Variant report

Variant	nsv524544
Chromosome Location	chr12:889902-922408
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	chr12:914118-914158	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:904508-904691	K562	blood:	n/a	n/a
3	ARID3A	chr12:899820-900011	K562	blood:	n/a	n/a
4	ARID3A	chr12:899446-899520	K562	blood:	n/a	n/a
5	ATF2	chr12:919620-920364	GM12878	blood:	n/a	n/a
6	ATF2	chr12:916459-916858	GM12878	blood:	n/a	n/a
7	ATF2	chr12:919616-920278	GM12878	blood:	n/a	n/a
8	ATF2	chr12:916414-916900	GM12878	blood:	n/a	n/a
9	BATF	chr12:901667-901904	GM12878	blood:	n/a	chr12:901756-901767
10	BATF	chr12:898909-899396	GM12878	blood:	n/a	chr12:899377-899386
11	BATF	chr12:919759-920261	GM12878	blood:	n/a	n/a
12	BATF	chr12:919770-920232	GM12878	blood:	n/a	n/a
13	BCL11A	chr12:916571-916782	GM12878	blood:	n/a	chr12:916732-916741
14	BCL11A	chr12:919798-920244	GM12878	blood:	n/a	n/a
15	BCL3	chr12:919780-920158	GM12878	blood:	n/a	n/a
16	BCLAF1	chr12:919710-920146	GM12878	blood:	n/a	n/a
17	BCLAF1	chr12:919660-920280	GM12878	blood:	n/a	n/a
18	BCLAF1	chr12:916411-916847	GM12878	blood:	n/a	chr12:916732-916741
19	BHLHE40	chr12:899138-899144	GM12878	blood:	n/a	n/a
20	BHLHE40	chr12:916497-916799	GM12878	blood:	n/a	n/a
21	BRCA1	chr12:915288-916262	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr12:913380-913664	IMR90	lung:	n/a	chr12:913526-913537
23	CEBPB	chr12:905401-905800	MCF-7	breast:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
24	CEBPB	chr12:913407-913609	H1-hESC	embryonic stem cell:	n/a	chr12:913526-913537
25	CEBPB	chr12:905392-905755	HepG2	liver:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
26	CEBPB	chr12:905298-905804	ECC-1	luminal epithelium:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
27	CEBPB	chr12:915246-916084	Hela-S3	cervix:	n/a	chr12:915952-915965 chr12:915485-915496
28	CEBPB	chr12:902966-903085	A549	lung:	n/a	n/a
29	CEBPB	chr12:915340-915667	HepG2	liver:	n/a	chr12:915485-915496
30	CEBPB	chr12:897316-897544	A549	lung:	n/a	chr12:897445-897456
31	CEBPB	chr12:905381-905772	K562	blood:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
32	CEBPB	chr12:913385-913617	HepG2	liver:	n/a	chr12:913526-913537
33	CEBPB	chr12:913365-913651	Hela-S3	cervix:	n/a	chr12:913526-913537
34	CEBPB	chr12:897329-897508	K562	blood:	n/a	chr12:897445-897456
35	CEBPB	chr12:905382-905775	Hela-S3	cervix:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
36	CEBPB	chr12:902952-903073	K562	blood:	n/a	n/a
37	CEBPB	chr12:915347-915635	K562	blood:	n/a	chr12:915485-915496
38	CEBPB	chr12:916904-916926	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr12:915306-915919	IMR90	lung:	n/a	chr12:915485-915496
40	CEBPB	chr12:905381-905768	IMR90	lung:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
41	CEBPB	chr12:915213-915805	A549	lung:	n/a	chr12:915485-915496
42	CEBPB	chr12:915360-915711	A549	lung:	n/a	chr12:915485-915496
43	CEBPB	chr12:897314-897616	HepG2	liver:	n/a	chr12:897445-897456
44	CEBPB	chr12:913368-913683	K562	blood:	n/a	chr12:913526-913537
45	CEBPB	chr12:905390-905769	A549	lung:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
46	CEBPB	chr12:905454-905615	K562	blood:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
47	CEBPB	chr12:905352-905829	HCT-116	colon:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
48	CEBPB	chr12:905259-905893	A549	lung:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584
49	CEBPB	chr12:897304-897610	IMR90	lung:	n/a	chr12:897445-897456
50	CEBPB	chr12:905367-905856	ECC-1	luminal epithelium:	n/a	chr12:905572-905583 chr12:905573-905582 chr12:905573-905582 chr12:905571-905584 chr12:905573-905582 chr12:905571-905584

No.	Distal block	Cell Line	Cell type
1	chr12:881327..883755-chr12:895131..898641,3	K562	blood:
2	chr12:906517..908148-chr12:911108..913048,2	K562	blood:
3	chr12:919540..922758-chr12:931539..933937,3	K562	blood:
4	chr12:918309..920299-chr12:1801890..1803898,2	K562	blood:
5	chr12:860140..862854-chr12:919115..921823,2	K562	blood:
6	chr12:906517..908148-chr12:911108..913048,2	K562	blood:
7	chr12:902748..905210-chr12:909004..911043,2	K562	blood:
8	chr12:881327..884915-chr12:893641..898608,4	K562	blood:
9	chr12:862452..864238-chr12:921433..923519,2	MCF-7	breast:
10	chr12:682408..684558-chr12:921412..923532,2	K562	blood:
11	chr12:860770..863546-chr12:920587..924774,4	MCF-7	breast:
12	chr12:860752..862615-chr12:913879..916697,2	K562	blood:
13	chr12:862374..864096-chr12:909523..912296,2	MCF-7	breast:
14	chr12:860587..863557-chr12:905754..908662,2	MCF-7	breast:
15	chr12:861876..864067-chr12:916033..918768,2	MCF-7	breast:
16	chr12:919866..922717-chr12:940854..943432,2	K562	blood:
17	chr12:689801..692487-chr12:897629..900163,2	K562	blood:
18	chr12:902748..905210-chr12:909004..911043,2	K562	blood:
19	chr12:899602..901917-chr13:59262650..59264676,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NINJ2-3	chr12:890139-890879	predAs_chen_BU787457_1

Variant related genes	Relation type
RNU4ATAC16P	TF binding region
ENSG00000060237	chromatin interactions

Extended variants
information (count: 1102 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1102 , 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	rs11064524	chr12:889902-889903	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs187035988	chr12:889959-889960	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs191511782	chr12:889999-890000	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs571751373	chr12:890042-890043	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs539097509	chr12:890068-890069	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs56131547	chr12:890069-890070	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs72647393	chr12:890116-890117	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs572097061	chr12:890133-890134	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs542819741	chr12:890179-890180	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs550727467	chr12:890192-890193	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs371432998	chr12:890195-890196	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs7968475	chr12:890205-890206	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs147783855	chr12:890237-890238	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs566801961	chr12:890247-890248	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs72647394	chr12:890253-890254	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs183607365	chr12:890255-890256	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs368510965	chr12:890267-890268	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs141473081	chr12:890273-890274	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs116463607	chr12:890274-890275	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs115614170	chr12:890275-890276	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs576447051	chr12:890277-890278	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs67262306	chr12:890279-890280	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs372492979	chr12:890281-890282	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs72647395	chr12:890289-890290	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs72647396	chr12:890295-890296	Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs11064525	chr12:890304-890305	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
27	rs11064526	chr12:890356-890357	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs559403770	chr12:890357-890358	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
29	rs568949013	chr12:890363-890364	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
30	rs72647397	chr12:890365-890366	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
31	rs371930021	chr12:890380-890381	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
32	rs189621387	chr12:890411-890412	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
33	rs561542147	chr12:890449-890450	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
34	rs140080278	chr12:890453-890454	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
35	rs550508857	chr12:890520-890521	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
36	rs146840635	chr12:890579-890580	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
37	rs72647398	chr12:890583-890584	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
38	rs76116945	chr12:890604-890605	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs539035686	chr12:890616-890617	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs547531733	chr12:890716-890717	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs182387363	chr12:890724-890725	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs536057142	chr12:890733-890734	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs554780021	chr12:890791-890792	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs575918736	chr12:890835-890836	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs185285926	chr12:890854-890855	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs558447528	chr12:890879-890880	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs576383099	chr12:890919-890920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs537684569	chr12:890948-890949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs541031472	chr12:890982-890983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs567165988	chr12:890983-890984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22844521	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1358 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:865200-895600	Weak transcription	Pancreas	Pancrea
2	chr12:881800-891400	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr12:883600-905200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr12:883800-923200	Weak transcription	Fetal Stomach	stomach
5	chr12:884000-891600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr12:884800-891600	Enhancers	Brain Hippocampus Middle	brain
7	chr12:884800-899000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr12:885200-890600	Enhancers	Brain Substantia Nigra	brain
9	chr12:885200-896000	Weak transcription	Dnd41	blood
10	chr12:885400-891800	Weak transcription	Fetal Thymus	thymus
11	chr12:885400-897000	Weak transcription	Fetal Intestine Small	intestine
12	chr12:885400-898400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr12:885400-904000	Weak transcription	Thymus	Thymus
14	chr12:885600-890000	Enhancers	Stomach Mucosa	stomach
15	chr12:885600-892000	Weak transcription	Ovary	ovary
16	chr12:886000-895800	Weak transcription	Lung	lung
17	chr12:886200-890600	Enhancers	Colon Smooth Muscle	Colon
18	chr12:886200-891600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr12:886600-890000	Enhancers	Primary T killer memory cells from peripheral blood	blood
20	chr12:886600-891400	Enhancers	Primary T helper naive cells from peripheral blood	blood
21	chr12:886600-895600	Weak transcription	Left Ventricle	heart
22	chr12:886800-890600	Enhancers	HepG2	liver
23	chr12:887000-890400	Enhancers	Skeletal Muscle Male	skeletal muscle
24	chr12:887600-890400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr12:887800-890000	Enhancers	NHEK	skin
26	chr12:887800-890400	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr12:887800-890600	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr12:887800-891800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr12:887800-895600	Weak transcription	Esophagus	oesophagus
30	chr12:888000-890200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr12:888000-890400	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr12:888000-890400	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr12:888000-891400	Enhancers	Hela-S3	cervix
34	chr12:888200-890800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr12:888200-891600	Enhancers	Fetal Heart	heart
36	chr12:888400-890600	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr12:888400-892200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
38	chr12:888600-890000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr12:888600-890200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr12:888600-890200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr12:888600-890400	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr12:888600-890800	Enhancers	Adipose Nuclei	Adipose
43	chr12:888800-890000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr12:888800-890000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr12:888800-890000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr12:888800-890400	Enhancers	Fetal Lung	lung
47	chr12:888800-890400	Enhancers	HMEC	breast
48	chr12:888800-890600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr12:888800-890600	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr12:888800-890600	Flanking Active TSS	GM12878-XiMat	blood

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