Variant report

Variant	rs73421553
Chromosome Location	chr12:121561921-121561922
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:121559257..121561994-chr12:121565943..121568175,2	K562	blood:
2	chr12:121561837..121563360-chr12:121583686..121585355,2	K562	blood:
3	chr12:121559081..121561979-chr12:121605012..121606674,2	MCF-7	breast:
4	chr12:121561171..121566774-chr12:121646455..121649214,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000135124	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10849842	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1169714	0.91[ASN][1000 genomes]
rs1180009	0.97[ASN][1000 genomes]
rs12320058	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12320178	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1718149	0.86[ASN][1000 genomes]
rs1794886	0.86[ASN][1000 genomes]
rs1794898	0.97[ASN][1000 genomes]
rs208288	0.83[ASN][1000 genomes]
rs35646440	0.83[ASN][1000 genomes]
rs3861795	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs487417	0.86[ASN][1000 genomes]
rs510660	0.86[ASN][1000 genomes]
rs511496	0.86[ASN][1000 genomes]
rs535557	0.86[ASN][1000 genomes]
rs56720891	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs568531	0.86[ASN][1000 genomes]
rs57263663	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57902817	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs590477	0.86[ASN][1000 genomes]
rs592340	0.86[ASN][1000 genomes]
rs593223	0.86[ASN][1000 genomes]
rs594423	0.86[ASN][1000 genomes]
rs607094	0.86[ASN][1000 genomes]
rs608425	0.86[ASN][1000 genomes]
rs622937	0.86[ASN][1000 genomes]
rs657995	0.91[ASN][1000 genomes]
rs669547	0.91[ASN][1000 genomes]
rs672140	0.86[ASN][1000 genomes]
rs73421546	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73421551	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv521928	chr12:121041728-121761800	Genic enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
2	nsv899559	chr12:121324727-121592689	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv899562	chr12:121376416-121565870	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	esv2758318	chr12:121415845-121584813	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	esv2759917	chr12:121415845-121584813	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
6	nsv832531	chr12:121440495-121604232	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv560454	chr12:121457073-121745742	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
8	nsv430537	chr12:121487632-121579955	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv1054878	chr12:121519880-121761800	Flanking Active TSS Genic enhancers Strong transcription Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
10	nsv455729	chr12:121525591-121761800	Enhancers Strong transcription Genic enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
11	nsv560455	chr12:121525591-121761800	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
12	nsv899563	chr12:121543011-121600529	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
13	nsv1050519	chr12:121552964-121756420	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121555400-121565800	Weak transcription	Gastric	stomach
2	chr12:121558600-121562200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr12:121559000-121563600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr12:121559600-121564000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr12:121560800-121562200	Enhancers	K562	blood
6	chr12:121560800-121562800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr12:121561000-121562800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr12:121561000-121563200	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr12:121561000-121563400	Enhancers	Placenta	Placenta
10	chr12:121561200-121562200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr12:121561200-121562600	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr12:121561200-121562600	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr12:121561200-121562800	Enhancers	Primary T cells from cord blood	blood
14	chr12:121561200-121562800	Enhancers	Primary T cells fromperipheralblood	blood
15	chr12:121561200-121562800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr12:121561200-121562800	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr12:121561400-121562600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr12:121561400-121562800	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr12:121561400-121563200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr12:121561400-121565800	Enhancers	HepG2	liver
21	chr12:121561600-121562200	Enhancers	Liver	Liver
22	chr12:121561600-121566200	Weak transcription	Thymus	Thymus
23	chr12:121561800-121562200	Weak transcription	Fetal Thymus	thymus
24	chr12:121561800-121562600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr12:121561800-121562600	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr12:121561800-121562600	Enhancers	A549	lung
27	chr12:121561800-121562600	Enhancers	NH-A	brain
28	chr12:121561800-121562600	Enhancers	NHLF	lung
29	chr12:121561800-121562800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr12:121561800-121562800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr12:121561800-121562800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr12:121561800-121562800	Enhancers	Fetal Heart	heart
33	chr12:121561800-121562800	Enhancers	Hela-S3	cervix
34	chr12:121561800-121562800	Enhancers	HMEC	breast
35	chr12:121561800-121562800	Enhancers	HSMM	muscle
36	chr12:121561800-121562800	Enhancers	HUVEC	blood vessel
37	chr12:121561800-121563000	Enhancers	NHEK	skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links