Variant report

Variant	nsv457172
Chromosome Location	chr15:58417895-58457507
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	chr15:58435113-58435606	K562	blood:	n/a	n/a
2	ATF1	chr15:58435080-58435720	K562	blood:	n/a	n/a
3	CCNT2	chr15:58435063-58435490	K562	blood:	n/a	n/a
4	CEBPB	chr15:58435045-58435391	Hela-S3	cervix:	n/a	chr15:58435216-58435227
5	CEBPB	chr15:58430253-58430528	HepG2	liver:	n/a	chr15:58430399-58430410 chr15:58430353-58430366
6	CEBPB	chr15:58439325-58439623	HepG2	liver:	n/a	chr15:58439465-58439476
7	CEBPB	chr15:58457192-58457397	HepG2	liver:	n/a	chr15:58457271-58457282
8	CEBPB	chr15:58430360-58430546	A549	lung:	n/a	chr15:58430399-58430410
9	CEBPB	chr15:58457168-58457399	A549	lung:	n/a	chr15:58457271-58457282
10	CEBPB	chr15:58435060-58435357	K562	blood:	n/a	chr15:58435216-58435227
11	CEBPB	chr15:58439346-58439592	A549	lung:	n/a	chr15:58439465-58439476
12	CEBPB	chr15:58435027-58435401	K562	blood:	n/a	chr15:58435216-58435227
13	CEBPB	chr15:58435119-58435301	IMR90	lung:	n/a	chr15:58435216-58435227
14	CEBPB	chr15:58457117-58457422	K562	blood:	n/a	chr15:58457271-58457282
15	CEBPB	chr15:58434995-58435463	K562	blood:	n/a	chr15:58435216-58435227
16	CEBPB	chr15:58435044-58435365	HepG2	liver:	n/a	chr15:58435216-58435227
17	CTCF	chr15:58454320-58454470	A549	lung:	n/a	n/a
18	CTCF	chr15:58454196-58454386	HUVEC	blood vessel:	n/a	chr15:58454278-58454299 chr15:58454276-58454294 chr15:58454281-58454291
19	CTCF	chr15:58440820-58440970	HFF-Myc	foreskin:	n/a	n/a
20	CTCF	chr15:58454268-58454340	Hela-S3	cervix:	n/a	chr15:58454278-58454299 chr15:58454276-58454294 chr15:58454281-58454291
21	CTCF	chr15:58433520-58433670	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr15:58456600-58456750	HRE	kidney:	n/a	n/a
23	CTCF	chr15:58454460-58454610	BE2_C	brain:	n/a	n/a
24	CUX1	chr15:58431180-58431359	K562	blood:	n/a	n/a
25	CUX1	chr15:58435905-58436041	K562	blood:	n/a	n/a
26	E2F4	chr15:58432275-58432514	MCF10A-Er-Src	breast:	n/a	n/a
27	EBF1	chr15:58430389-58430585	GM12878	blood:	n/a	n/a
28	EBF1	chr15:58439469-58439734	GM12878	blood:	n/a	n/a
29	EP300	chr15:58435062-58435750	K562	blood:	n/a	chr15:58435217-58435231
30	EP300	chr15:58427150-58427477	K562	blood:	n/a	n/a
31	ESR1	chr15:58439415-58439924	ECC-1	luminal epithelium:	n/a	n/a
32	ESR1	chr15:58438884-58439912	ECC-1	luminal epithelium:	n/a	chr15:58439054-58439069
33	ESR1	chr15:58439497-58439742	ECC-1	luminal epithelium:	n/a	n/a
34	ESR1	chr15:58439456-58439838	ECC-1	luminal epithelium:	n/a	n/a
35	ESR1	chr15:58438907-58439370	ECC-1	luminal epithelium:	n/a	chr15:58439054-58439069
36	ESR1	chr15:58438937-58439901	ECC-1	luminal epithelium:	n/a	chr15:58439054-58439069
37	ESR1	chr15:58439491-58439848	ECC-1	luminal epithelium:	n/a	n/a
38	ESR1	chr15:58439106-58439457	ECC-1	luminal epithelium:	n/a	n/a
39	FAM48A	chr15:58428964-58429072	GM12878	blood:	n/a	n/a
40	FOS	chr15:58431951-58432523	MCF10A-Er-Src	breast:	n/a	chr15:58432317-58432325 chr15:58432315-58432327 chr15:58432313-58432324
41	FOS	chr15:58455003-58455203	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr15:58430275-58430510	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr15:58430231-58430539	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr15:58439039-58439239	MCF10A-Er-Src	breast:	n/a	chr15:58439151-58439159 chr15:58439090-58439100 chr15:58439090-58439100 chr15:58439147-58439158 chr15:58439150-58439160
45	FOS	chr15:58431897-58432536	MCF10A-Er-Src	breast:	n/a	chr15:58432317-58432325 chr15:58432315-58432327 chr15:58432313-58432324
46	FOS	chr15:58439004-58439586	MCF10A-Er-Src	breast:	n/a	chr15:58439151-58439159 chr15:58439090-58439100 chr15:58439090-58439100 chr15:58439147-58439158 chr15:58439150-58439160
47	FOS	chr15:58438983-58439533	MCF10A-Er-Src	breast:	n/a	chr15:58439151-58439159 chr15:58439090-58439100 chr15:58439090-58439100 chr15:58439147-58439158 chr15:58439150-58439160
48	FOS	chr15:58431904-58432471	MCF10A-Er-Src	breast:	n/a	chr15:58432317-58432325 chr15:58432315-58432327 chr15:58432313-58432324
49	FOS	chr15:58447006-58447278	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr15:58439051-58439249	MCF10A-Er-Src	breast:	n/a	chr15:58439151-58439159 chr15:58439090-58439100 chr15:58439090-58439100 chr15:58439147-58439158 chr15:58439150-58439160

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:58429729-58429779	SK-N-SH	brain:	n/a
2	chr15:58429729-58429779	SK-N-SH	brain:	n/a
3	chr15:58429729-58429779	SKMC	muscle:	n/a
4	chr15:58430539-58430589	RPTEC	kidney:	n/a
5	chr15:58430682-58430732	ECC-1	luminal epithelium:	n/a
6	chr15:58430539-58430589	LNCaP	prostate:	n/a
7	chr15:58430539-58430589	HEEpiC	esophagus:	n/a
8	chr15:58429751-58429801	HIPEpiC	eye:	n/a
9	chr15:58430682-58430732	BE2_C	brain:	n/a
10	chr15:58430391-58430441	CMK	blood:	n/a
11	chr15:58430539-58430589	NHBE	bronchial:	n/a
12	chr15:58430539-58430589	BJ	skin:	n/a
13	chr15:58430391-58430441	BJ	skin:	n/a
14	chr15:58429751-58429801	NT2-D1	testis:	n/a
15	chr15:58429729-58429779	SAEC	small airway:	n/a
16	chr15:58429751-58429801	H1-hESC	embryonic stem cell:	embryo
17	chr15:58430539-58430589	AG04450	lung:	fetal
18	chr15:58430539-58430589	AG09319	gingival:	n/a
19	chr15:58430539-58430589	HRE	kidney:	n/a
20	chr15:58429751-58429801	IMR90	lung:	fetal
21	chr15:58429729-58429779	HRCEpiC	kidney:	n/a
22	chr15:58430391-58430441	K562	blood:	n/a
23	chr15:58430682-58430732	HCF	heart:	n/a
24	chr15:58430539-58430589	HIPEpiC	eye:	n/a
25	chr15:58430682-58430732	AG04450	lung:	fetal
26	chr15:58429729-58429779	HAEpiC	amniotic membrane:	n/a
27	chr15:58430539-58430589	T-47D	breast:	n/a
28	chr15:58429751-58429801	U87	brain:	n/a
29	chr15:58430391-58430441	NHDF-neo	bronchial:	n/a
30	chr15:58429751-58429801	HCM	heart:	n/a
31	chr15:58430391-58430441	HL-60	blood:	n/a
32	chr15:58430391-58430441	HEK293	kidney:	embryo
33	chr15:58430682-58430732	AG10803	skin:	n/a
34	chr15:58429729-58429779	SK-N-SH_RA	brain:	n/a
35	chr15:58430682-58430732	AG09309	skin:	n/a
36	chr15:58430391-58430441	GM12892	blood:	n/a
37	chr15:58429729-58429779	HL-60	blood:	n/a
38	chr15:58430682-58430732	NB4	blood:	n/a
39	chr15:58429729-58429779	GM12878	blood:	n/a
40	chr15:58429751-58429801	AG10803	skin:	n/a
41	chr15:58430539-58430589	SAEC	small airway:	n/a
42	chr15:58430391-58430441	IMR90	lung:	fetal
43	chr15:58429729-58429779	K562	blood:	n/a
44	chr15:58430391-58430441	AoSMC	blood vessel:	n/a
45	chr15:58430682-58430732	PANC-1	pancreas:	n/a
46	chr15:58430391-58430441	HAEpiC	amniotic membrane:	n/a
47	chr15:58430682-58430732	MCF10A-Er-Src	breast:	n/a
48	chr15:58430682-58430732	Hela-S3	cervix:	n/a
49	chr15:58429729-58429779	AG04449	skin:	fetal
50	chr15:58430682-58430732	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:58424607..58427157-chr15:58433686..58435502,2	K562	blood:
2	chr15:58451875..58456386-chr15:58457557..58459744,5	K562	blood:
3	chr15:58415494..58417791-chr15:58424997..58426623,2	K562	blood:
4	chr15:58457163..58460249-chr15:58468233..58471898,3	K562	blood:
5	chr15:58435593..58437807-chr15:58437844..58439525,2	K562	blood:
6	chr15:58414406..58417362-chr15:58440343..58442016,3	K562	blood:
7	chr15:58433881..58435963-chr15:58440042..58441729,2	K562	blood:
8	chr15:58433341..58435310-chr15:58436697..58438419,2	K562	blood:
9	chr15:58240183..58241922-chr15:58434571..58436348,2	K562	blood:
10	chr15:58451065..58452651-chr15:58454983..58457554,2	K562	blood:
11	chr15:58451065..58452651-chr15:58454983..58457554,2	K562	blood:
12	chr15:58424607..58427157-chr15:58433686..58435502,2	K562	blood:
13	chr15:58401521..58404295-chr15:58452218..58454934,2	K562	blood:
14	chr15:58435593..58437807-chr15:58437844..58439525,2	K562	blood:
15	chr15:58433881..58435963-chr15:58440042..58441729,2	K562	blood:
16	chr15:58452711..58455369-chr15:58457890..58460728,2	MCF-7	breast:
17	chr15:58433341..58435310-chr15:58436697..58438419,2	K562	blood:
18	chr15:58451875..58454675-chr15:58458002..58459744,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LIPC-7	chr15:58430462-58430875	NONHSAT044094
2	lnc-LIPC-7	chr15:58438921-58439094	NONHSAT044094
3	lnc-LIPC-4	chr15:58443232-58444712	NONHSAT044098
4	lnc-LIPC-2	chr15:58447159-58448260	NONHSAT044100
5	lnc-ADAM10-9	chr15:58430646-58430771	NONHSAT044095
6	lnc-ADAM10-9	chr15:58430646-58430771	NONHSAT044093
7	lnc-LIPC-3	chr15:58444805-58446606	NONHSAT044099
8	lnc-LIPC-6	chr15:58442474-58442762	NONHSAT044096
9	lnc-LIPC-5	chr15:58442834-58443161	NONHSAT044097
10	lnc-ADAM10-9	chr15:58430646-58430771	NONHSAT044089
11	lnc-ADAM10-9	chr15:58456151-58456343	NONHSAT044095

Variant related genes	Relation type
ENSG00000259626	TF binding region
ENSG00000259651	TF binding region
AQP9	TF binding region
ENSG00000259379	TF binding region
ENSG00000259671	TF binding region
ENSG00000259600	TF binding region
ALDH1A2	TF binding region
ENSG00000259626	CpG island
ENSG00000259651	CpG island
AQP9	CpG island
ENSG00000259379	CpG island
ENSG00000259671	CpG island
ENSG00000259600	CpG island
ALDH1A2	CpG island

Extended variants
information (count: 1351 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1351 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7180019	chr15:58425383-58425384	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570635301	chr15:58425441-58425442	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs7162304	chr15:58425456-58425457	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs569751982	chr15:58425517-58425518	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs2642628	chr15:58425529-58425530	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs374829471	chr15:58425542-58425543	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs183443307	chr15:58425543-58425544	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs373945449	chr15:58425592-58425593	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs574318853	chr15:58425629-58425630	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs536432431	chr15:58425649-58425650	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs553500329	chr15:58425672-58425673	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs556746329	chr15:58425697-58425698	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs186628431	chr15:58425736-58425737	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs545115597	chr15:58425776-58425777	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs556177093	chr15:58425779-58425780	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs386784407	chr15:58425804-58425805	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs572111811	chr15:58425823-58425824	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs2642629	chr15:58425825-58425826	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs541264596	chr15:58425861-58425862	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs561015099	chr15:58425878-58425879	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs530036468	chr15:58425891-58425892	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs549686435	chr15:58425923-58425924	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs76302487	chr15:58425931-58425932	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs75404679	chr15:58425932-58425933	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs563494070	chr15:58425944-58425945	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs532209550	chr15:58425987-58425988	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs139447970	chr15:58426009-58426010	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs565630431	chr15:58426010-58426011	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs534317313	chr15:58426058-58426059	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs28369432	chr15:58426072-58426073	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs191433644	chr15:58426073-58426074	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs536976631	chr15:58426077-58426078	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs556305691	chr15:58426078-58426079	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs147578026	chr15:58426082-58426083	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs139577150	chr15:58426117-58426118	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs558624461	chr15:58426170-58426171	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs576280193	chr15:58426201-58426202	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs572542717	chr15:58426204-58426205	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs541052122	chr15:58426215-58426216	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs372861292	chr15:58426224-58426225	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs17571313	chr15:58426242-58426243	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs73426124	chr15:58426298-58426299	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs34590779	chr15:58426360-58426361	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs372694925	chr15:58426415-58426416	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs184658253	chr15:58426521-58426522	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs543713815	chr15:58426535-58426536	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs572454872	chr15:58426548-58426549	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs532347070	chr15:58426570-58426571	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs541242790	chr15:58426599-58426600	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs541368302	chr15:58426604-58426605	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	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
Colorectal cancer	16774939	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
Prostate cancer	16573809	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	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:207 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58427000-58428800	Enhancers	K562	blood
2	chr15:58427200-58431000	Enhancers	HMEC	breast
3	chr15:58427400-58429800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr15:58427400-58430800	Enhancers	NHEK	skin
5	chr15:58427400-58431200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr15:58427600-58429800	Enhancers	Muscle Satellite Cultured Cells	--
7	chr15:58427600-58430800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr15:58428000-58429200	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr15:58428400-58429400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr15:58428400-58430600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr15:58428600-58429800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr15:58428800-58431600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr15:58428800-58433600	Weak transcription	K562	blood
14	chr15:58429000-58429600	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr15:58429000-58430400	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr15:58429200-58430000	Enhancers	Liver	Liver
17	chr15:58429200-58430600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
18	chr15:58429400-58429600	Bivalent Enhancer	Primary B cells from cord blood	blood
19	chr15:58429400-58430600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr15:58429600-58429800	Enhancers	Adipose Nuclei	Adipose
21	chr15:58429600-58430000	Bivalent/Poised TSS	Primary B cells from cord blood	blood
22	chr15:58429600-58432000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
23	chr15:58429600-58436800	Active TSS	Primary hematopoietic stem cells	blood
24	chr15:58429800-58430200	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr15:58429800-58430600	Weak transcription	Adipose Nuclei	Adipose
26	chr15:58429800-58431600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr15:58430000-58430400	Flanking Active TSS	Liver	Liver
28	chr15:58430000-58436000	Active TSS	Primary B cells from cord blood	blood
29	chr15:58430200-58430800	Enhancers	Muscle Satellite Cultured Cells	--
30	chr15:58430400-58430600	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr15:58430400-58430800	Active TSS	Duodenum Smooth Muscle	Duodenum
32	chr15:58430400-58430800	Enhancers	Fetal Lung	lung
33	chr15:58430400-58431000	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr15:58430400-58431600	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr15:58430400-58432400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
36	chr15:58430400-58433200	Active TSS	Liver	Liver
37	chr15:58430600-58431000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
38	chr15:58430600-58431200	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr15:58430600-58431600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr15:58430600-58431600	Enhancers	NHDF-Ad	bronchial
41	chr15:58430600-58432000	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr15:58430600-58432000	Enhancers	Adipose Nuclei	Adipose
43	chr15:58430600-58432600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr15:58430600-58432800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr15:58430600-58432800	Active TSS	Primary neutrophils fromperipheralblood	blood
46	chr15:58430800-58431200	Weak transcription	Fetal Lung	lung
47	chr15:58430800-58431600	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr15:58430800-58431600	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr15:58430800-58431800	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr15:58430800-58431800	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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