Variant report

Variant	rs369588102
Chromosome Location	chr22:27611143-27611144
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

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	nsv917333	chr22:26931825-27692024	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	142 gene(s)	inside rSNPs	diseases
2	esv34168	chr22:27289097-27678031	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	esv3413125	chr22:27404463-28121577	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
4	nsv459860	chr22:27527005-28181436	Strong transcription Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
5	nsv588872	chr22:27527005-28181436	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
6	nsv1064910	chr22:27609597-27648408	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	esv3412268	chr22:27610882-27611195	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:27606800-27620000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr22:27607000-27611400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr22:27607600-27611400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr22:27608000-27611600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr22:27608000-27611600	Enhancers	Osteobl	bone
6	chr22:27608000-27611800	Enhancers	Adipose Nuclei	Adipose
7	chr22:27608200-27611200	Enhancers	Spleen	Spleen
8	chr22:27608200-27611600	Enhancers	Ovary	ovary
9	chr22:27608200-27611800	Enhancers	Fetal Stomach	stomach
10	chr22:27608600-27611200	Enhancers	Stomach Smooth Muscle	stomach
11	chr22:27608600-27612200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr22:27608800-27611200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
13	chr22:27608800-27612800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr22:27609200-27615800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr22:27609400-27611200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr22:27609400-27613000	Weak transcription	A549	lung
17	chr22:27610000-27611200	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr22:27610000-27613400	Weak transcription	Right Atrium	heart
19	chr22:27610200-27616000	Weak transcription	Fetal Intestine Small	intestine
20	chr22:27610600-27612200	Enhancers	Rectal Smooth Muscle	rectum
21	chr22:27610800-27611200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
22	chr22:27611000-27611400	Enhancers	Duodenum Smooth Muscle	Duodenum
23	chr22:27611000-27611600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr22:27611000-27611800	Enhancers	Colon Smooth Muscle	Colon
25	chr22:27611000-27614200	Weak transcription	Fetal Muscle Leg	muscle
26	chr22:27611000-27615800	Weak transcription	NH-A	brain

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