Variant report

Variant	rs73909247
Chromosome Location	chr21:46126946-46126947
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr21:46123174..46125281-chr21:46125754..46127602,2	K562	blood:
2	chr21:46126774..46129621-chr21:46133926..46136280,3	MCF-7	breast:
3	chr21:46004403..46006273-chr21:46126860..46128813,2	MCF-7	breast:

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs2838667	1.00[AMR][1000 genomes]
rs57334195	0.91[AFR][1000 genomes]
rs58001811	1.00[AMR][1000 genomes]
rs59073447	1.00[AMR][1000 genomes]
rs59189711	1.00[AMR][1000 genomes]
rs59337865	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60085696	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7280175	1.00[AMR][1000 genomes]
rs73906917	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916258	chr21:45995986-46624705	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	102 gene(s)	inside rSNPs	diseases
2	nsv913956	chr21:46096964-46279505	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	nsv1062245	chr21:46096964-46332587	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
4	nsv544478	chr21:46096964-46332587	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:46122800-46129400	Weak transcription	Right Atrium	heart
2	chr21:46124400-46127000	ZNF genes & repeats	Spleen	Spleen
3	chr21:46125800-46128400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
4	chr21:46126000-46127000	Bivalent/Poised TSS	Primary T cells from cord blood	blood
5	chr21:46126000-46127000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
6	chr21:46126000-46127000	Bivalent Enhancer	Fetal Brain Male	brain
7	chr21:46126000-46127000	Bivalent Enhancer	Fetal Stomach	stomach
8	chr21:46126000-46127400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr21:46126000-46129000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
10	chr21:46126000-46129400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
11	chr21:46126000-46132600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
12	chr21:46126200-46127000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
13	chr21:46126200-46127200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
14	chr21:46126200-46127400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
15	chr21:46126200-46127600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr21:46126200-46128600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
17	chr21:46126200-46132000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr21:46126400-46132800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
19	chr21:46126600-46127000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr21:46126600-46128000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
21	chr21:46126600-46128200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
22	chr21:46126600-46128600	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr21:46126800-46127000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
24	chr21:46126800-46127400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
25	chr21:46126800-46127800	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
26	chr21:46126800-46128200	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr21:46126800-46129400	Weak transcription	Pancreas	Pancrea

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links