Variant report

Variant	esv33424
Chromosome Location	chr15:43888955-43995223
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	chr15:43930649-43931067	GM12878	blood:	n/a	n/a
3	ATF2	chr15:43937824-43938301	GM12878	blood:	n/a	n/a
4	BATF	chr15:43937914-43938101	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	chr15:43982183-43982550	GM12878	blood:	n/a	n/a
8	BATF	chr15:43931144-43931498	GM12878	blood:	n/a	n/a
9	BATF	chr15:43931124-43931473	GM12878	blood:	n/a	n/a
10	BCL11A	chr15:43938746-43939054	GM12878	blood:	n/a	n/a
11	BCL11A	chr15:43982262-43982477	GM12878	blood:	n/a	n/a
12	BCL11A	chr15:43938810-43938992	GM12878	blood:	n/a	n/a
13	BCL11A	chr15:43930652-43931058	GM12878	blood:	n/a	chr15:43930990-43930999
14	BCL11A	chr15:43930706-43930979	GM12878	blood:	n/a	n/a
15	BCLAF1	chr15:43930701-43931083	GM12878	blood:	n/a	chr15:43930990-43930999
16	BHLHE40	chr15:43939045-43939348	GM12878	blood:	n/a	n/a
17	CBX3	chr15:43982138-43982749	K562	blood:	n/a	chr15:43982622-43982633
18	CBX3	chr15:43982182-43982556	K562	blood:	n/a	n/a
19	CBX3	chr15:43985411-43986004	K562	blood:	n/a	n/a
20	CEBPB	chr15:43913566-43913782	HepG2	liver:	n/a	chr15:43913662-43913673
21	CEBPB	chr15:43933839-43934039	K562	blood:	n/a	n/a
22	CEBPB	chr15:43933963-43933971	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr15:43982162-43982682	GM12878	blood:	n/a	n/a
24	CEBPB	chr15:43913554-43913750	K562	blood:	n/a	chr15:43913662-43913673
25	CEBPB	chr15:43894468-43894801	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr15:43914526-43914540	Hela-S3	cervix:	n/a	n/a
27	CEBPD	chr15:43962726-43963199	K562	blood:	n/a	n/a
28	CHD2	chr15:43931127-43931189	GM12878	blood:	n/a	n/a
29	CHD2	chr15:43894517-43894780	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr15:43902588-43902631	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr15:43903539-43903775	K562	blood:	n/a	n/a
32	CTCF	chr15:43982182-43982515	GM19239	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
33	CTCF	chr15:43941279-43941373	HepG2	liver:	n/a	n/a
34	CTCF	chr15:43938709-43938821	Lung_OC	lung:	n/a	n/a
35	CTCF	chr15:43982204-43982517	MCF-7	breast:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
36	CTCF	chr15:43982016-43982654	K562	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
37	CTCF	chr15:43941262-43941391	GM12891	blood:	n/a	n/a
38	CTCF	chr15:43982157-43982511	GM12891	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
39	CTCF	chr15:43982226-43982490	GM10248	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
40	CTCF	chr15:43941268-43941360	GM19240	blood:	n/a	n/a
41	CTCF	chr15:43903572-43903813	K562	blood:	n/a	n/a
42	CTCF	chr15:43981939-43982021	GM12891	blood:	n/a	n/a
43	CTCF	chr15:43973064-43973112	Pancreas_OC	pancreas:	n/a	n/a
44	CTCF	chr15:43982189-43982507	Lung_OC	lung:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
45	CTCF	chr15:43985510-43985549	GM13976	blood:	n/a	n/a
46	CTCF	chr15:43941236-43941376	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr15:43982190-43982491	H1-hESC	embryonic stem cell:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
48	CTCF	chr15:43982194-43982490	MCF-7	breast:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
49	CTCF	chr15:43982212-43982534	Medullo	brain:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
50	CTCF	chr15:43904781-43904802	GM13977	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43941034-43941084	AG04449	skin:	fetal
2	chr15:43941642-43941692	HRPEpiC	eye:	n/a
3	chr15:43942014-43942064	PANC-1	pancreas:	n/a
4	chr15:43912221-43912271	HRPEpiC	eye:	n/a
5	chr15:43893898-43893948	HEK293	kidney:	embryo
6	chr15:43941407-43941457	SKMC	muscle:	n/a
7	chr15:43931742-43931792	HRCEpiC	kidney:	n/a
8	chr15:43941563-43941613	SK-N-MC	brain:	n/a
9	chr15:43941871-43941921	GM19239	blood:	n/a
10	chr15:43940867-43940917	SK-N-SH	brain:	n/a
11	chr15:43941642-43941692	NB4	blood:	n/a
12	chr15:43941407-43941457	Hepatocyte	liver:	n/a
13	chr15:43941563-43941613	Hela-S3	cervix:	n/a
14	chr15:43941034-43941084	HMEC	breast:	n/a
15	chr15:43891480-43891530	T-47D	breast:	n/a
16	chr15:43889864-43889914	NB4	blood:	n/a
17	chr15:43937339-43937389	GM06990	blood:	n/a
18	chr15:43984922-43984972	HNPCEpiC	eye:	n/a
19	chr15:43984922-43984972	PrEC	prostate:	n/a
20	chr15:43912221-43912271	CMK	blood:	n/a
21	chr15:43893898-43893948	HCM	heart:	n/a
22	chr15:43941042-43941092	K562	blood:	n/a
23	chr15:43931742-43931792	U87	brain:	n/a
24	chr15:43942440-43942490	NHDF-neo	bronchial:	n/a
25	chr15:43891480-43891530	GM06990	blood:	n/a
26	chr15:43942014-43942064	SK-N-SH	brain:	n/a
27	chr15:43941642-43941692	HCM	heart:	n/a
28	chr15:43940867-43940917	NHDF-neo	bronchial:	n/a
29	chr15:43983306-43983356	ECC-1	luminal epithelium:	n/a
30	chr15:43983306-43983356	ProgFib	skin:	n/a
31	chr15:43941407-43941457	SK-N-MC	brain:	n/a
32	chr15:43889864-43889914	NHDF-neo	bronchial:	n/a
33	chr15:43941407-43941457	ECC-1	luminal epithelium:	n/a
34	chr15:43941042-43941092	AoSMC	blood vessel:	n/a
35	chr15:43941407-43941457	Jurkat	blood:	n/a
36	chr15:43989074-43989124	HRE	kidney:	n/a
37	chr15:43991375-43991425	AG04450	lung:	fetal
38	chr15:43893898-43893948	H1-hESC	embryonic stem cell:	embryo
39	chr15:43941407-43941457	HMEC	breast:	n/a
40	chr15:43893898-43893948	PANC-1	pancreas:	n/a
41	chr15:43942014-43942064	AG04450	lung:	fetal
42	chr15:43893898-43893948	NH-A	brain:	n/a
43	chr15:43942440-43942490	PrEC	prostate:	n/a
44	chr15:43891480-43891530	BJ	skin:	n/a
45	chr15:43984922-43984972	HPAEpiC	pulmonary alveolar:	n/a
46	chr15:43940867-43940917	Hela-S3	cervix:	n/a
47	chr15:43931742-43931792	NHDF-neo	bronchial:	n/a
48	chr15:43937339-43937389	HepG2	liver:	n/a
49	chr15:43984922-43984972	Hepatocyte	liver:	n/a
50	chr15:43889864-43889914	AG04450	lung:	fetal

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

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

Variant related genes	Relation type
RNU6-353P	TF binding region
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
RNU6-353P	CpG island
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
ENSG00000242028	chromatin interactions
ENSG00000166763	chromatin interactions
ENSG00000167004	chromatin interactions
ENSG00000205771	chromatin interactions
ENSG00000067369	chromatin interactions
ENSG00000242866	chromatin interactions
ENSG00000140264	chromatin interactions
ENSG00000221792	chromatin interactions
ENSG00000238494	chromatin interactions

Extended variants
information (count: 2561 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2561 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10518820	chr15:43888976-43888977	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547962967	chr15:43888989-43888990	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs367857351	chr15:43889004-43889005	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539473811	chr15:43889083-43889084	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555854754	chr15:43889093-43889094	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569281291	chr15:43889094-43889095	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs66507262	chr15:43889122-43889123	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554978022	chr15:43889148-43889149	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs28475234	chr15:43889188-43889189	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs541011698	chr15:43889190-43889191	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs28535466	chr15:43889191-43889192	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557884688	chr15:43889193-43889194	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374104864	chr15:43889217-43889218	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs367647980	chr15:43889221-43889222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577773062	chr15:43889222-43889223	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115932989	chr15:43889254-43889255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
17	rs562994291	chr15:43889318-43889319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs576640095	chr15:43889367-43889368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542229730	chr15:43889398-43889399	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112761636	chr15:43889471-43889472	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527983292	chr15:43889524-43889525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547778709	chr15:43889528-43889529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191824279	chr15:43889677-43889678	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2467425	chr15:43889696-43889697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558385296	chr15:43889709-43889710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533369688	chr15:43889711-43889712	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs144248819	chr15:43889714-43889715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs147768609	chr15:43889715-43889716	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570562100	chr15:43889731-43889732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs3890552	chr15:43889734-43889735	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145282983	chr15:43889738-43889739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs117088361	chr15:43889834-43889835	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553252842	chr15:43889854-43889855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183438908	chr15:43889864-43889865	Weak transcription Strong transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
35	rs574675070	chr15:43889892-43889893	Weak transcription Strong transcription	CpG island	2 gene(s)	Overlapped CNVs	n/a
36	rs188100282	chr15:43889935-43889936	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537222176	chr15:43889947-43889948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557230395	chr15:43889952-43889953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576602344	chr15:43889989-43889990	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs112130628	chr15:43890003-43890004	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs113771631	chr15:43890013-43890014	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs150988672	chr15:43890048-43890049	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs562068663	chr15:43890078-43890079	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs572360090	chr15:43890079-43890080	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs535757429	chr15:43890103-43890104	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs75726580	chr15:43890116-43890117	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs564602883	chr15:43890131-43890132	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs192732445	chr15:43890132-43890133	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs150135252	chr15:43890138-43890139	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs563584935	chr15:43890144-43890145	Weak transcription Strong transcription	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:312 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43851800-43889600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr15:43871400-43898000	Weak transcription	Gastric	stomach
3	chr15:43885200-43889800	Weak transcription	Duodenum Mucosa	Duodenum
4	chr15:43887400-43889600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr15:43887400-43892800	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr15:43887400-43894200	Weak transcription	Placenta	Placenta
7	chr15:43887400-43894400	Weak transcription	Colonic Mucosa	Colon
8	chr15:43887400-43894400	Weak transcription	HMEC	breast
9	chr15:43887400-43894400	Weak transcription	NHEK	skin
10	chr15:43887600-43894000	Weak transcription	Rectal Smooth Muscle	rectum
11	chr15:43887800-43890200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr15:43888200-43889800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr15:43888200-43894400	Weak transcription	Esophagus	oesophagus
14	chr15:43888600-43889400	Strong transcription	Rectal Mucosa Donor 29	rectum
15	chr15:43888600-43891600	Strong transcription	Rectal Mucosa Donor 31	rectum
16	chr15:43888800-43889200	Strong transcription	H9 Cell Line	embryonic stem cell
17	chr15:43888800-43890000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr15:43888800-43890400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr15:43889200-43891800	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr15:43889200-43893600	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr15:43889400-43894800	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr15:43889600-43890000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr15:43889600-43891200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr15:43889800-43890200	Strong transcription	Duodenum Mucosa	Duodenum
25	chr15:43889800-43890400	Strong transcription	HUES48 Cell Line	embryonic stem cell
26	chr15:43890000-43894400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr15:43890000-43894400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr15:43890200-43891000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr15:43890200-43891200	Weak transcription	Duodenum Mucosa	Duodenum
30	chr15:43890400-43890800	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr15:43890400-43894400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr15:43890800-43891400	Strong transcription	HUES48 Cell Line	embryonic stem cell
33	chr15:43891200-43891600	Strong transcription	Duodenum Mucosa	Duodenum
34	chr15:43891200-43892600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr15:43891400-43894400	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr15:43891600-43893600	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr15:43891600-43896600	Weak transcription	Duodenum Mucosa	Duodenum
38	chr15:43892000-43894400	Weak transcription	Fetal Intestine Small	intestine
39	chr15:43892600-43893000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr15:43892800-43893000	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr15:43893000-43897200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr15:43893600-43893800	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr15:43893600-43894400	Enhancers	Hela-S3	cervix
44	chr15:43894200-43894600	Enhancers	Placenta	Placenta
45	chr15:43894200-43894800	Bivalent Enhancer	Fetal Muscle Leg	muscle
46	chr15:43894400-43894600	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr15:43894400-43894600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr15:43894400-43894600	Enhancers	Esophagus	oesophagus
49	chr15:43894400-43894600	Enhancers	NHEK	skin
50	chr15:43895400-43895600	Bivalent Enhancer	Fetal Muscle Leg	muscle

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