Variant report

Variant	rs570358048
Chromosome Location	chr15:56273833-56273834
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:56272827..56275263-chr15:56276968..56278689,2	MCF-7	breast:
2	chr15:56271136..56275778-chr15:56283975..56288276,6	K562	blood:
3	chr15:56271720..56275778-chr15:56283975..56286935,4	K562	blood:

Variant related genes	Relation type
ENSG00000069869	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

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	esv2761872	chr15:56211065-56426501	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv904245	chr15:56229760-56324451	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv457159	chr15:56255774-56321854	Strong transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv569543	chr15:56255774-56321854	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv457160	chr15:56273446-56320235	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	n/a
6	nsv569544	chr15:56273446-56320235	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56229600-56282600	Weak transcription	NHLF	lung
2	chr15:56231400-56284200	Weak transcription	Stomach Smooth Muscle	stomach
3	chr15:56236200-56276000	Weak transcription	HUVEC	blood vessel
4	chr15:56236800-56282800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr15:56243200-56276200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr15:56248200-56285200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr15:56251600-56281600	Weak transcription	Osteobl	bone
8	chr15:56253600-56282400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr15:56257600-56281600	Weak transcription	Fetal Intestine Large	intestine
10	chr15:56257600-56283600	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr15:56257600-56283800	Weak transcription	Primary T cells from cord blood	blood
12	chr15:56262800-56274200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr15:56262800-56276200	Weak transcription	NHEK	skin
14	chr15:56262800-56276400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr15:56262800-56276600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr15:56262800-56276600	Weak transcription	HMEC	breast
17	chr15:56263000-56275400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr15:56263800-56282400	Weak transcription	Fetal Intestine Small	intestine
19	chr15:56269400-56282400	Weak transcription	Primary hematopoietic stem cells	blood
20	chr15:56270400-56281600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr15:56272600-56274000	Enhancers	HSMM	muscle
22	chr15:56272600-56284200	Weak transcription	Lung	lung
23	chr15:56272800-56281600	Weak transcription	Psoas Muscle	Psoas
24	chr15:56273000-56281600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr15:56273000-56283000	Weak transcription	HSMMtube	muscle
26	chr15:56273600-56274800	Enhancers	Muscle Satellite Cultured Cells	--
27	chr15:56273800-56274800	Enhancers	A549	lung
28	chr15:56273800-56277000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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