Variant report

Variant	nsv1022273
Chromosome Location	chr8:110026712-110146600
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:751)
CpG islands
(count:672)
Chromatin interactive
region (count:31)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:751 , 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	ARID3A	chr8:110078075-110078690	K562	blood:	n/a	n/a
2	ARID3A	chr8:110076210-110076604	K562	blood:	n/a	n/a
3	ARID3A	chr8:110084674-110084872	K562	blood:	n/a	chr8:110084769-110084785
4	ATF1	chr8:110078044-110078293	K562	blood:	n/a	n/a
5	ATF2	chr8:110064596-110065146	GM12878	blood:	n/a	n/a
6	ATF3	chr8:110076282-110076655	K562	blood:	n/a	n/a
7	BACH1	chr8:110084658-110085028	H1-hESC	embryonic stem cell:	n/a	chr8:110084846-110084860
8	BACH1	chr8:110144881-110145050	H1-hESC	embryonic stem cell:	n/a	chr8:110144969-110144983
9	BACH1	chr8:110084678-110085051	K562	blood:	n/a	chr8:110084846-110084860
10	BATF	chr8:110064524-110065098	GM12878	blood:	n/a	n/a
11	BATF	chr8:110064802-110065084	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:110064833-110065052	GM12878	blood:	n/a	n/a
13	BCL11A	chr8:110064491-110065070	GM12878	blood:	n/a	n/a
14	BCL3	chr8:110064416-110065174	A549	lung:	n/a	n/a
15	BHLHE40	chr8:110099056-110099077	A549	lung:	n/a	n/a
16	BHLHE40	chr8:110077970-110078297	K562	blood:	n/a	n/a
17	BHLHE40	chr8:110045948-110046185	K562	blood:	n/a	n/a
18	BHLHE40	chr8:110071027-110071336	K562	blood:	n/a	n/a
19	BRCA1	chr8:110138556-110138590	GM12878	blood:	n/a	n/a
20	CBX3	chr8:110054329-110054749	HCT-116	colon:	n/a	n/a
21	CBX3	chr8:110054280-110054853	HCT-116	colon:	n/a	n/a
22	CBX3	chr8:110076273-110076662	K562	blood:	n/a	n/a
23	CCNT2	chr8:110071310-110071531	K562	blood:	n/a	n/a
24	CCNT2	chr8:110078073-110078335	K562	blood:	n/a	n/a
25	CEBPB	chr8:110114326-110114336	K562	blood:	n/a	n/a
26	CEBPB	chr8:110064588-110065209	A549	lung:	n/a	n/a
27	CEBPB	chr8:110080497-110080820	HepG2	liver:	n/a	n/a
28	CEBPB	chr8:110100855-110100997	K562	blood:	n/a	chr8:110100916-110100927 chr8:110100916-110100925
29	CEBPB	chr8:110064568-110065141	A549	lung:	n/a	n/a
30	CEBPB	chr8:110055008-110055311	A549	lung:	n/a	n/a
31	CEBPB	chr8:110093901-110093999	HepG2	liver:	n/a	chr8:110093920-110093931
32	CEBPB	chr8:110066356-110066556	HepG2	liver:	n/a	chr8:110066448-110066459
33	CEBPB	chr8:110035025-110035421	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr8:110076028-110076309	K562	blood:	n/a	n/a
35	CEBPB	chr8:110145299-110145789	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr8:110055096-110055252	K562	blood:	n/a	n/a
37	CEBPB	chr8:110109875-110110176	HepG2	liver:	n/a	chr8:110110014-110110025 chr8:110110158-110110171
38	CEBPB	chr8:110031943-110032097	A549	lung:	n/a	n/a
39	CEBPB	chr8:110054992-110055315	A549	lung:	n/a	n/a
40	CEBPB	chr8:110094761-110095166	Hela-S3	cervix:	n/a	chr8:110094822-110094833
41	CEBPB	chr8:110100925-110100968	A549	lung:	n/a	n/a
42	CEBPB	chr8:110114191-110114473	HepG2	liver:	n/a	chr8:110114323-110114334
43	CEBPB	chr8:110054169-110054813	HCT-116	colon:	n/a	chr8:110054706-110054719
44	CEBPB	chr8:110109945-110110160	IMR90	lung:	n/a	chr8:110110014-110110025
45	CEBPB	chr8:110107970-110108839	ECC-1	luminal epithelium:	n/a	n/a
46	CEBPB	chr8:110141604-110142010	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr8:110054256-110054810	A549	lung:	n/a	chr8:110054706-110054719
48	CEBPB	chr8:110109852-110110168	A549	lung:	n/a	chr8:110110014-110110025
49	CEBPB	chr8:110054884-110055432	A549	lung:	n/a	n/a
50	CEBPB	chr8:110037586-110038136	HCT-116	colon:	n/a	chr8:110038071-110038082

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:110082656-110082706	HCPEpiC	choroid plexus:	n/a
2	chr8:110082656-110082706	HCPEpiC	choroid plexus:	n/a
3	chr8:110116031-110116081	HMEC	breast:	n/a
4	chr8:110082656-110082706	HepG2	liver:	n/a
5	chr8:110082656-110082706	MCF10A-Er-Src	breast:	n/a
6	chr8:110132541-110132591	HCM	heart:	n/a
7	chr8:110082656-110082706	AG04450	lung:	fetal
8	chr8:110116031-110116081	AG09319	gingival:	n/a
9	chr8:110100005-110100055	Hela-S3	cervix:	n/a
10	chr8:110098866-110098916	NHBE	bronchial:	n/a
11	chr8:110082656-110082706	Jurkat	blood:	n/a
12	chr8:110082656-110082706	ProgFib	skin:	n/a
13	chr8:110145814-110145864	HCF	heart:	n/a
14	chr8:110100005-110100055	HEEpiC	esophagus:	n/a
15	chr8:110100005-110100055	HNPCEpiC	eye:	n/a
16	chr8:110132541-110132591	NHBE	bronchial:	n/a
17	chr8:110099683-110099733	SKMC	muscle:	n/a
18	chr8:110099750-110099800	PANC-1	pancreas:	n/a
19	chr8:110145814-110145864	AG10803	skin:	n/a
20	chr8:110100005-110100055	BE2_C	brain:	n/a
21	chr8:110098866-110098916	RPTEC	kidney:	n/a
22	chr8:110116031-110116081	H1-hESC	embryonic stem cell:	embryo
23	chr8:110100005-110100055	MCF10A-Er-Src	breast:	n/a
24	chr8:110116031-110116081	SK-N-SH	brain:	n/a
25	chr8:110099582-110099632	K562	blood:	n/a
26	chr8:110098866-110098916	GM12892	blood:	n/a
27	chr8:110098844-110098894	A549	lung:	n/a
28	chr8:110100005-110100055	BJ	skin:	n/a
29	chr8:110145814-110145864	HEK293	kidney:	embryo
30	chr8:110098923-110098973	HEK293	kidney:	embryo
31	chr8:110099750-110099800	CMK	blood:	n/a
32	chr8:110098844-110098894	PANC-1	pancreas:	n/a
33	chr8:110082656-110082706	SK-N-MC	brain:	n/a
34	chr8:110099683-110099733	ECC-1	luminal epithelium:	n/a
35	chr8:110145814-110145864	HRCEpiC	kidney:	n/a
36	chr8:110116031-110116081	ovcar-3	ovarian:	n/a
37	chr8:110145814-110145864	IMR90	lung:	fetal
38	chr8:110082656-110082706	GM12878	blood:	n/a
39	chr8:110145814-110145864	GM12891	blood:	n/a
40	chr8:110099582-110099632	SK-N-MC	brain:	n/a
41	chr8:110099582-110099632	HCM	heart:	n/a
42	chr8:110100005-110100055	Caco-2	colon:	n/a
43	chr8:110116031-110116081	HRE	kidney:	n/a
44	chr8:110132541-110132591	HEK293	kidney:	embryo
45	chr8:110116031-110116081	HCM	heart:	n/a
46	chr8:110116031-110116081	BE2_C	brain:	n/a
47	chr8:110082656-110082706	HAEpiC	amniotic membrane:	n/a
48	chr8:110145814-110145864	HMEC	breast:	n/a
49	chr8:110099582-110099632	MCF-7	breast:	n/a
50	chr8:110098923-110098973	ECC-1	luminal epithelium:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:110027745..110030017-chr8:110034035..110036010,2	MCF-7	breast:
2	chr8:110032538..110034538-chr8:110037178..110038775,2	K562	blood:
3	chr8:110106215..110109190-chr8:110112713..110114586,2	K562	blood:
4	chr8:110064627..110066916-chr8:110068551..110070751,3	K562	blood:
5	chr8:110096767..110098879-chr8:110100924..110103388,2	MCF-7	breast:
6	chr8:110144829..110147238-chr8:110238883..110241671,2	MCF-7	breast:
7	chr8:110123945..110126295-chr8:110127481..110129348,2	MCF-7	breast:
8	chr8:110064627..110066916-chr8:110068551..110070751,3	K562	blood:
9	chr8:110032538..110034538-chr8:110037178..110038775,2	K562	blood:
10	chr8:109912911..109915524-chr8:110051304..110053442,2	K562	blood:
11	chr8:110084963..110087132-chr8:110090550..110092121,2	MCF-7	breast:
12	chr8:110051446..110054408-chr8:110240885..110242830,2	MCF-7	breast:
13	chr8:110084963..110087132-chr8:110090550..110092121,2	MCF-7	breast:
14	chr8:110070694..110072266-chr8:110073492..110075488,2	K562	blood:
15	chr1:117352800..117353337-chr8:110126161..110126984,2	MCF-7	breast:
16	chr8:110077392..110079634-chr8:110134593..110136611,2	K562	blood:
17	chr8:110136298..110138304-chr8:110140145..110142017,2	MCF-7	breast:
18	chr8:110036524..110038466-chr8:110041307..110043822,2	K562	blood:
19	chr8:110077392..110079634-chr8:110134593..110136611,2	K562	blood:
20	chr8:110106215..110109190-chr8:110112713..110114586,2	K562	blood:
21	chr8:110036524..110038466-chr8:110041307..110043822,2	K562	blood:
22	chr8:110123945..110126295-chr8:110127481..110129348,2	MCF-7	breast:
23	chr8:110142753..110145243-chr8:110152469..110155392,3	K562	blood:
24	chr8:110136298..110138304-chr8:110140145..110142017,2	MCF-7	breast:
25	chr8:110145280..110147423-chr8:110148598..110150919,2	K562	blood:
26	chr8:110111135..110113678-chr8:110116104..110117999,2	K562	blood:
27	chr8:109930361..109931149-chr8:110047177..110047714,3	MCF-7	breast:
28	chr8:110070694..110072266-chr8:110073492..110075488,2	K562	blood:
29	chr8:110111135..110113678-chr8:110116104..110117999,2	K562	blood:
30	chr8:110130537..110131463-chr8:110294292..110294801,2	MCF-7	breast:
31	chr8:110027745..110030017-chr8:110034035..110036010,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM74-1	chr8:110075518-110075646	ENSG00000253796.1
2	lnc-TMEM74-1	chr8:110056285-110056356	ENSG00000253796.1
3	lnc-TMEM74-1	chr8:110055906-110055968	ENSG00000253796.1

No data

Variant related genes	Relation type
TRHR	TF binding region
ENSG00000253796	TF binding region
TRHR	CpG island
ENSG00000253796	CpG island
ENSG00000253796	chromatin interactions
ENSG00000174417	chromatin interactions

Extended variants
information (count: 3846 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:3846 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184067722	chr8:110026786-110026787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs188745574	chr8:110026789-110026790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528146975	chr8:110026808-110026809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551190316	chr8:110026832-110026833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs36180078	chr8:110026835-110026836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565038173	chr8:110026906-110026907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368709283	chr8:110026922-110026923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs60357696	chr8:110026939-110026940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs77128790	chr8:110026946-110026947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs149032132	chr8:110026950-110026951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145807558	chr8:110026951-110026952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs13282524	chr8:110026956-110026957	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs34814491	chr8:110026986-110026987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536568738	chr8:110027013-110027014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112217831	chr8:110027042-110027043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12550701	chr8:110027057-110027058	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs181475867	chr8:110027062-110027063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs34207171	chr8:110027094-110027095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs386413645	chr8:110027095-110027096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs386413646	chr8:110027108-110027109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs57719292	chr8:110027109-110027110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141807722	chr8:110027128-110027129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558782556	chr8:110027131-110027132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575848653	chr8:110027132-110027133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566261731	chr8:110027146-110027147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537227977	chr8:110027147-110027148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs147118391	chr8:110027214-110027215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565378886	chr8:110027227-110027228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200383132	chr8:110027264-110027265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148136148	chr8:110027316-110027317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs118119345	chr8:110027321-110027322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548865009	chr8:110027327-110027328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547600920	chr8:110027332-110027333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs12543567	chr8:110027347-110027348	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs572747133	chr8:110027348-110027349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs75750204	chr8:110027358-110027359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs117297639	chr8:110027376-110027377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs147530216	chr8:110027400-110027401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs71305920	chr8:110027405-110027406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs141962154	chr8:110027434-110027435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184538114	chr8:110027504-110027505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570241537	chr8:110027529-110027530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536515017	chr8:110027545-110027546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150640499	chr8:110027583-110027584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373087245	chr8:110027609-110027610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539142489	chr8:110027622-110027623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546982275	chr8:110027662-110027663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567202951	chr8:110027683-110027684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs115133645	chr8:110027696-110027697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552787727	chr8:110027759-110027760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	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
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
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
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Multiple myeloma	16461302	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	22539939	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Chronic myeloid leukemia	21384125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:304 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:110023000-110028800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr8:110026400-110026800	Enhancers	Left Ventricle	heart
3	chr8:110026800-110027200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr8:110028200-110030600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr8:110028200-110031000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr8:110028800-110033400	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr8:110030600-110031600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr8:110030800-110032200	Enhancers	Primary hematopoietic stem cells	blood
9	chr8:110031000-110031400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr8:110031000-110043000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr8:110031200-110031600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr8:110031400-110032800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr8:110031600-110032200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr8:110031600-110033200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr8:110032000-110032600	Enhancers	Adipose Nuclei	Adipose
16	chr8:110032200-110032600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr8:110032600-110037600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr8:110032800-110033200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr8:110033200-110033600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr8:110036200-110036400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr8:110036200-110036400	Enhancers	HUVEC	blood vessel
22	chr8:110036400-110037400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr8:110036400-110037400	Weak transcription	HUVEC	blood vessel
24	chr8:110036800-110037200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr8:110037000-110038800	Enhancers	HMEC	breast
26	chr8:110037200-110038200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr8:110037400-110038200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr8:110037400-110038800	Enhancers	HUVEC	blood vessel
29	chr8:110037600-110038400	Enhancers	Muscle Satellite Cultured Cells	--
30	chr8:110037600-110039200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr8:110038000-110038400	Enhancers	HSMM	muscle
32	chr8:110038000-110038400	Enhancers	Osteobl	bone
33	chr8:110038000-110038600	Enhancers	Stomach Mucosa	stomach
34	chr8:110038200-110038600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr8:110038200-110038600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr8:110038200-110038600	Enhancers	Adipose Nuclei	Adipose
37	chr8:110038200-110038600	Enhancers	Fetal Lung	lung
38	chr8:110038200-110038600	Enhancers	NH-A	brain
39	chr8:110038200-110039000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr8:110038600-110039200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr8:110038800-110042000	Weak transcription	HUVEC	blood vessel
42	chr8:110039000-110042600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr8:110042000-110043200	Enhancers	HUVEC	blood vessel
44	chr8:110042600-110043400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr8:110047800-110053200	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr8:110051200-110051600	Enhancers	A549	lung
47	chr8:110051600-110052800	Weak transcription	A549	lung
48	chr8:110052800-110053000	Enhancers	A549	lung
49	chr8:110052800-110055200	Enhancers	HMEC	breast
50	chr8:110052800-110055400	Enhancers	HSMM	muscle

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