Variant report

Variant	rs137976137
Chromosome Location	chr10:97062209-97062210
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:97054091..97056343-chr10:97062077..97064550,2	K562	blood:
2	chr10:97058437..97060123-chr10:97062143..97063800,2	K562	blood:
3	chr10:97057079..97058801-chr10:97061706..97063249,2	K562	blood:
4	chr10:97047645..97051954-chr10:97061072..97065962,7	MCF-7	breast:
5	chr10:97049641..97052402-chr10:97061641..97064043,3	K562	blood:

Variant related genes	Relation type
ENSG00000107438	Chromatin interaction

Extended variants
information (count: 4 )
Associated
traits (count: 0)

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	nsv529726	chr10:96632494-97106315	Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	esv15160	chr10:96942869-97074756	Bivalent Enhancer Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS 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 miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv552021	chr10:97053404-97071334	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv3407243	chr10:97061412-97063885	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	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	chr10:97055600-97063400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr10:97055600-97072800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr10:97055800-97063200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr10:97055800-97063200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr10:97055800-97063200	Weak transcription	Lung	lung
6	chr10:97055800-97063400	Weak transcription	NHEK	skin
7	chr10:97055800-97063800	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr10:97055800-97067600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr10:97057600-97064000	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr10:97057600-97070200	Weak transcription	Spleen	Spleen
11	chr10:97057800-97063200	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr10:97057800-97063200	Weak transcription	Left Ventricle	heart
13	chr10:97057800-97063400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr10:97057800-97063400	Weak transcription	Right Atrium	heart
15	chr10:97057800-97064600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr10:97058000-97068200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr10:97058200-97067600	Weak transcription	GM12878-XiMat	blood
18	chr10:97058400-97063200	Weak transcription	K562	blood
19	chr10:97060400-97062800	Weak transcription	Fetal Heart	heart
20	chr10:97060400-97063200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr10:97060600-97063400	Weak transcription	Gastric	stomach
22	chr10:97060800-97063200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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