Variant report

Variant	nsv519376
Chromosome Location	chr8:10611708-10691993
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1848)
CpG islands
(count:1406)
Chromatin interactive
region (count:92)
LncRNA
region (count:11)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1848 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:10665773-10666115	K562	blood:	n/a	n/a
2	ARID3A	chr8:10629194-10629470	K562	blood:	n/a	n/a
3	ARID3A	chr8:10631175-10631647	K562	blood:	n/a	n/a
4	ARID3A	chr8:10638845-10638952	K562	blood:	n/a	n/a
5	ARID3A	chr8:10656082-10656601	K562	blood:	n/a	n/a
6	ARID3A	chr8:10657288-10657802	K562	blood:	n/a	n/a
7	ARID3A	chr8:10618425-10619055	K562	blood:	n/a	n/a
8	ARID3A	chr8:10634540-10635222	K562	blood:	n/a	n/a
9	ARID3A	chr8:10676462-10676890	K562	blood:	n/a	n/a
10	ARID3A	chr8:10653397-10654025	K562	blood:	n/a	n/a
11	ARID3A	chr8:10632964-10633416	K562	blood:	n/a	n/a
12	ARID3A	chr8:10657152-10657846	HepG2	liver:	n/a	n/a
13	ATF1	chr8:10653494-10654054	K562	blood:	n/a	n/a
14	ATF1	chr8:10671700-10671979	K562	blood:	n/a	n/a
15	ATF1	chr8:10629162-10629538	K562	blood:	n/a	n/a
16	ATF1	chr8:10618426-10618829	K562	blood:	n/a	n/a
17	ATF1	chr8:10657290-10657727	K562	blood:	n/a	n/a
18	ATF1	chr8:10634783-10635469	K562	blood:	n/a	n/a
19	ATF2	chr8:10646076-10646653	GM12878	blood:	n/a	n/a
20	ATF2	chr8:10646115-10646583	GM12878	blood:	n/a	n/a
21	ATF2	chr8:10641097-10641653	GM12878	blood:	n/a	n/a
22	ATF2	chr8:10641139-10641593	GM12878	blood:	n/a	n/a
23	ATF3	chr8:10634812-10635209	K562	blood:	n/a	n/a
24	ATF3	chr8:10657391-10657631	K562	blood:	n/a	n/a
25	ATF3	chr8:10657250-10657724	K562	blood:	n/a	n/a
26	BACH1	chr8:10676446-10676803	K562	blood:	n/a	n/a
27	BACH1	chr8:10634535-10634552	K562	blood:	n/a	n/a
28	BACH1	chr8:10618657-10618682	K562	blood:	n/a	n/a
29	BATF	chr8:10641195-10641508	GM12878	blood:	n/a	chr8:10641369-10641380
30	BATF	chr8:10646148-10646551	GM12878	blood:	n/a	chr8:10646312-10646323
31	BATF	chr8:10663103-10663760	GM12878	blood:	n/a	n/a
32	BATF	chr8:10641154-10641577	GM12878	blood:	n/a	chr8:10641369-10641380
33	BCL11A	chr8:10641274-10641544	GM12878	blood:	n/a	n/a
34	BCL11A	chr8:10663503-10663756	GM12878	blood:	n/a	n/a
35	BCL11A	chr8:10646180-10646518	GM12878	blood:	n/a	n/a
36	BCL3	chr8:10646199-10646599	GM12878	blood:	n/a	n/a
37	BHLHE40	chr8:10653533-10653798	K562	blood:	n/a	n/a
38	BHLHE40	chr8:10675975-10676782	K562	blood:	n/a	chr8:10676166-10676175 chr8:10676166-10676175 chr8:10676160-10676181 chr8:10676525-10676541 chr8:10676165-10676174
39	BHLHE40	chr8:10618383-10618969	K562	blood:	n/a	n/a
40	BHLHE40	chr8:10634083-10635624	K562	blood:	n/a	n/a
41	BHLHE40	chr8:10657309-10657639	K562	blood:	n/a	n/a
42	BHLHE40	chr8:10648112-10648199	K562	blood:	n/a	n/a
43	BHLHE40	chr8:10646418-10646431	K562	blood:	n/a	n/a
44	BHLHE40	chr8:10633148-10633444	K562	blood:	n/a	n/a
45	BHLHE40	chr8:10682842-10683140	GM12878	blood:	n/a	n/a
46	BHLHE40	chr8:10629130-10629563	K562	blood:	n/a	n/a
47	BRCA1	chr8:10645582-10645644	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr8:10682855-10683017	GM12878	blood:	n/a	n/a
49	BRCA1	chr8:10657228-10657844	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr8:10647677-10647797	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1406 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:10657514-10657564	CMK	blood:	n/a
2	chr8:10649960-10650010	HCM	heart:	n/a
3	chr8:10617063-10617113	SK-N-SH_RA	brain:	n/a
4	chr8:10657514-10657564	CMK	blood:	n/a
5	chr8:10649960-10650010	HCM	heart:	n/a
6	chr8:10617063-10617113	SK-N-SH_RA	brain:	n/a
7	chr8:10683044-10683094	Hepatocyte	liver:	n/a
8	chr8:10683266-10683316	HRCEpiC	kidney:	n/a
9	chr8:10686021-10686071	H1-hESC	embryonic stem cell:	embryo
10	chr8:10622887-10622937	GM06990	blood:	n/a
11	chr8:10686070-10686120	NB4	blood:	n/a
12	chr8:10643634-10643684	GM19239	blood:	n/a
13	chr8:10683044-10683094	SK-N-MC	brain:	n/a
14	chr8:10621801-10621851	SKMC	muscle:	n/a
15	chr8:10683167-10683217	ovcar-3	ovarian:	n/a
16	chr8:10646690-10646740	NH-A	brain:	n/a
17	chr8:10623038-10623088	MCF-7	breast:	n/a
18	chr8:10686021-10686071	HRCEpiC	kidney:	n/a
19	chr8:10623534-10623584	PFSK-1	brain:	n/a
20	chr8:10686070-10686120	AG09319	gingival:	n/a
21	chr8:10650046-10650096	PFSK-1	brain:	n/a
22	chr8:10623344-10623394	HMEC	breast:	n/a
23	chr8:10650046-10650096	CMK	blood:	n/a
24	chr8:10621935-10621985	HPAEpiC	pulmonary alveolar:	n/a
25	chr8:10621874-10621924	MCF10A-Er-Src	breast:	n/a
26	chr8:10650046-10650096	HPAEpiC	pulmonary alveolar:	n/a
27	chr8:10622887-10622937	HL-60	blood:	n/a
28	chr8:10650046-10650096	HRE	kidney:	n/a
29	chr8:10621935-10621985	A549	lung:	n/a
30	chr8:10617394-10617444	IMR90	lung:	fetal
31	chr8:10621874-10621924	GM12892	blood:	n/a
32	chr8:10683167-10683217	PFSK-1	brain:	n/a
33	chr8:10657514-10657564	HMEC	breast:	n/a
34	chr8:10683139-10683189	AG09319	gingival:	n/a
35	chr8:10621935-10621985	HepG2	liver:	n/a
36	chr8:10657514-10657564	AoSMC	blood vessel:	n/a
37	chr8:10622805-10622855	K562	blood:	n/a
38	chr8:10635419-10635469	T-47D	breast:	n/a
39	chr8:10617063-10617113	HCT-116	colon:	n/a
40	chr8:10683139-10683189	GM19239	blood:	n/a
41	chr8:10646690-10646740	HMEC	breast:	n/a
42	chr8:10621935-10621985	HNPCEpiC	eye:	n/a
43	chr8:10623344-10623394	AG09319	gingival:	n/a
44	chr8:10621935-10621985	HCM	heart:	n/a
45	chr8:10686021-10686071	Jurkat	blood:	n/a
46	chr8:10617394-10617444	BJ	skin:	n/a
47	chr8:10683139-10683189	T-47D	breast:	n/a
48	chr8:10621801-10621851	MCF10A-Er-Src	breast:	n/a
49	chr8:10683188-10683238	HRE	kidney:	n/a
50	chr8:10683044-10683094	CMK	blood:	n/a

(count:92 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:10675871..10677525-chr8:10687580..10689455,2	MCF-7	breast:
2	chr8:10654838..10657527-chr8:10667570..10669417,2	K562	blood:
3	chr8:10663898..10666534-chr8:10670905..10672921,2	K562	blood:
4	chr8:10592393..10594061-chr8:10610774..10613759,2	K562	blood:
5	chr8:10670666..10672714-chr8:10674903..10676605,2	K562	blood:
6	chr8:10674524..10677009-chr8:10677940..10682794,6	K562	blood:
7	chr8:10447726..10448226-chr8:10680360..10680981,2	K562	blood:
8	chr8:10634439..10636776-chr8:10637920..10639941,2	K562	blood:
9	chr8:10683547..10686608-chr8:10694341..10697878,5	K562	blood:
10	chr8:10675871..10677525-chr8:10687580..10689455,2	MCF-7	breast:
11	chr8:10648353..10650941-chr8:10651549..10653303,2	K562	blood:
12	chr8:10635373..10637028-chr8:10639267..10640869,2	MCF-7	breast:
13	chr8:10671204..10673781-chr8:10675039..10678414,4	K562	blood:
14	chr8:10628530..10631997-chr8:10633640..10636320,4	K562	blood:
15	chr8:10444773..10445405-chr8:10656129..10656744,2	MCF-7	breast:
16	chr8:10634439..10636776-chr8:10637920..10639941,2	K562	blood:
17	chr8:10687146..10690339-chr8:10690695..10692954,3	K562	blood:
18	chr8:10655273..10657441-chr8:10673003..10675779,2	MCF-7	breast:
19	chr8:10651485..10654382-chr8:10658663..10661335,2	K562	blood:
20	chr8:10447312..10448291-chr8:10671241..10672318,3	MCF-7	breast:
21	chr8:10674954..10678350-chr8:10693952..10697087,3	K562	blood:
22	chr8:10447282..10448390-chr8:10682147..10683493,10	MCF-7	breast:
23	chr8:10615290..10617626-chr8:10678525..10680394,2	K562	blood:
24	chr8:10659319..10661970-chr8:10670204..10672080,2	K562	blood:
25	chr8:10613644..10615982-chr8:10616006..10618005,2	MCF-7	breast:
26	chr8:10659319..10661970-chr8:10670204..10672080,2	K562	blood:
27	chr8:10444970..10445545-chr8:10682548..10683133,2	K562	blood:
28	chr8:10461544..10463468-chr8:10674781..10677553,2	K562	blood:
29	chr8:10442713..10444669-chr8:10687154..10689359,2	K562	blood:
30	chr8:10687103..10689280-chr8:10695921..10698730,3	MCF-7	breast:
31	chr8:10407992..10408718-chr8:10682226..10683074,2	MCF-7	breast:
32	chr8:10648269..10650512-chr8:10653379..10655643,2	K562	blood:
33	chr8:10615290..10617626-chr8:10678525..10680394,2	K562	blood:
34	chr8:10633410..10636281-chr8:10695946..10698229,2	K562	blood:
35	chr8:10447388..10448227-chr8:10671479..10672292,5	MCF-7	breast:
36	chr8:10661041..10663071-chr8:10663223..10664921,2	MCF-7	breast:
37	chr8:10515210..10517092-chr8:10648053..10650432,2	K562	blood:
38	chr8:10447720..10448261-chr8:10675847..10676686,2	K562	blood:
39	chr8:10620237..10621942-chr8:10624836..10626716,2	K562	blood:
40	chr8:10651485..10654382-chr8:10658663..10661335,2	K562	blood:
41	chr8:10616130..10621063-chr8:10631004..10634975,5	K562	blood:
42	chr8:10444886..10445502-chr8:10682512..10683360,2	MCF-7	breast:
43	chr8:10447404..10448576-chr8:10655982..10656998,11	MCF-7	breast:
44	chr8:10444549..10445532-chr8:10658177..10659296,3	K562	blood:
45	chr8:10631743..10634256-chr8:10658449..10660185,2	K562	blood:
46	chr8:10654838..10657527-chr8:10667570..10669417,2	K562	blood:
47	chr8:10640744..10643813-chr8:10646247..10648006,3	K562	blood:
48	chr8:10591978..10593893-chr8:10610774..10613689,2	K562	blood:
49	chr8:10447366..10448118-chr8:10670992..10671978,2	K562	blood:
50	chr8:10611693..10613429-chr8:10616715..10619425,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PINX1-1	chr8:10615296-10618693	NONHSAT125016
2	lnc-C8orf74-1	chr8:10628705-10628902	ENSG00000248896
3	lnc-C8orf74-4	chr8:10624234-10624550	ucscGeneNc_uc003wtg_1
4	lnc-C8orf74-1	chr8:10611712-10611828	ENSG00000248896
5	lnc-C8orf74-1	chr8:10611712-10611828	NONHSAT125014
6	lnc-C8orf74-1	chr8:10621847-10622667	NONHSAT125014
7	lnc-C8orf74-1	chr8:10621847-10622233	ENSG00000248896
8	lnc-C8orf74-1	chr8:10622680-10622686	NONHSAT125014
9	lnc-C8orf74-4	chr8:10649122-10649238	ucscGeneNc_uc003wtg_1
10	lnc-RP1L1-7	chr8:10660588-10662320	NONHSAT125018
11	lnc-C8orf74-4	chr8:10659257-10660077	ucscGeneNc_uc003wtg_1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1322	chr8:10682885-10682903	MIMAT0005953

No data

Variant related genes	Relation type
ENSG00000252565	TF binding region
PINX1	TF binding region
ENSG00000252565	CpG island
PINX1	CpG island
ENSG00000258724	chromatin interactions
ENSG00000253695	chromatin interactions
ENSG00000252565	chromatin interactions
ENSG00000254093	chromatin interactions
HSPA1B	miRNA target sites

Extended variants
information (count: 4630 )
Associated
traits (count: 149 )

Variant overlapped rSNPs/rCNVs (count:4630 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1073913	chr8:10611708-10611709	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553791857	chr8:10611724-10611725	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs577032771	chr8:10611770-10611771	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs10106138	chr8:10611785-10611786	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs138381344	chr8:10611794-10611795	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs188226420	chr8:10611812-10611813	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs112586643	chr8:10611878-10611879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143929748	chr8:10611879-10611880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs557038412	chr8:10611881-10611882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs7014285	chr8:10611882-10611883	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs144298754	chr8:10611889-10611890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs547326926	chr8:10611893-10611894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560645675	chr8:10611922-10611923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532870339	chr8:10611923-10611924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs180790761	chr8:10611935-10611936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545766845	chr8:10611976-10611977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs376084428	chr8:10611984-10611985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553111856	chr8:10611985-10611986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569151293	chr8:10611989-10611990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538047546	chr8:10612025-10612026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572813233	chr8:10612033-10612034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568502722	chr8:10612053-10612054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs6981530	chr8:10612067-10612068	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs7018334	chr8:10612075-10612076	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs577145791	chr8:10612109-10612110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575529805	chr8:10612115-10612116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556485615	chr8:10612190-10612191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576348691	chr8:10612194-10612195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541997253	chr8:10612209-10612210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs544089863	chr8:10612223-10612224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561774294	chr8:10612229-10612230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572081341	chr8:10612235-10612236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs6980549	chr8:10612261-10612262	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs564146386	chr8:10612338-10612339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7001530	chr8:10612362-10612363	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs187193121	chr8:10612388-10612389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192125474	chr8:10612405-10612406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562796214	chr8:10612437-10612438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs73662614	chr8:10612486-10612487	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs563387852	chr8:10612503-10612504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77430620	chr8:10612530-10612531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs148342784	chr8:10612580-10612581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141521961	chr8:10612585-10612586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150903243	chr8:10612604-10612605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532380806	chr8:10612628-10612629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4562276	chr8:10612671-10612672	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs193051143	chr8:10612760-10612761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533382921	chr8:10612780-10612781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs4840513	chr8:10612806-10612807	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs62492345	chr8:10612843-10612844	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance

Variant related diseases (count:149)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	21215367	CNVD
Osteosarcoma	21215367	CNVD
Schizophrenia	23813976	CNVD
Autism	20531469	CNVD

Chromatin state (count:2274 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10609600-10614000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:10609600-10616200	Weak transcription	Primary T cells from cord blood	blood
3	chr8:10610000-10621400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr8:10610400-10614200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr8:10610600-10620400	Weak transcription	HepG2	liver
6	chr8:10610800-10622200	Weak transcription	Primary B cells from cord blood	blood
7	chr8:10610800-10662000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr8:10611200-10624400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr8:10612600-10612800	Weak transcription	Pancreas	Pancrea
10	chr8:10612600-10617600	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr8:10612600-10621600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr8:10612800-10621600	Weak transcription	Spleen	Spleen
13	chr8:10613200-10613400	ZNF genes & repeats	Aorta	Aorta
14	chr8:10613200-10622600	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr8:10613400-10621600	Weak transcription	Aorta	Aorta
16	chr8:10613600-10614800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr8:10613600-10614800	Enhancers	HMEC	breast
18	chr8:10613600-10618400	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr8:10613600-10618800	Weak transcription	Fetal Muscle Leg	muscle
20	chr8:10613800-10617800	Weak transcription	Ovary	ovary
21	chr8:10614000-10614800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr8:10614000-10614800	Enhancers	Esophagus	oesophagus
23	chr8:10614000-10614800	Enhancers	Placenta	Placenta
24	chr8:10614200-10614400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr8:10614200-10614800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr8:10614200-10614800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr8:10614200-10614800	Enhancers	Hela-S3	cervix
28	chr8:10614200-10614800	Enhancers	NHEK	skin
29	chr8:10614200-10616600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr8:10614200-10621400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr8:10614400-10614800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr8:10614400-10634200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr8:10614600-10616600	Weak transcription	K562	blood
34	chr8:10614800-10616000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr8:10614800-10616800	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr8:10614800-10617200	Weak transcription	Esophagus	oesophagus
37	chr8:10614800-10617400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr8:10614800-10617600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr8:10614800-10617600	Weak transcription	HMEC	breast
40	chr8:10614800-10617600	Weak transcription	NHEK	skin
41	chr8:10614800-10617800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr8:10614800-10618400	Weak transcription	Placenta	Placenta
43	chr8:10614800-10618600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr8:10614800-10621400	Weak transcription	Left Ventricle	heart
45	chr8:10614800-10621400	Weak transcription	Lung	lung
46	chr8:10614800-10621800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr8:10614800-10622000	Weak transcription	Hela-S3	cervix
48	chr8:10615000-10621400	Weak transcription	Adipose Nuclei	Adipose
49	chr8:10615200-10618400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr8:10615400-10620800	Weak transcription	Primary T helper cells fromperipheralblood	blood

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