Variant report

Variant	nsv1019168
Chromosome Location	chr8:100324341-100361194
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:159)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:159 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr8:100334302-100334493	K562	blood:	n/a	n/a
2	CCNT2	chr8:100332298-100332498	K562	blood:	n/a	n/a
3	CEBPB	chr8:100328430-100328776	HepG2	liver:	n/a	chr8:100328593-100328604
4	CEBPB	chr8:100335969-100336430	ECC-1	luminal epithelium:	n/a	n/a
5	CEBPB	chr8:100329518-100329524	A549	lung:	n/a	n/a
6	CEBPB	chr8:100328436-100328727	A549	lung:	n/a	chr8:100328593-100328604
7	CEBPB	chr8:100328452-100328768	MCF-7	breast:	n/a	chr8:100328593-100328604
8	CEBPB	chr8:100328445-100328642	K562	blood:	n/a	chr8:100328593-100328604
9	CEBPB	chr8:100328511-100328711	H1-hESC	embryonic stem cell:	n/a	chr8:100328593-100328604
10	CTCF	chr8:100352985-100353106	Fibrobl	skin:	n/a	n/a
11	CTCF	chr8:100353080-100353230	HBMEC	blood vessel:	n/a	n/a
12	CTCF	chr8:100359786-100359883	GM12891	blood:	n/a	n/a
13	CTCF	chr8:100353120-100353270	GM06990	blood:	n/a	n/a
14	CTCF	chr8:100353092-100353259	Medullo	brain:	n/a	n/a
15	CTCF	chr8:100353021-100353195	MCF-7	breast:	n/a	n/a
16	CTCF	chr8:100355880-100356030	AG10803	skin:	n/a	n/a
17	CTCF	chr8:100353060-100353210	RPTEC	kidney:	n/a	n/a
18	CTCF	chr8:100353060-100353350	HCT-116	colon:	n/a	n/a
19	CTCF	chr8:100353039-100353330	K562	blood:	n/a	n/a
20	CTCF	chr8:100352973-100353234	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr8:100359784-100359851	GM12892	blood:	n/a	n/a
22	CTCF	chr8:100353041-100353226	HepG2	liver:	n/a	n/a
23	CTCF	chr8:100353094-100353221	GM19238	blood:	n/a	n/a
24	CTCF	chr8:100359763-100359886	GM19238	blood:	n/a	n/a
25	CTCF	chr8:100353101-100353180	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr8:100354689-100354741	GM13976	blood:	n/a	n/a
27	CTCF	chr8:100359759-100359898	MCF-7	breast:	n/a	n/a
28	CTCF	chr8:100353780-100353930	AG09319	gingival:	n/a	n/a
29	CTCF	chr8:100353100-100353250	BE2_C	brain:	n/a	n/a
30	CTCF	chr8:100325687-100325700	Pancreas_OC	pancreas:	n/a	n/a
31	CTCF	chr8:100353080-100353230	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr8:100352997-100353004	MCF-7	breast:	n/a	n/a
33	CTCF	chr8:100352949-100353065	MCF-7	breast:	n/a	n/a
34	CTCF	chr8:100353040-100353190	HRE	kidney:	n/a	n/a
35	CTCF	chr8:100353126-100353240	HepG2	liver:	n/a	n/a
36	CTCF	chr8:100359799-100359873	NHEK	skin:	n/a	n/a
37	CTCF	chr8:100359801-100359857	A549	lung:	n/a	n/a
38	CTCF	chr8:100353060-100353210	K562	blood:	n/a	n/a
39	CTCF	chr8:100353083-100353244	MCF-7	breast:	n/a	n/a
40	CTCF	chr8:100353111-100353115	A549	lung:	n/a	n/a
41	CTCF	chr8:100353060-100353210	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr8:100353095-100353172	MCF-7	breast:	n/a	n/a
43	CTCF	chr8:100353118-100353155	A549	lung:	n/a	n/a
44	CTCF	chr8:100359802-100359866	HepG2	liver:	n/a	n/a
45	CTCF	chr8:100359743-100359900	MCF-7	breast:	n/a	n/a
46	CTCF	chr8:100353000-100353150	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr8:100359778-100359871	MCF-7	breast:	n/a	n/a
48	CTCF	chr8:100353080-100353230	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr8:100353080-100353230	Caco-2	colon:	n/a	n/a
50	CTCF	chr8:100352983-100353176	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:100334620-100334670	GM19239	blood:	n/a
2	chr8:100334620-100334670	A549	lung:	n/a
3	chr8:100334620-100334670	HRE	kidney:	n/a
4	chr8:100334620-100334670	HCM	heart:	n/a
5	chr8:100334620-100334670	HEEpiC	esophagus:	n/a
6	chr8:100334620-100334670	PFSK-1	brain:	n/a
7	chr8:100334620-100334670	GM12891	blood:	n/a
8	chr8:100334620-100334670	Hela-S3	cervix:	n/a
9	chr8:100334620-100334670	ECC-1	luminal epithelium:	n/a
10	chr8:100334620-100334670	Hepatocyte	liver:	n/a
11	chr8:100334620-100334670	GM06990	blood:	n/a
12	chr8:100334620-100334670	HCF	heart:	n/a
13	chr8:100334620-100334670	HL-60	blood:	n/a
14	chr8:100334620-100334670	HepG2	liver:	n/a
15	chr8:100334620-100334670	AG04449	skin:	fetal
16	chr8:100334620-100334670	PANC-1	pancreas:	n/a
17	chr8:100334620-100334670	AG10803	skin:	n/a
18	chr8:100334620-100334670	HEK293	kidney:	embryo
19	chr8:100334620-100334670	GM12892	blood:	n/a
20	chr8:100334620-100334670	HIPEpiC	eye:	n/a
21	chr8:100334620-100334670	AG09309	skin:	n/a
22	chr8:100334620-100334670	CMK	blood:	n/a
23	chr8:100334620-100334670	MCF10A-Er-Src	breast:	n/a
24	chr8:100334620-100334670	U87	brain:	n/a
25	chr8:100334620-100334670	BJ	skin:	n/a
26	chr8:100334620-100334670	ProgFib	skin:	n/a
27	chr8:100334620-100334670	H1-hESC	embryonic stem cell:	embryo
28	chr8:100334620-100334670	Caco-2	colon:	n/a
29	chr8:100334620-100334670	SK-N-SH_RA	brain:	n/a
30	chr8:100334620-100334670	HUVEC	blood vessel:	n/a
31	chr8:100334620-100334670	HAEpiC	amniotic membrane:	n/a
32	chr8:100334620-100334670	HNPCEpiC	eye:	n/a
33	chr8:100334620-100334670	SKMC	muscle:	n/a
34	chr8:100334620-100334670	HCPEpiC	choroid plexus:	n/a
35	chr8:100334620-100334670	HRCEpiC	kidney:	n/a
36	chr8:100334620-100334670	NB4	blood:	n/a
37	chr8:100334620-100334670	AG09319	gingival:	n/a
38	chr8:100334620-100334670	LNCaP	prostate:	n/a
39	chr8:100334620-100334670	AoSMC	blood vessel:	n/a
40	chr8:100334620-100334670	SK-N-MC	brain:	n/a
41	chr8:100334620-100334670	HMEC	breast:	n/a
42	chr8:100334620-100334670	HCT-116	colon:	n/a
43	chr8:100334620-100334670	NH-A	brain:	n/a
44	chr8:100334620-100334670	PrEC	prostate:	n/a
45	chr8:100334620-100334670	K562	blood:	n/a
46	chr8:100334620-100334670	AG04450	lung:	fetal
47	chr8:100334620-100334670	RPTEC	kidney:	n/a
48	chr8:100334620-100334670	NHBE	bronchial:	n/a
49	chr8:100334620-100334670	Jurkat	blood:	n/a
50	chr8:100334620-100334670	SK-N-SH	brain:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:100340207..100341801-chr8:100343989..100346691,2	MCF-7	breast:
2	chr8:100327325..100329198-chr8:100340079..100342358,2	MCF-7	breast:
3	chr8:100323481..100327206-chr8:100331154..100333171,3	MCF-7	breast:
4	chr8:100332741..100335703-chr8:100337137..100341568,3	MCF-7	breast:
5	chr8:100327325..100329198-chr8:100340079..100342358,2	MCF-7	breast:
6	chr8:100356710..100358343-chr8:100358891..100361073,2	K562	blood:
7	chr8:100340207..100341801-chr8:100343989..100346691,2	MCF-7	breast:
8	chr8:100357228..100359296-chr8:100360534..100362578,2	MCF-7	breast:
9	chr8:100323481..100327206-chr8:100331154..100333171,3	MCF-7	breast:
10	chr8:100024635..100026607-chr8:100339207..100341437,2	MCF-7	breast:
11	chr8:100343791..100346575-chr8:100348119..100349870,2	MCF-7	breast:
12	chr8:100360393..100360964-chr8:100816462..100817102,2	MCF-7	breast:
13	chr8:100329098..100330856-chr8:100331177..100332983,2	MCF-7	breast:
14	chr8:100343791..100346575-chr8:100348119..100349870,2	MCF-7	breast:
15	chr8:100329098..100330856-chr8:100331177..100332983,2	MCF-7	breast:
16	chr8:100355778..100358210-chr8:100359573..100361952,2	K562	blood:
17	chr8:100357228..100359296-chr8:100360534..100362578,2	MCF-7	breast:
18	chr8:99717161..99717948-chr8:100352640..100353640,2	K562	blood:
19	chr8:100332741..100335703-chr8:100337137..100341568,3	MCF-7	breast:
20	chr8:100354480..100357120-chr8:100365143..100367945,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STK3-6	chr8:100352533-100353989	NONHSAT127951
2	lnc-STK3-7	chr8:100358280-100360484	NONHSAT127952

No data

Variant related genes	Relation type
ENSG00000237704	TF binding region
ENSG00000225017	TF binding region
ENSG00000237704	CpG island
ENSG00000225017	CpG island
ENSG00000253948	chromatin interactions
ENSG00000225017	chromatin interactions
ENSG00000253912	chromatin interactions
ENSG00000132549	chromatin interactions

Extended variants
information (count: 1263 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:1263 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529945967	chr8:100324351-100324352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs538868214	chr8:100324355-100324356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148527840	chr8:100324379-100324380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563467825	chr8:100324423-100324424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372370409	chr8:100324438-100324439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571042069	chr8:100324441-100324442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565341827	chr8:100324446-100324447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533627435	chr8:100324534-100324535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147728921	chr8:100324598-100324599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191433252	chr8:100324599-100324600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567800945	chr8:100324614-100324615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs183103768	chr8:100324653-100324654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573567868	chr8:100324689-100324690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556502698	chr8:100324692-100324693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs199717733	chr8:100324696-100324697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs538965572	chr8:100324697-100324698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs559199215	chr8:100324710-100324711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs572512732	chr8:100324719-100324720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs541418340	chr8:100324722-100324723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs142518839	chr8:100324743-100324744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200582100	chr8:100324748-100324749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536200546	chr8:100324773-100324774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187692126	chr8:100324774-100324775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563348809	chr8:100324777-100324778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532289279	chr8:100324821-100324822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs367622108	chr8:100324843-100324844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545827407	chr8:100324854-100324855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559216338	chr8:100324857-100324858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201246222	chr8:100324887-100324888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368443778	chr8:100324910-100324911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528110157	chr8:100324954-100324955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547762708	chr8:100324970-100324971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567690904	chr8:100324978-100324979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs116147815	chr8:100324986-100324987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550603295	chr8:100325001-100325002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191068469	chr8:100325002-100325003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556520574	chr8:100325083-100325084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs199782901	chr8:100325113-100325114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570199900	chr8:100325122-100325123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539212856	chr8:100325129-100325130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559326758	chr8:100325144-100325145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs147586309	chr8:100325155-100325156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs140718382	chr8:100325164-100325165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182260463	chr8:100325188-100325189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187771524	chr8:100325189-100325190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs72672359	chr8:100325215-100325216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543557709	chr8:100325216-100325217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557427696	chr8:100325224-100325225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368610195	chr8:100325253-100325254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577007756	chr8:100325257-100325258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
Breast cancer	21611746	CNVD
Cohen syndrome	20461111	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:174 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:100310400-100325600	Weak transcription	Fetal Stomach	stomach
2	chr8:100319400-100325800	Weak transcription	Fetal Lung	lung
3	chr8:100320200-100326000	Weak transcription	Liver	Liver
4	chr8:100321800-100325800	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr8:100323800-100325600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr8:100325400-100325800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr8:100325400-100327000	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr8:100325600-100325800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr8:100325600-100326200	ZNF genes & repeats	Left Ventricle	heart
10	chr8:100325600-100326400	ZNF genes & repeats	Primary T cells from cord blood	blood
11	chr8:100325600-100326400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr8:100325600-100327000	ZNF genes & repeats	Fetal Intestine Small	intestine
13	chr8:100325600-100327000	ZNF genes & repeats	Fetal Stomach	stomach
14	chr8:100325800-100326000	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
15	chr8:100325800-100326200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
16	chr8:100325800-100326400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr8:100325800-100326400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr8:100325800-100326400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr8:100325800-100326400	ZNF genes & repeats	Fetal Lung	lung
20	chr8:100325800-100327000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:100325800-100327000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
22	chr8:100325800-100327000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr8:100325800-100327000	ZNF genes & repeats	Aorta	Aorta
24	chr8:100325800-100327200	ZNF genes & repeats	Primary B cells from peripheral blood	blood
25	chr8:100325800-100327600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr8:100326000-100326400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
27	chr8:100326000-100326400	ZNF genes & repeats	Liver	Liver
28	chr8:100326000-100326400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
29	chr8:100326200-100326400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
30	chr8:100326200-100326400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr8:100326200-100327600	ZNF genes & repeats	Dnd41	blood
32	chr8:100326400-100326800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr8:100326400-100327800	Weak transcription	Liver	Liver
34	chr8:100326400-100328400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr8:100326400-100328400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr8:100326400-100354600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr8:100326600-100326800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
38	chr8:100327000-100327600	Weak transcription	Fetal Intestine Small	intestine
39	chr8:100327000-100328200	Weak transcription	Fetal Stomach	stomach
40	chr8:100327000-100329200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr8:100327000-100334200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr8:100327000-100361800	Weak transcription	Aorta	Aorta
43	chr8:100327600-100327800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr8:100327600-100328400	Weak transcription	Dnd41	blood
45	chr8:100327600-100329000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr8:100327800-100329000	ZNF genes & repeats	Fetal Intestine Small	intestine
47	chr8:100328200-100328600	ZNF genes & repeats	Fetal Stomach	stomach
48	chr8:100328200-100328800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr8:100328200-100334800	Weak transcription	Primary B cells from cord blood	blood
50	chr8:100328400-100328600	ZNF genes & repeats	Lung	lung

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