Variant report

Variant	nsv1048655
Chromosome Location	chr15:41978391-42049360
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:412)
CpG islands
(count:122)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:41982134-41982630	K562	blood:	n/a	n/a
2	ARID3A	chr15:41982942-41983062	K562	blood:	n/a	n/a
3	ARID3A	chr15:41988287-41988466	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:42022846-42023059	K562	blood:	n/a	n/a
5	ATF1	chr15:41988263-41988565	K562	blood:	n/a	n/a
6	ATF1	chr15:42022883-42023145	K562	blood:	n/a	n/a
7	BACH1	chr15:42025720-42025784	K562	blood:	n/a	n/a
8	BRCA1	chr15:42020879-42020886	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr15:41987922-41988217	IMR90	lung:	n/a	n/a
10	CEBPB	chr15:42041787-42042091	IMR90	lung:	n/a	n/a
11	CEBPB	chr15:41982017-41982396	IMR90	lung:	n/a	chr15:41982196-41982207
12	CEBPB	chr15:41981996-41982481	ECC-1	luminal epithelium:	n/a	chr15:41982196-41982207
13	CEBPB	chr15:41983646-41983885	K562	blood:	n/a	n/a
14	CEBPB	chr15:41981998-41982417	H1-hESC	embryonic stem cell:	n/a	chr15:41982196-41982207
15	CEBPB	chr15:41981983-41982397	A549	lung:	n/a	chr15:41982196-41982207
16	CEBPB	chr15:41982029-41982392	HepG2	liver:	n/a	chr15:41982196-41982207
17	CEBPB	chr15:42039047-42039408	IMR90	lung:	n/a	n/a
18	CEBPB	chr15:41982070-41982265	HepG2	liver:	n/a	chr15:41982196-41982207
19	CEBPB	chr15:42039058-42039391	HepG2	liver:	n/a	n/a
20	CEBPB	chr15:41981966-41982412	HCT-116	colon:	n/a	chr15:41982196-41982207
21	CEBPB	chr15:41982905-41983105	Hela-S3	cervix:	n/a	chr15:41983027-41983038
22	CEBPB	chr15:41981927-41982556	K562	blood:	n/a	chr15:41982196-41982207
23	CEBPB	chr15:42022791-42023141	K562	blood:	n/a	chr15:42022944-42022955 chr15:42022956-42022968
24	CEBPB	chr15:41983000-41983128	H1-hESC	embryonic stem cell:	n/a	chr15:41983027-41983038
25	CEBPB	chr15:42039095-42039357	K562	blood:	n/a	n/a
26	CEBPB	chr15:42018827-42019014	IMR90	lung:	n/a	chr15:42018877-42018888
27	CEBPB	chr15:42039188-42039290	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr15:42018772-42019037	K562	blood:	n/a	chr15:42018877-42018888
29	CEBPB	chr15:42039027-42039417	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr15:42018839-42018924	HepG2	liver:	n/a	chr15:42018877-42018888
31	CEBPB	chr15:41981960-41982423	K562	blood:	n/a	chr15:41982196-41982207
32	CEBPB	chr15:41982026-41982379	ECC-1	luminal epithelium:	n/a	chr15:41982196-41982207
33	CEBPB	chr15:41982025-41982395	A549	lung:	n/a	chr15:41982196-41982207
34	CEBPB	chr15:41987997-41988144	K562	blood:	n/a	n/a
35	CEBPB	chr15:42039062-42039376	A549	lung:	n/a	n/a
36	CEBPB	chr15:41982880-41983156	HepG2	liver:	n/a	chr15:41983027-41983038
37	CEBPB	chr15:41982013-41982401	Hela-S3	cervix:	n/a	chr15:41982196-41982207
38	CEBPB	chr15:41981848-41983220	K562	blood:	n/a	chr15:41982196-41982207 chr15:41983027-41983038
39	CEBPB	chr15:41981972-41982305	HepG2	liver:	n/a	chr15:41982196-41982207
40	CEBPB	chr15:41981975-41982563	A549	lung:	n/a	chr15:41982196-41982207
41	CEBPB	chr15:42041780-42042039	K562	blood:	n/a	n/a
42	CEBPB	chr15:41982899-41983189	K562	blood:	n/a	chr15:41983027-41983038
43	CEBPB	chr15:42041788-42041975	A549	lung:	n/a	n/a
44	CEBPB	chr15:42018823-42018996	H1-hESC	embryonic stem cell:	n/a	chr15:42018877-42018888
45	CEBPB	chr15:41982830-41983209	K562	blood:	n/a	chr15:41983027-41983038
46	CEBPB	chr15:41982896-41983179	HepG2	liver:	n/a	chr15:41983027-41983038
47	CEBPD	chr15:41982004-41982490	K562	blood:	n/a	n/a
48	CEBPD	chr15:41981963-41982481	K562	blood:	n/a	n/a
49	CTCF	chr15:41988260-41988410	NHLF	lung:	n/a	n/a
50	CTCF	chr15:41988320-41988470	GM12864	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:41983773-41983823	NHBE	bronchial:	n/a
2	chr15:41983773-41983823	SK-N-MC	brain:	n/a
3	chr15:41982969-41983019	HMEC	breast:	n/a
4	chr15:41982969-41983019	AG09319	gingival:	n/a
5	chr15:41982969-41983019	HPAEpiC	pulmonary alveolar:	n/a
6	chr15:41982969-41983019	SK-N-MC	brain:	n/a
7	chr15:41982969-41983019	HL-60	blood:	n/a
8	chr15:41982969-41983019	ovcar-3	ovarian:	n/a
9	chr15:41982969-41983019	PFSK-1	brain:	n/a
10	chr15:41983773-41983823	HEEpiC	esophagus:	n/a
11	chr15:41983773-41983823	U87	brain:	n/a
12	chr15:41983773-41983823	SAEC	small airway:	n/a
13	chr15:41982969-41983019	HRCEpiC	kidney:	n/a
14	chr15:41983773-41983823	NH-A	brain:	n/a
15	chr15:41983773-41983823	HRPEpiC	eye:	n/a
16	chr15:41982969-41983019	NT2-D1	testis:	n/a
17	chr15:41982969-41983019	HEK293	kidney:	embryo
18	chr15:41983773-41983823	HIPEpiC	eye:	n/a
19	chr15:41982969-41983019	GM12878	blood:	n/a
20	chr15:41983773-41983823	GM12878	blood:	n/a
21	chr15:41983773-41983823	NHDF-neo	bronchial:	n/a
22	chr15:41982969-41983019	AG04449	skin:	fetal
23	chr15:41982969-41983019	T-47D	breast:	n/a
24	chr15:41983773-41983823	ProgFib	skin:	n/a
25	chr15:41982969-41983019	PrEC	prostate:	n/a
26	chr15:41983773-41983823	AG09319	gingival:	n/a
27	chr15:41983773-41983823	Hela-S3	cervix:	n/a
28	chr15:41983773-41983823	GM12892	blood:	n/a
29	chr15:41982969-41983019	BE2_C	brain:	n/a
30	chr15:41982969-41983019	Jurkat	blood:	n/a
31	chr15:41983773-41983823	A549	lung:	n/a
32	chr15:41982969-41983019	SK-N-SH	brain:	n/a
33	chr15:41982969-41983019	Caco-2	colon:	n/a
34	chr15:41982969-41983019	LNCaP	prostate:	n/a
35	chr15:41983773-41983823	SK-N-SH_RA	brain:	n/a
36	chr15:41983773-41983823	HCPEpiC	choroid plexus:	n/a
37	chr15:41982969-41983019	GM19239	blood:	n/a
38	chr15:41982969-41983019	HCF	heart:	n/a
39	chr15:41982969-41983019	HAEpiC	amniotic membrane:	n/a
40	chr15:41983773-41983823	ovcar-3	ovarian:	n/a
41	chr15:41983773-41983823	NT2-D1	testis:	n/a
42	chr15:41983773-41983823	NB4	blood:	n/a
43	chr15:41983773-41983823	HRCEpiC	kidney:	n/a
44	chr15:41983773-41983823	CMK	blood:	n/a
45	chr15:41982969-41983019	HCM	heart:	n/a
46	chr15:41982969-41983019	HRE	kidney:	n/a
47	chr15:41983773-41983823	HPAEpiC	pulmonary alveolar:	n/a
48	chr15:41982969-41983019	GM12891	blood:	n/a
49	chr15:41982969-41983019	AG04450	lung:	fetal
50	chr15:41983773-41983823	HCT-116	colon:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:42041841..42044077-chr15:42045967..42047583,2	K562	blood:
2	chr15:42030668..42033706-chr15:42033784..42035660,3	MCF-7	breast:
3	chr15:41998731..42000633-chr15:42001430..42003781,2	K562	blood:
4	chr15:42039177..42040902-chr15:42043568..42045872,2	MCF-7	breast:
5	chr15:42030668..42033706-chr15:42033784..42035660,3	MCF-7	breast:
6	chr15:41987207..41988924-chr15:41992415..41994588,2	MCF-7	breast:
7	chr15:42043169..42045092-chr15:42049532..42051518,2	MCF-7	breast:
8	chr15:42034159..42036679-chr15:42048298..42050430,2	K562	blood:
9	chr15:41998731..42000633-chr15:42001430..42003781,2	K562	blood:
10	chr15:42024047..42026644-chr15:42028448..42031222,2	K562	blood:
11	chr15:42028222..42030756-chr15:42044005..42046072,2	K562	blood:
12	chr15:42019750..42022278-chr15:42036338..42038977,2	K562	blood:
13	chr15:41967640..41970567-chr15:41975944..41978799,2	K562	blood:
14	chr15:41966089..41968665-chr15:41992958..41994638,2	K562	blood:
15	chr15:41987539..41989124-chr15:42004942..42006906,2	K562	blood:
16	chr15:42035386..42037537-chr15:42041123..42043627,2	MCF-7	breast:
17	chr15:42028588..42031786-chr15:42034789..42036907,3	K562	blood:
18	chr15:42024047..42026644-chr15:42028448..42031222,2	K562	blood:
19	chr15:42010789..42012329-chr15:42064397..42066596,2	K562	blood:
20	chr15:42019750..42022278-chr15:42036338..42038977,2	K562	blood:
21	chr15:42040960..42042477-chr15:42049684..42052512,2	MCF-7	breast:
22	chr15:41851006..41852814-chr15:41978575..41981340,2	K562	blood:
23	chr15:41950960..41953076-chr15:41988289..41990930,2	MCF-7	breast:
24	chr15:41971306..41973909-chr15:41977084..41979725,2	K562	blood:
25	chr15:42041841..42044077-chr15:42045967..42047583,2	K562	blood:
26	chr15:41988022..41988696-chr15:42103354..42104252,2	K562	blood:
27	chr15:42018096..42020182-chr15:42050911..42053494,2	K562	blood:
28	chr15:41873416..41873928-chr15:41987720..41988426,2	MCF-7	breast:
29	chr15:42035386..42037537-chr15:42041123..42043627,2	MCF-7	breast:
30	chr15:42039177..42040902-chr15:42043568..42045872,2	MCF-7	breast:
31	chr15:42028588..42031786-chr15:42034789..42036907,3	K562	blood:
32	chr15:41987207..41988924-chr15:41992415..41994588,2	MCF-7	breast:
33	chr15:41973132..41976112-chr15:41981516..41983125,2	K562	blood:
34	chr15:42005381..42008216-chr15:42025990..42028220,2	MCF-7	breast:
35	chr15:41987539..41989124-chr15:42004942..42006906,2	K562	blood:
36	chr15:42049130..42051110-chr15:42082054..42084370,2	MCF-7	breast:
37	chr15:42028222..42030756-chr15:42044005..42046072,2	K562	blood:
38	chr15:42034159..42036679-chr15:42048298..42050430,2	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-626	chr15:41983843-41983861	MIMAT0003295

No data

Variant related genes	Relation type
MIR626	TF binding region
ENSG00000270702	TF binding region
MGA	TF binding region
MIR626	CpG island
ENSG00000270702	CpG island
MGA	CpG island
ENSG00000260814	chromatin interactions
ENSG00000092445	chromatin interactions
ENSG00000174197	chromatin interactions
SLC7A5	Mature miRNA region

Extended variants
information (count: 2720 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:2720 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368247141	chr15:41978400-41978401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs143079519	chr15:41978417-41978418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574545980	chr15:41978423-41978424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183862490	chr15:41978449-41978450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565070776	chr15:41978469-41978470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562501674	chr15:41978476-41978477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540339013	chr15:41978492-41978493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs187662378	chr15:41978507-41978508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548883166	chr15:41978527-41978528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs79775403	chr15:41978605-41978606	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs111765150	chr15:41978631-41978632	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs111972812	chr15:41978645-41978646	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs111709099	chr15:41978660-41978661	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs568784939	chr15:41978720-41978721	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs572698518	chr15:41978725-41978726	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs192672939	chr15:41978735-41978736	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs547970513	chr15:41978736-41978737	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs554975380	chr15:41978764-41978765	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs575948529	chr15:41978847-41978848	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs570814933	chr15:41978852-41978853	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs560425771	chr15:41978871-41978872	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs539910332	chr15:41978940-41978941	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs556425973	chr15:41978991-41978992	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs75116764	chr15:41978993-41978994	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs139231302	chr15:41978994-41978995	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs8043069	chr15:41979033-41979034	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs145872623	chr15:41979040-41979041	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs184101176	chr15:41979056-41979057	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs533700250	chr15:41979108-41979109	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs553924853	chr15:41979141-41979142	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs116004169	chr15:41979178-41979179	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs187016561	chr15:41979179-41979180	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs563183577	chr15:41979184-41979185	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs192271421	chr15:41979188-41979189	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs148996159	chr15:41979230-41979231	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs76891658	chr15:41979306-41979307	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs184372372	chr15:41979361-41979362	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs149562880	chr15:41979372-41979373	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs562321035	chr15:41979382-41979383	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs558648629	chr15:41979403-41979404	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs11858452	chr15:41979472-41979473	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs547814772	chr15:41979524-41979525	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs564696456	chr15:41979532-41979533	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs190057407	chr15:41979595-41979596	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs11634033	chr15:41979608-41979609	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs114506556	chr15:41979651-41979652	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs11858513	chr15:41979659-41979660	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs4923908	chr15:41979672-41979673	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs182215038	chr15:41979709-41979710	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs548976918	chr15:41979770-41979771	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2100 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41954400-41978600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr15:41954400-41982800	Weak transcription	Small Intestine	intestine
3	chr15:41954600-41983800	Weak transcription	Thymus	Thymus
4	chr15:41954600-42001000	Weak transcription	Colonic Mucosa	Colon
5	chr15:41954800-41980800	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr15:41955000-41988200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr15:41958400-41978400	Weak transcription	Pancreas	Pancrea
8	chr15:41959400-41988600	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr15:41959400-41989000	Weak transcription	NHDF-Ad	bronchial
10	chr15:41959600-41981000	Weak transcription	Osteobl	bone
11	chr15:41961800-41990600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr15:41962000-41980200	Weak transcription	Duodenum Mucosa	Duodenum
13	chr15:41962000-41983800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr15:41962000-41988400	Weak transcription	Adipose Nuclei	Adipose
15	chr15:41962000-41990800	Weak transcription	NH-A	brain
16	chr15:41962000-41991200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr15:41962000-42001400	Weak transcription	Gastric	stomach
18	chr15:41962200-41984400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr15:41962200-42001000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr15:41962600-41981400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr15:41962600-41981800	Weak transcription	Primary hematopoietic stem cells	blood
22	chr15:41962600-41983400	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr15:41962600-41983600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr15:41962600-41984000	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr15:41962600-41988400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr15:41963400-41988400	Weak transcription	Placenta	Placenta
27	chr15:41963600-41987800	Weak transcription	Primary B cells from cord blood	blood
28	chr15:41964600-41981000	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr15:41964600-41982200	Weak transcription	Ovary	ovary
30	chr15:41964800-41983800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr15:41965000-41980600	Weak transcription	K562	blood
32	chr15:41965000-41982400	Weak transcription	Brain Anterior Caudate	brain
33	chr15:41966600-41984400	Weak transcription	Left Ventricle	heart
34	chr15:41966600-41988400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr15:41967600-41982600	Weak transcription	GM12878-XiMat	blood
36	chr15:41967800-41980600	Weak transcription	Dnd41	blood
37	chr15:41968400-41982200	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr15:41968800-41988600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr15:41971200-41980600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr15:41971200-41980800	Weak transcription	Colon Smooth Muscle	Colon
41	chr15:41971600-41980400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr15:41971600-41980400	Weak transcription	Fetal Stomach	stomach
43	chr15:41971600-41983600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr15:41971600-41988200	Weak transcription	Fetal Thymus	thymus
45	chr15:41971600-41997400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr15:41972000-41980800	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr15:41972000-41989600	Weak transcription	Fetal Intestine Small	intestine
48	chr15:41972400-42065200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr15:41972800-41999600	Weak transcription	Fetal Brain Female	brain
50	chr15:41973200-41981000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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