Variant report

Variant	nsv528965
Chromosome Location	chr15:56489159-56504598
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr15:56495751-56495990	K562	blood:	n/a	n/a
2	ATF2	chr15:56491341-56491707	GM12878	blood:	n/a	n/a
3	BATF	chr15:56491354-56491563	GM12878	blood:	n/a	chr15:56491479-56491490
4	BATF	chr15:56491314-56491646	GM12878	blood:	n/a	chr15:56491479-56491490
5	BCL11A	chr15:56495769-56496002	GM12878	blood:	n/a	n/a
6	BCL11A	chr15:56491303-56491591	GM12878	blood:	n/a	chr15:56491479-56491488 chr15:56491478-56491487
7	BCLAF1	chr15:56499195-56499659	GM12878	blood:	n/a	n/a
8	CEBPB	chr15:56500205-56500943	IMR90	lung:	n/a	chr15:56500790-56500801
9	CEBPB	chr15:56500649-56500879	A549	lung:	n/a	chr15:56500790-56500801
10	CEBPB	chr15:56500743-56500947	HepG2	liver:	n/a	chr15:56500790-56500801
11	CHD1	chr15:56499596-56499953	GM12878	blood:	n/a	n/a
12	CTCF	chr15:56492286-56492417	MCF-7	breast:	n/a	chr15:56492321-56492342 chr15:56492331-56492339 chr15:56492327-56492343 chr15:56492326-56492344
13	CTCF	chr15:56492240-56492390	HCFaa	heart:	n/a	chr15:56492321-56492342 chr15:56492331-56492339 chr15:56492327-56492343 chr15:56492326-56492344
14	CTCF	chr15:56492315-56492369	MCF-7	breast:	n/a	chr15:56492321-56492342 chr15:56492331-56492339 chr15:56492327-56492343 chr15:56492326-56492344
15	CTCF	chr15:56492280-56492430	SAEC	small airway:	n/a	chr15:56492321-56492342 chr15:56492331-56492339 chr15:56492327-56492343 chr15:56492326-56492344
16	CTCF	chr15:56500480-56500630	GM12871	blood:	n/a	n/a
17	CTCF	chr15:56492296-56492360	Hela-S3	cervix:	n/a	chr15:56492321-56492342 chr15:56492331-56492339 chr15:56492327-56492343 chr15:56492326-56492344
18	CTCF	chr15:56492280-56492430	MCF-7	breast:	n/a	chr15:56492321-56492342 chr15:56492331-56492339 chr15:56492327-56492343 chr15:56492326-56492344
19	CUX1	chr15:56496950-56497111	GM12878	blood:	n/a	n/a
20	CUX1	chr15:56499950-56499979	GM12878	blood:	n/a	n/a
21	E2F4	chr15:56497315-56497518	MCF10A-Er-Src	breast:	n/a	n/a
22	EBF1	chr15:56499343-56499613	GM12878	blood:	n/a	n/a
23	EBF1	chr15:56499294-56499584	GM12878	blood:	n/a	n/a
24	EBF1	chr15:56499308-56499595	GM12878	blood:	n/a	n/a
25	EBF1	chr15:56491419-56491551	GM12878	blood:	n/a	n/a
26	EGR1	chr15:56495799-56495974	K562	blood:	n/a	n/a
27	EGR1	chr15:56495799-56496028	K562	blood:	n/a	n/a
28	ELK1	chr15:56499538-56499555	GM12878	blood:	n/a	n/a
29	EP300	chr15:56499383-56499556	GM12878	blood:	n/a	n/a
30	FOS	chr15:56491335-56491499	MCF10A-Er-Src	breast:	n/a	chr15:56491478-56491487 chr15:56491479-56491487 chr15:56491479-56491486 chr15:56491478-56491488
31	FOS	chr15:56491430-56491611	MCF10A-Er-Src	breast:	n/a	chr15:56491478-56491487 chr15:56491479-56491487 chr15:56491479-56491486 chr15:56491478-56491488
32	FOS	chr15:56497346-56497454	MCF10A-Er-Src	breast:	n/a	chr15:56497389-56497397
33	FOS	chr15:56503872-56504152	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr15:56497761-56498216	HUVEC	blood vessel:	n/a	n/a
35	FOS	chr15:56497795-56497995	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr15:56495098-56495249	MCF10A-Er-Src	breast:	n/a	chr15:56495238-56495248
37	FOS	chr15:56491349-56491590	MCF10A-Er-Src	breast:	n/a	chr15:56491478-56491487 chr15:56491479-56491487 chr15:56491479-56491486 chr15:56491478-56491488
38	FOXA1	chr15:56504316-56504655	HepG2	liver:	n/a	n/a
39	FOXA1	chr15:56501470-56501775	HepG2	liver:	n/a	n/a
40	FOXM1	chr15:56491264-56491687	GM12878	blood:	n/a	n/a
41	GATA2	chr15:56495651-56495939	K562	blood:	n/a	n/a
42	GATA3	chr15:56492559-56492634	SH-SY5Y	brain:	n/a	n/a
43	IKZF1	chr15:56491313-56491632	GM12878	blood:	n/a	n/a
44	IKZF1	chr15:56501125-56501364	GM12878	blood:	n/a	n/a
45	IKZF1	chr15:56499968-56500375	GM12878	blood:	n/a	n/a
46	IKZF1	chr15:56497422-56497816	GM12878	blood:	n/a	n/a
47	IKZF1	chr15:56500782-56500863	GM12878	blood:	n/a	n/a
48	IRF4	chr15:56491235-56491611	GM12878	blood:	n/a	n/a
49	IRF4	chr15:56499215-56499698	GM12878	blood:	n/a	n/a
50	JUN	chr15:56503932-56504066	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:56480897..56483144-chr15:56491302..56493429,2	MCF-7	breast:
2	chr15:56502619..56504153-chr15:56505058..56507337,2	MCF-7	breast:
3	chr15:56496910..56499892-chr15:56507573..56509355,2	K562	blood:
4	chr15:56499669..56501343-chr15:56501763..56504338,2	K562	blood:
5	chr15:56485304..56488129-chr15:56488802..56490331,2	MCF-7	breast:
6	chr15:56498392..56501238-chr15:56507855..56509963,2	K562	blood:
7	chr15:56500425..56503148-chr15:56514379..56516558,2	K562	blood:
8	chr15:56492206..56494642-chr15:56495488..56498069,2	MCF-7	breast:
9	chr15:56499669..56501343-chr15:56501763..56504338,2	K562	blood:
10	chr15:56503289..56505951-chr15:56511015..56513534,2	K562	blood:
11	chr15:56484644..56486204-chr15:56489295..56491358,2	K562	blood:
12	chr15:56495337..56498069-chr15:56534935..56537509,2	K562	blood:
13	chr15:56494171..56496972-chr15:56541763..56543619,2	K562	blood:
14	chr15:56492206..56494642-chr15:56495488..56498069,2	MCF-7	breast:
15	chr15:56467090..56469731-chr15:56488365..56490022,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000261072	TF binding region
ENSG00000261072	chromatin interactions
ENSG00000151575	chromatin interactions
ENSG00000181827	chromatin interactions

Extended variants
information (count: 571 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:571 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1879347	chr15:56489159-56489160	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs372708467	chr15:56489191-56489192	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs370823886	chr15:56489202-56489203	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs538464179	chr15:56489217-56489218	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs188026791	chr15:56489220-56489221	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs373756362	chr15:56489311-56489312	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs190893710	chr15:56489318-56489319	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs558050644	chr15:56489404-56489405	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs540750108	chr15:56489426-56489427	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs183105050	chr15:56489459-56489460	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs540188367	chr15:56489495-56489496	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs188467371	chr15:56489534-56489535	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs192726786	chr15:56489541-56489542	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs563154011	chr15:56489560-56489561	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs578215156	chr15:56489572-56489573	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs185035205	chr15:56489607-56489608	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs150303502	chr15:56489622-56489623	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs540539186	chr15:56489630-56489631	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs565100764	chr15:56489642-56489643	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs527719011	chr15:56489660-56489661	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs553035980	chr15:56489715-56489716	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs137965292	chr15:56489738-56489739	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs76500804	chr15:56489794-56489795	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs572460537	chr15:56489826-56489827	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs536753386	chr15:56489846-56489847	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs561906808	chr15:56489885-56489886	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs550350352	chr15:56489908-56489909	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs570284062	chr15:56489949-56489950	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs539302729	chr15:56490055-56490056	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs12439682	chr15:56490057-56490058	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs149062170	chr15:56490151-56490152	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs534658327	chr15:56490207-56490208	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs2725871	chr15:56490268-56490269	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs16976805	chr15:56490276-56490277	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs574979587	chr15:56490283-56490284	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs543119643	chr15:56490360-56490361	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs555514066	chr15:56490379-56490380	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs376395414	chr15:56490462-56490463	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs147575832	chr15:56490485-56490486	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs576644405	chr15:56490489-56490490	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs397946383	chr15:56490493-56490494	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs545765714	chr15:56490512-56490513	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs16976808	chr15:56490525-56490526	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs527683504	chr15:56490527-56490528	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs11634455	chr15:56490549-56490550	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs145910087	chr15:56490569-56490570	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs530189307	chr15:56490635-56490636	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs12917493	chr15:56490737-56490738	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs187956459	chr15:56490830-56490831	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs368206862	chr15:56490832-56490833	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	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
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
Acute lymphoblastic leukemia	21339820	CNVD
Gastric adenocarcinoma	19115996	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD

Chromatin state (count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56453600-56515000	Weak transcription	NHLF	lung
2	chr15:56457400-56500400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr15:56458400-56496200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr15:56459200-56511000	Weak transcription	Esophagus	oesophagus
5	chr15:56463600-56496600	Weak transcription	NHEK	skin
6	chr15:56464600-56497800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr15:56465400-56496600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr15:56465800-56496000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr15:56465800-56496600	Weak transcription	HMEC	breast
10	chr15:56466000-56497000	Weak transcription	HSMMtube	muscle
11	chr15:56466000-56500000	Weak transcription	Thymus	Thymus
12	chr15:56466000-56514200	Weak transcription	Duodenum Mucosa	Duodenum
13	chr15:56466200-56494800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr15:56466400-56495400	Weak transcription	Fetal Stomach	stomach
15	chr15:56466800-56494600	Weak transcription	Fetal Intestine Large	intestine
16	chr15:56467000-56500400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr15:56467000-56511600	Weak transcription	Fetal Intestine Small	intestine
18	chr15:56469600-56491400	Weak transcription	A549	lung
19	chr15:56470200-56498800	Weak transcription	Dnd41	blood
20	chr15:56470800-56496400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr15:56470800-56503800	Weak transcription	Fetal Lung	lung
22	chr15:56474200-56495000	Weak transcription	K562	blood
23	chr15:56476600-56496200	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr15:56477000-56495800	Weak transcription	Primary B cells from cord blood	blood
25	chr15:56477000-56500400	Weak transcription	Liver	Liver
26	chr15:56477200-56497000	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr15:56479800-56496200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr15:56480000-56495000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr15:56480000-56496200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr15:56480000-56496600	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr15:56480000-56500000	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr15:56480200-56494600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr15:56480200-56497000	Weak transcription	HUVEC	blood vessel
34	chr15:56480200-56515400	Weak transcription	Hela-S3	cervix
35	chr15:56480800-56489800	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr15:56480800-56492600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr15:56480800-56496200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr15:56481400-56497800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr15:56482600-56497000	Weak transcription	NH-A	brain
40	chr15:56482600-56500200	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr15:56482800-56489200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr15:56483000-56491400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr15:56483000-56491600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr15:56483400-56495000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
45	chr15:56484200-56492200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr15:56484200-56492200	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chr15:56484800-56496200	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr15:56484800-56500000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr15:56485000-56489800	Weak transcription	GM12878-XiMat	blood
50	chr15:56485000-56502800	Weak transcription	Gastric	stomach

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