Variant report

Variant	rs73344421
Chromosome Location	chr5:177966216-177966217
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:177893036..177895122-chr5:177964444..177967291,2	K562	blood:

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs59019490	0.90[AFR][1000 genomes]
rs73342656	1.00[AMR][1000 genomes]
rs73342699	0.90[AFR][1000 genomes]
rs73344410	0.90[AFR][1000 genomes]
rs73344415	0.82[AFR][1000 genomes]
rs73344420	1.00[AMR][1000 genomes]
rs73344429	0.80[AFR][1000 genomes]
rs73344439	0.80[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948342	chr5:177384542-178168737	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	141 gene(s)	inside rSNPs	diseases
2	nsv1029398	chr5:177502106-178070654	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	136 gene(s)	inside rSNPs	diseases
3	nsv427739	chr5:177766033-177966666	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers 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	6 gene(s)	inside rSNPs	diseases
4	nsv883210	chr5:177771925-177980792	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv462570	chr5:177860454-178010145	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv600423	chr5:177860454-178010145	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv883214	chr5:177876309-178047217	Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv600427	chr5:177954516-177968251	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv883215	chr5:177961860-177980792	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv527857	chr5:177964317-177966921	Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177954600-177973800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr5:177960400-177969400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr5:177963000-177968800	Weak transcription	Left Ventricle	heart
4	chr5:177963000-177971200	Weak transcription	Right Atrium	heart
5	chr5:177963200-177968600	Weak transcription	Fetal Heart	heart
6	chr5:177963800-177968000	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr5:177964400-177968800	Weak transcription	Right Ventricle	heart
8	chr5:177965000-177966400	Enhancers	Stomach Smooth Muscle	stomach
9	chr5:177965000-177967600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr5:177965200-177969400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr5:177965200-177971600	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr5:177965600-177967000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr5:177965600-177969400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr5:177965800-177966400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
15	chr5:177965800-177972400	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr5:177966000-177966400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
17	chr5:177966000-177968400	Weak transcription	Fetal Stomach	stomach
18	chr5:177966000-177968800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr5:177966000-177969400	Weak transcription	Fetal Lung	lung
20	chr5:177966200-177968600	Weak transcription	Cortex derived primary cultured neurospheres	brain

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