Variant report

Variant	nsv1020630
Chromosome Location	chr7:38384841-38415389
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1981)
CpG islands
(count:488)
Chromatin interactive
region (count:12)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1981 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:38414156-38414377	K562	blood:	n/a	n/a
2	ATF1	chr7:38389490-38389669	K562	blood:	n/a	n/a
3	ATF2	chr7:38409406-38409844	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:38409481-38409625	K562	blood:	n/a	n/a
5	BATF	chr7:38393104-38393312	GM12878	blood:	n/a	n/a
6	BATF	chr7:38397831-38398310	GM12878	blood:	n/a	n/a
7	BATF	chr7:38397936-38398227	GM12878	blood:	n/a	n/a
8	BATF	chr7:38414007-38414347	GM12878	blood:	n/a	n/a
9	BATF	chr7:38385112-38385446	GM12878	blood:	n/a	n/a
10	BATF	chr7:38402244-38402635	GM12878	blood:	n/a	chr7:38402448-38402459
11	BATF	chr7:38388739-38389137	GM12878	blood:	n/a	n/a
12	BATF	chr7:38389336-38389771	GM12878	blood:	n/a	n/a
13	BATF	chr7:38393728-38393936	GM12878	blood:	n/a	n/a
14	BATF	chr7:38406981-38407278	GM12878	blood:	n/a	n/a
15	BATF	chr7:38388801-38389033	GM12878	blood:	n/a	n/a
16	BATF	chr7:38398491-38398925	GM12878	blood:	n/a	n/a
17	BATF	chr7:38406983-38407263	GM12878	blood:	n/a	n/a
18	BATF	chr7:38407600-38408059	GM12878	blood:	n/a	n/a
19	BATF	chr7:38402249-38402527	GM12878	blood:	n/a	chr7:38402448-38402459
20	BATF	chr7:38393104-38393355	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:38402227-38402452	GM12878	blood:	n/a	chr7:38402374-38402383
22	BCL11A	chr7:38407578-38407819	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:38398493-38398682	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:38393701-38393947	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:38406978-38407187	GM12878	blood:	n/a	chr7:38407111-38407120
26	BCL11A	chr7:38397653-38398122	GM12878	blood:	n/a	chr7:38398022-38398031
27	BCLAF1	chr7:38407679-38408065	GM12878	blood:	n/a	n/a
28	BCLAF1	chr7:38385200-38385540	GM12878	blood:	n/a	n/a
29	BCLAF1	chr7:38389556-38389732	GM12878	blood:	n/a	n/a
30	BHLHE40	chr7:38407782-38408093	GM12878	blood:	n/a	n/a
31	BHLHE40	chr7:38409415-38409953	GM12878	blood:	n/a	n/a
32	BHLHE40	chr7:38393917-38394132	K562	blood:	n/a	n/a
33	BHLHE40	chr7:38403094-38403268	K562	blood:	n/a	n/a
34	BHLHE40	chr7:38389643-38389696	GM12878	blood:	n/a	n/a
35	BHLHE40	chr7:38385332-38385486	K562	blood:	n/a	n/a
36	BHLHE40	chr7:38385297-38385497	GM12878	blood:	n/a	n/a
37	BHLHE40	chr7:38409540-38409919	HepG2	liver:	n/a	n/a
38	BHLHE40	chr7:38403131-38403176	GM12878	blood:	n/a	n/a
39	BHLHE40	chr7:38398804-38399002	K562	blood:	n/a	n/a
40	BHLHE40	chr7:38407780-38408107	K562	blood:	n/a	n/a
41	BHLHE40	chr7:38409538-38409840	K562	blood:	n/a	n/a
42	BRCA1	chr7:38408981-38409171	Hela-S3	cervix:	n/a	n/a
43	CBX3	chr7:38398578-38399039	K562	blood:	n/a	n/a
44	CBX3	chr7:38393853-38394294	K562	blood:	n/a	n/a
45	CBX3	chr7:38403002-38403403	K562	blood:	n/a	n/a
46	CBX3	chr7:38407677-38408137	K562	blood:	n/a	n/a
47	CBX3	chr7:38389461-38389863	K562	blood:	n/a	n/a
48	CBX3	chr7:38407763-38408208	HCT-116	colon:	n/a	n/a
49	CBX3	chr7:38409444-38409763	K562	blood:	n/a	n/a
50	CEBPB	chr7:38400447-38400672	A549	lung:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38398839-38398889	HRCEpiC	kidney:	n/a
2	chr7:38398836-38398886	AG04449	skin:	fetal
3	chr7:38398836-38398886	NB4	blood:	n/a
4	chr7:38389659-38389709	SK-N-SH	brain:	n/a
5	chr7:38398836-38398886	AG10803	skin:	n/a
6	chr7:38389685-38389735	HCM	heart:	n/a
7	chr7:38389991-38390041	HMEC	breast:	n/a
8	chr7:38389991-38390041	AoSMC	blood vessel:	n/a
9	chr7:38389659-38389709	RPTEC	kidney:	n/a
10	chr7:38403507-38403557	HEEpiC	esophagus:	n/a
11	chr7:38403507-38403557	T-47D	breast:	n/a
12	chr7:38408106-38408156	MCF10A-Er-Src	breast:	n/a
13	chr7:38403507-38403557	ProgFib	skin:	n/a
14	chr7:38409725-38409775	A549	lung:	n/a
15	chr7:38398836-38398886	K562	blood:	n/a
16	chr7:38389685-38389735	Jurkat	blood:	n/a
17	chr7:38409725-38409775	Hepatocyte	liver:	n/a
18	chr7:38398836-38398886	SK-N-MC	brain:	n/a
19	chr7:38408106-38408156	PANC-1	pancreas:	n/a
20	chr7:38398839-38398889	NHDF-neo	bronchial:	n/a
21	chr7:38398839-38398889	AG09319	gingival:	n/a
22	chr7:38408106-38408156	MCF-7	breast:	n/a
23	chr7:38409725-38409775	ovcar-3	ovarian:	n/a
24	chr7:38398836-38398886	RPTEC	kidney:	n/a
25	chr7:38389685-38389735	NT2-D1	testis:	n/a
26	chr7:38398836-38398886	PFSK-1	brain:	n/a
27	chr7:38398839-38398889	HCF	heart:	n/a
28	chr7:38408106-38408156	HMEC	breast:	n/a
29	chr7:38403507-38403557	NB4	blood:	n/a
30	chr7:38389685-38389735	HMEC	breast:	n/a
31	chr7:38398839-38398889	HMEC	breast:	n/a
32	chr7:38398839-38398889	HRPEpiC	eye:	n/a
33	chr7:38389685-38389735	CMK	blood:	n/a
34	chr7:38403507-38403557	HUVEC	blood vessel:	n/a
35	chr7:38408106-38408156	IMR90	lung:	fetal
36	chr7:38398836-38398886	HCF	heart:	n/a
37	chr7:38403507-38403557	GM12892	blood:	n/a
38	chr7:38389659-38389709	NT2-D1	testis:	n/a
39	chr7:38409725-38409775	NB4	blood:	n/a
40	chr7:38408106-38408156	HCF	heart:	n/a
41	chr7:38389685-38389735	ovcar-3	ovarian:	n/a
42	chr7:38408106-38408156	HCT-116	colon:	n/a
43	chr7:38389991-38390041	HEEpiC	esophagus:	n/a
44	chr7:38403507-38403557	HAEpiC	amniotic membrane:	n/a
45	chr7:38389659-38389709	AG10803	skin:	n/a
46	chr7:38389991-38390041	ProgFib	skin:	n/a
47	chr7:38389685-38389735	Hepatocyte	liver:	n/a
48	chr7:38389685-38389735	HCF	heart:	n/a
49	chr7:38408106-38408156	H1-hESC	embryonic stem cell:	embryo
50	chr7:38389991-38390041	SK-N-SH	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:38146965..38147587-chr7:38385316..38385987,2	MCF-7	breast:
2	chr7:38268103..38269784-chr7:38382757..38385051,2	K562	blood:
3	chr7:38385094..38385817-chr7:38407469..38408173,2	MCF-7	breast:
4	chr7:38385094..38385817-chr7:38407469..38408173,2	MCF-7	breast:
5	chr7:38409691..38411244-chr7:38417623..38419459,2	K562	blood:
6	chr7:38415288..38417406-chr7:38417942..38420287,3	K562	blood:
7	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
8	chr7:38378957..38381571-chr7:38387227..38389473,2	K562	blood:
9	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
10	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:
11	chr7:38375070..38375771-chr7:38393808..38394547,2	MCF-7	breast:
12	chr7:38413282..38415935-chr7:38416823..38418449,3	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMPH-1	chr7:38407614-38407746	XLOC_006412
2	lnc-STARD3NL-1	chr7:38415158-38418238	ENSG00000250924
3	lnc-STARD3NL-6	chr7:38405093-38405440	NONHSAT120185
4	lnc-STARD3NL-5	chr7:38404346-38404812	NONHSAT120184
5	lnc-AMPH-4	chr7:38394799-38395026	NONHSAT120180
6	lnc-STARD3NL-1	chr7:38385622-38385728	NONHSAT120179
7	lnc-STARD3NL-3	chr7:38397521-38397735	NONHSAT120182
8	lnc-STARD3NL-1	chr7:38385622-38385728	ENSG00000250924
9	lnc-STARD3NL-1	chr7:38389947-38390051	NONHSAT120179
10	lnc-STARD3NL-1	chr7:38389947-38390051	ENSG00000250924
11	lnc-AMPH-1	chr7:38407246-38407494	XLOC_006412
12	lnc-STARD3NL-4	chr7:38400418-38400732	NONHSAT120183
13	lnc-STARD3NL-7	chr7:38405699-38406016	NONHSAT120186
14	lnc-AMPH-3	chr7:38395172-38395463	NONHSAT120181
15	lnc-STARD3NL-1	chr7:38415158-38418238	NONHSAT120179

No data

Variant related genes	Relation type
TRGV2	TF binding region
TRGV5	TF binding region
TRGV1	TF binding region
TRGV6	TF binding region
TRGV4	TF binding region
TRGV3	TF binding region
TRGV5P	TF binding region
TRGV2	CpG island
TRGV5	CpG island
TRGV1	CpG island
TRGV6	CpG island
TRGV4	CpG island
TRGV3	CpG island
TRGV5P	CpG island
ENSG00000211701	chromatin interactions
ENSG00000228668	chromatin interactions
ENSG00000211697	chromatin interactions
ENSG00000226212	chromatin interactions
ENSG00000249978	chromatin interactions
FAM120C	miRNA target sites
RAB5A	miRNA target sites
SERTAD3	miRNA target sites

Extended variants
information (count: 1822 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1822 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12532845	chr7:38384841-38384842	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs527439048	chr7:38384889-38384890	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs77157249	chr7:38384908-38384909	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs207467792	chr7:38384915-38384916	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs113129415	chr7:38384916-38384917	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs570308503	chr7:38384931-38384932	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs532967866	chr7:38384935-38384936	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs17853440	chr7:38384938-38384939	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs28527485	chr7:38384952-38384953	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs549632581	chr7:38384954-38384955	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs569650347	chr7:38384959-38384960	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs74542140	chr7:38385007-38385008	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
13	rs555190351	chr7:38385016-38385017	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs568206895	chr7:38385018-38385019	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs13307324	chr7:38385051-38385052	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs533995470	chr7:38385053-38385054	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs13307653	chr7:38385063-38385064	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs554241747	chr7:38385067-38385068	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs577135789	chr7:38385083-38385084	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs13307431	chr7:38385084-38385085	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs13307355	chr7:38385085-38385086	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs13307701	chr7:38385092-38385093	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs536331034	chr7:38385097-38385098	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs556877591	chr7:38385102-38385103	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs13307706	chr7:38385109-38385110	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs13307707	chr7:38385112-38385113	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs13307440	chr7:38385130-38385131	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs576834448	chr7:38385134-38385135	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs13307331	chr7:38385143-38385144	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs190822284	chr7:38385145-38385146	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs13307714	chr7:38385149-38385150	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs540743904	chr7:38385150-38385151	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs111885782	chr7:38385158-38385159	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs13307372	chr7:38385162-38385163	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs13307717	chr7:38385173-38385174	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs532775824	chr7:38385175-38385176	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs549393569	chr7:38385198-38385199	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs200779905	chr7:38385227-38385228	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs529191665	chr7:38385245-38385246	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs548874130	chr7:38385247-38385248	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs62445003	chr7:38385255-38385256	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs62445004	chr7:38385260-38385261	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	mRNA abundance
43	rs139625300	chr7:38385266-38385267	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs375994707	chr7:38385307-38385308	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs386712321	chr7:38385336-38385337	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs368435694	chr7:38385337-38385338	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs111530608	chr7:38385364-38385365	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs148285231	chr7:38385384-38385385	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs577467672	chr7:38385401-38385402	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs371743546	chr7:38385415-38385416	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	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:882 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38381200-38389200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr7:38381400-38385000	Weak transcription	Fetal Muscle Leg	muscle
3	chr7:38381400-38385400	Weak transcription	Adipose Nuclei	Adipose
4	chr7:38381400-38385600	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr7:38381400-38389200	Weak transcription	Fetal Stomach	stomach
6	chr7:38381400-38408000	Weak transcription	Right Atrium	heart
7	chr7:38381800-38388800	Weak transcription	Duodenum Mucosa	Duodenum
8	chr7:38382000-38385200	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr7:38382000-38385600	Weak transcription	Pancreas	Pancrea
10	chr7:38382000-38389200	Weak transcription	Fetal Intestine Small	intestine
11	chr7:38382600-38385200	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr7:38383600-38385200	Enhancers	Dnd41	blood
13	chr7:38383600-38389000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:38383800-38386000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr7:38383800-38386200	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr7:38384000-38385200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
17	chr7:38384000-38386000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr7:38384200-38385000	Enhancers	Primary T killer memory cells from peripheral blood	blood
19	chr7:38384200-38385600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
20	chr7:38384200-38385600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chr7:38384200-38385800	Enhancers	Primary B cells from cord blood	blood
22	chr7:38384200-38385800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
23	chr7:38384200-38385800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr7:38384200-38385800	Enhancers	GM12878-XiMat	blood
25	chr7:38384200-38386000	Enhancers	Primary B cells from peripheral blood	blood
26	chr7:38384200-38386000	Enhancers	Primary hematopoietic stem cells	blood
27	chr7:38384200-38386000	Enhancers	Primary T helper cells fromperipheralblood	blood
28	chr7:38384400-38385200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr7:38384400-38385400	Enhancers	K562	blood
30	chr7:38384600-38385000	Enhancers	Placenta	Placenta
31	chr7:38384600-38385000	Enhancers	Spleen	Spleen
32	chr7:38384600-38385800	Flanking Active TSS	Fetal Thymus	thymus
33	chr7:38384800-38385000	Enhancers	Primary T cells from cord blood	blood
34	chr7:38384800-38385400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
35	chr7:38384800-38385800	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr7:38384800-38385800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
37	chr7:38384800-38386200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr7:38384800-38386400	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr7:38384800-38390800	Active TSS	Thymus	Thymus
40	chr7:38385000-38385200	Flanking Active TSS	Primary T cells from cord blood	blood
41	chr7:38385000-38385400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
42	chr7:38385000-38385400	Enhancers	Fetal Muscle Leg	muscle
43	chr7:38385000-38385800	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr7:38385000-38388800	Weak transcription	Spleen	Spleen
45	chr7:38385200-38385600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
46	chr7:38385200-38385600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr7:38385200-38385800	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr7:38385200-38386000	Enhancers	Primary T cells from cord blood	blood
49	chr7:38385200-38386200	Flanking Active TSS	Dnd41	blood
50	chr7:38385400-38385800	Enhancers	Adipose Nuclei	Adipose

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