Variant report

Variant	rs1847528
Chromosome Location	chr15:78735100-78735101
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	chr15:78734814..78737530-chr15:78775565..78778054,2	K562	blood:
2	chr15:78733161..78735105-chr15:78831790..78834378,2	K562	blood:

Variant related genes	Relation type
ENSG00000041357	Chromatin interaction
ENSG00000136381	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11072767	0.93[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12441256	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2036530	0.86[YRI][hapmap]
rs2036531	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2055587	1.00[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2230940	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2568484	1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2568486	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2568491	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2568492	0.93[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2656060	1.00[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2656064	0.95[AFR][1000 genomes]
rs2656066	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2656067	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2938672	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2958720	1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4886569	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4886570	1.00[AMR][1000 genomes]
rs4887060	1.00[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6495302	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7168018	1.00[AMR][1000 genomes]
rs73463009	1.00[AMR][1000 genomes]
rs73463024	1.00[AMR][1000 genomes]
rs73463098	1.00[AMR][1000 genomes]
rs8023649	0.85[YRI][hapmap]
rs8026728	1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs905741	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs905742	1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9788758	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9972290	0.93[YRI][hapmap];0.89[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529491	chr15:77932659-78751516	Genic enhancers Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS 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 miRNA target site	80 gene(s)	inside rSNPs	diseases
2	nsv917303	chr15:78491050-79205255	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS 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	122 gene(s)	inside rSNPs	diseases
3	nsv833063	chr15:78605215-78754945	Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78731400-78745400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr15:78731600-78736800	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
3	chr15:78731600-78740600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr15:78731600-78742800	Weak transcription	Esophagus	oesophagus
5	chr15:78731600-78742800	Weak transcription	Right Ventricle	heart
6	chr15:78731600-78756400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr15:78731600-78760200	Weak transcription	Aorta	Aorta
8	chr15:78731800-78738200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr15:78731800-78738200	Weak transcription	Colonic Mucosa	Colon
10	chr15:78731800-78740400	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr15:78731800-78740800	Weak transcription	Stomach Mucosa	stomach
12	chr15:78732000-78735200	Genic enhancers	Fetal Lung	lung
13	chr15:78732000-78736000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr15:78732200-78735200	Genic enhancers	Primary T cells from cord blood	blood
15	chr15:78732200-78735800	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr15:78732200-78735800	Genic enhancers	Fetal Intestine Large	intestine
17	chr15:78732200-78736000	Strong transcription	H1 Cell Line	embryonic stem cell
18	chr15:78732200-78737000	Genic enhancers	Primary T helper cells PMA-I stimulated	--
19	chr15:78732200-78738400	Weak transcription	Brain Substantia Nigra	brain
20	chr15:78732200-78738800	Genic enhancers	Primary T helper cells fromperipheralblood	blood
21	chr15:78732200-78739000	Strong transcription	Placenta	Placenta
22	chr15:78732200-78739600	Strong transcription	HUES48 Cell Line	embryonic stem cell
23	chr15:78732200-78739800	Strong transcription	HUES6 Cell Line	embryonic stem cell
24	chr15:78732200-78740400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
25	chr15:78732200-78740400	Strong transcription	Fetal Muscle Trunk	muscle
26	chr15:78732200-78741800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr15:78732200-78742800	Strong transcription	HUES64 Cell Line	embryonic stem cell
28	chr15:78732200-78747600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr15:78732200-78799400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr15:78732400-78735200	Strong transcription	HSMMtube	muscle
31	chr15:78732400-78735400	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr15:78732400-78735800	Genic enhancers	Duodenum Mucosa	Duodenum
33	chr15:78732400-78739600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr15:78732400-78740200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr15:78732400-78740600	Strong transcription	Fetal Stomach	stomach
36	chr15:78732400-78740800	Strong transcription	Primary neutrophils fromperipheralblood	blood
37	chr15:78732400-78742800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
38	chr15:78732400-78744400	Weak transcription	Fetal Kidney	kidney
39	chr15:78732600-78735200	Genic enhancers	A549	lung
40	chr15:78732600-78739400	Strong transcription	Osteobl	bone
41	chr15:78732800-78736000	Genic enhancers	Adipose Nuclei	Adipose
42	chr15:78732800-78740000	Strong transcription	Primary B cells from peripheral blood	blood
43	chr15:78732800-78758600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr15:78733000-78735600	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr15:78733200-78736000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr15:78733200-78737600	Strong transcription	NHDF-Ad	bronchial
47	chr15:78733200-78738000	Weak transcription	Psoas Muscle	Psoas
48	chr15:78733200-78739200	Strong transcription	NH-A	brain
49	chr15:78733200-78742200	Strong transcription	Fetal Thymus	thymus
50	chr15:78733400-78735200	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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