Variant report

Variant	nsv569298
Chromosome Location	chr15:44401266-44513090
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1354)
CpG islands
(count:1039)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1354 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:44487398-44487636	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:44491625-44492037	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:44450024-44450224	HepG2	liver:	n/a	n/a
4	ATF3	chr15:44449721-44450460	HCT-116	colon:	n/a	n/a
5	BACH1	chr15:44485966-44485975	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr15:44445635-44445910	GM12878	blood:	n/a	n/a
7	BCL3	chr15:44449875-44450383	A549	lung:	n/a	chr15:44450002-44450011 chr15:44449902-44449911 chr15:44449935-44449944 chr15:44450001-44450010
8	BHLHE40	chr15:44487373-44487862	HepG2	liver:	n/a	n/a
9	BHLHE40	chr15:44491634-44491971	HepG2	liver:	n/a	n/a
10	BHLHE40	chr15:44487368-44487684	A549	lung:	n/a	n/a
11	BHLHE40	chr15:44487395-44487682	GM12878	blood:	n/a	n/a
12	BRCA1	chr15:44487455-44487861	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr15:44487437-44487846	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr15:44487478-44487480	HepG2	liver:	n/a	n/a
15	CBX3	chr15:44449724-44450528	HCT-116	colon:	n/a	n/a
16	CBX3	chr15:44449686-44450670	HCT-116	colon:	n/a	n/a
17	CBX3	chr15:44429850-44430351	HCT-116	colon:	n/a	n/a
18	CBX3	chr15:44507637-44508247	HCT-116	colon:	n/a	n/a
19	CEBPB	chr15:44486307-44486816	IMR90	lung:	n/a	n/a
20	CEBPB	chr15:44486543-44486881	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr15:44473522-44473858	K562	blood:	n/a	chr15:44473555-44473566
22	CEBPB	chr15:44487636-44487867	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr15:44469774-44469976	HepG2	liver:	n/a	chr15:44469841-44469852
24	CEBPB	chr15:44507716-44508085	IMR90	lung:	n/a	n/a
25	CEBPB	chr15:44486611-44486722	K562	blood:	n/a	n/a
26	CEBPB	chr15:44449697-44450482	HCT-116	colon:	n/a	n/a
27	CEBPB	chr15:44449931-44450369	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr15:44473434-44473878	IMR90	lung:	n/a	chr15:44473555-44473566
29	CEBPB	chr15:44473384-44473701	HepG2	liver:	n/a	chr15:44473555-44473566
30	CEBPB	chr15:44431137-44431358	K562	blood:	n/a	chr15:44431248-44431259
31	CEBPB	chr15:44449905-44450291	IMR90	lung:	n/a	n/a
32	CEBPB	chr15:44449531-44450891	HCT-116	colon:	n/a	n/a
33	CEBPB	chr15:44431207-44431284	HepG2	liver:	n/a	chr15:44431248-44431259
34	CEBPB	chr15:44455279-44455461	K562	blood:	n/a	n/a
35	CEBPB	chr15:44473455-44473738	A549	lung:	n/a	chr15:44473555-44473566
36	CEBPB	chr15:44429993-44430247	Hela-S3	cervix:	n/a	chr15:44430060-44430073
37	CEBPB	chr15:44431131-44431385	IMR90	lung:	n/a	chr15:44431248-44431259
38	CEBPB	chr15:44507624-44508277	HCT-116	colon:	n/a	n/a
39	CEBPB	chr15:44410930-44411130	IMR90	lung:	n/a	chr15:44411029-44411040
40	CEBPB	chr15:44449782-44450409	A549	lung:	n/a	n/a
41	CEBPB	chr15:44473511-44473802	Hela-S3	cervix:	n/a	chr15:44473555-44473566
42	CEBPB	chr15:44410929-44411166	HepG2	liver:	n/a	chr15:44411029-44411040
43	CEBPZ	chr15:44487425-44487790	HepG2	liver:	n/a	n/a
44	CHD1	chr15:44487578-44487980	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD1	chr15:44486909-44487044	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr15:44487356-44487808	HepG2	liver:	n/a	n/a
47	CHD2	chr15:44487427-44487839	GM12878	blood:	n/a	n/a
48	CHD2	chr15:44487364-44488027	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr15:44486605-44486999	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr15:44487265-44487971	Hela-S3	cervix:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:44507997-44508047	ovcar-3	ovarian:	n/a
2	chr15:44487788-44487838	Hepatocyte	liver:	n/a
3	chr15:44507997-44508047	ovcar-3	ovarian:	n/a
4	chr15:44487788-44487838	Hepatocyte	liver:	n/a
5	chr15:44491027-44491077	AG09319	gingival:	n/a
6	chr15:44507997-44508047	GM12878	blood:	n/a
7	chr15:44491027-44491077	HAEpiC	amniotic membrane:	n/a
8	chr15:44487547-44487597	RPTEC	kidney:	n/a
9	chr15:44491027-44491077	AG10803	skin:	n/a
10	chr15:44487192-44487242	PrEC	prostate:	n/a
11	chr15:44487545-44487595	HRCEpiC	kidney:	n/a
12	chr15:44487547-44487597	ovcar-3	ovarian:	n/a
13	chr15:44487192-44487242	AG04449	skin:	fetal
14	chr15:44487910-44487960	BJ	skin:	n/a
15	chr15:44486207-44486257	PANC-1	pancreas:	n/a
16	chr15:44486450-44486500	BE2_C	brain:	n/a
17	chr15:44486562-44486612	T-47D	breast:	n/a
18	chr15:44507997-44508047	LNCaP	prostate:	n/a
19	chr15:44484200-44484250	HCT-116	colon:	n/a
20	chr15:44487910-44487960	NHBE	bronchial:	n/a
21	chr15:44487192-44487242	Caco-2	colon:	n/a
22	chr15:44487788-44487838	SK-N-SH_RA	brain:	n/a
23	chr15:44487192-44487242	HCPEpiC	choroid plexus:	n/a
24	chr15:44487910-44487960	HAEpiC	amniotic membrane:	n/a
25	chr15:44486621-44486671	HNPCEpiC	eye:	n/a
26	chr15:44487605-44487655	GM19239	blood:	n/a
27	chr15:44487547-44487597	ProgFib	skin:	n/a
28	chr15:44487547-44487597	PrEC	prostate:	n/a
29	chr15:44487605-44487655	BE2_C	brain:	n/a
30	chr15:44487788-44487838	HAEpiC	amniotic membrane:	n/a
31	chr15:44487547-44487597	GM19239	blood:	n/a
32	chr15:44487292-44487342	GM12891	blood:	n/a
33	chr15:44487545-44487595	H1-hESC	embryonic stem cell:	embryo
34	chr15:44487788-44487838	SK-N-SH	brain:	n/a
35	chr15:44486621-44486671	Hepatocyte	liver:	n/a
36	chr15:44487545-44487595	SAEC	small airway:	n/a
37	chr15:44487547-44487597	HAEpiC	amniotic membrane:	n/a
38	chr15:44486562-44486612	SK-N-MC	brain:	n/a
39	chr15:44487192-44487242	NH-A	brain:	n/a
40	chr15:44486621-44486671	HUVEC	blood vessel:	n/a
41	chr15:44486450-44486500	HNPCEpiC	eye:	n/a
42	chr15:44486450-44486500	HEK293	kidney:	embryo
43	chr15:44487924-44487974	GM12878	blood:	n/a
44	chr15:44487545-44487595	MCF-7	breast:	n/a
45	chr15:44507997-44508047	AG04450	lung:	fetal
46	chr15:44487728-44487778	AoSMC	blood vessel:	n/a
47	chr15:44507997-44508047	HepG2	liver:	n/a
48	chr15:44487308-44487358	GM12891	blood:	n/a
49	chr15:44486621-44486671	RPTEC	kidney:	n/a
50	chr15:44486207-44486257	SK-N-SH_RA	brain:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:44505864..44508334-chr15:44517714..44520133,2	K562	blood:
2	chr15:44498063..44499784-chr15:44504783..44507604,2	MCF-7	breast:
3	chr15:44195722..44196644-chr15:44511206..44512558,6	MCF-7	breast:
4	chr15:44391833..44394389-chr15:44398230..44401286,3	K562	blood:
5	chr15:44164813..44165436-chr15:44511999..44512879,2	MCF-7	breast:
6	chr15:44484355..44486935-chr15:44492288..44495192,2	MCF-7	breast:
7	chr15:44384733..44389004-chr15:44397743..44401359,3	K562	blood:
8	chr15:44192068..44194069-chr15:44510547..44512771,2	K562	blood:
9	chr15:44420856..44423555-chr15:44432395..44435096,2	K562	blood:
10	chr15:44510075..44512914-chr15:44817653..44819556,2	K562	blood:
11	chr15:44466277..44468385-chr15:44468539..44472676,4	MCF-7	breast:
12	chr15:44475513..44478627-chr15:44480233..44482535,3	K562	blood:
13	chr15:44475513..44478627-chr15:44480233..44482535,3	K562	blood:
14	chr15:44428775..44431085-chr15:44432139..44433893,2	MCF-7	breast:
15	chr15:44483275..44485560-chr15:44485692..44487954,2	K562	blood:
16	chr15:44358212..44359040-chr15:44511974..44512476,2	MCF-7	breast:
17	chr15:44420856..44423555-chr15:44432395..44435096,2	K562	blood:
18	chr15:44428775..44431085-chr15:44432139..44433893,2	MCF-7	breast:
19	chr15:44498063..44499784-chr15:44504783..44507604,2	MCF-7	breast:
20	chr15:44450623..44452763-chr15:44479639..44481622,2	MCF-7	breast:
21	chr15:44454686..44456749-chr15:44461504..44463965,2	K562	blood:
22	chr15:44448968..44451672-chr15:65596750..65598435,2	MCF-7	breast:
23	chr15:44496752..44498344-chr15:44833726..44836502,2	K562	blood:
24	chr15:44195949..44196699-chr15:44511446..44512539,4	K562	blood:
25	chr15:44411819..44414113-chr15:44419254..44421661,2	MCF-7	breast:
26	chr15:44482443..44484815-chr15:44485783..44488334,2	MCF-7	breast:
27	chr15:44450623..44452763-chr15:44479639..44481622,2	MCF-7	breast:
28	chr15:44466277..44468385-chr15:44468539..44472676,4	MCF-7	breast:
29	chr15:44411819..44414113-chr15:44419254..44421661,2	MCF-7	breast:
30	chr15:44454686..44456749-chr15:44461504..44463965,2	K562	blood:
31	chr15:44486877..44488833-chr15:44490905..44493302,2	MCF-7	breast:

No data

Variant related genes	Relation type
FRMD5	TF binding region
FRMD5	CpG island
ENSG00000200156	chromatin interactions
ENSG00000171877	chromatin interactions

Extended variants
information (count: 3751 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:3751 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2623016	chr15:44401266-44401267	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs571741674	chr15:44401268-44401269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs180713337	chr15:44401275-44401276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570677809	chr15:44401281-44401282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539347874	chr15:44401294-44401295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564086324	chr15:44401364-44401365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183783064	chr15:44401391-44401392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78656483	chr15:44401402-44401403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563465732	chr15:44401410-44401411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372927504	chr15:44401452-44401453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574653775	chr15:44401682-44401683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538657531	chr15:44401705-44401706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543078509	chr15:44401735-44401736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs527731500	chr15:44401773-44401774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148602688	chr15:44401774-44401775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200948614	chr15:44401776-44401777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182032052	chr15:44401784-44401785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142231935	chr15:44401840-44401841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531889958	chr15:44401849-44401850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35425269	chr15:44401860-44401861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs550128608	chr15:44401861-44401862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186014732	chr15:44401927-44401928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543892063	chr15:44401937-44401938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565486358	chr15:44401974-44401975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs34412466	chr15:44401977-44401978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs150805178	chr15:44402013-44402014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547368475	chr15:44402070-44402071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555082114	chr15:44402109-44402110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565434340	chr15:44402191-44402192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534321960	chr15:44402269-44402270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557291629	chr15:44402277-44402278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577876529	chr15:44402375-44402376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543675583	chr15:44402391-44402392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191725800	chr15:44402578-44402579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs558949566	chr15:44402594-44402595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575529084	chr15:44402650-44402651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562164799	chr15:44402666-44402667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs527743294	chr15:44402674-44402675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs541450779	chr15:44402749-44402750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs368968680	chr15:44402878-44402879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564475640	chr15:44402879-44402880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs565774033	chr15:44402896-44402897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533150750	chr15:44402904-44402905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs548094065	chr15:44402937-44402938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs566275726	chr15:44402961-44402962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs181794573	chr15:44403023-44403024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186348444	chr15:44403032-44403033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs549120064	chr15:44403033-44403034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs565448798	chr15:44403080-44403081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs534381709	chr15:44403086-44403087	Weak transcription Enhancers	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
Oral squamous cell carcinoma	17134496	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
Renal cell carcinoma	18765545	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
Mental retardation	17124404	CNVD
Melanoma	17363583	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:1265 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:44395000-44408000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr15:44396000-44408400	Weak transcription	HSMMtube	muscle
3	chr15:44396200-44402400	Weak transcription	Brain Angular Gyrus	brain
4	chr15:44396200-44413000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr15:44396400-44409800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr15:44398800-44402600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr15:44399200-44402600	Weak transcription	Brain Substantia Nigra	brain
8	chr15:44399600-44406400	Weak transcription	Brain Anterior Caudate	brain
9	chr15:44399800-44402400	Weak transcription	Brain Cingulate Gyrus	brain
10	chr15:44400000-44402400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr15:44400200-44403000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr15:44400200-44405200	Weak transcription	Fetal Heart	heart
13	chr15:44400200-44407800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr15:44400800-44401800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr15:44401000-44402400	Weak transcription	Brain Hippocampus Middle	brain
16	chr15:44402400-44404000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr15:44402400-44404000	Enhancers	Brain Angular Gyrus	brain
18	chr15:44402400-44404000	Enhancers	Brain Cingulate Gyrus	brain
19	chr15:44402400-44404000	Enhancers	Brain Hippocampus Middle	brain
20	chr15:44402600-44402800	Enhancers	Brain Substantia Nigra	brain
21	chr15:44402600-44404000	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr15:44402800-44403400	Weak transcription	Brain Substantia Nigra	brain
23	chr15:44403200-44403400	Enhancers	Fetal Brain Female	brain
24	chr15:44403200-44404000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr15:44403400-44404000	Enhancers	Brain Substantia Nigra	brain
26	chr15:44403400-44408000	Weak transcription	Fetal Brain Female	brain
27	chr15:44404000-44405200	Weak transcription	Brain Angular Gyrus	brain
28	chr15:44404000-44405200	Weak transcription	Brain Hippocampus Middle	brain
29	chr15:44404000-44405400	Weak transcription	Brain Substantia Nigra	brain
30	chr15:44404000-44405800	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr15:44404000-44406400	Weak transcription	Brain Cingulate Gyrus	brain
32	chr15:44405200-44405400	Enhancers	Brain Hippocampus Middle	brain
33	chr15:44405200-44405400	Enhancers	Fetal Heart	heart
34	chr15:44405200-44407200	Enhancers	Brain Angular Gyrus	brain
35	chr15:44405400-44405800	Weak transcription	Brain Hippocampus Middle	brain
36	chr15:44405400-44406000	Weak transcription	Fetal Heart	heart
37	chr15:44405400-44409800	Enhancers	Brain Substantia Nigra	brain
38	chr15:44405800-44406000	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr15:44405800-44410000	Enhancers	Brain Hippocampus Middle	brain
40	chr15:44406000-44406400	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr15:44406000-44406800	Enhancers	Fetal Heart	heart
42	chr15:44406400-44406800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr15:44406400-44407000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr15:44406400-44409000	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr15:44406400-44409600	Enhancers	Brain Anterior Caudate	brain
46	chr15:44406400-44411000	Enhancers	Brain Cingulate Gyrus	brain
47	chr15:44406600-44408800	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr15:44406800-44407800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr15:44406800-44408600	Weak transcription	Fetal Heart	heart
50	chr15:44407000-44409000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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