Variant report

Variant	nsv831802
Chromosome Location	chr10:19449261-19585888
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	BACH1	chr10:19523717-19523813	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr10:19457572-19457738	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr10:19458718-19458920	HepG2	liver:	n/a	n/a
4	CEBPB	chr10:19481079-19481325	HepG2	liver:	n/a	chr10:19481196-19481207
5	CEBPB	chr10:19483831-19484090	HepG2	liver:	n/a	chr10:19483936-19483947
6	CEBPB	chr10:19481040-19481301	IMR90	lung:	n/a	chr10:19481196-19481207
7	CEBPB	chr10:19498334-19498682	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr10:19498249-19498750	MCF-7	breast:	n/a	n/a
9	CEBPB	chr10:19455086-19455203	HepG2	liver:	n/a	chr10:19455162-19455173
10	CHD2	chr10:19457614-19457815	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr10:19457623-19457753	SK-N-SH_RA	brain:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
12	CTCF	chr10:19457600-19457750	GM12875	blood:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
13	CTCF	chr10:19457580-19457730	RPTEC	kidney:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
14	CTCF	chr10:19519937-19520251	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr10:19457620-19457770	HFF	foreskin:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
16	CTCF	chr10:19493381-19493396	MCF-7	breast:	n/a	n/a
17	CTCF	chr10:19493360-19493510	AG04450	lung:	n/a	n/a
18	CTCF	chr10:19457660-19457810	HepG2	liver:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
19	CTCF	chr10:19457600-19457750	SK-N-SH_RA	brain:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
20	CTCF	chr10:19493340-19493490	NHEK	skin:	n/a	n/a
21	CTCF	chr10:19457560-19457710	HA-sp	spinal cord:	n/a	chr10:19457699-19457708
22	CTCF	chr10:19457653-19457766	Fibrobl	skin:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
23	CTCF	chr10:19465733-19465812	MCF-7	breast:	n/a	n/a
24	CTCF	chr10:19457620-19457770	GM12873	blood:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
25	CTCF	chr10:19457540-19457690	GM12867	blood:	n/a	n/a
26	CTCF	chr10:19457620-19457770	HCFaa	heart:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
27	CTCF	chr10:19457605-19457829	Gliobla	brain:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
28	CTCF	chr10:19565919-19565946	ProgFib	skin:	n/a	n/a
29	CTCF	chr10:19457660-19457810	AG04450	lung:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
30	CTCF	chr10:19520140-19520290	HCFaa	heart:	n/a	n/a
31	CTCF	chr10:19457660-19457810	HCM	heart:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
32	CTCF	chr10:19457640-19457790	Hela-S3	cervix:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
33	CTCF	chr10:19457515-19457852	H1-hESC	embryonic stem cell:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
34	CTCF	chr10:19520171-19520208	HepG2	liver:	n/a	n/a
35	CTCF	chr10:19493300-19493450	MCF-7	breast:	n/a	n/a
36	CTCF	chr10:19520080-19520230	MCF-7	breast:	n/a	n/a
37	CTCF	chr10:19457620-19457770	GM12874	blood:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
38	CTCF	chr10:19457600-19457750	GM12878	blood:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
39	CTCF	chr10:19457960-19458110	AG04450	lung:	n/a	n/a
40	CTCF	chr10:19457600-19457750	SAEC	small airway:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
41	CTCF	chr10:19457640-19457790	MCF-7	breast:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
42	CTCF	chr10:19457620-19457770	BE2_C	brain:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
43	CTCF	chr10:19520112-19520210	NHEK	skin:	n/a	n/a
44	CTCF	chr10:19460458-19460539	Medullo	brain:	n/a	n/a
45	CTCF	chr10:19457580-19457730	HPAF	blood vessel:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
46	CTCF	chr10:19457521-19457842	H1-hESC	embryonic stem cell:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
47	CTCF	chr10:19457634-19457777	A549	lung:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
48	CTCF	chr10:19457616-19457788	NHEK	skin:	n/a	chr10:19457699-19457708 chr10:19457698-19457711 chr10:19457693-19457711
49	CTCF	chr10:19465716-19465852	MCF-7	breast:	n/a	n/a
50	CTCF	chr10:19493220-19493370	HAc	cerebellar:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:19540759-19540809	U87	brain:	n/a
2	chr10:19540759-19540809	AG04449	skin:	fetal
3	chr10:19540759-19540809	HL-60	blood:	n/a
4	chr10:19540759-19540809	NB4	blood:	n/a
5	chr10:19540759-19540809	HRE	kidney:	n/a
6	chr10:19540759-19540809	HepG2	liver:	n/a
7	chr10:19540759-19540809	HMEC	breast:	n/a
8	chr10:19540759-19540809	NT2-D1	testis:	n/a
9	chr10:19540759-19540809	CMK	blood:	n/a
10	chr10:19540759-19540809	HNPCEpiC	eye:	n/a
11	chr10:19540759-19540809	PrEC	prostate:	n/a
12	chr10:19540759-19540809	SK-N-MC	brain:	n/a
13	chr10:19540759-19540809	HRCEpiC	kidney:	n/a
14	chr10:19540759-19540809	HPAEpiC	pulmonary alveolar:	n/a
15	chr10:19540759-19540809	SAEC	small airway:	n/a
16	chr10:19540759-19540809	GM06990	blood:	n/a
17	chr10:19540759-19540809	HEEpiC	esophagus:	n/a
18	chr10:19540759-19540809	HUVEC	blood vessel:	n/a
19	chr10:19540759-19540809	LNCaP	prostate:	n/a
20	chr10:19540759-19540809	HCM	heart:	n/a
21	chr10:19540759-19540809	HAEpiC	amniotic membrane:	n/a
22	chr10:19540759-19540809	H1-hESC	embryonic stem cell:	embryo
23	chr10:19540759-19540809	AoSMC	blood vessel:	n/a
24	chr10:19540759-19540809	NHBE	bronchial:	n/a
25	chr10:19540759-19540809	AG09309	skin:	n/a
26	chr10:19540759-19540809	Hepatocyte	liver:	n/a
27	chr10:19540759-19540809	ECC-1	luminal epithelium:	n/a
28	chr10:19540759-19540809	SK-N-SH	brain:	n/a
29	chr10:19540759-19540809	AG09319	gingival:	n/a
30	chr10:19540759-19540809	GM12892	blood:	n/a
31	chr10:19540759-19540809	RPTEC	kidney:	n/a
32	chr10:19540759-19540809	MCF-7	breast:	n/a
33	chr10:19540759-19540809	BE2_C	brain:	n/a
34	chr10:19540759-19540809	HIPEpiC	eye:	n/a
35	chr10:19540759-19540809	SK-N-SH_RA	brain:	n/a
36	chr10:19540759-19540809	IMR90	lung:	fetal
37	chr10:19540759-19540809	GM19239	blood:	n/a
38	chr10:19540759-19540809	ovcar-3	ovarian:	n/a
39	chr10:19540759-19540809	HCPEpiC	choroid plexus:	n/a
40	chr10:19540759-19540809	MCF10A-Er-Src	breast:	n/a
41	chr10:19540759-19540809	BJ	skin:	n/a
42	chr10:19540759-19540809	NHDF-neo	bronchial:	n/a
43	chr10:19540759-19540809	GM12891	blood:	n/a
44	chr10:19540759-19540809	HRPEpiC	eye:	n/a
45	chr10:19540759-19540809	Jurkat	blood:	n/a
46	chr10:19540759-19540809	HEK293	kidney:	embryo
47	chr10:19540759-19540809	HCT-116	colon:	n/a
48	chr10:19540759-19540809	AG10803	skin:	n/a
49	chr10:19540759-19540809	PFSK-1	brain:	n/a
50	chr10:19540759-19540809	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr10:19458075..19458575-chr18:36304626..36305400,2	MCF-7	breast:
2	chr10:19496117..19498249-chr10:19507924..19510695,2	MCF-7	breast:
3	chr10:19510172..19510750-chr10:19521065..19522003,2	MCF-7	breast:
4	chr10:19466484..19467327-chr10:19521039..19521911,3	MCF-7	breast:
5	chr10:19510172..19510750-chr10:19521065..19522003,2	MCF-7	breast:
6	chr10:19547526..19550166-chr10:19551019..19552884,2	MCF-7	breast:
7	chr10:19502635..19505234-chr10:19507325..19509106,2	MCF-7	breast:
8	chr10:19544299..19547180-chr10:19549327..19551757,2	MCF-7	breast:
9	chr10:19466484..19467332-chr10:19521028..19521911,4	MCF-7	breast:
10	chr10:19534164..19535892-chr10:19543312..19545061,2	MCF-7	breast:
11	chr10:19578194..19580695-chr10:19582089..19585004,2	K562	blood:
12	chr10:19497233..19499735-chr10:19518305..19520335,2	MCF-7	breast:
13	chr10:19544299..19547180-chr10:19549327..19551757,2	MCF-7	breast:
14	chr10:19502635..19505234-chr10:19507325..19509106,2	MCF-7	breast:
15	chr10:19551633..19554617-chr10:19556322..19558693,2	K562	blood:
16	chr10:19534164..19535892-chr10:19543312..19545061,2	MCF-7	breast:
17	chr10:19466484..19467327-chr10:19521039..19521911,3	MCF-7	breast:
18	chr10:19082548..19083519-chr10:19457655..19458211,2	MCF-7	breast:
19	chr10:19547526..19550166-chr10:19551019..19552884,2	MCF-7	breast:
20	chr10:19551633..19554617-chr10:19556322..19558693,2	K562	blood:
21	chr10:19497233..19499735-chr10:19518305..19520335,2	MCF-7	breast:
22	chr10:19496117..19498249-chr10:19507924..19510695,2	MCF-7	breast:
23	chr10:19466484..19467332-chr10:19521028..19521911,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NSUN6-6	chr10:19580351-19580409	XLOC_008744
2	lnc-NSUN6-6	chr10:19579152-19579395	XLOC_008744

Variant related genes	Relation type
MALRD1	TF binding region
ENSG00000227734	TF binding region
MALRD1	CpG island
ENSG00000227734	CpG island
ENSG00000227734	chromatin interactions

Extended variants
information (count: 6493 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:6493 , 50 per page) page: 1 2 3 4 5 6 7 ... 130

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34358819	chr10:19449297-19449298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs543289496	chr10:19449345-19449346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554927304	chr10:19449375-19449376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573501337	chr10:19449389-19449390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570148149	chr10:19449391-19449392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565482195	chr10:19449451-19449452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537200064	chr10:19449512-19449513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12413696	chr10:19449536-19449537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543952429	chr10:19449549-19449550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562124816	chr10:19449555-19449556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529677566	chr10:19449569-19449570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548185710	chr10:19449624-19449625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566627536	chr10:19449677-19449678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs527586989	chr10:19449688-19449689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552046479	chr10:19449740-19449741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs11008715	chr10:19449806-19449807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375895583	chr10:19449839-19449840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557524240	chr10:19449843-19449844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201092347	chr10:19449870-19449871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569387350	chr10:19449882-19449883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190423021	chr10:19449938-19449939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554949789	chr10:19449945-19449946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573414630	chr10:19449948-19449949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540964177	chr10:19450020-19450021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558725933	chr10:19450031-19450032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs71497262	chr10:19450068-19450069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543890517	chr10:19450077-19450078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376342416	chr10:19450122-19450123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201257022	chr10:19450152-19450153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201705544	chr10:19450175-19450176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529819258	chr10:19450177-19450178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12780830	chr10:19450199-19450200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201504561	chr10:19450214-19450215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527587909	chr10:19450250-19450251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182701387	chr10:19450311-19450312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564256084	chr10:19450323-19450324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531498806	chr10:19450355-19450356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11817290	chr10:19450364-19450365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188228878	chr10:19450369-19450370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192562499	chr10:19450371-19450372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs11815933	chr10:19450399-19450400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs202079210	chr10:19450441-19450442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566906547	chr10:19450442-19450443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200782972	chr10:19450455-19450456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs34437737	chr10:19450468-19450469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138734718	chr10:19450469-19450470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs397847563	chr10:19450477-19450478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372714601	chr10:19450479-19450480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200420990	chr10:19450480-19450481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs74672766	chr10:19450495-19450496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:43)

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
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	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	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:19438400-19489000	Weak transcription	Fetal Intestine Small	intestine
2	chr10:19446000-19450600	Weak transcription	Duodenum Mucosa	Duodenum
3	chr10:19448800-19454600	Weak transcription	Fetal Intestine Large	intestine
4	chr10:19450600-19451000	Strong transcription	Duodenum Mucosa	Duodenum
5	chr10:19451000-19454600	Weak transcription	Duodenum Mucosa	Duodenum
6	chr10:19453200-19453800	Enhancers	NHEK	skin
7	chr10:19454600-19457600	Strong transcription	Duodenum Mucosa	Duodenum
8	chr10:19454600-19457600	Strong transcription	Fetal Intestine Large	intestine
9	chr10:19457600-19457800	Genic enhancers	Fetal Intestine Large	intestine
10	chr10:19457600-19475800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr10:19457800-19458200	Enhancers	Fetal Intestine Large	intestine
12	chr10:19458200-19465800	Weak transcription	Fetal Intestine Large	intestine
13	chr10:19465600-19465800	Enhancers	Pancreas	Pancrea
14	chr10:19465800-19468000	Enhancers	Fetal Intestine Large	intestine
15	chr10:19467000-19467400	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr10:19467400-19467600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
17	chr10:19467600-19467800	Active TSS	Pancreatic Islets	Pancreatic Islet
18	chr10:19467600-19468000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr10:19467800-19468000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
20	chr10:19468000-19468400	Active TSS	Pancreatic Islets	Pancreatic Islet
21	chr10:19468000-19475800	Weak transcription	Fetal Intestine Large	intestine
22	chr10:19473000-19473200	Enhancers	Fetal Lung	lung
23	chr10:19473800-19474600	Active TSS	Fetal Lung	lung
24	chr10:19474600-19474800	Enhancers	Fetal Lung	lung
25	chr10:19475800-19477600	Strong transcription	Fetal Intestine Large	intestine
26	chr10:19475800-19477800	Strong transcription	Duodenum Mucosa	Duodenum
27	chr10:19477600-19477800	ZNF genes & repeats	Fetal Intestine Large	intestine
28	chr10:19477800-19492200	Weak transcription	Duodenum Mucosa	Duodenum
29	chr10:19481000-19481200	Enhancers	Fetal Intestine Large	intestine
30	chr10:19481200-19488400	Weak transcription	Fetal Intestine Large	intestine
31	chr10:19486400-19486800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr10:19487600-19496800	Weak transcription	Small Intestine	intestine
33	chr10:19488400-19490000	Enhancers	Fetal Intestine Large	intestine
34	chr10:19488800-19489200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr10:19489000-19489600	Enhancers	Fetal Intestine Small	intestine
36	chr10:19489600-19493200	Weak transcription	Fetal Intestine Small	intestine
37	chr10:19490000-19492400	Weak transcription	Fetal Intestine Large	intestine
38	chr10:19492200-19501400	Strong transcription	Duodenum Mucosa	Duodenum
39	chr10:19492400-19496000	Strong transcription	Fetal Intestine Large	intestine
40	chr10:19492600-19493200	Enhancers	Fetal Lung	lung
41	chr10:19493200-19494800	Strong transcription	Fetal Intestine Small	intestine
42	chr10:19494800-19499800	Weak transcription	Fetal Intestine Small	intestine
43	chr10:19496000-19498200	Weak transcription	Fetal Intestine Large	intestine
44	chr10:19498200-19500400	Strong transcription	Fetal Intestine Large	intestine
45	chr10:19499800-19500800	Strong transcription	Fetal Intestine Small	intestine
46	chr10:19500400-19518600	Weak transcription	Fetal Intestine Large	intestine
47	chr10:19500600-19501600	Enhancers	Fetal Lung	lung
48	chr10:19500800-19502200	Weak transcription	Fetal Intestine Small	intestine
49	chr10:19501400-19502800	Weak transcription	Duodenum Mucosa	Duodenum
50	chr10:19501600-19502800	Weak transcription	Fetal Lung	lung

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