Variant report

Variant	rs73440772
Chromosome Location	chr21:40107103-40107104
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr21:40106344..40108151-chr21:40152083..40153978,2	MCF-7	breast:
2	chr21:40104619..40107467-chr21:40182654..40185637,2	K562	blood:
3	chr21:40104645..40107795-chr21:40176588..40180305,3	K562	blood:
4	chr21:40106234..40108594-chr21:40335676..40338028,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000157557	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs2187306	1.00[AMR][1000 genomes]
rs59592764	1.00[AMR][1000 genomes]
rs59907098	1.00[AMR][1000 genomes]
rs73432978	1.00[AMR][1000 genomes]
rs73433002	1.00[AMR][1000 genomes]
rs73434824	1.00[AMR][1000 genomes]
rs73440728	1.00[AMR][1000 genomes]
rs73440730	1.00[AMR][1000 genomes]
rs73440743	1.00[AMR][1000 genomes]
rs73440746	1.00[AMR][1000 genomes]
rs73440751	1.00[AMR][1000 genomes]
rs73440753	1.00[AMR][1000 genomes]
rs73440758	1.00[AMR][1000 genomes]
rs73442739	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73446336	1.00[AMR][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	nsv1060405	chr21:40095523-40159813	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1057356	chr21:40103881-40147363	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv913739	chr21:40103951-40152372	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv913740	chr21:40103951-40157124	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:40102600-40124800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr21:40106000-40107200	Active TSS	iPS-20b Cell Line	embryonic stem cell
3	chr21:40106000-40107200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
4	chr21:40106000-40107200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr21:40106000-40107200	Enhancers	HepG2	liver
6	chr21:40106000-40107200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
7	chr21:40106200-40107200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
8	chr21:40106400-40107200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr21:40106400-40107800	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr21:40106400-40108400	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr21:40106400-40111800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr21:40106600-40107200	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr21:40106600-40107200	Enhancers	Adipose Nuclei	Adipose
14	chr21:40106600-40107400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
15	chr21:40106600-40107600	Weak transcription	Liver	Liver
16	chr21:40106600-40107800	Weak transcription	Right Atrium	heart
17	chr21:40106600-40108000	Weak transcription	Aorta	Aorta
18	chr21:40106600-40108600	Enhancers	Fetal Intestine Large	intestine
19	chr21:40106600-40112800	Weak transcription	Colonic Mucosa	Colon
20	chr21:40106800-40107200	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr21:40106800-40107400	Weak transcription	Duodenum Mucosa	Duodenum
22	chr21:40106800-40108000	Weak transcription	Fetal Intestine Small	intestine
23	chr21:40106800-40108400	Enhancers	Dnd41	blood
24	chr21:40107000-40107200	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr21:40107000-40107400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr21:40107000-40107600	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr21:40107000-40107800	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr21:40107000-40108000	Weak transcription	Fetal Lung	lung
29	chr21:40107000-40108200	Enhancers	Primary hematopoietic stem cells	blood
30	chr21:40107000-40108400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr21:40107000-40108400	Enhancers	Small Intestine	intestine
32	chr21:40107000-40113000	Weak transcription	Primary T cells from cord blood	blood

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