Variant report

Variant	esv2760613
Chromosome Location	chr2:234650604-234662263
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	chr2:234653885-234654544	A549	lung:	n/a	n/a
4	BCL3	chr2:234653958-234654499	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	chr2:234656935-234657273	A549	lung:	n/a	chr2:234657082-234657093 chr2:234657082-234657093 chr2:234657104-234657115
8	CEBPB	chr2:234653902-234654598	HepG2	liver:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
9	CEBPB	chr2:234654020-234654389	A549	lung:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
10	CEBPB	chr2:234653892-234654497	A549	lung:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
11	CEBPB	chr2:234653908-234654385	HepG2	liver:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
12	CEBPB	chr2:234657008-234657264	IMR90	lung:	n/a	chr2:234657082-234657093 chr2:234657082-234657093 chr2:234657104-234657115
13	CEBPB	chr2:234653979-234654335	HepG2	liver:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
14	CEBPB	chr2:234653943-234654318	A549	lung:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
15	CEBPB	chr2:234656934-234657289	HepG2	liver:	n/a	chr2:234657082-234657093 chr2:234657082-234657093 chr2:234657104-234657115
16	CEBPB	chr2:234653961-234654410	HepG2	liver:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
17	CEBPD	chr2:234654049-234654478	HepG2	liver:	n/a	n/a
18	CHD2	chr2:234654164-234654273	HepG2	liver:	n/a	n/a
19	CREB1	chr2:234654062-234654459	A549	lung:	n/a	n/a
20	CREB1	chr2:234654194-234654509	A549	lung:	n/a	n/a
21	CREB1	chr2:234653968-234654547	HepG2	liver:	n/a	n/a
22	CREB1	chr2:234653888-234654608	HepG2	liver:	n/a	n/a
23	CTCF	chr2:234651956-234652041	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr2:234651938-234652009	GM20000	blood:	n/a	n/a
25	EP300	chr2:234653933-234654548	HepG2	liver:	n/a	chr2:234654068-234654082
26	EP300	chr2:234653868-234654574	HepG2	liver:	n/a	chr2:234654068-234654082
27	EP300	chr2:234653700-234654700	A549	lung:	n/a	chr2:234654068-234654082 chr2:234653862-234653871
28	EP300	chr2:234653810-234654542	A549	lung:	n/a	chr2:234654068-234654082 chr2:234653862-234653871
29	EP300	chr2:234654030-234654453	HepG2	liver:	n/a	chr2:234654068-234654082
30	FOSL2	chr2:234653946-234654485	HepG2	liver:	n/a	n/a
31	FOSL2	chr2:234654004-234654404	A549	lung:	n/a	n/a
32	FOSL2	chr2:234653860-234654613	A549	lung:	n/a	n/a
33	FOSL2	chr2:234654000-234654628	HepG2	liver:	n/a	n/a
34	FOXA1	chr2:234653871-234654608	HepG2	liver:	n/a	n/a
35	FOXA1	chr2:234653906-234654589	HepG2	liver:	n/a	n/a
36	FOXA1	chr2:234653830-234654570	HepG2	liver:	n/a	n/a
37	FOXA1	chr2:234653527-234654585	HepG2	liver:	n/a	n/a
38	FOXA2	chr2:234653884-234654483	HepG2	liver:	n/a	n/a
39	FOXA2	chr2:234653954-234654644	A549	lung:	n/a	n/a
40	FOXA2	chr2:234653696-234654749	HepG2	liver:	n/a	n/a
41	FOXA2	chr2:234653649-234654629	A549	lung:	n/a	n/a
42	GATA3	chr2:234653893-234654633	A549	lung:	n/a	n/a
43	GATA3	chr2:234653885-234654644	A549	lung:	n/a	n/a
44	HDAC2	chr2:234653853-234654551	HepG2	liver:	n/a	n/a
45	HDAC2	chr2:234653902-234654531	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	chr2:234654029-234654486	HepG2	liver:	n/a	chr2:234654285-234654298 chr2:234654285-234654300 chr2:234654281-234654303 chr2:234654233-234654248 chr2:234654285-234654298
49	HNF4A	chr2:234653992-234654483	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	chr2:234661536-234661586	PrEC	prostate:	n/a
2	chr2:234661536-234661586	PrEC	prostate:	n/a
3	chr2:234651850-234651900	SKMC	muscle:	n/a
4	chr2:234652601-234652651	Hela-S3	cervix:	n/a
5	chr2:234651850-234651900	Caco-2	colon:	n/a
6	chr2:234652363-234652413	NHBE	bronchial:	n/a
7	chr2:234653891-234653941	SKMC	muscle:	n/a
8	chr2:234652681-234652731	Hepatocyte	liver:	n/a
9	chr2:234651850-234651900	GM19239	blood:	n/a
10	chr2:234652669-234652719	RPTEC	kidney:	n/a
11	chr2:234661536-234661586	SKMC	muscle:	n/a
12	chr2:234652466-234652516	HAEpiC	amniotic membrane:	n/a
13	chr2:234652681-234652731	HCT-116	colon:	n/a
14	chr2:234655709-234655759	ProgFib	skin:	n/a
15	chr2:234652681-234652731	K562	blood:	n/a
16	chr2:234650765-234650815	GM12892	blood:	n/a
17	chr2:234653891-234653941	AG10803	skin:	n/a
18	chr2:234652601-234652651	Jurkat	blood:	n/a
19	chr2:234652669-234652719	GM12878	blood:	n/a
20	chr2:234652669-234652719	HRCEpiC	kidney:	n/a
21	chr2:234661536-234661586	AG09309	skin:	n/a
22	chr2:234652601-234652651	HCPEpiC	choroid plexus:	n/a
23	chr2:234653891-234653941	MCF10A-Er-Src	breast:	n/a
24	chr2:234652466-234652516	LNCaP	prostate:	n/a
25	chr2:234651850-234651900	SAEC	small airway:	n/a
26	chr2:234652466-234652516	IMR90	lung:	fetal
27	chr2:234652601-234652651	NHBE	bronchial:	n/a
28	chr2:234650765-234650815	HRE	kidney:	n/a
29	chr2:234650765-234650815	HMEC	breast:	n/a
30	chr2:234652601-234652651	HRPEpiC	eye:	n/a
31	chr2:234652681-234652731	MCF-7	breast:	n/a
32	chr2:234652681-234652731	SK-N-MC	brain:	n/a
33	chr2:234650765-234650815	NB4	blood:	n/a
34	chr2:234652681-234652731	HL-60	blood:	n/a
35	chr2:234652363-234652413	BE2_C	brain:	n/a
36	chr2:234652669-234652719	HPAEpiC	pulmonary alveolar:	n/a
37	chr2:234655709-234655759	AG04450	lung:	fetal
38	chr2:234650765-234650815	H1-hESC	embryonic stem cell:	embryo
39	chr2:234661536-234661586	HepG2	liver:	n/a
40	chr2:234651850-234651900	MCF-7	breast:	n/a
41	chr2:234650765-234650815	Caco-2	colon:	n/a
42	chr2:234650765-234650815	GM12891	blood:	n/a
43	chr2:234650765-234650815	HCT-116	colon:	n/a
44	chr2:234652601-234652651	HEK293	kidney:	embryo
45	chr2:234652466-234652516	GM19239	blood:	n/a
46	chr2:234652466-234652516	HepG2	liver:	n/a
47	chr2:234652466-234652516	AoSMC	blood vessel:	n/a
48	chr2:234652601-234652651	GM12891	blood:	n/a
49	chr2:234650765-234650815	AG09309	skin:	n/a
50	chr2:234653891-234653941	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:234651385..234654197-chr2:234659573..234662296,2	MCF-7	breast:
2	chr17:63274126..63274957-chr2:234657055..234657979,2	MCF-7	breast:
3	2:234543708-234558325..2:234649753-234657866	Hela-S3	cervix:
4	chr2:234660399..234662742-chr2:234667989..234670944,2	MCF-7	breast:
5	chr2:234650134..234652973-chr2:234653062..234655371,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT1A1-1	chr2:234661849-234662302	NONHSAT077510
2	lnc-UGT1A1-1	chr2:234660991-234661189	NONHSAT077510
3	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
ENSG00000242515	chromatin interactions
ENSG00000227802	chromatin interactions
ENSG00000241635	chromatin interactions
ENSG00000234143	chromatin interactions
ENSG00000242366	chromatin interactions

Extended variants
information (count: 582 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:582 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs386656371	chr2:234650604-234650605	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs115311938	chr2:234650605-234650606	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs573640732	chr2:234650652-234650653	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs115965783	chr2:234650662-234650663	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs553186051	chr2:234650685-234650686	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs371861111	chr2:234650693-234650694	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs146940550	chr2:234650698-234650699	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs180718670	chr2:234650703-234650704	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs74500985	chr2:234650706-234650707	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs185159129	chr2:234650714-234650715	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs147639323	chr2:234650718-234650719	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs539350164	chr2:234650736-234650737	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs544656761	chr2:234650755-234650756	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs368055004	chr2:234650759-234650760	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs142315410	chr2:234650765-234650766	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs569949528	chr2:234650787-234650788	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs114514275	chr2:234650794-234650795	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs146169334	chr2:234650826-234650827	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs191023728	chr2:234650870-234650871	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs557222655	chr2:234650874-234650875	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs571045989	chr2:234650882-234650883	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs530513116	chr2:234650921-234650922	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs113985330	chr2:234650927-234650928	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs4663966	chr2:234650964-234650965	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs566927246	chr2:234650996-234650997	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs536204491	chr2:234651008-234651009	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs553013500	chr2:234651040-234651041	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs566737557	chr2:234651057-234651058	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs114948883	chr2:234651067-234651068	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs62191917	chr2:234651071-234651072	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs112027081	chr2:234651088-234651089	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs376180640	chr2:234651142-234651143	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs35688951	chr2:234651157-234651158	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs544718368	chr2:234651220-234651221	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs28900373	chr2:234651223-234651224	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs150422783	chr2:234651248-234651249	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs540595235	chr2:234651254-234651255	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs138236964	chr2:234651261-234651262	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs532826876	chr2:234651275-234651276	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs546122146	chr2:234651359-234651360	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs17863795	chr2:234651369-234651370	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs181572285	chr2:234651390-234651391	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs550270409	chr2:234651427-234651428	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs76952857	chr2:234651428-234651429	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs564880841	chr2:234651459-234651460	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs546559267	chr2:234651492-234651493	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs186747767	chr2:234651539-234651540	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs28900374	chr2:234651542-234651543	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs558840772	chr2:234651561-234651562	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs78644424	chr2:234651582-234651583	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 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:57 , 50 per page) page: 1 2

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	chr2:234646400-234651000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr2:234646400-234666600	Weak transcription	Stomach Mucosa	stomach
6	chr2:234647800-234652200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr2:234647800-234655000	Weak transcription	Gastric	stomach
8	chr2:234649800-234652200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr2:234649800-234658800	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr2:234650400-234652600	Genic enhancers	Liver	Liver
11	chr2:234651000-234652800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr2:234652200-234652600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr2:234652200-234652600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr2:234652200-234652600	ZNF genes & repeats	Esophagus	oesophagus
15	chr2:234652200-234652800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr2:234652400-234652600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr2:234652600-234654400	Enhancers	Liver	Liver
18	chr2:234652600-234654600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr2:234652800-234658200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr2:234652800-234659200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr2:234653200-234654400	Enhancers	HepG2	liver
22	chr2:234653200-234655600	Enhancers	Fetal Intestine Small	intestine
23	chr2:234653400-234653800	Enhancers	A549	lung
24	chr2:234653800-234654200	Active TSS	A549	lung
25	chr2:234654200-234654800	Enhancers	Small Intestine	intestine
26	chr2:234654200-234655000	Enhancers	A549	lung
27	chr2:234654200-234655400	Enhancers	Duodenum Mucosa	Duodenum
28	chr2:234654200-234655400	Enhancers	Fetal Intestine Large	intestine
29	chr2:234654400-234654600	Flanking Active TSS	HepG2	liver
30	chr2:234654400-234656000	Flanking Active TSS	Liver	Liver
31	chr2:234654600-234655800	Bivalent Enhancer	HepG2	liver
32	chr2:234655000-234655200	Flanking Active TSS	A549	lung
33	chr2:234655000-234655600	Enhancers	Gastric	stomach
34	chr2:234655200-234655400	Enhancers	A549	lung
35	chr2:234655400-234655600	Flanking Active TSS	A549	lung
36	chr2:234655400-234656200	Enhancers	Pancreas	Pancrea
37	chr2:234655600-234656200	Enhancers	A549	lung
38	chr2:234656000-234656600	Enhancers	Liver	Liver
39	chr2:234656200-234659000	Weak transcription	A549	lung
40	chr2:234656600-234657000	Flanking Active TSS	Liver	Liver
41	chr2:234657000-234657200	Enhancers	Liver	Liver
42	chr2:234657200-234657600	Flanking Active TSS	Liver	Liver
43	chr2:234657600-234658000	Active TSS	Liver	Liver
44	chr2:234658000-234658200	Flanking Active TSS	Liver	Liver
45	chr2:234658200-234660600	Enhancers	Liver	Liver
46	chr2:234658200-234664000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr2:234659200-234659800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr2:234659600-234660200	ZNF genes & repeats	Colonic Mucosa	Colon
49	chr2:234659600-234660800	ZNF genes & repeats	Fetal Intestine Small	intestine
50	chr2:234659800-234661800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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