Variant report

Variant	rs28470973
Chromosome Location	chr16:71951357-71951358
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:7)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:7 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr16:71951353-71952199	K562	blood:	n/a	n/a
2	TCF12	chr16:71951313-71952363	SK-N-SH	brain:	n/a	n/a
3	NFIC	chr16:71951325-71952304	SK-N-SH	brain:	n/a	n/a
4	GATA3	chr16:71951300-71952300	SK-N-SH	brain:	n/a	n/a
5	PBX3	chr16:71951330-71952235	SK-N-SH	brain:	n/a	n/a
6	TCF12	chr16:71951344-71952386	SK-N-SH	brain:	n/a	n/a
7	GATA3	chr16:71951306-71952390	SK-N-SH	brain:	n/a	n/a

No data

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:71951184..71953960-chr16:72042535..72044526,2	MCF-7	breast:
2	chr16:71949724..71951506-chr16:71954411..71956772,2	MCF-7	breast:
3	chr16:71931575..71934137-chr16:71950822..71953492,2	MCF-7	breast:
4	chr16:71951326..71953519-chr16:71958185..71960042,2	K562	blood:

No data

Variant related genes	Relation type
IST1	TF binding region
ENSG00000261337	Chromatin interaction
ENSG00000182149	Chromatin interaction
ENSG00000102967	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs28539250	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9929683	0.95[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3347477	chr16:71555148-71985177	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Bivalent Enhancer 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	56 gene(s)	inside rSNPs	diseases
2	nsv948468	chr16:71727571-72651914	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
3	nsv1056439	chr16:71916498-72051144	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking 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	28 gene(s)	inside rSNPs	diseases
4	nsv1055854	chr16:71922144-72082886	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
5	nsv906893	chr16:71922663-71988728	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:71930800-71951800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr16:71931200-71956200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr16:71932600-71951800	Weak transcription	Colonic Mucosa	Colon
4	chr16:71937200-71952000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr16:71942200-71951400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr16:71942200-71951600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr16:71945200-71959000	Strong transcription	Primary T cells from cord blood	blood
8	chr16:71946000-71956000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr16:71948200-71952800	Strong transcription	Primary B cells from peripheral blood	blood
10	chr16:71948400-71953400	Strong transcription	HUES6 Cell Line	embryonic stem cell
11	chr16:71948400-71965600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr16:71948600-71952800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr16:71948600-71964000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
14	chr16:71948800-71952800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
15	chr16:71948800-71953000	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr16:71948800-71953200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr16:71948800-71966000	Strong transcription	HUES64 Cell Line	embryonic stem cell
18	chr16:71948800-71966200	Strong transcription	HUES48 Cell Line	embryonic stem cell
19	chr16:71948800-71968800	Strong transcription	Dnd41	blood
20	chr16:71948800-71969600	Strong transcription	Fetal Intestine Large	intestine
21	chr16:71949000-71952200	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr16:71949000-71952800	Strong transcription	ES-I3 Cell Line	embryonic stem cell
23	chr16:71949000-71952800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
24	chr16:71949000-71964600	Strong transcription	A549	lung
25	chr16:71949000-71966200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr16:71949200-71951800	Weak transcription	Fetal Heart	heart
27	chr16:71949200-71953000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr16:71949200-71953000	Weak transcription	Brain Angular Gyrus	brain
29	chr16:71949200-71954800	Strong transcription	Primary T cells fromperipheralblood	blood
30	chr16:71949200-71956000	Weak transcription	Small Intestine	intestine
31	chr16:71949200-71963000	Strong transcription	K562	blood
32	chr16:71949200-71966600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
33	chr16:71949200-71969600	Strong transcription	Fetal Thymus	thymus
34	chr16:71949400-71952800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr16:71949400-71952800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr16:71949400-71956600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr16:71949400-71960000	Strong transcription	Cortex derived primary cultured neurospheres	brain
38	chr16:71949400-71960400	Strong transcription	Rectal Mucosa Donor 29	rectum
39	chr16:71949400-71963600	Strong transcription	Fetal Kidney	kidney
40	chr16:71949400-71963800	Strong transcription	Fetal Lung	lung
41	chr16:71949400-71965200	Strong transcription	H1 Cell Line	embryonic stem cell
42	chr16:71949400-71965800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr16:71949600-71951400	Strong transcription	Stomach Smooth Muscle	stomach
44	chr16:71949600-71952800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr16:71949600-71952800	Strong transcription	Primary neutrophils fromperipheralblood	blood
46	chr16:71949600-71953000	Strong transcription	NHEK	skin
47	chr16:71949600-71960400	Strong transcription	Placenta	Placenta
48	chr16:71949600-71964800	Strong transcription	Primary T helper cells PMA-I stimulated	--
49	chr16:71949800-71951400	Strong transcription	NHDF-Ad	bronchial
50	chr16:71949800-71952200	Genic enhancers	Skeletal Muscle Female	skeletal muscle

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