Variant report

Variant	rs35699974
Chromosome Location	chr5:57385397-57385398
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:57378894..57391869-chr5:57753957..57758751,18	MCF-7	breast:
2	chr5:57385340..57390728-chr5:57748892..57752531,5	MCF-7	breast:
3	chr5:57377812..57380487-chr5:57383162..57386088,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000145632	Chromatin interaction

Extended variants
information (count: 102 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:101)

rs_ID	r²[population]
rs10461644	0.98[EUR][1000 genomes]
rs10461645	0.98[EUR][1000 genomes]
rs10491418	0.93[EUR][1000 genomes]
rs10491419	0.93[EUR][1000 genomes]
rs1125324	0.98[EUR][1000 genomes]
rs13152942	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13153091	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13155421	0.88[EUR][1000 genomes]
rs13159010	0.93[EUR][1000 genomes]
rs13159117	0.93[EUR][1000 genomes]
rs13160117	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13164786	0.96[EUR][1000 genomes]
rs13168168	0.88[EUR][1000 genomes]
rs13170721	0.88[EUR][1000 genomes]
rs13176924	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13177963	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13178678	0.95[EUR][1000 genomes]
rs13179148	0.93[EUR][1000 genomes]
rs13181962	0.93[EUR][1000 genomes]
rs13185082	0.93[EUR][1000 genomes]
rs13185712	0.88[EUR][1000 genomes]
rs13186152	0.93[EUR][1000 genomes]
rs13186306	0.93[EUR][1000 genomes]
rs13187466	0.93[EUR][1000 genomes]
rs13190103	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1549244	0.86[EUR][1000 genomes]
rs1565335	0.96[EUR][1000 genomes]
rs17367557	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17367866	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17368537	0.93[EUR][1000 genomes]
rs17368635	0.93[EUR][1000 genomes]
rs17368691	0.93[EUR][1000 genomes]
rs17368889	0.93[EUR][1000 genomes]
rs17368931	0.93[EUR][1000 genomes]
rs17368965	0.86[EUR][1000 genomes]
rs17369063	0.93[EUR][1000 genomes]
rs17369443	0.93[EUR][1000 genomes]
rs17369506	0.93[EUR][1000 genomes]
rs17369617	0.93[EUR][1000 genomes]
rs17369645	0.93[EUR][1000 genomes]
rs17370357	0.86[EUR][1000 genomes]
rs17433232	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17433281	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17433351	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17433413	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17433449	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17433525	0.93[EUR][1000 genomes]
rs17433602	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17433644	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17434105	0.89[EUR][1000 genomes]
rs17434147	0.93[EUR][1000 genomes]
rs17434756	0.93[EUR][1000 genomes]
rs17434985	0.93[EUR][1000 genomes]
rs17435116	0.93[EUR][1000 genomes]
rs17750857	0.88[EUR][1000 genomes]
rs17750946	0.88[EUR][1000 genomes]
rs17750970	0.95[EUR][1000 genomes]
rs17751024	0.88[EUR][1000 genomes]
rs2130362	0.85[EUR][1000 genomes]
rs2409072	0.95[EUR][1000 genomes]
rs2898084	0.95[EUR][1000 genomes]
rs34028264	0.93[EUR][1000 genomes]
rs34088369	0.96[EUR][1000 genomes]
rs34140627	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34145550	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34183980	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34283705	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34357926	0.93[EUR][1000 genomes]
rs34362402	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34393614	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34469485	0.93[EUR][1000 genomes]
rs34486088	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34540977	0.95[EUR][1000 genomes]
rs34558865	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34561456	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34563650	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34668052	0.93[EUR][1000 genomes]
rs34728348	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34739332	0.95[EUR][1000 genomes]
rs34839607	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34900511	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34911212	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35020899	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35102344	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35132533	0.88[EUR][1000 genomes]
rs35288659	0.93[EUR][1000 genomes]
rs35474010	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35480511	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35493107	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35559784	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35585983	0.93[EUR][1000 genomes]
rs35637947	0.93[EUR][1000 genomes]
rs36003001	0.93[EUR][1000 genomes]
rs36056213	0.93[EUR][1000 genomes]
rs36118761	0.93[EUR][1000 genomes]
rs4328995	0.93[EUR][1000 genomes]
rs58405952	0.91[EUR][1000 genomes]
rs71624184	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71624185	0.93[EUR][1000 genomes]
rs7734877	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7735526	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	nsv1033051	chr5:57380218-57471801	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:57380400-57386800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr5:57384200-57389400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr5:57384600-57385400	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr5:57384600-57385400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr5:57384600-57385800	Enhancers	Stomach Mucosa	stomach
6	chr5:57384600-57385800	Enhancers	HUVEC	blood vessel
7	chr5:57384600-57385800	Enhancers	K562	blood
8	chr5:57384800-57385400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr5:57385000-57385400	Enhancers	Adipose Nuclei	Adipose
10	chr5:57385000-57385800	Enhancers	A549	lung
11	chr5:57385200-57389400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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