Variant report

Variant	rs72777381
Chromosome Location	chr2:10906315-10906316
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:10905694..10908583-chr2:10912957..10914642,3	MCF-7	breast:
2	chr2:10905117..10907508-chr2:10909439..10912391,2	K562	blood:
3	chr2:10905922..10908917-chr2:10914932..10916687,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000272275	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1198844	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1198845	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1198846	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12464402	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12464513	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12468989	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12477285	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17365181	0.80[EUR][1000 genomes]
rs17365209	0.80[EUR][1000 genomes]
rs17365216	0.80[EUR][1000 genomes]
rs17456162	0.80[EUR][1000 genomes]
rs2046793	0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2306922	0.80[EUR][1000 genomes]
rs3856466	0.93[EUR][1000 genomes]
rs55648622	0.82[EUR][1000 genomes]
rs55675740	0.91[EUR][1000 genomes]
rs55906240	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56093996	0.81[EUR][1000 genomes]
rs56140102	0.80[EUR][1000 genomes]
rs56143168	0.93[EUR][1000 genomes]
rs56147885	0.80[EUR][1000 genomes]
rs56195743	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs56264212	0.82[EUR][1000 genomes]
rs66538971	0.98[EUR][1000 genomes]
rs72777378	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72777379	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72777384	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72777388	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72777393	0.93[EUR][1000 genomes]
rs72779425	0.80[EUR][1000 genomes]
rs72779433	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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
5	esv3427047	chr2:10900130-10906802	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	5 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	chr2:10897800-10906400	Enhancers	Placenta	Placenta
2	chr2:10899800-10908200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr2:10903400-10908200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr2:10903400-10908200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr2:10903400-10914400	Weak transcription	Right Atrium	heart
6	chr2:10903600-10908200	Weak transcription	Right Ventricle	heart
7	chr2:10903600-10914400	Weak transcription	Gastric	stomach
8	chr2:10904200-10916400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr2:10904400-10908200	Weak transcription	Fetal Muscle Leg	muscle
10	chr2:10904600-10916400	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr2:10904800-10915200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:10905000-10906400	Enhancers	Fetal Intestine Large	intestine
13	chr2:10905200-10906400	Enhancers	Fetal Intestine Small	intestine
14	chr2:10905600-10907600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr2:10905600-10918000	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr2:10905800-10906400	Active TSS	Spleen	Spleen
17	chr2:10906000-10914200	Weak transcription	Esophagus	oesophagus
18	chr2:10906200-10908000	Weak transcription	Hela-S3	cervix
19	chr2:10906200-10908400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr2:10906200-10918200	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr2:10906200-10918400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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