Variant report

Variant	nsv530640
Chromosome Location	chr14:38702117-38927901
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:38888665-38888979	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:38759899-38760181	HepG2	liver:	n/a	n/a
3	BACH1	chr14:38724550-38724659	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr14:38724903-38725003	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr14:38871703-38871784	K562	blood:	n/a	n/a
6	BRCA1	chr14:38808824-38809269	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr14:38755725-38756081	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr14:38832431-38832802	IMR90	lung:	n/a	n/a
9	CEBPB	chr14:38902684-38902958	IMR90	lung:	n/a	chr14:38902797-38902808 chr14:38902797-38902810 chr14:38902799-38902808 chr14:38902799-38902808 chr14:38902799-38902808 chr14:38902799-38902810 chr14:38902797-38902810 chr14:38902799-38902808
10	CEBPB	chr14:38725780-38725897	HepG2	liver:	n/a	chr14:38725812-38725823
11	CEBPB	chr14:38847428-38847654	IMR90	lung:	n/a	chr14:38847572-38847583
12	CEBPB	chr14:38869893-38870190	HepG2	liver:	n/a	chr14:38870011-38870022 chr14:38870010-38870023
13	CEBPB	chr14:38713192-38713257	A549	lung:	n/a	chr14:38713219-38713230
14	CEBPB	chr14:38798332-38799130	MCF-7	breast:	n/a	chr14:38798610-38798622
15	CEBPB	chr14:38889276-38889650	IMR90	lung:	n/a	chr14:38889459-38889470 chr14:38889625-38889638 chr14:38889458-38889471
16	CEBPB	chr14:38841409-38841675	HepG2	liver:	n/a	chr14:38841542-38841553
17	CEBPB	chr14:38725626-38725956	IMR90	lung:	n/a	chr14:38725812-38725823
18	CEBPB	chr14:38798418-38798889	Hela-S3	cervix:	n/a	chr14:38798610-38798622
19	CEBPB	chr14:38832502-38832641	HepG2	liver:	n/a	n/a
20	CEBPB	chr14:38812523-38812675	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr14:38730891-38731169	A549	lung:	n/a	chr14:38731020-38731031
22	CEBPB	chr14:38783479-38783703	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr14:38725636-38725973	H1-hESC	embryonic stem cell:	n/a	chr14:38725812-38725823
24	CEBPB	chr14:38759740-38760510	Hela-S3	cervix:	n/a	chr14:38760217-38760234 chr14:38760220-38760231
25	CEBPB	chr14:38893182-38893462	HepG2	liver:	n/a	chr14:38893309-38893320
26	CEBPB	chr14:38812529-38812740	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr14:38763040-38763149	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr14:38815044-38815240	HepG2	liver:	n/a	chr14:38815085-38815096
29	CEBPB	chr14:38873183-38874100	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr14:38713066-38713373	HepG2	liver:	n/a	chr14:38713219-38713230
31	CEBPB	chr14:38730845-38731197	HepG2	liver:	n/a	chr14:38731020-38731031
32	CEBPB	chr14:38726757-38727088	IMR90	lung:	n/a	chr14:38726951-38726964
33	CEBPB	chr14:38917178-38917466	HepG2	liver:	n/a	chr14:38917314-38917325
34	CEBPB	chr14:38889311-38889589	HepG2	liver:	n/a	chr14:38889459-38889470 chr14:38889458-38889471
35	CEBPB	chr14:38759954-38760380	HepG2	liver:	n/a	chr14:38760217-38760234 chr14:38760220-38760231
36	CEBPB	chr14:38798471-38798883	MCF-7	breast:	n/a	chr14:38798610-38798622
37	CEBPB	chr14:38909457-38909722	HepG2	liver:	n/a	chr14:38909582-38909593
38	CEBPB	chr14:38730845-38731204	Hela-S3	cervix:	n/a	chr14:38731020-38731031
39	CEBPB	chr14:38726753-38727143	Hela-S3	cervix:	n/a	chr14:38726951-38726964
40	CEBPB	chr14:38847425-38847711	A549	lung:	n/a	chr14:38847664-38847675 chr14:38847572-38847583
41	CEBPB	chr14:38755205-38756343	Hela-S3	cervix:	n/a	chr14:38755965-38755978 chr14:38755966-38755977
42	CEBPB	chr14:38832423-38832804	HepG2	liver:	n/a	n/a
43	CEBPB	chr14:38832470-38832730	A549	lung:	n/a	n/a
44	CEBPB	chr14:38909482-38909703	A549	lung:	n/a	chr14:38909582-38909593
45	CEBPB	chr14:38751469-38751487	HepG2	liver:	n/a	chr14:38751475-38751486 chr14:38751476-38751487
46	CEBPB	chr14:38794267-38794426	HepG2	liver:	n/a	chr14:38794391-38794402
47	CEBPB	chr14:38847404-38847738	HepG2	liver:	n/a	chr14:38847664-38847675 chr14:38847572-38847583
48	CEBPB	chr14:38721632-38721832	HepG2	liver:	n/a	n/a
49	CEBPB	chr14:38746895-38748156	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr14:38832406-38832824	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:38725312-38725362	AG09309	skin:	n/a
2	chr14:38725650-38725700	HNPCEpiC	eye:	n/a
3	chr14:38724675-38724725	SK-N-SH_RA	brain:	n/a
4	chr14:38723500-38723550	HepG2	liver:	n/a
5	chr14:38723500-38723550	SK-N-SH	brain:	n/a
6	chr14:38728932-38728982	HCT-116	colon:	n/a
7	chr14:38724675-38724725	H1-hESC	embryonic stem cell:	embryo
8	chr14:38728932-38728982	GM06990	blood:	n/a
9	chr14:38724255-38724305	NB4	blood:	n/a
10	chr14:38728932-38728982	HAEpiC	amniotic membrane:	n/a
11	chr14:38727014-38727064	HepG2	liver:	n/a
12	chr14:38726189-38726239	AG09309	skin:	n/a
13	chr14:38724945-38724995	MCF-7	breast:	n/a
14	chr14:38724255-38724305	HIPEpiC	eye:	n/a
15	chr14:38725750-38725800	AG09309	skin:	n/a
16	chr14:38725750-38725800	AG09319	gingival:	n/a
17	chr14:38724648-38724698	HCF	heart:	n/a
18	chr14:38725312-38725362	HepG2	liver:	n/a
19	chr14:38725650-38725700	HCT-116	colon:	n/a
20	chr14:38726189-38726239	AG04449	skin:	fetal
21	chr14:38725312-38725362	PFSK-1	brain:	n/a
22	chr14:38723500-38723550	K562	blood:	n/a
23	chr14:38723500-38723550	HNPCEpiC	eye:	n/a
24	chr14:38725656-38725706	RPTEC	kidney:	n/a
25	chr14:38725750-38725800	HMEC	breast:	n/a
26	chr14:38725710-38725760	HUVEC	blood vessel:	n/a
27	chr14:38724255-38724305	MCF-7	breast:	n/a
28	chr14:38725656-38725706	HIPEpiC	eye:	n/a
29	chr14:38724648-38724698	K562	blood:	n/a
30	chr14:38725750-38725800	HEK293	kidney:	embryo
31	chr14:38725312-38725362	T-47D	breast:	n/a
32	chr14:38727014-38727064	HEK293	kidney:	embryo
33	chr14:38725750-38725800	BJ	skin:	n/a
34	chr14:38725312-38725362	IMR90	lung:	fetal
35	chr14:38725312-38725362	GM12878	blood:	n/a
36	chr14:38726189-38726239	ECC-1	luminal epithelium:	n/a
37	chr14:38725536-38725586	HUVEC	blood vessel:	n/a
38	chr14:38725656-38725706	HMEC	breast:	n/a
39	chr14:38728932-38728982	HEK293	kidney:	embryo
40	chr14:38724648-38724698	PANC-1	pancreas:	n/a
41	chr14:38725312-38725362	ovcar-3	ovarian:	n/a
42	chr14:38725750-38725800	SAEC	small airway:	n/a
43	chr14:38724255-38724305	AG04450	lung:	fetal
44	chr14:38725650-38725700	HEEpiC	esophagus:	n/a
45	chr14:38876825-38876875	Jurkat	blood:	n/a
46	chr14:38725750-38725800	PFSK-1	brain:	n/a
47	chr14:38727014-38727064	GM06990	blood:	n/a
48	chr14:38725750-38725800	PrEC	prostate:	n/a
49	chr14:38724255-38724305	HMEC	breast:	n/a
50	chr14:38726189-38726239	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:38689000..38690587-chr14:38700372..38702993,2	K562	blood:
2	chr14:38794042..38795587-chr14:38809316..38811122,2	MCF-7	breast:
3	chr14:38747104..38750006-chr14:38750069..38751673,2	MCF-7	breast:
4	chr14:38743017..38744664-chr14:38746124..38747867,2	MCF-7	breast:
5	chr14:38747104..38750006-chr14:38750069..38751673,2	MCF-7	breast:
6	chr14:38741056..38743314-chr14:38745242..38747930,2	MCF-7	breast:
7	chr14:38743017..38744664-chr14:38746124..38747867,2	MCF-7	breast:
8	chr14:38758479..38760563-chr14:38765715..38768374,2	MCF-7	breast:
9	chr14:38898733..38900505-chr14:38900803..38902931,2	K562	blood:
10	chr14:38862979..38864532-chr14:38872147..38873752,2	MCF-7	breast:
11	chr14:38898733..38900505-chr14:38900803..38902931,2	K562	blood:
12	chr14:38741056..38743314-chr14:38745242..38747930,2	MCF-7	breast:
13	chr14:38794042..38795587-chr14:38809316..38811122,2	MCF-7	breast:
14	chr14:38862979..38864532-chr14:38872147..38873752,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SSTR1-2	chr14:38767718-38767808	XLOC_010809
2	lnc-SSTR1-2	chr14:38780991-38781134	ENSG00000259072
3	lnc-SSTR1-2	chr14:38780991-38780995	XLOC_010809
4	lnc-SSTR1-2	chr14:38767718-38768015	ENSG00000259072
5	lnc-SSTR1-2	chr14:38761411-38761575	ENSG00000259072
6	lnc-SSTR1-2	chr14:38760157-38760593	ENSG00000259072
7	lnc-SSTR1-2	chr14:38761469-38761575	XLOC_010809

Variant related genes	Relation type
CLEC14A	TF binding region
ENSG00000259072	TF binding region
ENSG00000264234	TF binding region
CLEC14A	CpG island
ENSG00000259072	CpG island
ENSG00000264234	CpG island
ENSG00000259072	chromatin interactions

Extended variants
information (count: 4427 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:4427 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535461373	chr14:38706605-38706606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs555390809	chr14:38706653-38706654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs111546136	chr14:38706678-38706679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs8021894	chr14:38706711-38706712	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs538181779	chr14:38706858-38706859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs563346143	chr14:38706943-38706944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs140693052	chr14:38707012-38707013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs143366290	chr14:38707083-38707084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188000938	chr14:38707125-38707126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs372803119	chr14:38707128-38707129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192591399	chr14:38707216-38707217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573631475	chr14:38707244-38707245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs370875367	chr14:38707247-38707248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542640872	chr14:38707250-38707251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs112637334	chr14:38707301-38707302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531620836	chr14:38707382-38707383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573769246	chr14:38707386-38707387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139505561	chr14:38707413-38707414	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs146165660	chr14:38707443-38707444	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs199924930	chr14:38707444-38707445	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs66983470	chr14:38707446-38707447	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs61370486	chr14:38707452-38707453	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs61180959	chr14:38707453-38707454	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs201284963	chr14:38707454-38707455	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs374444956	chr14:38707456-38707457	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs565694651	chr14:38707457-38707458	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs545003313	chr14:38707459-38707460	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs28481819	chr14:38707502-38707503	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs569493213	chr14:38707516-38707517	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs527510146	chr14:38707530-38707531	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs182148607	chr14:38707541-38707542	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs112220997	chr14:38707598-38707599	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs542729542	chr14:38707607-38707608	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs529388504	chr14:38707626-38707627	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs548950591	chr14:38707720-38707721	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs148576130	chr14:38707732-38707733	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs538123640	chr14:38707745-38707746	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs142926617	chr14:38707811-38707812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs7144914	chr14:38707826-38707827	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs534130812	chr14:38707846-38707847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369611735	chr14:38707848-38707849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534696654	chr14:38707855-38707856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs554388964	chr14:38707890-38707891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs151080019	chr14:38707949-38707950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs542776075	chr14:38707958-38707959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs115721985	chr14:38707967-38707968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576127817	chr14:38708042-38708043	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs545254180	chr14:38708077-38708078	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs565041391	chr14:38708099-38708100	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs5001880	chr14:38708117-38708118	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Intellectual disability	21811512	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:739 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:38706600-38707400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr14:38706600-38708400	Enhancers	Muscle Satellite Cultured Cells	--
3	chr14:38707000-38708400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr14:38707000-38708400	Enhancers	NHDF-Ad	bronchial
5	chr14:38707400-38707800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr14:38707400-38708200	Enhancers	NHLF	lung
7	chr14:38707400-38708600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr14:38707400-38708600	Enhancers	Hela-S3	cervix
9	chr14:38707800-38708000	Enhancers	HSMMtube	muscle
10	chr14:38707800-38708800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr14:38708000-38708200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr14:38708000-38708400	Enhancers	HSMM	muscle
13	chr14:38708000-38708400	Active TSS	HSMMtube	muscle
14	chr14:38708200-38708400	Enhancers	HUVEC	blood vessel
15	chr14:38708400-38708800	Enhancers	HSMMtube	muscle
16	chr14:38708400-38716200	Weak transcription	HUVEC	blood vessel
17	chr14:38715000-38719000	Weak transcription	Lung	lung
18	chr14:38716200-38718400	Genic enhancers	HUVEC	blood vessel
19	chr14:38716400-38716800	Enhancers	Left Ventricle	heart
20	chr14:38716600-38716800	Enhancers	Pancreas	Pancrea
21	chr14:38716600-38716800	Enhancers	Right Atrium	heart
22	chr14:38716800-38719000	Weak transcription	Left Ventricle	heart
23	chr14:38717400-38726200	Active TSS	Right Atrium	heart
24	chr14:38718000-38718600	Enhancers	Adipose Nuclei	Adipose
25	chr14:38718400-38718600	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr14:38718400-38722000	Transcr. at gene 5' and 3'	HUVEC	blood vessel
27	chr14:38718600-38718800	Flanking Active TSS	Adipose Nuclei	Adipose
28	chr14:38718600-38719000	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr14:38718800-38719200	Active TSS	Right Ventricle	heart
30	chr14:38718800-38723800	Active TSS	Adipose Nuclei	Adipose
31	chr14:38719000-38719400	Active TSS	Lung	lung
32	chr14:38719000-38719600	Active TSS	Skeletal Muscle Male	skeletal muscle
33	chr14:38719000-38720400	Active TSS	Left Ventricle	heart
34	chr14:38719200-38720000	Weak transcription	Right Ventricle	heart
35	chr14:38719200-38723800	Active TSS	Psoas Muscle	Psoas
36	chr14:38719400-38722400	Weak transcription	Lung	lung
37	chr14:38719600-38720000	Enhancers	Muscle Satellite Cultured Cells	--
38	chr14:38719600-38720800	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr14:38719800-38720000	Enhancers	Fetal Lung	lung
40	chr14:38720000-38723800	Active TSS	Right Ventricle	heart
41	chr14:38720000-38724400	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr14:38720200-38721600	Active TSS	Duodenum Smooth Muscle	Duodenum
43	chr14:38720200-38721600	Active TSS	Pancreatic Islets	Pancreatic Islet
44	chr14:38720400-38721400	Weak transcription	Left Ventricle	heart
45	chr14:38720800-38722800	Active TSS	Skeletal Muscle Male	skeletal muscle
46	chr14:38721000-38722000	Active TSS	Ovary	ovary
47	chr14:38721400-38723000	Active TSS	Left Ventricle	heart
48	chr14:38721400-38723600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
49	chr14:38721600-38722000	Active TSS	Skeletal Muscle Female	skeletal muscle
50	chr14:38721600-38722600	Weak transcription	Pancreatic Islets	Pancreatic Islet

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