Variant report

Variant	nsv891202
Chromosome Location	chr8:95445660-95456986
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:464)
CpG islands
(count:122)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:464 , 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	chr8:95448362-95449296	HepG2	liver:	n/a	chr8:95449228-95449244
2	ARID3A	chr8:95447244-95447764	K562	blood:	n/a	n/a
3	ARID3A	chr8:95452765-95453180	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:95451921-95452167	K562	blood:	n/a	n/a
5	ARID3A	chr8:95447327-95447807	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:95451413-95451707	K562	blood:	n/a	n/a
7	ARID3A	chr8:95448302-95449929	K562	blood:	n/a	chr8:95449228-95449244 chr8:95449498-95449514
8	ATF1	chr8:95451522-95451812	K562	blood:	n/a	n/a
9	ATF1	chr8:95449032-95449740	K562	blood:	n/a	n/a
10	ATF2	chr8:95453145-95453482	GM12878	blood:	n/a	n/a
11	ATF2	chr8:95452534-95453556	GM12878	blood:	n/a	n/a
12	ATF2	chr8:95452576-95453135	GM12878	blood:	n/a	n/a
13	BACH1	chr8:95448992-95449005	K562	blood:	n/a	n/a
14	BATF	chr8:95453067-95453464	GM12878	blood:	n/a	n/a
15	BATF	chr8:95453147-95453458	GM12878	blood:	n/a	n/a
16	BATF	chr8:95452687-95453034	GM12878	blood:	n/a	n/a
17	BATF	chr8:95454975-95455234	GM12878	blood:	n/a	n/a
18	BCL11A	chr8:95452736-95453536	GM12878	blood:	n/a	n/a
19	BCLAF1	chr8:95452579-95453544	GM12878	blood:	n/a	n/a
20	BCLAF1	chr8:95452636-95453482	GM12878	blood:	n/a	n/a
21	BHLHE40	chr8:95449084-95449498	K562	blood:	n/a	n/a
22	BHLHE40	chr8:95452655-95453538	GM12878	blood:	n/a	n/a
23	BHLHE40	chr8:95453865-95454268	GM12878	blood:	n/a	n/a
24	CCNT2	chr8:95446305-95446437	K562	blood:	n/a	n/a
25	CEBPB	chr8:95454953-95455254	A549	lung:	n/a	chr8:95455092-95455103
26	CEBPB	chr8:95449154-95449752	K562	blood:	n/a	n/a
27	CEBPB	chr8:95452555-95453671	GM12878	blood:	n/a	n/a
28	CEBPB	chr8:95455026-95455166	HepG2	liver:	n/a	chr8:95455092-95455103
29	CEBPD	chr8:95451813-95452310	K562	blood:	n/a	n/a
30	CHD1	chr8:95448542-95449483	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD1	chr8:95447360-95448171	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr8:95452657-95454151	GM12878	blood:	n/a	n/a
33	CHD1	chr8:95447421-95448091	GM12878	blood:	n/a	n/a
34	CHD1	chr8:95448841-95449650	GM12878	blood:	n/a	n/a
35	CHD2	chr8:95452740-95454065	GM12878	blood:	n/a	n/a
36	CHD2	chr8:95448377-95449015	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr8:95448598-95448728	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr8:95448560-95448710	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr8:95448560-95448710	HAc	cerebellar:	n/a	n/a
40	CTCF	chr8:95448520-95448670	AG04449	skin:	n/a	n/a
41	CTCF	chr8:95448540-95448690	GM12878	blood:	n/a	n/a
42	CTCF	chr8:95448580-95448730	HMF	breast:	n/a	n/a
43	CTCF	chr8:95448598-95448730	Medullo	brain:	n/a	n/a
44	CTCF	chr8:95448560-95448710	BJ	skin:	n/a	n/a
45	CTCF	chr8:95448620-95448770	SAEC	small airway:	n/a	n/a
46	CTCF	chr8:95448535-95448756	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr8:95448560-95448710	HRE	kidney:	n/a	n/a
48	CTCF	chr8:95448620-95448770	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr8:95448620-95448770	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr8:95449120-95449270	RPTEC	kidney:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:95448685-95448735	HCPEpiC	choroid plexus:	n/a
2	chr8:95448685-95448735	U87	brain:	n/a
3	chr8:95449946-95449996	SKMC	muscle:	n/a
4	chr8:95449946-95449996	Caco-2	colon:	n/a
5	chr8:95449946-95449996	SAEC	small airway:	n/a
6	chr8:95448685-95448735	HCT-116	colon:	n/a
7	chr8:95449946-95449996	HIPEpiC	eye:	n/a
8	chr8:95448685-95448735	NH-A	brain:	n/a
9	chr8:95448685-95448735	GM12892	blood:	n/a
10	chr8:95449946-95449996	T-47D	breast:	n/a
11	chr8:95449946-95449996	HCF	heart:	n/a
12	chr8:95449946-95449996	NHBE	bronchial:	n/a
13	chr8:95449946-95449996	HCPEpiC	choroid plexus:	n/a
14	chr8:95448685-95448735	PrEC	prostate:	n/a
15	chr8:95448685-95448735	GM06990	blood:	n/a
16	chr8:95448685-95448735	NHBE	bronchial:	n/a
17	chr8:95449946-95449996	IMR90	lung:	fetal
18	chr8:95448685-95448735	HRE	kidney:	n/a
19	chr8:95448685-95448735	ProgFib	skin:	n/a
20	chr8:95449946-95449996	GM06990	blood:	n/a
21	chr8:95449946-95449996	ECC-1	luminal epithelium:	n/a
22	chr8:95449946-95449996	HCT-116	colon:	n/a
23	chr8:95449946-95449996	AG04450	lung:	fetal
24	chr8:95448685-95448735	ECC-1	luminal epithelium:	n/a
25	chr8:95449946-95449996	NT2-D1	testis:	n/a
26	chr8:95449946-95449996	U87	brain:	n/a
27	chr8:95448685-95448735	Caco-2	colon:	n/a
28	chr8:95449946-95449996	ProgFib	skin:	n/a
29	chr8:95449946-95449996	AoSMC	blood vessel:	n/a
30	chr8:95448685-95448735	HMEC	breast:	n/a
31	chr8:95449946-95449996	GM12892	blood:	n/a
32	chr8:95448685-95448735	MCF10A-Er-Src	breast:	n/a
33	chr8:95449946-95449996	HEEpiC	esophagus:	n/a
34	chr8:95448685-95448735	HUVEC	blood vessel:	n/a
35	chr8:95448685-95448735	NB4	blood:	n/a
36	chr8:95449946-95449996	HepG2	liver:	n/a
37	chr8:95448685-95448735	T-47D	breast:	n/a
38	chr8:95449946-95449996	PrEC	prostate:	n/a
39	chr8:95448685-95448735	LNCaP	prostate:	n/a
40	chr8:95448685-95448735	HCF	heart:	n/a
41	chr8:95448685-95448735	Hepatocyte	liver:	n/a
42	chr8:95448685-95448735	HCM	heart:	n/a
43	chr8:95448685-95448735	AG04449	skin:	fetal
44	chr8:95448685-95448735	NT2-D1	testis:	n/a
45	chr8:95448685-95448735	A549	lung:	n/a
46	chr8:95448685-95448735	HEK293	kidney:	embryo
47	chr8:95448685-95448735	PANC-1	pancreas:	n/a
48	chr8:95448685-95448735	HPAEpiC	pulmonary alveolar:	n/a
49	chr8:95449946-95449996	CMK	blood:	n/a
50	chr8:95448685-95448735	H1-hESC	embryonic stem cell:	embryo

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:95451952..95453657-chr8:95456672..95458632,2	MCF-7	breast:
2	chr8:95447010..95451504-chr8:95455439..95460158,7	MCF-7	breast:
3	chr8:95448469..95450952-chr8:95730677..95732921,2	K562	blood:
4	chr8:95449237..95450737-chr8:95564769..95566376,2	K562	blood:
5	chr8:95449447..95452097-chr8:95455615..95457152,2	K562	blood:
6	chr8:95434502..95438276-chr8:95441146..95446197,5	K562	blood:
7	chr8:95447931..95449885-chr8:95451720..95455035,3	K562	blood:
8	chr8:95446159..95448906-chr8:95449268..95451697,2	K562	blood:
9	chr8:95455164..95456684-chr8:95467591..95470115,2	MCF-7	breast:
10	chr8:95449447..95452097-chr8:95455615..95457152,2	K562	blood:
11	chr8:95426007..95427555-chr8:95444022..95446517,2	MCF-7	breast:
12	chr8:95448512..95450630-chr8:95487309..95488900,2	K562	blood:
13	chr8:95437761..95439579-chr8:95445352..95447331,2	MCF-7	breast:
14	chr8:95451952..95453657-chr8:95456672..95458632,2	MCF-7	breast:
15	chr8:95446159..95448906-chr8:95449268..95451697,2	K562	blood:
16	chr8:95447931..95449655-chr8:95451874..95454373,2	K562	blood:

No data

Variant related genes	Relation type
FSBP	TF binding region
FSBP	CpG island
ENSG00000164944	chromatin interactions
ENSG00000253704	chromatin interactions
ENSG00000197275	chromatin interactions
ENSG00000265817	chromatin interactions
ENSG00000156162	chromatin interactions

Extended variants
information (count: 391 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3136428	chr8:95445660-95445661	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs573631312	chr8:95445787-95445788	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs535089069	chr8:95445836-95445837	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs531433369	chr8:95445848-95445849	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs191187671	chr8:95445875-95445876	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs142392716	chr8:95445886-95445887	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs544523361	chr8:95445892-95445893	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs542378260	chr8:95445904-95445905	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs3136417	chr8:95445908-95445909	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs577807994	chr8:95445917-95445918	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs540366710	chr8:95445920-95445921	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs3136427	chr8:95445930-95445931	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs369744426	chr8:95445937-95445938	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs531570616	chr8:95445994-95445995	Weak transcription Strong transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs373167090	chr8:95446147-95446148	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs180892612	chr8:95446162-95446163	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs145810120	chr8:95446224-95446225	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs77045500	chr8:95446271-95446272	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs527676471	chr8:95446360-95446361	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187178017	chr8:95446417-95446418	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192024801	chr8:95446463-95446464	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs3019154	chr8:95446508-95446509	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs565329153	chr8:95446545-95446546	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs3019278	chr8:95446567-95446568	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs3136414	chr8:95446633-95446634	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs3136413	chr8:95446635-95446636	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs143808824	chr8:95446665-95446666	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs548546076	chr8:95446702-95446703	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568547048	chr8:95446742-95446743	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs537740494	chr8:95446759-95446760	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558077958	chr8:95446779-95446780	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182901090	chr8:95446798-95446799	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs143051264	chr8:95446892-95446893	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs3136412	chr8:95446895-95446896	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs201936625	chr8:95446898-95446899	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs534002514	chr8:95446925-95446926	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368265368	chr8:95446984-95446985	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs3136411	chr8:95446998-95446999	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs187621721	chr8:95447000-95447001	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574203743	chr8:95447031-95447032	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs117519512	chr8:95447055-95447056	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs3136410	chr8:95447088-95447089	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs2930963	chr8:95447120-95447121	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs576425775	chr8:95447214-95447215	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545377291	chr8:95447260-95447261	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs3136409	chr8:95447262-95447263	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs3136408	chr8:95447282-95447283	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs547603806	chr8:95447317-95447318	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs3136407	chr8:95447381-95447382	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs138540568	chr8:95447388-95447389	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

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
Acute lymphoblastic leukemia	18458336	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
Epilepsy	20502679	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	17847001	CNVD
Neuropsychiatric disorder	20069037	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17142309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:727 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95393200-95447000	Weak transcription	K562	blood
2	chr8:95412200-95447200	Weak transcription	Fetal Thymus	thymus
3	chr8:95429600-95446200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr8:95430400-95447200	Weak transcription	Fetal Intestine Small	intestine
5	chr8:95430600-95446400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr8:95430600-95447000	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr8:95430600-95447400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr8:95430800-95446400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr8:95431000-95446800	Weak transcription	HMEC	breast
10	chr8:95431000-95447400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr8:95431000-95447400	Weak transcription	HSMM	muscle
12	chr8:95431000-95447400	Weak transcription	NHDF-Ad	bronchial
13	chr8:95431000-95448600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr8:95431000-95448600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr8:95432400-95478600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:95433600-95446400	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr8:95433800-95447200	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr8:95434000-95447400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr8:95438200-95447600	Weak transcription	Primary hematopoietic stem cells	blood
20	chr8:95441400-95446400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr8:95441400-95446400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr8:95441400-95446400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr8:95441800-95446400	Weak transcription	Brain Germinal Matrix	brain
24	chr8:95441800-95448600	Weak transcription	Hela-S3	cervix
25	chr8:95442000-95447600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr8:95442200-95447200	Weak transcription	Right Ventricle	heart
27	chr8:95442200-95447200	Weak transcription	HUVEC	blood vessel
28	chr8:95442400-95447200	Weak transcription	Fetal Kidney	kidney
29	chr8:95442600-95465400	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr8:95443200-95446000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr8:95443200-95446400	Weak transcription	Fetal Lung	lung
32	chr8:95443200-95447200	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr8:95443200-95447200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr8:95443400-95446000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr8:95443600-95446400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr8:95443600-95446600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr8:95443800-95446400	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr8:95444000-95447200	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr8:95444000-95447200	Weak transcription	NH-A	brain
40	chr8:95444000-95447400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr8:95444000-95447400	Weak transcription	NHEK	skin
42	chr8:95444000-95448800	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr8:95444200-95446600	Weak transcription	Brain Anterior Caudate	brain
44	chr8:95444400-95447200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr8:95444600-95447200	Weak transcription	Adipose Nuclei	Adipose
46	chr8:95444600-95447200	Weak transcription	Ovary	ovary
47	chr8:95444800-95449600	Active TSS	GM12878-XiMat	blood
48	chr8:95445000-95445800	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr8:95445000-95446200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr8:95445000-95446600	Weak transcription	Primary T cells from cord blood	blood

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