Variant report

Variant	nsv551956
Chromosome Location	chr10:96446632-96632253
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	chr10:96447569-96447764	HepG2	liver:	n/a	n/a
2	CEBPB	chr10:96485747-96485947	IMR90	lung:	n/a	n/a
3	CEBPB	chr10:96487896-96488218	IMR90	lung:	n/a	chr10:96488055-96488066
4	CEBPB	chr10:96610935-96611206	A549	lung:	n/a	chr10:96611099-96611110
5	CEBPB	chr10:96453074-96453300	K562	blood:	n/a	chr10:96453142-96453153
6	CEBPB	chr10:96543674-96543836	HepG2	liver:	n/a	chr10:96543736-96543747
7	CEBPB	chr10:96487903-96488237	HepG2	liver:	n/a	chr10:96488055-96488066
8	CEBPB	chr10:96581454-96581783	HepG2	liver:	n/a	chr10:96581633-96581644
9	CEBPB	chr10:96485885-96485913	K562	blood:	n/a	n/a
10	CEBPB	chr10:96452997-96453294	HepG2	liver:	n/a	chr10:96453142-96453153
11	CEBPB	chr10:96487899-96488178	A549	lung:	n/a	chr10:96488055-96488066
12	CEBPB	chr10:96487954-96488117	H1-hESC	embryonic stem cell:	n/a	chr10:96488055-96488066
13	CEBPB	chr10:96610998-96611149	K562	blood:	n/a	chr10:96611099-96611110
14	CEBPB	chr10:96504015-96504089	HepG2	liver:	n/a	chr10:96504062-96504073
15	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
16	CEBPB	chr10:96485737-96485940	A549	lung:	n/a	n/a
17	CEBPB	chr10:96507808-96507867	A549	lung:	n/a	n/a
18	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
19	CEBPB	chr10:96581486-96581791	A549	lung:	n/a	chr10:96581633-96581644
20	CEBPB	chr10:96610925-96611288	HepG2	liver:	n/a	chr10:96611099-96611110
21	CEBPB	chr10:96610933-96611257	IMR90	lung:	n/a	chr10:96611099-96611110
22	CEBPB	chr10:96543674-96543868	A549	lung:	n/a	chr10:96543736-96543747
23	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
24	CTCF	chr10:96516926-96516994	Medullo	brain:	n/a	n/a
25	CTCF	chr10:96626963-96627063	LNCaP	prostate:	n/a	n/a
26	CTCF	chr10:96563100-96563250	MCF-7	breast:	n/a	n/a
27	CTCF	chr10:96530910-96530967	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr10:96577722-96577829	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr10:96512231-96512340	MCF-7	breast:	n/a	n/a
30	CTCF	chr10:96563080-96563230	RPTEC	kidney:	n/a	n/a
31	CTCF	chr10:96505096-96505149	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr10:96562980-96563130	RPTEC	kidney:	n/a	n/a
33	CTCF	chr10:96570817-96570874	GM13976	blood:	n/a	n/a
34	CTCF	chr10:96621754-96621802	LNCaP	prostate:	n/a	n/a
35	CTCF	chr10:96512257-96512384	MCF-7	breast:	n/a	n/a
36	CTCF	chr10:96596395-96596418	LNCaP	prostate:	n/a	n/a
37	CTCF	chr10:96618977-96619055	MCF-7	breast:	n/a	n/a
38	CTCF	chr10:96517820-96517970	HepG2	liver:	n/a	n/a
39	CTCF	chr10:96534991-96535093	GM20000	blood:	n/a	n/a
40	CTCF	chr10:96530820-96530970	HEK293	kidney:	n/a	n/a
41	CTCF	chr10:96552160-96552310	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr10:96563126-96563151	HepG2	liver:	n/a	n/a
43	E2F4	chr10:96511121-96511131	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr10:96485613-96486005	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr10:96485593-96486022	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr10:96545074-96545211	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr10:96485608-96485959	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr10:96485600-96485967	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr10:96545059-96545259	MCF10A-Er-Src	breast:	n/a	n/a
50	FOSL2	chr10:96485580-96486030	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:96522433-96522483	K562	blood:	n/a
2	chr10:96521152-96521202	AoSMC	blood vessel:	n/a
3	chr10:96522433-96522483	NHBE	bronchial:	n/a
4	chr10:96523248-96523298	HEK293	kidney:	embryo
5	chr10:96446783-96446833	SKMC	muscle:	n/a
6	chr10:96446783-96446833	HMEC	breast:	n/a
7	chr10:96522433-96522483	PFSK-1	brain:	n/a
8	chr10:96521086-96521136	AG04449	skin:	fetal
9	chr10:96447464-96447514	Jurkat	blood:	n/a
10	chr10:96521086-96521136	AG09319	gingival:	n/a
11	chr10:96521086-96521136	LNCaP	prostate:	n/a
12	chr10:96523347-96523397	HRPEpiC	eye:	n/a
13	chr10:96447464-96447514	SK-N-SH	brain:	n/a
14	chr10:96446783-96446833	Jurkat	blood:	n/a
15	chr10:96521152-96521202	ECC-1	luminal epithelium:	n/a
16	chr10:96523248-96523298	H1-hESC	embryonic stem cell:	embryo
17	chr10:96521152-96521202	BJ	skin:	n/a
18	chr10:96523347-96523397	HPAEpiC	pulmonary alveolar:	n/a
19	chr10:96523347-96523397	AoSMC	blood vessel:	n/a
20	chr10:96522433-96522483	SKMC	muscle:	n/a
21	chr10:96523248-96523298	GM12891	blood:	n/a
22	chr10:96521086-96521136	HRCEpiC	kidney:	n/a
23	chr10:96447464-96447514	NH-A	brain:	n/a
24	chr10:96521152-96521202	PFSK-1	brain:	n/a
25	chr10:96523248-96523298	BE2_C	brain:	n/a
26	chr10:96523248-96523298	A549	lung:	n/a
27	chr10:96446783-96446833	T-47D	breast:	n/a
28	chr10:96521152-96521202	HL-60	blood:	n/a
29	chr10:96521152-96521202	SK-N-SH	brain:	n/a
30	chr10:96522433-96522483	GM06990	blood:	n/a
31	chr10:96521152-96521202	ProgFib	skin:	n/a
32	chr10:96447464-96447514	NT2-D1	testis:	n/a
33	chr10:96521152-96521202	Hela-S3	cervix:	n/a
34	chr10:96522433-96522483	RPTEC	kidney:	n/a
35	chr10:96521086-96521136	HRPEpiC	eye:	n/a
36	chr10:96521086-96521136	HCT-116	colon:	n/a
37	chr10:96523248-96523298	PANC-1	pancreas:	n/a
38	chr10:96446783-96446833	U87	brain:	n/a
39	chr10:96446783-96446833	AG09319	gingival:	n/a
40	chr10:96447464-96447514	HAEpiC	amniotic membrane:	n/a
41	chr10:96522433-96522483	AG04450	lung:	fetal
42	chr10:96521152-96521202	Hepatocyte	liver:	n/a
43	chr10:96521152-96521202	HRE	kidney:	n/a
44	chr10:96447464-96447514	GM12891	blood:	n/a
45	chr10:96522433-96522483	LNCaP	prostate:	n/a
46	chr10:96523347-96523397	BJ	skin:	n/a
47	chr10:96521086-96521136	NHDF-neo	bronchial:	n/a
48	chr10:96521152-96521202	AG04449	skin:	fetal
49	chr10:96523248-96523298	IMR90	lung:	fetal
50	chr10:96521086-96521136	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:96479612..96481874-chr10:96483604..96486212,2	MCF-7	breast:
2	chr10:96479612..96481874-chr10:96483604..96486212,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP2C8-4	chr10:96625946-96626096	NONHSAT015740
2	lnc-CYP2C8-4	chr10:96625609-96625760	NONHSAT015740

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

Extended variants
information (count: 8923 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:8923 , 50 per page) page: 1 2 3 4 5 6 7 ... 179

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1010570	chr10:96446632-96446633	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs79855020	chr10:96446639-96446640	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189077219	chr10:96446688-96446689	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547943633	chr10:96446690-96446691	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116017169	chr10:96446738-96446739	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530085920	chr10:96446739-96446740	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs116337528	chr10:96446741-96446742	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs550846947	chr10:96446742-96446743	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs115110027	chr10:96446749-96446750	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs111810443	chr10:96446783-96446784	Active TSS Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs532083425	chr10:96446870-96446871	Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs552433217	chr10:96446894-96446895	Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs2148552	chr10:96446899-96446900	Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs377416180	chr10:96446917-96446918	Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs565967296	chr10:96446947-96446948	Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs139996619	chr10:96447009-96447010	Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs554292592	chr10:96447100-96447101	Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs181467356	chr10:96447196-96447197	Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs563698410	chr10:96447218-96447219	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs79362265	chr10:96447235-96447236	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs184598934	chr10:96447251-96447252	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs189107757	chr10:96447256-96447257	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs529312809	chr10:96447279-96447280	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs181445839	chr10:96447285-96447286	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs576733156	chr10:96447322-96447323	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs186076273	chr10:96447352-96447353	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs559667945	chr10:96447371-96447372	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs35215359	chr10:96447390-96447391	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs189618219	chr10:96447407-96447408	Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs536859048	chr10:96447465-96447466	Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs141719908	chr10:96447517-96447518	Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs143341184	chr10:96447544-96447545	Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs146239394	chr10:96447551-96447552	Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs202113535	chr10:96447552-96447553	Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs372279673	chr10:96447561-96447562	Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs41291550	chr10:96447562-96447563	Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs375505433	chr10:96447580-96447581	Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs143695270	chr10:96447587-96447588	Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs368264095	chr10:96447597-96447598	Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs372444081	chr10:96447624-96447625	Flanking Active TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs550117143	chr10:96447626-96447627	Flanking Active TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs200398730	chr10:96447641-96447642	Flanking Active TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs145731435	chr10:96447683-96447684	Flanking Active TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs563730614	chr10:96447685-96447686	Flanking Active TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs375456478	chr10:96447691-96447692	Flanking Active TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs576478468	chr10:96447701-96447702	Flanking Active TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs367844838	chr10:96447707-96447708	Flanking Active TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs201140921	chr10:96447715-96447716	Flanking Active TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs199721510	chr10:96447726-96447727	Flanking Active TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs371698646	chr10:96447732-96447733	Flanking Active TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	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:282 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96442400-96447000	Active TSS	Liver	Liver
2	chr10:96443200-96446800	Active TSS	Duodenum Mucosa	Duodenum
3	chr10:96443200-96447200	Active TSS	Stomach Mucosa	stomach
4	chr10:96445200-96449600	Weak transcription	Esophagus	oesophagus
5	chr10:96445200-96449600	Weak transcription	Gastric	stomach
6	chr10:96445600-96446800	Weak transcription	Fetal Intestine Small	intestine
7	chr10:96445800-96447600	Weak transcription	Fetal Intestine Large	intestine
8	chr10:96446800-96447200	Flanking Active TSS	Duodenum Mucosa	Duodenum
9	chr10:96446800-96448000	ZNF genes & repeats	Fetal Intestine Small	intestine
10	chr10:96447000-96447800	Flanking Active TSS	Liver	Liver
11	chr10:96447200-96447400	Enhancers	Duodenum Mucosa	Duodenum
12	chr10:96447200-96504800	Weak transcription	Stomach Mucosa	stomach
13	chr10:96447400-96447800	Genic enhancers	Duodenum Mucosa	Duodenum
14	chr10:96447400-96448000	Enhancers	HepG2	liver
15	chr10:96447600-96449200	Strong transcription	Fetal Intestine Large	intestine
16	chr10:96447800-96448600	Transcr. at gene 5' and 3'	Liver	Liver
17	chr10:96447800-96450000	Strong transcription	Duodenum Mucosa	Duodenum
18	chr10:96448000-96449600	Weak transcription	Fetal Intestine Small	intestine
19	chr10:96448000-96450200	Weak transcription	Small Intestine	intestine
20	chr10:96448600-96449200	Strong transcription	Liver	Liver
21	chr10:96449200-96450000	ZNF genes & repeats	Liver	Liver
22	chr10:96449200-96450000	ZNF genes & repeats	Fetal Intestine Large	intestine
23	chr10:96449600-96449800	ZNF genes & repeats	Esophagus	oesophagus
24	chr10:96449600-96449800	ZNF genes & repeats	Gastric	stomach
25	chr10:96449600-96450000	ZNF genes & repeats	Fetal Intestine Small	intestine
26	chr10:96449800-96455000	Weak transcription	Esophagus	oesophagus
27	chr10:96449800-96456400	Weak transcription	Gastric	stomach
28	chr10:96450000-96450600	Strong transcription	Liver	Liver
29	chr10:96450000-96453000	Weak transcription	Fetal Intestine Small	intestine
30	chr10:96450000-96455200	Weak transcription	Duodenum Mucosa	Duodenum
31	chr10:96450000-96471400	Weak transcription	Fetal Intestine Large	intestine
32	chr10:96450600-96453000	Weak transcription	Liver	Liver
33	chr10:96453000-96453400	ZNF genes & repeats	Fetal Intestine Small	intestine
34	chr10:96453000-96456200	Strong transcription	Liver	Liver
35	chr10:96453400-96455000	Weak transcription	Fetal Intestine Small	intestine
36	chr10:96455000-96455600	ZNF genes & repeats	Esophagus	oesophagus
37	chr10:96455000-96456600	ZNF genes & repeats	Fetal Intestine Small	intestine
38	chr10:96455200-96456200	ZNF genes & repeats	Duodenum Mucosa	Duodenum
39	chr10:96456200-96462800	Weak transcription	Liver	Liver
40	chr10:96456200-96463800	Weak transcription	Duodenum Mucosa	Duodenum
41	chr10:96456600-96462800	Weak transcription	Fetal Intestine Small	intestine
42	chr10:96462800-96463200	ZNF genes & repeats	Fetal Intestine Small	intestine
43	chr10:96462800-96469800	Strong transcription	Liver	Liver
44	chr10:96463200-96465200	Strong transcription	Fetal Intestine Small	intestine
45	chr10:96463800-96468000	Strong transcription	Duodenum Mucosa	Duodenum
46	chr10:96464600-96466000	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr10:96465000-96465600	Enhancers	Colonic Mucosa	Colon
48	chr10:96465200-96467000	Weak transcription	Fetal Intestine Small	intestine
49	chr10:96465400-96465800	Enhancers	Rectal Mucosa Donor 29	rectum
50	chr10:96466000-96466400	Weak transcription	Rectal Mucosa Donor 31	rectum

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