Variant report

Variant	nsv606668
Chromosome Location	chr7:38388889-38403455
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:38389490-38389669	K562	blood:	n/a	n/a
2	BATF	chr7:38388801-38389033	GM12878	blood:	n/a	n/a
3	BATF	chr7:38397936-38398227	GM12878	blood:	n/a	n/a
4	BATF	chr7:38388739-38389137	GM12878	blood:	n/a	n/a
5	BATF	chr7:38393728-38393936	GM12878	blood:	n/a	n/a
6	BATF	chr7:38397831-38398310	GM12878	blood:	n/a	n/a
7	BATF	chr7:38393104-38393312	GM12878	blood:	n/a	n/a
8	BATF	chr7:38402249-38402527	GM12878	blood:	n/a	chr7:38402448-38402459
9	BATF	chr7:38389336-38389771	GM12878	blood:	n/a	n/a
10	BATF	chr7:38402244-38402635	GM12878	blood:	n/a	chr7:38402448-38402459
11	BATF	chr7:38393104-38393355	GM12878	blood:	n/a	n/a
12	BATF	chr7:38398491-38398925	GM12878	blood:	n/a	n/a
13	BCL11A	chr7:38393701-38393947	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:38402227-38402452	GM12878	blood:	n/a	chr7:38402374-38402383
15	BCL11A	chr7:38397653-38398122	GM12878	blood:	n/a	chr7:38398022-38398031
16	BCL11A	chr7:38398493-38398682	GM12878	blood:	n/a	n/a
17	BCLAF1	chr7:38389556-38389732	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:38403094-38403268	K562	blood:	n/a	n/a
19	BHLHE40	chr7:38398804-38399002	K562	blood:	n/a	n/a
20	BHLHE40	chr7:38403131-38403176	GM12878	blood:	n/a	n/a
21	BHLHE40	chr7:38393917-38394132	K562	blood:	n/a	n/a
22	BHLHE40	chr7:38389643-38389696	GM12878	blood:	n/a	n/a
23	CBX3	chr7:38389461-38389863	K562	blood:	n/a	n/a
24	CBX3	chr7:38403002-38403403	K562	blood:	n/a	n/a
25	CBX3	chr7:38398578-38399039	K562	blood:	n/a	n/a
26	CBX3	chr7:38393853-38394294	K562	blood:	n/a	n/a
27	CEBPB	chr7:38391385-38391451	IMR90	lung:	n/a	n/a
28	CEBPB	chr7:38400447-38400672	A549	lung:	n/a	n/a
29	CEBPB	chr7:38402455-38402609	HepG2	liver:	n/a	n/a
30	CHD1	chr7:38402581-38402583	GM12878	blood:	n/a	n/a
31	CHD1	chr7:38389454-38389506	GM12878	blood:	n/a	n/a
32	CHD2	chr7:38398814-38398836	GM12878	blood:	n/a	n/a
33	CHD2	chr7:38403060-38403224	GM12878	blood:	n/a	n/a
34	CTCF	chr7:38398595-38399049	K562	blood:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
35	CTCF	chr7:38398741-38398858	HepG2	liver:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
36	CTCF	chr7:38398700-38398850	HCM	heart:	n/a	n/a
37	CTCF	chr7:38398689-38399100	GM12891	blood:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
38	CTCF	chr7:38389580-38389730	GM12866	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
39	CTCF	chr7:38398680-38398830	GM12868	blood:	n/a	n/a
40	CTCF	chr7:38389580-38389730	GM12867	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
41	CTCF	chr7:38392385-38392427	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr7:38389570-38389815	GM20000	blood:	n/a	chr7:38389677-38389698 chr7:38389683-38389699 chr7:38389684-38389697 chr7:38389682-38389700
43	CTCF	chr7:38403080-38403230	AG04450	lung:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
44	CTCF	chr7:38403140-38403290	HPAF	blood vessel:	n/a	chr7:38403193-38403209 chr7:38403192-38403210 chr7:38403194-38403207 chr7:38403187-38403208 chr7:38403194-38403207
45	CTCF	chr7:38403040-38403190	HFF	foreskin:	n/a	n/a
46	CTCF	chr7:38398785-38399009	IMR90	lung:	n/a	chr7:38398837-38398853 chr7:38398838-38398851 chr7:38398838-38398851 chr7:38398831-38398852 chr7:38398836-38398854
47	CTCF	chr7:38398560-38398830	HRE	kidney:	n/a	n/a
48	CTCF	chr7:38393880-38394030	GM12864	blood:	n/a	n/a
49	CTCF	chr7:38393940-38394090	WERI-Rb-1	eye:	n/a	chr7:38394049-38394065 chr7:38394050-38394063 chr7:38394050-38394063 chr7:38394043-38394064 chr7:38394048-38394066
50	CTCF	chr7:38398680-38398830	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38398836-38398886	GM12878	blood:	n/a
2	chr7:38389685-38389735	T-47D	breast:	n/a
3	chr7:38398836-38398886	AoSMC	blood vessel:	n/a
4	chr7:38398836-38398886	Hepatocyte	liver:	n/a
5	chr7:38398839-38398889	HUVEC	blood vessel:	n/a
6	chr7:38398839-38398889	NHDF-neo	bronchial:	n/a
7	chr7:38398836-38398886	AG04449	skin:	fetal
8	chr7:38398839-38398889	AG10803	skin:	n/a
9	chr7:38389685-38389735	LNCaP	prostate:	n/a
10	chr7:38398839-38398889	MCF-7	breast:	n/a
11	chr7:38389685-38389735	HNPCEpiC	eye:	n/a
12	chr7:38398839-38398889	HL-60	blood:	n/a
13	chr7:38389685-38389735	PFSK-1	brain:	n/a
14	chr7:38389991-38390041	H1-hESC	embryonic stem cell:	embryo
15	chr7:38389659-38389709	HCT-116	colon:	n/a
16	chr7:38389685-38389735	CMK	blood:	n/a
17	chr7:38389991-38390041	HRCEpiC	kidney:	n/a
18	chr7:38389991-38390041	AG10803	skin:	n/a
19	chr7:38389659-38389709	SK-N-SH_RA	brain:	n/a
20	chr7:38389659-38389709	SAEC	small airway:	n/a
21	chr7:38398839-38398889	CMK	blood:	n/a
22	chr7:38389685-38389735	HL-60	blood:	n/a
23	chr7:38389685-38389735	NB4	blood:	n/a
24	chr7:38398839-38398889	Hepatocyte	liver:	n/a
25	chr7:38398836-38398886	ProgFib	skin:	n/a
26	chr7:38398836-38398886	LNCaP	prostate:	n/a
27	chr7:38389659-38389709	HIPEpiC	eye:	n/a
28	chr7:38389659-38389709	HNPCEpiC	eye:	n/a
29	chr7:38398836-38398886	GM12892	blood:	n/a
30	chr7:38389659-38389709	BJ	skin:	n/a
31	chr7:38389659-38389709	HepG2	liver:	n/a
32	chr7:38389991-38390041	T-47D	breast:	n/a
33	chr7:38398836-38398886	HNPCEpiC	eye:	n/a
34	chr7:38389991-38390041	MCF10A-Er-Src	breast:	n/a
35	chr7:38398839-38398889	HAEpiC	amniotic membrane:	n/a
36	chr7:38389659-38389709	HPAEpiC	pulmonary alveolar:	n/a
37	chr7:38389991-38390041	ProgFib	skin:	n/a
38	chr7:38389685-38389735	SAEC	small airway:	n/a
39	chr7:38398836-38398886	AG09309	skin:	n/a
40	chr7:38398836-38398886	HepG2	liver:	n/a
41	chr7:38398839-38398889	SKMC	muscle:	n/a
42	chr7:38389659-38389709	AG10803	skin:	n/a
43	chr7:38398836-38398886	ovcar-3	ovarian:	n/a
44	chr7:38398839-38398889	HEEpiC	esophagus:	n/a
45	chr7:38398836-38398886	Caco-2	colon:	n/a
46	chr7:38389991-38390041	SAEC	small airway:	n/a
47	chr7:38398839-38398889	K562	blood:	n/a
48	chr7:38398839-38398889	IMR90	lung:	fetal
49	chr7:38398839-38398889	HRCEpiC	kidney:	n/a
50	chr7:38398836-38398886	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:
2	chr7:38375070..38375771-chr7:38393808..38394547,2	MCF-7	breast:
3	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
4	chr7:38378957..38381571-chr7:38387227..38389473,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMPH-3	chr7:38395172-38395463	NONHSAT120181
2	lnc-STARD3NL-4	chr7:38400418-38400732	NONHSAT120183
3	lnc-STARD3NL-3	chr7:38397521-38397735	NONHSAT120182
4	lnc-STARD3NL-1	chr7:38389947-38390051	NONHSAT120179
5	lnc-STARD3NL-1	chr7:38389947-38390051	ENSG00000250924
6	lnc-AMPH-4	chr7:38394799-38395026	NONHSAT120180

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

Extended variants
information (count: 1049 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1049 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1810378	chr7:38388889-38388890	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs564031126	chr7:38388890-38388891	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs76205258	chr7:38388895-38388896	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs113354949	chr7:38388910-38388911	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs373371179	chr7:38388923-38388924	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs186143895	chr7:38388927-38388928	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs199664656	chr7:38388944-38388945	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs376662728	chr7:38388959-38388960	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs569923294	chr7:38388978-38388979	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs535656396	chr7:38388987-38388988	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs548379989	chr7:38388992-38388993	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs112420338	chr7:38389014-38389015	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs190777554	chr7:38389017-38389018	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs183241065	chr7:38389020-38389021	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs533935312	chr7:38389037-38389038	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs370803388	chr7:38389053-38389054	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs374363918	chr7:38389062-38389063	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs187227295	chr7:38389088-38389089	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs192044855	chr7:38389101-38389102	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs200569323	chr7:38389103-38389104	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs367715379	chr7:38389113-38389114	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs371587360	chr7:38389129-38389130	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs144218291	chr7:38389145-38389146	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs368224611	chr7:38389149-38389150	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs372324933	chr7:38389157-38389158	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs200167157	chr7:38389165-38389166	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs556918270	chr7:38389168-38389169	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs576674436	chr7:38389173-38389174	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs542443202	chr7:38389184-38389185	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs555145944	chr7:38389191-38389192	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs572147697	chr7:38389220-38389221	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs200972963	chr7:38389233-38389234	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs563693060	chr7:38389237-38389238	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs368513160	chr7:38389243-38389244	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs532786663	chr7:38389246-38389247	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs372931753	chr7:38389272-38389273	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs563279942	chr7:38389276-38389277	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs374793407	chr7:38389278-38389279	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs375909784	chr7:38389283-38389284	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs369193835	chr7:38389285-38389286	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs148292986	chr7:38389290-38389291	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
42	rs143036661	chr7:38389291-38389292	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
43	rs116888943	chr7:38389317-38389318	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs369333697	chr7:38389331-38389332	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs534699558	chr7:38389332-38389333	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs183835962	chr7:38389341-38389342	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs373102591	chr7:38389343-38389344	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs147535583	chr7:38389353-38389354	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs187884826	chr7:38389370-38389371	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs373951811	chr7:38389373-38389374	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 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:472 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38381200-38389200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr7:38381400-38389200	Weak transcription	Fetal Stomach	stomach
3	chr7:38381400-38408000	Weak transcription	Right Atrium	heart
4	chr7:38382000-38389200	Weak transcription	Fetal Intestine Small	intestine
5	chr7:38383600-38389000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr7:38384800-38390800	Active TSS	Thymus	Thymus
7	chr7:38385600-38389000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr7:38385800-38389000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr7:38385800-38389000	Weak transcription	GM12878-XiMat	blood
10	chr7:38385800-38389200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr7:38385800-38389200	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr7:38386000-38389000	Weak transcription	Primary T cells from cord blood	blood
13	chr7:38386000-38389000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr7:38386000-38389000	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr7:38386000-38389200	Weak transcription	Primary hematopoietic stem cells	blood
16	chr7:38386000-38389200	Weak transcription	K562	blood
17	chr7:38386800-38390600	Enhancers	Primary B cells from cord blood	blood
18	chr7:38387400-38389200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr7:38388200-38389000	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr7:38388200-38389200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr7:38388400-38389200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr7:38388600-38389000	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr7:38388600-38389200	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr7:38388600-38390200	Flanking Active TSS	Fetal Thymus	thymus
25	chr7:38388600-38390400	Active TSS	Primary T killer memory cells from peripheral blood	blood
26	chr7:38388600-38391000	Enhancers	Primary B cells from peripheral blood	blood
27	chr7:38388800-38389000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr7:38388800-38389200	Active TSS	Dnd41	blood
29	chr7:38388800-38389600	Enhancers	Spleen	Spleen
30	chr7:38388800-38390000	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
31	chr7:38388800-38390600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
32	chr7:38388800-38390600	Active TSS	Duodenum Mucosa	Duodenum
33	chr7:38388800-38391800	Active TSS	Primary T cells fromperipheralblood	blood
34	chr7:38388800-38394200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr7:38389000-38389200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
36	chr7:38389000-38389200	Active TSS	Primary T helper cells fromperipheralblood	blood
37	chr7:38389000-38389200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
38	chr7:38389000-38389200	Flanking Active TSS	GM12878-XiMat	blood
39	chr7:38389000-38389400	Active TSS	Primary T cells from cord blood	blood
40	chr7:38389000-38389400	Enhancers	HUVEC	blood vessel
41	chr7:38389000-38389600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
42	chr7:38389000-38389600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
43	chr7:38389000-38390000	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr7:38389000-38390200	Active TSS	Primary T helper naive cells from peripheral blood	blood
45	chr7:38389000-38390400	Active TSS	Primary T helper cells PMA-I stimulated	--
46	chr7:38389000-38390400	Active TSS	Rectal Mucosa Donor 29	rectum
47	chr7:38389000-38390600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr7:38389200-38389400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
49	chr7:38389200-38389400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr7:38389200-38389400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood

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