Variant report

Variant	nsv6227
Chromosome Location	chr8:63892087-63936952
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:614)
CpG islands
(count:183)
Chromatin interactive
region (count:21)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:614 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:63896383-63896947	HepG2	liver:	n/a	chr8:63896502-63896518
2	ARID3A	chr8:63921081-63921400	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:63922381-63923118	HepG2	liver:	n/a	n/a
4	ATF2	chr8:63920286-63920745	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr8:63921687-63922087	GM12878	blood:	n/a	n/a
6	BCL11A	chr8:63921810-63922084	GM12878	blood:	n/a	chr8:63921969-63921982
7	BHLHE40	chr8:63924460-63924621	GM12878	blood:	n/a	n/a
8	BHLHE40	chr8:63922648-63923096	GM12878	blood:	n/a	n/a
9	CEBPB	chr8:63920412-63920769	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr8:63920280-63920923	MCF-7	breast:	n/a	n/a
11	CEBPB	chr8:63914760-63915121	HepG2	liver:	n/a	chr8:63914940-63914951
12	CEBPB	chr8:63922434-63922866	HepG2	liver:	n/a	n/a
13	CEBPB	chr8:63921044-63921390	H1-hESC	embryonic stem cell:	n/a	chr8:63921195-63921208 chr8:63921197-63921206 chr8:63921195-63921206
14	CEBPB	chr8:63921148-63921314	HepG2	liver:	n/a	chr8:63921195-63921208 chr8:63921197-63921206 chr8:63921195-63921206
15	CEBPB	chr8:63920219-63920921	MCF-7	breast:	n/a	n/a
16	CEBPB	chr8:63921119-63921304	K562	blood:	n/a	chr8:63921195-63921208 chr8:63921197-63921206 chr8:63921195-63921206
17	CEBPB	chr8:63920966-63921409	HepG2	liver:	n/a	chr8:63921195-63921208 chr8:63921197-63921206 chr8:63921195-63921206
18	CEBPB	chr8:63920484-63920739	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr8:63921004-63921489	HepG2	liver:	n/a	chr8:63921195-63921208 chr8:63921197-63921206 chr8:63921195-63921206
20	CEBPB	chr8:63914806-63915032	K562	blood:	n/a	chr8:63914940-63914951
21	CEBPD	chr8:63921016-63921303	HepG2	liver:	n/a	n/a
22	CEBPZ	chr8:63922828-63922925	HepG2	liver:	n/a	n/a
23	CHD1	chr8:63921803-63921985	GM12878	blood:	n/a	n/a
24	CHD2	chr8:63921030-63921334	HepG2	liver:	n/a	n/a
25	CHD2	chr8:63896292-63896380	GM12878	blood:	n/a	n/a
26	CHD2	chr8:63922543-63922783	HepG2	liver:	n/a	n/a
27	CHD2	chr8:63920395-63920706	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTBP2	chr8:63920465-63921054	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr8:63896720-63896870	AG04450	lung:	n/a	chr8:63896787-63896808
30	CTCF	chr8:63924460-63924610	NHEK	skin:	n/a	chr8:63924475-63924496
31	CTCF	chr8:63902140-63902290	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr8:63896660-63896810	GM12864	blood:	n/a	chr8:63896787-63896808
33	CTCF	chr8:63924400-63924550	AG09319	gingival:	n/a	chr8:63924475-63924496
34	CTCF	chr8:63924360-63924510	NHEK	skin:	n/a	chr8:63924475-63924496
35	CTCF	chr8:63896627-63896905	HepG2	liver:	n/a	chr8:63896787-63896808
36	CTCF	chr8:63924640-63924790	GM12871	blood:	n/a	n/a
37	CTCF	chr8:63924340-63924490	RPTEC	kidney:	n/a	n/a
38	CTCF	chr8:63896720-63896870	HPAF	blood vessel:	n/a	chr8:63896787-63896808
39	CTCF	chr8:63924440-63924590	WERI-Rb-1	eye:	n/a	chr8:63924475-63924496
40	CTCF	chr8:63924380-63924530	GM12878	blood:	n/a	chr8:63924475-63924496
41	CTCF	chr8:63924420-63924570	AG10803	skin:	n/a	chr8:63924475-63924496
42	CTCF	chr8:63924420-63924570	NHDF-neo	bronchial:	n/a	chr8:63924475-63924496
43	CTCF	chr8:63924400-63924550	AG09309	skin:	n/a	chr8:63924475-63924496
44	CTCF	chr8:63896651-63896891	SK-N-SH_RA	brain:	n/a	chr8:63896787-63896808
45	CTCF	chr8:63896800-63896950	HVMF	connective:	n/a	n/a
46	CTCF	chr8:63924720-63924870	GM12872	blood:	n/a	n/a
47	CTCF	chr8:63924376-63924669	MCF-7	breast:	n/a	chr8:63924475-63924496
48	CTCF	chr8:63896660-63896810	WI-38	lung:	n/a	chr8:63896787-63896808
49	CTCF	chr8:63924460-63924610	HEEpiC	esophagus:	n/a	chr8:63924475-63924496
50	CTCF	chr8:63924423-63924623	MCF-7	breast:	n/a	chr8:63924475-63924496

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:63921966-63922016	Hela-S3	cervix:	n/a
2	chr8:63903574-63903624	CMK	blood:	n/a
3	chr8:63903574-63903624	HL-60	blood:	n/a
4	chr8:63921966-63922016	MCF-7	breast:	n/a
5	chr8:63921966-63922016	GM12891	blood:	n/a
6	chr8:63921966-63922016	ovcar-3	ovarian:	n/a
7	chr8:63903574-63903624	HIPEpiC	eye:	n/a
8	chr8:63895823-63895873	AG09319	gingival:	n/a
9	chr8:63903574-63903624	Caco-2	colon:	n/a
10	chr8:63903574-63903624	Jurkat	blood:	n/a
11	chr8:63903574-63903624	HepG2	liver:	n/a
12	chr8:63921966-63922016	SKMC	muscle:	n/a
13	chr8:63895823-63895873	GM12878	blood:	n/a
14	chr8:63895823-63895873	GM19239	blood:	n/a
15	chr8:63903574-63903624	AG04450	lung:	fetal
16	chr8:63921966-63922016	HepG2	liver:	n/a
17	chr8:63921966-63922016	A549	lung:	n/a
18	chr8:63903574-63903624	HRPEpiC	eye:	n/a
19	chr8:63903574-63903624	HCPEpiC	choroid plexus:	n/a
20	chr8:63903574-63903624	HUVEC	blood vessel:	n/a
21	chr8:63921966-63922016	IMR90	lung:	fetal
22	chr8:63903574-63903624	AoSMC	blood vessel:	n/a
23	chr8:63903574-63903624	ovcar-3	ovarian:	n/a
24	chr8:63895823-63895873	Caco-2	colon:	n/a
25	chr8:63921966-63922016	Hepatocyte	liver:	n/a
26	chr8:63903574-63903624	A549	lung:	n/a
27	chr8:63903574-63903624	HEK293	kidney:	embryo
28	chr8:63895823-63895873	NB4	blood:	n/a
29	chr8:63903574-63903624	HAEpiC	amniotic membrane:	n/a
30	chr8:63921966-63922016	HAEpiC	amniotic membrane:	n/a
31	chr8:63895823-63895873	BJ	skin:	n/a
32	chr8:63895823-63895873	IMR90	lung:	fetal
33	chr8:63921966-63922016	CMK	blood:	n/a
34	chr8:63895823-63895873	NHDF-neo	bronchial:	n/a
35	chr8:63895823-63895873	ovcar-3	ovarian:	n/a
36	chr8:63895823-63895873	HUVEC	blood vessel:	n/a
37	chr8:63903574-63903624	HCM	heart:	n/a
38	chr8:63921966-63922016	GM12878	blood:	n/a
39	chr8:63895823-63895873	A549	lung:	n/a
40	chr8:63903574-63903624	GM12878	blood:	n/a
41	chr8:63903574-63903624	ProgFib	skin:	n/a
42	chr8:63921966-63922016	NB4	blood:	n/a
43	chr8:63921966-63922016	AG09319	gingival:	n/a
44	chr8:63903574-63903624	HNPCEpiC	eye:	n/a
45	chr8:63895823-63895873	AG09309	skin:	n/a
46	chr8:63895823-63895873	GM12891	blood:	n/a
47	chr8:63895823-63895873	ProgFib	skin:	n/a
48	chr8:63903574-63903624	SAEC	small airway:	n/a
49	chr8:63903574-63903624	AG09319	gingival:	n/a
50	chr8:63903574-63903624	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:63878030..63880245-chr8:63911061..63912789,2	K562	blood:
2	chr8:63544521..63545096-chr8:63924008..63924706,2	MCF-7	breast:
3	chr8:63925295..63930979-chr8:63933165..63939315,7	K562	blood:
4	chr8:63925295..63930979-chr8:63933165..63939315,7	K562	blood:
5	chr8:63935416..63938127-chr8:63942225..63943777,2	K562	blood:
6	chr8:62722292..62723197-chr8:63896539..63897247,2	MCF-7	breast:
7	chr8:63925803..63927464-chr8:63930970..63933121,2	K562	blood:
8	chr8:63925803..63927464-chr8:63930970..63933121,2	K562	blood:
9	chr8:63932707..63934846-chr8:63939491..63942277,2	MCF-7	breast:
10	chr8:63925789..63928059-chr8:63949158..63951177,2	MCF-7	breast:
11	chr8:63926789..63928933-chr8:63950143..63952400,2	K562	blood:
12	chr8:63917789..63919405-chr8:63920362..63922527,2	MCF-7	breast:
13	chr8:63917789..63919405-chr8:63920362..63922527,2	MCF-7	breast:
14	chr8:63932840..63934408-chr8:63951913..63953581,2	K562	blood:
15	chr8:63896894..63899189-chr8:63921841..63923926,2	MCF-7	breast:
16	chr8:63932030..63935472-chr8:63949746..63951856,3	K562	blood:
17	chr8:63925216..63928918-chr8:63929188..63932470,3	K562	blood:
18	chr8:63896894..63899189-chr8:63921841..63923926,2	MCF-7	breast:
19	chr6:128163382..128164089-chr8:63934415..63935240,2	MCF-7	breast:
20	chr8:63925216..63928918-chr8:63929188..63932470,3	K562	blood:
21	chr8:63931185..63932747-chr8:63937234..63938983,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NKAIN3-1	chr8:63924580-63924728	XLOC_006819
2	lnc-NKAIN3-1	chr8:63925517-63925933	XLOC_006819
3	lnc-RP11-32K4.2.1-6	chr8:63894179-63897460	NONHSAT126910
4	lnc-NKAIN3-1	chr8:63925627-63925653	ENSG00000240915.2
5	lnc-NKAIN3-2	chr8:63936931-63937550	ENSG00000253121.1
6	lnc-NKAIN3-1	chr8:63926718-63927240	ENSG00000240915.2
7	lnc-RP11-32K4.2.1-6	chr8:63890420-63897460	NONHSAT126909

No data

Variant related genes	Relation type
ENSG00000240915	TF binding region
ENSG00000253121	TF binding region
GGH	TF binding region
ENSG00000240915	CpG island
ENSG00000253121	CpG island
GGH	CpG island
ENSG00000253121	chromatin interactions
ENSG00000240915	chromatin interactions
ENSG00000137563	chromatin interactions
TSKU	miRNA target sites
TSN	miRNA target sites

Extended variants
information (count: 1700 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1700 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539089945	chr8:63892129-63892130	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs138286340	chr8:63892133-63892134	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs149587343	chr8:63892135-63892136	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs144306193	chr8:63892142-63892143	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs536175066	chr8:63892160-63892161	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs371884741	chr8:63892203-63892204	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs561819135	chr8:63892204-63892205	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs148706211	chr8:63892217-63892218	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs544485083	chr8:63892266-63892267	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs142274035	chr8:63892312-63892313	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs147211496	chr8:63892314-63892315	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs566506637	chr8:63892333-63892334	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs552326600	chr8:63892360-63892361	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs60280139	chr8:63892392-63892393	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs528611970	chr8:63892396-63892397	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs184756771	chr8:63892402-63892403	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs546696789	chr8:63892406-63892407	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs552349520	chr8:63892414-63892415	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs114933245	chr8:63892420-63892421	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs535672346	chr8:63892421-63892422	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs565928882	chr8:63892422-63892423	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs189234438	chr8:63892452-63892453	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs569484257	chr8:63892468-63892469	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs539409880	chr8:63892476-63892477	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs74400605	chr8:63892491-63892492	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs566467396	chr8:63892498-63892499	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs533833352	chr8:63892519-63892520	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs145900738	chr8:63892530-63892531	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs555516936	chr8:63892543-63892544	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs16930023	chr8:63892585-63892586	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs544450272	chr8:63892667-63892668	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs147818625	chr8:63892700-63892701	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs577901225	chr8:63892715-63892716	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs546177761	chr8:63892751-63892752	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs140347912	chr8:63892757-63892758	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs192616449	chr8:63892759-63892760	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs540298283	chr8:63892769-63892770	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs558457557	chr8:63892771-63892772	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs561872872	chr8:63892775-63892776	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs529430642	chr8:63892777-63892778	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs550934395	chr8:63892789-63892790	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs66790008	chr8:63892800-63892801	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs547570792	chr8:63892813-63892814	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs533411860	chr8:63892829-63892830	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs552061407	chr8:63892842-63892843	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs566312398	chr8:63892858-63892859	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs533792512	chr8:63892860-63892861	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs184886868	chr8:63892869-63892870	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs373414207	chr8:63892877-63892878	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs567406146	chr8:63892894-63892895	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
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
Salivary gland tumor	18059337	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
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	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
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
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
Colorectal cancer	21645411	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:401 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63868600-63895800	Weak transcription	Fetal Brain Female	brain
2	chr8:63892000-63892600	Enhancers	Brain Germinal Matrix	brain
3	chr8:63892200-63892600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr8:63895200-63896200	Enhancers	Fetal Intestine Large	intestine
5	chr8:63895400-63895600	Bivalent Enhancer	A549	lung
6	chr8:63895400-63896200	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr8:63895400-63896400	Enhancers	Fetal Intestine Small	intestine
8	chr8:63895400-63896600	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr8:63895400-63896800	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr8:63895400-63896800	Enhancers	Fetal Kidney	kidney
11	chr8:63895600-63896200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
12	chr8:63895800-63896600	Enhancers	Fetal Brain Male	brain
13	chr8:63895800-63896600	Enhancers	Fetal Brain Female	brain
14	chr8:63895800-63896600	Enhancers	HepG2	liver
15	chr8:63896000-63896400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr8:63896000-63896400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr8:63896000-63896400	Bivalent Enhancer	NH-A	brain
18	chr8:63896000-63896600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr8:63896000-63896600	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr8:63896000-63896600	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr8:63896000-63896600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr8:63896000-63896800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr8:63896200-63896600	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr8:63896200-63896600	Enhancers	H1 Cell Line	embryonic stem cell
25	chr8:63896200-63896600	Enhancers	Liver	Liver
26	chr8:63896200-63896800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr8:63896200-63896800	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr8:63896200-63896800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
29	chr8:63896200-63897600	Weak transcription	Fetal Intestine Large	intestine
30	chr8:63896400-63896600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr8:63896400-63896600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
32	chr8:63896400-63898800	Weak transcription	Fetal Intestine Small	intestine
33	chr8:63896400-63901000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr8:63896600-63900600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr8:63896800-63897000	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr8:63897000-63897400	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr8:63897400-63898200	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr8:63897600-63897800	Enhancers	Esophagus	oesophagus
39	chr8:63897600-63898800	Enhancers	Fetal Intestine Large	intestine
40	chr8:63897800-63898000	Enhancers	Fetal Stomach	stomach
41	chr8:63897800-63899800	Weak transcription	Esophagus	oesophagus
42	chr8:63898000-63898600	Weak transcription	Fetal Stomach	stomach
43	chr8:63898600-63899200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr8:63898600-63899200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr8:63898600-63899200	Enhancers	Fetal Stomach	stomach
46	chr8:63898800-63899000	Enhancers	Fetal Intestine Small	intestine
47	chr8:63900600-63901000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
48	chr8:63905000-63905600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr8:63905400-63906600	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr8:63905600-63906000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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