Variant report

Variant	esv1812422
Chromosome Location	chr11:45419113-45431510
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:251)
CpG islands
(count:183)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:251 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr11:45422566-45422789	GM12878	blood:	n/a	n/a
2	BATF	chr11:45420774-45420989	GM12878	blood:	n/a	n/a
3	CTCF	chr11:45427920-45428070	GM12865	blood:	n/a	n/a
4	CTCF	chr11:45427920-45428070	HUVEC	blood vessel:	n/a	n/a
5	CTCF	chr11:45427944-45428094	GM10248	blood:	n/a	n/a
6	CTCF	chr11:45427940-45428090	HMF	breast:	n/a	n/a
7	CTCF	chr11:45427884-45428155	Medullo	brain:	n/a	n/a
8	CTCF	chr11:45420808-45420890	MCF-7	breast:	n/a	n/a
9	CTCF	chr11:45427687-45428420	A549	lung:	n/a	n/a
10	CTCF	chr11:45427880-45428030	GM12874	blood:	n/a	n/a
11	CTCF	chr11:45427920-45428070	NHEK	skin:	n/a	n/a
12	CTCF	chr11:45427887-45428114	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr11:45427880-45428030	HUVEC	blood vessel:	n/a	n/a
14	CTCF	chr11:45427900-45428050	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr11:45427920-45428070	AoAF	blood vessel:	n/a	n/a
16	CTCF	chr11:45427820-45427970	MCF-7	breast:	n/a	n/a
17	CTCF	chr11:45427900-45428050	SAEC	small airway:	n/a	n/a
18	CTCF	chr11:45427920-45428070	NB4	blood:	n/a	n/a
19	CTCF	chr11:45427940-45428090	HepG2	liver:	n/a	n/a
20	CTCF	chr11:45420826-45420871	Spleen_OC	spleen:	n/a	n/a
21	CTCF	chr11:45427900-45428050	Caco-2	colon:	n/a	n/a
22	CTCF	chr11:45427940-45428090	AG04449	skin:	n/a	n/a
23	CTCF	chr11:45427880-45428030	GM12878	blood:	n/a	n/a
24	CTCF	chr11:45427960-45428110	AG10803	skin:	n/a	n/a
25	CTCF	chr11:45420681-45420974	HepG2	liver:	n/a	n/a
26	CTCF	chr11:45427940-45428090	HL-60	blood:	n/a	n/a
27	CTCF	chr11:45428000-45428150	HCT-116	colon:	n/a	n/a
28	CTCF	chr11:45419847-45419906	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr11:45428160-45428310	GM12870	blood:	n/a	n/a
30	CTCF	chr11:45427939-45428058	GM10266	blood:	n/a	n/a
31	CTCF	chr11:45427980-45428130	GM12864	blood:	n/a	n/a
32	CTCF	chr11:45427920-45428070	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr11:45423700-45423850	GM12866	blood:	n/a	n/a
34	CTCF	chr11:45428020-45428170	HVMF	connective:	n/a	n/a
35	CTCF	chr11:45420843-45420874	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr11:45427900-45428050	GM12870	blood:	n/a	n/a
37	CTCF	chr11:45427880-45428030	GM12875	blood:	n/a	n/a
38	CTCF	chr11:45427900-45428118	LNCaP	prostate:	n/a	n/a
39	CTCF	chr11:45427960-45428110	AG04449	skin:	n/a	n/a
40	CTCF	chr11:45427920-45428070	HEK293	kidney:	n/a	n/a
41	CTCF	chr11:45427882-45428061	HepG2	liver:	n/a	n/a
42	CTCF	chr11:45427920-45428070	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr11:45427940-45428090	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr11:45427920-45428070	AG09309	skin:	n/a	n/a
45	CTCF	chr11:45427920-45428070	GM12868	blood:	n/a	n/a
46	CTCF	chr11:45427910-45428284	HCT-116	colon:	n/a	n/a
47	CTCF	chr11:45427920-45428070	HPF	lung:	n/a	n/a
48	CTCF	chr11:45419880-45420030	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr11:45419860-45420010	HepG2	liver:	n/a	n/a
50	CTCF	chr11:45419845-45419953	MCF-7	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:45420388-45420438	RPTEC	kidney:	n/a
2	chr11:45420442-45420492	A549	lung:	n/a
3	chr11:45420388-45420438	SK-N-SH	brain:	n/a
4	chr11:45420355-45420405	SK-N-SH	brain:	n/a
5	chr11:45420442-45420492	LNCaP	prostate:	n/a
6	chr11:45420355-45420405	A549	lung:	n/a
7	chr11:45420442-45420492	HRCEpiC	kidney:	n/a
8	chr11:45420388-45420438	BE2_C	brain:	n/a
9	chr11:45420355-45420405	GM19239	blood:	n/a
10	chr11:45420355-45420405	HepG2	liver:	n/a
11	chr11:45420388-45420438	ProgFib	skin:	n/a
12	chr11:45420355-45420405	HMEC	breast:	n/a
13	chr11:45420355-45420405	NHDF-neo	bronchial:	n/a
14	chr11:45420388-45420438	Caco-2	colon:	n/a
15	chr11:45420442-45420492	GM12878	blood:	n/a
16	chr11:45420442-45420492	GM12891	blood:	n/a
17	chr11:45420442-45420492	GM06990	blood:	n/a
18	chr11:45420388-45420438	HEEpiC	esophagus:	n/a
19	chr11:45420355-45420405	GM12892	blood:	n/a
20	chr11:45420355-45420405	HAEpiC	amniotic membrane:	n/a
21	chr11:45420442-45420492	NT2-D1	testis:	n/a
22	chr11:45420388-45420438	ECC-1	luminal epithelium:	n/a
23	chr11:45420355-45420405	HRPEpiC	eye:	n/a
24	chr11:45420388-45420438	K562	blood:	n/a
25	chr11:45420355-45420405	Hela-S3	cervix:	n/a
26	chr11:45420355-45420405	HEK293	kidney:	embryo
27	chr11:45420355-45420405	SKMC	muscle:	n/a
28	chr11:45420388-45420438	NB4	blood:	n/a
29	chr11:45420388-45420438	GM19239	blood:	n/a
30	chr11:45420355-45420405	HEEpiC	esophagus:	n/a
31	chr11:45420442-45420492	HIPEpiC	eye:	n/a
32	chr11:45420442-45420492	HCPEpiC	choroid plexus:	n/a
33	chr11:45420388-45420438	SAEC	small airway:	n/a
34	chr11:45420355-45420405	HCF	heart:	n/a
35	chr11:45420355-45420405	CMK	blood:	n/a
36	chr11:45420442-45420492	Jurkat	blood:	n/a
37	chr11:45420388-45420438	AG09309	skin:	n/a
38	chr11:45420442-45420492	NHDF-neo	bronchial:	n/a
39	chr11:45420388-45420438	HNPCEpiC	eye:	n/a
40	chr11:45420388-45420438	BJ	skin:	n/a
41	chr11:45420442-45420492	HCT-116	colon:	n/a
42	chr11:45420442-45420492	Hepatocyte	liver:	n/a
43	chr11:45420355-45420405	MCF10A-Er-Src	breast:	n/a
44	chr11:45420355-45420405	U87	brain:	n/a
45	chr11:45420442-45420492	GM12892	blood:	n/a
46	chr11:45420388-45420438	HPAEpiC	pulmonary alveolar:	n/a
47	chr11:45420355-45420405	HCM	heart:	n/a
48	chr11:45420355-45420405	NT2-D1	testis:	n/a
49	chr11:45420442-45420492	U87	brain:	n/a
50	chr11:45420355-45420405	K562	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:45427988..45430237-chr11:45431939..45433599,2	K562	blood:
2	chr11:45418856..45421391-chr11:45421484..45423655,2	K562	blood:
3	chr11:45413154..45414877-chr11:45416826..45419299,2	K562	blood:
4	chr11:45427814..45428397-chr11:45676543..45677286,2	MCF-7	breast:
5	chr11:45427597..45428482-chr11:45792562..45793604,3	MCF-7	breast:
6	chr11:45392504..45393419-chr11:45427914..45428464,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRDM11-5	chr11:45421636-45422078	ENSG00000254651
2	lnc-PRDM11-5	chr11:45420998-45421115	ENSG00000254651

No data

Variant related genes	Relation type
ENSG00000254651	TF binding region
ENSG00000254651	CpG island
ENSG00000255267	chromatin interactions
ENSG00000254651	chromatin interactions
ENSG00000205106	chromatin interactions

Extended variants
information (count: 473 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:473 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11038440	chr11:45419113-45419114	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs546070142	chr11:45419114-45419115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189363021	chr11:45419120-45419121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149516755	chr11:45419129-45419130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs112708848	chr11:45419225-45419226	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs561904715	chr11:45419259-45419260	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs572122232	chr11:45419358-45419359	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs182322992	chr11:45419421-45419422	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs564268493	chr11:45419490-45419491	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs186217468	chr11:45419508-45419509	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs550066812	chr11:45419524-45419525	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs527874388	chr11:45419613-45419614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563910460	chr11:45419628-45419629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145989738	chr11:45419705-45419706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs549668615	chr11:45419826-45419827	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs568048224	chr11:45419866-45419867	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs2044871	chr11:45419879-45419880	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs547514479	chr11:45420034-45420035	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs11276867	chr11:45420041-45420042	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs11279126	chr11:45420045-45420046	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs200941672	chr11:45420046-45420047	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs72396839	chr11:45420052-45420053	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs201624935	chr11:45420063-45420064	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs188973260	chr11:45420084-45420085	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs370912163	chr11:45420095-45420096	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs539526606	chr11:45420104-45420105	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs139976872	chr11:45420149-45420150	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs533693144	chr11:45420151-45420152	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs112605085	chr11:45420175-45420176	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs75918525	chr11:45420197-45420198	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs112166950	chr11:45420198-45420199	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs146755863	chr11:45420207-45420208	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs368383172	chr11:45420218-45420219	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs34042421	chr11:45420233-45420234	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs572085822	chr11:45420241-45420242	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs541073349	chr11:45420250-45420251	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs11038441	chr11:45420251-45420252	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs577669419	chr11:45420254-45420255	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs181362369	chr11:45420261-45420262	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs11602299	chr11:45420279-45420280	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs528856849	chr11:45420284-45420285	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs373208155	chr11:45420285-45420286	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs112566697	chr11:45420299-45420300	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs147091504	chr11:45420316-45420317	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs549392268	chr11:45420317-45420318	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs11827138	chr11:45420332-45420333	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs112987499	chr11:45420341-45420342	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs527272025	chr11:45420350-45420351	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs185548769	chr11:45420351-45420352	Weak transcription Enhancers Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs142640554	chr11:45420355-45420356	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	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
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45405400-45434800	Weak transcription	Right Atrium	heart
2	chr11:45407000-45421000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr11:45412600-45420400	Weak transcription	Gastric	stomach
4	chr11:45413600-45420200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr11:45415200-45421000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr11:45415400-45419600	Weak transcription	Brain Germinal Matrix	brain
7	chr11:45415800-45421000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr11:45416000-45420200	Weak transcription	Lung	lung
9	chr11:45416000-45423400	Weak transcription	Spleen	Spleen
10	chr11:45417800-45419800	Weak transcription	Fetal Brain Male	brain
11	chr11:45418800-45421400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr11:45419400-45420200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr11:45419600-45420400	Enhancers	Brain Germinal Matrix	brain
14	chr11:45419800-45420400	Enhancers	Fetal Brain Male	brain
15	chr11:45420000-45420200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr11:45420000-45420600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr11:45420200-45420600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr11:45420200-45420600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr11:45420200-45420600	ZNF genes & repeats	Lung	lung
20	chr11:45420200-45423800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr11:45420400-45420600	Active TSS	Gastric	stomach
22	chr11:45420600-45421600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr11:45420600-45421800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr11:45420600-45423000	Weak transcription	Lung	lung
25	chr11:45421000-45421800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr11:45421000-45421800	Enhancers	Muscle Satellite Cultured Cells	--
27	chr11:45421000-45422000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr11:45421000-45422000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr11:45421000-45422400	Enhancers	HSMM	muscle
30	chr11:45421000-45422600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr11:45421000-45423200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr11:45421000-45423200	Enhancers	Osteobl	bone
33	chr11:45421000-45423400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr11:45421200-45423200	Enhancers	HUVEC	blood vessel
35	chr11:45421400-45421800	Enhancers	NH-A	brain
36	chr11:45421400-45422000	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr11:45421400-45422000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr11:45421400-45423000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr11:45421400-45423200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr11:45421400-45423200	Enhancers	NHDF-Ad	bronchial
41	chr11:45421600-45422000	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr11:45421600-45422000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr11:45421600-45422000	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr11:45421600-45423200	Bivalent Enhancer	HepG2	liver
45	chr11:45421600-45423200	Enhancers	NHLF	lung
46	chr11:45421800-45422000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr11:45421800-45422600	Flanking Active TSS	NH-A	brain
48	chr11:45421800-45422800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
49	chr11:45421800-45431600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr11:45422000-45422200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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