Variant report

Variant	rs4729746
Chromosome Location	chr7:101257574-101257575
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:101255927..101262461-chr7:101262750..101268268,7	MCF-7	breast:

Extended variants
information (count: 18 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1541425	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1636444	1.00[ASN][1000 genomes]
rs2410856	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28850410	1.00[ASN][1000 genomes]
rs6465823	1.00[ASN][1000 genomes]
rs6968978	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7786466	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7794024	1.00[ASN][1000 genomes]
rs7812158	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 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	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
4	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
5	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
6	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
7	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
8	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
9	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:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101252600-101257800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr7:101252800-101257800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:101252800-101257800	Weak transcription	HMEC	breast
4	chr7:101252800-101258000	Weak transcription	Right Atrium	heart
5	chr7:101252800-101260800	Weak transcription	Esophagus	oesophagus
6	chr7:101256200-101258600	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr7:101256200-101258800	Enhancers	H1 Cell Line	embryonic stem cell
8	chr7:101256200-101258800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr7:101256200-101258800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr7:101256200-101259000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr7:101256200-101259400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr7:101256200-101259600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
13	chr7:101256200-101259600	Enhancers	Fetal Muscle Leg	muscle
14	chr7:101256400-101258800	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr7:101256400-101258800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr7:101256600-101257600	Enhancers	Aorta	Aorta
17	chr7:101256600-101258200	Weak transcription	Gastric	stomach
18	chr7:101256800-101257800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr7:101256800-101257800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr7:101256800-101257800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:101256800-101258400	Weak transcription	Ovary	ovary
22	chr7:101256800-101258600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr7:101257000-101258000	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr7:101257000-101258000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr7:101257000-101258200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr7:101257200-101257600	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr7:101257200-101257600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr7:101257200-101258200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr7:101257200-101262800	Enhancers	Placenta	Placenta
30	chr7:101257400-101257600	Bivalent Enhancer	Fetal Stomach	stomach
31	chr7:101257400-101257600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
32	chr7:101257400-101258000	Enhancers	Fetal Thymus	thymus
33	chr7:101257400-101259000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links