Variant report

Variant	rs10282329
Chromosome Location	chr7:6483877-6483878
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:6481370..6483042-chr7:6483146..6485535,2	MCF-7	breast:
2	chr7:6482815..6485017-chr7:6485346..6488810,3	MCF-7	breast:
3	chr7:6473644..6475592-chr7:6483600..6485102,2	K562	blood:
4	chr7:6475431..6480249-chr7:6480514..6484908,6	MCF-7	breast:
5	chr7:6474528..6479669-chr7:6479864..6485085,5	MCF-7	breast:
6	chr7:6474092..6477009-chr7:6483600..6487126,3	K562	blood:

Variant related genes	Relation type
ENSG00000164535	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10224776	1.00[AMR][1000 genomes]
rs10230345	1.00[AMR][1000 genomes]
rs10232409	1.00[AMR][1000 genomes]
rs10237734	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10239689	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10265923	1.00[AMR][1000 genomes]
rs10267075	1.00[AMR][1000 genomes]
rs10273790	1.00[AMR][1000 genomes]
rs28624716	1.00[AMR][1000 genomes]
rs35767264	1.00[AMR][1000 genomes]
rs36099272	1.00[AMR][1000 genomes]
rs57649911	1.00[AMR][1000 genomes]
rs58107700	1.00[AMR][1000 genomes]
rs6961782	1.00[AMR][1000 genomes]
rs73344970	1.00[AMR][1000 genomes]
rs73344979	1.00[AMR][1000 genomes]
rs73346969	1.00[AMR][1000 genomes]
rs73346993	1.00[AMR][1000 genomes]
rs73348720	1.00[AMR][1000 genomes]

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	nsv948912	chr7:5803903-6623553	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
2	nsv1034060	chr7:5814823-6745710	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	138 gene(s)	inside rSNPs	diseases
3	nsv538711	chr7:5814823-6745710	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	138 gene(s)	inside rSNPs	diseases
4	nsv1028242	chr7:5819084-6645024	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers 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	127 gene(s)	inside rSNPs	diseases
5	nsv538712	chr7:5819084-6645024	Weak transcription Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	127 gene(s)	inside rSNPs	diseases
6	nsv949531	chr7:5949371-6753694	Strong transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	129 gene(s)	inside rSNPs	diseases
7	nsv1020236	chr7:6248930-6690377	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
8	nsv497874	chr7:6296768-6614902	Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
9	esv1824738	chr7:6431933-6554222	Transcr. at gene 5' and 3' Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
10	esv1825865	chr7:6431933-6554222	Strong transcription Genic enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 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	chr7:6453000-6486800	Weak transcription	Small Intestine	intestine
2	chr7:6456800-6486800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr7:6465000-6486600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr7:6465800-6486400	Weak transcription	Colonic Mucosa	Colon
5	chr7:6466000-6486400	Weak transcription	Aorta	Aorta
6	chr7:6475400-6484400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr7:6476000-6484200	Weak transcription	K562	blood
8	chr7:6476200-6486400	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr7:6476400-6486400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr7:6478400-6485000	Strong transcription	Fetal Brain Female	brain
11	chr7:6478800-6485600	Strong transcription	Fetal Intestine Small	intestine
12	chr7:6478800-6486000	Strong transcription	HUES6 Cell Line	embryonic stem cell
13	chr7:6478800-6486600	Weak transcription	Fetal Heart	heart
14	chr7:6479000-6485400	Strong transcription	Fetal Intestine Large	intestine
15	chr7:6479000-6485400	Strong transcription	Stomach Smooth Muscle	stomach
16	chr7:6479000-6486000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr7:6479200-6486400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr7:6479400-6486400	Weak transcription	Right Atrium	heart
19	chr7:6479600-6485600	Strong transcription	Fetal Muscle Leg	muscle
20	chr7:6479800-6485800	Strong transcription	Fetal Thymus	thymus
21	chr7:6480000-6485600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr7:6480600-6485600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr7:6481000-6485800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr7:6481200-6485600	Strong transcription	Duodenum Mucosa	Duodenum
25	chr7:6481200-6485800	Strong transcription	HUES48 Cell Line	embryonic stem cell
26	chr7:6481200-6486000	Strong transcription	HUES64 Cell Line	embryonic stem cell
27	chr7:6481200-6486000	Strong transcription	Fetal Stomach	stomach
28	chr7:6481400-6484200	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr7:6481400-6484200	Genic enhancers	Lung	lung
30	chr7:6481400-6484600	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr7:6481400-6484600	Strong transcription	Dnd41	blood
32	chr7:6481400-6484800	Genic enhancers	HSMM	muscle
33	chr7:6481400-6485000	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr7:6481400-6485000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr7:6481400-6485200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr7:6481400-6485200	Strong transcription	Ovary	ovary
37	chr7:6481400-6485400	Strong transcription	H9 Cell Line	embryonic stem cell
38	chr7:6481400-6485400	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr7:6481400-6485400	Strong transcription	Duodenum Smooth Muscle	Duodenum
40	chr7:6481400-6485400	Strong transcription	Thymus	Thymus
41	chr7:6481400-6485400	Strong transcription	HepG2	liver
42	chr7:6481400-6485800	Strong transcription	H1 Cell Line	embryonic stem cell
43	chr7:6481400-6485800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
44	chr7:6481400-6485800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
45	chr7:6481400-6485800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr7:6481400-6485800	Genic enhancers	Primary monocytes fromperipheralblood	blood
47	chr7:6481400-6485800	Strong transcription	Cortex derived primary cultured neurospheres	brain
48	chr7:6481400-6485800	Strong transcription	Fetal Muscle Trunk	muscle
49	chr7:6481400-6486400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr7:6481600-6484400	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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