Variant report

Variant	rs7170877
Chromosome Location	chr15:77832019-77832020
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:77795830..77799057-chr15:77830706..77834217,3	MCF-7	breast:
2	chr15:77789053..77790918-chr15:77831495..77833590,2	MCF-7	breast:
3	chr15:77819974..77827062-chr15:77831334..77836599,8	MCF-7	breast:

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1005752	0.95[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.87[YRI][hapmap];0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1022172	0.86[EUR][1000 genomes]
rs11072653	0.85[CHB][hapmap];0.84[JPT][hapmap]
rs11633054	0.91[CEU][hapmap];0.85[CHB][hapmap];0.95[JPT][hapmap];0.85[EUR][1000 genomes]
rs11854328	0.84[CHB][hapmap];0.89[JPT][hapmap];0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11857450	0.95[CEU][hapmap];0.84[CHB][hapmap];0.95[JPT][hapmap];0.91[EUR][1000 genomes]
rs11857860	0.95[JPT][hapmap];0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1191196	0.84[CHB][hapmap];0.84[JPT][hapmap]
rs12324627	0.88[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs12900004	0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs12901130	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs12901503	0.95[CEU][hapmap];0.89[CHB][hapmap];0.95[JPT][hapmap];0.87[YRI][hapmap];0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12904938	0.80[EUR][1000 genomes]
rs12907746	0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs12910361	0.85[EUR][1000 genomes]
rs1473922	0.85[CHB][hapmap];0.84[JPT][hapmap]
rs1565756	0.91[CEU][hapmap];0.85[CHB][hapmap];0.84[JPT][hapmap];0.84[EUR][1000 genomes]
rs2055901	0.90[CEU][hapmap];0.84[CHB][hapmap];0.95[JPT][hapmap];0.81[YRI][hapmap];0.85[EUR][1000 genomes]
rs34591043	0.90[CEU][hapmap];0.84[CHB][hapmap];0.84[JPT][hapmap];0.81[YRI][hapmap];0.81[EUR][1000 genomes]
rs4886866	0.85[CHB][hapmap];0.84[JPT][hapmap]
rs4886869	0.84[CHB][hapmap];0.95[JPT][hapmap]
rs4886875	0.85[CHB][hapmap];0.95[JPT][hapmap];0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs4886876	0.85[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs4886877	0.85[CHB][hapmap];0.95[JPT][hapmap];0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs59153558	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62009090	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6495240	0.88[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.85[EUR][1000 genomes]
rs7162637	0.86[JPT][hapmap]
rs7171448	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7172144	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7177055	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7178572	0.90[CEU][hapmap];0.84[CHB][hapmap];0.95[JPT][hapmap];0.81[YRI][hapmap];0.84[EUR][1000 genomes]
rs8024485	0.90[CEU][hapmap];0.84[CHB][hapmap];0.84[JPT][hapmap];0.81[EUR][1000 genomes]
rs8034133	0.90[CEU][hapmap];0.85[CHB][hapmap];0.95[JPT][hapmap];0.85[EUR][1000 genomes]
rs869301	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs907369	0.84[ASN][1000 genomes]
rs907372	0.84[JPT][hapmap]
rs907388	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs952471	0.83[EUR][1000 genomes]
rs952472	0.85[EUR][1000 genomes]
rs965480	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040852	chr15:77160237-78137541	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv916323	chr15:77485765-78121259	Enhancers Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv1043284	chr15:77740632-77884026	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
4	nsv570139	chr15:77762493-77865459	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	nsv570140	chr15:77787469-77851535	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv833060	chr15:77816654-78035204	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	esv1806097	chr15:77817889-78301377	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77822000-77833600	Weak transcription	Right Atrium	heart
2	chr15:77827000-77833200	Weak transcription	HSMMtube	muscle
3	chr15:77827000-77835400	Weak transcription	Psoas Muscle	Psoas
4	chr15:77827000-77845400	Weak transcription	Fetal Kidney	kidney
5	chr15:77827600-77832400	Enhancers	Pancreas	Pancrea
6	chr15:77827600-77834000	Enhancers	Primary B cells from peripheral blood	blood
7	chr15:77828400-77832400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr15:77828400-77833400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr15:77828400-77835400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr15:77828400-77835400	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr15:77828400-77835400	Enhancers	Brain Anterior Caudate	brain
12	chr15:77828600-77833200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr15:77828600-77834000	Enhancers	Primary B cells from cord blood	blood
14	chr15:77828600-77834200	Enhancers	Brain Substantia Nigra	brain
15	chr15:77828800-77832200	Enhancers	Brain Cingulate Gyrus	brain
16	chr15:77828800-77833400	Weak transcription	K562	blood
17	chr15:77829000-77833000	Weak transcription	Fetal Intestine Large	intestine
18	chr15:77829400-77835000	Enhancers	Fetal Muscle Trunk	muscle
19	chr15:77829400-77844800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr15:77829600-77835400	Enhancers	Fetal Stomach	stomach
21	chr15:77829800-77835400	Enhancers	Fetal Brain Female	brain
22	chr15:77830000-77832200	Enhancers	Fetal Thymus	thymus
23	chr15:77830000-77835200	Enhancers	Fetal Muscle Leg	muscle
24	chr15:77830200-77833000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr15:77830400-77833600	Weak transcription	Fetal Intestine Small	intestine
26	chr15:77830600-77832800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr15:77831000-77832200	Enhancers	Gastric	stomach
28	chr15:77831000-77832200	Enhancers	Stomach Mucosa	stomach
29	chr15:77831200-77832200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr15:77831200-77832400	Enhancers	Stomach Smooth Muscle	stomach
31	chr15:77831200-77833400	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr15:77831200-77835000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr15:77831400-77832200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr15:77831400-77832200	Enhancers	NHLF	lung
35	chr15:77831400-77833200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr15:77831400-77833200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr15:77831400-77833600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr15:77831400-77833600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr15:77831400-77833800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr15:77831400-77834000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr15:77831400-77835200	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr15:77831600-77832200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr15:77831600-77832200	Enhancers	Placenta	Placenta
44	chr15:77831600-77832400	Enhancers	Lung	lung
45	chr15:77831600-77832400	Enhancers	NHDF-Ad	bronchial
46	chr15:77831600-77832600	Weak transcription	Brain Germinal Matrix	brain
47	chr15:77831600-77833000	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr15:77831600-77833000	Weak transcription	Fetal Brain Male	brain
49	chr15:77831600-77833000	Weak transcription	Fetal Heart	heart
50	chr15:77831600-77833400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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