Variant report

Variant	rs74015071
Chromosome Location	chr16:31159095-31159096
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:31149322..31163059-chr16:31188531..31198512,46	MCF-7	breast:
2	chr16:31157660..31164019-chr16:31188659..31195219,17	MCF-7	breast:
3	chr16:31158383..31160788-chr16:31186021..31187746,2	K562	blood:
4	chr16:31158034..31160388-chr16:31169650..31172147,2	MCF-7	breast:
5	chr16:31149707..31163529-chr16:31187237..31198825,44	K562	blood:
6	chr16:31151687..31162079-chr16:31189046..31201898,43	K562	blood:
7	chr16:30994877..30997297-chr16:31156140..31160263,3	MCF-7	breast:
8	chr16:31008122..31010429-chr16:31157760..31160273,2	MCF-7	breast:
9	chr16:31127615..31129162-chr16:31157743..31159403,2	MCF-7	breast:
10	chr16:31151491..31155912-chr16:31157765..31163894,11	MCF-7	breast:
11	chr16:31152927..31156733-chr16:31157447..31161176,6	MCF-7	breast:
12	chr16:31157423..31159789-chr16:31170400..31172208,2	MCF-7	breast:
13	chr16:30967607..30969891-chr16:31158023..31159706,2	MCF-7	breast:
14	chr16:31157885..31160193-chr16:31199237..31201496,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000089280	Chromatin interaction
ENSG00000260304	Chromatin interaction
ENSG00000099377	Chromatin interaction
ENSG00000103510	Chromatin interaction
ENSG00000099365	Chromatin interaction
ENSG00000178226	Chromatin interaction
ENSG00000099381	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs13331793	1.00[AMR][1000 genomes]
rs13339393	1.00[AMR][1000 genomes]
rs28428182	1.00[AMR][1000 genomes]
rs28637378	1.00[AMR][1000 genomes]
rs34107331	1.00[AMR][1000 genomes]
rs34259949	1.00[AMR][1000 genomes]
rs34831291	1.00[AMR][1000 genomes]
rs34889904	1.00[AMR][1000 genomes]
rs55886037	0.82[AFR][1000 genomes]
rs56196402	1.00[AMR][1000 genomes]
rs59076556	1.00[AMR][1000 genomes]
rs61237574	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74015066	1.00[AMR][1000 genomes]
rs74015068	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74015069	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74015099	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74018303	1.00[AMR][1000 genomes]
rs9888851	1.00[AMR][1000 genomes]
rs9922051	1.00[AMR][1000 genomes]
rs9933960	1.00[AMR][1000 genomes]
rs9940181	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062456	chr16:30442166-31253997	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
2	nsv542898	chr16:30442166-31253997	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
3	nsv905729	chr16:30642867-31247924	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	387 gene(s)	inside rSNPs	diseases
4	nsv431451	chr16:30682399-31340999	Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	350 gene(s)	inside rSNPs	diseases
5	nsv905734	chr16:30877544-31191482	Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
6	nsv905735	chr16:30890538-31247924	Strong transcription Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	264 gene(s)	inside rSNPs	diseases
7	nsv457483	chr16:30903679-31191482	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
8	nsv571820	chr16:30903679-31191482	Enhancers Genic enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
9	esv1797877	chr16:30948643-31188432	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
10	nsv905740	chr16:31066249-31232437	Flanking Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	202 gene(s)	inside rSNPs	diseases
11	nsv905741	chr16:31066249-31247924	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	202 gene(s)	inside rSNPs	diseases
12	nsv905742	chr16:31102321-31247924	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	188 gene(s)	inside rSNPs	diseases
13	nsv542900	chr16:31137352-31197027	Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	165 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31154400-31159400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr16:31154400-31159400	Weak transcription	Pancreas	Pancrea
3	chr16:31154400-31160600	Weak transcription	Hela-S3	cervix
4	chr16:31154400-31190400	Weak transcription	Right Atrium	heart
5	chr16:31154600-31159400	Weak transcription	Liver	Liver
6	chr16:31154600-31159400	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr16:31154600-31161800	Weak transcription	Primary hematopoietic stem cells	blood
8	chr16:31154800-31159200	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr16:31155000-31159400	Weak transcription	Gastric	stomach
10	chr16:31155000-31159400	Weak transcription	Spleen	Spleen
11	chr16:31155400-31159800	Weak transcription	Esophagus	oesophagus
12	chr16:31155400-31160400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr16:31157400-31159600	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr16:31157400-31159600	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr16:31157400-31161200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr16:31158800-31159200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
17	chr16:31159000-31159400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr16:31159000-31159400	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr16:31159000-31160000	Bivalent Enhancer	Placenta	Placenta
20	chr16:31159000-31160200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin

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