Variant report

Variant	rs191126406
Chromosome Location	chrX:65819043-65819044
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv995042	chrX:65121634-65953299	Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	40 gene(s)	inside rSNPs	diseases
2	nsv916917	chrX:65628203-65966658	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
3	nsv498092	chrX:65628203-66170369	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
4	nsv949354	chrX:65705774-65952293	Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv432334	chrX:65705774-66018207	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
6	nsv520630	chrX:65706079-66017027	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
7	nsv529910	chrX:65738026-66025016	Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
8	nsv532867	chrX:65768210-65926263	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv532866	chrX:65768210-65927478	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv532865	chrX:65768210-65952059	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
11	nsv432336	chrX:65808595-65913868	Active TSS Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	nsv534422	chrX:65815490-65894956	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	nsv534223	chrX:65815490-65895015	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:65810200-65827400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chrX:65811400-65819400	Weak transcription	HMEC	breast
3	chrX:65811800-65821000	Weak transcription	NHDF-Ad	bronchial
4	chrX:65812800-65823400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chrX:65812800-65825600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chrX:65814200-65821200	Strong transcription	HUES64 Cell Line	embryonic stem cell
7	chrX:65814800-65823200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chrX:65815000-65819600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chrX:65815000-65820400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chrX:65815000-65825400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chrX:65815400-65827800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chrX:65815400-65852200	Weak transcription	HepG2	liver
13	chrX:65815600-65822400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chrX:65815600-65823800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chrX:65815800-65822600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chrX:65816200-65825200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chrX:65816400-65823400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chrX:65816600-65822800	Strong transcription	HSMMtube	muscle
19	chrX:65817000-65821400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chrX:65817000-65823600	Strong transcription	HSMM	muscle
21	chrX:65817200-65819200	Strong transcription	GM12878-XiMat	blood
22	chrX:65817200-65820000	Strong transcription	Ovary	ovary
23	chrX:65817200-65823000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chrX:65817200-65823400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chrX:65817600-65821000	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chrX:65817600-65824800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chrX:65817800-65820400	Strong transcription	NH-A	brain
28	chrX:65817800-65821600	Weak transcription	Muscle Satellite Cultured Cells	--
29	chrX:65818000-65819400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chrX:65818000-65821600	Weak transcription	Brain Hippocampus Middle	brain
31	chrX:65818000-65823400	Strong transcription	HUES6 Cell Line	embryonic stem cell
32	chrX:65818000-65824200	Weak transcription	Pancreas	Pancrea
33	chrX:65818000-65834200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chrX:65818400-65819600	Weak transcription	H9 Cell Line	embryonic stem cell
35	chrX:65818400-65822200	Weak transcription	A549	lung
36	chrX:65818800-65820200	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chrX:65819000-65819400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
38	chrX:65819000-65819400	Strong transcription	Aorta	Aorta
39	chrX:65819000-65819800	Strong transcription	H1 Cell Line	embryonic stem cell
40	chrX:65819000-65821200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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