Variant report

Variant	rs1564783
Chromosome Location	chr15:74614913-74614914
allele	C/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:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:74607624..74610095-chr15:74613523..74615057,2	MCF-7	breast:
2	chr15:74419675..74420458-chr15:74614358..74615274,5	MCF-7	breast:
3	chr15:74243196..74243740-chr15:74614599..74615555,2	K562	blood:
4	chr15:74614889..74615521-chr3:120277797..120278349,2	MCF-7	breast:
5	chr15:74419576..74420529-chr15:74614579..74615595,4	K562	blood:
6	chr15:74614136..74616902-chr15:74617695..74620669,2	K562	blood:
7	chr15:74358127..74358835-chr15:74614868..74615479,2	MCF-7	breast:
8	chr15:74346287..74347045-chr15:74614632..74615538,3	MCF-7	breast:
9	chr15:74604086..74605037-chr15:74614467..74615451,3	K562	blood:
10	chr15:74418976..74421640-chr15:74612670..74615162,3	K562	blood:
11	chr15:74604204..74604761-chr15:74614716..74615372,2	MCF-7	breast:
12	chr15:74340832..74341338-chr15:74614392..74615111,2	K562	blood:
13	chr15:74340758..74341346-chr15:74614631..74615308,2	MCF-7	breast:
14	chr15:74423851..74425420-chr15:74614158..74616775,2	K562	blood:
15	chr15:74265166..74265894-chr15:74614554..74615483,3	MCF-7	breast:
16	chr15:74603562..74604487-chr15:74614598..74615365,4	MCF-7	breast:
17	chr15:74346094..74347046-chr15:74614640..74615508,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000167178	Chromatin interaction
ENSG00000248540	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11072478	0.82[CEU][hapmap]
rs11631552	0.82[EUR][1000 genomes]
rs11632698	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs11635047	0.96[CEU][hapmap];0.80[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11638442	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs12440952	0.85[CEU][hapmap];0.85[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs12900028	0.93[CEU][hapmap];0.86[EUR][1000 genomes]
rs12905100	0.81[CEU][hapmap]
rs12906092	0.85[CEU][hapmap];0.85[EUR][1000 genomes]
rs12912592	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12917295	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs12917557	0.88[CEU][hapmap];0.84[EUR][1000 genomes]
rs1484210	0.89[CEU][hapmap];0.80[EUR][1000 genomes]
rs1564782	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs1809500	0.84[EUR][1000 genomes]
rs2277605	0.91[AFR][1000 genomes]
rs2279356	0.87[YRI][hapmap];0.88[AFR][1000 genomes]
rs2899825	0.85[CEU][hapmap];0.81[JPT][hapmap];0.82[EUR][1000 genomes]
rs2930291	0.84[CEU][hapmap]
rs2930302	0.82[CEU][hapmap]
rs2959003	0.81[EUR][1000 genomes]
rs2959008	0.82[CEU][hapmap]
rs2959011	0.92[CEU][hapmap];0.91[EUR][1000 genomes]
rs34578565	0.91[EUR][1000 genomes]
rs35807116	0.85[EUR][1000 genomes]
rs4887134	0.96[CEU][hapmap];0.90[EUR][1000 genomes]
rs4887135	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs56339065	0.91[EUR][1000 genomes]
rs7173655	0.81[EUR][1000 genomes]
rs751527	0.94[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs900798	0.81[EUR][1000 genomes]
rs900801	0.89[CEU][hapmap];0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833054	chr15:74457643-74625283	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv428641	chr15:74555113-74724630	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
3	nsv482615	chr15:74593625-74757962	Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	58 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74604800-74623400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr15:74611000-74617200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr15:74612000-74657800	Weak transcription	Right Atrium	heart
4	chr15:74612800-74617400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr15:74612800-74618600	Weak transcription	Ovary	ovary
6	chr15:74613000-74618800	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr15:74613200-74615000	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr15:74613200-74615200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr15:74613200-74617600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr15:74613200-74617600	Weak transcription	Fetal Thymus	thymus
11	chr15:74613200-74619000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr15:74613200-74619000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr15:74613400-74615400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr15:74613400-74618800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr15:74613400-74618800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr15:74613400-74618800	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr15:74613400-74619200	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr15:74614200-74615800	Enhancers	Placenta	Placenta
19	chr15:74614400-74615600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr15:74614600-74615600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr15:74614800-74615000	Enhancers	Fetal Muscle Leg	muscle
22	chr15:74614800-74615200	Enhancers	Hela-S3	cervix
23	chr15:74614800-74615400	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr15:74614800-74615400	Enhancers	H1 Cell Line	embryonic stem cell
25	chr15:74614800-74615400	Enhancers	Fetal Muscle Trunk	muscle
26	chr15:74614800-74615600	Enhancers	Spleen	Spleen

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