Variant report

Variant	nsv6229
Chromosome Location	chr8:64282018-64326530
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:550)
CpG islands
(count:122)
Chromatin interactive
region (count:10)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:550 , 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	ATF1	chr8:64321036-64321329	K562	blood:	n/a	n/a
2	ATF1	chr8:64303952-64304219	K562	blood:	n/a	n/a
3	ATF2	chr8:64303842-64304356	GM12878	blood:	n/a	n/a
4	ATF2	chr8:64314425-64314930	GM12878	blood:	n/a	n/a
5	ATF2	chr8:64314395-64315013	GM12878	blood:	n/a	n/a
6	BATF	chr8:64314237-64314987	GM12878	blood:	n/a	n/a
7	BATF	chr8:64310972-64311227	GM12878	blood:	n/a	n/a
8	BATF	chr8:64314441-64314884	GM12878	blood:	n/a	n/a
9	BCL11A	chr8:64314466-64314835	GM12878	blood:	n/a	n/a
10	BCL11A	chr8:64314408-64314907	GM12878	blood:	n/a	n/a
11	BCL3	chr8:64314462-64314861	GM12878	blood:	n/a	n/a
12	BCLAF1	chr8:64314332-64314896	GM12878	blood:	n/a	n/a
13	BCLAF1	chr8:64303837-64304335	GM12878	blood:	n/a	chr8:64304235-64304244
14	BCLAF1	chr8:64314337-64314923	GM12878	blood:	n/a	n/a
15	BHLHE40	chr8:64310725-64310839	GM12878	blood:	n/a	n/a
16	BHLHE40	chr8:64314247-64314836	GM12878	blood:	n/a	n/a
17	BRCA1	chr8:64322994-64322999	GM12878	blood:	n/a	n/a
18	BRCA1	chr8:64312740-64312775	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr8:64303984-64304145	HepG2	liver:	n/a	n/a
20	CEBPB	chr8:64303841-64304212	MCF-7	breast:	n/a	n/a
21	CEBPB	chr8:64303935-64304281	A549	lung:	n/a	chr8:64304265-64304276 chr8:64304265-64304278 chr8:64304265-64304276
22	CEBPB	chr8:64306494-64306625	HepG2	liver:	n/a	n/a
23	CEBPB	chr8:64314298-64315056	GM12878	blood:	n/a	n/a
24	CEBPB	chr8:64303904-64304268	K562	blood:	n/a	n/a
25	CEBPB	chr8:64307291-64307645	A549	lung:	n/a	chr8:64307461-64307472 chr8:64307463-64307472 chr8:64307463-64307474
26	CEBPB	chr8:64307303-64307646	HepG2	liver:	n/a	chr8:64307461-64307472 chr8:64307463-64307472 chr8:64307463-64307474
27	CEBPB	chr8:64303891-64304396	HepG2	liver:	n/a	chr8:64304265-64304276 chr8:64304265-64304278 chr8:64304265-64304276
28	CEBPB	chr8:64303863-64304283	Hela-S3	cervix:	n/a	chr8:64304265-64304276 chr8:64304265-64304278 chr8:64304265-64304276
29	CEBPB	chr8:64307334-64307622	IMR90	lung:	n/a	chr8:64307461-64307472 chr8:64307463-64307472 chr8:64307463-64307474
30	CEBPB	chr8:64303909-64304227	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr8:64303880-64304390	IMR90	lung:	n/a	chr8:64304265-64304276 chr8:64304265-64304278 chr8:64304265-64304276
32	CEBPB	chr8:64307387-64307524	H1-hESC	embryonic stem cell:	n/a	chr8:64307461-64307472 chr8:64307463-64307472 chr8:64307463-64307474
33	CHD2	chr8:64314426-64314847	GM12878	blood:	n/a	n/a
34	CREB1	chr8:64310839-64311382	GM12878	blood:	n/a	n/a
35	CTCF	chr8:64303814-64304277	GM12878	blood:	n/a	n/a
36	CTCF	chr8:64303958-64304151	MCF-7	breast:	n/a	n/a
37	CTCF	chr8:64302981-64303054	Fibrobl	skin:	n/a	n/a
38	CTCF	chr8:64315220-64315370	GM12868	blood:	n/a	n/a
39	CTCF	chr8:64303881-64304158	Lung_OC	lung:	n/a	n/a
40	CTCF	chr8:64315220-64315370	GM12864	blood:	n/a	n/a
41	CTCF	chr8:64303960-64304110	GM12871	blood:	n/a	n/a
42	CTCF	chr8:64303913-64304163	HepG2	liver:	n/a	n/a
43	CTCF	chr8:64315299-64315375	MCF-7	breast:	n/a	n/a
44	CTCF	chr8:64303896-64304145	GM13977	blood:	n/a	n/a
45	CTCF	chr8:64315260-64315410	GM12865	blood:	n/a	n/a
46	CTCF	chr8:64303980-64304130	HEK293	kidney:	n/a	n/a
47	CTCF	chr8:64303940-64304090	GM06990	blood:	n/a	n/a
48	CTCF	chr8:64303829-64304115	A549	lung:	n/a	n/a
49	CTCF	chr8:64303931-64304181	GM12892	blood:	n/a	n/a
50	CTCF	chr8:64303960-64304110	Caco-2	colon:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:64314339-64314389	MCF10A-Er-Src	breast:	n/a
2	chr8:64314339-64314389	AG04449	skin:	fetal
3	chr8:64314339-64314389	NT2-D1	testis:	n/a
4	chr8:64314339-64314389	PFSK-1	brain:	n/a
5	chr8:64325777-64325827	SK-N-SH_RA	brain:	n/a
6	chr8:64314339-64314389	T-47D	breast:	n/a
7	chr8:64325777-64325827	BE2_C	brain:	n/a
8	chr8:64325777-64325827	HPAEpiC	pulmonary alveolar:	n/a
9	chr8:64314339-64314389	HRPEpiC	eye:	n/a
10	chr8:64314339-64314389	HCPEpiC	choroid plexus:	n/a
11	chr8:64325777-64325827	AG10803	skin:	n/a
12	chr8:64314339-64314389	ECC-1	luminal epithelium:	n/a
13	chr8:64314339-64314389	HNPCEpiC	eye:	n/a
14	chr8:64325777-64325827	GM06990	blood:	n/a
15	chr8:64325777-64325827	HEEpiC	esophagus:	n/a
16	chr8:64325777-64325827	PANC-1	pancreas:	n/a
17	chr8:64314339-64314389	RPTEC	kidney:	n/a
18	chr8:64314339-64314389	GM12892	blood:	n/a
19	chr8:64325777-64325827	HCT-116	colon:	n/a
20	chr8:64325777-64325827	ProgFib	skin:	n/a
21	chr8:64325777-64325827	Jurkat	blood:	n/a
22	chr8:64325777-64325827	Hepatocyte	liver:	n/a
23	chr8:64314339-64314389	SK-N-SH_RA	brain:	n/a
24	chr8:64314339-64314389	HCM	heart:	n/a
25	chr8:64314339-64314389	IMR90	lung:	fetal
26	chr8:64314339-64314389	HRE	kidney:	n/a
27	chr8:64314339-64314389	GM12891	blood:	n/a
28	chr8:64325777-64325827	HEK293	kidney:	embryo
29	chr8:64325777-64325827	ECC-1	luminal epithelium:	n/a
30	chr8:64325777-64325827	HL-60	blood:	n/a
31	chr8:64314339-64314389	Jurkat	blood:	n/a
32	chr8:64325777-64325827	NB4	blood:	n/a
33	chr8:64314339-64314389	SK-N-SH	brain:	n/a
34	chr8:64325777-64325827	SK-N-MC	brain:	n/a
35	chr8:64314339-64314389	PANC-1	pancreas:	n/a
36	chr8:64314339-64314389	SK-N-MC	brain:	n/a
37	chr8:64314339-64314389	HPAEpiC	pulmonary alveolar:	n/a
38	chr8:64314339-64314389	HAEpiC	amniotic membrane:	n/a
39	chr8:64325777-64325827	IMR90	lung:	fetal
40	chr8:64314339-64314389	HEEpiC	esophagus:	n/a
41	chr8:64325777-64325827	AG04449	skin:	fetal
42	chr8:64325777-64325827	HUVEC	blood vessel:	n/a
43	chr8:64314339-64314389	H1-hESC	embryonic stem cell:	embryo
44	chr8:64314339-64314389	GM06990	blood:	n/a
45	chr8:64325777-64325827	HCPEpiC	choroid plexus:	n/a
46	chr8:64325777-64325827	HMEC	breast:	n/a
47	chr8:64325777-64325827	GM12892	blood:	n/a
48	chr8:64325777-64325827	LNCaP	prostate:	n/a
49	chr8:64314339-64314389	AG09309	skin:	n/a
50	chr8:64314339-64314389	BE2_C	brain:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:64318299..64320307-chr8:64323831..64325883,2	K562	blood:
2	chr8:64303593..64304820-chr8:65294224..65295292,6	MCF-7	breast:
3	chr8:64303536..64304445-chr8:65294376..65295331,4	MCF-7	breast:
4	chr8:64318299..64320307-chr8:64323831..64325883,2	K562	blood:
5	chr8:64318299..64319986-chr8:64323561..64325883,2	K562	blood:
6	chr8:64312553..64315389-chr8:64317911..64320594,2	K562	blood:
7	chr8:64303514..64304353-chr8:65176496..65177185,3	MCF-7	breast:
8	chr8:64312553..64315389-chr8:64317911..64320594,2	K562	blood:
9	chr8:64305743..64306564-chr8:65294350..65295283,2	K562	blood:
10	chr8:64318299..64319986-chr8:64323561..64325883,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTPA-1	chr8:64323466-64323527	XLOC_007100
2	lnc-TTPA-1	chr8:64325669-64325809	ENSG00000253205
3	lnc-TTPA-1	chr8:64298421-64298464	ENSG00000253205
4	lnc-TTPA-1	chr8:64323466-64323527	ENSG00000253205
5	lnc-TTPA-1	chr8:64325669-64325809	NONHSAT126934
6	lnc-TTPA-1	chr8:64298167-64298464	ENSG00000253205
7	lnc-TTPA-1	chr8:64325669-64325809	XLOC_007100
8	lnc-TTPA-1	chr8:64297397-64298464	XLOC_007100
9	lnc-TTPA-1	chr8:64323466-64323527	ENSG00000253205
10	lnc-TTPA-1	chr8:64298436-64298464	NONHSAT126934
11	lnc-TTPA-1	chr8:64323466-64323527	NONHSAT126934
12	lnc-TTPA-1	chr8:64326191-64326275	ENSG00000253205

No data

Variant related genes	Relation type
IFITM8P	TF binding region
IFITM8P	CpG island

Extended variants
information (count: 1082 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1082 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190078035	chr8:64282073-64282074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs529738945	chr8:64282112-64282113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs4737642	chr8:64282126-64282127	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs563409117	chr8:64282129-64282130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs6472097	chr8:64282215-64282216	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs552132457	chr8:64282354-64282355	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7818456	chr8:64282381-64282382	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs369594176	chr8:64282395-64282396	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570648279	chr8:64282437-64282438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546887739	chr8:64282473-64282474	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567986534	chr8:64282484-64282485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546363574	chr8:64282494-64282495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554535389	chr8:64282520-64282521	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561465595	chr8:64282540-64282541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138997567	chr8:64282569-64282570	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558741776	chr8:64282581-64282582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375842427	chr8:64282621-64282622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531358620	chr8:64282624-64282625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577386957	chr8:64282776-64282777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs574105820	chr8:64286256-64286257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs376448994	chr8:64286306-64286307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114817975	chr8:64286357-64286358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533458118	chr8:64286373-64286374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs115659464	chr8:64286428-64286429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560320019	chr8:64286516-64286517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs7841909	chr8:64286567-64286568	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs73262764	chr8:64294604-64294605	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs575605466	chr8:64294679-64294680	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs569833712	chr8:64294700-64294701	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs370092645	chr8:64294701-64294702	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs538276606	chr8:64294704-64294705	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs556132138	chr8:64294735-64294736	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs571257265	chr8:64294741-64294742	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs550065351	chr8:64294746-64294747	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs7464324	chr8:64294773-64294774	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs553818622	chr8:64294778-64294779	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs572624897	chr8:64294795-64294796	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs191940606	chr8:64294802-64294803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs143661324	chr8:64294824-64294825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576655486	chr8:64294825-64294826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543451746	chr8:64294859-64294860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564877397	chr8:64294867-64294868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532110425	chr8:64294879-64294880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs541149417	chr8:64295013-64295014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs374542788	chr8:64295017-64295018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559467009	chr8:64295037-64295038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529932655	chr8:64295068-64295069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs146819939	chr8:64295070-64295071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs569979443	chr8:64295163-64295164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530714920	chr8:64295180-64295181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	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
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
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
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
Colorectal cancer	21645411	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:175 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:64281000-64282200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:64281400-64282200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr8:64281400-64282800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr8:64281600-64282400	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr8:64281600-64282400	Enhancers	Brain Germinal Matrix	brain
6	chr8:64281600-64282800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:64281800-64282600	Enhancers	H9 Cell Line	embryonic stem cell
8	chr8:64281800-64282600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr8:64281800-64282800	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr8:64282200-64282400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr8:64282400-64282800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr8:64282600-64282800	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr8:64286200-64286600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr8:64294600-64294800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr8:64294800-64295600	Enhancers	Brain Germinal Matrix	brain
16	chr8:64294800-64300600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr8:64295600-64304000	Weak transcription	Brain Germinal Matrix	brain
18	chr8:64302200-64302800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr8:64302200-64302800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr8:64302200-64303000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr8:64302200-64303000	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr8:64302200-64303400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr8:64302400-64303000	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr8:64302400-64303600	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr8:64302600-64303000	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr8:64302800-64303600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr8:64302800-64304000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr8:64303000-64303600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr8:64303000-64303800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr8:64303000-64304000	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr8:64303000-64308800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr8:64303400-64304000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr8:64303600-64304000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr8:64303600-64304000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr8:64303600-64304800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr8:64303800-64304000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr8:64303800-64304000	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr8:64303800-64304000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr8:64303800-64304000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr8:64303800-64304000	Enhancers	Adipose Nuclei	Adipose
41	chr8:64303800-64304000	Enhancers	Brain Cingulate Gyrus	brain
42	chr8:64303800-64304000	Enhancers	Dnd41	blood
43	chr8:64303800-64304400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr8:64303800-64304800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr8:64304000-64304200	Active TSS	Primary monocytes fromperipheralblood	blood
46	chr8:64304000-64304200	Enhancers	Primary B cells from peripheral blood	blood
47	chr8:64304000-64304200	Active TSS	Primary T cells fromperipheralblood	blood
48	chr8:64304000-64304200	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr8:64304000-64304200	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr8:64304000-64304200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood

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