Variant report

Variant	rs372389961
Chromosome Location	chr19:41194466-41194467
allele	-/ACAG
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr19:41194296-41195647	GM12878	blood:	n/a	n/a
2	STAT5A	chr19:41193052-41195402	K562	blood:	n/a	n/a
3	POLR2A	chr19:41193287-41197366	IMR90	lung:	n/a	n/a
4	MAZ	chr19:41194429-41197886	IMR90	lung:	n/a	chr19:41197262-41197271 chr19:41197258-41197273 chr19:41197265-41197275 chr19:41197260-41197269 chr19:41197261-41197268 chr19:41197251-41197267
5	MXI1	chr19:41192631-41197581	IMR90	lung:	n/a	chr19:41193038-41193053 chr19:41193021-41193036
6	MXI1	chr19:41193489-41197689	SK-N-SH	brain:	n/a	n/a
7	MAX	chr19:41194363-41197840	A549	lung:	n/a	chr19:41197262-41197271 chr19:41197258-41197273 chr19:41197265-41197275 chr19:41197260-41197269 chr19:41197261-41197268 chr19:41197251-41197267 chr19:41194393-41194403
8	POLR2A	chr19:41194391-41197325	HUVEC	blood vessel:	n/a	n/a
9	MAX	chr19:41193238-41194546	K562	blood:	n/a	chr19:41193826-41193835 chr19:41193824-41193835 chr19:41193823-41193836 chr19:41193825-41193834 chr19:41193825-41193834 chr19:41193823-41193836 chr19:41193825-41193834 chr19:41193824-41193835 chr19:41194393-41194403
10	CHD1	chr19:41192595-41197591	IMR90	lung:	n/a	chr19:41196943-41196953 chr19:41196593-41196603
11	STAT5A	chr19:41193198-41195366	GM12878	blood:	n/a	n/a
12	BCL3	chr19:41194463-41195376	GM12878	blood:	n/a	n/a
13	NFATC1	chr19:41194152-41195486	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:41193561..41199772-chr19:41221208..41225709,11	K562	blood:
2	chr19:41193560..41201987-chr19:41206623..41212331,16	K562	blood:
3	chr19:41186952..41192144-chr19:41192156..41195982,8	MCF-7	breast:
4	chr19:41185972..41188881-chr19:41192870..41195079,2	K562	blood:
5	chr19:41191573..41194549-chr19:41222613..41224121,2	K562	blood:
6	chr19:41193720..41198590-chr19:41218677..41224410,19	MCF-7	breast:
7	chr19:41191702..41194594-chr19:41196563..41198200,2	MCF-7	breast:
8	chr19:41193182..41199089-chr19:41206241..41209564,9	MCF-7	breast:
9	chr19:41194241..41200533-chr19:41254244..41257966,10	K562	blood:
10	chr19:41194241..41198233-chr19:41254859..41260401,9	K562	blood:
11	chr19:41191453..41200740-chr19:41219595..41226457,20	MCF-7	breast:

Variant related genes	Relation type
NUMBL	TF binding region
ENSG00000123815	Chromatin interaction
ENSG00000077312	Chromatin interaction
ENSG00000188493	Chromatin interaction
ENSG00000086544	Chromatin interaction
ENSG00000105245	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1830682	chr19:40880127-41270055	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
2	nsv911723	chr19:41075990-41195279	Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv911727	chr19:41111069-41200511	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
4	nsv911728	chr19:41111069-41211056	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
5	esv1800615	chr19:41127465-41270055	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
6	nsv1058707	chr19:41146147-41200820	Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	20 gene(s)	inside rSNPs	diseases
7	nsv1067017	chr19:41185992-41231251	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	36 gene(s)	inside rSNPs	diseases
8	esv3432319	chr19:41190112-41196510	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
9	esv3391681	chr19:41192212-41196610	Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
10	nsv820299	chr19:41193264-41195994	Active TSS Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41169800-41195400	Weak transcription	Psoas Muscle	Psoas
2	chr19:41175800-41196000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr19:41176000-41195200	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr19:41176200-41195600	Weak transcription	Small Intestine	intestine
5	chr19:41179200-41194800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr19:41179200-41195800	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr19:41179800-41196000	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr19:41181200-41195200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr19:41184600-41194800	Weak transcription	Fetal Thymus	thymus
10	chr19:41187000-41195600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr19:41187200-41195200	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr19:41187200-41195800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr19:41187400-41195200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr19:41187600-41195800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr19:41188800-41195800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr19:41191800-41194800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr19:41191800-41194800	Weak transcription	HMEC	breast
18	chr19:41191800-41195600	Weak transcription	Primary hematopoietic stem cells	blood
19	chr19:41192000-41194800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr19:41192000-41195000	Weak transcription	Fetal Intestine Large	intestine
21	chr19:41192000-41195200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr19:41192000-41195200	Weak transcription	Brain Substantia Nigra	brain
23	chr19:41192200-41194600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr19:41192600-41194600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr19:41192600-41195200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr19:41192600-41195200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr19:41192600-41195800	Weak transcription	Liver	Liver
28	chr19:41192600-41196000	Enhancers	Primary B cells from peripheral blood	blood
29	chr19:41192600-41196000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr19:41192800-41194600	Enhancers	Placenta	Placenta
31	chr19:41192800-41194800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr19:41192800-41194800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr19:41192800-41194800	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr19:41192800-41194800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr19:41192800-41194800	Weak transcription	Dnd41	blood
36	chr19:41192800-41195000	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr19:41192800-41195000	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr19:41192800-41195200	Enhancers	Primary B cells from cord blood	blood
39	chr19:41192800-41195200	Enhancers	Sigmoid Colon	Sigmoid Colon
40	chr19:41192800-41195600	Weak transcription	Thymus	Thymus
41	chr19:41193000-41194600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr19:41193000-41194800	Enhancers	NHEK	skin
43	chr19:41193000-41195000	Enhancers	Right Atrium	heart
44	chr19:41193200-41194600	Enhancers	Esophagus	oesophagus
45	chr19:41193200-41194600	Genic enhancers	A549	lung
46	chr19:41193200-41194800	Weak transcription	Primary T cells from cord blood	blood
47	chr19:41193200-41194800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr19:41193200-41194800	Weak transcription	Fetal Intestine Small	intestine
49	chr19:41193200-41195000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr19:41193200-41195000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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