Variant report

Variant	nsv1040976
Chromosome Location	chr10:96405296-96516804
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	chr10:96440204-96440693	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:96447569-96447764	HepG2	liver:	n/a	n/a
3	ATF1	chr10:96433424-96433649	K562	blood:	n/a	n/a
4	ATF3	chr10:96433388-96433701	HCT-116	colon:	n/a	n/a
5	BCL3	chr10:96440125-96440773	A549	lung:	n/a	n/a
6	BRCA1	chr10:96440359-96440638	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr10:96407816-96408111	H1-hESC	embryonic stem cell:	n/a	chr10:96407961-96407974 chr10:96407963-96407974 chr10:96407961-96407974 chr10:96407961-96407972
8	CEBPB	chr10:96440358-96440615	MCF-7	breast:	n/a	chr10:96440500-96440511
9	CEBPB	chr10:96433362-96433720	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr10:96485737-96485940	A549	lung:	n/a	n/a
11	CEBPB	chr10:96440287-96440606	MCF-7	breast:	n/a	chr10:96440500-96440511
12	CEBPB	chr10:96433387-96433694	HepG2	liver:	n/a	n/a
13	CEBPB	chr10:96436301-96436615	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr10:96426245-96426536	IMR90	lung:	n/a	chr10:96426349-96426360
15	CEBPB	chr10:96487899-96488178	A549	lung:	n/a	chr10:96488055-96488066
16	CEBPB	chr10:96485885-96485913	K562	blood:	n/a	n/a
17	CEBPB	chr10:96433472-96433592	K562	blood:	n/a	n/a
18	CEBPB	chr10:96438272-96438617	A549	lung:	n/a	chr10:96438440-96438451
19	CEBPB	chr10:96487896-96488218	IMR90	lung:	n/a	chr10:96488055-96488066
20	CEBPB	chr10:96487954-96488117	H1-hESC	embryonic stem cell:	n/a	chr10:96488055-96488066
21	CEBPB	chr10:96438271-96438623	HepG2	liver:	n/a	chr10:96438440-96438451
22	CEBPB	chr10:96440255-96440680	Hela-S3	cervix:	n/a	chr10:96440500-96440511
23	CEBPB	chr10:96440251-96440706	A549	lung:	n/a	chr10:96440500-96440511
24	CEBPB	chr10:96426194-96426529	A549	lung:	n/a	chr10:96426349-96426360
25	CEBPB	chr10:96407802-96408115	HepG2	liver:	n/a	chr10:96407961-96407974 chr10:96407963-96407974 chr10:96407961-96407974 chr10:96407961-96407972
26	CEBPB	chr10:96440103-96440886	A549	lung:	n/a	chr10:96440500-96440511
27	CEBPB	chr10:96426220-96426538	HepG2	liver:	n/a	chr10:96426349-96426360
28	CEBPB	chr10:96452997-96453294	HepG2	liver:	n/a	chr10:96453142-96453153
29	CEBPB	chr10:96407836-96408083	A549	lung:	n/a	chr10:96407961-96407974 chr10:96407963-96407974 chr10:96407961-96407974 chr10:96407961-96407972
30	CEBPB	chr10:96507808-96507867	A549	lung:	n/a	n/a
31	CEBPB	chr10:96440242-96440692	HepG2	liver:	n/a	chr10:96440500-96440511
32	CEBPB	chr10:96504015-96504089	HepG2	liver:	n/a	chr10:96504062-96504073
33	CEBPB	chr10:96407891-96408016	K562	blood:	n/a	chr10:96407961-96407974 chr10:96407963-96407974 chr10:96407961-96407974 chr10:96407961-96407972
34	CEBPB	chr10:96438306-96438602	Hela-S3	cervix:	n/a	chr10:96438440-96438451
35	CEBPB	chr10:96440299-96440668	HepG2	liver:	n/a	chr10:96440500-96440511
36	CEBPB	chr10:96440321-96440589	IMR90	lung:	n/a	chr10:96440500-96440511
37	CEBPB	chr10:96437529-96437557	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr10:96433393-96433726	A549	lung:	n/a	n/a
39	CEBPB	chr10:96438283-96438592	IMR90	lung:	n/a	chr10:96438440-96438451
40	CEBPB	chr10:96487903-96488237	HepG2	liver:	n/a	chr10:96488055-96488066
41	CEBPB	chr10:96426231-96426446	H1-hESC	embryonic stem cell:	n/a	chr10:96426349-96426360
42	CEBPB	chr10:96485747-96485947	IMR90	lung:	n/a	n/a
43	CEBPB	chr10:96440269-96440616	HepG2	liver:	n/a	chr10:96440500-96440511
44	CEBPB	chr10:96440328-96440581	HepG2	liver:	n/a	chr10:96440500-96440511
45	CEBPB	chr10:96433429-96433686	IMR90	lung:	n/a	n/a
46	CEBPB	chr10:96453074-96453300	K562	blood:	n/a	chr10:96453142-96453153
47	CEBPB	chr10:96440299-96440699	A549	lung:	n/a	chr10:96440500-96440511
48	CEBPD	chr10:96440299-96440574	HepG2	liver:	n/a	n/a
49	CHD1	chr10:96405418-96405426	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr10:96440311-96440767	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:96442154-96442204	NHDF-neo	bronchial:	n/a
2	chr10:96442154-96442204	NHDF-neo	bronchial:	n/a
3	chr10:96443165-96443215	AG09319	gingival:	n/a
4	chr10:96443071-96443121	BE2_C	brain:	n/a
5	chr10:96442674-96442724	BJ	skin:	n/a
6	chr10:96442154-96442204	NHBE	bronchial:	n/a
7	chr10:96447464-96447514	HAEpiC	amniotic membrane:	n/a
8	chr10:96442031-96442081	GM19239	blood:	n/a
9	chr10:96443195-96443245	HEK293	kidney:	embryo
10	chr10:96446783-96446833	NHBE	bronchial:	n/a
11	chr10:96443195-96443245	MCF10A-Er-Src	breast:	n/a
12	chr10:96443071-96443121	AoSMC	blood vessel:	n/a
13	chr10:96443195-96443245	HCPEpiC	choroid plexus:	n/a
14	chr10:96443165-96443215	HRCEpiC	kidney:	n/a
15	chr10:96446783-96446833	MCF-7	breast:	n/a
16	chr10:96447464-96447514	BJ	skin:	n/a
17	chr10:96446783-96446833	HepG2	liver:	n/a
18	chr10:96442154-96442204	AoSMC	blood vessel:	n/a
19	chr10:96447464-96447514	SKMC	muscle:	n/a
20	chr10:96447464-96447514	HRCEpiC	kidney:	n/a
21	chr10:96442031-96442081	SK-N-SH_RA	brain:	n/a
22	chr10:96446783-96446833	AG04449	skin:	fetal
23	chr10:96442674-96442724	HCF	heart:	n/a
24	chr10:96447464-96447514	Hepatocyte	liver:	n/a
25	chr10:96442154-96442204	GM06990	blood:	n/a
26	chr10:96443165-96443215	Hela-S3	cervix:	n/a
27	chr10:96443165-96443215	AG09309	skin:	n/a
28	chr10:96443071-96443121	ProgFib	skin:	n/a
29	chr10:96443383-96443433	HEEpiC	esophagus:	n/a
30	chr10:96443071-96443121	AG04450	lung:	fetal
31	chr10:96442154-96442204	CMK	blood:	n/a
32	chr10:96443071-96443121	U87	brain:	n/a
33	chr10:96443071-96443121	HRPEpiC	eye:	n/a
34	chr10:96442031-96442081	Jurkat	blood:	n/a
35	chr10:96442674-96442724	A549	lung:	n/a
36	chr10:96443383-96443433	AG04450	lung:	fetal
37	chr10:96442154-96442204	A549	lung:	n/a
38	chr10:96442674-96442724	AG09309	skin:	n/a
39	chr10:96446783-96446833	HL-60	blood:	n/a
40	chr10:96446783-96446833	HEEpiC	esophagus:	n/a
41	chr10:96442031-96442081	HRCEpiC	kidney:	n/a
42	chr10:96442674-96442724	MCF-7	breast:	n/a
43	chr10:96442154-96442204	HIPEpiC	eye:	n/a
44	chr10:96446783-96446833	HCPEpiC	choroid plexus:	n/a
45	chr10:96443383-96443433	HNPCEpiC	eye:	n/a
46	chr10:96442031-96442081	HL-60	blood:	n/a
47	chr10:96442154-96442204	AG10803	skin:	n/a
48	chr10:96443383-96443433	HCT-116	colon:	n/a
49	chr10:96443071-96443121	SAEC	small airway:	n/a
50	chr10:96443383-96443433	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:96429982..96431947-chr10:96435733..96437659,2	K562	blood:
2	chr10:96429982..96431947-chr10:96435733..96437659,2	K562	blood:
3	chr10:96479612..96481874-chr10:96483604..96486212,2	MCF-7	breast:
4	chr10:96479612..96481874-chr10:96483604..96486212,2	MCF-7	breast:

Variant related genes	Relation type
CYP2C18	TF binding region
CYP2C19	TF binding region
CTBP2P2	TF binding region
CYP2C18	CpG island
CYP2C19	CpG island
CTBP2P2	CpG island

Extended variants
information (count: 4273 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:4273 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542702137	chr10:96405299-96405300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs370184721	chr10:96405300-96405301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182469756	chr10:96405304-96405305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147025055	chr10:96405322-96405323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12772169	chr10:96405329-96405330	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
6	rs528479714	chr10:96405336-96405337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138334462	chr10:96405342-96405343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs143913174	chr10:96405356-96405357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531221280	chr10:96405431-96405432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs59510388	chr10:96405478-96405479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs370312697	chr10:96405501-96405502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs12777823	chr10:96405502-96405503	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
13	rs11188046	chr10:96405513-96405514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564338371	chr10:96405515-96405516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532906117	chr10:96405585-96405586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546302186	chr10:96405652-96405653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536822434	chr10:96405655-96405656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs7099346	chr10:96405671-96405672	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs871532	chr10:96405692-96405693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115150159	chr10:96405711-96405712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569089479	chr10:96405730-96405731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs538120339	chr10:96405759-96405760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs374080154	chr10:96405765-96405766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577902537	chr10:96405769-96405770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs74616289	chr10:96405774-96405775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs111261647	chr10:96405806-96405807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575943046	chr10:96405834-96405835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553526308	chr10:96405866-96405867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147280600	chr10:96405868-96405869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs35428261	chr10:96405876-96405877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541893488	chr10:96405885-96405886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562092990	chr10:96405892-96405893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575897260	chr10:96405893-96405894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544491949	chr10:96405932-96405933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564396248	chr10:96405977-96405978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533349072	chr10:96405983-96405984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546765757	chr10:96405998-96405999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs60234155	chr10:96406013-96406014	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs191878568	chr10:96406028-96406029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369660079	chr10:96406051-96406052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs79544495	chr10:96406066-96406067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568832566	chr10:96406074-96406075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs117215113	chr10:96406092-96406093	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
44	rs374623266	chr10:96406108-96406109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184786582	chr10:96406112-96406113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148660949	chr10:96406113-96406114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141241025	chr10:96406122-96406123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574110584	chr10:96406124-96406125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553993391	chr10:96406147-96406148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs74150870	chr10:96406166-96406167	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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
Pancreatic cancer	17952125	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oligozoospermia	20877625	CNVD

Chromatin state (count:230 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96400400-96407200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr10:96404200-96405800	Enhancers	GM12878-XiMat	blood
3	chr10:96407200-96407400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr10:96407400-96413000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr10:96411400-96412000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr10:96422200-96423800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr10:96422600-96423000	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr10:96422600-96423400	Enhancers	H1 Cell Line	embryonic stem cell
9	chr10:96422600-96423600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr10:96422600-96423800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr10:96422800-96423600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr10:96422800-96423800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr10:96422800-96423800	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr10:96423000-96423200	Enhancers	Gastric	stomach
15	chr10:96423000-96423400	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr10:96423000-96424000	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr10:96423200-96423600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr10:96423200-96424200	Weak transcription	Gastric	stomach
19	chr10:96423400-96423600	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr10:96423400-96423800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr10:96423400-96424000	Enhancers	Stomach Mucosa	stomach
22	chr10:96423600-96426200	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr10:96423800-96424200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr10:96424000-96426200	Weak transcription	Stomach Mucosa	stomach
25	chr10:96424200-96424400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr10:96424200-96424600	Enhancers	Gastric	stomach
27	chr10:96424400-96424600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr10:96424600-96424800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr10:96424600-96434200	Weak transcription	Gastric	stomach
30	chr10:96426000-96426600	Enhancers	Fetal Intestine Large	intestine
31	chr10:96426200-96426400	Enhancers	Duodenum Mucosa	Duodenum
32	chr10:96426200-96426600	Enhancers	Fetal Intestine Small	intestine
33	chr10:96426200-96426800	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr10:96426200-96426800	Enhancers	Stomach Mucosa	stomach
35	chr10:96426200-96433400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr10:96426800-96430400	Weak transcription	Stomach Mucosa	stomach
37	chr10:96430400-96431800	Enhancers	Stomach Mucosa	stomach
38	chr10:96431800-96433400	Weak transcription	Stomach Mucosa	stomach
39	chr10:96433400-96433800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr10:96433400-96438200	Enhancers	Stomach Mucosa	stomach
41	chr10:96433800-96434000	Enhancers	Fetal Intestine Small	intestine
42	chr10:96434000-96436400	Weak transcription	Fetal Intestine Small	intestine
43	chr10:96434200-96434400	Enhancers	Gastric	stomach
44	chr10:96434400-96435000	Weak transcription	Gastric	stomach
45	chr10:96435000-96435200	Enhancers	Gastric	stomach
46	chr10:96435200-96444800	Weak transcription	Gastric	stomach
47	chr10:96435800-96439600	Enhancers	Liver	Liver
48	chr10:96436000-96443400	Enhancers	Fetal Intestine Large	intestine
49	chr10:96436200-96436400	Enhancers	Rectal Mucosa Donor 29	rectum
50	chr10:96436400-96436600	Enhancers	Small Intestine	intestine

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