Variant report

Variant	nsv569908
Chromosome Location	chr15:72154000-72218036
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:181)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:181 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:72213921-72213933	K562	blood:	n/a	n/a
2	ARID3A	chr15:72212595-72212649	K562	blood:	n/a	n/a
3	ATF2	chr15:72206368-72206921	GM12878	blood:	n/a	n/a
4	BATF	chr15:72206431-72206854	GM12878	blood:	n/a	chr15:72206656-72206667
5	BATF	chr15:72166614-72167024	GM12878	blood:	n/a	n/a
6	BATF	chr15:72172137-72172404	GM12878	blood:	n/a	n/a
7	BATF	chr15:72206435-72206822	GM12878	blood:	n/a	chr15:72206656-72206667
8	BATF	chr15:72172158-72172394	GM12878	blood:	n/a	n/a
9	BCL11A	chr15:72206400-72206839	GM12878	blood:	n/a	n/a
10	BCL11A	chr15:72206377-72206869	GM12878	blood:	n/a	n/a
11	BCL3	chr15:72206413-72206809	GM12878	blood:	n/a	n/a
12	BHLHE40	chr15:72183574-72183575	K562	blood:	n/a	n/a
13	BHLHE40	chr15:72166665-72166809	GM12878	blood:	n/a	n/a
14	BHLHE40	chr15:72168244-72168288	GM12878	blood:	n/a	n/a
15	CEBPB	chr15:72157924-72158099	K562	blood:	n/a	n/a
16	CEBPB	chr15:72179288-72179290	A549	lung:	n/a	n/a
17	CHD1	chr15:72166676-72166792	GM12878	blood:	n/a	n/a
18	CTCF	chr15:72196712-72196751	GM20000	blood:	n/a	n/a
19	CTCF	chr15:72192683-72192728	GM13977	blood:	n/a	n/a
20	CTCF	chr15:72163938-72163954	MCF-7	breast:	n/a	n/a
21	CTCF	chr15:72213308-72213341	GM20000	blood:	n/a	n/a
22	CTCF	chr15:72154195-72154236	Kidney_OC	kidney:	n/a	n/a
23	CUX1	chr15:72183584-72183722	GM12878	blood:	n/a	n/a
24	E2F4	chr15:72175804-72176004	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr15:72170025-72170225	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr15:72155377-72155486	MCF10A-Er-Src	breast:	n/a	n/a
27	EBF1	chr15:72206533-72206945	GM12878	blood:	n/a	n/a
28	EBF1	chr15:72181133-72181443	GM12878	blood:	n/a	n/a
29	EBF1	chr15:72206458-72206945	GM12878	blood:	n/a	n/a
30	EBF1	chr15:72178617-72178803	GM12878	blood:	n/a	n/a
31	EBF1	chr15:72181148-72181474	GM12878	blood:	n/a	n/a
32	EBF1	chr15:72206577-72206859	GM12878	blood:	n/a	n/a
33	ELF1	chr15:72183461-72183819	K562	blood:	n/a	chr15:72183665-72183676 chr15:72183664-72183677
34	EP300	chr15:72208178-72209967	SK-N-SH	brain:	n/a	chr15:72208194-72208203 chr15:72208265-72208279 chr15:72208546-72208560
35	EP300	chr15:72168335-72168338	GM12878	blood:	n/a	n/a
36	EP300	chr15:72180946-72180948	K562	blood:	n/a	n/a
37	EP300	chr15:72166834-72166905	GM12878	blood:	n/a	n/a
38	EP300	chr15:72168239-72168430	GM12878	blood:	n/a	n/a
39	EP300	chr15:72206391-72206842	GM12878	blood:	n/a	n/a
40	EP300	chr15:72181099-72181626	GM12878	blood:	n/a	chr15:72181189-72181198
41	EP300	chr15:72206466-72206861	GM12878	blood:	n/a	n/a
42	EP300	chr15:72209135-72209491	SK-N-SH_RA	brain:	n/a	n/a
43	EP300	chr15:72181791-72182114	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr15:72209204-72209651	SK-N-SH_RA	brain:	n/a	n/a
45	FOS	chr15:72213622-72213745	MCF10A-Er-Src	breast:	n/a	chr15:72213704-72213715
46	FOS	chr15:72213561-72213747	MCF10A-Er-Src	breast:	n/a	chr15:72213704-72213715
47	FOXA1	chr15:72209091-72209667	T-47D	breast:	n/a	n/a
48	FOXA1	chr15:72209131-72209513	T-47D	breast:	n/a	n/a
49	FOXM1	chr15:72206318-72206871	GM12878	blood:	n/a	n/a
50	GATA2	chr15:72181811-72182063	SH-SY5Y	brain:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:72178118-72178168	IMR90	lung:	fetal
2	chr15:72178118-72178168	HepG2	liver:	n/a
3	chr15:72178118-72178168	T-47D	breast:	n/a
4	chr15:72178118-72178168	NHBE	bronchial:	n/a
5	chr15:72178118-72178168	AG10803	skin:	n/a
6	chr15:72178118-72178168	SK-N-MC	brain:	n/a
7	chr15:72178118-72178168	HRCEpiC	kidney:	n/a
8	chr15:72178118-72178168	SKMC	muscle:	n/a
9	chr15:72178118-72178168	Hepatocyte	liver:	n/a
10	chr15:72178118-72178168	AG09309	skin:	n/a
11	chr15:72178118-72178168	HL-60	blood:	n/a
12	chr15:72178118-72178168	LNCaP	prostate:	n/a
13	chr15:72178118-72178168	CMK	blood:	n/a
14	chr15:72178118-72178168	HMEC	breast:	n/a
15	chr15:72178118-72178168	AG04449	skin:	fetal
16	chr15:72178118-72178168	PFSK-1	brain:	n/a
17	chr15:72178118-72178168	HPAEpiC	pulmonary alveolar:	n/a
18	chr15:72178118-72178168	HIPEpiC	eye:	n/a
19	chr15:72178118-72178168	Hela-S3	cervix:	n/a
20	chr15:72178118-72178168	PrEC	prostate:	n/a
21	chr15:72178118-72178168	HCM	heart:	n/a
22	chr15:72178118-72178168	HAEpiC	amniotic membrane:	n/a
23	chr15:72178118-72178168	NH-A	brain:	n/a
24	chr15:72178118-72178168	A549	lung:	n/a
25	chr15:72178118-72178168	BJ	skin:	n/a
26	chr15:72178118-72178168	K562	blood:	n/a
27	chr15:72178118-72178168	SK-N-SH	brain:	n/a
28	chr15:72178118-72178168	MCF10A-Er-Src	breast:	n/a
29	chr15:72178118-72178168	H1-hESC	embryonic stem cell:	embryo
30	chr15:72178118-72178168	HEK293	kidney:	embryo
31	chr15:72178118-72178168	HRPEpiC	eye:	n/a
32	chr15:72178118-72178168	SAEC	small airway:	n/a
33	chr15:72178118-72178168	HUVEC	blood vessel:	n/a
34	chr15:72178118-72178168	NB4	blood:	n/a
35	chr15:72178118-72178168	U87	brain:	n/a
36	chr15:72178118-72178168	GM12892	blood:	n/a
37	chr15:72178118-72178168	HRE	kidney:	n/a
38	chr15:72178118-72178168	GM19239	blood:	n/a
39	chr15:72178118-72178168	AG09319	gingival:	n/a
40	chr15:72178118-72178168	RPTEC	kidney:	n/a
41	chr15:72178118-72178168	ovcar-3	ovarian:	n/a
42	chr15:72178118-72178168	BE2_C	brain:	n/a
43	chr15:72178118-72178168	HEEpiC	esophagus:	n/a
44	chr15:72178118-72178168	HNPCEpiC	eye:	n/a
45	chr15:72178118-72178168	Caco-2	colon:	n/a
46	chr15:72178118-72178168	PANC-1	pancreas:	n/a
47	chr15:72178118-72178168	ProgFib	skin:	n/a
48	chr15:72178118-72178168	GM12878	blood:	n/a
49	chr15:72178118-72178168	GM12891	blood:	n/a
50	chr15:72178118-72178168	HCT-116	colon:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:72138309..72141068-chr15:72175580..72177408,2	MCF-7	breast:
2	chr15:72197435..72199145-chr15:72206196..72207927,2	K562	blood:
3	chr15:72173982..72176259-chr15:72181202..72184060,3	K562	blood:
4	chr15:72197435..72199145-chr15:72206196..72207927,2	K562	blood:
5	chr15:72204090..72205988-chr15:72208798..72210918,2	K562	blood:
6	chr15:72187197..72189830-chr15:72197152..72199761,2	K562	blood:
7	chr15:72177869..72180074-chr15:72180572..72182469,2	MCF-7	breast:
8	chr15:72190232..72191910-chr15:72203994..72206448,2	MCF-7	breast:
9	chr15:72168681..72170784-chr15:72179926..72181699,2	MCF-7	breast:
10	chr15:72183241..72185017-chr15:72188166..72190098,2	MCF-7	breast:
11	chr15:72187197..72189830-chr15:72197152..72199761,2	K562	blood:
12	chr15:72173982..72176259-chr15:72181202..72184060,3	K562	blood:
13	chr15:72183241..72185017-chr15:72188166..72190098,2	MCF-7	breast:
14	chr15:72180763..72183209-chr15:72189285..72191973,2	MCF-7	breast:
15	chr15:72204090..72205988-chr15:72208798..72210918,2	K562	blood:
16	chr15:72143069..72145942-chr15:72153528..72155127,2	K562	blood:
17	chr15:72176973..72179854-chr15:72407858..72409826,2	MCF-7	breast:
18	chr15:72180763..72183209-chr15:72189285..72191973,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRAMD2-4	chr15:72185803-72186119	NONHSAT047057
2	lnc-GRAMD2-4	chr15:72189802-72190154	NONHSAT047057

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MYO9A	hsa-let-7c-5p	chr15:72183618-72183640

Variant related genes	Relation type
MYO9A	TF binding region
MYO9A	CpG island
ENSG00000166192	chromatin interactions
ENSG00000066933	chromatin interactions

Extended variants
information (count: 2170 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:2170 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7497104	chr15:72154000-72154001	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs375623076	chr15:72154021-72154022	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs550978969	chr15:72154032-72154033	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs530263925	chr15:72154033-72154034	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs183206463	chr15:72154034-72154035	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs372277426	chr15:72154041-72154042	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs66598621	chr15:72154042-72154043	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs28363671	chr15:72154043-72154044	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
9	rs570240189	chr15:72154046-72154047	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs537297834	chr15:72154050-72154051	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs375486722	chr15:72154070-72154071	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs571120154	chr15:72154158-72154159	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs538610919	chr15:72154176-72154177	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs75790411	chr15:72154188-72154189	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs34957368	chr15:72154221-72154222	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs571800789	chr15:72154226-72154227	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs12439494	chr15:72154358-72154359	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs563797539	chr15:72154364-72154365	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs149736484	chr15:72154365-72154366	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs113419531	chr15:72154367-72154368	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs551494967	chr15:72154373-72154374	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs552368431	chr15:72154479-72154480	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs376353065	chr15:72154494-72154495	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs187453400	chr15:72154498-72154499	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs565172103	chr15:72154527-72154528	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs532332904	chr15:72154557-72154558	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs541432710	chr15:72154563-72154564	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs56087519	chr15:72154577-72154578	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs530176791	chr15:72154580-72154581	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs79069157	chr15:72154602-72154603	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs548703754	chr15:72154609-72154610	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs117164880	chr15:72154617-72154618	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs531148194	chr15:72154650-72154651	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs192625660	chr15:72154709-72154710	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs571102146	chr15:72154748-72154749	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs185550098	chr15:72154773-72154774	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs145500964	chr15:72154878-72154879	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs375713583	chr15:72154889-72154890	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs138105643	chr15:72154914-72154915	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs370270618	chr15:72154921-72154922	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs142695910	chr15:72154932-72154933	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs373719174	chr15:72154955-72154956	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs527306019	chr15:72154988-72154989	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs370691034	chr15:72154989-72154990	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs200087998	chr15:72155003-72155004	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs565343582	chr15:72155015-72155016	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs112426426	chr15:72155068-72155069	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs554259894	chr15:72155100-72155101	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs567577202	chr15:72155225-72155226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs144094945	chr15:72155231-72155232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
Autism	20678247	CNVD
Retinoblastoma	21504564	CNVD
Matthew-Wood syndrome	21085971	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Urothelial cell carcinoma	18451213	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Mental retardation	17621639	CNVD
Autism	20808228	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Urothelial carcinoma	21177765	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Renal cell carcinoma	21215367	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1151 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:72114600-72190600	Weak transcription	Pancreas	Pancrea
2	chr15:72119200-72171800	Weak transcription	Psoas Muscle	Psoas
3	chr15:72122200-72189400	Weak transcription	Right Ventricle	heart
4	chr15:72122400-72195000	Weak transcription	NHEK	skin
5	chr15:72122600-72171800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr15:72122600-72185200	Weak transcription	Esophagus	oesophagus
7	chr15:72122600-72195800	Weak transcription	Gastric	stomach
8	chr15:72131800-72192800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr15:72137000-72156400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr15:72138200-72172400	Weak transcription	HUVEC	blood vessel
11	chr15:72140200-72171800	Weak transcription	HMEC	breast
12	chr15:72141400-72174200	Weak transcription	Fetal Brain Male	brain
13	chr15:72142600-72154000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr15:72142600-72154600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr15:72142600-72166400	Weak transcription	GM12878-XiMat	blood
16	chr15:72142600-72170200	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr15:72142600-72171800	Weak transcription	NH-A	brain
18	chr15:72142600-72183400	Weak transcription	Brain Angular Gyrus	brain
19	chr15:72142600-72189600	Weak transcription	NHLF	lung
20	chr15:72142600-72199200	Weak transcription	Hela-S3	cervix
21	chr15:72142800-72170000	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr15:72142800-72171800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr15:72142800-72172000	Weak transcription	Dnd41	blood
24	chr15:72142800-72176000	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr15:72142800-72184800	Weak transcription	A549	lung
26	chr15:72142800-72190200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr15:72143000-72163400	Weak transcription	Fetal Intestine Small	intestine
28	chr15:72143000-72172200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr15:72143000-72190600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr15:72143000-72190600	Weak transcription	Colonic Mucosa	Colon
31	chr15:72143800-72160200	Weak transcription	Aorta	Aorta
32	chr15:72143800-72172000	Weak transcription	Brain Germinal Matrix	brain
33	chr15:72144000-72166400	Weak transcription	Ovary	ovary
34	chr15:72144200-72170400	Weak transcription	NHDF-Ad	bronchial
35	chr15:72144600-72170200	Weak transcription	Colon Smooth Muscle	Colon
36	chr15:72144600-72223400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr15:72145200-72170000	Weak transcription	Fetal Brain Female	brain
38	chr15:72145400-72163400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr15:72145400-72163400	Weak transcription	Fetal Stomach	stomach
40	chr15:72145400-72190600	Weak transcription	Spleen	Spleen
41	chr15:72145600-72170600	Weak transcription	Primary T cells fromperipheralblood	blood
42	chr15:72145600-72182800	Weak transcription	Brain Cingulate Gyrus	brain
43	chr15:72145600-72184800	Weak transcription	Lung	lung
44	chr15:72145800-72170400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr15:72146000-72170000	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr15:72146200-72160200	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr15:72146200-72171800	Weak transcription	Brain Hippocampus Middle	brain
48	chr15:72146200-72171800	Weak transcription	Left Ventricle	heart
49	chr15:72146200-72172000	Weak transcription	Brain Anterior Caudate	brain
50	chr15:72146400-72169000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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