Variant report

Variant	nsv1038991
Chromosome Location	chr15:43914737-44024490
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	chr15:43937873-43938217	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	chr15:43931124-43931473	GM12878	blood:	n/a	n/a
5	BATF	chr15:43982183-43982550	GM12878	blood:	n/a	n/a
6	BATF	chr15:43931144-43931498	GM12878	blood:	n/a	n/a
7	BATF	chr15:43930739-43931096	GM12878	blood:	n/a	n/a
8	BATF	chr15:43937842-43938114	GM12878	blood:	n/a	n/a
9	BATF	chr15:43937914-43938101	GM12878	blood:	n/a	n/a
10	BCL11A	chr15:43938746-43939054	GM12878	blood:	n/a	n/a
11	BCL11A	chr15:43930652-43931058	GM12878	blood:	n/a	chr15:43930990-43930999
12	BCL11A	chr15:43930706-43930979	GM12878	blood:	n/a	n/a
13	BCL11A	chr15:43938810-43938992	GM12878	blood:	n/a	n/a
14	BCL11A	chr15:43982262-43982477	GM12878	blood:	n/a	n/a
15	BCL3	chr15:44013070-44013288	GM12878	blood:	n/a	n/a
16	BCLAF1	chr15:43930701-43931083	GM12878	blood:	n/a	chr15:43930990-43930999
17	BHLHE40	chr15:43939045-43939348	GM12878	blood:	n/a	n/a
18	CBX3	chr15:43982138-43982749	K562	blood:	n/a	chr15:43982622-43982633
19	CBX3	chr15:43985411-43986004	K562	blood:	n/a	n/a
20	CBX3	chr15:43982182-43982556	K562	blood:	n/a	n/a
21	CEBPB	chr15:44017050-44017346	HepG2	liver:	n/a	chr15:44017219-44017230
22	CEBPB	chr15:43933839-43934039	K562	blood:	n/a	n/a
23	CEBPB	chr15:43933963-43933971	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr15:44013072-44013307	A549	lung:	n/a	chr15:44013128-44013139
25	CEBPB	chr15:44017169-44017255	Hela-S3	cervix:	n/a	chr15:44017219-44017230
26	CEBPB	chr15:44013006-44013314	HepG2	liver:	n/a	chr15:44013128-44013139
27	CEBPB	chr15:44013108-44013199	IMR90	lung:	n/a	chr15:44013128-44013139
28	CEBPB	chr15:44013009-44013290	K562	blood:	n/a	chr15:44013128-44013139
29	CEBPB	chr15:43982162-43982682	GM12878	blood:	n/a	n/a
30	CEBPD	chr15:43962726-43963199	K562	blood:	n/a	n/a
31	CHD2	chr15:43931127-43931189	GM12878	blood:	n/a	n/a
32	CTCF	chr15:43982201-43982511	GM13976	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
33	CTCF	chr15:43941258-43941416	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr15:43982209-43982521	K562	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
35	CTCF	chr15:43981939-43982021	GM12891	blood:	n/a	n/a
36	CTCF	chr15:44003056-44003184	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr15:43982194-43982490	MCF-7	breast:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
38	CTCF	chr15:43969430-43969584	K562	blood:	n/a	n/a
39	CTCF	chr15:43980419-43980439	GM12878	blood:	n/a	n/a
40	CTCF	chr15:43982210-43982513	HepG2	liver:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
41	CTCF	chr15:43941284-43941422	GM19239	blood:	n/a	n/a
42	CTCF	chr15:43982113-43982127	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr15:43982204-43982500	LNCaP	prostate:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
44	CTCF	chr15:43982148-43982551	A549	lung:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
45	CTCF	chr15:44003045-44003213	HepG2	liver:	n/a	n/a
46	CTCF	chr15:44002969-44003267	K562	blood:	n/a	n/a
47	CTCF	chr15:43941279-43941373	HepG2	liver:	n/a	n/a
48	CTCF	chr15:43982079-43982503	K562	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
49	CTCF	chr15:43982211-43982504	GM20000	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
50	CTCF	chr15:44010454-44010457	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43942440-43942490	SK-N-SH	brain:	n/a
2	chr15:43941563-43941613	CMK	blood:	n/a
3	chr15:43942440-43942490	SK-N-SH	brain:	n/a
4	chr15:43941563-43941613	CMK	blood:	n/a
5	chr15:43941034-43941084	HRCEpiC	kidney:	n/a
6	chr15:43940867-43940917	HepG2	liver:	n/a
7	chr15:43983306-43983356	HIPEpiC	eye:	n/a
8	chr15:43941034-43941084	AoSMC	blood vessel:	n/a
9	chr15:43937339-43937389	HCF	heart:	n/a
10	chr15:43941871-43941921	HEK293	kidney:	embryo
11	chr15:43989074-43989124	HepG2	liver:	n/a
12	chr15:43941407-43941457	HAEpiC	amniotic membrane:	n/a
13	chr15:43931742-43931792	NB4	blood:	n/a
14	chr15:43983306-43983356	AG09309	skin:	n/a
15	chr15:43991375-43991425	NHDF-neo	bronchial:	n/a
16	chr15:43941407-43941457	GM12892	blood:	n/a
17	chr15:43942440-43942490	HUVEC	blood vessel:	n/a
18	chr15:43984922-43984972	NB4	blood:	n/a
19	chr15:43941563-43941613	ECC-1	luminal epithelium:	n/a
20	chr15:43941072-43941122	H1-hESC	embryonic stem cell:	embryo
21	chr15:43941034-43941084	GM12892	blood:	n/a
22	chr15:43940140-43940190	T-47D	breast:	n/a
23	chr15:43941642-43941692	AoSMC	blood vessel:	n/a
24	chr15:43991375-43991425	RPTEC	kidney:	n/a
25	chr15:43984922-43984972	HPAEpiC	pulmonary alveolar:	n/a
26	chr15:43937339-43937389	Jurkat	blood:	n/a
27	chr15:43941042-43941092	HIPEpiC	eye:	n/a
28	chr15:43989074-43989124	AG04450	lung:	fetal
29	chr15:43991375-43991425	T-47D	breast:	n/a
30	chr15:43941407-43941457	HCPEpiC	choroid plexus:	n/a
31	chr15:43937339-43937389	RPTEC	kidney:	n/a
32	chr15:43941642-43941692	SAEC	small airway:	n/a
33	chr15:43941871-43941921	Hepatocyte	liver:	n/a
34	chr15:43941407-43941457	HRE	kidney:	n/a
35	chr15:43941042-43941092	GM12891	blood:	n/a
36	chr15:43931742-43931792	A549	lung:	n/a
37	chr15:43941871-43941921	HMEC	breast:	n/a
38	chr15:43941042-43941092	ovcar-3	ovarian:	n/a
39	chr15:43937339-43937389	ECC-1	luminal epithelium:	n/a
40	chr15:43941042-43941092	U87	brain:	n/a
41	chr15:43941563-43941613	Hepatocyte	liver:	n/a
42	chr15:43941034-43941084	HEEpiC	esophagus:	n/a
43	chr15:43942014-43942064	HMEC	breast:	n/a
44	chr15:43941871-43941921	HIPEpiC	eye:	n/a
45	chr15:43941072-43941122	AG04449	skin:	fetal
46	chr15:43941642-43941692	ovcar-3	ovarian:	n/a
47	chr15:43984922-43984972	HCPEpiC	choroid plexus:	n/a
48	chr15:43941072-43941122	HMEC	breast:	n/a
49	chr15:43989074-43989124	ovcar-3	ovarian:	n/a
50	chr15:43991375-43991425	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	15:43924442-43930824..15:44015129-44020909	GM12878	blood:
2	15:43807815-43812531..15:44001645-44015047	Hela-S3	cervix:
3	chr15:44022701..44024388-chr15:44037503..44040006,2	K562	blood:
4	15:43916541-43924442..15:44034348-44042259	K562	blood:
5	15:43802874-43806906..15:44001645-44015047	Hela-S3	cervix:
6	15:43782117-43785993..15:44015129-44020909	GM12878	blood:
7	chr15:43821060..43823469-chr15:43995355..43996867,2	K562	blood:
8	15:43792489-43802874..15:44015129-44020909	GM12878	blood:
9	chr15:43946007..43947781-chr15:43949371..43952173,2	K562	blood:
10	15:43782117-43785993..15:44001645-44015047	GM12878	blood:
11	15:43792489-43802874..15:44001645-44015047	GM12878	blood:
12	15:43916541-43924442..15:44080886-44089111	GM12878	blood:
13	15:43792489-43802874..15:43916541-43924442	Hela-S3	cervix:
14	15:43924442-43930824..15:44001645-44015047	GM12878	blood:
15	chr15:43946007..43947781-chr15:43949371..43952173,2	K562	blood:
16	15:43924442-43930824..15:44001645-44015047	GM12878	blood:
17	15:43782117-43785993..15:43931042-43936532	GM12878	blood:
18	15:44001645-44015047..15:44080886-44089111	Hela-S3	cervix:
19	15:43889977-43895899..15:44001645-44015047	GM12878	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TP53BP1-5	chr15:43924915-43925417	NONHSAT042101
2	lnc-TP53BP1-5	chr15:43924469-43924561	NONHSAT042101

Variant related genes	Relation type
RNU6-353P	TF binding region
CATSPER2	TF binding region
CATSPER2P1	TF binding region
ENSG00000238494	TF binding region
PDIA3P2	TF binding region
STRC	TF binding region
RNU6-610P	TF binding region
CKMT1A	TF binding region
STRCP1	TF binding region
ENSG00000249839	TF binding region
RNU6-353P	CpG island
CATSPER2	CpG island
CATSPER2P1	CpG island
ENSG00000238494	CpG island
PDIA3P2	CpG island
STRC	CpG island
RNU6-610P	CpG island
CKMT1A	CpG island
STRCP1	CpG island
ENSG00000249839	CpG island
ENSG00000242866	chromatin interactions
ENSG00000221792	chromatin interactions
ENSG00000237289	chromatin interactions
ENSG00000140264	chromatin interactions
ENSG00000238494	chromatin interactions
ENSG00000166763	chromatin interactions
ENSG00000205771	chromatin interactions
ENSG00000166963	chromatin interactions
ENSG00000206991	chromatin interactions
ENSG00000067369	chromatin interactions
ENSG00000166762	chromatin interactions
ENSG00000242028	chromatin interactions
ENSG00000222398	chromatin interactions
ENSG00000167004	chromatin interactions

Extended variants
information (count: 2825 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2825 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528452005	chr15:43914745-43914746	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs551525238	chr15:43914757-43914758	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs571905088	chr15:43914799-43914800	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs551838414	chr15:43914882-43914883	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs34400110	chr15:43914897-43914898	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs147090764	chr15:43914996-43914997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550726307	chr15:43915001-43915002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs567875856	chr15:43915007-43915008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs536325683	chr15:43915056-43915057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189252487	chr15:43915113-43915114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573010816	chr15:43915121-43915122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544983338	chr15:43915234-43915235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562735869	chr15:43915241-43915242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531982457	chr15:43915337-43915338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs546267767	chr15:43915342-43915343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558318467	chr15:43915360-43915361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575452819	chr15:43915361-43915362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs544191915	chr15:43915410-43915411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138441322	chr15:43915411-43915412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529814696	chr15:43915416-43915417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191882077	chr15:43915419-43915420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140789078	chr15:43915426-43915427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528609869	chr15:43915437-43915438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187846570	chr15:43915445-43915446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150105521	chr15:43915501-43915502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184361259	chr15:43915588-43915589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531202143	chr15:43915591-43915592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539588669	chr15:43915596-43915597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138433862	chr15:43915600-43915601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs567989599	chr15:43915601-43915602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2927070	chr15:43915626-43915627	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs569085989	chr15:43915640-43915641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs71476497	chr15:43915643-43915644	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs547257163	chr15:43915647-43915648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566572567	chr15:43915649-43915650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186872248	chr15:43915679-43915680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146181753	chr15:43915711-43915712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs138161286	chr15:43915722-43915723	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs537874328	chr15:43915730-43915731	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs567951697	chr15:43915733-43915734	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs535285751	chr15:43915853-43915854	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs547388075	chr15:43915878-43915879	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs191771249	chr15:43915893-43915894	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs540033673	chr15:43915897-43915898	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs142621276	chr15:43915971-43915972	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs17727763	chr15:43916071-43916072	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs545186554	chr15:43916113-43916114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs377226259	chr15:43916140-43916141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565256765	chr15:43916180-43916181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371124705	chr15:43916213-43916214	Weak transcription	n/a	n/a	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:290 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43914600-43937400	Weak transcription	Fetal Intestine Small	intestine
2	chr15:43915000-43915400	Enhancers	Hela-S3	cervix
3	chr15:43915400-43941000	Weak transcription	Hela-S3	cervix
4	chr15:43917000-43918000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr15:43917200-43917800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr15:43917400-43918000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr15:43917600-43917800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr15:43919600-43941600	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr15:43920400-43941400	Weak transcription	Brain Hippocampus Middle	brain
10	chr15:43921000-43940600	Weak transcription	Gastric	stomach
11	chr15:43921400-43950400	Weak transcription	Aorta	Aorta
12	chr15:43921800-43952600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr15:43922200-43922600	Enhancers	Placenta	Placenta
14	chr15:43922800-43937600	Weak transcription	Fetal Intestine Large	intestine
15	chr15:43923200-43937400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr15:43923200-43951800	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr15:43924200-43924800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr15:43925200-43939200	Weak transcription	Brain Angular Gyrus	brain
19	chr15:43925200-43939800	Weak transcription	Brain Anterior Caudate	brain
20	chr15:43929600-43940200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr15:43929800-43937600	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr15:43930200-43930800	Enhancers	GM12878-XiMat	blood
23	chr15:43930600-43931200	Enhancers	Left Ventricle	heart
24	chr15:43930800-43931400	Flanking Active TSS	GM12878-XiMat	blood
25	chr15:43931000-43931200	Enhancers	Duodenum Smooth Muscle	Duodenum
26	chr15:43931000-43931400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr15:43931000-43931400	Enhancers	Duodenum Mucosa	Duodenum
28	chr15:43931200-43931400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr15:43931200-43943600	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr15:43931200-43952000	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr15:43931200-43952600	Weak transcription	Left Ventricle	heart
32	chr15:43931400-43939000	Weak transcription	Duodenum Mucosa	Duodenum
33	chr15:43931400-43942400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr15:43932800-43943600	Weak transcription	NHEK	skin
35	chr15:43933800-43941000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr15:43934200-43939200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr15:43934200-43939600	Weak transcription	Lung	lung
38	chr15:43934200-43940200	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr15:43934200-43941400	Weak transcription	Fetal Stomach	stomach
40	chr15:43934200-43941600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr15:43935200-43942200	Weak transcription	Esophagus	oesophagus
42	chr15:43935400-43943200	Weak transcription	Ovary	ovary
43	chr15:43935800-43937400	Weak transcription	Brain Cingulate Gyrus	brain
44	chr15:43935800-43938200	Weak transcription	Stomach Smooth Muscle	stomach
45	chr15:43935800-43940800	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr15:43935800-43941000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr15:43935800-43941200	Weak transcription	Fetal Brain Female	brain
48	chr15:43936000-43939600	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr15:43936000-43940200	Weak transcription	Colon Smooth Muscle	Colon
50	chr15:43936000-43940200	Weak transcription	Right Ventricle	heart

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