Variant report

Variant	nsv883012
Chromosome Location	chr5:145589542-145672431
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	chr5:145592962-145593348	K562	blood:	n/a	n/a
2	ARID3A	chr5:145670992-145671314	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:145593038-145593693	HepG2	liver:	n/a	n/a
4	BACH1	chr5:145620815-145620864	K562	blood:	n/a	n/a
5	BATF	chr5:145618600-145618803	GM12878	blood:	n/a	chr5:145618713-145618724
6	BHLHE40	chr5:145646919-145646923	K562	blood:	n/a	n/a
7	BHLHE40	chr5:145597993-145598128	K562	blood:	n/a	n/a
8	CBX3	chr5:145662776-145663477	HCT-116	colon:	n/a	chr5:145662797-145662808
9	CCNT2	chr5:145645217-145645417	K562	blood:	n/a	n/a
10	CEBPB	chr5:145659295-145659475	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr5:145663105-145663406	Hela-S3	cervix:	n/a	chr5:145663337-145663348 chr5:145663284-145663301
12	CEBPB	chr5:145593046-145593553	A549	lung:	n/a	chr5:145593475-145593486 chr5:145593299-145593310 chr5:145593298-145593311
13	CEBPB	chr5:145602778-145603060	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr5:145593104-145593643	HepG2	liver:	n/a	chr5:145593475-145593486 chr5:145593299-145593310 chr5:145593298-145593311
15	CEBPB	chr5:145593160-145593495	MCF-7	breast:	n/a	chr5:145593475-145593486 chr5:145593299-145593310 chr5:145593298-145593311
16	CEBPB	chr5:145602752-145603193	A549	lung:	n/a	n/a
17	CEBPB	chr5:145602736-145603055	K562	blood:	n/a	n/a
18	CEBPB	chr5:145659238-145659442	A549	lung:	n/a	n/a
19	CEBPB	chr5:145668257-145668465	K562	blood:	n/a	n/a
20	CEBPB	chr5:145602761-145603093	A549	lung:	n/a	n/a
21	CEBPB	chr5:145593088-145593597	Hela-S3	cervix:	n/a	chr5:145593475-145593486 chr5:145593299-145593310 chr5:145593298-145593311
22	CEBPB	chr5:145602786-145603066	A549	lung:	n/a	n/a
23	CEBPB	chr5:145669992-145670232	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr5:145593126-145593654	K562	blood:	n/a	chr5:145593475-145593486 chr5:145593299-145593310 chr5:145593298-145593311
25	CEBPB	chr5:145593019-145593455	MCF-7	breast:	n/a	chr5:145593299-145593310 chr5:145593298-145593311
26	CEBPB	chr5:145593124-145593648	A549	lung:	n/a	chr5:145593475-145593486 chr5:145593299-145593310 chr5:145593298-145593311
27	CEBPB	chr5:145593200-145593379	HepG2	liver:	n/a	chr5:145593299-145593310 chr5:145593298-145593311
28	CEBPB	chr5:145647342-145647592	IMR90	lung:	n/a	n/a
29	CEBPB	chr5:145602753-145603105	IMR90	lung:	n/a	n/a
30	CEBPB	chr5:145602739-145603127	K562	blood:	n/a	n/a
31	CEBPB	chr5:145593160-145593577	IMR90	lung:	n/a	chr5:145593475-145593486 chr5:145593299-145593310 chr5:145593298-145593311
32	CEBPB	chr5:145593110-145593479	ECC-1	luminal epithelium:	n/a	chr5:145593299-145593310 chr5:145593298-145593311
33	CEBPB	chr5:145593105-145593492	K562	blood:	n/a	chr5:145593475-145593486 chr5:145593299-145593310 chr5:145593298-145593311
34	CEBPB	chr5:145593149-145593439	K562	blood:	n/a	chr5:145593299-145593310 chr5:145593298-145593311
35	CEBPB	chr5:145602753-145603097	HepG2	liver:	n/a	n/a
36	CEBPB	chr5:145659226-145659464	IMR90	lung:	n/a	n/a
37	CEBPB	chr5:145602766-145603103	Hela-S3	cervix:	n/a	n/a
38	CEBPD	chr5:145593120-145593361	HepG2	liver:	n/a	chr5:145593298-145593309
39	CREB1	chr5:145670937-145671506	K562	blood:	n/a	n/a
40	CTCF	chr5:145671160-145671310	HA-sp	spinal cord:	n/a	chr5:145671213-145671231
41	CTCF	chr5:145671140-145671290	HPAF	blood vessel:	n/a	chr5:145671213-145671231
42	CTCF	chr5:145671132-145671307	GM10248	blood:	n/a	chr5:145671213-145671231
43	CTCF	chr5:145671134-145671300	H1-hESC	embryonic stem cell:	n/a	chr5:145671213-145671231
44	CTCF	chr5:145671200-145671350	GM12864	blood:	n/a	chr5:145671213-145671231
45	CTCF	chr5:145671113-145671316	Pancreas_OC	pancreas:	n/a	chr5:145671213-145671231
46	CTCF	chr5:145671164-145671288	MCF-7	breast:	n/a	chr5:145671213-145671231
47	CTCF	chr5:145671140-145671290	HEEpiC	esophagus:	n/a	chr5:145671213-145671231
48	CTCF	chr5:145671160-145671310	HCFaa	heart:	n/a	chr5:145671213-145671231
49	CTCF	chr5:145671140-145671290	AG04450	lung:	n/a	chr5:145671213-145671231
50	CTCF	chr5:145671140-145671290	Hela-S3	cervix:	n/a	chr5:145671213-145671231

No.	Distal block	Cell Line	Cell type
1	chr5:145560154..145562997-chr5:145607826..145610384,3	K562	blood:
2	chr5:145661955..145664023-chr5:145664235..145668387,3	K562	blood:
3	chr5:145661955..145664023-chr5:145664235..145668387,3	K562	blood:
4	chr5:145647167..145649031-chr5:145653206..145654859,2	K562	blood:
5	chr5:145612339..145614307-chr5:145615895..145618813,2	MCF-7	breast:
6	chr5:145643342..145645989-chr5:145650081..145652639,2	K562	blood:
7	chr5:145596366..145598063-chr5:145648958..145650482,2	K562	blood:
8	chr5:145670705..145671717-chr5:145769549..145770704,7	MCF-7	breast:
9	chr5:145594426..145596514-chr5:145599170..145601456,2	K562	blood:
10	chr5:145582535..145584854-chr5:145588808..145592360,5	MCF-7	breast:
11	chr5:145595165..145597126-chr5:145598903..145601685,2	K562	blood:
12	chr5:145653852..145655797-chr5:145658433..145661229,2	K562	blood:
13	chr5:145670731..145671269-chr5:145912930..145913474,2	K562	blood:
14	chr5:145643342..145645989-chr5:145650081..145652639,2	K562	blood:
15	chr5:145625443..145628007-chr5:145629715..145633107,5	K562	blood:
16	chr5:145581226..145585152-chr5:145585587..145593073,9	K562	blood:
17	chr5:145559745..145561849-chr5:145588233..145589890,2	K562	blood:
18	chr5:145625869..145628007-chr5:145631607..145633546,2	K562	blood:
19	chr5:145661955..145664023-chr5:145664235..145667190,2	K562	blood:
20	chr5:145625814..145628687-chr5:145636719..145638380,2	K562	blood:
21	chr5:145625814..145628687-chr5:145636719..145638380,2	K562	blood:
22	chr5:145625869..145628007-chr5:145631607..145633546,2	K562	blood:
23	chr5:145601632..145604303-chr5:145605562..145607960,2	MCF-7	breast:
24	chr5:145607480..145610119-chr5:145611867..145613573,2	MCF-7	breast:
25	chr5:145661955..145664023-chr5:145664235..145667190,2	K562	blood:
26	chr5:145615949..145618767-chr5:145647272..145650054,2	K562	blood:
27	chr5:145564948..145567866-chr5:145592052..145594140,2	K562	blood:
28	chr5:145670701..145671468-chr5:145806285..145807382,6	MCF-7	breast:
29	chr5:145582693..145585612-chr5:145586430..145590293,7	MCF-7	breast:
30	chr5:145591065..145593762-chr5:145596165..145598951,2	K562	blood:
31	chr5:145647167..145649031-chr5:145653206..145654859,2	K562	blood:
32	chr5:145670751..145671608-chr5:145806467..145807165,3	MCF-7	breast:
33	chr5:145587938..145589813-chr5:145591754..145593477,2	K562	blood:
34	chr5:145591065..145593762-chr5:145596165..145598951,2	K562	blood:
35	chr5:145564650..145566770-chr5:145588134..145589874,2	K562	blood:
36	chr5:145596366..145598063-chr5:145648958..145650482,2	K562	blood:
37	chr5:145615949..145618767-chr5:145647272..145650054,2	K562	blood:
38	chr5:145596117..145598265-chr5:145605012..145606909,2	K562	blood:
39	chr5:145670545..145671841-chr5:145804277..145805196,11	MCF-7	breast:
40	chr5:145670280..145672735-chr5:145688584..145691508,2	K562	blood:
41	chr5:145581405..145584024-chr5:145596123..145597883,2	K562	blood:
42	chr5:145588075..145590940-chr5:145591754..145595862,4	K562	blood:
43	chr5:145601632..145604303-chr5:145605562..145607960,2	MCF-7	breast:
44	chr5:145612339..145614307-chr5:145615895..145618813,2	MCF-7	breast:
45	chr5:145594426..145596514-chr5:145599170..145601456,2	K562	blood:
46	chr5:145607480..145610119-chr5:145611867..145613573,2	MCF-7	breast:
47	chr5:145670825..145671778-chr5:145806423..145807376,4	K562	blood:
48	chr5:145588075..145590940-chr5:145591754..145595862,4	K562	blood:
49	chr5:145558240..145560527-chr5:145600863..145603054,2	K562	blood:
50	chr5:145596117..145598265-chr5:145605012..145606909,2	K562	blood:

No.	miRNA target gene	miRNA name	Chromosome Location
1	RBM27	hsa-miR-25-3p	chr5:145668659-145668665
2	RBM27	hsa-miR-186-5p	chr5:145666629-145666653
3	RBM27	hsa-miR-92a-3p	chr5:145668659-145668665

Variant related genes	Relation type
RBM27	TF binding region
RNU7-180P	TF binding region
ENSG00000091009	chromatin interactions
ENSG00000133706	chromatin interactions

Extended variants
information (count: 2999 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2999 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13171939	chr5:145589542-145589543	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576693391	chr5:145589551-145589552	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs187227648	chr5:145589620-145589621	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs552546256	chr5:145589629-145589630	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs370585039	chr5:145589666-145589667	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs373717054	chr5:145589669-145589670	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs6887090	chr5:145589675-145589676	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs12656470	chr5:145589733-145589734	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs112544746	chr5:145589763-145589764	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs560539388	chr5:145589804-145589805	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs530540917	chr5:145589810-145589811	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs543995327	chr5:145589811-145589812	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs193099499	chr5:145589812-145589813	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs185580065	chr5:145589885-145589886	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs375803493	chr5:145589886-145589887	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs187650620	chr5:145589894-145589895	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs566072778	chr5:145589926-145589927	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs528447284	chr5:145589930-145589931	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs2963932	chr5:145589978-145589979	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs562504005	chr5:145590025-145590026	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs545217525	chr5:145590046-145590047	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs568515011	chr5:145590072-145590073	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs374596627	chr5:145590112-145590113	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs537164350	chr5:145590140-145590141	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs77881465	chr5:145590152-145590153	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs139848555	chr5:145590237-145590238	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs34141601	chr5:145590248-145590249	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs552807776	chr5:145590249-145590250	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs200986485	chr5:145590276-145590277	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs573055295	chr5:145590281-145590282	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs541779919	chr5:145590287-145590288	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs555080583	chr5:145590303-145590304	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs575280626	chr5:145590338-145590339	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs544353660	chr5:145590370-145590371	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs563012281	chr5:145590382-145590383	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs192667573	chr5:145590426-145590427	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs532796751	chr5:145590427-145590428	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs113431420	chr5:145590441-145590442	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs184284465	chr5:145590488-145590489	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs532047497	chr5:145590496-145590497	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs201750144	chr5:145590510-145590511	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs75237267	chr5:145590511-145590512	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs371980729	chr5:145590607-145590608	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs527848308	chr5:145590629-145590630	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs550701234	chr5:145590634-145590635	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs570621150	chr5:145590650-145590651	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs188676852	chr5:145590652-145590653	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs551668438	chr5:145590655-145590656	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs546408798	chr5:145590732-145590733	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs79709937	chr5:145590750-145590751	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	16864856	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	20864512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2182 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:145584400-145598800	Weak transcription	NH-A	brain
2	chr5:145584400-145606600	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr5:145584600-145595600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr5:145584600-145606400	Weak transcription	Stomach Smooth Muscle	stomach
5	chr5:145584800-145597200	Weak transcription	Fetal Muscle Trunk	muscle
6	chr5:145584800-145599000	Weak transcription	Fetal Muscle Leg	muscle
7	chr5:145584800-145608000	Weak transcription	Esophagus	oesophagus
8	chr5:145584800-145631200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr5:145585000-145590200	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr5:145585000-145590600	Weak transcription	Left Ventricle	heart
11	chr5:145585000-145593000	Weak transcription	Brain Substantia Nigra	brain
12	chr5:145585000-145593600	Weak transcription	Fetal Lung	lung
13	chr5:145585000-145598800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr5:145585000-145599000	Weak transcription	Fetal Brain Female	brain
15	chr5:145585000-145602600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr5:145585200-145592800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr5:145585200-145593000	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr5:145585200-145593000	Weak transcription	Primary hematopoietic stem cells	blood
19	chr5:145585200-145593000	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr5:145585200-145598600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr5:145585200-145598600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr5:145585200-145598800	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr5:145585200-145598800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr5:145585200-145598800	Weak transcription	HMEC	breast
25	chr5:145585200-145598800	Weak transcription	NHEK	skin
26	chr5:145585200-145609200	Weak transcription	Brain Anterior Caudate	brain
27	chr5:145585400-145597400	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr5:145585400-145598200	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr5:145585400-145598200	Weak transcription	HUVEC	blood vessel
30	chr5:145585400-145598400	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr5:145585400-145609000	Weak transcription	Brain Cingulate Gyrus	brain
32	chr5:145585600-145597400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr5:145585600-145599000	Weak transcription	Thymus	Thymus
34	chr5:145585600-145599200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr5:145585600-145601000	Weak transcription	Right Atrium	heart
36	chr5:145585600-145610200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr5:145585800-145598400	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr5:145585800-145598800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr5:145585800-145601800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr5:145586000-145599000	Weak transcription	HSMM	muscle
41	chr5:145586200-145597000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr5:145586400-145594600	Weak transcription	Lung	lung
43	chr5:145586400-145595600	Weak transcription	Pancreas	Pancrea
44	chr5:145586400-145598800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr5:145586400-145604000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr5:145586400-145616800	Weak transcription	Right Ventricle	heart
47	chr5:145586600-145592800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr5:145586800-145589600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr5:145586800-145593000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr5:145586800-145598600	Weak transcription	Rectal Mucosa Donor 29	rectum

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