Variant report

Variant	esv12437
Chromosome Location	chr7:38384509-38388845
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	BATF	chr7:38388739-38389137	GM12878	blood:	n/a	n/a
2	BATF	chr7:38388801-38389033	GM12878	blood:	n/a	n/a
3	BATF	chr7:38384403-38384723	GM12878	blood:	n/a	n/a
4	BATF	chr7:38385112-38385446	GM12878	blood:	n/a	n/a
5	BATF	chr7:38384447-38384746	GM12878	blood:	n/a	n/a
6	BCL11A	chr7:38384321-38384734	GM12878	blood:	n/a	chr7:38384540-38384549
7	BCLAF1	chr7:38385200-38385540	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:38385332-38385486	K562	blood:	n/a	n/a
9	BHLHE40	chr7:38385297-38385497	GM12878	blood:	n/a	n/a
10	CHD2	chr7:38385235-38385424	GM12878	blood:	n/a	n/a
11	CTCF	chr7:38385300-38385450	AG09319	gingival:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
12	CTCF	chr7:38385300-38385450	HCFaa	heart:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
13	CTCF	chr7:38385300-38385450	GM12874	blood:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
14	CTCF	chr7:38385300-38385450	AG04450	lung:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
15	CTCF	chr7:38385340-38385490	GM12864	blood:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
16	CTCF	chr7:38385320-38385470	HEEpiC	esophagus:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
17	CTCF	chr7:38385201-38385661	GM19240	blood:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
18	CTCF	chr7:38385019-38385641	K562	blood:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
19	CTCF	chr7:38385320-38385470	GM12870	blood:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
20	CTCF	chr7:38384497-38384574	Spleen_OC	spleen:	n/a	n/a
21	CTCF	chr7:38385320-38385470	HUVEC	blood vessel:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
22	CTCF	chr7:38385320-38385470	SAEC	small airway:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
23	CTCF	chr7:38385220-38385370	GM12866	blood:	n/a	n/a
24	CTCF	chr7:38385220-38385370	GM12872	blood:	n/a	n/a
25	CTCF	chr7:38385180-38385330	HCM	heart:	n/a	n/a
26	CTCF	chr7:38385244-38385501	GM10266	blood:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
27	CTCF	chr7:38385320-38385470	AoAF	blood vessel:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
28	CTCF	chr7:38385020-38385170	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr7:38385142-38385523	A549	lung:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
30	CTCF	chr7:38385256-38385463	HUVEC	blood vessel:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
31	CTCF	chr7:38385252-38385476	HepG2	liver:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
32	CTCF	chr7:38385300-38385450	HL-60	blood:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
33	CTCF	chr7:38385300-38385450	SAEC	small airway:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
34	CTCF	chr7:38385300-38385450	AG10803	skin:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
35	CTCF	chr7:38385660-38385810	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr7:38385320-38385470	NHEK	skin:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
37	CTCF	chr7:38385242-38385513	Lung_OC	lung:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
38	CTCF	chr7:38385220-38385370	BE2_C	brain:	n/a	n/a
39	CTCF	chr7:38385232-38385408	ECC-1	luminal epithelium:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
40	CTCF	chr7:38385270-38385473	GM20000	blood:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
41	CTCF	chr7:38385260-38385410	GM06990	blood:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
42	CTCF	chr7:38385400-38385550	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr7:38385066-38385100	GM19240	blood:	n/a	n/a
44	CTCF	chr7:38385300-38385450	Hela-S3	cervix:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
45	CTCF	chr7:38385192-38385604	GM19238	blood:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
46	CTCF	chr7:38385240-38385404	ECC-1	luminal epithelium:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
47	CTCF	chr7:38385300-38385450	AG04449	skin:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
48	CTCF	chr7:38385300-38385450	AoAF	blood vessel:	n/a	chr7:38385352-38385373 chr7:38385358-38385374 chr7:38385359-38385372 chr7:38385357-38385375 chr7:38385359-38385372
49	CTCF	chr7:38385200-38385350	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr7:38385220-38385370	A549	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:38146965..38147587-chr7:38385316..38385987,2	MCF-7	breast:
2	chr7:38385094..38385817-chr7:38407469..38408173,2	MCF-7	breast:
3	chr7:38268103..38269784-chr7:38382757..38385051,2	K562	blood:
4	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
5	chr7:38378957..38381571-chr7:38387227..38389473,2	K562	blood:
6	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STARD3NL-1	chr7:38385622-38385728	NONHSAT120179
2	lnc-STARD3NL-1	chr7:38385622-38385728	ENSG00000250924
3	lnc-STARD3NL-1	chr7:38381683-38384763	ucscGeneNc_uc003tgp_1

Variant related genes	Relation type
TRGV6	TF binding region
TRGV5P	TF binding region
ENSG00000211701	chromatin interactions
ENSG00000226212	chromatin interactions
ENSG00000211697	chromatin interactions
ENSG00000228668	chromatin interactions
SERTAD3	miRNA target sites

Extended variants
information (count: 305 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572405107	chr7:38384526-38384527	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
2	rs111405005	chr7:38384542-38384543	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	mRNA abundance
3	rs555260415	chr7:38384555-38384556	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs76591336	chr7:38384564-38384565	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	mRNA abundance
5	rs369055935	chr7:38384567-38384568	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs2736949	chr7:38384577-38384578	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs563029431	chr7:38384595-38384596	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs12532780	chr7:38384612-38384613	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs577706553	chr7:38384616-38384617	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs142965452	chr7:38384633-38384634	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs544563226	chr7:38384635-38384636	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs527260698	chr7:38384641-38384642	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs539949432	chr7:38384649-38384650	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs181538836	chr7:38384678-38384679	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs559720166	chr7:38384712-38384713	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs370990448	chr7:38384714-38384715	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs556428357	chr7:38384730-38384731	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs151125037	chr7:38384741-38384742	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs186237750	chr7:38384745-38384746	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs549096790	chr7:38384749-38384750	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs190116245	chr7:38384759-38384760	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs568555374	chr7:38384774-38384775	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs12532842	chr7:38384786-38384787	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs12535490	chr7:38384794-38384795	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs182760137	chr7:38384795-38384796	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs187694336	chr7:38384798-38384799	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs12535491	chr7:38384804-38384805	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	n/a
28	rs12532792	chr7:38384817-38384818	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	n/a
29	rs550724331	chr7:38384831-38384832	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs542473151	chr7:38384840-38384841	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	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
32	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
33	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
34	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
35	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
36	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
37	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
38	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
39	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
40	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
41	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
42	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
43	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
44	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
45	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
46	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
47	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
48	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
49	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
50	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

Variant related diseases (count:81)

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

Chromatin state (count:131 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38381200-38384600	Weak transcription	Spleen	Spleen
2	chr7:38381200-38389200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr7:38381400-38384800	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr7:38381400-38385000	Weak transcription	Fetal Muscle Leg	muscle
5	chr7:38381400-38385400	Weak transcription	Adipose Nuclei	Adipose
6	chr7:38381400-38385600	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr7:38381400-38389200	Weak transcription	Fetal Stomach	stomach
8	chr7:38381400-38408000	Weak transcription	Right Atrium	heart
9	chr7:38381600-38384800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr7:38381800-38388800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr7:38382000-38384600	Weak transcription	Placenta	Placenta
12	chr7:38382000-38384600	Enhancers	Fetal Thymus	thymus
13	chr7:38382000-38384800	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr7:38382000-38384800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr7:38382000-38384800	Weak transcription	Thymus	Thymus
16	chr7:38382000-38385200	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr7:38382000-38385600	Weak transcription	Pancreas	Pancrea
18	chr7:38382000-38389200	Weak transcription	Fetal Intestine Small	intestine
19	chr7:38382600-38385200	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr7:38383600-38385200	Enhancers	Dnd41	blood
21	chr7:38383600-38389000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr7:38383800-38386000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr7:38383800-38386200	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr7:38384000-38384600	Enhancers	Primary T cells from cord blood	blood
25	chr7:38384000-38385200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr7:38384000-38386000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr7:38384200-38384800	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr7:38384200-38385000	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr7:38384200-38385600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
30	chr7:38384200-38385600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr7:38384200-38385800	Enhancers	Primary B cells from cord blood	blood
32	chr7:38384200-38385800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr7:38384200-38385800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr7:38384200-38385800	Enhancers	GM12878-XiMat	blood
35	chr7:38384200-38386000	Enhancers	Primary B cells from peripheral blood	blood
36	chr7:38384200-38386000	Enhancers	Primary hematopoietic stem cells	blood
37	chr7:38384200-38386000	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr7:38384400-38385200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr7:38384400-38385400	Enhancers	K562	blood
40	chr7:38384600-38384800	Flanking Active TSS	Primary T cells from cord blood	blood
41	chr7:38384600-38385000	Enhancers	Placenta	Placenta
42	chr7:38384600-38385000	Enhancers	Spleen	Spleen
43	chr7:38384600-38385800	Flanking Active TSS	Fetal Thymus	thymus
44	chr7:38384800-38385000	Enhancers	Primary T cells from cord blood	blood
45	chr7:38384800-38385400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
46	chr7:38384800-38385800	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr7:38384800-38385800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr7:38384800-38386200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr7:38384800-38386400	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr7:38384800-38390800	Active TSS	Thymus	Thymus

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