Variant report

Variant	rs7781710
Chromosome Location	chr7:15056045-15056046
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:14757081..14758001-chr7:15054605..15056087,5	MCF-7	breast:
2	chr7:14737644..14738448-chr7:15055761..15056392,2	MCF-7	breast:
3	chr7:14756304..14757028-chr7:15055834..15056611,2	MCF-7	breast:
4	chr7:15046835..15047773-chr7:15055487..15056275,2	MCF-7	breast:
5	chr7:14757467..14758291-chr7:15055705..15056411,2	MCF-7	breast:

Extended variants
information (count: 58 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10238161	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10238625	0.90[EUR][1000 genomes]
rs10249299	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10264063	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10264723	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10266209	0.89[EUR][1000 genomes]
rs10267273	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10487796	0.80[AMR][1000 genomes]
rs10807778	0.90[EUR][1000 genomes]
rs10950546	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10950548	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10950549	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10950550	0.81[AMR][1000 genomes]
rs11514706	0.81[EUR][1000 genomes]
rs12113083	0.84[EUR][1000 genomes]
rs12538003	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12538043	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12540947	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12666046	0.82[EUR][1000 genomes]
rs12699673	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13220985	0.81[AMR][1000 genomes]
rs2191346	0.90[EUR][1000 genomes]
rs2215381	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2215382	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2358158	0.90[EUR][1000 genomes]
rs2358159	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4719430	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4719433	0.80[AMR][1000 genomes]
rs4721400	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62448644	0.84[EUR][1000 genomes]
rs6461153	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6960043	0.84[EUR][1000 genomes]
rs6962498	0.82[EUR][1000 genomes]
rs6972333	0.84[EUR][1000 genomes]
rs6972516	0.84[EUR][1000 genomes]
rs6976086	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6978885	0.83[EUR][1000 genomes]
rs7784091	0.86[EUR][1000 genomes]
rs7786873	0.80[EUR][1000 genomes]
rs7798124	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7798360	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758104	chr7:14896877-15299786	Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv2759512	chr7:14896877-15299786	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1032569	chr7:14905287-15597069	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1021172	chr7:14944318-15548794	Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv538743	chr7:14944318-15548794	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv887719	chr7:14995522-15072029	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv464389	chr7:15008138-15098004	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv606285	chr7:15008138-15098004	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv887720	chr7:15008714-15072029	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv517876	chr7:15010824-15198589	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv830910	chr7:15011028-15212309	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv887721	chr7:15025332-15163610	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv1017308	chr7:15047280-15074656	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
14	esv2761127	chr7:15051210-15152813	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
15	nsv1029986	chr7:15051210-15152813	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
16	nsv522499	chr7:15051754-15148454	Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
17	nsv1018434	chr7:15054190-15144078	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:15055000-15056200	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr7:15055200-15056600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr7:15055200-15056600	Enhancers	Colon Smooth Muscle	Colon
4	chr7:15055200-15056600	Enhancers	Rectal Smooth Muscle	rectum
5	chr7:15055200-15057000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr7:15055400-15056200	Enhancers	Muscle Satellite Cultured Cells	--
7	chr7:15055400-15056400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:15055800-15056200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr7:15055800-15056200	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr7:15055800-15056200	Enhancers	Fetal Brain Female	brain
11	chr7:15055800-15056400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr7:15055800-15056600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr7:15055800-15056600	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr7:15055800-15056600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr7:15055800-15056800	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr7:15055800-15056800	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr7:15055800-15057000	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr7:15055800-15057000	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr7:15055800-15057000	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr7:15055800-15057000	Enhancers	Fetal Intestine Large	intestine
21	chr7:15055800-15057000	Enhancers	Fetal Kidney	kidney
22	chr7:15055800-15057000	Enhancers	Hela-S3	cervix
23	chr7:15055800-15057000	Enhancers	HMEC	breast
24	chr7:15055800-15057200	Enhancers	NHEK	skin
25	chr7:15056000-15056200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr7:15056000-15056200	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr7:15056000-15056200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr7:15056000-15056400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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