Variant report

Variant	nsv1024525
Chromosome Location	chr8:47125996-47285399
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:345)
CpG islands
(count:1284)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:47263663-47264034	K562	blood:	n/a	n/a
2	BRCA1	chr8:47213331-47213535	GM12878	blood:	n/a	n/a
3	BRCA1	chr8:47128832-47128850	HepG2	liver:	n/a	n/a
4	CEBPB	chr8:47144487-47144545	K562	blood:	n/a	n/a
5	CEBPB	chr8:47214532-47214751	HepG2	liver:	n/a	chr8:47214612-47214623
6	CEBPB	chr8:47214503-47214753	A549	lung:	n/a	chr8:47214612-47214623
7	CEBPB	chr8:47214461-47214801	IMR90	lung:	n/a	chr8:47214612-47214623
8	CTCF	chr8:47154337-47154442	MCF-7	breast:	n/a	n/a
9	CTCF	chr8:47130638-47130796	A549	lung:	n/a	n/a
10	CTCF	chr8:47130555-47130949	K562	blood:	n/a	n/a
11	CTCF	chr8:47130435-47131168	SK-N-SH	brain:	n/a	n/a
12	CTCF	chr8:47130577-47131059	K562	blood:	n/a	n/a
13	CTCF	chr8:47131043-47131051	MCF-7	breast:	n/a	n/a
14	CTCF	chr8:47162059-47162138	Fibrobl	skin:	n/a	n/a
15	CTCF	chr8:47144398-47144575	HepG2	liver:	n/a	n/a
16	CTCF	chr8:47130631-47130851	K562	blood:	n/a	n/a
17	CTCF	chr8:47130631-47130844	A549	lung:	n/a	n/a
18	CTCF	chr8:47168596-47168802	MCF-7	breast:	n/a	n/a
19	CTCF	chr8:47144343-47144614	HepG2	liver:	n/a	n/a
20	CTCF	chr8:47144305-47144578	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr8:47144384-47144640	MCF-7	breast:	n/a	n/a
22	CTCF	chr8:47156882-47157133	K562	blood:	n/a	n/a
23	CTCF	chr8:47168476-47168932	MCF-7	breast:	n/a	n/a
24	CTCF	chr8:47131024-47131025	MCF-7	breast:	n/a	n/a
25	CTCF	chr8:47169772-47169783	MCF-7	breast:	n/a	n/a
26	CTCF	chr8:47130618-47130871	LNCaP	prostate:	n/a	n/a
27	CTCF	chr8:47168590-47168807	MCF-7	breast:	n/a	n/a
28	CTCF	chr8:47130681-47130815	HepG2	liver:	n/a	n/a
29	CTCF	chr8:47165203-47165271	MCF-7	breast:	n/a	n/a
30	CTCF	chr8:47243320-47243470	GM12866	blood:	n/a	n/a
31	CTCF	chr8:47171864-47171902	LNCaP	prostate:	n/a	n/a
32	CTCF	chr8:47130603-47130875	MCF-7	breast:	n/a	n/a
33	CTCF	chr8:47152187-47152288	MCF-7	breast:	n/a	n/a
34	CTCF	chr8:47130658-47130848	LNCaP	prostate:	n/a	n/a
35	CTCF	chr8:47130677-47130776	Fibrobl	skin:	n/a	n/a
36	CTCF	chr8:47130610-47130802	A549	lung:	n/a	n/a
37	CTCF	chr8:47154364-47154441	K562	blood:	n/a	n/a
38	CTCF	chr8:47152157-47152306	MCF-7	breast:	n/a	n/a
39	CTCF	chr8:47177440-47177481	GM13976	blood:	n/a	n/a
40	CTCF	chr8:47168569-47168759	K562	blood:	n/a	n/a
41	CTCF	chr8:47144305-47144642	T-47D	breast:	n/a	n/a
42	CTCF	chr8:47148155-47148199	GM13976	blood:	n/a	n/a
43	CTCF	chr8:47168594-47168762	HepG2	liver:	n/a	n/a
44	CTCF	chr8:47165184-47165267	Gliobla	brain:	n/a	n/a
45	CTCF	chr8:47144384-47144555	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr8:47144353-47144574	K562	blood:	n/a	n/a
47	CTCF	chr8:47130499-47131024	MCF-7	breast:	n/a	n/a
48	CTCF	chr8:47130611-47130886	Gliobla	brain:	n/a	n/a
49	CTCF	chr8:47130499-47131013	HCT-116	colon:	n/a	n/a
50	CTCF	chr8:47168596-47168815	LNCaP	prostate:	n/a	n/a

(count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:47145527-47145577	SK-N-SH	brain:	n/a
2	chr8:47144915-47144965	NHBE	bronchial:	n/a
3	chr8:47140781-47140831	HIPEpiC	eye:	n/a
4	chr8:47145527-47145577	SK-N-SH	brain:	n/a
5	chr8:47144915-47144965	NHBE	bronchial:	n/a
6	chr8:47140781-47140831	HIPEpiC	eye:	n/a
7	chr8:47165466-47165516	NB4	blood:	n/a
8	chr8:47174026-47174076	HRE	kidney:	n/a
9	chr8:47130822-47130872	HRPEpiC	eye:	n/a
10	chr8:47140781-47140831	HCPEpiC	choroid plexus:	n/a
11	chr8:47174057-47174107	GM06990	blood:	n/a
12	chr8:47156875-47156925	NH-A	brain:	n/a
13	chr8:47156875-47156925	HAEpiC	amniotic membrane:	n/a
14	chr8:47156687-47156737	HAEpiC	amniotic membrane:	n/a
15	chr8:47171826-47171876	HRE	kidney:	n/a
16	chr8:47130822-47130872	SKMC	muscle:	n/a
17	chr8:47174057-47174107	SK-N-SH_RA	brain:	n/a
18	chr8:47171826-47171876	GM12891	blood:	n/a
19	chr8:47165887-47165937	GM12892	blood:	n/a
20	chr8:47156875-47156925	SAEC	small airway:	n/a
21	chr8:47142166-47142216	HAEpiC	amniotic membrane:	n/a
22	chr8:47160830-47160880	MCF-7	breast:	n/a
23	chr8:47174057-47174107	BE2_C	brain:	n/a
24	chr8:47174026-47174076	K562	blood:	n/a
25	chr8:47171722-47171772	AG04450	lung:	fetal
26	chr8:47174026-47174076	HCF	heart:	n/a
27	chr8:47160830-47160880	SK-N-SH	brain:	n/a
28	chr8:47142166-47142216	HCT-116	colon:	n/a
29	chr8:47130822-47130872	AG04449	skin:	fetal
30	chr8:47171826-47171876	HCPEpiC	choroid plexus:	n/a
31	chr8:47165466-47165516	HAEpiC	amniotic membrane:	n/a
32	chr8:47156687-47156737	HepG2	liver:	n/a
33	chr8:47144915-47144965	MCF10A-Er-Src	breast:	n/a
34	chr8:47142089-47142139	GM12878	blood:	n/a
35	chr8:47165887-47165937	HAEpiC	amniotic membrane:	n/a
36	chr8:47165887-47165937	Jurkat	blood:	n/a
37	chr8:47145556-47145606	NHBE	bronchial:	n/a
38	chr8:47145556-47145606	NHDF-neo	bronchial:	n/a
39	chr8:47144915-47144965	AG09319	gingival:	n/a
40	chr8:47171826-47171876	NHDF-neo	bronchial:	n/a
41	chr8:47156687-47156737	HMEC	breast:	n/a
42	chr8:47171826-47171876	CMK	blood:	n/a
43	chr8:47144363-47144413	HRE	kidney:	n/a
44	chr8:47145527-47145577	HRE	kidney:	n/a
45	chr8:47156687-47156737	NH-A	brain:	n/a
46	chr8:47145556-47145606	Caco-2	colon:	n/a
47	chr8:47144915-47144965	HPAEpiC	pulmonary alveolar:	n/a
48	chr8:47142166-47142216	CMK	blood:	n/a
49	chr8:47165466-47165516	K562	blood:	n/a
50	chr8:47130777-47130827	H1-hESC	embryonic stem cell:	embryo

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:47144016..47144925-chr8:47484500..47485152,3	MCF-7	breast:
2	chr8:46940855..46941726-chr8:47130252..47130754,2	K562	blood:
3	chr8:47152207..47152786-chr8:47399264..47399945,2	MCF-7	breast:
4	chr8:47168205..47168775-chr8:47479656..47480472,2	MCF-7	breast:
5	chr8:46940678..46941746-chr8:47130003..47131748,8	MCF-7	breast:
6	chr2:86830620..86831120-chr8:47284541..47285069,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000255915	TF binding region
ENSG00000255915	CpG island

Extended variants
information (count: 7488 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:7488 , 50 per page) page: 1 2 3 4 5 6 7 ... 150

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142137143	chr8:47125998-47125999	ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs193287086	chr8:47126006-47126007	ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs529618636	chr8:47126016-47126017	ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs145901447	chr8:47126019-47126020	ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs377406796	chr8:47126064-47126065	ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs569455946	chr8:47126069-47126070	ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs59184965	chr8:47126073-47126074	ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs538467301	chr8:47126104-47126105	ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs557964111	chr8:47126112-47126113	ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs34387565	chr8:47126131-47126132	ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs147792894	chr8:47126136-47126137	ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs533900399	chr8:47126145-47126146	ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529325240	chr8:47126207-47126208	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148837231	chr8:47126224-47126225	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185611015	chr8:47126270-47126271	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs530537104	chr8:47126271-47126272	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556074627	chr8:47126288-47126289	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188546641	chr8:47126313-47126314	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545235978	chr8:47126324-47126325	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564822220	chr8:47126328-47126329	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs527394136	chr8:47126345-47126346	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192905179	chr8:47126367-47126368	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560963403	chr8:47126384-47126385	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs529747366	chr8:47126388-47126389	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549674275	chr8:47126391-47126392	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566923445	chr8:47126416-47126417	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs374692849	chr8:47126438-47126439	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs536099518	chr8:47126469-47126470	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs35412547	chr8:47126471-47126472	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs563219799	chr8:47126505-47126506	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs546527295	chr8:47126516-47126517	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531929607	chr8:47126535-47126536	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs566327319	chr8:47126537-47126538	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551959250	chr8:47126549-47126550	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143441948	chr8:47126562-47126563	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs534322418	chr8:47126564-47126565	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs538855389	chr8:47126583-47126584	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547439753	chr8:47126589-47126590	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs183999579	chr8:47126594-47126595	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188824319	chr8:47126604-47126605	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556038301	chr8:47126623-47126624	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs371220546	chr8:47126634-47126635	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs575972230	chr8:47126651-47126652	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538417531	chr8:47126661-47126662	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs180793456	chr8:47126673-47126674	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs575658640	chr8:47126677-47126678	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183929768	chr8:47126693-47126694	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs116017681	chr8:47126701-47126702	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs560991471	chr8:47126715-47126716	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs574478972	chr8:47126737-47126738	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	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
Oral cancer	21386901	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	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
Glioblastoma multiforme	21080181	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
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	20607354	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	20409316	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Schizophrenia	20967226	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Autism	20841430	CNVD
Tetralogy of Fallot	22912587	CNVD

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:47086400-47175600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:47106200-47128000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:47123800-47126200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr8:47126200-47135400	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr8:47127000-47127400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr8:47129800-47130600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr8:47129800-47131000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr8:47130200-47134000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr8:47130600-47132200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr8:47130800-47131000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
11	chr8:47130800-47132600	ZNF genes & repeats	Placenta	Placenta
12	chr8:47130800-47134400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:47131000-47132200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr8:47132200-47132600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr8:47132200-47133400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr8:47132400-47133000	Enhancers	Osteobl	bone
17	chr8:47132600-47133200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr8:47132600-47133200	Enhancers	Placenta	Placenta
19	chr8:47132600-47136200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr8:47133200-47133400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr8:47133200-47134400	ZNF genes & repeats	Placenta	Placenta
22	chr8:47135400-47135600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr8:47135600-47137000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr8:47137000-47138000	Active TSS	Primary T cells from cord blood	blood
25	chr8:47137000-47139200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr8:47137400-47159400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr8:47138000-47138200	ZNF genes & repeats	Brain Germinal Matrix	brain
28	chr8:47138000-47143600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr8:47139200-47139400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr8:47139400-47143800	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr8:47140400-47141000	Active TSS	Spleen	Spleen
32	chr8:47141200-47142400	Active TSS	Primary T cells from cord blood	blood
33	chr8:47141200-47142400	ZNF genes & repeats	Placenta	Placenta
34	chr8:47141800-47142200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr8:47142400-47143200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
36	chr8:47143200-47143400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr8:47143600-47143800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr8:47143800-47144400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
39	chr8:47144400-47144600	Active TSS	Breast Myoepithelial Primary Cells	Breast
40	chr8:47144400-47144600	Active TSS	Osteobl	bone
41	chr8:47144400-47144800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr8:47144400-47145600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr8:47144600-47144800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
44	chr8:47144600-47144800	Flanking Active TSS	Osteobl	bone
45	chr8:47144800-47145000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr8:47144800-47145200	Active TSS	Breast Myoepithelial Primary Cells	Breast
47	chr8:47145000-47147200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr8:47145200-47146400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
49	chr8:47146400-47146600	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr8:47146600-47146800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast

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