Variant report

Variant	nsv508522
Chromosome Location	chr8:105532034-105614403
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1289)
CpG islands
(count:734)
Chromatin interactive
region (count:74)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1289 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:105535835-105536069	K562	blood:	n/a	n/a
2	ARID3A	chr8:105548454-105548727	K562	blood:	n/a	n/a
3	ARID3A	chr8:105546470-105546519	K562	blood:	n/a	n/a
4	ARID3A	chr8:105541891-105542077	K562	blood:	n/a	n/a
5	ARID3A	chr8:105545234-105545610	K562	blood:	n/a	n/a
6	ARID3A	chr8:105591028-105591067	K562	blood:	n/a	n/a
7	ARID3A	chr8:105547231-105547709	K562	blood:	n/a	n/a
8	ARID3A	chr8:105601451-105601651	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:105597914-105598480	K562	blood:	n/a	n/a
10	ARID3A	chr8:105601357-105601729	K562	blood:	n/a	n/a
11	ARID3A	chr8:105583887-105583984	K562	blood:	n/a	n/a
12	ARID3A	chr8:105542573-105542845	K562	blood:	n/a	n/a
13	ARID3A	chr8:105550199-105551121	K562	blood:	n/a	n/a
14	ARID3A	chr8:105599810-105600452	K562	blood:	n/a	n/a
15	ARID3A	chr8:105552095-105552249	K562	blood:	n/a	n/a
16	ARID3A	chr8:105606601-105606865	K562	blood:	n/a	n/a
17	ARID3A	chr8:105602106-105602508	K562	blood:	n/a	n/a
18	ARID3A	chr8:105549052-105549937	K562	blood:	n/a	n/a
19	ARID3A	chr8:105594331-105594513	K562	blood:	n/a	n/a
20	ATF1	chr8:105542473-105542751	K562	blood:	n/a	n/a
21	ATF1	chr8:105597961-105598402	K562	blood:	n/a	n/a
22	ATF1	chr8:105586788-105586793	K562	blood:	n/a	n/a
23	ATF1	chr8:105535875-105536075	K562	blood:	n/a	n/a
24	ATF2	chr8:105587609-105588188	GM12878	blood:	n/a	n/a
25	ATF2	chr8:105597809-105598513	GM12878	blood:	n/a	n/a
26	ATF2	chr8:105601314-105601715	GM12878	blood:	n/a	n/a
27	ATF2	chr8:105587606-105588280	GM12878	blood:	n/a	n/a
28	ATF2	chr8:105601390-105601694	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr8:105558250-105558294	K562	blood:	n/a	n/a
30	BACH1	chr8:105598131-105598195	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr8:105601449-105601494	K562	blood:	n/a	n/a
32	BACH1	chr8:105598034-105598343	K562	blood:	n/a	n/a
33	BACH1	chr8:105601254-105602100	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr8:105600417-105600945	H1-hESC	embryonic stem cell:	n/a	n/a
35	BATF	chr8:105587771-105588108	GM12878	blood:	n/a	chr8:105587890-105587901
36	BATF	chr8:105580942-105581245	GM12878	blood:	n/a	chr8:105581123-105581134
37	BATF	chr8:105587624-105588145	GM12878	blood:	n/a	chr8:105587890-105587901
38	BATF	chr8:105601344-105601694	GM12878	blood:	n/a	n/a
39	BATF	chr8:105597912-105598347	GM12878	blood:	n/a	n/a
40	BATF	chr8:105597981-105598300	GM12878	blood:	n/a	n/a
41	BATF	chr8:105580959-105581283	GM12878	blood:	n/a	chr8:105581123-105581134
42	BCL11A	chr8:105597888-105598372	GM12878	blood:	n/a	n/a
43	BCL11A	chr8:105587733-105588169	GM12878	blood:	n/a	n/a
44	BCL11A	chr8:105587805-105588061	GM12878	blood:	n/a	n/a
45	BCL11A	chr8:105601500-105601660	GM12878	blood:	n/a	n/a
46	BCL3	chr8:105597706-105598304	A549	lung:	n/a	n/a
47	BCL3	chr8:105597909-105598381	GM12878	blood:	n/a	n/a
48	BCLAF1	chr8:105597954-105598429	GM12878	blood:	n/a	n/a
49	BCLAF1	chr8:105601331-105601682	GM12878	blood:	n/a	n/a
50	BCLAF1	chr8:105587472-105588067	GM12878	blood:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:105605548-105605598	CMK	blood:	n/a
2	chr8:105598224-105598274	RPTEC	kidney:	n/a
3	chr8:105605548-105605598	CMK	blood:	n/a
4	chr8:105598224-105598274	RPTEC	kidney:	n/a
5	chr8:105601862-105601912	AG10803	skin:	n/a
6	chr8:105600724-105600774	HAEpiC	amniotic membrane:	n/a
7	chr8:105601615-105601665	IMR90	lung:	fetal
8	chr8:105601835-105601885	HRCEpiC	kidney:	n/a
9	chr8:105605548-105605598	MCF10A-Er-Src	breast:	n/a
10	chr8:105605548-105605598	HRCEpiC	kidney:	n/a
11	chr8:105605548-105605598	T-47D	breast:	n/a
12	chr8:105601862-105601912	HIPEpiC	eye:	n/a
13	chr8:105601615-105601665	SK-N-MC	brain:	n/a
14	chr8:105601696-105601746	SAEC	small airway:	n/a
15	chr8:105601615-105601665	HNPCEpiC	eye:	n/a
16	chr8:105600242-105600292	HEEpiC	esophagus:	n/a
17	chr8:105601835-105601885	HepG2	liver:	n/a
18	chr8:105600724-105600774	HIPEpiC	eye:	n/a
19	chr8:105605548-105605598	NHBE	bronchial:	n/a
20	chr8:105600242-105600292	AG09309	skin:	n/a
21	chr8:105601047-105601097	U87	brain:	n/a
22	chr8:105601835-105601885	HCT-116	colon:	n/a
23	chr8:105601696-105601746	HRCEpiC	kidney:	n/a
24	chr8:105601047-105601097	IMR90	lung:	fetal
25	chr8:105601641-105601691	SK-N-MC	brain:	n/a
26	chr8:105601036-105601086	HIPEpiC	eye:	n/a
27	chr8:105600242-105600292	RPTEC	kidney:	n/a
28	chr8:105605548-105605598	MCF-7	breast:	n/a
29	chr8:105601641-105601691	HNPCEpiC	eye:	n/a
30	chr8:105601862-105601912	NHDF-neo	bronchial:	n/a
31	chr8:105601047-105601097	ProgFib	skin:	n/a
32	chr8:105601696-105601746	PANC-1	pancreas:	n/a
33	chr8:105601036-105601086	HUVEC	blood vessel:	n/a
34	chr8:105600242-105600292	HIPEpiC	eye:	n/a
35	chr8:105601615-105601665	HCF	heart:	n/a
36	chr8:105598224-105598274	T-47D	breast:	n/a
37	chr8:105601047-105601097	MCF-7	breast:	n/a
38	chr8:105601862-105601912	HPAEpiC	pulmonary alveolar:	n/a
39	chr8:105601615-105601665	CMK	blood:	n/a
40	chr8:105601047-105601097	HCT-116	colon:	n/a
41	chr8:105601036-105601086	HCT-116	colon:	n/a
42	chr8:105601835-105601885	CMK	blood:	n/a
43	chr8:105600242-105600292	GM06990	blood:	n/a
44	chr8:105601641-105601691	SKMC	muscle:	n/a
45	chr8:105601615-105601665	Jurkat	blood:	n/a
46	chr8:105605548-105605598	HMEC	breast:	n/a
47	chr8:105601696-105601746	Caco-2	colon:	n/a
48	chr8:105601036-105601086	AG04449	skin:	fetal
49	chr8:105601615-105601665	PANC-1	pancreas:	n/a
50	chr8:105601641-105601691	HRE	kidney:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:105597422..105599476-chr8:105599959..105601722,3	MCF-7	breast:
2	chr8:105587608..105589528-chr8:105597267..105600152,2	K562	blood:
3	chr8:105536142..105538633-chr8:105600457..105602580,2	MCF-7	breast:
4	chr8:105549086..105551378-chr8:105574063..105575720,2	K562	blood:
5	chr8:105604121..105606507-chr8:105689435..105691482,2	K562	blood:
6	chr8:105607303..105609924-chr8:105610357..105613113,2	MCF-7	breast:
7	chr8:105533738..105535742-chr8:105540260..105542167,2	MCF-7	breast:
8	chr8:105599361..105601982-chr8:105602248..105604776,3	MCF-7	breast:
9	chr8:105546044..105547694-chr8:105549682..105551996,2	K562	blood:
10	chr8:105599361..105601982-chr8:105602248..105604776,3	MCF-7	breast:
11	chr8:105564767..105567386-chr8:105599921..105602701,2	MCF-7	breast:
12	chr8:105590187..105593939-chr8:105599095..105602249,3	MCF-7	breast:
13	chr8:105578550..105580666-chr8:105596704..105598646,2	K562	blood:
14	chr8:105529593..105532262-chr8:105532296..105533876,2	K562	blood:
15	chr8:105550559..105552900-chr8:105554736..105557129,2	MCF-7	breast:
16	chr8:105596040..105597564-chr8:105603152..105604788,2	MCF-7	breast:
17	chr8:105539636..105541987-chr8:105546259..105549133,2	K562	blood:
18	chr8:105572145..105574529-chr8:105581183..105583326,2	K562	blood:
19	chr8:105544664..105547366-chr8:105749781..105751384,2	MCF-7	breast:
20	chr8:105543714..105545305-chr8:105608007..105609799,2	K562	blood:
21	chr8:105529380..105531604-chr8:105534787..105536889,2	K562	blood:
22	chr8:105571197..105572822-chr8:105600384..105602252,2	K562	blood:
23	chr8:105556248..105558457-chr8:105560436..105562817,2	MCF-7	breast:
24	chr8:105603605..105606287-chr8:105614491..105616469,2	K562	blood:
25	chr8:105528612..105531312-chr8:105607615..105609704,2	K562	blood:
26	chr8:105534479..105537318-chr8:105685417..105687384,2	K562	blood:
27	chr8:105565492..105567421-chr8:105600088..105601868,2	MCF-7	breast:
28	chr8:105607424..105610207-chr8:105615952..105617508,2	K562	blood:
29	chr8:105547753..105551944-chr8:105551987..105556104,4	K562	blood:
30	chr8:105609190..105611773-chr8:105612258..105615333,3	K562	blood:
31	chr8:105596815..105598399-chr8:105654955..105657445,2	K562	blood:
32	chr8:105608581..105611555-chr8:105688371..105691323,2	K562	blood:
33	chr8:105603605..105610207-chr8:105613658..105617508,6	K562	blood:
34	chr8:105609190..105611773-chr8:105612258..105615333,3	K562	blood:
35	chr8:105539636..105541250-chr8:105546259..105548784,2	K562	blood:
36	chr8:105583573..105585685-chr8:105598077..105599877,2	K562	blood:
37	chr8:105533738..105535742-chr8:105540260..105542167,2	MCF-7	breast:
38	chr8:105590457..105593310-chr8:105600135..105602594,4	K562	blood:
39	chr8:105541937..105546028-chr8:105546808..105551808,5	K562	blood:
40	chr8:105541186..105543623-chr8:105675952..105678475,2	K562	blood:
41	chr8:105594673..105597308-chr8:105598908..105601422,3	MCF-7	breast:
42	chr8:105548452..105551549-chr8:105551987..105555312,4	K562	blood:
43	chr8:105596040..105597564-chr8:105603152..105604788,2	MCF-7	breast:
44	chr8:105583196..105585939-chr8:105600741..105602751,2	K562	blood:
45	chr8:105560103..105561664-chr8:105601162..105603797,2	K562	blood:
46	chr8:105539636..105541250-chr8:105546259..105548784,2	K562	blood:
47	chr8:105548452..105551549-chr8:105551987..105555312,4	K562	blood:
48	chr8:105543820..105546530-chr8:105760722..105763113,2	K562	blood:
49	chr8:105543714..105545305-chr8:105608007..105609799,2	K562	blood:
50	chr8:105572145..105574529-chr8:105581183..105583326,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-127H5.1.1-2	chr8:105578314-105578657	NONHSAT128220

No data

Variant related genes	Relation type
NDUFA5P2	TF binding region
ENSG00000253350	TF binding region
LRP12	TF binding region
NDUFA5P2	CpG island
ENSG00000253350	CpG island
LRP12	CpG island
ENSG00000147650	chromatin interactions
ENSG00000253350	chromatin interactions

Extended variants
information (count: 3128 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:3128 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558913950	chr8:105532043-105532044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs77204605	chr8:105532121-105532122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs376157732	chr8:105532123-105532124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs35767747	chr8:105532154-105532155	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs563369445	chr8:105532225-105532226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs371849068	chr8:105532296-105532297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs141198226	chr8:105532297-105532298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530746123	chr8:105532298-105532299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs71520893	chr8:105532302-105532303	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs111765557	chr8:105532305-105532306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs528368817	chr8:105532321-105532322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547862271	chr8:105532325-105532326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556330514	chr8:105532339-105532340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs75139456	chr8:105532346-105532347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs35967695	chr8:105532349-105532350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs569540350	chr8:105532394-105532395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs140600608	chr8:105532427-105532428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs150415753	chr8:105532432-105532433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs138133348	chr8:105532459-105532460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs149174507	chr8:105532487-105532488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555639858	chr8:105532518-105532519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs34493777	chr8:105532547-105532548	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs112585677	chr8:105532575-105532576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs373828811	chr8:105532587-105532588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541323053	chr8:105532640-105532641	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552574847	chr8:105532647-105532648	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577199977	chr8:105532650-105532651	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs16871538	chr8:105532670-105532671	Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs16871540	chr8:105532731-105532732	Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs182576321	chr8:105532743-105532744	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs146487176	chr8:105532794-105532795	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs115074328	chr8:105532820-105532821	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528423958	chr8:105532849-105532850	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546901345	chr8:105532931-105532932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574723426	chr8:105532956-105532957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565143102	chr8:105532959-105532960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188893680	chr8:105533011-105533012	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73295127	chr8:105533033-105533034	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs7813481	chr8:105533090-105533091	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs192095961	chr8:105533113-105533114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549599595	chr8:105533143-105533144	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567734590	chr8:105533152-105533153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535016141	chr8:105533153-105533154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182872987	chr8:105533193-105533194	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553264444	chr8:105533251-105533252	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78103771	chr8:105533252-105533253	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138135048	chr8:105533269-105533270	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs556675762	chr8:105533270-105533271	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575347427	chr8:105533287-105533288	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187472082	chr8:105533360-105533361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

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
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
Sezary syndrome	18413736	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:1068 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:105499200-105542200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:105503800-105535800	Weak transcription	NHDF-Ad	bronchial
3	chr8:105509600-105535800	Weak transcription	Aorta	Aorta
4	chr8:105510200-105546200	Weak transcription	HMEC	breast
5	chr8:105510400-105539400	Weak transcription	HSMMtube	muscle
6	chr8:105511800-105532600	Weak transcription	HSMM	muscle
7	chr8:105511800-105550200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr8:105512800-105542000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr8:105512800-105550200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr8:105515200-105542400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr8:105519800-105534400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr8:105520400-105534800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr8:105520600-105537400	Weak transcription	NH-A	brain
14	chr8:105520800-105536600	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr8:105521000-105540000	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr8:105521400-105540000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr8:105521800-105568800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr8:105527200-105543000	Weak transcription	Primary hematopoietic stem cells	blood
19	chr8:105527400-105535600	Weak transcription	K562	blood
20	chr8:105527600-105534000	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr8:105527800-105549600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr8:105530200-105532600	Enhancers	Dnd41	blood
23	chr8:105530200-105540000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr8:105530200-105542600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr8:105531400-105534400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr8:105531400-105544600	Weak transcription	Brain Anterior Caudate	brain
27	chr8:105531600-105540000	Weak transcription	Fetal Thymus	thymus
28	chr8:105531600-105540400	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr8:105531600-105542200	Weak transcription	Thymus	Thymus
30	chr8:105531800-105534400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr8:105532600-105532800	Genic enhancers	Dnd41	blood
32	chr8:105532600-105533200	Strong transcription	HSMM	muscle
33	chr8:105532800-105533400	Strong transcription	Dnd41	blood
34	chr8:105533200-105551400	Weak transcription	HSMM	muscle
35	chr8:105533400-105534600	Weak transcription	Brain Hippocampus Middle	brain
36	chr8:105533400-105535800	Weak transcription	Dnd41	blood
37	chr8:105533400-105539000	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr8:105534000-105540000	Weak transcription	Brain Germinal Matrix	brain
39	chr8:105534400-105534800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr8:105534400-105535200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr8:105534400-105535800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr8:105534600-105534800	Enhancers	Brain Hippocampus Middle	brain
43	chr8:105534800-105535200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr8:105534800-105535600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr8:105534800-105535800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr8:105534800-105535800	Enhancers	GM12878-XiMat	blood
47	chr8:105534800-105536200	Enhancers	A549	lung
48	chr8:105534800-105544400	Weak transcription	Brain Hippocampus Middle	brain
49	chr8:105534800-105549400	Weak transcription	Osteobl	bone
50	chr8:105535200-105535800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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