Variant report

Variant	nsv904390
Chromosome Location	chr15:75795177-75840943
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:608)
CpG islands
(count:61)
Chromatin interactive
region (count:29)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:608 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:75824822-75825149	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:75837428-75837557	K562	blood:	n/a	n/a
3	ATF1	chr15:75837337-75837610	K562	blood:	n/a	n/a
4	ATF1	chr15:75824867-75825158	K562	blood:	n/a	n/a
5	BACH1	chr15:75824813-75824969	K562	blood:	n/a	n/a
6	BRCA1	chr15:75824914-75825048	HepG2	liver:	n/a	n/a
7	BRCA1	chr15:75809037-75809075	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr15:75803056-75803289	HepG2	liver:	n/a	chr15:75803160-75803171
9	CEBPB	chr15:75823823-75824098	K562	blood:	n/a	n/a
10	CEBPB	chr15:75815407-75815626	HepG2	liver:	n/a	chr15:75815529-75815540
11	CEBPB	chr15:75815382-75815671	Hela-S3	cervix:	n/a	chr15:75815529-75815540
12	CEBPB	chr15:75808981-75809098	A549	lung:	n/a	n/a
13	CEBPB	chr15:75812433-75812469	K562	blood:	n/a	n/a
14	CEBPB	chr15:75815418-75815659	K562	blood:	n/a	chr15:75815529-75815540
15	CEBPB	chr15:75834608-75834914	K562	blood:	n/a	n/a
16	CEBPB	chr15:75820264-75820294	K562	blood:	n/a	n/a
17	CEBPB	chr15:75815267-75815739	HCT-116	colon:	n/a	chr15:75815529-75815540
18	CEBPB	chr15:75812315-75812526	A549	lung:	n/a	chr15:75812421-75812432
19	CEBPB	chr15:75834613-75834972	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr15:75834604-75834964	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr15:75808888-75809157	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr15:75803083-75803304	Hela-S3	cervix:	n/a	chr15:75803160-75803171
23	CEBPB	chr15:75803049-75803314	A549	lung:	n/a	chr15:75803160-75803171
24	CEBPB	chr15:75815384-75815675	K562	blood:	n/a	chr15:75815529-75815540
25	CEBPB	chr15:75812259-75812505	HepG2	liver:	n/a	chr15:75812421-75812432
26	CEBPB	chr15:75835683-75835995	A549	lung:	n/a	n/a
27	CEBPB	chr15:75803007-75803340	IMR90	lung:	n/a	chr15:75803160-75803171
28	CEBPB	chr15:75812294-75812488	IMR90	lung:	n/a	chr15:75812421-75812432
29	CEBPD	chr15:75834788-75835238	K562	blood:	n/a	n/a
30	CEBPD	chr15:75834696-75835215	K562	blood:	n/a	n/a
31	CREB1	chr15:75824847-75825109	A549	lung:	n/a	n/a
32	CTCF	chr15:75824900-75825050	MCF-7	breast:	n/a	chr15:75824928-75824937
33	CTCF	chr15:75824860-75825010	GM12865	blood:	n/a	chr15:75824928-75824937
34	CTCF	chr15:75801400-75801550	HBMEC	blood vessel:	n/a	chr15:75801461-75801470
35	CTCF	chr15:75824840-75824990	HPAF	blood vessel:	n/a	chr15:75824928-75824937
36	CTCF	chr15:75801400-75801550	HPAF	blood vessel:	n/a	chr15:75801461-75801470
37	CTCF	chr15:75825080-75825230	GM12872	blood:	n/a	chr15:75825114-75825123
38	CTCF	chr15:75801400-75801550	BE2_C	brain:	n/a	chr15:75801461-75801470
39	CTCF	chr15:75824920-75825070	HMEC	breast:	n/a	chr15:75824928-75824937
40	CTCF	chr15:75824840-75824990	Caco-2	colon:	n/a	chr15:75824928-75824937
41	CTCF	chr15:75801373-75801560	Kidney_OC	kidney:	n/a	chr15:75801461-75801470
42	CTCF	chr15:75824820-75824970	RPTEC	kidney:	n/a	chr15:75824928-75824937
43	CTCF	chr15:75824860-75825010	K562	blood:	n/a	chr15:75824928-75824937
44	CTCF	chr15:75824920-75825070	HFF-Myc	foreskin:	n/a	chr15:75824928-75824937
45	CTCF	chr15:75824828-75825060	HepG2	liver:	n/a	chr15:75824928-75824937
46	CTCF	chr15:75801400-75801550	NHLF	lung:	n/a	chr15:75801461-75801470
47	CTCF	chr15:75824840-75824990	GM12873	blood:	n/a	chr15:75824928-75824937
48	CTCF	chr15:75801380-75801530	GM12878	blood:	n/a	chr15:75801461-75801470
49	CTCF	chr15:75801400-75801550	GM12868	blood:	n/a	chr15:75801461-75801470
50	CTCF	chr15:75824840-75824990	NHDF-neo	bronchial:	n/a	chr15:75824928-75824937

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:75835738-75835788	AG09319	gingival:	n/a
2	chr15:75835738-75835788	LNCaP	prostate:	n/a
3	chr15:75835738-75835788	NHBE	bronchial:	n/a
4	chr15:75835738-75835788	HL-60	blood:	n/a
5	chr15:75835738-75835788	ProgFib	skin:	n/a
6	chr15:75835738-75835788	HRPEpiC	eye:	n/a
7	chr15:75835738-75835788	K562	blood:	n/a
8	chr15:75835738-75835788	HRE	kidney:	n/a
9	chr15:75835738-75835788	HMEC	breast:	n/a
10	chr15:75835738-75835788	AoSMC	blood vessel:	n/a
11	chr15:75835738-75835788	SK-N-SH_RA	brain:	n/a
12	chr15:75835738-75835788	Hela-S3	cervix:	n/a
13	chr15:75835738-75835788	HAEpiC	amniotic membrane:	n/a
14	chr15:75835738-75835788	H1-hESC	embryonic stem cell:	embryo
15	chr15:75835738-75835788	PrEC	prostate:	n/a
16	chr15:75835738-75835788	HNPCEpiC	eye:	n/a
17	chr15:75835738-75835788	MCF-7	breast:	n/a
18	chr15:75835738-75835788	HEEpiC	esophagus:	n/a
19	chr15:75835738-75835788	U87	brain:	n/a
20	chr15:75835738-75835788	ECC-1	luminal epithelium:	n/a
21	chr15:75835738-75835788	PANC-1	pancreas:	n/a
22	chr15:75835738-75835788	Jurkat	blood:	n/a
23	chr15:75835738-75835788	NB4	blood:	n/a
24	chr15:75835738-75835788	BE2_C	brain:	n/a
25	chr15:75835738-75835788	Hepatocyte	liver:	n/a
26	chr15:75835738-75835788	HCT-116	colon:	n/a
27	chr15:75835738-75835788	RPTEC	kidney:	n/a
28	chr15:75835738-75835788	Caco-2	colon:	n/a
29	chr15:75835738-75835788	HCF	heart:	n/a
30	chr15:75835738-75835788	HCPEpiC	choroid plexus:	n/a
31	chr15:75835738-75835788	HRCEpiC	kidney:	n/a
32	chr15:75835738-75835788	GM06990	blood:	n/a
33	chr15:75835738-75835788	AG04450	lung:	fetal
34	chr15:75835738-75835788	GM12892	blood:	n/a
35	chr15:75835738-75835788	HCM	heart:	n/a
36	chr15:75835738-75835788	MCF10A-Er-Src	breast:	n/a
37	chr15:75835738-75835788	HPAEpiC	pulmonary alveolar:	n/a
38	chr15:75835738-75835788	BJ	skin:	n/a
39	chr15:75835738-75835788	A549	lung:	n/a
40	chr15:75835738-75835788	ovcar-3	ovarian:	n/a
41	chr15:75835738-75835788	SKMC	muscle:	n/a
42	chr15:75835738-75835788	CMK	blood:	n/a
43	chr15:75835738-75835788	NT2-D1	testis:	n/a
44	chr15:75835738-75835788	HEK293	kidney:	embryo
45	chr15:75835738-75835788	GM19239	blood:	n/a
46	chr15:75835738-75835788	SAEC	small airway:	n/a
47	chr15:75835738-75835788	HUVEC	blood vessel:	n/a
48	chr15:75835738-75835788	NH-A	brain:	n/a
49	chr15:75835738-75835788	IMR90	lung:	fetal
50	chr15:75835738-75835788	AG10803	skin:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:75817321..75818967-chr15:75847702..75849379,2	K562	blood:
2	chr15:75829509..75831948-chr15:75932181..75934351,2	MCF-7	breast:
3	chr15:75745002..75747584-chr15:75825328..75827934,2	K562	blood:
4	chr15:75805149..75807118-chr15:75809873..75811436,2	K562	blood:
5	chr15:75823461..75825727-chr15:75832256..75834760,2	K562	blood:
6	chr15:75835718..75837782-chr15:75838863..75841785,2	K562	blood:
7	chr15:75840878..75843615-chr15:75844264..75846206,2	K562	blood:
8	chr15:75824690..75826344-chr15:75835953..75838472,2	K562	blood:
9	chr15:75812434..75814085-chr15:75817248..75818845,2	K562	blood:
10	chr15:75748585..75750516-chr15:75799662..75801280,2	K562	blood:
11	chr15:75812709..75814869-chr15:75930872..75932533,2	MCF-7	breast:
12	chr15:75816718..75819055-chr15:75823449..75825405,3	MCF-7	breast:
13	chr15:75748494..75750085-chr15:75799130..75801162,2	K562	blood:
14	chr15:75830608..75832951-chr15:75924851..75928314,3	MCF-7	breast:
15	chr15:75823394..75827667-chr15:75930118..75933171,4	MCF-7	breast:
16	chr15:75817263..75819395-chr15:75931775..75934175,2	MCF-7	breast:
17	chr15:75799442..75801004-chr15:75975056..75976624,2	MCF-7	breast:
18	chr15:75812434..75814085-chr15:75817248..75818845,2	K562	blood:
19	chr15:75835718..75837782-chr15:75838863..75841785,2	K562	blood:
20	chr15:75808443..75810760-chr15:75862466..75865367,2	K562	blood:
21	chr15:75745273..75747975-chr15:75823616..75825294,2	MCF-7	breast:
22	chr15:75744318..75747084-chr15:75809053..75812043,2	MCF-7	breast:
23	chr15:75823461..75825727-chr15:75832256..75834760,2	K562	blood:
24	chr15:75799580..75804058-chr15:75932687..75934537,4	MCF-7	breast:
25	chr15:75828987..75830600-chr15:75834894..75837866,2	MCF-7	breast:
26	chr15:75801019..75801846-chr15:75975674..75976616,2	MCF-7	breast:
27	chr15:75816718..75819055-chr15:75823449..75825405,3	MCF-7	breast:
28	chr15:75814778..75817471-chr15:75819035..75821931,2	K562	blood:
29	chr15:75824690..75826344-chr15:75835953..75838472,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNX33-4	chr15:75797279-75797803	NONHSAT047350
2	lnc-SIN3A-4	chr15:75805111-75805381	NONHSAT047351

No data

Variant related genes	Relation type
PTPN9	TF binding region
ENSG00000259931	TF binding region
ENSG00000203473	TF binding region
PTPN9	CpG island
ENSG00000259931	CpG island
ENSG00000203473	CpG island
ENSG00000169375	chromatin interactions
ENSG00000259931	chromatin interactions
ENSG00000177971	chromatin interactions
ENSG00000203473	chromatin interactions
ENSG00000169410	chromatin interactions

Extended variants
information (count: 1517 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1517 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112505891	chr15:75795177-75795178	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs376471056	chr15:75795217-75795218	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs184036316	chr15:75795240-75795241	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs571809201	chr15:75795283-75795284	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs535987520	chr15:75795339-75795340	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs554333238	chr15:75795371-75795372	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs371578692	chr15:75795390-75795391	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs543679638	chr15:75795441-75795442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555836148	chr15:75795491-75795492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565055510	chr15:75795506-75795507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577936249	chr15:75795551-75795552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545083282	chr15:75795569-75795570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188792294	chr15:75795585-75795586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs527786584	chr15:75795589-75795590	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549541706	chr15:75795613-75795614	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs28609186	chr15:75795628-75795629	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs531829906	chr15:75795662-75795663	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs28731305	chr15:75795664-75795665	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs28402820	chr15:75795711-75795712	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs578142556	chr15:75795737-75795738	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs201178249	chr15:75795860-75795861	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs202127033	chr15:75795884-75795885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs62027169	chr15:75795917-75795918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556970835	chr15:75795937-75795938	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111700924	chr15:75795940-75795941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373469203	chr15:75796051-75796052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571854460	chr15:75796065-75796066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532082774	chr15:75796070-75796071	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546984641	chr15:75796085-75796086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560139024	chr15:75796111-75796112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565376517	chr15:75796167-75796168	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs535926596	chr15:75796183-75796184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113179403	chr15:75796236-75796237	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554272052	chr15:75796354-75796355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569804482	chr15:75796399-75796400	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374676031	chr15:75796472-75796473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536872154	chr15:75796479-75796480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62027170	chr15:75796491-75796492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558767958	chr15:75796539-75796540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577070398	chr15:75796567-75796568	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200420869	chr15:75796598-75796599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541375505	chr15:75796729-75796730	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554203417	chr15:75796741-75796742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572498320	chr15:75796757-75796758	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs9744367	chr15:75796823-75796824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200312445	chr15:75796858-75796859	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561393035	chr15:75796884-75796885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531889537	chr15:75796942-75796943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543665756	chr15:75797007-75797008	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565516854	chr15:75797026-75797027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	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
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
small cell lung cancer	20016488	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
Congenital diaphragmatic hernia	21085971	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21364760	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1572 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75749000-75797800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr15:75762200-75798000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr15:75762400-75797800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr15:75762400-75798000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr15:75763800-75797800	Weak transcription	Brain Substantia Nigra	brain
6	chr15:75765600-75797800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr15:75766800-75798000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr15:75772000-75797800	Weak transcription	NHEK	skin
9	chr15:75772400-75797800	Weak transcription	Fetal Brain Male	brain
10	chr15:75772400-75797800	Weak transcription	Right Ventricle	heart
11	chr15:75772400-75797800	Weak transcription	Spleen	Spleen
12	chr15:75772400-75798000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr15:75775200-75795400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr15:75775200-75795400	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr15:75775400-75795400	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr15:75775800-75798000	Weak transcription	Fetal Heart	heart
17	chr15:75776000-75795400	Strong transcription	Fetal Stomach	stomach
18	chr15:75776200-75795400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr15:75777200-75816800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr15:75777600-75795400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr15:75777600-75812000	Weak transcription	Small Intestine	intestine
22	chr15:75778400-75795400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr15:75779000-75795200	Strong transcription	HUES48 Cell Line	embryonic stem cell
24	chr15:75780200-75797800	Weak transcription	Colonic Mucosa	Colon
25	chr15:75780200-75812200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr15:75780600-75797800	Weak transcription	Rectal Smooth Muscle	rectum
27	chr15:75781000-75797800	Weak transcription	Pancreas	Pancrea
28	chr15:75782000-75797800	Weak transcription	Left Ventricle	heart
29	chr15:75782600-75797800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr15:75782600-75797800	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr15:75782600-75797800	Weak transcription	NHDF-Ad	bronchial
32	chr15:75782600-75815200	Weak transcription	K562	blood
33	chr15:75782800-75797800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr15:75782800-75797800	Weak transcription	Placenta	Placenta
35	chr15:75782800-75797800	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr15:75782800-75797800	Weak transcription	GM12878-XiMat	blood
37	chr15:75783400-75797800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr15:75783400-75797800	Weak transcription	Aorta	Aorta
39	chr15:75785000-75797800	Weak transcription	NHLF	lung
40	chr15:75785000-75798000	Weak transcription	Hela-S3	cervix
41	chr15:75785200-75797800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr15:75785200-75797800	Weak transcription	Fetal Kidney	kidney
43	chr15:75785200-75798000	Weak transcription	NH-A	brain
44	chr15:75785400-75797800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr15:75785400-75798000	Weak transcription	Primary T cells from cord blood	blood
46	chr15:75785600-75814200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr15:75785800-75795400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr15:75786000-75797800	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr15:75786000-75797800	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr15:75786000-75798000	Weak transcription	Primary B cells from cord blood	blood

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