Variant report

Variant	nsv1026442
Chromosome Location	chr8:100075230-100561451
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2785)
CpG islands
(count:795)
Chromatin interactive
region (count:211)
LncRNA
region (count:11)
Mature miRNA
region (count: 3)
miRNA target
sites (count:1)

(count:2785 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:100445541-100445734	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:100124728-100124858	K562	blood:	n/a	n/a
3	ARID3A	chr8:100370824-100371122	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:100510905-100511524	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:100476490-100476616	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:100416524-100416817	K562	blood:	n/a	n/a
7	ARID3A	chr8:100370860-100371168	K562	blood:	n/a	n/a
8	ARID3A	chr8:100400144-100400181	K562	blood:	n/a	n/a
9	ARID3A	chr8:100519158-100519359	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:100103092-100103687	K562	blood:	n/a	n/a
11	ARID3A	chr8:100298952-100299271	HepG2	liver:	n/a	n/a
12	ARID3A	chr8:100149959-100150472	K562	blood:	n/a	n/a
13	ATF1	chr8:100150113-100150549	K562	blood:	n/a	n/a
14	ATF1	chr8:100135547-100135703	K562	blood:	n/a	n/a
15	ATF1	chr8:100416505-100416787	K562	blood:	n/a	n/a
16	ATF1	chr8:100249602-100249617	K562	blood:	n/a	n/a
17	ATF1	chr8:100515482-100515487	K562	blood:	n/a	n/a
18	ATF1	chr8:100103355-100103611	K562	blood:	n/a	n/a
19	ATF1	chr8:100177666-100177787	K562	blood:	n/a	n/a
20	ATF1	chr8:100370807-100371120	K562	blood:	n/a	n/a
21	ATF1	chr8:100468108-100468135	K562	blood:	n/a	n/a
22	ATF1	chr8:100278899-100278960	K562	blood:	n/a	n/a
23	ATF2	chr8:100093166-100093626	GM12878	blood:	n/a	n/a
24	ATF2	chr8:100092901-100093701	GM12878	blood:	n/a	n/a
25	ATF3	chr8:100103253-100103550	K562	blood:	n/a	n/a
26	ATF3	chr8:100150017-100150481	K562	blood:	n/a	n/a
27	BACH1	chr8:100389266-100389270	K562	blood:	n/a	n/a
28	BACH1	chr8:100150185-100150441	K562	blood:	n/a	n/a
29	BACH1	chr8:100395401-100395488	K562	blood:	n/a	n/a
30	BACH1	chr8:100182411-100182437	H1-hESC	embryonic stem cell:	n/a	n/a
31	BATF	chr8:100510858-100511111	GM12878	blood:	n/a	chr8:100510967-100510978
32	BATF	chr8:100093290-100093609	GM12878	blood:	n/a	n/a
33	BATF	chr8:100093275-100093603	GM12878	blood:	n/a	n/a
34	BATF	chr8:100510819-100511214	GM12878	blood:	n/a	chr8:100510967-100510978
35	BATF	chr8:100253079-100253361	GM12878	blood:	n/a	n/a
36	BATF	chr8:100460709-100460986	GM12878	blood:	n/a	chr8:100460813-100460824
37	BATF	chr8:100508028-100508205	GM12878	blood:	n/a	n/a
38	BATF	chr8:100507953-100508207	GM12878	blood:	n/a	n/a
39	BATF	chr8:100460738-100460975	GM12878	blood:	n/a	chr8:100460813-100460824
40	BCL11A	chr8:100305139-100305357	GM12878	blood:	n/a	n/a
41	BCL11A	chr8:100508034-100508288	H1-hESC	embryonic stem cell:	n/a	n/a
42	BCL11A	chr8:100093229-100093561	GM12878	blood:	n/a	chr8:100093423-100093432
43	BCL11A	chr8:100508018-100508319	GM12878	blood:	n/a	n/a
44	BCL11A	chr8:100508036-100508276	GM12878	blood:	n/a	n/a
45	BCL3	chr8:100510825-100511538	A549	lung:	n/a	n/a
46	BCLAF1	chr8:100092916-100093613	GM12878	blood:	n/a	chr8:100093423-100093432
47	BCLAF1	chr8:100510821-100511230	GM12878	blood:	n/a	n/a
48	BHLHE40	chr8:100370878-100370919	A549	lung:	n/a	n/a
49	BHLHE40	chr8:100150155-100150410	K562	blood:	n/a	n/a
50	BHLHE40	chr8:100404161-100404287	K562	blood:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:100549776-100549826	NT2-D1	testis:	n/a
2	chr8:100157208-100157258	AG10803	skin:	n/a
3	chr8:100549776-100549826	NT2-D1	testis:	n/a
4	chr8:100157208-100157258	AG10803	skin:	n/a
5	chr8:100464878-100464928	AG04449	skin:	fetal
6	chr8:100262768-100262818	NB4	blood:	n/a
7	chr8:100104103-100104153	NB4	blood:	n/a
8	chr8:100157208-100157258	ProgFib	skin:	n/a
9	chr8:100559503-100559553	ECC-1	luminal epithelium:	n/a
10	chr8:100549776-100549826	GM12891	blood:	n/a
11	chr8:100104103-100104153	MCF10A-Er-Src	breast:	n/a
12	chr8:100104103-100104153	AG04449	skin:	fetal
13	chr8:100493491-100493541	PANC-1	pancreas:	n/a
14	chr8:100559503-100559553	GM12891	blood:	n/a
15	chr8:100246786-100246836	HAEpiC	amniotic membrane:	n/a
16	chr8:100246786-100246836	NHDF-neo	bronchial:	n/a
17	chr8:100262768-100262818	HRE	kidney:	n/a
18	chr8:100549849-100549899	HRE	kidney:	n/a
19	chr8:100104103-100104153	HEEpiC	esophagus:	n/a
20	chr8:100230864-100230914	HCM	heart:	n/a
21	chr8:100493491-100493541	HIPEpiC	eye:	n/a
22	chr8:100252466-100252516	GM19239	blood:	n/a
23	chr8:100493491-100493541	HRCEpiC	kidney:	n/a
24	chr8:100262768-100262818	GM19239	blood:	n/a
25	chr8:100246786-100246836	HCPEpiC	choroid plexus:	n/a
26	chr8:100252466-100252516	GM06990	blood:	n/a
27	chr8:100230864-100230914	ProgFib	skin:	n/a
28	chr8:100549849-100549899	HUVEC	blood vessel:	n/a
29	chr8:100559503-100559553	NHBE	bronchial:	n/a
30	chr8:100493491-100493541	AG09309	skin:	n/a
31	chr8:100549849-100549899	LNCaP	prostate:	n/a
32	chr8:100230864-100230914	HRPEpiC	eye:	n/a
33	chr8:100549849-100549899	RPTEC	kidney:	n/a
34	chr8:100464878-100464928	K562	blood:	n/a
35	chr8:100493491-100493541	AG04449	skin:	fetal
36	chr8:100230864-100230914	NB4	blood:	n/a
37	chr8:100549849-100549899	Hepatocyte	liver:	n/a
38	chr8:100262768-100262818	NHBE	bronchial:	n/a
39	chr8:100246786-100246836	SK-N-SH_RA	brain:	n/a
40	chr8:100252466-100252516	MCF10A-Er-Src	breast:	n/a
41	chr8:100230864-100230914	RPTEC	kidney:	n/a
42	chr8:100230864-100230914	HEEpiC	esophagus:	n/a
43	chr8:100252466-100252516	HCPEpiC	choroid plexus:	n/a
44	chr8:100246786-100246836	RPTEC	kidney:	n/a
45	chr8:100252466-100252516	ovcar-3	ovarian:	n/a
46	chr8:100549849-100549899	Caco-2	colon:	n/a
47	chr8:100246786-100246836	HepG2	liver:	n/a
48	chr8:100493491-100493541	GM06990	blood:	n/a
49	chr8:100493491-100493541	HPAEpiC	pulmonary alveolar:	n/a
50	chr8:100297748-100297798	Hepatocyte	liver:	n/a

(count:211 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr8:100513095..100514805-chr8:100516611..100518159,2	MCF-7	breast:
2	chr8:100298711..100300024-chr8:100370075..100371268,5	MCF-7	breast:
3	chr5:56110114..56112436-chr8:100221279..100223933,2	MCF-7	breast:
4	chr8:100217626..100220133-chr8:100221301..100223694,2	K562	blood:
5	chr8:100544046..100548556-chr8:100548656..100552103,4	K562	blood:
6	chr8:100525847..100527559-chr8:100529820..100532768,2	MCF-7	breast:
7	chr8:100486979..100489783-chr8:100490347..100493276,2	MCF-7	breast:
8	chr8:100354480..100357120-chr8:100365143..100367945,2	K562	blood:
9	chr8:100539051..100543758-chr8:100545879..100549609,5	K562	blood:
10	chr8:99995141..99996042-chr8:100118104..100118628,2	MCF-7	breast:
11	chr8:100266373..100268336-chr8:100270835..100272790,2	K562	blood:
12	chr8:100024284..100027084-chr8:100113982..100120280,5	MCF-7	breast:
13	chr8:100253354..100255632-chr8:100258136..100261117,2	MCF-7	breast:
14	chr8:100048867..100050500-chr8:100268956..100271777,2	MCF-7	breast:
15	chr8:100506206..100508940-chr8:100515378..100517666,2	MCF-7	breast:
16	chr8:100109729..100112333-chr8:100147157..100149231,2	K562	blood:
17	chr8:100266373..100268336-chr8:100270835..100272790,2	K562	blood:
18	chr8:100494882..100496542-chr8:100496740..100499297,2	MCF-7	breast:
19	chr8:100103552..100105106-chr8:100109674..100111736,2	K562	blood:
20	chr8:100189672..100191957-chr8:100789803..100791931,2	MCF-7	breast:
21	chr8:100247496..100249230-chr8:100251577..100253709,2	K562	blood:
22	chr8:100368561..100370943-chr8:100372272..100375246,2	K562	blood:
23	chr8:100180104..100181200-chr8:100370523..100371154,5	MCF-7	breast:
24	chr8:100550054..100551658-chr8:100559009..100560949,2	K562	blood:
25	chr8:100403606..100404633-chr8:100616940..100618032,4	MCF-7	breast:
26	chr8:100495717..100498178-chr8:100505651..100508035,2	K562	blood:
27	chr8:100247496..100249230-chr8:100251577..100253709,2	K562	blood:
28	chr8:100550054..100551658-chr8:100559009..100560949,2	K562	blood:
29	chr8:100534887..100536607-chr8:100537446..100539997,2	K562	blood:
30	chr8:100021568..100024441-chr8:100255336..100257958,2	MCF-7	breast:
31	chr8:100125265..100128114-chr8:100129986..100133353,3	K562	blood:
32	chr8:100145698..100148364-chr8:100156045..100158193,2	MCF-7	breast:
33	chr8:100180037..100180965-chr8:100818919..100819673,2	MCF-7	breast:
34	chr8:100440991..100443912-chr8:100444936..100447073,2	K562	blood:
35	chr8:100222308..100224756-chr8:100228347..100230627,2	K562	blood:
36	chr8:100360393..100360964-chr8:100816462..100817102,2	MCF-7	breast:
37	chr8:100235746..100237944-chr8:100240108..100241895,2	K562	blood:
38	chr8:99955457..99958039-chr8:100115422..100117482,3	MCF-7	breast:
39	chr8:100187208..100189859-chr8:100191478..100193795,2	MCF-7	breast:
40	chr8:100534887..100536607-chr8:100537446..100539997,2	K562	blood:
41	chr8:100024034..100025700-chr8:100109623..100113452,3	MCF-7	breast:
42	chr8:100459116..100461634-chr8:100473693..100476496,2	MCF-7	breast:
43	chr8:100403279..100404684-chr8:100871403..100872860,7	MCF-7	breast:
44	chr8:100145698..100148364-chr8:100156045..100158193,2	MCF-7	breast:
45	chr8:99717161..99717948-chr8:100352640..100353640,2	K562	blood:
46	chr8:100103552..100105106-chr8:100109674..100111736,2	K562	blood:
47	chr8:100197794..100200560-chr8:100203500..100205350,2	MCF-7	breast:
48	chr8:100012703..100016134-chr8:100151109..100154697,3	MCF-7	breast:
49	chr8:100190689..100193029-chr8:100201859..100204401,2	K562	blood:
50	chr8:100444521..100447261-chr8:100451811..100454572,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OSR2-2	chr8:100132332-100132809	ENSG00000253532.1
2	lnc-OSR2-2	chr8:100131580-100131696	ENSG00000253532.1
3	lnc-STK3-3	chr8:100103966-100104326	ENSG00000253562.1
4	lnc-OSR2-7	chr8:100441798-100441875	NONHSAT127953
5	lnc-STK3-3	chr8:100106157-100106288	ENSG00000253562.1
6	lnc-OSR2-7	chr8:100443749-100443892	NONHSAT127953
7	lnc-OSR2-7	chr8:100454629-100454639	NONHSAT127953
8	lnc-STK3-7	chr8:100358280-100360484	NONHSAT127952
9	lnc-OSR2-7	chr8:100403785-100403932	NONHSAT127953
10	lnc-OSR2-7	chr8:100401844-100401948	NONHSAT127953
11	lnc-STK3-6	chr8:100352533-100353989	NONHSAT127951

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

(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
VPS13B	TF binding region
ENSG00000253562	TF binding region
ENSG00000206699	TF binding region
ENSG00000237704	TF binding region
MIR599	TF binding region
ENSG00000225017	TF binding region
ENSG00000236583	TF binding region
ENSG00000253532	TF binding region
MIR875	TF binding region
VPS13B	CpG island
ENSG00000253562	CpG island
ENSG00000206699	CpG island
ENSG00000237704	CpG island
MIR599	CpG island
ENSG00000225017	CpG island
ENSG00000236583	CpG island
ENSG00000253532	CpG island
MIR875	CpG island
ENSG00000271930	chromatin interactions
ENSG00000206699	chromatin interactions
ENSG00000207804	chromatin interactions
ENSG00000009307	chromatin interactions
ENSG00000004779	chromatin interactions
ENSG00000132549	chromatin interactions
ENSG00000253912	chromatin interactions
ENSG00000225017	chromatin interactions
ENSG00000188029	chromatin interactions
ENSG00000253532	chromatin interactions
ENSG00000253948	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000253180	chromatin interactions
ENSG00000164920	chromatin interactions
ENSG00000095015	chromatin interactions
ENSG00000270135	chromatin interactions
ENSG00000216069	chromatin interactions

Extended variants
information (count: 16356 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:16356 , 50 per page) page: 1 2 3 4 5 6 7 ... 328

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113586011	chr8:100075242-100075243	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs200462811	chr8:100075243-100075244	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs527432419	chr8:100075279-100075280	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs547607206	chr8:100075288-100075289	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs528837572	chr8:100075321-100075322	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs187921422	chr8:100075339-100075340	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs561278474	chr8:100075393-100075394	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs191225209	chr8:100075422-100075423	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549777375	chr8:100075436-100075437	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569523917	chr8:100075490-100075491	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183522194	chr8:100075494-100075495	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538363381	chr8:100075506-100075507	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369075669	chr8:100075508-100075509	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571510162	chr8:100075521-100075522	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549270036	chr8:100075523-100075524	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187925007	chr8:100075524-100075525	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs192557073	chr8:100075564-100075565	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141573402	chr8:100075598-100075599	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576315960	chr8:100075628-100075629	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562631875	chr8:100075648-100075649	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs545519674	chr8:100075692-100075693	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184895906	chr8:100075701-100075702	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189963726	chr8:100075709-100075710	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs541264064	chr8:100075717-100075718	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560907210	chr8:100075741-100075742	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375091032	chr8:100075810-100075811	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530025657	chr8:100075848-100075849	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549774817	chr8:100075915-100075916	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113207186	chr8:100075960-100075961	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531936558	chr8:100075999-100076000	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11985761	chr8:100076001-100076002	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs565479565	chr8:100076021-100076022	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569105036	chr8:100076022-100076023	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534391485	chr8:100076045-100076046	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547992554	chr8:100076054-100076055	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201936258	chr8:100076194-100076195	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs567722712	chr8:100076231-100076232	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs536960062	chr8:100076254-100076255	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs182133936	chr8:100076292-100076293	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs570358042	chr8:100076374-100076375	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs539072499	chr8:100076382-100076383	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs558978395	chr8:100076388-100076389	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs572603142	chr8:100076394-100076395	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs80335094	chr8:100076440-100076441	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs541140159	chr8:100076449-100076450	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs184840238	chr8:100076450-100076451	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs371590206	chr8:100076520-100076521	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs6992480	chr8:100076537-100076538	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs571440359	chr8:100076543-100076544	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs543703688	chr8:100076559-100076560	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	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:4639 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:100026600-100083800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr8:100029600-100086200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr8:100032200-100084000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr8:100032400-100077800	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr8:100032600-100086200	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr8:100040600-100086800	Weak transcription	Brain Angular Gyrus	brain
7	chr8:100044400-100083600	Weak transcription	Aorta	Aorta
8	chr8:100044400-100083800	Weak transcription	Left Ventricle	heart
9	chr8:100044600-100077600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr8:100045000-100075400	Weak transcription	Thymus	Thymus
11	chr8:100048600-100078000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr8:100049200-100088200	Weak transcription	HSMM	muscle
13	chr8:100051400-100100400	Weak transcription	Osteobl	bone
14	chr8:100051800-100088000	Weak transcription	A549	lung
15	chr8:100057200-100083600	Weak transcription	Brain Hippocampus Middle	brain
16	chr8:100057400-100076000	Weak transcription	Liver	Liver
17	chr8:100057400-100083600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr8:100057400-100083800	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr8:100057600-100075400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr8:100058600-100076000	Weak transcription	Colonic Mucosa	Colon
21	chr8:100060200-100083400	Weak transcription	Esophagus	oesophagus
22	chr8:100062200-100076000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr8:100062400-100083600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr8:100062800-100075400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr8:100064000-100076200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr8:100064000-100076200	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr8:100064200-100075800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr8:100065000-100076000	Weak transcription	Dnd41	blood
29	chr8:100065600-100089600	Weak transcription	Rectal Smooth Muscle	rectum
30	chr8:100066000-100083400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr8:100066200-100075400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr8:100066600-100075400	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr8:100066600-100076200	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr8:100066600-100083400	Weak transcription	Stomach Smooth Muscle	stomach
35	chr8:100066600-100083600	Weak transcription	Duodenum Mucosa	Duodenum
36	chr8:100066600-100083600	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr8:100066600-100083600	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr8:100066600-100088000	Weak transcription	NHDF-Ad	bronchial
39	chr8:100066600-100094000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
40	chr8:100066800-100083400	Weak transcription	Gastric	stomach
41	chr8:100067000-100077600	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr8:100067600-100075400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr8:100067600-100075400	Weak transcription	Primary B cells from peripheral blood	blood
44	chr8:100067600-100075800	Weak transcription	Primary T cells from cord blood	blood
45	chr8:100067600-100078200	Weak transcription	Brain Cingulate Gyrus	brain
46	chr8:100067600-100079200	Weak transcription	Fetal Brain Male	brain
47	chr8:100067600-100083600	Weak transcription	Ovary	ovary
48	chr8:100067600-100088400	Weak transcription	NHEK	skin
49	chr8:100068000-100076200	Weak transcription	Fetal Kidney	kidney
50	chr8:100068400-100075400	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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