Variant report

Variant	rs183697614
Chromosome Location	chrX:76812681-76812682
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531129	chrX:76703995-77038914	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
2	nsv529412	chrX:76711812-76957972	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
3	esv3382160	chrX:76731246-76970544	Weak transcription Genic enhancers Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
4	esv3368873	chrX:76731246-77122844	Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	esv3367037	chrX:76731346-77001644	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
6	esv3431028	chrX:76731396-76822344	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases
7	esv3399586	chrX:76799846-77022144	Strong transcription ZNF genes & repeats Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	esv3413031	chrX:76808046-76981644	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:76756600-76845600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chrX:76766400-76833600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chrX:76766800-76834000	Weak transcription	Thymus	Thymus
4	chrX:76767000-76869800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chrX:76769200-76821800	Weak transcription	Fetal Intestine Small	intestine
6	chrX:76775400-76820200	Weak transcription	Primary T cells from cord blood	blood
7	chrX:76776800-76812800	Weak transcription	Fetal Intestine Large	intestine
8	chrX:76777200-76852000	Weak transcription	HSMM	muscle
9	chrX:76778800-76818200	Weak transcription	Primary hematopoietic stem cells	blood
10	chrX:76778800-76833400	Weak transcription	Duodenum Mucosa	Duodenum
11	chrX:76779200-76820000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chrX:76783400-76851000	Weak transcription	H1 Cell Line	embryonic stem cell
13	chrX:76783800-76819400	Weak transcription	Fetal Stomach	stomach
14	chrX:76784000-76821800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chrX:76793000-76833600	Weak transcription	Fetal Thymus	thymus
16	chrX:76799200-76851000	Weak transcription	Rectal Smooth Muscle	rectum
17	chrX:76799400-76818000	Weak transcription	Fetal Lung	lung
18	chrX:76801800-76820200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chrX:76802400-76819600	Weak transcription	Primary B cells from cord blood	blood
20	chrX:76802400-76843000	Weak transcription	Hela-S3	cervix
21	chrX:76802600-76838600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chrX:76802600-76872400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chrX:76802800-76814600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chrX:76803000-76819400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chrX:76807000-76914800	Weak transcription	NHDF-Ad	bronchial
26	chrX:76807600-76821400	Weak transcription	Liver	Liver
27	chrX:76808400-76813000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chrX:76808400-76820200	Weak transcription	Left Ventricle	heart
29	chrX:76808600-76833400	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chrX:76808600-76833400	Weak transcription	Fetal Brain Female	brain
31	chrX:76808600-76853400	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chrX:76809000-76817600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chrX:76809000-76819200	Weak transcription	Fetal Muscle Leg	muscle
34	chrX:76809000-76822200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chrX:76809000-76889200	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chrX:76809200-76820000	Weak transcription	HMEC	breast
37	chrX:76809400-76827600	Weak transcription	Osteobl	bone
38	chrX:76809600-76820000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chrX:76810000-76814200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chrX:76810000-76815600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chrX:76810200-76825800	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chrX:76810400-76833400	Weak transcription	Fetal Muscle Trunk	muscle
43	chrX:76810800-76817200	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chrX:76811000-76820200	Weak transcription	Brain Anterior Caudate	brain
45	chrX:76811200-76833400	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chrX:76811400-76813200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
47	chrX:76811400-76814400	Weak transcription	GM12878-XiMat	blood
48	chrX:76811400-76877000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
49	chrX:76811600-76814800	Weak transcription	Muscle Satellite Cultured Cells	--
50	chrX:76811600-76844600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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