/a
15	chr5:89770685-89770735	PFSK-1	brain:	n/a
16	chr5:89755537-89755587	AG10803	skin:	n/a
17	chr5:89770306-89770356	GM12892	blood:	n/a
18	chr5:89770577-89770627	Hepatocyte	liver:	n/a
19	chr5:89769860-89769910	AoSMC	blood vessel:	n/a
20	chr5:89767709-89767759	H1-hESC	embryonic stem cell:	embryo
21	chr5:89770306-89770356	AG09309	skin:	n/a
22	chr5:89770490-89770540	GM06990	blood:	n/a
23	chr5:89770687-89770737	GM06990	blood:	n/a
24	chr5:89770579-89770629	NB4	blood:	n/a
25	chr5:89767709-89767759	HCM	heart:	n/a
26	chr5:89770751-89770801	NT2-D1	testis:	n/a
27	chr5:89770685-89770735	PrEC	prostate:	n/a
28	chr5:89770455-89770505	A549	lung:	n/a
29	chr5:89770699-89770749	PANC-1	pancreas:	n/a
30	chr5:89770600-89770650	CMK	blood:	n/a
31	chr5:89770751-89770801	HCT-116	colon:	n/a
32	chr5:89769642-89769692	SK-N-SH_RA	brain:	n/a
33	chr5:89772071-89772121	K562	blood:	n/a
34	chr5:89770579-89770629	AoSMC	blood vessel:	n/a
35	chr5:89770685-89770735	HMEC	breast:	n/a
36	chr5:89767709-89767759	U87	brain:	n/a
37	chr5:89769860-89769910	GM12891	blood:	n/a
38	chr5:89767709-89767759	T-47D	breast:	n/a
39	chr5:89765967-89766017	BE2_C	brain:	n/a
40	chr5:89806996-89807046	HPAEpiC	pulmonary alveolar:	n/a
41	chr5:89770685-89770735	U87	brain:	n/a
42	chr5:89771460-89771510	NH-A	brain:	n/a
43	chr5:89806996-89807046	BE2_C	brain:	n/a
44	chr5:89770751-89770801	ProgFib	skin:	n/a
45	chr5:89770393-89770443	NB4	blood:	n/a
46	chr5:89770451-89770501	GM06990	blood:	n/a
47	chr5:89770490-89770540	HUVEC	blood vessel:	n/a
48	chr5:89770751-89770801	ovcar-3	ovarian:	n/a
49	chr5:89769860-89769910	HL-60	blood:	n/a
50	chr5:89755537-89755587	HepG2	liver:	n/a

(count:100 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:89702296..89704546-chr5:89766463..89768000,2	K562	blood:
2	chr5:89704413..89707772-chr5:89751873..89754605,3	K562	blood:
3	chr5:89735143..89736756-chr5:89793768..89795673,2	K562	blood:
4	chr3:48754066..48754971-chr5:89770292..89770812,2	Hela-S3	cervix:
5	chr5:89770745..89773686-chr5:89789440..89792433,3	K562	blood:
6	chr5:89797561..89800163-chr5:89806524..89808529,2	K562	blood:
7	chr5:89703543..89706963-chr5:89767513..89771420,6	MCF-7	breast:
8	chr5:89760831..89763273-chr5:89763943..89766948,3	K562	blood:
9	chr5:89759858..89763860-chr5:89768823..89772030,5	MCF-7	breast:
10	chr5:89798219..89802006-chr5:89813801..89815608,3	K562	blood:
11	chr5:89703597..89706583-chr5:89780566..89782809,3	K562	blood:
12	chr5:89774118..89776549-chr5:89797426..89799656,2	K562	blood:
13	chr5:89780327..89783012-chr5:89790179..89792320,2	K562	blood:
14	chr5:89768617..89771955-chr5:89774063..89779125,7	MCF-7	breast:
15	chr5:89772669..89774767-chr5:89820227..89822408,2	K562	blood:
16	chr5:89764343..89768380-chr5:89768675..89771583,10	MCF-7	breast:
17	chr5:89755571..89758307-chr5:89852744..89855321,2	K562	blood:
18	chr5:89703969..89706957-chr5:89807176..89809846,2	K562	blood:
19	chr5:89705794..89707376-chr5:89755475..89757618,2	K562	blood:
20	chr5:89769110..89772331-chr5:90086907..90091587,4	K562	blood:
21	chr5:89765101..89767054-chr5:89819920..89822582,2	K562	blood:
22	chr5:89774118..89776549-chr5:89797426..89799656,2	K562	blood:
23	chr5:89742653..89745217-chr5:89752023..89754805,2	K562	blood:
24	chr5:89752466..89754308-chr5:89769045..89771515,2	K562	blood:
25	chr5:40835401..40836355-chr5:89770182..89770686,2	Hela-S3	cervix:
26	chr5:89761339..89763295-chr5:89824966..89826659,2	MCF-7	breast:
27	chr5:89787516..89789972-chr5:89796977..89800489,3	K562	blood:
28	chr5:89704491..89706992-chr5:89769088..89771566,3	MCF-7	breast:
29	chr5:89782175..89784403-chr5:89901956..89904362,2	MCF-7	breast:
30	chr5:89769482..89772726-chr5:89779643..89782858,4	MCF-7	breast:
31	chr5:89768855..89773751-chr5:89822671..89829297,12	K562	blood:
32	chr5:89745902..89748472-chr5:89767709..89770788,5	K562	blood:
33	chr5:89763652..89766204-chr5:89766216..89768442,2	K562	blood:
34	chr5:89787239..89791726-chr5:89792887..89795524,4	K562	blood:
35	chr5:89776558..89779410-chr5:89779694..89781697,3	K562	blood:
36	chr5:89801341..89803372-chr5:89815675..89817477,2	MCF-7	breast:
37	chr5:89801527..89803796-chr5:89803997..89806887,2	K562	blood:
38	chr5:89777835..89781277-chr5:89821033..89823702,3	K562	blood:
39	chr5:89760831..89763273-chr5:89763943..89766948,3	K562	blood:
40	chr5:89752385..89754792-chr5:89760288..89762882,3	MCF-7	breast:
41	chr5:89770106..89771750-chr5:112311690..112313641,2	K562	blood:
42	chr5:89797561..89800163-chr5:89806524..89808529,2	K562	blood:
43	chr5:89787516..89790569-chr5:89797724..89800540,3	K562	blood:
44	chr5:89780920..89782434-chr5:89853716..89856481,2	MCF-7	breast:
45	chr5:89803083..89805276-chr5:89823748..89825574,3	K562	blood:
46	chr5:89701553..89708894-chr5:89768084..89771807,14	K562	blood:
47	chr5:89752607..89755470-chr5:89857714..89859860,2	MCF-7	breast:
48	chr5:89703741..89706905-chr5:89793187..89795864,3	K562	blood:
49	chr5:89768691..89773005-chr5:89822332..89827140,9	MCF-7	breast:
50	chr5:89762579..89764211-chr5:89823157..89825268,2	K562	blood:

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	POLR3G	hsa-miR-26b-5p	chr5:89808262-89808269
2	MBLAC2	hsa-miR-155-5p	chr5:89754607-89754629
3	POLR3G	hsa-miR-26b-5p	chr5:89808249-89808269
4	POLR3G	hsa-miR-26b-5p	chr5:89808371-89808391
5	POLR3G	hsa-miR-26b-5p	chr5:89808385-89808391

Variant related genes	Relation type
MBLAC2	TF binding region
POLR3G	TF binding region
MBLAC2	CpG island
POLR3G	CpG island
ENSG00000102103	chromatin interactions
ENSG00000145592	chromatin interactions
ENSG00000153140	chromatin interactions
ENSG00000250571	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000113356	chromatin interactions
ENSG00000176055	chromatin interactions
ENSG00000126768	chromatin interactions
ENSG00000265565	chromatin interactions
ENSG00000184825	chromatin interactions
ENSG00000164199	chromatin interactions
ENSG00000012061	chromatin interactions
ENSG00000113369	chromatin interactions
ENSG00000126821	chromatin interactions
ENSG00000200972	chromatin interactions
ENSG00000255647	chromatin interactions
ENSG00000068745	chromatin interactions
ENSG00000172795	chromatin interactions
ENSG00000176018	chromatin interactions

Extended variants
information (count: 1993 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1993 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10214167	chr5:89748142-89748143	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563981657	chr5:89748182-89748183	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs6872360	chr5:89748234-89748235	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs566636760	chr5:89748269-89748270	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs560789309	chr5:89748280-89748281	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs369556745	chr5:89748350-89748351	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs115811413	chr5:89748476-89748477	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs531499592	chr5:89748483-89748484	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs569245319	chr5:89748599-89748600	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs559977359	chr5:89748603-89748604	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs558476419	chr5:89748610-89748611	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs187781292	chr5:89748635-89748636	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs534160900	chr5:89748647-89748648	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs78632229	chr5:89748660-89748661	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs141786028	chr5:89748699-89748700	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs59742368	chr5:89748836-89748837	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs551435903	chr5:89748868-89748869	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs575238955	chr5:89748896-89748897	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs376653625	chr5:89748936-89748937	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs60410599	chr5:89748957-89748958	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs543837879	chr5:89748969-89748970	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs61610742	chr5:89749005-89749006	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs533281078	chr5:89749042-89749043	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs2963695	chr5:89749043-89749044	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs192660674	chr5:89749045-89749046	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs529060099	chr5:89749074-89749075	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs138150431	chr5:89749092-89749093	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs569248983	chr5:89749118-89749119	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs531760759	chr5:89749125-89749126	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs551472048	chr5:89749181-89749182	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs571276033	chr5:89749224-89749225	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs534244833	chr5:89749232-89749233	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs554000010	chr5:89749351-89749352	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs182875199	chr5:89749395-89749396	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs72781074	chr5:89749427-89749428	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs76211353	chr5:89749450-89749451	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs575231916	chr5:89749497-89749498	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs115704902	chr5:89749527-89749528	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs188767288	chr5:89749567-89749568	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs111629951	chr5:89749582-89749583	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs577664304	chr5:89749583-89749584	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs142635565	chr5:89749591-89749592	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs192649819	chr5:89749623-89749624	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs529148672	chr5:89749641-89749642	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs542437448	chr5:89749701-89749702	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs563036174	chr5:89749709-89749710	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs531730442	chr5:89749755-89749756	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs565721986	chr5:89749774-89749775	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs150617929	chr5:89749785-89749786	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs184950782	chr5:89749825-89749826	Weak transcription	Chromatin interactive region	2 gene(s)	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
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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	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
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19592390	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1120 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89734600-89769000	Weak transcription	Pancreas	Pancrea
2	chr5:89736000-89753000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:89736400-89754400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr5:89736400-89767600	Weak transcription	Hela-S3	cervix
5	chr5:89736400-89768400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr5:89737600-89751800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr5:89737600-89757000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr5:89742800-89750400	Weak transcription	Liver	Liver
9	chr5:89743800-89751000	Weak transcription	Fetal Stomach	stomach
10	chr5:89743800-89767800	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr5:89744000-89750600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr5:89744200-89759000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr5:89744400-89751600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr5:89744400-89768600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr5:89745400-89765800	Weak transcription	A549	lung
16	chr5:89746200-89750600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr5:89746400-89765200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr5:89747200-89750600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr5:89747400-89768600	Weak transcription	NHDF-Ad	bronchial
20	chr5:89747600-89760200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr5:89748000-89768400	Weak transcription	Duodenum Mucosa	Duodenum
22	chr5:89748200-89757400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr5:89748200-89759600	Weak transcription	Primary T cells from cord blood	blood
24	chr5:89748400-89768600	Weak transcription	Adipose Nuclei	Adipose
25	chr5:89748600-89750600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr5:89748600-89750800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr5:89748600-89754400	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr5:89748600-89768200	Weak transcription	Osteobl	bone
29	chr5:89748800-89753000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr5:89749000-89754400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr5:89749200-89751000	Weak transcription	Fetal Intestine Small	intestine
32	chr5:89749200-89768400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr5:89749200-89768800	Weak transcription	Brain Germinal Matrix	brain
34	chr5:89749200-89768800	Weak transcription	Ovary	ovary
35	chr5:89749200-89769000	Weak transcription	Left Ventricle	heart
36	chr5:89749400-89767600	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr5:89749400-89768600	Weak transcription	Fetal Intestine Large	intestine
38	chr5:89749800-89754000	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr5:89749800-89768600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr5:89750000-89752600	Weak transcription	Fetal Muscle Leg	muscle
41	chr5:89750000-89754800	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr5:89750200-89756600	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr5:89750200-89768800	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr5:89750400-89752600	Strong transcription	Liver	Liver
45	chr5:89750600-89750800	Active TSS	Primary hematopoietic stem cells	blood
46	chr5:89750600-89751400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr5:89750600-89752200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr5:89750600-89753200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
49	chr5:89750600-89755000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr5:89750600-89759000	Weak transcription	Lung	lung

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