Variant report

Variant	rs7714075
Chromosome Location	chr5:177843832-177843833
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:177841800..177844284-chr5:177969427..177971380,2	K562	blood:
2	chr5:177764211..177766744-chr5:177842337..177844246,2	MCF-7	breast:

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs60540959	0.88[AFR][1000 genomes]
rs73350809	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73350818	0.93[AFR][1000 genomes]
rs73350820	0.89[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 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	nsv1019404	chr5:177507080-177859089	Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Active TSS Weak transcription Genic enhancers 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	126 gene(s)	inside rSNPs	diseases
4	nsv1024689	chr5:177638936-177926244	Enhancers Bivalent Enhancer Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
5	nsv537968	chr5:177638936-177926244	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
6	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
7	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
8	nsv883213	chr5:177811754-177947771	Enhancers Bivalent Enhancer Weak transcription Active TSS 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	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177838800-177844000	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr5:177838800-177844200	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr5:177840000-177855000	Weak transcription	Right Atrium	heart
4	chr5:177841200-177844200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr5:177841200-177845600	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr5:177841200-177846000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr5:177841200-177854400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr5:177841800-177844600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr5:177842400-177848000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr5:177842600-177844000	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr5:177843400-177844400	Genic enhancers	Fetal Thymus	thymus
12	chr5:177843800-177844200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr5:177843800-177844200	Weak transcription	Thymus	Thymus
14	chr5:177843800-177844400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr5:177843800-177844400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr5:177843800-177844600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr5:177843800-177844600	Enhancers	NHDF-Ad	bronchial
18	chr5:177843800-177844800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr5:177843800-177845000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr5:177843800-177845200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr5:177843800-177846000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr5:177843800-177846800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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