Variant report

Variant	esv1825455
Chromosome Location	chr8:108504907-108518274
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:650)
CpG islands
(count:550)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:650 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:108507521-108507714	K562	blood:	n/a	n/a
2	ARID3A	chr8:108508084-108508490	K562	blood:	n/a	n/a
3	ATF1	chr8:108509570-108509767	K562	blood:	n/a	n/a
4	ATF1	chr8:108507182-108507614	K562	blood:	n/a	n/a
5	ATF1	chr8:108511798-108512110	K562	blood:	n/a	n/a
6	ATF1	chr8:108508076-108508478	K562	blood:	n/a	n/a
7	ATF1	chr8:108516735-108516955	K562	blood:	n/a	n/a
8	BACH1	chr8:108510092-108510388	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr8:108509292-108509700	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr8:108508071-108508438	K562	blood:	n/a	n/a
11	BACH1	chr8:108507381-108508744	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr8:108507353-108507568	GM12878	blood:	n/a	chr8:108507473-108507483 chr8:108507472-108507483
13	BHLHE40	chr8:108507613-108507809	K562	blood:	n/a	n/a
14	BHLHE40	chr8:108509316-108509391	K562	blood:	n/a	n/a
15	BHLHE40	chr8:108512087-108512160	K562	blood:	n/a	n/a
16	CBX3	chr8:108511563-108511961	K562	blood:	n/a	n/a
17	CBX3	chr8:108507978-108508422	K562	blood:	n/a	n/a
18	CEBPB	chr8:108506654-108506856	HepG2	liver:	n/a	n/a
19	CEBPB	chr8:108511629-108512013	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr8:108513528-108513941	IMR90	lung:	n/a	n/a
21	CEBPB	chr8:108510707-108511051	IMR90	lung:	n/a	chr8:108510870-108510881
22	CEBPB	chr8:108506742-108506744	A549	lung:	n/a	n/a
23	CEBPB	chr8:108509553-108510383	IMR90	lung:	n/a	n/a
24	CHD2	chr8:108511680-108511937	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr8:108508160-108508310	HPF	lung:	n/a	n/a
26	CTCF	chr8:108508100-108508250	HA-sp	spinal cord:	n/a	n/a
27	CTCF	chr8:108508053-108508514	MCF-7	breast:	n/a	n/a
28	CTCF	chr8:108511714-108511716	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr8:108508117-108508352	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr8:108508200-108508350	AG04450	lung:	n/a	n/a
31	CTCF	chr8:108511683-108511953	K562	blood:	n/a	n/a
32	CTCF	chr8:108509200-108509350	HFF	foreskin:	n/a	n/a
33	CTCF	chr8:108511613-108512018	IMR90	lung:	n/a	n/a
34	CTCF	chr8:108508050-108508353	A549	lung:	n/a	n/a
35	CTCF	chr8:108507900-108508050	HRE	kidney:	n/a	n/a
36	CTCF	chr8:108511756-108511910	GM10248	blood:	n/a	n/a
37	CTCF	chr8:108511760-108511910	GM12871	blood:	n/a	n/a
38	CTCF	chr8:108511880-108512030	MCF-7	breast:	n/a	n/a
39	CTCF	chr8:108508140-108508290	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr8:108508180-108508330	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr8:108511780-108511930	RPTEC	kidney:	n/a	n/a
42	CTCF	chr8:108508180-108508330	MCF-7	breast:	n/a	n/a
43	CTCF	chr8:108508180-108508330	AG09319	gingival:	n/a	n/a
44	CTCF	chr8:108509280-108509430	AG04449	skin:	n/a	n/a
45	CTCF	chr8:108508160-108508310	GM12875	blood:	n/a	n/a
46	CTCF	chr8:108509340-108509490	AG09309	skin:	n/a	n/a
47	CTCF	chr8:108509340-108509490	AG04449	skin:	n/a	n/a
48	CTCF	chr8:108509316-108509414	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr8:108508167-108508312	GM13976	blood:	n/a	n/a
50	CTCF	chr8:108508120-108508270	HVMF	connective:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:108510286-108510336	ECC-1	luminal epithelium:	n/a
2	chr8:108510286-108510336	ECC-1	luminal epithelium:	n/a
3	chr8:108511700-108511750	LNCaP	prostate:	n/a
4	chr8:108510286-108510336	CMK	blood:	n/a
5	chr8:108510096-108510146	HCM	heart:	n/a
6	chr8:108510314-108510364	NHBE	bronchial:	n/a
7	chr8:108511174-108511224	HepG2	liver:	n/a
8	chr8:108510096-108510146	HCPEpiC	choroid plexus:	n/a
9	chr8:108510286-108510336	HEEpiC	esophagus:	n/a
10	chr8:108510096-108510146	IMR90	lung:	fetal
11	chr8:108510096-108510146	K562	blood:	n/a
12	chr8:108509756-108509806	T-47D	breast:	n/a
13	chr8:108510314-108510364	HRPEpiC	eye:	n/a
14	chr8:108510096-108510146	HPAEpiC	pulmonary alveolar:	n/a
15	chr8:108510286-108510336	HRCEpiC	kidney:	n/a
16	chr8:108509756-108509806	NHDF-neo	bronchial:	n/a
17	chr8:108509756-108509806	H1-hESC	embryonic stem cell:	embryo
18	chr8:108510314-108510364	HCPEpiC	choroid plexus:	n/a
19	chr8:108510292-108510342	Jurkat	blood:	n/a
20	chr8:108510292-108510342	AG10803	skin:	n/a
21	chr8:108510096-108510146	PFSK-1	brain:	n/a
22	chr8:108510292-108510342	A549	lung:	n/a
23	chr8:108511700-108511750	BJ	skin:	n/a
24	chr8:108510286-108510336	Hela-S3	cervix:	n/a
25	chr8:108509756-108509806	HEK293	kidney:	embryo
26	chr8:108511700-108511750	Jurkat	blood:	n/a
27	chr8:108510096-108510146	BJ	skin:	n/a
28	chr8:108509756-108509806	AoSMC	blood vessel:	n/a
29	chr8:108510292-108510342	HCPEpiC	choroid plexus:	n/a
30	chr8:108510292-108510342	RPTEC	kidney:	n/a
31	chr8:108510286-108510336	NHDF-neo	bronchial:	n/a
32	chr8:108510096-108510146	Jurkat	blood:	n/a
33	chr8:108510292-108510342	HEK293	kidney:	embryo
34	chr8:108511621-108511671	SK-N-SH	brain:	n/a
35	chr8:108510096-108510146	HL-60	blood:	n/a
36	chr8:108511621-108511671	NHBE	bronchial:	n/a
37	chr8:108510314-108510364	HRE	kidney:	n/a
38	chr8:108511174-108511224	LNCaP	prostate:	n/a
39	chr8:108511700-108511750	SK-N-MC	brain:	n/a
40	chr8:108510286-108510336	SK-N-SH_RA	brain:	n/a
41	chr8:108510286-108510336	SKMC	muscle:	n/a
42	chr8:108510292-108510342	T-47D	breast:	n/a
43	chr8:108510343-108510393	LNCaP	prostate:	n/a
44	chr8:108510286-108510336	HEK293	kidney:	embryo
45	chr8:108510286-108510336	ProgFib	skin:	n/a
46	chr8:108509756-108509806	HMEC	breast:	n/a
47	chr8:108510096-108510146	BE2_C	brain:	n/a
48	chr8:108509756-108509806	GM12878	blood:	n/a
49	chr8:108511700-108511750	HPAEpiC	pulmonary alveolar:	n/a
50	chr8:108511700-108511750	RPTEC	kidney:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:66671180..66672114-chr8:108507497..108508036,2	MCF-7	breast:
2	chr8:108510326..108512343-chr8:108512433..108514232,2	K562	blood:
3	chr8:108510326..108512343-chr8:108512433..108514232,2	K562	blood:
4	chr8:108507981..108510207-chr8:108513209..108515922,2	K562	blood:
5	chr8:108080564..108081493-chr8:108508119..108508723,3	MCF-7	breast:
6	chr8:108511470..108511977-chr8:108793503..108794373,2	MCF-7	breast:
7	chr8:107857692..107858790-chr8:108507689..108508327,3	MCF-7	breast:
8	chr8:108516351..108518369-chr8:108521717..108523798,2	K562	blood:
9	chr8:108507981..108510207-chr8:108513209..108515922,2	K562	blood:

No data

Variant related genes	Relation type
ANGPT1	TF binding region
ANGPT1	CpG island

Extended variants
information (count: 412 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577011796	chr8:108504944-108504945	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs147517724	chr8:108504956-108504957	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs562478794	chr8:108504957-108504958	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs139305754	chr8:108504976-108504977	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs66520979	chr8:108504980-108504981	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs559662742	chr8:108504982-108504983	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs578067427	chr8:108505021-108505022	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs62514487	chr8:108505085-108505086	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs17302560	chr8:108505219-108505220	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs547574983	chr8:108505257-108505258	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs192214448	chr8:108505360-108505361	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs150020573	chr8:108505412-108505413	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs115101185	chr8:108505424-108505425	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs184301850	chr8:108505457-108505458	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs536176455	chr8:108505485-108505486	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs138836750	chr8:108505486-108505487	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs200940008	chr8:108505487-108505488	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs554565468	chr8:108505568-108505569	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs567967831	chr8:108505569-108505570	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs144206715	chr8:108505579-108505580	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs535771306	chr8:108505592-108505593	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs576955354	chr8:108505601-108505602	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs187185742	chr8:108505650-108505651	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs148717670	chr8:108505653-108505654	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs192921171	chr8:108505654-108505655	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs541728643	chr8:108505666-108505667	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs561698348	chr8:108505722-108505723	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs527729883	chr8:108505836-108505837	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs541503051	chr8:108505837-108505838	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs184591193	chr8:108505898-108505899	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs533546895	chr8:108505900-108505901	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs550368720	chr8:108505983-108505984	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs1283721	chr8:108505986-108505987	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs550677929	chr8:108506028-108506029	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs60357123	chr8:108506068-108506069	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs189525781	chr8:108506069-108506070	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs568039657	chr8:108506080-108506081	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs533588822	chr8:108506254-108506255	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs538638279	chr8:108506354-108506355	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs373234060	chr8:108506408-108506409	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs141147012	chr8:108506419-108506420	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs539164585	chr8:108506455-108506456	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs555897577	chr8:108506485-108506486	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs575833517	chr8:108506499-108506500	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs535356258	chr8:108506512-108506513	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs180770392	chr8:108506518-108506519	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs143349042	chr8:108506537-108506538	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs570550367	chr8:108506601-108506602	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs151207550	chr8:108506617-108506618	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs185033569	chr8:108506681-108506682	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Multiple myeloma	16461302	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	22539939	CNVD
Non-small cell lung cancer	19010865	CNVD
Prostate cancer	22341455	CNVD
Colorectal cancer	21645411	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:700 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:108497800-108508400	Weak transcription	Left Ventricle	heart
2	chr8:108498200-108506800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr8:108498400-108506800	Weak transcription	Brain Hippocampus Middle	brain
4	chr8:108498400-108507400	Weak transcription	Brain Cingulate Gyrus	brain
5	chr8:108499000-108506600	Weak transcription	Brain Substantia Nigra	brain
6	chr8:108499400-108507000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr8:108499600-108506800	Weak transcription	Fetal Thymus	thymus
8	chr8:108499800-108506800	Weak transcription	Aorta	Aorta
9	chr8:108500400-108507200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr8:108501800-108505200	Weak transcription	Fetal Kidney	kidney
11	chr8:108502400-108507600	Weak transcription	Psoas Muscle	Psoas
12	chr8:108502600-108506800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr8:108502800-108505400	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr8:108502800-108506400	Weak transcription	NHDF-Ad	bronchial
15	chr8:108502800-108506400	Weak transcription	NHLF	lung
16	chr8:108502800-108506600	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr8:108502800-108506600	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr8:108502800-108506600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr8:108502800-108506600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr8:108502800-108506600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr8:108502800-108506600	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr8:108502800-108506600	Weak transcription	Brain Germinal Matrix	brain
23	chr8:108502800-108506600	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr8:108502800-108506800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr8:108502800-108506800	Weak transcription	Fetal Brain Female	brain
26	chr8:108502800-108507000	Weak transcription	Ovary	ovary
27	chr8:108502800-108507200	Weak transcription	A549	lung
28	chr8:108502800-108507600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr8:108502800-108509200	Weak transcription	NHEK	skin
30	chr8:108503000-108505200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr8:108503000-108505200	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr8:108503000-108505800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr8:108503000-108506600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr8:108503000-108506600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr8:108503000-108506600	Weak transcription	Colon Smooth Muscle	Colon
36	chr8:108503000-108506800	Weak transcription	Adipose Nuclei	Adipose
37	chr8:108503000-108507400	Weak transcription	Rectal Smooth Muscle	rectum
38	chr8:108503000-108508400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr8:108503200-108505400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr8:108503200-108506200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr8:108503600-108505200	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr8:108503600-108506400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr8:108503800-108505400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr8:108503800-108506200	Weak transcription	Osteobl	bone
45	chr8:108503800-108506800	Weak transcription	Brain Anterior Caudate	brain
46	chr8:108503800-108506800	Weak transcription	Stomach Smooth Muscle	stomach
47	chr8:108504000-108505200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr8:108504000-108505200	Enhancers	Primary hematopoietic stem cells	blood
49	chr8:108504000-108506400	Weak transcription	Fetal Lung	lung
50	chr8:108504000-108506600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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