Variant report

Variant	nsv584705
Chromosome Location	chr2:234658623-234665537
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	ATF3	chr2:234665232-234665880	A549	lung:	n/a	n/a
3	ATF3	chr2:234665180-234665897	A549	lung:	n/a	n/a
4	BCL3	chr2:234665053-234665927	A549	lung:	n/a	n/a
5	BCL3	chr2:234665162-234665915	A549	lung:	n/a	n/a
6	BHLHE40	chr2:234665457-234665720	HepG2	liver:	n/a	n/a
7	BHLHE40	chr2:234665426-234665807	HepG2	liver:	n/a	n/a
8	CBX3	chr2:234659353-234659614	K562	blood:	n/a	n/a
9	CEBPB	chr2:234665245-234665826	HepG2	liver:	n/a	chr2:234665476-234665488 chr2:234665429-234665440
10	CEBPB	chr2:234665269-234665761	A549	lung:	n/a	chr2:234665476-234665488 chr2:234665429-234665440
11	CEBPB	chr2:234665395-234665774	HepG2	liver:	n/a	chr2:234665476-234665488 chr2:234665429-234665440
12	CEBPB	chr2:234665312-234665783	A549	lung:	n/a	chr2:234665476-234665488 chr2:234665429-234665440
13	CEBPB	chr2:234665270-234665777	HepG2	liver:	n/a	chr2:234665476-234665488 chr2:234665429-234665440
14	CEBPB	chr2:234665343-234665750	HepG2	liver:	n/a	chr2:234665476-234665488 chr2:234665429-234665440
15	CEBPB	chr2:234665229-234665946	A549	lung:	n/a	chr2:234665476-234665488 chr2:234665429-234665440
16	CEBPD	chr2:234665351-234665763	HepG2	liver:	n/a	n/a
17	CEBPD	chr2:234665334-234665685	HepG2	liver:	n/a	n/a
18	CREB1	chr2:234665450-234665902	A549	lung:	n/a	n/a
19	CREB1	chr2:234665410-234665788	A549	lung:	n/a	n/a
20	CTCF	chr2:234665140-234665221	GM10248	blood:	n/a	n/a
21	ELF1	chr2:234665287-234665705	A549	lung:	n/a	n/a
22	ELF1	chr2:234665363-234665770	HepG2	liver:	n/a	n/a
23	EP300	chr2:234665382-234665803	HepG2	liver:	n/a	n/a
24	EP300	chr2:234665041-234665982	A549	lung:	n/a	chr2:234665216-234665225
25	EP300	chr2:234665194-234665902	HepG2	liver:	n/a	chr2:234665216-234665225
26	EP300	chr2:234665228-234665863	HepG2	liver:	n/a	n/a
27	EP300	chr2:234664946-234666071	A549	lung:	n/a	chr2:234665216-234665225
28	ETS1	chr2:234665254-234665806	A549	lung:	n/a	n/a
29	FOSL2	chr2:234665355-234665937	HepG2	liver:	n/a	n/a
30	FOSL2	chr2:234665276-234665787	A549	lung:	n/a	n/a
31	FOSL2	chr2:234665168-234665967	A549	lung:	n/a	n/a
32	FOSL2	chr2:234665356-234665899	HepG2	liver:	n/a	n/a
33	FOXA1	chr2:234664847-234665924	HepG2	liver:	n/a	n/a
34	FOXA1	chr2:234665190-234665843	HepG2	liver:	n/a	n/a
35	FOXA1	chr2:234665076-234665877	HepG2	liver:	n/a	n/a
36	FOXA1	chr2:234665199-234665867	HepG2	liver:	n/a	n/a
37	FOXA2	chr2:234665036-234665882	HepG2	liver:	n/a	n/a
38	FOXA2	chr2:234664889-234665876	A549	lung:	n/a	n/a
39	FOXA2	chr2:234665202-234665815	HepG2	liver:	n/a	n/a
40	FOXA2	chr2:234665158-234665999	A549	lung:	n/a	n/a
41	GABPA	chr2:234665373-234665756	A549	lung:	n/a	n/a
42	GABPA	chr2:234665175-234665784	A549	lung:	n/a	n/a
43	GATA3	chr2:234665065-234665940	A549	lung:	n/a	n/a
44	GATA3	chr2:234665206-234665942	A549	lung:	n/a	n/a
45	HDAC2	chr2:234665213-234665928	HepG2	liver:	n/a	n/a
46	HDAC2	chr2:234665224-234665850	HepG2	liver:	n/a	n/a
47	HNF4A	chr2:234665304-234665827	HepG2	liver:	n/a	chr2:234665643-234665656 chr2:234665643-234665656 chr2:234665591-234665606 chr2:234665642-234665657 chr2:234665639-234665661
48	HNF4A	chr2:234665383-234665813	HepG2	liver:	n/a	chr2:234665643-234665656 chr2:234665643-234665656 chr2:234665591-234665606 chr2:234665642-234665657 chr2:234665639-234665661
49	HNF4A	chr2:234665337-234665848	HepG2	liver:	n/a	chr2:234665643-234665656 chr2:234665643-234665656 chr2:234665591-234665606 chr2:234665642-234665657 chr2:234665639-234665661
50	HNF4G	chr2:234665340-234665801	HepG2	liver:	n/a	chr2:234665643-234665656 chr2:234665643-234665656 chr2:234665639-234665661

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:234661536-234661586	ProgFib	skin:	n/a
2	chr2:234662759-234662809	HRE	kidney:	n/a
3	chr2:234661536-234661586	PrEC	prostate:	n/a
4	chr2:234664336-234664386	NH-A	brain:	n/a
5	chr2:234662401-234662451	NT2-D1	testis:	n/a
6	chr2:234663937-234663987	HRE	kidney:	n/a
7	chr2:234663900-234663950	GM06990	blood:	n/a
8	chr2:234663900-234663950	PFSK-1	brain:	n/a
9	chr2:234661536-234661586	HIPEpiC	eye:	n/a
10	chr2:234663729-234663779	AoSMC	blood vessel:	n/a
11	chr2:234663729-234663779	AG09319	gingival:	n/a
12	chr2:234663729-234663779	AG09309	skin:	n/a
13	chr2:234664336-234664386	HNPCEpiC	eye:	n/a
14	chr2:234663900-234663950	SK-N-SH_RA	brain:	n/a
15	chr2:234663937-234663987	ovcar-3	ovarian:	n/a
16	chr2:234661536-234661586	HCPEpiC	choroid plexus:	n/a
17	chr2:234662401-234662451	U87	brain:	n/a
18	chr2:234663729-234663779	K562	blood:	n/a
19	chr2:234663900-234663950	Hela-S3	cervix:	n/a
20	chr2:234663729-234663779	HEEpiC	esophagus:	n/a
21	chr2:234663937-234663987	ECC-1	luminal epithelium:	n/a
22	chr2:234664336-234664386	GM12878	blood:	n/a
23	chr2:234663729-234663779	SKMC	muscle:	n/a
24	chr2:234664336-234664386	PFSK-1	brain:	n/a
25	chr2:234664336-234664386	MCF10A-Er-Src	breast:	n/a
26	chr2:234663900-234663950	GM12891	blood:	n/a
27	chr2:234661536-234661586	AG09319	gingival:	n/a
28	chr2:234663729-234663779	NH-A	brain:	n/a
29	chr2:234661536-234661586	AG04449	skin:	fetal
30	chr2:234663900-234663950	NHBE	bronchial:	n/a
31	chr2:234662759-234662809	HepG2	liver:	n/a
32	chr2:234663729-234663779	LNCaP	prostate:	n/a
33	chr2:234662759-234662809	HNPCEpiC	eye:	n/a
34	chr2:234663900-234663950	K562	blood:	n/a
35	chr2:234662759-234662809	SK-N-SH_RA	brain:	n/a
36	chr2:234663937-234663987	Caco-2	colon:	n/a
37	chr2:234663729-234663779	Hepatocyte	liver:	n/a
38	chr2:234664336-234664386	SKMC	muscle:	n/a
39	chr2:234663900-234663950	AG09309	skin:	n/a
40	chr2:234662401-234662451	NHBE	bronchial:	n/a
41	chr2:234662759-234662809	HPAEpiC	pulmonary alveolar:	n/a
42	chr2:234663937-234663987	CMK	blood:	n/a
43	chr2:234662401-234662451	HPAEpiC	pulmonary alveolar:	n/a
44	chr2:234662759-234662809	U87	brain:	n/a
45	chr2:234662759-234662809	ovcar-3	ovarian:	n/a
46	chr2:234663900-234663950	BE2_C	brain:	n/a
47	chr2:234661536-234661586	HCF	heart:	n/a
48	chr2:234662759-234662809	IMR90	lung:	fetal
49	chr2:234664336-234664386	SAEC	small airway:	n/a
50	chr2:234663729-234663779	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:234651385..234654197-chr2:234659573..234662296,2	MCF-7	breast:
2	chr2:234660399..234662742-chr2:234667989..234670944,2	MCF-7	breast:

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

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

Extended variants
information (count: 330 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:330 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2221198	chr2:234658623-234658624	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs551997072	chr2:234658640-234658641	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs570611446	chr2:234658693-234658694	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs140494674	chr2:234658708-234658709	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556183809	chr2:234658709-234658710	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs12987866	chr2:234658712-234658713	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs535406029	chr2:234658719-234658720	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs187295904	chr2:234658801-234658802	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs571998663	chr2:234658827-234658828	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs569592101	chr2:234658830-234658831	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192238866	chr2:234658862-234658863	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577374317	chr2:234658925-234658926	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs543565956	chr2:234658963-234658964	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148166585	chr2:234658997-234658998	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs2885296	chr2:234659061-234659062	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs542993869	chr2:234659103-234659104	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs565350753	chr2:234659156-234659157	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs532642092	chr2:234659157-234659158	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560132107	chr2:234659164-234659165	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528794181	chr2:234659167-234659168	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552056379	chr2:234659173-234659174	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs575907211	chr2:234659212-234659213	ZNF genes & repeats Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs571880040	chr2:234659222-234659223	ZNF genes & repeats Strong transcription Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs531101043	chr2:234659242-234659243	ZNF genes & repeats Strong transcription Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs528497272	chr2:234659293-234659294	ZNF genes & repeats Strong transcription Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs370950467	chr2:234659296-234659297	ZNF genes & repeats Strong transcription Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs370445295	chr2:234659297-234659298	ZNF genes & repeats Strong transcription Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs370642557	chr2:234659308-234659309	ZNF genes & repeats Strong transcription Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs569716311	chr2:234659360-234659361	ZNF genes & repeats Strong transcription Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs183516703	chr2:234659402-234659403	ZNF genes & repeats Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544770541	chr2:234659420-234659421	ZNF genes & repeats Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs139213832	chr2:234659421-234659422	ZNF genes & repeats Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555312200	chr2:234659435-234659436	ZNF genes & repeats Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs62191919	chr2:234659471-234659472	ZNF genes & repeats Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534611009	chr2:234659493-234659494	ZNF genes & repeats Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs28899469	chr2:234659502-234659503	ZNF genes & repeats Strong transcription Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs577435588	chr2:234659534-234659535	ZNF genes & repeats Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543579784	chr2:234659540-234659541	ZNF genes & repeats Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147161885	chr2:234659552-234659553	ZNF genes & repeats Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574072604	chr2:234659555-234659556	ZNF genes & repeats Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542704180	chr2:234659576-234659577	ZNF genes & repeats Strong transcription Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs188955971	chr2:234659614-234659615	ZNF genes & repeats Strong transcription Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs140441181	chr2:234659633-234659634	ZNF genes & repeats Strong transcription Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs545732182	chr2:234659637-234659638	ZNF genes & repeats Strong transcription Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs560264893	chr2:234659645-234659646	ZNF genes & repeats Strong transcription Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs74787288	chr2:234659667-234659668	ZNF genes & repeats Strong transcription Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs193102367	chr2:234659669-234659670	ZNF genes & repeats Strong transcription Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs112081091	chr2:234659684-234659685	ZNF genes & repeats Strong transcription Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs531044910	chr2:234659758-234659759	ZNF genes & repeats Strong transcription Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs138900465	chr2:234659765-234659766	ZNF genes & repeats Strong transcription Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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	21293372	CNVD

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234620400-234659200	Weak transcription	Colonic Mucosa	Colon
2	chr2:234626600-234668400	Weak transcription	NHEK	skin
3	chr2:234646400-234666600	Weak transcription	Stomach Mucosa	stomach
4	chr2:234649800-234658800	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr2:234652800-234659200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr2:234656200-234659000	Weak transcription	A549	lung
7	chr2:234658200-234660600	Enhancers	Liver	Liver
8	chr2:234658200-234664000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr2:234659200-234659800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr2:234659600-234660200	ZNF genes & repeats	Colonic Mucosa	Colon
11	chr2:234659600-234660800	ZNF genes & repeats	Fetal Intestine Small	intestine
12	chr2:234659800-234661800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr2:234660000-234666200	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr2:234660200-234666400	Weak transcription	Colonic Mucosa	Colon
15	chr2:234660600-234663800	Weak transcription	Liver	Liver
16	chr2:234661400-234662000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr2:234661400-234662200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr2:234661800-234662200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr2:234661800-234664200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr2:234663600-234664000	ZNF genes & repeats	A549	lung
21	chr2:234663800-234664000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr2:234663800-234664000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr2:234663800-234664000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr2:234663800-234664000	Genic enhancers	Liver	Liver
25	chr2:234663800-234664000	Enhancers	Esophagus	oesophagus
26	chr2:234663800-234664000	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
27	chr2:234664000-234664200	Weak transcription	Liver	Liver
28	chr2:234664000-234664200	Weak transcription	A549	lung
29	chr2:234664000-234666400	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr2:234664000-234669000	Weak transcription	Esophagus	oesophagus
31	chr2:234664000-234669200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr2:234664200-234664600	Enhancers	A549	lung
33	chr2:234664200-234668800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr2:234664200-234669000	Enhancers	Liver	Liver
35	chr2:234664400-234664800	Bivalent Enhancer	HepG2	liver
36	chr2:234664400-234665200	Enhancers	Fetal Intestine Large	intestine
37	chr2:234664600-234664800	Flanking Active TSS	A549	lung
38	chr2:234664800-234665200	Enhancers	A549	lung
39	chr2:234664800-234666400	Enhancers	HepG2	liver
40	chr2:234664800-234671000	Enhancers	Fetal Intestine Small	intestine
41	chr2:234665200-234665400	Flanking Active TSS	A549	lung
42	chr2:234665200-234665600	Weak transcription	Fetal Intestine Large	intestine
43	chr2:234665200-234669200	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr2:234665400-234665600	Enhancers	A549	lung
45	chr2:234665400-234665600	Enhancers	Osteobl	bone

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