Variant report

Variant	nsv831283
Chromosome Location	chr8:34501243-34662634
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:394)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:394 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:34635478-34635568	K562	blood:	n/a	n/a
2	BACH1	chr8:34593814-34593967	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr8:34535698-34535742	A549	lung:	n/a	chr8:34535722-34535733 chr8:34535722-34535733 chr8:34535723-34535734 chr8:34535722-34535735 chr8:34535722-34535735
4	CEBPB	chr8:34592816-34593113	IMR90	lung:	n/a	chr8:34592925-34592936
5	CEBPB	chr8:34592826-34593009	K562	blood:	n/a	chr8:34592925-34592936
6	CEBPB	chr8:34594156-34594356	A549	lung:	n/a	chr8:34594208-34594219
7	CEBPB	chr8:34510956-34511207	A549	lung:	n/a	chr8:34511058-34511069
8	CEBPB	chr8:34627420-34627515	A549	lung:	n/a	n/a
9	CEBPB	chr8:34503111-34503453	IMR90	lung:	n/a	chr8:34503367-34503378 chr8:34503292-34503303 chr8:34503292-34503305
10	CEBPB	chr8:34510922-34511229	HepG2	liver:	n/a	chr8:34511058-34511069
11	CEBPB	chr8:34510902-34511233	IMR90	lung:	n/a	chr8:34511058-34511069
12	CEBPB	chr8:34535630-34535855	HepG2	liver:	n/a	chr8:34535722-34535733 chr8:34535722-34535733 chr8:34535723-34535734 chr8:34535722-34535735 chr8:34535722-34535735
13	CEBPB	chr8:34633426-34633445	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr8:34539280-34539549	HepG2	liver:	n/a	chr8:34539352-34539363 chr8:34539467-34539480
15	CEBPB	chr8:34594096-34594341	HepG2	liver:	n/a	chr8:34594208-34594219
16	CEBPB	chr8:34503146-34503472	HepG2	liver:	n/a	chr8:34503367-34503378 chr8:34503292-34503303 chr8:34503292-34503305
17	CEBPB	chr8:34592773-34593081	HepG2	liver:	n/a	chr8:34592925-34592936
18	CEBPB	chr8:34510949-34511191	H1-hESC	embryonic stem cell:	n/a	chr8:34511058-34511069
19	CEBPB	chr8:34638946-34639265	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr8:34535848-34535854	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr8:34541700-34541850	BJ	skin:	n/a	n/a
22	CTCF	chr8:34586080-34586230	HEEpiC	esophagus:	n/a	n/a
23	CTCF	chr8:34541740-34541890	GM12878	blood:	n/a	n/a
24	CTCF	chr8:34541789-34541878	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr8:34627780-34627930	HPAF	blood vessel:	n/a	n/a
26	CTCF	chr8:34541780-34541930	HMEC	breast:	n/a	n/a
27	CTCF	chr8:34627720-34627870	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr8:34541813-34541857	GM10266	blood:	n/a	n/a
29	CTCF	chr8:34541760-34541910	RPTEC	kidney:	n/a	n/a
30	CTCF	chr8:34541718-34541943	LNCaP	prostate:	n/a	n/a
31	CTCF	chr8:34544523-34544556	GM10248	blood:	n/a	n/a
32	CTCF	chr8:34586140-34586290	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr8:34541507-34541581	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr8:34627780-34627930	HAc	cerebellar:	n/a	n/a
35	CTCF	chr8:34541700-34541850	GM12873	blood:	n/a	n/a
36	CTCF	chr8:34541800-34541950	NHEK	skin:	n/a	n/a
37	CTCF	chr8:34541740-34541890	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr8:34586060-34586210	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr8:34586040-34586190	HRE	kidney:	n/a	n/a
40	CTCF	chr8:34541740-34541890	NB4	blood:	n/a	n/a
41	CTCF	chr8:34541762-34541919	Gliobla	brain:	n/a	n/a
42	CTCF	chr8:34541600-34541750	GM12866	blood:	n/a	n/a
43	CTCF	chr8:34541800-34541950	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr8:34627752-34627879	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr8:34541760-34541910	A549	lung:	n/a	n/a
46	CTCF	chr8:34656538-34656621	GM10248	blood:	n/a	n/a
47	CTCF	chr8:34541760-34541910	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr8:34541780-34541930	GM12875	blood:	n/a	n/a
49	CTCF	chr8:34593641-34593709	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr8:34541740-34541890	Caco-2	colon:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:34533034-34533084	HCF	heart:	n/a
2	chr8:34533034-34533084	HRE	kidney:	n/a
3	chr8:34533034-34533084	SK-N-SH_RA	brain:	n/a
4	chr8:34533034-34533084	SK-N-MC	brain:	n/a
5	chr8:34533034-34533084	HNPCEpiC	eye:	n/a
6	chr8:34533034-34533084	HCT-116	colon:	n/a
7	chr8:34533034-34533084	AG04450	lung:	fetal
8	chr8:34533034-34533084	NB4	blood:	n/a
9	chr8:34533034-34533084	AG04449	skin:	fetal
10	chr8:34533034-34533084	NHBE	bronchial:	n/a
11	chr8:34533034-34533084	GM06990	blood:	n/a
12	chr8:34533034-34533084	AG09309	skin:	n/a
13	chr8:34533034-34533084	PFSK-1	brain:	n/a
14	chr8:34533034-34533084	ovcar-3	ovarian:	n/a
15	chr8:34533034-34533084	ProgFib	skin:	n/a
16	chr8:34533034-34533084	T-47D	breast:	n/a
17	chr8:34533034-34533084	HEK293	kidney:	embryo
18	chr8:34533034-34533084	Hela-S3	cervix:	n/a
19	chr8:34533034-34533084	RPTEC	kidney:	n/a
20	chr8:34533034-34533084	A549	lung:	n/a
21	chr8:34533034-34533084	BJ	skin:	n/a
22	chr8:34533034-34533084	GM12891	blood:	n/a
23	chr8:34533034-34533084	MCF-7	breast:	n/a
24	chr8:34533034-34533084	GM19239	blood:	n/a
25	chr8:34533034-34533084	AG09319	gingival:	n/a
26	chr8:34533034-34533084	GM12878	blood:	n/a
27	chr8:34533034-34533084	ECC-1	luminal epithelium:	n/a
28	chr8:34533034-34533084	Jurkat	blood:	n/a
29	chr8:34533034-34533084	NT2-D1	testis:	n/a
30	chr8:34533034-34533084	HAEpiC	amniotic membrane:	n/a
31	chr8:34533034-34533084	BE2_C	brain:	n/a
32	chr8:34533034-34533084	HepG2	liver:	n/a
33	chr8:34533034-34533084	PrEC	prostate:	n/a
34	chr8:34533034-34533084	HCPEpiC	choroid plexus:	n/a
35	chr8:34533034-34533084	IMR90	lung:	fetal
36	chr8:34533034-34533084	GM12892	blood:	n/a
37	chr8:34533034-34533084	U87	brain:	n/a
38	chr8:34533034-34533084	H1-hESC	embryonic stem cell:	embryo
39	chr8:34533034-34533084	NH-A	brain:	n/a
40	chr8:34533034-34533084	HPAEpiC	pulmonary alveolar:	n/a
41	chr8:34533034-34533084	CMK	blood:	n/a
42	chr8:34533034-34533084	SAEC	small airway:	n/a
43	chr8:34533034-34533084	HUVEC	blood vessel:	n/a
44	chr8:34533034-34533084	HL-60	blood:	n/a
45	chr8:34533034-34533084	K562	blood:	n/a
46	chr8:34533034-34533084	PANC-1	pancreas:	n/a
47	chr8:34533034-34533084	MCF10A-Er-Src	breast:	n/a
48	chr8:34533034-34533084	SKMC	muscle:	n/a
49	chr8:34533034-34533084	LNCaP	prostate:	n/a
50	chr8:34533034-34533084	Caco-2	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:34623416..34626015-chr8:34627513..34629810,2	K562	blood:
2	chr8:34623416..34626015-chr8:34627513..34629810,2	K562	blood:
3	chr8:34606757..34608580-chr8:34608809..34610409,2	K562	blood:
4	chr8:34621951..34624916-chr8:34628310..34630031,2	K562	blood:
5	chr8:34631157..34633123-chr8:34636753..34638642,2	K562	blood:
6	chr8:34621951..34624916-chr8:34628310..34630031,2	K562	blood:
7	chr8:34606757..34608580-chr8:34608809..34610409,2	K562	blood:
8	chr8:34631157..34633123-chr8:34636753..34638642,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC5D-3	chr8:34650275-34650462	NONHSAT125996
2	lnc-UNC5D-3	chr8:34642569-34642589	NONHSAT125996
3	lnc-UNC5D-3	chr8:34642570-34642589	XLOC_006770
4	lnc-UNC5D-7	chr8:34537870-34538122	NONHSAT125994
5	lnc-UNC5D-3	chr8:34650276-34650462	XLOC_006770
6	lnc-UNC5D-7	chr8:34540946-34541081	NONHSAT125994

No data

Variant related genes	Relation type
ENSG00000254344	TF binding region
ENSG00000254344	CpG island

Extended variants
information (count: 2102 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:2102 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368202940	chr8:34501245-34501246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs78383814	chr8:34501299-34501300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572943277	chr8:34501311-34501312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142405892	chr8:34501335-34501336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189692791	chr8:34501362-34501363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574171474	chr8:34501416-34501417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182316459	chr8:34501433-34501434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs575098111	chr8:34501500-34501501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs4342589	chr8:34501546-34501547	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs533658113	chr8:34501566-34501567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551845386	chr8:34501609-34501610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565297700	chr8:34501628-34501629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs79544950	chr8:34501652-34501653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188754782	chr8:34501671-34501672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs193292055	chr8:34501672-34501673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549226873	chr8:34501709-34501710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs567721952	chr8:34501719-34501720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535273398	chr8:34501741-34501742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs145933484	chr8:34501763-34501764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs375174466	chr8:34501782-34501783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185097586	chr8:34501806-34501807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs138778254	chr8:34501872-34501873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs561860941	chr8:34501897-34501898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs74820604	chr8:34501899-34501900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188760629	chr8:34501947-34501948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs141872496	chr8:34501953-34501954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550799879	chr8:34502004-34502005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200258229	chr8:34502041-34502042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192182859	chr8:34502043-34502044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368721655	chr8:34502102-34502103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541443702	chr8:34502127-34502128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544856905	chr8:34502200-34502201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556791775	chr8:34502256-34502257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376650360	chr8:34502279-34502280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs578256866	chr8:34502322-34502323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs80022475	chr8:34502350-34502351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527707832	chr8:34502439-34502440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs4463416	chr8:34502571-34502572	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs552101243	chr8:34502588-34502589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548066197	chr8:34502596-34502597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561236634	chr8:34502703-34502704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531682901	chr8:34502724-34502725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550411252	chr8:34502761-34502762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566400646	chr8:34502805-34502806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568692325	chr8:34502824-34502825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533093620	chr8:34502970-34502971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs144575398	chr8:34503006-34503007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566711094	chr8:34503028-34503029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs79063780	chr8:34503087-34503088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs148457111	chr8:34503093-34503094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	21806811	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	20459607	CNVD
Renal cell carcinoma	18765545	CNVD
Colorectal cancer	16912164	CNVD
Neuroticism	17667963	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	18382360	CNVD
Ductal carcinoma	18381933	CNVD
Breast cancer	21328542	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Intellectual disability	22045946	CNVD
Lung cancer	17925434	CNVD
Uveal melanoma	20484589	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34500800-34501400	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr8:34501200-34502000	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr8:34501200-34503200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:34503200-34503400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:34503600-34504400	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr8:34503800-34504400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr8:34503800-34504400	Enhancers	Brain Hippocampus Middle	brain
8	chr8:34504000-34504800	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr8:34521000-34521800	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr8:34521200-34521800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr8:34521800-34522400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr8:34522400-34522800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr8:34522600-34523000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr8:34522600-34523400	Enhancers	Fetal Kidney	kidney
15	chr8:34522600-34524600	Enhancers	HUVEC	blood vessel
16	chr8:34523000-34524400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr8:34523400-34524400	Weak transcription	Fetal Kidney	kidney
18	chr8:34524000-34524800	Enhancers	Brain Anterior Caudate	brain
19	chr8:34524400-34524600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr8:34524400-34524600	Enhancers	Fetal Kidney	kidney
21	chr8:34524600-34524800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr8:34528600-34531000	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr8:34531600-34533000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr8:34532400-34533000	Enhancers	H9 Cell Line	embryonic stem cell
25	chr8:34532600-34533200	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr8:34536000-34536600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr8:34547800-34548600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr8:34548600-34553400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr8:34549600-34550000	Enhancers	Fetal Brain Male	brain
30	chr8:34549600-34550000	Enhancers	Fetal Brain Female	brain
31	chr8:34553400-34553800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr8:34571000-34576800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr8:34571800-34572600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
34	chr8:34603400-34603800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr8:34606800-34607000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr8:34606800-34607200	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr8:34607000-34607200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr8:34607000-34607200	Enhancers	Brain Germinal Matrix	brain
39	chr8:34607200-34609600	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr8:34607200-34609600	Weak transcription	Brain Germinal Matrix	brain
41	chr8:34607400-34610000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr8:34608800-34609400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr8:34609000-34610000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr8:34609200-34610000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr8:34609400-34610000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr8:34609400-34610000	Enhancers	Fetal Brain Female	brain
47	chr8:34609400-34610200	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr8:34609400-34611000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr8:34609400-34611800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr8:34609600-34609800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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