Variant report

Variant	nsv1030323
Chromosome Location	chr8:6268228-6279511
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:181)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:181 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:6270786-6270943	K562	blood:	n/a	n/a
2	ATF2	chr8:6274564-6275935	GM12878	blood:	n/a	n/a
3	ATF2	chr8:6274572-6275754	GM12878	blood:	n/a	n/a
4	ATF2	chr8:6273689-6274273	GM12878	blood:	n/a	n/a
5	BATF	chr8:6275084-6275784	GM12878	blood:	n/a	n/a
6	BATF	chr8:6274761-6275058	GM12878	blood:	n/a	n/a
7	BATF	chr8:6274819-6275423	GM12878	blood:	n/a	n/a
8	BCL11A	chr8:6275121-6275398	GM12878	blood:	n/a	n/a
9	BCL11A	chr8:6274723-6275701	GM12878	blood:	n/a	n/a
10	BCLAF1	chr8:6275116-6275837	GM12878	blood:	n/a	n/a
11	BCLAF1	chr8:6274613-6275965	GM12878	blood:	n/a	n/a
12	BHLHE40	chr8:6273910-6274154	GM12878	blood:	n/a	n/a
13	BHLHE40	chr8:6274528-6275764	GM12878	blood:	n/a	n/a
14	BRCA1	chr8:6274702-6274765	GM12878	blood:	n/a	n/a
15	CEBPB	chr8:6274778-6275140	HepG2	liver:	n/a	n/a
16	CEBPB	chr8:6274739-6275622	GM12878	blood:	n/a	n/a
17	CEBPB	chr8:6274826-6275059	A549	lung:	n/a	n/a
18	CEBPB	chr8:6274756-6275110	K562	blood:	n/a	n/a
19	CEBPB	chr8:6274761-6275124	A549	lung:	n/a	n/a
20	CEBPB	chr8:6274791-6275145	K562	blood:	n/a	n/a
21	CEBPB	chr8:6274802-6275022	HepG2	liver:	n/a	n/a
22	CEBPB	chr8:6274796-6275153	ECC-1	luminal epithelium:	n/a	n/a
23	CHD1	chr8:6274611-6275958	GM12878	blood:	n/a	n/a
24	CHD2	chr8:6274656-6275905	GM12878	blood:	n/a	n/a
25	CTCF	chr8:6275672-6275692	GM12878	blood:	n/a	n/a
26	CTCF	chr8:6277515-6277517	GM12878	blood:	n/a	n/a
27	CTCF	chr8:6276820-6276970	GM12873	blood:	n/a	n/a
28	CUX1	chr8:6270749-6270770	GM12878	blood:	n/a	n/a
29	CUX1	chr8:6274554-6275855	GM12878	blood:	n/a	n/a
30	CUX1	chr8:6273825-6274072	GM12878	blood:	n/a	n/a
31	CUX1	chr8:6269929-6270049	K562	blood:	n/a	n/a
32	CUX1	chr8:6273426-6273474	GM12878	blood:	n/a	n/a
33	E2F4	chr8:6270011-6270236	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr8:6274978-6275071	GM12878	blood:	n/a	n/a
35	EBF1	chr8:6273823-6274009	GM12878	blood:	n/a	n/a
36	EBF1	chr8:6274739-6275944	GM12878	blood:	n/a	n/a
37	ELK1	chr8:6273431-6273474	GM12878	blood:	n/a	n/a
38	ELK1	chr8:6275152-6275785	GM12878	blood:	n/a	n/a
39	ELK1	chr8:6274702-6274730	GM12878	blood:	n/a	n/a
40	EP300	chr8:6273740-6274158	GM12878	blood:	n/a	n/a
41	EP300	chr8:6273769-6274181	GM12878	blood:	n/a	n/a
42	EP300	chr8:6270813-6270874	K562	blood:	n/a	n/a
43	EP300	chr8:6273743-6274135	GM12878	blood:	n/a	n/a
44	EP300	chr8:6274597-6275870	GM12878	blood:	n/a	n/a
45	EP300	chr8:6274652-6275767	GM12878	blood:	n/a	n/a
46	EP300	chr8:6274756-6275563	GM12878	blood:	n/a	n/a
47	ESRRA	chr8:6273609-6276128	GM12878	blood:	n/a	n/a
48	FOS	chr8:6273766-6273916	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr8:6273723-6273957	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr8:6273716-6273980	MCF10A-Er-Src	breast:	n/a	n/a

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:6260743..6265726-chr8:6271007..6273930,5	K562	blood:
2	chr8:6277390..6279333-chr8:6576770..6578776,2	K562	blood:
3	chr8:6274685..6276639-chr8:6565162..6567770,2	MCF-7	breast:
4	chr8:6262451..6265274-chr8:6277590..6279636,2	MCF-7	breast:
5	chr8:6275765..6277346-chr8:6279948..6281566,2	K562	blood:
6	chr8:6267107..6268741-chr8:6565301..6567337,2	K562	blood:
7	chr8:6261231..6262782-chr8:6268049..6270486,2	K562	blood:
8	chr8:6262086..6265734-chr8:6266423..6270611,6	MCF-7	breast:
9	chr8:6277995..6281670-chr8:6564311..6568348,3	MCF-7	breast:
10	chr8:6269409..6272361-chr8:6283113..6285800,2	K562	blood:
11	chr8:6264019..6265631-chr8:6276024..6277548,2	K562	blood:
12	chr8:6266687..6268429-chr8:6271780..6273371,2	K562	blood:
13	chr8:6266687..6268429-chr8:6271780..6273371,2	K562	blood:
14	chr8:6263426..6264997-chr8:6273721..6275248,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000246089	TF binding region
ENSG00000155189	chromatin interactions
ENSG00000246089	chromatin interactions
ENSG00000147316	chromatin interactions
ENSG00000249898	chromatin interactions

Extended variants
information (count: 805 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:805 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546930562	chr8:6268230-6268231	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs560385039	chr8:6268272-6268273	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs187279068	chr8:6268319-6268320	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs191673962	chr8:6268323-6268324	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs569457903	chr8:6268328-6268329	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs146126243	chr8:6268382-6268383	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs548896829	chr8:6268385-6268386	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs377137768	chr8:6268442-6268443	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs566366642	chr8:6268456-6268457	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs76907500	chr8:6268464-6268465	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs543930450	chr8:6268485-6268486	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs369120325	chr8:6268487-6268488	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs185336585	chr8:6268493-6268494	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs568364286	chr8:6268504-6268505	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs111921654	chr8:6268543-6268544	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs572876292	chr8:6268575-6268576	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs189820722	chr8:6268582-6268583	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs142363805	chr8:6268589-6268590	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs56981469	chr8:6268595-6268596	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs544137888	chr8:6268601-6268602	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs61048567	chr8:6268612-6268613	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs372663519	chr8:6268618-6268619	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs78103271	chr8:6268632-6268633	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs151239523	chr8:6268643-6268644	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs560503410	chr8:6268644-6268645	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs532532361	chr8:6268651-6268652	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs139246496	chr8:6268665-6268666	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs563122195	chr8:6268704-6268705	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs149995252	chr8:6268710-6268711	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs73514774	chr8:6268714-6268715	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs568774660	chr8:6268732-6268733	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs193254856	chr8:6268734-6268735	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs75665611	chr8:6268736-6268737	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs566449305	chr8:6268742-6268743	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs538386443	chr8:6268779-6268780	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs59244869	chr8:6268782-6268783	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs538424814	chr8:6268786-6268787	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs116818595	chr8:6268787-6268788	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs376014985	chr8:6268788-6268789	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs537652015	chr8:6268799-6268800	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs554313070	chr8:6268806-6268807	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs574659150	chr8:6268810-6268811	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs558364848	chr8:6268811-6268812	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs368798509	chr8:6268821-6268822	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs540504245	chr8:6268834-6268835	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs553906906	chr8:6268837-6268838	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs142281064	chr8:6268842-6268843	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs565330650	chr8:6268869-6268870	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs562981718	chr8:6268954-6268955	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs531793173	chr8:6268962-6268963	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:137)

Disease	PMID	Source
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
Prostate cancer	16573809	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
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	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
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Autism	20685689	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:646 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6265000-6272600	Weak transcription	Esophagus	oesophagus
2	chr8:6265000-6272600	Weak transcription	Gastric	stomach
3	chr8:6265000-6286600	Weak transcription	Small Intestine	intestine
4	chr8:6265000-6339200	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr8:6265200-6269200	Weak transcription	Aorta	Aorta
6	chr8:6265200-6269400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr8:6265200-6269600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr8:6265200-6269600	Weak transcription	Pancreas	Pancrea
9	chr8:6265200-6281800	Weak transcription	Right Atrium	heart
10	chr8:6265200-6281800	Weak transcription	Right Ventricle	heart
11	chr8:6265200-6282600	Weak transcription	Colonic Mucosa	Colon
12	chr8:6265200-6302200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:6265400-6268600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr8:6265400-6268600	Weak transcription	Stomach Mucosa	stomach
15	chr8:6265400-6269600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr8:6265400-6270000	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr8:6265400-6272600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr8:6265400-6278200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr8:6265400-6287400	Weak transcription	Psoas Muscle	Psoas
20	chr8:6265400-6303800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr8:6265600-6268600	Weak transcription	Fetal Heart	heart
22	chr8:6265600-6268800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr8:6265600-6276400	Weak transcription	Fetal Brain Male	brain
24	chr8:6265600-6290000	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr8:6265800-6269200	Weak transcription	Hela-S3	cervix
26	chr8:6266000-6275800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr8:6266000-6275800	Strong transcription	Fetal Muscle Leg	muscle
28	chr8:6266200-6268600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr8:6266200-6270400	Strong transcription	Fetal Stomach	stomach
30	chr8:6266600-6268400	Strong transcription	Primary T cells fromperipheralblood	blood
31	chr8:6266600-6268400	Strong transcription	NHEK	skin
32	chr8:6266600-6269000	Genic enhancers	Dnd41	blood
33	chr8:6266600-6269200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr8:6266600-6269200	Strong transcription	Placenta	Placenta
35	chr8:6266600-6269600	Strong transcription	Duodenum Mucosa	Duodenum
36	chr8:6266600-6269600	Strong transcription	Left Ventricle	heart
37	chr8:6266600-6269800	Strong transcription	Cortex derived primary cultured neurospheres	brain
38	chr8:6266600-6269800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr8:6266600-6269800	Strong transcription	HUVEC	blood vessel
40	chr8:6266600-6270400	Strong transcription	HUES64 Cell Line	embryonic stem cell
41	chr8:6266600-6270400	Strong transcription	Fetal Muscle Trunk	muscle
42	chr8:6266600-6270600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr8:6266600-6270600	Strong transcription	Stomach Smooth Muscle	stomach
44	chr8:6266600-6270800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr8:6266600-6271000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr8:6266600-6271000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr8:6266600-6271000	Strong transcription	Fetal Intestine Large	intestine
48	chr8:6266600-6271000	Strong transcription	Skeletal Muscle Female	skeletal muscle
49	chr8:6266600-6271200	Strong transcription	Fetal Thymus	thymus
50	chr8:6266600-6275200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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