Variant report

Variant	rs10495568
Chromosome Location	chr2:9784399-9784400
allele	A/T
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:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:9768781..9770412-chr2:9782843..9784568,2	K562	blood:
2	chr2:9774726..9777001-chr2:9783752..9786208,2	MCF-7	breast:
3	chr2:9782754..9784911-chr2:9790958..9792910,2	K562	blood:
4	chr2:9770340..9772882-chr2:9783880..9785966,3	MCF-7	breast:
5	chr2:9730159..9735372-chr2:9781969..9785269,4	K562	blood:
6	chr2:9776669..9780406-chr2:9782873..9785983,5	MCF-7	breast:
7	chr2:9779400..9780949-chr2:9782818..9785036,2	K562	blood:
8	chr2:9782654..9789334-chr2:9794560..9799702,7	MCF-7	breast:
9	chr2:9781325..9786143-chr2:9786474..9789625,5	K562	blood:
10	chr2:9769023..9772880-chr2:9783334..9787114,8	MCF-7	breast:
11	chr2:9782904..9785147-chr2:9789937..9793084,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000134308	Chromatin interaction
ENSG00000240687	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10187701	1.00[ASN][1000 genomes]
rs10203320	1.00[ASN][1000 genomes]
rs11695174	1.00[ASN][1000 genomes]
rs1534043	1.00[ASN][1000 genomes]
rs16867104	1.00[ASN][1000 genomes]
rs17453871	1.00[ASN][1000 genomes]
rs55921604	1.00[ASN][1000 genomes]
rs62121160	1.00[ASN][1000 genomes]
rs62121164	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62121165	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62129867	1.00[ASN][1000 genomes]
rs62129868	1.00[ASN][1000 genomes]
rs6747234	0.95[CEU][hapmap];0.85[EUR][1000 genomes]
rs72777055	1.00[ASN][1000 genomes]
rs72777067	1.00[ASN][1000 genomes]
rs72780951	1.00[ASN][1000 genomes]
rs868095	1.00[YRI][hapmap];1.00[ASN][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	nsv580915	chr2:9308148-9844178	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
2	nsv1011802	chr2:9766171-9808284	Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	nsv518363	chr2:9777229-9788315	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:9778800-9788400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:9779400-9784800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr2:9779400-9786400	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr2:9779600-9789400	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr2:9779800-9784400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr2:9779800-9784400	Weak transcription	Fetal Intestine Small	intestine
7	chr2:9780000-9786400	Weak transcription	HSMMtube	muscle
8	chr2:9780200-9786400	Weak transcription	Lung	lung
9	chr2:9780200-9786400	Weak transcription	HSMM	muscle
10	chr2:9780400-9785200	Weak transcription	Fetal Lung	lung
11	chr2:9780800-9788000	Weak transcription	Fetal Heart	heart
12	chr2:9781000-9784600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr2:9781000-9785400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr2:9781000-9785400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr2:9781000-9786400	Weak transcription	Ovary	ovary
16	chr2:9783000-9784600	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr2:9783000-9786400	Weak transcription	Brain Hippocampus Middle	brain
18	chr2:9783000-9786600	Weak transcription	Brain Cingulate Gyrus	brain
19	chr2:9783200-9784800	Weak transcription	Placenta	Placenta
20	chr2:9783200-9786400	Weak transcription	Brain Angular Gyrus	brain
21	chr2:9783200-9788400	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr2:9783200-9789200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr2:9783600-9785000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr2:9783800-9784600	Enhancers	Esophagus	oesophagus
25	chr2:9783800-9784600	Enhancers	Placenta Amnion	Placenta Amnion
26	chr2:9783800-9784600	Enhancers	NHEK	skin
27	chr2:9783800-9785000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr2:9783800-9786400	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr2:9783800-9786600	Enhancers	Pancreas	Pancrea
30	chr2:9784000-9786000	Enhancers	Fetal Intestine Large	intestine
31	chr2:9784000-9792400	Weak transcription	Brain Substantia Nigra	brain
32	chr2:9784200-9784400	Weak transcription	Spleen	Spleen
33	chr2:9784200-9785200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr2:9784200-9785800	Enhancers	HMEC	breast

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