Variant report

Variant	esv1000322
Chromosome Location	chr11:72109327-72116806
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	ARID3A	chr11:72109061-72109639	HepG2	liver:	n/a	n/a
2	CEBPB	chr11:72109083-72109830	HepG2	liver:	n/a	chr11:72109573-72109585
3	CEBPB	chr11:72108896-72109576	ECC-1	luminal epithelium:	n/a	n/a
4	CEBPB	chr11:72109113-72109491	HepG2	liver:	n/a	n/a
5	CEBPB	chr11:72109038-72109469	ECC-1	luminal epithelium:	n/a	n/a
6	CEBPB	chr11:72109063-72109494	MCF-7	breast:	n/a	n/a
7	CEBPB	chr11:72109202-72109368	HepG2	liver:	n/a	n/a
8	CEBPD	chr11:72109096-72109479	HepG2	liver:	n/a	n/a
9	EGR1	chr11:72109009-72109576	ECC-1	luminal epithelium:	n/a	chr11:72109302-72109313 chr11:72109302-72109313
10	EGR1	chr11:72109018-72109566	HCT-116	colon:	n/a	chr11:72109302-72109313 chr11:72109302-72109313
11	EGR1	chr11:72108906-72109633	HCT-116	colon:	n/a	chr11:72109302-72109313 chr11:72109302-72109313
12	EGR1	chr11:72109055-72109485	MCF-7	breast:	n/a	chr11:72109302-72109313 chr11:72109302-72109313
13	EGR1	chr11:72108954-72109598	ECC-1	luminal epithelium:	n/a	chr11:72109302-72109313 chr11:72109302-72109313
14	EGR1	chr11:72108990-72109634	MCF-7	breast:	n/a	chr11:72109302-72109313 chr11:72109302-72109313
15	ELF1	chr11:72109101-72109402	HepG2	liver:	n/a	n/a
16	ELK1	chr11:72116491-72116495	GM12878	blood:	n/a	n/a
17	EP300	chr11:72108866-72109571	ECC-1	luminal epithelium:	n/a	n/a
18	EP300	chr11:72108936-72109552	HepG2	liver:	n/a	n/a
19	EP300	chr11:72109086-72109705	HepG2	liver:	n/a	chr11:72109590-72109604
20	EP300	chr11:72109004-72109576	MCF-7	breast:	n/a	n/a
21	EP300	chr11:72108860-72109768	ECC-1	luminal epithelium:	n/a	chr11:72109590-72109604
22	EP300	chr11:72108923-72109975	HepG2	liver:	n/a	chr11:72109590-72109604
23	ESR1	chr11:72108973-72109449	ECC-1	luminal epithelium:	n/a	n/a
24	ESR1	chr11:72108961-72109534	ECC-1	luminal epithelium:	n/a	n/a
25	ESR1	chr11:72108836-72109602	ECC-1	luminal epithelium:	n/a	n/a
26	ESR1	chr11:72108905-72109581	ECC-1	luminal epithelium:	n/a	n/a
27	ESR1	chr11:72108863-72109572	ECC-1	luminal epithelium:	n/a	n/a
28	ESR1	chr11:72108968-72109468	ECC-1	luminal epithelium:	n/a	n/a
29	FOXA1	chr11:72108976-72109973	HepG2	liver:	n/a	n/a
30	FOXA1	chr11:72108974-72109443	ECC-1	luminal epithelium:	n/a	n/a
31	FOXA1	chr11:72109098-72109381	T-47D	breast:	n/a	n/a
32	FOXA1	chr11:72108875-72110084	HepG2	liver:	n/a	n/a
33	FOXA1	chr11:72108929-72109885	HepG2	liver:	n/a	n/a
34	FOXA1	chr11:72109019-72109979	HepG2	liver:	n/a	n/a
35	FOXA1	chr11:72108923-72109542	ECC-1	luminal epithelium:	n/a	n/a
36	FOXA2	chr11:72108993-72110078	HepG2	liver:	n/a	n/a
37	FOXA2	chr11:72108966-72109973	HepG2	liver:	n/a	n/a
38	FOXM1	chr11:72108816-72109595	ECC-1	luminal epithelium:	n/a	n/a
39	FOXM1	chr11:72108719-72109619	ECC-1	luminal epithelium:	n/a	n/a
40	GATA3	chr11:72111459-72111590	SH-SY5Y	brain:	n/a	n/a
41	HDAC2	chr11:72109001-72109932	HepG2	liver:	n/a	chr11:72109591-72109605 chr11:72109271-72109280
42	HDAC2	chr11:72109103-72109570	MCF-7	breast:	n/a	chr11:72109271-72109280
43	HDAC2	chr11:72109014-72109945	HepG2	liver:	n/a	chr11:72109591-72109605 chr11:72109271-72109280
44	HNF4A	chr11:72109118-72109380	HepG2	liver:	n/a	chr11:72109273-72109281
45	HNF4A	chr11:72109065-72109509	HepG2	liver:	n/a	chr11:72109273-72109281
46	HNF4A	chr11:72109585-72109818	HepG2	liver:	n/a	chr11:72109721-72109733 chr11:72109718-72109736 chr11:72109720-72109735 chr11:72109721-72109734 chr11:72109719-72109734 chr11:72109721-72109733
47	HNF4A	chr11:72109546-72109865	HepG2	liver:	n/a	chr11:72109721-72109733 chr11:72109718-72109736 chr11:72109720-72109735 chr11:72109721-72109734 chr11:72109719-72109734 chr11:72109721-72109733
48	HNF4A	chr11:72109066-72109895	HepG2	liver:	n/a	chr11:72109721-72109733 chr11:72109718-72109736 chr11:72109720-72109735 chr11:72109721-72109734 chr11:72109719-72109734 chr11:72109273-72109281 chr11:72109721-72109733
49	HNF4G	chr11:72108992-72109860	HepG2	liver:	n/a	chr11:72109721-72109733 chr11:72109718-72109736 chr11:72109720-72109735 chr11:72109721-72109734 chr11:72109273-72109281 chr11:72109721-72109733
50	JUND	chr11:72109122-72109358	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:72108026..72111129-chr11:72112803..72115357,3	MCF-7	breast:
2	chr11:72110960..72113581-chr11:72114884..72118274,3	K562	blood:
3	chr11:72107648..72109723-chr11:72110877..72114081,3	K562	blood:
4	chr11:71813989..71816363-chr11:72110601..72112826,2	K562	blood:
5	chr11:72091599..72093441-chr11:72109431..72111887,2	MCF-7	breast:
6	chr11:72110960..72113581-chr11:72114884..72118274,3	K562	blood:
7	chr11:72108026..72111129-chr11:72112803..72115357,3	MCF-7	breast:
8	chr11:72113346..72115251-chr11:72116984..72119752,2	MCF-7	breast:
9	chr11:72107648..72109723-chr11:72110877..72114081,3	K562	blood:
10	chr11:72113681..72116356-chr11:72118762..72120337,2	K562	blood:

Variant related genes	Relation type
ENSG00000256403	TF binding region
ENSG00000149357	chromatin interactions
ENSG00000238768	chromatin interactions

Extended variants
information (count: 255 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:255 , 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	rs563297366	chr11:72109334-72109335	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs371543749	chr11:72109354-72109355	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs530837138	chr11:72109433-72109434	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs548997647	chr11:72109452-72109453	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs567528384	chr11:72109531-72109532	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs534654396	chr11:72109534-72109535	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs546762637	chr11:72109563-72109564	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs574530891	chr11:72109567-72109568	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs376270357	chr11:72109571-72109572	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs147280307	chr11:72109572-72109573	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs186294212	chr11:72109615-72109616	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs189893355	chr11:72109641-72109642	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs575076110	chr11:72109658-72109659	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs60132455	chr11:72109667-72109668	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs563884208	chr11:72109737-72109738	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs536240167	chr11:72109759-72109760	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs117515611	chr11:72109776-72109777	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs574272125	chr11:72109894-72109895	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs77931970	chr11:72109920-72109921	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs564907546	chr11:72109956-72109957	Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs532048282	chr11:72110036-72110037	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs578114536	chr11:72110042-72110043	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545073030	chr11:72110049-72110050	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs563423970	chr11:72110052-72110053	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs75696806	chr11:72110198-72110199	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542606637	chr11:72110229-72110230	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs139127446	chr11:72110242-72110243	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs528347272	chr11:72110264-72110265	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546581314	chr11:72110346-72110347	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs116579655	chr11:72110389-72110390	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs532361383	chr11:72110415-72110416	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550829430	chr11:72110422-72110423	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs568952989	chr11:72110444-72110445	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs370203339	chr11:72110462-72110463	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536398378	chr11:72110650-72110651	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs554540392	chr11:72110651-72110652	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs74694395	chr11:72110705-72110706	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs535280041	chr11:72110740-72110741	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs546515003	chr11:72110746-72110747	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs553414335	chr11:72110753-72110754	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs79828265	chr11:72110813-72110814	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs180723339	chr11:72110816-72110817	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs73530762	chr11:72110834-72110835	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs575322171	chr11:72110908-72110909	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs542761382	chr11:72110996-72110997	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs185779769	chr11:72111030-72111031	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs191284546	chr11:72111035-72111036	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs540485593	chr11:72111067-72111068	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs144665032	chr11:72111184-72111185	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs77327924	chr11:72111236-72111237	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	19153074	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:295 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:72065000-72110800	Weak transcription	Hela-S3	cervix
2	chr11:72069400-72111400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr11:72090400-72123000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr11:72091400-72109600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr11:72091400-72111400	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr11:72091600-72119200	Weak transcription	Thymus	Thymus
7	chr11:72093800-72109400	Weak transcription	Pancreas	Pancrea
8	chr11:72095200-72112800	Weak transcription	Fetal Stomach	stomach
9	chr11:72095800-72110600	Weak transcription	Dnd41	blood
10	chr11:72096200-72110600	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr11:72099200-72110600	Weak transcription	HSMM	muscle
12	chr11:72099200-72110800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr11:72099200-72111200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr11:72099200-72111400	Weak transcription	HSMMtube	muscle
15	chr11:72099200-72111600	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr11:72099200-72111600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr11:72099200-72112800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr11:72099200-72112800	Weak transcription	Fetal Muscle Leg	muscle
19	chr11:72099200-72112800	Weak transcription	Lung	lung
20	chr11:72099200-72115000	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr11:72099200-72115600	Weak transcription	NHDF-Ad	bronchial
22	chr11:72099200-72122800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr11:72099600-72125000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr11:72099600-72125000	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr11:72100200-72111400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr11:72100400-72117400	Weak transcription	HMEC	breast
27	chr11:72101400-72111600	Weak transcription	Gastric	stomach
28	chr11:72102000-72110800	Weak transcription	Primary hematopoietic stem cells	blood
29	chr11:72102000-72111400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr11:72102400-72111400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr11:72102600-72112600	Weak transcription	Fetal Intestine Small	intestine
32	chr11:72103400-72111400	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr11:72103400-72120000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr11:72103600-72111600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr11:72103600-72111600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr11:72103600-72116000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr11:72104000-72111000	Weak transcription	Primary neutrophils fromperipheralblood	blood
38	chr11:72104200-72111400	Weak transcription	Primary B cells from peripheral blood	blood
39	chr11:72104200-72111400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr11:72104200-72111600	Weak transcription	Spleen	Spleen
41	chr11:72104200-72113600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr11:72104400-72111800	Weak transcription	Fetal Muscle Trunk	muscle
43	chr11:72105000-72122200	Weak transcription	GM12878-XiMat	blood
44	chr11:72105400-72124800	Weak transcription	A549	lung
45	chr11:72106000-72115800	Strong transcription	Monocytes-CD14+_RO01746	blood
46	chr11:72106200-72111600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr11:72106200-72112400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr11:72106200-72113200	Weak transcription	Psoas Muscle	Psoas
49	chr11:72106200-72113600	Weak transcription	NHEK	skin
50	chr11:72106200-72121200	Weak transcription	Duodenum Smooth Muscle	Duodenum

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