Variant report

Variant	nsv818497
Chromosome Location	chr7:38318590-38380446
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1450)
CpG islands
(count:1892)
Chromatin interactive
region (count:50)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1450 , 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	chr7:38375261-38375775	K562	blood:	n/a	n/a
2	ARID3A	chr7:38333909-38333936	HepG2	liver:	n/a	n/a
3	ATF1	chr7:38375958-38376139	K562	blood:	n/a	n/a
4	ATF1	chr7:38379898-38380061	K562	blood:	n/a	n/a
5	ATF1	chr7:38332074-38332345	K562	blood:	n/a	n/a
6	ATF1	chr7:38358478-38358765	K562	blood:	n/a	n/a
7	ATF1	chr7:38375268-38375593	K562	blood:	n/a	n/a
8	ATF1	chr7:38319668-38320070	K562	blood:	n/a	n/a
9	ATF2	chr7:38375154-38375534	GM12878	blood:	n/a	n/a
10	ATF2	chr7:38358345-38358831	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr7:38375126-38375565	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr7:38375159-38375625	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr7:38375250-38375572	K562	blood:	n/a	n/a
14	BACH1	chr7:38375296-38375468	K562	blood:	n/a	n/a
15	BACH1	chr7:38371330-38371815	H1-hESC	embryonic stem cell:	n/a	chr7:38371628-38371642
16	BATF	chr7:38375071-38375552	GM12878	blood:	n/a	n/a
17	BATF	chr7:38335608-38335962	GM12878	blood:	n/a	n/a
18	BATF	chr7:38335625-38335952	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:38335645-38335867	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:38335675-38335915	GM12878	blood:	n/a	n/a
21	BCL3	chr7:38375082-38375686	A549	lung:	n/a	chr7:38375198-38375207
22	BCLAF1	chr7:38375138-38375654	GM12878	blood:	n/a	chr7:38375198-38375207
23	BCLAF1	chr7:38375115-38375667	GM12878	blood:	n/a	chr7:38375198-38375207
24	BHLHE40	chr7:38370489-38370864	K562	blood:	n/a	n/a
25	BHLHE40	chr7:38339818-38340010	K562	blood:	n/a	n/a
26	BHLHE40	chr7:38374979-38376051	K562	blood:	n/a	n/a
27	BHLHE40	chr7:38330740-38331111	K562	blood:	n/a	n/a
28	BHLHE40	chr7:38335593-38335955	GM12878	blood:	n/a	n/a
29	BHLHE40	chr7:38379902-38380060	K562	blood:	n/a	n/a
30	BHLHE40	chr7:38351349-38351381	GM12878	blood:	n/a	n/a
31	BHLHE40	chr7:38351090-38351531	K562	blood:	n/a	n/a
32	BHLHE40	chr7:38330775-38331007	HepG2	liver:	n/a	n/a
33	BHLHE40	chr7:38375174-38375547	GM12878	blood:	n/a	n/a
34	BHLHE40	chr7:38358558-38358736	K562	blood:	n/a	n/a
35	BRCA1	chr7:38375364-38375495	HepG2	liver:	n/a	n/a
36	CBX3	chr7:38375046-38375715	K562	blood:	n/a	n/a
37	CBX3	chr7:38350978-38351579	K562	blood:	n/a	n/a
38	CBX3	chr7:38375149-38375641	K562	blood:	n/a	n/a
39	CBX3	chr7:38370432-38370850	K562	blood:	n/a	n/a
40	CCNT2	chr7:38375300-38375668	K562	blood:	n/a	n/a
41	CCNT2	chr7:38350861-38351244	K562	blood:	n/a	n/a
42	CEBPB	chr7:38350358-38350709	K562	blood:	n/a	chr7:38350562-38350575
43	CEBPB	chr7:38357963-38358244	ECC-1	luminal epithelium:	n/a	chr7:38358095-38358108
44	CEBPB	chr7:38321761-38322047	K562	blood:	n/a	chr7:38321909-38321920
45	CEBPB	chr7:38361024-38361459	IMR90	lung:	n/a	chr7:38361262-38361275
46	CEBPB	chr7:38358105-38358116	K562	blood:	n/a	n/a
47	CEBPB	chr7:38375302-38375655	K562	blood:	n/a	n/a
48	CEBPB	chr7:38345755-38346111	MCF-7	breast:	n/a	n/a
49	CEBPB	chr7:38330530-38330719	K562	blood:	n/a	n/a
50	CEBPB	chr7:38357938-38358233	H1-hESC	embryonic stem cell:	n/a	chr7:38358095-38358108

(count:1892 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38355100-38355150	HEK293	kidney:	embryo
2	chr7:38355100-38355150	HEK293	kidney:	embryo
3	chr7:38370676-38370726	HRPEpiC	eye:	n/a
4	chr7:38357047-38357097	U87	brain:	n/a
5	chr7:38356865-38356915	HAEpiC	amniotic membrane:	n/a
6	chr7:38340103-38340153	BJ	skin:	n/a
7	chr7:38351094-38351144	BE2_C	brain:	n/a
8	chr7:38357047-38357097	SAEC	small airway:	n/a
9	chr7:38344934-38344984	T-47D	breast:	n/a
10	chr7:38356729-38356779	MCF10A-Er-Src	breast:	n/a
11	chr7:38351154-38351204	GM12878	blood:	n/a
12	chr7:38358429-38358479	HRCEpiC	kidney:	n/a
13	chr7:38350921-38350971	HRE	kidney:	n/a
14	chr7:38375485-38375535	BJ	skin:	n/a
15	chr7:38350464-38350514	AG04449	skin:	fetal
16	chr7:38370676-38370726	K562	blood:	n/a
17	chr7:38370664-38370714	NHDF-neo	bronchial:	n/a
18	chr7:38344934-38344984	AoSMC	blood vessel:	n/a
19	chr7:38344983-38345033	HRE	kidney:	n/a
20	chr7:38344934-38344984	GM06990	blood:	n/a
21	chr7:38332633-38332683	NHBE	bronchial:	n/a
22	chr7:38356865-38356915	Caco-2	colon:	n/a
23	chr7:38370874-38370924	PFSK-1	brain:	n/a
24	chr7:38370988-38371038	K562	blood:	n/a
25	chr7:38370676-38370726	SK-N-SH	brain:	n/a
26	chr7:38356729-38356779	AG09319	gingival:	n/a
27	chr7:38361199-38361249	HNPCEpiC	eye:	n/a
28	chr7:38370874-38370924	HUVEC	blood vessel:	n/a
29	chr7:38356729-38356779	HNPCEpiC	eye:	n/a
30	chr7:38370988-38371038	SAEC	small airway:	n/a
31	chr7:38332633-38332683	SK-N-SH_RA	brain:	n/a
32	chr7:38356865-38356915	AG04449	skin:	fetal
33	chr7:38344983-38345033	HRCEpiC	kidney:	n/a
34	chr7:38370874-38370924	ECC-1	luminal epithelium:	n/a
35	chr7:38340103-38340153	T-47D	breast:	n/a
36	chr7:38350921-38350971	GM12891	blood:	n/a
37	chr7:38370874-38370924	SK-N-SH	brain:	n/a
38	chr7:38344934-38344984	K562	blood:	n/a
39	chr7:38370676-38370726	HUVEC	blood vessel:	n/a
40	chr7:38355100-38355150	IMR90	lung:	fetal
41	chr7:38351226-38351276	A549	lung:	n/a
42	chr7:38358683-38358733	AG09319	gingival:	n/a
43	chr7:38370988-38371038	Hela-S3	cervix:	n/a
44	chr7:38355100-38355150	HEEpiC	esophagus:	n/a
45	chr7:38370874-38370924	A549	lung:	n/a
46	chr7:38332633-38332683	ECC-1	luminal epithelium:	n/a
47	chr7:38370874-38370924	HRE	kidney:	n/a
48	chr7:38361199-38361249	PANC-1	pancreas:	n/a
49	chr7:38370988-38371038	HMEC	breast:	n/a
50	chr7:38351094-38351144	HCF	heart:	n/a

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

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

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

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

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
TRGJP1	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
TRGJP1	CpG island
TRGVA	CpG island
ENSG00000231916	CpG island
TRGV9	CpG island
ENSG00000182919	chromatin interactions
ENSG00000204472	chromatin interactions
ENSG00000226212	chromatin interactions
ENSG00000245146	chromatin interactions
ENSG00000249978	chromatin interactions
ENSG00000106993	chromatin interactions
ENSG00000228668	chromatin interactions
ENSG00000211696	chromatin interactions
ENSG00000211691	chromatin interactions
ENSG00000211693	chromatin interactions
ENSG00000272908	chromatin interactions
ENSG00000211695	chromatin interactions
ENSG00000185129	chromatin interactions
ENSG00000211698	chromatin interactions
ENSG00000211694	chromatin interactions
ENSG00000225992	chromatin interactions
ENSG00000231202	chromatin interactions
ENSG00000273061	chromatin interactions
ENSG00000231916	chromatin interactions
ENSG00000166012	chromatin interactions
PTEN	miRNA target sites

Extended variants
information (count: 2596 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2596 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7782269	chr7:38318590-38318591	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs575349218	chr7:38318614-38318615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs544045520	chr7:38318621-38318622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs7782311	chr7:38318664-38318665	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs376326162	chr7:38318669-38318670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559263753	chr7:38318719-38318720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150442885	chr7:38318783-38318784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs117563655	chr7:38318809-38318810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182187981	chr7:38318825-38318826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545644964	chr7:38318839-38318840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs67646873	chr7:38318842-38318843	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs35084352	chr7:38318891-38318892	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs186742204	chr7:38318914-38318915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs75451924	chr7:38318918-38318919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529844937	chr7:38318951-38318952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs75261872	chr7:38319004-38319005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190821224	chr7:38319067-38319068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552720961	chr7:38319096-38319097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538259571	chr7:38319153-38319154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552443450	chr7:38319190-38319191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs183330881	chr7:38319193-38319194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537631707	chr7:38319236-38319237	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs563642488	chr7:38319237-38319238	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs201685967	chr7:38319238-38319239	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs188548961	chr7:38319261-38319262	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs575799025	chr7:38319273-38319274	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs2240826	chr7:38319339-38319340	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs6973776	chr7:38319378-38319379	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs532261503	chr7:38319427-38319428	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs138282155	chr7:38319435-38319436	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs2240827	chr7:38319436-38319437	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs573146423	chr7:38319459-38319460	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs192906458	chr7:38319471-38319472	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs559299299	chr7:38319508-38319509	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs2240828	chr7:38319513-38319514	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs35539722	chr7:38319536-38319537	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs116484089	chr7:38319587-38319588	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs574358708	chr7:38319598-38319599	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs561431688	chr7:38319631-38319632	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs183102990	chr7:38319643-38319644	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs28469212	chr7:38319672-38319673	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs77798705	chr7:38319741-38319742	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs375445390	chr7:38319752-38319753	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs369171573	chr7:38319753-38319754	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs2240829	chr7:38319774-38319775	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs377265288	chr7:38319837-38319838	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs145851844	chr7:38319867-38319868	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs566409153	chr7:38319904-38319905	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs371166643	chr7:38319917-38319918	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs537718031	chr7:38319976-38319977	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Cancer	20164919	CNVD
Neuroblastoma	19536264	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1198 , 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	chr7:38317000-38321400	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr7:38317000-38322000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr7:38317200-38321600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr7:38317200-38321800	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr7:38317200-38322400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr7:38317600-38318600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr7:38317600-38321800	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr7:38318200-38323000	Weak transcription	Primary hematopoietic stem cells	blood
11	chr7:38318600-38319000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr7:38319000-38322200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr7:38320200-38323800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr7:38321000-38321800	Enhancers	Adipose Nuclei	Adipose
15	chr7:38321400-38323200	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr7:38321600-38325200	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr7:38321800-38323200	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr7:38321800-38324200	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr7:38322000-38325000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr7:38322200-38322600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr7:38322400-38325000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr7:38322600-38325200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr7:38323000-38324200	Enhancers	Fetal Thymus	thymus
24	chr7:38323000-38325000	Enhancers	Primary hematopoietic stem cells	blood
25	chr7:38323200-38323600	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr7:38323200-38323600	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr7:38323400-38324800	Enhancers	Fetal Heart	heart
28	chr7:38323400-38324800	Enhancers	GM12878-XiMat	blood
29	chr7:38323600-38324200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr7:38323600-38325200	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr7:38323600-38325400	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr7:38324000-38324400	Enhancers	Right Atrium	heart
33	chr7:38324000-38324600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr7:38324200-38324600	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr7:38324200-38324600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
36	chr7:38324400-38325400	Enhancers	Primary B cells from cord blood	blood
37	chr7:38324600-38324800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr7:38324600-38324800	Enhancers	Left Ventricle	heart
39	chr7:38324600-38325000	Enhancers	Primary T cells from cord blood	blood
40	chr7:38324600-38325400	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr7:38325200-38326600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr7:38325200-38328200	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr7:38325200-38334400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr7:38325400-38327800	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr7:38325400-38328000	Weak transcription	Monocytes-CD14+_RO01746	blood
46	chr7:38327800-38329000	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr7:38328000-38328600	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr7:38329600-38330800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr7:38329800-38351000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr7:38330800-38331000	Enhancers	K562	blood

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