Variant report

Variant	esv3445313
Chromosome Location	chr8:38886844-38936643
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:690)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:690 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:38895681-38896135	K562	blood:	n/a	n/a
2	ARID3A	chr8:38895656-38896176	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:38916726-38917084	HepG2	liver:	n/a	n/a
4	ATF1	chr8:38895603-38896031	K562	blood:	n/a	n/a
5	ATF1	chr8:38887650-38887653	K562	blood:	n/a	n/a
6	ATF1	chr8:38913849-38914015	K562	blood:	n/a	n/a
7	ATF3	chr8:38899369-38900114	A549	lung:	n/a	n/a
8	ATF3	chr8:38895714-38896020	K562	blood:	n/a	n/a
9	ATF3	chr8:38895581-38896049	A549	lung:	n/a	n/a
10	ATF3	chr8:38895569-38896104	A549	lung:	n/a	n/a
11	BATF	chr8:38895654-38895924	GM12878	blood:	n/a	chr8:38895834-38895845
12	BATF	chr8:38895649-38895958	GM12878	blood:	n/a	chr8:38895834-38895845
13	BCL3	chr8:38889740-38890326	A549	lung:	n/a	n/a
14	BCL3	chr8:38895502-38896069	A549	lung:	n/a	n/a
15	BCL3	chr8:38889640-38890361	A549	lung:	n/a	n/a
16	BCL3	chr8:38899361-38900044	A549	lung:	n/a	n/a
17	BCL3	chr8:38899478-38900083	A549	lung:	n/a	n/a
18	BCL3	chr8:38895357-38896520	A549	lung:	n/a	n/a
19	BHLHE40	chr8:38895664-38895994	K562	blood:	n/a	n/a
20	BHLHE40	chr8:38899520-38899658	HepG2	liver:	n/a	n/a
21	CBX3	chr8:38895352-38896140	HCT-116	colon:	n/a	n/a
22	CBX3	chr8:38895573-38895996	K562	blood:	n/a	n/a
23	CBX3	chr8:38895242-38896138	HCT-116	colon:	n/a	n/a
24	CBX3	chr8:38899375-38899921	HCT-116	colon:	n/a	n/a
25	CCNT2	chr8:38895714-38895967	K562	blood:	n/a	n/a
26	CEBPB	chr8:38895691-38896359	IMR90	lung:	n/a	n/a
27	CEBPB	chr8:38916668-38916956	HepG2	liver:	n/a	n/a
28	CEBPB	chr8:38889424-38889609	HepG2	liver:	n/a	n/a
29	CEBPB	chr8:38895642-38896424	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr8:38908227-38908339	HepG2	liver:	n/a	chr8:38908270-38908281
31	CEBPB	chr8:38913760-38913960	A549	lung:	n/a	n/a
32	CEBPB	chr8:38896075-38896399	A549	lung:	n/a	n/a
33	CEBPB	chr8:38895720-38896429	A549	lung:	n/a	n/a
34	CEBPB	chr8:38896169-38896285	HepG2	liver:	n/a	n/a
35	CEBPB	chr8:38895512-38896531	A549	lung:	n/a	n/a
36	CEBPB	chr8:38899390-38900167	A549	lung:	n/a	n/a
37	CEBPB	chr8:38895125-38896583	HCT-116	colon:	n/a	n/a
38	CEBPD	chr8:38886622-38886995	K562	blood:	n/a	n/a
39	CREB1	chr8:38889725-38890186	A549	lung:	n/a	n/a
40	CTCF	chr8:38899546-38899642	GM19240	blood:	n/a	n/a
41	CTCF	chr8:38899469-38899675	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr8:38899500-38899650	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr8:38899520-38899670	BE2_C	brain:	n/a	n/a
44	CTCF	chr8:38899520-38899670	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr8:38899553-38899615	GM13976	blood:	n/a	n/a
46	CTCF	chr8:38899522-38899664	NHEK	skin:	n/a	n/a
47	CTCF	chr8:38899399-38899769	MCF-7	breast:	n/a	n/a
48	CTCF	chr8:38899287-38899718	HCT-116	colon:	n/a	n/a
49	CTCF	chr8:38899520-38899670	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr8:38899500-38899650	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:38898857-38898907	SK-N-MC	brain:	n/a
2	chr8:38898857-38898907	K562	blood:	n/a
3	chr8:38898857-38898907	HEEpiC	esophagus:	n/a
4	chr8:38898857-38898907	GM06990	blood:	n/a
5	chr8:38898857-38898907	CMK	blood:	n/a
6	chr8:38898857-38898907	ovcar-3	ovarian:	n/a
7	chr8:38898857-38898907	AG09309	skin:	n/a
8	chr8:38898857-38898907	Hela-S3	cervix:	n/a
9	chr8:38898857-38898907	HCT-116	colon:	n/a
10	chr8:38898857-38898907	HMEC	breast:	n/a
11	chr8:38898857-38898907	HRE	kidney:	n/a
12	chr8:38898857-38898907	SKMC	muscle:	n/a
13	chr8:38898857-38898907	T-47D	breast:	n/a
14	chr8:38898857-38898907	IMR90	lung:	fetal
15	chr8:38898857-38898907	MCF-7	breast:	n/a
16	chr8:38898857-38898907	GM12892	blood:	n/a
17	chr8:38898857-38898907	HL-60	blood:	n/a
18	chr8:38898857-38898907	H1-hESC	embryonic stem cell:	embryo
19	chr8:38898857-38898907	RPTEC	kidney:	n/a
20	chr8:38898857-38898907	MCF10A-Er-Src	breast:	n/a
21	chr8:38898857-38898907	NB4	blood:	n/a
22	chr8:38898857-38898907	HAEpiC	amniotic membrane:	n/a
23	chr8:38898857-38898907	AG09319	gingival:	n/a
24	chr8:38898857-38898907	AG04450	lung:	fetal
25	chr8:38898857-38898907	Jurkat	blood:	n/a
26	chr8:38898857-38898907	BE2_C	brain:	n/a
27	chr8:38898857-38898907	NHDF-neo	bronchial:	n/a
28	chr8:38898857-38898907	A549	lung:	n/a
29	chr8:38898857-38898907	AoSMC	blood vessel:	n/a
30	chr8:38898857-38898907	PFSK-1	brain:	n/a
31	chr8:38898857-38898907	HIPEpiC	eye:	n/a
32	chr8:38898857-38898907	HCF	heart:	n/a
33	chr8:38898857-38898907	SK-N-SH_RA	brain:	n/a
34	chr8:38898857-38898907	BJ	skin:	n/a
35	chr8:38898857-38898907	GM19239	blood:	n/a
36	chr8:38898857-38898907	HEK293	kidney:	embryo
37	chr8:38898857-38898907	Hepatocyte	liver:	n/a
38	chr8:38898857-38898907	ProgFib	skin:	n/a
39	chr8:38898857-38898907	AG10803	skin:	n/a
40	chr8:38898857-38898907	GM12878	blood:	n/a
41	chr8:38898857-38898907	SAEC	small airway:	n/a
42	chr8:38898857-38898907	HRPEpiC	eye:	n/a
43	chr8:38898857-38898907	NT2-D1	testis:	n/a
44	chr8:38898857-38898907	HRCEpiC	kidney:	n/a
45	chr8:38898857-38898907	HCM	heart:	n/a
46	chr8:38898857-38898907	GM12891	blood:	n/a
47	chr8:38898857-38898907	SK-N-SH	brain:	n/a
48	chr8:38898857-38898907	HepG2	liver:	n/a
49	chr8:38898857-38898907	AG04449	skin:	fetal
50	chr8:38898857-38898907	PANC-1	pancreas:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:38928615..38931127-chr8:38932750..38935591,2	K562	blood:
2	chr8:38915849..38919016-chr8:38921261..38923485,4	K562	blood:
3	chr8:38853505..38856171-chr8:38893000..38895883,3	K562	blood:
4	chr8:38928387..38930115-chr8:38932750..38934544,2	K562	blood:
5	chr8:38920268..38922257-chr8:38925771..38928354,3	K562	blood:
6	chr8:38920268..38922257-chr8:38925771..38928354,3	K562	blood:
7	chr8:38933732..38936418-chr8:38947721..38949546,2	MCF-7	breast:
8	chr8:38854112..38856391-chr8:38888365..38892463,3	MCF-7	breast:
9	chr8:38898390..38901319-chr8:38947288..38950284,2	K562	blood:
10	chr8:38853640..38855398-chr8:38893873..38896745,2	MCF-7	breast:
11	chr8:38895697..38898348-chr8:38953067..38955793,2	K562	blood:
12	chr8:38915849..38919016-chr8:38921261..38923485,4	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ADAM9	hsa-miR-23a-3p	chr8:38912000-38912008
2	ADAM9	hsa-miR-23a-3p	chr8:38899625-38899636

Variant related genes	Relation type
ADAM9	TF binding region
ADAM9	CpG island
ENSG00000168615	chromatin interactions
ENSG00000169490	chromatin interactions

Extended variants
information (count: 1813 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1813 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140891138	chr8:38886860-38886861	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs554649028	chr8:38886886-38886887	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73602703	chr8:38886899-38886900	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs543906742	chr8:38887109-38887110	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs573699920	chr8:38887117-38887118	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182191290	chr8:38887147-38887148	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563787355	chr8:38887176-38887177	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs10809000	chr8:38887192-38887193	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs185226954	chr8:38887197-38887198	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs113316633	chr8:38887206-38887207	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs79421382	chr8:38887222-38887223	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528765894	chr8:38887223-38887224	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs548893545	chr8:38887243-38887244	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs150175405	chr8:38887266-38887267	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs530518708	chr8:38887334-38887335	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529658966	chr8:38887339-38887340	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549427948	chr8:38887349-38887350	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs569418029	chr8:38887379-38887380	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538396270	chr8:38887426-38887427	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552074989	chr8:38887437-38887438	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs565899511	chr8:38887441-38887442	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs189941865	chr8:38887505-38887506	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138904631	chr8:38887527-38887528	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs574850703	chr8:38887586-38887587	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542662437	chr8:38887590-38887591	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537451655	chr8:38887608-38887609	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs557444594	chr8:38887651-38887652	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs141172499	chr8:38887655-38887656	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558932367	chr8:38887658-38887659	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs370122016	chr8:38887739-38887740	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs73602704	chr8:38887758-38887759	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs559671083	chr8:38887784-38887785	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532718520	chr8:38887802-38887803	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs573407887	chr8:38887809-38887810	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs542126257	chr8:38887834-38887835	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs562417580	chr8:38887978-38887979	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs529599635	chr8:38887980-38887981	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs549365471	chr8:38887992-38887993	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs372061451	chr8:38888026-38888027	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562982329	chr8:38888046-38888047	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs183007027	chr8:38888070-38888071	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532059020	chr8:38888080-38888081	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs7846203	chr8:38888123-38888124	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs188542548	chr8:38888145-38888146	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534831527	chr8:38888154-38888155	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs139001064	chr8:38888199-38888200	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs146927864	chr8:38888230-38888231	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs113112979	chr8:38888264-38888265	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs35108724	chr8:38888285-38888286	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs568365437	chr8:38888289-38888290	Enhancers Weak transcription Strong transcription Genic enhancers 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:1494 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:38856600-38889600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr8:38856800-38889600	Weak transcription	Colonic Mucosa	Colon
3	chr8:38865000-38887200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr8:38865000-38889600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr8:38865200-38887400	Strong transcription	HUES64 Cell Line	embryonic stem cell
6	chr8:38865400-38887800	Strong transcription	HSMM	muscle
7	chr8:38865400-38888800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr8:38865600-38888200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr8:38865600-38889000	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr8:38866000-38888400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr8:38869600-38902800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr8:38869800-38888400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr8:38872000-38890400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr8:38872400-38888200	Strong transcription	Fetal Intestine Large	intestine
15	chr8:38872600-38889600	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr8:38872600-38889800	Weak transcription	Primary B cells from peripheral blood	blood
17	chr8:38872800-38888000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr8:38874400-38888800	Strong transcription	Hela-S3	cervix
19	chr8:38875000-38888400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:38875200-38888800	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr8:38875400-38889400	Weak transcription	Esophagus	oesophagus
22	chr8:38875400-38890200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr8:38875800-38895400	Weak transcription	Brain Angular Gyrus	brain
24	chr8:38876400-38888000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr8:38876600-38888000	Strong transcription	Placenta	Placenta
26	chr8:38877400-38887400	Strong transcription	Fetal Muscle Leg	muscle
27	chr8:38878600-38888600	Strong transcription	Dnd41	blood
28	chr8:38879000-38887200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
29	chr8:38879000-38888000	Strong transcription	HUES6 Cell Line	embryonic stem cell
30	chr8:38879000-38888400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
31	chr8:38879200-38887000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
32	chr8:38879200-38887200	Strong transcription	Placenta Amnion	Placenta Amnion
33	chr8:38879200-38887800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr8:38879200-38888000	Strong transcription	Duodenum Smooth Muscle	Duodenum
35	chr8:38879200-38888400	Strong transcription	Cortex derived primary cultured neurospheres	brain
36	chr8:38879800-38888000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr8:38880200-38888000	Strong transcription	Sigmoid Colon	Sigmoid Colon
38	chr8:38880600-38887200	Weak transcription	Fetal Thymus	thymus
39	chr8:38880600-38888000	Strong transcription	Duodenum Mucosa	Duodenum
40	chr8:38880600-38888200	Strong transcription	GM12878-XiMat	blood
41	chr8:38881000-38887800	Strong transcription	Brain Hippocampus Middle	brain
42	chr8:38881200-38888000	Strong transcription	NHEK	skin
43	chr8:38882000-38913600	Weak transcription	Fetal Kidney	kidney
44	chr8:38882400-38889600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr8:38882800-38895000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr8:38882800-38895000	Weak transcription	Rectal Smooth Muscle	rectum
47	chr8:38883000-38889600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr8:38883000-38889600	Weak transcription	Lung	lung
49	chr8:38883000-38895000	Weak transcription	Spleen	Spleen
50	chr8:38883000-38913000	Weak transcription	Rectal Mucosa Donor 29	rectum

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