Variant report

Variant	rs376042744
Chromosome Location	chr19:35791039-35791040
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:35785237..35787422-chr19:35789802..35791961,2	MCF-7	breast:
2	chr19:35788326..35791177-chr19:35803354..35807024,3	MCF-7	breast:
3	chr19:35757970..35762827-chr19:35790905..35794858,6	K562	blood:
4	chr19:35740050..35742142-chr19:35790657..35792710,2	K562	blood:
5	chr19:35791001..35793580-chr19:35794123..35796268,2	MCF-7	breast:
6	chr19:35788362..35791092-chr19:35794304..35796037,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000105698	Chromatin interaction
ENSG00000105699	Chromatin interaction

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	nsv432045	chr19:35556260-36520760	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	nsv1060100	chr19:35658505-36170042	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv543993	chr19:35658505-36170042	Enhancers Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
4	nsv510765	chr19:35708226-35890668	Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
5	esv2758497	chr19:35711078-35887113	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
6	esv2758758	chr19:35711078-35887113	Bivalent Enhancer Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
7	nsv911618	chr19:35734107-35807845	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
8	nsv833810	chr19:35782588-35971959	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	29 gene(s)	inside rSNPs	diseases
9	esv3329030	chr19:35786312-35791110	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	n/a
10	esv3379757	chr19:35786412-35791110	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	5 gene(s)	inside rSNPs	n/a
11	esv3447618	chr19:35786412-35791110	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	n/a
12	esv3391577	chr19:35789737-35792285	Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription	Chromatin interactive region	5 gene(s)	inside rSNPs	n/a
13	esv3380994	chr19:35789962-35792160	Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:35774800-35809600	Weak transcription	Right Atrium	heart
2	chr19:35788200-35791800	Genic enhancers	Brain Substantia Nigra	brain
3	chr19:35788800-35791400	Genic enhancers	Brain Inferior Temporal Lobe	brain
4	chr19:35788800-35795000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr19:35789200-35793400	Weak transcription	Spleen	Spleen
6	chr19:35789200-35796800	Genic enhancers	Brain Cingulate Gyrus	brain
7	chr19:35789400-35794600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr19:35789600-35796200	Weak transcription	Primary B cells from peripheral blood	blood
9	chr19:35789600-35796600	Weak transcription	Primary hematopoietic stem cells	blood
10	chr19:35789800-35791200	Weak transcription	Gastric	stomach
11	chr19:35790000-35791200	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr19:35790000-35797800	Weak transcription	Fetal Kidney	kidney
13	chr19:35790200-35791200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr19:35790200-35792200	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr19:35790200-35794000	Weak transcription	Brain Anterior Caudate	brain
16	chr19:35790200-35794200	Weak transcription	Brain Angular Gyrus	brain
17	chr19:35790200-35796400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr19:35790400-35791600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr19:35790400-35792200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr19:35790600-35791200	Active TSS	HUES6 Cell Line	embryonic stem cell
21	chr19:35790600-35791200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr19:35791000-35791200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
23	chr19:35791000-35791200	Enhancers	H1 Cell Line	embryonic stem cell
24	chr19:35791000-35791200	Weak transcription	Brain Hippocampus Middle	brain
25	chr19:35791000-35791200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
26	chr19:35791000-35791400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
27	chr19:35791000-35791400	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr19:35791000-35791400	Bivalent Enhancer	Placenta	Placenta
29	chr19:35791000-35791400	Enhancers	Pancreas	Pancrea
30	chr19:35791000-35791600	Flanking Active TSS	K562	blood

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