Variant report

Variant	nsv570021
Chromosome Location	chr15:76813920-76978139
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:677)
CpG islands
(count:122)
Chromatin interactive
region (count:20)
LncRNA
region (count:1)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:677 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:76935433-76935442	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:76865111-76865365	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:76825612-76826689	HepG2	liver:	n/a	n/a
4	ATF2	chr15:76867574-76868256	GM12878	blood:	n/a	n/a
5	ATF2	chr15:76867545-76868188	GM12878	blood:	n/a	n/a
6	BATF	chr15:76907151-76907359	GM12878	blood:	n/a	n/a
7	BATF	chr15:76867553-76868299	GM12878	blood:	n/a	n/a
8	BATF	chr15:76907137-76907384	GM12878	blood:	n/a	n/a
9	BATF	chr15:76946679-76946925	GM12878	blood:	n/a	n/a
10	BATF	chr15:76946672-76946896	GM12878	blood:	n/a	n/a
11	BATF	chr15:76867629-76868083	GM12878	blood:	n/a	n/a
12	BATF	chr15:76868780-76869125	GM12878	blood:	n/a	n/a
13	BCL11A	chr15:76867646-76868017	GM12878	blood:	n/a	n/a
14	BCL11A	chr15:76946684-76946864	GM12878	blood:	n/a	n/a
15	BCL11A	chr15:76867571-76868071	GM12878	blood:	n/a	n/a
16	BCL3	chr15:76867594-76868106	GM12878	blood:	n/a	n/a
17	BCL3	chr15:76825763-76826141	GM12878	blood:	n/a	n/a
18	BCL3	chr15:76825735-76826094	GM12878	blood:	n/a	n/a
19	BCL3	chr15:76867671-76868118	GM12878	blood:	n/a	n/a
20	BCLAF1	chr15:76867603-76868092	GM12878	blood:	n/a	n/a
21	BCLAF1	chr15:76867350-76868205	GM12878	blood:	n/a	n/a
22	BHLHE40	chr15:76867676-76868010	GM12878	blood:	n/a	n/a
23	BHLHE40	chr15:76946680-76946809	GM12878	blood:	n/a	n/a
24	BRCA1	chr15:76969668-76969722	H1-hESC	embryonic stem cell:	n/a	n/a
25	CBX3	chr15:76928484-76928676	K562	blood:	n/a	n/a
26	CBX3	chr15:76928439-76928711	K562	blood:	n/a	n/a
27	CEBPB	chr15:76825717-76826086	A549	lung:	n/a	chr15:76825991-76826004 chr15:76825947-76825958
28	CEBPB	chr15:76825807-76825998	HepG2	liver:	n/a	chr15:76825947-76825958
29	CEBPB	chr15:76963560-76963674	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr15:76908855-76909056	HepG2	liver:	n/a	chr15:76908970-76908981
31	CEBPB	chr15:76960844-76961108	A549	lung:	n/a	n/a
32	CEBPB	chr15:76953585-76953673	A549	lung:	n/a	n/a
33	CEBPB	chr15:76839190-76839507	HepG2	liver:	n/a	chr15:76839336-76839347
34	CEBPB	chr15:76825743-76826204	HepG2	liver:	n/a	chr15:76825991-76826004 chr15:76825947-76825958
35	CEBPB	chr15:76826343-76826767	IMR90	lung:	n/a	n/a
36	CEBPB	chr15:76857129-76857461	A549	lung:	n/a	chr15:76857283-76857294
37	CEBPB	chr15:76865289-76865622	HepG2	liver:	n/a	chr15:76865442-76865453
38	CEBPB	chr15:76869014-76869478	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr15:76825694-76826267	MCF-7	breast:	n/a	chr15:76825991-76826004 chr15:76825947-76825958
40	CEBPB	chr15:76857118-76857460	HepG2	liver:	n/a	chr15:76857283-76857294
41	CEBPB	chr15:76867691-76868041	GM12878	blood:	n/a	n/a
42	CEBPB	chr15:76839201-76839452	A549	lung:	n/a	chr15:76839336-76839347
43	CEBPB	chr15:76852010-76852215	A549	lung:	n/a	n/a
44	CEBPB	chr15:76825760-76826178	A549	lung:	n/a	chr15:76825991-76826004 chr15:76825947-76825958
45	CEBPB	chr15:76825775-76826096	IMR90	lung:	n/a	chr15:76825991-76826004 chr15:76825947-76825958
46	CEBPB	chr15:76837027-76837186	IMR90	lung:	n/a	chr15:76837087-76837098
47	CEBPB	chr15:76865278-76865665	Hela-S3	cervix:	n/a	chr15:76865442-76865453
48	CEBPB	chr15:76839240-76839462	K562	blood:	n/a	chr15:76839336-76839347
49	CEBPB	chr15:76867534-76868241	GM12878	blood:	n/a	n/a
50	CEBPB	chr15:76857146-76857335	Hela-S3	cervix:	n/a	chr15:76857283-76857294

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:76901065-76901115	HRPEpiC	eye:	n/a
2	chr15:76901065-76901115	HepG2	liver:	n/a
3	chr15:76868964-76869014	BE2_C	brain:	n/a
4	chr15:76868964-76869014	IMR90	lung:	fetal
5	chr15:76868964-76869014	HMEC	breast:	n/a
6	chr15:76868964-76869014	MCF-7	breast:	n/a
7	chr15:76868964-76869014	CMK	blood:	n/a
8	chr15:76868964-76869014	PrEC	prostate:	n/a
9	chr15:76868964-76869014	HAEpiC	amniotic membrane:	n/a
10	chr15:76868964-76869014	HIPEpiC	eye:	n/a
11	chr15:76901065-76901115	AG04450	lung:	fetal
12	chr15:76901065-76901115	SK-N-SH	brain:	n/a
13	chr15:76868964-76869014	HCM	heart:	n/a
14	chr15:76868964-76869014	ECC-1	luminal epithelium:	n/a
15	chr15:76901065-76901115	HUVEC	blood vessel:	n/a
16	chr15:76901065-76901115	HMEC	breast:	n/a
17	chr15:76901065-76901115	GM19239	blood:	n/a
18	chr15:76901065-76901115	SKMC	muscle:	n/a
19	chr15:76901065-76901115	HCF	heart:	n/a
20	chr15:76901065-76901115	AoSMC	blood vessel:	n/a
21	chr15:76901065-76901115	SK-N-MC	brain:	n/a
22	chr15:76901065-76901115	Hela-S3	cervix:	n/a
23	chr15:76901065-76901115	Hepatocyte	liver:	n/a
24	chr15:76868964-76869014	HCF	heart:	n/a
25	chr15:76868964-76869014	HRE	kidney:	n/a
26	chr15:76901065-76901115	GM12891	blood:	n/a
27	chr15:76868964-76869014	SK-N-SH_RA	brain:	n/a
28	chr15:76868964-76869014	Caco-2	colon:	n/a
29	chr15:76868964-76869014	AG04450	lung:	fetal
30	chr15:76868964-76869014	NHBE	bronchial:	n/a
31	chr15:76901065-76901115	GM06990	blood:	n/a
32	chr15:76868964-76869014	GM19239	blood:	n/a
33	chr15:76868964-76869014	HL-60	blood:	n/a
34	chr15:76868964-76869014	HRPEpiC	eye:	n/a
35	chr15:76868964-76869014	AG09309	skin:	n/a
36	chr15:76868964-76869014	AoSMC	blood vessel:	n/a
37	chr15:76868964-76869014	SK-N-MC	brain:	n/a
38	chr15:76868964-76869014	BJ	skin:	n/a
39	chr15:76901065-76901115	NT2-D1	testis:	n/a
40	chr15:76901065-76901115	HNPCEpiC	eye:	n/a
41	chr15:76901065-76901115	PANC-1	pancreas:	n/a
42	chr15:76901065-76901115	GM12892	blood:	n/a
43	chr15:76901065-76901115	HIPEpiC	eye:	n/a
44	chr15:76901065-76901115	AG10803	skin:	n/a
45	chr15:76901065-76901115	MCF-7	breast:	n/a
46	chr15:76901065-76901115	Caco-2	colon:	n/a
47	chr15:76901065-76901115	HRE	kidney:	n/a
48	chr15:76901065-76901115	HCM	heart:	n/a
49	chr15:76901065-76901115	HRCEpiC	kidney:	n/a
50	chr15:76868964-76869014	HCT-116	colon:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:76877558..76879609-chr15:76881319..76882907,2	K562	blood:
2	chr15:76964455..76968844-chr15:76969640..76972722,4	K562	blood:
3	chr15:76959064..76961382-chr15:76964223..76965946,2	MCF-7	breast:
4	chr15:76855877..76857707-chr15:76866696..76869240,2	MCF-7	breast:
5	chr15:76855877..76857707-chr15:76866696..76869240,2	MCF-7	breast:
6	chr15:76821101..76824629-chr15:76825214..76826999,4	K562	blood:
7	chr15:76812872..76815537-chr15:76817323..76820278,2	MCF-7	breast:
8	chr15:76812872..76815537-chr15:76817323..76820278,2	MCF-7	breast:
9	chr15:76934226..76937075-chr15:76948287..76950112,2	MCF-7	breast:
10	chr15:76493051..76495991-chr15:76813493..76815400,2	MCF-7	breast:
11	chr15:76821101..76824629-chr15:76825214..76826999,4	K562	blood:
12	chr15:76934226..76937075-chr15:76948287..76950112,2	MCF-7	breast:
13	chr15:76967596..76970375-chr15:76976896..76979262,2	K562	blood:
14	chr15:76934897..76935640-chr15:77158999..77159764,3	MCF-7	breast:
15	chr15:76967596..76970375-chr15:76976896..76979262,2	K562	blood:
16	chr15:76934737..76935336-chr15:77133237..77133799,2	MCF-7	breast:
17	chr15:76969596..76972550-chr15:76979737..76981959,2	MCF-7	breast:
18	chr15:76810534..76813037-chr15:76815373..76817326,2	MCF-7	breast:
19	chr15:76964455..76968844-chr15:76969640..76972722,4	K562	blood:
20	chr15:76959064..76961382-chr15:76964223..76965946,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ETFA-5	chr15:76833537-76833934	NONHSAT047406

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3713	chr15:76878988-76879007	MIMAT0018164

No data

Variant related genes	Relation type
SCAPER	TF binding region
MIR3713	TF binding region
SCAPER	CpG island
MIR3713	CpG island
ENSG00000266449	chromatin interactions

Extended variants
information (count: 5583 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:5583 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566422490	chr15:76813920-76813921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs549053778	chr15:76813963-76813964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141469376	chr15:76813969-76813970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546103744	chr15:76813980-76813981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568597103	chr15:76813982-76813983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187988379	chr15:76814017-76814018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs375166137	chr15:76814043-76814044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572827334	chr15:76814061-76814062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537226745	chr15:76814091-76814092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561335425	chr15:76814092-76814093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs143160785	chr15:76814202-76814203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs8039601	chr15:76814227-76814228	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs562464324	chr15:76814265-76814266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs193074151	chr15:76814376-76814377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551270049	chr15:76814390-76814391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566688225	chr15:76814440-76814441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183929131	chr15:76814442-76814443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547156773	chr15:76814465-76814466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146651043	chr15:76814493-76814494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187852718	chr15:76814504-76814505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs62030360	chr15:76814570-76814571	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs191906751	chr15:76814604-76814605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184466983	chr15:76814632-76814633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114579908	chr15:76814672-76814673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558063209	chr15:76814680-76814681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573422394	chr15:76814714-76814715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140238503	chr15:76814881-76814882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555046430	chr15:76814908-76814909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188526875	chr15:76814955-76814956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs116533748	chr15:76815010-76815011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150803385	chr15:76815030-76815031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562178482	chr15:76815069-76815070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs61273691	chr15:76815226-76815227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150313959	chr15:76815244-76815245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192964083	chr15:76815275-76815276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560079614	chr15:76815286-76815287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368954815	chr15:76815375-76815376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11855816	chr15:76815378-76815379	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs547071055	chr15:76815472-76815473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541995900	chr15:76815555-76815556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184256052	chr15:76815597-76815598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529273108	chr15:76815618-76815619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562194404	chr15:76815625-76815626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189313866	chr15:76815661-76815662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569279762	chr15:76815667-76815668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs494268	chr15:76815713-76815714	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs74965006	chr15:76815787-76815788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566903213	chr15:76815846-76815847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534145069	chr15:76815917-76815918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201014407	chr15:76815959-76815960	Weak 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
Wilms tumour	21544195	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
early-passage human iPS cells	21368824	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:991 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76797400-76825000	Weak transcription	Primary B cells from cord blood	blood
2	chr15:76805600-76845800	Weak transcription	Primary T cells from cord blood	blood
3	chr15:76807600-76817800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr15:76808000-76816200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr15:76808400-76825000	Weak transcription	Fetal Intestine Small	intestine
6	chr15:76808400-76825600	Weak transcription	Fetal Intestine Large	intestine
7	chr15:76811200-76825400	Weak transcription	Fetal Stomach	stomach
8	chr15:76813000-76821600	Weak transcription	Left Ventricle	heart
9	chr15:76816200-76816800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr15:76816200-76819400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr15:76817200-76818400	Weak transcription	Fetal Brain Male	brain
12	chr15:76817800-76818000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr15:76818000-76819800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr15:76818400-76818600	Enhancers	Fetal Brain Male	brain
15	chr15:76819400-76828400	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr15:76819800-76820000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr15:76822400-76822800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr15:76823600-76823800	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr15:76823800-76825200	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr15:76825000-76825400	Enhancers	Primary B cells from cord blood	blood
21	chr15:76825000-76826800	Enhancers	Fetal Intestine Small	intestine
22	chr15:76825000-76826800	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr15:76825000-76826800	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr15:76825200-76825800	Enhancers	Duodenum Mucosa	Duodenum
25	chr15:76825200-76826800	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr15:76825200-76826800	Enhancers	Stomach Mucosa	stomach
27	chr15:76825200-76826800	Enhancers	A549	lung
28	chr15:76825200-76826800	Enhancers	HepG2	liver
29	chr15:76825400-76826600	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr15:76825400-76827600	Enhancers	Fetal Stomach	stomach
31	chr15:76825600-76826800	Enhancers	Fetal Intestine Large	intestine
32	chr15:76825800-76826200	Enhancers	Fetal Brain Male	brain
33	chr15:76826000-76826800	Enhancers	Duodenum Smooth Muscle	Duodenum
34	chr15:76826000-76826800	Enhancers	Fetal Lung	lung
35	chr15:76826000-76826800	Enhancers	Rectal Mucosa Donor 29	rectum
36	chr15:76826000-76826800	Enhancers	Small Intestine	intestine
37	chr15:76826400-76826800	Enhancers	Colon Smooth Muscle	Colon
38	chr15:76826400-76827000	Enhancers	NHLF	lung
39	chr15:76835800-76836200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr15:76837600-76838200	Enhancers	Fetal Heart	heart
41	chr15:76842000-76844200	Weak transcription	Fetal Stomach	stomach
42	chr15:76842200-76845400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr15:76842400-76845600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr15:76842600-76845400	Weak transcription	Primary T cells fromperipheralblood	blood
45	chr15:76842600-76845600	Weak transcription	Lung	lung
46	chr15:76842600-76845800	Weak transcription	Spleen	Spleen
47	chr15:76842800-76843000	ZNF genes & repeats	Primary B cells from cord blood	blood
48	chr15:76842800-76846200	Weak transcription	Primary T helper cells fromperipheralblood	blood
49	chr15:76843000-76844200	Weak transcription	Fetal Intestine Small	intestine
50	chr15:76843000-76844600	Weak transcription	Pancreas	Pancrea

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