Variant report

Variant	rs11937789
Chromosome Location	chr4:127608111-127608112
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:127606260..127608204-chr4:127695271..127697298,2	K562	blood:
2	chr4:127605123..127609029-chr4:127609783..127616585,6	K562	blood:
3	chr4:127606260..127608427-chr4:127694328..127697298,2	K562	blood:
4	chr4:127599658..127603060-chr4:127607594..127612436,4	K562	blood:

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10005082	0.89[ASN][1000 genomes]
rs1160368	0.83[ASN][1000 genomes]
rs13134248	0.90[ASN][1000 genomes]
rs1552665	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs167504	0.94[ASN][1000 genomes]
rs167505	0.87[ASN][1000 genomes]
rs16896	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17011412	0.84[AMR][1000 genomes]
rs17011435	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17011443	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs170195	0.94[ASN][1000 genomes]
rs170196	0.99[ASN][1000 genomes]
rs17200542	0.91[ASN][1000 genomes]
rs17261025	0.86[EUR][1000 genomes]
rs178299	0.94[ASN][1000 genomes]
rs186366	0.93[ASN][1000 genomes]
rs2391077	0.83[ASN][1000 genomes]
rs313046	0.94[ASN][1000 genomes]
rs313047	0.95[ASN][1000 genomes]
rs313048	0.95[ASN][1000 genomes]
rs313049	0.93[ASN][1000 genomes]
rs313050	0.95[ASN][1000 genomes]
rs313063	0.95[ASN][1000 genomes]
rs313066	0.95[ASN][1000 genomes]
rs313067	0.95[ASN][1000 genomes]
rs313069	0.99[ASN][1000 genomes]
rs313070	0.99[ASN][1000 genomes]
rs313071	0.99[ASN][1000 genomes]
rs313072	0.99[ASN][1000 genomes]
rs434002	0.84[ASN][1000 genomes]
rs435220	0.99[ASN][1000 genomes]
rs450453	0.85[ASN][1000 genomes]
rs56348808	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62322732	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62322733	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62324174	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62324175	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62324176	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6816353	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6845383	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6857039	0.99[ASN][1000 genomes]
rs7691175	0.93[CEU][hapmap];0.94[CHB][hapmap];0.93[JPT][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012833	chr4:127468474-127760933	Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv537242	chr4:127468474-127760933	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv524850	chr4:127470903-127768849	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1013854	chr4:127508969-127663216	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1009499	chr4:127532856-127659010	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv537243	chr4:127532856-127659010	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1007477	chr4:127561735-127726291	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv537244	chr4:127561735-127726291	Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv2752024	chr4:127584697-127671942	Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv595386	chr4:127597069-127668828	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv1028609	chr4:127597319-127664629	Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:127586800-127608800	Weak transcription	K562	blood
2	chr4:127607400-127608600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr4:127608000-127608400	Weak transcription	Fetal Lung	lung

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