Variant report

Variant	nsv1022346
Chromosome Location	chr8:5761956-5808225
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:139)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:139 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:5765727-5765858	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr8:5766581-5766595	A549	lung:	n/a	n/a
3	CTCF	chr8:5790273-5790369	HUVEC	blood vessel:	n/a	n/a
4	CTCF	chr8:5790174-5790455	GM12878	blood:	n/a	n/a
5	CTCF	chr8:5790180-5790330	RPTEC	kidney:	n/a	n/a
6	CTCF	chr8:5765000-5765150	GM12866	blood:	n/a	n/a
7	CTCF	chr8:5798357-5798574	MCF-7	breast:	n/a	n/a
8	CTCF	chr8:5790263-5790411	K562	blood:	n/a	n/a
9	CTCF	chr8:5790220-5790370	HCT-116	colon:	n/a	n/a
10	CTCF	chr8:5798360-5798510	BE2_C	brain:	n/a	n/a
11	CTCF	chr8:5798480-5798630	A549	lung:	n/a	n/a
12	CTCF	chr8:5798330-5798542	LNCaP	prostate:	n/a	n/a
13	CTCF	chr8:5798264-5798632	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr8:5790240-5790390	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr8:5790220-5790370	MCF-7	breast:	n/a	n/a
16	CTCF	chr8:5798441-5798516	Gliobla	brain:	n/a	n/a
17	CTCF	chr8:5798329-5798521	HepG2	liver:	n/a	n/a
18	CTCF	chr8:5790235-5790336	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr8:5798340-5798490	HFF-Myc	foreskin:	n/a	n/a
20	CTCF	chr8:5798340-5798490	MCF-7	breast:	n/a	n/a
21	CTCF	chr8:5798326-5798597	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr8:5798374-5798543	MCF-7	breast:	n/a	n/a
23	CTCF	chr8:5798420-5798570	Caco-2	colon:	n/a	n/a
24	CTCF	chr8:5798380-5798530	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr8:5790240-5790390	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr8:5790200-5790350	NHDF-neo	bronchial:	n/a	n/a
27	CTCF	chr8:5798353-5798573	MCF-7	breast:	n/a	n/a
28	CTCF	chr8:5790260-5790410	BE2_C	brain:	n/a	n/a
29	CTCF	chr8:5798351-5798551	GM12878	blood:	n/a	n/a
30	CTCF	chr8:5790269-5790386	Medullo	brain:	n/a	n/a
31	CTCF	chr8:5790240-5790390	A549	lung:	n/a	n/a
32	CTCF	chr8:5790601-5790700	Gliobla	brain:	n/a	n/a
33	CTCF	chr8:5790260-5790410	HepG2	liver:	n/a	n/a
34	CTCF	chr8:5790281-5790360	HepG2	liver:	n/a	n/a
35	CTCF	chr8:5790220-5790370	GM12866	blood:	n/a	n/a
36	CTCF	chr8:5790240-5790390	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr8:5790260-5790410	NHEK	skin:	n/a	n/a
38	CTCF	chr8:5798268-5798623	MCF-7	breast:	n/a	n/a
39	CTCF	chr8:5790238-5790466	LNCaP	prostate:	n/a	n/a
40	CTCF	chr8:5798440-5798590	HepG2	liver:	n/a	n/a
41	CTCF	chr8:5790260-5790410	NB4	blood:	n/a	n/a
42	CTCF	chr8:5790260-5790410	GM12869	blood:	n/a	n/a
43	CTCF	chr8:5790240-5790390	MCF-7	breast:	n/a	n/a
44	CTCF	chr8:5790251-5790406	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr8:5790254-5790377	MCF-7	breast:	n/a	n/a
46	CTCF	chr8:5790300-5790450	RPTEC	kidney:	n/a	n/a
47	CTCF	chr8:5798360-5798510	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr8:5790220-5790370	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr8:5798380-5798530	Caco-2	colon:	n/a	n/a
50	CTCF	chr8:5796519-5796555	LNCaP	prostate:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:5762990-5763040	HPAEpiC	pulmonary alveolar:	n/a
2	chr8:5762990-5763040	IMR90	lung:	fetal
3	chr8:5762944-5762994	BE2_C	brain:	n/a
4	chr8:5762990-5763040	HCM	heart:	n/a
5	chr8:5762990-5763040	SK-N-SH_RA	brain:	n/a
6	chr8:5762990-5763040	Jurkat	blood:	n/a
7	chr8:5762990-5763040	AG09319	gingival:	n/a
8	chr8:5762944-5762994	HRCEpiC	kidney:	n/a
9	chr8:5762944-5762994	HUVEC	blood vessel:	n/a
10	chr8:5762990-5763040	AG04450	lung:	fetal
11	chr8:5762990-5763040	T-47D	breast:	n/a
12	chr8:5762990-5763040	HepG2	liver:	n/a
13	chr8:5762944-5762994	NHDF-neo	bronchial:	n/a
14	chr8:5762990-5763040	ProgFib	skin:	n/a
15	chr8:5762944-5762994	SKMC	muscle:	n/a
16	chr8:5762944-5762994	SAEC	small airway:	n/a
17	chr8:5762990-5763040	HRE	kidney:	n/a
18	chr8:5762944-5762994	BJ	skin:	n/a
19	chr8:5762944-5762994	PANC-1	pancreas:	n/a
20	chr8:5762944-5762994	A549	lung:	n/a
21	chr8:5762990-5763040	HCT-116	colon:	n/a
22	chr8:5762990-5763040	CMK	blood:	n/a
23	chr8:5762944-5762994	HMEC	breast:	n/a
24	chr8:5762944-5762994	SK-N-SH_RA	brain:	n/a
25	chr8:5762944-5762994	ovcar-3	ovarian:	n/a
26	chr8:5762944-5762994	SK-N-SH	brain:	n/a
27	chr8:5762944-5762994	GM06990	blood:	n/a
28	chr8:5762990-5763040	GM12892	blood:	n/a
29	chr8:5762990-5763040	K562	blood:	n/a
30	chr8:5762990-5763040	RPTEC	kidney:	n/a
31	chr8:5762990-5763040	AG04449	skin:	fetal
32	chr8:5762944-5762994	HCPEpiC	choroid plexus:	n/a
33	chr8:5762944-5762994	GM12878	blood:	n/a
34	chr8:5762944-5762994	NH-A	brain:	n/a
35	chr8:5762944-5762994	K562	blood:	n/a
36	chr8:5762990-5763040	NHDF-neo	bronchial:	n/a
37	chr8:5762990-5763040	Hela-S3	cervix:	n/a
38	chr8:5762944-5762994	GM12891	blood:	n/a
39	chr8:5762944-5762994	HRE	kidney:	n/a
40	chr8:5762944-5762994	H1-hESC	embryonic stem cell:	embryo
41	chr8:5762944-5762994	ECC-1	luminal epithelium:	n/a
42	chr8:5762944-5762994	ProgFib	skin:	n/a
43	chr8:5762944-5762994	SK-N-MC	brain:	n/a
44	chr8:5762944-5762994	NT2-D1	testis:	n/a
45	chr8:5762944-5762994	HEK293	kidney:	embryo
46	chr8:5762944-5762994	CMK	blood:	n/a
47	chr8:5762990-5763040	LNCaP	prostate:	n/a
48	chr8:5762990-5763040	NT2-D1	testis:	n/a
49	chr8:5762990-5763040	AG10803	skin:	n/a
50	chr8:5762944-5762994	Jurkat	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:5797855..5798416-chr8:5934095..5934883,2	MCF-7	breast:
2	chr8:5775799..5778570-chr8:6262790..6264825,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANGPT2-12	chr8:5768467-5768758	NONHSAT124763

No data

Variant related genes	Relation type
RN7SKP159	TF binding region
RN7SKP159	CpG island
ENSG00000147316	chromatin interactions
ENSG00000246089	chromatin interactions

Extended variants
information (count: 1069 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:1069 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569316756	chr8:5761975-5761976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs562684800	chr8:5761978-5761979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527916909	chr8:5761983-5761984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540656394	chr8:5761994-5761995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116897279	chr8:5762072-5762073	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564285090	chr8:5762098-5762099	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531680847	chr8:5762128-5762129	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs550156128	chr8:5762142-5762143	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561884348	chr8:5762153-5762154	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs149839487	chr8:5762159-5762160	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547340623	chr8:5762170-5762171	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565963890	chr8:5762176-5762177	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539692981	chr8:5762179-5762180	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145714894	chr8:5762196-5762197	Enhancers Active TSS Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370326685	chr8:5762202-5762203	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs537589088	chr8:5762210-5762211	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs569776451	chr8:5762228-5762229	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs141510434	chr8:5762247-5762248	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs189647458	chr8:5762250-5762251	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs549214569	chr8:5762266-5762267	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs181699437	chr8:5762271-5762272	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs111928671	chr8:5762277-5762278	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs554073858	chr8:5762280-5762281	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs79296022	chr8:5762295-5762296	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs546026836	chr8:5762308-5762309	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs545405805	chr8:5762326-5762327	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs181771310	chr8:5762335-5762336	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs147688589	chr8:5762356-5762357	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs543523112	chr8:5762398-5762399	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs562129416	chr8:5762402-5762403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186774704	chr8:5762417-5762418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529303106	chr8:5762433-5762434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189173840	chr8:5762438-5762439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559726435	chr8:5762444-5762445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142200823	chr8:5762446-5762447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182017972	chr8:5762453-5762454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs75549531	chr8:5762461-5762462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537168699	chr8:5762489-5762490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs548842928	chr8:5762493-5762494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567334300	chr8:5762521-5762522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185073678	chr8:5762535-5762536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552539160	chr8:5762583-5762584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572412679	chr8:5762586-5762587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539695510	chr8:5762589-5762590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557948306	chr8:5762619-5762620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576525624	chr8:5762626-5762627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145928237	chr8:5762662-5762663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs377202981	chr8:5762668-5762669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570791821	chr8:5762674-5762675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562067858	chr8:5762686-5762687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:126)

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
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic myeloid leukemia	21384125	CNVD
Tetralogy of Fallot	22912587	CNVD
Type 2 diabetes	21526130	CNVD
Medulloblastoma	16783165	CNVD
Schizophrenia	20967226	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:5761400-5762000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:5761400-5763400	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr8:5761600-5762000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr8:5761600-5763400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr8:5761600-5763400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr8:5762000-5762200	Enhancers	H1 Cell Line	embryonic stem cell
7	chr8:5762000-5762200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr8:5762000-5762400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr8:5762200-5764000	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr8:5762200-5764600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr8:5763400-5763600	Enhancers	H9 Cell Line	embryonic stem cell
12	chr8:5763400-5764200	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr8:5763400-5764600	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr8:5763400-5765600	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr8:5763400-5765800	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr8:5763600-5764200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr8:5763600-5764600	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr8:5763800-5764600	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr8:5764000-5764200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr8:5764000-5764600	Enhancers	H1 Cell Line	embryonic stem cell
21	chr8:5764600-5765000	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr8:5764600-5765400	Enhancers	H9 Cell Line	embryonic stem cell
23	chr8:5764600-5765600	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr8:5765000-5765600	Enhancers	H1 Cell Line	embryonic stem cell
25	chr8:5772600-5774600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr8:5773000-5774800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr8:5792200-5794800	Enhancers	Dnd41	blood
28	chr8:5796200-5796600	Enhancers	Fetal Heart	heart
29	chr8:5806600-5809600	Weak transcription	Fetal Heart	heart

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