Variant report

Variant	nsv606651
Chromosome Location	chr7:38321653-38380446
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1441)
CpG islands
(count:1895)
Chromatin interactive
region (count:49)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1441 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:38333909-38333936	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:38375261-38375775	K562	blood:	n/a	n/a
3	ATF1	chr7:38358478-38358765	K562	blood:	n/a	n/a
4	ATF1	chr7:38375268-38375593	K562	blood:	n/a	n/a
5	ATF1	chr7:38379898-38380061	K562	blood:	n/a	n/a
6	ATF1	chr7:38332074-38332345	K562	blood:	n/a	n/a
7	ATF1	chr7:38375958-38376139	K562	blood:	n/a	n/a
8	ATF2	chr7:38358345-38358831	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr7:38375154-38375534	GM12878	blood:	n/a	n/a
10	ATF2	chr7:38375126-38375565	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr7:38375159-38375625	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr7:38375250-38375572	K562	blood:	n/a	n/a
13	BACH1	chr7:38375296-38375468	K562	blood:	n/a	n/a
14	BACH1	chr7:38371330-38371815	H1-hESC	embryonic stem cell:	n/a	chr7:38371628-38371642
15	BATF	chr7:38335608-38335962	GM12878	blood:	n/a	n/a
16	BATF	chr7:38375071-38375552	GM12878	blood:	n/a	n/a
17	BATF	chr7:38335625-38335952	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:38335675-38335915	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:38335645-38335867	GM12878	blood:	n/a	n/a
20	BCL3	chr7:38375082-38375686	A549	lung:	n/a	chr7:38375198-38375207
21	BCLAF1	chr7:38375138-38375654	GM12878	blood:	n/a	chr7:38375198-38375207
22	BCLAF1	chr7:38375115-38375667	GM12878	blood:	n/a	chr7:38375198-38375207
23	BHLHE40	chr7:38339818-38340010	K562	blood:	n/a	n/a
24	BHLHE40	chr7:38370489-38370864	K562	blood:	n/a	n/a
25	BHLHE40	chr7:38375174-38375547	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:38351090-38351531	K562	blood:	n/a	n/a
27	BHLHE40	chr7:38335593-38335955	GM12878	blood:	n/a	n/a
28	BHLHE40	chr7:38330775-38331007	HepG2	liver:	n/a	n/a
29	BHLHE40	chr7:38351349-38351381	GM12878	blood:	n/a	n/a
30	BHLHE40	chr7:38330740-38331111	K562	blood:	n/a	n/a
31	BHLHE40	chr7:38374979-38376051	K562	blood:	n/a	n/a
32	BHLHE40	chr7:38358558-38358736	K562	blood:	n/a	n/a
33	BHLHE40	chr7:38379902-38380060	K562	blood:	n/a	n/a
34	BRCA1	chr7:38375364-38375495	HepG2	liver:	n/a	n/a
35	CBX3	chr7:38370432-38370850	K562	blood:	n/a	n/a
36	CBX3	chr7:38350978-38351579	K562	blood:	n/a	n/a
37	CBX3	chr7:38375149-38375641	K562	blood:	n/a	n/a
38	CBX3	chr7:38375046-38375715	K562	blood:	n/a	n/a
39	CCNT2	chr7:38350861-38351244	K562	blood:	n/a	n/a
40	CCNT2	chr7:38375300-38375668	K562	blood:	n/a	n/a
41	CEBPB	chr7:38330530-38330719	K562	blood:	n/a	n/a
42	CEBPB	chr7:38375302-38375655	K562	blood:	n/a	n/a
43	CEBPB	chr7:38357938-38358233	H1-hESC	embryonic stem cell:	n/a	chr7:38358095-38358108
44	CEBPB	chr7:38361024-38361459	IMR90	lung:	n/a	chr7:38361262-38361275
45	CEBPB	chr7:38321761-38322047	K562	blood:	n/a	chr7:38321909-38321920
46	CEBPB	chr7:38345755-38346111	MCF-7	breast:	n/a	n/a
47	CEBPB	chr7:38350358-38350709	K562	blood:	n/a	chr7:38350562-38350575
48	CEBPB	chr7:38357963-38358244	ECC-1	luminal epithelium:	n/a	chr7:38358095-38358108
49	CEBPB	chr7:38358105-38358116	K562	blood:	n/a	n/a
50	CEBPB	chr7:38375195-38375630	K562	blood:	n/a	n/a

(count:1895 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38370664-38370714	HEEpiC	esophagus:	n/a
2	chr7:38332633-38332683	AG09309	skin:	n/a
3	chr7:38358683-38358733	RPTEC	kidney:	n/a
4	chr7:38348929-38348979	H1-hESC	embryonic stem cell:	embryo
5	chr7:38370664-38370714	HEEpiC	esophagus:	n/a
6	chr7:38332633-38332683	AG09309	skin:	n/a
7	chr7:38358683-38358733	RPTEC	kidney:	n/a
8	chr7:38348929-38348979	H1-hESC	embryonic stem cell:	embryo
9	chr7:38358683-38358733	GM06990	blood:	n/a
10	chr7:38348929-38348979	SK-N-MC	brain:	n/a
11	chr7:38358429-38358479	PrEC	prostate:	n/a
12	chr7:38344934-38344984	HL-60	blood:	n/a
13	chr7:38351154-38351204	RPTEC	kidney:	n/a
14	chr7:38370874-38370924	NH-A	brain:	n/a
15	chr7:38375376-38375426	ProgFib	skin:	n/a
16	chr7:38344934-38344984	PANC-1	pancreas:	n/a
17	chr7:38356865-38356915	K562	blood:	n/a
18	chr7:38350464-38350514	Caco-2	colon:	n/a
19	chr7:38347775-38347825	SAEC	small airway:	n/a
20	chr7:38351468-38351518	GM06990	blood:	n/a
21	chr7:38350938-38350988	NH-A	brain:	n/a
22	chr7:38358683-38358733	ECC-1	luminal epithelium:	n/a
23	chr7:38331753-38331803	ProgFib	skin:	n/a
24	chr7:38351094-38351144	AG04450	lung:	fetal
25	chr7:38356865-38356915	NHDF-neo	bronchial:	n/a
26	chr7:38351226-38351276	PrEC	prostate:	n/a
27	chr7:38357684-38357734	AG09309	skin:	n/a
28	chr7:38356865-38356915	HCM	heart:	n/a
29	chr7:38370874-38370924	HEK293	kidney:	embryo
30	chr7:38350938-38350988	HUVEC	blood vessel:	n/a
31	chr7:38348929-38348979	AG09309	skin:	n/a
32	chr7:38351226-38351276	GM12878	blood:	n/a
33	chr7:38358683-38358733	NH-A	brain:	n/a
34	chr7:38375376-38375426	A549	lung:	n/a
35	chr7:38351094-38351144	A549	lung:	n/a
36	chr7:38331871-38331921	SK-N-SH_RA	brain:	n/a
37	chr7:38370988-38371038	IMR90	lung:	fetal
38	chr7:38370664-38370714	HL-60	blood:	n/a
39	chr7:38351154-38351204	HUVEC	blood vessel:	n/a
40	chr7:38370676-38370726	AG09319	gingival:	n/a
41	chr7:38348929-38348979	HAEpiC	amniotic membrane:	n/a
42	chr7:38375485-38375535	SKMC	muscle:	n/a
43	chr7:38370676-38370726	GM12891	blood:	n/a
44	chr7:38357047-38357097	NHBE	bronchial:	n/a
45	chr7:38370988-38371038	SK-N-MC	brain:	n/a
46	chr7:38350938-38350988	MCF-7	breast:	n/a
47	chr7:38358683-38358733	PANC-1	pancreas:	n/a
48	chr7:38351226-38351276	MCF-7	breast:	n/a
49	chr7:38357047-38357097	GM12878	blood:	n/a
50	chr7:38356865-38356915	HAEpiC	amniotic membrane:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:38372590..38377698-chr7:38377994..38383669,12	K562	blood:
2	chr5:139487048..139487856-chr7:38339265..38339924,2	NB4	blood:
3	chr7:38350491..38352001-chr7:38373860..38376555,2	K562	blood:
4	chr7:38320521..38322943-chr7:38347615..38349997,2	K562	blood:
5	chr7:38333908..38338085-chr7:38338653..38341388,3	K562	blood:
6	chr11:93474211..93474958-chr7:38350865..38351599,2	NB4	blood:
7	chr7:38369534..38372460-chr7:38378778..38381886,3	K562	blood:
8	chr7:38338259..38344316-chr7:38349234..38354817,8	K562	blood:
9	chr7:38327903..38329443-chr7:38331082..38333824,2	MCF-7	breast:
10	chr7:37940728..37941537-chr7:38358496..38359055,2	MCF-7	breast:
11	chr7:38365694..38367640-chr7:38368298..38369847,2	K562	blood:
12	chr7:38338259..38341713-chr7:38349234..38353582,4	K562	blood:
13	chr7:38316692..38319374-chr7:38324142..38325804,2	MCF-7	breast:
14	chr7:38369664..38372472-chr7:38373590..38376789,3	K562	blood:
15	chr7:38369664..38372472-chr7:38373590..38376789,3	K562	blood:
16	chr7:38338259..38341713-chr7:38349234..38353582,4	K562	blood:
17	chr7:38255022..38255645-chr7:38375302..38376120,3	MCF-7	breast:
18	chr7:38269978..38272526-chr7:38377435..38379545,2	K562	blood:
19	chr7:38337293..38339358-chr7:38341457..38343029,2	K562	blood:
20	chr7:38320521..38322943-chr7:38347615..38349997,2	K562	blood:
21	chr7:38342202..38344316-chr7:38351382..38353535,2	K562	blood:
22	chr7:38322069..38325279-chr7:38325414..38329966,4	K562	blood:
23	chr7:38268526..38271338-chr7:38351636..38353674,2	K562	blood:
24	chr7:38350491..38353138-chr7:38373860..38375500,2	K562	blood:
25	chr7:38369534..38372460-chr7:38378778..38381886,3	K562	blood:
26	chr7:38375070..38375771-chr7:38393808..38394547,2	MCF-7	breast:
27	chr7:38375472..38376033-chr7:38384935..38385704,2	MCF-7	breast:
28	chr7:38145396..38146142-chr7:38358527..38359113,2	MCF-7	breast:
29	chr7:38312675..38315674-chr7:38326850..38329772,2	K562	blood:
30	chr7:38309718..38312267-chr7:38320422..38323270,2	MCF-7	breast:
31	chr7:38333908..38338085-chr7:38338653..38341388,3	K562	blood:
32	chr6:31583767..31584372-chr7:38349943..38350554,2	NB4	blood:
33	chr7:38350491..38352001-chr7:38373860..38376555,2	K562	blood:
34	chr7:38350441..38353889-chr7:38368470..38373744,5	K562	blood:
35	chr7:38357958..38360447-chr7:38360808..38363317,4	K562	blood:
36	chr7:38322069..38325279-chr7:38325414..38329966,4	K562	blood:
37	chr7:38272138..38275044-chr7:38351799..38354206,2	K562	blood:
38	chr7:38357958..38360447-chr7:38360808..38363317,4	K562	blood:
39	chr7:38338259..38344316-chr7:38349234..38354817,8	K562	blood:
40	chr7:38337293..38339358-chr7:38341457..38343029,2	K562	blood:
41	chr7:38350441..38353889-chr7:38368470..38373744,5	K562	blood:
42	chr7:38329299..38330977-chr7:38349932..38352366,2	K562	blood:
43	chr7:38372590..38377698-chr7:38377994..38383669,12	K562	blood:
44	chr7:38350491..38353138-chr7:38373860..38375500,2	K562	blood:
45	chr7:38350855..38351410-chr9:4679053..4679680,2	NB4	blood:
46	chr5:150068580..150069370-chr7:38338298..38339028,2	NB4	blood:
47	chr7:38325300..38328102-chr7:38356981..38359031,2	K562	blood:
48	chr7:38342202..38344316-chr7:38351382..38353535,2	K562	blood:
49	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMPH-6	chr7:38368841-38369244	ENSG00000272908.1
2	lnc-AMPH-10	chr7:38356621-38356709	NONHSAT120162
3	lnc-STARD3NL-1	chr7:38356472-38356576	ucscGeneNc_uc003tgp_1
4	lnc-AMPH-6	chr7:38365671-38367234	ENSG00000272908.1
5	lnc-AMPH-10	chr7:38356623-38356709	NONHSAT120170
6	lnc-AMPH-10	chr7:38356616-38356709	NONHSAT120169
7	lnc-AMPH-2	chr7:38342383-38343224	ENSG00000244971
8	lnc-AMPH-2	chr7:38342349-38343224	NONHSAT120173
9	lnc-AMPH-10	chr7:38356621-38356709	NONHSAT120161
10	lnc-AMPH-2	chr7:38343487-38343773	NONHSAT120173
11	lnc-STARD3NL-1	chr7:38347741-38347925	ucscGeneNc_uc003tgp_1
12	lnc-AMPH-7	chr7:38362047-38362331	NONHSAT120176
13	lnc-AMPH-10	chr7:38356605-38356709	NONHSAT120166
14	lnc-AMPH-5	chr7:38374642-38374951	NONHSAT120177
15	lnc-AMPH-2	chr7:38343487-38343773	ENSG00000244971
16	lnc-AMPH-2	chr7:38344265-38344378	NONHSAT120173
17	lnc-AMPH-5	chr7:38375073-38375115	NONHSAT120177
18	lnc-AMPH-10	chr7:38356622-38356709	NONHSAT120167
19	lnc-STARD3NL-1	chr7:38352147-38352253	ucscGeneNc_uc003tgp_1
20	lnc-AMPH-2	chr7:38344265-38345247	ENSG00000244971
21	lnc-AMPH-8	chr7:38335364-38335834	NONHSAT120172

No data

Variant related genes	Relation type
ENSG00000272908	TF binding region
TRGV7	TF binding region
TRGV10	TF binding region
TRGV11	TF binding region
TRGV8	TF binding region
TRGVB	TF binding region
TRGVA	TF binding region
ENSG00000231916	TF binding region
TRGV9	TF binding region
ENSG00000272908	CpG island
TRGV7	CpG island
TRGV10	CpG island
TRGV11	CpG island
TRGV8	CpG island
TRGVB	CpG island
TRGVA	CpG island
ENSG00000231916	CpG island
TRGV9	CpG island
ENSG00000211696	chromatin interactions
ENSG00000273061	chromatin interactions
ENSG00000185129	chromatin interactions
ENSG00000225992	chromatin interactions
ENSG00000231202	chromatin interactions
ENSG00000211695	chromatin interactions
ENSG00000249978	chromatin interactions
ENSG00000228668	chromatin interactions
ENSG00000211694	chromatin interactions
ENSG00000182919	chromatin interactions
ENSG00000211698	chromatin interactions
ENSG00000226212	chromatin interactions
ENSG00000231916	chromatin interactions
ENSG00000166012	chromatin interactions
ENSG00000211691	chromatin interactions
ENSG00000106993	chromatin interactions
ENSG00000245146	chromatin interactions
ENSG00000204472	chromatin interactions
ENSG00000211693	chromatin interactions
ENSG00000272908	chromatin interactions
PTEN	miRNA target sites

Extended variants
information (count: 2491 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2491 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2191310	chr7:38321653-38321654	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs75670217	chr7:38321755-38321756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181689573	chr7:38321821-38321822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs17171318	chr7:38321842-38321843	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs554454621	chr7:38321852-38321853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574734806	chr7:38321854-38321855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs143409065	chr7:38321863-38321864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs187154002	chr7:38321876-38321877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs17171319	chr7:38321887-38321888	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs386712310	chr7:38321925-38321926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs7784741	chr7:38321927-38321928	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs541404220	chr7:38321964-38321965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs561321031	chr7:38321966-38321967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575740842	chr7:38322080-38322081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs188450065	chr7:38322103-38322104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs573581092	chr7:38322118-38322119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs11380125	chr7:38322119-38322120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs397766325	chr7:38322132-38322133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs540919676	chr7:38322156-38322157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs1990359	chr7:38322168-38322169	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs371947616	chr7:38322242-38322243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532972855	chr7:38322251-38322252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs1990360	chr7:38322259-38322260	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs146087098	chr7:38322281-38322282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140097502	chr7:38322282-38322283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs111247671	chr7:38322316-38322317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs370297854	chr7:38322318-38322319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568421711	chr7:38322385-38322386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534203102	chr7:38322406-38322407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs373568259	chr7:38322407-38322408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547773537	chr7:38322432-38322433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs368128267	chr7:38322436-38322437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs145709913	chr7:38322460-38322461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs148996053	chr7:38322471-38322472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556367108	chr7:38322614-38322615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs207467791	chr7:38322667-38322668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs34648752	chr7:38322741-38322742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs199826050	chr7:38322742-38322743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs62443346	chr7:38322743-38322744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576252011	chr7:38322744-38322745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs141476066	chr7:38322752-38322753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs200379666	chr7:38322753-38322754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530471831	chr7:38322775-38322776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs535144725	chr7:38322831-38322832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs529661642	chr7:38322865-38322866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs142987937	chr7:38322887-38322888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541060277	chr7:38322900-38322901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs2270167	chr7:38322908-38322909	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs2270168	chr7:38322922-38322923	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs113153642	chr7:38322928-38322929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Neuroblastoma	19536264	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1194 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38316800-38323000	Weak transcription	Fetal Thymus	thymus
2	chr7:38316800-38323400	Weak transcription	GM12878-XiMat	blood
3	chr7:38317000-38322000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr7:38317200-38321800	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr7:38317200-38322400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr7:38317600-38321800	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr7:38318200-38323000	Weak transcription	Primary hematopoietic stem cells	blood
8	chr7:38319000-38322200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr7:38320200-38323800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr7:38321000-38321800	Enhancers	Adipose Nuclei	Adipose
11	chr7:38321400-38323200	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr7:38321600-38325200	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr7:38321800-38323200	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr7:38321800-38324200	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr7:38322000-38325000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr7:38322200-38322600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr7:38322400-38325000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr7:38322600-38325200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr7:38323000-38324200	Enhancers	Fetal Thymus	thymus
20	chr7:38323000-38325000	Enhancers	Primary hematopoietic stem cells	blood
21	chr7:38323200-38323600	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr7:38323200-38323600	Weak transcription	Primary neutrophils fromperipheralblood	blood
23	chr7:38323400-38324800	Enhancers	Fetal Heart	heart
24	chr7:38323400-38324800	Enhancers	GM12878-XiMat	blood
25	chr7:38323600-38324200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr7:38323600-38325200	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr7:38323600-38325400	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr7:38324000-38324400	Enhancers	Right Atrium	heart
29	chr7:38324000-38324600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr7:38324200-38324600	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr7:38324200-38324600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
32	chr7:38324400-38325400	Enhancers	Primary B cells from cord blood	blood
33	chr7:38324600-38324800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr7:38324600-38324800	Enhancers	Left Ventricle	heart
35	chr7:38324600-38325000	Enhancers	Primary T cells from cord blood	blood
36	chr7:38324600-38325400	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr7:38325200-38326600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr7:38325200-38328200	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr7:38325200-38334400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr7:38325400-38327800	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr7:38325400-38328000	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr7:38327800-38329000	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr7:38328000-38328600	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr7:38329600-38330800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr7:38329800-38351000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr7:38330800-38331000	Enhancers	K562	blood
47	chr7:38330800-38331200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr7:38330800-38331200	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr7:38330800-38332000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr7:38331000-38331200	Flanking Active TSS	K562	blood

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