Variant report

Variant	rs115677533
Chromosome Location	chr15:74556133-74556134
allele	A/G
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	chr15:74555739-74556988	H1-neurons	neurons:	n/a	n/a
2	REST	chr15:74555643-74556327	PFSK-1	brain:	n/a	chr15:74555689-74555703
3	REST	chr15:74555762-74556252	PFSK-1	brain:	n/a	n/a
4	CTCF	chr15:74556040-74556190	HAc	cerebellar:	n/a	n/a
5	REST	chr15:74555552-74557904	H1-neurons	neurons:	n/a	chr15:74557566-74557575 chr15:74557574-74557584 chr15:74557567-74557585 chr15:74556945-74556958 chr15:74555689-74555703 chr15:74557566-74557586 chr15:74557566-74557586 chr15:74557569-74557582 chr15:74557566-74557586 chr15:74557569-74557582 chr15:74557566-74557579 chr15:74557572-74557586
6	POLR2A	chr15:74555703-74556937	H1-neurons	neurons:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:74550593..74553035-chr15:74555004..74556677,2	K562	blood:
2	chr15:74555453..74556406-chr15:74595045..74595674,2	MCF-7	breast:
3	chr15:74555720..74556384-chr15:74594990..74595654,2	MCF-7	breast:

Variant related genes	Relation type
CCDC33	TF binding region
ENSG00000261384	Chromatin interaction

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833054	chr15:74457643-74625283	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1035367	chr15:74554972-74586538	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv428641	chr15:74555113-74724630	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74548600-74558000	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr15:74549200-74556200	Enhancers	Brain Germinal Matrix	brain
3	chr15:74549400-74557800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr15:74550000-74557800	Enhancers	Fetal Brain Male	brain
5	chr15:74553200-74556600	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr15:74553800-74556400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
7	chr15:74553800-74557400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr15:74554400-74557600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr15:74555200-74557600	Enhancers	Fetal Brain Female	brain
10	chr15:74555600-74556200	Bivalent Enhancer	Fetal Lung	lung
11	chr15:74555600-74556400	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr15:74555600-74556400	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr15:74555600-74557000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr15:74555600-74557000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr15:74555600-74557400	Enhancers	H1 Cell Line	embryonic stem cell
16	chr15:74555600-74557600	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr15:74555600-74557600	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr15:74555800-74556200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr15:74555800-74556400	Enhancers	Brain Hippocampus Middle	brain
20	chr15:74555800-74557000	Enhancers	Fetal Stomach	stomach
21	chr15:74555800-74557200	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr15:74555800-74557600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr15:74556000-74556200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr15:74556000-74556200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr15:74556000-74556200	Bivalent Enhancer	Brain Angular Gyrus	brain
26	chr15:74556000-74556200	Enhancers	Fetal Heart	heart
27	chr15:74556000-74556200	Enhancers	Fetal Kidney	kidney
28	chr15:74556000-74556400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr15:74556000-74556400	Enhancers	Brain Substantia Nigra	brain
30	chr15:74556000-74556600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr15:74556000-74556800	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr15:74556000-74557000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
33	chr15:74556000-74557000	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr15:74556000-74557000	Enhancers	Spleen	Spleen
35	chr15:74556000-74557200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr15:74556000-74557200	Enhancers	H9 Cell Line	embryonic stem cell
37	chr15:74556000-74557200	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr15:74556000-74557200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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