Variant report

Variant	rs11951833
Chromosome Location	chr5:114465987-114465988
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	chr5:114465952..114468354-chr5:114469870..114471606,2	K562	blood:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11954156	0.94[AFR][1000 genomes]
rs56203091	1.00[AMR][1000 genomes]
rs56239364	1.00[AMR][1000 genomes]
rs57056024	1.00[AMR][1000 genomes]
rs59813245	0.94[AFR][1000 genomes]
rs60895403	0.89[AFR][1000 genomes]
rs61011322	1.00[AMR][1000 genomes]
rs73780049	1.00[AMR][1000 genomes]
rs73780057	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73780058	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73780072	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73780076	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73780078	0.94[AFR][1000 genomes]
rs73780079	1.00[AMR][1000 genomes]
rs73780080	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73782639	1.00[AMR][1000 genomes]
rs73782641	1.00[AMR][1000 genomes]
rs73782662	1.00[AMR][1000 genomes]
rs73782663	1.00[AMR][1000 genomes]
rs7732755	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882729	chr5:113743628-114497708	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv830453	chr5:114277261-114546536	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	nsv462398	chr5:114445023-114475774	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
4	nsv599476	chr5:114445023-114475774	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
5	nsv462399	chr5:114445023-114526010	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
6	nsv599477	chr5:114445023-114526010	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
7	nsv830454	chr5:114453864-114607159	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:114453800-114500600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:114460000-114476000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr5:114460400-114470800	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr5:114460400-114486800	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr5:114460600-114466000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr5:114460600-114468000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr5:114460800-114489200	Weak transcription	Aorta	Aorta
8	chr5:114461000-114489200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr5:114461800-114467400	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr5:114462000-114472400	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr5:114463200-114469200	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr5:114464000-114478400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr5:114464400-114469400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr5:114464600-114466400	Strong transcription	Cortex derived primary cultured neurospheres	brain
15	chr5:114464600-114466600	Strong transcription	Fetal Brain Female	brain
16	chr5:114464800-114471400	Weak transcription	Fetal Brain Male	brain
17	chr5:114465000-114466200	Weak transcription	Duodenum Mucosa	Duodenum
18	chr5:114465000-114466400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr5:114465000-114473200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr5:114465400-114470000	Weak transcription	Colonic Mucosa	Colon
21	chr5:114465400-114486800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr5:114465600-114482800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr5:114465800-114467800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr5:114465800-114468200	Strong transcription	Brain Germinal Matrix	brain

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