Variant report

Variant	nsv1039818
Chromosome Location	chr15:43845410-43988541
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	ATF2	chr15:43930649-43931067	GM12878	blood:	n/a	n/a
2	ATF2	chr15:43937824-43938301	GM12878	blood:	n/a	n/a
3	ATF2	chr15:43937873-43938217	GM12878	blood:	n/a	n/a
4	BATF	chr15:43882351-43882718	GM12878	blood:	n/a	n/a
5	BATF	chr15:43930739-43931096	GM12878	blood:	n/a	n/a
6	BATF	chr15:43982183-43982550	GM12878	blood:	n/a	n/a
7	BATF	chr15:43937914-43938101	GM12878	blood:	n/a	n/a
8	BATF	chr15:43931124-43931473	GM12878	blood:	n/a	n/a
9	BATF	chr15:43937842-43938114	GM12878	blood:	n/a	n/a
10	BATF	chr15:43931144-43931498	GM12878	blood:	n/a	n/a
11	BCL11A	chr15:43930706-43930979	GM12878	blood:	n/a	n/a
12	BCL11A	chr15:43982262-43982477	GM12878	blood:	n/a	n/a
13	BCL11A	chr15:43882430-43882645	GM12878	blood:	n/a	n/a
14	BCL11A	chr15:43930652-43931058	GM12878	blood:	n/a	chr15:43930990-43930999
15	BCL11A	chr15:43938810-43938992	GM12878	blood:	n/a	n/a
16	BCL11A	chr15:43938746-43939054	GM12878	blood:	n/a	n/a
17	BCLAF1	chr15:43930701-43931083	GM12878	blood:	n/a	chr15:43930990-43930999
18	BHLHE40	chr15:43939045-43939348	GM12878	blood:	n/a	n/a
19	CBX3	chr15:43882308-43883030	K562	blood:	n/a	chr15:43882790-43882801
20	CBX3	chr15:43885528-43886169	K562	blood:	n/a	n/a
21	CBX3	chr15:43985411-43986004	K562	blood:	n/a	n/a
22	CBX3	chr15:43982182-43982556	K562	blood:	n/a	n/a
23	CBX3	chr15:43982138-43982749	K562	blood:	n/a	chr15:43982622-43982633
24	CBX3	chr15:43885781-43886051	K562	blood:	n/a	n/a
25	CEBPB	chr15:43894468-43894801	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr15:43982162-43982682	GM12878	blood:	n/a	n/a
27	CEBPB	chr15:43913554-43913750	K562	blood:	n/a	chr15:43913662-43913673
28	CEBPB	chr15:43933839-43934039	K562	blood:	n/a	n/a
29	CEBPB	chr15:43882346-43882722	K562	blood:	n/a	n/a
30	CEBPB	chr15:43914526-43914540	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr15:43913566-43913782	HepG2	liver:	n/a	chr15:43913662-43913673
32	CEBPB	chr15:43933963-43933971	Hela-S3	cervix:	n/a	n/a
33	CEBPD	chr15:43962726-43963199	K562	blood:	n/a	n/a
34	CEBPD	chr15:43882316-43882670	K562	blood:	n/a	n/a
35	CEBPD	chr15:43863161-43863508	K562	blood:	n/a	n/a
36	CHD2	chr15:43931127-43931189	GM12878	blood:	n/a	n/a
37	CHD2	chr15:43894517-43894780	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr15:43882248-43882687	GM12891	blood:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
39	CTCF	chr15:43882375-43882673	LNCaP	prostate:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
40	CTCF	chr15:43903608-43903750	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr15:43882360-43882688	Kidney_OC	kidney:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
42	CTCF	chr15:43982016-43982654	K562	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
43	CTCF	chr15:43903572-43903813	K562	blood:	n/a	n/a
44	CTCF	chr15:43982191-43982515	Fibrobl	skin:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
45	CTCF	chr15:43985777-43985779	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr15:43982171-43982497	MCF-7	breast:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
47	CTCF	chr15:43857288-43857401	GM13976	blood:	n/a	n/a
48	CTCF	chr15:43882358-43882694	Gliobla	brain:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
49	CTCF	chr15:43882377-43882727	GM10266	blood:	n/a	chr15:43882525-43882541 chr15:43882524-43882542 chr15:43882530-43882539 chr15:43882519-43882540
50	CTCF	chr15:43856051-43856096	GM13976	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43942440-43942490	HIPEpiC	eye:	n/a
2	chr15:43941072-43941122	AG09309	skin:	n/a
3	chr15:43893898-43893948	CMK	blood:	n/a
4	chr15:43942440-43942490	HIPEpiC	eye:	n/a
5	chr15:43941072-43941122	AG09309	skin:	n/a
6	chr15:43893898-43893948	CMK	blood:	n/a
7	chr15:43941407-43941457	HAEpiC	amniotic membrane:	n/a
8	chr15:43880680-43880730	AG10803	skin:	n/a
9	chr15:43891480-43891530	HRCEpiC	kidney:	n/a
10	chr15:43941034-43941084	SK-N-MC	brain:	n/a
11	chr15:43941642-43941692	LNCaP	prostate:	n/a
12	chr15:43940140-43940190	AG10803	skin:	n/a
13	chr15:43880680-43880730	U87	brain:	n/a
14	chr15:43883474-43883524	HUVEC	blood vessel:	n/a
15	chr15:43941407-43941457	MCF-7	breast:	n/a
16	chr15:43941072-43941122	HPAEpiC	pulmonary alveolar:	n/a
17	chr15:43941563-43941613	GM19239	blood:	n/a
18	chr15:43891480-43891530	HCF	heart:	n/a
19	chr15:43937339-43937389	MCF-7	breast:	n/a
20	chr15:43941642-43941692	MCF10A-Er-Src	breast:	n/a
21	chr15:43983306-43983356	SK-N-SH_RA	brain:	n/a
22	chr15:43941563-43941613	HUVEC	blood vessel:	n/a
23	chr15:43941563-43941613	HEEpiC	esophagus:	n/a
24	chr15:43940140-43940190	AG04450	lung:	fetal
25	chr15:43942440-43942490	RPTEC	kidney:	n/a
26	chr15:43941042-43941092	PFSK-1	brain:	n/a
27	chr15:43883469-43883519	ProgFib	skin:	n/a
28	chr15:43984922-43984972	HUVEC	blood vessel:	n/a
29	chr15:43941407-43941457	GM12891	blood:	n/a
30	chr15:43942014-43942064	Jurkat	blood:	n/a
31	chr15:43942440-43942490	GM12892	blood:	n/a
32	chr15:43941042-43941092	HCPEpiC	choroid plexus:	n/a
33	chr15:43941072-43941122	HRE	kidney:	n/a
34	chr15:43983306-43983356	Jurkat	blood:	n/a
35	chr15:43940867-43940917	IMR90	lung:	fetal
36	chr15:43912221-43912271	ECC-1	luminal epithelium:	n/a
37	chr15:43941034-43941084	HRCEpiC	kidney:	n/a
38	chr15:43937339-43937389	HCT-116	colon:	n/a
39	chr15:43883474-43883524	IMR90	lung:	fetal
40	chr15:43883469-43883519	SK-N-SH_RA	brain:	n/a
41	chr15:43937339-43937389	GM12891	blood:	n/a
42	chr15:43941042-43941092	GM12878	blood:	n/a
43	chr15:43941072-43941122	HRPEpiC	eye:	n/a
44	chr15:43942014-43942064	HRE	kidney:	n/a
45	chr15:43983306-43983356	BJ	skin:	n/a
46	chr15:43941871-43941921	MCF-7	breast:	n/a
47	chr15:43983306-43983356	ovcar-3	ovarian:	n/a
48	chr15:43885090-43885140	HRCEpiC	kidney:	n/a
49	chr15:43942440-43942490	SK-N-SH_RA	brain:	n/a
50	chr15:43984922-43984972	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type
1	chr15:43946007..43947781-chr15:43949371..43952173,2	K562	blood:
2	15:43889977-43895899..15:44001645-44015047	GM12878	blood:
3	15:43916541-43924442..15:44080886-44089111	GM12878	blood:
4	15:43924442-43930824..15:44001645-44015047	GM12878	blood:
5	15:43792489-43802874..15:43916541-43924442	Hela-S3	cervix:
6	15:43916541-43924442..15:44034348-44042259	K562	blood:
7	15:43782117-43785993..15:43931042-43936532	GM12878	blood:
8	chr15:43946007..43947781-chr15:43949371..43952173,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CKMT1A-1	chr15:43886893-43887305	NONHSAT042091
2	lnc-TP53BP1-5	chr15:43924915-43925417	NONHSAT042101
3	lnc-MAP1A-1	chr15:43896982-43897099	ENSG00000240430.1
4	lnc-CKMT1A-1	chr15:43886893-43887142	NONHSAT042092
5	lnc-CKMT1A-1	chr15:43886243-43886620	NONHSAT042090
6	lnc-MAP1A-1	chr15:43891590-43891731	ENSG00000240430.1
7	lnc-CKMT1A-1	chr15:43885406-43885469	NONHSAT042091
8	lnc-CKMT1A-1	chr15:43886243-43886565	NONHSAT042091
9	lnc-CKMT1A-1	chr15:43885285-43885469	NONHSAT042090
10	lnc-CKMT1A-1	chr15:43886217-43886565	NONHSAT042092
11	lnc-TP53BP1-5	chr15:43924469-43924561	NONHSAT042101

Variant related genes	Relation type
CATSPER2	TF binding region
PDIA3P2	TF binding region
RNU6-554P	TF binding region
STRC	TF binding region
PPIP5K1	TF binding region
RNU6-610P	TF binding region
CKMT1A	TF binding region
CKMT1B	TF binding region
ENSG00000249839	TF binding region
ENSG00000238535	TF binding region
CATSPER2	CpG island
PDIA3P2	CpG island
RNU6-554P	CpG island
STRC	CpG island
PPIP5K1	CpG island
RNU6-610P	CpG island
CKMT1A	CpG island
CKMT1B	CpG island
ENSG00000249839	CpG island
ENSG00000238535	CpG island
ENSG00000167004	chromatin interactions
ENSG00000067369	chromatin interactions
ENSG00000242866	chromatin interactions
ENSG00000242028	chromatin interactions
ENSG00000221792	chromatin interactions
ENSG00000238494	chromatin interactions
ENSG00000205771	chromatin interactions
ENSG00000140264	chromatin interactions
ENSG00000166763	chromatin interactions

Extended variants
information (count: 2737 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2737 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148833506	chr15:43845457-43845458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs544457903	chr15:43845494-43845495	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569585635	chr15:43845527-43845528	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs77250044	chr15:43845551-43845552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs62020615	chr15:43845553-43845554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
6	rs188413633	chr15:43845568-43845569	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs143434879	chr15:43845597-43845598	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs191776523	chr15:43845613-43845614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184894544	chr15:43845619-43845620	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565003067	chr15:43845633-43845634	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560145545	chr15:43845637-43845638	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189387516	chr15:43845638-43845639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552411660	chr15:43845682-43845683	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569077243	chr15:43845694-43845695	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531659739	chr15:43845764-43845765	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548064040	chr15:43845765-43845766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567953824	chr15:43845766-43845767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs34427127	chr15:43845838-43845839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140985800	chr15:43845839-43845840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564313930	chr15:43845844-43845845	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs71111822	chr15:43845845-43845846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112289725	chr15:43845846-43845847	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2439842	chr15:43845859-43845860	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2470133	chr15:43845875-43845876	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181032918	chr15:43845906-43845907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185671575	chr15:43845991-43845992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566495330	chr15:43845992-43845993	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566857801	chr15:43846031-43846032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2439843	chr15:43846036-43846037	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs558939356	chr15:43846077-43846078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141782389	chr15:43846090-43846091	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201516252	chr15:43846135-43846136	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12906300	chr15:43846139-43846140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2255051	chr15:43846161-43846162	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs555201752	chr15:43846217-43846218	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189478281	chr15:43846319-43846320	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540287092	chr15:43846350-43846351	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560302595	chr15:43846388-43846389	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150564796	chr15:43846437-43846438	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545457731	chr15:43846450-43846451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562537296	chr15:43846456-43846457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374547519	chr15:43846541-43846542	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs79636941	chr15:43846641-43846642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548511292	chr15:43846646-43846647	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138779421	chr15:43846685-43846686	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143925117	chr15:43846698-43846699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538413981	chr15:43846725-43846726	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546661935	chr15:43846775-43846776	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566605989	chr15:43846789-43846790	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs35264809	chr15:43846819-43846820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43818000-43852600	Weak transcription	Rectal Smooth Muscle	rectum
2	chr15:43818200-43851600	Weak transcription	Primary hematopoietic stem cells	blood
3	chr15:43823800-43852600	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr15:43824800-43853000	Weak transcription	GM12878-XiMat	blood
5	chr15:43824800-43853200	Weak transcription	Hela-S3	cervix
6	chr15:43827200-43849800	Weak transcription	Colonic Mucosa	Colon
7	chr15:43827400-43852600	Weak transcription	Left Ventricle	heart
8	chr15:43827400-43854000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr15:43827600-43846800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr15:43827600-43848400	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr15:43827600-43848600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr15:43827600-43849000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr15:43827600-43849400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr15:43827600-43851200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr15:43827600-43851400	Weak transcription	Right Ventricle	heart
16	chr15:43827600-43851800	Weak transcription	Primary B cells from peripheral blood	blood
17	chr15:43827600-43852800	Weak transcription	Lung	lung
18	chr15:43827600-43854000	Weak transcription	Aorta	Aorta
19	chr15:43827600-43855400	Weak transcription	Ovary	ovary
20	chr15:43827800-43848200	Weak transcription	Brain Germinal Matrix	brain
21	chr15:43827800-43848600	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr15:43827800-43848800	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr15:43827800-43849600	Weak transcription	Spleen	Spleen
24	chr15:43827800-43850000	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr15:43827800-43850400	Weak transcription	Primary B cells from cord blood	blood
26	chr15:43827800-43850800	Weak transcription	Esophagus	oesophagus
27	chr15:43827800-43851600	Weak transcription	Thymus	Thymus
28	chr15:43827800-43852800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr15:43828000-43851400	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr15:43829000-43850400	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr15:43829000-43852600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr15:43829200-43848800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr15:43831800-43848800	Weak transcription	Brain Cingulate Gyrus	brain
34	chr15:43832000-43848400	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr15:43832000-43849000	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr15:43834400-43848800	Weak transcription	Adipose Nuclei	Adipose
37	chr15:43835400-43848800	Weak transcription	Placenta	Placenta
38	chr15:43837000-43851200	Strong transcription	Fetal Intestine Small	intestine
39	chr15:43837200-43851400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr15:43839800-43853000	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr15:43840000-43848800	Weak transcription	Brain Hippocampus Middle	brain
42	chr15:43840000-43848800	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr15:43840200-43847000	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr15:43840200-43848800	Weak transcription	Primary T cells from cord blood	blood
45	chr15:43840200-43848800	Weak transcription	Fetal Brain Female	brain
46	chr15:43840200-43849000	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr15:43840200-43852600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr15:43840200-43853200	Weak transcription	HMEC	breast
49	chr15:43840400-43851800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
50	chr15:43840600-43848400	Weak transcription	Fetal Intestine Large	intestine

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