Variant report

Variant	esv1808288
Chromosome Location	chr2:234648708-234659502
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	chr2:234653961-234654410	HepG2	liver:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
8	CEBPB	chr2:234656934-234657289	HepG2	liver:	n/a	chr2:234657082-234657093 chr2:234657082-234657093 chr2:234657104-234657115
9	CEBPB	chr2:234653943-234654318	A549	lung:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
10	CEBPB	chr2:234654020-234654389	A549	lung:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
11	CEBPB	chr2:234656935-234657273	A549	lung:	n/a	chr2:234657082-234657093 chr2:234657082-234657093 chr2:234657104-234657115
12	CEBPB	chr2:234653902-234654598	HepG2	liver:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
13	CEBPB	chr2:234653979-234654335	HepG2	liver:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
14	CEBPB	chr2:234653908-234654385	HepG2	liver:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
15	CEBPB	chr2:234657008-234657264	IMR90	lung:	n/a	chr2:234657082-234657093 chr2:234657082-234657093 chr2:234657104-234657115
16	CEBPB	chr2:234653892-234654497	A549	lung:	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	chr2:234653968-234654547	HepG2	liver:	n/a	n/a
20	CREB1	chr2:234654194-234654509	A549	lung:	n/a	n/a
21	CREB1	chr2:234654062-234654459	A549	lung:	n/a	n/a
22	CREB1	chr2:234653888-234654608	HepG2	liver:	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	chr2:234653700-234654700	A549	lung:	n/a	chr2:234654068-234654082 chr2:234653862-234653871
26	EP300	chr2:234653868-234654574	HepG2	liver:	n/a	chr2:234654068-234654082
27	EP300	chr2:234654030-234654453	HepG2	liver:	n/a	chr2:234654068-234654082
28	EP300	chr2:234653933-234654548	HepG2	liver:	n/a	chr2:234654068-234654082
29	EP300	chr2:234653810-234654542	A549	lung:	n/a	chr2:234654068-234654082 chr2:234653862-234653871
30	FOSL2	chr2:234654000-234654628	HepG2	liver:	n/a	n/a
31	FOSL2	chr2:234653946-234654485	HepG2	liver:	n/a	n/a
32	FOSL2	chr2:234654004-234654404	A549	lung:	n/a	n/a
33	FOSL2	chr2:234653860-234654613	A549	lung:	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	chr2:234653696-234654749	HepG2	liver:	n/a	n/a
39	FOXA2	chr2:234653649-234654629	A549	lung:	n/a	n/a
40	FOXA2	chr2:234653884-234654483	HepG2	liver:	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	chr2:234653853-234654551	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	chr2:234653992-234654483	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	chr2:234653857-234654583	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	chr2:234653891-234653941	BJ	skin:	n/a
2	chr2:234651850-234651900	AoSMC	blood vessel:	n/a
3	chr2:234651850-234651900	NHDF-neo	bronchial:	n/a
4	chr2:234652601-234652651	HIPEpiC	eye:	n/a
5	chr2:234652466-234652516	MCF-7	breast:	n/a
6	chr2:234653891-234653941	NHBE	bronchial:	n/a
7	chr2:234651850-234651900	AG09309	skin:	n/a
8	chr2:234649204-234649254	HMEC	breast:	n/a
9	chr2:234652466-234652516	HCM	heart:	n/a
10	chr2:234652363-234652413	MCF10A-Er-Src	breast:	n/a
11	chr2:234652466-234652516	PANC-1	pancreas:	n/a
12	chr2:234650765-234650815	Caco-2	colon:	n/a
13	chr2:234652363-234652413	HCPEpiC	choroid plexus:	n/a
14	chr2:234651850-234651900	SK-N-SH	brain:	n/a
15	chr2:234652363-234652413	U87	brain:	n/a
16	chr2:234653891-234653941	SKMC	muscle:	n/a
17	chr2:234650765-234650815	AG09309	skin:	n/a
18	chr2:234651850-234651900	AG10803	skin:	n/a
19	chr2:234652681-234652731	GM12891	blood:	n/a
20	chr2:234652466-234652516	SAEC	small airway:	n/a
21	chr2:234650765-234650815	GM06990	blood:	n/a
22	chr2:234652466-234652516	HRCEpiC	kidney:	n/a
23	chr2:234652601-234652651	HPAEpiC	pulmonary alveolar:	n/a
24	chr2:234652466-234652516	CMK	blood:	n/a
25	chr2:234652363-234652413	GM12878	blood:	n/a
26	chr2:234652363-234652413	HPAEpiC	pulmonary alveolar:	n/a
27	chr2:234655709-234655759	GM06990	blood:	n/a
28	chr2:234652669-234652719	ECC-1	luminal epithelium:	n/a
29	chr2:234653891-234653941	HNPCEpiC	eye:	n/a
30	chr2:234649204-234649254	MCF-7	breast:	n/a
31	chr2:234650765-234650815	HIPEpiC	eye:	n/a
32	chr2:234651850-234651900	HepG2	liver:	n/a
33	chr2:234652363-234652413	AG04450	lung:	fetal
34	chr2:234651850-234651900	ProgFib	skin:	n/a
35	chr2:234655709-234655759	HRE	kidney:	n/a
36	chr2:234651850-234651900	HMEC	breast:	n/a
37	chr2:234649204-234649254	HAEpiC	amniotic membrane:	n/a
38	chr2:234652681-234652731	MCF-7	breast:	n/a
39	chr2:234650765-234650815	HAEpiC	amniotic membrane:	n/a
40	chr2:234652681-234652731	HIPEpiC	eye:	n/a
41	chr2:234652601-234652651	SK-N-SH_RA	brain:	n/a
42	chr2:234653891-234653941	SK-N-MC	brain:	n/a
43	chr2:234652681-234652731	A549	lung:	n/a
44	chr2:234650765-234650815	ProgFib	skin:	n/a
45	chr2:234652466-234652516	HCT-116	colon:	n/a
46	chr2:234652681-234652731	SK-N-SH	brain:	n/a
47	chr2:234649204-234649254	HEK293	kidney:	embryo
48	chr2:234650765-234650815	RPTEC	kidney:	n/a
49	chr2:234655709-234655759	IMR90	lung:	fetal
50	chr2:234651850-234651900	GM06990	blood:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT1A1-2	chr2:234649334-234649521	NONHSAT077507
2	lnc-UGT1A1-1	chr2:234659263-234659366	NONHSAT077510
3	lnc-UGT1A1-2	chr2:234650166-234650603	NONHSAT077507

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
ENSG00000227802	chromatin interactions
ENSG00000242515	chromatin interactions
ENSG00000234143	chromatin interactions

Extended variants
information (count: 552 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:552 , 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	rs6740653	chr2:234648708-234648709	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs375117222	chr2:234648727-234648728	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs17862874	chr2:234648746-234648747	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs143794870	chr2:234648780-234648781	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs565737138	chr2:234648790-234648791	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs534667918	chr2:234648797-234648798	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs578012287	chr2:234648802-234648803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571818278	chr2:234648805-234648806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537677937	chr2:234648814-234648815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191572005	chr2:234648816-234648817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573081380	chr2:234648832-234648833	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543664272	chr2:234648838-234648839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2018985	chr2:234648860-234648861	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs183860423	chr2:234648866-234648867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs6746419	chr2:234648883-234648884	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs540642726	chr2:234648910-234648911	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564436017	chr2:234648948-234648949	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533064296	chr2:234648977-234648978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543256832	chr2:234649022-234649023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542925034	chr2:234649122-234649123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567256454	chr2:234649133-234649134	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529004725	chr2:234649154-234649155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139363796	chr2:234649163-234649164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566003594	chr2:234649181-234649182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113995315	chr2:234649186-234649187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs60932271	chr2:234649204-234649205	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs571941766	chr2:234649205-234649206	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537335169	chr2:234649250-234649251	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs17862875	chr2:234649302-234649303	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs567869462	chr2:234649313-234649314	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536808969	chr2:234649323-234649324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145524882	chr2:234649393-234649394	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs189465133	chr2:234649412-234649413	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs541057948	chr2:234649423-234649424	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs557461962	chr2:234649444-234649445	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs528081181	chr2:234649516-234649517	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs557749460	chr2:234649534-234649535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543313311	chr2:234649543-234649544	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563199217	chr2:234649570-234649571	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10714492	chr2:234649574-234649575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576442434	chr2:234649623-234649624	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192915169	chr2:234649648-234649649	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs537141786	chr2:234649649-234649650	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs17868338	chr2:234649665-234649666	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs559824040	chr2:234649747-234649748	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs528561296	chr2:234649764-234649765	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs200537082	chr2:234649775-234649776	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs28900368	chr2:234649808-234649809	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs565131356	chr2:234649870-234649871	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs28900369	chr2:234649878-234649879	Weak transcription	Chromatin interactive region	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:54 , 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	chr2:234646400-234648800	Bivalent Enhancer	HepG2	liver
6	chr2:234646400-234651000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr2:234646400-234666600	Weak transcription	Stomach Mucosa	stomach
8	chr2:234647800-234652200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr2:234647800-234655000	Weak transcription	Gastric	stomach
10	chr2:234648000-234649800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr2:234648600-234649200	Weak transcription	Duodenum Mucosa	Duodenum
12	chr2:234648600-234649200	Weak transcription	A549	lung
13	chr2:234648600-234650400	Weak transcription	Liver	Liver
14	chr2:234649600-234649800	Enhancers	Rectal Mucosa Donor 29	rectum
15	chr2:234649800-234652200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr2:234649800-234658800	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr2:234650400-234652600	Genic enhancers	Liver	Liver
18	chr2:234651000-234652800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr2:234652200-234652600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr2:234652200-234652600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr2:234652200-234652600	ZNF genes & repeats	Esophagus	oesophagus
22	chr2:234652200-234652800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr2:234652400-234652600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr2:234652600-234654400	Enhancers	Liver	Liver
25	chr2:234652600-234654600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr2:234652800-234658200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr2:234652800-234659200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr2:234653200-234654400	Enhancers	HepG2	liver
29	chr2:234653200-234655600	Enhancers	Fetal Intestine Small	intestine
30	chr2:234653400-234653800	Enhancers	A549	lung
31	chr2:234653800-234654200	Active TSS	A549	lung
32	chr2:234654200-234654800	Enhancers	Small Intestine	intestine
33	chr2:234654200-234655000	Enhancers	A549	lung
34	chr2:234654200-234655400	Enhancers	Duodenum Mucosa	Duodenum
35	chr2:234654200-234655400	Enhancers	Fetal Intestine Large	intestine
36	chr2:234654400-234654600	Flanking Active TSS	HepG2	liver
37	chr2:234654400-234656000	Flanking Active TSS	Liver	Liver
38	chr2:234654600-234655800	Bivalent Enhancer	HepG2	liver
39	chr2:234655000-234655200	Flanking Active TSS	A549	lung
40	chr2:234655000-234655600	Enhancers	Gastric	stomach
41	chr2:234655200-234655400	Enhancers	A549	lung
42	chr2:234655400-234655600	Flanking Active TSS	A549	lung
43	chr2:234655400-234656200	Enhancers	Pancreas	Pancrea
44	chr2:234655600-234656200	Enhancers	A549	lung
45	chr2:234656000-234656600	Enhancers	Liver	Liver
46	chr2:234656200-234659000	Weak transcription	A549	lung
47	chr2:234656600-234657000	Flanking Active TSS	Liver	Liver
48	chr2:234657000-234657200	Enhancers	Liver	Liver
49	chr2:234657200-234657600	Flanking Active TSS	Liver	Liver
50	chr2:234657600-234658000	Active TSS	Liver	Liver

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