Variant report

Variant	rs703836
Chromosome Location	chr12:57912556-57912557
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:46)
CpG islands
(count:0)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:46 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr12:57911692-57912575	U87	brain:	n/a	n/a
2	POLR2A	chr12:57908101-57916508	PANC-1	pancreas:	n/a	n/a
3	POLR2A	chr12:57907839-57915181	PFSK-1	brain:	n/a	n/a
4	POLR2A	chr12:57912393-57912575	GM12878	blood:	n/a	n/a
5	POLR2A	chr12:57911713-57919299	SK-N-MC	brain:	n/a	n/a
6	HEY1	chr12:57909567-57914433	K562	blood:	n/a	n/a
7	POLR2A	chr12:57908219-57914828	A549	lung:	n/a	n/a
8	POLR2A	chr12:57904506-57914962	K562	blood:	n/a	n/a
9	POLR2A	chr12:57908236-57914960	HepG2	liver:	n/a	n/a
10	CEBPB	chr12:57912395-57912684	HepG2	liver:	n/a	chr12:57912499-57912510
11	POLR2A	chr12:57908014-57914558	U87	brain:	n/a	n/a
12	POLR2A	chr12:57908255-57914954	IMR90	lung:	n/a	n/a
13	POLR2A	chr12:57908093-57915086	PANC-1	pancreas:	n/a	n/a
14	POLR2A	chr12:57908382-57921207	K562	blood:	n/a	n/a
15	POLR2A	chr12:57911720-57912610	GM12892	blood:	n/a	n/a
16	POLR2A	chr12:57908268-57914527	GM12878	blood:	n/a	n/a
17	POLR2A	chr12:57908090-57915139	K562	blood:	n/a	n/a
18	POLR2A	chr12:57912411-57914996	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr12:57912166-57912577	K562	blood:	n/a	chr12:57912499-57912510
20	POLR2A	chr12:57908062-57920927	K562	blood:	n/a	n/a
21	HEY1	chr12:57912099-57912580	HepG2	liver:	n/a	n/a
22	POLR2A	chr12:57911693-57914961	HCT-116	colon:	n/a	n/a
23	POLR2A	chr12:57908262-57912570	K562	blood:	n/a	n/a
24	CEBPB	chr12:57912319-57912663	IMR90	lung:	n/a	chr12:57912499-57912510
25	POLR2A	chr12:57908188-57914911	Hela-S3	cervix:	n/a	n/a
26	POLR2A	chr12:57911827-57914966	HepG2	liver:	n/a	n/a
27	TEAD4	chr12:57912016-57912591	K562	blood:	n/a	n/a
28	CEBPB	chr12:57912340-57912657	A549	lung:	n/a	chr12:57912499-57912510
29	POLR2A	chr12:57907934-57915067	U87	brain:	n/a	n/a
30	POLR2A	chr12:57911759-57912578	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr12:57912465-57912570	A549	lung:	n/a	n/a
32	POLR2A	chr12:57911765-57915711	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr12:57907994-57915073	U87	brain:	n/a	n/a
34	HEY1	chr12:57911693-57912595	K562	blood:	n/a	n/a
35	POLR2A	chr12:57908294-57917206	HepG2	liver:	n/a	n/a
36	PML	chr12:57908507-57912597	K562	blood:	n/a	chr12:57912079-57912087
37	CEBPB	chr12:57912316-57912664	K562	blood:	n/a	chr12:57912499-57912510
38	POLR2A	chr12:57908734-57914513	GM12878	blood:	n/a	n/a
39	POLR2A	chr12:57911609-57912577	HCT-116	colon:	n/a	n/a
40	POLR2A	chr12:57912482-57912566	HUVEC	blood vessel:	n/a	n/a
41	POLR2A	chr12:57911702-57912578	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr12:57911545-57915016	PFSK-1	brain:	n/a	n/a
43	POLR2A	chr12:57908118-57912577	K562	blood:	n/a	n/a
44	POLR2A	chr12:57911723-57912597	HepG2	liver:	n/a	n/a
45	POLR2A	chr12:57911695-57912584	GM12892	blood:	n/a	n/a
46	POLR2A	chr12:57912391-57912603	GM12878	blood:	n/a	n/a

No data

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:57911286..57913384-chr12:58133067..58135116,2	K562	blood:
2	chr12:57896559..57899422-chr12:57912129..57915670,4	MCF-7	breast:
3	chr12:57911911..57916321-chr12:58013702..58018076,7	K562	blood:
4	chr12:57912267..57913858-chr12:58118505..58121411,2	MCF-7	breast:
5	chr12:57879207..57888227-chr12:57906247..57918451,36	K562	blood:
6	chr12:57849885..57859254-chr12:57908711..57915821,16	K562	blood:
7	chr12:57911913..57914667-chr12:58122854..58126849,5	K562	blood:
8	chr12:57909973..57915898-chr12:58127755..58134567,15	K562	blood:
9	chr12:57910924..57913637-chr12:58087334..58089189,3	K562	blood:
10	chr12:57844795..57846828-chr12:57912360..57915235,2	K562	blood:
11	chr12:57912095..57914310-chr12:58137199..58139977,2	MCF-7	breast:
12	chr12:57908910..57916122-chr12:58022622..58031573,17	K562	blood:
13	chr12:57912185..57914600-chr12:58159460..58162214,2	MCF-7	breast:
14	chr12:57912351..57915137-chr12:123457151..123459849,2	MCF-7	breast:
15	chr12:57911754..57916322-chr12:58006406..58010716,5	K562	blood:
16	chr12:57852034..57858739-chr12:57911478..57917144,8	MCF-7	breast:
17	chr12:57890573..57894514-chr12:57912146..57915649,5	MCF-7	breast:
18	chr12:57871859..57875002-chr12:57911901..57914526,3	K562	blood:
19	chr12:57850154..57858218-chr12:57910899..57919538,20	K562	blood:
20	chr12:57909291..57914221-chr12:58144639..58148673,6	K562	blood:
21	chr12:57912525..57914628-chr12:58024523..58026539,2	MCF-7	breast:
22	chr12:57911462..57914270-chr12:58144691..58146581,3	MCF-7	breast:
23	chr12:57911699..57918406-chr12:58000825..58010019,18	K562	blood:
24	chr12:57889487..57901620-chr12:57907600..57919310,30	K562	blood:
25	chr12:57912257..57915408-chr12:58000825..58006358,4	K562	blood:
26	chr12:57880356..57884964-chr12:57910434..57915758,10	MCF-7	breast:
27	chr12:57912181..57914315-chr12:58008996..58011925,2	MCF-7	breast:
28	chr12:57879869..57888452-chr12:57905809..57918310,36	K562	blood:
29	chr12:57881044..57886958-chr12:57910925..57918058,16	MCF-7	breast:
30	chr12:57908910..57916403-chr12:58022622..58028885,15	K562	blood:
31	chr12:57911596..57914324-chr12:58165059..58166579,2	MCF-7	breast:
32	chr12:57909076..57912703-chr12:58030683..58034118,3	K562	blood:

No data

Variant related genes	Relation type
MBD6	TF binding region
ENSG00000111325	Chromatin interaction
ENSG00000135452	Chromatin interaction
ENSG00000139269	Chromatin interaction
ENSG00000255737	Chromatin interaction
ENSG00000135454	Chromatin interaction
ENSG00000135439	Chromatin interaction
ENSG00000135506	Chromatin interaction
ENSG00000123329	Chromatin interaction
ENSG00000166986	Chromatin interaction
ENSG00000135446	Chromatin interaction
ENSG00000037897	Chromatin interaction
ENSG00000178498	Chromatin interaction
ENSG00000224713	Chromatin interaction
ENSG00000111087	Chromatin interaction
ENSG00000111012	Chromatin interaction
ENSG00000150967	Chromatin interaction
ENSG00000123427	Chromatin interaction
ENSG00000240771	Chromatin interaction
ENSG00000135502	Chromatin interaction
ENSG00000257499	Chromatin interaction

Extended variants
information (count: 60 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1148553	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1148554	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1148555	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1148557	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1284465	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1284605	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1284606	0.83[AMR][1000 genomes]
rs1299737	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1629410	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1669294	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1669296	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1669297	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1678537	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1679368	0.86[EUR][1000 genomes]
rs1709871	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1709874	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2127318	0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2620677	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2620679	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2928382	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2943696	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3782129	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3847699	0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs474544	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4760273	0.85[EUR][1000 genomes]
rs496245	0.90[EUR][1000 genomes]
rs511752	0.83[AMR][1000 genomes]
rs697221	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs703835	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs703837	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs703838	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs703839	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7299631	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs747340	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs775236	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs775237	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs775241	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs775323	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs775324	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs776038	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs776039	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7964074	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs796546	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7969683	0.84[EUR][1000 genomes]
rs9737891	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899117	chr12:57811414-57926472	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
2	nsv899118	chr12:57811414-57946477	Weak transcription Strong transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	106 gene(s)	inside rSNPs	diseases
3	esv1812398	chr12:57829733-58001868	Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
4	esv2758310	chr12:57829733-58001868	Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
5	esv2759901	chr12:57829733-58001868	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
6	nsv428283	chr12:57829733-58001868	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
7	nsv469411	chr12:57844049-57921188	Active TSS Flanking Active TSS Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
8	nsv559032	chr12:57844049-57921188	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
9	nsv559033	chr12:57848639-57946477	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
10	nsv899119	chr12:57851182-57923451	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
11	nsv559034	chr12:57859932-58012233	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
12	nsv1038741	chr12:57877355-58174506	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
13	nsv541503	chr12:57877355-58174506	Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
14	nsv899120	chr12:57886609-57921188	Active TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
15	nsv559036	chr12:57911212-57916042	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	68 gene(s)	inside rSNPs	n/a

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs703836	DCTN2	cis	Muscle Skeletal	GTEx

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:57900600-57912800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr12:57902400-57912800	Strong transcription	Fetal Brain Female	brain
3	chr12:57902800-57912600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
4	chr12:57903000-57912600	Strong transcription	Brain Germinal Matrix	brain
5	chr12:57903800-57912600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr12:57908200-57912600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr12:57910600-57913200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr12:57910600-57913200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr12:57910600-57914200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr12:57910800-57913200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr12:57910800-57913600	Transcr. at gene 5' and 3'	Breast Myoepithelial Primary Cells	Breast
12	chr12:57910800-57913800	Transcr. at gene 5' and 3'	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr12:57911000-57913000	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr12:57911200-57912800	Genic enhancers	Primary T helper cells PMA-I stimulated	--
15	chr12:57911200-57913000	Transcr. at gene 5' and 3'	NHDF-Ad	bronchial
16	chr12:57911200-57913200	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr12:57911400-57912800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr12:57911400-57913000	Weak transcription	Fetal Brain Male	brain
19	chr12:57911400-57913000	Enhancers	Pancreas	Pancrea
20	chr12:57911400-57913200	Weak transcription	Esophagus	oesophagus
21	chr12:57911400-57913200	Weak transcription	Small Intestine	intestine
22	chr12:57911400-57913800	Flanking Active TSS	Stomach Smooth Muscle	stomach
23	chr12:57911600-57912600	Genic enhancers	Sigmoid Colon	Sigmoid Colon
24	chr12:57911600-57912600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
25	chr12:57911600-57912800	Genic enhancers	Fetal Muscle Trunk	muscle
26	chr12:57911600-57913000	Genic enhancers	Fetal Thymus	thymus
27	chr12:57911600-57913400	Transcr. at gene 5' and 3'	Hela-S3	cervix
28	chr12:57911800-57912600	Genic enhancers	Primary T cells from cord blood	blood
29	chr12:57911800-57913000	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr12:57911800-57913000	Enhancers	Fetal Lung	lung
31	chr12:57911800-57913400	Transcr. at gene 5' and 3'	HUES48 Cell Line	embryonic stem cell
32	chr12:57911800-57913400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr12:57911800-57913600	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr12:57911800-57913800	Transcr. at gene 5' and 3'	K562	blood
35	chr12:57911800-57913800	Transcr. at gene 5' and 3'	Osteobl	bone
36	chr12:57911800-57914000	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--
37	chr12:57911800-57914000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
38	chr12:57911800-57914200	Transcr. at gene 5' and 3'	Dnd41	blood
39	chr12:57911800-57914200	Transcr. at gene 5' and 3'	NHEK	skin
40	chr12:57911800-57915000	Active TSS	Right Ventricle	heart
41	chr12:57912000-57912600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr12:57912000-57912600	Genic enhancers	Primary B cells from cord blood	blood
43	chr12:57912000-57912600	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
44	chr12:57912000-57912600	Flanking Active TSS	Brain Angular Gyrus	brain
45	chr12:57912000-57912600	Flanking Active TSS	Brain Hippocampus Middle	brain
46	chr12:57912000-57912600	Flanking Active TSS	Ovary	ovary
47	chr12:57912000-57912800	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr12:57912000-57912800	Genic enhancers	HUES64 Cell Line	embryonic stem cell
49	chr12:57912000-57912800	Genic enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr12:57912000-57912800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links