Variant report

Variant	nsv523502
Chromosome Location	chr5:145588483-145639987
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:324)
CpG islands
(count:0)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:324 , 50 per page) page: 1 2 3 4 5 6 7

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	chr5:145593038-145593693	HepG2	liver:	n/a	n/a
3	BACH1	chr5:145620815-145620864	K562	blood:	n/a	n/a
4	BATF	chr5:145618600-145618803	GM12878	blood:	n/a	chr5:145618713-145618724
5	BHLHE40	chr5:145597993-145598128	K562	blood:	n/a	n/a
6	CEBPB	chr5:145593160-145593495	MCF-7	breast:	n/a	chr5:145593475-145593486 chr5:145593299-145593310 chr5:145593298-145593311
7	CEBPB	chr5:145602753-145603097	HepG2	liver:	n/a	n/a
8	CEBPB	chr5:145593104-145593643	HepG2	liver:	n/a	chr5:145593475-145593486 chr5:145593299-145593310 chr5:145593298-145593311
9	CEBPB	chr5:145593149-145593439	K562	blood:	n/a	chr5:145593299-145593310 chr5:145593298-145593311
10	CEBPB	chr5:145602752-145603193	A549	lung:	n/a	n/a
11	CEBPB	chr5:145593200-145593379	HepG2	liver:	n/a	chr5:145593299-145593310 chr5:145593298-145593311
12	CEBPB	chr5:145593088-145593597	Hela-S3	cervix:	n/a	chr5:145593475-145593486 chr5:145593299-145593310 chr5:145593298-145593311
13	CEBPB	chr5:145602766-145603103	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr5:145593019-145593455	MCF-7	breast:	n/a	chr5:145593299-145593310 chr5:145593298-145593311
15	CEBPB	chr5:145593046-145593553	A549	lung:	n/a	chr5:145593475-145593486 chr5:145593299-145593310 chr5:145593298-145593311
16	CEBPB	chr5:145602736-145603055	K562	blood:	n/a	n/a
17	CEBPB	chr5:145602786-145603066	A549	lung:	n/a	n/a
18	CEBPB	chr5:145602761-145603093	A549	lung:	n/a	n/a
19	CEBPB	chr5:145602753-145603105	IMR90	lung:	n/a	n/a
20	CEBPB	chr5:145602739-145603127	K562	blood:	n/a	n/a
21	CEBPB	chr5:145593105-145593492	K562	blood:	n/a	chr5:145593475-145593486 chr5:145593299-145593310 chr5:145593298-145593311
22	CEBPB	chr5:145593160-145593577	IMR90	lung:	n/a	chr5:145593475-145593486 chr5:145593299-145593310 chr5:145593298-145593311
23	CEBPB	chr5:145593110-145593479	ECC-1	luminal epithelium:	n/a	chr5:145593299-145593310 chr5:145593298-145593311
24	CEBPB	chr5:145593126-145593654	K562	blood:	n/a	chr5:145593475-145593486 chr5:145593299-145593310 chr5:145593298-145593311
25	CEBPB	chr5:145593124-145593648	A549	lung:	n/a	chr5:145593475-145593486 chr5:145593299-145593310 chr5:145593298-145593311
26	CEBPB	chr5:145602778-145603060	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPD	chr5:145593120-145593361	HepG2	liver:	n/a	chr5:145593298-145593309
28	CTCF	chr5:145588800-145588950	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr5:145588820-145588970	GM12801	blood:	n/a	n/a
30	CTCF	chr5:145588840-145588990	GM12864	blood:	n/a	n/a
31	CTCF	chr5:145588780-145588930	NHEK	skin:	n/a	n/a
32	CTCF	chr5:145588860-145589010	GM12865	blood:	n/a	n/a
33	CTCF	chr5:145588820-145588970	HVMF	connective:	n/a	n/a
34	CTCF	chr5:145588720-145588870	HMEC	breast:	n/a	n/a
35	CTCF	chr5:145588840-145588990	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr5:145588780-145588930	AG04449	skin:	n/a	n/a
37	CTCF	chr5:145588780-145588930	HMF	breast:	n/a	n/a
38	CTCF	chr5:145588820-145588970	AG04450	lung:	n/a	n/a
39	CTCF	chr5:145588780-145588930	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr5:145588840-145588990	HepG2	liver:	n/a	n/a
41	CTCF	chr5:145588840-145588990	HMF	breast:	n/a	n/a
42	CTCF	chr5:145588820-145588970	GM12873	blood:	n/a	n/a
43	CTCF	chr5:145588800-145588950	AG04450	lung:	n/a	n/a
44	CTCF	chr5:145588840-145588990	HEK293	kidney:	n/a	n/a
45	CTCF	chr5:145588820-145588970	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr5:145588800-145588950	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr5:145588755-145589011	K562	blood:	n/a	n/a
48	CTCF	chr5:145588780-145588930	HCM	heart:	n/a	n/a
49	CTCF	chr5:145588860-145589010	HRE	kidney:	n/a	n/a
50	CTCF	chr5:145588780-145588930	MCF-7	breast:	n/a	n/a

No data

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:145625869..145628007-chr5:145631607..145633546,2	K562	blood:
2	chr5:145591065..145593762-chr5:145596165..145598951,2	K562	blood:
3	chr5:145558240..145560527-chr5:145600863..145603054,2	K562	blood:
4	chr5:145596117..145598265-chr5:145605012..145606909,2	K562	blood:
5	chr5:145625869..145628007-chr5:145631607..145633546,2	K562	blood:
6	chr5:145594426..145596514-chr5:145599170..145601456,2	K562	blood:
7	chr5:145587290..145589374-chr5:145604476..145606867,3	K562	blood:
8	chr5:145612339..145614307-chr5:145615895..145618813,2	MCF-7	breast:
9	chr5:145595165..145597126-chr5:145598903..145601685,2	K562	blood:
10	chr5:145582693..145585612-chr5:145586430..145590293,7	MCF-7	breast:
11	chr5:145582359..145584728-chr5:145597576..145599110,2	MCF-7	breast:
12	chr5:145591065..145593762-chr5:145596165..145598951,2	K562	blood:
13	chr5:145601632..145604303-chr5:145605562..145607960,2	MCF-7	breast:
14	chr5:145564650..145566770-chr5:145588134..145589874,2	K562	blood:
15	chr5:145615949..145618767-chr5:145647272..145650054,2	K562	blood:
16	chr5:145595165..145597126-chr5:145598903..145601685,2	K562	blood:
17	chr5:145559745..145561849-chr5:145588233..145589890,2	K562	blood:
18	chr5:145581405..145584024-chr5:145596123..145597883,2	K562	blood:
19	chr5:145588075..145590940-chr5:145591754..145595862,4	K562	blood:
20	chr5:145587290..145589374-chr5:145604476..145606867,3	K562	blood:
21	chr5:145560154..145562997-chr5:145607826..145610384,3	K562	blood:
22	chr5:145625443..145628007-chr5:145629715..145633107,5	K562	blood:
23	chr5:145612339..145614307-chr5:145615895..145618813,2	MCF-7	breast:
24	chr5:145582535..145584854-chr5:145588808..145592360,5	MCF-7	breast:
25	chr5:145596117..145598265-chr5:145605012..145606909,2	K562	blood:
26	chr5:145581226..145585152-chr5:145585587..145593073,9	K562	blood:
27	chr5:145564948..145567866-chr5:145592052..145594140,2	K562	blood:
28	chr5:145596366..145598063-chr5:145648958..145650482,2	K562	blood:
29	chr5:145587938..145589813-chr5:145591754..145593477,2	K562	blood:
30	chr5:145587938..145589813-chr5:145591754..145593477,2	K562	blood:
31	chr5:145607480..145610119-chr5:145611867..145613573,2	MCF-7	breast:
32	chr5:145601632..145604303-chr5:145605562..145607960,2	MCF-7	breast:
33	chr5:145588075..145590940-chr5:145591754..145595862,4	K562	blood:
34	chr5:145594426..145596514-chr5:145599170..145601456,2	K562	blood:
35	chr5:145625814..145628687-chr5:145636719..145638380,2	K562	blood:
36	chr5:145625814..145628687-chr5:145636719..145638380,2	K562	blood:
37	chr5:145625443..145628007-chr5:145629715..145633107,5	K562	blood:
38	chr5:145607480..145610119-chr5:145611867..145613573,2	MCF-7	breast:

No data

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

Extended variants
information (count: 1909 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1909 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6881180	chr5:145588483-145588484	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565102271	chr5:145588497-145588498	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs563202822	chr5:145588550-145588551	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs576730501	chr5:145588591-145588592	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs559554370	chr5:145588617-145588618	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs150479378	chr5:145588637-145588638	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs572976913	chr5:145588674-145588675	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs377000269	chr5:145588696-145588697	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs138350440	chr5:145588716-145588717	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs369693749	chr5:145588763-145588764	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs572746854	chr5:145588780-145588781	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs190682147	chr5:145588805-145588806	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs528153210	chr5:145588895-145588896	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs115313231	chr5:145588941-145588942	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs182855106	chr5:145588993-145588994	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs149614207	chr5:145589001-145589002	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs550108519	chr5:145589062-145589063	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs570334086	chr5:145589143-145589144	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs147300240	chr5:145589158-145589159	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs140774929	chr5:145589187-145589188	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs566109951	chr5:145589200-145589201	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs534807249	chr5:145589219-145589220	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs373545047	chr5:145589287-145589288	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs555088899	chr5:145589426-145589427	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs568471743	chr5:145589459-145589460	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs143125881	chr5:145589514-145589515	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs539941657	chr5:145589518-145589519	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs13171939	chr5:145589542-145589543	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs576693391	chr5:145589551-145589552	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs187227648	chr5:145589620-145589621	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs552546256	chr5:145589629-145589630	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs370585039	chr5:145589666-145589667	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs373717054	chr5:145589669-145589670	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs6887090	chr5:145589675-145589676	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs12656470	chr5:145589733-145589734	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs112544746	chr5:145589763-145589764	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs560539388	chr5:145589804-145589805	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs530540917	chr5:145589810-145589811	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs543995327	chr5:145589811-145589812	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs193099499	chr5:145589812-145589813	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs185580065	chr5:145589885-145589886	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs375803493	chr5:145589886-145589887	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs187650620	chr5:145589894-145589895	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs566072778	chr5:145589926-145589927	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs528447284	chr5:145589930-145589931	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs2963932	chr5:145589978-145589979	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs562504005	chr5:145590025-145590026	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs545217525	chr5:145590046-145590047	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs568515011	chr5:145590072-145590073	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs374596627	chr5:145590112-145590113	Weak transcription Enhancers	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:1479 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:145583800-145589000	Weak transcription	Small Intestine	intestine
2	chr5:145584200-145588800	Weak transcription	Fetal Intestine Small	intestine
3	chr5:145584400-145598800	Weak transcription	NH-A	brain
4	chr5:145584400-145606600	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr5:145584600-145588800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr5:145584600-145595600	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr5:145584600-145606400	Weak transcription	Stomach Smooth Muscle	stomach
8	chr5:145584800-145597200	Weak transcription	Fetal Muscle Trunk	muscle
9	chr5:145584800-145599000	Weak transcription	Fetal Muscle Leg	muscle
10	chr5:145584800-145608000	Weak transcription	Esophagus	oesophagus
11	chr5:145584800-145631200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr5:145585000-145588800	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr5:145585000-145588800	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr5:145585000-145589200	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr5:145585000-145590200	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr5:145585000-145590600	Weak transcription	Left Ventricle	heart
17	chr5:145585000-145593000	Weak transcription	Brain Substantia Nigra	brain
18	chr5:145585000-145593600	Weak transcription	Fetal Lung	lung
19	chr5:145585000-145598800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr5:145585000-145599000	Weak transcription	Fetal Brain Female	brain
21	chr5:145585000-145602600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr5:145585200-145589000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr5:145585200-145589000	Weak transcription	Fetal Kidney	kidney
24	chr5:145585200-145592800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr5:145585200-145593000	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr5:145585200-145593000	Weak transcription	Primary hematopoietic stem cells	blood
27	chr5:145585200-145593000	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr5:145585200-145598600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr5:145585200-145598600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr5:145585200-145598800	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr5:145585200-145598800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr5:145585200-145598800	Weak transcription	HMEC	breast
33	chr5:145585200-145598800	Weak transcription	NHEK	skin
34	chr5:145585200-145609200	Weak transcription	Brain Anterior Caudate	brain
35	chr5:145585400-145597400	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr5:145585400-145598200	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr5:145585400-145598200	Weak transcription	HUVEC	blood vessel
38	chr5:145585400-145598400	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr5:145585400-145609000	Weak transcription	Brain Cingulate Gyrus	brain
40	chr5:145585600-145597400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr5:145585600-145599000	Weak transcription	Thymus	Thymus
42	chr5:145585600-145599200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr5:145585600-145601000	Weak transcription	Right Atrium	heart
44	chr5:145585600-145610200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr5:145585800-145588800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr5:145585800-145589000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr5:145585800-145598400	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr5:145585800-145598800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr5:145585800-145601800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr5:145586000-145599000	Weak transcription	HSMM	muscle

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