Variant report

Variant	nsv824079
Chromosome Location	chr7:38385529-38395465
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	chr7:38388801-38389033	GM12878	blood:	n/a	n/a
3	BATF	chr7:38389336-38389771	GM12878	blood:	n/a	n/a
4	BATF	chr7:38393104-38393355	GM12878	blood:	n/a	n/a
5	BATF	chr7:38393728-38393936	GM12878	blood:	n/a	n/a
6	BATF	chr7:38388739-38389137	GM12878	blood:	n/a	n/a
7	BATF	chr7:38393104-38393312	GM12878	blood:	n/a	n/a
8	BCL11A	chr7:38393701-38393947	GM12878	blood:	n/a	n/a
9	BCLAF1	chr7:38385200-38385540	GM12878	blood:	n/a	n/a
10	BCLAF1	chr7:38389556-38389732	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:38389643-38389696	GM12878	blood:	n/a	n/a
12	BHLHE40	chr7:38393917-38394132	K562	blood:	n/a	n/a
13	CBX3	chr7:38393853-38394294	K562	blood:	n/a	n/a
14	CBX3	chr7:38389461-38389863	K562	blood:	n/a	n/a
15	CEBPB	chr7:38391385-38391451	IMR90	lung:	n/a	n/a
16	CHD1	chr7:38389454-38389506	GM12878	blood:	n/a	n/a
17	CTCF	chr7:38393980-38394130	BJ	skin:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
18	CTCF	chr7:38393980-38394130	HBMEC	blood vessel:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
19	CTCF	chr7:38393980-38394130	HPF	lung:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
20	CTCF	chr7:38389560-38389710	HCFaa	heart:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
21	CTCF	chr7:38389453-38389789	MCF-7	breast:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
22	CTCF	chr7:38389521-38389898	Gliobla	brain:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
23	CTCF	chr7:38385637-38385754	GM19238	blood:	n/a	n/a
24	CTCF	chr7:38394000-38394150	HAc	cerebellar:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
25	CTCF	chr7:38389586-38389815	NHEK	skin:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
26	CTCF	chr7:38393920-38394070	HFF	foreskin:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
27	CTCF	chr7:38393948-38394212	LNCaP	prostate:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
28	CTCF	chr7:38389580-38389730	GM12868	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
29	CTCF	chr7:38389560-38389710	HA-sp	spinal cord:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
30	CTCF	chr7:38389577-38389813	A549	lung:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
31	CTCF	chr7:38385029-38385651	A549	lung:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
32	CTCF	chr7:38389608-38389835	HepG2	liver:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
33	CTCF	chr7:38389549-38389567	GM20000	blood:	n/a	n/a
34	CTCF	chr7:38389594-38389779	MCF-7	breast:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
35	CTCF	chr7:38389466-38390000	GM19238	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
36	CTCF	chr7:38389560-38389710	HMF	breast:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
37	CTCF	chr7:38393855-38394198	GM13976	blood:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
38	CTCF	chr7:38393936-38394181	A549	lung:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
39	CTCF	chr7:38393916-38394199	IMR90	lung:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
40	CTCF	chr7:38385192-38385604	GM19238	blood:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
41	CTCF	chr7:38389431-38390041	K562	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
42	CTCF	chr7:38385620-38385770	HMF	breast:	n/a	n/a
43	CTCF	chr7:38389600-38389750	MCF-7	breast:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
44	CTCF	chr7:38393901-38394222	Gliobla	brain:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
45	CTCF	chr7:38389560-38389710	GM12865	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
46	CTCF	chr7:38394220-38394370	GM12874	blood:	n/a	n/a
47	CTCF	chr7:38393955-38394137	ECC-1	luminal epithelium:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
48	CTCF	chr7:38393912-38394199	MCF-7	breast:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
49	CTCF	chr7:38389560-38389710	HBMEC	blood vessel:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
50	CTCF	chr7:38394000-38394150	BE2_C	brain:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38389991-38390041	MCF-7	breast:	n/a
2	chr7:38389685-38389735	HUVEC	blood vessel:	n/a
3	chr7:38389659-38389709	SK-N-SH	brain:	n/a
4	chr7:38389685-38389735	HRPEpiC	eye:	n/a
5	chr7:38389991-38390041	SK-N-SH	brain:	n/a
6	chr7:38389991-38390041	IMR90	lung:	fetal
7	chr7:38389685-38389735	HCM	heart:	n/a
8	chr7:38389991-38390041	HEEpiC	esophagus:	n/a
9	chr7:38389991-38390041	HCPEpiC	choroid plexus:	n/a
10	chr7:38389991-38390041	ProgFib	skin:	n/a
11	chr7:38389659-38389709	AG04449	skin:	fetal
12	chr7:38389659-38389709	AG09309	skin:	n/a
13	chr7:38389685-38389735	AG09319	gingival:	n/a
14	chr7:38389659-38389709	HRE	kidney:	n/a
15	chr7:38389685-38389735	HPAEpiC	pulmonary alveolar:	n/a
16	chr7:38389685-38389735	K562	blood:	n/a
17	chr7:38389991-38390041	HL-60	blood:	n/a
18	chr7:38389659-38389709	GM12891	blood:	n/a
19	chr7:38389991-38390041	GM12891	blood:	n/a
20	chr7:38389991-38390041	Hepatocyte	liver:	n/a
21	chr7:38389991-38390041	GM12892	blood:	n/a
22	chr7:38389685-38389735	NT2-D1	testis:	n/a
23	chr7:38389685-38389735	U87	brain:	n/a
24	chr7:38389991-38390041	GM12878	blood:	n/a
25	chr7:38389659-38389709	HepG2	liver:	n/a
26	chr7:38389991-38390041	HepG2	liver:	n/a
27	chr7:38389685-38389735	HAEpiC	amniotic membrane:	n/a
28	chr7:38389659-38389709	CMK	blood:	n/a
29	chr7:38389991-38390041	NH-A	brain:	n/a
30	chr7:38389659-38389709	HCF	heart:	n/a
31	chr7:38389991-38390041	HRPEpiC	eye:	n/a
32	chr7:38389685-38389735	HRE	kidney:	n/a
33	chr7:38389685-38389735	NHBE	bronchial:	n/a
34	chr7:38389991-38390041	ECC-1	luminal epithelium:	n/a
35	chr7:38389991-38390041	HRCEpiC	kidney:	n/a
36	chr7:38389659-38389709	Hepatocyte	liver:	n/a
37	chr7:38389685-38389735	Caco-2	colon:	n/a
38	chr7:38389685-38389735	GM06990	blood:	n/a
39	chr7:38389659-38389709	K562	blood:	n/a
40	chr7:38389991-38390041	GM19239	blood:	n/a
41	chr7:38389659-38389709	GM06990	blood:	n/a
42	chr7:38389685-38389735	AG04450	lung:	fetal
43	chr7:38389685-38389735	SKMC	muscle:	n/a
44	chr7:38389991-38390041	AoSMC	blood vessel:	n/a
45	chr7:38389685-38389735	A549	lung:	n/a
46	chr7:38389991-38390041	RPTEC	kidney:	n/a
47	chr7:38389685-38389735	IMR90	lung:	fetal
48	chr7:38389991-38390041	HCM	heart:	n/a
49	chr7:38389991-38390041	SK-N-MC	brain:	n/a
50	chr7:38389659-38389709	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:38375070..38375771-chr7:38393808..38394547,2	MCF-7	breast:
2	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
3	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
4	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:
5	chr7:38146965..38147587-chr7:38385316..38385987,2	MCF-7	breast:
6	chr7:38378957..38381571-chr7:38387227..38389473,2	K562	blood:
7	chr7:38385094..38385817-chr7:38407469..38408173,2	MCF-7	breast:

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

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
ENSG00000228668	chromatin interactions
ENSG00000249978	chromatin interactions
ENSG00000226212	chromatin interactions
ENSG00000211697	chromatin interactions
ENSG00000211701	chromatin interactions
SERTAD3	miRNA target sites
RAB5A	miRNA target sites

Extended variants
information (count: 657 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:657 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111848856	chr7:38385534-38385535	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs369716119	chr7:38385542-38385543	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs548141122	chr7:38385546-38385547	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs146341763	chr7:38385553-38385554	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs376959604	chr7:38385556-38385557	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs117394082	chr7:38385558-38385559	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs200632841	chr7:38385594-38385595	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs76445820	chr7:38385602-38385603	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs60083729	chr7:38385612-38385613	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs73694032	chr7:38385624-38385625	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
11	rs183014559	chr7:38385645-38385646	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
12	rs113577386	chr7:38385654-38385655	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	mRNA abundance
13	rs534903070	chr7:38385663-38385664	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs558372553	chr7:38385694-38385695	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs118041532	chr7:38385712-38385713	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
16	rs550300547	chr7:38385713-38385714	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
17	rs375724910	chr7:38385747-38385748	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs528225798	chr7:38385748-38385749	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs116402297	chr7:38385754-38385755	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs60040858	chr7:38385755-38385756	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs61527547	chr7:38385822-38385823	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs57817940	chr7:38385828-38385829	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs188762637	chr7:38385842-38385843	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs145404441	chr7:38385845-38385846	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs397833658	chr7:38385861-38385862	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs13307718	chr7:38385883-38385884	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs538645106	chr7:38385933-38385934	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs2534587	chr7:38385938-38385939	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs57642344	chr7:38385940-38385941	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs542572004	chr7:38385941-38385942	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs565048427	chr7:38385987-38385988	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs530749322	chr7:38385997-38385998	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs2534588	chr7:38386006-38386007	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs192639207	chr7:38386197-38386198	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs570200816	chr7:38386212-38386213	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs529286182	chr7:38386224-38386225	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs367800633	chr7:38386266-38386267	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs78772946	chr7:38386274-38386275	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs566233433	chr7:38386276-38386277	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs535285175	chr7:38386277-38386278	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs558171510	chr7:38386281-38386282	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs7786580	chr7:38386296-38386297	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs182762829	chr7:38386316-38386317	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs35845111	chr7:38386358-38386359	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs398004446	chr7:38386361-38386362	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs573429430	chr7:38386367-38386368	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs35161308	chr7:38386370-38386371	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs112955705	chr7:38386385-38386386	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs542251779	chr7:38386395-38386396	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs552971285	chr7:38386440-38386441	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	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:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38381200-38389200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr7:38381400-38385600	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr7:38381400-38389200	Weak transcription	Fetal Stomach	stomach
4	chr7:38381400-38408000	Weak transcription	Right Atrium	heart
5	chr7:38381800-38388800	Weak transcription	Duodenum Mucosa	Duodenum
6	chr7:38382000-38385600	Weak transcription	Pancreas	Pancrea
7	chr7:38382000-38389200	Weak transcription	Fetal Intestine Small	intestine
8	chr7:38383600-38389000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr7:38383800-38386000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr7:38383800-38386200	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr7:38384000-38386000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
12	chr7:38384200-38385600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
13	chr7:38384200-38385600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr7:38384200-38385800	Enhancers	Primary B cells from cord blood	blood
15	chr7:38384200-38385800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr7:38384200-38385800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr7:38384200-38385800	Enhancers	GM12878-XiMat	blood
18	chr7:38384200-38386000	Enhancers	Primary B cells from peripheral blood	blood
19	chr7:38384200-38386000	Enhancers	Primary hematopoietic stem cells	blood
20	chr7:38384200-38386000	Enhancers	Primary T helper cells fromperipheralblood	blood
21	chr7:38384600-38385800	Flanking Active TSS	Fetal Thymus	thymus
22	chr7:38384800-38385800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr7:38384800-38385800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
24	chr7:38384800-38386200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr7:38384800-38386400	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr7:38384800-38390800	Active TSS	Thymus	Thymus
27	chr7:38385000-38385800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr7:38385000-38388800	Weak transcription	Spleen	Spleen
29	chr7:38385200-38385600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
30	chr7:38385200-38385600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr7:38385200-38385800	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr7:38385200-38386000	Enhancers	Primary T cells from cord blood	blood
33	chr7:38385200-38386200	Flanking Active TSS	Dnd41	blood
34	chr7:38385400-38385800	Enhancers	Adipose Nuclei	Adipose
35	chr7:38385400-38386000	Enhancers	Primary T helper naive cells from peripheral blood	blood
36	chr7:38385400-38386000	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr7:38385400-38386000	Enhancers	Brain Cingulate Gyrus	brain
38	chr7:38385400-38386000	Genic enhancers	K562	blood
39	chr7:38385600-38385800	Enhancers	Primary T cells fromperipheralblood	blood
40	chr7:38385600-38385800	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr7:38385600-38385800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
42	chr7:38385600-38385800	Enhancers	Pancreas	Pancrea
43	chr7:38385600-38386000	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr7:38385600-38389000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr7:38385800-38386200	Active TSS	Fetal Thymus	thymus
46	chr7:38385800-38386800	Weak transcription	Primary B cells from cord blood	blood
47	chr7:38385800-38386800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr7:38385800-38387000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr7:38385800-38387400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr7:38385800-38388800	Weak transcription	Primary T cells fromperipheralblood	blood

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