Variant report

Variant	rs9903631
Chromosome Location	chr17:19908995-19908996
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	chr17:19908823..19910742-chr17:19910847..19912569,3	K562	blood:

Variant related genes	Relation type
ENSG00000261033	Chromatin interaction

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs16960545	1.00[EUR][1000 genomes]
rs16960602	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28410781	0.91[ASN][1000 genomes]
rs28424266	1.00[EUR][1000 genomes]
rs28581607	1.00[EUR][1000 genomes]
rs28653561	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28713561	0.91[ASN][1000 genomes]
rs28767032	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28830504	0.88[ASN][1000 genomes]
rs28865331	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3909257	0.88[ASN][1000 genomes]
rs6587207	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6587208	0.91[ASN][1000 genomes]
rs6587212	0.88[ASN][1000 genomes]
rs7207459	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7207702	0.88[ASN][1000 genomes]
rs7208033	0.91[ASN][1000 genomes]
rs7210076	0.91[ASN][1000 genomes]
rs7210751	0.88[ASN][1000 genomes]
rs7214107	0.91[ASN][1000 genomes]
rs7215639	1.00[EUR][1000 genomes]
rs7215769	1.00[EUR][1000 genomes]
rs7217387	0.91[ASN][1000 genomes]
rs7217862	0.84[ASN][1000 genomes]
rs7217868	0.84[ASN][1000 genomes]
rs7217928	1.00[EUR][1000 genomes]
rs7218251	1.00[EUR][1000 genomes]
rs7218919	0.88[ASN][1000 genomes]
rs7219153	0.88[ASN][1000 genomes]
rs7220490	0.84[ASN][1000 genomes]
rs7221669	0.88[ASN][1000 genomes]
rs7223323	0.88[ASN][1000 genomes]
rs7224373	0.91[ASN][1000 genomes]
rs7224419	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7224567	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7224713	1.00[EUR][1000 genomes]
rs7224875	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8065122	1.00[EUR][1000 genomes]
rs8068015	1.00[EUR][1000 genomes]
rs8068488	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8071670	1.00[EUR][1000 genomes]
rs8079093	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8079487	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8080190	0.98[ASN][1000 genomes]
rs8082671	0.91[ASN][1000 genomes]
rs9889938	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9891008	0.91[ASN][1000 genomes]
rs9892175	0.88[ASN][1000 genomes]
rs9892271	1.00[EUR][1000 genomes]
rs9893185	0.91[ASN][1000 genomes]
rs9893296	1.00[EUR][1000 genomes]
rs9894666	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9896010	0.91[ASN][1000 genomes]
rs9896387	0.91[ASN][1000 genomes]
rs9896499	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9896633	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9896641	1.00[EUR][1000 genomes]
rs9897430	1.00[EUR][1000 genomes]
rs9897607	0.88[ASN][1000 genomes]
rs9898618	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9900393	0.91[ASN][1000 genomes]
rs9900441	0.91[ASN][1000 genomes]
rs9900510	1.00[EUR][1000 genomes]
rs9901862	0.91[ASN][1000 genomes]
rs9902663	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9904059	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9908415	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9909011	0.91[ASN][1000 genomes]
rs9909012	0.88[ASN][1000 genomes]
rs9909242	0.91[ASN][1000 genomes]
rs9909544	0.91[ASN][1000 genomes]
rs9911408	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9911872	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9912184	1.00[EUR][1000 genomes]
rs9912648	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9912657	0.91[ASN][1000 genomes]
rs9913858	1.00[EUR][1000 genomes]
rs9914328	0.86[ASN][1000 genomes]
rs9914429	0.91[ASN][1000 genomes]
rs9915039	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9915413	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062853	chr17:19547912-20206601	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
2	nsv907868	chr17:19768924-20217122	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv907869	chr17:19795774-19926836	Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv833394	chr17:19827714-19999577	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv1060337	chr17:19828636-20204872	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv543257	chr17:19828636-20204872	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
7	nsv907870	chr17:19871922-20001612	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
8	esv3382860	chr17:19894909-19918588	Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:19896600-19911600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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