Variant report

Variant	nsv3215
Chromosome Location	chr2:234631123-234670276
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	ARID3A	chr2:234665213-234665815	HepG2	liver:	n/a	n/a
3	ATF3	chr2:234653988-234654486	A549	lung:	n/a	n/a
4	ATF3	chr2:234665232-234665880	A549	lung:	n/a	n/a
5	ATF3	chr2:234665180-234665897	A549	lung:	n/a	n/a
6	BCL3	chr2:234665162-234665915	A549	lung:	n/a	n/a
7	BCL3	chr2:234665053-234665927	A549	lung:	n/a	n/a
8	BCL3	chr2:234653885-234654544	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	chr2:234668687-234669015	HepG2	liver:	n/a	chr2:234668830-234668839 chr2:234668830-234668839 chr2:234668831-234668840 chr2:234668828-234668841 chr2:234668824-234668845 chr2:234668829-234668838
12	BHLHE40	chr2:234665426-234665807	HepG2	liver:	n/a	n/a
13	BHLHE40	chr2:234665457-234665720	HepG2	liver:	n/a	n/a
14	CBX3	chr2:234659353-234659614	K562	blood:	n/a	n/a
15	CEBPB	chr2:234665312-234665783	A549	lung:	n/a	chr2:234665476-234665488 chr2:234665429-234665440
16	CEBPB	chr2:234654020-234654389	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	chr2:234639004-234639011	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr2:234670054-234670364	IMR90	lung:	n/a	n/a
20	CEBPB	chr2:234638863-234639204	IMR90	lung:	n/a	chr2:234639027-234639038
21	CEBPB	chr2:234656934-234657289	HepG2	liver:	n/a	chr2:234657082-234657093 chr2:234657082-234657093 chr2:234657104-234657115
22	CEBPB	chr2:234638962-234639116	Hela-S3	cervix:	n/a	chr2:234639027-234639038
23	CEBPB	chr2:234665395-234665774	HepG2	liver:	n/a	chr2:234665476-234665488 chr2:234665429-234665440
24	CEBPB	chr2:234665343-234665750	HepG2	liver:	n/a	chr2:234665476-234665488 chr2:234665429-234665440
25	CEBPB	chr2:234638858-234639186	HepG2	liver:	n/a	chr2:234639027-234639038
26	CEBPB	chr2:234653943-234654318	A549	lung:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
27	CEBPB	chr2:234656935-234657273	A549	lung:	n/a	chr2:234657082-234657093 chr2:234657082-234657093 chr2:234657104-234657115
28	CEBPB	chr2:234653902-234654598	HepG2	liver:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
29	CEBPB	chr2:234645458-234645657	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:234638876-234639151	K562	blood:	n/a	chr2:234639027-234639038
31	CEBPB	chr2:234653892-234654497	A549	lung:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
32	CEBPB	chr2:234665270-234665777	HepG2	liver:	n/a	chr2:234665476-234665488 chr2:234665429-234665440
33	CEBPB	chr2:234653908-234654385	HepG2	liver:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
34	CEBPB	chr2:234665269-234665761	A549	lung:	n/a	chr2:234665476-234665488 chr2:234665429-234665440
35	CEBPB	chr2:234657008-234657264	IMR90	lung:	n/a	chr2:234657082-234657093 chr2:234657082-234657093 chr2:234657104-234657115
36	CEBPB	chr2:234638913-234639194	A549	lung:	n/a	chr2:234639027-234639038
37	CEBPB	chr2:234665229-234665946	A549	lung:	n/a	chr2:234665476-234665488 chr2:234665429-234665440
38	CEBPB	chr2:234639642-234639778	HepG2	liver:	n/a	n/a
39	CEBPB	chr2:234653961-234654410	HepG2	liver:	n/a	chr2:234654071-234654082 chr2:234654069-234654086 chr2:234654118-234654130
40	CEBPB	chr2:234665245-234665826	HepG2	liver:	n/a	chr2:234665476-234665488 chr2:234665429-234665440
41	CEBPD	chr2:234665351-234665763	HepG2	liver:	n/a	n/a
42	CEBPD	chr2:234665334-234665685	HepG2	liver:	n/a	n/a
43	CEBPD	chr2:234654049-234654478	HepG2	liver:	n/a	n/a
44	CHD2	chr2:234668019-234668042	HepG2	liver:	n/a	n/a
45	CHD2	chr2:234654164-234654273	HepG2	liver:	n/a	n/a
46	CREB1	chr2:234654194-234654509	A549	lung:	n/a	n/a
47	CREB1	chr2:234665410-234665788	A549	lung:	n/a	n/a
48	CREB1	chr2:234665450-234665902	A549	lung:	n/a	n/a
49	CREB1	chr2:234653968-234654547	HepG2	liver:	n/a	n/a
50	CREB1	chr2:234654062-234654459	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:234668930-234668980	HL-60	blood:	n/a
2	chr2:234652681-234652731	AG04450	lung:	fetal
3	chr2:234668930-234668980	HL-60	blood:	n/a
4	chr2:234652681-234652731	AG04450	lung:	fetal
5	chr2:234663937-234663987	AG04450	lung:	fetal
6	chr2:234662401-234662451	GM12892	blood:	n/a
7	chr2:234649204-234649254	Caco-2	colon:	n/a
8	chr2:234637306-234637356	PrEC	prostate:	n/a
9	chr2:234652363-234652413	AoSMC	blood vessel:	n/a
10	chr2:234661536-234661586	HCM	heart:	n/a
11	chr2:234637667-234637717	HRE	kidney:	n/a
12	chr2:234667988-234668038	SK-N-SH	brain:	n/a
13	chr2:234668834-234668884	GM06990	blood:	n/a
14	chr2:234655709-234655759	GM12891	blood:	n/a
15	chr2:234637667-234637717	HRCEpiC	kidney:	n/a
16	chr2:234650765-234650815	HPAEpiC	pulmonary alveolar:	n/a
17	chr2:234637306-234637356	A549	lung:	n/a
18	chr2:234637574-234637624	NH-A	brain:	n/a
19	chr2:234669166-234669216	ProgFib	skin:	n/a
20	chr2:234637574-234637624	CMK	blood:	n/a
21	chr2:234638269-234638319	SK-N-MC	brain:	n/a
22	chr2:234663900-234663950	HRCEpiC	kidney:	n/a
23	chr2:234636389-234636439	LNCaP	prostate:	n/a
24	chr2:234638269-234638319	U87	brain:	n/a
25	chr2:234637667-234637717	HRPEpiC	eye:	n/a
26	chr2:234637306-234637356	CMK	blood:	n/a
27	chr2:234668042-234668092	PrEC	prostate:	n/a
28	chr2:234668930-234668980	ProgFib	skin:	n/a
29	chr2:234662759-234662809	AG10803	skin:	n/a
30	chr2:234667777-234667827	HAEpiC	amniotic membrane:	n/a
31	chr2:234637574-234637624	AoSMC	blood vessel:	n/a
32	chr2:234652601-234652651	GM06990	blood:	n/a
33	chr2:234668834-234668884	AG04449	skin:	fetal
34	chr2:234668930-234668980	HEK293	kidney:	embryo
35	chr2:234667988-234668038	SAEC	small airway:	n/a
36	chr2:234661536-234661586	HUVEC	blood vessel:	n/a
37	chr2:234652601-234652651	AG04449	skin:	fetal
38	chr2:234638269-234638319	HEEpiC	esophagus:	n/a
39	chr2:234652669-234652719	BE2_C	brain:	n/a
40	chr2:234653891-234653941	HNPCEpiC	eye:	n/a
41	chr2:234652669-234652719	Hela-S3	cervix:	n/a
42	chr2:234637667-234637717	Hela-S3	cervix:	n/a
43	chr2:234662759-234662809	PrEC	prostate:	n/a
44	chr2:234668355-234668405	HRE	kidney:	n/a
45	chr2:234651850-234651900	BE2_C	brain:	n/a
46	chr2:234652681-234652731	A549	lung:	n/a
47	chr2:234655709-234655759	SK-N-MC	brain:	n/a
48	chr2:234662401-234662451	HMEC	breast:	n/a
49	chr2:234667777-234667827	BE2_C	brain:	n/a
50	chr2:234662759-234662809	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	2:234543708-234558325..2:234649753-234657866	Hela-S3	cervix:
2	chr2:234660399..234662742-chr2:234667989..234670944,2	MCF-7	breast:
3	chr2:234650134..234652973-chr2:234653062..234655371,2	MCF-7	breast:
4	chr2:234651385..234654197-chr2:234659573..234662296,2	MCF-7	breast:
5	chr17:63274126..63274957-chr2:234657055..234657979,2	MCF-7	breast:
6	chr2:234637896..234640536-chr2:234645854..234647790,2	MCF-7	breast:
7	2:234635414-234639782..2:234772667-234780240	Hela-S3	cervix:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT1A1-1	chr2:234661849-234662302	NONHSAT077510
2	lnc-HJURP-4	chr2:234662962-234663437	NR_037696
3	lnc-UGT1A1-2	chr2:234647598-234647701	NONHSAT077507
4	lnc-HJURP-4	chr2:234663790-234663991	NR_037696
5	lnc-UGT1A1-1	chr2:234659263-234659366	NONHSAT077510
6	lnc-UGT1A1-1	chr2:234660991-234661189	NONHSAT077510
7	lnc-UGT1A1-2	chr2:234649334-234649521	NONHSAT077507
8	lnc-UGT1A1-2	chr2:234650166-234650603	NONHSAT077507

Variant related genes	Relation type
UGT1A2P	TF binding region
ENSG00000248705	TF binding region
ENSG00000178836	TF binding region
ENSG00000248114	TF binding region
UGT1A1	TF binding region
UGT1A8	TF binding region
DNAJB3	TF binding region
UGT1A3	TF binding region
RPL17P11	TF binding region
UGT1A2P	CpG island
ENSG00000248705	CpG island
ENSG00000178836	CpG island
ENSG00000248114	CpG island
UGT1A1	CpG island
UGT1A8	CpG island
DNAJB3	CpG island
UGT1A3	CpG island
RPL17P11	CpG island
ENSG00000242366	chromatin interactions
ENSG00000234143	chromatin interactions
ENSG00000241635	chromatin interactions
ENSG00000242515	chromatin interactions
ENSG00000248114	chromatin interactions
ENSG00000224287	chromatin interactions
ENSG00000227802	chromatin interactions

Extended variants
information (count: 1860 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1860 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147045039	chr2:234631136-234631137	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs147743220	chr2:234631143-234631144	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs188387982	chr2:234631153-234631154	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs558356938	chr2:234631245-234631246	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs571426683	chr2:234631273-234631274	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs370007116	chr2:234631409-234631410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192371212	chr2:234631484-234631485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs61550889	chr2:234631491-234631492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537122940	chr2:234631501-234631502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs397977696	chr2:234631505-234631506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183532563	chr2:234631638-234631639	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs573698030	chr2:234631801-234631802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551785642	chr2:234631840-234631841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111421853	chr2:234631845-234631846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs11677089	chr2:234631847-234631848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201420005	chr2:234631860-234631861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573450645	chr2:234631864-234631865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545296603	chr2:234631918-234631919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs537062236	chr2:234631919-234631920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6760025	chr2:234631921-234631922	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs557278496	chr2:234631935-234631936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543534197	chr2:234631947-234631948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563319275	chr2:234631948-234631949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs528884709	chr2:234632076-234632077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548922303	chr2:234632102-234632103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs6750992	chr2:234632130-234632131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370719058	chr2:234632183-234632184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370680353	chr2:234632188-234632189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200608956	chr2:234632305-234632306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113785176	chr2:234633092-234633093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528357739	chr2:234633101-234633102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551187141	chr2:234633106-234633107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568755731	chr2:234633121-234633122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571092299	chr2:234633135-234633136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563437519	chr2:234633147-234633148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200973045	chr2:234633166-234633167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557040072	chr2:234633177-234633178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs202203863	chr2:234633242-234633243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536726765	chr2:234633253-234633254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553228713	chr2:234633263-234633264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536267654	chr2:234633303-234633304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376440949	chr2:234633317-234633318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138869941	chr2:234633345-234633346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573485749	chr2:234633361-234633362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545669110	chr2:234633398-234633399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559235136	chr2:234633445-234633446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs62191902	chr2:234633459-234633460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372493213	chr2:234633468-234633469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377063392	chr2:234633469-234633470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370433880	chr2:234633520-234633521	Weak transcription	n/a	n/a	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:200 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234617800-234631600	Weak transcription	Gastric	stomach
2	chr2:234620400-234659200	Weak transcription	Colonic Mucosa	Colon
3	chr2:234620600-234652200	Weak transcription	Esophagus	oesophagus
4	chr2:234626000-234634600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr2:234626200-234649600	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr2:234626600-234668400	Weak transcription	NHEK	skin
7	chr2:234627600-234637200	Weak transcription	Duodenum Mucosa	Duodenum
8	chr2:234627800-234636000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr2:234630800-234634000	Weak transcription	A549	lung
10	chr2:234631000-234631400	Active TSS	Liver	Liver
11	chr2:234631400-234635800	Weak transcription	Liver	Liver
12	chr2:234633600-234634000	ZNF genes & repeats	Right Atrium	heart
13	chr2:234633800-234634000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr2:234634000-234634600	Enhancers	A549	lung
15	chr2:234634600-234639400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr2:234634600-234648400	Weak transcription	A549	lung
17	chr2:234635200-234637000	Weak transcription	Stomach Mucosa	stomach
18	chr2:234635800-234636600	Genic enhancers	Liver	Liver
19	chr2:234636000-234639000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr2:234636200-234636600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr2:234636200-234638400	Enhancers	Fetal Intestine Small	intestine
22	chr2:234636600-234637200	Enhancers	Liver	Liver
23	chr2:234636600-234637200	Weak transcription	Gastric	stomach
24	chr2:234637000-234638200	Enhancers	Stomach Mucosa	stomach
25	chr2:234637200-234637400	Flanking Active TSS	Liver	Liver
26	chr2:234637200-234637600	Enhancers	Duodenum Mucosa	Duodenum
27	chr2:234637200-234638000	Enhancers	Gastric	stomach
28	chr2:234637400-234637800	Enhancers	Liver	Liver
29	chr2:234637600-234638200	Bivalent Enhancer	HepG2	liver
30	chr2:234637800-234638600	Flanking Active TSS	Liver	Liver
31	chr2:234638400-234640200	Weak transcription	Fetal Intestine Small	intestine
32	chr2:234638600-234638800	Active TSS	Liver	Liver
33	chr2:234638800-234639400	Transcr. at gene 5' and 3'	Liver	Liver
34	chr2:234639000-234645600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr2:234639400-234639600	Active TSS	Liver	Liver
36	chr2:234639400-234645800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr2:234639600-234641000	Weak transcription	Liver	Liver
38	chr2:234641000-234641600	Enhancers	Liver	Liver
39	chr2:234641600-234642400	Weak transcription	Liver	Liver
40	chr2:234642400-234645000	Enhancers	Liver	Liver
41	chr2:234643400-234645000	Enhancers	HepG2	liver
42	chr2:234644000-234645000	Weak transcription	Fetal Intestine Small	intestine
43	chr2:234645000-234645400	Flanking Active TSS	Liver	Liver
44	chr2:234645000-234646200	Enhancers	Fetal Intestine Small	intestine
45	chr2:234645000-234646200	Flanking Active TSS	HepG2	liver
46	chr2:234645400-234648600	Enhancers	Liver	Liver
47	chr2:234645600-234646400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr2:234645600-234647000	Enhancers	Duodenum Mucosa	Duodenum
49	chr2:234645800-234646200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr2:234646200-234646400	Enhancers	Stomach Mucosa	stomach

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