Variant report

Variant	rs61758856
Chromosome Location	chr5:96430797-96430798
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:96425190..96428341-chr5:96429686..96433552,4	K562	blood:

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs17087310	0.87[EUR][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	nsv432755	chr5:95987984-96657483	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv598962	chr5:96057891-96893164	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv4924	chr5:96391451-96437233	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv830412	chr5:96427305-96606619	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 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	chr5:96425200-96437000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:96426400-96437200	Weak transcription	Primary B cells from peripheral blood	blood
3	chr5:96428200-96432600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr5:96428400-96440000	Weak transcription	K562	blood
5	chr5:96428800-96430800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr5:96429000-96432000	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr5:96429200-96431000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr5:96429200-96431400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr5:96429400-96431600	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr5:96430000-96434600	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr5:96430200-96430800	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr5:96430200-96431000	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr5:96430200-96431200	Strong transcription	Fetal Muscle Leg	muscle
14	chr5:96430200-96432800	Strong transcription	Primary B cells from cord blood	blood
15	chr5:96430400-96430800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr5:96430400-96430800	Enhancers	Fetal Thymus	thymus
17	chr5:96430400-96431200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr5:96430400-96431400	Enhancers	Dnd41	blood
19	chr5:96430600-96431000	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr5:96430600-96431200	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr5:96430600-96432200	Flanking Active TSS	GM12878-XiMat	blood
22	chr5:96430600-96438000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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