Variant report

Variant	nsv947321
Chromosome Location	chr1:150007387-150030042
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:292)
CpG islands
(count:0)
Chromatin interactive
region (count:72)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:292 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:150022594-150022894	HepG2	liver:	n/a	n/a
2	ATF1	chr1:150007597-150007748	K562	blood:	n/a	n/a
3	BHLHE40	chr1:150022643-150022843	GM12878	blood:	n/a	n/a
4	BRCA1	chr1:150022536-150022830	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr1:150021969-150022260	HepG2	liver:	n/a	chr1:150022121-150022132
6	CEBPB	chr1:150023010-150023203	A549	lung:	n/a	chr1:150023157-150023168
7	CEBPB	chr1:150022520-150022857	H1-hESC	embryonic stem cell:	n/a	chr1:150022649-150022662 chr1:150022648-150022665 chr1:150022649-150022662
8	CEBPB	chr1:150023010-150023247	K562	blood:	n/a	chr1:150023157-150023168
9	CEBPB	chr1:150023096-150023377	MCF-7	breast:	n/a	chr1:150023157-150023168
10	CEBPB	chr1:150022024-150022169	K562	blood:	n/a	chr1:150022121-150022132
11	CEBPB	chr1:150022517-150022891	Hela-S3	cervix:	n/a	chr1:150022649-150022662 chr1:150022648-150022665 chr1:150022649-150022662
12	CEBPB	chr1:150023011-150023205	HepG2	liver:	n/a	chr1:150023157-150023168
13	CEBPB	chr1:150022579-150022847	ECC-1	luminal epithelium:	n/a	chr1:150022649-150022662 chr1:150022648-150022665 chr1:150022649-150022662
14	CEBPB	chr1:150022062-150022165	A549	lung:	n/a	chr1:150022121-150022132
15	CEBPB	chr1:150022023-150022181	HepG2	liver:	n/a	chr1:150022121-150022132
16	CEBPB	chr1:150023089-150023202	H1-hESC	embryonic stem cell:	n/a	chr1:150023157-150023168
17	CEBPB	chr1:150021888-150022169	HepG2	liver:	n/a	chr1:150022121-150022132
18	CEBPB	chr1:150022066-150022241	H1-hESC	embryonic stem cell:	n/a	chr1:150022121-150022132
19	CEBPB	chr1:150022476-150022953	MCF-7	breast:	n/a	chr1:150022649-150022662 chr1:150022648-150022665 chr1:150022649-150022662
20	CTCF	chr1:150022560-150022911	ECC-1	luminal epithelium:	n/a	n/a
21	CTCF	chr1:150022618-150022882	K562	blood:	n/a	n/a
22	CTCF	chr1:150022540-150022690	HAc	cerebellar:	n/a	n/a
23	CTCF	chr1:150023080-150023230	HCFaa	heart:	n/a	n/a
24	CTCF	chr1:150022674-150022845	GM13976	blood:	n/a	n/a
25	CTCF	chr1:150022506-150022964	HCT-116	colon:	n/a	n/a
26	CTCF	chr1:150022714-150022789	MCF-7	breast:	n/a	n/a
27	CTCF	chr1:150022589-150022875	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr1:150022680-150022830	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr1:150022624-150022885	Pancreas_OC	pancreas:	n/a	n/a
30	CTCF	chr1:150022600-150022750	HFF-Myc	foreskin:	n/a	n/a
31	CTCF	chr1:150022530-150022880	A549	lung:	n/a	n/a
32	CTCF	chr1:150022620-150022770	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr1:150022700-150022850	GM12870	blood:	n/a	n/a
34	CTCF	chr1:150022660-150022810	Caco-2	colon:	n/a	n/a
35	CTCF	chr1:150022642-150022923	Lung_OC	lung:	n/a	n/a
36	CTCF	chr1:150022621-150022915	Spleen_OC	spleen:	n/a	n/a
37	CTCF	chr1:150022680-150022830	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr1:150022720-150022870	HCM	heart:	n/a	n/a
39	CTCF	chr1:150022660-150022810	GM12865	blood:	n/a	n/a
40	CTCF	chr1:150022680-150022830	AoAF	blood vessel:	n/a	n/a
41	CTCF	chr1:150022680-150022830	GM12866	blood:	n/a	n/a
42	CTCF	chr1:150022660-150022810	GM12873	blood:	n/a	n/a
43	CTCF	chr1:150022633-150022882	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr1:150022660-150022810	GM12864	blood:	n/a	n/a
45	CTCF	chr1:150022700-150022850	GM06990	blood:	n/a	n/a
46	CTCF	chr1:150022720-150022870	GM12875	blood:	n/a	n/a
47	CTCF	chr1:150022680-150022830	GM12865	blood:	n/a	n/a
48	CTCF	chr1:150022660-150022810	BE2_C	brain:	n/a	n/a
49	CTCF	chr1:150022740-150022890	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr1:150022660-150022810	Hela-S3	cervix:	n/a	n/a

No data

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:149932228..149936162-chr1:150020648..150023324,4	MCF-7	breast:
2	chr1:150023241..150025135-chr1:150032252..150034875,2	K562	blood:
3	chr1:150003285..150005353-chr1:150007041..150008892,2	MCF-7	breast:
4	chr1:149858594..149860168-chr1:150024352..150026596,2	MCF-7	breast:
5	chr1:149875657..149877242-chr1:150022210..150023854,2	K562	blood:
6	chr1:150013902..150015822-chr1:150017587..150020723,3	K562	blood:
7	chr1:150028686..150031993-chr1:150039075..150042074,4	K562	blood:
8	chr1:149933676..149934376-chr1:150022343..150023190,2	K562	blood:
9	chr1:149857742..149859968-chr1:150011110..150013121,2	MCF-7	breast:
10	chr1:150001605..150003568-chr1:150005160..150008934,3	K562	blood:
11	chr1:150022553..150024320-chr1:150157694..150159816,2	K562	blood:
12	chr1:150028352..150029866-chr1:150038625..150040747,2	MCF-7	breast:
13	chr1:150011132..150013163-chr1:150013455..150015637,2	K562	blood:
14	chr1:149949620..149952507-chr1:150022418..150024343,2	MCF-7	breast:
15	chr1:150020211..150024864-chr1:150037839..150041365,4	MCF-7	breast:
16	chr1:150005167..150006817-chr1:150009728..150012726,2	K562	blood:
17	chr1:149937397..149939684-chr1:150018242..150019838,2	MCF-7	breast:
18	chr1:149988828..149991415-chr1:150020920..150022808,2	MCF-7	breast:
19	chr1:149855348..149862315-chr1:150015478..150024375,18	MCF-7	breast:
20	chr1:149856755..149861735-chr1:150014773..150024288,21	MCF-7	breast:
21	chr1:150017927..150020825-chr1:150022056..150024781,3	MCF-7	breast:
22	chr1:149980202..149982705-chr1:150004768..150008210,3	MCF-7	breast:
23	chr1:149993776..149995889-chr1:150021300..150024191,2	MCF-7	breast:
24	chr1:149859746..149862142-chr1:150028326..150031401,5	K562	blood:
25	chr1:149858084..149861835-chr1:150019287..150023815,6	K562	blood:
26	chr1:149938841..149939614-chr1:150022722..150023249,3	MCF-7	breast:
27	chr1:149931408..149935324-chr1:150013770..150016857,4	K562	blood:
28	chr1:149980850..149983474-chr1:150009041..150010679,2	MCF-7	breast:
29	chr1:149980917..149983265-chr1:150029531..150031224,2	MCF-7	breast:
30	chr1:149984937..149987085-chr1:150017568..150019929,2	MCF-7	breast:
31	chr1:150013358..150016185-chr1:150037875..150040285,2	MCF-7	breast:
32	chr1:149980827..149982338-chr1:150010206..150012167,2	K562	blood:
33	chr1:150020045..150025053-chr1:150028781..150033753,5	MCF-7	breast:
34	chr1:149943671..149946306-chr1:150017241..150019364,2	MCF-7	breast:
35	chr1:150029169..150032073-chr1:150037083..150039053,2	K562	blood:
36	chr1:150011021..150013684-chr1:150016711..150019672,2	MCF-7	breast:
37	chr1:150003443..150005819-chr1:150028195..150029802,2	MCF-7	breast:
38	chr1:150025906..150027967-chr1:150037390..150039741,3	MCF-7	breast:
39	chr1:150014322..150016066-chr1:150017789..150019617,2	K562	blood:
40	chr1:150027925..150032582-chr1:150032961..150038144,5	K562	blood:
41	chr1:149933269..149934631-chr1:150022302..150023872,9	MCF-7	breast:
42	chr1:150015530..150017614-chr1:150019646..150022042,2	MCF-7	breast:
43	chr1:150019180..150020773-chr1:150021063..150023287,2	MCF-7	breast:
44	chr1:150011132..150013163-chr1:150013455..150015637,2	K562	blood:
45	chr1:149853918..149856291-chr1:150026219..150029011,2	K562	blood:
46	chr1:149908283..149911513-chr1:150013231..150017247,5	MCF-7	breast:
47	chr1:150014674..150017255-chr1:150017933..150019625,2	MCF-7	breast:
48	chr1:150014674..150017255-chr1:150017933..150019625,2	MCF-7	breast:
49	chr1:149857111..149861042-chr1:150027596..150032191,5	MCF-7	breast:
50	chr1:150006260..150008663-chr1:150039616..150042430,3	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VPS45-2	chr1:150029942-150030345	ucscGeneNc_uc001eze_2
2	lnc-VPS45-4	chr1:150017290-150018641	NONHSAT006266

No data

Variant related genes	Relation type
ENSG00000223945	TF binding region
ENSG00000184260	chromatin interactions
ENSG00000178096	chromatin interactions
ENSG00000163113	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000014914	chromatin interactions
ENSG00000184270	chromatin interactions
ENSG00000136631	chromatin interactions

Extended variants
information (count: 705 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:705 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186065560	chr1:150007409-150007410	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs191137007	chr1:150007423-150007424	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs374413247	chr1:150007573-150007574	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs587746644	chr1:150007590-150007591	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs587650553	chr1:150007598-150007599	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs76753828	chr1:150007699-150007700	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs587604615	chr1:150007718-150007719	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs75099959	chr1:150007813-150007814	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs370874586	chr1:150007836-150007837	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs140865581	chr1:150007854-150007855	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs144609667	chr1:150007861-150007862	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs35891929	chr1:150007924-150007925	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs370916662	chr1:150007968-150007969	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs587673510	chr1:150007990-150007991	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs587745549	chr1:150008024-150008025	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs587613304	chr1:150008033-150008034	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs587675948	chr1:150008034-150008035	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs151235755	chr1:150008089-150008090	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs587635950	chr1:150008096-150008097	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs140456905	chr1:150008120-150008121	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs183461052	chr1:150008179-150008180	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs587641769	chr1:150008192-150008193	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs111751705	chr1:150008212-150008213	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs587641202	chr1:150008233-150008234	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs587702713	chr1:150008291-150008292	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs587760743	chr1:150008293-150008294	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs187739791	chr1:150008300-150008301	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs113767824	chr1:150008372-150008373	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs587597295	chr1:150008390-150008391	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs145659979	chr1:150008431-150008432	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs189874794	chr1:150008478-150008479	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs77391665	chr1:150008584-150008585	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs182614345	chr1:150008600-150008601	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs587737126	chr1:150008616-150008617	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs587654054	chr1:150008654-150008655	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs16833299	chr1:150008681-150008682	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs587762206	chr1:150008734-150008735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12073359	chr1:150008790-150008791	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs71578461	chr1:150008810-150008811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs61808080	chr1:150008818-150008819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188162555	chr1:150008833-150008834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs587630031	chr1:150008877-150008878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs587680952	chr1:150008924-150008925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192891751	chr1:150008929-150008930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185301401	chr1:150009022-150009023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187297452	chr1:150009125-150009126	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs191976634	chr1:150009145-150009146	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs202067976	chr1:150009188-150009189	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs184761633	chr1:150009205-150009206	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs189169959	chr1:150009211-150009212	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Cancer	23975201	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:135 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:149985600-150022000	Weak transcription	Brain Substantia Nigra	brain
2	chr1:149996600-150037000	Weak transcription	Left Ventricle	heart
3	chr1:150003800-150022400	Weak transcription	Fetal Intestine Small	intestine
4	chr1:150006600-150022400	Weak transcription	Brain Hippocampus Middle	brain
5	chr1:150007400-150010800	Weak transcription	Right Atrium	heart
6	chr1:150015000-150016000	Enhancers	Sigmoid Colon	Sigmoid Colon
7	chr1:150016800-150024000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:150017600-150018400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr1:150017600-150022400	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr1:150017600-150026200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr1:150017600-150037600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr1:150017800-150025800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:150017800-150026000	Weak transcription	Osteobl	bone
14	chr1:150018000-150018200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr1:150018000-150018400	Enhancers	Brain Cingulate Gyrus	brain
16	chr1:150018000-150022600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr1:150018000-150031600	Weak transcription	Stomach Smooth Muscle	stomach
18	chr1:150018000-150033400	Weak transcription	Fetal Stomach	stomach
19	chr1:150018200-150022400	Weak transcription	Rectal Smooth Muscle	rectum
20	chr1:150018200-150038600	Weak transcription	Fetal Muscle Trunk	muscle
21	chr1:150018400-150022400	Weak transcription	Brain Cingulate Gyrus	brain
22	chr1:150018400-150024000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr1:150018600-150022400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr1:150018600-150022800	Weak transcription	Colon Smooth Muscle	Colon
25	chr1:150019000-150021000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr1:150019400-150023200	Weak transcription	A549	lung
27	chr1:150020400-150021200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr1:150021200-150021600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr1:150021600-150022200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr1:150021800-150022600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr1:150021800-150023000	Enhancers	HepG2	liver
32	chr1:150022000-150022800	Enhancers	Brain Substantia Nigra	brain
33	chr1:150022000-150023000	Enhancers	Liver	Liver
34	chr1:150022000-150023200	Enhancers	H1 Cell Line	embryonic stem cell
35	chr1:150022200-150022600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr1:150022200-150022800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr1:150022200-150025800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr1:150022400-150022600	Enhancers	Brain Hippocampus Middle	brain
39	chr1:150022400-150022800	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr1:150022400-150022800	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr1:150022400-150022800	Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr1:150022400-150022800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr1:150022400-150022800	Enhancers	Brain Angular Gyrus	brain
44	chr1:150022400-150022800	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr1:150022400-150022800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
46	chr1:150022400-150022800	Enhancers	Duodenum Smooth Muscle	Duodenum
47	chr1:150022400-150022800	Enhancers	Fetal Intestine Small	intestine
48	chr1:150022400-150022800	Enhancers	Rectal Smooth Muscle	rectum
49	chr1:150022400-150022800	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr1:150022400-150022800	Enhancers	Stomach Mucosa	stomach

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