Variant report

Variant	esv2421427
Chromosome Location	chr15:43885118-43988553
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	chr15:43937914-43938101	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	chr15:43931144-43931498	GM12878	blood:	n/a	n/a
8	BATF	chr15:43937842-43938114	GM12878	blood:	n/a	n/a
9	BATF	chr15:43931124-43931473	GM12878	blood:	n/a	n/a
10	BCL11A	chr15:43930706-43930979	GM12878	blood:	n/a	n/a
11	BCL11A	chr15:43930652-43931058	GM12878	blood:	n/a	chr15:43930990-43930999
12	BCL11A	chr15:43938810-43938992	GM12878	blood:	n/a	n/a
13	BCL11A	chr15:43982262-43982477	GM12878	blood:	n/a	n/a
14	BCL11A	chr15:43938746-43939054	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	chr15:43982182-43982556	K562	blood:	n/a	n/a
18	CBX3	chr15:43885528-43886169	K562	blood:	n/a	n/a
19	CBX3	chr15:43885781-43886051	K562	blood:	n/a	n/a
20	CBX3	chr15:43982138-43982749	K562	blood:	n/a	chr15:43982622-43982633
21	CBX3	chr15:43985411-43986004	K562	blood:	n/a	n/a
22	CEBPB	chr15:43914526-43914540	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr15:43982162-43982682	GM12878	blood:	n/a	n/a
24	CEBPB	chr15:43933839-43934039	K562	blood:	n/a	n/a
25	CEBPB	chr15:43933963-43933971	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr15:43913554-43913750	K562	blood:	n/a	chr15:43913662-43913673
27	CEBPB	chr15:43913566-43913782	HepG2	liver:	n/a	chr15:43913662-43913673
28	CEBPB	chr15:43894468-43894801	Hela-S3	cervix:	n/a	n/a
29	CEBPD	chr15:43962726-43963199	K562	blood:	n/a	n/a
30	CHD2	chr15:43931127-43931189	GM12878	blood:	n/a	n/a
31	CHD2	chr15:43894517-43894780	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr15:43969460-43969486	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr15:43982088-43982521	GM12892	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
34	CTCF	chr15:43969430-43969584	K562	blood:	n/a	n/a
35	CTCF	chr15:43941276-43941415	MCF-7	breast:	n/a	n/a
36	CTCF	chr15:43912160-43912310	SAEC	small airway:	n/a	n/a
37	CTCF	chr15:43982182-43982515	GM19239	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
38	CTCF	chr15:43982246-43982499	A549	lung:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372
39	CTCF	chr15:43982201-43982511	GM13976	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
40	CTCF	chr15:43982221-43982517	HUVEC	blood vessel:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
41	CTCF	chr15:43922822-43922936	GM13976	blood:	n/a	n/a
42	CTCF	chr15:43982165-43982167	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr15:43903637-43903732	GM12892	blood:	n/a	n/a
44	CTCF	chr15:43982206-43982501	LNCaP	prostate:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
45	CTCF	chr15:43982193-43982515	GM19240	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
46	CTCF	chr15:43982226-43982490	GM10248	blood:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
47	CTCF	chr15:43982179-43982187	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr15:43973064-43973112	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr15:43982204-43982500	LNCaP	prostate:	n/a	chr15:43982357-43982373 chr15:43982356-43982374 chr15:43982362-43982371 chr15:43982351-43982372 chr15:43982228-43982236
50	CTCF	chr15:43981816-43981820	GM19239	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43912221-43912271	MCF10A-Er-Src	breast:	n/a
2	chr15:43941642-43941692	HEK293	kidney:	embryo
3	chr15:43941642-43941692	SKMC	muscle:	n/a
4	chr15:43942014-43942064	K562	blood:	n/a
5	chr15:43885090-43885140	HEK293	kidney:	embryo
6	chr15:43940140-43940190	AoSMC	blood vessel:	n/a
7	chr15:43941034-43941084	HCT-116	colon:	n/a
8	chr15:43940867-43940917	SKMC	muscle:	n/a
9	chr15:43941034-43941084	HCM	heart:	n/a
10	chr15:43984922-43984972	GM06990	blood:	n/a
11	chr15:43941871-43941921	HMEC	breast:	n/a
12	chr15:43942440-43942490	Hepatocyte	liver:	n/a
13	chr15:43940867-43940917	GM12878	blood:	n/a
14	chr15:43885090-43885140	Jurkat	blood:	n/a
15	chr15:43891480-43891530	SKMC	muscle:	n/a
16	chr15:43931742-43931792	SK-N-SH_RA	brain:	n/a
17	chr15:43984922-43984972	ovcar-3	ovarian:	n/a
18	chr15:43937339-43937389	HEK293	kidney:	embryo
19	chr15:43941034-43941084	AG09309	skin:	n/a
20	chr15:43931742-43931792	MCF10A-Er-Src	breast:	n/a
21	chr15:43941034-43941084	NB4	blood:	n/a
22	chr15:43931742-43931792	ECC-1	luminal epithelium:	n/a
23	chr15:43942014-43942064	AG04450	lung:	fetal
24	chr15:43941072-43941122	HCT-116	colon:	n/a
25	chr15:43941642-43941692	HRE	kidney:	n/a
26	chr15:43937339-43937389	RPTEC	kidney:	n/a
27	chr15:43942440-43942490	GM06990	blood:	n/a
28	chr15:43941042-43941092	HUVEC	blood vessel:	n/a
29	chr15:43941642-43941692	SK-N-SH_RA	brain:	n/a
30	chr15:43942014-43942064	HUVEC	blood vessel:	n/a
31	chr15:43983306-43983356	HL-60	blood:	n/a
32	chr15:43937339-43937389	NT2-D1	testis:	n/a
33	chr15:43941072-43941122	NB4	blood:	n/a
34	chr15:43940867-43940917	HCPEpiC	choroid plexus:	n/a
35	chr15:43885090-43885140	HIPEpiC	eye:	n/a
36	chr15:43941642-43941692	GM19239	blood:	n/a
37	chr15:43983306-43983356	MCF10A-Er-Src	breast:	n/a
38	chr15:43984922-43984972	NT2-D1	testis:	n/a
39	chr15:43941642-43941692	Hepatocyte	liver:	n/a
40	chr15:43984922-43984972	Hela-S3	cervix:	n/a
41	chr15:43941034-43941084	HRE	kidney:	n/a
42	chr15:43941042-43941092	PrEC	prostate:	n/a
43	chr15:43941563-43941613	NB4	blood:	n/a
44	chr15:43937339-43937389	HPAEpiC	pulmonary alveolar:	n/a
45	chr15:43941407-43941457	SK-N-SH	brain:	n/a
46	chr15:43941034-43941084	BE2_C	brain:	n/a
47	chr15:43984922-43984972	ECC-1	luminal epithelium:	n/a
48	chr15:43941871-43941921	AG09309	skin:	n/a
49	chr15:43941871-43941921	HL-60	blood:	n/a
50	chr15:43889864-43889914	SAEC	small airway:	n/a

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

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-TP53BP1-5	chr15:43924915-43925417	NONHSAT042101
4	lnc-CKMT1A-1	chr15:43886893-43887305	NONHSAT042091
5	lnc-CKMT1A-1	chr15:43886893-43887142	NONHSAT042092
6	lnc-TP53BP1-5	chr15:43924469-43924561	NONHSAT042101
7	lnc-MAP1A-1	chr15:43896982-43897099	ENSG00000240430.1
8	lnc-CKMT1A-1	chr15:43886243-43886620	NONHSAT042090
9	lnc-CKMT1A-1	chr15:43886217-43886565	NONHSAT042092
10	lnc-CKMT1A-1	chr15:43885406-43885469	NONHSAT042091
11	lnc-CKMT1A-1	chr15:43886243-43886565	NONHSAT042091

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

Extended variants
information (count: 2286 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2286 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149445565	chr15:43885133-43885134	Enhancers Weak transcription Active TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
2	rs527496902	chr15:43885138-43885139	Enhancers Weak transcription Active TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
3	rs540339384	chr15:43885139-43885140	Enhancers Weak transcription Active TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
4	rs560612310	chr15:43885166-43885167	Enhancers Weak transcription Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs532530403	chr15:43885392-43885393	Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs146365139	chr15:43885395-43885396	Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs199809720	chr15:43885434-43885435	Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs549097733	chr15:43885529-43885530	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs553488518	chr15:43886182-43886183	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs143878241	chr15:43887435-43887436	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs148622895	chr15:43887512-43887513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112098208	chr15:43887526-43887527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144516907	chr15:43887981-43887982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552532443	chr15:43888309-43888310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs565348580	chr15:43888331-43888332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569317565	chr15:43888391-43888392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531998037	chr15:43888485-43888486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548911205	chr15:43888538-43888539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568638041	chr15:43888541-43888542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371987094	chr15:43888554-43888555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149230297	chr15:43888677-43888678	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs199826616	chr15:43888689-43888690	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554099912	chr15:43888715-43888716	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376120318	chr15:43888743-43888744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146365795	chr15:43888744-43888745	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374661313	chr15:43888753-43888754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555737933	chr15:43888761-43888762	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201489142	chr15:43888772-43888773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189827985	chr15:43888774-43888775	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541687320	chr15:43888787-43888788	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555262009	chr15:43888803-43888804	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572277175	chr15:43888850-43888851	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs77834292	chr15:43888852-43888853	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564165376	chr15:43888863-43888864	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532632372	chr15:43888864-43888865	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546319506	chr15:43888868-43888869	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113292887	chr15:43888877-43888878	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547616289	chr15:43888890-43888891	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183186835	chr15:43888907-43888908	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187911665	chr15:43888915-43888916	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs10518820	chr15:43888976-43888977	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs547962967	chr15:43888989-43888990	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs367857351	chr15:43889004-43889005	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539473811	chr15:43889083-43889084	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555854754	chr15:43889093-43889094	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs569281291	chr15:43889094-43889095	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs66507262	chr15:43889122-43889123	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554978022	chr15:43889148-43889149	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs28475234	chr15:43889188-43889189	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs541011698	chr15:43889190-43889191	Strong transcription 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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:289 , 50 per page) page: 1 2 3 4 5 6

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	chr15:43885000-43885200	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr15:43885000-43885200	Active TSS	Duodenum Mucosa	Duodenum
5	chr15:43885000-43885200	Active TSS	Rectal Mucosa Donor 29	rectum
6	chr15:43885000-43885200	Enhancers	K562	blood
7	chr15:43885200-43888600	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr15:43885200-43889800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr15:43885400-43886200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr15:43887000-43888600	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr15:43887000-43888800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr15:43887200-43888800	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr15:43887200-43888800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr15:43887400-43889600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr15:43887400-43892800	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr15:43887400-43894200	Weak transcription	Placenta	Placenta
17	chr15:43887400-43894400	Weak transcription	Colonic Mucosa	Colon
18	chr15:43887400-43894400	Weak transcription	HMEC	breast
19	chr15:43887400-43894400	Weak transcription	NHEK	skin
20	chr15:43887600-43894000	Weak transcription	Rectal Smooth Muscle	rectum
21	chr15:43887800-43890200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr15:43888200-43889800	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr15:43888200-43894400	Weak transcription	Esophagus	oesophagus
24	chr15:43888600-43889400	Strong transcription	Rectal Mucosa Donor 29	rectum
25	chr15:43888600-43891600	Strong transcription	Rectal Mucosa Donor 31	rectum
26	chr15:43888800-43889200	Strong transcription	H9 Cell Line	embryonic stem cell
27	chr15:43888800-43890000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
28	chr15:43888800-43890400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr15:43889200-43891800	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr15:43889200-43893600	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr15:43889400-43894800	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr15:43889600-43890000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr15:43889600-43891200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr15:43889800-43890200	Strong transcription	Duodenum Mucosa	Duodenum
35	chr15:43889800-43890400	Strong transcription	HUES48 Cell Line	embryonic stem cell
36	chr15:43890000-43894400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr15:43890000-43894400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr15:43890200-43891000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr15:43890200-43891200	Weak transcription	Duodenum Mucosa	Duodenum
40	chr15:43890400-43890800	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr15:43890400-43894400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr15:43890800-43891400	Strong transcription	HUES48 Cell Line	embryonic stem cell
43	chr15:43891200-43891600	Strong transcription	Duodenum Mucosa	Duodenum
44	chr15:43891200-43892600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr15:43891400-43894400	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr15:43891600-43893600	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr15:43891600-43896600	Weak transcription	Duodenum Mucosa	Duodenum
48	chr15:43892000-43894400	Weak transcription	Fetal Intestine Small	intestine
49	chr15:43892600-43893000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr15:43892800-43893000	Enhancers	Sigmoid Colon	Sigmoid Colon

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