Variant report

Variant	esv3344949
Chromosome Location	chr10:96443874-96666028
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	chr10:96662368-96662780	A549	lung:	n/a	n/a
5	BCL3	chr10:96662227-96662843	A549	lung:	n/a	n/a
6	CEBPB	chr10:96487899-96488178	A549	lung:	n/a	chr10:96488055-96488066
7	CEBPB	chr10:96504015-96504089	HepG2	liver:	n/a	chr10:96504062-96504073
8	CEBPB	chr10:96662344-96662777	Hela-S3	cervix:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
9	CEBPB	chr10:96662406-96662733	MCF-7	breast:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
10	CEBPB	chr10:96485885-96485913	K562	blood:	n/a	n/a
11	CEBPB	chr10:96487903-96488237	HepG2	liver:	n/a	chr10:96488055-96488066
12	CEBPB	chr10:96662475-96662675	IMR90	lung:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
13	CEBPB	chr10:96487954-96488117	H1-hESC	embryonic stem cell:	n/a	chr10:96488055-96488066
14	CEBPB	chr10:96485737-96485940	A549	lung:	n/a	n/a
15	CEBPB	chr10:96664707-96664914	HepG2	liver:	n/a	chr10:96664829-96664840
16	CEBPB	chr10:96662366-96662879	MCF-7	breast:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
17	CEBPB	chr10:96662318-96662764	A549	lung:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
18	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
19	CEBPB	chr10:96581454-96581783	HepG2	liver:	n/a	chr10:96581633-96581644
20	CEBPB	chr10:96543674-96543836	HepG2	liver:	n/a	chr10:96543736-96543747
21	CEBPB	chr10:96581486-96581791	A549	lung:	n/a	chr10:96581633-96581644
22	CEBPB	chr10:96452997-96453294	HepG2	liver:	n/a	chr10:96453142-96453153
23	CEBPB	chr10:96610998-96611149	K562	blood:	n/a	chr10:96611099-96611110
24	CEBPB	chr10:96543674-96543868	A549	lung:	n/a	chr10:96543736-96543747
25	CEBPB	chr10:96487896-96488218	IMR90	lung:	n/a	chr10:96488055-96488066
26	CEBPB	chr10:96662320-96662841	A549	lung:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
27	CEBPB	chr10:96507808-96507867	A549	lung:	n/a	n/a
28	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
29	CEBPB	chr10:96662301-96662799	HepG2	liver:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
30	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
31	CEBPB	chr10:96453074-96453300	K562	blood:	n/a	chr10:96453142-96453153
32	CEBPB	chr10:96610925-96611288	HepG2	liver:	n/a	chr10:96611099-96611110
33	CEBPB	chr10:96610933-96611257	IMR90	lung:	n/a	chr10:96611099-96611110
34	CEBPB	chr10:96485747-96485947	IMR90	lung:	n/a	n/a
35	CEBPB	chr10:96610935-96611206	A549	lung:	n/a	chr10:96611099-96611110
36	CEBPB	chr10:96662174-96662987	A549	lung:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
37	CEBPB	chr10:96662376-96662710	HepG2	liver:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
38	CEBPB	chr10:96662333-96662805	HepG2	liver:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
39	CEBPB	chr10:96662349-96662739	HepG2	liver:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
40	CEBPD	chr10:96662356-96662705	HepG2	liver:	n/a	n/a
41	CTCF	chr10:96639640-96639790	RPTEC	kidney:	n/a	n/a
42	CTCF	chr10:96530820-96530970	HEK293	kidney:	n/a	n/a
43	CTCF	chr10:96639700-96639850	RPTEC	kidney:	n/a	n/a
44	CTCF	chr10:96650440-96650590	MCF-7	breast:	n/a	n/a
45	CTCF	chr10:96639813-96639932	K562	blood:	n/a	n/a
46	CTCF	chr10:96562980-96563130	RPTEC	kidney:	n/a	n/a
47	CTCF	chr10:96660839-96660858	ProgFib	skin:	n/a	n/a
48	CTCF	chr10:96516926-96516994	Medullo	brain:	n/a	n/a
49	CTCF	chr10:96650520-96650670	HEK293	kidney:	n/a	n/a
50	CTCF	chr10:96534991-96535093	GM20000	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:96521152-96521202	GM12892	blood:	n/a
2	chr10:96521152-96521202	SK-N-MC	brain:	n/a
3	chr10:96521152-96521202	GM12892	blood:	n/a
4	chr10:96521152-96521202	SK-N-MC	brain:	n/a
5	chr10:96446783-96446833	HRCEpiC	kidney:	n/a
6	chr10:96521086-96521136	T-47D	breast:	n/a
7	chr10:96523347-96523397	HCF	heart:	n/a
8	chr10:96522433-96522483	HRE	kidney:	n/a
9	chr10:96521152-96521202	PANC-1	pancreas:	n/a
10	chr10:96446783-96446833	PFSK-1	brain:	n/a
11	chr10:96522433-96522483	RPTEC	kidney:	n/a
12	chr10:96521152-96521202	SKMC	muscle:	n/a
13	chr10:96446783-96446833	LNCaP	prostate:	n/a
14	chr10:96523248-96523298	HepG2	liver:	n/a
15	chr10:96522433-96522483	Caco-2	colon:	n/a
16	chr10:96521152-96521202	HCT-116	colon:	n/a
17	chr10:96521086-96521136	AG04449	skin:	fetal
18	chr10:96521152-96521202	SK-N-SH	brain:	n/a
19	chr10:96446783-96446833	IMR90	lung:	fetal
20	chr10:96521152-96521202	LNCaP	prostate:	n/a
21	chr10:96523347-96523397	HEEpiC	esophagus:	n/a
22	chr10:96523347-96523397	HCM	heart:	n/a
23	chr10:96523248-96523298	AG09319	gingival:	n/a
24	chr10:96522433-96522483	HRCEpiC	kidney:	n/a
25	chr10:96523248-96523298	NHDF-neo	bronchial:	n/a
26	chr10:96521152-96521202	GM12891	blood:	n/a
27	chr10:96523248-96523298	MCF-7	breast:	n/a
28	chr10:96447464-96447514	HAEpiC	amniotic membrane:	n/a
29	chr10:96522433-96522483	LNCaP	prostate:	n/a
30	chr10:96523347-96523397	T-47D	breast:	n/a
31	chr10:96523347-96523397	PFSK-1	brain:	n/a
32	chr10:96447464-96447514	GM06990	blood:	n/a
33	chr10:96521086-96521136	ovcar-3	ovarian:	n/a
34	chr10:96522433-96522483	HIPEpiC	eye:	n/a
35	chr10:96521086-96521136	HCPEpiC	choroid plexus:	n/a
36	chr10:96523248-96523298	AG04449	skin:	fetal
37	chr10:96447464-96447514	HCF	heart:	n/a
38	chr10:96521086-96521136	Jurkat	blood:	n/a
39	chr10:96446783-96446833	HIPEpiC	eye:	n/a
40	chr10:96523248-96523298	Caco-2	colon:	n/a
41	chr10:96523347-96523397	HEK293	kidney:	embryo
42	chr10:96523347-96523397	HPAEpiC	pulmonary alveolar:	n/a
43	chr10:96523248-96523298	HEEpiC	esophagus:	n/a
44	chr10:96523347-96523397	K562	blood:	n/a
45	chr10:96523248-96523298	PrEC	prostate:	n/a
46	chr10:96523248-96523298	Hepatocyte	liver:	n/a
47	chr10:96522433-96522483	MCF10A-Er-Src	breast:	n/a
48	chr10:96447464-96447514	HPAEpiC	pulmonary alveolar:	n/a
49	chr10:96521152-96521202	GM06990	blood:	n/a
50	chr10:96523347-96523397	AG04450	lung:	fetal

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

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

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

Extended variants
information (count: 10729 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:10729 , 50 per page) page: 1 2 3 4 5 6 7 ... 215

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533848732	chr10:96443874-96443875	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs570832981	chr10:96443886-96443887	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547257622	chr10:96443887-96443888	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs532971615	chr10:96443897-96443898	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs56194519	chr10:96443908-96443909	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs555659067	chr10:96443915-96443916	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182474845	chr10:96443917-96443918	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs145396926	chr10:96443926-96443927	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565996150	chr10:96443933-96443934	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs538298910	chr10:96443942-96443943	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557883317	chr10:96443952-96443953	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534780066	chr10:96443973-96443974	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs114185568	chr10:96443997-96443998	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs114740046	chr10:96444047-96444048	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560754079	chr10:96444061-96444062	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574327482	chr10:96444069-96444070	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs34147801	chr10:96444175-96444176	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116946966	chr10:96444184-96444185	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563049975	chr10:96444214-96444215	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12774424	chr10:96444249-96444250	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12774426	chr10:96444254-96444255	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531313793	chr10:96444255-96444256	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577946945	chr10:96444270-96444271	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368069572	chr10:96444278-96444279	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570974995	chr10:96444285-96444286	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564746116	chr10:96444319-96444320	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs116414747	chr10:96444379-96444380	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs75038120	chr10:96444395-96444396	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187550913	chr10:96444399-96444400	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs74872019	chr10:96444408-96444409	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567212255	chr10:96444410-96444411	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs57431619	chr10:96444512-96444513	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs549720848	chr10:96444515-96444516	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556429448	chr10:96444565-96444566	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569799961	chr10:96444569-96444570	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs60421813	chr10:96444580-96444581	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs370835468	chr10:96444624-96444625	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558210618	chr10:96444672-96444673	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs377735654	chr10:96444680-96444681	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140684348	chr10:96444740-96444741	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113927077	chr10:96444781-96444782	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141385927	chr10:96444782-96444783	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569530412	chr10:96444785-96444786	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201548197	chr10:96444793-96444794	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200047253	chr10:96444795-96444796	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs59761621	chr10:96444796-96444797	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs559659089	chr10:96444807-96444808	Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs534178235	chr10:96444854-96444855	Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs554554849	chr10:96444934-96444935	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs74615912	chr10:96444979-96444980	Active TSS Flanking Active TSS	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:349 , 50 per page) page: 1 2 3 4 5 6 7

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	chr10:96443600-96444000	Active TSS	Rectal Mucosa Donor 31	rectum
9	chr10:96443600-96444200	Active TSS	Colonic Mucosa	Colon
10	chr10:96444000-96444200	Active TSS	Esophagus	oesophagus
11	chr10:96444000-96444600	Active TSS	Duodenum Smooth Muscle	Duodenum
12	chr10:96444000-96445600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr10:96444600-96444800	Enhancers	Esophagus	oesophagus
14	chr10:96444800-96445000	Flanking Active TSS	Esophagus	oesophagus
15	chr10:96444800-96445200	Active TSS	Gastric	stomach
16	chr10:96445000-96445200	Active TSS	Esophagus	oesophagus
17	chr10:96445200-96449600	Weak transcription	Esophagus	oesophagus
18	chr10:96445200-96449600	Weak transcription	Gastric	stomach
19	chr10:96445400-96445800	ZNF genes & repeats	Fetal Intestine Large	intestine
20	chr10:96445600-96446800	Weak transcription	Fetal Intestine Small	intestine
21	chr10:96445800-96447600	Weak transcription	Fetal Intestine Large	intestine
22	chr10:96446800-96447200	Flanking Active TSS	Duodenum Mucosa	Duodenum
23	chr10:96446800-96448000	ZNF genes & repeats	Fetal Intestine Small	intestine
24	chr10:96447000-96447800	Flanking Active TSS	Liver	Liver
25	chr10:96447200-96447400	Enhancers	Duodenum Mucosa	Duodenum
26	chr10:96447200-96504800	Weak transcription	Stomach Mucosa	stomach
27	chr10:96447400-96447800	Genic enhancers	Duodenum Mucosa	Duodenum
28	chr10:96447400-96448000	Enhancers	HepG2	liver
29	chr10:96447600-96449200	Strong transcription	Fetal Intestine Large	intestine
30	chr10:96447800-96448600	Transcr. at gene 5' and 3'	Liver	Liver
31	chr10:96447800-96450000	Strong transcription	Duodenum Mucosa	Duodenum
32	chr10:96448000-96449600	Weak transcription	Fetal Intestine Small	intestine
33	chr10:96448000-96450200	Weak transcription	Small Intestine	intestine
34	chr10:96448600-96449200	Strong transcription	Liver	Liver
35	chr10:96449200-96450000	ZNF genes & repeats	Liver	Liver
36	chr10:96449200-96450000	ZNF genes & repeats	Fetal Intestine Large	intestine
37	chr10:96449600-96449800	ZNF genes & repeats	Esophagus	oesophagus
38	chr10:96449600-96449800	ZNF genes & repeats	Gastric	stomach
39	chr10:96449600-96450000	ZNF genes & repeats	Fetal Intestine Small	intestine
40	chr10:96449800-96455000	Weak transcription	Esophagus	oesophagus
41	chr10:96449800-96456400	Weak transcription	Gastric	stomach
42	chr10:96450000-96450600	Strong transcription	Liver	Liver
43	chr10:96450000-96453000	Weak transcription	Fetal Intestine Small	intestine
44	chr10:96450000-96455200	Weak transcription	Duodenum Mucosa	Duodenum
45	chr10:96450000-96471400	Weak transcription	Fetal Intestine Large	intestine
46	chr10:96450600-96453000	Weak transcription	Liver	Liver
47	chr10:96453000-96453400	ZNF genes & repeats	Fetal Intestine Small	intestine
48	chr10:96453000-96456200	Strong transcription	Liver	Liver
49	chr10:96453400-96455000	Weak transcription	Fetal Intestine Small	intestine
50	chr10:96455000-96455600	ZNF genes & repeats	Esophagus	oesophagus

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