Variant report

Variant	nsv1001191
Chromosome Location	chr1:179097246-179120938
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:487)
CpG islands
(count:244)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:487 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:179120877-179121723	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:179098249-179098469	K562	blood:	n/a	n/a
3	ATF1	chr1:179098888-179099123	K562	blood:	n/a	n/a
4	BHLHE40	chr1:179098858-179099223	GM12878	blood:	n/a	n/a
5	BHLHE40	chr1:179099024-179099096	K562	blood:	n/a	n/a
6	BRCA1	chr1:179111943-179112801	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr1:179111882-179112853	HCT-116	colon:	n/a	n/a
8	CBX3	chr1:179098150-179098767	HCT-116	colon:	n/a	n/a
9	CBX3	chr1:179111987-179112814	HCT-116	colon:	n/a	n/a
10	CBX3	chr1:179098178-179098735	HCT-116	colon:	n/a	n/a
11	CEBPB	chr1:179112039-179112841	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr1:179106692-179107273	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr1:179110994-179111335	IMR90	lung:	n/a	n/a
14	CEBPB	chr1:179112036-179112895	A549	lung:	n/a	n/a
15	CEBPB	chr1:179120901-179121555	A549	lung:	n/a	n/a
16	CEBPB	chr1:179098230-179098609	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr1:179106709-179107051	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPB	chr1:179111010-179111408	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:179106777-179107031	K562	blood:	n/a	n/a
20	CEBPB	chr1:179112120-179112789	A549	lung:	n/a	n/a
21	CEBPB	chr1:179112005-179112813	IMR90	lung:	n/a	n/a
22	CEBPB	chr1:179112025-179112877	HCT-116	colon:	n/a	n/a
23	CEBPB	chr1:179113813-179114058	IMR90	lung:	n/a	n/a
24	CEBPB	chr1:179106718-179107091	IMR90	lung:	n/a	n/a
25	CEBPB	chr1:179111947-179112920	HCT-116	colon:	n/a	n/a
26	CHD2	chr1:179098869-179099084	GM12878	blood:	n/a	n/a
27	CTCF	chr1:179097796-179097935	LNCaP	prostate:	n/a	n/a
28	CTCF	chr1:179097800-179097950	SAEC	small airway:	n/a	n/a
29	CTCF	chr1:179106780-179106930	HCM	heart:	n/a	n/a
30	CTCF	chr1:179106880-179107030	HPF	lung:	n/a	n/a
31	CTCF	chr1:179106940-179107090	HMF	breast:	n/a	n/a
32	CTCF	chr1:179115825-179115946	Medullo	brain:	n/a	n/a
33	CTCF	chr1:179106860-179107010	HVMF	connective:	n/a	n/a
34	CTCF	chr1:179097772-179097964	MCF-7	breast:	n/a	n/a
35	CTCF	chr1:179106780-179106930	HVMF	connective:	n/a	n/a
36	CTCF	chr1:179106840-179106990	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr1:179106880-179107030	AG09319	gingival:	n/a	n/a
38	CTCF	chr1:179106840-179106990	HPF	lung:	n/a	n/a
39	CTCF	chr1:179106860-179107010	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr1:179097785-179097977	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:179112222-179112284	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr1:179097782-179097971	MCF-7	breast:	n/a	n/a
43	CTCF	chr1:179098880-179099030	AG10803	skin:	n/a	n/a
44	CTCF	chr1:179097769-179097975	MCF-7	breast:	n/a	n/a
45	CTCF	chr1:179106920-179107070	AG10803	skin:	n/a	n/a
46	CTCF	chr1:179113408-179113450	GM13977	blood:	n/a	n/a
47	CTCF	chr1:179106920-179107070	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr1:179106860-179107010	AG04450	lung:	n/a	n/a
49	CTCF	chr1:179106940-179107090	AG10803	skin:	n/a	n/a
50	CTCF	chr1:179106900-179107050	SAEC	small airway:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:179100500-179100550	HCPEpiC	choroid plexus:	n/a
2	chr1:179104011-179104061	HCM	heart:	n/a
3	chr1:179100500-179100550	NHBE	bronchial:	n/a
4	chr1:179100500-179100550	MCF10A-Er-Src	breast:	n/a
5	chr1:179100500-179100550	U87	brain:	n/a
6	chr1:179104011-179104061	BJ	skin:	n/a
7	chr1:179104011-179104061	Caco-2	colon:	n/a
8	chr1:179112077-179112127	NHDF-neo	bronchial:	n/a
9	chr1:179112077-179112127	GM19239	blood:	n/a
10	chr1:179108412-179108462	BE2_C	brain:	n/a
11	chr1:179108412-179108462	HEK293	kidney:	embryo
12	chr1:179108412-179108462	HRCEpiC	kidney:	n/a
13	chr1:179100500-179100550	SKMC	muscle:	n/a
14	chr1:179112077-179112127	Hela-S3	cervix:	n/a
15	chr1:179104011-179104061	PFSK-1	brain:	n/a
16	chr1:179100500-179100550	HEK293	kidney:	embryo
17	chr1:179104011-179104061	NHBE	bronchial:	n/a
18	chr1:179108412-179108462	Jurkat	blood:	n/a
19	chr1:179112077-179112127	MCF10A-Er-Src	breast:	n/a
20	chr1:179104011-179104061	Hela-S3	cervix:	n/a
21	chr1:179100500-179100550	AG04449	skin:	fetal
22	chr1:179104011-179104061	GM12891	blood:	n/a
23	chr1:179100500-179100550	HCT-116	colon:	n/a
24	chr1:179104011-179104061	ovcar-3	ovarian:	n/a
25	chr1:179104011-179104061	T-47D	breast:	n/a
26	chr1:179108412-179108462	NHDF-neo	bronchial:	n/a
27	chr1:179104011-179104061	HCF	heart:	n/a
28	chr1:179108412-179108462	PFSK-1	brain:	n/a
29	chr1:179112077-179112127	HRPEpiC	eye:	n/a
30	chr1:179112077-179112127	SK-N-MC	brain:	n/a
31	chr1:179100500-179100550	GM12892	blood:	n/a
32	chr1:179100500-179100550	T-47D	breast:	n/a
33	chr1:179100500-179100550	NHDF-neo	bronchial:	n/a
34	chr1:179112077-179112127	HCPEpiC	choroid plexus:	n/a
35	chr1:179100500-179100550	AG10803	skin:	n/a
36	chr1:179104011-179104061	HPAEpiC	pulmonary alveolar:	n/a
37	chr1:179104011-179104061	SK-N-SH_RA	brain:	n/a
38	chr1:179108412-179108462	HUVEC	blood vessel:	n/a
39	chr1:179112077-179112127	ECC-1	luminal epithelium:	n/a
40	chr1:179104011-179104061	HMEC	breast:	n/a
41	chr1:179100500-179100550	HCF	heart:	n/a
42	chr1:179100500-179100550	HNPCEpiC	eye:	n/a
43	chr1:179112077-179112127	Caco-2	colon:	n/a
44	chr1:179108412-179108462	ECC-1	luminal epithelium:	n/a
45	chr1:179108412-179108462	H1-hESC	embryonic stem cell:	embryo
46	chr1:179104011-179104061	AG04449	skin:	fetal
47	chr1:179100500-179100550	HPAEpiC	pulmonary alveolar:	n/a
48	chr1:179104011-179104061	SK-N-MC	brain:	n/a
49	chr1:179112077-179112127	GM12891	blood:	n/a
50	chr1:179104011-179104061	PANC-1	pancreas:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:179108694..179110499-chr1:179120494..179123045,2	MCF-7	breast:
2	chr1:179075971..179079448-chr1:179095385..179098448,3	MCF-7	breast:
3	chr1:179091554..179094304-chr1:179109132..179111261,2	MCF-7	breast:
4	chr1:179097406..179100383-chr1:179127242..179129431,2	MCF-7	breast:
5	chr1:179110656..179113275-chr1:179262488..179264481,2	K562	blood:
6	chr1:179097711..179098293-chr1:179162847..179163421,2	MCF-7	breast:
7	chr1:179108694..179110499-chr1:179120494..179123045,2	MCF-7	breast:
8	chr1:179095025..179097028-chr1:179098926..179100910,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000234041	TF binding region
ABL2	TF binding region
ENSG00000234041	CpG island
ABL2	CpG island
ENSG00000057252	chromatin interactions

Extended variants
information (count: 929 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:929 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141589993	chr1:179097282-179097283	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs370481101	chr1:179097283-179097284	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs2816166	chr1:179097295-179097296	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs150478272	chr1:179097421-179097422	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570313465	chr1:179097427-179097428	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs367778538	chr1:179097428-179097429	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535782448	chr1:179097433-179097434	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535698752	chr1:179097439-179097440	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs575754286	chr1:179097473-179097474	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115096409	chr1:179097574-179097575	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564602465	chr1:179097581-179097582	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182405552	chr1:179097673-179097674	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs141495129	chr1:179097697-179097698	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs377618760	chr1:179097703-179097704	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs12075304	chr1:179097798-179097799	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs78111870	chr1:179097807-179097808	Weak transcription Genic enhancers Active TSS Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs529142217	chr1:179097808-179097809	Weak transcription Genic enhancers Active TSS Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs549055366	chr1:179097812-179097813	Weak transcription Genic enhancers Active TSS Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs555925699	chr1:179097866-179097867	Weak transcription Genic enhancers Active TSS Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs557419678	chr1:179097887-179097888	Weak transcription Genic enhancers Active TSS Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs185918983	chr1:179097896-179097897	Weak transcription Genic enhancers Active TSS Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs191165001	chr1:179097994-179097995	Weak transcription Genic enhancers Active TSS Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs11583272	chr1:179098084-179098085	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs527785799	chr1:179098085-179098086	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs540048017	chr1:179098086-179098087	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs541549029	chr1:179098128-179098129	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs182457887	chr1:179098131-179098132	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs558239633	chr1:179098143-179098144	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs533656695	chr1:179098145-179098146	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs547131569	chr1:179098188-179098189	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs566953549	chr1:179098223-179098224	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs185358385	chr1:179098319-179098320	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs555825293	chr1:179098328-179098329	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs560425582	chr1:179098355-179098356	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs2486995	chr1:179098475-179098476	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs76072391	chr1:179098556-179098557	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs142700976	chr1:179098558-179098559	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs368046067	chr1:179098594-179098595	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs147342420	chr1:179098595-179098596	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs558203014	chr1:179098618-179098619	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs2486996	chr1:179098633-179098634	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs374911734	chr1:179098674-179098675	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs563466406	chr1:179098675-179098676	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs182747658	chr1:179098677-179098678	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs573797152	chr1:179098684-179098685	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs542893449	chr1:179098739-179098740	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs138057082	chr1:179098757-179098758	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs2486997	chr1:179098770-179098771	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs200746188	chr1:179098791-179098792	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs12077877	chr1:179098811-179098812	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Lung adenocarcinoma	21935476	CNVD
Gastric cancer	22014070	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:1021 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179063200-179112000	Weak transcription	Fetal Kidney	kidney
2	chr1:179064800-179097800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr1:179078600-179097600	Weak transcription	Stomach Mucosa	stomach
4	chr1:179079600-179109800	Weak transcription	Small Intestine	intestine
5	chr1:179080000-179097800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr1:179080000-179097800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr1:179080000-179098600	Weak transcription	Esophagus	oesophagus
8	chr1:179080200-179101600	Weak transcription	Fetal Brain Male	brain
9	chr1:179080400-179103800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr1:179080800-179098400	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr1:179080800-179099000	Weak transcription	Colonic Mucosa	Colon
12	chr1:179080800-179099000	Weak transcription	Spleen	Spleen
13	chr1:179086600-179105000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr1:179086800-179099000	Weak transcription	Right Ventricle	heart
15	chr1:179087800-179097800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr1:179087800-179113000	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr1:179088000-179097800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr1:179088000-179098400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr1:179088000-179098600	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr1:179088000-179099000	Weak transcription	Aorta	Aorta
21	chr1:179088200-179097800	Weak transcription	Primary B cells from cord blood	blood
22	chr1:179088200-179098800	Weak transcription	Brain Hippocampus Middle	brain
23	chr1:179088200-179102400	Weak transcription	Brain Germinal Matrix	brain
24	chr1:179088400-179099200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr1:179088400-179099400	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr1:179088600-179098800	Weak transcription	Ovary	ovary
27	chr1:179088600-179098800	Weak transcription	Rectal Smooth Muscle	rectum
28	chr1:179089000-179097800	Weak transcription	Primary B cells from peripheral blood	blood
29	chr1:179089200-179098400	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr1:179089200-179099400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr1:179089400-179097600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr1:179089400-179098400	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr1:179089400-179098400	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr1:179089600-179099000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr1:179090800-179097800	Weak transcription	K562	blood
36	chr1:179090800-179098400	Weak transcription	Duodenum Mucosa	Duodenum
37	chr1:179090800-179099200	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr1:179090800-179104400	Weak transcription	Fetal Brain Female	brain
39	chr1:179091000-179097800	Weak transcription	Fetal Thymus	thymus
40	chr1:179091000-179097800	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr1:179091000-179098000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr1:179091000-179098000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr1:179091000-179098200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr1:179091000-179098200	Weak transcription	HepG2	liver
45	chr1:179091000-179098400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr1:179091000-179098400	Weak transcription	Colon Smooth Muscle	Colon
47	chr1:179091000-179098400	Weak transcription	GM12878-XiMat	blood
48	chr1:179091000-179098600	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr1:179091000-179098800	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr1:179091000-179098800	Weak transcription	Brain Angular Gyrus	brain

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