Variant report

Variant	esv3380017
Chromosome Location	chr10:96439904-96662339
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	ARID3A	chr10:96440204-96440693	HepG2	liver:	n/a	n/a
4	ATF3	chr10:96662325-96662813	A549	lung:	n/a	n/a
5	BCL3	chr10:96662227-96662843	A549	lung:	n/a	n/a
6	BCL3	chr10:96440125-96440773	A549	lung:	n/a	n/a
7	BRCA1	chr10:96440359-96440638	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr10:96581486-96581791	A549	lung:	n/a	chr10:96581633-96581644
9	CEBPB	chr10:96485747-96485947	IMR90	lung:	n/a	n/a
10	CEBPB	chr10:96662320-96662841	A549	lung:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
11	CEBPB	chr10:96452997-96453294	HepG2	liver:	n/a	chr10:96453142-96453153
12	CEBPB	chr10:96485737-96485940	A549	lung:	n/a	n/a
13	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
14	CEBPB	chr10:96662333-96662805	HepG2	liver:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
15	CEBPB	chr10:96485885-96485913	K562	blood:	n/a	n/a
16	CEBPB	chr10:96662301-96662799	HepG2	liver:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
17	CEBPB	chr10:96610998-96611149	K562	blood:	n/a	chr10:96611099-96611110
18	CEBPB	chr10:96440255-96440680	Hela-S3	cervix:	n/a	chr10:96440500-96440511
19	CEBPB	chr10:96440328-96440581	HepG2	liver:	n/a	chr10:96440500-96440511
20	CEBPB	chr10:96543674-96543868	A549	lung:	n/a	chr10:96543736-96543747
21	CEBPB	chr10:96487903-96488237	HepG2	liver:	n/a	chr10:96488055-96488066
22	CEBPB	chr10:96440299-96440668	HepG2	liver:	n/a	chr10:96440500-96440511
23	CEBPB	chr10:96662174-96662987	A549	lung:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
24	CEBPB	chr10:96440299-96440699	A549	lung:	n/a	chr10:96440500-96440511
25	CEBPB	chr10:96440269-96440616	HepG2	liver:	n/a	chr10:96440500-96440511
26	CEBPB	chr10:96453074-96453300	K562	blood:	n/a	chr10:96453142-96453153
27	CEBPB	chr10:96662318-96662764	A549	lung:	n/a	chr10:96662487-96662500 chr10:96662487-96662498
28	CEBPB	chr10:96440358-96440615	MCF-7	breast:	n/a	chr10:96440500-96440511
29	CEBPB	chr10:96487954-96488117	H1-hESC	embryonic stem cell:	n/a	chr10:96488055-96488066
30	CEBPB	chr10:96504015-96504089	HepG2	liver:	n/a	chr10:96504062-96504073
31	CEBPB	chr10:96440242-96440692	HepG2	liver:	n/a	chr10:96440500-96440511
32	CEBPB	chr10:96440321-96440589	IMR90	lung:	n/a	chr10:96440500-96440511
33	CEBPB	chr10:96440287-96440606	MCF-7	breast:	n/a	chr10:96440500-96440511
34	CEBPB	chr10:96610925-96611288	HepG2	liver:	n/a	chr10:96611099-96611110
35	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
36	CEBPB	chr10:96487896-96488218	IMR90	lung:	n/a	chr10:96488055-96488066
37	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
38	CEBPB	chr10:96487899-96488178	A549	lung:	n/a	chr10:96488055-96488066
39	CEBPB	chr10:96440251-96440706	A549	lung:	n/a	chr10:96440500-96440511
40	CEBPB	chr10:96610935-96611206	A549	lung:	n/a	chr10:96611099-96611110
41	CEBPB	chr10:96543674-96543836	HepG2	liver:	n/a	chr10:96543736-96543747
42	CEBPB	chr10:96440103-96440886	A549	lung:	n/a	chr10:96440500-96440511
43	CEBPB	chr10:96610933-96611257	IMR90	lung:	n/a	chr10:96611099-96611110
44	CEBPB	chr10:96507808-96507867	A549	lung:	n/a	n/a
45	CEBPB	chr10:96581454-96581783	HepG2	liver:	n/a	chr10:96581633-96581644
46	CEBPD	chr10:96440299-96440574	HepG2	liver:	n/a	n/a
47	CREB1	chr10:96440361-96440702	HepG2	liver:	n/a	n/a
48	CREB1	chr10:96440311-96440767	HepG2	liver:	n/a	n/a
49	CTCF	chr10:96562980-96563130	RPTEC	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	chr10:96443383-96443433	HL-60	blood:	n/a
2	chr10:96442674-96442724	HEEpiC	esophagus:	n/a
3	chr10:96447464-96447514	T-47D	breast:	n/a
4	chr10:96443383-96443433	HL-60	blood:	n/a
5	chr10:96442674-96442724	HEEpiC	esophagus:	n/a
6	chr10:96447464-96447514	T-47D	breast:	n/a
7	chr10:96523248-96523298	Hela-S3	cervix:	n/a
8	chr10:96443071-96443121	Hepatocyte	liver:	n/a
9	chr10:96447464-96447514	HAEpiC	amniotic membrane:	n/a
10	chr10:96442031-96442081	HCPEpiC	choroid plexus:	n/a
11	chr10:96443195-96443245	AG04449	skin:	fetal
12	chr10:96447464-96447514	MCF10A-Er-Src	breast:	n/a
13	chr10:96442031-96442081	SK-N-SH_RA	brain:	n/a
14	chr10:96443165-96443215	HPAEpiC	pulmonary alveolar:	n/a
15	chr10:96442154-96442204	LNCaP	prostate:	n/a
16	chr10:96442154-96442204	NHDF-neo	bronchial:	n/a
17	chr10:96446783-96446833	NB4	blood:	n/a
18	chr10:96443383-96443433	SKMC	muscle:	n/a
19	chr10:96446783-96446833	K562	blood:	n/a
20	chr10:96443195-96443245	NHDF-neo	bronchial:	n/a
21	chr10:96442154-96442204	AG09319	gingival:	n/a
22	chr10:96442031-96442081	HNPCEpiC	eye:	n/a
23	chr10:96521086-96521136	GM12892	blood:	n/a
24	chr10:96443195-96443245	AG04450	lung:	fetal
25	chr10:96521086-96521136	Hepatocyte	liver:	n/a
26	chr10:96522433-96522483	ECC-1	luminal epithelium:	n/a
27	chr10:96446783-96446833	LNCaP	prostate:	n/a
28	chr10:96447464-96447514	ovcar-3	ovarian:	n/a
29	chr10:96522433-96522483	HCPEpiC	choroid plexus:	n/a
30	chr10:96443383-96443433	MCF10A-Er-Src	breast:	n/a
31	chr10:96443383-96443433	NH-A	brain:	n/a
32	chr10:96446783-96446833	NH-A	brain:	n/a
33	chr10:96443165-96443215	PANC-1	pancreas:	n/a
34	chr10:96521086-96521136	HCF	heart:	n/a
35	chr10:96443383-96443433	HRPEpiC	eye:	n/a
36	chr10:96442154-96442204	PrEC	prostate:	n/a
37	chr10:96523248-96523298	HIPEpiC	eye:	n/a
38	chr10:96446783-96446833	HNPCEpiC	eye:	n/a
39	chr10:96443383-96443433	NB4	blood:	n/a
40	chr10:96447464-96447514	Hepatocyte	liver:	n/a
41	chr10:96521086-96521136	NH-A	brain:	n/a
42	chr10:96447464-96447514	HPAEpiC	pulmonary alveolar:	n/a
43	chr10:96442674-96442724	GM06990	blood:	n/a
44	chr10:96521086-96521136	HEEpiC	esophagus:	n/a
45	chr10:96523248-96523298	HAEpiC	amniotic membrane:	n/a
46	chr10:96523347-96523397	NHDF-neo	bronchial:	n/a
47	chr10:96442031-96442081	HCT-116	colon:	n/a
48	chr10:96446783-96446833	IMR90	lung:	fetal
49	chr10:96442154-96442204	Caco-2	colon:	n/a
50	chr10:96446783-96446833	GM12892	blood:	n/a

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	chr10:96632715-96632886	NONHSAT015740
2	lnc-CYP2C8-4	chr10:96625946-96626096	NONHSAT015740
3	lnc-CYP2C8-4	chr10:96625609-96625760	NONHSAT015740
4	lnc-CYP2C19-1	chr10:96642311-96643100	NONHSAT015741

Variant related genes	Relation type
CYP2C58P	TF binding region
ENSG00000225354	TF binding region
MTND4P19	TF binding region
CYP2C18	TF binding region
CYP2C19	TF binding region
CYP2C58P	CpG island
ENSG00000225354	CpG island
MTND4P19	CpG island
CYP2C18	CpG island
CYP2C19	CpG island

Extended variants
information (count: 10701 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:10701 , 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	rs148083509	chr10:96439935-96439936	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs76232438	chr10:96439968-96439969	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs80025016	chr10:96439981-96439982	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559028897	chr10:96439982-96439983	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566362997	chr10:96440010-96440011	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs182709814	chr10:96440067-96440068	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs188074017	chr10:96440070-96440071	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs201074789	chr10:96440104-96440105	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs148253206	chr10:96440108-96440109	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs375329525	chr10:96440110-96440111	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs201616369	chr10:96440111-96440112	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs574658386	chr10:96440123-96440124	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs568694337	chr10:96440153-96440154	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs543135878	chr10:96440181-96440182	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs556998160	chr10:96440211-96440212	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs576796915	chr10:96440223-96440224	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs114389831	chr10:96440331-96440332	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs192682543	chr10:96440492-96440493	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs573177512	chr10:96440568-96440569	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs59080023	chr10:96440595-96440596	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs375171081	chr10:96440606-96440607	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs530694322	chr10:96440614-96440615	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs550324114	chr10:96440712-96440713	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs563796056	chr10:96440779-96440780	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs532451100	chr10:96440792-96440793	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs532009839	chr10:96440911-96440912	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs150621289	chr10:96440946-96440947	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs140771115	chr10:96441053-96441054	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs75404862	chr10:96441082-96441083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
30	rs548445697	chr10:96441183-96441184	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs568307885	chr10:96441192-96441193	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs537230671	chr10:96441260-96441261	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs185430088	chr10:96441274-96441275	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs188291911	chr10:96441278-96441279	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs717238	chr10:96441300-96441301	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs147403219	chr10:96441319-96441320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572840101	chr10:96441360-96441361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542164848	chr10:96441392-96441393	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs397844695	chr10:96441424-96441425	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs561940423	chr10:96441504-96441505	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs575552861	chr10:96441514-96441515	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs192592307	chr10:96441526-96441527	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs564081332	chr10:96441556-96441557	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs142661740	chr10:96441585-96441586	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs184586182	chr10:96441596-96441597	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs188202788	chr10:96441646-96441647	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs10736086	chr10:96441650-96441651	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs528447882	chr10:96441676-96441677	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs548507659	chr10:96441697-96441698	Flanking Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs371150771	chr10:96441729-96441730	Flanking Active TSS Enhancers Weak transcription	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:375 , 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	chr10:96436000-96443400	Enhancers	Fetal Intestine Large	intestine
3	chr10:96436400-96442000	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr10:96437800-96440200	Weak transcription	Hela-S3	cervix
5	chr10:96439200-96440000	Enhancers	Stomach Mucosa	stomach
6	chr10:96439600-96440200	Flanking Active TSS	Liver	Liver
7	chr10:96439600-96440200	Enhancers	Duodenum Mucosa	Duodenum
8	chr10:96439600-96442800	Enhancers	HepG2	liver
9	chr10:96439600-96443200	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr10:96439800-96440000	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr10:96439800-96440000	Enhancers	Small Intestine	intestine
12	chr10:96439800-96440200	Flanking Active TSS	Fetal Intestine Small	intestine
13	chr10:96439800-96440600	Enhancers	Fetal Kidney	kidney
14	chr10:96439800-96440800	Flanking Active TSS	A549	lung
15	chr10:96440000-96442000	Weak transcription	Stomach Mucosa	stomach
16	chr10:96440200-96440600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr10:96440200-96440800	Enhancers	Hela-S3	cervix
18	chr10:96440200-96441600	Enhancers	Liver	Liver
19	chr10:96440200-96442200	Weak transcription	Duodenum Mucosa	Duodenum
20	chr10:96440200-96443200	Enhancers	Fetal Intestine Small	intestine
21	chr10:96440800-96442600	Enhancers	A549	lung
22	chr10:96441600-96442000	Flanking Active TSS	Liver	Liver
23	chr10:96441600-96443400	Enhancers	Colonic Mucosa	Colon
24	chr10:96442000-96442200	Active TSS	Liver	Liver
25	chr10:96442000-96443200	Enhancers	Rectal Mucosa Donor 29	rectum
26	chr10:96442000-96443200	Enhancers	Stomach Mucosa	stomach
27	chr10:96442200-96442400	Flanking Active TSS	Liver	Liver
28	chr10:96442200-96443000	Enhancers	Duodenum Mucosa	Duodenum
29	chr10:96442200-96443200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr10:96442400-96442600	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr10:96442400-96442600	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr10:96442400-96443000	Enhancers	Adipose Nuclei	Adipose
33	chr10:96442400-96447000	Active TSS	Liver	Liver
34	chr10:96442800-96443600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr10:96443000-96443200	Flanking Active TSS	Duodenum Mucosa	Duodenum
36	chr10:96443000-96443400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr10:96443000-96443400	Enhancers	NHEK	skin
38	chr10:96443000-96443600	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr10:96443200-96443400	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr10:96443200-96443400	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr10:96443200-96443400	Flanking Active TSS	Fetal Intestine Small	intestine
42	chr10:96443200-96443600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
43	chr10:96443200-96446800	Active TSS	Duodenum Mucosa	Duodenum
44	chr10:96443200-96447200	Active TSS	Stomach Mucosa	stomach
45	chr10:96443400-96443600	Weak transcription	Colonic Mucosa	Colon
46	chr10:96443400-96445000	Active TSS	Fetal Stomach	stomach
47	chr10:96443400-96445400	Active TSS	Fetal Intestine Large	intestine
48	chr10:96443400-96445600	Active TSS	Fetal Intestine Small	intestine
49	chr10:96443600-96444000	Active TSS	Rectal Mucosa Donor 31	rectum
50	chr10:96443600-96444200	Active TSS	Colonic Mucosa	Colon

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