Variant report

Variant	esv2759587
Chromosome Location	chr8:6104977-6159854
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	chr8:6132470-6132485	HepG2	liver:	n/a	n/a
4	CEBPB	chr8:6128430-6128600	HepG2	liver:	n/a	n/a
5	CEBPB	chr8:6106882-6107194	H1-hESC	embryonic stem cell:	n/a	chr8:6107026-6107037 chr8:6107026-6107039 chr8:6107028-6107039 chr8:6107028-6107037
6	CEBPB	chr8:6128333-6128520	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr8:6106894-6107185	IMR90	lung:	n/a	chr8:6107026-6107037 chr8:6107026-6107039 chr8:6107028-6107039 chr8:6107028-6107037
8	CEBPB	chr8:6148528-6148743	HepG2	liver:	n/a	chr8:6148625-6148638 chr8:6148625-6148638 chr8:6148626-6148637 chr8:6148625-6148636
9	CEBPB	chr8:6106947-6107139	MCF-7	breast:	n/a	chr8:6107026-6107037 chr8:6107026-6107039 chr8:6107028-6107039 chr8:6107028-6107037
10	CEBPB	chr8:6106985-6107104	K562	blood:	n/a	chr8:6107026-6107037 chr8:6107026-6107039 chr8:6107028-6107039 chr8:6107028-6107037
11	CEBPB	chr8:6106856-6107207	HepG2	liver:	n/a	chr8:6107026-6107037 chr8:6107026-6107039 chr8:6107028-6107039 chr8:6107028-6107037
12	CEBPB	chr8:6128437-6128476	K562	blood:	n/a	n/a
13	CTCF	chr8:6116080-6116230	NB4	blood:	n/a	n/a
14	CTCF	chr8:6116120-6116270	GM12867	blood:	n/a	n/a
15	CTCF	chr8:6116120-6116270	SAEC	small airway:	n/a	n/a
16	CTCF	chr8:6140653-6140811	HepG2	liver:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
17	CTCF	chr8:6116180-6116330	RPTEC	kidney:	n/a	n/a
18	CTCF	chr8:6140680-6140830	MCF-7	breast:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
19	CTCF	chr8:6116163-6116242	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr8:6116140-6116290	GM12864	blood:	n/a	n/a
21	CTCF	chr8:6116051-6116307	Gliobla	brain:	n/a	n/a
22	CTCF	chr8:6115894-6116460	HCT-116	colon:	n/a	n/a
23	CTCF	chr8:6147180-6147330	WERI-Rb-1	eye:	n/a	chr8:6147257-6147270
24	CTCF	chr8:6116089-6116275	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr8:6116065-6116286	A549	lung:	n/a	n/a
26	CTCF	chr8:6116100-6116317	A549	lung:	n/a	n/a
27	CTCF	chr8:6147121-6147372	K562	blood:	n/a	chr8:6147257-6147270
28	CTCF	chr8:6147177-6147364	H1-hESC	embryonic stem cell:	n/a	chr8:6147257-6147270
29	CTCF	chr8:6116001-6116339	K562	blood:	n/a	n/a
30	CTCF	chr8:6116141-6116268	GM19239	blood:	n/a	n/a
31	CTCF	chr8:6140651-6140824	MCF-7	breast:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
32	CTCF	chr8:6140660-6140810	GM12864	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
33	CTCF	chr8:6109067-6109110	LNCaP	prostate:	n/a	n/a
34	CTCF	chr8:6140686-6140835	GM12892	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
35	CTCF	chr8:6115820-6115970	GM12878	blood:	n/a	n/a
36	CTCF	chr8:6116080-6116230	HRE	kidney:	n/a	n/a
37	CTCF	chr8:6140730-6140797	LNCaP	prostate:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
38	CTCF	chr8:6116050-6116354	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr8:6116140-6116290	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr8:6140600-6140750	SAEC	small airway:	n/a	n/a
41	CTCF	chr8:6140640-6140790	GM06990	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
42	CTCF	chr8:6115987-6116327	HepG2	liver:	n/a	n/a
43	CTCF	chr8:6116080-6116230	HCFaa	heart:	n/a	n/a
44	CTCF	chr8:6116080-6116230	HepG2	liver:	n/a	n/a
45	CTCF	chr8:6116020-6116170	HepG2	liver:	n/a	n/a
46	CTCF	chr8:6140660-6140810	K562	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
47	CTCF	chr8:6116060-6116210	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr8:6140682-6140798	HepG2	liver:	n/a	chr8:6140735-6140753 chr8:6140730-6140751
49	CTCF	chr8:6116020-6116170	HCT-116	colon:	n/a	n/a
50	CTCF	chr8:6140660-6140810	GM06990	blood:	n/a	chr8:6140735-6140753 chr8:6140730-6140751

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6118526-6118576	HNPCEpiC	eye:	n/a
2	chr8:6118575-6118625	GM19239	blood:	n/a
3	chr8:6118575-6118625	U87	brain:	n/a
4	chr8:6118575-6118625	HRCEpiC	kidney:	n/a
5	chr8:6118526-6118576	ECC-1	luminal epithelium:	n/a
6	chr8:6118575-6118625	Hela-S3	cervix:	n/a
7	chr8:6118526-6118576	BJ	skin:	n/a
8	chr8:6118575-6118625	H1-hESC	embryonic stem cell:	embryo
9	chr8:6118526-6118576	GM12892	blood:	n/a
10	chr8:6118575-6118625	GM12891	blood:	n/a
11	chr8:6118526-6118576	T-47D	breast:	n/a
12	chr8:6118526-6118576	HEK293	kidney:	embryo
13	chr8:6118575-6118625	A549	lung:	n/a
14	chr8:6118575-6118625	GM06990	blood:	n/a
15	chr8:6118526-6118576	HIPEpiC	eye:	n/a
16	chr8:6118526-6118576	HCT-116	colon:	n/a
17	chr8:6118526-6118576	PFSK-1	brain:	n/a
18	chr8:6118575-6118625	ovcar-3	ovarian:	n/a
19	chr8:6118575-6118625	IMR90	lung:	fetal
20	chr8:6118575-6118625	PFSK-1	brain:	n/a
21	chr8:6118575-6118625	LNCaP	prostate:	n/a
22	chr8:6118575-6118625	HEK293	kidney:	embryo
23	chr8:6118526-6118576	SK-N-MC	brain:	n/a
24	chr8:6118526-6118576	SK-N-SH_RA	brain:	n/a
25	chr8:6118526-6118576	LNCaP	prostate:	n/a
26	chr8:6118526-6118576	MCF10A-Er-Src	breast:	n/a
27	chr8:6118526-6118576	AG10803	skin:	n/a
28	chr8:6118526-6118576	K562	blood:	n/a
29	chr8:6118575-6118625	HCF	heart:	n/a
30	chr8:6118526-6118576	A549	lung:	n/a
31	chr8:6118526-6118576	NHDF-neo	bronchial:	n/a
32	chr8:6118526-6118576	HEEpiC	esophagus:	n/a
33	chr8:6118526-6118576	AG09309	skin:	n/a
34	chr8:6118575-6118625	HPAEpiC	pulmonary alveolar:	n/a
35	chr8:6118526-6118576	HPAEpiC	pulmonary alveolar:	n/a
36	chr8:6118575-6118625	T-47D	breast:	n/a
37	chr8:6118575-6118625	SK-N-SH_RA	brain:	n/a
38	chr8:6118526-6118576	AG09319	gingival:	n/a
39	chr8:6118526-6118576	RPTEC	kidney:	n/a
40	chr8:6118575-6118625	SAEC	small airway:	n/a
41	chr8:6118526-6118576	Hepatocyte	liver:	n/a
42	chr8:6118575-6118625	MCF-7	breast:	n/a
43	chr8:6118575-6118625	SK-N-SH	brain:	n/a
44	chr8:6118526-6118576	PrEC	prostate:	n/a
45	chr8:6118575-6118625	NB4	blood:	n/a
46	chr8:6118526-6118576	AG04449	skin:	fetal
47	chr8:6118575-6118625	BE2_C	brain:	n/a
48	chr8:6118526-6118576	BE2_C	brain:	n/a
49	chr8:6118575-6118625	HUVEC	blood vessel:	n/a
50	chr8:6118575-6118625	HCT-116	colon:	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	chr8:6115678..6116241-chr8:6687345..6688278,2	K562	blood:
4	chr8:6115787..6116559-chr8:6229328..6229869,2	MCF-7	breast:
5	chr8:6116111..6116635-chr8:6188825..6189362,2	MCF-7	breast:
6	chr8:6117190..6120021-chr8:6122326..6123985,2	K562	blood:
7	chr8:6145627..6147844-chr8:6162410..6164202,2	MCF-7	breast:
8	chr8:6106618..6108795-chr8:6113891..6116770,2	K562	blood:
9	chr8:6139049..6141857-chr8:6147372..6149538,2	K562	blood:

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: 3360 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:3360 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13273029	chr8:6104977-6104978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs78236303	chr8:6104989-6104990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149059506	chr8:6104993-6104994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567259541	chr8:6105022-6105023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs58499895	chr8:6105045-6105046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs34515085	chr8:6105046-6105047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs143124761	chr8:6105073-6105074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371805955	chr8:6105089-6105090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146663261	chr8:6105094-6105095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs566677980	chr8:6105117-6105118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs529341247	chr8:6105121-6105122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538421549	chr8:6105132-6105133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140261447	chr8:6105138-6105139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575147520	chr8:6105139-6105140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569140443	chr8:6105146-6105147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs75206370	chr8:6105168-6105169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs538252022	chr8:6105183-6105184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs118115325	chr8:6105206-6105207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574472147	chr8:6105231-6105232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187832764	chr8:6105255-6105256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs560350253	chr8:6105269-6105270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532753162	chr8:6105278-6105279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191202285	chr8:6105280-6105281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546037455	chr8:6105282-6105283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs184623826	chr8:6105294-6105295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs62505522	chr8:6105301-6105302	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs539602409	chr8:6105317-6105318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs548322964	chr8:6105333-6105334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs145151940	chr8:6105359-6105360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs529684456	chr8:6105365-6105366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187954587	chr8:6105370-6105371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553193900	chr8:6105382-6105383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs193010126	chr8:6105384-6105385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs184784094	chr8:6105390-6105391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs558516508	chr8:6105419-6105420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs190080076	chr8:6105425-6105426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs567667037	chr8:6105434-6105435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs537778015	chr8:6105445-6105446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554415246	chr8:6105446-6105447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574509031	chr8:6105461-6105462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs181654228	chr8:6105462-6105463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs533904257	chr8:6105507-6105508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs386721727	chr8:6105513-6105514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs73190780	chr8:6105514-6105515	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs12547647	chr8:6105531-6105532	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs563107228	chr8:6105544-6105545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576686511	chr8:6105545-6105546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs542558466	chr8:6105576-6105577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs562331600	chr8:6105612-6105613	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs535179112	chr8:6105628-6105629	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

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
Osteosarcoma	21215367	CNVD

Chromatin state (count:130 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6104000-6105600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr8:6104000-6106000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr8:6104400-6107400	Enhancers	Primary hematopoietic stem cells	blood
4	chr8:6104800-6105200	Enhancers	H1 Cell Line	embryonic stem cell
5	chr8:6105000-6107400	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr8:6105200-6105600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr8:6105600-6106400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr8:6106000-6106400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr8:6106400-6111200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr8:6106400-6111200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr8:6107000-6107200	Enhancers	H1 Cell Line	embryonic stem cell
12	chr8:6107400-6110200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr8:6107400-6110600	Weak transcription	Primary hematopoietic stem cells	blood
14	chr8:6110200-6110600	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr8:6110600-6111000	Enhancers	Primary hematopoietic stem cells	blood
16	chr8:6110600-6111800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr8:6111000-6112400	Weak transcription	Primary hematopoietic stem cells	blood
18	chr8:6111200-6112200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr8:6111200-6112200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr8:6111800-6112800	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr8:6112200-6112600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr8:6112200-6112800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr8:6112400-6112600	Enhancers	Primary hematopoietic stem cells	blood
24	chr8:6112800-6114800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr8:6114800-6115200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr8:6114800-6115200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr8:6119400-6120000	Enhancers	Brain Germinal Matrix	brain
28	chr8:6119400-6120000	Enhancers	Osteobl	bone
29	chr8:6119400-6120200	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr8:6120000-6121000	Weak transcription	Brain Germinal Matrix	brain
31	chr8:6120200-6120800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr8:6120800-6121200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr8:6121000-6121200	Enhancers	Brain Germinal Matrix	brain
34	chr8:6122200-6123200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr8:6128200-6128600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr8:6132000-6132800	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr8:6132200-6132800	Enhancers	Spleen	Spleen
38	chr8:6132200-6133600	Enhancers	Pancreas	Pancrea
39	chr8:6132800-6134800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr8:6132800-6149000	Weak transcription	Spleen	Spleen
41	chr8:6134800-6135000	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr8:6138400-6141200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr8:6140200-6140400	Active TSS	Breast Myoepithelial Primary Cells	Breast
44	chr8:6140800-6141000	Active TSS	Breast Myoepithelial Primary Cells	Breast
45	chr8:6141200-6141400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr8:6141400-6144400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr8:6144400-6144600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr8:6144600-6147200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr8:6147200-6147400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr8:6147200-6148200	Enhancers	Breast Myoepithelial Primary Cells	Breast

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