Variant report

Variant	esv1808921
Chromosome Location	chr2:234648954-234666236
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	chr2:234665213-234665815	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:234653876-234654428	HepG2	liver:	n/a	n/a
3	ATF3	chr2:234665180-234665897	A549	lung:	n/a	n/a
4	ATF3	chr2:234653988-234654486	A549	lung:	n/a	n/a
5	ATF3	chr2:234665232-234665880	A549	lung:	n/a	n/a
6	BCL3	chr2:234653885-234654544	A549	lung:	n/a	n/a
7	BCL3	chr2:234665053-234665927	A549	lung:	n/a	n/a
8	BCL3	chr2:234665162-234665915	A549	lung:	n/a	n/a
9	BCL3	chr2:234653958-234654499	A549	lung:	n/a	n/a
10	BHLHE40	chr2:234654058-234654451	HepG2	liver:	n/a	n/a
11	BHLHE40	chr2:234665457-234665720	HepG2	liver:	n/a	n/a
12	BHLHE40	chr2:234665426-234665807	HepG2	liver:	n/a	n/a
13	CBX3	chr2:234659353-234659614	K562	blood:	n/a	n/a
14	CEBPB	chr2:234653902-234654598	HepG2	liver:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
15	CEBPB	chr2:234653961-234654410	HepG2	liver:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
16	CEBPB	chr2:234653892-234654497	A549	lung:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
17	CEBPB	chr2:234653979-234654335	HepG2	liver:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
18	CEBPB	chr2:234653943-234654318	A549	lung:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
19	CEBPB	chr2:234665312-234665783	A549	lung:	n/a	chr2:234665476-234665488 chr2:234665429-234665440
20	CEBPB	chr2:234656934-234657289	HepG2	liver:	n/a	chr2:234657082-234657093 chr2:234657082-234657093 chr2:234657104-234657115
21	CEBPB	chr2:234665395-234665774	HepG2	liver:	n/a	chr2:234665476-234665488 chr2:234665429-234665440
22	CEBPB	chr2:234665245-234665826	HepG2	liver:	n/a	chr2:234665476-234665488 chr2:234665429-234665440
23	CEBPB	chr2:234665343-234665750	HepG2	liver:	n/a	chr2:234665476-234665488 chr2:234665429-234665440
24	CEBPB	chr2:234653908-234654385	HepG2	liver:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
25	CEBPB	chr2:234656935-234657273	A549	lung:	n/a	chr2:234657082-234657093 chr2:234657082-234657093 chr2:234657104-234657115
26	CEBPB	chr2:234654020-234654389	A549	lung:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
27	CEBPB	chr2:234657008-234657264	IMR90	lung:	n/a	chr2:234657082-234657093 chr2:234657082-234657093 chr2:234657104-234657115
28	CEBPB	chr2:234665270-234665777	HepG2	liver:	n/a	chr2:234665476-234665488 chr2:234665429-234665440
29	CEBPB	chr2:234665229-234665946	A549	lung:	n/a	chr2:234665476-234665488 chr2:234665429-234665440
30	CEBPB	chr2:234665269-234665761	A549	lung:	n/a	chr2:234665476-234665488 chr2:234665429-234665440
31	CEBPD	chr2:234654049-234654478	HepG2	liver:	n/a	n/a
32	CEBPD	chr2:234665334-234665685	HepG2	liver:	n/a	n/a
33	CEBPD	chr2:234665351-234665763	HepG2	liver:	n/a	n/a
34	CHD2	chr2:234654164-234654273	HepG2	liver:	n/a	n/a
35	CREB1	chr2:234653968-234654547	HepG2	liver:	n/a	n/a
36	CREB1	chr2:234665410-234665788	A549	lung:	n/a	n/a
37	CREB1	chr2:234665450-234665902	A549	lung:	n/a	n/a
38	CREB1	chr2:234654062-234654459	A549	lung:	n/a	n/a
39	CREB1	chr2:234653888-234654608	HepG2	liver:	n/a	n/a
40	CREB1	chr2:234654194-234654509	A549	lung:	n/a	n/a
41	CTCF	chr2:234665140-234665221	GM10248	blood:	n/a	n/a
42	CTCF	chr2:234651938-234652009	GM20000	blood:	n/a	n/a
43	CTCF	chr2:234651956-234652041	Kidney_OC	kidney:	n/a	n/a
44	ELF1	chr2:234665287-234665705	A549	lung:	n/a	n/a
45	ELF1	chr2:234665363-234665770	HepG2	liver:	n/a	n/a
46	EP300	chr2:234665194-234665902	HepG2	liver:	n/a	chr2:234665216-234665225
47	EP300	chr2:234654030-234654453	HepG2	liver:	n/a	chr2:234654068-234654082
48	EP300	chr2:234653810-234654542	A549	lung:	n/a	chr2:234654068-234654082 chr2:234653862-234653871
49	EP300	chr2:234653933-234654548	HepG2	liver:	n/a	chr2:234654068-234654082
50	EP300	chr2:234664946-234666071	A549	lung:	n/a	chr2:234665216-234665225

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:234663729-234663779	IMR90	lung:	fetal
2	chr2:234663729-234663779	HEEpiC	esophagus:	n/a
3	chr2:234663729-234663779	IMR90	lung:	fetal
4	chr2:234663729-234663779	HEEpiC	esophagus:	n/a
5	chr2:234652601-234652651	A549	lung:	n/a
6	chr2:234652681-234652731	Caco-2	colon:	n/a
7	chr2:234652669-234652719	AG09309	skin:	n/a
8	chr2:234663729-234663779	HPAEpiC	pulmonary alveolar:	n/a
9	chr2:234662401-234662451	AG09319	gingival:	n/a
10	chr2:234661536-234661586	U87	brain:	n/a
11	chr2:234652681-234652731	LNCaP	prostate:	n/a
12	chr2:234663729-234663779	Hela-S3	cervix:	n/a
13	chr2:234662401-234662451	ProgFib	skin:	n/a
14	chr2:234653891-234653941	PFSK-1	brain:	n/a
15	chr2:234663900-234663950	SAEC	small airway:	n/a
16	chr2:234662759-234662809	HEK293	kidney:	embryo
17	chr2:234663900-234663950	NHBE	bronchial:	n/a
18	chr2:234661536-234661586	NHBE	bronchial:	n/a
19	chr2:234652601-234652651	Jurkat	blood:	n/a
20	chr2:234664336-234664386	GM12891	blood:	n/a
21	chr2:234662759-234662809	BE2_C	brain:	n/a
22	chr2:234653891-234653941	Hepatocyte	liver:	n/a
23	chr2:234661536-234661586	HRE	kidney:	n/a
24	chr2:234663937-234663987	CMK	blood:	n/a
25	chr2:234655709-234655759	SAEC	small airway:	n/a
26	chr2:234652601-234652651	SK-N-MC	brain:	n/a
27	chr2:234663729-234663779	ovcar-3	ovarian:	n/a
28	chr2:234649204-234649254	HPAEpiC	pulmonary alveolar:	n/a
29	chr2:234651850-234651900	SK-N-SH_RA	brain:	n/a
30	chr2:234650765-234650815	GM19239	blood:	n/a
31	chr2:234649204-234649254	NH-A	brain:	n/a
32	chr2:234650765-234650815	NB4	blood:	n/a
33	chr2:234652669-234652719	HAEpiC	amniotic membrane:	n/a
34	chr2:234650765-234650815	BJ	skin:	n/a
35	chr2:234650765-234650815	HRE	kidney:	n/a
36	chr2:234652669-234652719	AoSMC	blood vessel:	n/a
37	chr2:234652363-234652413	A549	lung:	n/a
38	chr2:234652601-234652651	GM06990	blood:	n/a
39	chr2:234662759-234662809	AG09309	skin:	n/a
40	chr2:234662759-234662809	HMEC	breast:	n/a
41	chr2:234650765-234650815	Jurkat	blood:	n/a
42	chr2:234655709-234655759	HCM	heart:	n/a
43	chr2:234649204-234649254	NHBE	bronchial:	n/a
44	chr2:234664336-234664386	GM06990	blood:	n/a
45	chr2:234652601-234652651	HL-60	blood:	n/a
46	chr2:234652669-234652719	GM06990	blood:	n/a
47	chr2:234650765-234650815	BE2_C	brain:	n/a
48	chr2:234651850-234651900	HRCEpiC	kidney:	n/a
49	chr2:234652363-234652413	SK-N-SH_RA	brain:	n/a
50	chr2:234655709-234655759	T-47D	breast:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT1A1-1	chr2:234660991-234661189	NONHSAT077510
2	lnc-HJURP-4	chr2:234663790-234663991	NR_037696
3	lnc-UGT1A1-2	chr2:234649334-234649521	NONHSAT077507
4	lnc-UGT1A1-2	chr2:234650166-234650603	NONHSAT077507
5	lnc-UGT1A1-1	chr2:234661849-234662302	NONHSAT077510
6	lnc-UGT1A1-1	chr2:234659263-234659366	NONHSAT077510
7	lnc-HJURP-4	chr2:234662962-234663437	NR_037696

Variant related genes	Relation type
UGT1A2P	TF binding region
ENSG00000248705	TF binding region
ENSG00000178836	TF binding region
UGT1A1	TF binding region
UGT1A8	TF binding region
DNAJB3	TF binding region
UGT1A2P	CpG island
ENSG00000248705	CpG island
ENSG00000178836	CpG island
UGT1A1	CpG island
UGT1A8	CpG island
DNAJB3	CpG island
ENSG00000242366	chromatin interactions
ENSG00000241635	chromatin interactions
ENSG00000227802	chromatin interactions
ENSG00000242515	chromatin interactions
ENSG00000234143	chromatin interactions

Extended variants
information (count: 864 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:864 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533064296	chr2:234648977-234648978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs543256832	chr2:234649022-234649023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542925034	chr2:234649122-234649123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567256454	chr2:234649133-234649134	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529004725	chr2:234649154-234649155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139363796	chr2:234649163-234649164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566003594	chr2:234649181-234649182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113995315	chr2:234649186-234649187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs60932271	chr2:234649204-234649205	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs571941766	chr2:234649205-234649206	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537335169	chr2:234649250-234649251	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs17862875	chr2:234649302-234649303	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs567869462	chr2:234649313-234649314	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536808969	chr2:234649323-234649324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs145524882	chr2:234649393-234649394	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs189465133	chr2:234649412-234649413	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs541057948	chr2:234649423-234649424	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs557461962	chr2:234649444-234649445	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs528081181	chr2:234649516-234649517	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs557749460	chr2:234649534-234649535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543313311	chr2:234649543-234649544	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563199217	chr2:234649570-234649571	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10714492	chr2:234649574-234649575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576442434	chr2:234649623-234649624	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs192915169	chr2:234649648-234649649	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537141786	chr2:234649649-234649650	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs17868338	chr2:234649665-234649666	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs559824040	chr2:234649747-234649748	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs528561296	chr2:234649764-234649765	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs200537082	chr2:234649775-234649776	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs28900368	chr2:234649808-234649809	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs565131356	chr2:234649870-234649871	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs28900369	chr2:234649878-234649879	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs530886202	chr2:234649886-234649887	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs551312228	chr2:234649905-234649906	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs184999730	chr2:234649956-234649957	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs536876139	chr2:234649958-234649959	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs546865407	chr2:234649976-234649977	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs565810764	chr2:234650004-234650005	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs190389633	chr2:234650015-234650016	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs564848260	chr2:234650016-234650017	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs386656370	chr2:234650101-234650102	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs557790582	chr2:234650103-234650104	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs577572519	chr2:234650112-234650113	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs28900370	chr2:234650119-234650120	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs574132609	chr2:234650124-234650125	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs4663963	chr2:234650193-234650194	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs28900371	chr2:234650208-234650209	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs559274983	chr2:234650221-234650222	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
50	rs569891780	chr2:234650225-234650226	Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:95 , 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	chr2:234626200-234649600	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr2:234626600-234668400	Weak transcription	NHEK	skin
5	chr2:234646400-234651000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr2:234646400-234666600	Weak transcription	Stomach Mucosa	stomach
7	chr2:234647800-234652200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr2:234647800-234655000	Weak transcription	Gastric	stomach
9	chr2:234648000-234649800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr2:234648600-234649200	Weak transcription	Duodenum Mucosa	Duodenum
11	chr2:234648600-234649200	Weak transcription	A549	lung
12	chr2:234648600-234650400	Weak transcription	Liver	Liver
13	chr2:234649600-234649800	Enhancers	Rectal Mucosa Donor 29	rectum
14	chr2:234649800-234652200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr2:234649800-234658800	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr2:234650400-234652600	Genic enhancers	Liver	Liver
17	chr2:234651000-234652800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr2:234652200-234652600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr2:234652200-234652600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr2:234652200-234652600	ZNF genes & repeats	Esophagus	oesophagus
21	chr2:234652200-234652800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr2:234652400-234652600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr2:234652600-234654400	Enhancers	Liver	Liver
24	chr2:234652600-234654600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr2:234652800-234658200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr2:234652800-234659200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr2:234653200-234654400	Enhancers	HepG2	liver
28	chr2:234653200-234655600	Enhancers	Fetal Intestine Small	intestine
29	chr2:234653400-234653800	Enhancers	A549	lung
30	chr2:234653800-234654200	Active TSS	A549	lung
31	chr2:234654200-234654800	Enhancers	Small Intestine	intestine
32	chr2:234654200-234655000	Enhancers	A549	lung
33	chr2:234654200-234655400	Enhancers	Duodenum Mucosa	Duodenum
34	chr2:234654200-234655400	Enhancers	Fetal Intestine Large	intestine
35	chr2:234654400-234654600	Flanking Active TSS	HepG2	liver
36	chr2:234654400-234656000	Flanking Active TSS	Liver	Liver
37	chr2:234654600-234655800	Bivalent Enhancer	HepG2	liver
38	chr2:234655000-234655200	Flanking Active TSS	A549	lung
39	chr2:234655000-234655600	Enhancers	Gastric	stomach
40	chr2:234655200-234655400	Enhancers	A549	lung
41	chr2:234655400-234655600	Flanking Active TSS	A549	lung
42	chr2:234655400-234656200	Enhancers	Pancreas	Pancrea
43	chr2:234655600-234656200	Enhancers	A549	lung
44	chr2:234656000-234656600	Enhancers	Liver	Liver
45	chr2:234656200-234659000	Weak transcription	A549	lung
46	chr2:234656600-234657000	Flanking Active TSS	Liver	Liver
47	chr2:234657000-234657200	Enhancers	Liver	Liver
48	chr2:234657200-234657600	Flanking Active TSS	Liver	Liver
49	chr2:234657600-234658000	Active TSS	Liver	Liver
50	chr2:234658000-234658200	Flanking Active TSS	Liver	Liver

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