Variant report

Variant	esv1805167
Chromosome Location	chr7:6692073-6698297
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:139)
CpG islands
(count:671)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:139 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr7:6693791-6694049	GM12878	blood:	n/a	n/a
2	BCL3	chr7:6693271-6693492	GM12878	blood:	n/a	n/a
3	CCNT2	chr7:6694042-6694139	K562	blood:	n/a	n/a
4	ELF1	chr7:6694512-6694819	GM12878	blood:	n/a	n/a
5	ELF1	chr7:6693518-6693985	GM12878	blood:	n/a	n/a
6	GABPA	chr7:6693265-6693772	H1-hESC	embryonic stem cell:	n/a	n/a
7	GABPA	chr7:6693871-6694198	H1-hESC	embryonic stem cell:	n/a	n/a
8	HMGN3	chr7:6692437-6692466	K562	blood:	n/a	n/a
9	MTA3	chr7:6698232-6699458	GM12878	blood:	n/a	n/a
10	MYC	chr7:6696184-6696296	MCF-7	breast:	n/a	n/a
11	MYC	chr7:6693497-6693638	MCF-7	breast:	n/a	n/a
12	MYC	chr7:6692304-6692375	MCF-7	breast:	n/a	n/a
13	NFATC1	chr7:6697463-6697790	GM12878	blood:	n/a	n/a
14	NFATC1	chr7:6698086-6698995	GM12878	blood:	n/a	n/a
15	NFYB	chr7:6696321-6696616	GM12878	blood:	n/a	chr7:6696510-6696524 chr7:6696512-6696522 chr7:6696509-6696524 chr7:6696509-6696524 chr7:6696513-6696525 chr7:6696511-6696524 chr7:6696512-6696522
16	NFYB	chr7:6696292-6696642	K562	blood:	n/a	chr7:6696510-6696524 chr7:6696512-6696522 chr7:6696509-6696524 chr7:6696509-6696524 chr7:6696513-6696525 chr7:6696511-6696524 chr7:6696512-6696522
17	PAX5	chr7:6692399-6692566	GM12878	blood:	n/a	n/a
18	PAX5	chr7:6692282-6692683	GM12891	blood:	n/a	n/a
19	PAX5	chr7:6693740-6694153	GM12878	blood:	n/a	chr7:6693933-6693952
20	PAX5	chr7:6692292-6692760	GM12878	blood:	n/a	n/a
21	PAX5	chr7:6693717-6694116	GM12891	blood:	n/a	chr7:6693933-6693952
22	PAX5	chr7:6693823-6694038	GM12892	blood:	n/a	chr7:6693933-6693952
23	PAX5	chr7:6692203-6692749	GM12878	blood:	n/a	n/a
24	PAX5	chr7:6693471-6694164	GM12892	blood:	n/a	chr7:6693933-6693952
25	PAX5	chr7:6692302-6692682	GM12878	blood:	n/a	n/a
26	PAX5	chr7:6693543-6694257	GM12878	blood:	n/a	chr7:6693933-6693952
27	PAX5	chr7:6692099-6692801	GM12892	blood:	n/a	n/a
28	PAX5	chr7:6693715-6694061	GM12878	blood:	n/a	chr7:6693933-6693952
29	PBX3	chr7:6693289-6693652	GM12878	blood:	n/a	n/a
30	PBX3	chr7:6693877-6694030	GM12878	blood:	n/a	n/a
31	POLR2A	chr7:6692822-6693107	GM12878	blood:	n/a	n/a
32	POLR2A	chr7:6692152-6692184	K562	blood:	n/a	n/a
33	POLR2A	chr7:6693210-6694064	GM12878	blood:	n/a	n/a
34	POLR2A	chr7:6693515-6693701	MCF-7	breast:	n/a	n/a
35	POLR2A	chr7:6693843-6693956	K562	blood:	n/a	n/a
36	POLR2A	chr7:6695401-6695521	MCF-7	breast:	n/a	n/a
37	POLR2A	chr7:6696972-6697448	K562	blood:	n/a	n/a
38	POLR2A	chr7:6695299-6696002	GM12892	blood:	n/a	n/a
39	POLR2A	chr7:6693424-6693453	HUVEC	blood vessel:	n/a	n/a
40	POLR2A	chr7:6697345-6697450	MCF-7	breast:	n/a	n/a
41	POLR2A	chr7:6697882-6699303	SK-N-SH	brain:	n/a	n/a
42	POLR2A	chr7:6695500-6695512	MCF-7	breast:	n/a	n/a
43	POLR2A	chr7:6696611-6697422	HepG2	liver:	n/a	n/a
44	POLR2A	chr7:6695548-6695562	MCF-7	breast:	n/a	n/a
45	POLR2A	chr7:6697289-6697450	HUVEC	blood vessel:	n/a	n/a
46	POLR2A	chr7:6695333-6696019	GM12891	blood:	n/a	n/a
47	POLR2A	chr7:6694419-6698122	K562	blood:	n/a	n/a
48	POLR2A	chr7:6695246-6696805	K562	blood:	n/a	n/a
49	POLR2A	chr7:6697576-6697637	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr7:6696841-6697102	K562	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6692445-6692495	HCF	heart:	n/a
2	chr7:6694373-6694423	HL-60	blood:	n/a
3	chr7:6695092-6695142	PrEC	prostate:	n/a
4	chr7:6692873-6692923	NH-A	brain:	n/a
5	chr7:6696120-6696170	PrEC	prostate:	n/a
6	chr7:6692873-6692923	ovcar-3	ovarian:	n/a
7	chr7:6696120-6696170	GM06990	blood:	n/a
8	chr7:6693030-6693080	K562	blood:	n/a
9	chr7:6693334-6693384	U87	brain:	n/a
10	chr7:6693838-6693888	AG04450	lung:	fetal
11	chr7:6693838-6693888	HCF	heart:	n/a
12	chr7:6692873-6692923	ECC-1	luminal epithelium:	n/a
13	chr7:6694735-6694785	HCF	heart:	n/a
14	chr7:6694373-6694423	HMEC	breast:	n/a
15	chr7:6694373-6694423	AoSMC	blood vessel:	n/a
16	chr7:6696120-6696170	BJ	skin:	n/a
17	chr7:6694978-6695028	PANC-1	pancreas:	n/a
18	chr7:6693334-6693384	HRE	kidney:	n/a
19	chr7:6695092-6695142	GM06990	blood:	n/a
20	chr7:6693838-6693888	ECC-1	luminal epithelium:	n/a
21	chr7:6693838-6693888	MCF-7	breast:	n/a
22	chr7:6695092-6695142	RPTEC	kidney:	n/a
23	chr7:6695121-6695171	SK-N-MC	brain:	n/a
24	chr7:6694978-6695028	HepG2	liver:	n/a
25	chr7:6696120-6696170	HMEC	breast:	n/a
26	chr7:6693030-6693080	HL-60	blood:	n/a
27	chr7:6696120-6696170	U87	brain:	n/a
28	chr7:6696120-6696170	H1-hESC	embryonic stem cell:	embryo
29	chr7:6694978-6695028	IMR90	lung:	fetal
30	chr7:6694373-6694423	GM12891	blood:	n/a
31	chr7:6694735-6694785	ovcar-3	ovarian:	n/a
32	chr7:6693030-6693080	HEK293	kidney:	embryo
33	chr7:6693030-6693080	SAEC	small airway:	n/a
34	chr7:6692873-6692923	SKMC	muscle:	n/a
35	chr7:6693838-6693888	LNCaP	prostate:	n/a
36	chr7:6692445-6692495	AG10803	skin:	n/a
37	chr7:6692445-6692495	HMEC	breast:	n/a
38	chr7:6692873-6692923	HCM	heart:	n/a
39	chr7:6695121-6695171	GM12891	blood:	n/a
40	chr7:6694978-6695028	BE2_C	brain:	n/a
41	chr7:6692445-6692495	ProgFib	skin:	n/a
42	chr7:6694978-6695028	ProgFib	skin:	n/a
43	chr7:6692873-6692923	AG04450	lung:	fetal
44	chr7:6692445-6692495	SK-N-SH_RA	brain:	n/a
45	chr7:6693838-6693888	PrEC	prostate:	n/a
46	chr7:6693838-6693888	HCM	heart:	n/a
47	chr7:6693030-6693080	NHBE	bronchial:	n/a
48	chr7:6694978-6695028	A549	lung:	n/a
49	chr7:6694978-6695028	HIPEpiC	eye:	n/a
50	chr7:6696120-6696170	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr7:6674759..6677679-chr7:6692100..6694240,3	MCF-7	breast:
2	chr7:6694849..6698438-chr7:6699530..6702045,3	K562	blood:
3	chr7:6676518..6678447-chr7:6694438..6696514,2	MCF-7	breast:
4	chr7:6660093..6661828-chr7:6695492..6697100,2	MCF-7	breast:
5	chr7:6698245..6699981-chr7:6737287..6739036,2	MCF-7	breast:
6	chr7:6680998..6682837-chr7:6692889..6695214,2	MCF-7	breast:
7	chr7:6675838..6678415-chr7:6696567..6699140,4	MCF-7	breast:
8	chr7:6688371..6689911-chr7:6696909..6698726,2	K562	blood:
9	chr7:6679487..6682483-chr7:6695124..6696654,2	MCF-7	breast:
10	chr7:6696313..6698315-chr7:6745284..6746997,2	K562	blood:
11	chr7:6692466..6696366-chr7:6696714..6698992,3	MCF-7	breast:
12	chr7:6681267..6684799-chr7:6697447..6700610,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC073343.1-2	chr7:6694495-6696063	ENSG00000260054.1

No data

Variant related genes	Relation type
ENSG00000260054	TF binding region
ENSG00000260054	CpG island
ENSG00000205903	chromatin interactions
ENSG00000164631	chromatin interactions
ENSG00000260054	chromatin interactions

Extended variants
information (count: 257 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:257 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558639787	chr7:6692082-6692083	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs62439671	chr7:6692096-6692097	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs3735302	chr7:6692105-6692106	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs189975373	chr7:6692137-6692138	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs575646947	chr7:6692142-6692143	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs542820737	chr7:6692151-6692152	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs554793791	chr7:6692203-6692204	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs572839621	chr7:6692227-6692228	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs369484052	chr7:6692229-6692230	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs373742099	chr7:6692247-6692248	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs564679858	chr7:6692261-6692262	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs576451588	chr7:6692277-6692278	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs376495708	chr7:6692291-6692292	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs562825244	chr7:6692353-6692354	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs530373612	chr7:6692367-6692368	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs548489831	chr7:6692379-6692380	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs560747381	chr7:6692432-6692433	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs527738311	chr7:6692441-6692442	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs142128577	chr7:6692445-6692446	Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs570828662	chr7:6692453-6692454	Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs538228318	chr7:6692520-6692521	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs550230193	chr7:6692539-6692540	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs372507837	chr7:6692586-6692587	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs1474419	chr7:6692605-6692606	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs536588168	chr7:6692607-6692608	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs111969111	chr7:6692677-6692678	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs554424733	chr7:6692762-6692763	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs572995417	chr7:6692784-6692785	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs533623472	chr7:6692866-6692867	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs201597524	chr7:6692886-6692887	Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs558246420	chr7:6692928-6692929	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs576563252	chr7:6692933-6692934	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs543783463	chr7:6693009-6693010	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs112309818	chr7:6693102-6693103	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs181376207	chr7:6693114-6693115	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs574752465	chr7:6693147-6693148	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs186574282	chr7:6693160-6693161	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs560452714	chr7:6693165-6693166	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs527903972	chr7:6693342-6693343	Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs12533369	chr7:6693427-6693428	Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs6979882	chr7:6693438-6693439	Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs111851769	chr7:6693552-6693553	Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs564551833	chr7:6693621-6693622	Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs531886101	chr7:6693654-6693655	Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs2464875	chr7:6693775-6693776	Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs550187610	chr7:6693864-6693865	Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs568471883	chr7:6693910-6693911	Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs536108327	chr7:6693944-6693945	Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs548485488	chr7:6693975-6693976	Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs140137220	chr7:6694055-6694056	Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Autism	20685689	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6678200-6698200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr7:6679000-6692200	Strong transcription	Primary T cells from cord blood	blood
3	chr7:6679000-6692600	Strong transcription	Primary B cells from peripheral blood	blood
4	chr7:6679000-6695200	Strong transcription	Stomach Smooth Muscle	stomach
5	chr7:6679000-6695400	Strong transcription	Brain Inferior Temporal Lobe	brain
6	chr7:6679200-6695400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr7:6679400-6696400	Strong transcription	Brain Hippocampus Middle	brain
8	chr7:6679400-6703600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr7:6679600-6693200	Strong transcription	Rectal Smooth Muscle	rectum
10	chr7:6679600-6699200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr7:6679800-6695600	Strong transcription	Primary T helper cells fromperipheralblood	blood
12	chr7:6680000-6692600	Strong transcription	Primary T helper cells PMA-I stimulated	--
13	chr7:6680000-6692600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr7:6680000-6695200	Strong transcription	Duodenum Mucosa	Duodenum
15	chr7:6680400-6694600	Strong transcription	Brain Cingulate Gyrus	brain
16	chr7:6680400-6695200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr7:6680400-6695600	Strong transcription	Rectal Mucosa Donor 29	rectum
18	chr7:6680400-6698600	Weak transcription	Right Atrium	heart
19	chr7:6680600-6692600	Strong transcription	Primary T cells fromperipheralblood	blood
20	chr7:6680600-6695200	Strong transcription	Duodenum Smooth Muscle	Duodenum
21	chr7:6680600-6695400	Strong transcription	Brain Anterior Caudate	brain
22	chr7:6680800-6692400	Strong transcription	Skeletal Muscle Female	skeletal muscle
23	chr7:6681000-6693400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr7:6682400-6698800	Weak transcription	Fetal Kidney	kidney
25	chr7:6683200-6693400	Weak transcription	Stomach Mucosa	stomach
26	chr7:6683800-6696600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
27	chr7:6684600-6694000	Weak transcription	NHDF-Ad	bronchial
28	chr7:6684600-6698200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr7:6684800-6699000	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr7:6685600-6695600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr7:6686200-6692200	Weak transcription	NHEK	skin
32	chr7:6686800-6695600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
33	chr7:6687000-6692400	ZNF genes & repeats	GM12878-XiMat	blood
34	chr7:6687400-6692600	Strong transcription	Fetal Muscle Trunk	muscle
35	chr7:6687400-6693000	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
36	chr7:6687800-6692600	Strong transcription	Brain Substantia Nigra	brain
37	chr7:6687800-6692600	ZNF genes & repeats	Fetal Stomach	stomach
38	chr7:6687800-6695200	ZNF genes & repeats	Fetal Intestine Large	intestine
39	chr7:6687800-6695400	Strong transcription	Right Ventricle	heart
40	chr7:6687800-6695800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr7:6687800-6696600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr7:6688000-6693200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
43	chr7:6688000-6693200	Strong transcription	Fetal Lung	lung
44	chr7:6688000-6695800	Strong transcription	Skeletal Muscle Male	skeletal muscle
45	chr7:6688600-6692400	Strong transcription	Left Ventricle	heart
46	chr7:6688600-6695600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr7:6688800-6693000	ZNF genes & repeats	Primary B cells from cord blood	blood
48	chr7:6689000-6694600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr7:6689000-6695400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr7:6689000-6696000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin

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