Variant report

Variant	nsv523490
Chromosome Location	chr10:19974930-20041146
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:388)
CpG islands
(count:305)
Chromatin interactive
region (count:2)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:388 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr10:20019092-20019388	K562	blood:	n/a	n/a
2	ATF1	chr10:20031092-20031318	K562	blood:	n/a	n/a
3	ATF1	chr10:20024073-20024273	K562	blood:	n/a	n/a
4	BATF	chr10:20035644-20035814	GM12878	blood:	n/a	n/a
5	BATF	chr10:20035664-20035859	GM12878	blood:	n/a	n/a
6	BCL11A	chr10:20035655-20035827	GM12878	blood:	n/a	n/a
7	BCL11A	chr10:20036910-20037233	GM12878	blood:	n/a	n/a
8	BCL11A	chr10:20035672-20035886	GM12878	blood:	n/a	n/a
9	BHLHE40	chr10:20035652-20035896	HepG2	liver:	n/a	n/a
10	BHLHE40	chr10:20036959-20037247	HepG2	liver:	n/a	n/a
11	CEBPB	chr10:19991211-19991537	IMR90	lung:	n/a	n/a
12	CEBPB	chr10:19996466-19996579	A549	lung:	n/a	chr10:19996526-19996537 chr10:19996526-19996539
13	CEBPB	chr10:20040537-20040789	HepG2	liver:	n/a	chr10:20040659-20040670
14	CEBPB	chr10:20038041-20038360	HepG2	liver:	n/a	chr10:20038189-20038200
15	CEBPB	chr10:20002775-20003063	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr10:20023681-20023947	HepG2	liver:	n/a	n/a
17	CEBPB	chr10:20023742-20023942	A549	lung:	n/a	n/a
18	CEBPB	chr10:19996370-19996656	HepG2	liver:	n/a	chr10:19996526-19996537 chr10:19996526-19996539
19	CEBPB	chr10:20038058-20038599	Hela-S3	cervix:	n/a	chr10:20038189-20038200
20	CEBPB	chr10:20038015-20038653	IMR90	lung:	n/a	chr10:20038189-20038200
21	CEBPB	chr10:20038066-20038352	A549	lung:	n/a	chr10:20038189-20038200
22	CEBPB	chr10:20040519-20040846	IMR90	lung:	n/a	chr10:20040659-20040670
23	CEBPB	chr10:20031111-20031430	K562	blood:	n/a	n/a
24	CEBPB	chr10:20006851-20006880	HepG2	liver:	n/a	n/a
25	CEBPB	chr10:20038151-20038314	H1-hESC	embryonic stem cell:	n/a	chr10:20038189-20038200
26	CEBPB	chr10:20005435-20005535	A549	lung:	n/a	n/a
27	CTCF	chr10:19988420-19988570	GM12867	blood:	n/a	n/a
28	CTCF	chr10:20002766-20003025	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr10:20002860-20003010	MCF-7	breast:	n/a	n/a
30	CTCF	chr10:20002841-20002937	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr10:20002800-20002950	NHEK	skin:	n/a	n/a
32	CTCF	chr10:20003000-20003150	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr10:19988398-19988464	NHEK	skin:	n/a	n/a
34	CTCF	chr10:20002820-20002970	MCF-7	breast:	n/a	n/a
35	CTCF	chr10:20002858-20002900	HepG2	liver:	n/a	n/a
36	CTCF	chr10:19988364-19988484	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr10:20002860-20003010	HMEC	breast:	n/a	n/a
38	CTCF	chr10:20014063-20014138	GM10266	blood:	n/a	n/a
39	CTCF	chr10:20002820-20002970	SAEC	small airway:	n/a	n/a
40	CTCF	chr10:20038146-20038410	IMR90	lung:	n/a	n/a
41	CTCF	chr10:20002800-20002950	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr10:20038120-20038270	HVMF	connective:	n/a	n/a
43	CTCF	chr10:20002867-20002909	GM12891	blood:	n/a	n/a
44	CTCF	chr10:20002780-20002930	A549	lung:	n/a	n/a
45	CTCF	chr10:20038300-20038450	AG04450	lung:	n/a	n/a
46	CTCF	chr10:20002760-20002910	GM12871	blood:	n/a	n/a
47	CTCF	chr10:20038140-20038290	HVMF	connective:	n/a	n/a
48	CTCF	chr10:20002760-20002910	GM12874	blood:	n/a	n/a
49	CTCF	chr10:20002740-20002890	HAc	cerebellar:	n/a	n/a
50	CTCF	chr10:20002880-20003030	GM12872	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:20023014-20023064	HCT-116	colon:	n/a
2	chr10:19993393-19993443	GM06990	blood:	n/a
3	chr10:20009221-20009271	IMR90	lung:	fetal
4	chr10:20023014-20023064	HCM	heart:	n/a
5	chr10:20017996-20018046	T-47D	breast:	n/a
6	chr10:20019641-20019691	HRE	kidney:	n/a
7	chr10:20017996-20018046	Caco-2	colon:	n/a
8	chr10:19993393-19993443	HRCEpiC	kidney:	n/a
9	chr10:20019641-20019691	NHDF-neo	bronchial:	n/a
10	chr10:19993393-19993443	NB4	blood:	n/a
11	chr10:20017996-20018046	MCF10A-Er-Src	breast:	n/a
12	chr10:20009221-20009271	BJ	skin:	n/a
13	chr10:19993393-19993443	AG04450	lung:	fetal
14	chr10:20017996-20018046	RPTEC	kidney:	n/a
15	chr10:20023014-20023064	K562	blood:	n/a
16	chr10:20017996-20018046	SAEC	small airway:	n/a
17	chr10:20017996-20018046	PANC-1	pancreas:	n/a
18	chr10:20023014-20023064	HepG2	liver:	n/a
19	chr10:19993393-19993443	PrEC	prostate:	n/a
20	chr10:19993393-19993443	IMR90	lung:	fetal
21	chr10:20017996-20018046	U87	brain:	n/a
22	chr10:20019641-20019691	HEK293	kidney:	embryo
23	chr10:20023014-20023064	IMR90	lung:	fetal
24	chr10:20023014-20023064	U87	brain:	n/a
25	chr10:20017996-20018046	HEK293	kidney:	embryo
26	chr10:20017996-20018046	HUVEC	blood vessel:	n/a
27	chr10:20019641-20019691	HCPEpiC	choroid plexus:	n/a
28	chr10:19993393-19993443	SK-N-MC	brain:	n/a
29	chr10:20009221-20009271	Jurkat	blood:	n/a
30	chr10:20017996-20018046	NT2-D1	testis:	n/a
31	chr10:20019641-20019691	GM12891	blood:	n/a
32	chr10:20009221-20009271	SKMC	muscle:	n/a
33	chr10:20023014-20023064	MCF-7	breast:	n/a
34	chr10:20009221-20009271	SAEC	small airway:	n/a
35	chr10:20019641-20019691	HRPEpiC	eye:	n/a
36	chr10:19993393-19993443	RPTEC	kidney:	n/a
37	chr10:20009221-20009271	Caco-2	colon:	n/a
38	chr10:20019641-20019691	PrEC	prostate:	n/a
39	chr10:20019641-20019691	Caco-2	colon:	n/a
40	chr10:20009221-20009271	ECC-1	luminal epithelium:	n/a
41	chr10:20019641-20019691	A549	lung:	n/a
42	chr10:20023014-20023064	HL-60	blood:	n/a
43	chr10:20023014-20023064	NHDF-neo	bronchial:	n/a
44	chr10:19993393-19993443	HRE	kidney:	n/a
45	chr10:20017996-20018046	Jurkat	blood:	n/a
46	chr10:20019641-20019691	Hepatocyte	liver:	n/a
47	chr10:19993393-19993443	SK-N-SH	brain:	n/a
48	chr10:20023014-20023064	NB4	blood:	n/a
49	chr10:20019641-20019691	T-47D	breast:	n/a
50	chr10:20009221-20009271	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:20019487..20021486-chr10:20023021..20025929,2	K562	blood:
2	chr10:20020129..20021732-chr10:20034774..20036880,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NEBL-2	chr10:20010517-20011154	ENSG00000233968.2
2	lnc-NEBL-2	chr10:20010626-20011154	ENSG00000233968.1
3	lnc-NEBL-2	chr10:20005728-20005819	ENSG00000233968.1
4	lnc-NEBL-3	chr10:20039263-20040223	NONHSAT011670
5	lnc-NEBL-2	chr10:20010907-20011154	ENSG00000233968.1
6	lnc-NEBL-2	chr10:20011259-20011351	ENSG00000233968.1
7	lnc-NEBL-2	chr10:20017334-20017479	ENSG00000233968.1
8	lnc-NEBL-2	chr10:20011259-20011351	ENSG00000233968.1
9	lnc-C10orf112-1	chr10:19981387-19981483	NONHSAT011665
10	lnc-NEBL-2	chr10:20011259-20011517	ENSG00000233968.1
11	lnc-NEBL-3	chr10:20039270-20040223	ucscGeneNc_uc001iqf_2
12	lnc-NEBL-2	chr10:20011259-20011351	ENSG00000233968.2
13	lnc-C10orf112-1	chr10:19981239-19981290	NONHSAT011665
14	lnc-NEBL-2	chr10:20013856-20013910	ENSG00000233968.2
15	lnc-NEBL-2	chr10:20017334-20017479	ENSG00000233968.2
16	lnc-NEBL-2	chr10:19999257-20000217	ENSG00000233968.1
17	lnc-NEBL-2	chr10:20017334-20017479	ENSG00000233968.1
18	lnc-NEBL-2	chr10:20013856-20013910	ENSG00000233968.1
19	lnc-NEBL-2	chr10:20011043-20011154	ENSG00000233968.1
20	lnc-NEBL-2	chr10:20013856-20013910	ENSG00000233968.1
21	lnc-NEBL-2	chr10:20017334-20017479	ENSG00000233968.1

No data

Variant related genes	Relation type
MALRD1	TF binding region
MTND2P16	TF binding region
ENSG00000233968	TF binding region
MALRD1	CpG island
MTND2P16	CpG island
ENSG00000233968	CpG island
ENSG00000230818	chromatin interactions
ENSG00000204740	chromatin interactions

Extended variants
information (count: 2861 )
Associated
traits (count: 44 )

Variant overlapped rSNPs/rCNVs (count:2861 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4748608	chr10:19974930-19974931	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535380756	chr10:19974942-19974943	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs553496162	chr10:19974976-19974977	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs140955491	chr10:19974981-19974982	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs59849389	chr10:19975026-19975027	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs557914428	chr10:19975027-19975028	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs116505664	chr10:19975036-19975037	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs183835233	chr10:19975043-19975044	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs58978591	chr10:19975122-19975123	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs397742309	chr10:19975123-19975124	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs144771349	chr10:19975146-19975147	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs575036719	chr10:19975177-19975178	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs542168475	chr10:19975193-19975194	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs1326967	chr10:19975246-19975247	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs200537498	chr10:19975250-19975251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs11817661	chr10:19975292-19975293	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs187998008	chr10:19975293-19975294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564254205	chr10:19975296-19975297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531371511	chr10:19975302-19975303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs193007829	chr10:19975320-19975321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568301179	chr10:19975321-19975322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138709075	chr10:19975333-19975334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185141076	chr10:19975358-19975359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140383534	chr10:19975372-19975373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs540680912	chr10:19975397-19975398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs7909654	chr10:19975408-19975409	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs143589531	chr10:19975410-19975411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576227085	chr10:19975418-19975419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190382814	chr10:19975444-19975445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11011078	chr10:19975446-19975447	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs544448431	chr10:19975460-19975461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575019237	chr10:19975479-19975480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374791222	chr10:19975491-19975492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549840089	chr10:19975550-19975551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74119729	chr10:19975582-19975583	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs185009231	chr10:19975585-19975586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188143341	chr10:19975595-19975596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs7906553	chr10:19975626-19975627	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs1326966	chr10:19975645-19975646	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs553932752	chr10:19975679-19975680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531700341	chr10:19975720-19975721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543548666	chr10:19975774-19975775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561729837	chr10:19975819-19975820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529112054	chr10:19975847-19975848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7924093	chr10:19975850-19975851	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs180903777	chr10:19975865-19975866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs72782176	chr10:19975866-19975867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551400327	chr10:19975867-19975868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569727359	chr10:19975889-19975890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532308731	chr10:19975927-19975928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:44)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	22083797	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Myelofibrosis	22110671	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:216 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:19974800-19975200	ZNF genes & repeats	Fetal Intestine Small	intestine
2	chr10:19975200-19983800	Weak transcription	Fetal Intestine Small	intestine
3	chr10:19975800-19986600	Weak transcription	HepG2	liver
4	chr10:19976600-19986000	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr10:19980800-19981600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr10:19981000-19981600	ZNF genes & repeats	Fetal Intestine Large	intestine
7	chr10:19981200-19981600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr10:19981200-19981600	ZNF genes & repeats	Duodenum Mucosa	Duodenum
9	chr10:19981400-19981600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
10	chr10:19981600-19984800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr10:19981600-19984800	Weak transcription	Fetal Intestine Large	intestine
12	chr10:19981600-19986600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr10:19981600-19986800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr10:19981600-19987400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr10:19983800-19986000	Weak transcription	Fetal Stomach	stomach
16	chr10:19983800-19986800	Strong transcription	Fetal Intestine Small	intestine
17	chr10:19984800-19985400	Strong transcription	Duodenum Mucosa	Duodenum
18	chr10:19984800-19988400	Strong transcription	Fetal Intestine Large	intestine
19	chr10:19985400-19987200	Weak transcription	Duodenum Mucosa	Duodenum
20	chr10:19986800-20000400	Weak transcription	Fetal Intestine Small	intestine
21	chr10:19987200-19989200	Strong transcription	Duodenum Mucosa	Duodenum
22	chr10:19988400-19993200	Weak transcription	Fetal Intestine Large	intestine
23	chr10:19989200-20000400	Weak transcription	Duodenum Mucosa	Duodenum
24	chr10:19989600-19989800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr10:19990200-19990400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr10:19990400-19991800	Enhancers	HSMMtube	muscle
27	chr10:19990800-19991400	Enhancers	NH-A	brain
28	chr10:19990800-19991800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr10:19990800-19991800	Enhancers	Muscle Satellite Cultured Cells	--
30	chr10:19990800-19991800	Enhancers	NHEK	skin
31	chr10:19990800-19991800	Enhancers	Osteobl	bone
32	chr10:19990800-19992000	Enhancers	HSMM	muscle
33	chr10:19991000-19991400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr10:19991200-19991400	Enhancers	Aorta	Aorta
35	chr10:19991400-19991800	Weak transcription	NH-A	brain
36	chr10:19991400-19992200	Weak transcription	Aorta	Aorta
37	chr10:19991800-19992000	Enhancers	NH-A	brain
38	chr10:19991800-19993200	Weak transcription	Osteobl	bone
39	chr10:19992000-19992600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr10:19992000-19993200	Weak transcription	NH-A	brain
41	chr10:19992000-19994200	Weak transcription	HSMM	muscle
42	chr10:19992200-19992400	Enhancers	Aorta	Aorta
43	chr10:19992400-20000600	Weak transcription	Aorta	Aorta
44	chr10:19992600-19993000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr10:19993000-19994600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr10:19993200-19993400	Enhancers	Osteobl	bone
47	chr10:19993200-19993800	Enhancers	NH-A	brain
48	chr10:19993200-19994400	Strong transcription	Fetal Intestine Large	intestine
49	chr10:19993400-19993800	Weak transcription	Osteobl	bone
50	chr10:19993800-19994200	Weak transcription	NH-A	brain

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