Variant report

Variant	rs61467203
Chromosome Location	chr19:21925770-21925771
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:21925492..21929369-chr19:21945562..21949951,4	K562	blood:
2	chr19:21922579..21924244-chr19:21924294..21926193,2	K562	blood:

Variant related genes	Relation type
ENSG00000197020	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs57484704	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58560061	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7250493	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv911422	chr19:21752009-21973929	ZNF genes & repeats Strong transcription Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	esv3441368	chr19:21781459-22182822	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	esv3339694	chr19:21781479-22182792	Enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv1063115	chr19:21782104-22528039	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
5	nsv458525	chr19:21796943-22019697	Weak transcription ZNF genes & repeats Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv578969	chr19:21796943-22019697	ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
7	esv3392559	chr19:21798396-21965956	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv911424	chr19:21798441-22471156	Strong transcription Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
9	nsv833783	chr19:21821406-21991838	ZNF genes & repeats Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	esv1815274	chr19:21825750-21981855	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	nsv911425	chr19:21841379-22338142	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
12	nsv911426	chr19:21892040-21973929	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
13	nsv911427	chr19:21900898-21960407	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	nsv833784	chr19:21902647-22037153	ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
15	nsv578970	chr19:21906655-21973929	Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
16	nsv961193	chr19:21911308-21950500	Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
17	esv3342879	chr19:21913482-21968857	Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr19:21905600-21947200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr19:21906200-21927600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr19:21906200-21949200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr19:21908800-21948800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
5	chr19:21909200-21946000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr19:21911200-21935600	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr19:21911400-21930000	Weak transcription	Right Ventricle	heart
8	chr19:21913400-21941200	Weak transcription	NHDF-Ad	bronchial
9	chr19:21914000-21934600	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
10	chr19:21916200-21926800	ZNF genes & repeats	Fetal Brain Female	brain
11	chr19:21916600-21929800	Weak transcription	Brain Cingulate Gyrus	brain
12	chr19:21916800-21926800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr19:21916800-21944600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr19:21917200-21934200	Weak transcription	Colon Smooth Muscle	Colon
15	chr19:21917400-21933400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr19:21918000-21941200	Weak transcription	Brain Angular Gyrus	brain
17	chr19:21918000-21948400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr19:21918800-21934400	Weak transcription	NH-A	brain
19	chr19:21919400-21929200	Weak transcription	K562	blood
20	chr19:21919400-21943800	Strong transcription	Dnd41	blood
21	chr19:21919600-21930200	Weak transcription	Brain Substantia Nigra	brain
22	chr19:21919600-21933800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr19:21919800-21932600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr19:21920000-21927200	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr19:21920000-21927800	Strong transcription	Duodenum Smooth Muscle	Duodenum
26	chr19:21920200-21926600	Weak transcription	NHEK	skin
27	chr19:21920200-21933600	Weak transcription	HUVEC	blood vessel
28	chr19:21920200-21935600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr19:21920200-21949200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr19:21920400-21948600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr19:21920800-21949200	Weak transcription	NHLF	lung
32	chr19:21921200-21926600	Strong transcription	HUES48 Cell Line	embryonic stem cell
33	chr19:21921200-21926600	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr19:21921400-21926800	Strong transcription	H1 Cell Line	embryonic stem cell
35	chr19:21921400-21927000	Strong transcription	Adipose Nuclei	Adipose
36	chr19:21921600-21927600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
37	chr19:21921600-21930400	Weak transcription	Rectal Smooth Muscle	rectum
38	chr19:21921600-21932400	Strong transcription	Cortex derived primary cultured neurospheres	brain
39	chr19:21921800-21927600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr19:21921800-21948600	Weak transcription	Stomach Mucosa	stomach
41	chr19:21922000-21929600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr19:21922000-21929800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr19:21922000-21933600	Weak transcription	Spleen	Spleen
44	chr19:21922000-21938200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr19:21922000-21941400	Weak transcription	Stomach Smooth Muscle	stomach
46	chr19:21922000-21949400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr19:21922000-21949400	Weak transcription	HSMMtube	muscle
48	chr19:21922200-21934000	Weak transcription	Brain Hippocampus Middle	brain
49	chr19:21922400-21926200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr19:21922400-21927800	Strong transcription	HUES64 Cell Line	embryonic stem cell

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