Variant report

Variant	nsv521175
Chromosome Location	chr18:9615851-9623052
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:102)
CpG islands
(count:0)
Chromatin interactive
region (count:20)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:102 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:9616059-9616297	K562	blood:	n/a	n/a
2	ARID3A	chr18:9616735-9617052	K562	blood:	n/a	n/a
3	BACH1	chr18:9616289-9616297	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr18:9615794-9615952	K562	blood:	n/a	n/a
5	BCL3	chr18:9616006-9616377	GM12878	blood:	n/a	chr18:9616049-9616058
6	CEBPB	chr18:9620157-9620320	MCF-7	breast:	n/a	chr18:9620226-9620237
7	CEBPB	chr18:9620050-9620426	HepG2	liver:	n/a	chr18:9620226-9620237
8	CEBPB	chr18:9619942-9620341	A549	lung:	n/a	chr18:9620226-9620237
9	CEBPB	chr18:9619429-9620429	IMR90	lung:	n/a	chr18:9620226-9620237
10	CEBPB	chr18:9616225-9616335	K562	blood:	n/a	n/a
11	CEBPB	chr18:9620049-9620425	Hela-S3	cervix:	n/a	chr18:9620226-9620237
12	CEBPB	chr18:9620110-9620316	K562	blood:	n/a	chr18:9620226-9620237
13	CEBPB	chr18:9619958-9620303	K562	blood:	n/a	chr18:9620226-9620237
14	CEBPB	chr18:9620049-9620386	K562	blood:	n/a	chr18:9620226-9620237
15	CEBPB	chr18:9620051-9620417	A549	lung:	n/a	chr18:9620226-9620237
16	CEBPB	chr18:9620096-9620314	H1-hESC	embryonic stem cell:	n/a	chr18:9620226-9620237
17	CEBPB	chr18:9619999-9620321	A549	lung:	n/a	chr18:9620226-9620237
18	CEBPB	chr18:9620166-9620279	HepG2	liver:	n/a	chr18:9620226-9620237
19	CEBPB	chr18:9616794-9616914	K562	blood:	n/a	n/a
20	EP300	chr18:9615778-9616326	K562	blood:	n/a	chr18:9616049-9616063
21	EP300	chr18:9616929-9617099	GM12878	blood:	n/a	chr18:9616996-9617010
22	FOS	chr18:9619637-9619849	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr18:9619282-9619989	HUVEC	blood vessel:	n/a	n/a
24	FOS	chr18:9616011-9616405	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr18:9616168-9616418	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr18:9616041-9616404	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr18:9619697-9619859	MCF10A-Er-Src	breast:	n/a	n/a
28	GATA1	chr18:9615396-9617194	PBDE	blood:	n/a	n/a
29	GATA2	chr18:9616015-9616375	K562	blood:	n/a	n/a
30	GATA2	chr18:9619202-9619985	HUVEC	blood vessel:	n/a	n/a
31	GTF2F1	chr18:9616757-9616887	K562	blood:	n/a	n/a
32	HDAC2	chr18:9620132-9620347	K562	blood:	n/a	n/a
33	HDAC2	chr18:9619984-9620340	K562	blood:	n/a	n/a
34	IRF1	chr18:9615696-9616258	K562	blood:	n/a	chr18:9616048-9616058 chr18:9616050-9616059
35	IRF1	chr18:9616786-9617198	K562	blood:	n/a	chr18:9616995-9617005 chr18:9616995-9617009
36	JUN	chr18:9616039-9616352	K562	blood:	n/a	n/a
37	JUND	chr18:9616053-9616482	K562	blood:	n/a	n/a
38	MAFF	chr18:9616032-9616395	K562	blood:	n/a	chr18:9616237-9616255
39	MAFF	chr18:9616051-9616335	HepG2	liver:	n/a	chr18:9616237-9616255
40	MAFK	chr18:9616037-9616380	HepG2	liver:	n/a	chr18:9616238-9616253
41	MAFK	chr18:9616067-9616205	Hela-S3	cervix:	n/a	n/a
42	MAFK	chr18:9615973-9616382	IMR90	lung:	n/a	chr18:9616238-9616253
43	MAFK	chr18:9616000-9616370	K562	blood:	n/a	chr18:9616238-9616253
44	MAFK	chr18:9616060-9616162	H1-hESC	embryonic stem cell:	n/a	n/a
45	MAFK	chr18:9619219-9619980	IMR90	lung:	n/a	n/a
46	MAFK	chr18:9616034-9616372	HepG2	liver:	n/a	chr18:9616238-9616253
47	MXI1	chr18:9611932-9615928	SK-N-SH	brain:	n/a	n/a
48	MYC	chr18:9617165-9617281	NB4	blood:	n/a	n/a
49	POLR2A	chr18:9616500-9617170	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr18:9616603-9616672	HepG2	liver:	n/a	n/a

No data

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:9593651..9596050-chr18:9613258..9616024,2	MCF-7	breast:
2	chr18:9615287..9617165-chr18:9631128..9633561,2	K562	blood:
3	chr18:9614449..9616140-chr18:9677968..9679576,2	K562	blood:
4	chr18:9596087..9600746-chr18:9613522..9617540,6	MCF-7	breast:
5	chr18:9614482..9616420-chr18:9617986..9621274,5	K562	blood:
6	chr18:9614624..9617257-chr18:9707449..9709089,2	K562	blood:
7	chr18:9614482..9616420-chr18:9617986..9621274,5	K562	blood:
8	chr18:9594858..9597558-chr18:9614248..9616397,2	MCF-7	breast:
9	chr18:9615576..9617257-chr18:9706860..9708949,2	K562	blood:
10	chr18:9613045..9616469-chr18:9913547..9915707,4	K562	blood:
11	chr17:57970172..57971882-chr18:9614484..9616129,2	MCF-7	breast:
12	chr18:9615456..9617526-chr18:9895448..9898198,2	K562	blood:
13	chr18:9474922..9476536-chr18:9613527..9616238,2	MCF-7	breast:
14	chr18:9616424..9618415-chr18:9912586..9915951,3	MCF-7	breast:
15	chr18:9613570..9616156-chr18:9878427..9881071,2	K562	blood:
16	chr18:9569658..9574401-chr18:9612462..9616455,5	K562	blood:
17	chr18:9612628..9617891-chr18:9619605..9623342,5	MCF-7	breast:
18	chr18:9612544..9617098-chr18:9708301..9712595,6	MCF-7	breast:
19	chr18:9613016..9616228-chr18:9911513..9913644,4	K562	blood:
20	chr18:9614922..9615897-chrX:48815132..48816087,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RALBP1-2	chr18:9615186-9616194	NONHSAT057231
2	lnc-RALBP1-2	chr18:9619193-9619364	NONHSAT057230
3	lnc-RALBP1-2	chr18:9617146-9617283	ENSG00000263627.1
4	lnc-RALBP1-2	chr18:9617146-9617283	NONHSAT057230
5	lnc-RALBP1-2	chr18:9619193-9619361	ENSG00000263627.1

No data

Variant related genes	Relation type
PPP4R1	TF binding region
RNU6-903P	TF binding region
ENSG00000068308	chromatin interactions
ENSG00000017797	chromatin interactions
ENSG00000263627	chromatin interactions
ENSG00000168461	chromatin interactions
ENSG00000212572	chromatin interactions
ENSG00000265564	chromatin interactions
ENSG00000272799	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000264644	chromatin interactions
ENSG00000154845	chromatin interactions
ENSG00000101558	chromatin interactions
ENSG00000108423	chromatin interactions

Extended variants
information (count: 286 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8090926	chr18:9615851-9615852	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536687109	chr18:9615944-9615945	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
3	rs376820166	chr18:9615991-9615992	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
4	rs181321122	chr18:9616008-9616009	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
5	rs184633053	chr18:9616046-9616047	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
6	rs570100072	chr18:9616094-9616095	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	11 gene(s)	Overlapped CNVs	n/a
7	rs537041930	chr18:9616202-9616203	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs559252054	chr18:9616233-9616234	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs35547777	chr18:9616250-9616251	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs397691340	chr18:9616263-9616264	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs376756697	chr18:9616264-9616265	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs377378789	chr18:9616265-9616266	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs577473427	chr18:9616275-9616276	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs189757175	chr18:9616305-9616306	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs535285378	chr18:9616351-9616352	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs145408172	chr18:9616422-9616423	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs574662285	chr18:9616445-9616446	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs62088912	chr18:9616490-9616491	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs62088913	chr18:9616537-9616538	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs62088914	chr18:9616543-9616544	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs543047284	chr18:9616568-9616569	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs113642765	chr18:9616649-9616650	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs532312852	chr18:9616671-9616672	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs547634230	chr18:9616687-9616688	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs559616082	chr18:9616704-9616705	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs138526686	chr18:9616810-9616811	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs575016941	chr18:9616811-9616812	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs367641822	chr18:9616942-9616943	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs62088915	chr18:9616980-9616981	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs538729116	chr18:9616983-9616984	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs75280005	chr18:9616989-9616990	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs553183603	chr18:9617017-9617018	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs552301852	chr18:9617115-9617116	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs570793518	chr18:9617138-9617139	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs369394687	chr18:9617149-9617150	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
36	rs553227630	chr18:9617160-9617161	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
37	rs574723228	chr18:9617171-9617172	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
38	rs111785416	chr18:9617227-9617228	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
39	rs535642190	chr18:9617238-9617239	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
40	rs61749090	chr18:9617262-9617263	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs61749091	chr18:9617263-9617264	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs61740360	chr18:9617272-9617273	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs181008551	chr18:9617289-9617290	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs142716007	chr18:9617306-9617307	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs681297	chr18:9617335-9617336	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs559676453	chr18:9617401-9617402	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs528638139	chr18:9617416-9617417	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs529962791	chr18:9617492-9617493	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs556828302	chr18:9617525-9617526	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs542052291	chr18:9617533-9617534	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Breast cancer	21785460	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:242 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:9615000-9616000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr18:9615000-9616000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
3	chr18:9615000-9616200	Flanking Active TSS	K562	blood
4	chr18:9615200-9616000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
5	chr18:9615200-9616000	Flanking Active TSS	Brain Cingulate Gyrus	brain
6	chr18:9615200-9616000	Flanking Active TSS	HMEC	breast
7	chr18:9615200-9616200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr18:9615200-9616200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
9	chr18:9615400-9616000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr18:9615400-9616000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr18:9615400-9616000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
12	chr18:9615400-9618200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr18:9615600-9616000	Enhancers	Primary T helper cells PMA-I stimulated	--
14	chr18:9615600-9616000	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
15	chr18:9615600-9616000	Enhancers	Fetal Heart	heart
16	chr18:9615600-9616000	Enhancers	Stomach Mucosa	stomach
17	chr18:9615600-9616600	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr18:9615600-9616600	Enhancers	Left Ventricle	heart
19	chr18:9615600-9617000	Enhancers	Brain Substantia Nigra	brain
20	chr18:9615600-9617000	Enhancers	Placenta Amnion	Placenta Amnion
21	chr18:9615600-9617200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr18:9615600-9617400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr18:9615600-9617600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr18:9615600-9617600	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr18:9615600-9619200	Weak transcription	GM12878-XiMat	blood
26	chr18:9615800-9616000	Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr18:9615800-9616000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr18:9615800-9616000	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr18:9615800-9616000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr18:9615800-9616000	Enhancers	Liver	Liver
31	chr18:9615800-9616000	Enhancers	Brain Hippocampus Middle	brain
32	chr18:9615800-9616000	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr18:9615800-9616200	Enhancers	H9 Cell Line	embryonic stem cell
34	chr18:9615800-9616200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr18:9615800-9616200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr18:9615800-9616200	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr18:9615800-9616200	Enhancers	Colon Smooth Muscle	Colon
38	chr18:9615800-9616200	Enhancers	HSMMtube	muscle
39	chr18:9615800-9616400	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr18:9615800-9616400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
41	chr18:9615800-9616600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr18:9615800-9616800	Weak transcription	Primary hematopoietic stem cells	blood
43	chr18:9615800-9616800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr18:9615800-9616800	Enhancers	Fetal Brain Female	brain
45	chr18:9615800-9616800	Weak transcription	NH-A	brain
46	chr18:9615800-9617000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr18:9615800-9617000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
48	chr18:9615800-9617000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr18:9615800-9617000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr18:9615800-9617000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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