Variant report

Variant	nsv464431
Chromosome Location	chr7:38273305-38361625
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:967)
CpG islands
(count:2198)
Chromatin interactive
region (count:42)
LncRNA
region (count:33)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:967 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:38298340-38298378	K562	blood:	n/a	n/a
2	ARID3A	chr7:38333909-38333936	HepG2	liver:	n/a	n/a
3	ATF1	chr7:38358478-38358765	K562	blood:	n/a	n/a
4	ATF1	chr7:38285866-38286066	K562	blood:	n/a	n/a
5	ATF1	chr7:38278820-38279001	K562	blood:	n/a	n/a
6	ATF1	chr7:38285408-38285488	K562	blood:	n/a	n/a
7	ATF1	chr7:38332074-38332345	K562	blood:	n/a	n/a
8	ATF1	chr7:38298851-38299117	K562	blood:	n/a	n/a
9	ATF1	chr7:38296748-38296967	K562	blood:	n/a	n/a
10	ATF1	chr7:38319668-38320070	K562	blood:	n/a	n/a
11	ATF2	chr7:38358345-38358831	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr7:38289493-38289850	GM12878	blood:	n/a	n/a
13	BATF	chr7:38305616-38305913	GM12878	blood:	n/a	n/a
14	BATF	chr7:38289507-38289847	GM12878	blood:	n/a	n/a
15	BATF	chr7:38335608-38335962	GM12878	blood:	n/a	n/a
16	BATF	chr7:38289510-38289833	GM12878	blood:	n/a	n/a
17	BATF	chr7:38335625-38335952	GM12878	blood:	n/a	n/a
18	BATF	chr7:38305659-38305874	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:38335645-38335867	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:38305548-38305926	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:38305612-38305832	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:38289452-38289744	GM12878	blood:	n/a	chr7:38289640-38289649
23	BCL11A	chr7:38335675-38335915	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:38289442-38289823	GM12878	blood:	n/a	chr7:38289640-38289649
25	BHLHE40	chr7:38313008-38313126	K562	blood:	n/a	n/a
26	BHLHE40	chr7:38335593-38335955	GM12878	blood:	n/a	n/a
27	BHLHE40	chr7:38339818-38340010	K562	blood:	n/a	n/a
28	BHLHE40	chr7:38330740-38331111	K562	blood:	n/a	n/a
29	BHLHE40	chr7:38351090-38351531	K562	blood:	n/a	n/a
30	BHLHE40	chr7:38351349-38351381	GM12878	blood:	n/a	n/a
31	BHLHE40	chr7:38330775-38331007	HepG2	liver:	n/a	n/a
32	BHLHE40	chr7:38358558-38358736	K562	blood:	n/a	n/a
33	CBX3	chr7:38350978-38351579	K562	blood:	n/a	n/a
34	CCNT2	chr7:38350861-38351244	K562	blood:	n/a	n/a
35	CEBPB	chr7:38357938-38358233	H1-hESC	embryonic stem cell:	n/a	chr7:38358095-38358108
36	CEBPB	chr7:38361024-38361459	IMR90	lung:	n/a	chr7:38361262-38361275
37	CEBPB	chr7:38285344-38285395	K562	blood:	n/a	n/a
38	CEBPB	chr7:38282932-38283307	K562	blood:	n/a	chr7:38282939-38282951
39	CEBPB	chr7:38345755-38346111	MCF-7	breast:	n/a	n/a
40	CEBPB	chr7:38350358-38350709	K562	blood:	n/a	chr7:38350562-38350575
41	CEBPB	chr7:38321761-38322047	K562	blood:	n/a	chr7:38321909-38321920
42	CEBPB	chr7:38282957-38283329	A549	lung:	n/a	n/a
43	CEBPB	chr7:38282943-38283333	K562	blood:	n/a	n/a
44	CEBPB	chr7:38296681-38297002	K562	blood:	n/a	chr7:38296860-38296873
45	CEBPB	chr7:38282963-38283206	MCF-7	breast:	n/a	n/a
46	CEBPB	chr7:38330530-38330719	K562	blood:	n/a	n/a
47	CEBPB	chr7:38357963-38358244	ECC-1	luminal epithelium:	n/a	chr7:38358095-38358108
48	CEBPB	chr7:38321770-38322083	HepG2	liver:	n/a	chr7:38321909-38321920
49	CEBPB	chr7:38282957-38283270	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr7:38282956-38283330	IMR90	lung:	n/a	n/a

(count:2198 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38356865-38356915	AG09309	skin:	n/a
2	chr7:38350921-38350971	PANC-1	pancreas:	n/a
3	chr7:38356865-38356915	AG09309	skin:	n/a
4	chr7:38350921-38350971	PANC-1	pancreas:	n/a
5	chr7:38351154-38351204	AG09309	skin:	n/a
6	chr7:38331871-38331921	Hela-S3	cervix:	n/a
7	chr7:38316654-38316704	IMR90	lung:	fetal
8	chr7:38356808-38356858	AG09319	gingival:	n/a
9	chr7:38358683-38358733	K562	blood:	n/a
10	chr7:38351154-38351204	AG10803	skin:	n/a
11	chr7:38357047-38357097	ProgFib	skin:	n/a
12	chr7:38309984-38310034	HRCEpiC	kidney:	n/a
13	chr7:38350938-38350988	BE2_C	brain:	n/a
14	chr7:38331871-38331921	Caco-2	colon:	n/a
15	chr7:38344455-38344505	NH-A	brain:	n/a
16	chr7:38357684-38357734	SK-N-MC	brain:	n/a
17	chr7:38299481-38299531	GM12892	blood:	n/a
18	chr7:38351154-38351204	PFSK-1	brain:	n/a
19	chr7:38331753-38331803	LNCaP	prostate:	n/a
20	chr7:38351226-38351276	NHBE	bronchial:	n/a
21	chr7:38299481-38299531	MCF10A-Er-Src	breast:	n/a
22	chr7:38344934-38344984	RPTEC	kidney:	n/a
23	chr7:38358429-38358479	NT2-D1	testis:	n/a
24	chr7:38331753-38331803	HMEC	breast:	n/a
25	chr7:38303957-38304007	AG04450	lung:	fetal
26	chr7:38356808-38356858	SKMC	muscle:	n/a
27	chr7:38298966-38299016	A549	lung:	n/a
28	chr7:38358429-38358479	U87	brain:	n/a
29	chr7:38351094-38351144	Caco-2	colon:	n/a
30	chr7:38350938-38350988	RPTEC	kidney:	n/a
31	chr7:38351468-38351518	NB4	blood:	n/a
32	chr7:38315971-38316021	HEEpiC	esophagus:	n/a
33	chr7:38350464-38350514	PrEC	prostate:	n/a
34	chr7:38299481-38299531	CMK	blood:	n/a
35	chr7:38298966-38299016	H1-hESC	embryonic stem cell:	embryo
36	chr7:38312366-38312416	HAEpiC	amniotic membrane:	n/a
37	chr7:38344934-38344984	MCF-7	breast:	n/a
38	chr7:38350921-38350971	SK-N-SH	brain:	n/a
39	chr7:38361199-38361249	NB4	blood:	n/a
40	chr7:38331753-38331803	Hela-S3	cervix:	n/a
41	chr7:38351094-38351144	Hela-S3	cervix:	n/a
42	chr7:38315964-38316014	ProgFib	skin:	n/a
43	chr7:38344934-38344984	HPAEpiC	pulmonary alveolar:	n/a
44	chr7:38298966-38299016	GM19239	blood:	n/a
45	chr7:38298908-38298958	NHDF-neo	bronchial:	n/a
46	chr7:38331753-38331803	BE2_C	brain:	n/a
47	chr7:38351154-38351204	K562	blood:	n/a
48	chr7:38350938-38350988	HCT-116	colon:	n/a
49	chr7:38351154-38351204	ovcar-3	ovarian:	n/a
50	chr7:38303957-38304007	GM19239	blood:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:38333908..38338085-chr7:38338653..38341388,3	K562	blood:
2	chr7:38322069..38325279-chr7:38325414..38329966,4	K562	blood:
3	chr7:38301028..38303453-chr7:38304151..38306717,2	K562	blood:
4	chr7:38272138..38275044-chr7:38351799..38354206,2	K562	blood:
5	chr7:38272138..38275044-chr7:38351799..38354206,2	K562	blood:
6	chr5:150068580..150069370-chr7:38338298..38339028,2	NB4	blood:
7	chr7:38145396..38146142-chr7:38358527..38359113,2	MCF-7	breast:
8	chr7:38316692..38319374-chr7:38324142..38325804,2	MCF-7	breast:
9	chr19:47892610..47893302-chr7:38314653..38315604,2	NB4	blood:
10	chr7:38350441..38353889-chr7:38368470..38373744,5	K562	blood:
11	chr7:38350491..38353138-chr7:38373860..38375500,2	K562	blood:
12	chr7:38338259..38344316-chr7:38349234..38354817,8	K562	blood:
13	chr7:38263678..38267697-chr7:38270258..38274189,5	K562	blood:
14	chr6:31583767..31584372-chr7:38349943..38350554,2	NB4	blood:
15	chr7:38322069..38325279-chr7:38325414..38329966,4	K562	blood:
16	chr7:38309718..38312267-chr7:38320422..38323270,2	MCF-7	breast:
17	chr7:38350855..38351410-chr9:4679053..4679680,2	NB4	blood:
18	chr7:38337293..38339358-chr7:38341457..38343029,2	K562	blood:
19	chr7:38320521..38322943-chr7:38347615..38349997,2	K562	blood:
20	chr7:38342202..38344316-chr7:38351382..38353535,2	K562	blood:
21	chr7:38337293..38339358-chr7:38341457..38343029,2	K562	blood:
22	chr7:38325300..38328102-chr7:38356981..38359031,2	K562	blood:
23	chr7:38329299..38330977-chr7:38349932..38352366,2	K562	blood:
24	chr7:37940728..37941537-chr7:38358496..38359055,2	MCF-7	breast:
25	chr7:38338259..38344316-chr7:38349234..38354817,8	K562	blood:
26	chr7:38268526..38271338-chr7:38351636..38353674,2	K562	blood:
27	chr7:38309718..38312267-chr7:38320422..38323270,2	MCF-7	breast:
28	chr5:139487048..139487856-chr7:38339265..38339924,2	NB4	blood:
29	chr7:38338259..38341713-chr7:38349234..38353582,4	K562	blood:
30	chr11:93474211..93474958-chr7:38350865..38351599,2	NB4	blood:
31	chr7:38316692..38319374-chr7:38324142..38325804,2	MCF-7	breast:
32	chr7:38357958..38360447-chr7:38360808..38363317,4	K562	blood:
33	chr7:38342202..38344316-chr7:38351382..38353535,2	K562	blood:
34	chr7:38357958..38360447-chr7:38360808..38363317,4	K562	blood:
35	chr4:10118970..10119677-chr7:38276136..38276938,2	NB4	blood:
36	chr7:38327903..38329443-chr7:38331082..38333824,2	MCF-7	breast:
37	chr7:38333908..38338085-chr7:38338653..38341388,3	K562	blood:
38	chr7:38262524..38265185-chr7:38273332..38275255,2	K562	blood:
39	chr7:38320521..38322943-chr7:38347615..38349997,2	K562	blood:
40	chr7:38350491..38352001-chr7:38373860..38376555,2	K562	blood:
41	chr7:38338259..38341713-chr7:38349234..38353582,4	K562	blood:
42	chr7:38312675..38315674-chr7:38326850..38329772,2	K562	blood:

(count:33 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMPH-10	chr7:38356621-38356709	NONHSAT120161
2	lnc-AMPH-10	chr7:38289105-38289173	NONHSAT120162
3	lnc-AMPH-10	chr7:38289106-38289173	NONHSAT120166
4	lnc-AMPH-10	chr7:38356605-38356709	NONHSAT120166
5	lnc-AMPH-10	chr7:38310012-38310298	ucscGeneNc_uc003tgm_1
6	lnc-AMPH-10	chr7:38295939-38295993	NONHSAT120166
7	lnc-AMPH-8	chr7:38335364-38335834	NONHSAT120172
8	lnc-AMPH-10	chr7:38310790-38310903	ucscGeneNc_uc003tgm_1
9	lnc-AMPH-2	chr7:38343487-38343773	ENSG00000244971
10	lnc-AMPH-10	chr7:38295939-38296001	NONHSAT120167
11	lnc-AMPH-2	chr7:38344265-38344378	NONHSAT120173
12	lnc-AMPH-10	chr7:38356621-38356709	NONHSAT120162
13	lnc-STARD3NL-1	chr7:38352147-38352253	ucscGeneNc_uc003tgp_1
14	lnc-AMPH-10	chr7:38313188-38313242	NONHSAT120170
15	lnc-AMPH-9	chr7:38305937-38306406	ucscGeneNc_uc003tgl_1
16	lnc-AMPH-2	chr7:38344265-38345247	ENSG00000244971
17	lnc-AMPH-10	chr7:38313188-38313238	NONHSAT120169
18	lnc-AMPH-10	chr7:38292981-38293028	NONHSAT120161
19	lnc-AMPH-10	chr7:38356622-38356709	NONHSAT120167
20	lnc-AMPH-10	chr7:38289105-38289173	NONHSAT120161
21	lnc-STARD3NL-1	chr7:38347741-38347925	ucscGeneNc_uc003tgp_1
22	lnc-AMPH-10	chr7:38356623-38356709	NONHSAT120170
23	lnc-AMPH-10	chr7:38292981-38293025	NONHSAT120162
24	lnc-AMPH-2	chr7:38343487-38343773	NONHSAT120173
25	lnc-STARD3NL-1	chr7:38356472-38356576	ucscGeneNc_uc003tgp_1
26	lnc-AMPH-10	chr7:38305211-38305279	NONHSAT120170
27	lnc-AMPH-10	chr7:38293236-38293239	NONHSAT120162
28	lnc-AMPH-10	chr7:38308874-38309749	ucscGeneNc_uc003tgm_1
29	lnc-AMPH-2	chr7:38342349-38343224	NONHSAT120173
30	lnc-AMPH-10	chr7:38356616-38356709	NONHSAT120169
31	lnc-AMPH-10	chr7:38305211-38305279	NONHSAT120169
32	lnc-AMPH-10	chr7:38289106-38289173	NONHSAT120167
33	lnc-AMPH-2	chr7:38342383-38343224	ENSG00000244971

No data

Variant related genes	Relation type
TRGC2	TF binding region
TRGC1	TF binding region
TRGJP	TF binding region
TRGJP2	TF binding region
TRGV10	TF binding region
TRGV11	TF binding region
TRGJ2	TF binding region
TRGVB	TF binding region
TRGJP1	TF binding region
TRGJ1	TF binding region
ENSG00000231916	TF binding region
TRGV9	TF binding region
TRGC2	CpG island
TRGC1	CpG island
TRGJP	CpG island
TRGJP2	CpG island
TRGV10	CpG island
TRGV11	CpG island
TRGJ2	CpG island
TRGVB	CpG island
TRGJP1	CpG island
TRGJ1	CpG island
ENSG00000231916	CpG island
TRGV9	CpG island
ENSG00000272908	chromatin interactions
ENSG00000245146	chromatin interactions
ENSG00000211695	chromatin interactions
ENSG00000182919	chromatin interactions
ENSG00000225992	chromatin interactions
ENSG00000204472	chromatin interactions
ENSG00000185129	chromatin interactions
ENSG00000231916	chromatin interactions
ENSG00000231202	chromatin interactions
ENSG00000106993	chromatin interactions
ENSG00000211694	chromatin interactions
ENSG00000211696	chromatin interactions
ENSG00000249978	chromatin interactions
ENSG00000273061	chromatin interactions
ENSG00000166012	chromatin interactions
ENSG00000211689	chromatin interactions
ENSG00000211691	chromatin interactions
ENSG00000211693	chromatin interactions
PTEN	miRNA target sites

Extended variants
information (count: 4075 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:4075 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6462820	chr7:38273305-38273306	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs562686169	chr7:38273314-38273315	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs189602118	chr7:38273395-38273396	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs558374299	chr7:38273425-38273426	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs578157449	chr7:38273456-38273457	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs543108831	chr7:38273520-38273521	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs557034835	chr7:38273533-38273534	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs373083636	chr7:38273559-38273560	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs573527438	chr7:38273567-38273568	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs151058618	chr7:38273588-38273589	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs4720273	chr7:38273611-38273612	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs572789439	chr7:38273632-38273633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs181968872	chr7:38273672-38273673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564881828	chr7:38273708-38273709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185774634	chr7:38273837-38273838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549974850	chr7:38273838-38273839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs139804828	chr7:38273848-38273849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs377559523	chr7:38273895-38273896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs564963722	chr7:38273928-38273929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529437977	chr7:38273929-38273930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs549383677	chr7:38273955-38273956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs566119996	chr7:38273959-38273960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535333812	chr7:38274011-38274012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs564193515	chr7:38274071-38274072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs11319416	chr7:38274076-38274077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs373181996	chr7:38274086-38274087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs6956727	chr7:38274151-38274152	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs571714736	chr7:38274153-38274154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs537671729	chr7:38274213-38274214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557300414	chr7:38274284-38274285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573663968	chr7:38274298-38274299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs17171309	chr7:38274311-38274312	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs189808651	chr7:38274316-38274317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2534595	chr7:38274318-38274319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572506857	chr7:38274324-38274325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs544860086	chr7:38274358-38274359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565202399	chr7:38274381-38274382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575320311	chr7:38274386-38274387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544376427	chr7:38274434-38274435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs560960475	chr7:38274452-38274453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528938895	chr7:38274548-38274549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529397461	chr7:38274556-38274557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs2058268	chr7:38274586-38274587	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs117214629	chr7:38274587-38274588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs528510793	chr7:38274644-38274645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs551758624	chr7:38274648-38274649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571888429	chr7:38274660-38274661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs537378203	chr7:38274667-38274668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551142624	chr7:38274677-38274678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540003939	chr7:38274730-38274731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Sezary syndrome	18413736	CNVD
Gastric cancer	24379144	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Multiple sclerosis	20428171	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Neuroblastoma	19536264	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1086 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38259600-38273800	Weak transcription	Rectal Smooth Muscle	rectum
2	chr7:38260400-38273800	Weak transcription	Fetal Brain Male	brain
3	chr7:38261600-38274800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr7:38261600-38277200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr7:38269600-38273400	Weak transcription	Colon Smooth Muscle	Colon
6	chr7:38269600-38273800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr7:38269600-38274400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr7:38269600-38274400	Weak transcription	Brain Germinal Matrix	brain
9	chr7:38269800-38273400	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr7:38269800-38273600	Weak transcription	Stomach Smooth Muscle	stomach
11	chr7:38269800-38273800	Weak transcription	Brain Cingulate Gyrus	brain
12	chr7:38269800-38273800	Weak transcription	NH-A	brain
13	chr7:38269800-38274400	Weak transcription	Esophagus	oesophagus
14	chr7:38269800-38275400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr7:38269800-38275600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr7:38269800-38275600	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr7:38270000-38273600	Weak transcription	Gastric	stomach
18	chr7:38270000-38274600	Weak transcription	Fetal Intestine Large	intestine
19	chr7:38270200-38273400	Weak transcription	NHEK	skin
20	chr7:38270200-38273600	Weak transcription	Brain Angular Gyrus	brain
21	chr7:38270200-38273600	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr7:38270200-38273800	Weak transcription	Brain Anterior Caudate	brain
23	chr7:38270400-38273600	Weak transcription	NHDF-Ad	bronchial
24	chr7:38270400-38273800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr7:38270400-38274200	Weak transcription	Liver	Liver
26	chr7:38270400-38274200	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr7:38270400-38275800	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr7:38270600-38273600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr7:38270600-38273600	Weak transcription	Brain Hippocampus Middle	brain
30	chr7:38270600-38274000	Weak transcription	HUVEC	blood vessel
31	chr7:38270600-38274200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr7:38271000-38278200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr7:38271400-38273800	Enhancers	Thymus	Thymus
34	chr7:38271400-38274400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr7:38271400-38275400	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr7:38271400-38276800	Enhancers	Primary hematopoietic stem cells	blood
37	chr7:38271600-38273800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr7:38271600-38274600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr7:38271800-38274000	Weak transcription	Aorta	Aorta
40	chr7:38271800-38276200	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr7:38272000-38273600	Flanking Active TSS	Dnd41	blood
42	chr7:38272000-38273800	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr7:38272000-38273800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
44	chr7:38272000-38274400	Weak transcription	Fetal Intestine Small	intestine
45	chr7:38272000-38274400	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr7:38272000-38275800	Weak transcription	Adipose Nuclei	Adipose
47	chr7:38272200-38276400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr7:38272400-38273600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr7:38272400-38274000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr7:38272400-38274000	Weak transcription	Fetal Muscle Leg	muscle

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