Variant report

Variant	nsv890979
Chromosome Location	chr8:69176154-69252417
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:403)
CpG islands
(count:1281)
Chromatin interactive
region (count:3)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:69227774-69227939	K562	blood:	n/a	n/a
2	BACH1	chr8:69242862-69243752	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:69218330-69218530	K562	blood:	n/a	n/a
4	BACH1	chr8:69244369-69244445	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:69245992-69246194	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:69207698-69207805	K562	blood:	n/a	n/a
7	BCL3	chr8:69208381-69208746	GM12878	blood:	n/a	n/a
8	BHLHE40	chr8:69183640-69183747	GM12878	blood:	n/a	n/a
9	BHLHE40	chr8:69218442-69218815	K562	blood:	n/a	n/a
10	CEBPB	chr8:69242704-69243064	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr8:69181615-69181856	H1-hESC	embryonic stem cell:	n/a	chr8:69181693-69181704 chr8:69181692-69181705
12	CEBPB	chr8:69181605-69181846	HepG2	liver:	n/a	chr8:69181693-69181704 chr8:69181692-69181705
13	CEBPB	chr8:69250133-69250455	HepG2	liver:	n/a	chr8:69250296-69250305 chr8:69250294-69250305
14	CEBPB	chr8:69208457-69208763	MCF-7	breast:	n/a	n/a
15	CHD1	chr8:69211429-69211450	GM12878	blood:	n/a	n/a
16	CHD1	chr8:69218317-69218685	GM12878	blood:	n/a	n/a
17	CHD1	chr8:69243419-69244042	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD1	chr8:69179058-69179073	GM12878	blood:	n/a	n/a
19	CHD2	chr8:69242636-69243750	H1-hESC	embryonic stem cell:	n/a	chr8:69243224-69243234 chr8:69243121-69243131
20	CHD2	chr8:69218449-69218649	K562	blood:	n/a	n/a
21	CREB1	chr8:69242735-69243268	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTBP2	chr8:69242647-69243935	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr8:69243580-69243730	MCF-7	breast:	n/a	n/a
24	CTCF	chr8:69196020-69196170	NHDF-neo	bronchial:	n/a	n/a
25	CTCF	chr8:69243116-69243239	LNCaP	prostate:	n/a	chr8:69243128-69243138
26	CTCF	chr8:69246080-69246230	AG09319	gingival:	n/a	chr8:69246144-69246165
27	CTCF	chr8:69243084-69243218	Medullo	brain:	n/a	chr8:69243128-69243138
28	CTCF	chr8:69243080-69243230	NHDF-neo	bronchial:	n/a	chr8:69243128-69243138
29	CTCF	chr8:69242842-69242995	MCF-7	breast:	n/a	n/a
30	CTCF	chr8:69245900-69246050	HAc	cerebellar:	n/a	n/a
31	CTCF	chr8:69243080-69243230	HRE	kidney:	n/a	chr8:69243128-69243138
32	CTCF	chr8:69196100-69196250	HRPEpiC	eye:	n/a	n/a
33	CTCF	chr8:69196140-69196290	RPTEC	kidney:	n/a	n/a
34	CTCF	chr8:69229745-69229787	GM10248	blood:	n/a	n/a
35	CTCF	chr8:69245920-69246070	Caco-2	colon:	n/a	n/a
36	CTCF	chr8:69243040-69243190	NHDF-neo	bronchial:	n/a	chr8:69243128-69243138
37	CTCF	chr8:69242740-69242890	HEK293	kidney:	n/a	n/a
38	CTCF	chr8:69198020-69198170	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr8:69243060-69243210	HEK293	kidney:	n/a	chr8:69243128-69243138
40	CTCF	chr8:69243120-69243270	GM12874	blood:	n/a	chr8:69243128-69243138
41	CTCF	chr8:69196000-69196150	HMF	breast:	n/a	n/a
42	CTCF	chr8:69243100-69243250	HFF	foreskin:	n/a	chr8:69243128-69243138
43	CTCF	chr8:69246020-69246170	HRPEpiC	eye:	n/a	chr8:69246144-69246165
44	CTCF	chr8:69195940-69196090	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr8:69243120-69243270	HCM	heart:	n/a	chr8:69243128-69243138
46	CTCF	chr8:69219748-69219767	ProgFib	skin:	n/a	n/a
47	CTCF	chr8:69196020-69196170	HEK293	kidney:	n/a	n/a
48	CTCF	chr8:69243340-69243490	SAEC	small airway:	n/a	n/a
49	CTCF	chr8:69243566-69243899	NHEK	skin:	n/a	n/a
50	CTCF	chr8:69195960-69196110	BJ	skin:	n/a	n/a

(count:1281 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:69244553-69244603	MCF10A-Er-Src	breast:	n/a
2	chr8:69240774-69240824	A549	lung:	n/a
3	chr8:69216882-69216932	Hepatocyte	liver:	n/a
4	chr8:69241923-69241973	GM12892	blood:	n/a
5	chr8:69242921-69242971	AG09319	gingival:	n/a
6	chr8:69243904-69243954	NB4	blood:	n/a
7	chr8:69243904-69243954	HPAEpiC	pulmonary alveolar:	n/a
8	chr8:69243904-69243954	GM12891	blood:	n/a
9	chr8:69240774-69240824	ProgFib	skin:	n/a
10	chr8:69241923-69241973	PANC-1	pancreas:	n/a
11	chr8:69240774-69240824	NT2-D1	testis:	n/a
12	chr8:69244553-69244603	HepG2	liver:	n/a
13	chr8:69243510-69243560	NB4	blood:	n/a
14	chr8:69244734-69244784	Hepatocyte	liver:	n/a
15	chr8:69244553-69244603	PFSK-1	brain:	n/a
16	chr8:69240774-69240824	ECC-1	luminal epithelium:	n/a
17	chr8:69246056-69246106	HEEpiC	esophagus:	n/a
18	chr8:69244553-69244603	AG10803	skin:	n/a
19	chr8:69243510-69243560	SK-N-SH_RA	brain:	n/a
20	chr8:69242921-69242971	MCF-7	breast:	n/a
21	chr8:69243510-69243560	HNPCEpiC	eye:	n/a
22	chr8:69240774-69240824	HPAEpiC	pulmonary alveolar:	n/a
23	chr8:69241923-69241973	PrEC	prostate:	n/a
24	chr8:69243752-69243802	AG10803	skin:	n/a
25	chr8:69216882-69216932	HNPCEpiC	eye:	n/a
26	chr8:69243510-69243560	GM12878	blood:	n/a
27	chr8:69246056-69246106	H1-hESC	embryonic stem cell:	embryo
28	chr8:69240774-69240824	SK-N-SH_RA	brain:	n/a
29	chr8:69243602-69243652	IMR90	lung:	fetal
30	chr8:69246056-69246106	HRPEpiC	eye:	n/a
31	chr8:69243285-69243335	T-47D	breast:	n/a
32	chr8:69244205-69244255	Hela-S3	cervix:	n/a
33	chr8:69246056-69246106	PFSK-1	brain:	n/a
34	chr8:69243510-69243560	Hela-S3	cervix:	n/a
35	chr8:69244553-69244603	PrEC	prostate:	n/a
36	chr8:69242509-69242559	H1-hESC	embryonic stem cell:	embryo
37	chr8:69216882-69216932	MCF-7	breast:	n/a
38	chr8:69243486-69243536	HAEpiC	amniotic membrane:	n/a
39	chr8:69243904-69243954	PANC-1	pancreas:	n/a
40	chr8:69243486-69243536	CMK	blood:	n/a
41	chr8:69242921-69242971	Caco-2	colon:	n/a
42	chr8:69244152-69244202	GM12891	blood:	n/a
43	chr8:69243752-69243802	ProgFib	skin:	n/a
44	chr8:69243285-69243335	PANC-1	pancreas:	n/a
45	chr8:69244510-69244560	T-47D	breast:	n/a
46	chr8:69242974-69243024	NB4	blood:	n/a
47	chr8:69245801-69245851	NHDF-neo	bronchial:	n/a
48	chr8:69244152-69244202	AG04449	skin:	fetal
49	chr8:69243602-69243652	BJ	skin:	n/a
50	chr8:69245801-69245851	NH-A	brain:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:69172089..69174443-chr8:69177342..69179034,2	K562	blood:
2	chr8:69214227..69216220-chr8:69229088..69230981,2	K562	blood:
3	chr8:69214227..69216220-chr8:69229088..69230981,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-664D7.4.1-4	chr8:69218753-69218833	NONHSAT127094
2	lnc-RP11-664D7.4.1-5	chr8:69205681-69206053	NONHSAT127092
3	lnc-RP11-664D7.4.1-4	chr8:69214472-69216749	NONHSAT127093
4	lnc-RP11-664D7.4.1-4	chr8:69243542-69243726	NR_038877
5	lnc-RP11-664D7.4.1-4	chr8:69218753-69218833	NR_038877
6	lnc-RP11-664D7.4.1-4	chr8:69216867-69217036	NONHSAT127094
7	lnc-RP11-664D7.4.1-4	chr8:69224379-69224452	NONHSAT127094
8	lnc-RP11-664D7.4.1-4	chr8:69215703-69217036	NR_038877

No data

Variant related genes	Relation type
C8orf34	TF binding region
RPL31P40	TF binding region
ENSG00000248801	TF binding region
C8orf34	CpG island
RPL31P40	CpG island
ENSG00000248801	CpG island

Extended variants
information (count: 1580 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1580 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4737889	chr8:69176154-69176155	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs538235312	chr8:69176178-69176179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557819994	chr8:69176202-69176203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181172876	chr8:69176220-69176221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534005616	chr8:69176221-69176222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs554332066	chr8:69176273-69176274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573053988	chr8:69176297-69176298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs551212499	chr8:69176375-69176376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185437561	chr8:69176384-69176385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs74704109	chr8:69176385-69176386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566628041	chr8:69176408-69176409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs533782942	chr8:69176461-69176462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs544501228	chr8:69176578-69176579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563891689	chr8:69176580-69176581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs76277339	chr8:69176640-69176641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs117611666	chr8:69176673-69176674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559849291	chr8:69176686-69176687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529438239	chr8:69176697-69176698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs190985106	chr8:69176727-69176728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182321231	chr8:69176791-69176792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs79726682	chr8:69176814-69176815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs187391805	chr8:69176829-69176830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571525807	chr8:69176956-69176957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568930237	chr8:69176979-69176980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573405399	chr8:69176984-69176985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs148205711	chr8:69177061-69177062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188641331	chr8:69181611-69181612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs577516016	chr8:69181615-69181616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191742168	chr8:69181624-69181625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2103155	chr8:69181652-69181653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs113295814	chr8:69181668-69181669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs183984130	chr8:69181669-69181670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs148259417	chr8:69181674-69181675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs1404593	chr8:69181681-69181682	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs562073334	chr8:69181702-69181703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141326977	chr8:69181709-69181710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs77288166	chr8:69181730-69181731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs563500256	chr8:69181759-69181760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs376877191	chr8:69181796-69181797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201783051	chr8:69181820-69181821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561037365	chr8:69181879-69181880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566319418	chr8:69181969-69181970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs117461941	chr8:69181973-69181974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs376139774	chr8:69181979-69181980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs527529199	chr8:69181994-69181995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs145197764	chr8:69181997-69181998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs376363677	chr8:69182026-69182027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs3056813	chr8:69182057-69182058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs397837298	chr8:69182062-69182063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559363157	chr8:69182076-69182077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
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
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	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
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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
Salivary gland tumor	18059337	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
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
head and neck squamous cell carcinoma	16715129	CNVD
Prostate cancer	16461572	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Colorectal cancer	21645411	CNVD

Chromatin state (count:424 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69174400-69176600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:69174600-69176200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr8:69176200-69177200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr8:69176600-69177000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:69181600-69181800	Enhancers	NHEK	skin
6	chr8:69181600-69182000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr8:69181600-69182000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr8:69182000-69185600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr8:69182400-69182600	Enhancers	NHEK	skin
10	chr8:69183000-69184000	Enhancers	GM12878-XiMat	blood
11	chr8:69185600-69186600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr8:69188200-69188600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr8:69194800-69195400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr8:69204600-69205200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr8:69204600-69205200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr8:69207200-69207400	Enhancers	Lung	lung
17	chr8:69207400-69208400	Weak transcription	Lung	lung
18	chr8:69208200-69211000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr8:69208200-69211000	Enhancers	HMEC	breast
20	chr8:69208400-69208800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr8:69208400-69208800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr8:69208400-69209000	ZNF genes & repeats	Lung	lung
23	chr8:69208400-69211000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr8:69208600-69208800	Enhancers	NHEK	skin
25	chr8:69208600-69209400	Enhancers	Fetal Brain Female	brain
26	chr8:69208800-69209200	Enhancers	Fetal Brain Male	brain
27	chr8:69208800-69210600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr8:69209000-69216800	Weak transcription	Lung	lung
29	chr8:69209200-69210000	Weak transcription	Fetal Brain Male	brain
30	chr8:69209800-69211000	Enhancers	NHEK	skin
31	chr8:69210000-69210200	Enhancers	Fetal Brain Male	brain
32	chr8:69210000-69210800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr8:69210200-69210800	Weak transcription	Fetal Brain Male	brain
34	chr8:69210600-69211000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr8:69210800-69211000	Enhancers	Fetal Brain Male	brain
36	chr8:69212200-69212600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr8:69216800-69217000	ZNF genes & repeats	Lung	lung
38	chr8:69216800-69217000	ZNF genes & repeats	Pancreas	Pancrea
39	chr8:69217000-69219600	Weak transcription	Pancreas	Pancrea
40	chr8:69218200-69218400	Weak transcription	NHEK	skin
41	chr8:69218400-69218600	ZNF genes & repeats	NHDF-Ad	bronchial
42	chr8:69218400-69218600	ZNF genes & repeats	NHEK	skin
43	chr8:69218400-69218800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
44	chr8:69219600-69219800	ZNF genes & repeats	Pancreas	Pancrea
45	chr8:69219800-69221600	Weak transcription	Pancreas	Pancrea
46	chr8:69221600-69222000	ZNF genes & repeats	Pancreas	Pancrea
47	chr8:69222000-69225000	Weak transcription	Pancreas	Pancrea
48	chr8:69224400-69225200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr8:69225000-69225200	Enhancers	Pancreas	Pancrea
50	chr8:69229600-69229800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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