Variant report

Variant	rs558022236
Chromosome Location	chr18:39622561-39622562
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1066869	chr18:38742896-39680723	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv543685	chr18:38742896-39680723	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv949609	chr18:39126941-40070286	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer 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
4	nsv431979	chr18:39255558-39696452	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
5	nsv1066029	chr18:39322920-39623625	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv543686	chr18:39322920-39623625	Strong transcription Weak transcription Active TSS Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv909566	chr18:39327962-39688452	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
8	esv34153	chr18:39398768-39872265	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
9	nsv909567	chr18:39470190-39652939	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
10	nsv909568	chr18:39491873-39768746	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
11	nsv1057988	chr18:39618253-39713904	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
12	nsv1065792	chr18:39619676-39711798	Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
13	nsv1057790	chr18:39621947-39705550	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
14	esv2762006	chr18:39621947-39713916	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
15	nsv1063952	chr18:39621947-39718600	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:39536800-39633600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr18:39548400-39670000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr18:39572000-39654400	Weak transcription	Colonic Mucosa	Colon
4	chr18:39578400-39663200	Weak transcription	Fetal Heart	heart
5	chr18:39581000-39647400	Weak transcription	Spleen	Spleen
6	chr18:39581000-39666200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr18:39585000-39646000	Weak transcription	Pancreas	Pancrea
8	chr18:39585000-39658600	Weak transcription	Small Intestine	intestine
9	chr18:39585400-39627600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr18:39586600-39647400	Weak transcription	Thymus	Thymus
11	chr18:39590600-39668000	Weak transcription	Esophagus	oesophagus
12	chr18:39592200-39629400	Weak transcription	Fetal Brain Female	brain
13	chr18:39594600-39638800	Weak transcription	K562	blood
14	chr18:39599000-39646000	Weak transcription	Psoas Muscle	Psoas
15	chr18:39601600-39668200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr18:39606200-39628200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr18:39607400-39626000	Strong transcription	Primary neutrophils fromperipheralblood	blood
18	chr18:39607600-39634600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr18:39608600-39627400	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr18:39608800-39631400	Strong transcription	Primary T helper cells fromperipheralblood	blood
21	chr18:39609000-39625600	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr18:39609000-39628600	Strong transcription	HUES64 Cell Line	embryonic stem cell
23	chr18:39609200-39624000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr18:39609200-39624200	Strong transcription	Duodenum Smooth Muscle	Duodenum
25	chr18:39609200-39625800	Strong transcription	Primary T cells from cord blood	blood
26	chr18:39609200-39626000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr18:39609200-39626600	Strong transcription	Primary T helper cells PMA-I stimulated	--
28	chr18:39609200-39631400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr18:39609200-39631600	Strong transcription	Primary B cells from peripheral blood	blood
30	chr18:39609400-39626200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr18:39609800-39630400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr18:39610200-39626200	Strong transcription	Liver	Liver
33	chr18:39610600-39628000	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr18:39611600-39627600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr18:39612200-39623000	Weak transcription	Fetal Intestine Small	intestine
36	chr18:39612200-39647400	Weak transcription	Aorta	Aorta
37	chr18:39612200-39666400	Weak transcription	Gastric	stomach
38	chr18:39612200-39669800	Weak transcription	Fetal Stomach	stomach
39	chr18:39612200-39670000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr18:39612400-39624000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr18:39613400-39626200	Strong transcription	Duodenum Mucosa	Duodenum
42	chr18:39613800-39631200	Strong transcription	Primary T cells fromperipheralblood	blood
43	chr18:39613800-39631400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr18:39614200-39624000	Strong transcription	Rectal Mucosa Donor 31	rectum
45	chr18:39614400-39623000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr18:39614400-39631400	Strong transcription	Primary B cells from cord blood	blood
47	chr18:39615000-39649600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
48	chr18:39615400-39663400	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr18:39617000-39623800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr18:39617200-39622800	Strong transcription	HUES6 Cell Line	embryonic stem cell

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