Variant report

Variant	nsv548277
Chromosome Location	chr1:179319868-179333194
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:64)
CpG islands
(count:184)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:64 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:179332575-179332913	K562	blood:	n/a	n/a
2	ATF1	chr1:179332419-179332755	K562	blood:	n/a	n/a
3	BHLHE40	chr1:179332521-179332721	K562	blood:	n/a	n/a
4	CEBPB	chr1:179329778-179330058	HepG2	liver:	n/a	chr1:179329888-179329901
5	CEBPB	chr1:179321177-179321297	HepG2	liver:	n/a	n/a
6	CTCF	chr1:179327970-179328026	Lung_OC	lung:	n/a	n/a
7	E2F4	chr1:179325379-179325573	MCF10A-Er-Src	breast:	n/a	n/a
8	EP300	chr1:179332413-179332796	K562	blood:	n/a	n/a
9	FOS	chr1:179320526-179320711	MCF10A-Er-Src	breast:	n/a	chr1:179320598-179320607
10	FOS	chr1:179322805-179323074	MCF10A-Er-Src	breast:	n/a	n/a
11	FOS	chr1:179322829-179322913	MCF10A-Er-Src	breast:	n/a	n/a
12	FOSL2	chr1:179322690-179322963	HepG2	liver:	n/a	n/a
13	FOSL2	chr1:179322702-179323199	SK-N-SH	brain:	n/a	n/a
14	GATA2	chr1:179332443-179332967	HUVEC	blood vessel:	n/a	n/a
15	IRF1	chr1:179332206-179332336	K562	blood:	n/a	n/a
16	JUND	chr1:179332429-179332803	K562	blood:	n/a	n/a
17	JUND	chr1:179322747-179323031	HepG2	liver:	n/a	chr1:179322895-179322906
18	JUND	chr1:179322870-179323060	H1-hESC	embryonic stem cell:	n/a	chr1:179322895-179322906
19	JUND	chr1:179322774-179323075	K562	blood:	n/a	chr1:179322895-179322906
20	MAFK	chr1:179332585-179332723	K562	blood:	n/a	n/a
21	MAX	chr1:179332569-179332802	K562	blood:	n/a	n/a
22	MAZ	chr1:179332508-179332725	K562	blood:	n/a	n/a
23	MXI1	chr1:179322739-179322880	GM12878	blood:	n/a	n/a
24	MYC	chr1:179332290-179332626	K562	blood:	n/a	n/a
25	NR2F2	chr1:179332430-179332775	K562	blood:	n/a	n/a
26	PBX3	chr1:179322772-179323202	SK-N-SH	brain:	n/a	n/a
27	POLR2A	chr1:179329337-179329567	Hela-S3	cervix:	n/a	n/a
28	POLR2A	chr1:179332512-179332817	K562	blood:	n/a	n/a
29	POLR2A	chr1:179324271-179324305	A549	lung:	n/a	n/a
30	POLR2A	chr1:179330444-179330568	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr1:179328573-179328894	K562	blood:	n/a	n/a
32	POLR2A	chr1:179332035-179332135	K562	blood:	n/a	n/a
33	POLR2A	chr1:179326891-179326943	HepG2	liver:	n/a	n/a
34	POLR2A	chr1:179329086-179329302	HepG2	liver:	n/a	n/a
35	POLR2A	chr1:179328666-179328733	HepG2	liver:	n/a	n/a
36	POLR2A	chr1:179324080-179324223	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr1:179328508-179328541	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr1:179328356-179328630	HepG2	liver:	n/a	n/a
39	POLR2A	chr1:179323168-179323411	K562	blood:	n/a	n/a
40	POLR2A	chr1:179328588-179329025	Hela-S3	cervix:	n/a	n/a
41	POLR2A	chr1:179324262-179324814	K562	blood:	n/a	n/a
42	POLR2A	chr1:179329333-179329473	HepG2	liver:	n/a	n/a
43	POLR2A	chr1:179327769-179327884	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr1:179327924-179328083	K562	blood:	n/a	n/a
45	POLR2A	chr1:179325503-179327637	K562	blood:	n/a	n/a
46	POLR2A	chr1:179329353-179329476	GM12878	blood:	n/a	n/a
47	POLR2A	chr1:179326845-179326890	HepG2	liver:	n/a	n/a
48	POLR2A	chr1:179327415-179327763	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr1:179331037-179331459	K562	blood:	n/a	n/a
50	POLR2A	chr1:179329529-179329556	HepG2	liver:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:179322762-179322812	BJ	skin:	n/a
2	chr1:179322762-179322812	BJ	skin:	n/a
3	chr1:179324199-179324249	SK-N-SH	brain:	n/a
4	chr1:179332148-179332198	PANC-1	pancreas:	n/a
5	chr1:179324199-179324249	Hepatocyte	liver:	n/a
6	chr1:179324199-179324249	Hela-S3	cervix:	n/a
7	chr1:179332148-179332198	GM19239	blood:	n/a
8	chr1:179324199-179324249	Caco-2	colon:	n/a
9	chr1:179332148-179332198	AG09319	gingival:	n/a
10	chr1:179332148-179332198	GM12891	blood:	n/a
11	chr1:179324199-179324249	HCPEpiC	choroid plexus:	n/a
12	chr1:179322762-179322812	AG04449	skin:	fetal
13	chr1:179332148-179332198	Caco-2	colon:	n/a
14	chr1:179332148-179332198	GM06990	blood:	n/a
15	chr1:179322762-179322812	Hela-S3	cervix:	n/a
16	chr1:179332148-179332198	GM12878	blood:	n/a
17	chr1:179322762-179322812	ProgFib	skin:	n/a
18	chr1:179324199-179324249	HL-60	blood:	n/a
19	chr1:179322762-179322812	SK-N-MC	brain:	n/a
20	chr1:179322762-179322812	T-47D	breast:	n/a
21	chr1:179324199-179324249	ovcar-3	ovarian:	n/a
22	chr1:179322762-179322812	Jurkat	blood:	n/a
23	chr1:179324199-179324249	U87	brain:	n/a
24	chr1:179322762-179322812	HepG2	liver:	n/a
25	chr1:179332148-179332198	Jurkat	blood:	n/a
26	chr1:179322762-179322812	GM12892	blood:	n/a
27	chr1:179324199-179324249	AoSMC	blood vessel:	n/a
28	chr1:179324199-179324249	IMR90	lung:	fetal
29	chr1:179322762-179322812	MCF10A-Er-Src	breast:	n/a
30	chr1:179322762-179322812	SK-N-SH	brain:	n/a
31	chr1:179332148-179332198	AG04449	skin:	fetal
32	chr1:179322762-179322812	AG09309	skin:	n/a
33	chr1:179324199-179324249	Jurkat	blood:	n/a
34	chr1:179332148-179332198	HepG2	liver:	n/a
35	chr1:179322762-179322812	CMK	blood:	n/a
36	chr1:179322762-179322812	ovcar-3	ovarian:	n/a
37	chr1:179324199-179324249	K562	blood:	n/a
38	chr1:179322762-179322812	HAEpiC	amniotic membrane:	n/a
39	chr1:179332148-179332198	SK-N-MC	brain:	n/a
40	chr1:179332148-179332198	AG10803	skin:	n/a
41	chr1:179324199-179324249	HRPEpiC	eye:	n/a
42	chr1:179332148-179332198	HUVEC	blood vessel:	n/a
43	chr1:179324199-179324249	HEK293	kidney:	embryo
44	chr1:179332148-179332198	K562	blood:	n/a
45	chr1:179332148-179332198	NT2-D1	testis:	n/a
46	chr1:179324199-179324249	HAEpiC	amniotic membrane:	n/a
47	chr1:179324199-179324249	MCF-7	breast:	n/a
48	chr1:179324199-179324249	SK-N-SH_RA	brain:	n/a
49	chr1:179322762-179322812	HRE	kidney:	n/a
50	chr1:179322762-179322812	HL-60	blood:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:179332952..179336574-chr1:179337996..179342859,7	MCF-7	breast:
2	chr1:179048972..179052099-chr1:179331450..179336701,5	MCF-7	breast:
3	chr1:179049229..179051266-chr1:179328606..179330148,2	MCF-7	breast:
4	chr1:179324764..179330437-chr1:179332106..179336685,6	K562	blood:
5	chr1:179050571..179052997-chr1:179322581..179325112,2	MCF-7	breast:
6	chr1:179317813..179319571-chr1:179319821..179322785,2	K562	blood:
7	chr1:179316253..179318749-chr1:179321719..179323631,3	MCF-7	breast:
8	chr1:179315825..179319571-chr1:179319821..179322785,4	K562	blood:
9	chr1:179319158..179320695-chr1:179327831..179330357,2	K562	blood:
10	chr1:179319218..179322738-chr1:179324103..179326545,3	K562	blood:
11	chr1:179317813..179320620-chr1:179325439..179328200,3	MCF-7	breast:
12	chr1:179319158..179320695-chr1:179327831..179330357,2	K562	blood:
13	chr1:179325938..179328666-chr1:179330165..179332477,2	K562	blood:
14	chr1:179303201..179305368-chr1:179327214..179329206,2	MCF-7	breast:
15	chr1:179323629..179325492-chr1:179329945..179332466,2	MCF-7	breast:
16	chr1:179319218..179322738-chr1:179324103..179326545,3	K562	blood:
17	chr1:179315802..179317742-chr1:179327309..179329268,2	K562	blood:
18	chr1:179329907..179332888-chr1:179333300..179336235,2	MCF-7	breast:
19	chr1:179314011..179316743-chr1:179317198..179320043,2	K562	blood:
20	chr1:179323629..179325492-chr1:179329945..179332466,2	MCF-7	breast:
21	chr1:179321788..179324308-chr1:179333616..179335747,3	MCF-7	breast:
22	chr1:179317813..179320620-chr1:179325439..179328200,3	MCF-7	breast:
23	chr1:179330939..179332441-chr1:179334465..179336040,2	MCF-7	breast:
24	chr1:179325938..179328666-chr1:179330165..179332477,2	K562	blood:

No data

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SOAT1	hsa-miR-192-5p	chr1:179323373-179323394
2	SOAT1	hsa-miR-215-5p	chr1:179322901-179322921
3	SOAT1	hsa-miR-192-5p	chr1:179322901-179322921
4	SOAT1	hsa-miR-192-5p	chr1:179323550-179323571
5	SOAT1	hsa-miR-215-5p	chr1:179323373-179323394
6	SOAT1	hsa-miR-215-5p	chr1:179323550-179323571

Variant related genes	Relation type
RN7SL374P	TF binding region
AXDND1	TF binding region
RN7SL374P	CpG island
AXDND1	CpG island
ENSG00000263633	chromatin interactions
ENSG00000186283	chromatin interactions
ENSG00000162779	chromatin interactions

Extended variants
information (count: 552 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10913734	chr1:179319868-179319869	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs75929253	chr1:179319869-179319870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185100117	chr1:179319870-179319871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555516959	chr1:179319877-179319878	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370491059	chr1:179319910-179319911	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140065470	chr1:179319955-179319956	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs190097450	chr1:179319956-179319957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs563953080	chr1:179320020-179320021	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116224034	chr1:179320089-179320090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546121237	chr1:179320114-179320115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559594111	chr1:179320137-179320138	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79875667	chr1:179320139-179320140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs201449849	chr1:179320157-179320158	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12045396	chr1:179320160-179320161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs12045399	chr1:179320169-179320170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs202206253	chr1:179320173-179320174	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200510703	chr1:179320182-179320183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561782064	chr1:179320183-179320184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs13306727	chr1:179320249-179320250	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs568467469	chr1:179320253-179320254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531082761	chr1:179320263-179320264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs13306730	chr1:179320279-179320280	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs372288622	chr1:179320333-179320334	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555236880	chr1:179320366-179320367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372653119	chr1:179320367-179320368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192941228	chr1:179320379-179320380	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138504513	chr1:179320466-179320467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184723206	chr1:179320477-179320478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs139216715	chr1:179320484-179320485	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189625699	chr1:179320492-179320493	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149504397	chr1:179320507-179320508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144676710	chr1:179320540-179320541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200291571	chr1:179320575-179320576	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs13306731	chr1:179320578-179320579	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs180878250	chr1:179320593-179320594	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs199593729	chr1:179320597-179320598	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs13306732	chr1:179320665-179320666	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs373875383	chr1:179320684-179320685	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544334552	chr1:179320698-179320699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs557551616	chr1:179320708-179320709	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185431453	chr1:179320750-179320751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs13306733	chr1:179320758-179320759	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs139344930	chr1:179320798-179320799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs56303406	chr1:179320845-179320846	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs71901753	chr1:179320857-179320858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375921751	chr1:179320872-179320873	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs76542429	chr1:179320873-179320874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528717412	chr1:179320893-179320894	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542116739	chr1:179320917-179320918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562155497	chr1:179320922-179320923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	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
Glioblastoma multiforme	21080181	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
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	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
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Breast cancer	16397240	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	23248035	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:303 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179264800-179334200	Weak transcription	Colon Smooth Muscle	Colon
2	chr1:179266400-179322800	Weak transcription	Small Intestine	intestine
3	chr1:179292400-179328000	Weak transcription	Rectal Smooth Muscle	rectum
4	chr1:179293000-179322600	Weak transcription	Fetal Heart	heart
5	chr1:179294200-179324600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr1:179296800-179327800	Weak transcription	Colonic Mucosa	Colon
7	chr1:179297400-179321600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr1:179298600-179324200	Weak transcription	Thymus	Thymus
9	chr1:179300400-179334600	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr1:179300600-179322400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr1:179301800-179322800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr1:179303200-179324600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr1:179303400-179322600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr1:179304200-179320000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr1:179304200-179324400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:179304200-179324400	Strong transcription	Primary T cells fromperipheralblood	blood
17	chr1:179304200-179324600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr1:179304200-179325200	Strong transcription	Primary T helper cells fromperipheralblood	blood
19	chr1:179304400-179324400	Strong transcription	Primary T helper cells PMA-I stimulated	--
20	chr1:179304600-179324200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr1:179305200-179327200	Weak transcription	Right Ventricle	heart
22	chr1:179305600-179334200	Weak transcription	Pancreas	Pancrea
23	chr1:179305800-179322600	Weak transcription	Brain Cingulate Gyrus	brain
24	chr1:179306000-179321000	Strong transcription	Dnd41	blood
25	chr1:179306800-179324600	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr1:179307400-179325800	Weak transcription	Esophagus	oesophagus
27	chr1:179307600-179322600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr1:179307600-179325200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr1:179307800-179322200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr1:179308000-179321000	Weak transcription	Fetal Brain Male	brain
31	chr1:179308000-179324400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr1:179308400-179322600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr1:179308600-179322000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr1:179308800-179320800	Strong transcription	Osteobl	bone
35	chr1:179309800-179326400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr1:179310000-179325200	Strong transcription	Primary T cells from cord blood	blood
37	chr1:179310200-179322000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr1:179310200-179323000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr1:179310400-179322800	Weak transcription	Aorta	Aorta
40	chr1:179310400-179324400	Strong transcription	Primary B cells from peripheral blood	blood
41	chr1:179311200-179325200	Strong transcription	Monocytes-CD14+_RO01746	blood
42	chr1:179311600-179320800	Strong transcription	Sigmoid Colon	Sigmoid Colon
43	chr1:179311600-179326400	Strong transcription	Primary monocytes fromperipheralblood	blood
44	chr1:179311800-179321200	Strong transcription	Duodenum Mucosa	Duodenum
45	chr1:179312000-179324200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr1:179312000-179324800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr1:179312200-179322400	Weak transcription	HMEC	breast
48	chr1:179312200-179322600	Weak transcription	Stomach Mucosa	stomach
49	chr1:179312200-179325200	Strong transcription	Liver	Liver
50	chr1:179312600-179320800	Strong transcription	Rectal Mucosa Donor 31	rectum

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