Variant report

No.	Distal block	Cell Line	Cell type
1	chrX:109637443..109639454-chrX:109642435..109645799,3	K562	blood:
2	chrX:109632843..109635409-chrX:109636308..109639551,3	K562	blood:
3	chrX:109626748..109629484-chrX:109635802..109638311,2	MCF-7	breast:
4	chrX:109633892..109639812-chrX:109645953..109649648,6	MCF-7	breast:
5	chrX:109421031..109422719-chrX:109637799..109640538,2	K562	blood:
6	chrX:109560266..109562217-chrX:109637723..109640288,4	K562	blood:

Variant related genes	Relation type
ENSG00000101935	Chromatin interaction

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	nsv530248	chrX:109436208-109743686	Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	esv2758583	chrX:109581771-109711481	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	esv2758884	chrX:109581771-109711481	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	nsv438150	chrX:109635217-109640055	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:109626400-109638000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chrX:109635000-109638200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chrX:109636000-109642200	Enhancers	K562	blood
4	chrX:109637200-109638400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chrX:109637400-109639200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chrX:109637600-109638200	Enhancers	Ovary	ovary
7	chrX:109637600-109638400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chrX:109637600-109642000	Enhancers	HMEC	breast
9	chrX:109637800-109638400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chrX:109637800-109638400	Enhancers	NHEK	skin
11	chrX:109637800-109639000	Enhancers	Placenta	Placenta
12	chrX:109637800-109639200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
13	chrX:109637800-109640000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chrX:109637800-109640200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chrX:109637800-109640600	Enhancers	Muscle Satellite Cultured Cells	--
16	chrX:109637800-109640600	Enhancers	HSMMtube	muscle
17	chrX:109637800-109641400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chrX:109637800-109641400	Enhancers	NHDF-Ad	bronchial
19	chrX:109637800-109641600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chrX:109637800-109641600	Enhancers	HSMM	muscle
21	chrX:109637800-109641800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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