Variant report

Variant	rs1955662
Chromosome Location	chr14:65110840-65110841
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	chr14:65005413..65007156-chr14:65110465..65112406,2	MCF-7	breast:
2	chr14:65102703..65104469-chr14:65109001..65111503,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000259116	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10130241	0.81[ASN][1000 genomes]
rs10130755	0.87[ASN][1000 genomes]
rs10132794	0.93[CHB][hapmap];0.81[ASN][1000 genomes]
rs10133861	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10134770	0.94[CHB][hapmap];0.80[CHD][hapmap];0.83[JPT][hapmap];0.88[ASN][1000 genomes]
rs10138611	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10140678	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10144661	0.94[CHB][hapmap]
rs10145003	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10145101	1.00[CEU][hapmap];0.94[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10145275	1.00[CEU][hapmap];0.94[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10145844	0.85[ASN][1000 genomes]
rs10151656	0.94[CHB][hapmap];0.80[CHD][hapmap];0.87[ASN][1000 genomes]
rs10467818	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10498516	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11158547	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11158548	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11158549	1.00[ASW][hapmap];0.94[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];1.00[LWK][hapmap];0.88[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11158550	0.90[AFR][1000 genomes]
rs11158551	0.90[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs11844669	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11846008	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11846264	0.83[CHB][hapmap];0.88[GIH][hapmap]
rs11848587	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11850291	0.94[CHB][hapmap];0.83[ASN][1000 genomes]
rs12586275	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12588437	0.83[ASN][1000 genomes]
rs12588509	0.94[CHB][hapmap];0.83[ASN][1000 genomes]
rs17101956	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1955661	1.00[CEU][hapmap];0.94[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1955663	1.00[CEU][hapmap];0.94[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2123458	0.81[ASN][1000 genomes]
rs28714198	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28761289	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2884269	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56039018	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56396472	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58268586	0.90[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs58273663	0.90[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs61067746	0.90[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs61987036	0.83[ASN][1000 genomes]
rs61987038	0.82[ASN][1000 genomes]
rs7140482	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7148864	0.94[CHB][hapmap];0.82[CHD][hapmap];0.88[JPT][hapmap];0.91[ASN][1000 genomes]
rs7153518	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7156649	1.00[CEU][hapmap];0.94[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.89[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7160131	0.88[CHB][hapmap]
rs74056339	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs74056358	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs74056359	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8006017	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049097	chr14:65027753-65202018	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs1955662	ZBTB25	cis	cerebellum	SCAN
rs1955662	ZBTB25	cis	lymphoblastoid	seeQTL

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65099400-65111600	Weak transcription	Osteobl	bone
2	chr14:65103400-65111000	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr14:65103800-65111400	Weak transcription	Rectal Smooth Muscle	rectum
4	chr14:65103800-65111600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr14:65103800-65111800	Weak transcription	Fetal Heart	heart
6	chr14:65103800-65112400	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr14:65106800-65111600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr14:65106800-65111600	Weak transcription	NHLF	lung
9	chr14:65106800-65112600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr14:65106800-65112600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr14:65106800-65115400	Weak transcription	Fetal Intestine Small	intestine
12	chr14:65107000-65111200	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr14:65107000-65111800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr14:65107000-65112000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr14:65107000-65112000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr14:65108000-65111800	Weak transcription	HMEC	breast
17	chr14:65108200-65112000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr14:65108800-65111000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr14:65108800-65111800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr14:65110200-65111600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr14:65110600-65111200	ZNF genes & repeats	A549	lung
22	chr14:65110600-65116200	Enhancers	Placenta	Placenta
23	chr14:65110800-65111000	Weak transcription	HSMM	muscle
24	chr14:65110800-65111200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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