Variant report

Variant	nsv569246
Chromosome Location	chr15:43891512-43980721
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:375)
CpG islands
(count:977)
Chromatin interactive
region (count:8)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:375 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr15:43937873-43938217	GM12878	blood:	n/a	n/a
2	ATF2	chr15:43937824-43938301	GM12878	blood:	n/a	n/a
3	ATF2	chr15:43930649-43931067	GM12878	blood:	n/a	n/a
4	BATF	chr15:43931144-43931498	GM12878	blood:	n/a	n/a
5	BATF	chr15:43930739-43931096	GM12878	blood:	n/a	n/a
6	BATF	chr15:43937842-43938114	GM12878	blood:	n/a	n/a
7	BATF	chr15:43931124-43931473	GM12878	blood:	n/a	n/a
8	BATF	chr15:43937914-43938101	GM12878	blood:	n/a	n/a
9	BCL11A	chr15:43930652-43931058	GM12878	blood:	n/a	chr15:43930990-43930999
10	BCL11A	chr15:43930706-43930979	GM12878	blood:	n/a	n/a
11	BCL11A	chr15:43938746-43939054	GM12878	blood:	n/a	n/a
12	BCL11A	chr15:43938810-43938992	GM12878	blood:	n/a	n/a
13	BCLAF1	chr15:43930701-43931083	GM12878	blood:	n/a	chr15:43930990-43930999
14	BHLHE40	chr15:43939045-43939348	GM12878	blood:	n/a	n/a
15	CEBPB	chr15:43914526-43914540	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr15:43933963-43933971	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr15:43933839-43934039	K562	blood:	n/a	n/a
18	CEBPB	chr15:43894468-43894801	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr15:43913554-43913750	K562	blood:	n/a	chr15:43913662-43913673
20	CEBPB	chr15:43913566-43913782	HepG2	liver:	n/a	chr15:43913662-43913673
21	CEBPD	chr15:43962726-43963199	K562	blood:	n/a	n/a
22	CHD2	chr15:43894517-43894780	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr15:43931127-43931189	GM12878	blood:	n/a	n/a
24	CTCF	chr15:43941291-43941401	GM12892	blood:	n/a	n/a
25	CTCF	chr15:43922929-43922982	LNCaP	prostate:	n/a	n/a
26	CTCF	chr15:43903384-43903840	K562	blood:	n/a	n/a
27	CTCF	chr15:43904781-43904802	GM13977	blood:	n/a	n/a
28	CTCF	chr15:43955748-43955784	MCF-7	breast:	n/a	n/a
29	CTCF	chr15:43912160-43912310	SAEC	small airway:	n/a	n/a
30	CTCF	chr15:43903598-43903709	GM12878	blood:	n/a	n/a
31	CTCF	chr15:43898257-43898297	LNCaP	prostate:	n/a	n/a
32	CTCF	chr15:43969430-43969584	K562	blood:	n/a	n/a
33	CTCF	chr15:43941284-43941422	GM19239	blood:	n/a	n/a
34	CTCF	chr15:43973064-43973112	Pancreas_OC	pancreas:	n/a	n/a
35	CTCF	chr15:43941236-43941376	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr15:43941306-43941392	MCF-7	breast:	n/a	n/a
37	CTCF	chr15:43903672-43903694	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr15:43980419-43980439	GM12878	blood:	n/a	n/a
39	CTCF	chr15:43903608-43903750	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr15:43969453-43969569	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr15:43941276-43941415	MCF-7	breast:	n/a	n/a
42	CTCF	chr15:43941270-43941358	GM12878	blood:	n/a	n/a
43	CTCF	chr15:43941279-43941373	HepG2	liver:	n/a	n/a
44	CTCF	chr15:43941277-43941388	GM19238	blood:	n/a	n/a
45	CTCF	chr15:43903630-43903723	HepG2	liver:	n/a	n/a
46	CTCF	chr15:43941258-43941416	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr15:43969462-43969553	MCF-7	breast:	n/a	n/a
48	CTCF	chr15:43926469-43926503	LNCaP	prostate:	n/a	n/a
49	CTCF	chr15:43941945-43942043	GM20000	blood:	n/a	n/a
50	CTCF	chr15:43941268-43941360	GM19240	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43941072-43941122	Caco-2	colon:	n/a
2	chr15:43941072-43941122	Caco-2	colon:	n/a
3	chr15:43937339-43937389	GM06990	blood:	n/a
4	chr15:43941871-43941921	RPTEC	kidney:	n/a
5	chr15:43941042-43941092	H1-hESC	embryonic stem cell:	embryo
6	chr15:43931742-43931792	HUVEC	blood vessel:	n/a
7	chr15:43937339-43937389	MCF10A-Er-Src	breast:	n/a
8	chr15:43891480-43891530	HRCEpiC	kidney:	n/a
9	chr15:43940867-43940917	T-47D	breast:	n/a
10	chr15:43937339-43937389	H1-hESC	embryonic stem cell:	embryo
11	chr15:43942440-43942490	GM12891	blood:	n/a
12	chr15:43941642-43941692	LNCaP	prostate:	n/a
13	chr15:43912221-43912271	HRPEpiC	eye:	n/a
14	chr15:43941072-43941122	PANC-1	pancreas:	n/a
15	chr15:43942440-43942490	NB4	blood:	n/a
16	chr15:43931742-43931792	HepG2	liver:	n/a
17	chr15:43941563-43941613	RPTEC	kidney:	n/a
18	chr15:43941407-43941457	HRPEpiC	eye:	n/a
19	chr15:43941407-43941457	HepG2	liver:	n/a
20	chr15:43941072-43941122	Hepatocyte	liver:	n/a
21	chr15:43941407-43941457	HCM	heart:	n/a
22	chr15:43940140-43940190	HEEpiC	esophagus:	n/a
23	chr15:43931742-43931792	CMK	blood:	n/a
24	chr15:43931742-43931792	GM12878	blood:	n/a
25	chr15:43941563-43941613	AoSMC	blood vessel:	n/a
26	chr15:43893898-43893948	HAEpiC	amniotic membrane:	n/a
27	chr15:43893898-43893948	MCF10A-Er-Src	breast:	n/a
28	chr15:43912221-43912271	SAEC	small airway:	n/a
29	chr15:43941072-43941122	AG10803	skin:	n/a
30	chr15:43941042-43941092	SK-N-MC	brain:	n/a
31	chr15:43941563-43941613	SAEC	small airway:	n/a
32	chr15:43941563-43941613	GM12878	blood:	n/a
33	chr15:43941034-43941084	GM12878	blood:	n/a
34	chr15:43931742-43931792	BE2_C	brain:	n/a
35	chr15:43891480-43891530	PANC-1	pancreas:	n/a
36	chr15:43912221-43912271	GM12892	blood:	n/a
37	chr15:43941563-43941613	A549	lung:	n/a
38	chr15:43941042-43941092	HepG2	liver:	n/a
39	chr15:43941563-43941613	NHDF-neo	bronchial:	n/a
40	chr15:43941407-43941457	ProgFib	skin:	n/a
41	chr15:43942440-43942490	HCF	heart:	n/a
42	chr15:43891480-43891530	HCM	heart:	n/a
43	chr15:43931742-43931792	GM12891	blood:	n/a
44	chr15:43941407-43941457	HMEC	breast:	n/a
45	chr15:43940867-43940917	PFSK-1	brain:	n/a
46	chr15:43941407-43941457	NT2-D1	testis:	n/a
47	chr15:43941407-43941457	AG09319	gingival:	n/a
48	chr15:43941642-43941692	GM12892	blood:	n/a
49	chr15:43941042-43941092	HCT-116	colon:	n/a
50	chr15:43931742-43931792	SAEC	small airway:	n/a

(count:8 , 50 per page) page: 1

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

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAP1A-1	chr15:43891590-43891731	ENSG00000240430.1
2	lnc-TP53BP1-5	chr15:43924469-43924561	NONHSAT042101
3	lnc-TP53BP1-5	chr15:43924915-43925417	NONHSAT042101
4	lnc-MAP1A-1	chr15:43896982-43897099	ENSG00000240430.1

No data

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

Extended variants
information (count: 2079 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2079 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2439	chr15:43891512-43891513	Weak transcription Strong transcription	CpG island Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs200506674	chr15:43891518-43891519	Weak transcription Strong transcription	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs557843521	chr15:43891558-43891559	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs191555202	chr15:43891560-43891561	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs537028277	chr15:43891666-43891667	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs556972566	chr15:43891670-43891671	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs574244085	chr15:43891689-43891690	Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
8	rs546676861	chr15:43891780-43891781	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs537002499	chr15:43891814-43891815	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs553244472	chr15:43892030-43892031	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs573393756	chr15:43892037-43892038	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs544745249	chr15:43892098-43892099	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs564996151	chr15:43892101-43892102	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs575443944	chr15:43892126-43892127	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs370640437	chr15:43892145-43892146	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs374714345	chr15:43892165-43892166	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs544216441	chr15:43892194-43892195	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs200770543	chr15:43892197-43892198	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs201899170	chr15:43892206-43892207	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs139956283	chr15:43892209-43892210	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs141749062	chr15:43892218-43892219	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs375848386	chr15:43892227-43892228	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs368600593	chr15:43892245-43892246	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs372685255	chr15:43892247-43892248	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs568263767	chr15:43892256-43892257	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs377184465	chr15:43892311-43892312	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs372113043	chr15:43892329-43892330	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs546879457	chr15:43892348-43892349	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs375561385	chr15:43892361-43892362	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs532356677	chr15:43892574-43892575	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs574813814	chr15:43892629-43892630	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs551979899	chr15:43892637-43892638	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs571393973	chr15:43892640-43892641	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs537190397	chr15:43892646-43892647	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs535616758	chr15:43892648-43892649	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs370742823	chr15:43892649-43892650	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs369759232	chr15:43892724-43892725	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs369652730	chr15:43892761-43892762	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs200327107	chr15:43892766-43892767	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs556988243	chr15:43892777-43892778	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs550560949	chr15:43892797-43892798	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs567655009	chr15:43892798-43892799	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs2920791	chr15:43892807-43892808	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs2860666	chr15:43892808-43892809	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs2915791	chr15:43892822-43892823	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs375284306	chr15:43892837-43892838	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs12438025	chr15:43892847-43892848	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs139683375	chr15:43892862-43892863	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs184909019	chr15:43892880-43892881	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs369417288	chr15:43892883-43892884	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:236 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43871400-43898000	Weak transcription	Gastric	stomach
2	chr15:43887400-43892800	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr15:43887400-43894200	Weak transcription	Placenta	Placenta
4	chr15:43887400-43894400	Weak transcription	Colonic Mucosa	Colon
5	chr15:43887400-43894400	Weak transcription	HMEC	breast
6	chr15:43887400-43894400	Weak transcription	NHEK	skin
7	chr15:43887600-43894000	Weak transcription	Rectal Smooth Muscle	rectum
8	chr15:43888200-43894400	Weak transcription	Esophagus	oesophagus
9	chr15:43888600-43891600	Strong transcription	Rectal Mucosa Donor 31	rectum
10	chr15:43889200-43891800	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr15:43889200-43893600	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr15:43889400-43894800	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr15:43890000-43894400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr15:43890000-43894400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr15:43890400-43894400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr15:43891200-43891600	Strong transcription	Duodenum Mucosa	Duodenum
17	chr15:43891200-43892600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr15:43891400-43894400	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr15:43891600-43893600	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr15:43891600-43896600	Weak transcription	Duodenum Mucosa	Duodenum
21	chr15:43892000-43894400	Weak transcription	Fetal Intestine Small	intestine
22	chr15:43892600-43893000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr15:43892800-43893000	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr15:43893000-43897200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr15:43893600-43893800	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr15:43893600-43894400	Enhancers	Hela-S3	cervix
27	chr15:43894200-43894600	Enhancers	Placenta	Placenta
28	chr15:43894200-43894800	Bivalent Enhancer	Fetal Muscle Leg	muscle
29	chr15:43894400-43894600	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr15:43894400-43894600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr15:43894400-43894600	Enhancers	Esophagus	oesophagus
32	chr15:43894400-43894600	Enhancers	NHEK	skin
33	chr15:43895400-43895600	Bivalent Enhancer	Fetal Muscle Leg	muscle
34	chr15:43913400-43914400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr15:43914000-43914400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr15:43914200-43914600	Enhancers	Fetal Intestine Small	intestine
37	chr15:43914600-43937400	Weak transcription	Fetal Intestine Small	intestine
38	chr15:43915000-43915400	Enhancers	Hela-S3	cervix
39	chr15:43915400-43941000	Weak transcription	Hela-S3	cervix
40	chr15:43917000-43918000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr15:43917200-43917800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr15:43917400-43918000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr15:43917600-43917800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr15:43919600-43941600	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr15:43920400-43941400	Weak transcription	Brain Hippocampus Middle	brain
46	chr15:43921000-43940600	Weak transcription	Gastric	stomach
47	chr15:43921400-43950400	Weak transcription	Aorta	Aorta
48	chr15:43921800-43952600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr15:43922200-43922600	Enhancers	Placenta	Placenta
50	chr15:43922800-43937600	Weak transcription	Fetal Intestine Large	intestine

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