Variant report

Variant	rs236428
Chromosome Location	chr6:36733474-36733475
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:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:36731587..36733687-chr6:36952350..36954273,2	MCF-7	breast:
2	chr6:36731859..36733721-chr6:36744461..36746494,2	MCF-7	breast:
3	chr6:36724584..36727925-chr6:36730250..36733668,5	MCF-7	breast:
4	chr6:36731113..36733577-chr6:36757707..36759344,2	MCF-7	breast:
5	chr6:36726753..36730019-chr6:36730894..36734737,3	K562	blood:
6	chr6:36732942..36735975-chr6:36816237..36818800,3	MCF-7	breast:
7	chr6:36732357..36734281-chr6:36851932..36853693,2	MCF-7	breast:
8	chr6:36723524..36726204-chr6:36732546..36734917,2	K562	blood:
9	chr6:36733415..36734583-chr6:36985207..36986995,7	MCF-7	breast:
10	chr6:36732636..36735426-chr6:36737432..36739720,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000198663	Chromatin interaction
ENSG00000124772	Chromatin interaction
ENSG00000137409	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs236422	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs236425	0.91[CHB][hapmap];1.00[JPT][hapmap];0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs236427	0.87[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs236429	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs236430	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs236432	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs236433	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs236441	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs763046	0.81[CHB][hapmap]
rs86707	0.93[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9380597	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023171	chr6:36686935-36880899	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv538202	chr6:36686935-36880899	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv1033261	chr6:36687424-36837315	Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv524053	chr6:36695223-36747406	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:36722800-36748200	Weak transcription	Fetal Kidney	kidney
2	chr6:36723800-36736200	Weak transcription	Right Atrium	heart
3	chr6:36724000-36736200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr6:36724800-36734400	Weak transcription	Right Ventricle	heart
5	chr6:36725600-36733800	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr6:36725800-36735400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr6:36726000-36736200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr6:36726800-36733800	Weak transcription	Pancreas	Pancrea
9	chr6:36727000-36733800	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr6:36727200-36734000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr6:36727200-36736400	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr6:36727400-36735200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr6:36727400-36736200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr6:36729600-36733600	Weak transcription	Brain Anterior Caudate	brain
15	chr6:36732000-36733600	Enhancers	H1 Cell Line	embryonic stem cell
16	chr6:36732000-36733800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr6:36732200-36733600	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr6:36732200-36733600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr6:36732400-36733600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr6:36732400-36733600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr6:36732400-36734200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr6:36732400-36734600	Enhancers	Fetal Brain Male	brain
23	chr6:36732400-36738600	Enhancers	Fetal Muscle Leg	muscle
24	chr6:36732600-36734200	Enhancers	Ovary	ovary
25	chr6:36732600-36734600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:36732800-36733600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr6:36732800-36734400	Enhancers	Fetal Brain Female	brain
28	chr6:36732800-36734600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr6:36732800-36738800	Enhancers	Primary B cells from cord blood	blood
30	chr6:36732800-36739000	Enhancers	Primary B cells from peripheral blood	blood
31	chr6:36732800-36739600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr6:36732800-36739800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr6:36733000-36733800	Enhancers	Colonic Mucosa	Colon
34	chr6:36733000-36734000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr6:36733000-36734000	Enhancers	Spleen	Spleen
36	chr6:36733000-36734200	Enhancers	Brain Substantia Nigra	brain
37	chr6:36733000-36734400	Enhancers	Brain Cingulate Gyrus	brain
38	chr6:36733000-36734400	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr6:36733000-36734400	Enhancers	Placenta	Placenta
40	chr6:36733000-36734400	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr6:36733000-36734400	Enhancers	Stomach Smooth Muscle	stomach
42	chr6:36733000-36734600	Enhancers	Brain Hippocampus Middle	brain
43	chr6:36733000-36734600	Enhancers	Fetal Thymus	thymus
44	chr6:36733200-36733600	Enhancers	Brain Germinal Matrix	brain
45	chr6:36733200-36733800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr6:36733200-36733800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr6:36733200-36733800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr6:36733200-36734000	Genic enhancers	Cortex derived primary cultured neurospheres	brain
49	chr6:36733200-36734000	Enhancers	Fetal Stomach	stomach
50	chr6:36733200-36734000	Enhancers	NHDF-Ad	bronchial

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