Variant report

Variant	rs17717651
Chromosome Location	chr4:143453079-143453080
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:143390775..143397216-chr4:143452311..143461627,17	MCF-7	breast:
2	chr4:143393273..143395827-chr4:143451885..143454348,2	MCF-7	breast:
3	chr4:143451539..143454827-chr4:143468974..143471578,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000109452	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10519649	0.95[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11100748	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11100749	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11728822	0.87[JPT][hapmap]
rs11930912	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12504375	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12504378	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12504418	0.81[JPT][hapmap]
rs12504770	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1425518	0.82[CEU][hapmap];0.84[CHB][hapmap];0.87[JPT][hapmap];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1425519	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1476122	0.86[EUR][1000 genomes]
rs16998558	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs16998560	0.83[JPT][hapmap]
rs17016344	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17016354	0.83[CHB][hapmap];0.80[EUR][1000 genomes]
rs2059510	0.95[CEU][hapmap];0.92[CHB][hapmap];0.93[JPT][hapmap];0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2059511	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2059513	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2217016	0.82[CEU][hapmap];0.85[CHB][hapmap];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35854467	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4246729	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4524461	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4975306	0.95[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4975313	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4975316	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4975317	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4975318	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58899027	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs60329859	0.86[AMR][1000 genomes]
rs61104737	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6537109	0.82[CEU][hapmap];0.80[EUR][1000 genomes]
rs6537110	0.80[EUR][1000 genomes]
rs6816875	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7671198	0.82[EUR][1000 genomes];0.81[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	nsv498005	chr4:142515689-143502988	Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv461660	chr4:143437219-143538179	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv595605	chr4:143437219-143538179	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:143438800-143462800	Weak transcription	Aorta	Aorta
2	chr4:143444400-143456400	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr4:143444800-143468400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:143451000-143454400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr4:143451400-143455400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr4:143451800-143453600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr4:143452200-143453200	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr4:143452200-143453400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr4:143452200-143453400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr4:143452200-143453400	Weak transcription	Left Ventricle	heart
11	chr4:143452200-143453800	Enhancers	Fetal Heart	heart
12	chr4:143452400-143453400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr4:143452800-143458800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr4:143453000-143453600	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr4:143453000-143453800	Enhancers	Primary hematopoietic stem cells	blood
16	chr4:143453000-143453800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr4:143453000-143464000	Weak transcription	Fetal Intestine Small	intestine

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