Variant report

Variant	nsv977055
Chromosome Location	chr15:45949717-45957214
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:111)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:111 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr15:45954589-45954766	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr15:45955811-45955950	HepG2	liver:	n/a	chr15:45955915-45955926
3	CEBPB	chr15:45955850-45955977	H1-hESC	embryonic stem cell:	n/a	chr15:45955915-45955926
4	CHD1	chr15:45954739-45954750	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr15:45952460-45952610	GM06990	blood:	n/a	n/a
6	CTCF	chr15:45952420-45952570	HEK293	kidney:	n/a	n/a
7	CTCF	chr15:45952420-45952622	MCF-7	breast:	n/a	n/a
8	CTCF	chr15:45952454-45952566	HUVEC	blood vessel:	n/a	n/a
9	CTCF	chr15:45952520-45952670	NHEK	skin:	n/a	n/a
10	CTCF	chr15:45952439-45952567	GM10248	blood:	n/a	n/a
11	CTCF	chr15:45952440-45952590	RPTEC	kidney:	n/a	n/a
12	CTCF	chr15:45952420-45952570	SK-N-SH_RA	brain:	n/a	n/a
13	CTCF	chr15:45952480-45952630	GM12872	blood:	n/a	n/a
14	CTCF	chr15:45952440-45952590	HCPEpiC	choroid plexus:	n/a	n/a
15	CTCF	chr15:45952380-45952530	HRE	kidney:	n/a	n/a
16	CTCF	chr15:45952500-45952650	HCT-116	colon:	n/a	n/a
17	CTCF	chr15:45952440-45952590	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr15:45952380-45952530	HepG2	liver:	n/a	n/a
19	CTCF	chr15:45952440-45952590	SAEC	small airway:	n/a	n/a
20	CTCF	chr15:45952489-45952522	GM13977	blood:	n/a	n/a
21	CTCF	chr15:45952360-45952510	K562	blood:	n/a	n/a
22	CTCF	chr15:45954678-45954843	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr15:45954680-45954830	K562	blood:	n/a	n/a
24	CTCF	chr15:45952430-45952589	MCF-7	breast:	n/a	n/a
25	CTCF	chr15:45952455-45952551	GM10266	blood:	n/a	n/a
26	CTCF	chr15:45952480-45952630	HA-sp	spinal cord:	n/a	n/a
27	CTCF	chr15:45952440-45952590	A549	lung:	n/a	n/a
28	CTCF	chr15:45952439-45952543	NHEK	skin:	n/a	n/a
29	CTCF	chr15:45952520-45952670	BE2_C	brain:	n/a	n/a
30	CTCF	chr15:45952382-45952689	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr15:45952380-45952530	GM12872	blood:	n/a	n/a
32	CTCF	chr15:45954612-45954879	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr15:45954588-45954905	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr15:45952440-45952590	K562	blood:	n/a	n/a
35	CTCF	chr15:45952400-45952550	HVMF	connective:	n/a	n/a
36	CTCF	chr15:45954680-45954830	GM06990	blood:	n/a	n/a
37	CTCF	chr15:45952640-45952790	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr15:45952380-45952530	HPF	lung:	n/a	n/a
39	CTCF	chr15:45952400-45952550	HMEC	breast:	n/a	n/a
40	CTCF	chr15:45952420-45952570	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr15:45952661-45952730	LNCaP	prostate:	n/a	n/a
42	CTCF	chr15:45952420-45952570	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr15:45952320-45952470	BE2_C	brain:	n/a	n/a
44	CTCF	chr15:45952420-45952570	HCT-116	colon:	n/a	n/a
45	CTCF	chr15:45952420-45952570	BE2_C	brain:	n/a	n/a
46	CTCF	chr15:45952468-45952523	GM12878	blood:	n/a	n/a
47	CTCF	chr15:45952431-45952473	GM19238	blood:	n/a	n/a
48	CTCF	chr15:45952480-45952630	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr15:45952400-45952550	NB4	blood:	n/a	n/a
50	CTCF	chr15:45954700-45954850	NB4	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:45952725-45952775	NHBE	bronchial:	n/a
2	chr15:45952725-45952775	AoSMC	blood vessel:	n/a
3	chr15:45952725-45952775	GM12892	blood:	n/a
4	chr15:45952725-45952775	HRE	kidney:	n/a
5	chr15:45952725-45952775	BE2_C	brain:	n/a
6	chr15:45952725-45952775	ProgFib	skin:	n/a
7	chr15:45952725-45952775	Jurkat	blood:	n/a
8	chr15:45952725-45952775	MCF10A-Er-Src	breast:	n/a
9	chr15:45952725-45952775	HEK293	kidney:	embryo
10	chr15:45952725-45952775	ECC-1	luminal epithelium:	n/a
11	chr15:45952725-45952775	AG09319	gingival:	n/a
12	chr15:45952725-45952775	IMR90	lung:	fetal
13	chr15:45952725-45952775	HCF	heart:	n/a
14	chr15:45952725-45952775	T-47D	breast:	n/a
15	chr15:45952725-45952775	HepG2	liver:	n/a
16	chr15:45952725-45952775	HEEpiC	esophagus:	n/a
17	chr15:45952725-45952775	NT2-D1	testis:	n/a
18	chr15:45952725-45952775	AG10803	skin:	n/a
19	chr15:45952725-45952775	PANC-1	pancreas:	n/a
20	chr15:45952725-45952775	HUVEC	blood vessel:	n/a
21	chr15:45952725-45952775	HRPEpiC	eye:	n/a
22	chr15:45952725-45952775	NHDF-neo	bronchial:	n/a
23	chr15:45952725-45952775	CMK	blood:	n/a
24	chr15:45952725-45952775	PFSK-1	brain:	n/a
25	chr15:45952725-45952775	U87	brain:	n/a
26	chr15:45952725-45952775	HPAEpiC	pulmonary alveolar:	n/a
27	chr15:45952725-45952775	HL-60	blood:	n/a
28	chr15:45952725-45952775	GM06990	blood:	n/a
29	chr15:45952725-45952775	K562	blood:	n/a
30	chr15:45952725-45952775	SAEC	small airway:	n/a
31	chr15:45952725-45952775	SK-N-MC	brain:	n/a
32	chr15:45952725-45952775	HRCEpiC	kidney:	n/a
33	chr15:45952725-45952775	AG04450	lung:	fetal
34	chr15:45952725-45952775	A549	lung:	n/a
35	chr15:45952725-45952775	HMEC	breast:	n/a
36	chr15:45952725-45952775	H1-hESC	embryonic stem cell:	embryo
37	chr15:45952725-45952775	Hepatocyte	liver:	n/a
38	chr15:45952725-45952775	ovcar-3	ovarian:	n/a
39	chr15:45952725-45952775	BJ	skin:	n/a
40	chr15:45952725-45952775	HNPCEpiC	eye:	n/a
41	chr15:45952725-45952775	MCF-7	breast:	n/a
42	chr15:45952725-45952775	RPTEC	kidney:	n/a
43	chr15:45952725-45952775	PrEC	prostate:	n/a
44	chr15:45952725-45952775	AG04449	skin:	fetal
45	chr15:45952725-45952775	Caco-2	colon:	n/a
46	chr15:45952725-45952775	Hela-S3	cervix:	n/a
47	chr15:45952725-45952775	SK-N-SH_RA	brain:	n/a
48	chr15:45952725-45952775	LNCaP	prostate:	n/a
49	chr15:45952725-45952775	HCPEpiC	choroid plexus:	n/a
50	chr15:45952725-45952775	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr15:45951100..45953645-chr15:45956649..45958912,2	MCF-7	breast:
2	chr15:45926784..45929101-chr15:45955336..45958856,3	MCF-7	breast:
3	chr15:45932766..45934482-chr15:45951327..45953164,2	MCF-7	breast:

No data

Variant related genes	Relation type
SQRDL	TF binding region
SQRDL	CpG island
ENSG00000137767	chromatin interactions

Extended variants
information (count: 340 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149173971	chr15:45949726-45949727	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs564364145	chr15:45949728-45949729	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs577345699	chr15:45949741-45949742	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs572178974	chr15:45949743-45949744	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs540713088	chr15:45949779-45949780	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs144755182	chr15:45949828-45949829	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs138694885	chr15:45949844-45949845	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs36071952	chr15:45949865-45949866	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs35540030	chr15:45949874-45949875	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs662592	chr15:45949886-45949887	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs532011945	chr15:45949914-45949915	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs548639003	chr15:45949926-45949927	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs141816783	chr15:45949927-45949928	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs185890831	chr15:45949943-45949944	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs674117	chr15:45949983-45949984	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs570916335	chr15:45950046-45950047	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs35349519	chr15:45950052-45950053	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs539955076	chr15:45950078-45950079	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs146276378	chr15:45950081-45950082	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs569978180	chr15:45950087-45950088	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs674638	chr15:45950138-45950139	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs674676	chr15:45950159-45950160	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs572200786	chr15:45950215-45950216	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs534463417	chr15:45950238-45950239	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs147503257	chr15:45950256-45950257	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs663992	chr15:45950259-45950260	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs141628914	chr15:45950270-45950271	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs150521293	chr15:45950273-45950274	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs573595975	chr15:45950287-45950288	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs542506800	chr15:45950305-45950306	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs562198186	chr15:45950311-45950312	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs528001119	chr15:45950322-45950323	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs192409224	chr15:45950351-45950352	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs675599	chr15:45950367-45950368	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs546672890	chr15:45950376-45950377	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs561788892	chr15:45950389-45950390	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs664768	chr15:45950391-45950392	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs550040501	chr15:45950409-45950410	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs664824	chr15:45950435-45950436	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs16946621	chr15:45950481-45950482	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs549360112	chr15:45950484-45950485	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs72715082	chr15:45950523-45950524	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs73422332	chr15:45950528-45950529	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs535013459	chr15:45950551-45950552	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs676476	chr15:45950569-45950570	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs533757435	chr15:45950591-45950592	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs183733495	chr15:45950640-45950641	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs536742669	chr15:45950648-45950649	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs78096414	chr15:45950679-45950680	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs573684250	chr15:45950682-45950683	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Melanoma	17363583	CNVD
Acute myeloid leukemia	19651601	CNVD
Marfan syndrome	17492313	CNVD
Esophageal adenocarcinoma	18820669	CNVD

Chromatin state (count:396 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:45933800-45951200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr15:45934200-45961600	Weak transcription	Fetal Kidney	kidney
3	chr15:45938400-45950400	Weak transcription	Brain Hippocampus Middle	brain
4	chr15:45938600-45951000	Weak transcription	Primary B cells from cord blood	blood
5	chr15:45938600-45952600	Weak transcription	Adipose Nuclei	Adipose
6	chr15:45938800-45954200	Weak transcription	Aorta	Aorta
7	chr15:45941400-45950600	Weak transcription	Primary T cells from cord blood	blood
8	chr15:45941600-45951800	Weak transcription	Thymus	Thymus
9	chr15:45941600-45952400	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr15:45941600-45952600	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr15:45941600-45954000	Weak transcription	Hela-S3	cervix
12	chr15:45941600-45966800	Weak transcription	NHLF	lung
13	chr15:45942200-45950800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr15:45942200-45951600	Weak transcription	NHEK	skin
15	chr15:45942600-45950600	Weak transcription	HMEC	breast
16	chr15:45942800-45950800	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr15:45942800-45951000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr15:45942800-45951800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr15:45942800-45952800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr15:45943800-45950400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr15:45943800-45950600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr15:45943800-45956600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr15:45944000-45950600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr15:45945600-45951200	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr15:45945800-45951200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr15:45945800-45953600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr15:45946000-45950600	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr15:45946000-45951200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr15:45946200-45950000	Weak transcription	Lung	lung
30	chr15:45946200-45950400	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr15:45946200-45950600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr15:45946200-45951600	Weak transcription	Primary B cells from peripheral blood	blood
33	chr15:45946200-45952000	Weak transcription	Left Ventricle	heart
34	chr15:45946200-45952000	Weak transcription	Right Atrium	heart
35	chr15:45946200-45952200	Weak transcription	NHDF-Ad	bronchial
36	chr15:45946200-45953400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr15:45946200-45953600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr15:45946200-45953600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr15:45946200-45954600	Weak transcription	Right Ventricle	heart
40	chr15:45946400-45949800	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr15:45946400-45951600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr15:45946600-45950200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr15:45946600-45950800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr15:45946600-45953800	Weak transcription	Primary hematopoietic stem cells	blood
45	chr15:45946800-45954000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr15:45947000-45950000	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr15:45947000-45951400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr15:45947000-45954000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr15:45947200-45949800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr15:45947200-45950000	Weak transcription	Spleen	Spleen

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