Variant report

Variant	rs6918923
Chromosome Location	chr6:132266127-132266128
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	6:132259484-132267655..6:132269655-132282174	Hela-S3	cervix:
2	chr6:132266076..132267882-chr6:132270565..132272216,2	MCF-7	breast:
3	6:132182612-132191683..6:132259484-132267655	H1-hESC	embryonic stem cell:	embryo
4	6:132176847-132180372..6:132259484-132267655	GM12878	blood:

Variant related genes	Relation type
ENSG00000197594	Chromatin interaction
ENSG00000227220	Chromatin interaction
ENSG00000118523	Chromatin interaction

Extended variants
information (count: 3 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs1931003	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6918698	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv7968	chr6:131917172-132321099	Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 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	chr6:132259200-132271000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr6:132259400-132269800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr6:132259400-132270400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:132259400-132271000	Weak transcription	Liver	Liver
5	chr6:132259600-132267600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr6:132259600-132268800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr6:132259600-132269400	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr6:132259600-132269400	Weak transcription	HMEC	breast
9	chr6:132259600-132270000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:132259800-132268200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr6:132260000-132271000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr6:132260200-132267000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr6:132260200-132267200	Weak transcription	NHLF	lung
14	chr6:132260200-132268200	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr6:132260400-132268600	Weak transcription	A549	lung
16	chr6:132260600-132267800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr6:132260600-132268000	Weak transcription	HSMM	muscle
18	chr6:132262400-132268000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:132265400-132267200	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr6:132265600-132266400	Weak transcription	Osteobl	bone
21	chr6:132265600-132266600	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr6:132265600-132266600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr6:132265800-132267000	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr6:132265800-132269400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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