Variant report

Variant	esv3511406
Chromosome Location	chr5:118409810-118459495
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:221)
CpG islands
(count:61)
Chromatin interactive
region (count:23)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:221 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:118414951-118415381	K562	blood:	n/a	n/a
2	ARID3A	chr5:118409996-118410235	K562	blood:	n/a	n/a
3	ATF1	chr5:118410040-118410119	K562	blood:	n/a	n/a
4	ATF2	chr5:118409921-118410605	GM12878	blood:	n/a	n/a
5	ATF2	chr5:118409872-118410675	GM12878	blood:	n/a	n/a
6	BACH1	chr5:118414944-118415775	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr5:118415197-118415534	GM12878	blood:	n/a	n/a
8	BATF	chr5:118410023-118410530	GM12878	blood:	n/a	n/a
9	BATF	chr5:118409998-118410330	GM12878	blood:	n/a	n/a
10	BATF	chr5:118415147-118415603	GM12878	blood:	n/a	n/a
11	BCL11A	chr5:118410073-118410262	GM12878	blood:	n/a	chr5:118410231-118410240
12	BCL11A	chr5:118415243-118415608	GM12878	blood:	n/a	n/a
13	BCLAF1	chr5:118409916-118410653	GM12878	blood:	n/a	chr5:118410231-118410240
14	BHLHE40	chr5:118412086-118412242	GM12878	blood:	n/a	n/a
15	BHLHE40	chr5:118413129-118413462	K562	blood:	n/a	n/a
16	BHLHE40	chr5:118410102-118410677	GM12878	blood:	n/a	n/a
17	CBX3	chr5:118421618-118422203	K562	blood:	n/a	n/a
18	CBX3	chr5:118410936-118411366	K562	blood:	n/a	n/a
19	CCNT2	chr5:118417240-118417440	K562	blood:	n/a	n/a
20	CEBPB	chr5:118414460-118414811	IMR90	lung:	n/a	n/a
21	CEBPB	chr5:118414374-118414625	HepG2	liver:	n/a	n/a
22	CEBPB	chr5:118430489-118430589	K562	blood:	n/a	n/a
23	CEBPB	chr5:118425375-118425408	A549	lung:	n/a	n/a
24	CEBPB	chr5:118414432-118414681	K562	blood:	n/a	n/a
25	CEBPB	chr5:118409798-118410657	GM12878	blood:	n/a	n/a
26	CHD1	chr5:118409910-118410713	GM12878	blood:	n/a	n/a
27	CHD1	chr5:118414851-118415284	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr5:118409924-118410526	GM12878	blood:	n/a	n/a
29	CHD2	chr5:118414885-118415681	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr5:118409978-118410643	GM12878	blood:	n/a	n/a
31	CTCF	chr5:118455294-118455343	Lung_OC	lung:	n/a	n/a
32	CTCF	chr5:118444165-118444224	ProgFib	skin:	n/a	n/a
33	CTCF	chr5:118444124-118444172	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr5:118413234-118413304	MCF-7	breast:	n/a	n/a
35	CUX1	chr5:118414880-118415010	GM12878	blood:	n/a	n/a
36	CUX1	chr5:118446029-118446106	GM12878	blood:	n/a	n/a
37	CUX1	chr5:118415380-118415580	K562	blood:	n/a	n/a
38	E2F6	chr5:118413198-118413399	K562	blood:	n/a	n/a
39	EBF1	chr5:118410085-118410583	GM12878	blood:	n/a	n/a
40	EGR1	chr5:118411124-118411244	GM12878	blood:	n/a	n/a
41	EGR1	chr5:118411035-118411329	K562	blood:	n/a	n/a
42	EGR1	chr5:118411049-118411347	K562	blood:	n/a	n/a
43	ELF1	chr5:118409532-118409898	K562	blood:	n/a	chr5:118409692-118409705
44	EP300	chr5:118409997-118410397	GM12878	blood:	n/a	chr5:118410226-118410240 chr5:118410052-118410066
45	EP300	chr5:118411671-118411769	GM12878	blood:	n/a	chr5:118411684-118411698 chr5:118411685-118411699 chr5:118411688-118411702 chr5:118411690-118411704
46	EP300	chr5:118414919-118415531	K562	blood:	n/a	n/a
47	EP300	chr5:118410016-118410508	GM12878	blood:	n/a	chr5:118410226-118410240 chr5:118410052-118410066
48	EP300	chr5:118415087-118415733	H1-hESC	embryonic stem cell:	n/a	n/a
49	EP300	chr5:118413943-118414017	GM12878	blood:	n/a	chr5:118413980-118413994
50	EP300	chr5:118409990-118410570	GM12878	blood:	n/a	chr5:118410226-118410240 chr5:118410052-118410066

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:118416915-118416965	SK-N-MC	brain:	n/a
2	chr5:118416915-118416965	HIPEpiC	eye:	n/a
3	chr5:118416915-118416965	GM19239	blood:	n/a
4	chr5:118416915-118416965	CMK	blood:	n/a
5	chr5:118416915-118416965	SKMC	muscle:	n/a
6	chr5:118416915-118416965	BE2_C	brain:	n/a
7	chr5:118416915-118416965	HCPEpiC	choroid plexus:	n/a
8	chr5:118416915-118416965	Caco-2	colon:	n/a
9	chr5:118416915-118416965	A549	lung:	n/a
10	chr5:118416915-118416965	IMR90	lung:	fetal
11	chr5:118416915-118416965	MCF10A-Er-Src	breast:	n/a
12	chr5:118416915-118416965	GM12892	blood:	n/a
13	chr5:118416915-118416965	AG09309	skin:	n/a
14	chr5:118416915-118416965	AG04450	lung:	fetal
15	chr5:118416915-118416965	GM06990	blood:	n/a
16	chr5:118416915-118416965	RPTEC	kidney:	n/a
17	chr5:118416915-118416965	H1-hESC	embryonic stem cell:	embryo
18	chr5:118416915-118416965	U87	brain:	n/a
19	chr5:118416915-118416965	K562	blood:	n/a
20	chr5:118416915-118416965	MCF-7	breast:	n/a
21	chr5:118416915-118416965	HCT-116	colon:	n/a
22	chr5:118416915-118416965	Hela-S3	cervix:	n/a
23	chr5:118416915-118416965	HepG2	liver:	n/a
24	chr5:118416915-118416965	HEEpiC	esophagus:	n/a
25	chr5:118416915-118416965	NHBE	bronchial:	n/a
26	chr5:118416915-118416965	BJ	skin:	n/a
27	chr5:118416915-118416965	SAEC	small airway:	n/a
28	chr5:118416915-118416965	HCF	heart:	n/a
29	chr5:118416915-118416965	GM12891	blood:	n/a
30	chr5:118416915-118416965	HEK293	kidney:	embryo
31	chr5:118416915-118416965	HMEC	breast:	n/a
32	chr5:118416915-118416965	ovcar-3	ovarian:	n/a
33	chr5:118416915-118416965	LNCaP	prostate:	n/a
34	chr5:118416915-118416965	HPAEpiC	pulmonary alveolar:	n/a
35	chr5:118416915-118416965	AG09319	gingival:	n/a
36	chr5:118416915-118416965	HCM	heart:	n/a
37	chr5:118416915-118416965	NH-A	brain:	n/a
38	chr5:118416915-118416965	Hepatocyte	liver:	n/a
39	chr5:118416915-118416965	HNPCEpiC	eye:	n/a
40	chr5:118416915-118416965	ProgFib	skin:	n/a
41	chr5:118416915-118416965	AG10803	skin:	n/a
42	chr5:118416915-118416965	T-47D	breast:	n/a
43	chr5:118416915-118416965	PFSK-1	brain:	n/a
44	chr5:118416915-118416965	GM12878	blood:	n/a
45	chr5:118416915-118416965	SK-N-SH_RA	brain:	n/a
46	chr5:118416915-118416965	HRPEpiC	eye:	n/a
47	chr5:118416915-118416965	PANC-1	pancreas:	n/a
48	chr5:118416915-118416965	HRE	kidney:	n/a
49	chr5:118416915-118416965	NT2-D1	testis:	n/a
50	chr5:118416915-118416965	HL-60	blood:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:118405803..118408184-chr5:118416454..118418702,2	MCF-7	breast:
2	chr5:118450875..118452560-chr5:118453902..118455943,2	K562	blood:
3	chr5:118416688..118419081-chr5:118737050..118740009,2	K562	blood:
4	chr5:118442391..118447973-chr5:118448057..118454025,9	K562	blood:
5	chr5:118415616..118417740-chr5:118600067..118602902,2	MCF-7	breast:
6	chr5:118406208..118409819-chr5:118421498..118424768,4	MCF-7	breast:
7	chr5:118450748..118453641-chr5:118458726..118460761,2	K562	blood:
8	chr5:118450875..118452560-chr5:118453902..118455943,2	K562	blood:
9	chr5:118443410..118445340-chr5:118449495..118451851,2	K562	blood:
10	chr5:118405957..118409296-chr5:118409304..118413767,5	MCF-7	breast:
11	chr5:118405552..118407163-chr5:118413181..118416258,3	K562	blood:
12	chr5:118416875..118419760-chr5:118654118..118656007,2	K562	blood:
13	chr5:118407762..118409623-chr5:118414700..118416296,2	K562	blood:
14	chr5:118408484..118411107-chr5:118751959..118754643,2	K562	blood:
15	chr5:118450748..118453641-chr5:118458726..118460761,2	K562	blood:
16	chr5:118453288..118453823-chr5:118482934..118483702,2	K562	blood:
17	chr5:118405385..118408063-chr5:118418201..118420659,2	K562	blood:
18	chr5:118443410..118445340-chr5:118449495..118451851,2	K562	blood:
19	chr5:118406491..118408879-chr5:118423582..118425820,2	MCF-7	breast:
20	chr5:118442391..118447973-chr5:118448057..118454025,9	K562	blood:
21	chr5:118442538..118444845-chr5:118444949..118447296,2	K562	blood:
22	chr5:118442538..118444845-chr5:118444949..118447296,2	K562	blood:
23	chr5:118406683..118408484-chr5:118448040..118450335,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DMXL1-5	chr5:118439823-118439975	NONHSAT103415
2	lnc-DMXL1-5	chr5:118437630-118437905	NONHSAT103419
3	lnc-DMXL1-5	chr5:118433674-118433799	NONHSAT103415
4	lnc-DMXL1-5	chr5:118436296-118436366	NONHSAT103419
5	lnc-DMXL1-5	chr5:118437630-118437701	NONHSAT103415

No data

Variant related genes	Relation type
ENSG00000249494	TF binding region
ENSG00000239011	TF binding region
DMXL1	TF binding region
ENSG00000249494	CpG island
ENSG00000239011	CpG island
DMXL1	CpG island
ENSG00000172869	chromatin interactions
ENSG00000249494	chromatin interactions

Extended variants
information (count: 2324 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2324 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538062436	chr5:118409863-118409864	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs551997032	chr5:118409869-118409870	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs571416035	chr5:118409871-118409872	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs533852089	chr5:118409874-118409875	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs4493704	chr5:118409934-118409935	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs141908260	chr5:118409961-118409962	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs192531738	chr5:118409992-118409993	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs202062311	chr5:118410023-118410024	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs1375163	chr5:118410049-118410050	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs147345369	chr5:118410074-118410075	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs576275817	chr5:118410100-118410101	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs544921700	chr5:118410112-118410113	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs558307727	chr5:118410133-118410134	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs373451767	chr5:118410161-118410162	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs185064606	chr5:118410209-118410210	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs560184489	chr5:118410259-118410260	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs529272618	chr5:118410289-118410290	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs190296934	chr5:118410292-118410293	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs552944313	chr5:118410306-118410307	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs564653023	chr5:118410388-118410389	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs116254186	chr5:118410428-118410429	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs532031408	chr5:118410430-118410431	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs552033678	chr5:118410431-118410432	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs571855618	chr5:118410433-118410434	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs139458356	chr5:118410440-118410441	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs142530999	chr5:118410481-118410482	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs181221007	chr5:118410526-118410527	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs535879430	chr5:118410536-118410537	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs74589253	chr5:118410617-118410618	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs528722545	chr5:118410685-118410686	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs547085357	chr5:118410759-118410760	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs569878651	chr5:118410795-118410796	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs140791902	chr5:118410871-118410872	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs34916964	chr5:118410916-118410917	Enhancers Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs201065387	chr5:118410936-118410937	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs201088042	chr5:118410937-118410938	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs558396025	chr5:118410972-118410973	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs571929145	chr5:118411056-118411057	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs548443934	chr5:118411068-118411069	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs540778894	chr5:118411080-118411081	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs186675681	chr5:118411099-118411100	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs553855449	chr5:118411159-118411160	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs574068376	chr5:118411164-118411165	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs369080336	chr5:118411170-118411171	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs150031597	chr5:118411176-118411177	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs372819928	chr5:118411177-118411178	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs568553903	chr5:118411186-118411187	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs576540331	chr5:118411187-118411188	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs545732243	chr5:118411196-118411197	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs146610586	chr5:118411197-118411198	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
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
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
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	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
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1262 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:118405200-118410000	Active TSS	K562	blood
2	chr5:118405600-118410000	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr5:118405600-118410800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:118406000-118411000	Active TSS	GM12878-XiMat	blood
5	chr5:118407200-118410800	Flanking Active TSS	Primary B cells from cord blood	blood
6	chr5:118407600-118413000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr5:118407600-118423600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr5:118407800-118410600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
9	chr5:118407800-118410600	Enhancers	Brain Anterior Caudate	brain
10	chr5:118407800-118410600	Enhancers	Colon Smooth Muscle	Colon
11	chr5:118407800-118412400	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr5:118407800-118413800	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr5:118407800-118421600	Weak transcription	Fetal Muscle Trunk	muscle
14	chr5:118407800-118456600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr5:118408000-118410400	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr5:118408000-118410600	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr5:118408000-118414600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr5:118408000-118414600	Weak transcription	HSMM	muscle
19	chr5:118408200-118410600	Enhancers	Adipose Nuclei	Adipose
20	chr5:118408200-118412200	Enhancers	Primary T helper cells fromperipheralblood	blood
21	chr5:118408400-118451800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr5:118408600-118410200	Active TSS	Rectal Mucosa Donor 29	rectum
23	chr5:118408600-118410600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr5:118408600-118412200	Enhancers	Liver	Liver
25	chr5:118408600-118414400	Weak transcription	Osteobl	bone
26	chr5:118408600-118414600	Weak transcription	Fetal Intestine Small	intestine
27	chr5:118408600-118414800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr5:118408800-118410000	Active TSS	HUES6 Cell Line	embryonic stem cell
29	chr5:118408800-118410000	Enhancers	Duodenum Smooth Muscle	Duodenum
30	chr5:118408800-118410200	Enhancers	Rectal Smooth Muscle	rectum
31	chr5:118408800-118410600	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr5:118408800-118411800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr5:118408800-118414600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr5:118408800-118414800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr5:118409000-118410000	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr5:118409000-118410000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr5:118409000-118410400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr5:118409000-118410400	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr5:118409000-118410800	Enhancers	HepG2	liver
40	chr5:118409000-118411400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr5:118409000-118411800	Weak transcription	Brain Germinal Matrix	brain
42	chr5:118409000-118412800	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr5:118409000-118413200	Weak transcription	Fetal Brain Male	brain
44	chr5:118409000-118414200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr5:118409000-118414200	Weak transcription	Right Ventricle	heart
46	chr5:118409000-118414400	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr5:118409000-118414400	Weak transcription	NHEK	skin
48	chr5:118409000-118414800	Weak transcription	Right Atrium	heart
49	chr5:118409000-118415600	Weak transcription	Left Ventricle	heart
50	chr5:118409000-118415800	Weak transcription	Fetal Muscle Leg	muscle

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