Variant report

Variant	nsv831331
Chromosome Location	chr8:60770382-60959633
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:760)
CpG islands
(count:183)
Chromatin interactive
region (count:21)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:760 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:60774816-60774965	K562	blood:	n/a	n/a
2	ATF2	chr8:60881172-60882020	GM12878	blood:	n/a	n/a
3	ATF2	chr8:60881187-60881985	GM12878	blood:	n/a	n/a
4	ATF2	chr8:60938834-60939465	GM12878	blood:	n/a	n/a
5	ATF2	chr8:60910897-60911483	GM12878	blood:	n/a	n/a
6	ATF2	chr8:60910949-60911402	GM12878	blood:	n/a	n/a
7	ATF2	chr8:60875802-60876553	GM12878	blood:	n/a	chr8:60875998-60876005
8	ATF2	chr8:60938575-60939406	GM12878	blood:	n/a	n/a
9	ATF2	chr8:60872845-60873437	GM12878	blood:	n/a	n/a
10	ATF2	chr8:60872935-60873372	GM12878	blood:	n/a	n/a
11	BATF	chr8:60832775-60832932	GM12878	blood:	n/a	chr8:60832859-60832870
12	BATF	chr8:60939045-60939360	GM12878	blood:	n/a	n/a
13	BATF	chr8:60885198-60885473	GM12878	blood:	n/a	n/a
14	BATF	chr8:60881374-60881844	GM12878	blood:	n/a	n/a
15	BATF	chr8:60873030-60873306	GM12878	blood:	n/a	n/a
16	BATF	chr8:60882612-60882882	GM12878	blood:	n/a	n/a
17	BATF	chr8:60910996-60911354	GM12878	blood:	n/a	n/a
18	BATF	chr8:60881355-60881813	GM12878	blood:	n/a	n/a
19	BATF	chr8:60882522-60882874	GM12878	blood:	n/a	n/a
20	BATF	chr8:60910951-60911405	GM12878	blood:	n/a	n/a
21	BATF	chr8:60939071-60939303	GM12878	blood:	n/a	n/a
22	BCL11A	chr8:60881418-60881810	GM12878	blood:	n/a	n/a
23	BCL11A	chr8:60938913-60939384	GM12878	blood:	n/a	chr8:60939166-60939175
24	BCL11A	chr8:60881286-60881827	GM12878	blood:	n/a	n/a
25	BCL11A	chr8:60882522-60882924	GM12878	blood:	n/a	n/a
26	BCL11A	chr8:60872992-60873372	GM12878	blood:	n/a	chr8:60873222-60873231
27	BCL11A	chr8:60875887-60876234	GM12878	blood:	n/a	n/a
28	BCL11A	chr8:60911017-60911346	GM12878	blood:	n/a	n/a
29	BCL3	chr8:60911004-60911430	GM12878	blood:	n/a	n/a
30	BCL3	chr8:60881371-60881769	GM12878	blood:	n/a	n/a
31	BCL3	chr8:60881278-60881859	GM12878	blood:	n/a	n/a
32	BCL3	chr8:60911142-60911443	GM12878	blood:	n/a	n/a
33	BCLAF1	chr8:60938946-60939457	GM12878	blood:	n/a	chr8:60939166-60939175
34	BCLAF1	chr8:60881252-60882012	GM12878	blood:	n/a	chr8:60881993-60882002
35	BCLAF1	chr8:60872906-60873436	GM12878	blood:	n/a	chr8:60873222-60873231
36	BCLAF1	chr8:60881385-60881881	GM12878	blood:	n/a	n/a
37	BHLHE40	chr8:60881360-60881873	GM12878	blood:	n/a	n/a
38	BHLHE40	chr8:60832767-60832901	GM12878	blood:	n/a	n/a
39	BHLHE40	chr8:60834373-60834433	GM12878	blood:	n/a	n/a
40	CEBPB	chr8:60825365-60825644	H1-hESC	embryonic stem cell:	n/a	chr8:60825546-60825557
41	CEBPB	chr8:60813374-60813485	A549	lung:	n/a	n/a
42	CEBPB	chr8:60926444-60926564	HepG2	liver:	n/a	chr8:60926474-60926485
43	CEBPB	chr8:60802987-60803059	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr8:60825405-60825712	HepG2	liver:	n/a	chr8:60825546-60825557
45	CEBPB	chr8:60806551-60806779	HepG2	liver:	n/a	n/a
46	CEBPB	chr8:60881201-60882003	GM12878	blood:	n/a	n/a
47	CEBPB	chr8:60825358-60825611	A549	lung:	n/a	chr8:60825546-60825557
48	CEBPB	chr8:60881429-60881752	GM12878	blood:	n/a	n/a
49	CEBPB	chr8:60872876-60873481	GM12878	blood:	n/a	n/a
50	CEBPB	chr8:60825419-60825717	K562	blood:	n/a	chr8:60825546-60825557

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:60844458-60844508	T-47D	breast:	n/a
2	chr8:60788116-60788166	BE2_C	brain:	n/a
3	chr8:60844458-60844508	A549	lung:	n/a
4	chr8:60834013-60834063	HIPEpiC	eye:	n/a
5	chr8:60788116-60788166	NHDF-neo	bronchial:	n/a
6	chr8:60844458-60844508	HUVEC	blood vessel:	n/a
7	chr8:60788116-60788166	H1-hESC	embryonic stem cell:	embryo
8	chr8:60844458-60844508	PrEC	prostate:	n/a
9	chr8:60788116-60788166	Hepatocyte	liver:	n/a
10	chr8:60844458-60844508	ovcar-3	ovarian:	n/a
11	chr8:60844458-60844508	ProgFib	skin:	n/a
12	chr8:60844458-60844508	NT2-D1	testis:	n/a
13	chr8:60834013-60834063	ProgFib	skin:	n/a
14	chr8:60788116-60788166	GM19239	blood:	n/a
15	chr8:60788116-60788166	A549	lung:	n/a
16	chr8:60834013-60834063	HepG2	liver:	n/a
17	chr8:60834013-60834063	GM19239	blood:	n/a
18	chr8:60844458-60844508	GM12878	blood:	n/a
19	chr8:60788116-60788166	K562	blood:	n/a
20	chr8:60788116-60788166	LNCaP	prostate:	n/a
21	chr8:60834013-60834063	NHDF-neo	bronchial:	n/a
22	chr8:60834013-60834063	HCPEpiC	choroid plexus:	n/a
23	chr8:60788116-60788166	CMK	blood:	n/a
24	chr8:60788116-60788166	NT2-D1	testis:	n/a
25	chr8:60834013-60834063	U87	brain:	n/a
26	chr8:60788116-60788166	HPAEpiC	pulmonary alveolar:	n/a
27	chr8:60844458-60844508	SKMC	muscle:	n/a
28	chr8:60844458-60844508	AG09319	gingival:	n/a
29	chr8:60834013-60834063	MCF-7	breast:	n/a
30	chr8:60834013-60834063	MCF10A-Er-Src	breast:	n/a
31	chr8:60834013-60834063	K562	blood:	n/a
32	chr8:60844458-60844508	HepG2	liver:	n/a
33	chr8:60834013-60834063	AG09309	skin:	n/a
34	chr8:60834013-60834063	AG09319	gingival:	n/a
35	chr8:60834013-60834063	NH-A	brain:	n/a
36	chr8:60788116-60788166	HCM	heart:	n/a
37	chr8:60844458-60844508	NH-A	brain:	n/a
38	chr8:60788116-60788166	SAEC	small airway:	n/a
39	chr8:60834013-60834063	PrEC	prostate:	n/a
40	chr8:60788116-60788166	HRCEpiC	kidney:	n/a
41	chr8:60834013-60834063	SAEC	small airway:	n/a
42	chr8:60844458-60844508	HMEC	breast:	n/a
43	chr8:60844458-60844508	PFSK-1	brain:	n/a
44	chr8:60834013-60834063	AG04449	skin:	fetal
45	chr8:60788116-60788166	HMEC	breast:	n/a
46	chr8:60834013-60834063	RPTEC	kidney:	n/a
47	chr8:60834013-60834063	HCM	heart:	n/a
48	chr8:60788116-60788166	Hela-S3	cervix:	n/a
49	chr8:60788116-60788166	HCT-116	colon:	n/a
50	chr8:60788116-60788166	AG04449	skin:	fetal

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:60955308..60958080-chr8:60958846..60961273,2	K562	blood:
2	chr8:60928178..60929748-chr8:60930851..60932873,2	K562	blood:
3	chr8:60127615..60128279-chr8:60833868..60834810,2	MCF-7	breast:
4	chr8:59720401..59721132-chr8:60833849..60834670,2	MCF-7	breast:
5	chr8:60773557..60775411-chr8:60775874..60778196,2	K562	blood:
6	chr8:59634286..59634829-chr8:60833735..60834731,2	MCF-7	breast:
7	chr8:60844306..60846738-chr8:60851041..60853636,2	K562	blood:
8	chr8:60955308..60958080-chr8:60958846..60961273,2	K562	blood:
9	chr8:60929909..60932479-chr8:60938404..60940502,2	K562	blood:
10	chr8:60773557..60775411-chr8:60775874..60778196,2	K562	blood:
11	chr8:60844306..60846738-chr8:60851041..60853636,2	K562	blood:
12	chr8:60928178..60929748-chr8:60930851..60932873,2	K562	blood:
13	chr8:60886348..60887855-chr8:60889671..60891351,2	K562	blood:
14	chr8:60886348..60887855-chr8:60889671..60891351,2	K562	blood:
15	chr5:12654971..12655664-chr8:60884734..60885526,2	MCF-7	breast:
16	chr8:60929909..60932479-chr8:60938404..60940502,2	K562	blood:
17	chr8:60740494..60743423-chr8:60825234..60828198,2	K562	blood:
18	chr8:59924451..59925349-chr8:60833829..60834732,3	MCF-7	breast:
19	chr8:60875870..60877485-chr8:60879560..60881950,2	K562	blood:
20	chr8:60909031..60911601-chr8:61562751..61565399,2	K562	blood:
21	chr8:60875870..60877485-chr8:60879560..60881950,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAB2A-1	chr8:60959352-60959496	XLOC_006814
2	lnc-RAB2A-1	chr8:60959326-60959496	NONHSAT126813
3	lnc-RAB2A-1	chr8:60959352-60959496	XLOC_006814

No data

Variant related genes	Relation type
ENSG00000254775	TF binding region
ENSG00000254775	CpG island
HNRNPA1	miRNA target sites

Extended variants
information (count: 3441 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:3441 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562152729	chr8:60775012-60775013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs10087623	chr8:60775038-60775039	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs137865488	chr8:60775054-60775055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141694803	chr8:60775056-60775057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183827598	chr8:60775122-60775123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs62509972	chr8:60775126-60775127	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs541995071	chr8:60775182-60775183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs372844042	chr8:60775186-60775187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs79748204	chr8:60775209-60775210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs574034696	chr8:60775233-60775234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs368524818	chr8:60775248-60775249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530627714	chr8:60775279-60775280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545937064	chr8:60775301-60775302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564245181	chr8:60775307-60775308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs150523888	chr8:60775333-60775334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs369852365	chr8:60775422-60775423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs546473944	chr8:60775525-60775526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs568142668	chr8:60775558-60775559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs372114539	chr8:60775593-60775594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs375196792	chr8:60775594-60775595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569292135	chr8:60775602-60775603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553065485	chr8:60775625-60775626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs62509973	chr8:60775627-60775628	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs74837921	chr8:60775689-60775690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs564730373	chr8:60775716-60775717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs7822560	chr8:60775727-60775728	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs75271775	chr8:60775740-60775741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556094285	chr8:60775771-60775772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574527844	chr8:60775823-60775824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372171054	chr8:60775832-60775833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376162724	chr8:60775850-60775851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556784109	chr8:60775852-60775853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374872339	chr8:60775883-60775884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567705271	chr8:60775889-60775890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575271103	chr8:60775900-60775901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186396012	chr8:60775903-60775904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563973752	chr8:60775905-60775906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs75121343	chr8:60775915-60775916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs74473982	chr8:60775920-60775921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs56203327	chr8:60775976-60775977	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs191157375	chr8:60775983-60775984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183479376	chr8:60775995-60775996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550903333	chr8:60776007-60776008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs80095852	chr8:60776027-60776028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533504933	chr8:60776031-60776032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs62509975	chr8:60776045-60776046	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs75559621	chr8:60776101-60776102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs139892150	chr8:60776105-60776106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186659756	chr8:60776161-60776162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs72659731	chr8:60776163-60776164	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:96)

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
Salivary gland tumor	18059337	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
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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16461572	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
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Colorectal cancer	21645411	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
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD

Chromatin state (count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:60775000-60775800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr8:60775800-60781600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr8:60781600-60781800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr8:60789200-60789600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr8:60789200-60789600	Enhancers	HMEC	breast
6	chr8:60801400-60802200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr8:60809400-60809800	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr8:60809400-60809800	Enhancers	Brain Germinal Matrix	brain
9	chr8:60809600-60810000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr8:60809800-60813200	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr8:60812000-60812600	Enhancers	Placenta	Placenta
12	chr8:60812200-60812400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:60813200-60813600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
14	chr8:60819600-60820000	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr8:60828200-60828400	Enhancers	Colon Smooth Muscle	Colon
16	chr8:60828200-60828400	Enhancers	Fetal Stomach	stomach
17	chr8:60828400-60828800	Enhancers	Stomach Smooth Muscle	stomach
18	chr8:60828400-60832200	Weak transcription	Colon Smooth Muscle	Colon
19	chr8:60828600-60834800	Weak transcription	Fetal Stomach	stomach
20	chr8:60828800-60834000	Weak transcription	Stomach Smooth Muscle	stomach
21	chr8:60829200-60830400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr8:60829800-60830200	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr8:60830000-60830200	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr8:60830000-60830400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr8:60830000-60831200	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr8:60830000-60834000	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr8:60830000-60834200	Enhancers	Primary B cells from peripheral blood	blood
28	chr8:60830200-60830400	Enhancers	GM12878-XiMat	blood
29	chr8:60830200-60833600	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr8:60830400-60831600	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr8:60830600-60831800	Weak transcription	GM12878-XiMat	blood
32	chr8:60830800-60831000	Enhancers	Rectal Smooth Muscle	rectum
33	chr8:60830800-60832600	Enhancers	Primary B cells from cord blood	blood
34	chr8:60831200-60833000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
35	chr8:60831400-60832000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
36	chr8:60831400-60833000	Enhancers	HUVEC	blood vessel
37	chr8:60831600-60832000	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr8:60831600-60833000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr8:60831600-60833600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr8:60831800-60833000	Enhancers	GM12878-XiMat	blood
41	chr8:60831800-60833000	Enhancers	NH-A	brain
42	chr8:60832200-60832800	Enhancers	Colon Smooth Muscle	Colon
43	chr8:60832400-60832600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr8:60832600-60832800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr8:60832600-60833000	Flanking Active TSS	Primary B cells from cord blood	blood
46	chr8:60832600-60833000	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr8:60832600-60833600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr8:60832800-60833000	Enhancers	NHDF-Ad	bronchial
49	chr8:60832800-60833000	Enhancers	Osteobl	bone
50	chr8:60832800-60834000	Weak transcription	Colon Smooth Muscle	Colon

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