Variant report

Variant	rs28715006
Chromosome Location	chr19:56811623-56811624
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10401852	1.00[EUR][1000 genomes]
rs12104157	1.00[EUR][1000 genomes]
rs12104316	1.00[EUR][1000 genomes]
rs58167140	1.00[EUR][1000 genomes]
rs58477337	1.00[EUR][1000 genomes]
rs60994843	1.00[EUR][1000 genomes]
rs73621065	1.00[EUR][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	nsv1064371	chr19:56418215-56842450	ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
2	nsv1057316	chr19:56418215-56849458	Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
3	nsv912516	chr19:56601298-56981382	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	93 gene(s)	inside rSNPs	diseases
4	nsv526325	chr19:56741186-56852035	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
5	nsv949121	chr19:56754719-57591038	ZNF genes & repeats Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
6	nsv1062341	chr19:56794070-57273332	Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
7	nsv544094	chr19:56794070-57273332	Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
8	nsv912517	chr19:56794645-56822466	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv1056713	chr19:56799151-57265682	ZNF genes & repeats Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
10	nsv544095	chr19:56799151-57265682	Strong transcription ZNF genes & repeats Active TSS Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
11	nsv1058026	chr19:56799847-56833153	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 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	chr19:56771400-56817200	Weak transcription	Fetal Brain Male	brain
2	chr19:56772800-56824200	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr19:56775800-56815600	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr19:56779600-56820200	Weak transcription	Hela-S3	cervix
5	chr19:56782800-56825200	Weak transcription	Psoas Muscle	Psoas
6	chr19:56783000-56825000	Weak transcription	Stomach Mucosa	stomach
7	chr19:56785400-56823600	Weak transcription	Osteobl	bone
8	chr19:56786800-56813000	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr19:56788200-56824400	Weak transcription	Rectal Smooth Muscle	rectum
10	chr19:56788800-56813000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr19:56789000-56817400	Weak transcription	Small Intestine	intestine
12	chr19:56789000-56823800	Weak transcription	Brain Angular Gyrus	brain
13	chr19:56790600-56820000	Weak transcription	Primary B cells from cord blood	blood
14	chr19:56794000-56813000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr19:56796400-56816600	Weak transcription	Fetal Kidney	kidney
16	chr19:56796600-56813000	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr19:56797600-56811800	Strong transcription	Fetal Stomach	stomach
18	chr19:56798200-56813000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr19:56799800-56825200	Weak transcription	Right Atrium	heart
20	chr19:56800800-56817400	Weak transcription	Fetal Brain Female	brain
21	chr19:56801400-56814800	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr19:56801600-56812800	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr19:56802400-56821800	Weak transcription	Primary B cells from peripheral blood	blood
24	chr19:56802800-56813000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr19:56803000-56812800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr19:56803000-56813000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr19:56803000-56816600	Weak transcription	Dnd41	blood
28	chr19:56803000-56824200	Weak transcription	Fetal Thymus	thymus
29	chr19:56803200-56825000	Weak transcription	Colon Smooth Muscle	Colon
30	chr19:56803600-56816600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr19:56804400-56825000	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr19:56804600-56815000	Weak transcription	HSMMtube	muscle
33	chr19:56804600-56825000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr19:56804800-56813000	Weak transcription	Primary T cells from cord blood	blood
35	chr19:56804800-56820200	Weak transcription	HSMM	muscle
36	chr19:56805200-56815200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr19:56805200-56825400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr19:56805600-56820200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr19:56806000-56825000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr19:56806400-56814200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr19:56806400-56815200	Weak transcription	Brain Cingulate Gyrus	brain
42	chr19:56806400-56816000	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr19:56806400-56825200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr19:56806400-56825200	Weak transcription	Brain Hippocampus Middle	brain
45	chr19:56806400-56825200	Weak transcription	NH-A	brain
46	chr19:56806600-56812800	Weak transcription	Brain Anterior Caudate	brain
47	chr19:56806600-56814200	Weak transcription	Brain Substantia Nigra	brain
48	chr19:56806600-56814200	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr19:56806600-56814400	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr19:56806600-56825000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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