Variant report

Variant	nsv551955
Chromosome Location	chr10:96444249-96690371
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	ARID3A	chr10:96662316-96662867	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:96447569-96447764	HepG2	liver:	n/a	n/a
3	ATF3	chr10:96662325-96662813	A549	lung:	n/a	n/a
4	BCL3	chr10:96662227-96662843	A549	lung:	n/a	n/a
5	BCL3	chr10:96662368-96662780	A549	lung:	n/a	n/a
6	CEBPB	chr10:96485747-96485947	IMR90	lung:	n/a	n/a
7	CEBPB	chr10:96507808-96507867	A549	lung:	n/a	n/a
8	CEBPB	chr10:96687947-96687969	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr10:96520913-96521049	A549	lung:	n/a	chr10:96520959-96520970 chr10:96520961-96520970 chr10:96520960-96520971 chr10:96520961-96520970 chr10:96520961-96520970 chr10:96520961-96520970
10	CEBPB	chr10:96662366-96662879	MCF-7	breast:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
11	CEBPB	chr10:96543674-96543836	HepG2	liver:	n/a	chr10:96543736-96543747
12	CEBPB	chr10:96487903-96488237	HepG2	liver:	n/a	chr10:96488055-96488066
13	CEBPB	chr10:96662301-96662799	HepG2	liver:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
14	CEBPB	chr10:96662174-96662987	A549	lung:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
15	CEBPB	chr10:96610933-96611257	IMR90	lung:	n/a	chr10:96611099-96611110
16	CEBPB	chr10:96453074-96453300	K562	blood:	n/a	chr10:96453142-96453153
17	CEBPB	chr10:96685653-96685786	IMR90	lung:	n/a	chr10:96685750-96685761
18	CEBPB	chr10:96662406-96662733	MCF-7	breast:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
19	CEBPB	chr10:96487954-96488117	H1-hESC	embryonic stem cell:	n/a	chr10:96488055-96488066
20	CEBPB	chr10:96662333-96662805	HepG2	liver:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
21	CEBPB	chr10:96662318-96662764	A549	lung:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
22	CEBPB	chr10:96610998-96611149	K562	blood:	n/a	chr10:96611099-96611110
23	CEBPB	chr10:96685708-96685784	A549	lung:	n/a	chr10:96685750-96685761
24	CEBPB	chr10:96487899-96488178	A549	lung:	n/a	chr10:96488055-96488066
25	CEBPB	chr10:96662376-96662710	HepG2	liver:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
26	CEBPB	chr10:96664707-96664914	HepG2	liver:	n/a	chr10:96664829-96664840
27	CEBPB	chr10:96685700-96685775	HepG2	liver:	n/a	chr10:96685750-96685761
28	CEBPB	chr10:96610935-96611206	A549	lung:	n/a	chr10:96611099-96611110
29	CEBPB	chr10:96520891-96521011	IMR90	lung:	n/a	chr10:96520959-96520970 chr10:96520961-96520970 chr10:96520960-96520971 chr10:96520961-96520970 chr10:96520961-96520970 chr10:96520961-96520970
30	CEBPB	chr10:96452997-96453294	HepG2	liver:	n/a	chr10:96453142-96453153
31	CEBPB	chr10:96662344-96662777	Hela-S3	cervix:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
32	CEBPB	chr10:96581486-96581791	A549	lung:	n/a	chr10:96581633-96581644
33	CEBPB	chr10:96662320-96662841	A549	lung:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
34	CEBPB	chr10:96662475-96662675	IMR90	lung:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
35	CEBPB	chr10:96520862-96521099	HepG2	liver:	n/a	chr10:96520959-96520970 chr10:96520961-96520970 chr10:96520960-96520971 chr10:96520961-96520970 chr10:96520961-96520970 chr10:96520961-96520970
36	CEBPB	chr10:96487896-96488218	IMR90	lung:	n/a	chr10:96488055-96488066
37	CEBPB	chr10:96543674-96543868	A549	lung:	n/a	chr10:96543736-96543747
38	CEBPB	chr10:96581454-96581783	HepG2	liver:	n/a	chr10:96581633-96581644
39	CEBPB	chr10:96504015-96504089	HepG2	liver:	n/a	chr10:96504062-96504073
40	CEBPB	chr10:96485737-96485940	A549	lung:	n/a	n/a
41	CEBPB	chr10:96662349-96662739	HepG2	liver:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
42	CEBPB	chr10:96610925-96611288	HepG2	liver:	n/a	chr10:96611099-96611110
43	CEBPB	chr10:96485885-96485913	K562	blood:	n/a	n/a
44	CEBPD	chr10:96662356-96662705	HepG2	liver:	n/a	n/a
45	CTCF	chr10:96516926-96516994	Medullo	brain:	n/a	n/a
46	CTCF	chr10:96650400-96650550	RPTEC	kidney:	n/a	n/a
47	CTCF	chr10:96563080-96563230	RPTEC	kidney:	n/a	n/a
48	CTCF	chr10:96660839-96660858	ProgFib	skin:	n/a	n/a
49	CTCF	chr10:96621754-96621802	LNCaP	prostate:	n/a	n/a
50	CTCF	chr10:96650518-96650626	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:96447464-96447514	NH-A	brain:	n/a
2	chr10:96447464-96447514	NH-A	brain:	n/a
3	chr10:96523347-96523397	SKMC	muscle:	n/a
4	chr10:96521086-96521136	AoSMC	blood vessel:	n/a
5	chr10:96521152-96521202	GM12878	blood:	n/a
6	chr10:96447464-96447514	GM06990	blood:	n/a
7	chr10:96521152-96521202	PANC-1	pancreas:	n/a
8	chr10:96523248-96523298	SK-N-SH	brain:	n/a
9	chr10:96521152-96521202	AoSMC	blood vessel:	n/a
10	chr10:96523347-96523397	ovcar-3	ovarian:	n/a
11	chr10:96523248-96523298	MCF-7	breast:	n/a
12	chr10:96447464-96447514	BJ	skin:	n/a
13	chr10:96523248-96523298	HUVEC	blood vessel:	n/a
14	chr10:96522433-96522483	AG04449	skin:	fetal
15	chr10:96523248-96523298	HEEpiC	esophagus:	n/a
16	chr10:96522433-96522483	BJ	skin:	n/a
17	chr10:96447464-96447514	AG09319	gingival:	n/a
18	chr10:96447464-96447514	HPAEpiC	pulmonary alveolar:	n/a
19	chr10:96523347-96523397	AoSMC	blood vessel:	n/a
20	chr10:96523248-96523298	H1-hESC	embryonic stem cell:	embryo
21	chr10:96446783-96446833	HRCEpiC	kidney:	n/a
22	chr10:96521086-96521136	U87	brain:	n/a
23	chr10:96521152-96521202	HCT-116	colon:	n/a
24	chr10:96523347-96523397	SK-N-SH_RA	brain:	n/a
25	chr10:96523347-96523397	GM19239	blood:	n/a
26	chr10:96523248-96523298	IMR90	lung:	fetal
27	chr10:96523347-96523397	K562	blood:	n/a
28	chr10:96446783-96446833	NT2-D1	testis:	n/a
29	chr10:96521152-96521202	A549	lung:	n/a
30	chr10:96523347-96523397	HPAEpiC	pulmonary alveolar:	n/a
31	chr10:96521152-96521202	AG09309	skin:	n/a
32	chr10:96521152-96521202	AG04450	lung:	fetal
33	chr10:96521152-96521202	H1-hESC	embryonic stem cell:	embryo
34	chr10:96523248-96523298	ovcar-3	ovarian:	n/a
35	chr10:96521086-96521136	HL-60	blood:	n/a
36	chr10:96523248-96523298	HEK293	kidney:	embryo
37	chr10:96523347-96523397	GM12891	blood:	n/a
38	chr10:96523347-96523397	BJ	skin:	n/a
39	chr10:96447464-96447514	MCF10A-Er-Src	breast:	n/a
40	chr10:96447464-96447514	SK-N-SH	brain:	n/a
41	chr10:96521086-96521136	Hela-S3	cervix:	n/a
42	chr10:96523347-96523397	CMK	blood:	n/a
43	chr10:96446783-96446833	NH-A	brain:	n/a
44	chr10:96447464-96447514	HEEpiC	esophagus:	n/a
45	chr10:96521152-96521202	BJ	skin:	n/a
46	chr10:96446783-96446833	MCF10A-Er-Src	breast:	n/a
47	chr10:96521152-96521202	NB4	blood:	n/a
48	chr10:96521152-96521202	AG10803	skin:	n/a
49	chr10:96446783-96446833	HAEpiC	amniotic membrane:	n/a
50	chr10:96523347-96523397	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:96644256..96646461-chr10:96648799..96651515,2	K562	blood:
2	chr10:96479612..96481874-chr10:96483604..96486212,2	MCF-7	breast:
3	chr10:96479612..96481874-chr10:96483604..96486212,2	MCF-7	breast:
4	chr10:96644256..96646461-chr10:96648799..96651515,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP2C8-4	chr10:96632715-96632886	NONHSAT015740
2	lnc-CYP2C8-4	chr10:96625946-96626096	NONHSAT015740
3	lnc-CYP2C19-1	chr10:96642311-96643100	NONHSAT015741
4	lnc-CYP2C8-4	chr10:96625609-96625760	NONHSAT015740

Variant related genes	Relation type
CYP2C58P	TF binding region
ENSG00000225354	TF binding region
MTND4P19	TF binding region
CYP2C19	TF binding region
CYP2C58P	CpG island
ENSG00000225354	CpG island
MTND4P19	CpG island
CYP2C19	CpG island

Extended variants
information (count: 11324 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:11324 , 50 per page) page: 1 2 3 4 5 6 7 ... 227

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12774424	chr10:96444249-96444250	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs12774426	chr10:96444254-96444255	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531313793	chr10:96444255-96444256	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577946945	chr10:96444270-96444271	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs368069572	chr10:96444278-96444279	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570974995	chr10:96444285-96444286	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564746116	chr10:96444319-96444320	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs116414747	chr10:96444379-96444380	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs75038120	chr10:96444395-96444396	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187550913	chr10:96444399-96444400	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs74872019	chr10:96444408-96444409	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567212255	chr10:96444410-96444411	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs57431619	chr10:96444512-96444513	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs549720848	chr10:96444515-96444516	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556429448	chr10:96444565-96444566	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569799961	chr10:96444569-96444570	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs60421813	chr10:96444580-96444581	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs370835468	chr10:96444624-96444625	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558210618	chr10:96444672-96444673	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs377735654	chr10:96444680-96444681	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140684348	chr10:96444740-96444741	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113927077	chr10:96444781-96444782	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141385927	chr10:96444782-96444783	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569530412	chr10:96444785-96444786	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201548197	chr10:96444793-96444794	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200047253	chr10:96444795-96444796	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs59761621	chr10:96444796-96444797	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559659089	chr10:96444807-96444808	Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs534178235	chr10:96444854-96444855	Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs554554849	chr10:96444934-96444935	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs74615912	chr10:96444979-96444980	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs117634501	chr10:96444991-96444992	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs527873116	chr10:96445007-96445008	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs371980461	chr10:96445014-96445015	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs80064739	chr10:96445042-96445043	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs562012772	chr10:96445070-96445071	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs142943032	chr10:96445088-96445089	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs138313662	chr10:96445094-96445095	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs191540333	chr10:96445096-96445097	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs149642358	chr10:96445156-96445157	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs540620150	chr10:96445167-96445168	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs552370260	chr10:96445226-96445227	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531042039	chr10:96445249-96445250	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570984342	chr10:96445254-96445255	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs75935150	chr10:96445258-96445259	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs397789494	chr10:96445259-96445260	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376870394	chr10:96445260-96445261	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370541483	chr10:96445261-96445262	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529954039	chr10:96445274-96445275	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182855916	chr10:96445295-96445296	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Intracranial aneurysm	16715129	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oligozoospermia	20877625	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:355 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96435200-96444800	Weak transcription	Gastric	stomach
2	chr10:96442400-96447000	Active TSS	Liver	Liver
3	chr10:96443200-96446800	Active TSS	Duodenum Mucosa	Duodenum
4	chr10:96443200-96447200	Active TSS	Stomach Mucosa	stomach
5	chr10:96443400-96445000	Active TSS	Fetal Stomach	stomach
6	chr10:96443400-96445400	Active TSS	Fetal Intestine Large	intestine
7	chr10:96443400-96445600	Active TSS	Fetal Intestine Small	intestine
8	chr10:96444000-96444600	Active TSS	Duodenum Smooth Muscle	Duodenum
9	chr10:96444000-96445600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr10:96444600-96444800	Enhancers	Esophagus	oesophagus
11	chr10:96444800-96445000	Flanking Active TSS	Esophagus	oesophagus
12	chr10:96444800-96445200	Active TSS	Gastric	stomach
13	chr10:96445000-96445200	Active TSS	Esophagus	oesophagus
14	chr10:96445200-96449600	Weak transcription	Esophagus	oesophagus
15	chr10:96445200-96449600	Weak transcription	Gastric	stomach
16	chr10:96445400-96445800	ZNF genes & repeats	Fetal Intestine Large	intestine
17	chr10:96445600-96446800	Weak transcription	Fetal Intestine Small	intestine
18	chr10:96445800-96447600	Weak transcription	Fetal Intestine Large	intestine
19	chr10:96446800-96447200	Flanking Active TSS	Duodenum Mucosa	Duodenum
20	chr10:96446800-96448000	ZNF genes & repeats	Fetal Intestine Small	intestine
21	chr10:96447000-96447800	Flanking Active TSS	Liver	Liver
22	chr10:96447200-96447400	Enhancers	Duodenum Mucosa	Duodenum
23	chr10:96447200-96504800	Weak transcription	Stomach Mucosa	stomach
24	chr10:96447400-96447800	Genic enhancers	Duodenum Mucosa	Duodenum
25	chr10:96447400-96448000	Enhancers	HepG2	liver
26	chr10:96447600-96449200	Strong transcription	Fetal Intestine Large	intestine
27	chr10:96447800-96448600	Transcr. at gene 5' and 3'	Liver	Liver
28	chr10:96447800-96450000	Strong transcription	Duodenum Mucosa	Duodenum
29	chr10:96448000-96449600	Weak transcription	Fetal Intestine Small	intestine
30	chr10:96448000-96450200	Weak transcription	Small Intestine	intestine
31	chr10:96448600-96449200	Strong transcription	Liver	Liver
32	chr10:96449200-96450000	ZNF genes & repeats	Liver	Liver
33	chr10:96449200-96450000	ZNF genes & repeats	Fetal Intestine Large	intestine
34	chr10:96449600-96449800	ZNF genes & repeats	Esophagus	oesophagus
35	chr10:96449600-96449800	ZNF genes & repeats	Gastric	stomach
36	chr10:96449600-96450000	ZNF genes & repeats	Fetal Intestine Small	intestine
37	chr10:96449800-96455000	Weak transcription	Esophagus	oesophagus
38	chr10:96449800-96456400	Weak transcription	Gastric	stomach
39	chr10:96450000-96450600	Strong transcription	Liver	Liver
40	chr10:96450000-96453000	Weak transcription	Fetal Intestine Small	intestine
41	chr10:96450000-96455200	Weak transcription	Duodenum Mucosa	Duodenum
42	chr10:96450000-96471400	Weak transcription	Fetal Intestine Large	intestine
43	chr10:96450600-96453000	Weak transcription	Liver	Liver
44	chr10:96453000-96453400	ZNF genes & repeats	Fetal Intestine Small	intestine
45	chr10:96453000-96456200	Strong transcription	Liver	Liver
46	chr10:96453400-96455000	Weak transcription	Fetal Intestine Small	intestine
47	chr10:96455000-96455600	ZNF genes & repeats	Esophagus	oesophagus
48	chr10:96455000-96456600	ZNF genes & repeats	Fetal Intestine Small	intestine
49	chr10:96455200-96456200	ZNF genes & repeats	Duodenum Mucosa	Duodenum
50	chr10:96456200-96462800	Weak transcription	Liver	Liver

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