Variant report

Variant	nsv977704
Chromosome Location	chr15:42123613-42125024
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:37)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:37 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr15:42124464-42124722	K562	blood:	n/a	chr15:42124601-42124612
2	CEBPB	chr15:42124429-42124791	A549	lung:	n/a	chr15:42124601-42124612
3	CEBPB	chr15:42124423-42124790	HepG2	liver:	n/a	chr15:42124601-42124612
4	CEBPB	chr15:42124434-42124790	IMR90	lung:	n/a	chr15:42124601-42124612
5	CEBPB	chr15:42124523-42124799	MCF-7	breast:	n/a	chr15:42124601-42124612
6	CEBPB	chr15:42124968-42125593	ECC-1	luminal epithelium:	n/a	n/a
7	CEBPB	chr15:42124921-42125585	ECC-1	luminal epithelium:	n/a	n/a
8	CEBPB	chr15:42124468-42124770	K562	blood:	n/a	chr15:42124601-42124612
9	CEBPB	chr15:42124453-42124846	ECC-1	luminal epithelium:	n/a	chr15:42124601-42124612
10	CEBPB	chr15:42124413-42124855	ECC-1	luminal epithelium:	n/a	chr15:42124601-42124612
11	CEBPB	chr15:42124462-42124755	Hela-S3	cervix:	n/a	chr15:42124601-42124612
12	CTCF	chr15:42123618-42123722	Spleen_OC	spleen:	n/a	n/a
13	EP300	chr15:42124790-42125606	ECC-1	luminal epithelium:	n/a	n/a
14	FOXM1	chr15:42124841-42125626	ECC-1	luminal epithelium:	n/a	n/a
15	FOXM1	chr15:42124851-42125568	ECC-1	luminal epithelium:	n/a	n/a
16	MAX	chr15:42124765-42125628	ECC-1	luminal epithelium:	n/a	n/a
17	MAX	chr15:42124754-42125715	ECC-1	luminal epithelium:	n/a	n/a
18	MYC	chr15:42124988-42125612	MCF10A-Er-Src	breast:	n/a	n/a
19	MYC	chr15:42125012-42125597	MCF10A-Er-Src	breast:	n/a	n/a
20	NFIC	chr15:42124918-42125580	ECC-1	luminal epithelium:	n/a	n/a
21	NFIC	chr15:42124871-42125611	ECC-1	luminal epithelium:	n/a	n/a
22	NR3C1	chr15:42124964-42125508	ECC-1	luminal epithelium:	n/a	n/a
23	POLR2A	chr15:42124975-42125520	ECC-1	luminal epithelium:	n/a	n/a
24	POLR2A	chr15:42124177-42124522	ECC-1	luminal epithelium:	n/a	n/a
25	POLR2A	chr15:42124388-42124588	GM12878	blood:	n/a	n/a
26	POLR2A	chr15:42124571-42125549	ECC-1	luminal epithelium:	n/a	n/a
27	POLR2A	chr15:42123667-42123798	HUVEC	blood vessel:	n/a	n/a
28	POLR2A	chr15:42125023-42125141	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr15:42125012-42125505	MCF10A-Er-Src	breast:	n/a	n/a
30	RAD21	chr15:42124912-42125568	ECC-1	luminal epithelium:	n/a	n/a
31	TCF12	chr15:42124762-42125768	ECC-1	luminal epithelium:	n/a	chr15:42125129-42125139
32	TCF12	chr15:42124861-42125592	ECC-1	luminal epithelium:	n/a	chr15:42125129-42125139
33	TEAD4	chr15:42124938-42125614	ECC-1	luminal epithelium:	n/a	n/a
34	TEAD4	chr15:42124900-42125722	ECC-1	luminal epithelium:	n/a	n/a
35	USF1	chr15:42124938-42125582	ECC-1	luminal epithelium:	n/a	n/a
36	USF1	chr15:42124983-42125508	ECC-1	luminal epithelium:	n/a	n/a
37	YY1	chr15:42125010-42125443	ECC-1	luminal epithelium:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:42123717-42123767	U87	brain:	n/a
2	chr15:42123717-42123767	AG04449	skin:	fetal
3	chr15:42123717-42123767	K562	blood:	n/a
4	chr15:42123717-42123767	NB4	blood:	n/a
5	chr15:42123717-42123767	MCF10A-Er-Src	breast:	n/a
6	chr15:42123717-42123767	HUVEC	blood vessel:	n/a
7	chr15:42123717-42123767	GM12891	blood:	n/a
8	chr15:42123717-42123767	AG04450	lung:	fetal
9	chr15:42123717-42123767	HEEpiC	esophagus:	n/a
10	chr15:42123717-42123767	ECC-1	luminal epithelium:	n/a
11	chr15:42123717-42123767	AG09319	gingival:	n/a
12	chr15:42123717-42123767	HepG2	liver:	n/a
13	chr15:42123717-42123767	CMK	blood:	n/a
14	chr15:42123717-42123767	Jurkat	blood:	n/a
15	chr15:42123717-42123767	IMR90	lung:	fetal
16	chr15:42123717-42123767	SKMC	muscle:	n/a
17	chr15:42123717-42123767	RPTEC	kidney:	n/a
18	chr15:42123717-42123767	MCF-7	breast:	n/a
19	chr15:42123717-42123767	HMEC	breast:	n/a
20	chr15:42123717-42123767	GM12878	blood:	n/a
21	chr15:42123717-42123767	AoSMC	blood vessel:	n/a
22	chr15:42123717-42123767	SK-N-SH_RA	brain:	n/a
23	chr15:42123717-42123767	HCT-116	colon:	n/a
24	chr15:42123717-42123767	LNCaP	prostate:	n/a
25	chr15:42123717-42123767	HRCEpiC	kidney:	n/a
26	chr15:42123717-42123767	NHBE	bronchial:	n/a
27	chr15:42123717-42123767	HPAEpiC	pulmonary alveolar:	n/a
28	chr15:42123717-42123767	AG10803	skin:	n/a
29	chr15:42123717-42123767	NH-A	brain:	n/a
30	chr15:42123717-42123767	Caco-2	colon:	n/a
31	chr15:42123717-42123767	BJ	skin:	n/a
32	chr15:42123717-42123767	HIPEpiC	eye:	n/a
33	chr15:42123717-42123767	HNPCEpiC	eye:	n/a
34	chr15:42123717-42123767	T-47D	breast:	n/a
35	chr15:42123717-42123767	GM12892	blood:	n/a
36	chr15:42123717-42123767	NT2-D1	testis:	n/a
37	chr15:42123717-42123767	H1-hESC	embryonic stem cell:	embryo
38	chr15:42123717-42123767	GM06990	blood:	n/a
39	chr15:42123717-42123767	NHDF-neo	bronchial:	n/a
40	chr15:42123717-42123767	SK-N-SH	brain:	n/a
41	chr15:42123717-42123767	HL-60	blood:	n/a
42	chr15:42123717-42123767	GM19239	blood:	n/a
43	chr15:42123717-42123767	PFSK-1	brain:	n/a
44	chr15:42123717-42123767	Hela-S3	cervix:	n/a
45	chr15:42123717-42123767	HRPEpiC	eye:	n/a
46	chr15:42123717-42123767	SAEC	small airway:	n/a
47	chr15:42123717-42123767	HEK293	kidney:	embryo
48	chr15:42123717-42123767	A549	lung:	n/a
49	chr15:42123717-42123767	PrEC	prostate:	n/a
50	chr15:42123717-42123767	ProgFib	skin:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:42121774..42125537-chr15:42128092..42132193,4	MCF-7	breast:
2	chr15:42122872..42126047-chr15:42126791..42131021,4	K562	blood:
3	chr15:42119169..42123691-chr15:42124459..42130624,7	MCF-7	breast:
4	chr15:42119641..42122495-chr15:42123255..42125312,3	K562	blood:
5	chr15:42119169..42123691-chr15:42124459..42130624,7	MCF-7	breast:

No data

Variant related genes	Relation type
PLA2G4B	TF binding region
JMJD7-PLA2G4B	TF binding region
ENSG00000250379	TF binding region
JMJD7	TF binding region
PLA2G4B	CpG island
JMJD7-PLA2G4B	CpG island
ENSG00000250379	CpG island
JMJD7	CpG island
ENSG00000250379	chromatin interactions
ENSG00000243708	chromatin interactions
ENSG00000243789	chromatin interactions
ENSG00000168970	chromatin interactions

Extended variants
information (count: 65 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:65 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144622142	chr15:42123618-42123619	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs543723039	chr15:42123682-42123683	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs557501672	chr15:42123706-42123707	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs138495036	chr15:42123717-42123718	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs149185661	chr15:42123747-42123748	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs558875789	chr15:42123782-42123783	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs575470724	chr15:42123829-42123830	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs116010150	chr15:42123864-42123865	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs551041005	chr15:42123888-42123889	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs565293526	chr15:42123893-42123894	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs557085989	chr15:42123910-42123911	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs533232076	chr15:42123960-42123961	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs549783009	chr15:42123984-42123985	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs76668620	chr15:42124040-42124041	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs2412640	chr15:42124082-42124083	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs373624482	chr15:42124102-42124103	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs143326533	chr15:42124171-42124172	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs377131564	chr15:42124208-42124209	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs35143822	chr15:42124272-42124273	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs565595106	chr15:42124296-42124297	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs116839520	chr15:42124325-42124326	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs557297474	chr15:42124349-42124350	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs570933006	chr15:42124354-42124355	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs536677240	chr15:42124359-42124360	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs557360463	chr15:42124367-42124368	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs2412641	chr15:42124399-42124400	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs367642682	chr15:42124407-42124408	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs373494387	chr15:42124414-42124415	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs553539890	chr15:42124466-42124467	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs78460360	chr15:42124485-42124486	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs545537890	chr15:42124508-42124509	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs565404315	chr15:42124519-42124520	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs186418811	chr15:42124539-42124540	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs545215803	chr15:42124556-42124557	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs192135688	chr15:42124559-42124560	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs563433807	chr15:42124563-42124564	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs78074678	chr15:42124573-42124574	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs548867498	chr15:42124593-42124594	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs565555622	chr15:42124608-42124609	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs182594618	chr15:42124611-42124612	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs148355037	chr15:42124626-42124627	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs11630242	chr15:42124643-42124644	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs536638764	chr15:42124656-42124657	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs11635067	chr15:42124673-42124674	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs567822581	chr15:42124675-42124676	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs536968215	chr15:42124700-42124701	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs553260617	chr15:42124709-42124710	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs573450289	chr15:42124717-42124718	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs141182186	chr15:42124732-42124733	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs150746351	chr15:42124775-42124776	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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	20164920	CNVD
Hodgkin''s lymphoma	18641027	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
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Maculopathy	20981449	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:205 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42121000-42147400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr15:42121200-42123800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr15:42121200-42124000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr15:42121200-42124200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr15:42121200-42124200	Enhancers	Fetal Thymus	thymus
6	chr15:42121200-42124400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr15:42121200-42124400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr15:42121200-42124400	Weak transcription	Right Atrium	heart
9	chr15:42121200-42126000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
10	chr15:42121200-42126600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr15:42121200-42130400	Weak transcription	Stomach Mucosa	stomach
12	chr15:42121400-42123800	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr15:42121400-42123800	Weak transcription	Fetal Lung	lung
14	chr15:42121400-42123800	Weak transcription	HSMM	muscle
15	chr15:42121400-42124000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr15:42121400-42124200	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr15:42121400-42124200	Weak transcription	Aorta	Aorta
18	chr15:42121400-42124200	Enhancers	Dnd41	blood
19	chr15:42121400-42124600	Weak transcription	HSMMtube	muscle
20	chr15:42121400-42124800	Weak transcription	K562	blood
21	chr15:42121400-42125200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr15:42121400-42125400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr15:42121400-42125400	Enhancers	Primary T helper naive cells from peripheral blood	blood
24	chr15:42121400-42126200	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr15:42121400-42126200	Weak transcription	Ovary	ovary
26	chr15:42121400-42129400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr15:42121400-42130400	Weak transcription	Psoas Muscle	Psoas
28	chr15:42121400-42133800	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr15:42121400-42138200	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr15:42121400-42138400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr15:42121400-42138400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr15:42121400-42138400	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr15:42121400-42138400	Weak transcription	Primary B cells from cord blood	blood
34	chr15:42121400-42147600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr15:42121400-42147600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr15:42121600-42123800	Weak transcription	Brain Cingulate Gyrus	brain
37	chr15:42121600-42123800	Weak transcription	Brain Germinal Matrix	brain
38	chr15:42121600-42124000	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr15:42121600-42124000	Weak transcription	Rectal Smooth Muscle	rectum
40	chr15:42121600-42124400	Weak transcription	Placenta	Placenta
41	chr15:42121600-42125400	Weak transcription	Fetal Kidney	kidney
42	chr15:42121600-42130200	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr15:42121600-42134000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr15:42121600-42137200	Weak transcription	Osteobl	bone
45	chr15:42121600-42137400	Weak transcription	Small Intestine	intestine
46	chr15:42121600-42138600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr15:42121600-42141400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr15:42121600-42141800	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr15:42121800-42136600	Weak transcription	Brain Substantia Nigra	brain
50	chr15:42121800-42140400	Weak transcription	Hela-S3	cervix

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