Variant report

Variant	nsv520101
Chromosome Location	chr11:18401531-18405510
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:334)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:334 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:18405509-18405570	K562	blood:	n/a	n/a
2	ATF2	chr11:18405190-18406276	GM12878	blood:	n/a	n/a
3	ATF2	chr11:18405250-18406175	GM12878	blood:	n/a	n/a
4	ATF3	chr11:18404979-18405669	A549	lung:	n/a	n/a
5	ATF3	chr11:18405049-18406253	A549	lung:	n/a	n/a
6	BACH1	chr11:18405354-18405361	K562	blood:	n/a	n/a
7	BATF	chr11:18405254-18405807	GM12878	blood:	n/a	n/a
8	BCL3	chr11:18405074-18406342	A549	lung:	n/a	chr11:18405880-18405888
9	BCL3	chr11:18404658-18406453	A549	lung:	n/a	chr11:18405880-18405888 chr11:18405033-18405042
10	BCLAF1	chr11:18405092-18405956	GM12878	blood:	n/a	chr11:18405880-18405888
11	BCLAF1	chr11:18405255-18405911	GM12878	blood:	n/a	chr11:18405880-18405888
12	BHLHE40	chr11:18405300-18406209	GM12878	blood:	n/a	n/a
13	BHLHE40	chr11:18405048-18405124	K562	blood:	n/a	n/a
14	BHLHE40	chr11:18405491-18405832	K562	blood:	n/a	n/a
15	BRCA1	chr11:18405494-18405516	HepG2	liver:	n/a	n/a
16	BRCA1	chr11:18404957-18406198	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr11:18405263-18406179	K562	blood:	n/a	n/a
18	CEBPB	chr11:18405307-18406294	A549	lung:	n/a	n/a
19	CEBPB	chr11:18403623-18403813	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr11:18404505-18404868	HepG2	liver:	n/a	chr11:18404676-18404687 chr11:18404678-18404689
21	CEBPB	chr11:18404490-18404776	HepG2	liver:	n/a	chr11:18404676-18404687 chr11:18404678-18404689
22	CEBPB	chr11:18404608-18404792	HepG2	liver:	n/a	chr11:18404676-18404687 chr11:18404678-18404689
23	CEBPB	chr11:18404533-18405024	A549	lung:	n/a	chr11:18404676-18404687 chr11:18404678-18404689
24	CEBPB	chr11:18405252-18405768	A549	lung:	n/a	n/a
25	CEBPB	chr11:18405083-18406285	GM12878	blood:	n/a	n/a
26	CEBPB	chr11:18404540-18404837	K562	blood:	n/a	chr11:18404676-18404687 chr11:18404678-18404689
27	CEBPB	chr11:18404506-18406294	Hela-S3	cervix:	n/a	chr11:18404676-18404687 chr11:18404678-18404689
28	CEBPB	chr11:18405141-18406475	A549	lung:	n/a	n/a
29	CEBPB	chr11:18404530-18406254	IMR90	lung:	n/a	chr11:18404676-18404687 chr11:18404678-18404689
30	CEBPD	chr11:18404621-18404797	HepG2	liver:	n/a	n/a
31	CHD1	chr11:18404993-18405330	GM12878	blood:	n/a	n/a
32	CHD2	chr11:18405104-18406278	GM12878	blood:	n/a	n/a
33	CHD2	chr11:18405386-18405411	K562	blood:	n/a	n/a
34	CHD2	chr11:18404836-18404973	HepG2	liver:	n/a	n/a
35	CHD2	chr11:18405087-18406231	Hela-S3	cervix:	n/a	n/a
36	CREB1	chr11:18405191-18405628	A549	lung:	n/a	n/a
37	CREB1	chr11:18405065-18405647	A549	lung:	n/a	n/a
38	CTCF	chr11:18405280-18405430	HCPEpiC	choroid plexus:	n/a	chr11:18405363-18405371
39	CTCF	chr11:18405433-18405544	K562	blood:	n/a	n/a
40	CTCF	chr11:18405240-18405390	A549	lung:	n/a	chr11:18405363-18405371
41	CTCF	chr11:18405340-18405490	HPAF	blood vessel:	n/a	chr11:18405363-18405371
42	CTCF	chr11:18405060-18405210	GM12870	blood:	n/a	n/a
43	CTCF	chr11:18405420-18405570	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr11:18405460-18405610	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr11:18405460-18405610	HEK293	kidney:	n/a	n/a
46	CTCF	chr11:18405400-18405550	HPF	lung:	n/a	n/a
47	CTCF	chr11:18405240-18405390	GM12873	blood:	n/a	chr11:18405363-18405371
48	CTCF	chr11:18405420-18405570	AG04449	skin:	n/a	n/a
49	CTCF	chr11:18405220-18405370	AG10803	skin:	n/a	n/a
50	CUX1	chr11:18405226-18405549	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:18405491-18405541	AG09319	gingival:	n/a
2	chr11:18405491-18405541	AG04449	skin:	fetal
3	chr11:18405491-18405541	HRE	kidney:	n/a
4	chr11:18405491-18405541	U87	brain:	n/a
5	chr11:18405491-18405541	BE2_C	brain:	n/a
6	chr11:18405491-18405541	SK-N-MC	brain:	n/a
7	chr11:18405491-18405541	MCF-7	breast:	n/a
8	chr11:18405491-18405541	HRPEpiC	eye:	n/a
9	chr11:18405491-18405541	Hepatocyte	liver:	n/a
10	chr11:18405491-18405541	GM12892	blood:	n/a
11	chr11:18405491-18405541	HRCEpiC	kidney:	n/a
12	chr11:18405491-18405541	NHDF-neo	bronchial:	n/a
13	chr11:18405491-18405541	LNCaP	prostate:	n/a
14	chr11:18405491-18405541	GM12878	blood:	n/a
15	chr11:18405491-18405541	H1-hESC	embryonic stem cell:	embryo
16	chr11:18405491-18405541	ECC-1	luminal epithelium:	n/a
17	chr11:18405491-18405541	AG09309	skin:	n/a
18	chr11:18405491-18405541	ovcar-3	ovarian:	n/a
19	chr11:18405491-18405541	MCF10A-Er-Src	breast:	n/a
20	chr11:18405491-18405541	HEK293	kidney:	embryo
21	chr11:18405491-18405541	AG10803	skin:	n/a
22	chr11:18405491-18405541	BJ	skin:	n/a
23	chr11:18405491-18405541	IMR90	lung:	fetal
24	chr11:18405491-18405541	GM19239	blood:	n/a
25	chr11:18405491-18405541	HPAEpiC	pulmonary alveolar:	n/a
26	chr11:18405491-18405541	PANC-1	pancreas:	n/a
27	chr11:18405491-18405541	Jurkat	blood:	n/a
28	chr11:18405491-18405541	NB4	blood:	n/a
29	chr11:18405491-18405541	NT2-D1	testis:	n/a
30	chr11:18405491-18405541	GM06990	blood:	n/a
31	chr11:18405491-18405541	HEEpiC	esophagus:	n/a
32	chr11:18405491-18405541	Caco-2	colon:	n/a
33	chr11:18405491-18405541	SK-N-SH_RA	brain:	n/a
34	chr11:18405491-18405541	AG04450	lung:	fetal
35	chr11:18405491-18405541	A549	lung:	n/a
36	chr11:18405491-18405541	Hela-S3	cervix:	n/a
37	chr11:18405491-18405541	NHBE	bronchial:	n/a
38	chr11:18405491-18405541	RPTEC	kidney:	n/a
39	chr11:18405491-18405541	T-47D	breast:	n/a
40	chr11:18405491-18405541	HCM	heart:	n/a
41	chr11:18405491-18405541	HIPEpiC	eye:	n/a
42	chr11:18405491-18405541	HAEpiC	amniotic membrane:	n/a
43	chr11:18405491-18405541	ProgFib	skin:	n/a
44	chr11:18405491-18405541	AoSMC	blood vessel:	n/a
45	chr11:18405491-18405541	SK-N-SH	brain:	n/a
46	chr11:18405491-18405541	GM12891	blood:	n/a
47	chr11:18405491-18405541	PrEC	prostate:	n/a
48	chr11:18405491-18405541	HCF	heart:	n/a
49	chr11:18405491-18405541	HepG2	liver:	n/a
50	chr11:18405491-18405541	PFSK-1	brain:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:18401037..18403856-chr11:18413417..18417997,5	K562	blood:
2	chr11:18405218..18405915-chr14:23299034..23299589,2	NB4	blood:
3	chr11:18402803..18405154-chr11:18406672..18408656,2	K562	blood:
4	chr11:18400049..18401686-chr11:18404314..18405882,2	K562	blood:
5	chr11:18405238..18405993-chr9:33817340..33817887,2	Hela-S3	cervix:
6	chr11:18385990..18389914-chr11:18403284..18406325,4	K562	blood:
7	chr11:18404260..18406442-chr11:18407385..18409678,2	MCF-7	breast:
8	chr11:18343373..18345684-chr11:18403945..18406882,4	MCF-7	breast:
9	chr11:18403635..18406093-chr11:18432067..18434105,2	MCF-7	breast:
10	chr11:18401460..18405154-chr11:18406672..18408749,3	K562	blood:
11	chr11:18400049..18401686-chr11:18404314..18405882,2	K562	blood:
12	chr11:18349981..18351945-chr11:18404895..18407239,2	MCF-7	breast:
13	chr11:18404463..18406104-chr11:18409610..18411729,2	K562	blood:
14	chr11:18404604..18407545-chr11:18408793..18411812,5	K562	blood:

No data

Variant related genes	Relation type
MIR3159	TF binding region
MIR3159	CpG island
ENSG00000110768	chromatin interactions
ENSG00000166796	chromatin interactions
ENSG00000107341	chromatin interactions
ENSG00000134333	chromatin interactions
ENSG00000110756	chromatin interactions
ENSG00000172590	chromatin interactions
ENSG00000264603	chromatin interactions

Extended variants
information (count: 166 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:166 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10766473	chr11:18401531-18401532	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs199644134	chr11:18401581-18401582	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs72868510	chr11:18401608-18401609	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs76089896	chr11:18401634-18401635	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs376207179	chr11:18401655-18401656	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs533895788	chr11:18401659-18401660	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs568454567	chr11:18401660-18401661	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs118022954	chr11:18401679-18401680	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs533484930	chr11:18401681-18401682	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs570661622	chr11:18401699-18401700	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs374241858	chr11:18401710-18401711	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs556335312	chr11:18401762-18401763	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs568962686	chr11:18401815-18401816	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs144151813	chr11:18401847-18401848	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs80105582	chr11:18401867-18401868	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
16	rs566326958	chr11:18401909-18401910	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs181710259	chr11:18401912-18401913	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs11024635	chr11:18401918-18401919	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs545841979	chr11:18401959-18401960	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs148668823	chr11:18401961-18401962	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs185906501	chr11:18401962-18401963	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs533744170	chr11:18401971-18401972	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs543501173	chr11:18402064-18402065	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs563098043	chr11:18402095-18402096	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs190280290	chr11:18402156-18402157	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs4756941	chr11:18402220-18402221	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs576968467	chr11:18402224-18402225	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs567083703	chr11:18402228-18402229	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs182539854	chr11:18402230-18402231	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs552196367	chr11:18402240-18402241	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs570474214	chr11:18402262-18402263	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs537955057	chr11:18402326-18402327	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs544431935	chr11:18402335-18402336	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs4586131	chr11:18402366-18402367	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs556385518	chr11:18402385-18402386	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs556356166	chr11:18402406-18402407	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs568262752	chr11:18402437-18402438	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs151282949	chr11:18402474-18402475	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs574834553	chr11:18402518-18402519	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs140440859	chr11:18402554-18402555	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs145393767	chr11:18402557-18402558	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs186866917	chr11:18402564-18402565	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs557795887	chr11:18402566-18402567	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs576060333	chr11:18402639-18402640	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs75572247	chr11:18402648-18402649	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs537922923	chr11:18402650-18402651	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs77322838	chr11:18402668-18402669	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs77357035	chr11:18402670-18402671	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs543522804	chr11:18402674-18402675	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs142594329	chr11:18402696-18402697	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:236 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18345000-18405000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:18387600-18404200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr11:18387600-18404400	Weak transcription	Esophagus	oesophagus
4	chr11:18387600-18404800	Weak transcription	Pancreas	Pancrea
5	chr11:18387800-18404400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr11:18388000-18405000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr11:18388400-18402600	Weak transcription	Hela-S3	cervix
8	chr11:18388800-18404400	Weak transcription	Brain Anterior Caudate	brain
9	chr11:18389200-18404600	Weak transcription	Thymus	Thymus
10	chr11:18390000-18404400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr11:18390000-18404400	Weak transcription	Fetal Brain Female	brain
12	chr11:18390200-18404200	Weak transcription	Fetal Thymus	thymus
13	chr11:18390400-18404000	Weak transcription	NHDF-Ad	bronchial
14	chr11:18390400-18404200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr11:18390400-18404200	Weak transcription	HMEC	breast
16	chr11:18390400-18404600	Weak transcription	Primary B cells from cord blood	blood
17	chr11:18390400-18404800	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr11:18390600-18404200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr11:18390600-18404200	Weak transcription	Adipose Nuclei	Adipose
20	chr11:18390600-18404200	Weak transcription	Osteobl	bone
21	chr11:18390800-18404200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr11:18391200-18404200	Weak transcription	HSMM	muscle
23	chr11:18391600-18404200	Weak transcription	A549	lung
24	chr11:18393000-18404200	Weak transcription	HSMMtube	muscle
25	chr11:18393000-18404400	Weak transcription	Primary T cells from cord blood	blood
26	chr11:18393600-18404200	Weak transcription	HepG2	liver
27	chr11:18399800-18401600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr11:18400400-18404200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr11:18400400-18404200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr11:18400400-18404200	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr11:18400400-18404400	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr11:18401200-18404200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr11:18401600-18404200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr11:18401600-18405000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr11:18402000-18402600	Enhancers	Psoas Muscle	Psoas
36	chr11:18402600-18404200	Enhancers	Hela-S3	cervix
37	chr11:18402600-18404400	Weak transcription	Psoas Muscle	Psoas
38	chr11:18402800-18404200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr11:18403400-18404000	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr11:18403400-18404800	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr11:18403600-18406600	Enhancers	Fetal Intestine Small	intestine
42	chr11:18404000-18404200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr11:18404000-18404200	Enhancers	NHDF-Ad	bronchial
44	chr11:18404000-18404200	Weak transcription	NHLF	lung
45	chr11:18404200-18404400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr11:18404200-18404400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr11:18404200-18404400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr11:18404200-18404400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr11:18404200-18404400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr11:18404200-18404400	Enhancers	Rectal Mucosa Donor 29	rectum

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