Variant report

Variant	nsv1015143
Chromosome Location	chr8:43413955-43824036
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3938)
CpG islands
(count:306)
Chromatin interactive
region (count:2)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3938 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:43819080-43819187	K562	blood:	n/a	n/a
2	ATF1	chr8:43785555-43785668	K562	blood:	n/a	n/a
3	ATF1	chr8:43786577-43787136	K562	blood:	n/a	n/a
4	ATF1	chr8:43792645-43793396	K562	blood:	n/a	n/a
5	BACH1	chr8:43818947-43819136	K562	blood:	n/a	n/a
6	BACH1	chr8:43572418-43572443	K562	blood:	n/a	n/a
7	BACH1	chr8:43790059-43790248	K562	blood:	n/a	n/a
8	BACH1	chr8:43779446-43779599	K562	blood:	n/a	n/a
9	BACH1	chr8:43820379-43820751	K562	blood:	n/a	n/a
10	BACH1	chr8:43654724-43654750	K562	blood:	n/a	n/a
11	BACH1	chr8:43717526-43717725	K562	blood:	n/a	n/a
12	BATF	chr8:43772038-43772467	GM12878	blood:	n/a	n/a
13	BATF	chr8:43760193-43760718	GM12878	blood:	n/a	n/a
14	BATF	chr8:43823636-43824118	GM12878	blood:	n/a	n/a
15	BATF	chr8:43781687-43781911	GM12878	blood:	n/a	n/a
16	BATF	chr8:43796850-43797049	GM12878	blood:	n/a	n/a
17	BATF	chr8:43761295-43761752	GM12878	blood:	n/a	n/a
18	BATF	chr8:43816105-43816326	GM12878	blood:	n/a	n/a
19	BATF	chr8:43759902-43760143	GM12878	blood:	n/a	n/a
20	BATF	chr8:43820362-43821200	GM12878	blood:	n/a	n/a
21	BATF	chr8:43801979-43802190	GM12878	blood:	n/a	n/a
22	BATF	chr8:43790147-43790722	GM12878	blood:	n/a	n/a
23	BATF	chr8:43816102-43816270	GM12878	blood:	n/a	n/a
24	BATF	chr8:43793735-43795027	GM12878	blood:	n/a	n/a
25	BATF	chr8:43783535-43783800	GM12878	blood:	n/a	n/a
26	BATF	chr8:43801942-43802323	GM12878	blood:	n/a	n/a
27	BATF	chr8:43781686-43781952	GM12878	blood:	n/a	n/a
28	BATF	chr8:43790368-43790722	GM12878	blood:	n/a	n/a
29	BATF	chr8:43813396-43813769	GM12878	blood:	n/a	n/a
30	BATF	chr8:43823238-43824120	GM12878	blood:	n/a	n/a
31	BATF	chr8:43805912-43806229	GM12878	blood:	n/a	n/a
32	BATF	chr8:43805047-43805337	GM12878	blood:	n/a	n/a
33	BATF	chr8:43821328-43821864	GM12878	blood:	n/a	n/a
34	BATF	chr8:43808539-43808737	GM12878	blood:	n/a	n/a
35	BATF	chr8:43810454-43810881	GM12878	blood:	n/a	n/a
36	BATF	chr8:43796330-43796659	GM12878	blood:	n/a	n/a
37	BATF	chr8:43821252-43822263	GM12878	blood:	n/a	n/a
38	BATF	chr8:43802641-43802856	GM12878	blood:	n/a	n/a
39	BATF	chr8:43803086-43803339	GM12878	blood:	n/a	n/a
40	BATF	chr8:43771212-43771629	GM12878	blood:	n/a	n/a
41	BATF	chr8:43805556-43805832	GM12878	blood:	n/a	n/a
42	BATF	chr8:43770392-43770728	GM12878	blood:	n/a	n/a
43	BATF	chr8:43822263-43823134	GM12878	blood:	n/a	n/a
44	BATF	chr8:43795705-43796262	GM12878	blood:	n/a	n/a
45	BATF	chr8:43800254-43800627	GM12878	blood:	n/a	n/a
46	BATF	chr8:43810945-43811236	GM12878	blood:	n/a	n/a
47	BATF	chr8:43800976-43801176	GM12878	blood:	n/a	n/a
48	BATF	chr8:43818749-43818924	GM12878	blood:	n/a	n/a
49	BATF	chr8:43771245-43771622	GM12878	blood:	n/a	n/a
50	BATF	chr8:43800956-43801154	GM12878	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:43417291-43417341	HCPEpiC	choroid plexus:	n/a
2	chr8:43417291-43417341	HCPEpiC	choroid plexus:	n/a
3	chr8:43417291-43417341	NHDF-neo	bronchial:	n/a
4	chr8:43418721-43418771	ProgFib	skin:	n/a
5	chr8:43417291-43417341	GM12878	blood:	n/a
6	chr8:43417050-43417100	T-47D	breast:	n/a
7	chr8:43418406-43418456	AG04449	skin:	fetal
8	chr8:43418406-43418456	GM12892	blood:	n/a
9	chr8:43418721-43418771	PFSK-1	brain:	n/a
10	chr8:43417050-43417100	AoSMC	blood vessel:	n/a
11	chr8:43417050-43417100	HEK293	kidney:	embryo
12	chr8:43417050-43417100	ProgFib	skin:	n/a
13	chr8:43417050-43417100	K562	blood:	n/a
14	chr8:43418721-43418771	GM06990	blood:	n/a
15	chr8:43794595-43794645	HEEpiC	esophagus:	n/a
16	chr8:43418406-43418456	SK-N-SH	brain:	n/a
17	chr8:43417291-43417341	AG10803	skin:	n/a
18	chr8:43418406-43418456	HCM	heart:	n/a
19	chr8:43418721-43418771	H1-hESC	embryonic stem cell:	embryo
20	chr8:43417291-43417341	AG09319	gingival:	n/a
21	chr8:43794595-43794645	PFSK-1	brain:	n/a
22	chr8:43417291-43417341	NH-A	brain:	n/a
23	chr8:43417291-43417341	MCF-7	breast:	n/a
24	chr8:43417050-43417100	Caco-2	colon:	n/a
25	chr8:43417291-43417341	SAEC	small airway:	n/a
26	chr8:43418406-43418456	MCF10A-Er-Src	breast:	n/a
27	chr8:43418406-43418456	LNCaP	prostate:	n/a
28	chr8:43418406-43418456	SK-N-MC	brain:	n/a
29	chr8:43417050-43417100	PANC-1	pancreas:	n/a
30	chr8:43417050-43417100	Hepatocyte	liver:	n/a
31	chr8:43418406-43418456	GM12891	blood:	n/a
32	chr8:43417291-43417341	HepG2	liver:	n/a
33	chr8:43417050-43417100	GM19239	blood:	n/a
34	chr8:43417050-43417100	GM12891	blood:	n/a
35	chr8:43418406-43418456	ProgFib	skin:	n/a
36	chr8:43417291-43417341	HCF	heart:	n/a
37	chr8:43794595-43794645	HAEpiC	amniotic membrane:	n/a
38	chr8:43794595-43794645	ECC-1	luminal epithelium:	n/a
39	chr8:43794595-43794645	HEK293	kidney:	embryo
40	chr8:43417291-43417341	SK-N-MC	brain:	n/a
41	chr8:43417291-43417341	PrEC	prostate:	n/a
42	chr8:43417291-43417341	HPAEpiC	pulmonary alveolar:	n/a
43	chr8:43794595-43794645	ovcar-3	ovarian:	n/a
44	chr8:43794595-43794645	A549	lung:	n/a
45	chr8:43418721-43418771	U87	brain:	n/a
46	chr8:43418406-43418456	PANC-1	pancreas:	n/a
47	chr8:43794595-43794645	NB4	blood:	n/a
48	chr8:43418406-43418456	Hela-S3	cervix:	n/a
49	chr8:43418721-43418771	HCT-116	colon:	n/a
50	chr8:43794595-43794645	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:63385860..63386443-chr8:43553599..43554374,2	MCF-7	breast:
2	chr8:43092429..43093269-chr8:43823893..43824414,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HGSNAT-12	chr8:43527966-43528218	NONHSAT126367
2	lnc-RNF170-9	chr8:43529413-43529734	NONHSAT126368

No data

Variant related genes	Relation type
ENSG00000221295	TF binding region
ENSG00000253845	TF binding region
ENSG00000253198	TF binding region
ENSG00000221295	CpG island
ENSG00000253845	CpG island
ENSG00000253198	CpG island

Extended variants
information (count: 25914 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:25914 , 50 per page) page: 1 2 3 4 5 6 7 ... 519

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4737117	chr8:43413955-43413956	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372133940	chr8:43413970-43413971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs146644341	chr8:43413984-43413985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs550868164	chr8:43414005-43414006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs4737118	chr8:43414015-43414016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs532160263	chr8:43414063-43414064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545511658	chr8:43414064-43414065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs565255563	chr8:43414066-43414067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188529501	chr8:43414114-43414115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7293798	chr8:43414155-43414156	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs7293751	chr8:43414170-43414171	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs530462432	chr8:43414192-43414193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs181257078	chr8:43414214-43414215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553133056	chr8:43414266-43414267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs73569638	chr8:43414276-43414277	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs185802085	chr8:43414288-43414289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188217821	chr8:43414316-43414317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565654058	chr8:43414324-43414325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568093997	chr8:43414326-43414327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554273260	chr8:43414343-43414344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs141412590	chr8:43414392-43414393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376255302	chr8:43414400-43414401	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs372413801	chr8:43414404-43414405	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs145117761	chr8:43414478-43414479	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs556814982	chr8:43414519-43414520	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs77998838	chr8:43414521-43414522	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs545694365	chr8:43414542-43414543	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs376447116	chr8:43414544-43414545	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs559455224	chr8:43414556-43414557	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs73569639	chr8:43414557-43414558	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs371820646	chr8:43414566-43414567	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs180924859	chr8:43414568-43414569	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs79116673	chr8:43414602-43414603	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs530103577	chr8:43414616-43414617	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs550525200	chr8:43414623-43414624	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs117187537	chr8:43414637-43414638	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs575212492	chr8:43414657-43414658	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs532821170	chr8:43414675-43414676	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs72635429	chr8:43414691-43414692	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs566219562	chr8:43414705-43414706	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs115913047	chr8:43414716-43414717	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs148955755	chr8:43414717-43414718	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs567745315	chr8:43414743-43414744	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs10105936	chr8:43414789-43414790	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs536669230	chr8:43414794-43414795	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs6981373	chr8:43414797-43414798	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs114429667	chr8:43414812-43414813	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs370951015	chr8:43414816-43414817	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs556503606	chr8:43414824-43414825	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs576734253	chr8:43414841-43414842	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Seminomas	18059402	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21785460	CNVD
Rhabdomyosarcoma	16790082	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	23813976	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19214233	CNVD

Chromatin state (count:1269 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:43413600-43414000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr8:43413800-43414400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr8:43414600-43415000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr8:43415400-43427200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr8:43416400-43417000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
6	chr8:43416400-43427200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:43417400-43419200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
8	chr8:43417400-43421000	ZNF genes & repeats	Fetal Stomach	stomach
9	chr8:43417800-43422800	ZNF genes & repeats	Adipose Nuclei	Adipose
10	chr8:43418800-43419200	ZNF genes & repeats	Colonic Mucosa	Colon
11	chr8:43418800-43423600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr8:43419000-43419200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr8:43419600-43421400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
14	chr8:43419600-43422400	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
15	chr8:43420400-43420800	ZNF genes & repeats	Brain Germinal Matrix	brain
16	chr8:43420400-43421000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr8:43420400-43421000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
18	chr8:43420400-43423600	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
19	chr8:43422800-43425800	ZNF genes & repeats	Fetal Muscle Trunk	muscle
20	chr8:43423800-43427400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
21	chr8:43424600-43426200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
22	chr8:43426800-43430800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr8:43427600-43428400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
24	chr8:43429200-43430000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
25	chr8:43429400-43430600	ZNF genes & repeats	Liver	Liver
26	chr8:43434000-43435000	ZNF genes & repeats	Liver	Liver
27	chr8:43434000-43454200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr8:43436400-43436800	ZNF genes & repeats	Liver	Liver
29	chr8:43439800-43443800	ZNF genes & repeats	Adipose Nuclei	Adipose
30	chr8:43441000-43453800	ZNF genes & repeats	Liver	Liver
31	chr8:43442400-43446800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
32	chr8:43444000-43445000	Weak transcription	Adipose Nuclei	Adipose
33	chr8:43444800-43453600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
34	chr8:43445000-43449800	ZNF genes & repeats	Adipose Nuclei	Adipose
35	chr8:43446800-43447200	Active TSS	Right Atrium	heart
36	chr8:43451000-43453600	ZNF genes & repeats	Adipose Nuclei	Adipose
37	chr8:43451200-43451800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr8:43451400-43453400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr8:43451800-43452800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr8:43452800-43458400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr8:43453400-43462000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
42	chr8:43455800-43456800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr8:43458000-43458800	ZNF genes & repeats	Liver	Liver
44	chr8:43458200-43460600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr8:43458400-43458600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr8:43462600-43466400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr8:43462600-43473600	ZNF genes & repeats	Liver	Liver
48	chr8:43463400-43464600	Active TSS	Right Atrium	heart
49	chr8:43469800-43474800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
50	chr8:43470200-43472000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell

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