Variant report

Variant	nsv871893
Chromosome Location	chr1:62767953-62819067
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:609)
CpG islands
(count:854)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:609 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:62785027-62785395	HepG2	liver:	n/a	n/a
2	BACH1	chr1:62803445-62803931	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:62803774-62803794	K562	blood:	n/a	n/a
4	BCL3	chr1:62812681-62812894	GM12878	blood:	n/a	n/a
5	BHLHE40	chr1:62809014-62809050	K562	blood:	n/a	n/a
6	BHLHE40	chr1:62804179-62804317	K562	blood:	n/a	n/a
7	BHLHE40	chr1:62801444-62801471	HepG2	liver:	n/a	n/a
8	BHLHE40	chr1:62808999-62809071	HepG2	liver:	n/a	n/a
9	BRCA1	chr1:62784036-62784179	HepG2	liver:	n/a	n/a
10	BRCA1	chr1:62773751-62774246	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr1:62787169-62787450	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr1:62790754-62791105	A549	lung:	n/a	chr1:62790867-62790878
13	CEBPB	chr1:62777297-62777609	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr1:62801401-62801609	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:62784852-62785343	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:62785032-62785313	K562	blood:	n/a	n/a
17	CEBPB	chr1:62784975-62785350	MCF-7	breast:	n/a	n/a
18	CEBPB	chr1:62790697-62791060	HepG2	liver:	n/a	chr1:62790867-62790878
19	CEBPB	chr1:62784999-62785311	A549	lung:	n/a	n/a
20	CEBPB	chr1:62773707-62774105	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr1:62784929-62785402	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr1:62784980-62785385	A549	lung:	n/a	n/a
23	CEBPB	chr1:62787066-62787565	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr1:62801368-62801538	K562	blood:	n/a	n/a
25	CEBPB	chr1:62790704-62791126	Hela-S3	cervix:	n/a	chr1:62790867-62790878
26	CEBPB	chr1:62784944-62785359	HepG2	liver:	n/a	n/a
27	CEBPB	chr1:62785040-62785323	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr1:62787244-62787473	A549	lung:	n/a	n/a
29	CEBPB	chr1:62787251-62787472	A549	lung:	n/a	n/a
30	CEBPB	chr1:62784973-62785355	HepG2	liver:	n/a	n/a
31	CEBPB	chr1:62784848-62785378	A549	lung:	n/a	n/a
32	CEBPB	chr1:62785014-62785300	HepG2	liver:	n/a	n/a
33	CEBPB	chr1:62784888-62785352	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr1:62790755-62791032	A549	lung:	n/a	chr1:62790867-62790878
35	CEBPD	chr1:62784989-62785316	HepG2	liver:	n/a	n/a
36	CEBPD	chr1:62784803-62785236	HepG2	liver:	n/a	n/a
37	CHD1	chr1:62777455-62777457	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr1:62784179-62784330	HepG2	liver:	n/a	n/a
39	CHD2	chr1:62787044-62787515	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr1:62790895-62791114	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr1:62773755-62774089	Hela-S3	cervix:	n/a	n/a
42	CREB1	chr1:62784915-62785415	HepG2	liver:	n/a	n/a
43	CREB1	chr1:62784647-62785436	HepG2	liver:	n/a	n/a
44	CTBP2	chr1:62783909-62785025	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr1:62800460-62800610	GM12865	blood:	n/a	n/a
46	CTCF	chr1:62804720-62804870	HA-sp	spinal cord:	n/a	chr1:62804749-62804756
47	CTCF	chr1:62803980-62804130	AG10803	skin:	n/a	n/a
48	CTCF	chr1:62801414-62801485	Lung_OC	lung:	n/a	n/a
49	CTCF	chr1:62801440-62801590	NB4	blood:	n/a	n/a
50	CTCF	chr1:62801480-62801630	WERI-Rb-1	eye:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:62785901-62785951	SK-N-MC	brain:	n/a
2	chr1:62784651-62784701	Caco-2	colon:	n/a
3	chr1:62784651-62784701	AoSMC	blood vessel:	n/a
4	chr1:62784269-62784319	SK-N-SH	brain:	n/a
5	chr1:62784802-62784852	BE2_C	brain:	n/a
6	chr1:62784651-62784701	GM12891	blood:	n/a
7	chr1:62786082-62786132	AG04450	lung:	fetal
8	chr1:62784332-62784382	HRCEpiC	kidney:	n/a
9	chr1:62784332-62784382	BJ	skin:	n/a
10	chr1:62787266-62787316	HCPEpiC	choroid plexus:	n/a
11	chr1:62784269-62784319	NH-A	brain:	n/a
12	chr1:62781737-62781787	K562	blood:	n/a
13	chr1:62785512-62785562	HL-60	blood:	n/a
14	chr1:62784651-62784701	ECC-1	luminal epithelium:	n/a
15	chr1:62784332-62784382	SK-N-MC	brain:	n/a
16	chr1:62784762-62784812	NHDF-neo	bronchial:	n/a
17	chr1:62785079-62785129	HIPEpiC	eye:	n/a
18	chr1:62785512-62785562	PANC-1	pancreas:	n/a
19	chr1:62785079-62785129	NB4	blood:	n/a
20	chr1:62784651-62784701	Hepatocyte	liver:	n/a
21	chr1:62784269-62784319	HCF	heart:	n/a
22	chr1:62783533-62783583	PFSK-1	brain:	n/a
23	chr1:62785901-62785951	GM12891	blood:	n/a
24	chr1:62785079-62785129	SKMC	muscle:	n/a
25	chr1:62784332-62784382	HCM	heart:	n/a
26	chr1:62787266-62787316	A549	lung:	n/a
27	chr1:62785901-62785951	GM06990	blood:	n/a
28	chr1:62781737-62781787	HUVEC	blood vessel:	n/a
29	chr1:62786082-62786132	Jurkat	blood:	n/a
30	chr1:62785454-62785504	BE2_C	brain:	n/a
31	chr1:62785079-62785129	HCT-116	colon:	n/a
32	chr1:62787266-62787316	HRE	kidney:	n/a
33	chr1:62785079-62785129	K562	blood:	n/a
34	chr1:62781737-62781787	HRE	kidney:	n/a
35	chr1:62784332-62784382	PrEC	prostate:	n/a
36	chr1:62784651-62784701	HL-60	blood:	n/a
37	chr1:62783533-62783583	A549	lung:	n/a
38	chr1:62785901-62785951	HRE	kidney:	n/a
39	chr1:62785454-62785504	NB4	blood:	n/a
40	chr1:62785079-62785129	HCF	heart:	n/a
41	chr1:62785512-62785562	GM06990	blood:	n/a
42	chr1:62785512-62785562	NHDF-neo	bronchial:	n/a
43	chr1:62785079-62785129	AG09309	skin:	n/a
44	chr1:62783533-62783583	ProgFib	skin:	n/a
45	chr1:62786082-62786132	A549	lung:	n/a
46	chr1:62784651-62784701	SKMC	muscle:	n/a
47	chr1:62785079-62785129	SK-N-SH_RA	brain:	n/a
48	chr1:62785079-62785129	HNPCEpiC	eye:	n/a
49	chr1:62784269-62784319	NB4	blood:	n/a
50	chr1:62781737-62781787	SKMC	muscle:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:62801173..62802961-chr1:62807029..62808736,2	K562	blood:
2	chr1:62801173..62802961-chr1:62807029..62808736,2	K562	blood:
3	chr1:62796227..62800204-chr1:62803015..62806082,4	K562	blood:
4	chr1:62786251..62788988-chr1:62790093..62792721,3	MCF-7	breast:
5	chr1:62786251..62788988-chr1:62790093..62792721,3	MCF-7	breast:
6	chr1:62810042..62812942-chr1:62813222..62814814,2	K562	blood:
7	chr1:62796227..62800204-chr1:62803015..62806082,4	K562	blood:
8	chr1:62810042..62812942-chr1:62813222..62814814,2	K562	blood:
9	chr1:62782472..62785250-chr1:62785761..62788536,3	MCF-7	breast:

No data

Variant related genes	Relation type
RNU6-371P	TF binding region
KANK4	TF binding region
RNU6-371P	CpG island
KANK4	CpG island
ENSG00000132854	chromatin interactions

Extended variants
information (count: 2018 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:2018 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12037499	chr1:62767953-62767954	Bivalent Enhancer Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs912896	chr1:62767968-62767969	Bivalent Enhancer Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs144444959	chr1:62767977-62767978	Bivalent Enhancer Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs12044289	chr1:62767993-62767994	Bivalent Enhancer Genic enhancers Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs548827669	chr1:62768006-62768007	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs370149451	chr1:62768017-62768018	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs187573528	chr1:62768026-62768027	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs912895	chr1:62768053-62768054	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs141020304	chr1:62768061-62768062	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs12037540	chr1:62768093-62768094	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs144968518	chr1:62768148-62768149	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs115780244	chr1:62768200-62768201	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs570054090	chr1:62768205-62768206	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs74078522	chr1:62768246-62768247	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs147506934	chr1:62768253-62768254	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190968938	chr1:62768288-62768289	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543064668	chr1:62768302-62768303	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564997566	chr1:62768373-62768374	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs182759188	chr1:62768389-62768390	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs912894	chr1:62768455-62768456	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs559773679	chr1:62768456-62768457	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs74078523	chr1:62768459-62768460	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs78416311	chr1:62768467-62768468	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188303606	chr1:62768474-62768475	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs531138369	chr1:62768614-62768615	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs17123413	chr1:62768632-62768633	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558588498	chr1:62768648-62768649	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs78103528	chr1:62768690-62768691	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs17123415	chr1:62768721-62768722	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs547007679	chr1:62768738-62768739	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs565828836	chr1:62768743-62768744	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs17123418	chr1:62768744-62768745	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs193180231	chr1:62768779-62768780	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs575788684	chr1:62768824-62768825	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs61264462	chr1:62768903-62768904	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs397947366	chr1:62768905-62768906	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184747902	chr1:62768961-62768962	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs558339021	chr1:62769048-62769049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188426881	chr1:62769098-62769099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576898262	chr1:62769099-62769100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs535447341	chr1:62769140-62769141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs75954052	chr1:62769144-62769145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs140052895	chr1:62769155-62769156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs145569513	chr1:62769190-62769191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs542495216	chr1:62769232-62769233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs55948475	chr1:62769240-62769241	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs191258931	chr1:62769268-62769269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552833825	chr1:62769270-62769271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs374615754	chr1:62769326-62769327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs554414438	chr1:62769362-62769363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21546498	CNVD

Chromatin state (count:771 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62754400-62773400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr1:62759800-62770800	Enhancers	Fetal Muscle Leg	muscle
3	chr1:62762200-62773200	Weak transcription	Fetal Lung	lung
4	chr1:62764800-62768000	Enhancers	Pancreas	Pancrea
5	chr1:62765000-62768000	Enhancers	Fetal Stomach	stomach
6	chr1:62766000-62768600	Weak transcription	Adipose Nuclei	Adipose
7	chr1:62766000-62770000	Weak transcription	Fetal Muscle Trunk	muscle
8	chr1:62766000-62770200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr1:62766800-62768000	Enhancers	H9 Cell Line	embryonic stem cell
10	chr1:62766800-62770200	Weak transcription	Gastric	stomach
11	chr1:62767000-62768000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr1:62767000-62769000	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr1:62767400-62768000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
14	chr1:62767600-62768000	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr1:62767600-62768000	Enhancers	Fetal Kidney	kidney
16	chr1:62767600-62780600	Weak transcription	HepG2	liver
17	chr1:62767800-62768000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
18	chr1:62767800-62768000	Enhancers	Fetal Heart	heart
19	chr1:62768000-62770000	Weak transcription	Pancreas	Pancrea
20	chr1:62768000-62772600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr1:62768000-62773600	Weak transcription	Fetal Stomach	stomach
22	chr1:62768000-62776800	Weak transcription	Fetal Kidney	kidney
23	chr1:62768600-62769000	Enhancers	Adipose Nuclei	Adipose
24	chr1:62769000-62770000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr1:62769000-62772800	Weak transcription	Adipose Nuclei	Adipose
26	chr1:62770000-62770800	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr1:62770000-62771000	Enhancers	Fetal Muscle Trunk	muscle
28	chr1:62770000-62772000	Enhancers	Pancreas	Pancrea
29	chr1:62770200-62770600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr1:62770200-62770800	Enhancers	Gastric	stomach
31	chr1:62770800-62773200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr1:62770800-62773200	Weak transcription	Fetal Muscle Leg	muscle
33	chr1:62770800-62775600	Weak transcription	Gastric	stomach
34	chr1:62771000-62773200	Weak transcription	Fetal Muscle Trunk	muscle
35	chr1:62772000-62772400	Weak transcription	Pancreas	Pancrea
36	chr1:62772400-62776000	Enhancers	Pancreas	Pancrea
37	chr1:62772600-62774400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr1:62772600-62776400	Enhancers	HMEC	breast
39	chr1:62772600-62776600	Enhancers	Placenta	Placenta
40	chr1:62772800-62776200	Enhancers	Adipose Nuclei	Adipose
41	chr1:62773200-62773400	Enhancers	Fetal Lung	lung
42	chr1:62773200-62773400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
43	chr1:62773200-62773600	Enhancers	Hela-S3	cervix
44	chr1:62773200-62774200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr1:62773200-62774400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
46	chr1:62773200-62774600	Enhancers	Fetal Muscle Leg	muscle
47	chr1:62773200-62774800	Enhancers	Fetal Muscle Trunk	muscle
48	chr1:62773200-62776000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr1:62773200-62776200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr1:62773200-62776200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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