Variant report

Variant	nsv977071
Chromosome Location	chr15:59509537-59519089
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:168)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:168 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr15:59514411-59514599	GM12878	blood:	n/a	n/a
2	CTCF	chr15:59513320-59513373	Fibrobl	skin:	n/a	n/a
3	CTCF	chr15:59515647-59515698	Pancreas_OC	pancreas:	n/a	n/a
4	EP300	chr15:59511903-59512191	GM12878	blood:	n/a	n/a
5	EP300	chr15:59514025-59514846	SK-N-SH	brain:	n/a	n/a
6	FOS	chr15:59510342-59510785	HUVEC	blood vessel:	n/a	chr15:59510497-59510508
7	FOS	chr15:59514310-59514692	HUVEC	blood vessel:	n/a	n/a
8	FOSL2	chr15:59514089-59514771	SK-N-SH	brain:	n/a	n/a
9	GATA2	chr15:59514211-59514575	HUVEC	blood vessel:	n/a	chr15:59514305-59514312
10	GATA2	chr15:59510048-59511159	HUVEC	blood vessel:	n/a	chr15:59510437-59510453 chr15:59510436-59510450 chr15:59510809-59510819
11	GATA2	chr15:59515191-59515507	SH-SY5Y	brain:	n/a	n/a
12	GATA3	chr15:59513919-59514852	SK-N-SH	brain:	n/a	chr15:59514305-59514312
13	GATA3	chr15:59513979-59514868	SK-N-SH	brain:	n/a	chr15:59514305-59514312
14	JUN	chr15:59510230-59510773	HUVEC	blood vessel:	n/a	n/a
15	JUND	chr15:59514103-59514795	SK-N-SH	brain:	n/a	n/a
16	JUND	chr15:59514178-59514791	SK-N-SH	brain:	n/a	n/a
17	MAFK	chr15:59514250-59514666	IMR90	lung:	n/a	chr15:59514404-59514420
18	MAX	chr15:59514295-59514713	SK-N-SH	brain:	n/a	n/a
19	MAZ	chr15:59517074-59517093	Hela-S3	cervix:	n/a	n/a
20	MEF2A	chr15:59514059-59514786	SK-N-SH	brain:	n/a	chr15:59514426-59514447
21	MXI1	chr15:59514276-59514940	IMR90	lung:	n/a	n/a
22	MYC	chr15:59510323-59510452	HUVEC	blood vessel:	n/a	n/a
23	MYC	chr15:59516805-59516834	HUVEC	blood vessel:	n/a	n/a
24	NR3C1	chr15:59515354-59515867	A549	lung:	n/a	n/a
25	NR3C1	chr15:59516001-59516324	A549	lung:	n/a	chr15:59516144-59516158
26	PBX3	chr15:59514016-59514817	SK-N-SH	brain:	n/a	n/a
27	PBX3	chr15:59514158-59514778	SK-N-SH	brain:	n/a	n/a
28	POLR2A	chr15:59510047-59511483	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr15:59509961-59510734	GM12891	blood:	n/a	n/a
30	POLR2A	chr15:59517074-59517878	GM12892	blood:	n/a	n/a
31	POLR2A	chr15:59511751-59512526	GM12892	blood:	n/a	n/a
32	POLR2A	chr15:59509886-59510369	Hela-S3	cervix:	n/a	n/a
33	POLR2A	chr15:59516987-59517048	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr15:59513375-59514018	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr15:59509698-59511648	GM12892	blood:	n/a	n/a
36	POLR2A	chr15:59516644-59516916	GM12878	blood:	n/a	n/a
37	POLR2A	chr15:59513567-59514065	GM12891	blood:	n/a	n/a
38	POLR2A	chr15:59516900-59517736	A549	lung:	n/a	n/a
39	POLR2A	chr15:59519004-59519559	Hela-S3	cervix:	n/a	n/a
40	POLR2A	chr15:59518997-59519834	GM12892	blood:	n/a	n/a
41	POLR2A	chr15:59511928-59512448	GM12892	blood:	n/a	n/a
42	POLR2A	chr15:59516743-59517121	GM12878	blood:	n/a	n/a
43	POLR2A	chr15:59510932-59511315	GM12891	blood:	n/a	n/a
44	POLR2A	chr15:59509828-59509851	Hela-S3	cervix:	n/a	n/a
45	POLR2A	chr15:59515406-59515859	GM12891	blood:	n/a	n/a
46	POLR2A	chr15:59517435-59517728	GM12878	blood:	n/a	n/a
47	POLR2A	chr15:59515972-59516651	GM12892	blood:	n/a	n/a
48	POLR2A	chr15:59514869-59517290	GM12892	blood:	n/a	n/a
49	POLR2A	chr15:59510794-59511397	GM12892	blood:	n/a	n/a
50	POLR2A	chr15:59517316-59517322	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:59514661-59514711	SK-N-MC	brain:	n/a
2	chr15:59514661-59514711	HEK293	kidney:	embryo
3	chr15:59514661-59514711	HCM	heart:	n/a
4	chr15:59514661-59514711	HIPEpiC	eye:	n/a
5	chr15:59514661-59514711	T-47D	breast:	n/a
6	chr15:59514661-59514711	SK-N-SH_RA	brain:	n/a
7	chr15:59514661-59514711	ovcar-3	ovarian:	n/a
8	chr15:59514661-59514711	GM06990	blood:	n/a
9	chr15:59514661-59514711	AG10803	skin:	n/a
10	chr15:59514661-59514711	NB4	blood:	n/a
11	chr15:59514661-59514711	GM12878	blood:	n/a
12	chr15:59514661-59514711	NT2-D1	testis:	n/a
13	chr15:59514661-59514711	Caco-2	colon:	n/a
14	chr15:59514661-59514711	CMK	blood:	n/a
15	chr15:59514661-59514711	SK-N-SH	brain:	n/a
16	chr15:59514661-59514711	MCF10A-Er-Src	breast:	n/a
17	chr15:59514661-59514711	HNPCEpiC	eye:	n/a
18	chr15:59514661-59514711	HAEpiC	amniotic membrane:	n/a
19	chr15:59514661-59514711	Hepatocyte	liver:	n/a
20	chr15:59514661-59514711	NH-A	brain:	n/a
21	chr15:59514661-59514711	BE2_C	brain:	n/a
22	chr15:59514661-59514711	K562	blood:	n/a
23	chr15:59514661-59514711	ECC-1	luminal epithelium:	n/a
24	chr15:59514661-59514711	HRPEpiC	eye:	n/a
25	chr15:59514661-59514711	H1-hESC	embryonic stem cell:	embryo
26	chr15:59514661-59514711	BJ	skin:	n/a
27	chr15:59514661-59514711	U87	brain:	n/a
28	chr15:59514661-59514711	SAEC	small airway:	n/a
29	chr15:59514661-59514711	HL-60	blood:	n/a
30	chr15:59514661-59514711	HEEpiC	esophagus:	n/a
31	chr15:59514661-59514711	PrEC	prostate:	n/a
32	chr15:59514661-59514711	HUVEC	blood vessel:	n/a
33	chr15:59514661-59514711	HMEC	breast:	n/a
34	chr15:59514661-59514711	NHBE	bronchial:	n/a
35	chr15:59514661-59514711	HepG2	liver:	n/a
36	chr15:59514661-59514711	AG04449	skin:	fetal
37	chr15:59514661-59514711	PANC-1	pancreas:	n/a
38	chr15:59514661-59514711	A549	lung:	n/a
39	chr15:59514661-59514711	MCF-7	breast:	n/a
40	chr15:59514661-59514711	AoSMC	blood vessel:	n/a
41	chr15:59514661-59514711	HCF	heart:	n/a
42	chr15:59514661-59514711	HRCEpiC	kidney:	n/a
43	chr15:59514661-59514711	GM12891	blood:	n/a
44	chr15:59514661-59514711	GM12892	blood:	n/a
45	chr15:59514661-59514711	AG09309	skin:	n/a
46	chr15:59514661-59514711	PFSK-1	brain:	n/a
47	chr15:59514661-59514711	ProgFib	skin:	n/a
48	chr15:59514661-59514711	IMR90	lung:	fetal
49	chr15:59514661-59514711	AG04450	lung:	fetal
50	chr15:59514661-59514711	HPAEpiC	pulmonary alveolar:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:59509480..59512109-chr15:59514954..59517211,4	K562	blood:
2	chr15:59518511..59521491-chr15:59664302..59666468,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNU4-80P	TF binding region
MYO1E	TF binding region
RNU4-80P	CpG island
MYO1E	CpG island
ENSG00000157483	chromatin interactions
ENSG00000157470	chromatin interactions

Extended variants
information (count: 442 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:442 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62004155	chr15:59509545-59509546	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs528772517	chr15:59509549-59509550	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs187660774	chr15:59509569-59509570	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs565235376	chr15:59509589-59509590	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs191139293	chr15:59509591-59509592	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs551342099	chr15:59509608-59509609	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs12439579	chr15:59509609-59509610	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs569062129	chr15:59509616-59509617	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs182618131	chr15:59509638-59509639	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs11638386	chr15:59509663-59509664	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs56192171	chr15:59509666-59509667	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs567428547	chr15:59509702-59509703	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs12913516	chr15:59509719-59509720	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs534919118	chr15:59509743-59509744	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs12439599	chr15:59509762-59509763	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs187318230	chr15:59509765-59509766	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs569331084	chr15:59509776-59509777	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs146855568	chr15:59509815-59509816	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs557299294	chr15:59509876-59509877	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs192139358	chr15:59509906-59509907	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs184552710	chr15:59509919-59509920	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs554748366	chr15:59509925-59509926	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs573151613	chr15:59509953-59509954	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs113881904	chr15:59510005-59510006	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188896100	chr15:59510009-59510010	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532820686	chr15:59510016-59510017	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs193114973	chr15:59510017-59510018	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs144686965	chr15:59510045-59510046	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs368275853	chr15:59510058-59510059	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372487333	chr15:59510117-59510118	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs146652440	chr15:59510132-59510133	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs200925200	chr15:59510136-59510137	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144731469	chr15:59510161-59510162	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2230155	chr15:59510189-59510190	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs141570155	chr15:59510219-59510220	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150397493	chr15:59510221-59510222	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546799247	chr15:59510226-59510227	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs112484008	chr15:59510247-59510248	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs145427071	chr15:59510275-59510276	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs148823974	chr15:59510278-59510279	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369132214	chr15:59510280-59510281	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs371620679	chr15:59510295-59510296	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs538894173	chr15:59510369-59510370	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs189096653	chr15:59510377-59510378	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569188107	chr15:59510382-59510383	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs536249710	chr15:59510387-59510388	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs116611542	chr15:59510393-59510394	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs554424326	chr15:59510405-59510406	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540454631	chr15:59510409-59510410	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs180975453	chr15:59510457-59510458	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
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
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
Mental retardation	17124404	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:381 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:59467800-59523200	Weak transcription	Fetal Brain Female	brain
2	chr15:59468200-59528600	Weak transcription	Stomach Mucosa	stomach
3	chr15:59468600-59521400	Strong transcription	Rectal Mucosa Donor 29	rectum
4	chr15:59475800-59517800	Strong transcription	HUES48 Cell Line	embryonic stem cell
5	chr15:59483200-59514000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr15:59485400-59515400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr15:59485600-59521200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr15:59487800-59524400	Weak transcription	Small Intestine	intestine
9	chr15:59489800-59512600	Strong transcription	HUES6 Cell Line	embryonic stem cell
10	chr15:59489800-59515600	Weak transcription	Right Atrium	heart
11	chr15:59490200-59510800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr15:59492000-59521600	Strong transcription	Rectal Mucosa Donor 31	rectum
13	chr15:59493000-59512000	Strong transcription	HSMM	muscle
14	chr15:59493000-59513800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr15:59493200-59513600	Strong transcription	Osteobl	bone
16	chr15:59493200-59513800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr15:59493200-59514400	Strong transcription	HMEC	breast
18	chr15:59493200-59523200	Strong transcription	Hela-S3	cervix
19	chr15:59494800-59514200	Strong transcription	A549	lung
20	chr15:59496800-59515200	Weak transcription	Spleen	Spleen
21	chr15:59496800-59515600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
22	chr15:59496800-59522000	Strong transcription	NHEK	skin
23	chr15:59497000-59514600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr15:59497000-59524800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr15:59497200-59517600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr15:59498000-59516000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr15:59498800-59522000	Strong transcription	GM12878-XiMat	blood
28	chr15:59499200-59512600	Strong transcription	Fetal Intestine Large	intestine
29	chr15:59500000-59509600	Weak transcription	Esophagus	oesophagus
30	chr15:59500000-59513600	Weak transcription	Fetal Kidney	kidney
31	chr15:59500000-59515000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr15:59500000-59515000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr15:59500000-59517600	Weak transcription	Fetal Lung	lung
34	chr15:59500000-59524400	Weak transcription	Right Ventricle	heart
35	chr15:59500600-59524600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr15:59501200-59509800	Weak transcription	Lung	lung
37	chr15:59501200-59510400	Weak transcription	Brain Angular Gyrus	brain
38	chr15:59501200-59514200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr15:59501200-59515000	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr15:59501200-59515000	Weak transcription	Pancreas	Pancrea
41	chr15:59501200-59521400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr15:59501200-59523400	Weak transcription	Ovary	ovary
43	chr15:59501200-59525600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr15:59501400-59514200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr15:59502400-59510600	Strong transcription	Placenta	Placenta
46	chr15:59502400-59513400	Strong transcription	NHDF-Ad	bronchial
47	chr15:59502800-59509800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr15:59502800-59513600	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr15:59502800-59525800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr15:59503200-59513600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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