Variant report

Variant	rs8134047
Chromosome Location	chr21:46375916-46375917
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr21:46348854..46378176-chr21:46489799..46500436,75	K562	blood:
2	chr21:46374315..46377421-chr21:46386112..46389411,4	K562	blood:
3	chr21:46363747..46379047-chr21:46484156..46498795,67	K562	blood:
4	chr21:46368791..46372085-chr21:46374524..46378071,4	MCF-7	breast:
5	chr21:46373821..46376741-chr21:46385880..46388857,2	MCF-7	breast:
6	chr21:46373591..46376395-chr21:46393601..46395111,2	MCF-7	breast:
7	chr21:46374813..46377391-chr21:46493131..46495030,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000197381	Chromatin interaction
ENSG00000235374	Chromatin interaction
ENSG00000268856	Chromatin interaction

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs2838748	1.00[EUR][1000 genomes]
rs55633511	1.00[EUR][1000 genomes]
rs55705724	1.00[EUR][1000 genomes]
rs55775492	1.00[EUR][1000 genomes]
rs55989453	1.00[EUR][1000 genomes]
rs56283815	1.00[EUR][1000 genomes]
rs56297608	1.00[EUR][1000 genomes]
rs57677709	1.00[EUR][1000 genomes]
rs58184639	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58929845	1.00[EUR][1000 genomes]
rs58951027	1.00[EUR][1000 genomes]
rs58977945	1.00[EUR][1000 genomes]
rs59163354	1.00[EUR][1000 genomes]
rs59226008	1.00[EUR][1000 genomes]
rs59267673	1.00[EUR][1000 genomes]
rs59281465	1.00[EUR][1000 genomes]
rs59318141	1.00[EUR][1000 genomes]
rs59444929	1.00[EUR][1000 genomes]
rs59573927	1.00[EUR][1000 genomes]
rs59730475	1.00[EUR][1000 genomes]
rs60088468	1.00[EUR][1000 genomes]
rs60725487	1.00[EUR][1000 genomes]
rs7276874	1.00[EUR][1000 genomes]
rs7277529	1.00[EUR][1000 genomes]
rs7278296	1.00[EUR][1000 genomes]
rs7278617	1.00[EUR][1000 genomes]
rs7283338	1.00[EUR][1000 genomes]
rs7283630	1.00[EUR][1000 genomes]
rs73376557	1.00[EUR][1000 genomes]
rs73906965	1.00[EUR][1000 genomes]
rs73906966	1.00[EUR][1000 genomes]
rs73906968	1.00[EUR][1000 genomes]
rs73906970	1.00[EUR][1000 genomes]
rs73906971	1.00[EUR][1000 genomes]
rs73906974	1.00[EUR][1000 genomes]
rs73906981	1.00[EUR][1000 genomes]
rs73906983	1.00[EUR][1000 genomes]
rs73906984	1.00[EUR][1000 genomes]
rs73906985	1.00[EUR][1000 genomes]
rs73907002	1.00[EUR][1000 genomes]
rs73909903	1.00[EUR][1000 genomes]
rs73909905	1.00[EUR][1000 genomes]
rs73909906	1.00[EUR][1000 genomes]
rs73909911	1.00[EUR][1000 genomes]
rs8127517	1.00[EUR][1000 genomes]
rs8129398	1.00[EUR][1000 genomes]
rs8130143	1.00[EUR][1000 genomes]
rs8130435	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916258	chr21:45995986-46624705	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	102 gene(s)	inside rSNPs	diseases
2	nsv1056513	chr21:46254075-46442759	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription 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	32 gene(s)	inside rSNPs	diseases
3	nsv913969	chr21:46279505-46472929	Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv913970	chr21:46305175-46487831	Bivalent Enhancer Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv913974	chr21:46306161-46430792	Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
6	nsv913975	chr21:46306161-46459432	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv913976	chr21:46306161-46487831	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh 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	26 gene(s)	inside rSNPs	diseases
8	nsv834110	chr21:46316183-46505151	Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
9	nsv1064518	chr21:46317690-46413159	Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
10	nsv913977	chr21:46335761-46454391	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
11	nsv913978	chr21:46335761-46466674	Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
12	nsv913979	chr21:46335761-46472929	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
13	nsv913980	chr21:46337565-46454391	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Weak transcription 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 lncRNA	23 gene(s)	inside rSNPs	diseases
14	nsv913981	chr21:46344426-46408790	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
15	nsv913982	chr21:46344426-46430792	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription 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	21 gene(s)	inside rSNPs	diseases
16	nsv913984	chr21:46344426-46435610	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
17	nsv913983	chr21:46344426-46440385	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
18	nsv913985	chr21:46344426-46448142	Weak transcription Genic enhancers Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
19	nsv913986	chr21:46344426-46466674	Strong transcription Enhancers 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	23 gene(s)	inside rSNPs	diseases
20	nsv913987	chr21:46344426-46472929	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
21	nsv913988	chr21:46356816-46408790	Genic enhancers Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
22	nsv913989	chr21:46356816-46430792	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
23	nsv913990	chr21:46356816-46448142	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
24	nsv913991	chr21:46356816-46472929	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
25	nsv544480	chr21:46364856-46413159	Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Bivalent Enhancer 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	13 gene(s)	inside rSNPs	diseases
26	nsv913992	chr21:46366547-46408790	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:46361000-46384200	Weak transcription	Fetal Kidney	kidney
2	chr21:46361400-46384600	Weak transcription	Small Intestine	intestine
3	chr21:46361600-46378000	Weak transcription	Stomach Mucosa	stomach
4	chr21:46361600-46378200	Weak transcription	NHDF-Ad	bronchial
5	chr21:46361600-46389200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr21:46362000-46382800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr21:46362400-46383200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
8	chr21:46363000-46382400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
9	chr21:46363400-46377400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr21:46363600-46378000	Strong transcription	Fetal Intestine Large	intestine
11	chr21:46363600-46378000	Strong transcription	NHLF	lung
12	chr21:46363600-46378600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr21:46364200-46391400	Strong transcription	Dnd41	blood
14	chr21:46364400-46377200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr21:46364800-46380400	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr21:46365600-46378200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr21:46366600-46376600	Weak transcription	Osteobl	bone
18	chr21:46367600-46376400	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr21:46367600-46382200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr21:46367800-46377600	Weak transcription	Ovary	ovary
21	chr21:46367800-46378000	Weak transcription	HUVEC	blood vessel
22	chr21:46368200-46376200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr21:46368800-46380600	Enhancers	Fetal Heart	heart
24	chr21:46368800-46382600	Genic enhancers	Fetal Muscle Leg	muscle
25	chr21:46369000-46383000	Genic enhancers	Fetal Muscle Trunk	muscle
26	chr21:46369800-46377800	Strong transcription	Gastric	stomach
27	chr21:46370000-46376600	Weak transcription	Brain Hippocampus Middle	brain
28	chr21:46370000-46378400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr21:46370000-46378400	Weak transcription	Brain Substantia Nigra	brain
30	chr21:46370000-46380200	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr21:46370000-46384200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr21:46370000-46385000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr21:46370200-46378000	Strong transcription	Fetal Intestine Small	intestine
34	chr21:46370200-46380800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr21:46370200-46382600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr21:46370200-46383400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr21:46370200-46383600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
38	chr21:46370400-46377400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr21:46370400-46378000	Strong transcription	Thymus	Thymus
40	chr21:46370600-46376800	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr21:46370600-46378400	Strong transcription	Fetal Thymus	thymus
42	chr21:46370600-46383000	Strong transcription	Primary T helper cells PMA-I stimulated	--
43	chr21:46370600-46384800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr21:46371000-46381200	Strong transcription	NHEK	skin
45	chr21:46371000-46382600	Strong transcription	Primary T helper cells fromperipheralblood	blood
46	chr21:46371000-46382800	Strong transcription	H1 Cell Line	embryonic stem cell
47	chr21:46371000-46383000	Strong transcription	HUES6 Cell Line	embryonic stem cell
48	chr21:46371000-46383200	Strong transcription	Primary T cells from cord blood	blood
49	chr21:46371200-46378600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr21:46371200-46384400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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