Variant report

Variant	nsv966930
Chromosome Location	chr7:56440900-56461705
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:299)
CpG islands
(count:307)
Chromatin interactive
region (count:0)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:299 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr7:56440976-56442496	GM12878	blood:	n/a	n/a
2	BATF	chr7:56442645-56442830	GM12878	blood:	n/a	n/a
3	BATF	chr7:56441021-56441428	GM12878	blood:	n/a	n/a
4	BATF	chr7:56441464-56441866	GM12878	blood:	n/a	n/a
5	BATF	chr7:56450946-56451228	GM12878	blood:	n/a	n/a
6	BCL11A	chr7:56440912-56442515	GM12878	blood:	n/a	n/a
7	BCL11A	chr7:56440941-56442557	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:56440907-56441906	HepG2	liver:	n/a	n/a
9	BHLHE40	chr7:56442086-56442477	HepG2	liver:	n/a	n/a
10	BRCA1	chr7:56441064-56441264	GM12878	blood:	n/a	n/a
11	CBX3	chr7:56441554-56442520	K562	blood:	n/a	n/a
12	CBX3	chr7:56440964-56441418	K562	blood:	n/a	n/a
13	CBX3	chr7:56440971-56442559	K562	blood:	n/a	n/a
14	CHD1	chr7:56441237-56441247	GM12878	blood:	n/a	n/a
15	CHD2	chr7:56441230-56441262	GM12878	blood:	n/a	n/a
16	CHD2	chr7:56441229-56441247	K562	blood:	n/a	n/a
17	CTCF	chr7:56441453-56441936	K562	blood:	n/a	n/a
18	CTCF	chr7:56441234-56441259	LNCaP	prostate:	n/a	n/a
19	CTCF	chr7:56442004-56442453	K562	blood:	n/a	n/a
20	CTCF	chr7:56441227-56441296	A549	lung:	n/a	n/a
21	CTCF	chr7:56441100-56441250	GM06990	blood:	n/a	n/a
22	CTCF	chr7:56448962-56449041	LNCaP	prostate:	n/a	n/a
23	CTCF	chr7:56441140-56441290	HA-sp	spinal cord:	n/a	n/a
24	CTCF	chr7:56441180-56441330	HFF-Myc	foreskin:	n/a	n/a
25	CTCF	chr7:56441160-56441310	HepG2	liver:	n/a	n/a
26	CTCF	chr7:56441100-56441250	HPF	lung:	n/a	n/a
27	CTCF	chr7:56445362-56445944	K562	blood:	n/a	chr7:56445507-56445520 chr7:56445507-56445516 chr7:56445506-56445527 chr7:56445509-56445519 chr7:56445448-56445461 chr7:56445504-56445522 chr7:56445763-56445781
28	CTCF	chr7:56441100-56441250	HA-sp	spinal cord:	n/a	n/a
29	CTCF	chr7:56441566-56441838	K562	blood:	n/a	n/a
30	CTCF	chr7:56441100-56441250	GM12872	blood:	n/a	n/a
31	CTCF	chr7:56442480-56442630	GM12867	blood:	n/a	n/a
32	CTCF	chr7:56454040-56454153	LNCaP	prostate:	n/a	n/a
33	CTCF	chr7:56441214-56441249	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr7:56446724-56447076	K562	blood:	n/a	n/a
35	CTCF	chr7:56441100-56441250	SAEC	small airway:	n/a	n/a
36	CTCF	chr7:56441120-56441270	AG04449	skin:	n/a	n/a
37	CTCF	chr7:56445216-56445941	K562	blood:	n/a	chr7:56445507-56445520 chr7:56445507-56445516 chr7:56445506-56445527 chr7:56445509-56445519 chr7:56445448-56445461 chr7:56445504-56445522 chr7:56445763-56445781
38	CTCF	chr7:56441100-56441250	HL-60	blood:	n/a	n/a
39	CTCF	chr7:56441160-56441310	RPTEC	kidney:	n/a	n/a
40	CTCF	chr7:56457900-56458050	NB4	blood:	n/a	chr7:56457962-56457972 chr7:56457954-56457975 chr7:56457959-56457977
41	CTCF	chr7:56441120-56441270	GM12866	blood:	n/a	n/a
42	CTCF	chr7:56441160-56441310	AG09309	skin:	n/a	n/a
43	CTCF	chr7:56441100-56441250	GM12878	blood:	n/a	n/a
44	CTCF	chr7:56441160-56441310	GM12869	blood:	n/a	n/a
45	CTCF	chr7:56441221-56441277	Gliobla	brain:	n/a	n/a
46	CTCF	chr7:56441120-56441270	GM12869	blood:	n/a	n/a
47	CTCF	chr7:56441120-56441270	GM12872	blood:	n/a	n/a
48	CTCF	chr7:56441140-56441290	BE2_C	brain:	n/a	n/a
49	CTCF	chr7:56441100-56441250	GM12874	blood:	n/a	n/a
50	CTCF	chr7:56445363-56445922	K562	blood:	n/a	chr7:56445507-56445520 chr7:56445507-56445516 chr7:56445506-56445527 chr7:56445509-56445519 chr7:56445448-56445461 chr7:56445504-56445522 chr7:56445763-56445781

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:56450073-56450123	SK-N-MC	brain:	n/a
2	chr7:56450073-56450123	HRCEpiC	kidney:	n/a
3	chr7:56450073-56450123	SK-N-MC	brain:	n/a
4	chr7:56450073-56450123	HRCEpiC	kidney:	n/a
5	chr7:56446385-56446435	NHBE	bronchial:	n/a
6	chr7:56450073-56450123	NH-A	brain:	n/a
7	chr7:56450073-56450123	GM12891	blood:	n/a
8	chr7:56446176-56446226	GM19239	blood:	n/a
9	chr7:56449947-56449997	T-47D	breast:	n/a
10	chr7:56450073-56450123	BJ	skin:	n/a
11	chr7:56450073-56450123	HRPEpiC	eye:	n/a
12	chr7:56446385-56446435	A549	lung:	n/a
13	chr7:56450073-56450123	ECC-1	luminal epithelium:	n/a
14	chr7:56450073-56450123	NHBE	bronchial:	n/a
15	chr7:56446385-56446435	AG04449	skin:	fetal
16	chr7:56449947-56449997	SAEC	small airway:	n/a
17	chr7:56442537-56442587	HEK293	kidney:	embryo
18	chr7:56449947-56449997	GM12878	blood:	n/a
19	chr7:56450073-56450123	PrEC	prostate:	n/a
20	chr7:56450073-56450123	AG09309	skin:	n/a
21	chr7:56446385-56446435	HRE	kidney:	n/a
22	chr7:56442537-56442587	RPTEC	kidney:	n/a
23	chr7:56449947-56449997	AG09309	skin:	n/a
24	chr7:56450073-56450123	AG04450	lung:	fetal
25	chr7:56449947-56449997	HCT-116	colon:	n/a
26	chr7:56442537-56442587	AG10803	skin:	n/a
27	chr7:56450073-56450123	HCT-116	colon:	n/a
28	chr7:56442537-56442587	T-47D	breast:	n/a
29	chr7:56450073-56450123	Hepatocyte	liver:	n/a
30	chr7:56446385-56446435	AG09319	gingival:	n/a
31	chr7:56446176-56446226	SK-N-SH	brain:	n/a
32	chr7:56449947-56449997	Caco-2	colon:	n/a
33	chr7:56446385-56446435	HEK293	kidney:	embryo
34	chr7:56446176-56446226	HRE	kidney:	n/a
35	chr7:56442537-56442587	HCF	heart:	n/a
36	chr7:56446176-56446226	PANC-1	pancreas:	n/a
37	chr7:56449947-56449997	BE2_C	brain:	n/a
38	chr7:56449947-56449997	NHDF-neo	bronchial:	n/a
39	chr7:56442537-56442587	SK-N-MC	brain:	n/a
40	chr7:56446176-56446226	H1-hESC	embryonic stem cell:	embryo
41	chr7:56449947-56449997	Hela-S3	cervix:	n/a
42	chr7:56442537-56442587	NHBE	bronchial:	n/a
43	chr7:56449947-56449997	MCF10A-Er-Src	breast:	n/a
44	chr7:56446176-56446226	HNPCEpiC	eye:	n/a
45	chr7:56450073-56450123	HAEpiC	amniotic membrane:	n/a
46	chr7:56446176-56446226	U87	brain:	n/a
47	chr7:56446176-56446226	SAEC	small airway:	n/a
48	chr7:56446385-56446435	GM12892	blood:	n/a
49	chr7:56442537-56442587	A549	lung:	n/a
50	chr7:56442537-56442587	GM12878	blood:	n/a

No data

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SUMF2-13	chr7:56448669-56449005	NONHSAT120750
2	lnc-RP4-725G10.1.1-2	chr7:56448433-56448602	XLOC_006455
3	lnc-RP4-725G10.1.1-2	chr7:56446322-56446398	XLOC_006455
4	lnc-RP4-725G10.1.1-2	chr7:56446010-56446229	XLOC_006455
5	lnc-RP4-725G10.1.1-2	chr7:56446340-56446379	XLOC_006455

No data

Variant related genes	Relation type
ENSG00000224370	TF binding region
ENSG00000224370	CpG island

Extended variants
information (count: 317 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:317 , 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	rs539344606	chr7:56440916-56440917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs202106937	chr7:56440919-56440920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559340924	chr7:56440951-56440952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs376807163	chr7:56440952-56440953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374403202	chr7:56440970-56440971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368332465	chr7:56440989-56440990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs4612295	chr7:56441084-56441085	ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs4072174	chr7:56441202-56441203	ZNF genes & repeats Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
9	rs375403262	chr7:56441240-56441241	ZNF genes & repeats Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
10	rs575892368	chr7:56441309-56441310	ZNF genes & repeats Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
11	rs4618651	chr7:56441366-56441367	ZNF genes & repeats Active TSS Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
12	rs4281080	chr7:56441454-56441455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs4398857	chr7:56441464-56441465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs4078490	chr7:56441501-56441502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4281081	chr7:56441503-56441504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs4339585	chr7:56441546-56441547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371714593	chr7:56441600-56441601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200183754	chr7:56441648-56441649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575840626	chr7:56441902-56441903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200623437	chr7:56441903-56441904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143274241	chr7:56442025-56442026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542892013	chr7:56442056-56442057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369320622	chr7:56442061-56442062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs71255685	chr7:56442160-56442161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561539515	chr7:56442161-56442162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528616021	chr7:56442183-56442184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs111505459	chr7:56442225-56442226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540349554	chr7:56442302-56442303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565001981	chr7:56442303-56442304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532402949	chr7:56442310-56442311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372018657	chr7:56442344-56442345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569896742	chr7:56442359-56442360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530845657	chr7:56442374-56442375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548961662	chr7:56442399-56442400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567478699	chr7:56442430-56442431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534777861	chr7:56442439-56442440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs377152893	chr7:56442440-56442441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553138669	chr7:56442454-56442455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs71545711	chr7:56442455-56442456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201288041	chr7:56442472-56442473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538685592	chr7:56442519-56442520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556905786	chr7:56442529-56442530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs374535322	chr7:56442534-56442535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181815632	chr7:56442537-56442538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377457311	chr7:56442540-56442541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536955955	chr7:56442541-56442542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549068189	chr7:56442545-56442546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186595582	chr7:56442548-56442549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573114884	chr7:56442560-56442561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540408930	chr7:56442563-56442564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Wilms tumour	21544195	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
Breast cancer	21364760	CNVD
Esophageal cancer	21851588	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
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Intracranial ependymoma	16609018	CNVD
Lung cancer	21911935	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17925434	CNVD
Glioma	24330732	CNVD
Lung adenocarcinoma	23938291	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
Medullary thyroid carcinoma	18765511	CNVD
small cell lung cancer	20016488	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:56439800-56441000	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr7:56439800-56441000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:56439800-56441000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr7:56439800-56441000	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr7:56439800-56441000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr7:56439800-56441000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr7:56439800-56441000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr7:56439800-56441000	Weak transcription	Aorta	Aorta
9	chr7:56439800-56441000	Weak transcription	Duodenum Mucosa	Duodenum
10	chr7:56439800-56441000	Weak transcription	Fetal Stomach	stomach
11	chr7:56439800-56441000	Weak transcription	Gastric	stomach
12	chr7:56439800-56441000	Weak transcription	Left Ventricle	heart
13	chr7:56439800-56441000	Weak transcription	Lung	lung
14	chr7:56439800-56441000	Weak transcription	Ovary	ovary
15	chr7:56439800-56441000	Weak transcription	Right Ventricle	heart
16	chr7:56439800-56441000	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr7:56439800-56441000	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr7:56439800-56441000	Weak transcription	Thymus	Thymus
19	chr7:56439800-56441000	Weak transcription	Spleen	Spleen
20	chr7:56439800-56441000	Weak transcription	Dnd41	blood
21	chr7:56439800-56442800	Weak transcription	Right Atrium	heart
22	chr7:56441000-56441200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr7:56441000-56441200	ZNF genes & repeats	Fetal Muscle Leg	muscle
24	chr7:56441000-56441200	Flanking Bivalent TSS/Enh	Placenta	Placenta
25	chr7:56441000-56441400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
26	chr7:56441000-56441400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr7:56441000-56441400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr7:56441000-56441400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
29	chr7:56441000-56441400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
30	chr7:56441000-56441400	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
31	chr7:56441000-56441400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
32	chr7:56441000-56441400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr7:56441000-56441400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr7:56441000-56441400	Active TSS	Primary T cells from cord blood	blood
35	chr7:56441000-56441400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
36	chr7:56441000-56441400	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
37	chr7:56441000-56441400	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
38	chr7:56441000-56441400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr7:56441000-56441400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
40	chr7:56441000-56441400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr7:56441000-56441400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr7:56441000-56441400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr7:56441000-56441400	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr7:56441000-56441400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr7:56441000-56441400	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
46	chr7:56441000-56441400	ZNF genes & repeats	Adipose Nuclei	Adipose
47	chr7:56441000-56441400	ZNF genes & repeats	Aorta	Aorta
48	chr7:56441000-56441400	ZNF genes & repeats	Liver	Liver
49	chr7:56441000-56441400	ZNF genes & repeats	Brain Anterior Caudate	brain
50	chr7:56441000-56441400	ZNF genes & repeats	Brain Germinal Matrix	brain

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