Variant report

Variant	rs73139219
Chromosome Location	chr5:96335567-96335568
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	chr5:96328610..96330249-chr5:96333541..96335673,2	K562	blood:

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1423567	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58748938	0.88[AFR][1000 genomes]
rs59959433	1.00[AMR][1000 genomes]
rs73135411	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73135415	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73135418	1.00[AMR][1000 genomes]
rs73135420	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73135421	1.00[AMR][1000 genomes]
rs73135423	1.00[AMR][1000 genomes]
rs73135424	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73137399	1.00[AMR][1000 genomes]
rs73139226	1.00[AMR][1000 genomes]
rs73139235	1.00[AMR][1000 genomes]
rs73139238	1.00[AMR][1000 genomes]
rs73139248	1.00[AMR][1000 genomes]
rs73139255	1.00[AMR][1000 genomes]
rs73141126	1.00[AMR][1000 genomes]
rs73141135	0.85[AFR][1000 genomes]
rs7728347	0.89[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432755	chr5:95987984-96657483	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv598962	chr5:96057891-96893164	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv948703	chr5:96078309-96368839	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv1027472	chr5:96081592-96337550	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv1028741	chr5:96082401-96372165	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv949058	chr5:96082433-96390619	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv598963	chr5:96084776-96363407	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96304600-96335600	Weak transcription	Stomach Mucosa	stomach
2	chr5:96304800-96346600	Weak transcription	Lung	lung
3	chr5:96304800-96359600	Weak transcription	Hela-S3	cervix
4	chr5:96313400-96342600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr5:96313400-96342600	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr5:96314000-96360200	Weak transcription	Fetal Brain Male	brain
7	chr5:96314200-96343600	Strong transcription	Primary B cells from peripheral blood	blood
8	chr5:96314200-96344000	Strong transcription	Primary B cells from cord blood	blood
9	chr5:96314200-96347600	Strong transcription	Fetal Thymus	thymus
10	chr5:96314400-96343800	Strong transcription	Dnd41	blood
11	chr5:96314800-96343200	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr5:96314800-96343800	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr5:96315400-96374800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr5:96315600-96335600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr5:96315600-96353400	Weak transcription	Pancreas	Pancrea
16	chr5:96315600-96358600	Weak transcription	Brain Substantia Nigra	brain
17	chr5:96316000-96338400	Weak transcription	Brain Hippocampus Middle	brain
18	chr5:96316000-96360000	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr5:96316200-96335800	Weak transcription	NHLF	lung
20	chr5:96316400-96336000	Weak transcription	Colonic Mucosa	Colon
21	chr5:96316400-96346600	Weak transcription	NH-A	brain
22	chr5:96320000-96357600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr5:96321000-96336200	Weak transcription	Rectal Smooth Muscle	rectum
24	chr5:96321200-96344600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr5:96321600-96344800	Weak transcription	Small Intestine	intestine
26	chr5:96322200-96348600	Weak transcription	Fetal Kidney	kidney
27	chr5:96322200-96349800	Weak transcription	Psoas Muscle	Psoas
28	chr5:96322400-96336000	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr5:96322400-96336200	Weak transcription	K562	blood
30	chr5:96322400-96353600	Weak transcription	Right Ventricle	heart
31	chr5:96322400-96358600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr5:96322400-96359600	Weak transcription	Gastric	stomach
33	chr5:96323800-96342200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr5:96325800-96338200	Strong transcription	Primary T helper cells PMA-I stimulated	--
35	chr5:96326400-96346600	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr5:96326800-96340200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr5:96327000-96339600	Weak transcription	Ovary	ovary
38	chr5:96327400-96339600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr5:96329800-96358800	Weak transcription	Brain Germinal Matrix	brain
40	chr5:96330000-96359800	Weak transcription	Aorta	Aorta
41	chr5:96330200-96340400	Weak transcription	Osteobl	bone
42	chr5:96330400-96335600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr5:96330400-96335800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr5:96330400-96336000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr5:96330400-96336400	Weak transcription	HSMMtube	muscle
46	chr5:96330400-96359400	Weak transcription	Fetal Brain Female	brain
47	chr5:96330600-96339000	Weak transcription	Fetal Lung	lung
48	chr5:96330600-96339800	Weak transcription	Brain Angular Gyrus	brain
49	chr5:96330600-96353600	Weak transcription	Esophagus	oesophagus
50	chr5:96330800-96339400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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