Variant report

Variant	nsv1551
Chromosome Location	chr15:58891639-58936580
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:224)
CpG islands
(count:62)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:224 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:58918774-58919007	HepG2	liver:	n/a	n/a
2	CBX3	chr15:58906522-58906965	K562	blood:	n/a	n/a
3	CBX3	chr15:58906532-58906857	K562	blood:	n/a	n/a
4	CCNT2	chr15:58919885-58919962	K562	blood:	n/a	n/a
5	CEBPB	chr15:58896483-58897272	MCF-7	breast:	n/a	chr15:58896839-58896852
6	CEBPB	chr15:58896831-58897146	HepG2	liver:	n/a	chr15:58896839-58896852
7	CEBPB	chr15:58896535-58897290	MCF-7	breast:	n/a	chr15:58896839-58896852
8	CEBPB	chr15:58936462-58936497	IMR90	lung:	n/a	n/a
9	CEBPB	chr15:58900320-58901027	IMR90	lung:	n/a	n/a
10	CEBPB	chr15:58918503-58918845	HepG2	liver:	n/a	n/a
11	CEBPB	chr15:58896676-58897139	HepG2	liver:	n/a	chr15:58896839-58896852
12	CEBPB	chr15:58912637-58912708	A549	lung:	n/a	chr15:58912684-58912695
13	CTCF	chr15:58904436-58904864	K562	blood:	n/a	n/a
14	CTCF	chr15:58904612-58904807	MCF-7	breast:	n/a	n/a
15	CTCF	chr15:58904638-58904709	A549	lung:	n/a	n/a
16	CTCF	chr15:58904701-58904739	NHEK	skin:	n/a	n/a
17	CTCF	chr15:58904580-58904730	Caco-2	colon:	n/a	n/a
18	CTCF	chr15:58895560-58895710	GM12873	blood:	n/a	n/a
19	CTCF	chr15:58904580-58904730	HRE	kidney:	n/a	n/a
20	CTCF	chr15:58904560-58904710	SAEC	small airway:	n/a	n/a
21	CTCF	chr15:58904680-58904830	HEK293	kidney:	n/a	n/a
22	CTCF	chr15:58904662-58904770	MCF-7	breast:	n/a	n/a
23	CTCF	chr15:58906320-58906470	GM06990	blood:	n/a	n/a
24	CTCF	chr15:58904688-58904734	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr15:58904560-58904710	NHEK	skin:	n/a	n/a
26	CTCF	chr15:58895664-58895735	GM10248	blood:	n/a	n/a
27	CTCF	chr15:58922017-58922120	Fibrobl	skin:	n/a	n/a
28	CTCF	chr15:58904640-58904790	SAEC	small airway:	n/a	n/a
29	CTCF	chr15:58904626-58904791	MCF-7	breast:	n/a	n/a
30	CTCF	chr15:58904611-58904671	GM10248	blood:	n/a	n/a
31	CTCF	chr15:58904691-58904720	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr15:58904700-58904850	GM12873	blood:	n/a	n/a
33	CTCF	chr15:58904682-58904757	HepG2	liver:	n/a	n/a
34	CTCF	chr15:58904727-58904751	GM12878	blood:	n/a	n/a
35	CTCF	chr15:58904735-58904737	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr15:58900280-58900430	HCM	heart:	n/a	n/a
37	CTCF	chr15:58904580-58904730	GM12871	blood:	n/a	n/a
38	CTCF	chr15:58904524-58904823	K562	blood:	n/a	n/a
39	CTCF	chr15:58916726-58916793	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr15:58904520-58904670	MCF-7	breast:	n/a	n/a
41	CTCF	chr15:58904620-58904770	Caco-2	colon:	n/a	n/a
42	CTCF	chr15:58904640-58904790	NHEK	skin:	n/a	n/a
43	CTCF	chr15:58904277-58904812	K562	blood:	n/a	n/a
44	CTCF	chr15:58904638-58904775	GM12891	blood:	n/a	n/a
45	CTCF	chr15:58907370-58907423	GM13976	blood:	n/a	n/a
46	CTCF	chr15:58904709-58904714	GM19240	blood:	n/a	n/a
47	CTCF	chr15:58904718-58904755	GM19240	blood:	n/a	n/a
48	CTCF	chr15:58904639-58904786	MCF-7	breast:	n/a	n/a
49	CTCF	chr15:58904740-58904890	A549	lung:	n/a	n/a
50	CTCF	chr15:58904640-58904790	GM12866	blood:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:58902656-58902706	Hepatocyte	liver:	n/a
2	chr15:58902656-58902706	Hepatocyte	liver:	n/a
3	chr15:58902656-58902706	NH-A	brain:	n/a
4	chr15:58902656-58902706	Jurkat	blood:	n/a
5	chr15:58902656-58902706	AG04450	lung:	fetal
6	chr15:58902656-58902706	A549	lung:	n/a
7	chr15:58902656-58902706	SK-N-MC	brain:	n/a
8	chr15:58902656-58902706	HEK293	kidney:	embryo
9	chr15:58902656-58902706	HCPEpiC	choroid plexus:	n/a
10	chr15:58902656-58902706	GM12878	blood:	n/a
11	chr15:58902656-58902706	AG04449	skin:	fetal
12	chr15:58902656-58902706	HEEpiC	esophagus:	n/a
13	chr15:58902656-58902706	CMK	blood:	n/a
14	chr15:58902656-58902706	IMR90	lung:	fetal
15	chr15:58902656-58902706	BJ	skin:	n/a
16	chr15:58902656-58902706	ECC-1	luminal epithelium:	n/a
17	chr15:58902656-58902706	HCF	heart:	n/a
18	chr15:58902656-58902706	H1-hESC	embryonic stem cell:	embryo
19	chr15:58902656-58902706	HAEpiC	amniotic membrane:	n/a
20	chr15:58902656-58902706	HIPEpiC	eye:	n/a
21	chr15:58902656-58902706	NT2-D1	testis:	n/a
22	chr15:58902656-58902706	HRCEpiC	kidney:	n/a
23	chr15:58902656-58902706	HNPCEpiC	eye:	n/a
24	chr15:58902656-58902706	GM19239	blood:	n/a
25	chr15:58902656-58902706	BE2_C	brain:	n/a
26	chr15:58902656-58902706	K562	blood:	n/a
27	chr15:58902656-58902706	PANC-1	pancreas:	n/a
28	chr15:58902656-58902706	NB4	blood:	n/a
29	chr15:58902656-58902706	AG09309	skin:	n/a
30	chr15:58902656-58902706	GM12891	blood:	n/a
31	chr15:58902656-58902706	GM12892	blood:	n/a
32	chr15:58902656-58902706	LNCaP	prostate:	n/a
33	chr15:58902656-58902706	HUVEC	blood vessel:	n/a
34	chr15:58902656-58902706	SAEC	small airway:	n/a
35	chr15:58902656-58902706	SK-N-SH_RA	brain:	n/a
36	chr15:58902656-58902706	HMEC	breast:	n/a
37	chr15:58902656-58902706	MCF10A-Er-Src	breast:	n/a
38	chr15:58902656-58902706	HPAEpiC	pulmonary alveolar:	n/a
39	chr15:58902656-58902706	SK-N-SH	brain:	n/a
40	chr15:58902656-58902706	HRPEpiC	eye:	n/a
41	chr15:58902656-58902706	ProgFib	skin:	n/a
42	chr15:58902656-58902706	AG09319	gingival:	n/a
43	chr15:58902656-58902706	AG10803	skin:	n/a
44	chr15:58902656-58902706	HL-60	blood:	n/a
45	chr15:58902656-58902706	Hela-S3	cervix:	n/a
46	chr15:58902656-58902706	NHDF-neo	bronchial:	n/a
47	chr15:58902656-58902706	HCT-116	colon:	n/a
48	chr15:58902656-58902706	HepG2	liver:	n/a
49	chr15:58902656-58902706	NHBE	bronchial:	n/a
50	chr15:58902656-58902706	HCM	heart:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:58898609..58900839-chr15:58904046..58906383,2	K562	blood:
2	chr15:58906314..58907814-chr15:99432678..99434601,2	MCF-7	breast:
3	chr15:58915714..58920888-chr15:58922126..58927407,8	K562	blood:
4	chr15:58894443..58897022-chr15:58897229..58899718,3	K562	blood:
5	chr15:58814045..58816618-chr15:58898707..58900922,2	MCF-7	breast:
6	chr15:58909393..58911330-chr15:58917319..58918979,2	K562	blood:
7	chr15:58919916..58921624-chr15:58929696..58932530,2	K562	blood:
8	chr15:58915714..58921238-chr15:58922986..58925558,6	K562	blood:
9	chr15:58909393..58911330-chr15:58917319..58918979,2	K562	blood:
10	chr15:58915714..58920888-chr15:58922126..58927407,8	K562	blood:
11	chr15:58928689..58931025-chr15:60688699..60690909,2	K562	blood:
12	chr15:58888706..58891622-chr15:58895276..58897701,2	MCF-7	breast:
13	chr15:58919916..58921624-chr15:58929696..58932530,2	K562	blood:
14	chr15:58898609..58900839-chr15:58904046..58906383,2	K562	blood:
15	chr15:58897720..58899751-chr15:59040032..59042523,2	MCF-7	breast:
16	chr15:58903672..58906413-chr15:58914641..58916719,2	K562	blood:
17	chr15:58927036..58929525-chr15:58931244..58932793,2	K562	blood:
18	chr15:58932722..58935543-chr15:58957168..58958694,2	K562	blood:
19	chr15:58892060..58893645-chr15:58896803..58898412,2	MCF-7	breast:
20	chr15:58903672..58906413-chr15:58914641..58916719,2	K562	blood:
21	chr15:58894443..58897022-chr15:58897229..58899718,3	K562	blood:
22	chr15:58888535..58891486-chr15:58900584..58902210,3	K562	blood:
23	chr15:58915714..58921238-chr15:58922986..58925558,6	K562	blood:
24	chr15:58895066..58897354-chr15:59040253..59042004,2	MCF-7	breast:
25	chr15:58623131..58625818-chr15:58896837..58898652,2	MCF-7	breast:
26	chr15:58890495..58893590-chr15:58895773..58898243,3	K562	blood:
27	chr15:58888127..58890448-chr15:58892630..58894989,2	MCF-7	breast:
28	chr15:58927036..58929525-chr15:58931244..58932793,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000239100	TF binding region
ADAM10	TF binding region
ENSG00000239100	CpG island
ADAM10	CpG island
ENSG00000239100	chromatin interactions
ENSG00000182718	chromatin interactions
ENSG00000128918	chromatin interactions
ENSG00000140443	chromatin interactions
ENSG00000137845	chromatin interactions

Extended variants
information (count: 1921 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1921 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181100749	chr15:58891672-58891673	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs376702289	chr15:58891700-58891701	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs548930862	chr15:58891732-58891733	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs150973637	chr15:58891749-58891750	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs202126699	chr15:58891766-58891767	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200630085	chr15:58891773-58891774	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531515326	chr15:58891781-58891782	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs201001771	chr15:58891812-58891813	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs374768516	chr15:58891828-58891829	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs202095530	chr15:58891840-58891841	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs200338212	chr15:58891842-58891843	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs35009923	chr15:58891861-58891862	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs199842003	chr15:58891867-58891868	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs140875224	chr15:58891903-58891904	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs144826830	chr15:58891906-58891907	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551538667	chr15:58891909-58891910	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532900944	chr15:58891950-58891951	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529521307	chr15:58891951-58891952	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs200550772	chr15:58891954-58891955	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs398078228	chr15:58891960-58891961	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs398027483	chr15:58891961-58891962	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184218416	chr15:58891967-58891968	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs114121756	chr15:58891996-58891997	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs547328844	chr15:58891997-58891998	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560578989	chr15:58892011-58892012	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567067150	chr15:58892038-58892039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370995725	chr15:58892097-58892098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs75112899	chr15:58892098-58892099	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373003976	chr15:58892114-58892115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563214109	chr15:58892116-58892117	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555762123	chr15:58892157-58892158	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575474372	chr15:58892159-58892160	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538047466	chr15:58892186-58892187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557835074	chr15:58892189-58892190	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188844866	chr15:58892194-58892195	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376075596	chr15:58892203-58892204	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368982339	chr15:58892214-58892215	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372701384	chr15:58892221-58892222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560513655	chr15:58892297-58892298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10601564	chr15:58892322-58892323	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201036701	chr15:58892323-58892324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs398057731	chr15:58892326-58892327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs56023019	chr15:58892328-58892329	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs75529953	chr15:58892329-58892330	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181595787	chr15:58892348-58892349	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376104125	chr15:58892391-58892392	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7166076	chr15:58892410-58892411	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs142310903	chr15:58892426-58892427	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs77403331	chr15:58892450-58892451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs377464351	chr15:58892458-58892459	Weak transcription Strong transcription	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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	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
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1870 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58878000-58898400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr15:58878000-58900000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr15:58878000-58900000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr15:58878400-58897800	Weak transcription	Brain Cingulate Gyrus	brain
5	chr15:58878400-58900200	Weak transcription	Brain Substantia Nigra	brain
6	chr15:58878600-58900200	Weak transcription	NHLF	lung
7	chr15:58878800-58904400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr15:58879200-58893800	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr15:58880200-58904600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr15:58880600-58920600	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr15:58882600-58904000	Weak transcription	Gastric	stomach
12	chr15:58882600-58907600	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr15:58883000-58901800	Weak transcription	HUVEC	blood vessel
14	chr15:58883200-58900400	Weak transcription	Fetal Heart	heart
15	chr15:58883200-58904600	Strong transcription	HSMM	muscle
16	chr15:58883400-58893800	Weak transcription	Fetal Kidney	kidney
17	chr15:58883400-58900000	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr15:58883800-58896600	Weak transcription	HepG2	liver
19	chr15:58884000-58894000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr15:58884000-58894400	Weak transcription	Aorta	Aorta
21	chr15:58884000-58895400	Strong transcription	Fetal Thymus	thymus
22	chr15:58884200-58891800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr15:58884200-58893800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr15:58884200-58894400	Weak transcription	Fetal Stomach	stomach
25	chr15:58884200-58894600	Weak transcription	Esophagus	oesophagus
26	chr15:58884400-58896200	Weak transcription	Lung	lung
27	chr15:58884400-58902600	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr15:58884600-58895600	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr15:58885200-58897000	Weak transcription	Colon Smooth Muscle	Colon
30	chr15:58885600-58891800	Strong transcription	Dnd41	blood
31	chr15:58885600-58897400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr15:58885800-58892200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr15:58885800-58892800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr15:58885800-58896200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr15:58885800-58906800	Weak transcription	Fetal Brain Male	brain
36	chr15:58886400-58899800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
37	chr15:58886800-58893800	Weak transcription	NHEK	skin
38	chr15:58887200-58906600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr15:58887400-58892000	Strong transcription	Primary B cells from peripheral blood	blood
40	chr15:58887400-58898200	Weak transcription	Brain Angular Gyrus	brain
41	chr15:58887600-58897600	Strong transcription	Primary T helper cells fromperipheralblood	blood
42	chr15:58887800-58905200	Weak transcription	Brain Germinal Matrix	brain
43	chr15:58888000-58906200	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr15:58888200-58891800	Strong transcription	Placenta	Placenta
45	chr15:58888200-58893200	Weak transcription	Stomach Mucosa	stomach
46	chr15:58888400-58891800	Strong transcription	GM12878-XiMat	blood
47	chr15:58888400-58900400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr15:58888400-58920000	Weak transcription	Rectal Smooth Muscle	rectum
49	chr15:58888600-58892000	Strong transcription	Primary B cells from cord blood	blood
50	chr15:58888600-58899600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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