Variant report

Variant	esv15840
Chromosome Location	chr7:57668539-57710061
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:163)
CpG islands
(count:366)
Chromatin interactive
region (count:0)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:163 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:57698544-57698607	HepG2	liver:	n/a	n/a
2	BACH1	chr7:57708717-57708917	K562	blood:	n/a	n/a
3	BHLHE40	chr7:57708547-57708919	K562	blood:	n/a	n/a
4	BRCA1	chr7:57698528-57698644	HepG2	liver:	n/a	n/a
5	CEBPB	chr7:57708544-57708746	K562	blood:	n/a	n/a
6	CEBPB	chr7:57695840-57696024	A549	lung:	n/a	n/a
7	CHD2	chr7:57708603-57708917	K562	blood:	n/a	n/a
8	CHD2	chr7:57698601-57698644	HepG2	liver:	n/a	n/a
9	CTCF	chr7:57683975-57684045	GM20000	blood:	n/a	n/a
10	CTCF	chr7:57684560-57684627	LNCaP	prostate:	n/a	n/a
11	CTCF	chr7:57704941-57704999	GM10266	blood:	n/a	n/a
12	CTCF	chr7:57707457-57707520	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr7:57699200-57699350	GM12873	blood:	n/a	n/a
14	CTCF	chr7:57703880-57703942	Kidney_OC	kidney:	n/a	n/a
15	CTCF	chr7:57703820-57703970	GM12873	blood:	n/a	n/a
16	CTCF	chr7:57698460-57698610	WI-38	lung:	n/a	n/a
17	CTCF	chr7:57680531-57680580	LNCaP	prostate:	n/a	n/a
18	CTCF	chr7:57671898-57672015	LNCaP	prostate:	n/a	n/a
19	CTCF	chr7:57695600-57695750	HEEpiC	esophagus:	n/a	n/a
20	CTCF	chr7:57695600-57695750	AG09309	skin:	n/a	n/a
21	CTCF	chr7:57705060-57705062	GM10248	blood:	n/a	n/a
22	CTCF	chr7:57708717-57708744	K562	blood:	n/a	n/a
23	CTCF	chr7:57704996-57705057	GM10248	blood:	n/a	n/a
24	CTCF	chr7:57696460-57696610	AG09309	skin:	n/a	n/a
25	CUX1	chr7:57708547-57708917	K562	blood:	n/a	n/a
26	ELK1	chr7:57708719-57708918	K562	blood:	n/a	n/a
27	EP300	chr7:57699512-57699873	GM12878	blood:	n/a	chr7:57699782-57699792
28	FOSL2	chr7:57696452-57696980	HepG2	liver:	n/a	n/a
29	FOSL2	chr7:57694659-57694963	HepG2	liver:	n/a	n/a
30	FOSL2	chr7:57699358-57699797	HepG2	liver:	n/a	n/a
31	FOSL2	chr7:57684614-57684939	HepG2	liver:	n/a	n/a
32	FOSL2	chr7:57679258-57679554	HepG2	liver:	n/a	n/a
33	FOSL2	chr7:57686735-57687524	HepG2	liver:	n/a	n/a
34	FOSL2	chr7:57683879-57684233	HepG2	liver:	n/a	n/a
35	FOSL2	chr7:57690659-57690903	HepG2	liver:	n/a	n/a
36	FOSL2	chr7:57673789-57674106	HepG2	liver:	n/a	n/a
37	FOSL2	chr7:57677704-57677957	HepG2	liver:	n/a	n/a
38	FOSL2	chr7:57700226-57700588	HepG2	liver:	n/a	n/a
39	FOSL2	chr7:57685016-57685273	HepG2	liver:	n/a	n/a
40	FOXA1	chr7:57699628-57699955	HepG2	liver:	n/a	chr7:57699779-57699791
41	FOXA1	chr7:57708987-57709144	T-47D	breast:	n/a	n/a
42	GABPA	chr7:57696554-57696931	Hela-S3	cervix:	n/a	n/a
43	HCFC1	chr7:57708709-57708747	K562	blood:	n/a	n/a
44	HEY1	chr7:57708573-57708861	K562	blood:	n/a	n/a
45	HEY1	chr7:57708574-57708880	K562	blood:	n/a	n/a
46	IRF4	chr7:57696300-57696737	GM12878	blood:	n/a	n/a
47	JUND	chr7:57679275-57679431	HepG2	liver:	n/a	n/a
48	JUND	chr7:57708548-57708918	K562	blood:	n/a	n/a
49	JUND	chr7:57699364-57699554	HepG2	liver:	n/a	n/a
50	JUND	chr7:57696532-57696722	HepG2	liver:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:57688265-57688315	RPTEC	kidney:	n/a
2	chr7:57698643-57698693	H1-hESC	embryonic stem cell:	embryo
3	chr7:57705910-57705960	HCM	heart:	n/a
4	chr7:57707202-57707252	NH-A	brain:	n/a
5	chr7:57706707-57706757	Caco-2	colon:	n/a
6	chr7:57705910-57705960	BJ	skin:	n/a
7	chr7:57698643-57698693	U87	brain:	n/a
8	chr7:57688265-57688315	GM12891	blood:	n/a
9	chr7:57707202-57707252	MCF-7	breast:	n/a
10	chr7:57707202-57707252	RPTEC	kidney:	n/a
11	chr7:57707202-57707252	SK-N-SH	brain:	n/a
12	chr7:57705910-57705960	ovcar-3	ovarian:	n/a
13	chr7:57705701-57705751	T-47D	breast:	n/a
14	chr7:57707202-57707252	PrEC	prostate:	n/a
15	chr7:57705910-57705960	HPAEpiC	pulmonary alveolar:	n/a
16	chr7:57707202-57707252	HRE	kidney:	n/a
17	chr7:57705701-57705751	A549	lung:	n/a
18	chr7:57706707-57706757	PrEC	prostate:	n/a
19	chr7:57698643-57698693	HepG2	liver:	n/a
20	chr7:57688265-57688315	NHBE	bronchial:	n/a
21	chr7:57688265-57688315	LNCaP	prostate:	n/a
22	chr7:57705910-57705960	GM12892	blood:	n/a
23	chr7:57705701-57705751	HRCEpiC	kidney:	n/a
24	chr7:57705910-57705960	NT2-D1	testis:	n/a
25	chr7:57688265-57688315	MCF-7	breast:	n/a
26	chr7:57698643-57698693	PFSK-1	brain:	n/a
27	chr7:57707202-57707252	NHDF-neo	bronchial:	n/a
28	chr7:57707202-57707252	NT2-D1	testis:	n/a
29	chr7:57705910-57705960	Hela-S3	cervix:	n/a
30	chr7:57707202-57707252	HL-60	blood:	n/a
31	chr7:57705701-57705751	BE2_C	brain:	n/a
32	chr7:57688265-57688315	HEEpiC	esophagus:	n/a
33	chr7:57688265-57688315	HIPEpiC	eye:	n/a
34	chr7:57705910-57705960	HNPCEpiC	eye:	n/a
35	chr7:57705701-57705751	ovcar-3	ovarian:	n/a
36	chr7:57688265-57688315	SK-N-SH	brain:	n/a
37	chr7:57698643-57698693	AG09319	gingival:	n/a
38	chr7:57706707-57706757	U87	brain:	n/a
39	chr7:57705910-57705960	HEK293	kidney:	embryo
40	chr7:57707202-57707252	AG09309	skin:	n/a
41	chr7:57688265-57688315	GM19239	blood:	n/a
42	chr7:57698643-57698693	HRE	kidney:	n/a
43	chr7:57698643-57698693	BJ	skin:	n/a
44	chr7:57688265-57688315	HNPCEpiC	eye:	n/a
45	chr7:57707202-57707252	HepG2	liver:	n/a
46	chr7:57705701-57705751	K562	blood:	n/a
47	chr7:57707202-57707252	GM19239	blood:	n/a
48	chr7:57698643-57698693	AG04450	lung:	fetal
49	chr7:57698643-57698693	HAEpiC	amniotic membrane:	n/a
50	chr7:57705701-57705751	PANC-1	pancreas:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF479-8	chr7:57703364-57703554	NONHSAT120850
2	lnc-ZNF479-8	chr7:57689787-57689961	NONHSAT120850
3	lnc-ZNF479-8	chr7:57696817-57696916	NONHSAT120850
4	lnc-ZNF479-8	chr7:57704747-57704895	NONHSAT120850
5	lnc-ZNF479-8	chr7:57689759-57689983	NONHSAT120847
6	lnc-ZNF479-8	chr7:57688185-57688268	NONHSAT120847
7	lnc-ZNF479-8	chr7:57688668-57688812	NONHSAT120848
8	lnc-ZNF479-8	chr7:57701610-57701660	NONHSAT120847
9	lnc-ZNF479-8	chr7:57689759-57689961	NONHSAT120848
10	lnc-ZNF479-8	chr7:57696818-57696916	NONHSAT120847
11	lnc-ZNF479-8	chr7:57703900-57703975	NONHSAT120850
12	lnc-ZNF479-8	chr7:57696817-57696917	NONHSAT120848

No data

Variant related genes	Relation type
ENSG00000237639	TF binding region
ENSG00000234085	TF binding region
ENSG00000229627	TF binding region
ENSG00000270749	TF binding region
ENSG00000243981	TF binding region
ENSG00000236261	TF binding region
ENSG00000237639	CpG island
ENSG00000234085	CpG island
ENSG00000229627	CpG island
ENSG00000270749	CpG island
ENSG00000243981	CpG island
ENSG00000236261	CpG island

Extended variants
information (count: 1294 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1294 , 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	rs4079171	chr7:57684829-57684830	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs62450194	chr7:57684842-57684843	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs113334011	chr7:57684987-57684988	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs199565488	chr7:57685175-57685176	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs141881598	chr7:57685796-57685797	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs550895918	chr7:57685804-57685805	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs201370641	chr7:57685816-57685817	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs535998306	chr7:57685817-57685818	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs548148108	chr7:57685854-57685855	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs376399882	chr7:57686750-57686751	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs534071408	chr7:57686765-57686766	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs199666989	chr7:57686927-57686928	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs200660681	chr7:57686930-57686931	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs190037027	chr7:57686989-57686990	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs183111495	chr7:57687009-57687010	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs558852757	chr7:57687031-57687032	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs186852512	chr7:57687033-57687034	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs191642520	chr7:57687056-57687057	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs577215774	chr7:57687061-57687062	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs183894600	chr7:57687069-57687070	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs199833493	chr7:57687088-57687089	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs200690497	chr7:57687089-57687090	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs538012472	chr7:57687092-57687093	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs556098855	chr7:57687106-57687107	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs575676482	chr7:57687141-57687142	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs201560097	chr7:57687183-57687184	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs542779727	chr7:57687284-57687285	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs200036335	chr7:57687354-57687355	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs1890863	chr7:57688308-57688309	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs113440720	chr7:57688688-57688689	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs368366277	chr7:57688697-57688698	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs371339338	chr7:57688703-57688704	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs373983715	chr7:57688726-57688727	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs544479345	chr7:57688793-57688794	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs376310191	chr7:57688794-57688795	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs540240982	chr7:57689864-57689865	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs200565476	chr7:57693734-57693735	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs201293501	chr7:57693798-57693799	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs202050978	chr7:57693976-57693977	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs111393497	chr7:57694005-57694006	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs369674794	chr7:57694481-57694482	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs201468454	chr7:57694518-57694519	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs199736564	chr7:57694562-57694563	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs62450200	chr7:57694618-57694619	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs62450201	chr7:57694650-57694651	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs111580307	chr7:57694668-57694669	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs201353465	chr7:57694714-57694715	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs62450202	chr7:57694736-57694737	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs62450203	chr7:57694821-57694822	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs111632664	chr7:57694822-57694823	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	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
Esophageal squamous carcinoma	21637470	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
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Biliary cancer	19435499	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Glioma	17634744	CNVD
Oral squamous cell carcinoma	19276369	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Lung cancer	20031968	CNVD
Glioblastoma	17090523	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Glioma	17123091	CNVD
Hodgkin''s lymphoma	18641027	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:57695600-57695800	Enhancers	Spleen	Spleen
2	chr7:57696400-57696600	ZNF genes & repeats	Fetal Kidney	kidney
3	chr7:57697800-57698800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
4	chr7:57697800-57698800	ZNF genes & repeats	Adipose Nuclei	Adipose
5	chr7:57697800-57699000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
6	chr7:57697800-57699400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
7	chr7:57698000-57698600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr7:57698000-57698800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr7:57698000-57698800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr7:57698000-57698800	ZNF genes & repeats	Esophagus	oesophagus
11	chr7:57698000-57698800	ZNF genes & repeats	Gastric	stomach
12	chr7:57698000-57698800	ZNF genes & repeats	Pancreas	Pancrea
13	chr7:57698000-57699400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
14	chr7:57698200-57698800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr7:57698400-57698800	ZNF genes & repeats	Fetal Stomach	stomach
16	chr7:57698400-57699000	ZNF genes & repeats	Brain Anterior Caudate	brain
17	chr7:57698600-57698800	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
18	chr7:57698800-57701200	Weak transcription	Gastric	stomach
19	chr7:57698800-57701200	Weak transcription	Pancreas	Pancrea
20	chr7:57699000-57701400	Weak transcription	Brain Anterior Caudate	brain
21	chr7:57701200-57701600	Active TSS	Primary T cells from cord blood	blood
22	chr7:57701200-57701800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
23	chr7:57701200-57701800	ZNF genes & repeats	Fetal Brain Male	brain
24	chr7:57701200-57701800	ZNF genes & repeats	Gastric	stomach
25	chr7:57701200-57701800	ZNF genes & repeats	Pancreas	Pancrea
26	chr7:57701200-57704000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
27	chr7:57701400-57701600	ZNF genes & repeats	Fetal Heart	heart
28	chr7:57701400-57701800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr7:57701400-57701800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
30	chr7:57701400-57701800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr7:57701400-57701800	ZNF genes & repeats	Brain Anterior Caudate	brain
32	chr7:57701400-57701800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
33	chr7:57701400-57702000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr7:57701600-57701800	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
35	chr7:57701600-57701800	ZNF genes & repeats	Colonic Mucosa	Colon
36	chr7:57701800-57703000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr7:57703000-57703800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr7:57705600-57707000	Active TSS	K562	blood
39	chr7:57705800-57710200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
40	chr7:57705800-57716600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
41	chr7:57706000-57715600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr7:57706400-57713800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr7:57707000-57707200	Flanking Active TSS	K562	blood
44	chr7:57707200-57708600	Weak transcription	K562	blood
45	chr7:57707400-57711000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
46	chr7:57708400-57709400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
47	chr7:57708400-57710200	ZNF genes & repeats	Duodenum Mucosa	Duodenum
48	chr7:57708400-57712200	ZNF genes & repeats	Adipose Nuclei	Adipose
49	chr7:57708600-57709000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr7:57708600-57709000	Active TSS	K562	blood

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