Variant report

Variant	nsv431712
Chromosome Location	chr1:62759369-62766001
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	CEBPB	chr1:62761906-62762043	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr1:62760229-62760469	A549	lung:	n/a	chr1:62760366-62760377
3	CEBPB	chr1:62760222-62760455	HepG2	liver:	n/a	chr1:62760366-62760377
4	CTCF	chr1:62759937-62760180	MCF-7	breast:	n/a	chr1:62760048-62760069
5	CTCF	chr1:62759960-62760110	BJ	skin:	n/a	chr1:62760048-62760069
6	CTCF	chr1:62759960-62760110	HPF	lung:	n/a	chr1:62760048-62760069
7	CTCF	chr1:62759936-62760315	MCF-7	breast:	n/a	chr1:62760048-62760069
8	CTCF	chr1:62759787-62760270	MCF-7	breast:	n/a	chr1:62760048-62760069
9	CTCF	chr1:62759940-62760090	HPAF	blood vessel:	n/a	chr1:62760048-62760069
10	CTCF	chr1:62759940-62760090	HCPEpiC	choroid plexus:	n/a	chr1:62760048-62760069
11	CTCF	chr1:62759880-62760030	HFF	foreskin:	n/a	n/a
12	CTCF	chr1:62759960-62760110	GM12878	blood:	n/a	chr1:62760048-62760069
13	CTCF	chr1:62760020-62760170	HEEpiC	esophagus:	n/a	chr1:62760048-62760069
14	CTCF	chr1:62760020-62760170	HFF-Myc	foreskin:	n/a	chr1:62760048-62760069
15	CTCF	chr1:62759971-62760122	LNCaP	prostate:	n/a	chr1:62760048-62760069
16	CTCF	chr1:62760024-62760078	Pancreas_OC	pancreas:	n/a	chr1:62760048-62760069
17	CTCF	chr1:62759955-62760165	Medullo	brain:	n/a	chr1:62760048-62760069
18	CTCF	chr1:62759849-62760236	HepG2	liver:	n/a	chr1:62760048-62760069
19	CTCF	chr1:62759980-62760130	HepG2	liver:	n/a	chr1:62760048-62760069
20	CTCF	chr1:62760006-62760123	GM10248	blood:	n/a	chr1:62760048-62760069
21	CTCF	chr1:62759980-62760130	Hela-S3	cervix:	n/a	chr1:62760048-62760069
22	CTCF	chr1:62759954-62760205	HepG2	liver:	n/a	chr1:62760048-62760069
23	CTCF	chr1:62759969-62760155	GM19238	blood:	n/a	chr1:62760048-62760069
24	CTCF	chr1:62759920-62760070	HFF-Myc	foreskin:	n/a	chr1:62760048-62760069
25	CTCF	chr1:62759860-62760010	GM12868	blood:	n/a	n/a
26	CTCF	chr1:62761800-62761950	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr1:62759960-62760126	HepG2	liver:	n/a	chr1:62760048-62760069
28	CTCF	chr1:62759980-62760130	GM12869	blood:	n/a	chr1:62760048-62760069
29	CTCF	chr1:62759960-62760110	NHEK	skin:	n/a	chr1:62760048-62760069
30	CTCF	chr1:62759960-62760110	HRPEpiC	eye:	n/a	chr1:62760048-62760069
31	CTCF	chr1:62760120-62760270	HCM	heart:	n/a	n/a
32	CTCF	chr1:62759920-62760193	GM12878	blood:	n/a	chr1:62760048-62760069
33	CTCF	chr1:62759920-62760070	HCFaa	heart:	n/a	chr1:62760048-62760069
34	CTCF	chr1:62759918-62760184	Gliobla	brain:	n/a	chr1:62760048-62760069
35	CTCF	chr1:62760005-62760009	GM19240	blood:	n/a	n/a
36	CTCF	chr1:62759934-62760257	A549	lung:	n/a	chr1:62760048-62760069
37	CTCF	chr1:62759920-62760070	NHLF	lung:	n/a	chr1:62760048-62760069
38	CTCF	chr1:62759960-62760110	AG10803	skin:	n/a	chr1:62760048-62760069
39	CTCF	chr1:62760000-62760150	HBMEC	blood vessel:	n/a	chr1:62760048-62760069
40	CTCF	chr1:62759980-62760130	WERI-Rb-1	eye:	n/a	chr1:62760048-62760069
41	CTCF	chr1:62759980-62760130	AoAF	blood vessel:	n/a	chr1:62760048-62760069
42	CTCF	chr1:62759949-62760151	A549	lung:	n/a	chr1:62760048-62760069
43	CTCF	chr1:62759980-62760130	GM12874	blood:	n/a	chr1:62760048-62760069
44	CTCF	chr1:62759940-62760090	SAEC	small airway:	n/a	chr1:62760048-62760069
45	CTCF	chr1:62759940-62760090	GM12875	blood:	n/a	chr1:62760048-62760069
46	CTCF	chr1:62759980-62760130	GM06990	blood:	n/a	chr1:62760048-62760069
47	CTCF	chr1:62759795-62760359	A549	lung:	n/a	chr1:62760048-62760069
48	CTCF	chr1:62759960-62760110	RPTEC	kidney:	n/a	chr1:62760048-62760069
49	CTCF	chr1:62760000-62760150	GM12873	blood:	n/a	chr1:62760048-62760069
50	CTCF	chr1:62759980-62760130	GM12873	blood:	n/a	chr1:62760048-62760069

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:62761846-62761896	SK-N-SH_RA	brain:	n/a
2	chr1:62761846-62761896	GM19239	blood:	n/a
3	chr1:62761846-62761896	AG09319	gingival:	n/a
4	chr1:62761846-62761896	Hela-S3	cervix:	n/a
5	chr1:62761846-62761896	AG04450	lung:	fetal
6	chr1:62761846-62761896	HRCEpiC	kidney:	n/a
7	chr1:62761846-62761896	GM12878	blood:	n/a
8	chr1:62761846-62761896	HEK293	kidney:	embryo
9	chr1:62761846-62761896	PrEC	prostate:	n/a
10	chr1:62761846-62761896	PFSK-1	brain:	n/a
11	chr1:62761846-62761896	GM06990	blood:	n/a
12	chr1:62761846-62761896	HCPEpiC	choroid plexus:	n/a
13	chr1:62761846-62761896	HPAEpiC	pulmonary alveolar:	n/a
14	chr1:62761846-62761896	SAEC	small airway:	n/a
15	chr1:62761846-62761896	LNCaP	prostate:	n/a
16	chr1:62761846-62761896	CMK	blood:	n/a
17	chr1:62761846-62761896	ProgFib	skin:	n/a
18	chr1:62761846-62761896	HAEpiC	amniotic membrane:	n/a
19	chr1:62761846-62761896	ECC-1	luminal epithelium:	n/a
20	chr1:62761846-62761896	HL-60	blood:	n/a
21	chr1:62761846-62761896	SK-N-SH	brain:	n/a
22	chr1:62761846-62761896	AoSMC	blood vessel:	n/a
23	chr1:62761846-62761896	Caco-2	colon:	n/a
24	chr1:62761846-62761896	MCF10A-Er-Src	breast:	n/a
25	chr1:62761846-62761896	Jurkat	blood:	n/a
26	chr1:62761846-62761896	HEEpiC	esophagus:	n/a
27	chr1:62761846-62761896	SK-N-MC	brain:	n/a
28	chr1:62761846-62761896	HRE	kidney:	n/a
29	chr1:62761846-62761896	NHBE	bronchial:	n/a
30	chr1:62761846-62761896	Hepatocyte	liver:	n/a
31	chr1:62761846-62761896	IMR90	lung:	fetal
32	chr1:62761846-62761896	NT2-D1	testis:	n/a
33	chr1:62761846-62761896	H1-hESC	embryonic stem cell:	embryo
34	chr1:62761846-62761896	HUVEC	blood vessel:	n/a
35	chr1:62761846-62761896	ovcar-3	ovarian:	n/a
36	chr1:62761846-62761896	HCF	heart:	n/a
37	chr1:62761846-62761896	BE2_C	brain:	n/a
38	chr1:62761846-62761896	NH-A	brain:	n/a
39	chr1:62761846-62761896	RPTEC	kidney:	n/a
40	chr1:62761846-62761896	HIPEpiC	eye:	n/a
41	chr1:62761846-62761896	GM12892	blood:	n/a
42	chr1:62761846-62761896	PANC-1	pancreas:	n/a
43	chr1:62761846-62761896	HepG2	liver:	n/a
44	chr1:62761846-62761896	HRPEpiC	eye:	n/a
45	chr1:62761846-62761896	BJ	skin:	n/a
46	chr1:62761846-62761896	A549	lung:	n/a
47	chr1:62761846-62761896	T-47D	breast:	n/a
48	chr1:62761846-62761896	K562	blood:	n/a
49	chr1:62761846-62761896	HCM	heart:	n/a
50	chr1:62761846-62761896	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:62695851..62696415-chr1:62759671..62760258,2	MCF-7	breast:
2	chr1:62759537..62760142-chr1:62872912..62873611,2	MCF-7	breast:
3	chr1:62759279..62761889-chr1:62763662..62766108,2	MCF-7	breast:

Variant related genes	Relation type
RNU6-371P	TF binding region
RNU6-371P	CpG island
ENSG00000201153	chromatin interactions

Extended variants
information (count: 250 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:250 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2765263	chr1:62759369-62759370	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs560184947	chr1:62759374-62759375	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs527811799	chr1:62759401-62759402	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs80156143	chr1:62759402-62759403	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs561377213	chr1:62759437-62759438	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs529172693	chr1:62759492-62759493	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs550802854	chr1:62759505-62759506	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs77946622	chr1:62759566-62759567	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs569180760	chr1:62759667-62759668	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs562549343	chr1:62759671-62759672	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs551620521	chr1:62759672-62759673	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs577820190	chr1:62759706-62759707	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs17314520	chr1:62759707-62759708	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs765692	chr1:62759729-62759730	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs6679889	chr1:62759792-62759793	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs555057841	chr1:62759793-62759794	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs567208810	chr1:62759826-62759827	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs75955598	chr1:62759843-62759844	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs765691	chr1:62759848-62759849	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs577938990	chr1:62759861-62759862	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs376158478	chr1:62759876-62759877	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs373883673	chr1:62759887-62759888	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs545178978	chr1:62759938-62759939	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs553982305	chr1:62759958-62759959	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs1325738	chr1:62759959-62759960	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs188888521	chr1:62759964-62759965	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs561226794	chr1:62759966-62759967	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs531689214	chr1:62759974-62759975	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs113438219	chr1:62760019-62760020	Enhancers Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs1325739	chr1:62760110-62760111	Enhancers Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs577247530	chr1:62760130-62760131	Enhancers Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs369508287	chr1:62760167-62760168	Enhancers Weak transcription Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs566713521	chr1:62760204-62760205	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs147035860	chr1:62760289-62760290	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs2765264	chr1:62760297-62760298	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs200374698	chr1:62760312-62760313	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs5774596	chr1:62760313-62760314	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs33950335	chr1:62760314-62760315	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs200614409	chr1:62760315-62760316	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs1886830	chr1:62760352-62760353	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs551632555	chr1:62760359-62760360	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs115481613	chr1:62760384-62760385	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs1886831	chr1:62760400-62760401	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs571455456	chr1:62760404-62760405	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs1886832	chr1:62760412-62760413	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs533643157	chr1:62760431-62760432	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs369908451	chr1:62760453-62760454	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs372934332	chr1:62760577-62760578	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs192224773	chr1:62760589-62760590	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs113899815	chr1:62760598-62760599	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	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:278 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62753200-62760000	Weak transcription	Fetal Stomach	stomach
2	chr1:62753200-62761600	Weak transcription	Pancreas	Pancrea
3	chr1:62753200-62761600	Weak transcription	Right Atrium	heart
4	chr1:62754200-62760200	Weak transcription	Placenta	Placenta
5	chr1:62754400-62773400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr1:62754800-62765200	Weak transcription	Fetal Heart	heart
7	chr1:62755000-62759800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr1:62755200-62759800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr1:62755600-62761000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr1:62756200-62765000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr1:62756400-62764800	Weak transcription	HepG2	liver
12	chr1:62757800-62760000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr1:62758400-62760000	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr1:62759600-62759800	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr1:62759600-62760200	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr1:62759800-62760000	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr1:62759800-62760000	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr1:62759800-62760000	Enhancers	HSMMtube	muscle
19	chr1:62759800-62760200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr1:62759800-62760200	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr1:62759800-62760400	Enhancers	HMEC	breast
22	chr1:62759800-62760600	Enhancers	H9 Cell Line	embryonic stem cell
23	chr1:62759800-62760600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr1:62759800-62761800	Enhancers	Fetal Muscle Trunk	muscle
25	chr1:62759800-62765400	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr1:62759800-62770800	Enhancers	Fetal Muscle Leg	muscle
27	chr1:62760000-62760200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr1:62760000-62760200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr1:62760000-62760200	Enhancers	Brain Hippocampus Middle	brain
30	chr1:62760000-62760200	Strong transcription	Fetal Stomach	stomach
31	chr1:62760000-62760400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr1:62760000-62760600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr1:62760000-62760600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr1:62760000-62760600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr1:62760000-62760800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr1:62760000-62760800	Bivalent Enhancer	Brain Cingulate Gyrus	brain
37	chr1:62760000-62761200	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr1:62760000-62761200	Weak transcription	HSMMtube	muscle
39	chr1:62760000-62761600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr1:62760000-62762400	Enhancers	H1 Cell Line	embryonic stem cell
41	chr1:62760200-62760400	Enhancers	Placenta	Placenta
42	chr1:62760200-62760400	Enhancers	Fetal Thymus	thymus
43	chr1:62760200-62761000	Weak transcription	Fetal Stomach	stomach
44	chr1:62760200-62761200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr1:62760200-62761200	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr1:62760200-62761200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr1:62760200-62761600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr1:62760200-62761600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr1:62760400-62760800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr1:62760400-62760800	Weak transcription	HMEC	breast

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