Variant report

Variant	nsv904219
Chromosome Location	chr15:51851999-51977159
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2145)
CpG islands
(count:1464)
Chromatin interactive
region (count:187)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2145 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:51871485-51871486	K562	blood:	n/a	n/a
2	ARID3A	chr15:51869305-51869743	K562	blood:	n/a	n/a
3	ARID3A	chr15:51913407-51913677	K562	blood:	n/a	n/a
4	ARID3A	chr15:51926895-51927114	K562	blood:	n/a	n/a
5	ARID3A	chr15:51873449-51874120	K562	blood:	n/a	n/a
6	ARID3A	chr15:51914057-51914328	K562	blood:	n/a	n/a
7	ARID3A	chr15:51915628-51916287	K562	blood:	n/a	n/a
8	ARID3A	chr15:51870029-51870641	K562	blood:	n/a	n/a
9	ARID3A	chr15:51943840-51944929	K562	blood:	n/a	n/a
10	ARID3A	chr15:51939094-51939751	K562	blood:	n/a	n/a
11	ARID3A	chr15:51965660-51965996	K562	blood:	n/a	n/a
12	ARID3A	chr15:51872535-51873050	K562	blood:	n/a	n/a
13	ARID3A	chr15:51912932-51913016	K562	blood:	n/a	n/a
14	ARID3A	chr15:51893648-51893900	K562	blood:	n/a	n/a
15	ARID3A	chr15:51895626-51895896	K562	blood:	n/a	n/a
16	ATF1	chr15:51869224-51869631	K562	blood:	n/a	n/a
17	ATF1	chr15:51964374-51964827	K562	blood:	n/a	n/a
18	ATF1	chr15:51939313-51939872	K562	blood:	n/a	n/a
19	ATF1	chr15:51944242-51944903	K562	blood:	n/a	n/a
20	ATF1	chr15:51915722-51916114	K562	blood:	n/a	n/a
21	ATF1	chr15:51942165-51942440	K562	blood:	n/a	n/a
22	ATF1	chr15:51973437-51973899	K562	blood:	n/a	chr15:51973584-51973598
23	ATF1	chr15:51872652-51872968	K562	blood:	n/a	n/a
24	ATF1	chr15:51926916-51927167	K562	blood:	n/a	n/a
25	ATF2	chr15:51914116-51914796	GM12878	blood:	n/a	n/a
26	ATF2	chr15:51942038-51942440	GM12878	blood:	n/a	n/a
27	ATF2	chr15:51917219-51918018	GM12878	blood:	n/a	n/a
28	ATF2	chr15:51917308-51917935	GM12878	blood:	n/a	n/a
29	ATF3	chr15:51973405-51973799	K562	blood:	n/a	chr15:51973587-51973607 chr15:51973759-51973768
30	ATF3	chr15:51939278-51939725	K562	blood:	n/a	n/a
31	ATF3	chr15:51892411-51892760	K562	blood:	n/a	n/a
32	ATF3	chr15:51895627-51896150	K562	blood:	n/a	n/a
33	BACH1	chr15:51893743-51893893	K562	blood:	n/a	n/a
34	BACH1	chr15:51915616-51916109	K562	blood:	n/a	n/a
35	BACH1	chr15:51973550-51974054	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr15:51964468-51964470	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr15:51907534-51907617	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr15:51939410-51939672	K562	blood:	n/a	n/a
39	BACH1	chr15:51914113-51914733	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr15:51915019-51915548	H1-hESC	embryonic stem cell:	n/a	n/a
41	BATF	chr15:51892416-51892715	GM12878	blood:	n/a	chr15:51892572-51892583
42	BCL11A	chr15:51917337-51917861	GM12878	blood:	n/a	n/a
43	BCL11A	chr15:51914213-51914609	GM12878	blood:	n/a	n/a
44	BCL11A	chr15:51917428-51917689	GM12878	blood:	n/a	n/a
45	BCL3	chr15:51914363-51915166	A549	lung:	n/a	chr15:51915134-51915147 chr15:51914934-51914947 chr15:51914930-51914943 chr15:51914933-51914942 chr15:51914930-51914939 chr15:51914931-51914944
46	BCL3	chr15:51914303-51914883	GM12878	blood:	n/a	n/a
47	BCL3	chr15:51921286-51921581	GM12878	blood:	n/a	n/a
48	BCL3	chr15:51921286-51921652	GM12878	blood:	n/a	n/a
49	BCLAF1	chr15:51917370-51917848	GM12878	blood:	n/a	n/a
50	BCLAF1	chr15:51914100-51914752	GM12878	blood:	n/a	n/a

(count:1464 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:51970968-51971018	AG04449	skin:	fetal
2	chr15:51915370-51915420	AG09319	gingival:	n/a
3	chr15:51973534-51973584	SK-N-SH	brain:	n/a
4	chr15:51973591-51973641	IMR90	lung:	fetal
5	chr15:51970968-51971018	NT2-D1	testis:	n/a
6	chr15:51973460-51973510	MCF10A-Er-Src	breast:	n/a
7	chr15:51972699-51972749	Caco-2	colon:	n/a
8	chr15:51915087-51915137	IMR90	lung:	fetal
9	chr15:51973534-51973584	AG09319	gingival:	n/a
10	chr15:51973920-51973970	HCT-116	colon:	n/a
11	chr15:51915395-51915445	LNCaP	prostate:	n/a
12	chr15:51910925-51910975	NH-A	brain:	n/a
13	chr15:51914952-51915002	HL-60	blood:	n/a
14	chr15:51947756-51947806	NB4	blood:	n/a
15	chr15:51915035-51915085	U87	brain:	n/a
16	chr15:51973224-51973274	GM19239	blood:	n/a
17	chr15:51970968-51971018	GM12878	blood:	n/a
18	chr15:51947756-51947806	K562	blood:	n/a
19	chr15:51973534-51973584	NHDF-neo	bronchial:	n/a
20	chr15:51914292-51914342	PANC-1	pancreas:	n/a
21	chr15:51915087-51915137	HUVEC	blood vessel:	n/a
22	chr15:51914292-51914342	HEK293	kidney:	embryo
23	chr15:51973764-51973814	MCF-7	breast:	n/a
24	chr15:51973661-51973711	HCM	heart:	n/a
25	chr15:51973224-51973274	MCF-7	breast:	n/a
26	chr15:51915035-51915085	HEK293	kidney:	embryo
27	chr15:51973534-51973584	SK-N-SH_RA	brain:	n/a
28	chr15:51970968-51971018	HCF	heart:	n/a
29	chr15:51915035-51915085	SK-N-MC	brain:	n/a
30	chr15:51973591-51973641	ProgFib	skin:	n/a
31	chr15:51918170-51918220	CMK	blood:	n/a
32	chr15:51914746-51914796	HepG2	liver:	n/a
33	chr15:51973661-51973711	HRPEpiC	eye:	n/a
34	chr15:51972699-51972749	MCF-7	breast:	n/a
35	chr15:51973661-51973711	RPTEC	kidney:	n/a
36	chr15:51973534-51973584	ovcar-3	ovarian:	n/a
37	chr15:51973764-51973814	HAEpiC	amniotic membrane:	n/a
38	chr15:51915035-51915085	HNPCEpiC	eye:	n/a
39	chr15:51915035-51915085	HIPEpiC	eye:	n/a
40	chr15:51947756-51947806	BE2_C	brain:	n/a
41	chr15:51915395-51915445	HRE	kidney:	n/a
42	chr15:51973661-51973711	HNPCEpiC	eye:	n/a
43	chr15:51947756-51947806	PANC-1	pancreas:	n/a
44	chr15:51915087-51915137	SK-N-SH	brain:	n/a
45	chr15:51918170-51918220	HCT-116	colon:	n/a
46	chr15:51973199-51973249	SK-N-SH_RA	brain:	n/a
47	chr15:51915413-51915463	GM19239	blood:	n/a
48	chr15:51964706-51964756	GM12891	blood:	n/a
49	chr15:51914952-51915002	ECC-1	luminal epithelium:	n/a
50	chr15:51973591-51973641	Hela-S3	cervix:	n/a

(count:187 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr15:51893271..51895082-chr15:51912831..51915334,2	K562	blood:
2	chr15:51860984..51863229-chr15:51878270..51880253,2	MCF-7	breast:
3	chr15:51976547..51978091-chr15:52028258..52031013,2	MCF-7	breast:
4	chr15:51904892..51907829-chr15:51916271..51917973,2	MCF-7	breast:
5	chr15:51960620..51962408-chr15:51966194..51968469,2	MCF-7	breast:
6	chr15:51923743..51925497-chr15:51937035..51939547,2	K562	blood:
7	chr15:51870572..51873309-chr15:51873394..51875007,2	MCF-7	breast:
8	chr15:51828883..51829809-chr15:51853123..51854092,2	MCF-7	breast:
9	chr15:51940521..51942581-chr15:52121824..52123791,2	MCF-7	breast:
10	chr14:51026899..51027640-chr15:51914645..51915479,2	HCT-116	colon:
11	chr15:51913840..51916895-chr15:51922199..51924980,3	MCF-7	breast:
12	chr15:51914090..51916828-chr15:51923962..51929306,7	MCF-7	breast:
13	chr15:51855034..51858623-chr15:51869913..51872025,3	MCF-7	breast:
14	chr15:51976806..51978342-chr15:51982300..51983965,2	MCF-7	breast:
15	chr15:51892783..51896070-chr15:51903536..51906578,4	K562	blood:
16	chr15:51877838..51880078-chr15:51913640..51915227,2	MCF-7	breast:
17	chr15:51914680..51916767-chr15:51938237..51940151,2	MCF-7	breast:
18	chr15:51915397..51918003-chr15:52069309..52070981,2	MCF-7	breast:
19	chr15:51913792..51916405-chr15:51942869..51945366,3	K562	blood:
20	chr15:51923743..51925497-chr15:51937035..51939547,2	K562	blood:
21	chr15:51970627..51972181-chr15:52008855..52011853,2	MCF-7	breast:
22	chr15:51933560..51938280-chr15:51939228..51942863,5	MCF-7	breast:
23	chr15:51880703..51883110-chr15:51892306..51895178,2	MCF-7	breast:
24	chr15:51941554..51943046-chr15:52068074..52069805,23	MCF-7	breast:
25	chr15:51835902..51838646-chr15:51851787..51853381,2	MCF-7	breast:
26	chr15:51830870..51833230-chr15:51850921..51853249,2	K562	blood:
27	chr15:51876863..51879432-chr15:51880781..51882627,2	MCF-7	breast:
28	chr15:51965668..51968596-chr15:51971807..51974578,3	K562	blood:
29	chr15:51914529..51916927-chr15:52121179..52124043,2	MCF-7	breast:
30	chr15:51950953..51953753-chr15:52026333..52028408,2	MCF-7	breast:
31	chr15:51922746..51924870-chr15:51925767..51927937,2	K562	blood:
32	chr15:51947467..51949887-chr15:51951692..51953338,2	MCF-7	breast:
33	chr15:51944446..51946253-chr15:52042557..52044525,2	K562	blood:
34	chr15:51867811..51869730-chr15:51913400..51915633,2	MCF-7	breast:
35	chr15:51975005..51977651-chr15:51984880..51987418,3	K562	blood:
36	chr15:51904383..51907963-chr15:51911974..51914714,3	K562	blood:
37	chr15:51859933..51862256-chr15:51866857..51869173,2	MCF-7	breast:
38	chr15:51854337..51857092-chr15:51860809..51862898,2	K562	blood:
39	chr15:51922579..51924292-chr5:34006602..34008870,2	MCF-7	breast:
40	chr15:51915278..51917337-chr15:51922529..51924335,2	K562	blood:
41	chr15:51912949..51917432-chr15:51917786..51922199,7	K562	blood:
42	chr15:51923873..51926717-chr15:51934100..51936928,2	MCF-7	breast:
43	chr15:51941765..51942808-chr15:52067729..52069864,21	K562	blood:
44	chr15:51892718..51895585-chr15:52310402..52312798,2	K562	blood:
45	chr15:51915278..51917337-chr15:51922529..51924335,2	K562	blood:
46	chr15:51694062..51694684-chr15:51881746..51882355,2	MCF-7	breast:
47	chr15:51939928..51943794-chr15:52067782..52071460,6	MCF-7	breast:
48	chr15:51909586..51911705-chr15:51923357..51924958,2	K562	blood:
49	chr15:51942152..51942788-chr15:52431755..52432640,2	K562	blood:
50	chr15:51943708..51945946-chr15:52042057..52044525,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000263437	TF binding region
SCG3	TF binding region
DMXL2	TF binding region
ENSG00000263437	CpG island
SCG3	CpG island
DMXL2	CpG island
ENSG00000128872	chromatin interactions
ENSG00000242110	chromatin interactions
ENSG00000104093	chromatin interactions
ENSG00000198513	chromatin interactions
ENSG00000140280	chromatin interactions
ENSG00000187742	chromatin interactions
ENSG00000259438	chromatin interactions
ENSG00000104112	chromatin interactions
ENSG00000069956	chromatin interactions
ENSG00000263437	chromatin interactions
ENSG00000138594	chromatin interactions
ENSG00000267302	chromatin interactions
ENSG00000065621	chromatin interactions
ENSG00000259377	chromatin interactions
ENSG00000069966	chromatin interactions
ENSG00000137842	chromatin interactions
ENSG00000166477	chromatin interactions
ENSG00000189050	chromatin interactions

Extended variants
information (count: 4420 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:4420 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4774594	chr15:51851999-51852000	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs558470033	chr15:51852015-51852016	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573615425	chr15:51852039-51852040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540945216	chr15:51852040-51852041	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562086743	chr15:51852056-51852057	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370245039	chr15:51852057-51852058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs544652597	chr15:51852131-51852132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562881503	chr15:51852253-51852254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532957126	chr15:51852256-51852257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs148579553	chr15:51852269-51852270	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559998163	chr15:51852289-51852290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76510433	chr15:51852308-51852309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549027074	chr15:51852447-51852448	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567204822	chr15:51852480-51852481	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537450678	chr15:51852525-51852526	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549846900	chr15:51852540-51852541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571285711	chr15:51852649-51852650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs151087341	chr15:51852663-51852664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12148382	chr15:51852699-51852700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536863046	chr15:51852722-51852723	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs66990182	chr15:51852728-51852729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187355938	chr15:51852739-51852740	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549125280	chr15:51852744-51852745	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370333600	chr15:51852746-51852747	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573500657	chr15:51852760-51852761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs142584041	chr15:51852776-51852777	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs76252910	chr15:51852820-51852821	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs193140089	chr15:51852847-51852848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544326827	chr15:51852860-51852861	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185523152	chr15:51852892-51852893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs35455221	chr15:51852901-51852902	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs74724306	chr15:51852908-51852909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1902591	chr15:51852920-51852921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs577747517	chr15:51852926-51852927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545113689	chr15:51852943-51852944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574143089	chr15:51852958-51852959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374292079	chr15:51853020-51853021	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559886122	chr15:51853047-51853048	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116375982	chr15:51853070-51853071	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189263542	chr15:51853081-51853082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368679081	chr15:51853129-51853130	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561066544	chr15:51853139-51853140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs34112292	chr15:51853143-51853144	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370775220	chr15:51853158-51853159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs75423878	chr15:51853173-51853174	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs35051365	chr15:51853191-51853192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs78179620	chr15:51853310-51853311	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192596249	chr15:51853386-51853387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532219763	chr15:51853407-51853408	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs577208724	chr15:51853481-51853482	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:1395 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:51776800-51855200	Weak transcription	Thymus	Thymus
2	chr15:51780400-51855800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr15:51781400-51863000	Weak transcription	HSMM	muscle
4	chr15:51787400-51855400	Weak transcription	Osteobl	bone
5	chr15:51794600-51861000	Weak transcription	Gastric	stomach
6	chr15:51809000-51854800	Weak transcription	Brain Hippocampus Middle	brain
7	chr15:51816000-51861000	Weak transcription	Pancreas	Pancrea
8	chr15:51817800-51862200	Weak transcription	Fetal Brain Male	brain
9	chr15:51818200-51855400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr15:51818200-51861600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr15:51818400-51853400	Weak transcription	Lung	lung
12	chr15:51818400-51861200	Weak transcription	Fetal Stomach	stomach
13	chr15:51819400-51852600	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr15:51819400-51853400	Weak transcription	Ovary	ovary
15	chr15:51819600-51853400	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr15:51819600-51861400	Weak transcription	Fetal Muscle Trunk	muscle
17	chr15:51819800-51863000	Weak transcription	Right Ventricle	heart
18	chr15:51824400-51854200	Weak transcription	Fetal Kidney	kidney
19	chr15:51824600-51855000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr15:51824600-51860600	Weak transcription	Brain Anterior Caudate	brain
21	chr15:51824600-51861000	Weak transcription	Left Ventricle	heart
22	chr15:51824800-51863200	Weak transcription	Primary hematopoietic stem cells	blood
23	chr15:51826000-51853400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr15:51827000-51861600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr15:51827400-51859800	Weak transcription	Fetal Intestine Small	intestine
26	chr15:51828600-51861200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr15:51828800-51868000	Weak transcription	Adipose Nuclei	Adipose
28	chr15:51828800-51868200	Weak transcription	Fetal Intestine Large	intestine
29	chr15:51829000-51853400	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr15:51829000-51855200	Weak transcription	Stomach Smooth Muscle	stomach
31	chr15:51829000-51856000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr15:51829000-51857000	Weak transcription	NHDF-Ad	bronchial
33	chr15:51829000-51859800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr15:51829000-51861000	Weak transcription	Fetal Lung	lung
35	chr15:51829000-51868800	Weak transcription	A549	lung
36	chr15:51829200-51861000	Weak transcription	Placenta	Placenta
37	chr15:51829400-51860600	Weak transcription	Fetal Brain Female	brain
38	chr15:51829400-51863200	Weak transcription	Dnd41	blood
39	chr15:51830000-51861000	Weak transcription	K562	blood
40	chr15:51831400-51868800	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr15:51836400-51861400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr15:51836600-51853400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr15:51836800-51858000	Weak transcription	Liver	Liver
44	chr15:51836800-51869000	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr15:51839400-51868600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr15:51846600-51861000	Weak transcription	HepG2	liver
47	chr15:51849600-51861000	Weak transcription	Spleen	Spleen
48	chr15:51850000-51852000	Genic enhancers	Primary monocytes fromperipheralblood	blood
49	chr15:51850600-51861000	Weak transcription	Duodenum Mucosa	Duodenum
50	chr15:51850800-51867400	Weak transcription	Cortex derived primary cultured neurospheres	brain

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