Variant report

Variant	nsv1027744
Chromosome Location	chr8:89526571-89609651
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:345)
CpG islands
(count:183)
Chromatin interactive
region (count:15)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr8:89577895-89578380	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr8:89604135-89604849	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr8:89577913-89578323	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr8:89604244-89604922	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr8:89602979-89603398	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr8:89572408-89572579	GM12878	blood:	n/a	chr8:89572504-89572515 chr8:89572532-89572543
7	BATF	chr8:89569033-89569373	GM12878	blood:	n/a	n/a
8	BCL11A	chr8:89578000-89578362	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr8:89604202-89604701	H1-hESC	embryonic stem cell:	n/a	n/a
10	CBX3	chr8:89566652-89567196	HCT-116	colon:	n/a	n/a
11	CEBPB	chr8:89555267-89555524	A549	lung:	n/a	chr8:89555372-89555383 chr8:89555370-89555383 chr8:89555372-89555381
12	CEBPB	chr8:89579799-89580176	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr8:89602844-89603444	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr8:89547516-89547766	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr8:89566843-89567140	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr8:89579911-89580100	K562	blood:	n/a	n/a
17	CEBPB	chr8:89609398-89609422	IMR90	lung:	n/a	n/a
18	CEBPB	chr8:89547501-89547802	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr8:89577973-89578315	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr8:89547544-89547773	IMR90	lung:	n/a	n/a
21	CHD1	chr8:89603657-89604328	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr8:89529892-89529909	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr8:89577995-89578256	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr8:89603122-89603569	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr8:89604052-89604708	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr8:89604248-89604757	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTBP2	chr8:89604181-89604935	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr8:89566891-89566938	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr8:89566780-89566930	Caco-2	colon:	n/a	n/a
30	CTCF	chr8:89558580-89558730	MCF-7	breast:	n/a	chr8:89558622-89558630
31	CTCF	chr8:89566860-89567010	AG10803	skin:	n/a	n/a
32	CTCF	chr8:89566840-89566990	AG09319	gingival:	n/a	n/a
33	CTCF	chr8:89566760-89566910	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr8:89597710-89597777	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr8:89566860-89567010	BJ	skin:	n/a	n/a
36	CTCF	chr8:89566840-89566990	BJ	skin:	n/a	n/a
37	CTCF	chr8:89566820-89566970	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr8:89566820-89566970	AG09319	gingival:	n/a	n/a
39	CTCF	chr8:89566780-89566930	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr8:89566993-89567082	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr8:89566860-89567010	HAc	cerebellar:	n/a	n/a
42	CTCF	chr8:89566800-89566950	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr8:89566780-89566930	GM12873	blood:	n/a	n/a
44	CTCF	chr8:89566580-89566730	HVMF	connective:	n/a	n/a
45	CTCF	chr8:89566786-89566979	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr8:89566879-89566951	GM12892	blood:	n/a	n/a
47	CTCF	chr8:89566800-89566950	RPTEC	kidney:	n/a	n/a
48	CTCF	chr8:89566782-89567074	MCF-7	breast:	n/a	n/a
49	CTCF	chr8:89566720-89567073	GM12878	blood:	n/a	n/a
50	CTCF	chr8:89566800-89566950	HEK293	kidney:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:89603364-89603414	AoSMC	blood vessel:	n/a
2	chr8:89555539-89555589	Caco-2	colon:	n/a
3	chr8:89578031-89578081	HEK293	kidney:	embryo
4	chr8:89603364-89603414	HAEpiC	amniotic membrane:	n/a
5	chr8:89578031-89578081	SK-N-MC	brain:	n/a
6	chr8:89603364-89603414	HRPEpiC	eye:	n/a
7	chr8:89555539-89555589	HRPEpiC	eye:	n/a
8	chr8:89555539-89555589	HEEpiC	esophagus:	n/a
9	chr8:89603364-89603414	HCM	heart:	n/a
10	chr8:89578031-89578081	Hepatocyte	liver:	n/a
11	chr8:89555539-89555589	Jurkat	blood:	n/a
12	chr8:89578031-89578081	NB4	blood:	n/a
13	chr8:89555539-89555589	HUVEC	blood vessel:	n/a
14	chr8:89603364-89603414	GM12891	blood:	n/a
15	chr8:89555539-89555589	GM06990	blood:	n/a
16	chr8:89555539-89555589	GM12892	blood:	n/a
17	chr8:89603364-89603414	HRCEpiC	kidney:	n/a
18	chr8:89578031-89578081	HMEC	breast:	n/a
19	chr8:89603364-89603414	ECC-1	luminal epithelium:	n/a
20	chr8:89603364-89603414	MCF-7	breast:	n/a
21	chr8:89578031-89578081	BE2_C	brain:	n/a
22	chr8:89555539-89555589	NT2-D1	testis:	n/a
23	chr8:89555539-89555589	AoSMC	blood vessel:	n/a
24	chr8:89578031-89578081	GM12892	blood:	n/a
25	chr8:89603364-89603414	HEEpiC	esophagus:	n/a
26	chr8:89555539-89555589	NB4	blood:	n/a
27	chr8:89555539-89555589	SK-N-SH_RA	brain:	n/a
28	chr8:89578031-89578081	Caco-2	colon:	n/a
29	chr8:89603364-89603414	SK-N-SH	brain:	n/a
30	chr8:89603364-89603414	SAEC	small airway:	n/a
31	chr8:89555539-89555589	HNPCEpiC	eye:	n/a
32	chr8:89578031-89578081	HRE	kidney:	n/a
33	chr8:89578031-89578081	HRCEpiC	kidney:	n/a
34	chr8:89578031-89578081	HCPEpiC	choroid plexus:	n/a
35	chr8:89555539-89555589	BE2_C	brain:	n/a
36	chr8:89603364-89603414	HUVEC	blood vessel:	n/a
37	chr8:89603364-89603414	HepG2	liver:	n/a
38	chr8:89603364-89603414	A549	lung:	n/a
39	chr8:89555539-89555589	A549	lung:	n/a
40	chr8:89578031-89578081	AG10803	skin:	n/a
41	chr8:89555539-89555589	MCF10A-Er-Src	breast:	n/a
42	chr8:89578031-89578081	AG04450	lung:	fetal
43	chr8:89578031-89578081	HPAEpiC	pulmonary alveolar:	n/a
44	chr8:89555539-89555589	LNCaP	prostate:	n/a
45	chr8:89578031-89578081	GM12878	blood:	n/a
46	chr8:89578031-89578081	NHDF-neo	bronchial:	n/a
47	chr8:89578031-89578081	HL-60	blood:	n/a
48	chr8:89578031-89578081	SAEC	small airway:	n/a
49	chr8:89578031-89578081	NH-A	brain:	n/a
50	chr8:89603364-89603414	Caco-2	colon:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:88592943..88594779-chr8:89566513..89567283,4	MCF-7	breast:
2	chr11:60667438..60667958-chr8:89531289..89532163,2	MCF-7	breast:
3	chr8:89302385..89303116-chr8:89566700..89567661,2	MCF-7	breast:
4	chr8:89301825..89302992-chr8:89566410..89567020,3	MCF-7	breast:
5	chr8:89304186..89304879-chr8:89566533..89567355,3	MCF-7	breast:
6	chr8:89340294..89341947-chr8:89566335..89567397,24	MCF-7	breast:
7	chr8:89340700..89341308-chr8:89537775..89538662,2	MCF-7	breast:
8	chr8:89604118..89605802-chr8:89608046..89610893,2	K562	blood:
9	chr8:89604118..89605802-chr8:89608046..89610893,2	K562	blood:
10	chr8:89332758..89333407-chr8:89566429..89566999,2	MCF-7	breast:
11	chr8:89340595..89341565-chr8:89566032..89567395,11	MCF-7	breast:
12	chr8:89483236..89485336-chr8:89557800..89560254,2	MCF-7	breast:
13	chr8:89566591..89567525-chr8:89823590..89824198,2	MCF-7	breast:
14	chr8:88707267..88708110-chr8:89566454..89567220,4	MCF-7	breast:
15	chr8:88844099..88844976-chr8:89566466..89567055,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNBD1-4	chr8:89554846-89555059	ENSG00000253553.1
2	lnc-MMP16-1	chr8:89578146-89578341	XLOC_007146
3	lnc-CNBD1-4	chr8:89554909-89554980	ENSG00000253553.1
4	lnc-CNBD1-4	chr8:89554833-89554988	ENSG00000253553.1
5	lnc-MMP16-1	chr8:89600620-89600696	XLOC_007146
6	lnc-CNBD1-4	chr8:89554909-89555039	ENSG00000253553.1
7	lnc-MMP16-1	chr8:89578175-89578341	XLOC_007146
8	lnc-MMP16-1	chr8:89578146-89578341	XLOC_007146

No data

Variant related genes	Relation type
ENSG00000253553	TF binding region
ENSG00000253553	CpG island
GXYLT1	miRNA target sites

Extended variants
information (count: 1830 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:1830 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182102030	chr8:89527802-89527803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs542877084	chr8:89527901-89527902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185172770	chr8:89527905-89527906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551163060	chr8:89527930-89527931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543693178	chr8:89527998-89527999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs565266135	chr8:89528068-89528069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs189830254	chr8:89528088-89528089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs111801905	chr8:89528109-89528110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs547813180	chr8:89528125-89528126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs565952186	chr8:89528126-89528127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569318258	chr8:89528136-89528137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182483366	chr8:89528137-89528138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs548418749	chr8:89528144-89528145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs16883962	chr8:89528148-89528149	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs538063606	chr8:89528159-89528160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs570699315	chr8:89528169-89528170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs10504863	chr8:89528229-89528230	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs146832956	chr8:89528267-89528268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs571108036	chr8:89528299-89528300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs538943235	chr8:89528315-89528316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs543530441	chr8:89534036-89534037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs557892956	chr8:89534051-89534052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs7834603	chr8:89534091-89534092	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs149155267	chr8:89534148-89534149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188075218	chr8:89534200-89534201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558940089	chr8:89534226-89534227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs573662206	chr8:89534231-89534232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs544263959	chr8:89534237-89534238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556287839	chr8:89534249-89534250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs563505571	chr8:89534251-89534252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544793644	chr8:89534363-89534364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560712372	chr8:89534378-89534379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs139110601	chr8:89534403-89534404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs572582867	chr8:89534429-89534430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542899112	chr8:89534436-89534437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561288856	chr8:89534440-89534441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs373471785	chr8:89534453-89534454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs549718377	chr8:89534469-89534470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs368597686	chr8:89534493-89534494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564946494	chr8:89534508-89534509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532604413	chr8:89534532-89534533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547595731	chr8:89534609-89534610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs114790798	chr8:89534620-89534621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs533778854	chr8:89534621-89534622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs549287272	chr8:89534647-89534648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs532335056	chr8:89534846-89534847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs146367938	chr8:89534848-89534849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs117573048	chr8:89534869-89534870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs577591740	chr8:89534921-89534922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs538706550	chr8:89534936-89534937	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Autism	22495311	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
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	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
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
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:89527800-89528400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr8:89534000-89535200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr8:89537400-89537800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr8:89537400-89537800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:89550000-89550400	Enhancers	Fetal Kidney	kidney
6	chr8:89554600-89556400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr8:89554800-89555000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr8:89554800-89555800	Enhancers	H9 Cell Line	embryonic stem cell
9	chr8:89554800-89556400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr8:89554800-89556400	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr8:89554800-89557000	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr8:89554800-89557200	Enhancers	H1 Cell Line	embryonic stem cell
13	chr8:89554800-89557200	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr8:89555000-89557200	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr8:89555200-89557000	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr8:89555600-89557200	Enhancers	NHDF-Ad	bronchial
17	chr8:89555600-89557400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr8:89556000-89557200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr8:89556200-89557200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr8:89556200-89557400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:89556400-89557200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr8:89557000-89560600	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr8:89560600-89561000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
24	chr8:89562600-89563400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr8:89562600-89563400	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr8:89576200-89576600	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr8:89576600-89577800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr8:89577000-89577600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr8:89577000-89578200	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr8:89577000-89579000	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr8:89577000-89579000	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr8:89577400-89577800	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr8:89577600-89578400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
34	chr8:89577600-89579400	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr8:89577800-89578200	Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr8:89577800-89578800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr8:89578200-89578400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr8:89578200-89578400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr8:89578200-89578800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
40	chr8:89578200-89578800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr8:89578400-89579000	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr8:89578400-89579400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr8:89578400-89579400	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr8:89579000-89579600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr8:89579000-89585400	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr8:89579600-89579800	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr8:89585400-89586000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
48	chr8:89585600-89587000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
49	chr8:89586000-89587000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
50	chr8:89587000-89596600	Weak transcription	H1 Cell Line	embryonic stem cell

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