Variant report

Variant	nsv904205
Chromosome Location	chr15:50228476-50286981
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	CEBPB	chr15:50244805-50245063	IMR90	lung:	n/a	chr15:50244943-50244954
2	CEBPB	chr15:50283418-50283665	IMR90	lung:	n/a	n/a
3	CEBPB	chr15:50244820-50244979	K562	blood:	n/a	chr15:50244943-50244954
4	CEBPB	chr15:50277117-50277315	K562	blood:	n/a	chr15:50277226-50277235 chr15:50277226-50277235 chr15:50277224-50277237 chr15:50277226-50277235 chr15:50277224-50277237 chr15:50277224-50277235 chr15:50277226-50277237 chr15:50277226-50277237 chr15:50277224-50277237 chr15:50277226-50277235
5	CEBPB	chr15:50254358-50254487	A549	lung:	n/a	n/a
6	CEBPB	chr15:50265660-50265875	HepG2	liver:	n/a	chr15:50265794-50265805
7	CEBPB	chr15:50244784-50245065	HepG2	liver:	n/a	chr15:50244943-50244954
8	CEBPB	chr15:50265730-50265838	Hela-S3	cervix:	n/a	chr15:50265794-50265805
9	CEBPB	chr15:50244843-50245052	MCF-7	breast:	n/a	chr15:50244943-50244954
10	CEBPB	chr15:50277075-50277249	HepG2	liver:	n/a	chr15:50277226-50277235 chr15:50277226-50277235 chr15:50277224-50277237 chr15:50277226-50277235 chr15:50277224-50277237 chr15:50277224-50277235 chr15:50277226-50277237 chr15:50277226-50277237 chr15:50277224-50277237 chr15:50277226-50277235
11	CEBPB	chr15:50244795-50245092	A549	lung:	n/a	chr15:50244943-50244954
12	CEBPB	chr15:50276536-50277317	MCF-7	breast:	n/a	chr15:50277226-50277235 chr15:50277226-50277235 chr15:50277224-50277237 chr15:50277226-50277235 chr15:50277224-50277237 chr15:50277224-50277235 chr15:50277226-50277237 chr15:50277226-50277237 chr15:50277224-50277237 chr15:50277226-50277235
13	CEBPB	chr15:50278713-50279006	A549	lung:	n/a	n/a
14	CEBPB	chr15:50265669-50265934	IMR90	lung:	n/a	chr15:50265794-50265805
15	CEBPB	chr15:50278741-50278953	HepG2	liver:	n/a	n/a
16	CEBPB	chr15:50244939-50244956	H1-hESC	embryonic stem cell:	n/a	chr15:50244943-50244954
17	CEBPB	chr15:50274778-50275207	IMR90	lung:	n/a	n/a
18	CHD2	chr15:50245658-50245684	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr15:50241351-50241407	GM20000	blood:	n/a	n/a
20	CTCF	chr15:50244904-50244921	GM10248	blood:	n/a	n/a
21	CTCF	chr15:50264053-50264129	Spleen_OC	spleen:	n/a	n/a
22	CTCF	chr15:50275860-50276010	HRE	kidney:	n/a	n/a
23	CTCF	chr15:50270680-50270830	HFF-Myc	foreskin:	n/a	n/a
24	CTCF	chr15:50245600-50245750	MCF-7	breast:	n/a	n/a
25	CTCF	chr15:50281776-50281814	GM20000	blood:	n/a	n/a
26	CTCF	chr15:50278660-50278810	BJ	skin:	n/a	n/a
27	EBF1	chr15:50284514-50284520	GM12878	blood:	n/a	n/a
28	ELK1	chr15:50248081-50248119	K562	blood:	n/a	n/a
29	EP300	chr15:50254474-50254738	SK-N-SH_RA	brain:	n/a	n/a
30	EP300	chr15:50238959-50239317	T-47D	breast:	n/a	n/a
31	EP300	chr15:50238922-50239273	T-47D	breast:	n/a	n/a
32	EP300	chr15:50254202-50254753	SK-N-SH_RA	brain:	n/a	chr15:50254304-50254312 chr15:50254303-50254317
33	EP300	chr15:50253966-50255019	SK-N-SH	brain:	n/a	chr15:50254304-50254312 chr15:50254303-50254317
34	ESR1	chr15:50276654-50277027	T-47D	breast:	n/a	n/a
35	ESR1	chr15:50276695-50277047	T-47D	breast:	n/a	n/a
36	ESR1	chr15:50276724-50276971	T-47D	breast:	n/a	n/a
37	ESR1	chr15:50239029-50239240	ECC-1	luminal epithelium:	n/a	n/a
38	ESR1	chr15:50276751-50277042	T-47D	breast:	n/a	n/a
39	ESR1	chr15:50276626-50277052	T-47D	breast:	n/a	n/a
40	FOS	chr15:50239016-50239238	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr15:50239038-50239238	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr15:50279777-50279820	MCF10A-Er-Src	breast:	n/a	chr15:50279779-50279788 chr15:50279779-50279786 chr15:50279777-50279789
43	FOSL2	chr15:50283396-50283703	SK-N-SH	brain:	n/a	n/a
44	FOXA1	chr15:50239011-50239273	ECC-1	luminal epithelium:	n/a	chr15:50239108-50239123
45	FOXA1	chr15:50258517-50258893	HepG2	liver:	n/a	n/a
46	FOXA1	chr15:50276629-50276951	T-47D	breast:	n/a	n/a
47	FOXA1	chr15:50238991-50239253	ECC-1	luminal epithelium:	n/a	chr15:50239108-50239123
48	FOXA1	chr15:50238964-50239356	T-47D	breast:	n/a	chr15:50239108-50239123
49	FOXA1	chr15:50238984-50239300	T-47D	breast:	n/a	chr15:50239108-50239123
50	FOXA2	chr15:50258485-50258860	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:50280871-50280921	Hepatocyte	liver:	n/a
2	chr15:50282326-50282376	RPTEC	kidney:	n/a
3	chr15:50274021-50274071	Caco-2	colon:	n/a
4	chr15:50282326-50282376	NB4	blood:	n/a
5	chr15:50280871-50280921	HMEC	breast:	n/a
6	chr15:50280871-50280921	HRCEpiC	kidney:	n/a
7	chr15:50280871-50280921	AG10803	skin:	n/a
8	chr15:50280871-50280921	GM12878	blood:	n/a
9	chr15:50280871-50280921	T-47D	breast:	n/a
10	chr15:50274021-50274071	HCPEpiC	choroid plexus:	n/a
11	chr15:50280871-50280921	PFSK-1	brain:	n/a
12	chr15:50274021-50274071	HCM	heart:	n/a
13	chr15:50274021-50274071	HEK293	kidney:	embryo
14	chr15:50282326-50282376	BE2_C	brain:	n/a
15	chr15:50274021-50274071	HAEpiC	amniotic membrane:	n/a
16	chr15:50282326-50282376	AoSMC	blood vessel:	n/a
17	chr15:50280871-50280921	U87	brain:	n/a
18	chr15:50282326-50282376	GM12878	blood:	n/a
19	chr15:50282326-50282376	SK-N-SH	brain:	n/a
20	chr15:50282326-50282376	MCF10A-Er-Src	breast:	n/a
21	chr15:50280871-50280921	HCM	heart:	n/a
22	chr15:50282326-50282376	HepG2	liver:	n/a
23	chr15:50282326-50282376	U87	brain:	n/a
24	chr15:50274021-50274071	SK-N-SH	brain:	n/a
25	chr15:50274021-50274071	GM12891	blood:	n/a
26	chr15:50280871-50280921	GM12891	blood:	n/a
27	chr15:50280871-50280921	GM06990	blood:	n/a
28	chr15:50282326-50282376	HRPEpiC	eye:	n/a
29	chr15:50274021-50274071	HCF	heart:	n/a
30	chr15:50274021-50274071	GM19239	blood:	n/a
31	chr15:50280871-50280921	NB4	blood:	n/a
32	chr15:50280871-50280921	HEEpiC	esophagus:	n/a
33	chr15:50274021-50274071	ECC-1	luminal epithelium:	n/a
34	chr15:50282326-50282376	BJ	skin:	n/a
35	chr15:50280871-50280921	MCF-7	breast:	n/a
36	chr15:50282326-50282376	AG09319	gingival:	n/a
37	chr15:50282326-50282376	IMR90	lung:	fetal
38	chr15:50280871-50280921	HNPCEpiC	eye:	n/a
39	chr15:50282326-50282376	SK-N-SH_RA	brain:	n/a
40	chr15:50280871-50280921	HepG2	liver:	n/a
41	chr15:50274021-50274071	HCT-116	colon:	n/a
42	chr15:50274021-50274071	RPTEC	kidney:	n/a
43	chr15:50280871-50280921	RPTEC	kidney:	n/a
44	chr15:50274021-50274071	HRPEpiC	eye:	n/a
45	chr15:50280871-50280921	K562	blood:	n/a
46	chr15:50280871-50280921	PANC-1	pancreas:	n/a
47	chr15:50274021-50274071	ProgFib	skin:	n/a
48	chr15:50274021-50274071	PrEC	prostate:	n/a
49	chr15:50282326-50282376	MCF-7	breast:	n/a
50	chr15:50280871-50280921	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:50269706..50272212-chr15:50276259..50278710,2	K562	blood:
2	chr15:50274598..50275298-chr17:37617590..37618180,2	NB4	blood:
3	chr1:115656548..115657326-chr15:50280165..50281026,2	MCF-7	breast:
4	chr15:50229689..50230313-chr6:58776456..58777229,2	MCF-7	breast:
5	chr15:50157609..50159636-chr15:50284420..50286036,2	MCF-7	breast:
6	chr15:50275595..50278547-chr15:50278669..50281707,3	K562	blood:
7	chr15:50275595..50278547-chr15:50278669..50281707,3	K562	blood:
8	chr15:50277715..50280459-chr15:50288291..50290867,2	MCF-7	breast:
9	chr15:50272105..50274274-chr15:50283581..50286177,2	MCF-7	breast:
10	chr15:50275991..50276690-chr6:82462543..82463331,2	NB4	blood:
11	chr15:50223443..50226093-chr15:50228959..50230928,2	K562	blood:
12	chr15:50272105..50274274-chr15:50283581..50286177,2	MCF-7	breast:
13	chr15:50269706..50272212-chr15:50276259..50278710,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C15orf33-1	chr15:50279709-50279746	NONHSAT042399

Variant related genes	Relation type
RNA5SP394	TF binding region
RNA5SP394	CpG island
ENSG00000167258	chromatin interactions

Extended variants
information (count: 2203 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2203 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2248985	chr15:50228476-50228477	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs533642854	chr15:50228515-50228516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555401866	chr15:50228635-50228636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573660581	chr15:50228714-50228715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543977039	chr15:50228737-50228738	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184399920	chr15:50228743-50228744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562545589	chr15:50228839-50228840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538539536	chr15:50228849-50228850	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs199709112	chr15:50228928-50228929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs371214908	chr15:50228929-50228930	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147777962	chr15:50228936-50228937	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368888409	chr15:50228943-50228944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs58957982	chr15:50228946-50228947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs28502034	chr15:50229015-50229016	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs368292774	chr15:50229059-50229060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143736309	chr15:50229070-50229071	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544946973	chr15:50229083-50229084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564312388	chr15:50229106-50229107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs28555213	chr15:50229108-50229109	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs561632950	chr15:50229137-50229138	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113805011	chr15:50229145-50229146	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562182418	chr15:50229177-50229178	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529422370	chr15:50229199-50229200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551181184	chr15:50229278-50229279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569501594	chr15:50229416-50229417	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533664512	chr15:50229451-50229452	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552144265	chr15:50229490-50229491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548513144	chr15:50229536-50229537	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567063210	chr15:50229645-50229646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533737793	chr15:50229650-50229651	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs36025803	chr15:50229651-50229652	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs140970125	chr15:50229687-50229688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189229456	chr15:50229708-50229709	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555934266	chr15:50229721-50229722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs145962940	chr15:50229741-50229742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575875358	chr15:50229798-50229799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577453543	chr15:50229803-50229804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73397002	chr15:50229915-50229916	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs553985546	chr15:50229922-50229923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75945351	chr15:50229926-50229927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540594779	chr15:50230002-50230003	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs142910970	chr15:50230007-50230008	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375911934	chr15:50230059-50230060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529391195	chr15:50230078-50230079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs147006246	chr15:50230132-50230133	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563069619	chr15:50230213-50230214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182409582	chr15:50230224-50230225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533516378	chr15:50230255-50230256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551690780	chr15:50230267-50230268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560801998	chr15:50230302-50230303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Myelofibrosis	22110671	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:50205400-50234400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
2	chr15:50210200-50232400	Strong transcription	Primary hematopoietic stem cells	blood
3	chr15:50211400-50232400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr15:50226000-50245200	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr15:50226400-50232400	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr15:50226400-50236000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr15:50228200-50229000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr15:50228200-50234200	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr15:50229000-50232200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr15:50232200-50232800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr15:50232400-50233000	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr15:50232400-50234200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
13	chr15:50232400-50241800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr15:50233000-50238800	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr15:50234200-50235200	Weak transcription	Primary hematopoietic stem cells	blood
16	chr15:50234200-50235400	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr15:50234400-50235400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr15:50235200-50236800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
19	chr15:50235400-50236200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
20	chr15:50235400-50236400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
21	chr15:50235600-50236800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr15:50236000-50236800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr15:50236200-50237800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
24	chr15:50236400-50237000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr15:50236400-50237800	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr15:50236800-50239000	Strong transcription	Primary hematopoietic stem cells	blood
27	chr15:50236800-50245000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr15:50237800-50238400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr15:50237800-50242600	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr15:50238400-50238800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
31	chr15:50238600-50239600	Enhancers	Liver	Liver
32	chr15:50238800-50242000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
33	chr15:50239000-50239200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr15:50239000-50239600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
35	chr15:50239000-50239600	Enhancers	Pancreas	Pancrea
36	chr15:50239200-50240600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr15:50239600-50243800	Weak transcription	Primary hematopoietic stem cells	blood
38	chr15:50240600-50240800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr15:50242000-50243200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr15:50243200-50246400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
41	chr15:50243600-50249000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr15:50243800-50245000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
43	chr15:50245000-50249400	Strong transcription	Primary hematopoietic stem cells	blood
44	chr15:50245000-50252200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr15:50245200-50246000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
46	chr15:50245200-50246400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
47	chr15:50245200-50248000	Strong transcription	Primary neutrophils fromperipheralblood	blood
48	chr15:50245400-50246000	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr15:50245400-50246000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr15:50245400-50246000	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood

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