Variant report

Variant	rs1797314
Chromosome Location	chr15:50486075-50486076
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:50485533..50488870-chr15:50492194..50494725,4	MCF-7	breast:
2	chr15:50485822..50488396-chr15:50488932..50490501,2	MCF-7	breast:
3	chr15:50471330..50473823-chr15:50485540..50487357,2	MCF-7	breast:
4	chr15:50468307..50471264-chr15:50485331..50487376,2	MCF-7	breast:
5	chr15:50483477..50486888-chr15:50488882..50492194,4	K562	blood:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11858285	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1529345	0.87[AFR][1000 genomes]
rs1648345	0.90[ASN][1000 genomes]
rs1648346	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1648349	0.84[ASN][1000 genomes]
rs16963406	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1797315	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1797316	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1797318	1.00[ASN][1000 genomes]
rs1797319	0.96[ASN][1000 genomes]
rs1797320	0.93[ASN][1000 genomes]
rs2433281	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2433283	0.89[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs2554884	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2554885	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2554886	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2555485	0.92[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2555487	0.96[ASN][1000 genomes]
rs2555488	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2555489	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28455006	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2899458	0.88[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs6493415	0.83[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs8024818	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8031851	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs933855	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs933857	0.89[AFR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044277	chr15:49921547-50702386	Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv542380	chr15:49921547-50702386	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv1035983	chr15:50223334-50595170	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv542382	chr15:50223334-50595170	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:50476000-50503400	Weak transcription	Colonic Mucosa	Colon
2	chr15:50476600-50498000	Weak transcription	Pancreas	Pancrea
3	chr15:50477600-50486200	Enhancers	HepG2	liver
4	chr15:50477600-50498000	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr15:50477600-50502200	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr15:50478000-50486400	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr15:50478400-50502400	Weak transcription	Placenta	Placenta
8	chr15:50478800-50487000	Enhancers	Fetal Intestine Large	intestine
9	chr15:50480000-50490000	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr15:50480400-50501600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr15:50482000-50502800	Weak transcription	Duodenum Mucosa	Duodenum
12	chr15:50482200-50487000	Strong transcription	Hela-S3	cervix
13	chr15:50482600-50501800	Weak transcription	A549	lung
14	chr15:50482800-50492600	Weak transcription	Primary hematopoietic stem cells	blood
15	chr15:50483000-50487000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr15:50483200-50497400	Weak transcription	K562	blood
17	chr15:50483800-50489600	Weak transcription	Liver	Liver
18	chr15:50483800-50490000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr15:50485200-50486600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr15:50485600-50486200	Enhancers	NHEK	skin
21	chr15:50485600-50486400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr15:50485600-50491000	Weak transcription	Fetal Intestine Small	intestine
23	chr15:50485800-50489800	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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