Variant report

Variant	rs531529107
Chromosome Location	chr19:18716632-18716633
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr19:18716009-18718542	HepG2	liver:	n/a	n/a
2	ZBTB7A	chr19:18716541-18717420	ECC-1	luminal epithelium:	n/a	chr19:18716546-18716554 chr19:18716946-18716954 chr19:18716935-18716943
3	MAX	chr19:18716141-18717800	HepG2	liver:	n/a	chr19:18717315-18717325 chr19:18716898-18716908 chr19:18716978-18716988 chr19:18716969-18716976 chr19:18716668-18716678
4	POLR2A	chr19:18716237-18716867	H1-neurons	neurons:	n/a	n/a
5	SUZ12	chr19:18716185-18716661	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:18713204..18718867-chr19:18719015..18725496,7	MCF-7	breast:
2	chr19:18714829..18718349-chr19:18723409..18727026,4	K562	blood:
3	chr19:18713933..18717054-chr19:18723624..18727026,3	K562	blood:
4	chr19:18715795..18719274-chr19:18719391..18724999,7	MCF-7	breast:
5	chr19:18546602..18548402-chr19:18715878..18718027,2	MCF-7	breast:
6	chr19:18714258..18716711-chr19:18719461..18722423,3	K562	blood:

Variant related genes	Relation type
TMEM59L	TF binding region
ENSG00000105655	Chromatin interaction
ENSG00000105696	Chromatin interaction

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

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1057795	chr19:18453362-18883844	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
2	nsv543925	chr19:18453362-18883844	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
3	nsv532615	chr19:18534867-18796031	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
4	nsv911281	chr19:18613917-18758255	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
5	nsv911282	chr19:18624964-18928480	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription 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	60 gene(s)	inside rSNPs	diseases
6	nsv833776	chr19:18638028-18782264	Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
7	nsv911286	chr19:18652844-18811112	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
8	nsv911287	chr19:18699333-18727913	Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	18 gene(s)	inside rSNPs	diseases
9	nsv911288	chr19:18700047-18739497	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	18 gene(s)	inside rSNPs	diseases
10	nsv911289	chr19:18700047-18811112	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
11	nsv911290	chr19:18701499-18720981	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
12	nsv911291	chr19:18701499-18726856	Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
13	nsv911292	chr19:18701499-18731658	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
14	esv1822476	chr19:18710535-18717425	Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
15	esv3392352	chr19:18715977-18718525	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18713600-18716800	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr19:18714000-18718200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr19:18714200-18717200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr19:18714400-18716800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr19:18714400-18717600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
6	chr19:18714400-18718400	Active TSS	HSMMtube	muscle
7	chr19:18714400-18719000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr19:18714800-18716800	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr19:18715000-18717000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
10	chr19:18715000-18718200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
11	chr19:18715400-18717000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
12	chr19:18715400-18717400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr19:18715400-18717400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
14	chr19:18715400-18718200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
15	chr19:18715400-18719000	Active TSS	HSMM	muscle
16	chr19:18715800-18717000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr19:18715800-18717200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
18	chr19:18716000-18717200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
19	chr19:18716000-18718800	Bivalent/Poised TSS	Osteobl	bone
20	chr19:18716200-18717000	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr19:18716200-18717200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
22	chr19:18716200-18717200	Transcr. at gene 5' and 3'	Right Atrium	heart
23	chr19:18716200-18718800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
24	chr19:18716200-18718800	Bivalent Enhancer	Colonic Mucosa	Colon
25	chr19:18716200-18719000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
26	chr19:18716400-18716800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr19:18716400-18716800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr19:18716400-18716800	Bivalent/Poised TSS	Brain Anterior Caudate	brain
29	chr19:18716400-18716800	Bivalent Enhancer	Brain Germinal Matrix	brain
30	chr19:18716400-18716800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
31	chr19:18716400-18716800	Flanking Active TSS	Pancreas	Pancrea
32	chr19:18716400-18716800	Enhancers	A549	lung
33	chr19:18716400-18717000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr19:18716400-18717000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr19:18716400-18717000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr19:18716400-18717000	Bivalent/Poised TSS	Esophagus	oesophagus
37	chr19:18716400-18717200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr19:18716400-18717200	Bivalent Enhancer	Brain Hippocampus Middle	brain
39	chr19:18716400-18717200	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr19:18716400-18717200	Bivalent Enhancer	Placenta	Placenta
41	chr19:18716400-18717200	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
42	chr19:18716400-18717200	Bivalent/Poised TSS	HepG2	liver
43	chr19:18716400-18717400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr19:18716400-18717400	Bivalent Enhancer	Spleen	Spleen
45	chr19:18716400-18718000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr19:18716400-18718200	Bivalent/Poised TSS	Left Ventricle	heart
47	chr19:18716400-18718600	Bivalent/Poised TSS	Psoas Muscle	Psoas
48	chr19:18716600-18716800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr19:18716600-18716800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
50	chr19:18716600-18716800	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle

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