Variant report

Variant	esv1801754
Chromosome Location	chr7:38383309-38411786
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1810)
CpG islands
(count:489)
Chromatin interactive
region (count:12)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1810 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

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	ATF2	chr7:38409406-38409844	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:38409481-38409625	K562	blood:	n/a	n/a
4	BATF	chr7:38389336-38389771	GM12878	blood:	n/a	n/a
5	BATF	chr7:38393104-38393312	GM12878	blood:	n/a	n/a
6	BATF	chr7:38388801-38389033	GM12878	blood:	n/a	n/a
7	BATF	chr7:38385112-38385446	GM12878	blood:	n/a	n/a
8	BATF	chr7:38398491-38398925	GM12878	blood:	n/a	n/a
9	BATF	chr7:38393728-38393936	GM12878	blood:	n/a	n/a
10	BATF	chr7:38388739-38389137	GM12878	blood:	n/a	n/a
11	BATF	chr7:38384403-38384723	GM12878	blood:	n/a	n/a
12	BATF	chr7:38384447-38384746	GM12878	blood:	n/a	n/a
13	BATF	chr7:38406981-38407278	GM12878	blood:	n/a	n/a
14	BATF	chr7:38393104-38393355	GM12878	blood:	n/a	n/a
15	BATF	chr7:38402244-38402635	GM12878	blood:	n/a	chr7:38402448-38402459
16	BATF	chr7:38397936-38398227	GM12878	blood:	n/a	n/a
17	BATF	chr7:38397831-38398310	GM12878	blood:	n/a	n/a
18	BATF	chr7:38407600-38408059	GM12878	blood:	n/a	n/a
19	BATF	chr7:38406983-38407263	GM12878	blood:	n/a	n/a
20	BATF	chr7:38402249-38402527	GM12878	blood:	n/a	chr7:38402448-38402459
21	BCL11A	chr7:38393701-38393947	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:38398493-38398682	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:38384321-38384734	GM12878	blood:	n/a	chr7:38384540-38384549
24	BCL11A	chr7:38407578-38407819	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:38402227-38402452	GM12878	blood:	n/a	chr7:38402374-38402383
26	BCL11A	chr7:38406978-38407187	GM12878	blood:	n/a	chr7:38407111-38407120
27	BCL11A	chr7:38397653-38398122	GM12878	blood:	n/a	chr7:38398022-38398031
28	BCLAF1	chr7:38385200-38385540	GM12878	blood:	n/a	n/a
29	BCLAF1	chr7:38407679-38408065	GM12878	blood:	n/a	n/a
30	BCLAF1	chr7:38389556-38389732	GM12878	blood:	n/a	n/a
31	BHLHE40	chr7:38403094-38403268	K562	blood:	n/a	n/a
32	BHLHE40	chr7:38393917-38394132	K562	blood:	n/a	n/a
33	BHLHE40	chr7:38398804-38399002	K562	blood:	n/a	n/a
34	BHLHE40	chr7:38389643-38389696	GM12878	blood:	n/a	n/a
35	BHLHE40	chr7:38403131-38403176	GM12878	blood:	n/a	n/a
36	BHLHE40	chr7:38407780-38408107	K562	blood:	n/a	n/a
37	BHLHE40	chr7:38409538-38409840	K562	blood:	n/a	n/a
38	BHLHE40	chr7:38409415-38409953	GM12878	blood:	n/a	n/a
39	BHLHE40	chr7:38409540-38409919	HepG2	liver:	n/a	n/a
40	BHLHE40	chr7:38385297-38385497	GM12878	blood:	n/a	n/a
41	BHLHE40	chr7:38407782-38408093	GM12878	blood:	n/a	n/a
42	BHLHE40	chr7:38385332-38385486	K562	blood:	n/a	n/a
43	BRCA1	chr7:38408981-38409171	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr7:38403002-38403403	K562	blood:	n/a	n/a
45	CBX3	chr7:38398578-38399039	K562	blood:	n/a	n/a
46	CBX3	chr7:38389461-38389863	K562	blood:	n/a	n/a
47	CBX3	chr7:38409444-38409763	K562	blood:	n/a	n/a
48	CBX3	chr7:38407763-38408208	HCT-116	colon:	n/a	n/a
49	CBX3	chr7:38407677-38408137	K562	blood:	n/a	n/a
50	CBX3	chr7:38393853-38394294	K562	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38408106-38408156	PFSK-1	brain:	n/a
2	chr7:38408106-38408156	PFSK-1	brain:	n/a
3	chr7:38398836-38398886	NHBE	bronchial:	n/a
4	chr7:38403507-38403557	ovcar-3	ovarian:	n/a
5	chr7:38403507-38403557	PANC-1	pancreas:	n/a
6	chr7:38408106-38408156	U87	brain:	n/a
7	chr7:38389685-38389735	IMR90	lung:	fetal
8	chr7:38389659-38389709	HUVEC	blood vessel:	n/a
9	chr7:38389685-38389735	HRPEpiC	eye:	n/a
10	chr7:38389991-38390041	T-47D	breast:	n/a
11	chr7:38409725-38409775	ProgFib	skin:	n/a
12	chr7:38403507-38403557	AG04449	skin:	fetal
13	chr7:38408106-38408156	ECC-1	luminal epithelium:	n/a
14	chr7:38389685-38389735	HCPEpiC	choroid plexus:	n/a
15	chr7:38389991-38390041	Hela-S3	cervix:	n/a
16	chr7:38389991-38390041	HL-60	blood:	n/a
17	chr7:38398839-38398889	SAEC	small airway:	n/a
18	chr7:38398839-38398889	HAEpiC	amniotic membrane:	n/a
19	chr7:38398836-38398886	HNPCEpiC	eye:	n/a
20	chr7:38408106-38408156	T-47D	breast:	n/a
21	chr7:38409725-38409775	HEK293	kidney:	embryo
22	chr7:38403507-38403557	HEK293	kidney:	embryo
23	chr7:38389659-38389709	BJ	skin:	n/a
24	chr7:38398839-38398889	GM12892	blood:	n/a
25	chr7:38389659-38389709	HCT-116	colon:	n/a
26	chr7:38398836-38398886	HL-60	blood:	n/a
27	chr7:38389659-38389709	HAEpiC	amniotic membrane:	n/a
28	chr7:38398836-38398886	ProgFib	skin:	n/a
29	chr7:38398839-38398889	AG09319	gingival:	n/a
30	chr7:38408106-38408156	MCF-7	breast:	n/a
31	chr7:38389685-38389735	AG09309	skin:	n/a
32	chr7:38389991-38390041	HNPCEpiC	eye:	n/a
33	chr7:38408106-38408156	HPAEpiC	pulmonary alveolar:	n/a
34	chr7:38398839-38398889	CMK	blood:	n/a
35	chr7:38403507-38403557	GM06990	blood:	n/a
36	chr7:38389991-38390041	MCF10A-Er-Src	breast:	n/a
37	chr7:38408106-38408156	HEK293	kidney:	embryo
38	chr7:38389685-38389735	LNCaP	prostate:	n/a
39	chr7:38398839-38398889	T-47D	breast:	n/a
40	chr7:38389685-38389735	HCT-116	colon:	n/a
41	chr7:38403507-38403557	AoSMC	blood vessel:	n/a
42	chr7:38389991-38390041	HIPEpiC	eye:	n/a
43	chr7:38389685-38389735	MCF10A-Er-Src	breast:	n/a
44	chr7:38389685-38389735	AG10803	skin:	n/a
45	chr7:38409725-38409775	HMEC	breast:	n/a
46	chr7:38389991-38390041	IMR90	lung:	fetal
47	chr7:38408106-38408156	NHBE	bronchial:	n/a
48	chr7:38409725-38409775	SKMC	muscle:	n/a
49	chr7:38398836-38398886	MCF-7	breast:	n/a
50	chr7:38389659-38389709	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:
2	chr7:38379860..38381671-chr7:38382000..38383618,2	K562	blood:
3	chr7:38375070..38375771-chr7:38393808..38394547,2	MCF-7	breast:
4	chr7:38385094..38385817-chr7:38407469..38408173,2	MCF-7	breast:
5	chr7:38372590..38377698-chr7:38377994..38383669,12	K562	blood:
6	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
7	chr7:38268103..38269784-chr7:38382757..38385051,2	K562	blood:
8	chr7:38146965..38147587-chr7:38385316..38385987,2	MCF-7	breast:
9	chr7:38378957..38381571-chr7:38387227..38389473,2	K562	blood:
10	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
11	chr7:38409691..38411244-chr7:38417623..38419459,2	K562	blood:
12	chr7:38385094..38385817-chr7:38407469..38408173,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STARD3NL-6	chr7:38405093-38405440	NONHSAT120185
2	lnc-STARD3NL-7	chr7:38405699-38406016	NONHSAT120186
3	lnc-AMPH-4	chr7:38394799-38395026	NONHSAT120180
4	lnc-STARD3NL-1	chr7:38385622-38385728	ENSG00000250924
5	lnc-STARD3NL-5	chr7:38404346-38404812	NONHSAT120184
6	lnc-STARD3NL-1	chr7:38389947-38390051	ENSG00000250924
7	lnc-STARD3NL-1	chr7:38389947-38390051	NONHSAT120179
8	lnc-AMPH-3	chr7:38395172-38395463	NONHSAT120181
9	lnc-STARD3NL-4	chr7:38400418-38400732	NONHSAT120183
10	lnc-AMPH-1	chr7:38407614-38407746	XLOC_006412
11	lnc-STARD3NL-3	chr7:38397521-38397735	NONHSAT120182
12	lnc-AMPH-1	chr7:38407246-38407494	XLOC_006412
13	lnc-STARD3NL-1	chr7:38385622-38385728	NONHSAT120179
14	lnc-STARD3NL-1	chr7:38381683-38384763	ucscGeneNc_uc003tgp_1

No data

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

Extended variants
information (count: 1805 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1805 , 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	rs529881741	chr7:38383317-38383318	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
2	rs182248765	chr7:38383318-38383319	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs187655092	chr7:38383322-38383323	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs34288843	chr7:38383340-38383341	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs397820167	chr7:38383342-38383343	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs193227097	chr7:38383362-38383363	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs551474214	chr7:38383364-38383365	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs111450376	chr7:38383406-38383407	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs113132429	chr7:38383413-38383414	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs60671613	chr7:38383432-38383433	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs530812079	chr7:38383436-38383437	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs111709720	chr7:38383437-38383438	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs567633348	chr7:38383488-38383489	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs536429659	chr7:38383514-38383515	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs553200865	chr7:38383545-38383546	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs2735141	chr7:38383547-38383548	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs538688161	chr7:38383556-38383557	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs2534580	chr7:38383561-38383562	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs2735140	chr7:38383599-38383600	Weak transcription Active TSS Enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs574154479	chr7:38383601-38383602	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs185570497	chr7:38383604-38383605	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs554888750	chr7:38383620-38383621	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs149199780	chr7:38383653-38383654	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs540424484	chr7:38383671-38383672	Weak transcription Enhancers Strong transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
25	rs560334878	chr7:38383716-38383717	Weak transcription Enhancers Strong transcription Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs188501659	chr7:38383721-38383722	Weak transcription Enhancers Strong transcription Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs534104768	chr7:38383725-38383726	Weak transcription Enhancers Strong transcription Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs192057973	chr7:38383735-38383736	Weak transcription Enhancers Strong transcription Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs58232536	chr7:38383771-38383772	Weak transcription Enhancers Strong transcription Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs530897792	chr7:38383799-38383800	Weak transcription Enhancers Strong transcription Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs10232528	chr7:38383823-38383824	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs561246035	chr7:38383848-38383849	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs117090244	chr7:38383867-38383868	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs184433846	chr7:38383876-38383877	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs372970670	chr7:38383896-38383897	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs201378402	chr7:38383901-38383902	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs188481895	chr7:38383906-38383907	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs181246572	chr7:38383911-38383912	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs552217134	chr7:38383918-38383919	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs183520892	chr7:38383929-38383930	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs578095633	chr7:38383935-38383936	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs66478351	chr7:38383938-38383939	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs536759004	chr7:38383951-38383952	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs372611482	chr7:38383952-38383953	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs553389266	chr7:38384067-38384068	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
46	rs573303959	chr7:38384069-38384070	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
47	rs376381198	chr7:38384070-38384071	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
48	rs554283057	chr7:38384071-38384072	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
49	rs111537562	chr7:38384072-38384073	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	mRNA abundance
50	rs573863448	chr7:38384081-38384082	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 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:864 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38381000-38383800	Active TSS	K562	blood
2	chr7:38381200-38384200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr7:38381200-38384600	Weak transcription	Spleen	Spleen
4	chr7:38381200-38389200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr7:38381400-38384200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr7:38381400-38384800	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr7:38381400-38385000	Weak transcription	Fetal Muscle Leg	muscle
8	chr7:38381400-38385400	Weak transcription	Adipose Nuclei	Adipose
9	chr7:38381400-38385600	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr7:38381400-38389200	Weak transcription	Fetal Stomach	stomach
11	chr7:38381400-38408000	Weak transcription	Right Atrium	heart
12	chr7:38381600-38384200	Weak transcription	Primary B cells from cord blood	blood
13	chr7:38381600-38384800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr7:38381800-38384000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr7:38381800-38384200	Weak transcription	Primary B cells from peripheral blood	blood
16	chr7:38381800-38388800	Weak transcription	Duodenum Mucosa	Duodenum
17	chr7:38382000-38383600	Active TSS	Primary T cells fromperipheralblood	blood
18	chr7:38382000-38383600	Weak transcription	Dnd41	blood
19	chr7:38382000-38383800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr7:38382000-38384200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr7:38382000-38384200	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr7:38382000-38384200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr7:38382000-38384200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr7:38382000-38384200	Weak transcription	GM12878-XiMat	blood
25	chr7:38382000-38384600	Weak transcription	Placenta	Placenta
26	chr7:38382000-38384600	Enhancers	Fetal Thymus	thymus
27	chr7:38382000-38384800	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr7:38382000-38384800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr7:38382000-38384800	Weak transcription	Thymus	Thymus
30	chr7:38382000-38385200	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr7:38382000-38385600	Weak transcription	Pancreas	Pancrea
32	chr7:38382000-38389200	Weak transcription	Fetal Intestine Small	intestine
33	chr7:38382200-38383600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr7:38382200-38384000	Weak transcription	Primary T cells from cord blood	blood
35	chr7:38382200-38384000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr7:38382200-38384200	Weak transcription	Primary hematopoietic stem cells	blood
37	chr7:38382600-38385200	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr7:38383200-38383400	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr7:38383200-38384200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr7:38383400-38383800	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr7:38383600-38384000	Weak transcription	Primary T cells fromperipheralblood	blood
42	chr7:38383600-38385200	Enhancers	Dnd41	blood
43	chr7:38383600-38389000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr7:38383800-38384200	Enhancers	K562	blood
45	chr7:38383800-38386000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr7:38383800-38386200	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr7:38384000-38384200	Enhancers	Primary T cells fromperipheralblood	blood
48	chr7:38384000-38384600	Enhancers	Primary T cells from cord blood	blood
49	chr7:38384000-38385200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr7:38384000-38386000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood

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