Variant report

Variant	nsv539695
Chromosome Location	chr8:100190356-100720313
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2908)
CpG islands
(count:1099)
Chromatin interactive
region (count:233)
LncRNA
region (count:8)
Mature miRNA
region (count: 3)
miRNA target
sites (count:1)

(count:2908 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:100298952-100299271	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:100649546-100649965	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:100694633-100695046	K562	blood:	n/a	n/a
4	ARID3A	chr8:100510905-100511524	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:100718258-100718424	K562	blood:	n/a	chr8:100718324-100718340
6	ARID3A	chr8:100476490-100476616	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:100416524-100416817	K562	blood:	n/a	n/a
8	ARID3A	chr8:100519158-100519359	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:100400144-100400181	K562	blood:	n/a	n/a
10	ARID3A	chr8:100370824-100371122	HepG2	liver:	n/a	n/a
11	ARID3A	chr8:100645951-100646742	HepG2	liver:	n/a	chr8:100645997-100646013
12	ARID3A	chr8:100370860-100371168	K562	blood:	n/a	n/a
13	ARID3A	chr8:100649502-100649902	K562	blood:	n/a	n/a
14	ARID3A	chr8:100445541-100445734	HepG2	liver:	n/a	n/a
15	ATF1	chr8:100370807-100371120	K562	blood:	n/a	n/a
16	ATF1	chr8:100654398-100654716	K562	blood:	n/a	n/a
17	ATF1	chr8:100718057-100718285	K562	blood:	n/a	n/a
18	ATF1	chr8:100609763-100609906	K562	blood:	n/a	n/a
19	ATF1	chr8:100617407-100617536	K562	blood:	n/a	n/a
20	ATF1	chr8:100649659-100649974	K562	blood:	n/a	n/a
21	ATF1	chr8:100416505-100416787	K562	blood:	n/a	n/a
22	ATF1	chr8:100249602-100249617	K562	blood:	n/a	n/a
23	ATF1	chr8:100515482-100515487	K562	blood:	n/a	n/a
24	ATF1	chr8:100468108-100468135	K562	blood:	n/a	n/a
25	ATF1	chr8:100278899-100278960	K562	blood:	n/a	n/a
26	ATF2	chr8:100675640-100676176	GM12878	blood:	n/a	n/a
27	ATF2	chr8:100675713-100676177	GM12878	blood:	n/a	n/a
28	ATF2	chr8:100667670-100668603	GM12878	blood:	n/a	n/a
29	ATF3	chr8:100717996-100718348	K562	blood:	n/a	n/a
30	BACH1	chr8:100395401-100395488	K562	blood:	n/a	n/a
31	BACH1	chr8:100694808-100695067	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr8:100389266-100389270	K562	blood:	n/a	n/a
33	BACH1	chr8:100694604-100695056	K562	blood:	n/a	n/a
34	BATF	chr8:100648147-100648397	GM12878	blood:	n/a	n/a
35	BATF	chr8:100460709-100460986	GM12878	blood:	n/a	chr8:100460813-100460824
36	BATF	chr8:100694790-100695087	GM12878	blood:	n/a	chr8:100694911-100694922
37	BATF	chr8:100507953-100508207	GM12878	blood:	n/a	n/a
38	BATF	chr8:100668709-100669157	GM12878	blood:	n/a	n/a
39	BATF	chr8:100253079-100253361	GM12878	blood:	n/a	n/a
40	BATF	chr8:100510858-100511111	GM12878	blood:	n/a	chr8:100510967-100510978
41	BATF	chr8:100667761-100668621	GM12878	blood:	n/a	n/a
42	BATF	chr8:100510819-100511214	GM12878	blood:	n/a	chr8:100510967-100510978
43	BATF	chr8:100692484-100692710	GM12878	blood:	n/a	n/a
44	BATF	chr8:100698390-100698700	GM12878	blood:	n/a	chr8:100698530-100698541
45	BATF	chr8:100691641-100691903	GM12878	blood:	n/a	n/a
46	BATF	chr8:100460738-100460975	GM12878	blood:	n/a	chr8:100460813-100460824
47	BATF	chr8:100694712-100695127	GM12878	blood:	n/a	chr8:100694911-100694922
48	BATF	chr8:100668748-100669124	GM12878	blood:	n/a	n/a
49	BATF	chr8:100508028-100508205	GM12878	blood:	n/a	n/a
50	BATF	chr8:100667811-100668195	GM12878	blood:	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	chr8:100716071-100716121	HUVEC	blood vessel:	n/a
2	chr8:100716071-100716121	HUVEC	blood vessel:	n/a
3	chr8:100549849-100549899	NHDF-neo	bronchial:	n/a
4	chr8:100667796-100667846	SAEC	small airway:	n/a
5	chr8:100246786-100246836	HCPEpiC	choroid plexus:	n/a
6	chr8:100708945-100708995	Hela-S3	cervix:	n/a
7	chr8:100262768-100262818	ECC-1	luminal epithelium:	n/a
8	chr8:100667796-100667846	AG09319	gingival:	n/a
9	chr8:100464878-100464928	HPAEpiC	pulmonary alveolar:	n/a
10	chr8:100464878-100464928	HIPEpiC	eye:	n/a
11	chr8:100708621-100708671	HEK293	kidney:	embryo
12	chr8:100297748-100297798	AoSMC	blood vessel:	n/a
13	chr8:100246786-100246836	HNPCEpiC	eye:	n/a
14	chr8:100708621-100708671	AG04449	skin:	fetal
15	chr8:100230864-100230914	GM19239	blood:	n/a
16	chr8:100667796-100667846	HEEpiC	esophagus:	n/a
17	chr8:100252466-100252516	PrEC	prostate:	n/a
18	chr8:100252466-100252516	HIPEpiC	eye:	n/a
19	chr8:100708945-100708995	HRCEpiC	kidney:	n/a
20	chr8:100246786-100246836	GM12891	blood:	n/a
21	chr8:100246786-100246836	NT2-D1	testis:	n/a
22	chr8:100667796-100667846	HRPEpiC	eye:	n/a
23	chr8:100559503-100559553	HCT-116	colon:	n/a
24	chr8:100716071-100716121	Caco-2	colon:	n/a
25	chr8:100334620-100334670	NHDF-neo	bronchial:	n/a
26	chr8:100262768-100262818	MCF-7	breast:	n/a
27	chr8:100549776-100549826	BE2_C	brain:	n/a
28	chr8:100493491-100493541	HPAEpiC	pulmonary alveolar:	n/a
29	chr8:100716071-100716121	A549	lung:	n/a
30	chr8:100252466-100252516	A549	lung:	n/a
31	chr8:100708545-100708595	SK-N-MC	brain:	n/a
32	chr8:100246786-100246836	IMR90	lung:	fetal
33	chr8:100230864-100230914	AG04450	lung:	fetal
34	chr8:100549776-100549826	HepG2	liver:	n/a
35	chr8:100493491-100493541	HepG2	liver:	n/a
36	chr8:100262768-100262818	IMR90	lung:	fetal
37	chr8:100252466-100252516	T-47D	breast:	n/a
38	chr8:100716071-100716121	U87	brain:	n/a
39	chr8:100464878-100464928	RPTEC	kidney:	n/a
40	chr8:100708545-100708595	Jurkat	blood:	n/a
41	chr8:100493491-100493541	GM12878	blood:	n/a
42	chr8:100649114-100649164	SK-N-MC	brain:	n/a
43	chr8:100708545-100708595	Hela-S3	cervix:	n/a
44	chr8:100635039-100635089	HPAEpiC	pulmonary alveolar:	n/a
45	chr8:100549776-100549826	CMK	blood:	n/a
46	chr8:100262768-100262818	GM19239	blood:	n/a
47	chr8:100559503-100559553	NHBE	bronchial:	n/a
48	chr8:100230864-100230914	AG09309	skin:	n/a
49	chr8:100559503-100559553	ProgFib	skin:	n/a
50	chr8:100334620-100334670	SK-N-SH_RA	brain:	n/a

(count:233 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr8:100180149..100180921-chr8:100370671..100371459,2	MCF-7	breast:
2	chr8:100218080..100220133-chr8:100221773..100223694,2	K562	blood:
3	chr8:100403788..100404692-chr8:100799555..100800231,3	MCF-7	breast:
4	chr8:100587220..100589733-chr8:100589949..100592234,2	K562	blood:
5	chr8:100607857..100609807-chr8:100619167..100621104,2	K562	blood:
6	chr8:100719725..100721462-chr8:100723554..100725582,2	K562	blood:
7	chr8:100253574..100255217-chr8:100258258..100260154,2	K562	blood:
8	chr11:74032580..74033199-chr8:100370794..100371470,2	MCF-7	breast:
9	chr8:100474939..100477291-chr8:100497932..100499895,2	MCF-7	breast:
10	chr8:100222308..100224756-chr8:100228347..100230627,2	K562	blood:
11	chr8:99717161..99717948-chr8:100352640..100353640,2	K562	blood:
12	chr5:56110114..56112436-chr8:100221279..100223933,2	MCF-7	breast:
13	chr8:100381765..100384655-chr8:100392997..100394529,2	K562	blood:
14	chr8:100464584..100466784-chr8:100489016..100491472,2	MCF-7	breast:
15	chr8:100629647..100631528-chr8:100671490..100673021,2	K562	blood:
16	chr8:100253354..100255632-chr8:100258136..100261117,2	MCF-7	breast:
17	chr8:100340207..100341801-chr8:100343989..100346691,2	MCF-7	breast:
18	chr8:100717456..100719730-chr8:100748168..100750293,2	MCF-7	breast:
19	chr8:100197794..100200560-chr8:100203500..100205350,2	MCF-7	breast:
20	chr8:100553009..100554706-chr8:100561096..100563189,2	K562	blood:
21	chr8:100506206..100508940-chr8:100515378..100517666,2	MCF-7	breast:
22	chr8:100197794..100200560-chr8:100203500..100205350,2	MCF-7	breast:
23	chr8:100210858..100212558-chr8:100220865..100223573,2	MCF-7	breast:
24	chr8:100559744..100561257-chr8:101041447..101043428,2	K562	blood:
25	chr8:100534887..100536607-chr8:100537446..100539997,2	K562	blood:
26	chr8:100693782..100695662-chr8:100781246..100783612,2	K562	blood:
27	chr8:100403606..100404633-chr8:100616940..100618032,4	MCF-7	breast:
28	chr8:100241348..100243532-chr8:101014262..101016207,2	MCF-7	breast:
29	chr8:100354480..100357120-chr8:100365143..100367945,2	K562	blood:
30	chr8:100368561..100370943-chr8:100372272..100375246,2	K562	blood:
31	chr8:100492530..100494149-chr8:100495886..100498811,2	MCF-7	breast:
32	chr8:100343791..100346575-chr8:100348119..100349870,2	MCF-7	breast:
33	chr8:100615293..100618024-chr8:100620811..100623753,2	MCF-7	breast:
34	chr8:100715387..100717513-chr8:100719961..100722930,2	K562	blood:
35	chr8:100263532..100265951-chr8:100267509..100269368,2	K562	blood:
36	chr8:100433051..100434745-chr9:90387715..90390439,2	MCF-7	breast:
37	chr8:100266373..100268336-chr8:100270835..100272790,2	K562	blood:
38	chr8:100433911..100436132-chr8:100443954..100446728,2	MCF-7	breast:
39	chr8:100357228..100359296-chr8:100360534..100362578,2	MCF-7	breast:
40	chr8:100707994..100711279-chr8:100711487..100714977,4	K562	blood:
41	chr8:100253785..100255699-chr8:100276390..100278151,2	MCF-7	breast:
42	chr8:100048867..100050500-chr8:100268956..100271777,2	MCF-7	breast:
43	chr8:100380996..100382939-chr8:100386454..100387970,2	K562	blood:
44	chr8:100525847..100527559-chr8:100529820..100532768,2	MCF-7	breast:
45	chr8:100711733..100714570-chr8:100716914..100719775,2	MCF-7	breast:
46	chr8:100712738..100714435-chr8:100716061..100717614,2	K562	blood:
47	chr8:100641638..100644745-chr8:100644767..100647893,3	K562	blood:
48	chr8:100532719..100535105-chr8:100539628..100541847,3	MCF-7	breast:
49	chr8:100459116..100461634-chr8:100473693..100476496,2	MCF-7	breast:
50	chr8:100214282..100216094-chr8:100216677..100219374,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OSR2-7	chr8:100401844-100401948	NONHSAT127953
2	lnc-STK3-7	chr8:100358280-100360484	NONHSAT127952
3	lnc-OSR2-7	chr8:100454629-100454639	NONHSAT127953
4	lnc-OSR2-7	chr8:100441798-100441875	NONHSAT127953
5	lnc-COX6C-2	chr8:100626014-100626306	NONHSAT127958
6	lnc-OSR2-7	chr8:100443749-100443892	NONHSAT127953
7	lnc-OSR2-7	chr8:100403785-100403932	NONHSAT127953
8	lnc-STK3-6	chr8:100352533-100353989	NONHSAT127951

miRNA name	Chromosome Location	mirBase accession
hsa-miR-875-3p	chr8:100549025-100549045	MIMAT0004923
hsa-miR-599	chr8:100548879-100548898	MIMAT0003267
hsa-miR-875-5p	chr8:100549058-100549079	MIMAT0004922

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	VPS13B	hsa-miR-186-5p	chr8:100221987-100222010

Variant related genes	Relation type
RN7SL350P	TF binding region
VPS13B	TF binding region
MIR599	TF binding region
ENSG00000225017	TF binding region
ENSG00000236583	TF binding region
MIR875	TF binding region
ENSG00000235683	TF binding region
ENSG00000206699	TF binding region
ENSG00000237704	TF binding region
RN7SL350P	CpG island
VPS13B	CpG island
MIR599	CpG island
ENSG00000225017	CpG island
ENSG00000236583	CpG island
MIR875	CpG island
ENSG00000235683	CpG island
ENSG00000206699	CpG island
ENSG00000237704	CpG island
ENSG00000207804	chromatin interactions
ENSG00000132549	chromatin interactions
ENSG00000095015	chromatin interactions
ENSG00000216069	chromatin interactions
ENSG00000235683	chromatin interactions
ENSG00000253948	chromatin interactions
ENSG00000188029	chromatin interactions
ENSG00000253912	chromatin interactions
ENSG00000270135	chromatin interactions
ENSG00000164920	chromatin interactions
ENSG00000225017	chromatin interactions
ENSG00000206699	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000009307	chromatin interactions
ENSG00000004779	chromatin interactions
ENSG00000243254	chromatin interactions

Extended variants
information (count: 17734 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:17734 , 50 per page) page: 1 2 3 4 5 6 7 ... 355

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7821383	chr8:100190375-100190376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566670642	chr8:100190378-100190379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563911996	chr8:100190383-100190384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs75348644	chr8:100190386-100190387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550168496	chr8:100190387-100190388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs527669325	chr8:100190388-100190389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs570029927	chr8:100190390-100190391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539022982	chr8:100190392-100190393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190707374	chr8:100190406-100190407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566177244	chr8:100190408-100190409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534861408	chr8:100190436-100190437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181903501	chr8:100190500-100190501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs142194646	chr8:100190502-100190503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536919088	chr8:100190564-100190565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556554663	chr8:100190569-100190570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576458811	chr8:100190576-100190577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145925258	chr8:100190678-100190679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545391325	chr8:100190721-100190722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs559061982	chr8:100190807-100190808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139156048	chr8:100190814-100190815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546649668	chr8:100190859-100190860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574928318	chr8:100190912-100190913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561294268	chr8:100190913-100190914	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186042082	chr8:100190918-100190919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190961032	chr8:100190936-100190937	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201306007	chr8:100190953-100190954	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183175532	chr8:100190972-100190973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs4615539	chr8:100190985-100190986	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs552597952	chr8:100191097-100191098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566189314	chr8:100191141-100191142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528531858	chr8:100191145-100191146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs188108650	chr8:100191146-100191147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529265982	chr8:100191191-100191192	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201206360	chr8:100191195-100191196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs115671952	chr8:100191214-100191215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs376856972	chr8:100191251-100191252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537228901	chr8:100191281-100191282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7826207	chr8:100191304-100191305	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs570402757	chr8:100191313-100191314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs569547995	chr8:100191367-100191368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs540014649	chr8:100191470-100191471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539054527	chr8:100191471-100191472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs143656714	chr8:100191535-100191536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs76129651	chr8:100191546-100191547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs112197286	chr8:100191630-100191631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552503258	chr8:100191719-100191720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572915144	chr8:100191743-100191744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs10808361	chr8:100191783-100191784	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs555422363	chr8:100191793-100191794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs10808362	chr8:100191814-100191815	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Colorectal cancer	19455253	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cohen syndrome	20461111	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:4733 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:100109200-100197600	Weak transcription	HUVEC	blood vessel
2	chr8:100109600-100198000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr8:100122000-100201200	Weak transcription	Gastric	stomach
4	chr8:100131800-100197600	Weak transcription	Lung	lung
5	chr8:100161400-100202000	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr8:100163000-100197000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr8:100163000-100198800	Weak transcription	HSMM	muscle
8	chr8:100163200-100197800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr8:100163400-100190400	Weak transcription	Fetal Brain Male	brain
10	chr8:100163400-100191000	Weak transcription	Ovary	ovary
11	chr8:100163400-100198200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr8:100163400-100214400	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr8:100163400-100224800	Weak transcription	Duodenum Mucosa	Duodenum
14	chr8:100163400-100225000	Weak transcription	Fetal Thymus	thymus
15	chr8:100163400-100226800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr8:100163400-100226800	Weak transcription	Fetal Muscle Trunk	muscle
17	chr8:100163400-100230600	Weak transcription	Right Ventricle	heart
18	chr8:100163600-100214200	Weak transcription	Dnd41	blood
19	chr8:100163600-100214400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr8:100163800-100206600	Weak transcription	GM12878-XiMat	blood
21	chr8:100164000-100205000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr8:100164000-100225600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr8:100164000-100229600	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr8:100164200-100245000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr8:100164800-100214400	Weak transcription	Liver	Liver
26	chr8:100165200-100206400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr8:100166800-100194400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr8:100169800-100192600	Weak transcription	Primary hematopoietic stem cells	blood
29	chr8:100170200-100192400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr8:100171200-100205000	Weak transcription	Primary T helper cells fromperipheralblood	blood
31	chr8:100171400-100214400	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr8:100173400-100191200	Weak transcription	NHDF-Ad	bronchial
33	chr8:100173400-100192400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr8:100173400-100198200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr8:100173400-100202400	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr8:100174800-100207800	Weak transcription	Primary B cells from peripheral blood	blood
37	chr8:100175400-100222800	Weak transcription	Fetal Stomach	stomach
38	chr8:100176200-100222600	Weak transcription	Fetal Intestine Large	intestine
39	chr8:100176400-100190800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr8:100178200-100194200	Weak transcription	Brain Anterior Caudate	brain
41	chr8:100178800-100245000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr8:100178800-100245000	Weak transcription	Fetal Intestine Small	intestine
43	chr8:100179200-100191800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr8:100179200-100199800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr8:100179200-100204800	Weak transcription	Primary B cells from cord blood	blood
46	chr8:100179200-100217000	Weak transcription	Adipose Nuclei	Adipose
47	chr8:100179200-100223000	Weak transcription	Fetal Muscle Leg	muscle
48	chr8:100179200-100229600	Weak transcription	Fetal Lung	lung
49	chr8:100179400-100197400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr8:100179400-100202600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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