Variant report

Variant	nsv872527
Chromosome Location	chr1:168327555-168375973
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:913)
CpG islands
(count:488)
Chromatin interactive
region (count:43)
LncRNA
region (count:4)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:913 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:168332394-168332589	K562	blood:	n/a	n/a
2	ARID3A	chr1:168368284-168368533	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:168343229-168343407	K562	blood:	n/a	n/a
4	ARID3A	chr1:168335503-168335579	K562	blood:	n/a	n/a
5	ARID3A	chr1:168337311-168337679	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:168368098-168368571	K562	blood:	n/a	n/a
7	ARID3A	chr1:168371924-168371935	K562	blood:	n/a	n/a
8	ARID3A	chr1:168335006-168335245	K562	blood:	n/a	n/a
9	ATF1	chr1:168330012-168330212	K562	blood:	n/a	n/a
10	ATF1	chr1:168373187-168373436	K562	blood:	n/a	n/a
11	ATF1	chr1:168332337-168332598	K562	blood:	n/a	n/a
12	ATF1	chr1:168342118-168342700	K562	blood:	n/a	n/a
13	ATF1	chr1:168343203-168343424	K562	blood:	n/a	n/a
14	ATF1	chr1:168335008-168335286	K562	blood:	n/a	n/a
15	ATF1	chr1:168341584-168341901	K562	blood:	n/a	n/a
16	ATF2	chr1:168356361-168357102	H1-hESC	embryonic stem cell:	n/a	chr1:168356575-168356589 chr1:168356577-168356588
17	ATF2	chr1:168356434-168356843	H1-hESC	embryonic stem cell:	n/a	chr1:168356575-168356589 chr1:168356577-168356588
18	ATF3	chr1:168368315-168368701	K562	blood:	n/a	n/a
19	ATF3	chr1:168343126-168343426	K562	blood:	n/a	n/a
20	ATF3	chr1:168368138-168368658	K562	blood:	n/a	n/a
21	ATF3	chr1:168355801-168356057	K562	blood:	n/a	n/a
22	BACH1	chr1:168356174-168356821	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr1:168361870-168362573	K562	blood:	n/a	chr1:168362330-168362344
24	BACH1	chr1:168361902-168361929	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr1:168334918-168335322	K562	blood:	n/a	n/a
26	BACH1	chr1:168362166-168362509	H1-hESC	embryonic stem cell:	n/a	chr1:168362330-168362344
27	BACH1	chr1:168357056-168357360	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr1:168368283-168368645	H1-hESC	embryonic stem cell:	n/a	chr1:168368437-168368451
29	BACH1	chr1:168368271-168368612	K562	blood:	n/a	chr1:168368437-168368451
30	BCL3	chr1:168348281-168348839	A549	lung:	n/a	chr1:168348563-168348572 chr1:168348562-168348571
31	BHLHE40	chr1:168368298-168368602	K562	blood:	n/a	n/a
32	BHLHE40	chr1:168347732-168348156	K562	blood:	n/a	n/a
33	BHLHE40	chr1:168332390-168332553	K562	blood:	n/a	n/a
34	BHLHE40	chr1:168371828-168371933	K562	blood:	n/a	n/a
35	BHLHE40	chr1:168343187-168343406	K562	blood:	n/a	n/a
36	BHLHE40	chr1:168367875-168367885	K562	blood:	n/a	n/a
37	BHLHE40	chr1:168335065-168335538	K562	blood:	n/a	n/a
38	BHLHE40	chr1:168362300-168362316	K562	blood:	n/a	n/a
39	BHLHE40	chr1:168341818-168342686	K562	blood:	n/a	n/a
40	BHLHE40	chr1:168338996-168339285	K562	blood:	n/a	n/a
41	BRCA1	chr1:168366205-168366816	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr1:168375019-168375412	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr1:168359647-168359700	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr1:168356568-168356732	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr1:168361083-168361740	Hela-S3	cervix:	n/a	n/a
46	CBX3	chr1:168374736-168375745	HCT-116	colon:	n/a	n/a
47	CBX3	chr1:168334932-168335691	K562	blood:	n/a	n/a
48	CBX3	chr1:168341561-168342695	K562	blood:	n/a	n/a
49	CBX3	chr1:168368139-168368604	K562	blood:	n/a	n/a
50	CCNT2	chr1:168371887-168372219	K562	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:168356537-168356587	Hepatocyte	liver:	n/a
2	chr1:168356537-168356587	AG10803	skin:	n/a
3	chr1:168356673-168356723	RPTEC	kidney:	n/a
4	chr1:168356537-168356587	HNPCEpiC	eye:	n/a
5	chr1:168343945-168343995	MCF10A-Er-Src	breast:	n/a
6	chr1:168343339-168343389	ovcar-3	ovarian:	n/a
7	chr1:168356673-168356723	MCF10A-Er-Src	breast:	n/a
8	chr1:168356591-168356641	SK-N-SH	brain:	n/a
9	chr1:168356591-168356641	SK-N-MC	brain:	n/a
10	chr1:168356606-168356656	SKMC	muscle:	n/a
11	chr1:168356606-168356656	BE2_C	brain:	n/a
12	chr1:168356591-168356641	HCF	heart:	n/a
13	chr1:168344264-168344314	Caco-2	colon:	n/a
14	chr1:168356606-168356656	HAEpiC	amniotic membrane:	n/a
15	chr1:168344264-168344314	SKMC	muscle:	n/a
16	chr1:168356537-168356587	HMEC	breast:	n/a
17	chr1:168356673-168356723	MCF-7	breast:	n/a
18	chr1:168356537-168356587	LNCaP	prostate:	n/a
19	chr1:168344184-168344234	GM12878	blood:	n/a
20	chr1:168356591-168356641	SK-N-SH_RA	brain:	n/a
21	chr1:168343339-168343389	LNCaP	prostate:	n/a
22	chr1:168343945-168343995	SK-N-SH	brain:	n/a
23	chr1:168344264-168344314	SK-N-MC	brain:	n/a
24	chr1:168344264-168344314	HRCEpiC	kidney:	n/a
25	chr1:168344184-168344234	Hela-S3	cervix:	n/a
26	chr1:168356537-168356587	GM19239	blood:	n/a
27	chr1:168356591-168356641	A549	lung:	n/a
28	chr1:168343339-168343389	HEEpiC	esophagus:	n/a
29	chr1:168356606-168356656	HPAEpiC	pulmonary alveolar:	n/a
30	chr1:168356673-168356723	HEEpiC	esophagus:	n/a
31	chr1:168344184-168344234	HCF	heart:	n/a
32	chr1:168356591-168356641	HCT-116	colon:	n/a
33	chr1:168356673-168356723	PFSK-1	brain:	n/a
34	chr1:168356673-168356723	AG09319	gingival:	n/a
35	chr1:168344264-168344314	LNCaP	prostate:	n/a
36	chr1:168356537-168356587	GM12878	blood:	n/a
37	chr1:168356591-168356641	Jurkat	blood:	n/a
38	chr1:168343945-168343995	A549	lung:	n/a
39	chr1:168356673-168356723	HNPCEpiC	eye:	n/a
40	chr1:168344264-168344314	AG04449	skin:	fetal
41	chr1:168343945-168343995	IMR90	lung:	fetal
42	chr1:168343339-168343389	PANC-1	pancreas:	n/a
43	chr1:168356673-168356723	LNCaP	prostate:	n/a
44	chr1:168356673-168356723	AG04450	lung:	fetal
45	chr1:168344264-168344314	HAEpiC	amniotic membrane:	n/a
46	chr1:168343339-168343389	PFSK-1	brain:	n/a
47	chr1:168356591-168356641	HL-60	blood:	n/a
48	chr1:168343339-168343389	GM19239	blood:	n/a
49	chr1:168344264-168344314	MCF10A-Er-Src	breast:	n/a
50	chr1:168343945-168343995	BJ	skin:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:168335359..168337795-chr1:168345574..168348326,2	K562	blood:
2	chr1:168335359..168337795-chr1:168345574..168348326,2	K562	blood:
3	chr1:168372698..168375484-chr1:168376700..168379733,3	K562	blood:
4	chr1:168348118..168353414-chr1:168355151..168359007,7	MCF-7	breast:
5	chr1:168334562..168336538-chr1:168357801..168359534,2	K562	blood:
6	chr1:168366951..168368452-chr1:168372047..168373905,2	K562	blood:
7	chr1:168312661..168313699-chr1:168334688..168335805,3	K562	blood:
8	chr1:168349449..168351805-chr1:168370757..168373468,2	K562	blood:
9	chr1:168355026..168356826-chr1:168398882..168401309,2	K562	blood:
10	chr1:168349449..168351805-chr1:168370757..168373468,2	K562	blood:
11	chr1:168338940..168340901-chr1:168341151..168343365,2	MCF-7	breast:
12	chr1:168346129..168348064-chr1:168353010..168355199,2	K562	blood:
13	chr1:168368481..168370115-chr1:168372441..168374527,2	K562	blood:
14	chr1:168338940..168340901-chr1:168341151..168343365,2	MCF-7	breast:
15	chr1:168187433..168189118-chr1:168341371..168344286,2	K562	blood:
16	chr1:168360896..168362544-chr1:168366659..168368237,2	K562	blood:
17	chr1:168341145..168343864-chr1:168357058..168358969,2	K562	blood:
18	chr1:168368481..168370115-chr1:168372441..168374527,2	K562	blood:
19	chr1:168311666..168312512-chr1:168334779..168335573,2	MCF-7	breast:
20	chr1:168357609..168359334-chr1:168366941..168369901,2	K562	blood:
21	chr1:168333149..168334696-chr1:168337018..168339175,2	K562	blood:
22	chr1:168348118..168353414-chr1:168355151..168359007,7	MCF-7	breast:
23	chr1:168356981..168360579-chr1:168363528..168366891,3	MCF-7	breast:
24	chr1:168366951..168368657-chr1:168370802..168373547,2	K562	blood:
25	chr1:168342866..168344756-chr1:168372914..168374516,2	K562	blood:
26	chr1:168342866..168344756-chr1:168372914..168374516,2	K562	blood:
27	chr1:168360896..168362544-chr1:168366659..168368237,2	K562	blood:
28	chr1:168311877..168312534-chr1:168334700..168335638,2	K562	blood:
29	chr1:168343623..168346188-chr1:168350297..168353036,3	K562	blood:
30	chr1:168324913..168327529-chr1:168329698..168331377,2	K562	blood:
31	chr1:168334562..168336538-chr1:168357801..168359534,2	K562	blood:
32	chr1:168346129..168348064-chr1:168353010..168355199,2	K562	blood:
33	chr1:168356981..168360579-chr1:168363528..168366891,3	MCF-7	breast:
34	chr1:168341145..168343864-chr1:168357058..168358969,2	K562	blood:
35	chr1:168328202..168331069-chr1:168335120..168337354,2	K562	blood:
36	chr1:168311676..168312490-chr1:168334705..168335594,4	MCF-7	breast:
37	chr1:168366951..168368657-chr1:168370802..168373547,2	K562	blood:
38	chr1:168328202..168331069-chr1:168335120..168337354,2	K562	blood:
39	chr1:168311642..168312682-chr1:168331951..168332907,6	K562	blood:
40	chr1:168311615..168313900-chr1:168348090..168350975,2	MCF-7	breast:
41	chr1:168344082..168345767-chr1:168346742..168349715,2	K562	blood:
42	chr1:168366951..168368452-chr1:168372047..168373905,2	K562	blood:
43	chr1:168357609..168359334-chr1:168366941..168369901,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-XCL2-2	chr1:168370067-168371581	XLOC_001083
2	lnc-XCL2-2	chr1:168369427-168371581	NONHSAT007437
3	lnc-XCL2-2	chr1:168370721-168370768	XLOC_001083
4	lnc-XCL2-2	chr1:168371277-168371581	XLOC_001083

miRNA name	Chromosome Location	mirBase accession
hsa-miR-557	chr1:168344822-168344844	MIMAT0003221

No data

Variant related genes	Relation type
MIR557	TF binding region
ENSG00000227722	TF binding region
MIR557	CpG island
ENSG00000227722	CpG island
ENSG00000207974	chromatin interactions
ENSG00000227722	chromatin interactions

Extended variants
information (count: 1788 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1788 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10800356	chr1:168327555-168327556	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs376053760	chr1:168327610-168327611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs76684195	chr1:168327613-168327614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570361010	chr1:168327615-168327616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528352092	chr1:168327673-168327674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531087973	chr1:168327694-168327695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546856151	chr1:168327698-168327699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182311158	chr1:168327714-168327715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529395867	chr1:168327716-168327717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185889526	chr1:168327725-168327726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552782040	chr1:168327745-168327746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190810108	chr1:168327772-168327773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553790112	chr1:168327795-168327796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs145188149	chr1:168327802-168327803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs144239134	chr1:168327807-168327808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566833864	chr1:168327809-168327810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368349055	chr1:168327812-168327813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141986994	chr1:168327845-168327846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555588529	chr1:168327881-168327882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374060411	chr1:168327938-168327939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs118003959	chr1:168327949-168327950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200237478	chr1:168327950-168327951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183122946	chr1:168327976-168327977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539296525	chr1:168328109-168328110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs386636546	chr1:168328119-168328120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs57956428	chr1:168328120-168328121	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs540511080	chr1:168328157-168328158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535453016	chr1:168328159-168328160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190354839	chr1:168328208-168328209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542087492	chr1:168328223-168328224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529101570	chr1:168328242-168328243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113238143	chr1:168328281-168328282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182979646	chr1:168328300-168328301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533230376	chr1:168328310-168328311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs562295043	chr1:168328314-168328315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs149590979	chr1:168328367-168328368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs566527095	chr1:168328453-168328454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528008227	chr1:168328494-168328495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549252901	chr1:168328548-168328549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567832635	chr1:168328565-168328566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528017396	chr1:168328679-168328680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556437301	chr1:168328718-168328719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568972330	chr1:168328733-168328734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539534741	chr1:168328784-168328785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4656583	chr1:168328834-168328835	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs572860440	chr1:168328835-168328836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540200493	chr1:168328843-168328844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187652476	chr1:168328912-168328913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2900726	chr1:168329037-168329038	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs12352147	chr1:168329039-168329040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:533 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:168318400-168329200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr1:168318400-168329400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr1:168318400-168329400	Weak transcription	Colon Smooth Muscle	Colon
4	chr1:168325000-168329200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr1:168325400-168330600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr1:168327200-168327600	Enhancers	HepG2	liver
7	chr1:168327600-168329400	Weak transcription	HepG2	liver
8	chr1:168329200-168329400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr1:168329200-168329400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr1:168329200-168329600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
11	chr1:168329200-168330400	Enhancers	Rectal Smooth Muscle	rectum
12	chr1:168329200-168330600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr1:168329200-168331200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr1:168329200-168331400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr1:168329200-168331600	Enhancers	Fetal Heart	heart
16	chr1:168329200-168332200	Enhancers	Placenta Amnion	Placenta Amnion
17	chr1:168329400-168329600	Enhancers	Primary T helper naive cells from peripheral blood	blood
18	chr1:168329400-168329600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr1:168329400-168329600	Enhancers	NHDF-Ad	bronchial
20	chr1:168329400-168329800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr1:168329400-168329800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr1:168329400-168330200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr1:168329400-168330200	Enhancers	HepG2	liver
24	chr1:168329400-168330400	Enhancers	Adipose Nuclei	Adipose
25	chr1:168329400-168330600	Enhancers	Fetal Intestine Large	intestine
26	chr1:168329400-168330800	Enhancers	Colon Smooth Muscle	Colon
27	chr1:168329400-168331200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr1:168329400-168331200	Enhancers	Fetal Lung	lung
29	chr1:168329400-168333200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
30	chr1:168329400-168333200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr1:168329400-168333800	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr1:168329400-168334600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr1:168329600-168329800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr1:168329600-168329800	Enhancers	Right Atrium	heart
35	chr1:168329600-168330000	Enhancers	Stomach Mucosa	stomach
36	chr1:168329600-168330200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr1:168329600-168330800	Enhancers	Fetal Intestine Small	intestine
38	chr1:168329600-168331800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr1:168329600-168331800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr1:168329600-168333600	Enhancers	Primary T killer memory cells from peripheral blood	blood
41	chr1:168329600-168334000	Enhancers	Primary T cells fromperipheralblood	blood
42	chr1:168329800-168330600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr1:168329800-168330600	Weak transcription	Right Atrium	heart
44	chr1:168330000-168331200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr1:168330200-168330800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr1:168330200-168332000	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr1:168330200-168333600	Weak transcription	HepG2	liver
48	chr1:168330600-168330800	Enhancers	Right Atrium	heart
49	chr1:168330800-168333000	Weak transcription	Right Atrium	heart
50	chr1:168331200-168333000	Enhancers	Primary T helper cells PMA-I stimulated	--

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