Variant report

Variant	rs7578933
Chromosome Location	chr2:9847152-9847153
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:9846347..9848775-chr2:9855960..9857602,2	K562	blood:
2	chr2:9847027..9849818-chr2:9850088..9852900,2	K562	blood:
3	chr2:9843482..9849818-chr2:9850036..9855209,6	K562	blood:
4	chr2:9716130..9717904-chr2:9846619..9848740,2	MCF-7	breast:
5	chr2:9845674..9847302-chr2:9868513..9870809,2	MCF-7	breast:
6	chr2:9769450..9771110-chr2:9846663..9848986,2	K562	blood:
7	chr2:9769741..9772155-chr2:9846974..9850798,3	MCF-7	breast:
8	chr2:9845748..9848155-chr2:9867890..9870403,2	K562	blood:

Variant related genes	Relation type
ENSG00000134308	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10202938	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10929596	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10929597	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10929598	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10929600	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10929602	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10929605	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11674642	0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs11680429	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11695437	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11892176	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11901380	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11902412	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12466594	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12472594	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13024852	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1877953	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2357263	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2357264	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2357265	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4459704	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4507070	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4668636	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4668637	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4668638	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4668639	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4668640	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4669427	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4669428	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4669429	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4669430	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4669432	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4669433	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4669435	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4669437	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4669441	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs5020306	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs58961346	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6432033	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6724483	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6735280	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6736421	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6738072	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7592044	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7602784	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7605675	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs885572	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv469405	chr2:9814374-9964947	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
2	nsv580930	chr2:9814374-9964947	Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:9837000-9849600	Weak transcription	Pancreas	Pancrea
2	chr2:9843800-9852000	Weak transcription	Left Ventricle	heart
3	chr2:9844000-9847200	Weak transcription	Fetal Heart	heart
4	chr2:9844000-9847200	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr2:9844200-9847400	Weak transcription	Gastric	stomach
6	chr2:9844200-9852000	Weak transcription	Esophagus	oesophagus
7	chr2:9844400-9848400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr2:9844400-9848800	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr2:9844400-9848800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr2:9844400-9849000	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr2:9844400-9849600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr2:9844400-9849600	Weak transcription	HMEC	breast
13	chr2:9844600-9849000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr2:9844600-9849800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr2:9844800-9848400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr2:9845000-9848000	Weak transcription	K562	blood
17	chr2:9845000-9849600	Weak transcription	Spleen	Spleen
18	chr2:9845000-9850000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr2:9845200-9849800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr2:9845200-9852000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr2:9845400-9847200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr2:9845400-9848000	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr2:9845400-9848200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr2:9845400-9860600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr2:9845600-9851600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr2:9846400-9848400	Bivalent Enhancer	HepG2	liver
27	chr2:9846600-9848400	Enhancers	A549	lung
28	chr2:9846800-9847400	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr2:9846800-9848000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr2:9846800-9854800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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