Variant report

Variant	esv3419326
Chromosome Location	chr2:234498411-234560470
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:314)
CpG islands
(count:550)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:314 , 50 per page) page: 1 2 3 4 5 6 7

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	chr2:234501781-234502299	GM12878	blood:	n/a	n/a
4	BATF	chr2:234501769-234502305	GM12878	blood:	n/a	n/a
5	BCL11A	chr2:234501789-234502263	GM12878	blood:	n/a	n/a
6	BCL11A	chr2:234501828-234502266	GM12878	blood:	n/a	n/a
7	BCLAF1	chr2:234501832-234502192	GM12878	blood:	n/a	n/a
8	BHLHE40	chr2:234501879-234502256	GM12878	blood:	n/a	n/a
9	CCNT2	chr2:234509214-234509461	K562	blood:	n/a	n/a
10	CEBPB	chr2:234512344-234512544	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:234521112-234521181	IMR90	lung:	n/a	n/a
12	CHD2	chr2:234501976-234502223	GM12878	blood:	n/a	n/a
13	CTCF	chr2:234522915-234522947	GM20000	blood:	n/a	n/a
14	CTCF	chr2:234551860-234552010	GM12865	blood:	n/a	n/a
15	CTCF	chr2:234551940-234552090	GM12868	blood:	n/a	n/a
16	CTCF	chr2:234551920-234552070	HPF	lung:	n/a	n/a
17	CTCF	chr2:234551900-234552050	GM12869	blood:	n/a	n/a
18	CTCF	chr2:234551920-234552070	GM12865	blood:	n/a	n/a
19	CTCF	chr2:234516863-234516899	GM12891	blood:	n/a	n/a
20	CTCF	chr2:234551909-234552096	MCF-7	breast:	n/a	n/a
21	CTCF	chr2:234551620-234551770	GM12868	blood:	n/a	n/a
22	CTCF	chr2:234547580-234547730	GM12864	blood:	n/a	n/a
23	CTCF	chr2:234551860-234552010	HMF	breast:	n/a	n/a
24	CTCF	chr2:234551820-234551970	HFF-Myc	foreskin:	n/a	n/a
25	CTCF	chr2:234551922-234552046	IMR90	lung:	n/a	n/a
26	CTCF	chr2:234551929-234552062	Gliobla	brain:	n/a	n/a
27	CTCF	chr2:234545228-234545302	NHEK	skin:	n/a	n/a
28	CTCF	chr2:234551920-234552070	HMEC	breast:	n/a	n/a
29	CTCF	chr2:234551920-234552070	AG04449	skin:	n/a	n/a
30	CTCF	chr2:234547634-234547721	GM12892	blood:	n/a	n/a
31	CTCF	chr2:234516851-234516858	GM12878	blood:	n/a	n/a
32	CTCF	chr2:234551920-234552070	AG09319	gingival:	n/a	n/a
33	CTCF	chr2:234551900-234552050	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr2:234547480-234547630	A549	lung:	n/a	n/a
35	CTCF	chr2:234551900-234552050	HAc	cerebellar:	n/a	n/a
36	CTCF	chr2:234551880-234552030	AG04450	lung:	n/a	n/a
37	CTCF	chr2:234551880-234552030	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr2:234551880-234552030	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr2:234547643-234547715	GM19240	blood:	n/a	n/a
40	CTCF	chr2:234551907-234552102	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:234551900-234552050	NHEK	skin:	n/a	n/a
42	CTCF	chr2:234551900-234552050	GM12867	blood:	n/a	n/a
43	CTCF	chr2:234551900-234552050	HVMF	connective:	n/a	n/a
44	CTCF	chr2:234547667-234547723	GM13977	blood:	n/a	n/a
45	CTCF	chr2:234551900-234552050	HFF	foreskin:	n/a	n/a
46	CTCF	chr2:234551800-234551950	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr2:234551820-234551970	BJ	skin:	n/a	n/a
48	CTCF	chr2:234551940-234552090	HCM	heart:	n/a	n/a
49	CTCF	chr2:234551820-234551970	A549	lung:	n/a	n/a
50	CTCF	chr2:234551898-234552073	GM19239	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	chr2:234545177-234545227	MCF-7	breast:	n/a
2	chr2:234545177-234545227	MCF-7	breast:	n/a
3	chr2:234544462-234544512	GM12878	blood:	n/a
4	chr2:234544995-234545045	K562	blood:	n/a
5	chr2:234545177-234545227	HCPEpiC	choroid plexus:	n/a
6	chr2:234526077-234526127	PrEC	prostate:	n/a
7	chr2:234526077-234526127	HCPEpiC	choroid plexus:	n/a
8	chr2:234526295-234526345	RPTEC	kidney:	n/a
9	chr2:234526077-234526127	Caco-2	colon:	n/a
10	chr2:234526295-234526345	BE2_C	brain:	n/a
11	chr2:234544462-234544512	H1-hESC	embryonic stem cell:	embryo
12	chr2:234545110-234545160	LNCaP	prostate:	n/a
13	chr2:234544271-234544321	BJ	skin:	n/a
14	chr2:234545110-234545160	HL-60	blood:	n/a
15	chr2:234544271-234544321	ProgFib	skin:	n/a
16	chr2:234526295-234526345	LNCaP	prostate:	n/a
17	chr2:234544271-234544321	SKMC	muscle:	n/a
18	chr2:234544462-234544512	T-47D	breast:	n/a
19	chr2:234545110-234545160	SK-N-SH_RA	brain:	n/a
20	chr2:234545110-234545160	SK-N-SH	brain:	n/a
21	chr2:234525618-234525668	AG04449	skin:	fetal
22	chr2:234545177-234545227	HEEpiC	esophagus:	n/a
23	chr2:234525618-234525668	HIPEpiC	eye:	n/a
24	chr2:234525618-234525668	RPTEC	kidney:	n/a
25	chr2:234545177-234545227	Hepatocyte	liver:	n/a
26	chr2:234525618-234525668	PANC-1	pancreas:	n/a
27	chr2:234526255-234526305	BJ	skin:	n/a
28	chr2:234544995-234545045	U87	brain:	n/a
29	chr2:234526295-234526345	AoSMC	blood vessel:	n/a
30	chr2:234526255-234526305	A549	lung:	n/a
31	chr2:234545177-234545227	AG04449	skin:	fetal
32	chr2:234526077-234526127	HEEpiC	esophagus:	n/a
33	chr2:234544995-234545045	HepG2	liver:	n/a
34	chr2:234526255-234526305	GM12892	blood:	n/a
35	chr2:234526295-234526345	HCPEpiC	choroid plexus:	n/a
36	chr2:234545110-234545160	GM19239	blood:	n/a
37	chr2:234526077-234526127	SK-N-MC	brain:	n/a
38	chr2:234545110-234545160	MCF-7	breast:	n/a
39	chr2:234526077-234526127	HNPCEpiC	eye:	n/a
40	chr2:234544462-234544512	NHBE	bronchial:	n/a
41	chr2:234544271-234544321	SAEC	small airway:	n/a
42	chr2:234544995-234545045	GM06990	blood:	n/a
43	chr2:234545110-234545160	PrEC	prostate:	n/a
44	chr2:234545177-234545227	HL-60	blood:	n/a
45	chr2:234526295-234526345	NHDF-neo	bronchial:	n/a
46	chr2:234544995-234545045	HRPEpiC	eye:	n/a
47	chr2:234545177-234545227	HUVEC	blood vessel:	n/a
48	chr2:234545177-234545227	SAEC	small airway:	n/a
49	chr2:234526255-234526305	CMK	blood:	n/a
50	chr2:234525618-234525668	CMK	blood:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	2:234498935-234505513..2:234743181-234749667	Hela-S3	cervix:
2	2:234543708-234558325..2:234649753-234657866	Hela-S3	cervix:
3	2:234492023-234494396..2:234543708-234558325	GM12878	blood:
4	2:234498935-234505513..2:234683624-234705119	K562	blood:
5	2:234498935-234505513..2:234666975-234672018	Hela-S3	cervix:
6	2:234543708-234558325..2:234772667-234780240	Hela-S3	cervix:
7	2:234498935-234505513..2:234543708-234558325	H1-hESC	embryonic stem cell:	embryo
8	2:234498935-234505513..2:234635414-234639782	Hela-S3	cervix:
9	chr2:234534086..234537809-chr2:234597332..234600775,3	MCF-7	breast:
10	2:234498935-234505513..2:234572898-234594986	K562	blood:
11	chr2:234559926..234563165-chr2:234564749..234566368,3	K562	blood:
12	2:234498935-234505513..2:234898811-234918017	Hela-S3	cervix:
13	2:234505513-234506682..2:234635414-234639782	Hela-S3	cervix:
14	2:234498935-234505513..2:234825998-234827518	Hela-S3	cervix:
15	2:234498935-234505513..2:234954947-234965240	Hela-S3	cervix:
16	chr2:234557472..234561426-chr2:234563315..234566249,3	K562	blood:
17	chr2:234544581..234547100-chr2:234548174..234549799,2	MCF-7	breast:
18	chr2:234448748..234450538-chr2:234553700..234555671,2	K562	blood:
19	chr2:234495064..234497019-chr2:234498487..234500716,2	K562	blood:
20	2:234498935-234505513..2:234835115-234838817	Hela-S3	cervix:

No data

Variant related genes	Relation type
UGT1A10	TF binding region
UGT1A13P	TF binding region
UGT1A11P	TF binding region
UGT1A8	TF binding region
UGT1A10	CpG island
UGT1A13P	CpG island
UGT1A11P	CpG island
UGT1A8	CpG island
ENSG00000244122	chromatin interactions
ENSG00000243135	chromatin interactions
ENSG00000242515	chromatin interactions
ENSG00000144481	chromatin interactions
ENSG00000167165	chromatin interactions
ENSG00000241119	chromatin interactions
ENSG00000228949	chromatin interactions
ENSG00000185038	chromatin interactions
ENSG00000227802	chromatin interactions
ENSG00000241635	chromatin interactions
ENSG00000228445	chromatin interactions
ENSG00000123485	chromatin interactions
ENSG00000224287	chromatin interactions
ENSG00000234143	chromatin interactions
ENSG00000242366	chromatin interactions
ENSG00000072080	chromatin interactions

Extended variants
information (count: 2152 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2152 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188101508	chr2:234498944-234498945	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
2	rs554848893	chr2:234499046-234499047	Bivalent Enhancer	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
3	rs538412468	chr2:234499064-234499065	Bivalent Enhancer	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
4	rs558636731	chr2:234499065-234499066	Bivalent Enhancer	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
5	rs6761848	chr2:234499168-234499169	Bivalent Enhancer	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs368690166	chr2:234499204-234499205	Bivalent Enhancer	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
7	rs113167317	chr2:234499212-234499213	Bivalent Enhancer	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
8	rs554659076	chr2:234499235-234499236	Bivalent Enhancer	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
9	rs534174103	chr2:234499241-234499242	Bivalent Enhancer	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
10	rs113544038	chr2:234499300-234499301	Bivalent Enhancer	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
11	rs10176427	chr2:234499326-234499327	Bivalent Enhancer	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs181076283	chr2:234499327-234499328	Bivalent Enhancer	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
13	rs554333837	chr2:234499347-234499348	Bivalent Enhancer	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
14	rs554415741	chr2:234499371-234499372	Bivalent Enhancer	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
15	rs147509194	chr2:234499379-234499380	Bivalent Enhancer	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
16	rs201587279	chr2:234499421-234499422	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
17	rs567806488	chr2:234499422-234499423	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
18	rs564975712	chr2:234499423-234499424	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
19	rs28658582	chr2:234499434-234499435	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
20	rs376898631	chr2:234499446-234499447	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
21	rs575408191	chr2:234499452-234499453	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
22	rs544234849	chr2:234499462-234499463	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
23	rs12611762	chr2:234499467-234499468	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
24	rs560705396	chr2:234499485-234499486	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
25	rs529665649	chr2:234499486-234499487	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
26	rs546595542	chr2:234499487-234499488	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
27	rs186507122	chr2:234499569-234499570	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
28	rs28966992	chr2:234499584-234499585	Inactive region	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs189736750	chr2:234499623-234499624	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
30	rs536853604	chr2:234499656-234499657	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
31	rs73123152	chr2:234499657-234499658	Inactive region	Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs186594313	chr2:234499676-234499677	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
33	rs190528571	chr2:234499681-234499682	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
34	rs568382690	chr2:234499689-234499690	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
35	rs140034405	chr2:234499729-234499730	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs183063232	chr2:234499772-234499773	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs186434616	chr2:234499805-234499806	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs528912914	chr2:234499942-234499943	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs540085840	chr2:234499950-234499951	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs146893715	chr2:234499984-234499985	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
41	rs556785337	chr2:234499997-234499998	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
42	rs145565413	chr2:234500029-234500030	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
43	rs71935517	chr2:234500048-234500049	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
44	rs17863752	chr2:234500064-234500065	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
45	rs561006167	chr2:234500165-234500166	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
46	rs574359240	chr2:234500174-234500175	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
47	rs540179290	chr2:234500255-234500256	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs560064765	chr2:234500278-234500279	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs367641750	chr2:234500279-234500280	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs371398485	chr2:234500283-234500284	Inactive region	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234499000-234499400	Bivalent Enhancer	HepG2	liver
2	chr2:234500600-234501200	ZNF genes & repeats	GM12878-XiMat	blood
3	chr2:234500600-234502200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr2:234501200-234501600	Weak transcription	GM12878-XiMat	blood
5	chr2:234501600-234502000	Enhancers	HMEC	breast
6	chr2:234501600-234502200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr2:234501600-234502200	Flanking Active TSS	GM12878-XiMat	blood
8	chr2:234501600-234502600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr2:234502000-234502600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr2:234502200-234503000	Enhancers	GM12878-XiMat	blood
11	chr2:234502600-234502800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr2:234505600-234506200	Enhancers	Esophagus	oesophagus
13	chr2:234505600-234507800	Enhancers	Fetal Kidney	kidney
14	chr2:234505800-234507200	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr2:234506000-234506800	Enhancers	Rectal Mucosa Donor 29	rectum
16	chr2:234506200-234507000	Enhancers	A549	lung
17	chr2:234506400-234507200	Enhancers	Colon Smooth Muscle	Colon
18	chr2:234506400-234508000	Enhancers	Liver	Liver
19	chr2:234506600-234507000	Enhancers	Placenta Amnion	Placenta Amnion
20	chr2:234507000-234507800	Flanking Active TSS	A549	lung
21	chr2:234507800-234508000	Enhancers	A549	lung
22	chr2:234508000-234511000	Weak transcription	Liver	Liver
23	chr2:234509000-234509400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr2:234509000-234509400	Enhancers	NHEK	skin
25	chr2:234509400-234510800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr2:234511000-234511200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr2:234511000-234514200	Enhancers	Liver	Liver
28	chr2:234512000-234512800	Enhancers	HepG2	liver
29	chr2:234514200-234516600	Weak transcription	Liver	Liver
30	chr2:234516600-234518200	Enhancers	Liver	Liver
31	chr2:234525600-234528200	Active TSS	Rectal Mucosa Donor 29	rectum
32	chr2:234525800-234526000	Enhancers	Duodenum Mucosa	Duodenum
33	chr2:234525800-234526200	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr2:234525800-234526400	Enhancers	NHEK	skin
35	chr2:234526000-234526600	Flanking Active TSS	Duodenum Mucosa	Duodenum
36	chr2:234526200-234526600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
37	chr2:234526600-234526800	Enhancers	Duodenum Mucosa	Duodenum
38	chr2:234526600-234526800	Active TSS	Rectal Mucosa Donor 31	rectum
39	chr2:234526800-234528800	Weak transcription	Duodenum Mucosa	Duodenum
40	chr2:234526800-234528800	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr2:234528800-234529000	Enhancers	Duodenum Mucosa	Duodenum
42	chr2:234528800-234529600	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr2:234537800-234538000	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
44	chr2:234538000-234544600	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr2:234544400-234545200	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr2:234544600-234544800	Enhancers	Duodenum Mucosa	Duodenum
47	chr2:234544600-234544800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
48	chr2:234544600-234545000	Enhancers	Colonic Mucosa	Colon
49	chr2:234544800-234547600	Active TSS	Duodenum Mucosa	Duodenum
50	chr2:234544800-234548400	Active TSS	Rectal Mucosa Donor 29	rectum

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