Variant report

Variant	nsv611808
Chromosome Location	chr8:99544765-99591736
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:500)
CpG islands
(count:0)
Chromatin interactive
region (count:49)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:500 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:99552839-99553223	K562	blood:	n/a	n/a
2	ARID3A	chr8:99570483-99570523	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:99547792-99547835	K562	blood:	n/a	n/a
4	ATF1	chr8:99552873-99553325	K562	blood:	n/a	n/a
5	BHLHE40	chr8:99553115-99553231	K562	blood:	n/a	n/a
6	CBX3	chr8:99552776-99553837	K562	blood:	n/a	n/a
7	CEBPB	chr8:99561495-99561715	A549	lung:	n/a	chr8:99561589-99561600
8	CEBPB	chr8:99552777-99553194	K562	blood:	n/a	n/a
9	CEBPB	chr8:99560786-99561050	HepG2	liver:	n/a	chr8:99560905-99560916
10	CEBPB	chr8:99552740-99553470	K562	blood:	n/a	n/a
11	CEBPB	chr8:99561492-99561744	IMR90	lung:	n/a	chr8:99561589-99561600
12	CEBPB	chr8:99584907-99585116	K562	blood:	n/a	chr8:99585037-99585050 chr8:99585037-99585050
13	CEBPB	chr8:99561461-99561666	K562	blood:	n/a	chr8:99561589-99561600
14	CEBPB	chr8:99561508-99561729	HepG2	liver:	n/a	chr8:99561589-99561600
15	CEBPB	chr8:99552821-99553181	HepG2	liver:	n/a	n/a
16	CEBPB	chr8:99552887-99553258	MCF-7	breast:	n/a	n/a
17	CEBPB	chr8:99560789-99561031	K562	blood:	n/a	chr8:99560905-99560916
18	CEBPB	chr8:99552838-99553199	IMR90	lung:	n/a	n/a
19	CEBPB	chr8:99552907-99553069	HepG2	liver:	n/a	n/a
20	CEBPB	chr8:99560817-99561041	IMR90	lung:	n/a	chr8:99560905-99560916
21	CEBPB	chr8:99552828-99553181	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr8:99552745-99553319	K562	blood:	n/a	n/a
23	CEBPB	chr8:99590960-99590965	A549	lung:	n/a	n/a
24	CEBPD	chr8:99552758-99553302	K562	blood:	n/a	n/a
25	CHD2	chr8:99553366-99553731	K562	blood:	n/a	n/a
26	CHD2	chr8:99552880-99553054	K562	blood:	n/a	n/a
27	CTCF	chr8:99570360-99570510	BJ	skin:	n/a	chr8:99570442-99570463 chr8:99570440-99570458
28	CTCF	chr8:99559245-99559467	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr8:99570300-99570450	NHDF-neo	bronchial:	n/a	n/a
30	CTCF	chr8:99559081-99559652	MCF-7	breast:	n/a	n/a
31	CTCF	chr8:99559260-99559410	Caco-2	colon:	n/a	n/a
32	CTCF	chr8:99559260-99559410	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr8:99567180-99567330	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr8:99559298-99559445	HepG2	liver:	n/a	n/a
35	CTCF	chr8:99567200-99567350	HMEC	breast:	n/a	n/a
36	CTCF	chr8:99567230-99567326	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr8:99559308-99559441	LNCaP	prostate:	n/a	n/a
38	CTCF	chr8:99563480-99563630	HCM	heart:	n/a	n/a
39	CTCF	chr8:99570360-99570510	Caco-2	colon:	n/a	chr8:99570442-99570463 chr8:99570440-99570458
40	CTCF	chr8:99570020-99570170	AG04449	skin:	n/a	n/a
41	CTCF	chr8:99570380-99570530	HMF	breast:	n/a	chr8:99570442-99570463 chr8:99570440-99570458
42	CTCF	chr8:99570240-99570390	HFF	foreskin:	n/a	n/a
43	CTCF	chr8:99569885-99570869	A549	lung:	n/a	chr8:99570442-99570463 chr8:99570440-99570458
44	CTCF	chr8:99559384-99559419	A549	lung:	n/a	n/a
45	CTCF	chr8:99570360-99570510	AG09319	gingival:	n/a	chr8:99570442-99570463 chr8:99570440-99570458
46	CTCF	chr8:99570300-99570450	HCM	heart:	n/a	n/a
47	CTCF	chr8:99559260-99559410	HRE	kidney:	n/a	n/a
48	CTCF	chr8:99573053-99573244	MCF-7	breast:	n/a	n/a
49	CTCF	chr8:99569880-99570030	NB4	blood:	n/a	n/a
50	CTCF	chr8:99559280-99559430	HPAF	blood vessel:	n/a	n/a

No data

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:99557700..99559329-chr8:100024185..100025880,2	MCF-7	breast:
2	chr8:99570092..99570986-chr8:100009815..100010452,2	MCF-7	breast:
3	chr8:99558355..99561109-chr8:99565802..99568182,2	MCF-7	breast:
4	chr8:99568854..99571836-chr8:99577056..99579865,2	K562	blood:
5	chr8:99580951..99583147-chr8:99585319..99588307,2	MCF-7	breast:
6	chr8:99536690..99539147-chr8:99552855..99554572,2	K562	blood:
7	chr8:99540019..99542563-chr8:99545669..99547224,2	K562	blood:
8	chr8:99547855..99550787-chr8:99555161..99557416,2	MCF-7	breast:
9	chr8:99552951..99554839-chr8:99564123..99567093,2	K562	blood:
10	chr8:99542296..99548423-chr8:99550336..99556395,6	K562	blood:
11	chr8:99305859..99308517-chr8:99567304..99569483,2	MCF-7	breast:
12	chr8:99558108..99560568-chr8:99561487..99563992,2	MCF-7	breast:
13	chr8:99568854..99571836-chr8:99577056..99579865,2	K562	blood:
14	chr8:99537016..99539977-chr8:99549369..99551043,2	K562	blood:
15	chr8:99562289..99564114-chr8:99567497..99569189,2	K562	blood:
16	chr8:99542296..99548423-chr8:99550336..99556395,6	K562	blood:
17	chr8:99542982..99544707-chr8:99547158..99548868,2	K562	blood:
18	chr8:99561270..99563959-chr8:99566385..99568748,2	MCF-7	breast:
19	chr8:99545068..99548423-chr8:99550336..99555475,4	K562	blood:
20	chr8:99552951..99554839-chr8:99564123..99567093,2	K562	blood:
21	chr8:99176565..99177464-chr8:99569990..99570552,2	MCF-7	breast:
22	chr8:99561270..99563959-chr8:99566385..99568748,2	MCF-7	breast:
23	chr8:99591533..99593708-chr8:99612212..99613959,2	MCF-7	breast:
24	chr8:99562289..99564114-chr8:99567497..99569189,2	K562	blood:
25	chr8:99581930..99583507-chr8:99587107..99589920,2	K562	blood:
26	chr7:100812765..100815379-chr8:99565140..99568111,2	MCF-7	breast:
27	chr8:99537550..99540460-chr8:99551301..99553310,2	MCF-7	breast:
28	chr8:99539907..99541519-chr8:99544944..99547169,2	K562	blood:
29	chr8:99586001..99587844-chr8:99593892..99596537,2	K562	blood:
30	chr8:99570440..99572311-chr8:99716067..99717678,2	MCF-7	breast:
31	chr8:99548557..99552364-chr8:99553180..99556021,3	MCF-7	breast:
32	chr8:99542843..99544364-chr8:99551083..99552848,2	K562	blood:
33	chr8:99570067..99570984-chr8:99843872..99844522,2	MCF-7	breast:
34	chr8:99574600..99576292-chr8:99955675..99958275,2	MCF-7	breast:
35	chr8:99548557..99552364-chr8:99553180..99556021,3	MCF-7	breast:
36	chr8:99569567..99570631-chr8:99717657..99718318,3	MCF-7	breast:
37	chr8:99548500..99551679-chr8:99552322..99555998,3	K562	blood:
38	chr8:99568406..99571836-chr8:99575589..99579865,3	K562	blood:
39	chr8:99580951..99583147-chr8:99585319..99588307,2	MCF-7	breast:
40	chr8:23385716..23387742-chr8:99554566..99556123,2	MCF-7	breast:
41	chr8:99568406..99571836-chr8:99575589..99579865,3	K562	blood:
42	chr8:99537267..99539977-chr8:99549523..99551043,2	K562	blood:
43	chr8:99570015..99570973-chr8:100370433..100371359,3	K562	blood:
44	chr8:99547855..99550787-chr8:99555161..99557416,2	MCF-7	breast:
45	chr8:99590385..99592004-chr8:100024205..100026832,2	MCF-7	breast:
46	chr8:99548500..99551679-chr8:99552322..99555998,3	K562	blood:
47	chr8:99567325..99572845-chr8:99952617..99957549,5	MCF-7	breast:
48	chr8:99545068..99548423-chr8:99550336..99555475,4	K562	blood:
49	chr8:99581930..99583507-chr8:99587107..99589920,2	K562	blood:

No data

Variant related genes	Relation type
STK3	TF binding region
ENSG00000253948	chromatin interactions
ENSG00000271930	chromatin interactions
ENSG00000147454	chromatin interactions
ENSG00000104361	chromatin interactions
ENSG00000164920	chromatin interactions
ENSG00000104375	chromatin interactions
ENSG00000132549	chromatin interactions

Extended variants
information (count: 1439 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:1439 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6651181	chr8:99544765-99544766	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563584129	chr8:99544803-99544804	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs148423938	chr8:99544823-99544824	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs576025058	chr8:99544845-99544846	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545013134	chr8:99544871-99544872	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs561355210	chr8:99544890-99544891	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs558942046	chr8:99544936-99544937	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs13268777	chr8:99544964-99544965	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs191732034	chr8:99544965-99544966	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs561152196	chr8:99544981-99544982	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs142523467	chr8:99545106-99545107	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs147552784	chr8:99545119-99545120	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs111444199	chr8:99545185-99545186	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs562830774	chr8:99545256-99545257	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142282797	chr8:99545276-99545277	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs144465741	chr8:99545307-99545308	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs551364741	chr8:99545319-99545320	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571265445	chr8:99545391-99545392	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184283046	chr8:99545397-99545398	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs55964698	chr8:99545408-99545409	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs567875154	chr8:99545433-99545434	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373435409	chr8:99545438-99545439	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs13270534	chr8:99545465-99545466	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs556266053	chr8:99545516-99545517	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566039129	chr8:99545543-99545544	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569651062	chr8:99545553-99545554	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs13272983	chr8:99545560-99545561	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs76133403	chr8:99545664-99545665	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs147848785	chr8:99545680-99545681	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs189071432	chr8:99545693-99545694	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11994001	chr8:99545697-99545698	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs11994002	chr8:99545700-99545701	ZNF genes & repeats Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs554547225	chr8:99545827-99545828	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs193198005	chr8:99545828-99545829	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs72666631	chr8:99545891-99545892	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs140339694	chr8:99545981-99545982	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557400845	chr8:99546026-99546027	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150345895	chr8:99546051-99546052	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145269324	chr8:99546058-99546059	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545063226	chr8:99546063-99546064	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs76321746	chr8:99546065-99546066	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527656328	chr8:99546072-99546073	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548102185	chr8:99546102-99546103	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567855551	chr8:99546134-99546135	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530367824	chr8:99546188-99546189	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577454111	chr8:99546204-99546205	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550114270	chr8:99546285-99546286	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570225393	chr8:99546299-99546300	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538755237	chr8:99546336-99546337	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185368829	chr8:99546338-99546339	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

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
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
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	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
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
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Colorectal cancer	19455253	CNVD
Sezary syndrome	18413736	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	21611746	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:533 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:99490400-99547600	Weak transcription	Ovary	ovary
2	chr8:99500400-99558800	Weak transcription	Aorta	Aorta
3	chr8:99515000-99550800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr8:99518800-99551000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr8:99519000-99548400	Weak transcription	Fetal Stomach	stomach
6	chr8:99525800-99576400	Weak transcription	Pancreas	Pancrea
7	chr8:99526200-99549400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr8:99531000-99569600	Weak transcription	HMEC	breast
9	chr8:99531200-99561800	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr8:99531400-99586400	Weak transcription	HSMM	muscle
11	chr8:99531600-99561800	Weak transcription	Esophagus	oesophagus
12	chr8:99532000-99548000	Weak transcription	HSMMtube	muscle
13	chr8:99533400-99566400	Weak transcription	NHLF	lung
14	chr8:99534600-99567200	Weak transcription	A549	lung
15	chr8:99534800-99549800	Weak transcription	Colon Smooth Muscle	Colon
16	chr8:99535400-99571600	Weak transcription	Gastric	stomach
17	chr8:99536800-99545000	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr8:99539200-99548200	Weak transcription	NHDF-Ad	bronchial
19	chr8:99539200-99553000	Weak transcription	HepG2	liver
20	chr8:99542000-99546600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr8:99542200-99545600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr8:99542600-99545000	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr8:99542600-99546000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
24	chr8:99542600-99546600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr8:99542800-99544800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
26	chr8:99542800-99546400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr8:99543000-99544800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
28	chr8:99543000-99544800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr8:99543000-99544800	Strong transcription	Fetal Intestine Large	intestine
30	chr8:99543000-99545000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr8:99543000-99545000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr8:99543000-99545400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr8:99543000-99546400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr8:99543000-99566800	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr8:99543200-99545400	ZNF genes & repeats	Dnd41	blood
36	chr8:99543600-99544800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr8:99543600-99553200	Weak transcription	Duodenum Mucosa	Duodenum
38	chr8:99543800-99544800	ZNF genes & repeats	Liver	Liver
39	chr8:99543800-99547600	Weak transcription	K562	blood
40	chr8:99543800-99548000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr8:99543800-99548400	Weak transcription	Adipose Nuclei	Adipose
42	chr8:99543800-99555000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr8:99544000-99544800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr8:99544000-99547600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr8:99544000-99547600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr8:99544000-99548600	Weak transcription	Fetal Kidney	kidney
47	chr8:99544000-99552400	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr8:99544000-99552400	Weak transcription	Placenta	Placenta
49	chr8:99544000-99552800	Weak transcription	Stomach Smooth Muscle	stomach
50	chr8:99544000-99559000	Weak transcription	Skeletal Muscle Male	skeletal muscle

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