Variant report

Variant	nsv904400
Chromosome Location	chr15:76772062-77085283
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1178)
CpG islands
(count:122)
Chromatin interactive
region (count:42)
LncRNA
region (count:2)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1178 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:76865111-76865365	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:76935433-76935442	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:76806361-76807005	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:76825612-76826689	HepG2	liver:	n/a	n/a
5	ATF2	chr15:76867574-76868256	GM12878	blood:	n/a	n/a
6	ATF2	chr15:77003703-77004047	GM12878	blood:	n/a	n/a
7	ATF2	chr15:77003716-77004122	GM12878	blood:	n/a	n/a
8	ATF2	chr15:76867545-76868188	GM12878	blood:	n/a	n/a
9	BATF	chr15:76946672-76946896	GM12878	blood:	n/a	n/a
10	BATF	chr15:76867629-76868083	GM12878	blood:	n/a	n/a
11	BATF	chr15:76946679-76946925	GM12878	blood:	n/a	n/a
12	BATF	chr15:76907137-76907384	GM12878	blood:	n/a	n/a
13	BATF	chr15:76996436-76996655	GM12878	blood:	n/a	n/a
14	BATF	chr15:76867553-76868299	GM12878	blood:	n/a	n/a
15	BATF	chr15:76996451-76996676	GM12878	blood:	n/a	n/a
16	BATF	chr15:76868780-76869125	GM12878	blood:	n/a	n/a
17	BATF	chr15:76907151-76907359	GM12878	blood:	n/a	n/a
18	BCL11A	chr15:77003618-77004150	GM12878	blood:	n/a	n/a
19	BCL11A	chr15:76867571-76868071	GM12878	blood:	n/a	n/a
20	BCL11A	chr15:76867646-76868017	GM12878	blood:	n/a	n/a
21	BCL11A	chr15:77003630-77004113	GM12878	blood:	n/a	n/a
22	BCL11A	chr15:76946684-76946864	GM12878	blood:	n/a	n/a
23	BCL3	chr15:76825763-76826141	GM12878	blood:	n/a	n/a
24	BCL3	chr15:76867671-76868118	GM12878	blood:	n/a	n/a
25	BCL3	chr15:76825735-76826094	GM12878	blood:	n/a	n/a
26	BCL3	chr15:76867594-76868106	GM12878	blood:	n/a	n/a
27	BCLAF1	chr15:77003650-77004026	GM12878	blood:	n/a	n/a
28	BCLAF1	chr15:76867350-76868205	GM12878	blood:	n/a	n/a
29	BCLAF1	chr15:76867603-76868092	GM12878	blood:	n/a	n/a
30	BHLHE40	chr15:77003580-77004137	GM12878	blood:	n/a	n/a
31	BHLHE40	chr15:76867676-76868010	GM12878	blood:	n/a	n/a
32	BHLHE40	chr15:76946680-76946809	GM12878	blood:	n/a	n/a
33	BRCA1	chr15:76969668-76969722	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr15:76805598-76805611	H1-hESC	embryonic stem cell:	n/a	n/a
35	CBX3	chr15:76928484-76928676	K562	blood:	n/a	n/a
36	CBX3	chr15:77055892-77056260	K562	blood:	n/a	n/a
37	CBX3	chr15:77069395-77069686	K562	blood:	n/a	n/a
38	CBX3	chr15:77069334-77069671	K562	blood:	n/a	n/a
39	CBX3	chr15:76928439-76928711	K562	blood:	n/a	n/a
40	CBX3	chr15:77055938-77056220	K562	blood:	n/a	n/a
41	CEBPB	chr15:76867534-76868241	GM12878	blood:	n/a	n/a
42	CEBPB	chr15:76796124-76796451	IMR90	lung:	n/a	chr15:76796282-76796293
43	CEBPB	chr15:76865274-76865637	IMR90	lung:	n/a	chr15:76865442-76865453
44	CEBPB	chr15:76825807-76825998	HepG2	liver:	n/a	chr15:76825947-76825958
45	CEBPB	chr15:76839201-76839452	A549	lung:	n/a	chr15:76839336-76839347
46	CEBPB	chr15:76803703-76803878	HepG2	liver:	n/a	n/a
47	CEBPB	chr15:76839240-76839462	K562	blood:	n/a	chr15:76839336-76839347
48	CEBPB	chr15:76865361-76865572	H1-hESC	embryonic stem cell:	n/a	chr15:76865442-76865453
49	CEBPB	chr15:77052043-77052208	A549	lung:	n/a	n/a
50	CEBPB	chr15:76837027-76837186	IMR90	lung:	n/a	chr15:76837087-76837098

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:76901065-76901115	HL-60	blood:	n/a
2	chr15:76901065-76901115	Hepatocyte	liver:	n/a
3	chr15:76901065-76901115	BE2_C	brain:	n/a
4	chr15:76868964-76869014	MCF10A-Er-Src	breast:	n/a
5	chr15:76901065-76901115	HRE	kidney:	n/a
6	chr15:76868964-76869014	HepG2	liver:	n/a
7	chr15:76901065-76901115	GM19239	blood:	n/a
8	chr15:76901065-76901115	NHBE	bronchial:	n/a
9	chr15:76901065-76901115	GM12878	blood:	n/a
10	chr15:76868964-76869014	HCM	heart:	n/a
11	chr15:76901065-76901115	MCF10A-Er-Src	breast:	n/a
12	chr15:76868964-76869014	GM12891	blood:	n/a
13	chr15:76901065-76901115	GM12891	blood:	n/a
14	chr15:76901065-76901115	HCF	heart:	n/a
15	chr15:76901065-76901115	SKMC	muscle:	n/a
16	chr15:76868964-76869014	SK-N-SH_RA	brain:	n/a
17	chr15:76868964-76869014	PFSK-1	brain:	n/a
18	chr15:76868964-76869014	HAEpiC	amniotic membrane:	n/a
19	chr15:76901065-76901115	Hela-S3	cervix:	n/a
20	chr15:76868964-76869014	Hela-S3	cervix:	n/a
21	chr15:76901065-76901115	HCM	heart:	n/a
22	chr15:76901065-76901115	PFSK-1	brain:	n/a
23	chr15:76868964-76869014	NB4	blood:	n/a
24	chr15:76901065-76901115	IMR90	lung:	fetal
25	chr15:76868964-76869014	Jurkat	blood:	n/a
26	chr15:76868964-76869014	HCPEpiC	choroid plexus:	n/a
27	chr15:76868964-76869014	HUVEC	blood vessel:	n/a
28	chr15:76901065-76901115	HIPEpiC	eye:	n/a
29	chr15:76868964-76869014	Hepatocyte	liver:	n/a
30	chr15:76901065-76901115	SK-N-SH	brain:	n/a
31	chr15:76901065-76901115	Caco-2	colon:	n/a
32	chr15:76868964-76869014	CMK	blood:	n/a
33	chr15:76868964-76869014	AG04449	skin:	fetal
34	chr15:76868964-76869014	PANC-1	pancreas:	n/a
35	chr15:76901065-76901115	AG09309	skin:	n/a
36	chr15:76868964-76869014	GM06990	blood:	n/a
37	chr15:76868964-76869014	BJ	skin:	n/a
38	chr15:76901065-76901115	AG04449	skin:	fetal
39	chr15:76868964-76869014	GM19239	blood:	n/a
40	chr15:76901065-76901115	SAEC	small airway:	n/a
41	chr15:76868964-76869014	HL-60	blood:	n/a
42	chr15:76868964-76869014	SK-N-SH	brain:	n/a
43	chr15:76901065-76901115	AG10803	skin:	n/a
44	chr15:76901065-76901115	RPTEC	kidney:	n/a
45	chr15:76901065-76901115	ProgFib	skin:	n/a
46	chr15:76901065-76901115	ovcar-3	ovarian:	n/a
47	chr15:76901065-76901115	BJ	skin:	n/a
48	chr15:76868964-76869014	NHBE	bronchial:	n/a
49	chr15:76868964-76869014	PrEC	prostate:	n/a
50	chr15:76901065-76901115	HepG2	liver:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:76482009..76484403-chr15:77035735..77037455,2	MCF-7	breast:
2	chr11:60896554..60897446-chr15:76806259..76806955,2	MCF-7	breast:
3	chr15:77017797..77020777-chr8:43093705..43096561,2	K562	blood:
4	chr15:76997314..76998845-chr15:77007470..77009179,2	MCF-7	breast:
5	chr15:76997314..76998845-chr15:77007470..77009179,2	MCF-7	breast:
6	chr15:77044758..77046845-chr15:77050241..77052508,2	MCF-7	breast:
7	chr15:77024348..77024882-chr15:77132939..77133789,2	MCF-7	breast:
8	chr15:76969596..76972550-chr15:76979737..76981959,2	MCF-7	breast:
9	chr15:76964455..76968844-chr15:76969640..76972722,4	K562	blood:
10	chr15:76812872..76815537-chr15:76817323..76820278,2	MCF-7	breast:
11	chr15:77052021..77055015-chr15:77055082..77056903,3	K562	blood:
12	chr15:76934226..76937075-chr15:76948287..76950112,2	MCF-7	breast:
13	chr15:76978559..76980160-chr15:76982250..76984451,2	MCF-7	breast:
14	chr15:76978559..76980160-chr15:76982250..76984451,2	MCF-7	breast:
15	chr15:77022336..77024619-chr15:77130860..77133173,2	MCF-7	breast:
16	chr15:76810534..76813037-chr15:76815373..76817326,2	MCF-7	breast:
17	chr15:76959064..76961382-chr15:76964223..76965946,2	MCF-7	breast:
18	chr15:76821101..76824629-chr15:76825214..76826999,4	K562	blood:
19	chr10:94276542..94277057-chr15:77040784..77041284,2	MCF-7	breast:
20	chr15:76812872..76815537-chr15:76817323..76820278,2	MCF-7	breast:
21	chr15:76969596..76972550-chr15:76979737..76981959,2	MCF-7	breast:
22	chr15:76803456..76806308-chr15:77131835..77134067,2	MCF-7	breast:
23	chr15:76877558..76879609-chr15:76881319..76882907,2	K562	blood:
24	chr15:76855877..76857707-chr15:76866696..76869240,2	MCF-7	breast:
25	chr15:76967596..76970375-chr15:76976896..76979262,2	K562	blood:
26	chr15:76934897..76935640-chr15:77158999..77159764,3	MCF-7	breast:
27	chr15:76934737..76935336-chr15:77133237..77133799,2	MCF-7	breast:
28	chr15:76964455..76968844-chr15:76969640..76972722,4	K562	blood:
29	chr15:77051074..77052943-chr15:77058188..77061067,2	K562	blood:
30	chr15:76789083..76790896-chr15:76806122..76808106,2	MCF-7	breast:
31	chr15:77052021..77055015-chr15:77055082..77056903,3	K562	blood:
32	chr15:76493051..76495991-chr15:76813493..76815400,2	MCF-7	breast:
33	chr15:76789083..76790896-chr15:76806122..76808106,2	MCF-7	breast:
34	chr15:77083317..77084988-chr15:77087176..77089675,2	K562	blood:
35	chr15:76934226..76937075-chr15:76948287..76950112,2	MCF-7	breast:
36	chr15:76810534..76813037-chr15:76815373..76817326,2	MCF-7	breast:
37	chr15:76821101..76824629-chr15:76825214..76826999,4	K562	blood:
38	chr15:76855877..76857707-chr15:76866696..76869240,2	MCF-7	breast:
39	chr15:77051074..77052943-chr15:77058188..77061067,2	K562	blood:
40	chr15:76959064..76961382-chr15:76964223..76965946,2	MCF-7	breast:
41	chr15:77044758..77046845-chr15:77050241..77052508,2	MCF-7	breast:
42	chr15:76967596..76970375-chr15:76976896..76979262,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RCN2-1	chr15:77028982-77029321	NONHSAT047408
2	lnc-ETFA-5	chr15:76833537-76833934	NONHSAT047406

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3713	chr15:76878988-76879007	MIMAT0018164

No data

Variant related genes	Relation type
SCAPER	TF binding region
RN7SKP217	TF binding region
MIR3713	TF binding region
SCAPER	CpG island
RN7SKP217	CpG island
MIR3713	CpG island
ENSG00000169758	chromatin interactions
ENSG00000266449	chromatin interactions

Extended variants
information (count: 10980 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:10980 , 50 per page) page: 1 2 3 4 5 6 7 ... 220

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2469249	chr15:76772062-76772063	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs548641543	chr15:76772168-76772169	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186395532	chr15:76772170-76772171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544721390	chr15:76772258-76772259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558534441	chr15:76772269-76772270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570761041	chr15:76772282-76772283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535005988	chr15:76772335-76772336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189593445	chr15:76772338-76772339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558892536	chr15:76772434-76772435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574956250	chr15:76772484-76772485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542107886	chr15:76772499-76772500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557012394	chr15:76772547-76772548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182212922	chr15:76772555-76772556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76744121	chr15:76772605-76772606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs564093000	chr15:76772615-76772616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs577897147	chr15:76772619-76772620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs35092831	chr15:76772661-76772662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs73442185	chr15:76772730-76772731	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs540506245	chr15:76772757-76772758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561860455	chr15:76772813-76772814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187564446	chr15:76772814-76772815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550541350	chr15:76772815-76772816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs372007611	chr15:76772827-76772828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs543321052	chr15:76772866-76772867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569772864	chr15:76772892-76772893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs377107142	chr15:76772914-76772915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs556927966	chr15:76772917-76772918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192658390	chr15:76772942-76772943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs147466125	chr15:76772954-76772955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570524940	chr15:76772991-76772992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369536608	chr15:76772995-76772996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs11854048	chr15:76773140-76773141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs547269893	chr15:76773157-76773158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs8026220	chr15:76773204-76773205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536010333	chr15:76773215-76773216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557278239	chr15:76773256-76773257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs367862779	chr15:76773263-76773264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575383679	chr15:76773282-76773283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559478917	chr15:76773284-76773285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370304833	chr15:76773314-76773315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572709832	chr15:76773319-76773320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1965492	chr15:76773326-76773327	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs557922519	chr15:76773327-76773328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572852590	chr15:76773335-76773336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368880159	chr15:76773356-76773357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183416049	chr15:76773361-76773362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562005629	chr15:76773364-76773365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573862158	chr15:76773367-76773368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544344646	chr15:76773420-76773421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145253151	chr15:76773457-76773458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
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
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:2787 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76725800-76812600	Weak transcription	Left Ventricle	heart
2	chr15:76760000-76772600	Weak transcription	GM12878-XiMat	blood
3	chr15:76760400-76773800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr15:76763000-76795000	Weak transcription	Primary B cells from cord blood	blood
5	chr15:76763600-76775200	Weak transcription	Liver	Liver
6	chr15:76771400-76772200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr15:76772600-76773200	Enhancers	GM12878-XiMat	blood
8	chr15:76775200-76776000	Enhancers	Liver	Liver
9	chr15:76775400-76776000	Enhancers	HepG2	liver
10	chr15:76785200-76786000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr15:76785400-76790400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr15:76785400-76799800	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr15:76786000-76786600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr15:76786600-76786800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr15:76786800-76790600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr15:76787800-76793200	Weak transcription	Colon Smooth Muscle	Colon
17	chr15:76788000-76788400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr15:76788000-76795200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr15:76788000-76796600	Weak transcription	HSMM	muscle
20	chr15:76788200-76788600	Enhancers	Fetal Intestine Small	intestine
21	chr15:76788200-76795000	Weak transcription	Primary T cells from cord blood	blood
22	chr15:76788200-76798400	Weak transcription	Dnd41	blood
23	chr15:76788400-76788600	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr15:76788400-76793800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr15:76788400-76813600	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr15:76788600-76792000	Weak transcription	Fetal Intestine Small	intestine
27	chr15:76789200-76789800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr15:76789200-76796200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr15:76789200-76796200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr15:76789200-76796600	Weak transcription	Adipose Nuclei	Adipose
31	chr15:76789600-76796400	Weak transcription	Stomach Smooth Muscle	stomach
32	chr15:76790000-76802000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr15:76790400-76790800	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr15:76790400-76791000	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr15:76790400-76791200	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr15:76790600-76790800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr15:76790600-76796200	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr15:76791000-76796200	Weak transcription	Primary hematopoietic stem cells	blood
39	chr15:76791200-76806200	Weak transcription	Fetal Muscle Leg	muscle
40	chr15:76792000-76796400	Enhancers	Fetal Intestine Small	intestine
41	chr15:76792600-76798600	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr15:76792600-76801800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr15:76792800-76794600	Enhancers	Duodenum Mucosa	Duodenum
44	chr15:76793200-76794400	Enhancers	Small Intestine	intestine
45	chr15:76793200-76796400	Enhancers	Fetal Intestine Large	intestine
46	chr15:76793800-76794200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr15:76793800-76796600	Weak transcription	Ovary	ovary
48	chr15:76793800-76798600	Weak transcription	Placenta	Placenta
49	chr15:76793800-76799400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr15:76794000-76794200	Enhancers	Gastric	stomach

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