Variant report

Variant	esv3325011
Chromosome Location	chr8:38899844-38936643
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	ARID3A	chr8:38916726-38917084	HepG2	liver:	n/a	n/a
2	ATF1	chr8:38913849-38914015	K562	blood:	n/a	n/a
3	ATF3	chr8:38899369-38900114	A549	lung:	n/a	n/a
4	BCL3	chr8:38899478-38900083	A549	lung:	n/a	n/a
5	BCL3	chr8:38899361-38900044	A549	lung:	n/a	n/a
6	CBX3	chr8:38899375-38899921	HCT-116	colon:	n/a	n/a
7	CEBPB	chr8:38899390-38900167	A549	lung:	n/a	n/a
8	CEBPB	chr8:38913760-38913960	A549	lung:	n/a	n/a
9	CEBPB	chr8:38908227-38908339	HepG2	liver:	n/a	chr8:38908270-38908281
10	CEBPB	chr8:38916668-38916956	HepG2	liver:	n/a	n/a
11	CTCF	chr8:38907540-38907690	HPAF	blood vessel:	n/a	n/a
12	CTCF	chr8:38899388-38900008	SK-N-SH	brain:	n/a	n/a
13	CTCF	chr8:38935120-38935270	BJ	skin:	n/a	n/a
14	CTCF	chr8:38907940-38908090	A549	lung:	n/a	n/a
15	CTCF	chr8:38904345-38904404	A549	lung:	n/a	n/a
16	CTCF	chr8:38922951-38923002	GM10248	blood:	n/a	n/a
17	E2F4	chr8:38899524-38899940	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F4	chr8:38927281-38927430	MCF10A-Er-Src	breast:	n/a	n/a
19	ELF1	chr8:38899420-38899905	A549	lung:	n/a	n/a
20	EP300	chr8:38899236-38900328	SK-N-SH	brain:	n/a	chr8:38900154-38900168 chr8:38900158-38900167
21	EP300	chr8:38899348-38900234	A549	lung:	n/a	chr8:38900154-38900168 chr8:38900158-38900167
22	EP300	chr8:38899605-38900051	SK-N-SH_RA	brain:	n/a	n/a
23	EP300	chr8:38899361-38900179	A549	lung:	n/a	chr8:38900154-38900168 chr8:38900158-38900167
24	EP300	chr8:38932627-38932917	SK-N-SH_RA	brain:	n/a	n/a
25	EP300	chr8:38899364-38900105	SK-N-SH	brain:	n/a	n/a
26	EP300	chr8:38899617-38900005	SK-N-SH_RA	brain:	n/a	n/a
27	EP300	chr8:38899476-38900189	SK-N-SH	brain:	n/a	chr8:38900154-38900168 chr8:38900158-38900167
28	FOS	chr8:38916944-38917182	MCF10A-Er-Src	breast:	n/a	chr8:38917062-38917073
29	FOS	chr8:38916886-38917124	MCF10A-Er-Src	breast:	n/a	chr8:38917062-38917073
30	FOS	chr8:38899600-38900063	HUVEC	blood vessel:	n/a	n/a
31	FOS	chr8:38917014-38917173	MCF10A-Er-Src	breast:	n/a	chr8:38917062-38917073
32	FOS	chr8:38899548-38899992	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr8:38899548-38900002	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr8:38899622-38899975	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr8:38916867-38917317	HUVEC	blood vessel:	n/a	chr8:38917062-38917073
36	FOS	chr8:38916890-38917091	MCF10A-Er-Src	breast:	n/a	chr8:38917062-38917073
37	FOSL1	chr8:38899371-38899995	HCT-116	colon:	n/a	chr8:38899411-38899423
38	FOSL2	chr8:38916830-38917324	SK-N-SH	brain:	n/a	n/a
39	FOSL2	chr8:38899456-38900148	SK-N-SH	brain:	n/a	n/a
40	FOSL2	chr8:38899433-38899993	A549	lung:	n/a	n/a
41	FOSL2	chr8:38899304-38900285	A549	lung:	n/a	chr8:38899411-38899423
42	FOXA1	chr8:38932914-38933130	A549	lung:	n/a	chr8:38933069-38933084
43	FOXA1	chr8:38914569-38914797	T-47D	breast:	n/a	n/a
44	FOXA2	chr8:38899525-38900130	A549	lung:	n/a	chr8:38899987-38899999
45	FOXA2	chr8:38899448-38900234	A549	lung:	n/a	chr8:38899987-38899999 chr8:38899450-38899462
46	FOXA2	chr8:38902844-38903092	A549	lung:	n/a	n/a
47	GABPA	chr8:38899392-38900006	A549	lung:	n/a	n/a
48	GATA1	chr8:38935609-38936309	PBDE	blood:	n/a	chr8:38935941-38935948 chr8:38935941-38935948 chr8:38935770-38935791 chr8:38935772-38935788 chr8:38935941-38935948 chr8:38935775-38935784
49	GATA3	chr8:38900753-38900930	SH-SY5Y	brain:	n/a	n/a
50	GATA3	chr8:38899251-38900343	A549	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:38933732..38936418-chr8:38947721..38949546,2	MCF-7	breast:
2	chr8:38928387..38930115-chr8:38932750..38934544,2	K562	blood:
3	chr8:38928615..38931127-chr8:38932750..38935591,2	K562	blood:
4	chr8:38920268..38922257-chr8:38925771..38928354,3	K562	blood:
5	chr8:38920268..38922257-chr8:38925771..38928354,3	K562	blood:
6	chr8:38915849..38919016-chr8:38921261..38923485,4	K562	blood:
7	chr8:38898390..38901319-chr8:38947288..38950284,2	K562	blood:
8	chr8:38915849..38919016-chr8:38921261..38923485,4	K562	blood:

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ADAM9	hsa-miR-23a-3p	chr8:38912000-38912008

Variant related genes	Relation type
ADAM9	TF binding region
ENSG00000168615	chromatin interactions

Extended variants
information (count: 1349 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1349 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536176990	chr8:38899886-38899887	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs554281509	chr8:38899926-38899927	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs188812772	chr8:38899966-38899967	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs56982260	chr8:38900018-38900019	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs111980663	chr8:38900089-38900090	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs181532750	chr8:38900094-38900095	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs397815127	chr8:38900101-38900102	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs545131130	chr8:38900323-38900324	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs565382896	chr8:38900358-38900359	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs572615484	chr8:38900388-38900389	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs566434059	chr8:38900395-38900396	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs113356388	chr8:38900423-38900424	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs561498084	chr8:38900443-38900444	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs530394026	chr8:38900451-38900452	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs550474631	chr8:38900502-38900503	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs144203746	chr8:38900534-38900535	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs531349070	chr8:38900655-38900656	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs148745238	chr8:38900677-38900678	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs535338662	chr8:38900723-38900724	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs533682190	chr8:38900730-38900731	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs547175666	chr8:38900740-38900741	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs4733970	chr8:38900746-38900747	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs536120970	chr8:38900786-38900787	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs187132731	chr8:38900795-38900796	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs556430061	chr8:38900832-38900833	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs576311790	chr8:38900872-38900873	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs539017943	chr8:38900907-38900908	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs369844990	chr8:38900974-38900975	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs578247435	chr8:38900980-38900981	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs559030574	chr8:38900997-38900998	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs536548788	chr8:38901019-38901020	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs572554261	chr8:38901049-38901050	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs541565222	chr8:38901051-38901052	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs555175295	chr8:38901059-38901060	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs372430495	chr8:38901117-38901118	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs371676460	chr8:38901124-38901125	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs368363836	chr8:38901140-38901141	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs112938703	chr8:38901159-38901160	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs4733903	chr8:38901267-38901268	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs141454879	chr8:38901322-38901323	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564014336	chr8:38901323-38901324	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs147409411	chr8:38901337-38901338	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs191823174	chr8:38901417-38901418	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs10108538	chr8:38901450-38901451	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs370071210	chr8:38901497-38901498	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs73602732	chr8:38901551-38901552	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs145214866	chr8:38901594-38901595	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs547104172	chr8:38901691-38901692	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs147653960	chr8:38901738-38901739	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs529901807	chr8:38901802-38901803	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	21979893	CNVD
Prostate cancer	16573809	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
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
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
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Myxofibrosarcoma	16751306	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
Endometrioid adenocarcinoma	16974079	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
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Non-muscle invasive bladder neoplasm	19445696	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
abnormal development	18461090	CNVD
Breast cancer	16620391	CNVD
Adrenocortical carcinoma	18281524	CNVD
Rhabdomyosarcoma	16790082	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21138945	CNVD
Lung cancer	21569311	CNVD
Breast cancer	21364760	CNVD
Prader-willi syndrome	20588305	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:958 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:38869600-38902800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:38882000-38913600	Weak transcription	Fetal Kidney	kidney
3	chr8:38883000-38913000	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr8:38885200-38902800	Weak transcription	Psoas Muscle	Psoas
5	chr8:38885400-38904400	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr8:38885600-38903600	Weak transcription	Fetal Brain Female	brain
7	chr8:38885800-38911200	Weak transcription	Ovary	ovary
8	chr8:38886400-38904400	Weak transcription	Fetal Muscle Trunk	muscle
9	chr8:38887400-38911200	Weak transcription	Aorta	Aorta
10	chr8:38888200-38904400	Weak transcription	GM12878-XiMat	blood
11	chr8:38888400-38905400	Weak transcription	Primary B cells from cord blood	blood
12	chr8:38888800-38901600	Weak transcription	Fetal Brain Male	brain
13	chr8:38890000-38904400	Weak transcription	Gastric	stomach
14	chr8:38890200-38904400	Weak transcription	Esophagus	oesophagus
15	chr8:38890200-38911200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:38890200-38914400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr8:38890400-38903400	Weak transcription	Fetal Muscle Leg	muscle
18	chr8:38890400-38904200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr8:38890400-38904200	Weak transcription	Fetal Intestine Small	intestine
20	chr8:38890400-38904200	Weak transcription	Lung	lung
21	chr8:38890400-38919800	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr8:38892600-38901000	Weak transcription	Dnd41	blood
23	chr8:38895600-38902000	Weak transcription	Right Ventricle	heart
24	chr8:38895600-38911200	Weak transcription	Fetal Stomach	stomach
25	chr8:38895800-38901600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr8:38896000-38901600	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr8:38896000-38918400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr8:38896000-38925000	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr8:38896200-38900600	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr8:38896200-38900800	Genic enhancers	HSMM	muscle
31	chr8:38896200-38901800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr8:38896200-38907600	Weak transcription	Duodenum Mucosa	Duodenum
33	chr8:38896200-38911200	Weak transcription	Placenta	Placenta
34	chr8:38896200-38911200	Weak transcription	Left Ventricle	heart
35	chr8:38896200-38916000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr8:38896400-38900200	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr8:38896400-38916400	Weak transcription	K562	blood
38	chr8:38896600-38905200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr8:38896600-38912800	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr8:38896800-38900200	Enhancers	Osteobl	bone
41	chr8:38896800-38900400	Weak transcription	Small Intestine	intestine
42	chr8:38896800-38904000	Weak transcription	Primary hematopoietic stem cells	blood
43	chr8:38896800-38911200	Weak transcription	Adipose Nuclei	Adipose
44	chr8:38897200-38900200	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr8:38897200-38907000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr8:38897200-38907800	Weak transcription	Brain Cingulate Gyrus	brain
47	chr8:38897200-38911200	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr8:38897400-38900000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr8:38897400-38900200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr8:38897400-38900200	Weak transcription	Skeletal Muscle Male	skeletal muscle

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