Variant report

Variant	nsv591824
Chromosome Location	chr3:133292746-133293438
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:593)
CpG islands
(count:306)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:593 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:133293326-133293655	HepG2	liver:	n/a	n/a
2	ATF2	chr3:133293175-133293723	GM12878	blood:	n/a	n/a
3	ATF2	chr3:133293160-133294099	GM12878	blood:	n/a	n/a
4	ATF3	chr3:133293112-133293707	GM12878	blood:	n/a	chr3:133293434-133293445
5	ATF3	chr3:133293118-133293400	HepG2	liver:	n/a	n/a
6	ATF3	chr3:133293098-133293392	K562	blood:	n/a	n/a
7	ATF3	chr3:133293088-133293348	GM12878	blood:	n/a	n/a
8	ATF3	chr3:133293083-133293387	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr3:133291718-133292900	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr3:133293281-133293612	GM12878	blood:	n/a	n/a
11	BATF	chr3:133293198-133293700	GM12878	blood:	n/a	n/a
12	BCL11A	chr3:133293259-133293647	GM12878	blood:	n/a	n/a
13	BCL11A	chr3:133293317-133293597	GM12878	blood:	n/a	n/a
14	BCL3	chr3:133293060-133293605	GM12878	blood:	n/a	n/a
15	BCLAF1	chr3:133292364-133293853	GM12878	blood:	n/a	chr3:133292366-133292379 chr3:133292672-133292681 chr3:133292720-133292733 chr3:133292540-133292553 chr3:133293658-133293666 chr3:133292639-133292652 chr3:133292648-133292661
16	BCLAF1	chr3:133293192-133293868	GM12878	blood:	n/a	chr3:133293658-133293666
17	BHLHE40	chr3:133291327-133293834	K562	blood:	n/a	chr3:133292670-133292686 chr3:133292636-133292652 chr3:133292628-133292644
18	BHLHE40	chr3:133291569-133293601	HepG2	liver:	n/a	chr3:133292670-133292686 chr3:133292636-133292652 chr3:133292628-133292644
19	BHLHE40	chr3:133292540-133292786	A549	lung:	n/a	chr3:133292670-133292686 chr3:133292636-133292652 chr3:133292628-133292644
20	BHLHE40	chr3:133291182-133293907	GM12878	blood:	n/a	chr3:133292670-133292686 chr3:133292636-133292652 chr3:133292628-133292644
21	BRCA1	chr3:133291829-133292903	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr3:133292574-133292752	HepG2	liver:	n/a	n/a
23	BRCA1	chr3:133293279-133293853	Hela-S3	cervix:	n/a	n/a
24	CCNT2	chr3:133291928-133293606	K562	blood:	n/a	chr3:133292264-133292273
25	CEBPB	chr3:133293224-133293808	Hela-S3	cervix:	n/a	n/a
26	CEBPD	chr3:133292326-133293281	HepG2	liver:	n/a	n/a
27	CHD1	chr3:133292466-133295357	GM12878	blood:	n/a	n/a
28	CHD1	chr3:133293203-133293597	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr3:133291159-133295702	IMR90	lung:	n/a	chr3:133292262-133292272 chr3:133292366-133292376
30	CHD1	chr3:133292529-133292915	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr3:133291191-133292830	GM12878	blood:	n/a	chr3:133292262-133292272 chr3:133292366-133292376
32	CHD2	chr3:133293245-133293468	HepG2	liver:	n/a	n/a
33	CHD2	chr3:133293187-133293474	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr3:133293200-133293820	GM12878	blood:	n/a	n/a
35	CHD2	chr3:133291881-133293595	Hela-S3	cervix:	n/a	chr3:133292262-133292272 chr3:133292366-133292376
36	CHD2	chr3:133292707-133292798	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr3:133291971-133292931	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr3:133293035-133293836	GM12878	blood:	n/a	n/a
39	CREB1	chr3:133293040-133293533	A549	lung:	n/a	n/a
40	CREB1	chr3:133293170-133293710	K562	blood:	n/a	n/a
41	CREB1	chr3:133291931-133292951	A549	lung:	n/a	n/a
42	CREB1	chr3:133293288-133293739	ECC-1	luminal epithelium:	n/a	n/a
43	CREB1	chr3:133293209-133293605	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr3:133291776-133293736	HepG2	liver:	n/a	n/a
45	CREB1	chr3:133293112-133293662	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr3:133291661-133292997	GM12878	blood:	n/a	n/a
47	CREB1	chr3:133293038-133294159	GM12878	blood:	n/a	n/a
48	CREB1	chr3:133291879-133292843	K562	blood:	n/a	n/a
49	CTCF	chr3:133293356-133293439	GM10266	blood:	n/a	chr3:133293390-133293397 chr3:133293373-133293386
50	CTCF	chr3:133293378-133293424	GM13977	blood:	n/a	chr3:133293390-133293397

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:133292899-133292949	AG09309	skin:	n/a
2	chr3:133292899-133292949	AG09309	skin:	n/a
3	chr3:133293165-133293215	HNPCEpiC	eye:	n/a
4	chr3:133293427-133293477	NHDF-neo	bronchial:	n/a
5	chr3:133293153-133293203	AG10803	skin:	n/a
6	chr3:133293427-133293477	T-47D	breast:	n/a
7	chr3:133293427-133293477	Jurkat	blood:	n/a
8	chr3:133293165-133293215	SK-N-MC	brain:	n/a
9	chr3:133293165-133293215	HAEpiC	amniotic membrane:	n/a
10	chr3:133292899-133292949	ovcar-3	ovarian:	n/a
11	chr3:133293165-133293215	HEK293	kidney:	embryo
12	chr3:133293146-133293196	U87	brain:	n/a
13	chr3:133293146-133293196	SK-N-MC	brain:	n/a
14	chr3:133293153-133293203	SKMC	muscle:	n/a
15	chr3:133293146-133293196	HRPEpiC	eye:	n/a
16	chr3:133292899-133292949	AG09319	gingival:	n/a
17	chr3:133293427-133293477	CMK	blood:	n/a
18	chr3:133292899-133292949	SKMC	muscle:	n/a
19	chr3:133293146-133293196	ProgFib	skin:	n/a
20	chr3:133293153-133293203	HNPCEpiC	eye:	n/a
21	chr3:133293146-133293196	HUVEC	blood vessel:	n/a
22	chr3:133293427-133293477	HepG2	liver:	n/a
23	chr3:133293153-133293203	PrEC	prostate:	n/a
24	chr3:133292899-133292949	GM19239	blood:	n/a
25	chr3:133292899-133292949	AoSMC	blood vessel:	n/a
26	chr3:133293146-133293196	LNCaP	prostate:	n/a
27	chr3:133293146-133293196	PFSK-1	brain:	n/a
28	chr3:133293146-133293196	Hela-S3	cervix:	n/a
29	chr3:133293146-133293196	Jurkat	blood:	n/a
30	chr3:133293153-133293203	GM19239	blood:	n/a
31	chr3:133293153-133293203	AG04450	lung:	fetal
32	chr3:133292899-133292949	CMK	blood:	n/a
33	chr3:133292899-133292949	IMR90	lung:	fetal
34	chr3:133292899-133292949	HRPEpiC	eye:	n/a
35	chr3:133293427-133293477	BJ	skin:	n/a
36	chr3:133293153-133293203	ECC-1	luminal epithelium:	n/a
37	chr3:133293427-133293477	AG04449	skin:	fetal
38	chr3:133293427-133293477	K562	blood:	n/a
39	chr3:133293146-133293196	GM12891	blood:	n/a
40	chr3:133293165-133293215	T-47D	breast:	n/a
41	chr3:133293165-133293215	HPAEpiC	pulmonary alveolar:	n/a
42	chr3:133293427-133293477	HPAEpiC	pulmonary alveolar:	n/a
43	chr3:133292899-133292949	SK-N-SH_RA	brain:	n/a
44	chr3:133293165-133293215	HIPEpiC	eye:	n/a
45	chr3:133293153-133293203	MCF10A-Er-Src	breast:	n/a
46	chr3:133292899-133292949	A549	lung:	n/a
47	chr3:133292899-133292949	ProgFib	skin:	n/a
48	chr3:133293165-133293215	U87	brain:	n/a
49	chr3:133292899-133292949	HIPEpiC	eye:	n/a
50	chr3:133292899-133292949	K562	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:132439752..132442432-chr3:133291591..133294160,3	K562	blood:
2	chr12:123380262..123380795-chr3:133292200..133293035,2	Hela-S3	cervix:
3	chr3:133207179..133209818-chr3:133291516..133294111,3	MCF-7	breast:
4	chr16:30006617..30007124-chr3:133292657..133293213,2	Hela-S3	cervix:
5	chr3:133164640..133168534-chr3:133291750..133294077,5	MCF-7	breast:
6	chr1:144533945..144534883-chr3:133292589..133293471,2	Hela-S3	cervix:
7	chr3:133207094..133210649-chr3:133290648..133294454,4	MCF-7	breast:
8	chr3:133169398..133190840-chr3:133288286..133298861,41	MCF-7	breast:
9	chr15:65596825..65597694-chr3:133292711..133293433,2	Hela-S3	cervix:
10	chr3:132440102..132442906-chr3:133291126..133294877,5	K562	blood:
11	chr20:57467067..57467853-chr3:133292915..133293441,2	Hela-S3	cervix:
12	chr21:38737416..38739692-chr3:133291408..133294289,2	MCF-7	breast:
13	chr10:71930068..71930946-chr3:133292953..133293844,2	Hela-S3	cervix:
14	chr19:47291403..47292001-chr3:133293045..133294029,2	NB4	blood:
15	chr3:133292322..133293201-chr3:142314859..142315610,2	HCT-116	colon:

No data

Variant related genes	Relation type
CDV3	TF binding region
CDV3	CpG island
ENSG00000201699	chromatin interactions
ENSG00000214301	chromatin interactions
ENSG00000105281	chromatin interactions
ENSG00000079332	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000120756	chromatin interactions
ENSG00000249993	chromatin interactions
ENSG00000139722	chromatin interactions
ENSG00000248724	chromatin interactions
ENSG00000169592	chromatin interactions
ENSG00000273210	chromatin interactions
ENSG00000113971	chromatin interactions
ENSG00000157540	chromatin interactions
ENSG00000087460	chromatin interactions
ENSG00000149929	chromatin interactions
ENSG00000170819	chromatin interactions

Extended variants
information (count: 24 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561646187	chr3:133292747-133292748	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
2	rs530840892	chr3:133292768-133292769	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
3	rs550544599	chr3:133292809-133292810	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
4	rs570627506	chr3:133292821-133292822	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
5	rs539518053	chr3:133292857-133292858	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
6	rs201192440	chr3:133292858-133292859	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
7	rs546879668	chr3:133292987-133292988	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
8	rs193280445	chr3:133293012-133293013	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
9	rs371742216	chr3:133293171-133293172	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
10	rs535661133	chr3:133293201-133293202	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
11	rs556070938	chr3:133293204-133293205	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
12	rs575995429	chr3:133293223-133293224	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
13	rs537061552	chr3:133293225-133293226	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
14	rs556971472	chr3:133293236-133293237	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
15	rs569973591	chr3:133293290-133293291	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
16	rs538540417	chr3:133293300-133293301	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
17	rs545843063	chr3:133293303-133293304	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
18	rs552374881	chr3:133293309-133293310	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
19	rs113254107	chr3:133293314-133293315	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
20	rs573040651	chr3:133293350-133293351	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
21	rs368431828	chr3:133293359-133293360	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
22	rs541638933	chr3:133293365-133293366	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
23	rs116707775	chr3:133293414-133293415	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
24	rs371446104	chr3:133293432-133293433	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Hailey-hailey disease	17597066	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:142 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:133289800-133293200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr3:133291200-133294000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:133291400-133293800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr3:133291600-133293600	Active TSS	Brain Cingulate Gyrus	brain
5	chr3:133291600-133293600	Active TSS	Brain Germinal Matrix	brain
6	chr3:133291600-133293600	Active TSS	Fetal Brain Female	brain
7	chr3:133291600-133293800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr3:133291600-133293800	Active TSS	Psoas Muscle	Psoas
9	chr3:133291600-133294000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr3:133291600-133294000	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr3:133291600-133294000	Active TSS	Right Ventricle	heart
12	chr3:133291600-133294400	Active TSS	Duodenum Smooth Muscle	Duodenum
13	chr3:133291600-133295000	Active TSS	Colonic Mucosa	Colon
14	chr3:133291600-133295000	Active TSS	Right Atrium	heart
15	chr3:133291800-133293400	Active TSS	Brain Hippocampus Middle	brain
16	chr3:133291800-133293600	Active TSS	Liver	Liver
17	chr3:133291800-133293800	Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr3:133291800-133293800	Active TSS	Fetal Stomach	stomach
19	chr3:133291800-133293800	Active TSS	Thymus	Thymus
20	chr3:133291800-133293800	Active TSS	A549	lung
21	chr3:133291800-133294000	Active TSS	iPS-15b Cell Line	embryonic stem cell
22	chr3:133291800-133294000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr3:133291800-133294000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr3:133291800-133294200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr3:133291800-133294200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr3:133291800-133294200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr3:133291800-133294200	Active TSS	Fetal Muscle Trunk	muscle
28	chr3:133291800-133294200	Active TSS	Ovary	ovary
29	chr3:133291800-133294200	Active TSS	Pancreas	Pancrea
30	chr3:133291800-133294800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr3:133291800-133295000	Active TSS	Left Ventricle	heart
32	chr3:133291800-133295400	Active TSS	Aorta	Aorta
33	chr3:133292000-133293200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
34	chr3:133292000-133293200	Weak transcription	Fetal Heart	heart
35	chr3:133292000-133293400	Active TSS	HUES6 Cell Line	embryonic stem cell
36	chr3:133292000-133293400	Active TSS	Primary B cells from cord blood	blood
37	chr3:133292000-133293400	Active TSS	Skeletal Muscle Female	skeletal muscle
38	chr3:133292000-133293400	Weak transcription	Stomach Mucosa	stomach
39	chr3:133292000-133293600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr3:133292000-133293600	Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr3:133292000-133293600	Active TSS	Primary hematopoietic stem cells short term culture	blood
42	chr3:133292000-133293600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr3:133292000-133293600	Active TSS	Adipose Nuclei	Adipose
44	chr3:133292000-133293600	Active TSS	Brain Anterior Caudate	brain
45	chr3:133292000-133293600	Active TSS	Brain Inferior Temporal Lobe	brain
46	chr3:133292000-133293600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
47	chr3:133292000-133293600	Active TSS	Brain Substantia Nigra	brain
48	chr3:133292000-133293600	Active TSS	Colon Smooth Muscle	Colon
49	chr3:133292000-133293600	Active TSS	Rectal Mucosa Donor 31	rectum
50	chr3:133292000-133293600	Active TSS	Skeletal Muscle Male	skeletal muscle

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