Variant report

Variant	rs11629762
Chromosome Location	chr15:58804106-58804107
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:58800669..58805424-chr15:58807712..58810883,4	K562	blood:
2	chr15:58797035..58800948-chr15:58803702..58808140,4	K562	blood:
3	chr15:58797460..58800451-chr15:58803881..58805523,2	K562	blood:
4	chr15:58801519..58805506-chr15:58811166..58813986,3	K562	blood:

Variant related genes	Relation type
ENSG00000259476	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11630152	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11630220	1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11633131	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11638347	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17190615	0.82[CHB][hapmap]
rs2899632	0.82[CHB][hapmap]
rs7174210	1.00[CEU][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7175593	0.82[CHB][hapmap]
rs8029592	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051058	chr15:58519922-59092530	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv542401	chr15:58519922-59092530	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv569598	chr15:58552606-58852463	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	esv3362898	chr15:58705732-58850860	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1043041	chr15:58744505-58876327	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv569601	chr15:58800766-58866156	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58791400-58809400	Weak transcription	Spleen	Spleen
2	chr15:58798600-58807800	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr15:58798600-58813200	Weak transcription	Aorta	Aorta
4	chr15:58798800-58807800	Weak transcription	Primary B cells from cord blood	blood
5	chr15:58798800-58812600	Weak transcription	Left Ventricle	heart
6	chr15:58799000-58804600	Weak transcription	Placenta	Placenta
7	chr15:58799000-58805000	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr15:58799000-58806000	Weak transcription	Psoas Muscle	Psoas
9	chr15:58799200-58807200	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr15:58799200-58809400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr15:58799400-58805000	Weak transcription	Fetal Thymus	thymus
12	chr15:58799400-58807800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr15:58800000-58804600	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr15:58801000-58806600	Enhancers	HSMMtube	muscle
15	chr15:58802400-58805000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr15:58802600-58805200	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr15:58802800-58806400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr15:58803200-58805000	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr15:58803400-58804200	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr15:58803400-58805600	Weak transcription	A549	lung
21	chr15:58803600-58805600	Weak transcription	NHDF-Ad	bronchial
22	chr15:58803600-58805800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr15:58803600-58807000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr15:58803600-58811800	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr15:58803800-58804800	Weak transcription	Fetal Muscle Leg	muscle
26	chr15:58803800-58805200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr15:58803800-58805400	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr15:58803800-58805600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr15:58803800-58805600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr15:58803800-58805800	Weak transcription	NHEK	skin
31	chr15:58803800-58807800	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr15:58803800-58812600	Weak transcription	Esophagus	oesophagus
33	chr15:58804000-58805000	Weak transcription	HSMM	muscle
34	chr15:58804000-58816200	Weak transcription	Liver	Liver

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