Variant report

Variant	esv1793350
Chromosome Location	chr8:50013702-50102628
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:515)
CpG islands
(count:61)
Chromatin interactive
region (count:40)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:515 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:50038776-50039400	K562	blood:	n/a	n/a
2	ARID3A	chr8:50037822-50038312	K562	blood:	n/a	n/a
3	ARID3A	chr8:50042305-50042634	K562	blood:	n/a	n/a
4	ARID3A	chr8:50033978-50034353	K562	blood:	n/a	n/a
5	ARID3A	chr8:50045458-50045469	K562	blood:	n/a	n/a
6	ARID3A	chr8:50022835-50023624	K562	blood:	n/a	n/a
7	ATF1	chr8:50042268-50042716	K562	blood:	n/a	n/a
8	ATF1	chr8:50022908-50023300	K562	blood:	n/a	n/a
9	ATF1	chr8:50043141-50043408	K562	blood:	n/a	n/a
10	ATF2	chr8:50064675-50065110	GM12878	blood:	n/a	n/a
11	ATF2	chr8:50063437-50063916	GM12878	blood:	n/a	n/a
12	ATF2	chr8:50063467-50063855	GM12878	blood:	n/a	n/a
13	ATF2	chr8:50064665-50065098	GM12878	blood:	n/a	n/a
14	ATF3	chr8:50042276-50042621	K562	blood:	n/a	chr8:50042553-50042561 chr8:50042553-50042563 chr8:50042549-50042564 chr8:50042551-50042564
15	ATF3	chr8:50022637-50023275	K562	blood:	n/a	n/a
16	BACH1	chr8:50039590-50039608	K562	blood:	n/a	n/a
17	BACH1	chr8:50021996-50022013	K562	blood:	n/a	n/a
18	BACH1	chr8:50033867-50033912	K562	blood:	n/a	n/a
19	BATF	chr8:50084554-50084785	GM12878	blood:	n/a	n/a
20	BATF	chr8:50064660-50065058	GM12878	blood:	n/a	n/a
21	BATF	chr8:50064654-50065062	GM12878	blood:	n/a	n/a
22	BCL11A	chr8:50084502-50084833	GM12878	blood:	n/a	n/a
23	BCL11A	chr8:50064635-50065082	GM12878	blood:	n/a	n/a
24	BCL11A	chr8:50063546-50063802	GM12878	blood:	n/a	n/a
25	BCLAF1	chr8:50064650-50065109	GM12878	blood:	n/a	n/a
26	BCLAF1	chr8:50063542-50063887	GM12878	blood:	n/a	n/a
27	BHLHE40	chr8:50044310-50044588	K562	blood:	n/a	n/a
28	BHLHE40	chr8:50064693-50065179	GM12878	blood:	n/a	n/a
29	BHLHE40	chr8:50059350-50059367	K562	blood:	n/a	n/a
30	BHLHE40	chr8:50022959-50023395	K562	blood:	n/a	n/a
31	BHLHE40	chr8:50084538-50084914	GM12878	blood:	n/a	n/a
32	BHLHE40	chr8:50037870-50038258	K562	blood:	n/a	n/a
33	BHLHE40	chr8:50063559-50063839	GM12878	blood:	n/a	n/a
34	BHLHE40	chr8:50084573-50084835	K562	blood:	n/a	n/a
35	BHLHE40	chr8:50042271-50042571	K562	blood:	n/a	n/a
36	CBX3	chr8:50044278-50044595	K562	blood:	n/a	n/a
37	CBX3	chr8:50037777-50038300	K562	blood:	n/a	n/a
38	CBX3	chr8:50044277-50044525	K562	blood:	n/a	n/a
39	CBX3	chr8:50016665-50016951	K562	blood:	n/a	n/a
40	CBX3	chr8:50016717-50017003	K562	blood:	n/a	n/a
41	CBX3	chr8:50022996-50023351	K562	blood:	n/a	n/a
42	CBX3	chr8:50022681-50023648	K562	blood:	n/a	n/a
43	CBX3	chr8:50042212-50042911	K562	blood:	n/a	n/a
44	CCNT2	chr8:50056003-50056202	K562	blood:	n/a	n/a
45	CCNT2	chr8:50044294-50044494	K562	blood:	n/a	n/a
46	CCNT2	chr8:50022923-50023681	K562	blood:	n/a	n/a
47	CEBPB	chr8:50030113-50030131	K562	blood:	n/a	n/a
48	CEBPB	chr8:50082488-50082719	A549	lung:	n/a	chr8:50082628-50082639
49	CEBPB	chr8:50042303-50042876	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr8:50079888-50080172	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:50020154-50020204	SK-N-SH	brain:	n/a
2	chr8:50020154-50020204	H1-hESC	embryonic stem cell:	embryo
3	chr8:50020154-50020204	GM06990	blood:	n/a
4	chr8:50020154-50020204	HL-60	blood:	n/a
5	chr8:50020154-50020204	MCF10A-Er-Src	breast:	n/a
6	chr8:50020154-50020204	HMEC	breast:	n/a
7	chr8:50020154-50020204	BJ	skin:	n/a
8	chr8:50020154-50020204	MCF-7	breast:	n/a
9	chr8:50020154-50020204	HNPCEpiC	eye:	n/a
10	chr8:50020154-50020204	ECC-1	luminal epithelium:	n/a
11	chr8:50020154-50020204	AG09319	gingival:	n/a
12	chr8:50020154-50020204	ProgFib	skin:	n/a
13	chr8:50020154-50020204	GM12892	blood:	n/a
14	chr8:50020154-50020204	SAEC	small airway:	n/a
15	chr8:50020154-50020204	HCT-116	colon:	n/a
16	chr8:50020154-50020204	AG04449	skin:	fetal
17	chr8:50020154-50020204	Hepatocyte	liver:	n/a
18	chr8:50020154-50020204	NH-A	brain:	n/a
19	chr8:50020154-50020204	PFSK-1	brain:	n/a
20	chr8:50020154-50020204	GM19239	blood:	n/a
21	chr8:50020154-50020204	HRCEpiC	kidney:	n/a
22	chr8:50020154-50020204	HCF	heart:	n/a
23	chr8:50020154-50020204	IMR90	lung:	fetal
24	chr8:50020154-50020204	HEEpiC	esophagus:	n/a
25	chr8:50020154-50020204	NHDF-neo	bronchial:	n/a
26	chr8:50020154-50020204	HIPEpiC	eye:	n/a
27	chr8:50020154-50020204	AG04450	lung:	fetal
28	chr8:50020154-50020204	RPTEC	kidney:	n/a
29	chr8:50020154-50020204	HRPEpiC	eye:	n/a
30	chr8:50020154-50020204	HEK293	kidney:	embryo
31	chr8:50020154-50020204	HepG2	liver:	n/a
32	chr8:50020154-50020204	CMK	blood:	n/a
33	chr8:50020154-50020204	HCPEpiC	choroid plexus:	n/a
34	chr8:50020154-50020204	HPAEpiC	pulmonary alveolar:	n/a
35	chr8:50020154-50020204	LNCaP	prostate:	n/a
36	chr8:50020154-50020204	NHBE	bronchial:	n/a
37	chr8:50020154-50020204	PrEC	prostate:	n/a
38	chr8:50020154-50020204	GM12878	blood:	n/a
39	chr8:50020154-50020204	NB4	blood:	n/a
40	chr8:50020154-50020204	AoSMC	blood vessel:	n/a
41	chr8:50020154-50020204	BE2_C	brain:	n/a
42	chr8:50020154-50020204	SK-N-MC	brain:	n/a
43	chr8:50020154-50020204	PANC-1	pancreas:	n/a
44	chr8:50020154-50020204	A549	lung:	n/a
45	chr8:50020154-50020204	GM12891	blood:	n/a
46	chr8:50020154-50020204	T-47D	breast:	n/a
47	chr8:50020154-50020204	Hela-S3	cervix:	n/a
48	chr8:50020154-50020204	Jurkat	blood:	n/a
49	chr8:50020154-50020204	U87	brain:	n/a
50	chr8:50020154-50020204	K562	blood:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:50083760..50086501-chr8:50089833..50092673,4	K562	blood:
2	chr8:50036565..50039449-chr8:50040680..50044061,3	K562	blood:
3	chr8:50023723..50026392-chr8:50033896..50036136,2	K562	blood:
4	chr8:50069109..50071962-chr8:50074924..50077500,3	K562	blood:
5	chr8:50052841..50054803-chr8:50061122..50063671,2	K562	blood:
6	chr8:50056870..50059672-chr8:50062118..50064411,2	K562	blood:
7	chr8:50031366..50035096-chr8:50036647..50040169,3	K562	blood:
8	chr8:50055914..50057439-chr8:50058331..50060895,2	MCF-7	breast:
9	chr8:50029029..50031186-chr8:50035515..50038037,2	K562	blood:
10	chr8:50055914..50057439-chr8:50058331..50060895,2	MCF-7	breast:
11	chr8:50083760..50086501-chr8:50089833..50092673,4	K562	blood:
12	chr8:50087104..50089647-chr8:50092325..50095180,2	K562	blood:
13	chr8:50052529..50054341-chr8:50060024..50062622,2	K562	blood:
14	chr8:50023484..50026392-chr8:50032948..50035396,2	K562	blood:
15	chr8:49978220..49980915-chr8:50057645..50059549,2	K562	blood:
16	chr8:50039038..50041267-chr8:50044782..50047548,2	K562	blood:
17	chr8:50032130..50034951-chr8:50036647..50039869,3	K562	blood:
18	chr8:50084279..50086501-chr8:50089833..50092255,3	K562	blood:
19	chr8:50031366..50035096-chr8:50036647..50040169,3	K562	blood:
20	chr8:49959355..49961119-chr8:50034461..50036687,2	K562	blood:
21	chr8:49957733..49959287-chr8:50036754..50039574,2	K562	blood:
22	chr8:50032130..50034951-chr8:50036647..50039869,3	K562	blood:
23	chr8:50078942..50082109-chr8:50083366..50086406,3	K562	blood:
24	chr8:50056870..50059672-chr8:50062118..50064411,2	K562	blood:
25	chr8:50003812..50005388-chr8:50034210..50037111,2	K562	blood:
26	chr8:50039038..50041267-chr8:50044782..50047548,2	K562	blood:
27	chr8:50087104..50089647-chr8:50092325..50095180,2	K562	blood:
28	chr8:50019288..50021191-chr8:50037884..50039646,2	K562	blood:
29	chr8:50069109..50071962-chr8:50074924..50077500,3	K562	blood:
30	chr8:50023723..50026392-chr8:50033896..50036136,2	K562	blood:
31	chr8:50029029..50031186-chr8:50035515..50038037,2	K562	blood:
32	chr8:50037357..50040620-chr8:50040803..50044061,4	K562	blood:
33	chr8:50037357..50040620-chr8:50040803..50044061,4	K562	blood:
34	chr8:50019288..50021191-chr8:50037884..50039646,2	K562	blood:
35	chr8:50080096..50082552-chr8:50086990..50089298,2	K562	blood:
36	chr8:50052529..50054341-chr8:50060024..50062622,2	K562	blood:
37	chr8:50084279..50086501-chr8:50089833..50092255,3	K562	blood:
38	chr8:50036565..50039449-chr8:50040680..50044061,3	K562	blood:
39	chr8:50052841..50054803-chr8:50061122..50063671,2	K562	blood:
40	chr8:50023484..50026392-chr8:50032948..50035396,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf22-2	chr8:50081241-50081368	ENSG00000253474
2	lnc-SNAI2-1	chr8:50047181-50047788	NONHSAT126505
3	lnc-C8orf22-2	chr8:50081243-50081368	XLOC_006793
4	lnc-C8orf22-2	chr8:50080642-50080861	XLOC_006793
5	lnc-C8orf22-2	chr8:50081243-50081368	XLOC_006793
6	lnc-C8orf22-2	chr8:50080641-50081407	NONHSAT126506
7	lnc-C8orf22-2	chr8:50080642-50081090	XLOC_006793
8	lnc-C8orf22-2	chr8:50081098-50081368	ENSG00000253474

No data

Variant related genes	Relation type
ENSG00000253474	TF binding region
ENSG00000253474	CpG island
ENSG00000253474	chromatin interactions

Extended variants
information (count: 1850 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1850 , 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	rs144137739	chr8:50013712-50013713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs191677395	chr8:50013720-50013721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs111632669	chr8:50013738-50013739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187795565	chr8:50013787-50013788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537334009	chr8:50013805-50013806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536291054	chr8:50013811-50013812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs193140905	chr8:50013823-50013824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566294391	chr8:50013883-50013884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538078194	chr8:50013912-50013913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531749717	chr8:50013928-50013929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533907072	chr8:50013944-50013945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185676350	chr8:50013960-50013961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs78998297	chr8:50013988-50013989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577401746	chr8:50014015-50014016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538032284	chr8:50014016-50014017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556485093	chr8:50014028-50014029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574783186	chr8:50014032-50014033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11997959	chr8:50014044-50014045	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs187544314	chr8:50014054-50014055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369084950	chr8:50014161-50014162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs13275723	chr8:50014220-50014221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10097472	chr8:50014240-50014241	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs146527649	chr8:50014282-50014283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533937117	chr8:50014308-50014309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532367262	chr8:50014365-50014366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554139368	chr8:50014424-50014425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs9643394	chr8:50014427-50014428	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs562630386	chr8:50014429-50014430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539937780	chr8:50014433-50014434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs9643395	chr8:50014500-50014501	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs201831275	chr8:50014507-50014508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557909745	chr8:50014549-50014550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548472861	chr8:50014579-50014580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566477311	chr8:50014614-50014615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192129773	chr8:50014706-50014707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569074322	chr8:50014725-50014726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368399806	chr8:50014745-50014746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577892768	chr8:50014757-50014758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs140019285	chr8:50014785-50014786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377429038	chr8:50014789-50014790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs10100956	chr8:50014814-50014815	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs575485999	chr8:50014822-50014823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544450743	chr8:50014880-50014881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375120633	chr8:50014897-50014898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563719169	chr8:50014940-50014941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535768650	chr8:50014985-50014986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554138478	chr8:50014990-50014991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572439584	chr8:50014992-50014993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545859645	chr8:50015000-50015001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558280362	chr8:50015037-50015038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:50008200-50015400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:50008200-50015600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:50015600-50016200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:50015600-50022400	Weak transcription	Gastric	stomach
5	chr8:50016000-50016200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr8:50016000-50016200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:50016000-50016800	Enhancers	HMEC	breast
8	chr8:50016200-50016600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr8:50016200-50016800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr8:50016200-50016800	Enhancers	NHEK	skin
11	chr8:50016200-50019400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr8:50016200-50022400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr8:50016600-50016800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr8:50016800-50022400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr8:50018800-50022400	Enhancers	K562	blood
16	chr8:50019000-50023400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr8:50019200-50023600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr8:50019400-50020000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr8:50019400-50020600	Enhancers	HSMMtube	muscle
20	chr8:50019400-50021800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr8:50019800-50020600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr8:50019800-50020600	Enhancers	Fetal Lung	lung
23	chr8:50019800-50020800	Enhancers	Stomach Mucosa	stomach
24	chr8:50020000-50020600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr8:50020000-50020800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr8:50020600-50025800	Weak transcription	Fetal Lung	lung
27	chr8:50020800-50022400	Weak transcription	Stomach Mucosa	stomach
28	chr8:50021800-50022400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr8:50022200-50023600	Enhancers	NHEK	skin
30	chr8:50022400-50022600	Enhancers	Gastric	stomach
31	chr8:50022400-50022600	Enhancers	Stomach Mucosa	stomach
32	chr8:50022400-50022600	Flanking Active TSS	K562	blood
33	chr8:50022400-50023200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr8:50022400-50023200	Enhancers	Pancreas	Pancrea
35	chr8:50022400-50023400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr8:50022400-50023400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr8:50022400-50023400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr8:50022400-50023400	Enhancers	HMEC	breast
39	chr8:50022600-50023000	Weak transcription	Stomach Mucosa	stomach
40	chr8:50022600-50023400	Weak transcription	Gastric	stomach
41	chr8:50022600-50023600	Enhancers	K562	blood
42	chr8:50022800-50023600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
43	chr8:50022800-50023600	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr8:50023000-50023600	Enhancers	Stomach Mucosa	stomach
45	chr8:50023200-50023400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
46	chr8:50023400-50023600	Enhancers	Gastric	stomach
47	chr8:50023400-50026200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr8:50023600-50024400	Weak transcription	Stomach Mucosa	stomach
49	chr8:50023600-50025200	Weak transcription	K562	blood
50	chr8:50024400-50024800	Enhancers	Stomach Mucosa	stomach

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