Variant report

Variant	nsv5707
Chromosome Location	chr7:38380984-38407182
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1577)
CpG islands
(count:366)
Chromatin interactive
region (count:12)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1577 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:38380924-38381236	K562	blood:	n/a	n/a
2	ATF1	chr7:38389490-38389669	K562	blood:	n/a	n/a
3	ATF1	chr7:38380742-38381291	K562	blood:	n/a	n/a
4	BATF	chr7:38406983-38407263	GM12878	blood:	n/a	n/a
5	BATF	chr7:38406981-38407278	GM12878	blood:	n/a	n/a
6	BATF	chr7:38389336-38389771	GM12878	blood:	n/a	n/a
7	BATF	chr7:38388801-38389033	GM12878	blood:	n/a	n/a
8	BATF	chr7:38388739-38389137	GM12878	blood:	n/a	n/a
9	BATF	chr7:38397936-38398227	GM12878	blood:	n/a	n/a
10	BATF	chr7:38385112-38385446	GM12878	blood:	n/a	n/a
11	BATF	chr7:38384447-38384746	GM12878	blood:	n/a	n/a
12	BATF	chr7:38393104-38393312	GM12878	blood:	n/a	n/a
13	BATF	chr7:38402249-38402527	GM12878	blood:	n/a	chr7:38402448-38402459
14	BATF	chr7:38398491-38398925	GM12878	blood:	n/a	n/a
15	BATF	chr7:38402244-38402635	GM12878	blood:	n/a	chr7:38402448-38402459
16	BATF	chr7:38397831-38398310	GM12878	blood:	n/a	n/a
17	BATF	chr7:38393104-38393355	GM12878	blood:	n/a	n/a
18	BATF	chr7:38393728-38393936	GM12878	blood:	n/a	n/a
19	BATF	chr7:38384403-38384723	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:38406978-38407187	GM12878	blood:	n/a	chr7:38407111-38407120
21	BCL11A	chr7:38397653-38398122	GM12878	blood:	n/a	chr7:38398022-38398031
22	BCL11A	chr7:38402227-38402452	GM12878	blood:	n/a	chr7:38402374-38402383
23	BCL11A	chr7:38393701-38393947	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:38384321-38384734	GM12878	blood:	n/a	chr7:38384540-38384549
25	BCL11A	chr7:38398493-38398682	GM12878	blood:	n/a	n/a
26	BCLAF1	chr7:38389556-38389732	GM12878	blood:	n/a	n/a
27	BCLAF1	chr7:38385200-38385540	GM12878	blood:	n/a	n/a
28	BHLHE40	chr7:38389643-38389696	GM12878	blood:	n/a	n/a
29	BHLHE40	chr7:38393917-38394132	K562	blood:	n/a	n/a
30	BHLHE40	chr7:38385297-38385497	GM12878	blood:	n/a	n/a
31	BHLHE40	chr7:38385332-38385486	K562	blood:	n/a	n/a
32	BHLHE40	chr7:38403131-38403176	GM12878	blood:	n/a	n/a
33	BHLHE40	chr7:38380767-38381281	K562	blood:	n/a	n/a
34	BHLHE40	chr7:38398804-38399002	K562	blood:	n/a	n/a
35	BHLHE40	chr7:38403094-38403268	K562	blood:	n/a	n/a
36	CBX3	chr7:38393853-38394294	K562	blood:	n/a	n/a
37	CBX3	chr7:38380820-38381270	K562	blood:	n/a	n/a
38	CBX3	chr7:38398578-38399039	K562	blood:	n/a	n/a
39	CBX3	chr7:38389461-38389863	K562	blood:	n/a	n/a
40	CBX3	chr7:38380733-38381387	K562	blood:	n/a	n/a
41	CBX3	chr7:38403002-38403403	K562	blood:	n/a	n/a
42	CCNT2	chr7:38380858-38381223	K562	blood:	n/a	n/a
43	CEBPB	chr7:38402455-38402609	HepG2	liver:	n/a	n/a
44	CEBPB	chr7:38400447-38400672	A549	lung:	n/a	n/a
45	CEBPB	chr7:38391385-38391451	IMR90	lung:	n/a	n/a
46	CEBPB	chr7:38380943-38381315	K562	blood:	n/a	n/a
47	CEBPD	chr7:38380772-38381308	K562	blood:	n/a	n/a
48	CHD1	chr7:38389454-38389506	GM12878	blood:	n/a	n/a
49	CHD1	chr7:38402581-38402583	GM12878	blood:	n/a	n/a
50	CHD2	chr7:38398814-38398836	GM12878	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38389991-38390041	BJ	skin:	n/a
2	chr7:38398839-38398889	U87	brain:	n/a
3	chr7:38389685-38389735	SK-N-SH	brain:	n/a
4	chr7:38398839-38398889	SK-N-SH_RA	brain:	n/a
5	chr7:38389991-38390041	HCM	heart:	n/a
6	chr7:38398839-38398889	GM12892	blood:	n/a
7	chr7:38403507-38403557	Caco-2	colon:	n/a
8	chr7:38389685-38389735	BE2_C	brain:	n/a
9	chr7:38389685-38389735	HNPCEpiC	eye:	n/a
10	chr7:38403507-38403557	GM12878	blood:	n/a
11	chr7:38398839-38398889	Jurkat	blood:	n/a
12	chr7:38398839-38398889	HCT-116	colon:	n/a
13	chr7:38389991-38390041	T-47D	breast:	n/a
14	chr7:38389991-38390041	SK-N-SH	brain:	n/a
15	chr7:38398836-38398886	NB4	blood:	n/a
16	chr7:38389659-38389709	HCF	heart:	n/a
17	chr7:38389685-38389735	Jurkat	blood:	n/a
18	chr7:38389659-38389709	T-47D	breast:	n/a
19	chr7:38398836-38398886	NHBE	bronchial:	n/a
20	chr7:38389659-38389709	SK-N-SH	brain:	n/a
21	chr7:38389685-38389735	HRE	kidney:	n/a
22	chr7:38403507-38403557	SKMC	muscle:	n/a
23	chr7:38403507-38403557	CMK	blood:	n/a
24	chr7:38403507-38403557	PrEC	prostate:	n/a
25	chr7:38389659-38389709	HRE	kidney:	n/a
26	chr7:38398839-38398889	Hela-S3	cervix:	n/a
27	chr7:38398836-38398886	CMK	blood:	n/a
28	chr7:38389991-38390041	GM19239	blood:	n/a
29	chr7:38403507-38403557	SK-N-SH_RA	brain:	n/a
30	chr7:38389991-38390041	HEK293	kidney:	embryo
31	chr7:38389991-38390041	Caco-2	colon:	n/a
32	chr7:38389991-38390041	AG04450	lung:	fetal
33	chr7:38398836-38398886	MCF10A-Er-Src	breast:	n/a
34	chr7:38389659-38389709	BE2_C	brain:	n/a
35	chr7:38389991-38390041	SK-N-SH_RA	brain:	n/a
36	chr7:38389685-38389735	Hela-S3	cervix:	n/a
37	chr7:38389659-38389709	PANC-1	pancreas:	n/a
38	chr7:38389659-38389709	SAEC	small airway:	n/a
39	chr7:38389991-38390041	ovcar-3	ovarian:	n/a
40	chr7:38389659-38389709	HPAEpiC	pulmonary alveolar:	n/a
41	chr7:38389659-38389709	PrEC	prostate:	n/a
42	chr7:38398839-38398889	A549	lung:	n/a
43	chr7:38389659-38389709	Jurkat	blood:	n/a
44	chr7:38389685-38389735	MCF-7	breast:	n/a
45	chr7:38389991-38390041	AG09309	skin:	n/a
46	chr7:38389991-38390041	GM12892	blood:	n/a
47	chr7:38389659-38389709	ProgFib	skin:	n/a
48	chr7:38389685-38389735	PANC-1	pancreas:	n/a
49	chr7:38389685-38389735	HCPEpiC	choroid plexus:	n/a
50	chr7:38403507-38403557	NHDF-neo	bronchial:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:38379860..38381671-chr7:38382000..38383618,2	K562	blood:
2	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:
3	chr7:38372590..38377698-chr7:38377994..38383669,12	K562	blood:
4	chr7:38268103..38269784-chr7:38382757..38385051,2	K562	blood:
5	chr7:38375070..38375771-chr7:38393808..38394547,2	MCF-7	breast:
6	chr7:38378957..38381571-chr7:38387227..38389473,2	K562	blood:
7	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
8	chr7:38369534..38372460-chr7:38378778..38381886,3	K562	blood:
9	chr7:38146965..38147587-chr7:38385316..38385987,2	MCF-7	breast:
10	chr7:38385094..38385817-chr7:38407469..38408173,2	MCF-7	breast:
11	chr7:38380741..38382401-chr7:38383649..38386131,2	K562	blood:
12	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STARD3NL-1	chr7:38381178-38381400	NONHSAT120179
2	lnc-STARD3NL-5	chr7:38404346-38404812	NONHSAT120184
3	lnc-STARD3NL-7	chr7:38405699-38406016	NONHSAT120186
4	lnc-AMPH-3	chr7:38395172-38395463	NONHSAT120181
5	lnc-STARD3NL-6	chr7:38405093-38405440	NONHSAT120185
6	lnc-STARD3NL-4	chr7:38400418-38400732	NONHSAT120183
7	lnc-STARD3NL-1	chr7:38381098-38381400	NONHSAT120178
8	lnc-STARD3NL-1	chr7:38385622-38385728	NONHSAT120179
9	lnc-STARD3NL-1	chr7:38381683-38384763	ucscGeneNc_uc003tgp_1
10	lnc-STARD3NL-1	chr7:38381216-38381400	ENSG00000250924
11	lnc-STARD3NL-3	chr7:38397521-38397735	NONHSAT120182
12	lnc-STARD3NL-1	chr7:38381747-38382154	NONHSAT120178
13	lnc-STARD3NL-1	chr7:38385622-38385728	ENSG00000250924
14	lnc-STARD3NL-1	chr7:38389947-38390051	ENSG00000250924
15	lnc-AMPH-4	chr7:38394799-38395026	NONHSAT120180
16	lnc-STARD3NL-1	chr7:38389947-38390051	NONHSAT120179

No data

Variant related genes	Relation type
TRGV5	TF binding region
TRGV6	TF binding region
TRGV4	TF binding region
TRGV3	TF binding region
TRGV2	TF binding region
TRGV5P	TF binding region
TRGV5	CpG island
TRGV6	CpG island
TRGV4	CpG island
TRGV3	CpG island
TRGV2	CpG island
TRGV5P	CpG island
ENSG00000226212	chromatin interactions
ENSG00000211697	chromatin interactions
ENSG00000211696	chromatin interactions
ENSG00000211701	chromatin interactions
ENSG00000228668	chromatin interactions
ENSG00000249978	chromatin interactions
CA13	miRNA target sites
RAB5A	miRNA target sites
SERTAD3	miRNA target sites

Extended variants
information (count: 1774 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1774 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535618284	chr7:38381003-38381004	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs374861834	chr7:38381080-38381081	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs150391595	chr7:38381081-38381082	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs113522558	chr7:38381117-38381118	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
5	rs73694030	chr7:38381152-38381153	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs1810381	chr7:38381179-38381180	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs375528443	chr7:38381180-38381181	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
8	rs370078194	chr7:38381203-38381204	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
9	rs374086369	chr7:38381250-38381251	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
10	rs2735148	chr7:38381265-38381266	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs563179658	chr7:38381290-38381291	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
12	rs531937333	chr7:38381313-38381314	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
13	rs548795080	chr7:38381345-38381346	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
14	rs562306939	chr7:38381359-38381360	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
15	rs527894129	chr7:38381428-38381429	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs201710775	chr7:38381433-38381434	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs570471729	chr7:38381437-38381438	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs57588347	chr7:38381439-38381440	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs78001223	chr7:38381451-38381452	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs76272040	chr7:38381452-38381453	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs1810380	chr7:38381456-38381457	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs1810379	chr7:38381475-38381476	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs561936528	chr7:38381476-38381477	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs569931824	chr7:38381541-38381542	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs2017031	chr7:38381543-38381544	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs555251765	chr7:38381563-38381564	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs565491793	chr7:38381570-38381571	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs534529996	chr7:38381574-38381575	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs371018815	chr7:38381588-38381589	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs2016974	chr7:38381593-38381594	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs564102870	chr7:38381603-38381604	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs577300461	chr7:38381619-38381620	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs191379318	chr7:38381627-38381628	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs183971727	chr7:38381644-38381645	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs532905018	chr7:38381663-38381664	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs556327684	chr7:38381666-38381667	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs367812778	chr7:38381685-38381686	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
38	rs2735147	chr7:38381693-38381694	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs57353813	chr7:38381701-38381702	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
40	rs542497609	chr7:38381702-38381703	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
41	rs375591305	chr7:38381706-38381707	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
42	rs386712319	chr7:38381713-38381714	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
43	rs117675066	chr7:38381728-38381729	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
44	rs187819535	chr7:38381750-38381751	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
45	rs193137151	chr7:38381752-38381753	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
46	rs550247793	chr7:38381765-38381766	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
47	rs570720380	chr7:38381804-38381805	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
48	rs145154823	chr7:38381809-38381810	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
49	rs532932620	chr7:38381817-38381818	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
50	rs548803944	chr7:38381822-38381823	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region lncRNA	4 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:746 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38376400-38381000	Weak transcription	Duodenum Mucosa	Duodenum
2	chr7:38379200-38381600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr7:38379600-38382000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr7:38379800-38381000	Enhancers	Primary T cells from cord blood	blood
5	chr7:38379800-38381000	Flanking Active TSS	K562	blood
6	chr7:38379800-38381200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr7:38379800-38381400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
8	chr7:38379800-38381400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr7:38379800-38381600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
10	chr7:38379800-38382000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr7:38379800-38382000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr7:38379800-38382000	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr7:38379800-38382000	Enhancers	Fetal Intestine Large	intestine
14	chr7:38379800-38382000	Enhancers	Fetal Intestine Small	intestine
15	chr7:38379800-38382000	Enhancers	Placenta	Placenta
16	chr7:38379800-38382200	Enhancers	Primary hematopoietic stem cells	blood
17	chr7:38380000-38381000	Enhancers	Fetal Lung	lung
18	chr7:38380000-38381200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr7:38380000-38381200	Enhancers	Spleen	Spleen
20	chr7:38380000-38381400	Enhancers	Fetal Stomach	stomach
21	chr7:38380000-38381600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
22	chr7:38380000-38382000	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr7:38380000-38382000	Enhancers	Primary T helper cells fromperipheralblood	blood
24	chr7:38380000-38382000	Enhancers	Pancreas	Pancrea
25	chr7:38380000-38382200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
26	chr7:38380200-38382000	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr7:38380400-38381000	Enhancers	A549	lung
28	chr7:38380400-38381200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr7:38380400-38381200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
30	chr7:38380400-38381400	Enhancers	Fetal Muscle Leg	muscle
31	chr7:38380400-38381800	Active TSS	Thymus	Thymus
32	chr7:38380400-38382000	Enhancers	GM12878-XiMat	blood
33	chr7:38380600-38381000	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr7:38380600-38381200	Enhancers	Fetal Muscle Trunk	muscle
35	chr7:38380600-38381400	Enhancers	Adipose Nuclei	Adipose
36	chr7:38380600-38381600	Enhancers	Primary B cells from cord blood	blood
37	chr7:38380600-38381800	Enhancers	Primary B cells from peripheral blood	blood
38	chr7:38380800-38381000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
39	chr7:38380800-38381000	Flanking Active TSS	Dnd41	blood
40	chr7:38380800-38381200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr7:38380800-38381200	Enhancers	Left Ventricle	heart
42	chr7:38380800-38381400	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr7:38380800-38381400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr7:38380800-38381400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr7:38380800-38381400	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr7:38380800-38381400	Enhancers	Muscle Satellite Cultured Cells	--
47	chr7:38380800-38381400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr7:38380800-38381400	Enhancers	Right Atrium	heart
49	chr7:38380800-38381800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr7:38380800-38382000	Enhancers	Primary T killer memory cells from peripheral blood	blood

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