Variant report

Variant	nsv946422
Chromosome Location	chr1:155716220-155722236
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:190)
CpG islands
(count:184)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:190 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr1:155720269-155720579	K562	blood:	n/a	n/a
2	CEBPB	chr1:155720357-155720519	IMR90	lung:	n/a	n/a
3	FOSL2	chr1:155715054-155716441	HepG2	liver:	n/a	n/a
4	FOSL2	chr1:155717188-155717424	HepG2	liver:	n/a	n/a
5	HEY1	chr1:155714959-155716438	K562	blood:	n/a	chr1:155715581-155715596 chr1:155715318-155715333
6	HEY1	chr1:155716760-155717703	K562	blood:	n/a	n/a
7	HEY1	chr1:155717015-155717577	K562	blood:	n/a	n/a
8	HEY1	chr1:155720187-155720532	K562	blood:	n/a	n/a
9	HEY1	chr1:155719087-155719336	K562	blood:	n/a	n/a
10	HEY1	chr1:155715003-155716572	K562	blood:	n/a	chr1:155715581-155715596 chr1:155715318-155715333
11	POLR2A	chr1:155720188-155720633	GM12891	blood:	n/a	n/a
12	POLR2A	chr1:155718077-155718319	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr1:155721715-155721732	GM12878	blood:	n/a	n/a
14	POLR2A	chr1:155720081-155720598	GM12891	blood:	n/a	n/a
15	POLR2A	chr1:155722150-155722480	Hela-S3	cervix:	n/a	n/a
16	POLR2A	chr1:155718377-155718600	GM12878	blood:	n/a	n/a
17	POLR2A	chr1:155714929-155716665	SK-N-MC	brain:	n/a	n/a
18	POLR2A	chr1:155714958-155716588	GM12891	blood:	n/a	n/a
19	POLR2A	chr1:155714999-155716580	GM12878	blood:	n/a	n/a
20	POLR2A	chr1:155715220-155716247	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr1:155716709-155716775	K562	blood:	n/a	n/a
22	POLR2A	chr1:155720195-155720647	PANC-1	pancreas:	n/a	n/a
23	POLR2A	chr1:155719969-155720567	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr1:155721249-155722551	K562	blood:	n/a	n/a
25	POLR2A	chr1:155721373-155722195	GM12892	blood:	n/a	n/a
26	POLR2A	chr1:155720356-155720508	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr1:155721256-155722489	GM12892	blood:	n/a	n/a
28	POLR2A	chr1:155722032-155722243	HepG2	liver:	n/a	n/a
29	POLR2A	chr1:155721518-155721819	GM12891	blood:	n/a	n/a
30	POLR2A	chr1:155716763-155716987	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr1:155721262-155722355	SK-N-MC	brain:	n/a	n/a
32	POLR2A	chr1:155716187-155716378	HepG2	liver:	n/a	n/a
33	POLR2A	chr1:155718969-155720014	GM12891	blood:	n/a	n/a
34	POLR2A	chr1:155718938-155718960	HepG2	liver:	n/a	n/a
35	POLR2A	chr1:155721537-155721704	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr1:155718470-155718527	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr1:155716138-155716328	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr1:155716724-155718710	GM12891	blood:	n/a	n/a
39	POLR2A	chr1:155718096-155718751	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr1:155721322-155722344	GM12878	blood:	n/a	n/a
41	POLR2A	chr1:155721591-155721641	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr1:155722001-155722253	A549	lung:	n/a	n/a
43	POLR2A	chr1:155721464-155721859	PANC-1	pancreas:	n/a	n/a
44	POLR2A	chr1:155721630-155722067	HUVEC	blood vessel:	n/a	n/a
45	POLR2A	chr1:155720319-155720559	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr1:155716772-155717638	GM12891	blood:	n/a	n/a
47	POLR2A	chr1:155722077-155722121	HUVEC	blood vessel:	n/a	n/a
48	POLR2A	chr1:155721692-155721720	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr1:155714591-155716469	PFSK-1	brain:	n/a	n/a
50	POLR2A	chr1:155718500-155718639	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:155718648-155718698	HCM	heart:	n/a
2	chr1:155718648-155718698	HCM	heart:	n/a
3	chr1:155717533-155717583	PrEC	prostate:	n/a
4	chr1:155720323-155720373	HEEpiC	esophagus:	n/a
5	chr1:155717533-155717583	GM12892	blood:	n/a
6	chr1:155717533-155717583	HRE	kidney:	n/a
7	chr1:155718648-155718698	PrEC	prostate:	n/a
8	chr1:155720323-155720373	MCF-7	breast:	n/a
9	chr1:155720323-155720373	CMK	blood:	n/a
10	chr1:155717533-155717583	PFSK-1	brain:	n/a
11	chr1:155718648-155718698	CMK	blood:	n/a
12	chr1:155720323-155720373	HCF	heart:	n/a
13	chr1:155718648-155718698	AG04450	lung:	fetal
14	chr1:155718648-155718698	GM12878	blood:	n/a
15	chr1:155720323-155720373	ECC-1	luminal epithelium:	n/a
16	chr1:155720323-155720373	HCT-116	colon:	n/a
17	chr1:155718648-155718698	HIPEpiC	eye:	n/a
18	chr1:155720323-155720373	HepG2	liver:	n/a
19	chr1:155717533-155717583	CMK	blood:	n/a
20	chr1:155718648-155718698	GM12891	blood:	n/a
21	chr1:155720323-155720373	SAEC	small airway:	n/a
22	chr1:155718648-155718698	AG04449	skin:	fetal
23	chr1:155717533-155717583	NT2-D1	testis:	n/a
24	chr1:155720323-155720373	PrEC	prostate:	n/a
25	chr1:155717533-155717583	NHBE	bronchial:	n/a
26	chr1:155717533-155717583	SK-N-SH	brain:	n/a
27	chr1:155720323-155720373	T-47D	breast:	n/a
28	chr1:155718648-155718698	AG09309	skin:	n/a
29	chr1:155717533-155717583	ovcar-3	ovarian:	n/a
30	chr1:155717533-155717583	PANC-1	pancreas:	n/a
31	chr1:155718648-155718698	HCF	heart:	n/a
32	chr1:155717533-155717583	NHDF-neo	bronchial:	n/a
33	chr1:155718648-155718698	HRE	kidney:	n/a
34	chr1:155718648-155718698	A549	lung:	n/a
35	chr1:155718648-155718698	MCF10A-Er-Src	breast:	n/a
36	chr1:155718648-155718698	HRPEpiC	eye:	n/a
37	chr1:155717533-155717583	HCM	heart:	n/a
38	chr1:155718648-155718698	BE2_C	brain:	n/a
39	chr1:155717533-155717583	A549	lung:	n/a
40	chr1:155720323-155720373	MCF10A-Er-Src	breast:	n/a
41	chr1:155720323-155720373	RPTEC	kidney:	n/a
42	chr1:155718648-155718698	AoSMC	blood vessel:	n/a
43	chr1:155720323-155720373	Hela-S3	cervix:	n/a
44	chr1:155720323-155720373	HIPEpiC	eye:	n/a
45	chr1:155718648-155718698	HEEpiC	esophagus:	n/a
46	chr1:155720323-155720373	Jurkat	blood:	n/a
47	chr1:155720323-155720373	SKMC	muscle:	n/a
48	chr1:155720323-155720373	U87	brain:	n/a
49	chr1:155720323-155720373	SK-N-SH_RA	brain:	n/a
50	chr1:155720323-155720373	SK-N-SH	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:155713796..155716545-chr1:155826802..155829458,2	K562	blood:
2	chr1:155714815..155717655-chr1:155717982..155720933,2	K562	blood:

No data

Variant related genes	Relation type
GON4L	TF binding region
GON4L	CpG island
ENSG00000116580	chromatin interactions
ENSG00000203761	chromatin interactions
ENSG00000132718	chromatin interactions

Extended variants
information (count: 220 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:220 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568905049	chr1:155716279-155716280	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs536385829	chr1:155716343-155716344	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs554625637	chr1:155716354-155716355	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs573526880	chr1:155716429-155716430	Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs481110	chr1:155716706-155716707	Weak transcription Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs534783937	chr1:155716732-155716733	Weak transcription Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs553003336	chr1:155716745-155716746	Weak transcription Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs577824437	chr1:155716771-155716772	Weak transcription Strong transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs544972619	chr1:155716809-155716810	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563339198	chr1:155716858-155716859	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575299441	chr1:155716871-155716872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542773995	chr1:155716890-155716891	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560938572	chr1:155716891-155716892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs528710171	chr1:155716937-155716938	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547129500	chr1:155716947-155716948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565440754	chr1:155717011-155717012	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532884458	chr1:155717026-155717027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550981739	chr1:155717095-155717096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568945103	chr1:155717110-155717111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536222937	chr1:155717215-155717216	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548293279	chr1:155717220-155717221	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566587465	chr1:155717292-155717293	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534521358	chr1:155717305-155717306	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553179904	chr1:155717323-155717324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs577756346	chr1:155717334-155717335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538960875	chr1:155717438-155717439	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs145509034	chr1:155717528-155717529	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575335803	chr1:155717529-155717530	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542608496	chr1:155717530-155717531	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs446900	chr1:155717533-155717534	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs560973077	chr1:155717542-155717543	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs35177764	chr1:155717548-155717549	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192357238	chr1:155717607-155717608	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs112737969	chr1:155717608-155717609	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs565514945	chr1:155717628-155717629	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369592602	chr1:155717632-155717633	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs532581093	chr1:155717640-155717641	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs200676591	chr1:155717654-155717655	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs148065907	chr1:155717677-155717678	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs530046530	chr1:155717683-155717684	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs1705486	chr1:155717701-155717702	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs397839749	chr1:155717705-155717706	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551440204	chr1:155717734-155717735	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs571379837	chr1:155717737-155717738	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs184430142	chr1:155717741-155717742	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566525258	chr1:155717751-155717752	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs534343069	chr1:155717770-155717771	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552377553	chr1:155717774-155717775	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs571449860	chr1:155717787-155717788	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530614846	chr1:155717790-155717791	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	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
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	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
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Dihydropyrimidine dehydrogenase deficiency	18421352	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155714000-155716800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr1:155714600-155716600	Active TSS	HMEC	breast
3	chr1:155714600-155716800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr1:155714800-155716600	Active TSS	GM12878-XiMat	blood
5	chr1:155715000-155716800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr1:155715200-155716600	Active TSS	Dnd41	blood
7	chr1:155715200-155716800	Active TSS	NHEK	skin
8	chr1:155715400-155717200	Weak transcription	Lung	lung
9	chr1:155715400-155720800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:155715400-155720800	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr1:155715400-155721200	Weak transcription	Colon Smooth Muscle	Colon
12	chr1:155715400-155723000	Weak transcription	Aorta	Aorta
13	chr1:155715400-155725600	Weak transcription	Fetal Brain Male	brain
14	chr1:155715400-155726200	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr1:155715400-155730000	Weak transcription	Stomach Mucosa	stomach
16	chr1:155715400-155739200	Weak transcription	Fetal Heart	heart
17	chr1:155715400-155789200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr1:155715600-155716600	Weak transcription	Fetal Intestine Small	intestine
19	chr1:155715600-155717200	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr1:155715600-155717400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr1:155715600-155717400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr1:155715600-155717400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr1:155715600-155717400	Weak transcription	Primary T cells from cord blood	blood
24	chr1:155715600-155717400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr1:155715600-155717400	Weak transcription	Adipose Nuclei	Adipose
26	chr1:155715600-155717400	Weak transcription	Brain Anterior Caudate	brain
27	chr1:155715600-155717400	Weak transcription	Duodenum Mucosa	Duodenum
28	chr1:155715600-155717400	Weak transcription	Ovary	ovary
29	chr1:155715600-155717400	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr1:155715600-155717600	Weak transcription	Liver	Liver
31	chr1:155715600-155717600	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr1:155715600-155717600	Weak transcription	Spleen	Spleen
33	chr1:155715600-155717800	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr1:155715600-155717800	Weak transcription	Brain Substantia Nigra	brain
35	chr1:155715600-155717800	Weak transcription	Thymus	Thymus
36	chr1:155715600-155718000	Weak transcription	K562	blood
37	chr1:155715600-155718400	Weak transcription	Primary B cells from peripheral blood	blood
38	chr1:155715600-155718400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr1:155715600-155718400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr1:155715600-155720600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr1:155715600-155720600	Weak transcription	Colonic Mucosa	Colon
42	chr1:155715600-155720600	Weak transcription	Fetal Lung	lung
43	chr1:155715600-155720800	Weak transcription	Primary B cells from cord blood	blood
44	chr1:155715600-155720800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr1:155715600-155720800	Weak transcription	HepG2	liver
46	chr1:155715600-155722800	Weak transcription	Fetal Kidney	kidney
47	chr1:155715600-155722800	Weak transcription	Gastric	stomach
48	chr1:155715600-155725000	Weak transcription	Small Intestine	intestine
49	chr1:155715600-155725200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr1:155715600-155725200	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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