Variant report

Variant	esv2761766
Chromosome Location	chr15:43834318-44014255
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1103)
CpG islands
(count:1588)
Chromatin interactive
region (count:19)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1103 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

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	chr15:43937873-43938217	GM12878	blood:	n/a	n/a
3	ATF2	chr15:43937824-43938301	GM12878	blood:	n/a	n/a
4	ATF3	chr15:43834019-43834357	K562	blood:	n/a	n/a
5	BACH1	chr15:43835107-43835121	K562	blood:	n/a	n/a
6	BATF	chr15:43882351-43882718	GM12878	blood:	n/a	n/a
7	BATF	chr15:43930739-43931096	GM12878	blood:	n/a	n/a
8	BATF	chr15:43937914-43938101	GM12878	blood:	n/a	n/a
9	BATF	chr15:43931144-43931498	GM12878	blood:	n/a	n/a
10	BATF	chr15:43982183-43982550	GM12878	blood:	n/a	n/a
11	BATF	chr15:43931124-43931473	GM12878	blood:	n/a	n/a
12	BATF	chr15:43937842-43938114	GM12878	blood:	n/a	n/a
13	BCL11A	chr15:43938810-43938992	GM12878	blood:	n/a	n/a
14	BCL11A	chr15:43882430-43882645	GM12878	blood:	n/a	n/a
15	BCL11A	chr15:43982262-43982477	GM12878	blood:	n/a	n/a
16	BCL11A	chr15:43930706-43930979	GM12878	blood:	n/a	n/a
17	BCL11A	chr15:43938746-43939054	GM12878	blood:	n/a	n/a
18	BCL11A	chr15:43930652-43931058	GM12878	blood:	n/a	chr15:43930990-43930999
19	BCL3	chr15:44013070-44013288	GM12878	blood:	n/a	n/a
20	BCLAF1	chr15:43930701-43931083	GM12878	blood:	n/a	chr15:43930990-43930999
21	BHLHE40	chr15:43939045-43939348	GM12878	blood:	n/a	n/a
22	BRCA1	chr15:43834036-43834319	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr15:43885781-43886051	K562	blood:	n/a	n/a
24	CBX3	chr15:43885528-43886169	K562	blood:	n/a	n/a
25	CBX3	chr15:43985411-43986004	K562	blood:	n/a	n/a
26	CBX3	chr15:43982182-43982556	K562	blood:	n/a	n/a
27	CBX3	chr15:43982138-43982749	K562	blood:	n/a	chr15:43982622-43982633
28	CBX3	chr15:43882308-43883030	K562	blood:	n/a	chr15:43882790-43882801
29	CEBPB	chr15:44013009-44013290	K562	blood:	n/a	chr15:44013128-44013139
30	CEBPB	chr15:43833979-43834365	A549	lung:	n/a	chr15:43834148-43834159 chr15:43834169-43834180
31	CEBPB	chr15:43933839-43934039	K562	blood:	n/a	n/a
32	CEBPB	chr15:43882346-43882722	K562	blood:	n/a	n/a
33	CEBPB	chr15:44013072-44013307	A549	lung:	n/a	chr15:44013128-44013139
34	CEBPB	chr15:43838707-43838732	K562	blood:	n/a	n/a
35	CEBPB	chr15:43834027-43834365	K562	blood:	n/a	chr15:43834148-43834159 chr15:43834169-43834180
36	CEBPB	chr15:43833951-43834402	K562	blood:	n/a	chr15:43834148-43834159 chr15:43834169-43834180
37	CEBPB	chr15:44013108-44013199	IMR90	lung:	n/a	chr15:44013128-44013139
38	CEBPB	chr15:43833976-43834362	IMR90	lung:	n/a	chr15:43834148-43834159 chr15:43834169-43834180
39	CEBPB	chr15:43834031-43834323	HepG2	liver:	n/a	chr15:43834148-43834159 chr15:43834169-43834180
40	CEBPB	chr15:43914526-43914540	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr15:43833894-43834399	Hela-S3	cervix:	n/a	chr15:43834148-43834159 chr15:43834169-43834180
42	CEBPB	chr15:43933963-43933971	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr15:43834051-43834474	HCT-116	colon:	n/a	chr15:43834148-43834159 chr15:43834169-43834180
44	CEBPB	chr15:43833857-43834489	K562	blood:	n/a	chr15:43834148-43834159 chr15:43834169-43834180
45	CEBPB	chr15:43833902-43834409	ECC-1	luminal epithelium:	n/a	chr15:43834148-43834159 chr15:43834169-43834180
46	CEBPB	chr15:43913554-43913750	K562	blood:	n/a	chr15:43913662-43913673
47	CEBPB	chr15:43833974-43834387	A549	lung:	n/a	chr15:43834148-43834159 chr15:43834169-43834180
48	CEBPB	chr15:43913566-43913782	HepG2	liver:	n/a	chr15:43913662-43913673
49	CEBPB	chr15:43894468-43894801	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr15:43833899-43834386	ECC-1	luminal epithelium:	n/a	chr15:43834148-43834159 chr15:43834169-43834180

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43941642-43941692	GM12892	blood:	n/a
2	chr15:43883474-43883524	ProgFib	skin:	n/a
3	chr15:43941642-43941692	GM12892	blood:	n/a
4	chr15:43883474-43883524	ProgFib	skin:	n/a
5	chr15:43941034-43941084	BE2_C	brain:	n/a
6	chr15:43942440-43942490	Hepatocyte	liver:	n/a
7	chr15:43941072-43941122	AG10803	skin:	n/a
8	chr15:43891480-43891530	NT2-D1	testis:	n/a
9	chr15:43941642-43941692	HRPEpiC	eye:	n/a
10	chr15:43940140-43940190	HNPCEpiC	eye:	n/a
11	chr15:43940140-43940190	Caco-2	colon:	n/a
12	chr15:43940867-43940917	HCPEpiC	choroid plexus:	n/a
13	chr15:43880680-43880730	PrEC	prostate:	n/a
14	chr15:43941871-43941921	PrEC	prostate:	n/a
15	chr15:43941034-43941084	RPTEC	kidney:	n/a
16	chr15:43883469-43883519	ProgFib	skin:	n/a
17	chr15:43893898-43893948	NHBE	bronchial:	n/a
18	chr15:43940867-43940917	HRPEpiC	eye:	n/a
19	chr15:43941642-43941692	PrEC	prostate:	n/a
20	chr15:43885090-43885140	HCM	heart:	n/a
21	chr15:43941042-43941092	NT2-D1	testis:	n/a
22	chr15:43893898-43893948	ovcar-3	ovarian:	n/a
23	chr15:43940867-43940917	AG09309	skin:	n/a
24	chr15:43891480-43891530	A549	lung:	n/a
25	chr15:43879335-43879385	CMK	blood:	n/a
26	chr15:43931742-43931792	AG09309	skin:	n/a
27	chr15:43942014-43942064	BJ	skin:	n/a
28	chr15:43989074-43989124	HEEpiC	esophagus:	n/a
29	chr15:43991375-43991425	Jurkat	blood:	n/a
30	chr15:43940140-43940190	ovcar-3	ovarian:	n/a
31	chr15:43984922-43984972	GM12892	blood:	n/a
32	chr15:43941871-43941921	Hela-S3	cervix:	n/a
33	chr15:43991375-43991425	HCF	heart:	n/a
34	chr15:43991375-43991425	SKMC	muscle:	n/a
35	chr15:43885090-43885140	HUVEC	blood vessel:	n/a
36	chr15:43989074-43989124	SKMC	muscle:	n/a
37	chr15:43942440-43942490	HUVEC	blood vessel:	n/a
38	chr15:43989074-43989124	SAEC	small airway:	n/a
39	chr15:43991375-43991425	CMK	blood:	n/a
40	chr15:43883474-43883524	HepG2	liver:	n/a
41	chr15:43937339-43937389	SK-N-MC	brain:	n/a
42	chr15:43984922-43984972	Caco-2	colon:	n/a
43	chr15:43889864-43889914	HEEpiC	esophagus:	n/a
44	chr15:43941034-43941084	GM12891	blood:	n/a
45	chr15:43940867-43940917	AG09319	gingival:	n/a
46	chr15:43885090-43885140	HEK293	kidney:	embryo
47	chr15:43941563-43941613	BE2_C	brain:	n/a
48	chr15:43942440-43942490	AG10803	skin:	n/a
49	chr15:43893898-43893948	IMR90	lung:	fetal
50	chr15:43983306-43983356	HAEpiC	amniotic membrane:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	15:43924442-43930824..15:44001645-44015047	GM12878	blood:
2	15:43916541-43924442..15:44080886-44089111	GM12878	blood:
3	15:43802874-43806906..15:44001645-44015047	Hela-S3	cervix:
4	chr15:43946007..43947781-chr15:43949371..43952173,2	K562	blood:
5	chr15:43814141..43815931-chr15:43837910..43839648,2	K562	blood:
6	15:43782117-43785993..15:43931042-43936532	GM12878	blood:
7	chr15:43828054..43831995-chr15:43833960..43836416,4	K562	blood:
8	15:44001645-44015047..15:44080886-44089111	Hela-S3	cervix:
9	15:43792489-43802874..15:44001645-44015047	GM12878	blood:
10	chr15:43946007..43947781-chr15:43949371..43952173,2	K562	blood:
11	15:43807815-43812531..15:44001645-44015047	Hela-S3	cervix:
12	15:43782117-43785993..15:44001645-44015047	GM12878	blood:
13	15:43889977-43895899..15:44001645-44015047	GM12878	blood:
14	15:43792489-43802874..15:43916541-43924442	Hela-S3	cervix:
15	chr15:43821060..43823469-chr15:43995355..43996867,2	K562	blood:
16	15:43889977-43895899..15:44001645-44015047	GM12878	blood:
17	15:43916541-43924442..15:44034348-44042259	K562	blood:
18	15:43924442-43930824..15:44001645-44015047	GM12878	blood:
19	chr15:43822573..43824658-chr15:43837005..43839748,2	K562	blood:

(count:11 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
RNU6-353P	TF binding region
CATSPER2	TF binding region
ENSG00000238494	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
STRCP1	TF binding region
CKMT1B	TF binding region
ENSG00000249839	TF binding region
ENSG00000238535	TF binding region
RNU6-353P	CpG island
CATSPER2	CpG island
ENSG00000238494	CpG island
PDIA3P2	CpG island
RNU6-554P	CpG island
STRC	CpG island
PPIP5K1	CpG island
RNU6-610P	CpG island
CKMT1A	CpG island
STRCP1	CpG island
CKMT1B	CpG island
ENSG00000249839	CpG island
ENSG00000238535	CpG island
ENSG00000166762	chromatin interactions
ENSG00000237289	chromatin interactions
ENSG00000238494	chromatin interactions
ENSG00000140264	chromatin interactions
ENSG00000222398	chromatin interactions
ENSG00000166963	chromatin interactions
ENSG00000166763	chromatin interactions
ENSG00000167004	chromatin interactions
ENSG00000242866	chromatin interactions
ENSG00000242028	chromatin interactions
ENSG00000205771	chromatin interactions
ENSG00000067369	chromatin interactions
ENSG00000206991	chromatin interactions
ENSG00000221792	chromatin interactions

Extended variants
information (count: 3832 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:3832 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2255042	chr15:43834318-43834319	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs550177320	chr15:43834330-43834331	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570066665	chr15:43834333-43834334	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541752912	chr15:43834369-43834370	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374241884	chr15:43834371-43834372	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs147752806	chr15:43834392-43834393	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs78223610	chr15:43834398-43834399	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142636524	chr15:43834457-43834458	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs367766367	chr15:43834499-43834500	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs35106975	chr15:43834500-43834501	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557396366	chr15:43834504-43834505	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577340460	chr15:43834506-43834507	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536775615	chr15:43834510-43834511	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs398027050	chr15:43834511-43834512	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs62020613	chr15:43834537-43834538	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs148340277	chr15:43834538-43834539	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573620767	chr15:43834592-43834593	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556825276	chr15:43834617-43834618	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs542552781	chr15:43834634-43834635	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs559609460	chr15:43834649-43834650	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs528851145	chr15:43834704-43834705	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs572918965	chr15:43834708-43834709	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545249017	chr15:43834716-43834717	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs550838290	chr15:43834747-43834748	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs565107729	chr15:43834759-43834760	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567844781	chr15:43834767-43834768	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs377388368	chr15:43834846-43834847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs550340080	chr15:43834862-43834863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs200652191	chr15:43834864-43834865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs67384524	chr15:43834894-43834895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs56361192	chr15:43834895-43834896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs2584709	chr15:43834900-43834901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs116502684	chr15:43834908-43834909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs150315817	chr15:43835042-43835043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs137918687	chr15:43835068-43835069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs534858594	chr15:43835203-43835204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs142384830	chr15:43835258-43835259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571541295	chr15:43835259-43835260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs183680730	chr15:43835364-43835365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs35341481	chr15:43835370-43835371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557064076	chr15:43835386-43835387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs553539763	chr15:43835421-43835422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377009482	chr15:43835464-43835465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573517859	chr15:43835476-43835477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536261264	chr15:43835477-43835478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs2470132	chr15:43835481-43835482	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
47	rs567016999	chr15:43835489-43835490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371757875	chr15:43835496-43835497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539147007	chr15:43835537-43835538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145932233	chr15:43835541-43835542	Weak 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:630 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43812000-43844400	Weak transcription	Fetal Brain Male	brain
2	chr15:43815800-43839400	Weak transcription	Stomach Mucosa	stomach
3	chr15:43818000-43835400	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr15:43818000-43852600	Weak transcription	Rectal Smooth Muscle	rectum
5	chr15:43818200-43851600	Weak transcription	Primary hematopoietic stem cells	blood
6	chr15:43822800-43842800	Weak transcription	HSMM	muscle
7	chr15:43823200-43835600	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr15:43823600-43837400	Weak transcription	Fetal Lung	lung
9	chr15:43823600-43840000	Weak transcription	Psoas Muscle	Psoas
10	chr15:43823800-43836400	Weak transcription	NHLF	lung
11	chr15:43823800-43852600	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr15:43824200-43842800	Weak transcription	HSMMtube	muscle
13	chr15:43824200-43845000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr15:43824800-43853000	Weak transcription	GM12878-XiMat	blood
15	chr15:43824800-43853200	Weak transcription	Hela-S3	cervix
16	chr15:43827200-43849800	Weak transcription	Colonic Mucosa	Colon
17	chr15:43827400-43839800	Weak transcription	Colon Smooth Muscle	Colon
18	chr15:43827400-43841400	Weak transcription	NHEK	skin
19	chr15:43827400-43842400	Weak transcription	Osteobl	bone
20	chr15:43827400-43852600	Weak transcription	Left Ventricle	heart
21	chr15:43827400-43854000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr15:43827600-43837000	Weak transcription	Gastric	stomach
23	chr15:43827600-43839200	Weak transcription	Primary T cells from cord blood	blood
24	chr15:43827600-43839200	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr15:43827600-43840400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr15:43827600-43840400	Weak transcription	Fetal Stomach	stomach
27	chr15:43827600-43846800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr15:43827600-43848400	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr15:43827600-43848600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr15:43827600-43849000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr15:43827600-43849400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr15:43827600-43851200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr15:43827600-43851400	Weak transcription	Right Ventricle	heart
34	chr15:43827600-43851800	Weak transcription	Primary B cells from peripheral blood	blood
35	chr15:43827600-43852800	Weak transcription	Lung	lung
36	chr15:43827600-43854000	Weak transcription	Aorta	Aorta
37	chr15:43827600-43855400	Weak transcription	Ovary	ovary
38	chr15:43827800-43835600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr15:43827800-43838600	Weak transcription	Duodenum Mucosa	Duodenum
40	chr15:43827800-43839800	Weak transcription	Brain Anterior Caudate	brain
41	chr15:43827800-43839800	Weak transcription	Brain Hippocampus Middle	brain
42	chr15:43827800-43839800	Weak transcription	HMEC	breast
43	chr15:43827800-43841000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr15:43827800-43841400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr15:43827800-43842800	Weak transcription	Brain Angular Gyrus	brain
46	chr15:43827800-43845200	Weak transcription	Liver	Liver
47	chr15:43827800-43845400	Weak transcription	Stomach Smooth Muscle	stomach
48	chr15:43827800-43848200	Weak transcription	Brain Germinal Matrix	brain
49	chr15:43827800-43848600	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr15:43827800-43848800	Weak transcription	Skeletal Muscle Male	skeletal muscle

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