Variant report

Variant	nsv9259
Chromosome Location	chr15:45317368-45326350
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:117)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:117 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:45319667-45319860	K562	blood:	n/a	n/a
2	ATF1	chr15:45321173-45321223	K562	blood:	n/a	n/a
3	CBX3	chr15:45323759-45324400	K562	blood:	n/a	n/a
4	CBX3	chr15:45323934-45324441	K562	blood:	n/a	n/a
5	CBX3	chr15:45321842-45322070	K562	blood:	n/a	n/a
6	CBX3	chr15:45321710-45322207	K562	blood:	n/a	n/a
7	CEBPB	chr15:45322992-45323243	K562	blood:	n/a	chr15:45323141-45323152
8	CEBPB	chr15:45317888-45318268	HepG2	liver:	n/a	chr15:45318077-45318088 chr15:45318077-45318090
9	CEBPB	chr15:45322965-45323330	K562	blood:	n/a	chr15:45323141-45323152
10	CEBPB	chr15:45317888-45318260	HepG2	liver:	n/a	chr15:45318077-45318088 chr15:45318077-45318090
11	CEBPB	chr15:45323785-45324250	K562	blood:	n/a	n/a
12	CEBPB	chr15:45319580-45319770	K562	blood:	n/a	n/a
13	CEBPB	chr15:45323012-45323267	HepG2	liver:	n/a	chr15:45323141-45323152
14	CEBPB	chr15:45317946-45318119	HepG2	liver:	n/a	chr15:45318077-45318088 chr15:45318077-45318090
15	CEBPB	chr15:45317852-45318158	HepG2	liver:	n/a	chr15:45318077-45318088 chr15:45318077-45318090
16	CEBPD	chr15:45323757-45324332	K562	blood:	n/a	n/a
17	CTCF	chr15:45326204-45326268	HepG2	liver:	n/a	n/a
18	CTCF	chr15:45326174-45326213	LNCaP	prostate:	n/a	n/a
19	CTCF	chr15:45318700-45318850	HPAF	blood vessel:	n/a	n/a
20	CTCF	chr15:45318680-45318830	HUVEC	blood vessel:	n/a	n/a
21	CTCF	chr15:45318600-45318750	GM12873	blood:	n/a	n/a
22	CTCF	chr15:45318660-45318810	GM12872	blood:	n/a	n/a
23	CTCF	chr15:45318900-45319050	RPTEC	kidney:	n/a	n/a
24	CTCF	chr15:45318600-45318750	GM12878	blood:	n/a	n/a
25	CTCF	chr15:45318580-45318730	GM12872	blood:	n/a	n/a
26	EP300	chr15:45320383-45321549	SK-N-SH	brain:	n/a	chr15:45321423-45321437 chr15:45321424-45321433 chr15:45321284-45321298
27	EP300	chr15:45319562-45319752	K562	blood:	n/a	n/a
28	EP300	chr15:45317814-45318168	HepG2	liver:	n/a	n/a
29	EP300	chr15:45318795-45320180	SK-N-SH	brain:	n/a	chr15:45319152-45319166
30	FAM48A	chr15:45323542-45323666	GM12878	blood:	n/a	n/a
31	FOSL2	chr15:45326331-45326608	HepG2	liver:	n/a	n/a
32	FOXA1	chr15:45326260-45326612	HepG2	liver:	n/a	n/a
33	FOXA1	chr15:45325712-45325970	HepG2	liver:	n/a	n/a
34	FOXA2	chr15:45317809-45318126	HepG2	liver:	n/a	n/a
35	GATA1	chr15:45323639-45324008	PBDE	blood:	n/a	chr15:45323963-45323979 chr15:45323963-45323979
36	GATA2	chr15:45320990-45321321	SH-SY5Y	brain:	n/a	n/a
37	GATA2	chr15:45323697-45324456	K562	blood:	n/a	chr15:45324075-45324084 chr15:45324027-45324043 chr15:45323963-45323979 chr15:45323963-45323979
38	GATA2	chr15:45318863-45319238	HUVEC	blood vessel:	n/a	chr15:45319014-45319024 chr15:45319014-45319021 chr15:45319154-45319165
39	GATA3	chr15:45320956-45321396	SH-SY5Y	brain:	n/a	n/a
40	HDAC2	chr15:45317842-45318139	HepG2	liver:	n/a	n/a
41	HNF4A	chr15:45317886-45318251	HepG2	liver:	n/a	n/a
42	HNF4A	chr15:45317799-45318158	HepG2	liver:	n/a	n/a
43	HNF4A	chr15:45317915-45318152	HepG2	liver:	n/a	n/a
44	HNF4G	chr15:45317867-45318183	HepG2	liver:	n/a	n/a
45	HNF4G	chr15:45317861-45318145	HepG2	liver:	n/a	n/a
46	JUND	chr15:45319377-45319804	K562	blood:	n/a	n/a
47	KAP1	chr15:45321685-45322280	K562	blood:	n/a	n/a
48	MAFF	chr15:45319522-45319729	K562	blood:	n/a	n/a
49	MAZ	chr15:45319007-45319282	K562	blood:	n/a	n/a
50	MYC	chr15:45319526-45319719	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:45319037-45319087	GM12891	blood:	n/a
2	chr15:45319037-45319087	HAEpiC	amniotic membrane:	n/a
3	chr15:45319037-45319087	AG09319	gingival:	n/a
4	chr15:45319037-45319087	ovcar-3	ovarian:	n/a
5	chr15:45319037-45319087	A549	lung:	n/a
6	chr15:45319037-45319087	HUVEC	blood vessel:	n/a
7	chr15:45319037-45319087	Jurkat	blood:	n/a
8	chr15:45319037-45319087	HCT-116	colon:	n/a
9	chr15:45319037-45319087	AoSMC	blood vessel:	n/a
10	chr15:45319037-45319087	HEK293	kidney:	embryo
11	chr15:45319037-45319087	AG10803	skin:	n/a
12	chr15:45319037-45319087	HRCEpiC	kidney:	n/a
13	chr15:45319037-45319087	NHBE	bronchial:	n/a
14	chr15:45319037-45319087	HCPEpiC	choroid plexus:	n/a
15	chr15:45319037-45319087	GM12892	blood:	n/a
16	chr15:45319037-45319087	RPTEC	kidney:	n/a
17	chr15:45319037-45319087	BE2_C	brain:	n/a
18	chr15:45319037-45319087	MCF-7	breast:	n/a
19	chr15:45319037-45319087	ProgFib	skin:	n/a
20	chr15:45319037-45319087	HNPCEpiC	eye:	n/a
21	chr15:45319037-45319087	NH-A	brain:	n/a
22	chr15:45319037-45319087	SKMC	muscle:	n/a
23	chr15:45319037-45319087	HCF	heart:	n/a
24	chr15:45319037-45319087	GM19239	blood:	n/a
25	chr15:45319037-45319087	HCM	heart:	n/a
26	chr15:45319037-45319087	AG04450	lung:	fetal
27	chr15:45319037-45319087	MCF10A-Er-Src	breast:	n/a
28	chr15:45319037-45319087	HepG2	liver:	n/a
29	chr15:45319037-45319087	SK-N-SH_RA	brain:	n/a
30	chr15:45319037-45319087	CMK	blood:	n/a
31	chr15:45319037-45319087	NHDF-neo	bronchial:	n/a
32	chr15:45319037-45319087	LNCaP	prostate:	n/a
33	chr15:45319037-45319087	GM06990	blood:	n/a
34	chr15:45319037-45319087	AG04449	skin:	fetal
35	chr15:45319037-45319087	HL-60	blood:	n/a
36	chr15:45319037-45319087	U87	brain:	n/a
37	chr15:45319037-45319087	SAEC	small airway:	n/a
38	chr15:45319037-45319087	T-47D	breast:	n/a
39	chr15:45319037-45319087	NB4	blood:	n/a
40	chr15:45319037-45319087	ECC-1	luminal epithelium:	n/a
41	chr15:45319037-45319087	AG09309	skin:	n/a
42	chr15:45319037-45319087	GM12878	blood:	n/a
43	chr15:45319037-45319087	SK-N-SH	brain:	n/a
44	chr15:45319037-45319087	SK-N-MC	brain:	n/a
45	chr15:45319037-45319087	NT2-D1	testis:	n/a
46	chr15:45319037-45319087	HPAEpiC	pulmonary alveolar:	n/a
47	chr15:45319037-45319087	PrEC	prostate:	n/a
48	chr15:45319037-45319087	PANC-1	pancreas:	n/a
49	chr15:45319037-45319087	Caco-2	colon:	n/a
50	chr15:45319037-45319087	K562	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:45313440..45317462-chr15:45317525..45323259,9	K562	blood:

No data

Variant related genes	Relation type
SORD	TF binding region
SORD	CpG island
ENSG00000140263	chromatin interactions

Extended variants
information (count: 489 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538824050	chr15:45317378-45317379	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs1808791	chr15:45317389-45317390	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs566220098	chr15:45317402-45317403	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs75064051	chr15:45317403-45317404	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs397832496	chr15:45317404-45317405	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs397746585	chr15:45317411-45317412	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs536741231	chr15:45317432-45317433	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs114949504	chr15:45317450-45317451	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs537897233	chr15:45317452-45317453	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs116557213	chr15:45317481-45317482	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs548658472	chr15:45317482-45317483	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs187014567	chr15:45317485-45317486	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs893098	chr15:45317492-45317493	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs140865848	chr15:45317511-45317512	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs576981463	chr15:45317536-45317537	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs570276285	chr15:45317567-45317568	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs537215376	chr15:45317571-45317572	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs371836041	chr15:45317615-45317616	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs78683343	chr15:45317631-45317632	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs201341772	chr15:45317633-45317634	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs191793185	chr15:45317642-45317643	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs183684775	chr15:45317732-45317733	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs576399128	chr15:45317781-45317782	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs559227436	chr15:45317803-45317804	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs34029087	chr15:45317822-45317823	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs138578157	chr15:45317869-45317870	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs2576081	chr15:45317895-45317896	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs114480171	chr15:45317896-45317897	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs2576080	chr15:45317898-45317899	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs62026025	chr15:45317911-45317912	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs11636774	chr15:45317915-45317916	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs182291326	chr15:45317969-45317970	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs185684066	chr15:45317970-45317971	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs552353401	chr15:45317972-45317973	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs116833727	chr15:45317978-45317979	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs73421320	chr15:45317995-45317996	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs112767360	chr15:45318015-45318016	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs548206931	chr15:45318030-45318031	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs113140210	chr15:45318031-45318032	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs146563116	chr15:45318041-45318042	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs139091557	chr15:45318052-45318053	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs577220564	chr15:45318053-45318054	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs539666444	chr15:45318070-45318071	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs2576079	chr15:45318080-45318081	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs556381348	chr15:45318149-45318150	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs111232134	chr15:45318212-45318213	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs576437293	chr15:45318218-45318219	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs542121758	chr15:45318232-45318233	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs561932634	chr15:45318240-45318241	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs143020556	chr15:45318251-45318252	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	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:362 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:45316000-45321600	Weak transcription	Aorta	Aorta
2	chr15:45316200-45326200	Weak transcription	Psoas Muscle	Psoas
3	chr15:45316200-45340600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr15:45316400-45317400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr15:45316400-45318000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr15:45316400-45318400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr15:45316400-45319200	Enhancers	Fetal Thymus	thymus
8	chr15:45316400-45320600	Weak transcription	Fetal Kidney	kidney
9	chr15:45316400-45321000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr15:45316400-45321400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr15:45316400-45321400	Weak transcription	Primary T cells from cord blood	blood
12	chr15:45316400-45321600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr15:45316400-45321600	Weak transcription	Right Atrium	heart
14	chr15:45316400-45321800	Weak transcription	Ovary	ovary
15	chr15:45316400-45323400	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr15:45316400-45327600	Weak transcription	Primary B cells from cord blood	blood
17	chr15:45316400-45329400	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr15:45316400-45333000	Weak transcription	Lung	lung
19	chr15:45316400-45341200	Weak transcription	Fetal Muscle Trunk	muscle
20	chr15:45316400-45342200	Weak transcription	HSMMtube	muscle
21	chr15:45316400-45342600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr15:45316600-45317400	Enhancers	Fetal Brain Female	brain
23	chr15:45316600-45317600	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr15:45316600-45317600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr15:45316600-45317600	Enhancers	Brain Hippocampus Middle	brain
26	chr15:45316600-45317600	Enhancers	Stomach Mucosa	stomach
27	chr15:45316600-45317800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr15:45316600-45317800	Enhancers	Brain Cingulate Gyrus	brain
29	chr15:45316600-45318000	Enhancers	Brain Substantia Nigra	brain
30	chr15:45316600-45318200	Weak transcription	HUVEC	blood vessel
31	chr15:45316600-45318600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr15:45316600-45318600	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr15:45316600-45318600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr15:45316600-45318800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr15:45316600-45318800	Weak transcription	A549	lung
36	chr15:45316600-45319000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr15:45316600-45319000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr15:45316600-45319000	Weak transcription	Duodenum Mucosa	Duodenum
39	chr15:45316600-45319000	Weak transcription	Left Ventricle	heart
40	chr15:45316600-45319000	Weak transcription	Right Ventricle	heart
41	chr15:45316600-45319400	Weak transcription	Brain Angular Gyrus	brain
42	chr15:45316600-45319400	Weak transcription	Brain Germinal Matrix	brain
43	chr15:45316600-45319800	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr15:45316600-45321200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr15:45316600-45321400	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr15:45316600-45321400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr15:45316600-45321400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr15:45316600-45321400	Weak transcription	Fetal Intestine Small	intestine
49	chr15:45316600-45321400	Weak transcription	Fetal Stomach	stomach
50	chr15:45316600-45321800	Weak transcription	Primary monocytes fromperipheralblood	blood

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