Variant report

Variant	nsv609987
Chromosome Location	chr8:6091254-6171324
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr8:6125905-6126127	GM12878	blood:	n/a	n/a
2	BHLHE40	chr8:6149426-6149734	GM12878	blood:	n/a	n/a
3	CEBPB	chr8:6106894-6107185	IMR90	lung:	n/a	chr8:6107026-6107037 chr8:6107026-6107039 chr8:6107028-6107039 chr8:6107028-6107037
4	CEBPB	chr8:6100264-6100476	A549	lung:	n/a	n/a
5	CEBPB	chr8:6165750-6165958	HepG2	liver:	n/a	chr8:6165822-6165835 chr8:6165824-6165833 chr8:6165822-6165833
6	CEBPB	chr8:6106856-6107207	HepG2	liver:	n/a	chr8:6107026-6107037 chr8:6107026-6107039 chr8:6107028-6107039 chr8:6107028-6107037
7	CEBPB	chr8:6165763-6166327	K562	blood:	n/a	chr8:6165822-6165835 chr8:6165824-6165833 chr8:6165822-6165833
8	CEBPB	chr8:6106882-6107194	H1-hESC	embryonic stem cell:	n/a	chr8:6107026-6107037 chr8:6107026-6107039 chr8:6107028-6107039 chr8:6107028-6107037
9	CEBPB	chr8:6148528-6148743	HepG2	liver:	n/a	chr8:6148625-6148638 chr8:6148625-6148638 chr8:6148626-6148637 chr8:6148625-6148636
10	CEBPB	chr8:6132470-6132485	HepG2	liver:	n/a	n/a
11	CEBPB	chr8:6128437-6128476	K562	blood:	n/a	n/a
12	CEBPB	chr8:6165750-6165950	IMR90	lung:	n/a	chr8:6165822-6165835 chr8:6165824-6165833 chr8:6165822-6165833
13	CEBPB	chr8:6165771-6165947	A549	lung:	n/a	chr8:6165822-6165835 chr8:6165824-6165833 chr8:6165822-6165833
14	CEBPB	chr8:6106985-6107104	K562	blood:	n/a	chr8:6107026-6107037 chr8:6107026-6107039 chr8:6107028-6107039 chr8:6107028-6107037
15	CEBPB	chr8:6128430-6128600	HepG2	liver:	n/a	n/a
16	CEBPB	chr8:6128333-6128520	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr8:6100276-6100536	HepG2	liver:	n/a	n/a
18	CEBPB	chr8:6106947-6107139	MCF-7	breast:	n/a	chr8:6107026-6107037 chr8:6107026-6107039 chr8:6107028-6107039 chr8:6107028-6107037
19	CTCF	chr8:6140600-6140750	SAEC	small airway:	n/a	n/a
20	CTCF	chr8:6116020-6116170	HCT-116	colon:	n/a	n/a
21	CTCF	chr8:6115960-6116110	A549	lung:	n/a	n/a
22	CTCF	chr8:6116140-6116290	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr8:6140640-6140790	HEEpiC	esophagus:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
24	CTCF	chr8:6116080-6116230	HPF	lung:	n/a	n/a
25	CTCF	chr8:6147164-6147366	H1-hESC	embryonic stem cell:	n/a	chr8:6147257-6147270
26	CTCF	chr8:6140640-6140790	Caco-2	colon:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
27	CTCF	chr8:6147920-6148070	GM12868	blood:	n/a	n/a
28	CTCF	chr8:6160454-6160522	GM10248	blood:	n/a	n/a
29	CTCF	chr8:6116051-6116307	Gliobla	brain:	n/a	n/a
30	CTCF	chr8:6140746-6140784	GM19240	blood:	n/a	n/a
31	CTCF	chr8:6115998-6116332	MCF-7	breast:	n/a	n/a
32	CTCF	chr8:6115964-6116428	K562	blood:	n/a	n/a
33	CTCF	chr8:6147276-6147301	Gliobla	brain:	n/a	n/a
34	CTCF	chr8:6140640-6140790	GM06990	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
35	CTCF	chr8:6116140-6116290	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr8:6128364-6128443	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr8:6140620-6140770	GM12874	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
38	CTCF	chr8:6140686-6140835	GM12892	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
39	CTCF	chr8:6115710-6116473	SK-N-SH	brain:	n/a	n/a
40	CTCF	chr8:6140640-6140790	GM12866	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
41	CTCF	chr8:6116077-6116278	HepG2	liver:	n/a	n/a
42	CTCF	chr8:6149920-6150070	GM12873	blood:	n/a	n/a
43	CTCF	chr8:6140660-6140810	K562	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
44	CTCF	chr8:6115820-6115970	GM12878	blood:	n/a	n/a
45	CTCF	chr8:6140561-6140824	H1-hESC	embryonic stem cell:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
46	CTCF	chr8:6116131-6116247	A549	lung:	n/a	n/a
47	CTCF	chr8:6169960-6170110	GM12872	blood:	n/a	n/a
48	CTCF	chr8:6116124-6116218	GM10266	blood:	n/a	n/a
49	CTCF	chr8:6116180-6116330	RPTEC	kidney:	n/a	n/a
50	CTCF	chr8:6116100-6116250	WERI-Rb-1	eye:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6118526-6118576	GM12878	blood:	n/a
2	chr8:6118526-6118576	GM12878	blood:	n/a
3	chr8:6118526-6118576	ECC-1	luminal epithelium:	n/a
4	chr8:6118575-6118625	HepG2	liver:	n/a
5	chr8:6118526-6118576	MCF10A-Er-Src	breast:	n/a
6	chr8:6118575-6118625	U87	brain:	n/a
7	chr8:6118526-6118576	HEK293	kidney:	embryo
8	chr8:6118526-6118576	U87	brain:	n/a
9	chr8:6118575-6118625	BJ	skin:	n/a
10	chr8:6118526-6118576	HPAEpiC	pulmonary alveolar:	n/a
11	chr8:6118575-6118625	PANC-1	pancreas:	n/a
12	chr8:6118526-6118576	HRPEpiC	eye:	n/a
13	chr8:6118526-6118576	HEEpiC	esophagus:	n/a
14	chr8:6118526-6118576	MCF-7	breast:	n/a
15	chr8:6118575-6118625	HCT-116	colon:	n/a
16	chr8:6118526-6118576	GM12891	blood:	n/a
17	chr8:6118575-6118625	HIPEpiC	eye:	n/a
18	chr8:6118526-6118576	AG09309	skin:	n/a
19	chr8:6118575-6118625	GM12892	blood:	n/a
20	chr8:6118526-6118576	Hepatocyte	liver:	n/a
21	chr8:6118575-6118625	Hela-S3	cervix:	n/a
22	chr8:6118575-6118625	HCPEpiC	choroid plexus:	n/a
23	chr8:6118526-6118576	HCM	heart:	n/a
24	chr8:6118526-6118576	Hela-S3	cervix:	n/a
25	chr8:6118526-6118576	AG04450	lung:	fetal
26	chr8:6118526-6118576	AG04449	skin:	fetal
27	chr8:6118526-6118576	GM06990	blood:	n/a
28	chr8:6118526-6118576	SK-N-SH_RA	brain:	n/a
29	chr8:6118575-6118625	T-47D	breast:	n/a
30	chr8:6118575-6118625	SK-N-MC	brain:	n/a
31	chr8:6118575-6118625	RPTEC	kidney:	n/a
32	chr8:6118575-6118625	HNPCEpiC	eye:	n/a
33	chr8:6118526-6118576	A549	lung:	n/a
34	chr8:6118526-6118576	PrEC	prostate:	n/a
35	chr8:6118575-6118625	BE2_C	brain:	n/a
36	chr8:6118575-6118625	HUVEC	blood vessel:	n/a
37	chr8:6118575-6118625	ProgFib	skin:	n/a
38	chr8:6118575-6118625	GM19239	blood:	n/a
39	chr8:6118575-6118625	AG10803	skin:	n/a
40	chr8:6118526-6118576	SK-N-SH	brain:	n/a
41	chr8:6118526-6118576	SKMC	muscle:	n/a
42	chr8:6118526-6118576	ovcar-3	ovarian:	n/a
43	chr8:6118575-6118625	LNCaP	prostate:	n/a
44	chr8:6118575-6118625	HCF	heart:	n/a
45	chr8:6118575-6118625	Hepatocyte	liver:	n/a
46	chr8:6118575-6118625	NT2-D1	testis:	n/a
47	chr8:6118526-6118576	GM19239	blood:	n/a
48	chr8:6118526-6118576	GM12892	blood:	n/a
49	chr8:6118575-6118625	NH-A	brain:	n/a
50	chr8:6118575-6118625	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:6139049..6141857-chr8:6147372..6149538,2	K562	blood:
2	chr8:6117190..6120021-chr8:6122326..6123985,2	K562	blood:
3	chr8:6117190..6120021-chr8:6122326..6123985,2	K562	blood:
4	chr8:6084910..6087836-chr8:6095267..6098254,2	K562	blood:
5	chr8:6145627..6147844-chr8:6162410..6164202,2	MCF-7	breast:
6	chr8:6106618..6108795-chr8:6113891..6116770,2	K562	blood:
7	chr8:6080157..6081666-chr8:6091415..6093477,2	MCF-7	breast:
8	chr8:6115678..6116241-chr8:6687345..6688278,2	K562	blood:
9	chr8:6145627..6147844-chr8:6162410..6164202,2	MCF-7	breast:
10	chr8:6115787..6116559-chr8:6229328..6229869,2	MCF-7	breast:
11	chr8:6139049..6141857-chr8:6147372..6149538,2	K562	blood:
12	chr8:6116111..6116635-chr8:6188825..6189362,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANGPT2-3	chr8:6114933-6115058	ENSG00000253880

Variant related genes	Relation type
ENSG00000253880	TF binding region
ENSG00000253880	CpG island
ENSG00000253880	chromatin interactions

Extended variants
information (count: 4368 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:4368 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146585169	chr8:6100201-6100202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs78747695	chr8:6100206-6100207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542341319	chr8:6100218-6100219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183031511	chr8:6100245-6100246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs527906555	chr8:6100268-6100269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs142279380	chr8:6100343-6100344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs369602583	chr8:6100356-6100357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564775196	chr8:6100358-6100359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs533719961	chr8:6100371-6100372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs151215356	chr8:6100377-6100378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568871263	chr8:6100384-6100385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs531186679	chr8:6100387-6100388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs187367252	chr8:6100389-6100390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs58882286	chr8:6100429-6100430	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs73520077	chr8:6100443-6100444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531622432	chr8:6100447-6100448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs371114962	chr8:6100461-6100462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs79986368	chr8:6100480-6100481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs551433233	chr8:6100485-6100486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs539387106	chr8:6100488-6100489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185423512	chr8:6100505-6100506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs527516865	chr8:6100531-6100532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs547054498	chr8:6100550-6100551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540033746	chr8:6100572-6100573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567044900	chr8:6100585-6100586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs541828141	chr8:6100590-6100591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs138963493	chr8:6104018-6104019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs186466402	chr8:6104025-6104026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs189719439	chr8:6104032-6104033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs6995691	chr8:6104057-6104058	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs542909519	chr8:6104077-6104078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs6982565	chr8:6104080-6104081	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs571691968	chr8:6104102-6104103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540794694	chr8:6104119-6104120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs6559122	chr8:6104157-6104158	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs73520095	chr8:6104170-6104171	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs543559143	chr8:6104174-6104175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs76494875	chr8:6104178-6104179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529245739	chr8:6104179-6104180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs549283208	chr8:6104198-6104199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs180951821	chr8:6104200-6104201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs528462208	chr8:6104215-6104216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551602007	chr8:6104221-6104222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs144724915	chr8:6104240-6104241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs186286106	chr8:6104246-6104247	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs557576744	chr8:6104267-6104268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs567508950	chr8:6104269-6104270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191579626	chr8:6104271-6104272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs6559123	chr8:6104273-6104274	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs571729436	chr8:6104274-6104275	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
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
Oral cancer	21386901	CNVD
Prostate cancer	21088497	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
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
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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	21364760	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	20688739	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:152 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6100200-6100600	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr8:6104000-6105600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr8:6104000-6106000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr8:6104400-6107400	Enhancers	Primary hematopoietic stem cells	blood
5	chr8:6104800-6105200	Enhancers	H1 Cell Line	embryonic stem cell
6	chr8:6105000-6107400	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr8:6105200-6105600	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr8:6105600-6106400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr8:6106000-6106400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr8:6106400-6111200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr8:6106400-6111200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr8:6107000-6107200	Enhancers	H1 Cell Line	embryonic stem cell
13	chr8:6107400-6110200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr8:6107400-6110600	Weak transcription	Primary hematopoietic stem cells	blood
15	chr8:6110200-6110600	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr8:6110600-6111000	Enhancers	Primary hematopoietic stem cells	blood
17	chr8:6110600-6111800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr8:6111000-6112400	Weak transcription	Primary hematopoietic stem cells	blood
19	chr8:6111200-6112200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr8:6111200-6112200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr8:6111800-6112800	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr8:6112200-6112600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr8:6112200-6112800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr8:6112400-6112600	Enhancers	Primary hematopoietic stem cells	blood
25	chr8:6112800-6114800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr8:6114800-6115200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr8:6114800-6115200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr8:6119400-6120000	Enhancers	Brain Germinal Matrix	brain
29	chr8:6119400-6120000	Enhancers	Osteobl	bone
30	chr8:6119400-6120200	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr8:6120000-6121000	Weak transcription	Brain Germinal Matrix	brain
32	chr8:6120200-6120800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr8:6120800-6121200	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr8:6121000-6121200	Enhancers	Brain Germinal Matrix	brain
35	chr8:6122200-6123200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr8:6128200-6128600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr8:6132000-6132800	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr8:6132200-6132800	Enhancers	Spleen	Spleen
39	chr8:6132200-6133600	Enhancers	Pancreas	Pancrea
40	chr8:6132800-6134800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr8:6132800-6149000	Weak transcription	Spleen	Spleen
42	chr8:6134800-6135000	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr8:6138400-6141200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr8:6140200-6140400	Active TSS	Breast Myoepithelial Primary Cells	Breast
45	chr8:6140800-6141000	Active TSS	Breast Myoepithelial Primary Cells	Breast
46	chr8:6141200-6141400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr8:6141400-6144400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr8:6144400-6144600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr8:6144600-6147200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr8:6147200-6147400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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