Variant report

Variant	esv3340085
Chromosome Location	chr2:234651714-234660160
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	chr2:234653876-234654428	HepG2	liver:	n/a	n/a
2	ATF3	chr2:234653988-234654486	A549	lung:	n/a	n/a
3	BCL3	chr2:234653958-234654499	A549	lung:	n/a	n/a
4	BCL3	chr2:234653885-234654544	A549	lung:	n/a	n/a
5	BHLHE40	chr2:234654058-234654451	HepG2	liver:	n/a	n/a
6	CBX3	chr2:234659353-234659614	K562	blood:	n/a	n/a
7	CEBPB	chr2:234656934-234657289	HepG2	liver:	n/a	chr2:234657082-234657093 chr2:234657082-234657093 chr2:234657104-234657115
8	CEBPB	chr2:234657008-234657264	IMR90	lung:	n/a	chr2:234657082-234657093 chr2:234657082-234657093 chr2:234657104-234657115
9	CEBPB	chr2:234653908-234654385	HepG2	liver:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
10	CEBPB	chr2:234653979-234654335	HepG2	liver:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
11	CEBPB	chr2:234653902-234654598	HepG2	liver:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
12	CEBPB	chr2:234653892-234654497	A549	lung:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
13	CEBPB	chr2:234653961-234654410	HepG2	liver:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
14	CEBPB	chr2:234654020-234654389	A549	lung:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
15	CEBPB	chr2:234653943-234654318	A549	lung:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
16	CEBPB	chr2:234656935-234657273	A549	lung:	n/a	chr2:234657082-234657093 chr2:234657082-234657093 chr2:234657104-234657115
17	CEBPD	chr2:234654049-234654478	HepG2	liver:	n/a	n/a
18	CHD2	chr2:234654164-234654273	HepG2	liver:	n/a	n/a
19	CREB1	chr2:234654194-234654509	A549	lung:	n/a	n/a
20	CREB1	chr2:234653888-234654608	HepG2	liver:	n/a	n/a
21	CREB1	chr2:234653968-234654547	HepG2	liver:	n/a	n/a
22	CREB1	chr2:234654062-234654459	A549	lung:	n/a	n/a
23	CTCF	chr2:234651938-234652009	GM20000	blood:	n/a	n/a
24	CTCF	chr2:234651956-234652041	Kidney_OC	kidney:	n/a	n/a
25	EP300	chr2:234654030-234654453	HepG2	liver:	n/a	chr2:234654068-234654082
26	EP300	chr2:234653810-234654542	A549	lung:	n/a	chr2:234654068-234654082 chr2:234653862-234653871
27	EP300	chr2:234653933-234654548	HepG2	liver:	n/a	chr2:234654068-234654082
28	EP300	chr2:234653700-234654700	A549	lung:	n/a	chr2:234654068-234654082 chr2:234653862-234653871
29	EP300	chr2:234653868-234654574	HepG2	liver:	n/a	chr2:234654068-234654082
30	FOSL2	chr2:234654004-234654404	A549	lung:	n/a	n/a
31	FOSL2	chr2:234654000-234654628	HepG2	liver:	n/a	n/a
32	FOSL2	chr2:234653860-234654613	A549	lung:	n/a	n/a
33	FOSL2	chr2:234653946-234654485	HepG2	liver:	n/a	n/a
34	FOXA1	chr2:234653527-234654585	HepG2	liver:	n/a	n/a
35	FOXA1	chr2:234653871-234654608	HepG2	liver:	n/a	n/a
36	FOXA1	chr2:234653830-234654570	HepG2	liver:	n/a	n/a
37	FOXA1	chr2:234653906-234654589	HepG2	liver:	n/a	n/a
38	FOXA2	chr2:234653884-234654483	HepG2	liver:	n/a	n/a
39	FOXA2	chr2:234653696-234654749	HepG2	liver:	n/a	n/a
40	FOXA2	chr2:234653649-234654629	A549	lung:	n/a	n/a
41	FOXA2	chr2:234653954-234654644	A549	lung:	n/a	n/a
42	GATA3	chr2:234653885-234654644	A549	lung:	n/a	n/a
43	GATA3	chr2:234653893-234654633	A549	lung:	n/a	n/a
44	HDAC2	chr2:234653902-234654531	HepG2	liver:	n/a	n/a
45	HDAC2	chr2:234653853-234654551	HepG2	liver:	n/a	n/a
46	HEY1	chr2:234652495-234652743	K562	blood:	n/a	n/a
47	HNF4A	chr2:234653907-234654493	HepG2	liver:	n/a	chr2:234654285-234654298 chr2:234654285-234654300 chr2:234654281-234654303 chr2:234654233-234654248 chr2:234654285-234654298
48	HNF4A	chr2:234653992-234654483	HepG2	liver:	n/a	chr2:234654285-234654298 chr2:234654285-234654300 chr2:234654281-234654303 chr2:234654233-234654248 chr2:234654285-234654298
49	HNF4A	chr2:234654029-234654486	HepG2	liver:	n/a	chr2:234654285-234654298 chr2:234654285-234654300 chr2:234654281-234654303 chr2:234654233-234654248 chr2:234654285-234654298
50	HNF4G	chr2:234653874-234654479	HepG2	liver:	n/a	chr2:234654285-234654298 chr2:234654285-234654300 chr2:234654281-234654303 chr2:234654285-234654298

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:234652669-234652719	Hepatocyte	liver:	n/a
2	chr2:234652669-234652719	Hepatocyte	liver:	n/a
3	chr2:234652601-234652651	HAEpiC	amniotic membrane:	n/a
4	chr2:234652669-234652719	ProgFib	skin:	n/a
5	chr2:234652466-234652516	NHBE	bronchial:	n/a
6	chr2:234655709-234655759	HMEC	breast:	n/a
7	chr2:234652466-234652516	NT2-D1	testis:	n/a
8	chr2:234652363-234652413	HCF	heart:	n/a
9	chr2:234653891-234653941	AG10803	skin:	n/a
10	chr2:234652601-234652651	NH-A	brain:	n/a
11	chr2:234655709-234655759	NB4	blood:	n/a
12	chr2:234652669-234652719	U87	brain:	n/a
13	chr2:234655709-234655759	AG09319	gingival:	n/a
14	chr2:234655709-234655759	SK-N-SH	brain:	n/a
15	chr2:234652601-234652651	ovcar-3	ovarian:	n/a
16	chr2:234652466-234652516	ECC-1	luminal epithelium:	n/a
17	chr2:234655709-234655759	BJ	skin:	n/a
18	chr2:234655709-234655759	Jurkat	blood:	n/a
19	chr2:234651850-234651900	SK-N-SH_RA	brain:	n/a
20	chr2:234652601-234652651	U87	brain:	n/a
21	chr2:234652681-234652731	GM06990	blood:	n/a
22	chr2:234652466-234652516	MCF10A-Er-Src	breast:	n/a
23	chr2:234652681-234652731	LNCaP	prostate:	n/a
24	chr2:234652466-234652516	NH-A	brain:	n/a
25	chr2:234652466-234652516	K562	blood:	n/a
26	chr2:234652669-234652719	NHBE	bronchial:	n/a
27	chr2:234652669-234652719	PANC-1	pancreas:	n/a
28	chr2:234652363-234652413	BJ	skin:	n/a
29	chr2:234652466-234652516	LNCaP	prostate:	n/a
30	chr2:234652466-234652516	CMK	blood:	n/a
31	chr2:234652601-234652651	HUVEC	blood vessel:	n/a
32	chr2:234653891-234653941	PANC-1	pancreas:	n/a
33	chr2:234653891-234653941	MCF10A-Er-Src	breast:	n/a
34	chr2:234652681-234652731	NT2-D1	testis:	n/a
35	chr2:234655709-234655759	HCT-116	colon:	n/a
36	chr2:234653891-234653941	NB4	blood:	n/a
37	chr2:234652681-234652731	HRPEpiC	eye:	n/a
38	chr2:234651850-234651900	MCF-7	breast:	n/a
39	chr2:234652681-234652731	HEEpiC	esophagus:	n/a
40	chr2:234652669-234652719	PFSK-1	brain:	n/a
41	chr2:234652601-234652651	LNCaP	prostate:	n/a
42	chr2:234651850-234651900	NB4	blood:	n/a
43	chr2:234651850-234651900	HMEC	breast:	n/a
44	chr2:234652363-234652413	HRPEpiC	eye:	n/a
45	chr2:234652466-234652516	ovcar-3	ovarian:	n/a
46	chr2:234652681-234652731	PFSK-1	brain:	n/a
47	chr2:234652363-234652413	H1-hESC	embryonic stem cell:	embryo
48	chr2:234652601-234652651	HPAEpiC	pulmonary alveolar:	n/a
49	chr2:234652601-234652651	HEEpiC	esophagus:	n/a
50	chr2:234652466-234652516	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:63274126..63274957-chr2:234657055..234657979,2	MCF-7	breast:
2	chr2:234651385..234654197-chr2:234659573..234662296,2	MCF-7	breast:
3	2:234543708-234558325..2:234649753-234657866	Hela-S3	cervix:
4	chr2:234650134..234652973-chr2:234653062..234655371,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT1A1-1	chr2:234659263-234659366	NONHSAT077510

Variant related genes	Relation type
UGT1A2P	TF binding region
ENSG00000248705	TF binding region
DNAJB3	TF binding region
UGT1A2P	CpG island
ENSG00000248705	CpG island
DNAJB3	CpG island
ENSG00000234143	chromatin interactions
ENSG00000242515	chromatin interactions
ENSG00000227802	chromatin interactions

Extended variants
information (count: 444 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:444 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs397839835	chr2:234651714-234651715	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs1054800	chr2:234651722-234651723	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs187768174	chr2:234651749-234651750	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs77486749	chr2:234651788-234651789	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs78331994	chr2:234651789-234651790	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs3796088	chr2:234651800-234651801	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs191127881	chr2:234651806-234651807	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs182109098	chr2:234651817-234651818	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs28900375	chr2:234651822-234651823	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs546323978	chr2:234651831-234651832	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs560095677	chr2:234651838-234651839	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs187896113	chr2:234651850-234651851	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs397839834	chr2:234651870-234651871	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs17863796	chr2:234651880-234651881	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs561592324	chr2:234651888-234651889	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs569147758	chr2:234651893-234651894	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs538069492	chr2:234651916-234651917	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs548391374	chr2:234651926-234651927	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs568503727	chr2:234651980-234651981	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs534297671	chr2:234651981-234651982	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs553930129	chr2:234652025-234652026	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs35742148	chr2:234652062-234652063	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs577178509	chr2:234652065-234652066	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs539413664	chr2:234652081-234652082	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs192671736	chr2:234652086-234652087	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs61736688	chr2:234652104-234652105	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs372766492	chr2:234652108-234652109	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs542057655	chr2:234652110-234652111	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs185061073	chr2:234652152-234652153	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs199947040	chr2:234652155-234652156	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs34135810	chr2:234652185-234652186	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs544018510	chr2:234652187-234652188	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs201114978	chr2:234652193-234652194	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs61744897	chr2:234652194-234652195	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs546286371	chr2:234652209-234652210	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs532152836	chr2:234652212-234652213	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs28900376	chr2:234652227-234652228	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs375891802	chr2:234652233-234652234	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs370692834	chr2:234652238-234652239	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs61729911	chr2:234652243-234652244	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs201940151	chr2:234652247-234652248	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs376857469	chr2:234652251-234652252	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs531629615	chr2:234652253-234652254	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs28900377	chr2:234652257-234652258	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs146398257	chr2:234652268-234652269	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs34150486	chr2:234652269-234652270	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs201123763	chr2:234652271-234652272	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs570829500	chr2:234652275-234652276	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs201446096	chr2:234652281-234652282	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs375962177	chr2:234652283-234652284	ZNF genes & repeats Strong transcription Genic enhancers Weak transcription	Chromatin interactive region	2 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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234620400-234659200	Weak transcription	Colonic Mucosa	Colon
2	chr2:234620600-234652200	Weak transcription	Esophagus	oesophagus
3	chr2:234626600-234668400	Weak transcription	NHEK	skin
4	chr2:234646400-234666600	Weak transcription	Stomach Mucosa	stomach
5	chr2:234647800-234652200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr2:234647800-234655000	Weak transcription	Gastric	stomach
7	chr2:234649800-234652200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr2:234649800-234658800	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr2:234650400-234652600	Genic enhancers	Liver	Liver
10	chr2:234651000-234652800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr2:234652200-234652600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr2:234652200-234652600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr2:234652200-234652600	ZNF genes & repeats	Esophagus	oesophagus
14	chr2:234652200-234652800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr2:234652400-234652600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr2:234652600-234654400	Enhancers	Liver	Liver
17	chr2:234652600-234654600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr2:234652800-234658200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr2:234652800-234659200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr2:234653200-234654400	Enhancers	HepG2	liver
21	chr2:234653200-234655600	Enhancers	Fetal Intestine Small	intestine
22	chr2:234653400-234653800	Enhancers	A549	lung
23	chr2:234653800-234654200	Active TSS	A549	lung
24	chr2:234654200-234654800	Enhancers	Small Intestine	intestine
25	chr2:234654200-234655000	Enhancers	A549	lung
26	chr2:234654200-234655400	Enhancers	Duodenum Mucosa	Duodenum
27	chr2:234654200-234655400	Enhancers	Fetal Intestine Large	intestine
28	chr2:234654400-234654600	Flanking Active TSS	HepG2	liver
29	chr2:234654400-234656000	Flanking Active TSS	Liver	Liver
30	chr2:234654600-234655800	Bivalent Enhancer	HepG2	liver
31	chr2:234655000-234655200	Flanking Active TSS	A549	lung
32	chr2:234655000-234655600	Enhancers	Gastric	stomach
33	chr2:234655200-234655400	Enhancers	A549	lung
34	chr2:234655400-234655600	Flanking Active TSS	A549	lung
35	chr2:234655400-234656200	Enhancers	Pancreas	Pancrea
36	chr2:234655600-234656200	Enhancers	A549	lung
37	chr2:234656000-234656600	Enhancers	Liver	Liver
38	chr2:234656200-234659000	Weak transcription	A549	lung
39	chr2:234656600-234657000	Flanking Active TSS	Liver	Liver
40	chr2:234657000-234657200	Enhancers	Liver	Liver
41	chr2:234657200-234657600	Flanking Active TSS	Liver	Liver
42	chr2:234657600-234658000	Active TSS	Liver	Liver
43	chr2:234658000-234658200	Flanking Active TSS	Liver	Liver
44	chr2:234658200-234660600	Enhancers	Liver	Liver
45	chr2:234658200-234664000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr2:234659200-234659800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr2:234659600-234660200	ZNF genes & repeats	Colonic Mucosa	Colon
48	chr2:234659600-234660800	ZNF genes & repeats	Fetal Intestine Small	intestine
49	chr2:234659800-234661800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr2:234660000-234666200	Weak transcription	Rectal Mucosa Donor 29	rectum

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