Variant report

Variant	nsv430318
Chromosome Location	chr11:8958492-8964319
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:52)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:52 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:8958557-8959209	GM12878	blood:	n/a	n/a
2	ATF2	chr11:8958641-8959164	GM12878	blood:	n/a	n/a
3	BATF	chr11:8958632-8959155	GM12878	blood:	n/a	n/a
4	BCL3	chr11:8958622-8959086	GM12878	blood:	n/a	n/a
5	BCL3	chr11:8958736-8959033	GM12878	blood:	n/a	n/a
6	BCLAF1	chr11:8958629-8959151	GM12878	blood:	n/a	n/a
7	BHLHE40	chr11:8963447-8963516	K562	blood:	n/a	n/a
8	BHLHE40	chr11:8958705-8959053	GM12878	blood:	n/a	n/a
9	CHD1	chr11:8963311-8963452	H1-hESC	embryonic stem cell:	n/a	n/a
10	CUX1	chr11:8958725-8958990	GM12878	blood:	n/a	n/a
11	E2F6	chr11:8959159-8959547	H1-hESC	embryonic stem cell:	n/a	n/a
12	E2F6	chr11:8959281-8959537	K562	blood:	n/a	n/a
13	EBF1	chr11:8958691-8959103	GM12878	blood:	n/a	n/a
14	EBF1	chr11:8958769-8959082	GM12878	blood:	n/a	n/a
15	EBF1	chr11:8958741-8959105	GM12878	blood:	n/a	n/a
16	ELF1	chr11:8958589-8959065	GM12878	blood:	n/a	n/a
17	ELF1	chr11:8958746-8959001	GM12878	blood:	n/a	n/a
18	ELF1	chr11:8963283-8963549	K562	blood:	n/a	n/a
19	FOXM1	chr11:8958726-8959150	GM12878	blood:	n/a	n/a
20	FOXM1	chr11:8958472-8959152	GM12878	blood:	n/a	n/a
21	IRF1	chr11:8958682-8958756	K562	blood:	n/a	chr11:8958683-8958700 chr11:8958688-8958701 chr11:8958687-8958698
22	JUND	chr11:8962832-8962838	K562	blood:	n/a	n/a
23	JUND	chr11:8963388-8963400	K562	blood:	n/a	n/a
24	MAX	chr11:8959428-8959701	K562	blood:	n/a	n/a
25	MAZ	chr11:8962852-8962912	HepG2	liver:	n/a	n/a
26	MTA3	chr11:8958642-8959127	GM12878	blood:	n/a	n/a
27	MYC	chr11:8962967-8963149	K562	blood:	n/a	n/a
28	NFATC1	chr11:8958614-8959165	GM12878	blood:	n/a	n/a
29	NFATC1	chr11:8958635-8959049	GM12878	blood:	n/a	n/a
30	NFIC	chr11:8958546-8959204	GM12878	blood:	n/a	n/a
31	NFIC	chr11:8958628-8959175	GM12878	blood:	n/a	n/a
32	PAX5	chr11:8958504-8959180	GM12878	blood:	n/a	chr11:8958846-8958855 chr11:8958845-8958864 chr11:8958846-8958864
33	PAX5	chr11:8958642-8958982	GM12878	blood:	n/a	chr11:8958846-8958855 chr11:8958845-8958864 chr11:8958846-8958864
34	PAX5	chr11:8958635-8959005	GM12878	blood:	n/a	chr11:8958846-8958855 chr11:8958845-8958864 chr11:8958846-8958864
35	PAX5	chr11:8958666-8959014	GM12891	blood:	n/a	chr11:8958846-8958855 chr11:8958845-8958864 chr11:8958846-8958864
36	PAX5	chr11:8958716-8958997	GM12892	blood:	n/a	chr11:8958846-8958855 chr11:8958845-8958864 chr11:8958846-8958864
37	PAX5	chr11:8958741-8959011	GM12892	blood:	n/a	chr11:8958846-8958855 chr11:8958845-8958864 chr11:8958846-8958864
38	PAX5	chr11:8958581-8959039	GM12891	blood:	n/a	chr11:8958846-8958855 chr11:8958845-8958864 chr11:8958846-8958864
39	PAX5	chr11:8958568-8959068	GM12878	blood:	n/a	chr11:8958846-8958855 chr11:8958845-8958864 chr11:8958846-8958864
40	POLR2A	chr11:8960806-8960911	H1-hESC	embryonic stem cell:	n/a	n/a
41	POU2F2	chr11:8958623-8959114	GM12891	blood:	n/a	chr11:8959071-8959084
42	POU2F2	chr11:8958586-8959071	GM12878	blood:	n/a	n/a
43	POU2F2	chr11:8958644-8959046	GM12891	blood:	n/a	n/a
44	POU2F2	chr11:8958606-8958969	GM12878	blood:	n/a	n/a
45	RCOR1	chr11:8962857-8962954	K562	blood:	n/a	n/a
46	RUNX3	chr11:8958617-8959171	GM12878	blood:	n/a	n/a
47	RUNX3	chr11:8958622-8959089	GM12878	blood:	n/a	n/a
48	TCF12	chr11:8958745-8958987	GM12878	blood:	n/a	chr11:8958945-8958955
49	TCF7L2	chr11:8962585-8962840	PANC-1	pancreas:	n/a	n/a
50	UBTF	chr11:8958837-8958848	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:8959438-8959488	H1-hESC	embryonic stem cell:	embryo
2	chr11:8959438-8959488	AG04450	lung:	fetal
3	chr11:8959438-8959488	MCF-7	breast:	n/a
4	chr11:8959438-8959488	HUVEC	blood vessel:	n/a
5	chr11:8959438-8959488	PrEC	prostate:	n/a
6	chr11:8959438-8959488	SAEC	small airway:	n/a
7	chr11:8959438-8959488	NB4	blood:	n/a
8	chr11:8959438-8959488	RPTEC	kidney:	n/a
9	chr11:8959438-8959488	AG09319	gingival:	n/a
10	chr11:8959438-8959488	ProgFib	skin:	n/a
11	chr11:8959438-8959488	PANC-1	pancreas:	n/a
12	chr11:8959438-8959488	GM12892	blood:	n/a
13	chr11:8959438-8959488	SKMC	muscle:	n/a
14	chr11:8959438-8959488	U87	brain:	n/a
15	chr11:8959438-8959488	Hela-S3	cervix:	n/a
16	chr11:8959438-8959488	Caco-2	colon:	n/a
17	chr11:8959438-8959488	HMEC	breast:	n/a
18	chr11:8959438-8959488	HAEpiC	amniotic membrane:	n/a
19	chr11:8959438-8959488	NHBE	bronchial:	n/a
20	chr11:8959438-8959488	K562	blood:	n/a
21	chr11:8959438-8959488	HCM	heart:	n/a
22	chr11:8959438-8959488	HL-60	blood:	n/a
23	chr11:8959438-8959488	GM12891	blood:	n/a
24	chr11:8959438-8959488	GM06990	blood:	n/a
25	chr11:8959438-8959488	ovcar-3	ovarian:	n/a
26	chr11:8959438-8959488	SK-N-SH	brain:	n/a
27	chr11:8959438-8959488	HNPCEpiC	eye:	n/a
28	chr11:8959438-8959488	T-47D	breast:	n/a
29	chr11:8959438-8959488	HCPEpiC	choroid plexus:	n/a
30	chr11:8959438-8959488	Hepatocyte	liver:	n/a
31	chr11:8959438-8959488	IMR90	lung:	fetal
32	chr11:8959438-8959488	SK-N-MC	brain:	n/a
33	chr11:8959438-8959488	GM19239	blood:	n/a
34	chr11:8959438-8959488	HPAEpiC	pulmonary alveolar:	n/a
35	chr11:8959438-8959488	NH-A	brain:	n/a
36	chr11:8959438-8959488	AG09309	skin:	n/a
37	chr11:8959438-8959488	HIPEpiC	eye:	n/a
38	chr11:8959438-8959488	AG10803	skin:	n/a
39	chr11:8959438-8959488	LNCaP	prostate:	n/a
40	chr11:8959438-8959488	HRCEpiC	kidney:	n/a
41	chr11:8959438-8959488	Jurkat	blood:	n/a
42	chr11:8959438-8959488	BE2_C	brain:	n/a
43	chr11:8959438-8959488	GM12878	blood:	n/a
44	chr11:8959438-8959488	MCF10A-Er-Src	breast:	n/a
45	chr11:8959438-8959488	HRE	kidney:	n/a
46	chr11:8959438-8959488	AG04449	skin:	fetal
47	chr11:8959438-8959488	AoSMC	blood vessel:	n/a
48	chr11:8959438-8959488	NT2-D1	testis:	n/a
49	chr11:8959438-8959488	CMK	blood:	n/a
50	chr11:8959438-8959488	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:8957976..8959649-chr11:8961738..8963442,2	K562	blood:
2	chr11:8961456..8964030-chr11:8978805..8982021,3	K562	blood:
3	chr11:8955859..8958646-chr11:8984465..8986441,3	MCF-7	breast:
4	chr11:8957976..8959649-chr11:8961738..8963442,2	K562	blood:
5	chr11:8955484..8958608-chr11:8984431..8986354,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C11orf16-1	chr11:8960581-8960712	NDM29
2	lnc-AKIP1-6	chr11:8958467-8958768	NONHSAT017892

No data

Variant related genes	Relation type
C11orf16	TF binding region
ASCL3	TF binding region
C11orf16	CpG island
ASCL3	CpG island
ENSG00000254860	chromatin interactions
ENSG00000175348	chromatin interactions

Extended variants
information (count: 294 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:294 , 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	rs7396042	chr11:8958492-8958493	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561363390	chr11:8958504-8958505	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs545975031	chr11:8958521-8958522	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
4	rs566534365	chr11:8958535-8958536	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs559296622	chr11:8958559-8958560	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs530399575	chr11:8958602-8958603	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs528158094	chr11:8958606-8958607	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
8	rs550467112	chr11:8958633-8958634	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
9	rs75038917	chr11:8958678-8958679	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs9300096	chr11:8958694-8958695	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs113128007	chr11:8958704-8958705	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs550198988	chr11:8958718-8958719	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs140780375	chr11:8958719-8958720	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs546768789	chr11:8958727-8958728	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs59489608	chr11:8958827-8958828	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs535100034	chr11:8958835-8958836	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs566967563	chr11:8958866-8958867	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs555063196	chr11:8958881-8958882	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs111273644	chr11:8958885-8958886	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs3751064	chr11:8958903-8958904	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs145910646	chr11:8958986-8958987	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs538240502	chr11:8959007-8959008	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs3751063	chr11:8959020-8959021	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs368390220	chr11:8959050-8959051	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs557695658	chr11:8959070-8959071	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs577464158	chr11:8959084-8959085	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs546137438	chr11:8959096-8959097	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs559473558	chr11:8959103-8959104	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs572928010	chr11:8959106-8959107	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs373082955	chr11:8959112-8959113	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs138490490	chr11:8959152-8959153	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs376186721	chr11:8959153-8959154	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs143210191	chr11:8959231-8959232	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs564169914	chr11:8959232-8959233	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs561616589	chr11:8959248-8959249	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs202106934	chr11:8959255-8959256	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs200856266	chr11:8959283-8959284	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs201014647	chr11:8959295-8959296	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs141980368	chr11:8959296-8959297	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs370503735	chr11:8959301-8959302	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs141568989	chr11:8959327-8959328	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs150668187	chr11:8959351-8959352	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs146206636	chr11:8959360-8959361	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs137922914	chr11:8959369-8959370	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs2742505	chr11:8959370-8959371	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs150867873	chr11:8959380-8959381	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs185371444	chr11:8959387-8959388	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs138891086	chr11:8959395-8959396	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs560348439	chr11:8959396-8959397	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs149388223	chr11:8959406-8959407	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
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
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Dysmorphic features	22052655	CNVD
Intellectual disability	22052655	CNVD
Obesity	22052655	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21785460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8942400-8959000	Weak transcription	Fetal Kidney	kidney
2	chr11:8943800-8969200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr11:8944600-8985000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr11:8945800-8974000	Weak transcription	Colon Smooth Muscle	Colon
5	chr11:8947000-8968800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr11:8947000-8977000	Weak transcription	Aorta	Aorta
7	chr11:8947400-8969000	Weak transcription	Thymus	Thymus
8	chr11:8947600-8969000	Weak transcription	Brain Cingulate Gyrus	brain
9	chr11:8948200-8969000	Weak transcription	Fetal Brain Female	brain
10	chr11:8948600-8969200	Weak transcription	Gastric	stomach
11	chr11:8948600-8969200	Weak transcription	Stomach Smooth Muscle	stomach
12	chr11:8951200-8974400	Weak transcription	HepG2	liver
13	chr11:8952600-8975800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr11:8952800-8968600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr11:8954400-8984400	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr11:8955200-8976200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr11:8955800-8968000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr11:8956800-8968600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr11:8956800-8969000	Weak transcription	Osteobl	bone
20	chr11:8957000-8962400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr11:8957000-8968000	Weak transcription	HSMM	muscle
22	chr11:8957000-8968800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr11:8957000-8968800	Weak transcription	Fetal Intestine Large	intestine
24	chr11:8957000-8969000	Weak transcription	HSMMtube	muscle
25	chr11:8957000-8969800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr11:8957000-8969800	Weak transcription	Fetal Stomach	stomach
27	chr11:8957000-8974200	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr11:8957000-8980800	Weak transcription	Fetal Heart	heart
29	chr11:8957200-8958800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr11:8957200-8968800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr11:8957200-8968800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr11:8957200-8969000	Weak transcription	A549	lung
33	chr11:8957200-8969200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr11:8957200-8970200	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr11:8957200-8973400	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr11:8957400-8958600	Weak transcription	Placenta	Placenta
37	chr11:8957400-8959200	Weak transcription	K562	blood
38	chr11:8957400-8960400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr11:8957400-8968600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr11:8957400-8968800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr11:8957400-8969000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr11:8957400-8969000	Weak transcription	Fetal Thymus	thymus
43	chr11:8957400-8969000	Weak transcription	NH-A	brain
44	chr11:8957400-8969800	Weak transcription	Spleen	Spleen
45	chr11:8958400-8959600	Enhancers	GM12878-XiMat	blood
46	chr11:8958600-8959000	Enhancers	Placenta	Placenta
47	chr11:8958800-8959000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr11:8958800-8969000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr11:8959000-8959200	Enhancers	Fetal Kidney	kidney
50	chr11:8959000-8968800	Weak transcription	Placenta	Placenta

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