Variant report

Variant	esv3336672
Chromosome Location	chr10:96543010-96711519
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	ATF3	chr10:96662325-96662813	A549	lung:	n/a	n/a
3	BCL3	chr10:96662368-96662780	A549	lung:	n/a	n/a
4	BCL3	chr10:96662227-96662843	A549	lung:	n/a	n/a
5	CBX3	chr10:96703425-96703936	HCT-116	colon:	n/a	n/a
6	CBX3	chr10:96703538-96703819	K562	blood:	n/a	n/a
7	CEBPB	chr10:96687947-96687969	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr10:96581486-96581791	A549	lung:	n/a	chr10:96581633-96581644
9	CEBPB	chr10:96610935-96611206	A549	lung:	n/a	chr10:96611099-96611110
10	CEBPB	chr10:96662406-96662733	MCF-7	breast:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
11	CEBPB	chr10:96685700-96685775	HepG2	liver:	n/a	chr10:96685750-96685761
12	CEBPB	chr10:96662320-96662841	A549	lung:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
13	CEBPB	chr10:96543674-96543836	HepG2	liver:	n/a	chr10:96543736-96543747
14	CEBPB	chr10:96685653-96685786	IMR90	lung:	n/a	chr10:96685750-96685761
15	CEBPB	chr10:96662174-96662987	A549	lung:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
16	CEBPB	chr10:96662344-96662777	Hela-S3	cervix:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
17	CEBPB	chr10:96697192-96697397	IMR90	lung:	n/a	n/a
18	CEBPB	chr10:96696670-96696759	A549	lung:	n/a	chr10:96696690-96696699 chr10:96696690-96696699
19	CEBPB	chr10:96697196-96697461	A549	lung:	n/a	n/a
20	CEBPB	chr10:96610925-96611288	HepG2	liver:	n/a	chr10:96611099-96611110
21	CEBPB	chr10:96662318-96662764	A549	lung:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
22	CEBPB	chr10:96662366-96662879	MCF-7	breast:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
23	CEBPB	chr10:96662376-96662710	HepG2	liver:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
24	CEBPB	chr10:96664707-96664914	HepG2	liver:	n/a	chr10:96664829-96664840
25	CEBPB	chr10:96581454-96581783	HepG2	liver:	n/a	chr10:96581633-96581644
26	CEBPB	chr10:96685708-96685784	A549	lung:	n/a	chr10:96685750-96685761
27	CEBPB	chr10:96662333-96662805	HepG2	liver:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
28	CEBPB	chr10:96662475-96662675	IMR90	lung:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
29	CEBPB	chr10:96662349-96662739	HepG2	liver:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
30	CEBPB	chr10:96662301-96662799	HepG2	liver:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
31	CEBPB	chr10:96610998-96611149	K562	blood:	n/a	chr10:96611099-96611110
32	CEBPB	chr10:96543674-96543868	A549	lung:	n/a	chr10:96543736-96543747
33	CEBPB	chr10:96610933-96611257	IMR90	lung:	n/a	chr10:96611099-96611110
34	CEBPD	chr10:96662356-96662705	HepG2	liver:	n/a	n/a
35	CTCF	chr10:96650520-96650670	HEK293	kidney:	n/a	n/a
36	CTCF	chr10:96687367-96687423	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr10:96698280-96698430	NHLF	lung:	n/a	n/a
38	CTCF	chr10:96650523-96650622	GM12878	blood:	n/a	n/a
39	CTCF	chr10:96562980-96563130	RPTEC	kidney:	n/a	n/a
40	CTCF	chr10:96639700-96639850	RPTEC	kidney:	n/a	n/a
41	CTCF	chr10:96696732-96696792	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr10:96650517-96650640	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr10:96639691-96639881	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr10:96650487-96650634	MCF-7	breast:	n/a	n/a
45	CTCF	chr10:96639300-96639450	RPTEC	kidney:	n/a	n/a
46	CTCF	chr10:96563080-96563230	RPTEC	kidney:	n/a	n/a
47	CTCF	chr10:96650518-96650626	A549	lung:	n/a	n/a
48	CTCF	chr10:96704959-96705046	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr10:96650415-96650676	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr10:96650440-96650590	Caco-2	colon:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:96698366-96698416	GM12891	blood:	n/a
2	chr10:96698366-96698416	MCF10A-Er-Src	breast:	n/a
3	chr10:96698366-96698416	SK-N-SH	brain:	n/a
4	chr10:96698366-96698416	PFSK-1	brain:	n/a
5	chr10:96697436-96697486	RPTEC	kidney:	n/a
6	chr10:96698366-96698416	K562	blood:	n/a
7	chr10:96697436-96697486	T-47D	breast:	n/a
8	chr10:96698366-96698416	A549	lung:	n/a
9	chr10:96697436-96697486	HNPCEpiC	eye:	n/a
10	chr10:96698366-96698416	AG04450	lung:	fetal
11	chr10:96698366-96698416	HEEpiC	esophagus:	n/a
12	chr10:96698366-96698416	RPTEC	kidney:	n/a
13	chr10:96697436-96697486	HPAEpiC	pulmonary alveolar:	n/a
14	chr10:96698366-96698416	AoSMC	blood vessel:	n/a
15	chr10:96697436-96697486	Hepatocyte	liver:	n/a
16	chr10:96698366-96698416	SKMC	muscle:	n/a
17	chr10:96697436-96697486	Jurkat	blood:	n/a
18	chr10:96697436-96697486	GM19239	blood:	n/a
19	chr10:96697436-96697486	HL-60	blood:	n/a
20	chr10:96698366-96698416	T-47D	breast:	n/a
21	chr10:96698366-96698416	H1-hESC	embryonic stem cell:	embryo
22	chr10:96697436-96697486	GM12878	blood:	n/a
23	chr10:96697436-96697486	PANC-1	pancreas:	n/a
24	chr10:96697436-96697486	AG04449	skin:	fetal
25	chr10:96698366-96698416	BE2_C	brain:	n/a
26	chr10:96698366-96698416	ECC-1	luminal epithelium:	n/a
27	chr10:96698366-96698416	AG04449	skin:	fetal
28	chr10:96698366-96698416	HUVEC	blood vessel:	n/a
29	chr10:96698366-96698416	HNPCEpiC	eye:	n/a
30	chr10:96698366-96698416	NHBE	bronchial:	n/a
31	chr10:96698366-96698416	ProgFib	skin:	n/a
32	chr10:96697436-96697486	NHBE	bronchial:	n/a
33	chr10:96698366-96698416	HCM	heart:	n/a
34	chr10:96697436-96697486	LNCaP	prostate:	n/a
35	chr10:96698366-96698416	HRPEpiC	eye:	n/a
36	chr10:96697436-96697486	HAEpiC	amniotic membrane:	n/a
37	chr10:96697436-96697486	HCM	heart:	n/a
38	chr10:96697436-96697486	SKMC	muscle:	n/a
39	chr10:96698366-96698416	HepG2	liver:	n/a
40	chr10:96697436-96697486	AG10803	skin:	n/a
41	chr10:96698366-96698416	HCT-116	colon:	n/a
42	chr10:96697436-96697486	NH-A	brain:	n/a
43	chr10:96698366-96698416	MCF-7	breast:	n/a
44	chr10:96697436-96697486	HCT-116	colon:	n/a
45	chr10:96698366-96698416	ovcar-3	ovarian:	n/a
46	chr10:96697436-96697486	SK-N-SH_RA	brain:	n/a
47	chr10:96697436-96697486	HEK293	kidney:	embryo
48	chr10:96698366-96698416	AG10803	skin:	n/a
49	chr10:96698366-96698416	HRE	kidney:	n/a
50	chr10:96697436-96697486	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:96644256..96646461-chr10:96648799..96651515,2	K562	blood:
2	chr10:96644256..96646461-chr10:96648799..96651515,2	K562	blood:

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

Variant related genes	Relation type
CYP2C9	TF binding region
CYP2C58P	TF binding region
MTND4P20	TF binding region
ENSG00000225354	TF binding region
CYP2C9	CpG island
CYP2C58P	CpG island
MTND4P20	CpG island
ENSG00000225354	CpG island

Extended variants
information (count: 7945 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:7945 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372034589	chr10:96543054-96543055	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs535997114	chr10:96543104-96543105	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555599929	chr10:96543106-96543107	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575538876	chr10:96543132-96543133	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544503798	chr10:96543252-96543253	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558049120	chr10:96543253-96543254	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577539576	chr10:96543255-96543256	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149235482	chr10:96543257-96543258	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186726257	chr10:96543288-96543289	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528952221	chr10:96543297-96543298	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542340772	chr10:96543301-96543302	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561928407	chr10:96543304-96543305	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376753877	chr10:96543313-96543314	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568888761	chr10:96543318-96543319	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191118873	chr10:96543374-96543375	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552950763	chr10:96543375-96543376	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369887474	chr10:96543388-96543389	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577324078	chr10:96543406-96543407	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531569515	chr10:96543426-96543427	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183782144	chr10:96543505-96543506	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146191614	chr10:96543521-96543522	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548192452	chr10:96543551-96543552	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188269722	chr10:96543562-96543563	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566919798	chr10:96543572-96543573	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535933212	chr10:96543596-96543597	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369464084	chr10:96543649-96543650	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs534225643	chr10:96543651-96543652	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs115159754	chr10:96543661-96543662	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574304273	chr10:96543670-96543671	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538066975	chr10:96543684-96543685	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560332387	chr10:96543719-96543720	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs139198915	chr10:96543731-96543732	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs80259168	chr10:96543753-96543754	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
34	rs192325147	chr10:96543754-96543755	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569966929	chr10:96543759-96543760	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183068024	chr10:96543782-96543783	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187746182	chr10:96543783-96543784	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35390752	chr10:96543823-96543824	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs562263433	chr10:96543824-96543825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530961624	chr10:96543826-96543827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369839143	chr10:96543830-96543831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144067211	chr10:96543831-96543832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561464260	chr10:96543865-96543866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191442080	chr10:96543879-96543880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371038548	chr10:96543886-96543887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547008423	chr10:96543947-96543948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566858774	chr10:96543976-96543977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs55734964	chr10:96543992-96543993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs397731667	chr10:96543997-96543998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529323219	chr10:96544056-96544057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	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:205 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96533000-96564600	Weak transcription	Gastric	stomach
2	chr10:96538000-96553400	Weak transcription	Fetal Intestine Small	intestine
3	chr10:96538200-96543800	Strong transcription	Liver	Liver
4	chr10:96540800-96547800	Weak transcription	Duodenum Mucosa	Duodenum
5	chr10:96542200-96545400	Weak transcription	Fetal Intestine Large	intestine
6	chr10:96543800-96545200	Weak transcription	Liver	Liver
7	chr10:96545200-96549400	Strong transcription	Liver	Liver
8	chr10:96545400-96546000	Strong transcription	Fetal Intestine Large	intestine
9	chr10:96546000-96553600	Weak transcription	Fetal Intestine Large	intestine
10	chr10:96547800-96548600	Strong transcription	Duodenum Mucosa	Duodenum
11	chr10:96548600-96552800	Weak transcription	Duodenum Mucosa	Duodenum
12	chr10:96549400-96550200	Weak transcription	Liver	Liver
13	chr10:96550200-96550400	Strong transcription	Liver	Liver
14	chr10:96550400-96552000	Weak transcription	Liver	Liver
15	chr10:96552000-96554600	Strong transcription	Liver	Liver
16	chr10:96552800-96554200	Strong transcription	Duodenum Mucosa	Duodenum
17	chr10:96553400-96554200	ZNF genes & repeats	Fetal Intestine Small	intestine
18	chr10:96553600-96554200	ZNF genes & repeats	Fetal Intestine Large	intestine
19	chr10:96554200-96560000	Weak transcription	Duodenum Mucosa	Duodenum
20	chr10:96554200-96560000	Weak transcription	Fetal Intestine Small	intestine
21	chr10:96554200-96560400	Weak transcription	Fetal Intestine Large	intestine
22	chr10:96554600-96560000	Weak transcription	Liver	Liver
23	chr10:96560000-96560800	Genic enhancers	Liver	Liver
24	chr10:96560000-96561200	ZNF genes & repeats	Fetal Intestine Small	intestine
25	chr10:96560000-96562200	Strong transcription	Duodenum Mucosa	Duodenum
26	chr10:96560400-96564600	Strong transcription	Fetal Intestine Large	intestine
27	chr10:96560800-96566200	Strong transcription	Liver	Liver
28	chr10:96561600-96562000	ZNF genes & repeats	Fetal Intestine Small	intestine
29	chr10:96562000-96563200	Weak transcription	Fetal Intestine Small	intestine
30	chr10:96562200-96563000	Weak transcription	Duodenum Mucosa	Duodenum
31	chr10:96563000-96564400	Strong transcription	Duodenum Mucosa	Duodenum
32	chr10:96563200-96563600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr10:96563200-96563800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr10:96563200-96564400	Strong transcription	Fetal Intestine Small	intestine
35	chr10:96564400-96565400	Weak transcription	Fetal Intestine Small	intestine
36	chr10:96564400-96565600	Weak transcription	Duodenum Mucosa	Duodenum
37	chr10:96564600-96565400	Weak transcription	Fetal Intestine Large	intestine
38	chr10:96565400-96565800	Strong transcription	Fetal Intestine Large	intestine
39	chr10:96565400-96565800	ZNF genes & repeats	Fetal Intestine Small	intestine
40	chr10:96565600-96565800	Strong transcription	Duodenum Mucosa	Duodenum
41	chr10:96565800-96566000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
42	chr10:96565800-96569800	Weak transcription	Fetal Intestine Small	intestine
43	chr10:96565800-96581600	Weak transcription	Fetal Intestine Large	intestine
44	chr10:96566000-96580200	Weak transcription	Duodenum Mucosa	Duodenum
45	chr10:96566200-96580200	Weak transcription	Liver	Liver
46	chr10:96569800-96570000	ZNF genes & repeats	Fetal Intestine Small	intestine
47	chr10:96570400-96570800	Weak transcription	Fetal Intestine Small	intestine
48	chr10:96577000-96580200	Weak transcription	Fetal Intestine Small	intestine
49	chr10:96580200-96581000	ZNF genes & repeats	Fetal Intestine Small	intestine
50	chr10:96580200-96581600	Strong transcription	Liver	Liver

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