Variant report

Variant	nsv518178
Chromosome Location	chr8:58328635-58542880
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1696)
CpG islands
(count:0)
Chromatin interactive
region (count:34)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1696 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:58476520-58477283	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:58462919-58463233	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:58492647-58493411	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:58499788-58500142	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:58500894-58501389	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:58333227-58333305	HepG2	liver:	n/a	n/a
7	ATF2	chr8:58492953-58493463	GM12878	blood:	n/a	n/a
8	ATF2	chr8:58333169-58333805	GM12878	blood:	n/a	n/a
9	ATF2	chr8:58390674-58391022	GM12878	blood:	n/a	n/a
10	BACH1	chr8:58347415-58347430	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr8:58428447-58428496	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr8:58354912-58354914	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr8:58379190-58379193	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr8:58390640-58391020	GM12878	blood:	n/a	n/a
15	BATF	chr8:58333475-58333713	GM12878	blood:	n/a	n/a
16	BATF	chr8:58493059-58493347	GM12878	blood:	n/a	chr8:58493204-58493215
17	BATF	chr8:58375688-58376050	GM12878	blood:	n/a	n/a
18	BATF	chr8:58390691-58391025	GM12878	blood:	n/a	n/a
19	BATF	chr8:58360119-58360363	GM12878	blood:	n/a	n/a
20	BATF	chr8:58375749-58376012	GM12878	blood:	n/a	n/a
21	BATF	chr8:58431541-58431841	GM12878	blood:	n/a	n/a
22	BCL11A	chr8:58431714-58432065	GM12878	blood:	n/a	chr8:58431723-58431732
23	BCL11A	chr8:58510285-58510560	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCL3	chr8:58476576-58477390	A549	lung:	n/a	n/a
25	BCLAF1	chr8:58333055-58333814	GM12878	blood:	n/a	n/a
26	BCLAF1	chr8:58333114-58333732	GM12878	blood:	n/a	n/a
27	BHLHE40	chr8:58333190-58333753	GM12878	blood:	n/a	n/a
28	BHLHE40	chr8:58431585-58431909	GM12878	blood:	n/a	n/a
29	BHLHE40	chr8:58500849-58501230	HepG2	liver:	n/a	n/a
30	CBX3	chr8:58510249-58510452	K562	blood:	n/a	n/a
31	CBX3	chr8:58510232-58510480	HCT-116	colon:	n/a	n/a
32	CEBPB	chr8:58476786-58477197	A549	lung:	n/a	n/a
33	CEBPB	chr8:58528378-58528615	A549	lung:	n/a	chr8:58528492-58528503
34	CEBPB	chr8:58365514-58365823	IMR90	lung:	n/a	chr8:58365647-58365658
35	CEBPB	chr8:58492944-58493340	HepG2	liver:	n/a	n/a
36	CEBPB	chr8:58500963-58501204	HepG2	liver:	n/a	n/a
37	CEBPB	chr8:58506299-58506568	HepG2	liver:	n/a	chr8:58506491-58506504 chr8:58506397-58506408
38	CEBPB	chr8:58518966-58519006	HepG2	liver:	n/a	n/a
39	CEBPB	chr8:58449571-58449863	MCF-7	breast:	n/a	n/a
40	CEBPB	chr8:58463011-58463359	HepG2	liver:	n/a	n/a
41	CEBPB	chr8:58476582-58477291	HepG2	liver:	n/a	n/a
42	CEBPB	chr8:58354024-58354259	A549	lung:	n/a	n/a
43	CEBPB	chr8:58500565-58500597	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr8:58361798-58362049	HepG2	liver:	n/a	chr8:58361892-58361903
45	CEBPB	chr8:58500390-58500522	A549	lung:	n/a	chr8:58500451-58500464
46	CEBPB	chr8:58494550-58494740	HepG2	liver:	n/a	chr8:58494697-58494708
47	CEBPB	chr8:58499731-58500732	MCF-7	breast:	n/a	chr8:58500451-58500464
48	CEBPB	chr8:58476753-58477143	HCT-116	colon:	n/a	n/a
49	CEBPB	chr8:58463015-58463318	MCF-7	breast:	n/a	n/a
50	CEBPB	chr8:58506312-58506591	A549	lung:	n/a	chr8:58506491-58506504 chr8:58506397-58506408

No data

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:58537334..58539259-chr8:58545738..58547653,2	K562	blood:
2	chr8:58334906..58335645-chr8:58403623..58404511,2	MCF-7	breast:
3	chr8:58458453..58461364-chr8:58462477..58464451,2	MCF-7	breast:
4	chr8:58332707..58333926-chr8:58403565..58404649,11	MCF-7	breast:
5	chr8:58404877..58405459-chr8:58487377..58488213,3	MCF-7	breast:
6	chr8:58332821..58333771-chr8:58403706..58404764,4	MCF-7	breast:
7	chr8:58489621..58490358-chr8:58651676..58652569,4	MCF-7	breast:
8	chr8:58489495..58490193-chr8:58651461..58652081,3	MCF-7	breast:
9	chr8:58332707..58333926-chr8:58403565..58404649,11	MCF-7	breast:
10	chr8:58460821..58463332-chr8:58465089..58467286,2	K562	blood:
11	chr8:58487590..58488096-chr8:59301318..59302266,2	MCF-7	breast:
12	chr8:58504798..58506738-chr8:58508959..58511696,2	MCF-7	breast:
13	chr8:58487549..58488499-chr8:59307870..59308447,3	MCF-7	breast:
14	chr8:58499798..58502598-chr8:59323213..59325065,2	MCF-7	breast:
15	chr8:58332657..58333329-chr8:58487609..58488171,2	MCF-7	breast:
16	chr8:58489931..58492018-chr8:58907170..58909246,2	MCF-7	breast:
17	chr8:58332553..58333478-chr8:59230571..59231163,3	K562	blood:
18	chr8:58334906..58335645-chr8:58403623..58404511,2	MCF-7	breast:
19	chr8:58487534..58488381-chr8:59156649..59157508,2	MCF-7	breast:
20	chr8:58332821..58333771-chr8:58403706..58404764,4	MCF-7	breast:
21	chr8:58460821..58463332-chr8:58465089..58467286,2	K562	blood:
22	chr8:58332657..58333329-chr8:58487609..58488171,2	MCF-7	breast:
23	chr8:58332845..58333756-chr8:59307075..59308444,4	K562	blood:
24	chr8:58504798..58506738-chr8:58508959..58511696,2	MCF-7	breast:
25	chr8:58458453..58461364-chr8:58462477..58464451,2	MCF-7	breast:
26	chr8:58489820..58490346-chr8:59307522..59308461,2	MCF-7	breast:
27	chr3:27395027..27395631-chr8:58500130..58500818,2	MCF-7	breast:
28	chr8:58487606..58488471-chr8:58651601..58652426,3	MCF-7	breast:
29	chr8:58462603..58464504-chr8:58491631..58493379,2	K562	blood:
30	chr8:58462603..58464504-chr8:58491631..58493379,2	K562	blood:
31	chr8:58512585..58515336-chr8:58516943..58518859,2	K562	blood:
32	chr8:58256197..58257142-chr8:58333343..58333895,2	MCF-7	breast:
33	chr8:58512585..58515336-chr8:58516943..58518859,2	K562	blood:
34	chr4:139291348..139291947-chr8:58507526..58508108,2	MCF-7	breast:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM110B-10	chr8:58421807-58422176	ucscGeneNc_uc003xth_2
2	lnc-FAM110B-11	chr8:58352607-58353048	l_3603_chr8:58348578-58353048_testes
3	lnc-FAM110B-4	chr8:58405443-58405534	ENSG00000253821
4	lnc-FAM110B-4	chr8:58375465-58375636	NONHSAT126755
5	lnc-FAM110B-4	chr8:58458028-58458502	ENSG00000253821
6	lnc-FAM110B-10	chr8:58420077-58420253	ucscGeneNc_uc003xth_2
7	lnc-FAM110B-4	chr8:58504039-58504118	ENSG00000253821
8	lnc-FAM110B-10	chr8:58427573-58427690	ucscGeneNc_uc003xth_2
9	lnc-FAM110B-4	chr8:58405426-58405506	NONHSAT126755
10	lnc-FAM110B-10	chr8:58432559-58432637	ucscGeneNc_uc003xth_2
11	lnc-FAM110B-4	chr8:58375466-58375636	XLOC_006808
12	lnc-FAM110B-4	chr8:58405402-58405534	NONHSAT126757
13	lnc-FAM110B-4	chr8:58405427-58405506	XLOC_006808
14	lnc-FAM110B-10	chr8:58418900-58419128	ucscGeneNc_uc003xth_2
15	lnc-FAM110B-10	chr8:58439655-58439967	ucscGeneNc_uc003xth_2
16	lnc-FAM110B-10	chr8:58423482-58423699	ucscGeneNc_uc003xth_2
17	lnc-FAM110B-4	chr8:58405458-58405534	ENSG00000253821
18	lnc-FAM110B-11	chr8:58348579-58351315	l_3603_chr8:58348578-58353048_testes
19	lnc-FAM110B-4	chr8:58458029-58463564	NONHSAT126757
20	lnc-FAM110B-10	chr8:58428384-58428521	ucscGeneNc_uc003xth_2
21	lnc-IMPAD1-2	chr8:58506725-58507021	ENSG00000253322
22	lnc-FAM110B-10	chr8:58422335-58422521	ucscGeneNc_uc003xth_2

No data

Variant related genes	Relation type
RNU7-174P	TF binding region
ENSG00000253821	TF binding region
ENSG00000253821	chromatin interactions
ENSG00000253871	chromatin interactions
ENSG00000215114	chromatin interactions

Extended variants
information (count: 6242 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:6242 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149613668	chr8:58329220-58329221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559702219	chr8:58329235-58329236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528449474	chr8:58329248-58329249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545732177	chr8:58329281-58329282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565612173	chr8:58329282-58329283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114461517	chr8:58329367-58329368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191843554	chr8:58329379-58329380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs372932526	chr8:58329398-58329399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183180003	chr8:58329399-58329400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs113332481	chr8:58329400-58329401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529804713	chr8:58329402-58329403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533622096	chr8:58329403-58329404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549604240	chr8:58329464-58329465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs75359710	chr8:58329481-58329482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538210285	chr8:58329492-58329493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551737379	chr8:58329561-58329562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112826520	chr8:58329577-58329578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188206083	chr8:58329578-58329579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs11991955	chr8:58329588-58329589	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs574502313	chr8:58329610-58329611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536774765	chr8:58329616-58329617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs375925808	chr8:58329636-58329637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553158442	chr8:58329638-58329639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573359645	chr8:58329643-58329644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574972038	chr8:58329653-58329654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs111979041	chr8:58329674-58329675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545446048	chr8:58329681-58329682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs13251689	chr8:58329703-58329704	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs144352954	chr8:58329725-58329726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191393208	chr8:58329741-58329742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565594816	chr8:58329746-58329747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs58702444	chr8:58329752-58329753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544877344	chr8:58329765-58329766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4486191	chr8:58329778-58329779	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs182273562	chr8:58329800-58329801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546688174	chr8:58329819-58329820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs116040846	chr8:58329831-58329832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532077346	chr8:58329889-58329890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551798765	chr8:58329948-58329949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4493896	chr8:58329956-58329957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs5891653	chr8:58329976-58329977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186539950	chr8:58330015-58330016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537753534	chr8:58330065-58330066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10504233	chr8:58330086-58330087	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs140173281	chr8:58330122-58330123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533781040	chr8:58330149-58330150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553910787	chr8:58330152-58330153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192535296	chr8:58330187-58330188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs4582544	chr8:58330194-58330195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs142262285	chr8:58330202-58330203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Renal cell carcinoma	21215367	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:843 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58329200-58333000	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr8:58330800-58331200	Enhancers	Liver	Liver
3	chr8:58331200-58333400	Weak transcription	Liver	Liver
4	chr8:58333000-58333200	Enhancers	Primary B cells from cord blood	blood
5	chr8:58333000-58333200	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr8:58333200-58333400	Active TSS	Primary T cells from cord blood	blood
7	chr8:58333200-58333400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr8:58333200-58333400	Active TSS	Muscle Satellite Cultured Cells	--
9	chr8:58333200-58333400	Active TSS	Brain Anterior Caudate	brain
10	chr8:58333200-58333400	Enhancers	Brain Cingulate Gyrus	brain
11	chr8:58333200-58333400	Active TSS	Duodenum Smooth Muscle	Duodenum
12	chr8:58333200-58333400	Active TSS	Fetal Kidney	kidney
13	chr8:58333200-58333400	Active TSS	NHDF-Ad	bronchial
14	chr8:58333200-58333600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr8:58333200-58333600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr8:58333200-58333600	Active TSS	Colon Smooth Muscle	Colon
17	chr8:58333200-58333600	Active TSS	Right Ventricle	heart
18	chr8:58333200-58333600	Active TSS	Skeletal Muscle Female	skeletal muscle
19	chr8:58333200-58333600	Active TSS	NHEK	skin
20	chr8:58333200-58333600	Active TSS	Osteobl	bone
21	chr8:58333200-58333800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr8:58333200-58333800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr8:58333200-58333800	Flanking Active TSS	Primary B cells from cord blood	blood
24	chr8:58333200-58333800	Active TSS	Adipose Nuclei	Adipose
25	chr8:58333200-58333800	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr8:58333200-58333800	Active TSS	Ovary	ovary
27	chr8:58333200-58333800	Active TSS	Right Atrium	heart
28	chr8:58333200-58333800	Active TSS	Skeletal Muscle Male	skeletal muscle
29	chr8:58333200-58333800	Active TSS	Stomach Smooth Muscle	stomach
30	chr8:58333200-58333800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
31	chr8:58333200-58334000	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr8:58333400-58333600	Bivalent/Poised TSS	Primary T cells from cord blood	blood
33	chr8:58333400-58333600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr8:58333400-58333600	Flanking Active TSS	Brain Anterior Caudate	brain
35	chr8:58333400-58333600	Enhancers	Duodenum Mucosa	Duodenum
36	chr8:58333400-58333600	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
37	chr8:58333400-58333600	Enhancers	Fetal Heart	heart
38	chr8:58333400-58333600	Enhancers	Fetal Intestine Large	intestine
39	chr8:58333400-58333600	Flanking Active TSS	Fetal Kidney	kidney
40	chr8:58333400-58333600	Enhancers	Fetal Lung	lung
41	chr8:58333400-58333600	Active TSS	Fetal Muscle Leg	muscle
42	chr8:58333400-58333600	Flanking Bivalent TSS/Enh	A549	lung
43	chr8:58333400-58333600	Enhancers	Dnd41	blood
44	chr8:58333400-58333600	Active TSS	GM12878-XiMat	blood
45	chr8:58333400-58333600	Enhancers	HepG2	liver
46	chr8:58333400-58333600	Enhancers	NH-A	brain
47	chr8:58333400-58333800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr8:58333400-58333800	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr8:58333400-58333800	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr8:58333400-58333800	Enhancers	iPS-20b Cell Line	embryonic stem cell

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