Variant report

Variant	nsv306
Chromosome Location	chr11:45414044-45444431
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:326)
CpG islands
(count:366)
Chromatin interactive
region (count:12)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:326 , 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	BATF	chr11:45422566-45422789	GM12878	blood:	n/a	n/a
2	BATF	chr11:45420774-45420989	GM12878	blood:	n/a	n/a
3	CEBPB	chr11:45434794-45435108	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr11:45434195-45434384	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr11:45419860-45419899	HepG2	liver:	n/a	n/a
6	CTCF	chr11:45427920-45428070	WERI-Rb-1	eye:	n/a	n/a
7	CTCF	chr11:45427920-45428070	HMEC	breast:	n/a	n/a
8	CTCF	chr11:45420681-45420974	HepG2	liver:	n/a	n/a
9	CTCF	chr11:45427920-45428070	BE2_C	brain:	n/a	n/a
10	CTCF	chr11:45427939-45428058	GM10266	blood:	n/a	n/a
11	CTCF	chr11:45427920-45428070	HCFaa	heart:	n/a	n/a
12	CTCF	chr11:45427960-45428110	HA-sp	spinal cord:	n/a	n/a
13	CTCF	chr11:45427880-45428030	HUVEC	blood vessel:	n/a	n/a
14	CTCF	chr11:45427920-45428070	SK-N-SH_RA	brain:	n/a	n/a
15	CTCF	chr11:45427900-45428050	HBMEC	blood vessel:	n/a	n/a
16	CTCF	chr11:45428220-45428370	HEK293	kidney:	n/a	n/a
17	CTCF	chr11:45427900-45428050	AG04450	lung:	n/a	n/a
18	CTCF	chr11:45427900-45428050	GM12872	blood:	n/a	n/a
19	CTCF	chr11:45427929-45428112	Lung_OC	lung:	n/a	n/a
20	CTCF	chr11:45427900-45428050	GM12870	blood:	n/a	n/a
21	CTCF	chr11:45428240-45428390	HVMF	connective:	n/a	n/a
22	CTCF	chr11:45427920-45428070	NB4	blood:	n/a	n/a
23	CTCF	chr11:45420852-45420922	MCF-7	breast:	n/a	n/a
24	CTCF	chr11:45427920-45428070	GM12872	blood:	n/a	n/a
25	CTCF	chr11:45427900-45428050	HRPEpiC	eye:	n/a	n/a
26	CTCF	chr11:45427640-45427790	NHEK	skin:	n/a	n/a
27	CTCF	chr11:45420843-45420874	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr11:45432691-45432710	Lung_OC	lung:	n/a	n/a
29	CTCF	chr11:45420748-45420937	HepG2	liver:	n/a	n/a
30	CTCF	chr11:45427900-45428050	SAEC	small airway:	n/a	n/a
31	CTCF	chr11:45420740-45420890	AG09309	skin:	n/a	n/a
32	CTCF	chr11:45427480-45427630	AG09319	gingival:	n/a	n/a
33	CTCF	chr11:45427920-45428070	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr11:45427940-45428090	AG04449	skin:	n/a	n/a
35	CTCF	chr11:45427920-45428070	WI-38	lung:	n/a	n/a
36	CTCF	chr11:45427920-45428070	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr11:45433060-45433210	AG09309	skin:	n/a	n/a
38	CTCF	chr11:45427900-45428050	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr11:45427980-45428130	NHLF	lung:	n/a	n/a
40	CTCF	chr11:45427910-45428284	HCT-116	colon:	n/a	n/a
41	CTCF	chr11:45427890-45428090	GM12878	blood:	n/a	n/a
42	CTCF	chr11:45420808-45420890	MCF-7	breast:	n/a	n/a
43	CTCF	chr11:45427900-45428050	GM12873	blood:	n/a	n/a
44	CTCF	chr11:45427960-45428110	HRE	kidney:	n/a	n/a
45	CTCF	chr11:45427880-45428030	GM12871	blood:	n/a	n/a
46	CTCF	chr11:45419863-45419935	MCF-7	breast:	n/a	n/a
47	CTCF	chr11:45427940-45428090	RPTEC	kidney:	n/a	n/a
48	CTCF	chr11:45427960-45428110	AG10803	skin:	n/a	n/a
49	CTCF	chr11:45419847-45419906	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr11:45427919-45428123	Pancreas_OC	pancreas:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:45433358-45433408	HEEpiC	esophagus:	n/a
2	chr11:45420388-45420438	SAEC	small airway:	n/a
3	chr11:45420442-45420492	Jurkat	blood:	n/a
4	chr11:45420355-45420405	PrEC	prostate:	n/a
5	chr11:45420355-45420405	HNPCEpiC	eye:	n/a
6	chr11:45420388-45420438	HEEpiC	esophagus:	n/a
7	chr11:45420355-45420405	U87	brain:	n/a
8	chr11:45420388-45420438	HUVEC	blood vessel:	n/a
9	chr11:45433229-45433279	AG09309	skin:	n/a
10	chr11:45420442-45420492	GM12878	blood:	n/a
11	chr11:45433358-45433408	HL-60	blood:	n/a
12	chr11:45433229-45433279	HRE	kidney:	n/a
13	chr11:45433229-45433279	H1-hESC	embryonic stem cell:	embryo
14	chr11:45420355-45420405	HL-60	blood:	n/a
15	chr11:45433358-45433408	HMEC	breast:	n/a
16	chr11:45433358-45433408	GM12878	blood:	n/a
17	chr11:45433009-45433059	AG04449	skin:	fetal
18	chr11:45420355-45420405	HepG2	liver:	n/a
19	chr11:45433229-45433279	HUVEC	blood vessel:	n/a
20	chr11:45420355-45420405	K562	blood:	n/a
21	chr11:45420442-45420492	HAEpiC	amniotic membrane:	n/a
22	chr11:45420442-45420492	AoSMC	blood vessel:	n/a
23	chr11:45433358-45433408	NT2-D1	testis:	n/a
24	chr11:45433229-45433279	HRPEpiC	eye:	n/a
25	chr11:45433009-45433059	HEEpiC	esophagus:	n/a
26	chr11:45420355-45420405	GM06990	blood:	n/a
27	chr11:45420442-45420492	LNCaP	prostate:	n/a
28	chr11:45420388-45420438	Hepatocyte	liver:	n/a
29	chr11:45420442-45420492	GM12892	blood:	n/a
30	chr11:45420388-45420438	BE2_C	brain:	n/a
31	chr11:45420442-45420492	AG04449	skin:	fetal
32	chr11:45420355-45420405	AG04449	skin:	fetal
33	chr11:45433009-45433059	Jurkat	blood:	n/a
34	chr11:45433358-45433408	PANC-1	pancreas:	n/a
35	chr11:45420355-45420405	AoSMC	blood vessel:	n/a
36	chr11:45420355-45420405	GM12878	blood:	n/a
37	chr11:45433229-45433279	GM06990	blood:	n/a
38	chr11:45420442-45420492	HCPEpiC	choroid plexus:	n/a
39	chr11:45420442-45420492	Caco-2	colon:	n/a
40	chr11:45433229-45433279	SKMC	muscle:	n/a
41	chr11:45433229-45433279	NT2-D1	testis:	n/a
42	chr11:45433358-45433408	HepG2	liver:	n/a
43	chr11:45420388-45420438	GM12891	blood:	n/a
44	chr11:45433229-45433279	HAEpiC	amniotic membrane:	n/a
45	chr11:45420388-45420438	HPAEpiC	pulmonary alveolar:	n/a
46	chr11:45433009-45433059	Hela-S3	cervix:	n/a
47	chr11:45433358-45433408	ECC-1	luminal epithelium:	n/a
48	chr11:45433229-45433279	Caco-2	colon:	n/a
49	chr11:45433229-45433279	HPAEpiC	pulmonary alveolar:	n/a
50	chr11:45420442-45420492	HCT-116	colon:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:45435401..45438353-chr11:45439674..45442968,4	K562	blood:
2	chr11:45413154..45414877-chr11:45416826..45419299,2	K562	blood:
3	chr11:45427814..45428397-chr11:45676543..45677286,2	MCF-7	breast:
4	chr11:45427597..45428482-chr11:45792562..45793604,3	MCF-7	breast:
5	chr11:45427988..45430237-chr11:45431939..45433599,2	K562	blood:
6	chr11:45435401..45438353-chr11:45439674..45442968,4	K562	blood:
7	chr11:45427988..45430237-chr11:45431939..45433599,2	K562	blood:
8	chr11:45434026..45435982-chr11:45444753..45447322,2	K562	blood:
9	chr11:45392504..45393419-chr11:45427914..45428464,2	MCF-7	breast:
10	chr11:45418856..45421391-chr11:45421484..45423655,2	K562	blood:
11	chr11:45441248..45443305-chr11:45447656..45449205,2	K562	blood:
12	chr11:45413154..45414877-chr11:45416826..45419299,2	K562	blood:

(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: 1137 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1137 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368038760	chr11:45414062-45414063	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs144594212	chr11:45414063-45414064	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs76212854	chr11:45414073-45414074	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs552121881	chr11:45414166-45414167	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs1545466	chr11:45414183-45414184	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs79652181	chr11:45414184-45414185	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs1545467	chr11:45414193-45414194	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs180685470	chr11:45414222-45414223	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs535628615	chr11:45414223-45414224	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs138605445	chr11:45414270-45414271	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs200723406	chr11:45414281-45414282	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs531810966	chr11:45414337-45414338	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs187568272	chr11:45414363-45414364	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs534580194	chr11:45414376-45414377	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs386753162	chr11:45414388-45414389	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs201105407	chr11:45414390-45414391	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs202024875	chr11:45414392-45414393	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs543458799	chr11:45414419-45414420	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs563434857	chr11:45414428-45414429	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs140270310	chr11:45414443-45414444	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs568374831	chr11:45414518-45414519	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs563646757	chr11:45414545-45414546	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs182319165	chr11:45414546-45414547	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs185969525	chr11:45414571-45414572	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs552086699	chr11:45414574-45414575	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs565603675	chr11:45414620-45414621	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs368227131	chr11:45414622-45414623	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs549842919	chr11:45414626-45414627	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs143347365	chr11:45414671-45414672	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs535157308	chr11:45414672-45414673	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs549082442	chr11:45414709-45414710	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs565722725	chr11:45414782-45414783	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs534536244	chr11:45414796-45414797	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs190487050	chr11:45414881-45414882	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs570737186	chr11:45414907-45414908	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs536959805	chr11:45414930-45414931	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs539861533	chr11:45415025-45415026	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs896331	chr11:45415035-45415036	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs542718325	chr11:45415042-45415043	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs559829858	chr11:45415047-45415048	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs573333341	chr11:45415057-45415058	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs386753163	chr11:45415061-45415062	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs116171886	chr11:45415062-45415063	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs75274948	chr11:45415103-45415104	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs551299726	chr11:45415106-45415107	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs12271560	chr11:45415146-45415147	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs528918186	chr11:45415193-45415194	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs74827412	chr11:45415300-45415301	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs565816780	chr11:45415362-45415363	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs535770034	chr11:45415367-45415368	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	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:286 , 50 per page) page: 1 2 3 4 5 6

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	chr11:45411200-45417000	Enhancers	Liver	Liver
4	chr11:45412200-45415400	Bivalent Enhancer	Fetal Stomach	stomach
5	chr11:45412200-45417600	Weak transcription	Fetal Brain Female	brain
6	chr11:45412600-45415200	Enhancers	Fetal Lung	lung
7	chr11:45412600-45420400	Weak transcription	Gastric	stomach
8	chr11:45413000-45414200	Enhancers	Fetal Intestine Small	intestine
9	chr11:45413000-45414800	Weak transcription	Brain Germinal Matrix	brain
10	chr11:45413600-45420200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr11:45413800-45414600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
12	chr11:45413800-45414600	Weak transcription	Ovary	ovary
13	chr11:45413800-45415200	Enhancers	HepG2	liver
14	chr11:45413800-45415400	Weak transcription	Lung	lung
15	chr11:45413800-45417000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr11:45414000-45414200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr11:45414000-45414200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr11:45414000-45414400	Weak transcription	Fetal Brain Male	brain
19	chr11:45414000-45415200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr11:45414400-45414600	Enhancers	Fetal Brain Male	brain
21	chr11:45414400-45415600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr11:45414600-45414800	Enhancers	Ovary	ovary
23	chr11:45414600-45417000	Weak transcription	Fetal Brain Male	brain
24	chr11:45414800-45415400	Enhancers	Brain Germinal Matrix	brain
25	chr11:45414800-45418000	Weak transcription	Ovary	ovary
26	chr11:45415200-45415600	Bivalent Enhancer	HepG2	liver
27	chr11:45415200-45421000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr11:45415400-45416000	Enhancers	Lung	lung
29	chr11:45415400-45419600	Weak transcription	Brain Germinal Matrix	brain
30	chr11:45415600-45415800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr11:45415600-45415800	Flanking Bivalent TSS/Enh	HepG2	liver
32	chr11:45415800-45416000	Enhancers	Spleen	Spleen
33	chr11:45415800-45416000	Flanking Active TSS	HepG2	liver
34	chr11:45415800-45421000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr11:45416000-45417000	Enhancers	HepG2	liver
36	chr11:45416000-45420200	Weak transcription	Lung	lung
37	chr11:45416000-45423400	Weak transcription	Spleen	Spleen
38	chr11:45417000-45417200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr11:45417000-45417800	Enhancers	Fetal Brain Male	brain
40	chr11:45417000-45418200	Bivalent Enhancer	HepG2	liver
41	chr11:45417600-45418000	Enhancers	Fetal Brain Female	brain
42	chr11:45417800-45419800	Weak transcription	Fetal Brain Male	brain
43	chr11:45418000-45418200	Enhancers	Ovary	ovary
44	chr11:45418400-45418600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr11:45418800-45421400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr11:45419400-45420200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr11:45419600-45420400	Enhancers	Brain Germinal Matrix	brain
48	chr11:45419800-45420400	Enhancers	Fetal Brain Male	brain
49	chr11:45420000-45420200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr11:45420000-45420600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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