Variant report

Variant	nsv608212
Chromosome Location	chr7:111157532-111323799
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1646)
CpG islands
(count:916)
Chromatin interactive
region (count:126)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1646 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:111290764-111291175	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:111290526-111290531	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:111157885-111158000	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:111199925-111200215	K562	blood:	n/a	n/a
5	ARID3A	chr7:111202247-111202264	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:111170171-111170509	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:111181171-111181430	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:111172220-111172476	K562	blood:	n/a	n/a
9	ARID3A	chr7:111202485-111202878	K562	blood:	n/a	n/a
10	ARID3A	chr7:111202492-111202797	HepG2	liver:	n/a	n/a
11	ATF1	chr7:111172136-111172453	K562	blood:	n/a	n/a
12	ATF1	chr7:111163232-111163327	K562	blood:	n/a	n/a
13	ATF1	chr7:111175451-111175458	K562	blood:	n/a	n/a
14	ATF1	chr7:111319096-111319299	K562	blood:	n/a	n/a
15	ATF2	chr7:111167522-111167997	GM12878	blood:	n/a	n/a
16	ATF2	chr7:111167450-111168045	GM12878	blood:	n/a	n/a
17	ATF2	chr7:111201787-111202190	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr7:111201918-111202678	K562	blood:	n/a	n/a
19	ATF3	chr7:111290708-111291147	A549	lung:	n/a	n/a
20	BACH1	chr7:111172186-111172416	K562	blood:	n/a	n/a
21	BACH1	chr7:111201779-111202839	K562	blood:	n/a	n/a
22	BACH1	chr7:111312247-111312255	K562	blood:	n/a	n/a
23	BACH1	chr7:111202015-111202410	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr7:111160755-111160869	K562	blood:	n/a	n/a
25	BACH1	chr7:111169257-111169277	K562	blood:	n/a	n/a
26	BACH1	chr7:111188905-111189076	K562	blood:	n/a	n/a
27	BATF	chr7:111228155-111228552	GM12878	blood:	n/a	chr7:111228280-111228290 chr7:111228384-111228394 chr7:111228383-111228394
28	BCL11A	chr7:111168484-111168730	GM12878	blood:	n/a	n/a
29	BCL3	chr7:111201738-111202909	A549	lung:	n/a	chr7:111202581-111202590 chr7:111202620-111202629 chr7:111202514-111202527 chr7:111202540-111202549
30	BCLAF1	chr7:111201762-111202357	GM12878	blood:	n/a	n/a
31	BCLAF1	chr7:111168247-111168782	GM12878	blood:	n/a	n/a
32	BCLAF1	chr7:111202426-111202931	GM12878	blood:	n/a	chr7:111202581-111202590 chr7:111202620-111202629 chr7:111202514-111202527 chr7:111202540-111202549
33	BHLHE40	chr7:111161346-111161405	K562	blood:	n/a	n/a
34	BHLHE40	chr7:111202134-111202334	A549	lung:	n/a	n/a
35	BHLHE40	chr7:111201889-111202773	HepG2	liver:	n/a	n/a
36	BHLHE40	chr7:111198942-111199292	GM12878	blood:	n/a	n/a
37	BHLHE40	chr7:111168429-111168772	GM12878	blood:	n/a	n/a
38	BHLHE40	chr7:111201850-111202859	GM12878	blood:	n/a	n/a
39	BHLHE40	chr7:111167550-111167999	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:111172180-111172524	K562	blood:	n/a	n/a
41	BHLHE40	chr7:111200634-111202933	K562	blood:	n/a	n/a
42	BRCA1	chr7:111202645-111202975	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr7:111202039-111202441	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr7:111172126-111172326	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr7:111201100-111201803	Hela-S3	cervix:	n/a	n/a
46	CBX3	chr7:111211729-111212168	K562	blood:	n/a	n/a
47	CBX3	chr7:111202484-111202951	K562	blood:	n/a	n/a
48	CBX3	chr7:111211688-111212363	K562	blood:	n/a	n/a
49	CBX3	chr7:111284643-111285027	K562	blood:	n/a	n/a
50	CBX3	chr7:111161699-111162145	K562	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:111202222-111202272	AoSMC	blood vessel:	n/a
2	chr7:111202222-111202272	AoSMC	blood vessel:	n/a
3	chr7:111200944-111200994	ovcar-3	ovarian:	n/a
4	chr7:111202679-111202729	NHDF-neo	bronchial:	n/a
5	chr7:111202395-111202445	HL-60	blood:	n/a
6	chr7:111202457-111202507	PFSK-1	brain:	n/a
7	chr7:111202679-111202729	RPTEC	kidney:	n/a
8	chr7:111249576-111249626	A549	lung:	n/a
9	chr7:111202755-111202805	HAEpiC	amniotic membrane:	n/a
10	chr7:111202679-111202729	NB4	blood:	n/a
11	chr7:111202666-111202716	HCPEpiC	choroid plexus:	n/a
12	chr7:111202389-111202439	HL-60	blood:	n/a
13	chr7:111202679-111202729	NH-A	brain:	n/a
14	chr7:111202679-111202729	IMR90	lung:	fetal
15	chr7:111202682-111202732	SK-N-MC	brain:	n/a
16	chr7:111198163-111198213	GM06990	blood:	n/a
17	chr7:111203008-111203058	HRCEpiC	kidney:	n/a
18	chr7:111202679-111202729	AG10803	skin:	n/a
19	chr7:111202457-111202507	Caco-2	colon:	n/a
20	chr7:111202222-111202272	IMR90	lung:	fetal
21	chr7:111204826-111204876	MCF10A-Er-Src	breast:	n/a
22	chr7:111202450-111202500	SK-N-SH	brain:	n/a
23	chr7:111249576-111249626	GM12891	blood:	n/a
24	chr7:111249576-111249626	NT2-D1	testis:	n/a
25	chr7:111202450-111202500	Jurkat	blood:	n/a
26	chr7:111202389-111202439	HEEpiC	esophagus:	n/a
27	chr7:111198163-111198213	NB4	blood:	n/a
28	chr7:111204826-111204876	SK-N-SH	brain:	n/a
29	chr7:111249576-111249626	HMEC	breast:	n/a
30	chr7:111202682-111202732	MCF-7	breast:	n/a
31	chr7:111202682-111202732	HCF	heart:	n/a
32	chr7:111202457-111202507	AG10803	skin:	n/a
33	chr7:111202222-111202272	PFSK-1	brain:	n/a
34	chr7:111198163-111198213	Hela-S3	cervix:	n/a
35	chr7:111204826-111204876	BE2_C	brain:	n/a
36	chr7:111249924-111249974	HIPEpiC	eye:	n/a
37	chr7:111202222-111202272	GM19239	blood:	n/a
38	chr7:111202395-111202445	SK-N-MC	brain:	n/a
39	chr7:111202666-111202716	Jurkat	blood:	n/a
40	chr7:111202389-111202439	GM12891	blood:	n/a
41	chr7:111202679-111202729	CMK	blood:	n/a
42	chr7:111249924-111249974	ECC-1	luminal epithelium:	n/a
43	chr7:111202389-111202439	NHDF-neo	bronchial:	n/a
44	chr7:111203008-111203058	PFSK-1	brain:	n/a
45	chr7:111202679-111202729	BE2_C	brain:	n/a
46	chr7:111203008-111203058	GM12892	blood:	n/a
47	chr7:111203008-111203058	SK-N-SH_RA	brain:	n/a
48	chr7:111202755-111202805	Hela-S3	cervix:	n/a
49	chr7:111202755-111202805	MCF-7	breast:	n/a
50	chr7:111202222-111202272	GM12892	blood:	n/a

(count:126 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:111199186..111200731-chr7:111244724..111246694,2	K562	blood:
2	chr7:111165046..111167501-chr7:111171827..111173680,2	K562	blood:
3	chr7:111198013..111199792-chr7:111239009..111241221,2	K562	blood:
4	chr7:111181285..111183708-chr7:111185192..111188559,3	K562	blood:
5	chr7:111156804..111158834-chr7:111201568..111203855,2	MCF-7	breast:
6	chr7:111299147..111302092-chr7:111316986..111318533,2	K562	blood:
7	chr7:111284627..111287307-chr7:111300910..111302600,2	K562	blood:
8	chr7:111174213..111177437-chr7:111200487..111202315,3	K562	blood:
9	chr7:111162292..111164581-chr7:111182567..111185234,2	K562	blood:
10	chr6:31619932..31621913-chr7:111169935..111172752,2	K562	blood:
11	chr7:111178493..111181177-chr7:111184776..111187564,2	K562	blood:
12	chr7:111149350..111150943-chr7:111156315..111157965,2	K562	blood:
13	chr7:111201240..111203723-chr7:111208743..111211882,3	K562	blood:
14	chr5:39074237..39075141-chr7:111201699..111202501,2	Hela-S3	cervix:
15	chr7:111198013..111199792-chr7:111239009..111241221,2	K562	blood:
16	chr7:111174213..111176704-chr7:111200682..111203644,3	K562	blood:
17	chr7:110685337..110687591-chr7:111322599..111325063,2	K562	blood:
18	chr7:111178053..111179952-chr7:111201249..111203327,2	MCF-7	breast:
19	chr7:111067141..111070112-chr7:111198227..111201087,2	K562	blood:
20	chr7:111172393..111173981-chr7:111189118..111191154,2	K562	blood:
21	chr7:111164432..111166766-chr7:111167043..111169484,2	MCF-7	breast:
22	chr7:111166819..111169168-chr7:111191445..111193799,2	K562	blood:
23	chr7:111299093..111300961-chr7:111312313..111315147,2	K562	blood:
24	chr7:111304451..111306356-chr7:111315376..111317800,2	MCF-7	breast:
25	chr7:111149997..111152577-chr7:111162240..111165050,2	K562	blood:
26	chr7:111114124..111115929-chr7:111199099..111201690,2	K562	blood:
27	chr7:111154605..111156613-chr7:111179034..111181673,2	K562	blood:
28	chr7:111310577..111313223-chr7:111316574..111319309,2	K562	blood:
29	chr7:111176865..111178433-chr7:111182046..111183894,2	K562	blood:
30	chr7:111252721..111255749-chr7:111259045..111261451,3	K562	blood:
31	chr1:231114585..231115155-chr7:111179137..111179637,2	NB4	blood:
32	chr7:111160191..111163357-chr7:111166833..111169527,4	K562	blood:
33	chr7:111309388..111312560-chr7:111313840..111315927,3	K562	blood:
34	chr7:111222849..111225723-chr7:111230601..111232352,2	K562	blood:
35	chr7:111238331..111240393-chr7:111247235..111250162,2	K562	blood:
36	chr7:111199186..111200731-chr7:111244724..111246694,2	K562	blood:
37	chr7:111299147..111302092-chr7:111316986..111318533,2	K562	blood:
38	chr7:111165987..111169659-chr7:111199981..111202962,6	K562	blood:
39	chr7:111201167..111202749-chr7:111247769..111250524,2	MCF-7	breast:
40	chr7:111284627..111287307-chr7:111300910..111302600,2	K562	blood:
41	chr7:111227327..111229119-chr7:111232502..111234968,2	K562	blood:
42	chr7:111299093..111300961-chr7:111312313..111315147,2	K562	blood:
43	chr7:111226016..111229076-chr7:111232229..111235664,3	K562	blood:
44	chr7:111198400..111201071-chr7:111297443..111299093,2	K562	blood:
45	chr7:108236133..108238229-chr7:111206520..111209026,2	K562	blood:
46	chr7:111199806..111203815-chr7:111204194..111208663,6	MCF-7	breast:
47	chr7:111252421..111255385-chr7:111257912..111259805,2	MCF-7	breast:
48	chr7:111182436..111184713-chr7:111201121..111202847,2	MCF-7	breast:
49	chr7:111200608..111203822-chr7:111213514..111217285,4	K562	blood:
50	chr7:111176865..111178433-chr7:111182046..111183894,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRN3-2	chr7:111235830-111235905	ucscGeneNc_uc003vfz_2
2	lnc-LRRN3-2	chr7:111246670-111249064	ucscGeneNc_uc003vfz_2

No data

Variant related genes	Relation type
IMMP2L	TF binding region
IMMP2L	CpG island
ENSG00000164327	chromatin interactions
ENSG00000143643	chromatin interactions
ENSG00000184903	chromatin interactions
ENSG00000214188	chromatin interactions
ENSG00000173812	chromatin interactions
ENSG00000204463	chromatin interactions
ENSG00000204444	chromatin interactions
ENSG00000240053	chromatin interactions
ENSG00000178951	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000102103	chromatin interactions
ENSG00000126768	chromatin interactions
ENSG00000141979	chromatin interactions
ENSG00000105085	chromatin interactions
ENSG00000173409	chromatin interactions

Extended variants
information (count: 4215 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:4215 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2613589	chr7:111157532-111157533	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs7805960	chr7:111157548-111157549	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs11972448	chr7:111157674-111157675	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs556522528	chr7:111157681-111157682	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs527784679	chr7:111157696-111157697	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs115758688	chr7:111157706-111157707	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs535445420	chr7:111157714-111157715	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs530296323	chr7:111157726-111157727	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs554321849	chr7:111157729-111157730	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs116149483	chr7:111157765-111157766	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs371537698	chr7:111157818-111157819	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs557929607	chr7:111157819-111157820	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs59888605	chr7:111157841-111157842	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs576258036	chr7:111157917-111157918	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs376725670	chr7:111157970-111157971	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs566136471	chr7:111157973-111157974	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs146769935	chr7:111157979-111157980	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs574298547	chr7:111158009-111158010	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs140321520	chr7:111158019-111158020	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs560102047	chr7:111158020-111158021	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs539479078	chr7:111158051-111158052	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs527386090	chr7:111158053-111158054	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs552347975	chr7:111158062-111158063	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs564249510	chr7:111158066-111158067	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs370368755	chr7:111158109-111158110	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs374054190	chr7:111158121-111158122	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs531568682	chr7:111158188-111158189	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs539821330	chr7:111158281-111158282	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs568234594	chr7:111158294-111158295	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs80009519	chr7:111158322-111158323	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs576326520	chr7:111158347-111158348	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs547467977	chr7:111158352-111158353	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs566115320	chr7:111158354-111158355	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs539527666	chr7:111158375-111158376	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs543337327	chr7:111158380-111158381	Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs75999753	chr7:111158443-111158444	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs532091364	chr7:111158465-111158466	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs199746113	chr7:111158529-111158530	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs148000604	chr7:111158567-111158568	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs555169739	chr7:111158586-111158587	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs555931854	chr7:111158638-111158639	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs78750061	chr7:111158687-111158688	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs541749469	chr7:111158696-111158697	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs559889041	chr7:111158716-111158717	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs572096545	chr7:111158717-111158718	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs181465696	chr7:111158728-111158729	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs185880366	chr7:111158768-111158769	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs112670386	chr7:111158792-111158793	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs548510800	chr7:111158806-111158807	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs549670086	chr7:111158829-111158830	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	19401682	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Autism	20841430	CNVD
Autism	20685689	CNVD
Cancer	20164919	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1225 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:111123000-111159000	Weak transcription	Aorta	Aorta
2	chr7:111146600-111159000	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:111147200-111161400	Weak transcription	Fetal Intestine Small	intestine
4	chr7:111149000-111161600	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr7:111149600-111161200	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr7:111149800-111163600	Weak transcription	HMEC	breast
7	chr7:111150400-111161800	Weak transcription	Primary B cells from cord blood	blood
8	chr7:111151000-111158400	Weak transcription	Adipose Nuclei	Adipose
9	chr7:111151000-111162000	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr7:111151000-111167200	Weak transcription	Left Ventricle	heart
11	chr7:111151000-111180600	Weak transcription	Pancreas	Pancrea
12	chr7:111151200-111158800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr7:111151200-111161800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr7:111151400-111158800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:111152000-111160400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr7:111152000-111163000	Weak transcription	Fetal Stomach	stomach
17	chr7:111152200-111158400	Weak transcription	K562	blood
18	chr7:111152400-111168000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr7:111153200-111160600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr7:111154200-111158200	Weak transcription	Primary B cells from peripheral blood	blood
21	chr7:111154200-111169000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr7:111155400-111159200	Weak transcription	Primary T cells from cord blood	blood
23	chr7:111155400-111161800	Weak transcription	Primary T cells fromperipheralblood	blood
24	chr7:111155600-111158200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr7:111156200-111157600	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr7:111156200-111160200	Weak transcription	NHLF	lung
27	chr7:111156400-111158400	Weak transcription	Hela-S3	cervix
28	chr7:111156400-111159600	Weak transcription	Colon Smooth Muscle	Colon
29	chr7:111156600-111158600	Flanking Active TSS	A549	lung
30	chr7:111156800-111157600	Enhancers	Duodenum Mucosa	Duodenum
31	chr7:111156800-111159000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr7:111157000-111158400	Weak transcription	Gastric	stomach
33	chr7:111157000-111158400	Weak transcription	Ovary	ovary
34	chr7:111157000-111161800	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr7:111157200-111157600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr7:111157200-111157600	Enhancers	Liver	Liver
37	chr7:111157200-111159800	Weak transcription	NHEK	skin
38	chr7:111157400-111159000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr7:111157400-111159000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr7:111157400-111159000	Weak transcription	Dnd41	blood
41	chr7:111157400-111170000	Weak transcription	Stomach Mucosa	stomach
42	chr7:111157600-111157800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr7:111157600-111157800	Flanking Active TSS	Liver	Liver
44	chr7:111157600-111158000	Weak transcription	Duodenum Mucosa	Duodenum
45	chr7:111157600-111161400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr7:111157600-111161800	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr7:111157600-111168200	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr7:111157800-111158200	Active TSS	Liver	Liver
49	chr7:111157800-111168000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
50	chr7:111157800-111178000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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