Variant report

Variant	nsv606230
Chromosome Location	chr7:12516170-12564128
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	ARID3A	chr7:12536356-12536848	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:12536532-12536802	K562	blood:	n/a	n/a
3	ARID3A	chr7:12529812-12530097	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:12533106-12533341	K562	blood:	n/a	n/a
5	ATF1	chr7:12529814-12530077	K562	blood:	n/a	n/a
6	BACH1	chr7:12532972-12533274	K562	blood:	n/a	n/a
7	BACH1	chr7:12532994-12533280	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr7:12524666-12525474	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:12533085-12533378	K562	blood:	n/a	n/a
10	BHLHE40	chr7:12521491-12521740	GM12878	blood:	n/a	n/a
11	CBX3	chr7:12557088-12557431	K562	blood:	n/a	n/a
12	CBX3	chr7:12557129-12557384	K562	blood:	n/a	n/a
13	CBX3	chr7:12558748-12559243	HCT-116	colon:	n/a	n/a
14	CCNT2	chr7:12533047-12533307	K562	blood:	n/a	n/a
15	CEBPB	chr7:12519662-12519793	A549	lung:	n/a	n/a
16	CEBPB	chr7:12534206-12534533	K562	blood:	n/a	n/a
17	CEBPB	chr7:12529839-12530092	A549	lung:	n/a	n/a
18	CEBPB	chr7:12536996-12537150	A549	lung:	n/a	n/a
19	CEBPB	chr7:12533125-12533486	K562	blood:	n/a	n/a
20	CEBPB	chr7:12521423-12521514	HepG2	liver:	n/a	chr7:12521454-12521465
21	CEBPB	chr7:12529776-12530104	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr7:12519704-12519859	K562	blood:	n/a	n/a
23	CEBPB	chr7:12521403-12521540	H1-hESC	embryonic stem cell:	n/a	chr7:12521454-12521465
24	CEBPD	chr7:12532996-12533568	K562	blood:	n/a	n/a
25	CHD2	chr7:12534687-12534708	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr7:12529840-12529990	HPAF	blood vessel:	n/a	chr7:12529922-12529938 chr7:12529916-12529937 chr7:12529921-12529939
27	CTCF	chr7:12558900-12559050	GM12871	blood:	n/a	n/a
28	CTCF	chr7:12536477-12536852	HCT-116	colon:	n/a	chr7:12536619-12536629 chr7:12536611-12536632 chr7:12536616-12536634 chr7:12536618-12536631 chr7:12536620-12536641 chr7:12536622-12536631 chr7:12536617-12536633
29	CTCF	chr7:12558825-12559102	GM12891	blood:	n/a	n/a
30	CTCF	chr7:12536580-12536730	HRE	kidney:	n/a	chr7:12536619-12536629 chr7:12536611-12536632 chr7:12536616-12536634 chr7:12536618-12536631 chr7:12536620-12536641 chr7:12536622-12536631 chr7:12536617-12536633
31	CTCF	chr7:12559140-12559290	A549	lung:	n/a	n/a
32	CTCF	chr7:12529706-12530062	ECC-1	luminal epithelium:	n/a	chr7:12529922-12529938 chr7:12529916-12529937 chr7:12529921-12529939
33	CTCF	chr7:12536533-12536744	Spleen_OC	spleen:	n/a	chr7:12536619-12536629 chr7:12536611-12536632 chr7:12536616-12536634 chr7:12536618-12536631 chr7:12536620-12536641 chr7:12536622-12536631 chr7:12536617-12536633
34	CTCF	chr7:12536560-12536710	AG04449	skin:	n/a	chr7:12536619-12536629 chr7:12536611-12536632 chr7:12536616-12536634 chr7:12536618-12536631 chr7:12536620-12536641 chr7:12536622-12536631 chr7:12536617-12536633
35	CTCF	chr7:12536640-12536790	NHEK	skin:	n/a	n/a
36	CTCF	chr7:12536599-12536671	GM13976	blood:	n/a	chr7:12536619-12536629 chr7:12536611-12536632 chr7:12536616-12536634 chr7:12536618-12536631 chr7:12536620-12536641 chr7:12536622-12536631 chr7:12536617-12536633
37	CTCF	chr7:12534400-12534550	HEEpiC	esophagus:	n/a	chr7:12534432-12534450 chr7:12534434-12534447 chr7:12534427-12534448
38	CTCF	chr7:12530520-12530670	AG04449	skin:	n/a	n/a
39	CTCF	chr7:12558600-12558750	GM12878	blood:	n/a	n/a
40	CTCF	chr7:12558900-12559050	AG04450	lung:	n/a	n/a
41	CTCF	chr7:12530340-12530490	BE2_C	brain:	n/a	n/a
42	CTCF	chr7:12558900-12559050	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr7:12529860-12530010	HA-sp	spinal cord:	n/a	chr7:12529922-12529938 chr7:12529916-12529937 chr7:12529921-12529939
44	CTCF	chr7:12534320-12534470	NHEK	skin:	n/a	chr7:12534432-12534450 chr7:12534434-12534447 chr7:12534427-12534448
45	CTCF	chr7:12529847-12530014	Pancreas_OC	pancreas:	n/a	chr7:12529922-12529938 chr7:12529916-12529937 chr7:12529921-12529939
46	CTCF	chr7:12536480-12536630	GM12873	blood:	n/a	chr7:12536619-12536629
47	CTCF	chr7:12529780-12529930	NB4	blood:	n/a	n/a
48	CTCF	chr7:12534293-12534617	GM12878	blood:	n/a	chr7:12534432-12534450 chr7:12534434-12534447 chr7:12534427-12534448
49	CTCF	chr7:12534340-12534490	GM06990	blood:	n/a	chr7:12534432-12534450 chr7:12534434-12534447 chr7:12534427-12534448
50	CTCF	chr7:12558880-12559030	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:12537108-12537158	Hela-S3	cervix:	n/a
2	chr7:12537108-12537158	AG09309	skin:	n/a
3	chr7:12537108-12537158	NHDF-neo	bronchial:	n/a
4	chr7:12537108-12537158	U87	brain:	n/a
5	chr7:12537108-12537158	Hepatocyte	liver:	n/a
6	chr7:12537108-12537158	GM12878	blood:	n/a
7	chr7:12537108-12537158	GM19239	blood:	n/a
8	chr7:12537108-12537158	CMK	blood:	n/a
9	chr7:12537108-12537158	HUVEC	blood vessel:	n/a
10	chr7:12537108-12537158	AG04449	skin:	fetal
11	chr7:12537108-12537158	HAEpiC	amniotic membrane:	n/a
12	chr7:12537108-12537158	NT2-D1	testis:	n/a
13	chr7:12537108-12537158	SK-N-SH	brain:	n/a
14	chr7:12537108-12537158	MCF-7	breast:	n/a
15	chr7:12537108-12537158	BJ	skin:	n/a
16	chr7:12537108-12537158	PANC-1	pancreas:	n/a
17	chr7:12537108-12537158	H1-hESC	embryonic stem cell:	embryo
18	chr7:12537108-12537158	PrEC	prostate:	n/a
19	chr7:12537108-12537158	ProgFib	skin:	n/a
20	chr7:12537108-12537158	GM06990	blood:	n/a
21	chr7:12537108-12537158	AoSMC	blood vessel:	n/a
22	chr7:12537108-12537158	HepG2	liver:	n/a
23	chr7:12537108-12537158	AG04450	lung:	fetal
24	chr7:12537108-12537158	GM12892	blood:	n/a
25	chr7:12537108-12537158	HRE	kidney:	n/a
26	chr7:12537108-12537158	LNCaP	prostate:	n/a
27	chr7:12537108-12537158	HRPEpiC	eye:	n/a
28	chr7:12537108-12537158	SKMC	muscle:	n/a
29	chr7:12537108-12537158	HNPCEpiC	eye:	n/a
30	chr7:12537108-12537158	HRCEpiC	kidney:	n/a
31	chr7:12537108-12537158	HCT-116	colon:	n/a
32	chr7:12537108-12537158	IMR90	lung:	fetal
33	chr7:12537108-12537158	NHBE	bronchial:	n/a
34	chr7:12537108-12537158	NB4	blood:	n/a
35	chr7:12537108-12537158	T-47D	breast:	n/a
36	chr7:12537108-12537158	NH-A	brain:	n/a
37	chr7:12537108-12537158	Caco-2	colon:	n/a
38	chr7:12537108-12537158	MCF10A-Er-Src	breast:	n/a
39	chr7:12537108-12537158	SK-N-MC	brain:	n/a
40	chr7:12537108-12537158	SAEC	small airway:	n/a
41	chr7:12537108-12537158	K562	blood:	n/a
42	chr7:12537108-12537158	BE2_C	brain:	n/a
43	chr7:12537108-12537158	HCM	heart:	n/a
44	chr7:12537108-12537158	ovcar-3	ovarian:	n/a
45	chr7:12537108-12537158	HL-60	blood:	n/a
46	chr7:12537108-12537158	A549	lung:	n/a
47	chr7:12537108-12537158	HEK293	kidney:	embryo
48	chr7:12537108-12537158	HEEpiC	esophagus:	n/a
49	chr7:12537108-12537158	AG10803	skin:	n/a
50	chr7:12537108-12537158	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:12497991..12498705-chr7:12529442..12530188,2	MCF-7	breast:
2	chr7:12497885..12498702-chr7:12558562..12559343,2	MCF-7	breast:
3	chr7:12473455..12474066-chr7:12536117..12536924,2	MCF-7	breast:
4	chr7:12485193..12487796-chr7:12515501..12517755,2	K562	blood:
5	chr7:12563798..12566063-chr7:12723431..12726105,2	K562	blood:
6	chr7:12473597..12474340-chr7:12529520..12530546,3	MCF-7	breast:
7	chr7:12497831..12498808-chr7:12529325..12530426,5	K562	blood:
8	chr7:12511799..12515284-chr7:12517629..12521714,3	K562	blood:
9	chr7:12563571..12565144-chr7:12668072..12670277,2	K562	blood:
10	chr7:12326033..12327864-chr7:12530775..12532531,2	K562	blood:
11	chr7:12520796..12522779-chr7:12527850..12529893,2	K562	blood:
12	chr7:12516830..12519772-chr7:12523106..12525607,3	K562	blood:
13	chr7:12511799..12514210-chr7:12517629..12520508,2	K562	blood:
14	chr7:12528914..12532541-chr7:12534824..12536655,4	K562	blood:
15	chr7:12473109..12473862-chr7:12558519..12559485,2	K562	blood:
16	chr7:12558622..12559420-chr7:12663224..12663821,2	MCF-7	breast:
17	chr7:12558451..12560515-chr7:12754100..12757020,2	K562	blood:
18	chr7:12249540..12251997-chr7:12556631..12559101,2	K562	blood:
19	chr7:12557824..12559651-chr7:12562613..12565542,2	K562	blood:
20	chr7:12497882..12499037-chr7:12533987..12535337,10	MCF-7	breast:
21	chr7:12558222..12560896-chr7:12563188..12565683,2	K562	blood:
22	chr7:12497870..12498820-chr7:12528972..12530631,10	MCF-7	breast:
23	chr7:12498003..12498630-chr7:12536129..12537096,2	K562	blood:
24	chr7:12558222..12560896-chr7:12563188..12565683,2	K562	blood:
25	chr7:12564097..12565730-chr7:12662861..12664188,13	K562	blood:
26	chr7:12557824..12559651-chr7:12562613..12565542,2	K562	blood:
27	chr7:12516830..12519772-chr7:12523106..12525607,3	K562	blood:
28	chr7:12528914..12532541-chr7:12534824..12536655,4	K562	blood:
29	chr7:12473418..12474056-chr7:12534375..12534896,2	MCF-7	breast:
30	chr7:12564069..12565148-chr7:12663270..12664407,15	MCF-7	breast:
31	chr7:12520796..12522779-chr7:12527850..12529893,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SCIN-3	chr7:12537187-12537243	l_3363_chr7:12529385-12547552_testes
2	lnc-SCIN-2	chr7:12544025-12544172	ENSG00000226690.2
3	lnc-SCIN-3	chr7:12545633-12545694	NONHSAT119232
4	lnc-SCIN-2	chr7:12544050-12544172	ENSG00000226690.2
5	lnc-SCIN-2	chr7:12536055-12536265	ENSG00000226690.2
6	lnc-SCIN-4	chr7:12530721-12531630	NONHSAT119228
7	lnc-SCIN-3	chr7:12546429-12546638	NONHSAT119232
8	lnc-SCIN-3	chr7:12535053-12535266	l_3363_chr7:12529385-12547552_testes
9	lnc-SCIN-3	chr7:12531971-12532055	l_3363_chr7:12529385-12547552_testes
10	lnc-SCIN-3	chr7:12547071-12547552	l_3363_chr7:12529385-12547552_testes
11	lnc-SCIN-3	chr7:12546915-12547104	NONHSAT119232
12	lnc-SCIN-3	chr7:12529386-12529577	l_3363_chr7:12529385-12547552_testes

Variant related genes	Relation type
ENSG00000224667	TF binding region
TAS2R2P	TF binding region
ENSG00000226690	TF binding region
ENSG00000224667	CpG island
TAS2R2P	CpG island
ENSG00000226690	CpG island
ENSG00000226690	chromatin interactions
ENSG00000106460	chromatin interactions
ENSG00000271253	chromatin interactions
ENSG00000203523	chromatin interactions

Extended variants
information (count: 1297 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1297 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs758281	chr7:12516170-12516171	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs573250085	chr7:12516215-12516216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545480670	chr7:12516255-12516256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565285438	chr7:12516281-12516282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547501725	chr7:12516325-12516326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530900455	chr7:12516335-12516336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543754303	chr7:12516397-12516398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs563417500	chr7:12516405-12516406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529111793	chr7:12516493-12516494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs6954423	chr7:12516509-12516510	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs370905858	chr7:12516621-12516622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182927486	chr7:12516622-12516623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539341459	chr7:12516677-12516678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs375228522	chr7:12516679-12516680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536636191	chr7:12516685-12516686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375547500	chr7:12516717-12516718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs115757713	chr7:12516719-12516720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145786314	chr7:12516720-12516721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185752726	chr7:12516733-12516734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536892614	chr7:12516799-12516800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10950402	chr7:12516800-12516801	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs573679749	chr7:12516812-12516813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573342459	chr7:12516813-12516814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371749428	chr7:12516819-12516820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375980142	chr7:12516820-12516821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568854293	chr7:12516821-12516822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539160089	chr7:12516830-12516831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191005513	chr7:12516837-12516838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182875917	chr7:12516861-12516862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148952933	chr7:12516874-12516875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563645102	chr7:12516905-12516906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs78828501	chr7:12516944-12516945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549772640	chr7:12516962-12516963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573106540	chr7:12516963-12516964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187782184	chr7:12516989-12516990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559285481	chr7:12517039-12517040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs1440016	chr7:12517056-12517057	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs1440017	chr7:12517066-12517067	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs564616728	chr7:12517088-12517089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs367673931	chr7:12517125-12517126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530471424	chr7:12517156-12517157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575313785	chr7:12517166-12517167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544450933	chr7:12517212-12517213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550297748	chr7:12517244-12517245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192698534	chr7:12517250-12517251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183411355	chr7:12517255-12517256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547245863	chr7:12517284-12517285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371811088	chr7:12517287-12517288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567086959	chr7:12517292-12517293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564332053	chr7:12517422-12517423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
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
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12513600-12516200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr7:12515600-12521000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr7:12521000-12521400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr7:12521000-12521600	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr7:12521000-12521600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
6	chr7:12521000-12521800	Enhancers	Primary T cells from cord blood	blood
7	chr7:12521000-12522400	Enhancers	GM12878-XiMat	blood
8	chr7:12521200-12521400	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr7:12521400-12521800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr7:12521400-12521800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr7:12521400-12521800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
12	chr7:12521400-12522000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr7:12521400-12522400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr7:12521600-12521800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
15	chr7:12521600-12522000	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr7:12521800-12522000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
17	chr7:12521800-12522000	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr7:12521800-12522200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr7:12522400-12522600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr7:12528000-12528200	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr7:12528000-12528400	Enhancers	Brain Germinal Matrix	brain
22	chr7:12528200-12529400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr7:12528400-12528800	Enhancers	Fetal Brain Male	brain
24	chr7:12528400-12530800	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr7:12528600-12530200	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr7:12528600-12530400	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr7:12528800-12531000	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr7:12529200-12529800	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr7:12529200-12530400	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr7:12529400-12529600	Enhancers	K562	blood
31	chr7:12529400-12530000	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr7:12529600-12536600	Weak transcription	K562	blood
33	chr7:12530000-12530400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr7:12530400-12530600	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr7:12530400-12536600	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr7:12530600-12536600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr7:12530800-12536600	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr7:12531000-12536200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr7:12533000-12534000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr7:12533200-12533800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr7:12533400-12536600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
42	chr7:12533600-12533800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr7:12536200-12537400	Active TSS	iPS-15b Cell Line	embryonic stem cell
44	chr7:12536400-12536600	Enhancers	Hela-S3	cervix
45	chr7:12536400-12536800	Active TSS	Pancreatic Islets	Pancreatic Islet
46	chr7:12536600-12536800	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr7:12536600-12537200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
48	chr7:12536600-12537200	Active TSS	iPS-18 Cell Line	embryonic stem cell
49	chr7:12536600-12537200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr7:12536600-12537200	Active TSS	Muscle Satellite Cultured Cells	--

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