Variant report

Variant	rs72777384
Chromosome Location	chr2:10909440-10909441
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:10908158..10909919-chr2:10911915..10914036,2	K562	blood:
2	chr2:10829824..10831420-chr2:10907947..10910452,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000243819	Chromatin interaction
ENSG00000115761	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1198844	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1198845	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1198846	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12464402	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12464513	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12468989	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12472302	0.81[ASN][1000 genomes]
rs12477285	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17365181	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17365209	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17365216	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17456162	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2046793	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2306922	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3856466	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55648622	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55675740	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55906240	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56093996	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs56140102	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs56143168	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs56147885	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs56195743	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56264212	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs66538971	1.00[EUR][1000 genomes]
rs72777378	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs72777379	0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72777381	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72777388	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72777393	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72779425	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72779433	0.80[EUR][1000 genomes];0.81[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	nsv1000953	chr2:10717304-10921805	Strong transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv535584	chr2:10717304-10921805	Bivalent Enhancer Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv833381	chr2:10723465-10911284	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv1000731	chr2:10758657-10943882	Strong transcription Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:10903400-10914400	Weak transcription	Right Atrium	heart
2	chr2:10903600-10914400	Weak transcription	Gastric	stomach
3	chr2:10904200-10916400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr2:10904600-10916400	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr2:10904800-10915200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr2:10905600-10918000	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr2:10906000-10914200	Weak transcription	Esophagus	oesophagus
8	chr2:10906200-10918200	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr2:10906200-10918400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr2:10906400-10912200	Weak transcription	Placenta	Placenta
11	chr2:10906400-10913000	Weak transcription	Fetal Intestine Small	intestine
12	chr2:10908000-10918200	Weak transcription	Pancreas	Pancrea
13	chr2:10908000-10918400	Weak transcription	Aorta	Aorta
14	chr2:10908600-10924400	Weak transcription	Psoas Muscle	Psoas
15	chr2:10908800-10917400	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr2:10908800-10918200	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr2:10909000-10913400	Weak transcription	Hela-S3	cervix
18	chr2:10909200-10914800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr2:10909400-10911400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr2:10909400-10911800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr2:10909400-10914200	Weak transcription	Right Ventricle	heart

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