Variant report

Variant	nsv882775
Chromosome Location	chr5:118669094-118691888
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1167)
CpG islands
(count:1038)
Chromatin interactive
region (count:24)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1167 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:118673259-118673296	K562	blood:	n/a	n/a
2	ARID3A	chr5:118670705-118671029	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:118675431-118676059	K562	blood:	n/a	n/a
4	ATF1	chr5:118670279-118670327	K562	blood:	n/a	n/a
5	ATF1	chr5:118679408-118679544	K562	blood:	n/a	n/a
6	ATF1	chr5:118677891-118678079	K562	blood:	n/a	n/a
7	ATF1	chr5:118676333-118677014	K562	blood:	n/a	n/a
8	ATF2	chr5:118675485-118677940	GM12878	blood:	n/a	n/a
9	ATF2	chr5:118670480-118670949	GM12878	blood:	n/a	n/a
10	ATF2	chr5:118691369-118691917	GM12878	blood:	n/a	n/a
11	ATF2	chr5:118689343-118690645	GM12878	blood:	n/a	n/a
12	ATF2	chr5:118679215-118679910	GM12878	blood:	n/a	n/a
13	ATF2	chr5:118679296-118679918	GM12878	blood:	n/a	n/a
14	ATF2	chr5:118689827-118690698	GM12878	blood:	n/a	n/a
15	ATF2	chr5:118667855-118669525	GM12878	blood:	n/a	n/a
16	ATF2	chr5:118675651-118678448	GM12878	blood:	n/a	n/a
17	ATF2	chr5:118691304-118692503	GM12878	blood:	n/a	n/a
18	BACH1	chr5:118685198-118685225	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr5:118690953-118691153	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr5:118682477-118682568	K562	blood:	n/a	n/a
21	BATF	chr5:118691377-118691933	GM12878	blood:	n/a	n/a
22	BATF	chr5:118691509-118691818	GM12878	blood:	n/a	n/a
23	BATF	chr5:118679359-118679844	GM12878	blood:	n/a	n/a
24	BATF	chr5:118676180-118676561	GM12878	blood:	n/a	n/a
25	BATF	chr5:118668825-118669139	GM12878	blood:	n/a	n/a
26	BATF	chr5:118677370-118677893	GM12878	blood:	n/a	n/a
27	BCL11A	chr5:118679324-118679822	GM12878	blood:	n/a	n/a
28	BCL11A	chr5:118691327-118691910	GM12878	blood:	n/a	chr5:118691526-118691539 chr5:118691546-118691559 chr5:118691527-118691540
29	BCL11A	chr5:118677374-118677698	GM12878	blood:	n/a	chr5:118677543-118677552
30	BCL11A	chr5:118676114-118676728	GM12878	blood:	n/a	chr5:118676341-118676350
31	BCL11A	chr5:118677312-118677762	GM12878	blood:	n/a	chr5:118677543-118677552
32	BCL11A	chr5:118676243-118676633	GM12878	blood:	n/a	chr5:118676341-118676350
33	BCL3	chr5:118691275-118691906	GM12878	blood:	n/a	chr5:118691526-118691539 chr5:118691546-118691559 chr5:118691527-118691540
34	BCL3	chr5:118670601-118671129	A549	lung:	n/a	n/a
35	BCL3	chr5:118676124-118676678	GM12878	blood:	n/a	chr5:118676341-118676350
36	BCLAF1	chr5:118691267-118692383	GM12878	blood:	n/a	chr5:118691526-118691539 chr5:118691546-118691559 chr5:118691527-118691540 chr5:118691998-118692011
37	BCLAF1	chr5:118677006-118678110	GM12878	blood:	n/a	chr5:118677543-118677552
38	BCLAF1	chr5:118690659-118691201	GM12878	blood:	n/a	n/a
39	BCLAF1	chr5:118676089-118676735	GM12878	blood:	n/a	chr5:118676341-118676350
40	BCLAF1	chr5:118676780-118678155	GM12878	blood:	n/a	chr5:118677543-118677552
41	BCLAF1	chr5:118668446-118669754	GM12878	blood:	n/a	n/a
42	BCLAF1	chr5:118676122-118676724	GM12878	blood:	n/a	chr5:118676341-118676350
43	BCLAF1	chr5:118679238-118679816	GM12878	blood:	n/a	n/a
44	BCLAF1	chr5:118691253-118692793	GM12878	blood:	n/a	chr5:118691526-118691539 chr5:118691546-118691559 chr5:118691527-118691540 chr5:118691998-118692011
45	BCLAF1	chr5:118679311-118679762	GM12878	blood:	n/a	n/a
46	BCLAF1	chr5:118689518-118690235	GM12878	blood:	n/a	n/a
47	BHLHE40	chr5:118676238-118677016	K562	blood:	n/a	n/a
48	BHLHE40	chr5:118675681-118678090	GM12878	blood:	n/a	n/a
49	BHLHE40	chr5:118675697-118675857	K562	blood:	n/a	n/a
50	BHLHE40	chr5:118690758-118692466	GM12878	blood:	n/a	chr5:118691457-118691473 chr5:118691449-118691465

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:118691066-118691116	HMEC	breast:	n/a
2	chr5:118691066-118691116	HMEC	breast:	n/a
3	chr5:118691561-118691611	GM06990	blood:	n/a
4	chr5:118689293-118689343	ovcar-3	ovarian:	n/a
5	chr5:118691033-118691083	HMEC	breast:	n/a
6	chr5:118691561-118691611	HNPCEpiC	eye:	n/a
7	chr5:118691751-118691801	ECC-1	luminal epithelium:	n/a
8	chr5:118691007-118691057	HRPEpiC	eye:	n/a
9	chr5:118689961-118690011	HRPEpiC	eye:	n/a
10	chr5:118691066-118691116	HIPEpiC	eye:	n/a
11	chr5:118691126-118691176	K562	blood:	n/a
12	chr5:118677172-118677222	HRPEpiC	eye:	n/a
13	chr5:118677172-118677222	HCT-116	colon:	n/a
14	chr5:118690955-118691005	HRPEpiC	eye:	n/a
15	chr5:118691561-118691611	RPTEC	kidney:	n/a
16	chr5:118691425-118691475	SK-N-SH_RA	brain:	n/a
17	chr5:118683890-118683940	Jurkat	blood:	n/a
18	chr5:118677172-118677222	ECC-1	luminal epithelium:	n/a
19	chr5:118691751-118691801	HEK293	kidney:	embryo
20	chr5:118691425-118691475	Hela-S3	cervix:	n/a
21	chr5:118691751-118691801	NHBE	bronchial:	n/a
22	chr5:118691066-118691116	Jurkat	blood:	n/a
23	chr5:118689961-118690011	HCF	heart:	n/a
24	chr5:118691033-118691083	PANC-1	pancreas:	n/a
25	chr5:118691561-118691611	HCF	heart:	n/a
26	chr5:118691007-118691057	LNCaP	prostate:	n/a
27	chr5:118691007-118691057	NB4	blood:	n/a
28	chr5:118691425-118691475	ovcar-3	ovarian:	n/a
29	chr5:118691694-118691744	HCF	heart:	n/a
30	chr5:118691697-118691747	NT2-D1	testis:	n/a
31	chr5:118691794-118691844	CMK	blood:	n/a
32	chr5:118689961-118690011	HEEpiC	esophagus:	n/a
33	chr5:118691794-118691844	Caco-2	colon:	n/a
34	chr5:118690955-118691005	BJ	skin:	n/a
35	chr5:118691033-118691083	ProgFib	skin:	n/a
36	chr5:118691126-118691176	MCF10A-Er-Src	breast:	n/a
37	chr5:118691751-118691801	SAEC	small airway:	n/a
38	chr5:118691066-118691116	HRPEpiC	eye:	n/a
39	chr5:118691697-118691747	LNCaP	prostate:	n/a
40	chr5:118691697-118691747	PFSK-1	brain:	n/a
41	chr5:118683890-118683940	BJ	skin:	n/a
42	chr5:118691697-118691747	HCM	heart:	n/a
43	chr5:118691694-118691744	MCF-7	breast:	n/a
44	chr5:118691066-118691116	PrEC	prostate:	n/a
45	chr5:118689293-118689343	NT2-D1	testis:	n/a
46	chr5:118691751-118691801	PFSK-1	brain:	n/a
47	chr5:118691751-118691801	ProgFib	skin:	n/a
48	chr5:118691415-118691465	ProgFib	skin:	n/a
49	chr5:118691794-118691844	SKMC	muscle:	n/a
50	chr5:118691425-118691475	IMR90	lung:	fetal

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:118669449..118670965-chr5:118681990..118684958,2	K562	blood:
2	chr5:118657976..118659657-chr5:118675627..118677194,2	MCF-7	breast:
3	chr5:118547322..118548106-chr5:118670433..118671294,2	MCF-7	breast:
4	chr5:118322596..118324427-chr5:118669439..118671541,2	MCF-7	breast:
5	chr5:118604157..118605993-chr5:118671344..118674136,2	MCF-7	breast:
6	chr5:118665304..118666908-chr5:118684151..118685664,2	K562	blood:
7	chr5:118686914..118688782-chr5:118689065..118691768,2	MCF-7	breast:
8	chr5:118666908..118671699-chr5:118672968..118679055,7	K562	blood:
9	chr5:118666448..118669414-chr5:118669488..118671183,2	MCF-7	breast:
10	chr5:118675434..118678874-chr5:118679948..118684456,6	K562	blood:
11	chr5:118654543..118656491-chr5:118674624..118677344,2	K562	blood:
12	chr5:118650756..118653747-chr5:118669086..118671011,2	MCF-7	breast:
13	chr5:118658870..118659716-chr5:118670433..118671147,2	MCF-7	breast:
14	chr5:118672680..118674679-chr5:118676635..118678463,2	K562	blood:
15	chr5:118651451..118652140-chr5:118670433..118670936,2	MCF-7	breast:
16	chr5:118671639..118673344-chr5:118704484..118706218,2	MCF-7	breast:
17	chr5:118670103..118672210-chr5:118744741..118746294,2	MCF-7	breast:
18	chr5:118405258..118407472-chr5:118664950..118669105,3	K562	blood:
19	chr5:118672680..118674679-chr5:118676635..118678463,2	K562	blood:
20	chr5:118669449..118670965-chr5:118681990..118684958,2	K562	blood:
21	chr5:118667237..118669895-chr5:118670074..118672597,2	K562	blood:
22	chr5:118675434..118678874-chr5:118679948..118684456,6	K562	blood:
23	chr5:118666728..118668661-chr5:118669320..118670898,2	MCF-7	breast:
24	chr5:118602801..118604637-chr5:118670249..118672077,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DMXL1-8	chr5:118677271-118680524	NONHSAT103433

No data

Variant related genes	Relation type
TNFAIP8	TF binding region
TNFAIP8	CpG island
ENSG00000169570	chromatin interactions
ENSG00000249494	chromatin interactions
ENSG00000172869	chromatin interactions
ENSG00000145779	chromatin interactions

Extended variants
information (count: 903 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:903 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs250306	chr5:118669094-118669095	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs530256965	chr5:118669160-118669161	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs549320274	chr5:118669166-118669167	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs550431348	chr5:118669173-118669174	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370446675	chr5:118669189-118669190	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564549263	chr5:118669191-118669192	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563875206	chr5:118669223-118669224	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs11959659	chr5:118669224-118669225	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs574049277	chr5:118669268-118669269	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs566146645	chr5:118669291-118669292	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs56329027	chr5:118669304-118669305	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs539866498	chr5:118669326-118669327	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs191584320	chr5:118669351-118669352	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs567186597	chr5:118669358-118669359	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534098639	chr5:118669377-118669378	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs557217355	chr5:118669386-118669387	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577066127	chr5:118669427-118669428	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs574507884	chr5:118669457-118669458	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs371058002	chr5:118669488-118669489	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs572572528	chr5:118669489-118669490	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs541500641	chr5:118669503-118669504	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs549617336	chr5:118669535-118669536	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs567713196	chr5:118669556-118669557	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs183141440	chr5:118669576-118669577	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs188075626	chr5:118669606-118669607	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs543659610	chr5:118669628-118669629	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs192652922	chr5:118669703-118669704	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs72786157	chr5:118669780-118669781	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs57346323	chr5:118669849-118669850	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs1895202	chr5:118669851-118669852	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs559762473	chr5:118670003-118670004	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs368532305	chr5:118670043-118670044	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs146684869	chr5:118670117-118670118	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs250305	chr5:118670120-118670121	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs372762103	chr5:118670123-118670124	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs35990456	chr5:118670168-118670169	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs539053086	chr5:118670186-118670187	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs111535980	chr5:118670188-118670189	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs182320784	chr5:118670225-118670226	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs187728442	chr5:118670235-118670236	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs77414488	chr5:118670282-118670283	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs148502522	chr5:118670319-118670320	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs374415234	chr5:118670320-118670321	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs570691660	chr5:118670350-118670351	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs59714206	chr5:118670352-118670353	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs72786159	chr5:118670361-118670362	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs552874021	chr5:118670366-118670367	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs71585211	chr5:118670368-118670369	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs535118748	chr5:118670388-118670389	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs559261542	chr5:118670391-118670392	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Gastric cancer	17229543	CNVD

Chromatin state (count:1227 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:118658200-118670400	Weak transcription	Lung	lung
2	chr5:118659600-118677800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr5:118660200-118675600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr5:118660200-118678600	Weak transcription	HepG2	liver
5	chr5:118660400-118670400	Weak transcription	Right Atrium	heart
6	chr5:118662600-118670400	Weak transcription	Right Ventricle	heart
7	chr5:118663000-118669600	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr5:118663800-118669200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
9	chr5:118664200-118671600	Weak transcription	Small Intestine	intestine
10	chr5:118664200-118673400	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr5:118664400-118678200	Weak transcription	Fetal Kidney	kidney
12	chr5:118664600-118669200	Enhancers	Colonic Mucosa	Colon
13	chr5:118664800-118670600	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr5:118664800-118673000	Weak transcription	HSMM	muscle
15	chr5:118665000-118670400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr5:118665000-118670600	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr5:118665000-118672600	Weak transcription	Hela-S3	cervix
18	chr5:118665200-118669200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr5:118665200-118670400	Weak transcription	Osteobl	bone
20	chr5:118665400-118670600	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr5:118665400-118670600	Weak transcription	NHLF	lung
22	chr5:118665400-118677000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr5:118665600-118670000	Genic enhancers	Dnd41	blood
24	chr5:118665600-118670400	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr5:118665600-118670400	Weak transcription	Aorta	Aorta
26	chr5:118665600-118670600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr5:118665800-118670600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr5:118665800-118672600	Weak transcription	Fetal Intestine Small	intestine
29	chr5:118665800-118673200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr5:118666200-118669400	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr5:118666200-118672200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr5:118666400-118669600	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr5:118666600-118670400	Weak transcription	Adipose Nuclei	Adipose
34	chr5:118666600-118672600	Weak transcription	Fetal Stomach	stomach
35	chr5:118666800-118671000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr5:118667000-118669600	Genic enhancers	K562	blood
37	chr5:118667200-118669200	Weak transcription	Colon Smooth Muscle	Colon
38	chr5:118667600-118669400	Weak transcription	Placenta	Placenta
39	chr5:118667600-118670200	Weak transcription	Spleen	Spleen
40	chr5:118667600-118670400	Weak transcription	Esophagus	oesophagus
41	chr5:118667600-118670400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr5:118667600-118670400	Weak transcription	Left Ventricle	heart
43	chr5:118667600-118670400	Weak transcription	Pancreas	Pancrea
44	chr5:118667600-118671200	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr5:118667600-118671800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr5:118667600-118673000	Weak transcription	Gastric	stomach
47	chr5:118667800-118670400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr5:118667800-118670400	Weak transcription	Liver	Liver
49	chr5:118668000-118669800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
50	chr5:118668000-118672200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood

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