Variant report

Variant	rs10277726
Chromosome Location	chr7:16836312-16836313
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:16836212..16838215-chr7:16926884..16928846,2	MCF-7	breast:
2	chr7:16835974..16838932-chr7:16840945..16844181,3	MCF-7	breast:
3	chr7:16829911..16832805-chr7:16833008..16837157,5	MCF-7	breast:
4	chr7:16832562..16837080-chr7:16918023..16922699,4	MCF-7	breast:
5	chr7:16835874..16837684-chr7:16837980..16840761,3	MCF-7	breast:
6	chr7:16687122..16688978-chr7:16834691..16836513,2	MCF-7	breast:
7	chr7:16834464..16837381-chr7:16917250..16920233,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000173467	Chromatin interaction
ENSG00000227965	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10265402	1.00[EUR][1000 genomes]
rs28626646	0.85[AFR][1000 genomes]
rs56937850	1.00[EUR][1000 genomes]
rs59696533	1.00[EUR][1000 genomes]
rs59726258	1.00[EUR][1000 genomes]
rs59800459	1.00[EUR][1000 genomes]
rs61100071	1.00[EUR][1000 genomes]
rs6461274	1.00[EUR][1000 genomes]
rs720587	1.00[EUR][1000 genomes]
rs73299640	1.00[EUR][1000 genomes]
rs73312785	1.00[EUR][1000 genomes]
rs7780556	1.00[EUR][1000 genomes]
rs7785269	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028125	chr7:16529160-16847225	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1024059	chr7:16639432-16836425	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv887761	chr7:16834361-17732490	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	nsv887762	chr7:16834361-17746628	Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv887763	chr7:16834361-17750811	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16814400-16843800	Weak transcription	Small Intestine	intestine
2	chr7:16815000-16838000	Weak transcription	K562	blood
3	chr7:16819800-16838000	Weak transcription	Placenta	Placenta
4	chr7:16823600-16843600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:16825800-16836600	Weak transcription	Left Ventricle	heart
6	chr7:16827400-16837000	Weak transcription	Primary B cells from cord blood	blood
7	chr7:16831800-16839200	Strong transcription	Placenta Amnion	Placenta Amnion
8	chr7:16832000-16839600	Strong transcription	Rectal Mucosa Donor 31	rectum
9	chr7:16832400-16838200	Strong transcription	Sigmoid Colon	Sigmoid Colon
10	chr7:16832400-16840000	Strong transcription	Rectal Mucosa Donor 29	rectum
11	chr7:16833600-16839600	Strong transcription	A549	lung
12	chr7:16834000-16842400	Weak transcription	Gastric	stomach
13	chr7:16834200-16839800	Strong transcription	Duodenum Mucosa	Duodenum
14	chr7:16834400-16837800	Strong transcription	Fetal Intestine Small	intestine
15	chr7:16834800-16837200	Weak transcription	Colonic Mucosa	Colon
16	chr7:16835000-16844200	Weak transcription	Psoas Muscle	Psoas
17	chr7:16835400-16836400	Enhancers	Fetal Brain Female	brain
18	chr7:16835600-16839000	Weak transcription	Fetal Heart	heart
19	chr7:16835800-16837600	Weak transcription	Stomach Mucosa	stomach
20	chr7:16835800-16838200	Weak transcription	Fetal Stomach	stomach
21	chr7:16835800-16840000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr7:16836000-16837200	Weak transcription	Fetal Intestine Large	intestine

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