Variant report

Variant	esv3380436
Chromosome Location	chr11:64982801-64985349
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:118)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:118 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:64983190-64983243	HepG2	liver:	n/a	n/a
2	ATF3	chr11:64983085-64983723	K562	blood:	n/a	n/a
3	ATF3	chr11:64983136-64983735	K562	blood:	n/a	n/a
4	BACH1	chr11:64983179-64983723	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr11:64983080-64983822	GM12878	blood:	n/a	n/a
6	BCL3	chr11:64983940-64984169	GM12878	blood:	n/a	n/a
7	BCL3	chr11:64982929-64984437	GM12878	blood:	n/a	n/a
8	CBX3	chr11:64982938-64983663	K562	blood:	n/a	n/a
9	CEBPB	chr11:64983021-64983308	K562	blood:	n/a	n/a
10	CEBPB	chr11:64982938-64983372	K562	blood:	n/a	n/a
11	CEBPB	chr11:64983065-64983326	HepG2	liver:	n/a	n/a
12	CTCF	chr11:64984560-64984710	GM12868	blood:	n/a	n/a
13	CTCF	chr11:64984400-64984550	HBMEC	blood vessel:	n/a	n/a
14	CTCF	chr11:64984300-64984450	GM12869	blood:	n/a	n/a
15	CTCF	chr11:64984400-64984550	HEK293	kidney:	n/a	n/a
16	CTCF	chr11:64984320-64984470	K562	blood:	n/a	n/a
17	CTCF	chr11:64984340-64984490	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr11:64984380-64984530	HL-60	blood:	n/a	n/a
19	CTCF	chr11:64984360-64984510	GM12864	blood:	n/a	n/a
20	CTCF	chr11:64984340-64984490	GM12871	blood:	n/a	n/a
21	CTCF	chr11:64984380-64984530	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr11:64984340-64984490	HCFaa	heart:	n/a	n/a
23	CTCF	chr11:64984400-64984550	AG04449	skin:	n/a	n/a
24	CTCF	chr11:64984400-64984550	GM12864	blood:	n/a	n/a
25	CTCF	chr11:64984360-64984510	GM12874	blood:	n/a	n/a
26	CTCF	chr11:64984340-64984490	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr11:64984360-64984510	GM12873	blood:	n/a	n/a
28	CTCF	chr11:64984420-64984570	K562	blood:	n/a	n/a
29	CTCF	chr11:64984340-64984490	NB4	blood:	n/a	n/a
30	CTCF	chr11:64984380-64984530	GM12872	blood:	n/a	n/a
31	CTCF	chr11:64984360-64984510	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr11:64984360-64984510	HepG2	liver:	n/a	n/a
33	CTCF	chr11:64984460-64984610	GM12871	blood:	n/a	n/a
34	CTCF	chr11:64984360-64984510	HEK293	kidney:	n/a	n/a
35	CTCF	chr11:64984360-64984510	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr11:64984420-64984570	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr11:64984340-64984490	GM12868	blood:	n/a	n/a
38	CTCF	chr11:64984320-64984470	NHEK	skin:	n/a	n/a
39	CTCF	chr11:64984400-64984550	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr11:64984340-64984490	GM12875	blood:	n/a	n/a
41	CTCF	chr11:64984360-64984510	HMF	breast:	n/a	n/a
42	CTCF	chr11:64984400-64984550	NHEK	skin:	n/a	n/a
43	CTCF	chr11:64984420-64984570	HRE	kidney:	n/a	n/a
44	CTCF	chr11:64984440-64984590	GM12873	blood:	n/a	n/a
45	CTCF	chr11:64984420-64984570	GM12872	blood:	n/a	n/a
46	CTCF	chr11:64984380-64984530	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr11:64984360-64984561	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr11:64984380-64984530	GM12873	blood:	n/a	n/a
49	CTCF	chr11:64984340-64984490	SAEC	small airway:	n/a	n/a
50	CTCF	chr11:64984380-64984530	GM12868	blood:	n/a	n/a

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:64981559..64983157-chr11:64987692..64989765,2	MCF-7	breast:
2	chr11:64983043..64986391-chr11:64991756..64994999,4	K562	blood:
3	chr11:64971880..64974071-chr11:64983696..64985630,2	K562	blood:
4	chr11:64983969..64987666-chr11:65274563..65276878,3	K562	blood:
5	chr11:64981290..64983424-chr11:64983464..64986635,3	K562	blood:
6	chr11:64981702..64983459-chr11:65028915..65031631,2	K562	blood:
7	chr11:64981666..64983514-chr11:65194659..65196523,2	K562	blood:
8	chr11:64981985..64982874-chr18:10585091..10585596,2	MCF-7	breast:
9	chr11:64936286..64938198-chr11:64981682..64983744,2	K562	blood:
10	chr11:64982257..64984604-chr11:64993334..64996229,2	MCF-7	breast:
11	chr11:64971045..64975621-chr11:64984238..64988273,4	MCF-7	breast:
12	chr11:64936316..64940123-chr11:64985070..64987472,4	K562	blood:
13	chr11:64981438..64983077-chr11:65020117..65022507,2	MCF-7	breast:

No data

Variant related genes	Relation type
SLC22A20	TF binding region
ENSG00000197847	chromatin interactions
ENSG00000014216	chromatin interactions
ENSG00000204710	chromatin interactions
ENSG00000014138	chromatin interactions

Extended variants
information (count: 137 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:137 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34709214	chr11:64982808-64982809	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs534021547	chr11:64982817-64982818	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs183527217	chr11:64982842-64982843	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs373169830	chr11:64982872-64982873	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs144743536	chr11:64982896-64982897	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs372256382	chr11:64982934-64982935	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs536213028	chr11:64982986-64982987	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs186364022	chr11:64983019-64983020	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs576633253	chr11:64983076-64983077	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs191218315	chr11:64983077-64983078	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs182098626	chr11:64983080-64983081	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs186965657	chr11:64983086-64983087	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs539738952	chr11:64983102-64983103	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs370254763	chr11:64983106-64983107	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs528098088	chr11:64983238-64983239	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs552791346	chr11:64983239-64983240	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs564489972	chr11:64983242-64983243	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs530930776	chr11:64983254-64983255	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs551018115	chr11:64983261-64983262	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs376908758	chr11:64983275-64983276	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs533420	chr11:64983278-64983279	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs562042705	chr11:64983312-64983313	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs371305141	chr11:64983326-64983327	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs560018323	chr11:64983358-64983359	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs201778044	chr11:64983376-64983377	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs114460465	chr11:64983378-64983379	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs148654562	chr11:64983390-64983391	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs183514092	chr11:64983396-64983397	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs188279478	chr11:64983398-64983399	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs373101026	chr11:64983403-64983404	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs645599	chr11:64983416-64983417	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs116555665	chr11:64983431-64983432	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs376093316	chr11:64983438-64983439	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs559119380	chr11:64983479-64983480	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs545639428	chr11:64983501-64983502	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs111065614	chr11:64983508-64983509	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs373829050	chr11:64983535-64983536	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs566811732	chr11:64983560-64983561	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs538891596	chr11:64983568-64983569	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs201397175	chr11:64983575-64983576	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs200294022	chr11:64983579-64983580	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs386754375	chr11:64983580-64983581	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs200365396	chr11:64983581-64983582	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs373863744	chr11:64983604-64983605	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs193047544	chr11:64983609-64983610	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs570361033	chr11:64983610-64983611	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs199669928	chr11:64983627-64983628	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs185219679	chr11:64983654-64983655	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs559239348	chr11:64983681-64983682	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs239260	chr11:64983703-64983704	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:100)

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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	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
Anaplastic thyroid cancer	18753363	CNVD
Prostate cancer	18779856	CNVD
Cancer	17160897	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
Chronic lymphocytic leukemia	22228453	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:132 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64950600-64992400	Weak transcription	Right Atrium	heart
2	chr11:64952400-64992800	Weak transcription	Fetal Heart	heart
3	chr11:64973800-64992600	Weak transcription	Fetal Kidney	kidney
4	chr11:64976600-64992600	Weak transcription	Psoas Muscle	Psoas
5	chr11:64977400-64998400	Weak transcription	Small Intestine	intestine
6	chr11:64977600-64993200	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr11:64978200-64986800	Weak transcription	HepG2	liver
8	chr11:64978400-64992200	Weak transcription	Stomach Mucosa	stomach
9	chr11:64978400-64992800	Weak transcription	HSMM	muscle
10	chr11:64978600-64992800	Weak transcription	HSMMtube	muscle
11	chr11:64978800-64987000	Weak transcription	NHDF-Ad	bronchial
12	chr11:64979200-64983000	Weak transcription	Brain Anterior Caudate	brain
13	chr11:64979200-64983400	Enhancers	Primary hematopoietic stem cells	blood
14	chr11:64979200-64986400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr11:64979200-64987000	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr11:64979200-64992400	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr11:64979200-64993000	Weak transcription	Aorta	Aorta
18	chr11:64979400-64984400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr11:64979400-64987000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr11:64979400-64992400	Weak transcription	A549	lung
21	chr11:64979600-64984800	Weak transcription	Fetal Brain Female	brain
22	chr11:64979600-64986400	Weak transcription	Stomach Smooth Muscle	stomach
23	chr11:64979600-64990600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr11:64979600-64992200	Weak transcription	NHEK	skin
25	chr11:64979800-64983200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr11:64979800-64984800	Weak transcription	Brain Germinal Matrix	brain
27	chr11:64979800-64984800	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr11:64979800-64989800	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr11:64979800-64992400	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr11:64979800-64993000	Weak transcription	Ovary	ovary
31	chr11:64980000-64983400	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr11:64980000-64986000	Weak transcription	Lung	lung
33	chr11:64980000-64989800	Weak transcription	Left Ventricle	heart
34	chr11:64980000-64992200	Weak transcription	HMEC	breast
35	chr11:64980200-64984600	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr11:64980200-64992200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr11:64980200-64992600	Weak transcription	Colonic Mucosa	Colon
38	chr11:64980200-64993000	Weak transcription	Gastric	stomach
39	chr11:64980400-64985400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr11:64980400-64990000	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr11:64980400-64992600	Weak transcription	Esophagus	oesophagus
42	chr11:64980400-64992600	Weak transcription	Rectal Smooth Muscle	rectum
43	chr11:64980400-64993000	Weak transcription	Pancreas	Pancrea
44	chr11:64980800-64983400	Active TSS	H9 Cell Line	embryonic stem cell
45	chr11:64981000-64992600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr11:64981200-64986400	Weak transcription	K562	blood
47	chr11:64981200-64986800	Weak transcription	Hela-S3	cervix
48	chr11:64981200-64987000	Weak transcription	NHLF	lung
49	chr11:64981200-64987200	Weak transcription	Adipose Nuclei	Adipose
50	chr11:64981200-64992200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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