Variant report

Variant	nsv932917
Chromosome Location	chr8:100074076-100193594
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:780)
CpG islands
(count:123)
Chromatin interactive
region (count:51)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:780 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:100103092-100103687	K562	blood:	n/a	n/a
2	ARID3A	chr8:100124728-100124858	K562	blood:	n/a	n/a
3	ARID3A	chr8:100149959-100150472	K562	blood:	n/a	n/a
4	ATF1	chr8:100150113-100150549	K562	blood:	n/a	n/a
5	ATF1	chr8:100103355-100103611	K562	blood:	n/a	n/a
6	ATF1	chr8:100135547-100135703	K562	blood:	n/a	n/a
7	ATF1	chr8:100177666-100177787	K562	blood:	n/a	n/a
8	ATF2	chr8:100092901-100093701	GM12878	blood:	n/a	n/a
9	ATF2	chr8:100093166-100093626	GM12878	blood:	n/a	n/a
10	ATF3	chr8:100103253-100103550	K562	blood:	n/a	n/a
11	ATF3	chr8:100150017-100150481	K562	blood:	n/a	n/a
12	BACH1	chr8:100182411-100182437	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr8:100150185-100150441	K562	blood:	n/a	n/a
14	BATF	chr8:100093290-100093609	GM12878	blood:	n/a	n/a
15	BATF	chr8:100093275-100093603	GM12878	blood:	n/a	n/a
16	BCL11A	chr8:100093229-100093561	GM12878	blood:	n/a	chr8:100093423-100093432
17	BCLAF1	chr8:100092916-100093613	GM12878	blood:	n/a	chr8:100093423-100093432
18	BHLHE40	chr8:100150155-100150410	K562	blood:	n/a	n/a
19	CBX3	chr8:100082907-100083212	K562	blood:	n/a	n/a
20	CBX3	chr8:100150104-100150431	K562	blood:	n/a	n/a
21	CBX3	chr8:100150051-100150770	K562	blood:	n/a	n/a
22	CCNT2	chr8:100150101-100150431	K562	blood:	n/a	n/a
23	CCNT2	chr8:100103316-100103587	K562	blood:	n/a	n/a
24	CEBPB	chr8:100150136-100150322	K562	blood:	n/a	n/a
25	CEBPB	chr8:100092989-100093315	HepG2	liver:	n/a	chr8:100093091-100093102 chr8:100093091-100093104
26	CEBPB	chr8:100077735-100077878	Hela-S3	cervix:	n/a	chr8:100077849-100077860
27	CEBPB	chr8:100077716-100077972	K562	blood:	n/a	chr8:100077849-100077860
28	CEBPB	chr8:100077668-100078038	K562	blood:	n/a	chr8:100077849-100077860
29	CEBPB	chr8:100077676-100077938	IMR90	lung:	n/a	chr8:100077849-100077860
30	CEBPB	chr8:100077718-100077940	K562	blood:	n/a	chr8:100077849-100077860
31	CEBPB	chr8:100076054-100076288	MCF-7	breast:	n/a	chr8:100076127-100076138
32	CEBPB	chr8:100082977-100082989	A549	lung:	n/a	n/a
33	CEBPB	chr8:100101954-100102308	K562	blood:	n/a	chr8:100102138-100102149
34	CEBPB	chr8:100100423-100100719	IMR90	lung:	n/a	chr8:100100587-100100600
35	CEBPB	chr8:100101981-100102305	Hela-S3	cervix:	n/a	chr8:100102138-100102149
36	CEBPB	chr8:100102052-100102257	H1-hESC	embryonic stem cell:	n/a	chr8:100102138-100102149
37	CEBPB	chr8:100117844-100118377	MCF-7	breast:	n/a	n/a
38	CEBPB	chr8:100150009-100150483	K562	blood:	n/a	n/a
39	CEBPB	chr8:100102069-100102315	HepG2	liver:	n/a	chr8:100102138-100102149
40	CEBPB	chr8:100101993-100102298	K562	blood:	n/a	chr8:100102138-100102149
41	CEBPB	chr8:100157064-100157434	IMR90	lung:	n/a	n/a
42	CEBPB	chr8:100077714-100078025	A549	lung:	n/a	chr8:100077849-100077860
43	CEBPB	chr8:100100439-100100639	K562	blood:	n/a	chr8:100100587-100100600
44	CEBPB	chr8:100101978-100102329	IMR90	lung:	n/a	chr8:100102138-100102149
45	CEBPB	chr8:100149955-100150424	K562	blood:	n/a	n/a
46	CEBPB	chr8:100075976-100076309	HepG2	liver:	n/a	chr8:100076127-100076138
47	CEBPB	chr8:100092961-100093259	IMR90	lung:	n/a	chr8:100093091-100093102 chr8:100093091-100093104
48	CEBPB	chr8:100173099-100173249	K562	blood:	n/a	n/a
49	CEBPB	chr8:100101978-100102309	A549	lung:	n/a	chr8:100102138-100102149
50	CEBPB	chr8:100077769-100077945	MCF-7	breast:	n/a	chr8:100077849-100077860

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:100157208-100157258	Jurkat	blood:	n/a
2	chr8:100157208-100157258	Jurkat	blood:	n/a
3	chr8:100104103-100104153	HCPEpiC	choroid plexus:	n/a
4	chr8:100157208-100157258	T-47D	breast:	n/a
5	chr8:100104103-100104153	HRPEpiC	eye:	n/a
6	chr8:100157208-100157258	HUVEC	blood vessel:	n/a
7	chr8:100104103-100104153	ovcar-3	ovarian:	n/a
8	chr8:100104103-100104153	U87	brain:	n/a
9	chr8:100157208-100157258	NHDF-neo	bronchial:	n/a
10	chr8:100104103-100104153	AoSMC	blood vessel:	n/a
11	chr8:100104103-100104153	BE2_C	brain:	n/a
12	chr8:100104103-100104153	SKMC	muscle:	n/a
13	chr8:100104103-100104153	Jurkat	blood:	n/a
14	chr8:100157208-100157258	HPAEpiC	pulmonary alveolar:	n/a
15	chr8:100104103-100104153	HepG2	liver:	n/a
16	chr8:100104103-100104153	HUVEC	blood vessel:	n/a
17	chr8:100157208-100157258	GM12892	blood:	n/a
18	chr8:100157208-100157258	HL-60	blood:	n/a
19	chr8:100157208-100157258	GM06990	blood:	n/a
20	chr8:100157208-100157258	BE2_C	brain:	n/a
21	chr8:100104103-100104153	HCM	heart:	n/a
22	chr8:100157208-100157258	NHBE	bronchial:	n/a
23	chr8:100157208-100157258	HCM	heart:	n/a
24	chr8:100104103-100104153	SK-N-SH	brain:	n/a
25	chr8:100157208-100157258	PFSK-1	brain:	n/a
26	chr8:100157208-100157258	HIPEpiC	eye:	n/a
27	chr8:100157208-100157258	GM12878	blood:	n/a
28	chr8:100157208-100157258	AG04450	lung:	fetal
29	chr8:100157208-100157258	HAEpiC	amniotic membrane:	n/a
30	chr8:100157208-100157258	Hela-S3	cervix:	n/a
31	chr8:100157208-100157258	SK-N-SH_RA	brain:	n/a
32	chr8:100104103-100104153	K562	blood:	n/a
33	chr8:100157208-100157258	Hepatocyte	liver:	n/a
34	chr8:100104103-100104153	Hepatocyte	liver:	n/a
35	chr8:100104103-100104153	AG04450	lung:	fetal
36	chr8:100157208-100157258	H1-hESC	embryonic stem cell:	embryo
37	chr8:100104103-100104153	HCT-116	colon:	n/a
38	chr8:100104103-100104153	NHBE	bronchial:	n/a
39	chr8:100157208-100157258	U87	brain:	n/a
40	chr8:100104103-100104153	SK-N-MC	brain:	n/a
41	chr8:100157208-100157258	ovcar-3	ovarian:	n/a
42	chr8:100104103-100104153	HRE	kidney:	n/a
43	chr8:100157208-100157258	HMEC	breast:	n/a
44	chr8:100104103-100104153	HNPCEpiC	eye:	n/a
45	chr8:100104103-100104153	AG10803	skin:	n/a
46	chr8:100104103-100104153	LNCaP	prostate:	n/a
47	chr8:100157208-100157258	GM12891	blood:	n/a
48	chr8:100157208-100157258	AG10803	skin:	n/a
49	chr8:100157208-100157258	HCT-116	colon:	n/a
50	chr8:100104103-100104153	PFSK-1	brain:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:99956376..99957970-chr8:100136435..100137944,2	MCF-7	breast:
2	chr8:100180284..100182081-chr8:100183993..100185529,2	K562	blood:
3	chr17:59467368..59468208-chr8:100108099..100109078,2	MCF-7	breast:
4	chr8:100181985..100183886-chr8:100189568..100191594,2	MCF-7	breast:
5	chr8:100180037..100180965-chr8:100818919..100819673,2	MCF-7	breast:
6	chr8:100024345..100027040-chr8:100106649..100108605,2	MCF-7	breast:
7	chr8:100103552..100105106-chr8:100109674..100111736,2	K562	blood:
8	chr8:100144557..100146496-chr8:100147591..100149372,3	MCF-7	breast:
9	chr8:100024034..100025700-chr8:100109623..100113452,3	MCF-7	breast:
10	chr8:100190689..100193029-chr8:100201859..100204401,2	K562	blood:
11	chr8:100109729..100112333-chr8:100147157..100149231,2	K562	blood:
12	chr8:100043379..100045451-chr8:100150795..100153462,2	MCF-7	breast:
13	chr8:100180104..100181200-chr8:100370523..100371154,5	MCF-7	breast:
14	chr8:100187208..100189859-chr8:100191478..100193795,2	MCF-7	breast:
15	chr8:100145698..100148364-chr8:100156045..100158193,2	MCF-7	breast:
16	chr8:100087357..100089175-chr8:100091437..100093600,2	MCF-7	breast:
17	chr8:100101168..100103542-chr8:100111717..100113562,2	K562	blood:
18	chr8:100165081..100167634-chr8:100170824..100172995,2	K562	blood:
19	chr8:100024284..100027084-chr8:100113982..100120280,5	MCF-7	breast:
20	chr8:99955457..99958039-chr8:100115422..100117482,3	MCF-7	breast:
21	chr8:100087357..100089175-chr8:100091437..100093600,2	MCF-7	breast:
22	chr8:100179836..100180811-chr8:101138118..101138640,2	MCF-7	breast:
23	chr8:100025833..100028756-chr8:100100624..100103335,2	MCF-7	breast:
24	chr8:100115261..100117016-chr8:100117428..100119133,2	K562	blood:
25	chr8:100136650..100138168-chr8:100240298..100242917,2	K562	blood:
26	chr8:100144557..100146496-chr8:100147591..100149372,3	MCF-7	breast:
27	chr8:100145698..100148364-chr8:100156045..100158193,2	MCF-7	breast:
28	chr8:100024787..100026436-chr8:100179759..100181890,2	MCF-7	breast:
29	chr8:100067262..100071049-chr8:100071737..100074698,3	MCF-7	breast:
30	chr8:100024118..100026755-chr8:100073445..100075343,2	MCF-7	breast:
31	chr8:100165081..100167634-chr8:100170824..100172995,2	K562	blood:
32	chr8:100103552..100105106-chr8:100109674..100111736,2	K562	blood:
33	chr8:100189672..100191957-chr8:100789803..100791931,2	MCF-7	breast:
34	chr8:100180284..100182081-chr8:100183993..100185529,2	K562	blood:
35	chr8:100024436..100026482-chr8:100177416..100178944,2	MCF-7	breast:
36	chr8:99995141..99996042-chr8:100118104..100118628,2	MCF-7	breast:
37	chr8:100024762..100026893-chr8:100106816..100109546,3	MCF-7	breast:
38	chr8:100187208..100189859-chr8:100191478..100193795,2	MCF-7	breast:
39	chr8:100023955..100026746-chr8:100146269..100148393,2	K562	blood:
40	chr8:100162823..100164704-chr8:100167097..100169098,2	K562	blood:
41	chr8:100130524..100132088-chr8:100135733..100138707,2	K562	blood:
42	chr8:100180149..100180921-chr8:100370671..100371459,2	MCF-7	breast:
43	chr8:100188351..100191240-chr8:100198710..100200651,2	K562	blood:
44	chr8:100181985..100183886-chr8:100189568..100191594,2	MCF-7	breast:
45	chr8:100109729..100112333-chr8:100147157..100149231,2	K562	blood:
46	chr8:100101168..100103542-chr8:100111717..100113562,2	K562	blood:
47	chr8:100125265..100128114-chr8:100129986..100133353,3	K562	blood:
48	chr8:100023368..100025355-chr8:100122244..100124287,2	MCF-7	breast:
49	chr8:100012703..100016134-chr8:100151109..100154697,3	MCF-7	breast:
50	chr8:100109070..100113299-chr8:100115182..100118080,5	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STK3-3	chr8:100103966-100104326	ENSG00000253562.1
2	lnc-OSR2-2	chr8:100131580-100131696	ENSG00000253532.1
3	lnc-STK3-3	chr8:100106157-100106288	ENSG00000253562.1
4	lnc-OSR2-2	chr8:100132332-100132809	ENSG00000253532.1

No data

Variant related genes	Relation type
VPS13B	TF binding region
ENSG00000253532	TF binding region
ENSG00000253562	TF binding region
VPS13B	CpG island
ENSG00000253532	CpG island
ENSG00000253562	CpG island
ENSG00000132549	chromatin interactions
ENSG00000253948	chromatin interactions
ENSG00000164920	chromatin interactions
ENSG00000271930	chromatin interactions
ENSG00000253180	chromatin interactions
ENSG00000253532	chromatin interactions

Extended variants
information (count: 4101 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:4101 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190276484	chr8:100074078-100074079	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs531487457	chr8:100074084-100074085	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs72670203	chr8:100074127-100074128	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs201871927	chr8:100074129-100074130	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs376706418	chr8:100074160-100074161	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs571601875	chr8:100074189-100074190	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs534057364	chr8:100074226-100074227	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs553823567	chr8:100074246-100074247	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs567235064	chr8:100074264-100074265	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs528165774	chr8:100074266-100074267	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs150254716	chr8:100074283-100074284	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs7829780	chr8:100074352-100074353	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs576055432	chr8:100074357-100074358	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs181925506	chr8:100074362-100074363	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs145796569	chr8:100074377-100074378	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs115636781	chr8:100074421-100074422	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs112625274	chr8:100074475-100074476	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs186578052	chr8:100074568-100074569	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs377360336	chr8:100074569-100074570	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs111333109	chr8:100074571-100074572	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs560131566	chr8:100074572-100074573	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs564200679	chr8:100074576-100074577	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs149065923	chr8:100074590-100074591	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs144634970	chr8:100074621-100074622	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs371656866	chr8:100074631-100074632	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs576744248	chr8:100074706-100074707	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs189799291	chr8:100074717-100074718	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs202181050	chr8:100074730-100074731	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs7830122	chr8:100074757-100074758	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs180988007	chr8:100074758-100074759	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs571438813	chr8:100074765-100074766	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs527597675	chr8:100074782-100074783	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs547673200	chr8:100074783-100074784	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs200074871	chr8:100074806-100074807	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs371681215	chr8:100074821-100074822	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs4236854	chr8:100074838-100074839	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs555879890	chr8:100074845-100074846	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs569769563	chr8:100074846-100074847	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs185610499	chr8:100074880-100074881	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs191073491	chr8:100074884-100074885	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs557954045	chr8:100074886-100074887	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs577782501	chr8:100074911-100074912	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs183339237	chr8:100074923-100074924	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs553998046	chr8:100074986-100074987	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs540299072	chr8:100074988-100074989	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs188225573	chr8:100075062-100075063	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs191887460	chr8:100075100-100075101	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs576501627	chr8:100075102-100075103	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs183228419	chr8:100075141-100075142	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs113586011	chr8:100075242-100075243	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

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

Chromatin state (count:1656 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

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	chr8:100066400-100074800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr8:100066600-100075400	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr8:100066600-100076200	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr8:100066600-100083400	Weak transcription	Stomach Smooth Muscle	stomach
36	chr8:100066600-100083600	Weak transcription	Duodenum Mucosa	Duodenum
37	chr8:100066600-100083600	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr8:100066600-100083600	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr8:100066600-100088000	Weak transcription	NHDF-Ad	bronchial
40	chr8:100066600-100094000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr8:100066800-100083400	Weak transcription	Gastric	stomach
42	chr8:100067000-100077600	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr8:100067600-100074600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr8:100067600-100075400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr8:100067600-100075400	Weak transcription	Primary B cells from peripheral blood	blood
46	chr8:100067600-100075800	Weak transcription	Primary T cells from cord blood	blood
47	chr8:100067600-100078200	Weak transcription	Brain Cingulate Gyrus	brain
48	chr8:100067600-100079200	Weak transcription	Fetal Brain Male	brain
49	chr8:100067600-100083600	Weak transcription	Ovary	ovary
50	chr8:100067600-100088400	Weak transcription	NHEK	skin

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