Variant report

Variant	nsv876014
Chromosome Location	chr2:234495742-234545861
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:149)
CpG islands
(count:550)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:149 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:234500843-234501043	K562	blood:	n/a	n/a
2	ATF2	chr2:234501691-234502188	GM12878	blood:	n/a	n/a
3	BATF	chr2:234501769-234502305	GM12878	blood:	n/a	n/a
4	BATF	chr2:234501781-234502299	GM12878	blood:	n/a	n/a
5	BATF	chr2:234495601-234495908	GM12878	blood:	n/a	n/a
6	BATF	chr2:234495653-234495913	GM12878	blood:	n/a	n/a
7	BCL11A	chr2:234501828-234502266	GM12878	blood:	n/a	n/a
8	BCL11A	chr2:234501789-234502263	GM12878	blood:	n/a	n/a
9	BCLAF1	chr2:234501832-234502192	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:234501879-234502256	GM12878	blood:	n/a	n/a
11	CCNT2	chr2:234509214-234509461	K562	blood:	n/a	n/a
12	CEBPB	chr2:234521112-234521181	IMR90	lung:	n/a	n/a
13	CEBPB	chr2:234512344-234512544	HepG2	liver:	n/a	n/a
14	CHD2	chr2:234501976-234502223	GM12878	blood:	n/a	n/a
15	CTCF	chr2:234504160-234504310	GM12871	blood:	n/a	n/a
16	CTCF	chr2:234518152-234518168	K562	blood:	n/a	n/a
17	CTCF	chr2:234545228-234545302	NHEK	skin:	n/a	n/a
18	CTCF	chr2:234504308-234504457	K562	blood:	n/a	n/a
19	CTCF	chr2:234504280-234504430	GM12866	blood:	n/a	n/a
20	CTCF	chr2:234516850-234516892	GM19240	blood:	n/a	n/a
21	CTCF	chr2:234504381-234504401	GM19238	blood:	n/a	n/a
22	CTCF	chr2:234500410-234500464	Kidney_OC	kidney:	n/a	n/a
23	CTCF	chr2:234516827-234516916	GM12892	blood:	n/a	n/a
24	CTCF	chr2:234545031-234545104	Pancreas_OC	pancreas:	n/a	n/a
25	CTCF	chr2:234512274-234512347	GM13976	blood:	n/a	n/a
26	CTCF	chr2:234516851-234516858	GM12878	blood:	n/a	n/a
27	CTCF	chr2:234523993-234524038	GM13977	blood:	n/a	n/a
28	CTCF	chr2:234504337-234504433	GM19240	blood:	n/a	n/a
29	CTCF	chr2:234504335-234504429	K562	blood:	n/a	n/a
30	CTCF	chr2:234505920-234506070	GM12867	blood:	n/a	n/a
31	CTCF	chr2:234504320-234504470	GM12865	blood:	n/a	n/a
32	CTCF	chr2:234516843-234516899	GM19239	blood:	n/a	n/a
33	CTCF	chr2:234516863-234516899	GM12891	blood:	n/a	n/a
34	CTCF	chr2:234504345-234504416	GM12892	blood:	n/a	n/a
35	CTCF	chr2:234504140-234504290	A549	lung:	n/a	n/a
36	CTCF	chr2:234507660-234507810	A549	lung:	n/a	n/a
37	CTCF	chr2:234495766-234495803	GM10266	blood:	n/a	n/a
38	CTCF	chr2:234522915-234522947	GM20000	blood:	n/a	n/a
39	CTCF	chr2:234504400-234504550	HepG2	liver:	n/a	n/a
40	CTCF	chr2:234526271-234526288	Pancreas_OC	pancreas:	n/a	n/a
41	CTCF	chr2:234516777-234516915	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr2:234516816-234516892	GM20000	blood:	n/a	n/a
43	CUX1	chr2:234502003-234502233	GM12878	blood:	n/a	n/a
44	E2F4	chr2:234509753-234509767	MCF10A-Er-Src	breast:	n/a	n/a
45	EBF1	chr2:234533840-234534107	GM12878	blood:	n/a	n/a
46	EBF1	chr2:234502757-234503201	GM12878	blood:	n/a	chr2:234503021-234503032
47	EBF1	chr2:234501858-234502343	GM12878	blood:	n/a	n/a
48	EBF1	chr2:234504943-234505513	GM12878	blood:	n/a	n/a
49	EP300	chr2:234509142-234509441	K562	blood:	n/a	n/a
50	EP300	chr2:234501868-234502299	GM12878	blood:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:234526255-234526305	Hepatocyte	liver:	n/a
2	chr2:234526255-234526305	Hepatocyte	liver:	n/a
3	chr2:234544271-234544321	HIPEpiC	eye:	n/a
4	chr2:234544271-234544321	MCF10A-Er-Src	breast:	n/a
5	chr2:234544271-234544321	SK-N-MC	brain:	n/a
6	chr2:234545110-234545160	HCPEpiC	choroid plexus:	n/a
7	chr2:234526295-234526345	Hela-S3	cervix:	n/a
8	chr2:234525618-234525668	HepG2	liver:	n/a
9	chr2:234544271-234544321	AoSMC	blood vessel:	n/a
10	chr2:234544995-234545045	MCF-7	breast:	n/a
11	chr2:234545177-234545227	GM12891	blood:	n/a
12	chr2:234526255-234526305	NT2-D1	testis:	n/a
13	chr2:234545177-234545227	U87	brain:	n/a
14	chr2:234526295-234526345	HPAEpiC	pulmonary alveolar:	n/a
15	chr2:234544995-234545045	AG09319	gingival:	n/a
16	chr2:234544462-234544512	BJ	skin:	n/a
17	chr2:234526255-234526305	A549	lung:	n/a
18	chr2:234545110-234545160	HCM	heart:	n/a
19	chr2:234545177-234545227	Hela-S3	cervix:	n/a
20	chr2:234526077-234526127	BE2_C	brain:	n/a
21	chr2:234526255-234526305	PFSK-1	brain:	n/a
22	chr2:234544995-234545045	PFSK-1	brain:	n/a
23	chr2:234526077-234526127	HUVEC	blood vessel:	n/a
24	chr2:234545110-234545160	GM12891	blood:	n/a
25	chr2:234545177-234545227	GM19239	blood:	n/a
26	chr2:234544271-234544321	ECC-1	luminal epithelium:	n/a
27	chr2:234526255-234526305	GM12878	blood:	n/a
28	chr2:234526255-234526305	HRPEpiC	eye:	n/a
29	chr2:234526255-234526305	HCT-116	colon:	n/a
30	chr2:234526295-234526345	U87	brain:	n/a
31	chr2:234544271-234544321	AG09309	skin:	n/a
32	chr2:234526077-234526127	SK-N-SH_RA	brain:	n/a
33	chr2:234525618-234525668	SKMC	muscle:	n/a
34	chr2:234526255-234526305	ECC-1	luminal epithelium:	n/a
35	chr2:234545110-234545160	Jurkat	blood:	n/a
36	chr2:234526295-234526345	H1-hESC	embryonic stem cell:	embryo
37	chr2:234526255-234526305	HPAEpiC	pulmonary alveolar:	n/a
38	chr2:234545177-234545227	HIPEpiC	eye:	n/a
39	chr2:234544462-234544512	SK-N-MC	brain:	n/a
40	chr2:234545110-234545160	H1-hESC	embryonic stem cell:	embryo
41	chr2:234525618-234525668	ProgFib	skin:	n/a
42	chr2:234544462-234544512	HNPCEpiC	eye:	n/a
43	chr2:234545110-234545160	GM06990	blood:	n/a
44	chr2:234526255-234526305	BJ	skin:	n/a
45	chr2:234544271-234544321	GM12892	blood:	n/a
46	chr2:234525618-234525668	HUVEC	blood vessel:	n/a
47	chr2:234525618-234525668	SK-N-SH_RA	brain:	n/a
48	chr2:234544271-234544321	HAEpiC	amniotic membrane:	n/a
49	chr2:234544995-234545045	U87	brain:	n/a
50	chr2:234544995-234545045	HUVEC	blood vessel:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	2:234505513-234506682..2:234635414-234639782	Hela-S3	cervix:
2	2:234498935-234505513..2:234683624-234705119	K562	blood:
3	chr2:234534086..234537809-chr2:234597332..234600775,3	MCF-7	breast:
4	2:234498935-234505513..2:234635414-234639782	Hela-S3	cervix:
5	chr2:234495064..234497019-chr2:234498487..234500716,2	K562	blood:
6	2:234543708-234558325..2:234649753-234657866	Hela-S3	cervix:
7	chr2:234492474..234494735-chr2:234496256..234497901,2	K562	blood:
8	2:234498935-234505513..2:234825998-234827518	Hela-S3	cervix:
9	2:234543708-234558325..2:234772667-234780240	Hela-S3	cervix:
10	2:234498935-234505513..2:234954947-234965240	Hela-S3	cervix:
11	chr2:234495064..234497019-chr2:234498487..234500716,2	K562	blood:
12	2:234498935-234505513..2:234835115-234838817	Hela-S3	cervix:
13	2:234498935-234505513..2:234898811-234918017	Hela-S3	cervix:
14	2:234498935-234505513..2:234543708-234558325	H1-hESC	embryonic stem cell:	embryo
15	2:234492023-234494396..2:234543708-234558325	GM12878	blood:
16	2:234498935-234505513..2:234743181-234749667	Hela-S3	cervix:
17	2:234498935-234505513..2:234666975-234672018	Hela-S3	cervix:
18	2:234498935-234505513..2:234572898-234594986	K562	blood:

No data

Variant related genes	Relation type
UGT1A11P	TF binding region
UGT1A8	TF binding region
UGT1A10	TF binding region
UGT1A11P	CpG island
UGT1A8	CpG island
UGT1A10	CpG island
ENSG00000234143	chromatin interactions
ENSG00000123485	chromatin interactions
ENSG00000167165	chromatin interactions
ENSG00000072080	chromatin interactions
ENSG00000242366	chromatin interactions
ENSG00000228949	chromatin interactions
ENSG00000243135	chromatin interactions
ENSG00000185038	chromatin interactions
ENSG00000242515	chromatin interactions
ENSG00000241119	chromatin interactions
ENSG00000241635	chromatin interactions
ENSG00000228445	chromatin interactions
ENSG00000144481	chromatin interactions
ENSG00000244122	chromatin interactions
ENSG00000224287	chromatin interactions
ENSG00000227802	chromatin interactions

Extended variants
information (count: 1633 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1633 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17864661	chr2:234495742-234495743	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535152586	chr2:234495760-234495761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555334282	chr2:234495778-234495779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572285221	chr2:234495781-234495782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs576456988	chr2:234495787-234495788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541979234	chr2:234495800-234495801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs144354579	chr2:234495804-234495805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577931085	chr2:234495823-234495824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562176335	chr2:234495870-234495871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551381412	chr2:234495953-234495954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs183329399	chr2:234495959-234495960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs28966989	chr2:234495960-234495961	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs186492368	chr2:234495996-234495997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147798589	chr2:234496037-234496038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs60368650	chr2:234496087-234496088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs13006014	chr2:234496124-234496125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs13006015	chr2:234496125-234496126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs12999759	chr2:234496157-234496158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs12989949	chr2:234496164-234496165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs141081890	chr2:234496186-234496187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150303011	chr2:234496187-234496188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs531017085	chr2:234496202-234496203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs12999956	chr2:234496213-234496214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs12999973	chr2:234496237-234496238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191292153	chr2:234496252-234496253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs541195124	chr2:234496267-234496268	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs368720509	chr2:234496286-234496287	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs57988503	chr2:234496298-234496299	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs569454673	chr2:234496315-234496316	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs535520228	chr2:234496344-234496345	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs114572579	chr2:234496345-234496346	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs564084316	chr2:234496371-234496372	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs565693086	chr2:234496428-234496429	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs534291010	chr2:234496443-234496444	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs183253592	chr2:234496491-234496492	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs112368820	chr2:234496492-234496493	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs17864662	chr2:234496534-234496535	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs188130946	chr2:234496608-234496609	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs574082471	chr2:234496620-234496621	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs193073667	chr2:234496646-234496647	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs374096622	chr2:234496678-234496679	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs115831140	chr2:234496687-234496688	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs573205467	chr2:234496708-234496709	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs28968505	chr2:234496725-234496726	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs138075615	chr2:234496764-234496765	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs528850471	chr2:234496765-234496766	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs550798011	chr2:234496784-234496785	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs1530957	chr2:234496796-234496797	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs185273095	chr2:234496832-234496833	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs114972376	chr2:234496846-234496847	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	22429812	CNVD
Bladder cancer	21909424	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
prenatal diagnosis	22389664	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mental retardation	20152051	CNVD
Cancer	21183584	CNVD
Albright''s disease	22277900	CNVD
Brachydactyly-Mental Retardation Syndrome	22470819	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Colorectal cancer	19359472	CNVD
Autism	18414403	CNVD
Chronic myeloid leukemia	21384125	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234495000-234497000	Enhancers	GM12878-XiMat	blood
2	chr2:234496600-234497000	Enhancers	Fetal Intestine Small	intestine
3	chr2:234496600-234497600	Enhancers	Fetal Intestine Large	intestine
4	chr2:234499000-234499400	Bivalent Enhancer	HepG2	liver
5	chr2:234500600-234501200	ZNF genes & repeats	GM12878-XiMat	blood
6	chr2:234500600-234502200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr2:234501200-234501600	Weak transcription	GM12878-XiMat	blood
8	chr2:234501600-234502000	Enhancers	HMEC	breast
9	chr2:234501600-234502200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr2:234501600-234502200	Flanking Active TSS	GM12878-XiMat	blood
11	chr2:234501600-234502600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr2:234502000-234502600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr2:234502200-234503000	Enhancers	GM12878-XiMat	blood
14	chr2:234502600-234502800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr2:234505600-234506200	Enhancers	Esophagus	oesophagus
16	chr2:234505600-234507800	Enhancers	Fetal Kidney	kidney
17	chr2:234505800-234507200	Enhancers	Rectal Mucosa Donor 31	rectum
18	chr2:234506000-234506800	Enhancers	Rectal Mucosa Donor 29	rectum
19	chr2:234506200-234507000	Enhancers	A549	lung
20	chr2:234506400-234507200	Enhancers	Colon Smooth Muscle	Colon
21	chr2:234506400-234508000	Enhancers	Liver	Liver
22	chr2:234506600-234507000	Enhancers	Placenta Amnion	Placenta Amnion
23	chr2:234507000-234507800	Flanking Active TSS	A549	lung
24	chr2:234507800-234508000	Enhancers	A549	lung
25	chr2:234508000-234511000	Weak transcription	Liver	Liver
26	chr2:234509000-234509400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr2:234509000-234509400	Enhancers	NHEK	skin
28	chr2:234509400-234510800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr2:234511000-234511200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr2:234511000-234514200	Enhancers	Liver	Liver
31	chr2:234512000-234512800	Enhancers	HepG2	liver
32	chr2:234514200-234516600	Weak transcription	Liver	Liver
33	chr2:234516600-234518200	Enhancers	Liver	Liver
34	chr2:234525600-234528200	Active TSS	Rectal Mucosa Donor 29	rectum
35	chr2:234525800-234526000	Enhancers	Duodenum Mucosa	Duodenum
36	chr2:234525800-234526200	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr2:234525800-234526400	Enhancers	NHEK	skin
38	chr2:234526000-234526600	Flanking Active TSS	Duodenum Mucosa	Duodenum
39	chr2:234526200-234526600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
40	chr2:234526600-234526800	Enhancers	Duodenum Mucosa	Duodenum
41	chr2:234526600-234526800	Active TSS	Rectal Mucosa Donor 31	rectum
42	chr2:234526800-234528800	Weak transcription	Duodenum Mucosa	Duodenum
43	chr2:234526800-234528800	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr2:234528800-234529000	Enhancers	Duodenum Mucosa	Duodenum
45	chr2:234528800-234529600	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr2:234537800-234538000	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
47	chr2:234538000-234544600	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr2:234544400-234545200	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr2:234544600-234544800	Enhancers	Duodenum Mucosa	Duodenum
50	chr2:234544600-234544800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum

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