Variant report

Variant	nsv904440
Chromosome Location	chr15:82524544-82591082
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1081)
CpG islands
(count:855)
Chromatin interactive
region (count:21)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1081 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:82555714-82556193	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:82559315-82559851	K562	blood:	n/a	chr15:82559334-82559350
3	ARID3A	chr15:82579685-82580009	K562	blood:	n/a	n/a
4	ARID3A	chr15:82554834-82555131	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:82524162-82524551	K562	blood:	n/a	n/a
6	ARID3A	chr15:82555062-82555139	K562	blood:	n/a	n/a
7	ATF1	chr15:82554940-82555263	K562	blood:	n/a	n/a
8	ATF1	chr15:82559461-82559850	K562	blood:	n/a	n/a
9	ATF1	chr15:82554221-82554539	K562	blood:	n/a	n/a
10	ATF1	chr15:82523950-82524615	K562	blood:	n/a	n/a
11	ATF1	chr15:82531947-82532068	K562	blood:	n/a	n/a
12	ATF1	chr15:82579653-82580093	K562	blood:	n/a	n/a
13	ATF2	chr15:82578497-82579260	GM12878	blood:	n/a	n/a
14	ATF2	chr15:82578573-82579183	GM12878	blood:	n/a	n/a
15	ATF2	chr15:82579381-82579874	GM12878	blood:	n/a	n/a
16	ATF2	chr15:82554787-82555221	GM12878	blood:	n/a	n/a
17	ATF3	chr15:82554649-82555249	A549	lung:	n/a	n/a
18	BATF	chr15:82535965-82536263	GM12878	blood:	n/a	n/a
19	BATF	chr15:82578776-82579109	GM12878	blood:	n/a	n/a
20	BATF	chr15:82579428-82579685	GM12878	blood:	n/a	chr15:82579569-82579580
21	BATF	chr15:82578169-82578348	GM12878	blood:	n/a	n/a
22	BATF	chr15:82554283-82554528	GM12878	blood:	n/a	n/a
23	BATF	chr15:82536053-82536235	GM12878	blood:	n/a	n/a
24	BATF	chr15:82578722-82579110	GM12878	blood:	n/a	n/a
25	BCL11A	chr15:82578753-82579028	GM12878	blood:	n/a	n/a
26	BCL11A	chr15:82578726-82579144	GM12878	blood:	n/a	n/a
27	BCL11A	chr15:82579447-82579672	GM12878	blood:	n/a	n/a
28	BCL3	chr15:82554620-82555192	A549	lung:	n/a	chr15:82555168-82555176
29	BCL3	chr15:82578562-82579223	GM12878	blood:	n/a	n/a
30	BCLAF1	chr15:82554710-82555318	GM12878	blood:	n/a	chr15:82555168-82555176
31	BCLAF1	chr15:82578750-82579243	GM12878	blood:	n/a	n/a
32	BCLAF1	chr15:82578792-82579220	GM12878	blood:	n/a	n/a
33	BHLHE40	chr15:82554476-82555224	HepG2	liver:	n/a	chr15:82554950-82554966 chr15:82554640-82554649 chr15:82554639-82554648 chr15:82554640-82554649 chr15:82554634-82554655
34	BHLHE40	chr15:82554365-82555276	K562	blood:	n/a	chr15:82554950-82554966 chr15:82554640-82554649 chr15:82554639-82554648 chr15:82554640-82554649 chr15:82554634-82554655
35	BHLHE40	chr15:82554471-82555241	GM12878	blood:	n/a	chr15:82554950-82554966 chr15:82554640-82554649 chr15:82554639-82554648 chr15:82554640-82554649 chr15:82554634-82554655
36	BHLHE40	chr15:82578705-82579224	GM12878	blood:	n/a	n/a
37	BRCA1	chr15:82554436-82554804	H1-hESC	embryonic stem cell:	n/a	n/a
38	BRCA1	chr15:82555010-82555075	GM12878	blood:	n/a	n/a
39	BRCA1	chr15:82554360-82555242	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr15:82555006-82555196	HepG2	liver:	n/a	n/a
41	CBX3	chr15:82554755-82555383	K562	blood:	n/a	n/a
42	CBX3	chr15:82524106-82524560	K562	blood:	n/a	n/a
43	CCNT2	chr15:82579685-82580075	K562	blood:	n/a	n/a
44	CCNT2	chr15:82554793-82555276	K562	blood:	n/a	chr15:82554850-82554859
45	CCNT2	chr15:82559609-82559822	K562	blood:	n/a	n/a
46	CEBPB	chr15:82556432-82556628	HepG2	liver:	n/a	chr15:82556467-82556478
47	CEBPB	chr15:82554200-82554576	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr15:82579879-82580072	K562	blood:	n/a	n/a
49	CEBPB	chr15:82554022-82554526	IMR90	lung:	n/a	n/a
50	CEBPB	chr15:82556396-82556592	K562	blood:	n/a	chr15:82556467-82556478

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:82555390-82555440	U87	brain:	n/a
2	chr15:82555390-82555440	U87	brain:	n/a
3	chr15:82558555-82558605	HUVEC	blood vessel:	n/a
4	chr15:82554886-82554936	NHDF-neo	bronchial:	n/a
5	chr15:82575848-82575898	ovcar-3	ovarian:	n/a
6	chr15:82554584-82554634	SK-N-SH	brain:	n/a
7	chr15:82554902-82554952	AG04449	skin:	fetal
8	chr15:82555113-82555163	H1-hESC	embryonic stem cell:	embryo
9	chr15:82555113-82555163	NB4	blood:	n/a
10	chr15:82551086-82551136	BE2_C	brain:	n/a
11	chr15:82554820-82554870	HEEpiC	esophagus:	n/a
12	chr15:82558555-82558605	ovcar-3	ovarian:	n/a
13	chr15:82575848-82575898	MCF10A-Er-Src	breast:	n/a
14	chr15:82555552-82555602	PANC-1	pancreas:	n/a
15	chr15:82555456-82555506	AoSMC	blood vessel:	n/a
16	chr15:82554820-82554870	GM06990	blood:	n/a
17	chr15:82554886-82554936	SK-N-SH	brain:	n/a
18	chr15:82575848-82575898	HNPCEpiC	eye:	n/a
19	chr15:82554820-82554870	NHBE	bronchial:	n/a
20	chr15:82551086-82551136	CMK	blood:	n/a
21	chr15:82554902-82554952	BJ	skin:	n/a
22	chr15:82574624-82574674	HCPEpiC	choroid plexus:	n/a
23	chr15:82554902-82554952	HNPCEpiC	eye:	n/a
24	chr15:82574624-82574674	U87	brain:	n/a
25	chr15:82554820-82554870	GM19239	blood:	n/a
26	chr15:82554886-82554936	AG09319	gingival:	n/a
27	chr15:82555390-82555440	GM12878	blood:	n/a
28	chr15:82554820-82554870	HNPCEpiC	eye:	n/a
29	chr15:82555336-82555386	SK-N-SH	brain:	n/a
30	chr15:82575848-82575898	HAEpiC	amniotic membrane:	n/a
31	chr15:82551086-82551136	PFSK-1	brain:	n/a
32	chr15:82554584-82554634	AG04450	lung:	fetal
33	chr15:82575848-82575898	HRPEpiC	eye:	n/a
34	chr15:82555456-82555506	PANC-1	pancreas:	n/a
35	chr15:82555336-82555386	ECC-1	luminal epithelium:	n/a
36	chr15:82554584-82554634	Hela-S3	cervix:	n/a
37	chr15:82555456-82555506	AG10803	skin:	n/a
38	chr15:82551086-82551136	K562	blood:	n/a
39	chr15:82554820-82554870	AG04450	lung:	fetal
40	chr15:82558555-82558605	HRCEpiC	kidney:	n/a
41	chr15:82555113-82555163	Caco-2	colon:	n/a
42	chr15:82554584-82554634	PFSK-1	brain:	n/a
43	chr15:82574624-82574674	HAEpiC	amniotic membrane:	n/a
44	chr15:82554902-82554952	PrEC	prostate:	n/a
45	chr15:82554886-82554936	HRPEpiC	eye:	n/a
46	chr15:82554584-82554634	PrEC	prostate:	n/a
47	chr15:82558555-82558605	NHBE	bronchial:	n/a
48	chr15:82555552-82555602	HL-60	blood:	n/a
49	chr15:82575848-82575898	H1-hESC	embryonic stem cell:	embryo
50	chr15:82574624-82574674	NT2-D1	testis:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:82550051..82552780-chr15:82552889..82555231,4	K562	blood:
2	chr15:82558957..82560704-chr15:82563268..82565317,2	K562	blood:
3	chr1:242011083..242011828-chr15:82554163..82555047,2	Hela-S3	cervix:
4	chr15:82524498..82526931-chr15:82528402..82530346,2	MCF-7	breast:
5	chr15:82546241..82548403-chr15:82550539..82552952,2	MCF-7	breast:
6	chr15:82544226..82545855-chr15:82550615..82553251,2	K562	blood:
7	chr15:82540150..82542827-chr15:82551322..82553905,2	K562	blood:
8	chr15:82554331..82555047-chr17:39845080..39845674,3	Hela-S3	cervix:
9	chr15:82557073..82558574-chr15:82565794..82567576,2	K562	blood:
10	chr15:82558957..82560704-chr15:82563268..82565317,2	K562	blood:
11	chr15:82557636..82558140-chr15:84740091..84741075,2	MCF-7	breast:
12	chr15:82556066..82557698-chr15:82564817..82567206,2	MCF-7	breast:
13	chr15:82550191..82552669-chr15:82553526..82555918,3	MCF-7	breast:
14	chr15:82556066..82557698-chr15:82564817..82567206,2	MCF-7	breast:
15	chr12:6862392..6862918-chr15:82554357..82555098,2	Hela-S3	cervix:
16	chr15:82540150..82542827-chr15:82551322..82553905,2	K562	blood:
17	chr15:82546241..82548403-chr15:82550539..82552952,2	MCF-7	breast:
18	chr15:82511968..82514595-chr15:82553137..82554662,2	K562	blood:
19	chr15:82337966..82340144-chr15:82550811..82553189,2	MCF-7	breast:
20	chr15:82554707..82555430-chr17:57915266..57915873,2	MCF-7	breast:
21	chr15:82557073..82558574-chr15:82565794..82567576,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GOLGA6L9-6	chr15:82557014-82557230	NONHSAT047773
2	lnc-GOLGA6L9-6	chr15:82555485-82555529	NONHSAT047773
3	lnc-GOLGA6L9-5	chr15:82573380-82573998	NONHSAT047774

No data

Variant related genes	Relation type
FAM154B	TF binding region
ADAMTS7P1	TF binding region
EFTUD1	TF binding region
FAM154B	CpG island
ADAMTS7P1	CpG island
EFTUD1	CpG island
ENSG00000173812	chromatin interactions
ENSG00000174371	chromatin interactions
ENSG00000183496	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000188659	chromatin interactions
ENSG00000140598	chromatin interactions
ENSG00000089693	chromatin interactions

Extended variants
information (count: 1803 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1803 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2134046	chr15:82524544-82524545	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs541002901	chr15:82524545-82524546	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs560761874	chr15:82524597-82524598	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs574190798	chr15:82524606-82524607	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs558391648	chr15:82524651-82524652	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs563101434	chr15:82524660-82524661	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs532199134	chr15:82524661-82524662	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs375916844	chr15:82524677-82524678	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs559582894	chr15:82524733-82524734	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs528416719	chr15:82524744-82524745	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs547769573	chr15:82524759-82524760	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs567669819	chr15:82524792-82524793	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs185632921	chr15:82524823-82524824	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs139382157	chr15:82524852-82524853	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs117104393	chr15:82524857-82524858	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539198649	chr15:82524882-82524883	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549142054	chr15:82524885-82524886	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115352906	chr15:82524899-82524900	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs572686456	chr15:82524965-82524966	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535054562	chr15:82525001-82525002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs554096254	chr15:82525042-82525043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs144138884	chr15:82525075-82525076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs543078793	chr15:82525142-82525143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs552333595	chr15:82525157-82525158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189310117	chr15:82525180-82525181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576900124	chr15:82525181-82525182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545969277	chr15:82525202-82525203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs559334024	chr15:82525222-82525223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs76768691	chr15:82525246-82525247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs528343442	chr15:82525270-82525271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs541770656	chr15:82525275-82525276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs561234269	chr15:82525279-82525280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs146497021	chr15:82525310-82525311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs531581168	chr15:82525409-82525410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs117016370	chr15:82525425-82525426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs78695705	chr15:82525431-82525432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs532536379	chr15:82525471-82525472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs180994273	chr15:82525486-82525487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs143735143	chr15:82525542-82525543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535282699	chr15:82525543-82525544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs151050601	chr15:82525567-82525568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs140940338	chr15:82525571-82525572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs536634486	chr15:82525577-82525578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs186433431	chr15:82525580-82525581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs576868579	chr15:82525591-82525592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs571468404	chr15:82525598-82525599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs28610286	chr15:82525655-82525656	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs553094224	chr15:82525675-82525676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572970969	chr15:82525691-82525692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs377181104	chr15:82525706-82525707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
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
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Congenital diaphragmatic hernia	20921022	CNVD
abnormal development	18461090	CNVD
Intellectual disability	22102821	CNVD
renal disease	17924346	CNVD
Breast cancer	20409316	CNVD
Mental retardation	17847001	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1418 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:82432600-82552800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr15:82481800-82553000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr15:82488200-82531200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr15:82496200-82532000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr15:82496400-82532000	Weak transcription	Fetal Brain Male	brain
6	chr15:82497000-82553600	Weak transcription	Rectal Smooth Muscle	rectum
7	chr15:82497600-82536000	Weak transcription	Fetal Heart	heart
8	chr15:82499000-82550800	Weak transcription	HUVEC	blood vessel
9	chr15:82499400-82553000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr15:82499600-82531400	Weak transcription	Colonic Mucosa	Colon
11	chr15:82501400-82532000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr15:82501800-82544600	Weak transcription	Brain Angular Gyrus	brain
13	chr15:82503000-82531800	Weak transcription	Colon Smooth Muscle	Colon
14	chr15:82503000-82531800	Weak transcription	NHDF-Ad	bronchial
15	chr15:82503000-82531800	Weak transcription	NHLF	lung
16	chr15:82503000-82542200	Weak transcription	Stomach Mucosa	stomach
17	chr15:82503200-82552800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr15:82503600-82553000	Weak transcription	Small Intestine	intestine
19	chr15:82503800-82553200	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr15:82504200-82553200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr15:82505200-82531200	Weak transcription	Brain Cingulate Gyrus	brain
22	chr15:82507400-82553000	Weak transcription	NH-A	brain
23	chr15:82508200-82553800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr15:82510400-82526000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr15:82510600-82531200	Weak transcription	Brain Substantia Nigra	brain
26	chr15:82510600-82532600	Weak transcription	Ovary	ovary
27	chr15:82510800-82531200	Weak transcription	Fetal Lung	lung
28	chr15:82510800-82554200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr15:82511000-82529200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr15:82511800-82530400	Weak transcription	Left Ventricle	heart
31	chr15:82511800-82534800	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr15:82511800-82554200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr15:82512000-82530400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr15:82512200-82531200	Weak transcription	Fetal Stomach	stomach
35	chr15:82512200-82531800	Weak transcription	Brain Germinal Matrix	brain
36	chr15:82512600-82531400	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr15:82512600-82539600	Weak transcription	Spleen	Spleen
38	chr15:82515800-82553600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr15:82518800-82525000	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr15:82519800-82531200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr15:82519800-82531200	Weak transcription	A549	lung
42	chr15:82519800-82532600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr15:82520000-82530600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr15:82520000-82531000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr15:82520000-82531800	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr15:82520000-82553000	Weak transcription	Gastric	stomach
47	chr15:82520000-82553000	Weak transcription	Right Ventricle	heart
48	chr15:82520000-82553400	Weak transcription	Brain Hippocampus Middle	brain
49	chr15:82520000-82554200	Weak transcription	Pancreas	Pancrea
50	chr15:82520200-82529200	Weak transcription	Thymus	Thymus

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