Variant report

Variant	rs577529787
Chromosome Location	chr22:34107404-34107405
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv934109	chr22:33722066-34339500	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv531588	chr22:33776857-34150188	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1055791	chr22:33822226-34159536	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	esv2763261	chr22:33831348-34288389	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
5	nsv917167	chr22:33852676-34137036	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1062832	chr22:33861531-34143295	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv544686	chr22:33861531-34143295	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1057450	chr22:33928913-34849012	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv934161	chr22:33979015-34118621	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv914990	chr22:34090440-34373293	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv1055203	chr22:34098417-34196685	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv914991	chr22:34106384-34293516	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv459878	chr22:34106745-34226592	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
14	nsv588936	chr22:34106745-34226592	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:34087000-34109400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr22:34091600-34115800	Weak transcription	Pancreas	Pancrea
3	chr22:34092400-34109200	Weak transcription	Fetal Intestine Large	intestine
4	chr22:34097000-34110000	Weak transcription	Ovary	ovary
5	chr22:34097200-34108000	Weak transcription	Fetal Intestine Small	intestine
6	chr22:34097200-34109200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr22:34097200-34109200	Weak transcription	Fetal Brain Female	brain
8	chr22:34097200-34109400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr22:34097600-34110200	Weak transcription	Stomach Smooth Muscle	stomach
10	chr22:34097600-34114600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr22:34098200-34110600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr22:34100400-34109000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr22:34100600-34108200	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr22:34100800-34110000	Weak transcription	Primary B cells from peripheral blood	blood
15	chr22:34101200-34108800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr22:34101200-34109600	Weak transcription	Fetal Stomach	stomach
17	chr22:34101200-34110000	Weak transcription	Aorta	Aorta
18	chr22:34103200-34110600	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr22:34104000-34110000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr22:34104200-34118800	Weak transcription	Right Ventricle	heart
21	chr22:34104600-34109400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr22:34105000-34109800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr22:34105200-34109800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr22:34105600-34133400	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr22:34106400-34110200	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr22:34106600-34109200	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr22:34106600-34109400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr22:34106600-34109400	Weak transcription	Brain Cingulate Gyrus	brain
29	chr22:34106600-34109400	Weak transcription	Brain Hippocampus Middle	brain
30	chr22:34106600-34110000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr22:34106800-34108400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr22:34107000-34107600	Genic enhancers	Left Ventricle	heart
33	chr22:34107200-34109800	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr22:34107200-34110000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr22:34107200-34110000	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr22:34107400-34107600	Enhancers	Stomach Mucosa	stomach
37	chr22:34107400-34107800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr22:34107400-34108200	Strong transcription	ES-I3 Cell Line	embryonic stem cell

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