Variant report

Variant	rs8069155
Chromosome Location	chr17:37668488-37668489
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	chr17:37617543..37619739-chr17:37667912..37670239,2	K562	blood:
2	chr17:37662451..37664162-chr17:37667239..37668949,2	K562	blood:

Variant related genes	Relation type
ENSG00000167258	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11656614	1.00[CHD][hapmap]
rs34518049	1.00[CHD][hapmap]
rs35829705	1.00[CHD][hapmap]

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	nsv932024	chr17:37192290-37850932	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	92 gene(s)	inside rSNPs	diseases
2	nsv1057655	chr17:37333956-37732451	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers 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	72 gene(s)	inside rSNPs	diseases
3	nsv1066033	chr17:37333956-37795617	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers 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	78 gene(s)	inside rSNPs	diseases
4	nsv543340	chr17:37333956-37795617	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	78 gene(s)	inside rSNPs	diseases
5	nsv908204	chr17:37349655-37682657	Genic enhancers Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
6	nsv1061951	chr17:37442228-37770903	Bivalent Enhancer Strong transcription Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
7	nsv543341	chr17:37442228-37770903	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
8	esv1825702	chr17:37487168-37876767	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
9	nsv532712	chr17:37521822-37768345	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
10	nsv1063848	chr17:37575622-37707592	Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	32 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	chr17:37624000-37680400	Weak transcription	Fetal Brain Male	brain
2	chr17:37624000-37690600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr17:37626600-37690600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr17:37628400-37682200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr17:37634200-37688600	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr17:37635200-37680600	Weak transcription	Fetal Heart	heart
7	chr17:37636200-37685800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
8	chr17:37640400-37691000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr17:37642000-37689600	Strong transcription	Fetal Thymus	thymus
10	chr17:37642600-37680400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr17:37643200-37688600	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr17:37643400-37689000	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr17:37643800-37668800	Strong transcription	Fetal Stomach	stomach
14	chr17:37644000-37685200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr17:37644400-37688200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr17:37645000-37669200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr17:37645000-37689000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr17:37645000-37689600	Strong transcription	Primary T cells fromperipheralblood	blood
19	chr17:37645400-37685600	Strong transcription	Fetal Muscle Trunk	muscle
20	chr17:37645600-37689200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr17:37646000-37684800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr17:37646000-37688400	Strong transcription	Primary neutrophils fromperipheralblood	blood
23	chr17:37646400-37668800	Strong transcription	Sigmoid Colon	Sigmoid Colon
24	chr17:37646400-37688200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr17:37646400-37688600	Strong transcription	Fetal Intestine Large	intestine
26	chr17:37646400-37689800	Strong transcription	HUES6 Cell Line	embryonic stem cell
27	chr17:37646600-37668600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr17:37646600-37687200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr17:37646600-37688200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr17:37646600-37688800	Strong transcription	Liver	Liver
31	chr17:37646600-37689600	Strong transcription	Dnd41	blood
32	chr17:37646600-37690200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr17:37646800-37682200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr17:37646800-37683800	Strong transcription	Rectal Mucosa Donor 29	rectum
35	chr17:37646800-37685600	Strong transcription	Duodenum Smooth Muscle	Duodenum
36	chr17:37646800-37686200	Strong transcription	Adipose Nuclei	Adipose
37	chr17:37646800-37688200	Strong transcription	Primary T helper cells PMA-I stimulated	--
38	chr17:37646800-37688600	Strong transcription	Primary T helper cells fromperipheralblood	blood
39	chr17:37646800-37688600	Strong transcription	Placenta	Placenta
40	chr17:37646800-37689000	Strong transcription	HUES48 Cell Line	embryonic stem cell
41	chr17:37646800-37689000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr17:37646800-37689000	Strong transcription	Primary B cells from peripheral blood	blood
43	chr17:37646800-37689200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
44	chr17:37646800-37689200	Strong transcription	HepG2	liver
45	chr17:37646800-37690000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr17:37647400-37668800	Strong transcription	Spleen	Spleen
47	chr17:37649000-37668800	Strong transcription	Brain Germinal Matrix	brain
48	chr17:37649200-37669600	Strong transcription	Fetal Brain Female	brain
49	chr17:37653800-37688400	Strong transcription	Stomach Smooth Muscle	stomach
50	chr17:37654000-37675000	Strong transcription	Primary hematopoietic stem cells	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links