Variant report

Variant	nsv559016
Chromosome Location	chr12:57095815-57112637
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:427)
CpG islands
(count:0)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:57104819-57105213	GM12878	blood:	n/a	n/a
2	BCL3	chr12:57104622-57104934	GM12878	blood:	n/a	n/a
3	BCL3	chr12:57104583-57105539	A549	lung:	n/a	chr12:57105438-57105447
4	CEBPB	chr12:57099897-57099920	IMR90	lung:	n/a	n/a
5	CEBPB	chr12:57099876-57100076	A549	lung:	n/a	n/a
6	CEBPB	chr12:57099900-57100044	K562	blood:	n/a	n/a
7	CEBPB	chr12:57099893-57100074	Hela-S3	cervix:	n/a	n/a
8	CHD2	chr12:57105136-57105191	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr12:57108304-57108514	T-47D	breast:	n/a	n/a
10	CTCF	chr12:57107257-57107569	T-47D	breast:	n/a	n/a
11	CTCF	chr12:57101209-57101294	Lung_OC	lung:	n/a	n/a
12	CTCF	chr12:57096622-57096684	Lung_OC	lung:	n/a	n/a
13	CTCF	chr12:57108084-57108267	T-47D	breast:	n/a	n/a
14	CTCF	chr12:57106517-57106713	T-47D	breast:	n/a	n/a
15	CTCF	chr12:57110520-57110670	GM12866	blood:	n/a	n/a
16	E2F4	chr12:57107182-57107357	MCF10A-Er-Src	breast:	n/a	n/a
17	EP300	chr12:57111556-57111748	GM12878	blood:	n/a	n/a
18	EP300	chr12:57111548-57111863	GM12878	blood:	n/a	n/a
19	FOS	chr12:57107122-57107540	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr12:57099952-57100119	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr12:57107133-57107538	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr12:57107139-57107436	MCF10A-Er-Src	breast:	n/a	n/a
23	FOSL2	chr12:57104596-57104844	HepG2	liver:	n/a	n/a
24	HEY1	chr12:57109521-57110035	K562	blood:	n/a	n/a
25	HEY1	chr12:57111470-57111835	K562	blood:	n/a	n/a
26	HEY1	chr12:57111440-57112682	K562	blood:	n/a	n/a
27	HEY1	chr12:57110928-57111323	K562	blood:	n/a	n/a
28	HEY1	chr12:57110055-57110696	K562	blood:	n/a	n/a
29	HEY1	chr12:57108778-57109021	K562	blood:	n/a	n/a
30	HEY1	chr12:57111571-57111955	HepG2	liver:	n/a	n/a
31	HEY1	chr12:57111540-57111862	HepG2	liver:	n/a	n/a
32	JUND	chr12:57104559-57104965	A549	lung:	n/a	n/a
33	JUND	chr12:57104865-57105031	H1-hESC	embryonic stem cell:	n/a	n/a
34	MTA3	chr12:57112012-57112430	GM12878	blood:	n/a	n/a
35	MTA3	chr12:57104517-57105513	GM12878	blood:	n/a	n/a
36	MTA3	chr12:57109628-57110229	GM12878	blood:	n/a	n/a
37	MTA3	chr12:57104913-57105392	GM12878	blood:	n/a	n/a
38	MYC	chr12:57107144-57107447	MCF10A-Er-Src	breast:	n/a	n/a
39	NFATC1	chr12:57104607-57105262	GM12878	blood:	n/a	n/a
40	NFATC1	chr12:57104572-57105512	GM12878	blood:	n/a	n/a
41	NFIC	chr12:57099806-57100366	ECC-1	luminal epithelium:	n/a	n/a
42	NFIC	chr12:57105012-57105434	GM12878	blood:	n/a	n/a
43	NFIC	chr12:57099781-57100414	ECC-1	luminal epithelium:	n/a	n/a
44	NFIC	chr12:57099962-57100355	SK-N-SH	brain:	n/a	n/a
45	NFIC	chr12:57104720-57105107	GM12878	blood:	n/a	n/a
46	NR2F2	chr12:57103801-57104042	K562	blood:	n/a	n/a
47	PML	chr12:57104690-57105634	GM12878	blood:	n/a	n/a
48	PML	chr12:57104769-57105442	K562	blood:	n/a	n/a
49	POLR2A	chr12:57104643-57104815	GM12878	blood:	n/a	n/a
50	POLR2A	chr12:57106452-57106760	MCF-7	breast:	n/a	n/a

No data

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:57098172..57100413-chr12:57108972..57110548,2	MCF-7	breast:
2	chr12:57074578..57085543-chr12:57108746..57121559,55	K562	blood:
3	chr12:57112603..57114130-chr12:57504633..57506166,2	K562	blood:
4	chr12:57080638..57082220-chr12:57105324..57106849,2	K562	blood:
5	chr12:57080452..57082981-chr12:57101571..57103409,2	K562	blood:
6	chr12:57089245..57091057-chr12:57096522..57098278,2	K562	blood:
7	chr12:57038464..57040434-chr12:57103579..57106506,2	K562	blood:
8	chr12:57112436..57114253-chr12:57144608..57146371,2	K562	blood:
9	chr12:57101910..57104991-chr12:57106569..57110622,4	MCF-7	breast:
10	chr12:56510526..56513327-chr12:57111291..57113363,2	K562	blood:
11	chr12:57077883..57080577-chr12:57094681..57096906,2	K562	blood:
12	chr12:57106579..57108709-chrX:20158606..20161019,2	K562	blood:
13	chr12:57098172..57100413-chr12:57108972..57110548,2	MCF-7	breast:
14	chr12:57093397..57096206-chr12:57097645..57099530,2	K562	blood:
15	chr12:57076071..57078890-chr12:57104142..57106874,2	K562	blood:
16	chr12:57076604..57085974-chr12:57112559..57120474,46	MCF-7	breast:
17	chr12:57082048..57083806-chr12:57102806..57104517,2	MCF-7	breast:
18	chr12:57093397..57096206-chr12:57097645..57099530,2	K562	blood:
19	chr12:57025967..57028369-chr12:57109076..57111615,2	K562	blood:
20	chr12:57098550..57104951-chr12:57116953..57119967,8	MCF-7	breast:
21	chr12:57029529..57031708-chr12:57108822..57111712,2	K562	blood:
22	chr12:57080452..57082852-chr12:57101909..57106660,4	K562	blood:
23	chr12:57027907..57030417-chr12:57100088..57101998,2	MCF-7	breast:
24	chr12:57071568..57074070-chr12:57103902..57106725,2	K562	blood:
25	chr12:57079048..57083970-chr12:57107938..57112602,6	K562	blood:
26	chr12:57075341..57085478-chr12:57112447..57121011,58	MCF-7	breast:
27	chr12:57088163..57090039-chr12:57103030..57105439,2	MCF-7	breast:
28	chr12:57082206..57082785-chr12:57103455..57104262,2	NB4	blood:
29	chr12:57111474..57114081-chr12:57143216..57146135,2	MCF-7	breast:
30	chr12:57078008..57083064-chr12:57107591..57112002,6	MCF-7	breast:
31	chr12:57094927..57096881-chr12:57105605..57107947,2	MCF-7	breast:

No data

Variant related genes	Relation type
NACA	TF binding region
ENSG00000110955	chromatin interactions
ENSG00000139641	chromatin interactions
ENSG00000135482	chromatin interactions
ENSG00000198056	chromatin interactions
ENSG00000229117	chromatin interactions
ENSG00000110958	chromatin interactions
ENSG00000207031	chromatin interactions
ENSG00000076108	chromatin interactions
ENSG00000166888	chromatin interactions
ENSG00000196531	chromatin interactions
ENSG00000173674	chromatin interactions
ENSG00000025423	chromatin interactions

Extended variants
information (count: 746 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:746 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566171105	chr12:57095922-57095923	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs536895131	chr12:57095954-57095955	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs143121605	chr12:57095960-57095961	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs560784404	chr12:57095986-57095987	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs201913318	chr12:57095995-57095996	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs545192164	chr12:57096020-57096021	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs7135720	chr12:57096030-57096031	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs371973432	chr12:57096049-57096050	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs548239349	chr12:57096075-57096076	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs537310242	chr12:57096098-57096099	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs187869287	chr12:57096115-57096116	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs568149508	chr12:57096142-57096143	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs150812693	chr12:57096146-57096147	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs373276176	chr12:57096147-57096148	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs530673826	chr12:57096167-57096168	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs12578477	chr12:57096168-57096169	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs375378753	chr12:57096175-57096176	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs527507864	chr12:57096192-57096193	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs552690041	chr12:57096214-57096215	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs184757412	chr12:57096245-57096246	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs189211049	chr12:57096272-57096273	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs192212115	chr12:57096304-57096305	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs7957300	chr12:57096343-57096344	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs546149503	chr12:57096412-57096413	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs184276693	chr12:57096416-57096417	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs367618625	chr12:57096421-57096422	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs189753602	chr12:57096430-57096431	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs142472994	chr12:57096453-57096454	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs181336345	chr12:57096475-57096476	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs186168472	chr12:57096480-57096481	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs559887216	chr12:57096481-57096482	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs535284122	chr12:57096488-57096489	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs548777364	chr12:57096535-57096536	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs570119334	chr12:57096536-57096537	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs537628756	chr12:57096548-57096549	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs189495223	chr12:57096604-57096605	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs570801058	chr12:57096636-57096637	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs534362776	chr12:57096668-57096669	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs4759254	chr12:57096674-57096675	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs116892336	chr12:57096678-57096679	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs150675588	chr12:57096748-57096749	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs180744710	chr12:57096755-57096756	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs75915474	chr12:57096761-57096762	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs556998338	chr12:57096762-57096763	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs144643723	chr12:57096798-57096799	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs546013861	chr12:57096799-57096800	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs573773240	chr12:57096805-57096806	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs564422060	chr12:57096903-57096904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573126090	chr12:57096920-57096921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs541442972	chr12:57096946-57096947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Wilms tumour	21544195	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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Bladder cancer	21909424	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	20531469	CNVD
Rhabdomyosarcoma	16790082	CNVD
Renal cell carcinoma	18765545	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21138945	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	21509527	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glycogen storage disease	18421352	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:638 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:57083800-57105200	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr12:57089000-57109600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:57090400-57104600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr12:57090400-57104800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr12:57093400-57104800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:57094800-57100200	Weak transcription	K562	blood
7	chr12:57094800-57104800	Weak transcription	NH-A	brain
8	chr12:57094800-57105000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr12:57095000-57104600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr12:57095000-57104800	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr12:57095000-57104800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr12:57095000-57104800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr12:57095000-57104800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr12:57095000-57104800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr12:57095000-57104800	Weak transcription	Primary B cells from peripheral blood	blood
16	chr12:57095000-57104800	Weak transcription	Osteobl	bone
17	chr12:57095000-57105000	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr12:57095000-57105000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr12:57095000-57105000	Weak transcription	Primary B cells from cord blood	blood
20	chr12:57095000-57105200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr12:57095200-57096200	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr12:57095200-57105000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr12:57095400-57096000	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr12:57095400-57100200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr12:57095400-57104800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr12:57095400-57104800	Weak transcription	Placenta	Placenta
27	chr12:57095600-57097400	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr12:57096200-57096600	Weak transcription	Primary monocytes fromperipheralblood	blood
29	chr12:57096600-57098200	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr12:57097400-57098000	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr12:57098000-57099400	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr12:57098200-57099400	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr12:57099400-57100600	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr12:57099400-57100800	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr12:57099600-57099800	Enhancers	A549	lung
36	chr12:57099600-57100800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr12:57099800-57104800	Weak transcription	A549	lung
38	chr12:57100000-57105200	Weak transcription	Thymus	Thymus
39	chr12:57100200-57100600	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr12:57100200-57100800	Enhancers	Skeletal Muscle Male	skeletal muscle
41	chr12:57100200-57101400	Enhancers	K562	blood
42	chr12:57100400-57100600	Enhancers	NHEK	skin
43	chr12:57100400-57100800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr12:57100400-57100800	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr12:57100400-57104800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr12:57100400-57105200	Weak transcription	GM12878-XiMat	blood
47	chr12:57100400-57106600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
48	chr12:57100600-57102800	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr12:57100600-57104800	Weak transcription	NHEK	skin
50	chr12:57100600-57105200	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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