Variant report

Variant	esv2758159
Chromosome Location	chr8:54474589-54737473
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2421)
CpG islands
(count:2077)
Chromatin interactive
region (count:85)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2421 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:54572160-54572506	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:54647105-54647471	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:54722562-54722623	K562	blood:	n/a	n/a
4	ARID3A	chr8:54637510-54637700	K562	blood:	n/a	n/a
5	ARID3A	chr8:54691337-54691687	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:54721367-54721603	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:54644917-54645356	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:54570398-54570858	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:54680405-54681240	K562	blood:	n/a	n/a
10	ATF1	chr8:54654608-54655219	K562	blood:	n/a	n/a
11	ATF1	chr8:54640297-54640735	K562	blood:	n/a	n/a
12	ATF1	chr8:54544519-54544528	K562	blood:	n/a	n/a
13	ATF1	chr8:54649329-54649510	K562	blood:	n/a	n/a
14	ATF1	chr8:54680670-54680980	K562	blood:	n/a	n/a
15	ATF1	chr8:54643653-54644232	K562	blood:	n/a	n/a
16	ATF1	chr8:54641216-54641511	K562	blood:	n/a	n/a
17	ATF1	chr8:54722553-54722705	K562	blood:	n/a	n/a
18	ATF2	chr8:54675032-54675540	GM12878	blood:	n/a	n/a
19	ATF2	chr8:54680660-54681618	GM12878	blood:	n/a	n/a
20	ATF2	chr8:54680671-54681379	GM12878	blood:	n/a	n/a
21	ATF2	chr8:54674017-54674831	GM12878	blood:	n/a	n/a
22	ATF3	chr8:54636219-54636386	GM12878	blood:	n/a	n/a
23	ATF3	chr8:54640308-54640659	K562	blood:	n/a	n/a
24	ATF3	chr8:54636102-54636510	GM12878	blood:	n/a	n/a
25	ATF3	chr8:54500590-54500893	K562	blood:	n/a	n/a
26	ATF3	chr8:54722373-54722713	K562	blood:	n/a	n/a
27	BACH1	chr8:54571949-54572309	H1-hESC	embryonic stem cell:	n/a	chr8:54572062-54572076
28	BACH1	chr8:54721328-54721601	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr8:54680763-54681149	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr8:54570235-54570628	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr8:54680666-54681200	K562	blood:	n/a	n/a
32	BATF	chr8:54504956-54505391	GM12878	blood:	n/a	n/a
33	BATF	chr8:54570319-54570744	GM12878	blood:	n/a	n/a
34	BATF	chr8:54680671-54681602	GM12878	blood:	n/a	n/a
35	BATF	chr8:54680721-54681233	GM12878	blood:	n/a	n/a
36	BATF	chr8:54500701-54500900	GM12878	blood:	n/a	n/a
37	BATF	chr8:54674043-54674335	GM12878	blood:	n/a	n/a
38	BATF	chr8:54500648-54500962	GM12878	blood:	n/a	n/a
39	BATF	chr8:54504995-54505293	GM12878	blood:	n/a	n/a
40	BATF	chr8:54674116-54674298	GM12878	blood:	n/a	n/a
41	BCL11A	chr8:54680671-54681266	GM12878	blood:	n/a	n/a
42	BCL11A	chr8:54680758-54681134	GM12878	blood:	n/a	n/a
43	BCL11A	chr8:54566743-54566909	GM12878	blood:	n/a	n/a
44	BCL11A	chr8:54570427-54570702	GM12878	blood:	n/a	n/a
45	BCL3	chr8:54680701-54681227	GM12878	blood:	n/a	n/a
46	BCLAF1	chr8:54680637-54681401	GM12878	blood:	n/a	n/a
47	BCLAF1	chr8:54674041-54674821	GM12878	blood:	n/a	n/a
48	BCLAF1	chr8:54680675-54681338	GM12878	blood:	n/a	n/a
49	BHLHE40	chr8:54636217-54636466	GM12878	blood:	n/a	n/a
50	BHLHE40	chr8:54570625-54570632	K562	blood:	n/a	n/a

(count:2077 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:54521834-54521884	GM06990	blood:	n/a
2	chr8:54641642-54641692	ECC-1	luminal epithelium:	n/a
3	chr8:54708636-54708686	BJ	skin:	n/a
4	chr8:54521834-54521884	GM06990	blood:	n/a
5	chr8:54641642-54641692	ECC-1	luminal epithelium:	n/a
6	chr8:54708636-54708686	BJ	skin:	n/a
7	chr8:54522246-54522296	AG04449	skin:	fetal
8	chr8:54507218-54507268	A549	lung:	n/a
9	chr8:54507218-54507268	MCF-7	breast:	n/a
10	chr8:54570293-54570343	HEK293	kidney:	embryo
11	chr8:54510816-54510866	NH-A	brain:	n/a
12	chr8:54562283-54562333	HEEpiC	esophagus:	n/a
13	chr8:54565721-54565771	HL-60	blood:	n/a
14	chr8:54671892-54671942	GM12878	blood:	n/a
15	chr8:54569999-54570049	NB4	blood:	n/a
16	chr8:54571020-54571070	HPAEpiC	pulmonary alveolar:	n/a
17	chr8:54573876-54573926	PANC-1	pancreas:	n/a
18	chr8:54671892-54671942	H1-hESC	embryonic stem cell:	embryo
19	chr8:54521834-54521884	U87	brain:	n/a
20	chr8:54687817-54687867	HL-60	blood:	n/a
21	chr8:54687817-54687867	HCF	heart:	n/a
22	chr8:54573876-54573926	HUVEC	blood vessel:	n/a
23	chr8:54573876-54573926	HCPEpiC	choroid plexus:	n/a
24	chr8:54507218-54507268	BJ	skin:	n/a
25	chr8:54571020-54571070	Jurkat	blood:	n/a
26	chr8:54507218-54507268	ECC-1	luminal epithelium:	n/a
27	chr8:54522246-54522296	LNCaP	prostate:	n/a
28	chr8:54605566-54605616	HEEpiC	esophagus:	n/a
29	chr8:54507532-54507582	HAEpiC	amniotic membrane:	n/a
30	chr8:54687817-54687867	Jurkat	blood:	n/a
31	chr8:54521834-54521884	HEEpiC	esophagus:	n/a
32	chr8:54605613-54605663	AG04450	lung:	fetal
33	chr8:54605788-54605838	HL-60	blood:	n/a
34	chr8:54570623-54570673	Caco-2	colon:	n/a
35	chr8:54720431-54720481	HEEpiC	esophagus:	n/a
36	chr8:54557599-54557649	AoSMC	blood vessel:	n/a
37	chr8:54605566-54605616	HepG2	liver:	n/a
38	chr8:54562283-54562333	ECC-1	luminal epithelium:	n/a
39	chr8:54505303-54505353	HepG2	liver:	n/a
40	chr8:54510816-54510866	MCF10A-Er-Src	breast:	n/a
41	chr8:54573841-54573891	AG04449	skin:	fetal
42	chr8:54720431-54720481	HCM	heart:	n/a
43	chr8:54573876-54573926	HNPCEpiC	eye:	n/a
44	chr8:54573841-54573891	K562	blood:	n/a
45	chr8:54562283-54562333	NHBE	bronchial:	n/a
46	chr8:54570623-54570673	SKMC	muscle:	n/a
47	chr8:54671892-54671942	ProgFib	skin:	n/a
48	chr8:54507118-54507168	GM19239	blood:	n/a
49	chr8:54504774-54504824	RPTEC	kidney:	n/a
50	chr8:54720431-54720481	GM12891	blood:	n/a

(count:85 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:54614266..54615818-chr8:54636955..54638612,2	K562	blood:
2	chr8:54707662..54709513-chr8:54713902..54716199,2	K562	blood:
3	chr8:54685671..54687300-chr8:54728905..54731468,2	MCF-7	breast:
4	chr8:54640506..54642635-chr8:54647079..54648821,2	K562	blood:
5	chr8:54577235..54579753-chr8:54579803..54581358,2	MCF-7	breast:
6	chr8:54709889..54711878-chr8:54714434..54716224,2	K562	blood:
7	chr8:54652211..54654707-chr8:54657866..54660858,2	MCF-7	breast:
8	chr8:54640318..54643345-chr8:54643961..54649280,5	MCF-7	breast:
9	chr8:54500891..54501616-chr8:54619259..54619767,2	MCF-7	breast:
10	chr8:54561725..54563448-chr8:54565234..54566808,2	K562	blood:
11	chr8:54629241..54631291-chr8:54638690..54641108,3	MCF-7	breast:
12	chr8:54669633..54671247-chr8:54674350..54676508,2	K562	blood:
13	chr8:54563689..54565236-chr8:54567231..54570214,2	K562	blood:
14	chr8:54654556..54656764-chr8:54720675..54722580,2	MCF-7	breast:
15	chr8:54627356..54630312-chr8:54633637..54635175,2	K562	blood:
16	chr8:54736720..54739090-chr8:54754502..54756079,2	K562	blood:
17	chr8:54620507..54623207-chr8:54638020..54640255,2	K562	blood:
18	chr8:54669747..54672193-chr8:54674369..54676508,2	K562	blood:
19	chr8:54547138..54549363-chr8:54573155..54575642,2	MCF-7	breast:
20	chr8:54614266..54615818-chr8:54636955..54638612,2	K562	blood:
21	chr8:54726065..54728887-chr8:54733160..54735179,2	MCF-7	breast:
22	chr8:54654853..54656684-chr8:54661881..54664357,2	MCF-7	breast:
23	chr8:54614151..54616881-chr8:54622890..54625467,2	MCF-7	breast:
24	chr8:54640506..54642635-chr8:54647079..54648821,2	K562	blood:
25	chr8:54702587..54705497-chr8:54714078..54716603,2	K562	blood:
26	chr8:54669633..54671247-chr8:54674350..54676508,2	K562	blood:
27	chr8:54632819..54637804-chr8:54638171..54641276,4	MCF-7	breast:
28	chr8:54647209..54647746-chr8:54721040..54721617,3	MCF-7	breast:
29	chr8:54733544..54735901-chr8:54752993..54755423,2	MCF-7	breast:
30	chr8:54667680..54670590-chr8:54671196..54673684,2	K562	blood:
31	chr8:54647209..54647746-chr8:54721040..54721617,3	MCF-7	breast:
32	chr5:151522783..151523283-chr8:54673594..54674407,2	NB4	blood:
33	chr8:54685269..54687285-chr8:54688387..54691070,4	K562	blood:
34	chr8:54547138..54549363-chr8:54573155..54575642,2	MCF-7	breast:
35	chr8:54631323..54633867-chr8:54635784..54637550,2	K562	blood:
36	chr8:54672064..54673646-chr8:54673878..54676217,2	MCF-7	breast:
37	chr8:54654375..54655195-chr8:54720875..54721883,7	MCF-7	breast:
38	chr8:54539383..54541156-chr8:54547912..54549422,2	K562	blood:
39	chr8:54690844..54693046-chr8:54700903..54703804,2	K562	blood:
40	chr8:53878134..53878972-chr8:54721059..54722142,3	K562	blood:
41	chr8:54662153..54663773-chr8:54755567..54757091,2	MCF-7	breast:
42	chr8:54569929..54571839-chr8:54577373..54579144,2	K562	blood:
43	chr8:54672064..54673646-chr8:54673878..54676217,2	MCF-7	breast:
44	chr8:54556956..54558528-chr8:54569373..54571068,2	MCF-7	breast:
45	chr8:54482970..54485884-chr8:54754833..54757181,2	MCF-7	breast:
46	chr8:54629241..54631291-chr8:54638690..54641108,3	MCF-7	breast:
47	chr8:54654375..54655195-chr8:54720875..54721883,7	MCF-7	breast:
48	chr8:54632819..54637804-chr8:54638171..54641276,4	MCF-7	breast:
49	chr8:54631323..54633867-chr8:54635784..54637550,2	K562	blood:
50	chr8:54651332..54653261-chr8:54754407..54756402,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V1H-6	chr8:54474642-54474950	l_3595_chr8:54474263-54476685_ovary
2	lnc-ATP6V1H-6	chr8:54474264-54474610	l_3595_chr8:54474263-54476685_ovary
3	lnc-ATP6V1H-6	chr8:54476593-54476685	l_3595_chr8:54474263-54476685_ovary
4	lnc-ATP6V1H-4	chr8:54590284-54592067	ucscGeneNc_uc003xrj_1
5	lnc-ATP6V1H-4	chr8:54598442-54599044	ucscGeneNc_uc003xrj_1

No data

Variant related genes	Relation type
ATP6V1H	TF binding region
ENSG00000253668	TF binding region
ATP6V1H	CpG island
ENSG00000253668	CpG island
ENSG00000253668	chromatin interactions
ENSG00000047249	chromatin interactions

Extended variants
information (count: 8976 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:8976 , 50 per page) page: 1 2 3 4 5 6 7 ... 180

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548608895	chr8:54474672-54474673	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs568454120	chr8:54474683-54474684	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs534320985	chr8:54474709-54474710	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs530139702	chr8:54474711-54474712	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs368892006	chr8:54474750-54474751	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs570924491	chr8:54474764-54474765	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs182230103	chr8:54474767-54474768	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs556434891	chr8:54474827-54474828	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs576721936	chr8:54474842-54474843	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs147644483	chr8:54474921-54474922	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs554585402	chr8:54474935-54474936	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs140826010	chr8:54474946-54474947	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs574071580	chr8:54474975-54474976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539812587	chr8:54474979-54474980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576746767	chr8:54476668-54476669	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs534300215	chr8:54476678-54476679	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs539546072	chr8:54476679-54476680	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs542050197	chr8:54476809-54476810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs2086072	chr8:54476824-54476825	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs537308082	chr8:54476854-54476855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs180879788	chr8:54476888-54476889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs557536067	chr8:54476908-54476909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564503019	chr8:54476929-54476930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs7461954	chr8:54476968-54476969	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs141519992	chr8:54476988-54476989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563637713	chr8:54477026-54477027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs150885333	chr8:54477049-54477050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs185122781	chr8:54477086-54477087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565925809	chr8:54477099-54477100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs535018227	chr8:54477188-54477189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551635282	chr8:54477192-54477193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571880522	chr8:54477193-54477194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190276233	chr8:54477194-54477195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs548433457	chr8:54477213-54477214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536784822	chr8:54477260-54477261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182543759	chr8:54477275-54477276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs186172015	chr8:54477277-54477278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191737688	chr8:54477278-54477279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs536938092	chr8:54477350-54477351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs371190054	chr8:54477357-54477358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs184025607	chr8:54477383-54477384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs370566054	chr8:54477405-54477406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs573478801	chr8:54477426-54477427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs541202393	chr8:54477440-54477441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs78737393	chr8:54477454-54477455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189055765	chr8:54477476-54477477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553487802	chr8:54477523-54477524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539200997	chr8:54477528-54477529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573302140	chr8:54477565-54477566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs193013561	chr8:54477594-54477595	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	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
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
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	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
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Uveal melanoma	20484589	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:4948 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:54474600-54475000	Enhancers	H9 Cell Line	embryonic stem cell
2	chr8:54476800-54478200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr8:54477000-54477400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:54477000-54477600	Enhancers	Colon Smooth Muscle	Colon
5	chr8:54477400-54477800	Enhancers	Placenta Amnion	Placenta Amnion
6	chr8:54486200-54486600	Enhancers	Esophagus	oesophagus
7	chr8:54486200-54486600	Enhancers	Pancreas	Pancrea
8	chr8:54492600-54495800	Enhancers	HUVEC	blood vessel
9	chr8:54494400-54495000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:54494400-54495200	Enhancers	Fetal Kidney	kidney
11	chr8:54495000-54496600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr8:54496600-54496800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr8:54496800-54500200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr8:54497400-54497600	Enhancers	Aorta	Aorta
15	chr8:54499600-54499800	Enhancers	H1 Cell Line	embryonic stem cell
16	chr8:54499800-54500800	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr8:54500000-54501400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr8:54500200-54501000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr8:54500200-54501000	Enhancers	Fetal Heart	heart
20	chr8:54500200-54501200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr8:54500200-54501200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr8:54500200-54501200	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr8:54500200-54501200	Enhancers	HSMMtube	muscle
24	chr8:54500200-54501400	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr8:54500400-54500800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr8:54500400-54500800	Weak transcription	Aorta	Aorta
27	chr8:54500400-54501200	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr8:54500400-54501200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr8:54500400-54501200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr8:54500600-54501200	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr8:54500600-54501200	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr8:54500600-54501200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr8:54500600-54501200	Enhancers	Fetal Lung	lung
34	chr8:54500800-54501000	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr8:54500800-54501000	Enhancers	Adipose Nuclei	Adipose
36	chr8:54500800-54501000	Enhancers	Fetal Muscle Leg	muscle
37	chr8:54500800-54501000	Enhancers	Pancreas	Pancrea
38	chr8:54500800-54501200	Enhancers	H1 Cell Line	embryonic stem cell
39	chr8:54500800-54501200	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr8:54500800-54501200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr8:54500800-54501200	Enhancers	Aorta	Aorta
42	chr8:54500800-54501200	Enhancers	Ovary	ovary
43	chr8:54500800-54501200	Enhancers	GM12878-XiMat	blood
44	chr8:54501000-54501200	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr8:54501000-54501400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr8:54501000-54502000	Weak transcription	Adipose Nuclei	Adipose
47	chr8:54501000-54502000	Weak transcription	Fetal Muscle Leg	muscle
48	chr8:54501000-54502000	Weak transcription	Pancreas	Pancrea
49	chr8:54501000-54504400	Weak transcription	Fetal Heart	heart
50	chr8:54501200-54502200	Weak transcription	Aorta	Aorta

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