Variant report

Variant	nsv824078
Chromosome Location	chr7:38382278-38395465
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:38389490-38389669	K562	blood:	n/a	n/a
2	BATF	chr7:38393104-38393312	GM12878	blood:	n/a	n/a
3	BATF	chr7:38393728-38393936	GM12878	blood:	n/a	n/a
4	BATF	chr7:38384403-38384723	GM12878	blood:	n/a	n/a
5	BATF	chr7:38388801-38389033	GM12878	blood:	n/a	n/a
6	BATF	chr7:38393104-38393355	GM12878	blood:	n/a	n/a
7	BATF	chr7:38384447-38384746	GM12878	blood:	n/a	n/a
8	BATF	chr7:38388739-38389137	GM12878	blood:	n/a	n/a
9	BATF	chr7:38389336-38389771	GM12878	blood:	n/a	n/a
10	BATF	chr7:38385112-38385446	GM12878	blood:	n/a	n/a
11	BCL11A	chr7:38393701-38393947	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:38384321-38384734	GM12878	blood:	n/a	chr7:38384540-38384549
13	BCLAF1	chr7:38389556-38389732	GM12878	blood:	n/a	n/a
14	BCLAF1	chr7:38385200-38385540	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:38393917-38394132	K562	blood:	n/a	n/a
16	BHLHE40	chr7:38385297-38385497	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:38385332-38385486	K562	blood:	n/a	n/a
18	BHLHE40	chr7:38389643-38389696	GM12878	blood:	n/a	n/a
19	CBX3	chr7:38389461-38389863	K562	blood:	n/a	n/a
20	CBX3	chr7:38393853-38394294	K562	blood:	n/a	n/a
21	CEBPB	chr7:38391385-38391451	IMR90	lung:	n/a	n/a
22	CHD1	chr7:38389454-38389506	GM12878	blood:	n/a	n/a
23	CHD2	chr7:38385235-38385424	GM12878	blood:	n/a	n/a
24	CTCF	chr7:38385019-38385641	K562	blood:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
25	CTCF	chr7:38385220-38385370	A549	lung:	n/a	n/a
26	CTCF	chr7:38389560-38389710	AG09309	skin:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
27	CTCF	chr7:38385220-38385533	GM12891	blood:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
28	CTCF	chr7:38389560-38389710	HRPEpiC	eye:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
29	CTCF	chr7:38389593-38389809	LNCaP	prostate:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
30	CTCF	chr7:38385380-38385530	HCM	heart:	n/a	n/a
31	CTCF	chr7:38394000-38394150	GM12874	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
32	CTCF	chr7:38385202-38385542	Spleen_OC	spleen:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
33	CTCF	chr7:38394000-38394150	GM12866	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
34	CTCF	chr7:38394220-38394370	GM12874	blood:	n/a	n/a
35	CTCF	chr7:38385400-38385550	HFF	foreskin:	n/a	n/a
36	CTCF	chr7:38389560-38389710	GM12878	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
37	CTCF	chr7:38385000-38385150	AG04450	lung:	n/a	n/a
38	CTCF	chr7:38389560-38389710	HRE	kidney:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
39	CTCF	chr7:38385320-38385470	HEEpiC	esophagus:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
40	CTCF	chr7:38389586-38389815	NHEK	skin:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
41	CTCF	chr7:38385102-38385512	HepG2	liver:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
42	CTCF	chr7:38385664-38385683	GM12878	blood:	n/a	n/a
43	CTCF	chr7:38394000-38394150	MCF-7	breast:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
44	CTCF	chr7:38389560-38389710	HCFaa	heart:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
45	CTCF	chr7:38394000-38394150	AG04450	lung:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
46	CTCF	chr7:38393880-38394030	GM06990	blood:	n/a	n/a
47	CTCF	chr7:38393960-38394110	GM12867	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
48	CTCF	chr7:38393855-38394198	GM13976	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
49	CTCF	chr7:38385560-38385710	AG09319	gingival:	n/a	n/a
50	CTCF	chr7:38389560-38389710	AG09319	gingival:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38389685-38389735	CMK	blood:	n/a
2	chr7:38389685-38389735	CMK	blood:	n/a
3	chr7:38389685-38389735	RPTEC	kidney:	n/a
4	chr7:38389685-38389735	NHDF-neo	bronchial:	n/a
5	chr7:38389659-38389709	AoSMC	blood vessel:	n/a
6	chr7:38389659-38389709	HCPEpiC	choroid plexus:	n/a
7	chr7:38389685-38389735	AG04449	skin:	fetal
8	chr7:38389991-38390041	RPTEC	kidney:	n/a
9	chr7:38389659-38389709	HUVEC	blood vessel:	n/a
10	chr7:38389685-38389735	HEEpiC	esophagus:	n/a
11	chr7:38389659-38389709	HRPEpiC	eye:	n/a
12	chr7:38389685-38389735	NHBE	bronchial:	n/a
13	chr7:38389991-38390041	Hepatocyte	liver:	n/a
14	chr7:38389685-38389735	HL-60	blood:	n/a
15	chr7:38389991-38390041	AG09309	skin:	n/a
16	chr7:38389685-38389735	U87	brain:	n/a
17	chr7:38389685-38389735	Jurkat	blood:	n/a
18	chr7:38389659-38389709	NHDF-neo	bronchial:	n/a
19	chr7:38389991-38390041	PrEC	prostate:	n/a
20	chr7:38389685-38389735	GM12892	blood:	n/a
21	chr7:38389685-38389735	HIPEpiC	eye:	n/a
22	chr7:38389991-38390041	AoSMC	blood vessel:	n/a
23	chr7:38389685-38389735	SAEC	small airway:	n/a
24	chr7:38389685-38389735	ovcar-3	ovarian:	n/a
25	chr7:38389991-38390041	GM12891	blood:	n/a
26	chr7:38389991-38390041	BE2_C	brain:	n/a
27	chr7:38389685-38389735	MCF10A-Er-Src	breast:	n/a
28	chr7:38389659-38389709	AG04449	skin:	fetal
29	chr7:38389685-38389735	SK-N-MC	brain:	n/a
30	chr7:38389685-38389735	HCM	heart:	n/a
31	chr7:38389659-38389709	NT2-D1	testis:	n/a
32	chr7:38389685-38389735	GM19239	blood:	n/a
33	chr7:38389685-38389735	PFSK-1	brain:	n/a
34	chr7:38389685-38389735	AG09309	skin:	n/a
35	chr7:38389659-38389709	HRE	kidney:	n/a
36	chr7:38389659-38389709	NHBE	bronchial:	n/a
37	chr7:38389991-38390041	CMK	blood:	n/a
38	chr7:38389685-38389735	ProgFib	skin:	n/a
39	chr7:38389991-38390041	SKMC	muscle:	n/a
40	chr7:38389659-38389709	MCF-7	breast:	n/a
41	chr7:38389659-38389709	BJ	skin:	n/a
42	chr7:38389991-38390041	GM19239	blood:	n/a
43	chr7:38389659-38389709	HEEpiC	esophagus:	n/a
44	chr7:38389685-38389735	IMR90	lung:	fetal
45	chr7:38389659-38389709	IMR90	lung:	fetal
46	chr7:38389685-38389735	Caco-2	colon:	n/a
47	chr7:38389991-38390041	K562	blood:	n/a
48	chr7:38389991-38390041	PANC-1	pancreas:	n/a
49	chr7:38389685-38389735	T-47D	breast:	n/a
50	chr7:38389991-38390041	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
2	chr7:38385094..38385817-chr7:38407469..38408173,2	MCF-7	breast:
3	chr7:38146965..38147587-chr7:38385316..38385987,2	MCF-7	breast:
4	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
5	chr7:38379860..38381671-chr7:38382000..38383618,2	K562	blood:
6	chr7:38380741..38382401-chr7:38383649..38386131,2	K562	blood:
7	chr7:38375070..38375771-chr7:38393808..38394547,2	MCF-7	breast:
8	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:
9	chr7:38378957..38381571-chr7:38387227..38389473,2	K562	blood:
10	chr7:38268103..38269784-chr7:38382757..38385051,2	K562	blood:
11	chr7:38372590..38377698-chr7:38377994..38383669,12	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STARD3NL-1	chr7:38381683-38384763	ucscGeneNc_uc003tgp_1
2	lnc-AMPH-3	chr7:38395172-38395463	NONHSAT120181
3	lnc-STARD3NL-1	chr7:38385622-38385728	NONHSAT120179
4	lnc-STARD3NL-1	chr7:38389947-38390051	ENSG00000250924
5	lnc-AMPH-4	chr7:38394799-38395026	NONHSAT120180
6	lnc-STARD3NL-1	chr7:38385622-38385728	ENSG00000250924
7	lnc-STARD3NL-1	chr7:38389947-38390051	NONHSAT120179

Variant related genes	Relation type
TRGV5	TF binding region
TRGV6	TF binding region
TRGV4	TF binding region
TRGV5P	TF binding region
TRGV5	CpG island
TRGV6	CpG island
TRGV4	CpG island
TRGV5P	CpG island
ENSG00000226212	chromatin interactions
ENSG00000211701	chromatin interactions
ENSG00000228668	chromatin interactions
ENSG00000211697	chromatin interactions
ENSG00000249978	chromatin interactions
RAB5A	miRNA target sites
SERTAD3	miRNA target sites

Extended variants
information (count: 911 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:911 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35574637	chr7:38382308-38382309	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
2	rs113688867	chr7:38382333-38382334	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs111309640	chr7:38382340-38382341	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
4	rs386712320	chr7:38382354-38382355	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs2975077	chr7:38382362-38382363	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs367985184	chr7:38382390-38382391	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs537251399	chr7:38382414-38382415	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs562101193	chr7:38382431-38382432	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs2975076	chr7:38382462-38382463	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs112582934	chr7:38382473-38382474	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs570200667	chr7:38382480-38382481	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs535829933	chr7:38382494-38382495	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs544670800	chr7:38382507-38382508	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs2975075	chr7:38382511-38382512	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs533479028	chr7:38382541-38382542	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs7802567	chr7:38382571-38382572	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs57765971	chr7:38382575-38382576	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs10227973	chr7:38382584-38382585	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs57410959	chr7:38382593-38382594	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs200917978	chr7:38382594-38382595	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs536255893	chr7:38382600-38382601	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs573429292	chr7:38382640-38382641	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs533818910	chr7:38382644-38382645	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs35116207	chr7:38382655-38382656	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs558962801	chr7:38382656-38382657	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs79966836	chr7:38382674-38382675	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs186773087	chr7:38382678-38382679	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs191608482	chr7:38382698-38382699	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs565204273	chr7:38382714-38382715	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs530605599	chr7:38382715-38382716	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs550782371	chr7:38382749-38382750	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs370376900	chr7:38382750-38382751	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
33	rs570162121	chr7:38382792-38382793	Weak transcription Active TSS Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
34	rs373698702	chr7:38382794-38382795	Weak transcription Active TSS Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
35	rs183169046	chr7:38382802-38382803	Weak transcription Active TSS Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
36	rs376807194	chr7:38382817-38382818	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs566033998	chr7:38382852-38382853	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs568029868	chr7:38382853-38382854	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs535039524	chr7:38382862-38382863	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs2975074	chr7:38382873-38382874	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs187133486	chr7:38382911-38382912	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs2215372	chr7:38382923-38382924	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs147427926	chr7:38382929-38382930	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs573390542	chr7:38382947-38382948	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs2975073	chr7:38382958-38382959	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs2975072	chr7:38382965-38382966	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs2975071	chr7:38382990-38382991	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs6974606	chr7:38382991-38382992	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs2975070	chr7:38383000-38383001	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs35486746	chr7:38383022-38383023	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:82)

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
lymphocytic leukemia	21291569	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
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38380800-38382600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr7:38381000-38383800	Active TSS	K562	blood
3	chr7:38381200-38384200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr7:38381200-38384600	Weak transcription	Spleen	Spleen
5	chr7:38381200-38389200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr7:38381400-38384200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr7:38381400-38384800	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr7:38381400-38385000	Weak transcription	Fetal Muscle Leg	muscle
9	chr7:38381400-38385400	Weak transcription	Adipose Nuclei	Adipose
10	chr7:38381400-38385600	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr7:38381400-38389200	Weak transcription	Fetal Stomach	stomach
12	chr7:38381400-38408000	Weak transcription	Right Atrium	heart
13	chr7:38381600-38384200	Weak transcription	Primary B cells from cord blood	blood
14	chr7:38381600-38384800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr7:38381800-38384000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr7:38381800-38384200	Weak transcription	Primary B cells from peripheral blood	blood
17	chr7:38381800-38388800	Weak transcription	Duodenum Mucosa	Duodenum
18	chr7:38382000-38383200	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr7:38382000-38383600	Active TSS	Primary T cells fromperipheralblood	blood
20	chr7:38382000-38383600	Weak transcription	Dnd41	blood
21	chr7:38382000-38383800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr7:38382000-38384200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr7:38382000-38384200	Weak transcription	Primary T helper cells fromperipheralblood	blood
24	chr7:38382000-38384200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr7:38382000-38384200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr7:38382000-38384200	Weak transcription	GM12878-XiMat	blood
27	chr7:38382000-38384600	Weak transcription	Placenta	Placenta
28	chr7:38382000-38384600	Enhancers	Fetal Thymus	thymus
29	chr7:38382000-38384800	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr7:38382000-38384800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr7:38382000-38384800	Weak transcription	Thymus	Thymus
32	chr7:38382000-38385200	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr7:38382000-38385600	Weak transcription	Pancreas	Pancrea
34	chr7:38382000-38389200	Weak transcription	Fetal Intestine Small	intestine
35	chr7:38382200-38382400	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr7:38382200-38383600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr7:38382200-38384000	Weak transcription	Primary T cells from cord blood	blood
38	chr7:38382200-38384000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr7:38382200-38384200	Weak transcription	Primary hematopoietic stem cells	blood
40	chr7:38382400-38382600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
41	chr7:38382600-38383200	Active TSS	Primary T helper naive cells from peripheral blood	blood
42	chr7:38382600-38385200	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr7:38383200-38383400	Enhancers	Primary T helper cells PMA-I stimulated	--
44	chr7:38383200-38384200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr7:38383400-38383800	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr7:38383600-38384000	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr7:38383600-38385200	Enhancers	Dnd41	blood
48	chr7:38383600-38389000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr7:38383800-38384200	Enhancers	K562	blood
50	chr7:38383800-38386000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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