Variant report

Variant	rs7794024
Chromosome Location	chr7:101245484-101245485
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:101245451..101246297-chr7:101914933..101915725,2	MCF-7	breast:
2	chr7:101242393..101247738-chr7:101456834..101460384,5	MCF-7	breast:
3	chr7:101245401..101246357-chr7:101879322..101880688,4	K562	blood:
4	chr7:101245468..101246352-chr7:101915597..101916163,4	K562	blood:
5	chr7:101245091..101246357-chr7:101457101..101458459,9	MCF-7	breast:
6	chr7:101244039..101255564-chr7:101454524..101463981,21	MCF-7	breast:
7	chr7:101239160..101242958-chr7:101243756..101248056,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000257923	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10244678	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1541425	1.00[ASN][1000 genomes]
rs1636444	1.00[ASN][1000 genomes]
rs2410856	1.00[ASN][1000 genomes]
rs28850410	1.00[ASN][1000 genomes]
rs4729746	1.00[ASN][1000 genomes]
rs6465823	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6968978	1.00[ASN][1000 genomes]
rs7786466	1.00[ASN][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	nsv933653	chr7:100701931-101515782	Active TSS ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv888821	chr7:101091470-101311540	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv831078	chr7:101094945-101257486	Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv888822	chr7:101105017-101330734	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv888824	chr7:101109073-101330734	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
6	nsv888825	chr7:101168283-101330734	Enhancers Genic enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv1018544	chr7:101225639-101424889	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv539045	chr7:101225639-101424889	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv888826	chr7:101230768-101277334	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv482758	chr7:101231458-101395219	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101241400-101246200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:101242200-101245600	Weak transcription	Brain Hippocampus Middle	brain
3	chr7:101242200-101249600	Weak transcription	Spleen	Spleen
4	chr7:101242400-101245800	Weak transcription	HMEC	breast
5	chr7:101242400-101246200	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr7:101242400-101248400	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr7:101242600-101245600	Weak transcription	Fetal Intestine Small	intestine
8	chr7:101242600-101245800	Weak transcription	Colonic Mucosa	Colon
9	chr7:101242600-101245800	Weak transcription	Pancreas	Pancrea
10	chr7:101242600-101248600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr7:101242600-101248800	Weak transcription	Fetal Lung	lung
12	chr7:101242800-101245600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr7:101242800-101246000	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr7:101242800-101246000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr7:101242800-101251600	Weak transcription	Gastric	stomach
16	chr7:101243000-101246000	Weak transcription	HSMMtube	muscle
17	chr7:101243200-101246000	Weak transcription	NHDF-Ad	bronchial
18	chr7:101243600-101245600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
19	chr7:101245000-101246400	Enhancers	Fetal Intestine Large	intestine
20	chr7:101245200-101245600	Bivalent Enhancer	Placenta	Placenta
21	chr7:101245200-101246600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
22	chr7:101245200-101246800	Enhancers	Fetal Muscle Leg	muscle
23	chr7:101245400-101245800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr7:101245400-101245800	Bivalent Enhancer	Stomach Mucosa	stomach
25	chr7:101245400-101245800	Enhancers	HepG2	liver
26	chr7:101245400-101246000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr7:101245400-101246400	Enhancers	Placenta Amnion	Placenta Amnion
28	chr7:101245400-101246400	Enhancers	HSMM	muscle
29	chr7:101245400-101246600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr7:101245400-101246600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr7:101245400-101246600	Bivalent Enhancer	Fetal Stomach	stomach
32	chr7:101245400-101246600	Enhancers	Skeletal Muscle Female	skeletal muscle

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