Variant report

Variant	nsv891293
Chromosome Location	chr8:111704563-111822043
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:317)
CpG islands
(count:61)
Chromatin interactive
region (count:26)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:317 , 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	ATF1	chr8:111804441-111804627	K562	blood:	n/a	n/a
2	ATF2	chr8:111758640-111758925	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr8:111758671-111758920	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:111719799-111719982	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr8:111758735-111758917	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr8:111758677-111758916	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr8:111719822-111720092	GM12878	blood:	n/a	n/a
8	CBX3	chr8:111810769-111811126	K562	blood:	n/a	n/a
9	CBX3	chr8:111810832-111811007	K562	blood:	n/a	n/a
10	CEBPB	chr8:111714073-111714166	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr8:111724257-111724440	HepG2	liver:	n/a	n/a
12	CEBPB	chr8:111708552-111709216	IMR90	lung:	n/a	n/a
13	CEBPB	chr8:111793912-111794250	IMR90	lung:	n/a	n/a
14	CEBPB	chr8:111769530-111769868	HepG2	liver:	n/a	chr8:111769695-111769706
15	CEBPB	chr8:111755449-111755533	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr8:111769522-111769876	IMR90	lung:	n/a	chr8:111769695-111769706
17	CEBPB	chr8:111793925-111794261	A549	lung:	n/a	n/a
18	CEBPB	chr8:111769540-111769842	Hela-S3	cervix:	n/a	chr8:111769695-111769706
19	CEBPB	chr8:111769556-111769845	A549	lung:	n/a	chr8:111769695-111769706
20	CEBPB	chr8:111757204-111757296	HepG2	liver:	n/a	n/a
21	CEBPB	chr8:111793930-111794262	HepG2	liver:	n/a	n/a
22	CEBPB	chr8:111816593-111816629	HepG2	liver:	n/a	n/a
23	CEBPB	chr8:111708632-111709146	HepG2	liver:	n/a	n/a
24	CEBPB	chr8:111794027-111794161	K562	blood:	n/a	n/a
25	CEBPB	chr8:111758683-111758901	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr8:111769516-111769877	H1-hESC	embryonic stem cell:	n/a	chr8:111769695-111769706
27	CEBPB	chr8:111793909-111794206	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr8:111758688-111758879	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr8:111726278-111726443	GM12878	blood:	n/a	n/a
30	CTCF	chr8:111746240-111746390	GM12873	blood:	n/a	n/a
31	CTCF	chr8:111746220-111746370	GM12865	blood:	n/a	n/a
32	CTCF	chr8:111746273-111746387	MCF-7	breast:	n/a	n/a
33	CTCF	chr8:111757567-111757594	GM10248	blood:	n/a	n/a
34	CTCF	chr8:111746240-111746390	GM12865	blood:	n/a	n/a
35	CTCF	chr8:111806240-111806390	BE2_C	brain:	n/a	n/a
36	CTCF	chr8:111746320-111746470	GM12866	blood:	n/a	n/a
37	CTCF	chr8:111746280-111746430	GM12871	blood:	n/a	n/a
38	CTCF	chr8:111806260-111806410	AG09309	skin:	n/a	n/a
39	CTCF	chr8:111746240-111746390	GM12867	blood:	n/a	n/a
40	CTCF	chr8:111746360-111746510	GM12864	blood:	n/a	n/a
41	CTCF	chr8:111806160-111806310	MCF-7	breast:	n/a	n/a
42	CTCF	chr8:111806220-111806370	HMEC	breast:	n/a	n/a
43	CTCF	chr8:111790021-111790061	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr8:111746260-111746410	GM12864	blood:	n/a	n/a
45	CTCF	chr8:111751881-111751972	MCF-7	breast:	n/a	n/a
46	CTCF	chr8:111746360-111746510	GM12866	blood:	n/a	n/a
47	CTCF	chr8:111746228-111746463	MCF-7	breast:	n/a	n/a
48	CTCF	chr8:111746220-111746370	GM12868	blood:	n/a	n/a
49	CTCF	chr8:111784400-111784550	BE2_C	brain:	n/a	n/a
50	CTCF	chr8:111726373-111726433	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:111707758-111707808	IMR90	lung:	fetal
2	chr8:111707758-111707808	HCT-116	colon:	n/a
3	chr8:111707758-111707808	HCM	heart:	n/a
4	chr8:111707758-111707808	SK-N-MC	brain:	n/a
5	chr8:111707758-111707808	NB4	blood:	n/a
6	chr8:111707758-111707808	MCF-7	breast:	n/a
7	chr8:111707758-111707808	AG09309	skin:	n/a
8	chr8:111707758-111707808	H1-hESC	embryonic stem cell:	embryo
9	chr8:111707758-111707808	HEK293	kidney:	embryo
10	chr8:111707758-111707808	CMK	blood:	n/a
11	chr8:111707758-111707808	NHBE	bronchial:	n/a
12	chr8:111707758-111707808	HRE	kidney:	n/a
13	chr8:111707758-111707808	AG10803	skin:	n/a
14	chr8:111707758-111707808	HNPCEpiC	eye:	n/a
15	chr8:111707758-111707808	AG04450	lung:	fetal
16	chr8:111707758-111707808	U87	brain:	n/a
17	chr8:111707758-111707808	AG04449	skin:	fetal
18	chr8:111707758-111707808	SK-N-SH	brain:	n/a
19	chr8:111707758-111707808	HAEpiC	amniotic membrane:	n/a
20	chr8:111707758-111707808	ECC-1	luminal epithelium:	n/a
21	chr8:111707758-111707808	PrEC	prostate:	n/a
22	chr8:111707758-111707808	HMEC	breast:	n/a
23	chr8:111707758-111707808	HepG2	liver:	n/a
24	chr8:111707758-111707808	ovcar-3	ovarian:	n/a
25	chr8:111707758-111707808	HEEpiC	esophagus:	n/a
26	chr8:111707758-111707808	Hela-S3	cervix:	n/a
27	chr8:111707758-111707808	GM06990	blood:	n/a
28	chr8:111707758-111707808	NT2-D1	testis:	n/a
29	chr8:111707758-111707808	HPAEpiC	pulmonary alveolar:	n/a
30	chr8:111707758-111707808	NH-A	brain:	n/a
31	chr8:111707758-111707808	SAEC	small airway:	n/a
32	chr8:111707758-111707808	HUVEC	blood vessel:	n/a
33	chr8:111707758-111707808	A549	lung:	n/a
34	chr8:111707758-111707808	Jurkat	blood:	n/a
35	chr8:111707758-111707808	SK-N-SH_RA	brain:	n/a
36	chr8:111707758-111707808	RPTEC	kidney:	n/a
37	chr8:111707758-111707808	HCF	heart:	n/a
38	chr8:111707758-111707808	ProgFib	skin:	n/a
39	chr8:111707758-111707808	K562	blood:	n/a
40	chr8:111707758-111707808	AoSMC	blood vessel:	n/a
41	chr8:111707758-111707808	BE2_C	brain:	n/a
42	chr8:111707758-111707808	GM12878	blood:	n/a
43	chr8:111707758-111707808	SKMC	muscle:	n/a
44	chr8:111707758-111707808	Caco-2	colon:	n/a
45	chr8:111707758-111707808	AG09319	gingival:	n/a
46	chr8:111707758-111707808	MCF10A-Er-Src	breast:	n/a
47	chr8:111707758-111707808	GM12892	blood:	n/a
48	chr8:111707758-111707808	T-47D	breast:	n/a
49	chr8:111707758-111707808	GM19239	blood:	n/a
50	chr8:111707758-111707808	HL-60	blood:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:43241796..43242729-chr8:111709968..111710717,2	MCF-7	breast:
2	chr8:111799556..111802962-chr8:111805139..111808019,3	MCF-7	breast:
3	chr8:111770515..111773370-chr8:111778420..111781176,2	K562	blood:
4	chr8:111815829..111818454-chr8:111818863..111820532,2	K562	blood:
5	chr8:111714002..111715922-chr8:111718938..111720595,2	K562	blood:
6	chr8:111712144..111713669-chr8:111724852..111727560,2	MCF-7	breast:
7	chr8:111731408..111733781-chr8:111735894..111737971,2	K562	blood:
8	chr8:111744937..111746990-chr8:111753666..111755908,2	K562	blood:
9	chr6:47444917..47447011-chr8:111717811..111719807,2	MCF-7	breast:
10	chr8:111705966..111708208-chr8:111719733..111721854,2	MCF-7	breast:
11	chr8:111780743..111782594-chr8:111785721..111788222,2	MCF-7	breast:
12	chr8:37622904..37623517-chr8:111713671..111714213,2	MCF-7	breast:
13	chr8:111731408..111733781-chr8:111735894..111737971,2	K562	blood:
14	chr8:111799556..111802962-chr8:111805139..111808019,3	MCF-7	breast:
15	chr8:111705966..111708208-chr8:111719733..111721854,2	MCF-7	breast:
16	chr8:111781609..111784016-chr8:111789603..111791637,2	MCF-7	breast:
17	chr8:111815829..111818454-chr8:111818863..111820532,2	K562	blood:
18	chr8:111702766..111704836-chr8:111705809..111708776,2	MCF-7	breast:
19	chr8:111744937..111746990-chr8:111753666..111755908,2	K562	blood:
20	chr8:111811884..111813878-chr8:111822855..111824615,2	K562	blood:
21	chr8:111712144..111713669-chr8:111724852..111727560,2	MCF-7	breast:
22	chr8:111702766..111704836-chr8:111705809..111708776,2	MCF-7	breast:
23	chr8:111781609..111784016-chr8:111789603..111791637,2	MCF-7	breast:
24	chr8:111780743..111782594-chr8:111785721..111788222,2	MCF-7	breast:
25	chr8:111661559..111663835-chr8:111734745..111737537,2	MCF-7	breast:
26	chr8:111714002..111715922-chr8:111718938..111720595,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-422N16.3.1-3	chr8:111779092-111779145	ENSG00000253717
2	lnc-KCNV1-5	chr8:111821623-111822123	NONHSAT128312
3	lnc-RP11-422N16.3.1-3	chr8:111784567-111784988	ENSG00000253717

No data

Variant related genes	Relation type
ENSG00000253717	TF binding region
ENSG00000253717	CpG island
ENSG00000198087	chromatin interactions
ENSG00000270761	chromatin interactions
ENSG00000253717	chromatin interactions

Extended variants
information (count: 2498 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2498 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2220822	chr8:111704563-111704564	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs6981046	chr8:111704584-111704585	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs558989588	chr8:111704594-111704595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184763425	chr8:111704687-111704688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs544492404	chr8:111704708-111704709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs561449406	chr8:111704720-111704721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs147748690	chr8:111704731-111704732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs200547430	chr8:111704765-111704766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540728627	chr8:111704769-111704770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560514336	chr8:111704797-111704798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532414710	chr8:111704841-111704842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552499982	chr8:111704863-111704864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs71526771	chr8:111704885-111704886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190441796	chr8:111704909-111704910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs77662499	chr8:111704916-111704917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375329700	chr8:111705073-111705074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs79699796	chr8:111705115-111705116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553415874	chr8:111705116-111705117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs535981293	chr8:111705176-111705177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs180888275	chr8:111705191-111705192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566183740	chr8:111705211-111705212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184642825	chr8:111705219-111705220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538278040	chr8:111705229-111705230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189155669	chr8:111705234-111705235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113739889	chr8:111705248-111705249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538508454	chr8:111705299-111705300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542562356	chr8:111705333-111705334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181358020	chr8:111705334-111705335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs185630344	chr8:111705359-111705360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs546823487	chr8:111705378-111705379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540789745	chr8:111705383-111705384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190691476	chr8:111705389-111705390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs377501854	chr8:111705392-111705393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545896517	chr8:111705395-111705396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74912801	chr8:111705441-111705442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181519452	chr8:111705469-111705470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs74751629	chr8:111705471-111705472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560807083	chr8:111705473-111705474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529839220	chr8:111705495-111705496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142661171	chr8:111705503-111705504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566460205	chr8:111705519-111705520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531170563	chr8:111705531-111705532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10102006	chr8:111705572-111705573	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs551913560	chr8:111705581-111705582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568830398	chr8:111705586-111705587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369790158	chr8:111705613-111705614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs143382392	chr8:111705614-111705615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555312319	chr8:111705658-111705659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs4735161	chr8:111705663-111705664	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs373561054	chr8:111705691-111705692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Liver carcinoma	19366792	CNVD
Seminomas	18059402	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
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
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:111703400-111707600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr8:111704400-111705000	Enhancers	Fetal Intestine Small	intestine
3	chr8:111706200-111706400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr8:111706200-111709000	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr8:111706400-111706600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr8:111706400-111707200	Enhancers	H9 Cell Line	embryonic stem cell
7	chr8:111706400-111707600	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr8:111706400-111708000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr8:111706400-111708200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:111706400-111708200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr8:111706600-111707200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr8:111706600-111708000	Enhancers	H1 Cell Line	embryonic stem cell
13	chr8:111706600-111708200	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr8:111706600-111709000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr8:111706600-111709400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr8:111706600-111709600	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr8:111706800-111707200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr8:111706800-111708000	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr8:111707000-111707200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr8:111707000-111708200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr8:111707200-111709400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr8:111707400-111708000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr8:111707600-111708000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr8:111707600-111708000	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr8:111707600-111708000	Enhancers	NH-A	brain
26	chr8:111707800-111708000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr8:111708000-111708200	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr8:111708000-111709600	Weak transcription	NH-A	brain
29	chr8:111708200-111709400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr8:111708200-111709400	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr8:111708200-111709400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr8:111709000-111711000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr8:111709400-111709800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr8:111709400-111710200	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr8:111709400-111710400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr8:111709400-111710400	Enhancers	HMEC	breast
37	chr8:111709400-111710400	Enhancers	NHEK	skin
38	chr8:111709400-111711400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr8:111709600-111709800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr8:111709600-111709800	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr8:111709600-111710200	Enhancers	NH-A	brain
42	chr8:111709600-111710400	Enhancers	Muscle Satellite Cultured Cells	--
43	chr8:111709600-111710400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr8:111709800-111710000	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr8:111709800-111710000	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr8:111710400-111711200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr8:111711200-111711400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr8:111716600-111717400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr8:111717200-111717600	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr8:111717400-111718400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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