Variant report

Variant	rs16955210
Chromosome Location	chr16:81411495-81411496
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:81399271..81400806-chr16:81410047..81412446,2	K562	blood:
2	chr16:81402764..81405493-chr16:81409051..81411986,2	K562	blood:
3	chr16:81410198..81413162-chr16:81434374..81435892,2	MCF-7	breast:
4	chr16:81406782..81409533-chr16:81410750..81415931,4	K562	blood:
5	chr16:81348439..81350259-chr16:81409837..81412238,3	MCF-7	breast:
6	chr16:81411383..81414632-chr16:81425808..81428318,4	MCF-7	breast:
7	chr16:81402764..81406733-chr16:81409051..81413423,3	K562	blood:
8	chr16:81409751..81411946-chr16:81415475..81417498,3	MCF-7	breast:
9	chr16:81409982..81413670-chr16:81414350..81417251,3	K562	blood:
10	chr16:81411221..81413980-chr16:81432249..81433979,2	MCF-7	breast:
11	chr16:81409982..81414172-chr16:81414350..81416327,5	K562	blood:

No data

Variant related genes	Relation type
ENSG00000261609	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1075352	0.85[EUR][1000 genomes]
rs1075353	1.00[TSI][hapmap];0.85[EUR][1000 genomes]
rs11643220	1.00[GIH][hapmap]
rs11861886	1.00[GIH][hapmap];1.00[TSI][hapmap]
rs11862778	1.00[GIH][hapmap];1.00[TSI][hapmap]
rs11866374	1.00[GIH][hapmap];1.00[TSI][hapmap]
rs16955031	1.00[GIH][hapmap];0.83[TSI][hapmap]
rs16955059	1.00[GIH][hapmap];0.83[TSI][hapmap]
rs16955067	1.00[GIH][hapmap];0.83[TSI][hapmap]
rs16955109	1.00[GIH][hapmap];0.83[TSI][hapmap]
rs16955113	1.00[GIH][hapmap];0.83[TSI][hapmap]
rs16955203	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];1.00[TSI][hapmap]
rs2290949	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];1.00[ASN][1000 genomes]
rs28561847	0.85[EUR][1000 genomes]
rs4386128	0.96[ASN][1000 genomes]
rs9935105	1.00[GIH][hapmap];0.83[TSI][hapmap]

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	nsv532569	chr16:80980356-81700149	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
2	nsv1058519	chr16:81177767-81735333	Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
3	nsv948448	chr16:81198147-81906766	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	37 gene(s)	inside rSNPs	diseases
4	nsv1061359	chr16:81349826-81471867	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
5	nsv542992	chr16:81349826-81471867	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:81382400-81418400	Weak transcription	Small Intestine	intestine
2	chr16:81384200-81434600	Weak transcription	NHLF	lung
3	chr16:81384200-81437400	Weak transcription	Fetal Brain Male	brain
4	chr16:81385600-81418200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr16:81386400-81424200	Weak transcription	Psoas Muscle	Psoas
6	chr16:81387000-81428600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr16:81387600-81415200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr16:81391200-81417600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr16:81392000-81428400	Weak transcription	Fetal Heart	heart
10	chr16:81397400-81426400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr16:81399000-81417400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr16:81399200-81431000	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr16:81399600-81413000	Weak transcription	Primary neutrophils fromperipheralblood	blood
14	chr16:81399800-81414000	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr16:81400000-81427200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr16:81400000-81434600	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr16:81401400-81411800	Strong transcription	Rectal Mucosa Donor 31	rectum
18	chr16:81402000-81415000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr16:81402200-81418000	Weak transcription	Brain Germinal Matrix	brain
20	chr16:81404400-81417200	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr16:81405200-81418400	Weak transcription	Right Atrium	heart
22	chr16:81406600-81423800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr16:81408200-81412000	Strong transcription	Fetal Stomach	stomach
24	chr16:81408800-81412000	Strong transcription	Fetal Intestine Small	intestine
25	chr16:81409000-81411800	Strong transcription	Duodenum Mucosa	Duodenum
26	chr16:81409000-81413400	Strong transcription	HUES48 Cell Line	embryonic stem cell
27	chr16:81409200-81411800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr16:81409200-81412200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr16:81409200-81412400	Strong transcription	Fetal Intestine Large	intestine
30	chr16:81409200-81413200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
31	chr16:81409400-81411800	Strong transcription	Brain Cingulate Gyrus	brain
32	chr16:81409400-81412000	Strong transcription	Stomach Smooth Muscle	stomach
33	chr16:81409400-81412400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr16:81409400-81412400	Strong transcription	Duodenum Smooth Muscle	Duodenum
35	chr16:81409400-81412400	Strong transcription	HepG2	liver
36	chr16:81409400-81415400	Strong transcription	Dnd41	blood
37	chr16:81409400-81415800	Strong transcription	Primary T cells from cord blood	blood
38	chr16:81409600-81411600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr16:81409600-81415400	Strong transcription	HUES64 Cell Line	embryonic stem cell
40	chr16:81409600-81415600	Strong transcription	Monocytes-CD14+_RO01746	blood
41	chr16:81409800-81412000	Strong transcription	Sigmoid Colon	Sigmoid Colon
42	chr16:81409800-81412200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr16:81409800-81412600	Strong transcription	Cortex derived primary cultured neurospheres	brain
44	chr16:81409800-81413000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr16:81409800-81413000	Strong transcription	Liver	Liver
46	chr16:81409800-81415800	Strong transcription	Rectal Mucosa Donor 29	rectum
47	chr16:81410200-81411800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr16:81410200-81412000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr16:81410200-81412000	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr16:81410200-81412400	Strong transcription	Skeletal Muscle Male	skeletal muscle

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