Variant report

Variant	nsv553590
Chromosome Location	chr11:17897414-17910664
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	BHLHE40	chr11:17899513-17899713	GM12878	blood:	n/a	n/a
2	CEBPB	chr11:17909449-17909661	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr11:17897560-17897710	GM12866	blood:	n/a	n/a
4	CTCF	chr11:17910380-17910530	HMF	breast:	n/a	n/a
5	CTCF	chr11:17909360-17909510	HCPEpiC	choroid plexus:	n/a	n/a
6	CTCF	chr11:17910460-17910610	HCM	heart:	n/a	n/a
7	CTCF	chr11:17902990-17903054	Lung_OC	lung:	n/a	n/a
8	CTCF	chr11:17910440-17910590	HCPEpiC	choroid plexus:	n/a	n/a
9	CTCF	chr11:17910400-17910550	HCPEpiC	choroid plexus:	n/a	n/a
10	CTCF	chr11:17910380-17910530	HPAF	blood vessel:	n/a	n/a
11	IRF1	chr11:17902423-17902430	K562	blood:	n/a	n/a
12	KAP1	chr11:17909130-17909658	U2OS	brain:	n/a	n/a
13	MAFK	chr11:17904839-17905040	HepG2	liver:	n/a	chr11:17904955-17904966
14	PAX5	chr11:17899544-17899760	GM12878	blood:	n/a	n/a
15	POLR2A	chr11:17909313-17909532	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr11:17905925-17906042	HepG2	liver:	n/a	n/a
17	POLR2A	chr11:17909329-17909652	H1-neurons	neurons:	n/a	n/a
18	POLR2A	chr11:17910156-17910220	HepG2	liver:	n/a	n/a
19	POLR2A	chr11:17902026-17902034	MCF10A-Er-Src	breast:	n/a	n/a
20	POLR2A	chr11:17910246-17910267	HepG2	liver:	n/a	n/a
21	POLR2A	chr11:17909386-17909571	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr11:17907061-17907088	GM12878	blood:	n/a	n/a
23	POLR2A	chr11:17904200-17904202	HepG2	liver:	n/a	n/a
24	REST	chr11:17898340-17898735	H1-hESC	embryonic stem cell:	n/a	chr11:17898529-17898543 chr11:17898528-17898537 chr11:17898523-17898543 chr11:17898523-17898543 chr11:17898524-17898542 chr11:17898526-17898539
25	REST	chr11:17898422-17898643	PFSK-1	brain:	n/a	chr11:17898529-17898543 chr11:17898528-17898537 chr11:17898523-17898543 chr11:17898523-17898543 chr11:17898524-17898542 chr11:17898526-17898539
26	REST	chr11:17898387-17898739	PFSK-1	brain:	n/a	chr11:17898529-17898543 chr11:17898528-17898537 chr11:17898523-17898543 chr11:17898523-17898543 chr11:17898524-17898542 chr11:17898526-17898539
27	REST	chr11:17898423-17898591	Hela-S3	cervix:	n/a	chr11:17898529-17898543 chr11:17898528-17898537 chr11:17898523-17898543 chr11:17898523-17898543 chr11:17898524-17898542 chr11:17898526-17898539
28	REST	chr11:17898479-17898570	GM12878	blood:	n/a	chr11:17898529-17898543 chr11:17898528-17898537 chr11:17898523-17898543 chr11:17898523-17898543 chr11:17898524-17898542 chr11:17898526-17898539
29	REST	chr11:17898361-17898627	MCF-7	breast:	n/a	chr11:17898529-17898543 chr11:17898528-17898537 chr11:17898523-17898543 chr11:17898523-17898543 chr11:17898524-17898542 chr11:17898526-17898539
30	REST	chr11:17898325-17898697	ECC-1	luminal epithelium:	n/a	chr11:17898529-17898543 chr11:17898528-17898537 chr11:17898523-17898543 chr11:17898523-17898543 chr11:17898524-17898542 chr11:17898526-17898539
31	REST	chr11:17898494-17898598	GM12878	blood:	n/a	chr11:17898529-17898543 chr11:17898528-17898537 chr11:17898523-17898543 chr11:17898523-17898543 chr11:17898524-17898542 chr11:17898526-17898539
32	REST	chr11:17898411-17898638	K562	blood:	n/a	chr11:17898529-17898543 chr11:17898528-17898537 chr11:17898523-17898543 chr11:17898523-17898543 chr11:17898524-17898542 chr11:17898526-17898539
33	REST	chr11:17898461-17898657	SK-N-SH	brain:	n/a	chr11:17898529-17898543 chr11:17898528-17898537 chr11:17898523-17898543 chr11:17898523-17898543 chr11:17898524-17898542 chr11:17898526-17898539
34	REST	chr11:17898365-17898668	H1-hESC	embryonic stem cell:	n/a	chr11:17898529-17898543 chr11:17898528-17898537 chr11:17898523-17898543 chr11:17898523-17898543 chr11:17898524-17898542 chr11:17898526-17898539
35	REST	chr11:17898297-17898773	HL-60	blood:	n/a	chr11:17898529-17898543 chr11:17898528-17898537 chr11:17898523-17898543 chr11:17898523-17898543 chr11:17898524-17898542 chr11:17898526-17898539
36	RUNX3	chr11:17899459-17899800	GM12878	blood:	n/a	n/a
37	RUNX3	chr11:17899458-17899789	GM12878	blood:	n/a	n/a
38	SIN3A	chr11:17898443-17898611	H1-hESC	embryonic stem cell:	n/a	chr11:17898527-17898537 chr11:17898528-17898542
39	TEAD4	chr11:17909252-17909671	H1-hESC	embryonic stem cell:	n/a	n/a
40	TEAD4	chr11:17909251-17909649	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:17907720-17907770	ECC-1	luminal epithelium:	n/a
2	chr11:17905750-17905800	HRPEpiC	eye:	n/a
3	chr11:17903316-17903366	PFSK-1	brain:	n/a
4	chr11:17905495-17905545	IMR90	lung:	fetal
5	chr11:17905879-17905929	NH-A	brain:	n/a
6	chr11:17905750-17905800	HAEpiC	amniotic membrane:	n/a
7	chr11:17898125-17898175	HRCEpiC	kidney:	n/a
8	chr11:17905495-17905545	AG09309	skin:	n/a
9	chr11:17898125-17898175	SK-N-SH_RA	brain:	n/a
10	chr11:17905972-17906022	HCT-116	colon:	n/a
11	chr11:17905750-17905800	IMR90	lung:	fetal
12	chr11:17905972-17906022	HepG2	liver:	n/a
13	chr11:17905879-17905929	CMK	blood:	n/a
14	chr11:17905972-17906022	GM12878	blood:	n/a
15	chr11:17905750-17905800	CMK	blood:	n/a
16	chr11:17905972-17906022	T-47D	breast:	n/a
17	chr11:17905879-17905929	HRPEpiC	eye:	n/a
18	chr11:17905495-17905545	AG04450	lung:	fetal
19	chr11:17905879-17905929	NHDF-neo	bronchial:	n/a
20	chr11:17903316-17903366	NB4	blood:	n/a
21	chr11:17905879-17905929	ECC-1	luminal epithelium:	n/a
22	chr11:17907720-17907770	PrEC	prostate:	n/a
23	chr11:17907720-17907770	HRPEpiC	eye:	n/a
24	chr11:17905972-17906022	AoSMC	blood vessel:	n/a
25	chr11:17905495-17905545	HCPEpiC	choroid plexus:	n/a
26	chr11:17898125-17898175	BE2_C	brain:	n/a
27	chr11:17905972-17906022	AG04450	lung:	fetal
28	chr11:17898125-17898175	GM12878	blood:	n/a
29	chr11:17905972-17906022	HEK293	kidney:	embryo
30	chr11:17905495-17905545	BJ	skin:	n/a
31	chr11:17905750-17905800	SK-N-MC	brain:	n/a
32	chr11:17905879-17905929	A549	lung:	n/a
33	chr11:17905972-17906022	NHDF-neo	bronchial:	n/a
34	chr11:17905879-17905929	AG09319	gingival:	n/a
35	chr11:17903316-17903366	GM06990	blood:	n/a
36	chr11:17905750-17905800	HepG2	liver:	n/a
37	chr11:17905972-17906022	Hepatocyte	liver:	n/a
38	chr11:17903316-17903366	H1-hESC	embryonic stem cell:	embryo
39	chr11:17907720-17907770	HEK293	kidney:	embryo
40	chr11:17898125-17898175	K562	blood:	n/a
41	chr11:17905750-17905800	Jurkat	blood:	n/a
42	chr11:17905750-17905800	K562	blood:	n/a
43	chr11:17907720-17907770	AG09309	skin:	n/a
44	chr11:17905495-17905545	U87	brain:	n/a
45	chr11:17905879-17905929	HEEpiC	esophagus:	n/a
46	chr11:17905750-17905800	SK-N-SH_RA	brain:	n/a
47	chr11:17898125-17898175	SAEC	small airway:	n/a
48	chr11:17907720-17907770	Hela-S3	cervix:	n/a
49	chr11:17905879-17905929	HAEpiC	amniotic membrane:	n/a
50	chr11:17905750-17905800	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:17896076..17899590-chr11:17904076..17908190,3	K562	blood:
2	chr11:17904340..17905932-chr11:17909489..17911647,2	MCF-7	breast:
3	chr11:17903051..17904653-chr11:17907402..17909230,2	K562	blood:
4	chr11:17896076..17899590-chr11:17904076..17908190,3	K562	blood:
5	chr11:17903444..17905952-chr11:17924658..17927370,2	K562	blood:
6	chr11:17903051..17904653-chr11:17907402..17909230,2	K562	blood:
7	chr11:17896076..17898646-chr11:17904076..17906937,2	K562	blood:
8	chr11:17904340..17905932-chr11:17909489..17911647,2	MCF-7	breast:
9	chr11:17909721..17912297-chr11:17913016..17915575,2	K562	blood:
10	chr11:17897357..17898994-chr11:17900707..17903680,2	MCF-7	breast:
11	chr11:17897357..17898994-chr11:17900707..17903680,2	MCF-7	breast:
12	chr11:17896076..17898646-chr11:17904076..17906937,2	K562	blood:
13	chr11:17904489..17907254-chr11:17912817..17916274,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SERGEF-1	chr11:17899755-17899791	NONHSAT018249

Variant related genes	Relation type
SERGEF	TF binding region
SERGEF	CpG island

Extended variants
information (count: 436 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:436 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2237929	chr11:17897414-17897415	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530618951	chr11:17897423-17897424	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534142505	chr11:17897424-17897425	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552798303	chr11:17897473-17897474	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571167939	chr11:17897523-17897524	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs538587805	chr11:17897530-17897531	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548872009	chr11:17897562-17897563	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs556589849	chr11:17897579-17897580	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs574922440	chr11:17897719-17897720	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190879270	chr11:17897728-17897729	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs368951360	chr11:17897779-17897780	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73426256	chr11:17897988-17897989	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567183360	chr11:17897989-17897990	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs553997033	chr11:17898031-17898032	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs74923501	chr11:17898084-17898085	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182143516	chr11:17898126-17898127	Enhancers Weak transcription Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs564352840	chr11:17898139-17898140	Enhancers Weak transcription Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs534713336	chr11:17898170-17898171	Enhancers Weak transcription Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs140565764	chr11:17898204-17898205	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2237928	chr11:17898208-17898209	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528878187	chr11:17898209-17898210	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547432732	chr11:17898258-17898259	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs559189842	chr11:17898259-17898260	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs17793144	chr11:17898263-17898264	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs2283244	chr11:17898288-17898289	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs2283243	chr11:17898289-17898290	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs538525034	chr11:17898359-17898360	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs111933995	chr11:17898361-17898362	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs148077473	chr11:17898390-17898391	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs34296672	chr11:17898397-17898398	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs557551571	chr11:17898427-17898428	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs554198713	chr11:17898446-17898447	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs572444673	chr11:17898458-17898459	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs539157383	chr11:17898481-17898482	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs539962461	chr11:17898490-17898491	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs117150966	chr11:17898563-17898564	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs76842098	chr11:17898607-17898608	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs140952730	chr11:17898612-17898613	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs575841302	chr11:17898632-17898633	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs536795398	chr11:17898635-17898636	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs543283024	chr11:17898696-17898697	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs74334417	chr11:17898719-17898720	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs573536809	chr11:17898728-17898729	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs551087319	chr11:17898844-17898845	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs150270619	chr11:17898894-17898895	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559349746	chr11:17898951-17898952	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543611463	chr11:17899013-17899014	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374323599	chr11:17899051-17899052	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564649046	chr11:17899054-17899055	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531964813	chr11:17899061-17899062	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:158 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17838400-17971600	Weak transcription	Gastric	stomach
2	chr11:17863800-17939200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr11:17864400-17944800	Weak transcription	Ovary	ovary
4	chr11:17864800-17899400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr11:17868600-17914000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr11:17869000-17909600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr11:17869000-17916400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr11:17872600-17926600	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr11:17876400-17900200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr11:17876800-17914000	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr11:17878200-17898600	Weak transcription	GM12878-XiMat	blood
12	chr11:17882800-17943800	Weak transcription	Rectal Smooth Muscle	rectum
13	chr11:17884400-17919800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr11:17885800-17939200	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr11:17886000-17965200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr11:17888200-17915600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr11:17888200-17916200	Weak transcription	HSMMtube	muscle
18	chr11:17889000-17898200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr11:17889600-17898400	Weak transcription	Fetal Stomach	stomach
20	chr11:17890600-17898000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr11:17891400-17907400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr11:17892000-17900600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr11:17893000-17901000	Strong transcription	Primary T cells from cord blood	blood
24	chr11:17893200-17897600	Strong transcription	Primary B cells from cord blood	blood
25	chr11:17894600-17899600	Strong transcription	Primary T helper cells fromperipheralblood	blood
26	chr11:17894600-17903000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr11:17894800-17898000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr11:17894800-17898800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr11:17895200-17897800	Enhancers	Left Ventricle	heart
30	chr11:17895200-17939000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr11:17895400-17899400	Strong transcription	Aorta	Aorta
32	chr11:17895400-17901800	Enhancers	Fetal Thymus	thymus
33	chr11:17895400-17901800	Enhancers	Thymus	Thymus
34	chr11:17895800-17898600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr11:17895800-17899800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr11:17895800-17914600	Weak transcription	Liver	Liver
37	chr11:17895800-17937200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr11:17895800-17943400	Weak transcription	Pancreas	Pancrea
39	chr11:17896000-17898400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr11:17896000-17909400	Weak transcription	Fetal Brain Female	brain
41	chr11:17896000-17914000	Weak transcription	Dnd41	blood
42	chr11:17896000-17914200	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr11:17896000-17915600	Weak transcription	Brain Anterior Caudate	brain
44	chr11:17896000-17944600	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr11:17896000-17968000	Weak transcription	Duodenum Mucosa	Duodenum
46	chr11:17896400-17898400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr11:17896400-17915800	Weak transcription	Fetal Intestine Small	intestine
48	chr11:17896400-17916400	Weak transcription	Right Ventricle	heart
49	chr11:17896400-17939200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr11:17896400-17968000	Weak transcription	Sigmoid Colon	Sigmoid Colon

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