Variant report

Variant	rs10051515
Chromosome Location	chr5:124339845-124339846
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	chr5:124144207..124147001-chr5:124338580..124340102,2	K562	blood:

Variant related genes	Relation type
ENSG00000242814	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10037351	1.00[EUR][1000 genomes]
rs10039152	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10051816	0.83[EUR][1000 genomes]
rs10051865	0.83[EUR][1000 genomes]
rs10056903	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10059820	0.83[EUR][1000 genomes]
rs10061638	0.83[EUR][1000 genomes]
rs10076719	0.83[EUR][1000 genomes]
rs10076822	0.83[EUR][1000 genomes]
rs10223088	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10478646	1.00[EUR][1000 genomes]
rs28379635	0.83[EUR][1000 genomes]
rs28442881	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28469490	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56878962	0.83[EUR][1000 genomes]
rs60081045	0.83[EUR][1000 genomes]
rs60582094	0.83[EUR][1000 genomes]
rs6862844	0.83[EUR][1000 genomes]
rs6862998	0.83[EUR][1000 genomes]
rs6867051	0.83[EUR][1000 genomes]
rs6867249	0.83[EUR][1000 genomes]
rs6870217	0.83[EUR][1000 genomes]
rs6874077	0.83[EUR][1000 genomes]
rs6874416	0.83[EUR][1000 genomes]
rs6875818	0.83[EUR][1000 genomes]
rs6891699	0.83[EUR][1000 genomes]
rs73306728	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73306768	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73308739	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882822	chr5:124250018-124449375	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv830474	chr5:124263628-124431299	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:124323400-124348600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:124326600-124342000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:124333000-124341000	Weak transcription	Brain Anterior Caudate	brain
4	chr5:124333800-124341400	Weak transcription	Fetal Kidney	kidney
5	chr5:124336400-124341800	Enhancers	Dnd41	blood
6	chr5:124336800-124343000	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr5:124337000-124343000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr5:124337000-124343000	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr5:124337200-124341800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr5:124337200-124342000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr5:124337400-124341800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr5:124337600-124342600	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr5:124337800-124342600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr5:124337800-124342800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr5:124338000-124343000	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr5:124338400-124340000	Enhancers	H9 Cell Line	embryonic stem cell
17	chr5:124338400-124343000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr5:124338400-124343000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr5:124338600-124340400	Enhancers	H1 Cell Line	embryonic stem cell
20	chr5:124338600-124340600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr5:124338800-124342800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr5:124339000-124340200	Weak transcription	Primary B cells from cord blood	blood
23	chr5:124339000-124340400	Weak transcription	Primary B cells from peripheral blood	blood
24	chr5:124339400-124340600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr5:124339400-124340800	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr5:124339400-124341000	Weak transcription	GM12878-XiMat	blood
27	chr5:124339600-124340000	Weak transcription	Fetal Brain Female	brain
28	chr5:124339600-124342200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr5:124339800-124340000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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