Variant report

Variant	rs145434816
Chromosome Location	chr12:49687881-49687882
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	KAP1	chr12:49686994-49689288	U2OS	brain:	n/a	chr12:49687857-49687865
2	KAP1	chr12:49686318-49689281	HEK293	kidney:	n/a	chr12:49687857-49687865

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:49660927..49665723-chr12:49685096..49688729,4	MCF-7	breast:
2	chr12:49686580..49692358-chr12:49712251..49718367,13	MCF-7	breast:
3	chr12:49656941..49662685-chr12:49687034..49693573,13	MCF-7	breast:
4	chr12:49685493..49694205-chr12:49728829..49734805,16	K562	blood:
5	chr12:49680691..49694205-chr12:49725987..49738512,25	K562	blood:
6	chr12:49656956..49663896-chr12:49681239..49693031,16	K562	blood:
7	chr12:49687485..49689033-chr12:49958204..49960498,2	K562	blood:
8	chr12:49686386..49687917-chr12:49689353..49691051,2	MCF-7	breast:
9	chr12:49665854..49668915-chr12:49685671..49689413,3	MCF-7	breast:
10	chr12:49654800..49660850-chr12:49685742..49692441,19	MCF-7	breast:

No data

Variant related genes	Relation type
PRPH	TF binding region
ENSG00000258232	Chromatin interaction
ENSG00000186897	Chromatin interaction
ENSG00000187778	Chromatin interaction
ENSG00000135451	Chromatin interaction
ENSG00000258334	Chromatin interaction
ENSG00000135406	Chromatin interaction
ENSG00000258101	Chromatin interaction
ENSG00000167553	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051161	chr12:49314550-49828473	Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Strong transcription Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
2	nsv541489	chr12:49314550-49828473	Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
3	nsv1036452	chr12:49376285-49867760	Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	315 gene(s)	inside rSNPs	diseases
4	nsv428801	chr12:49536659-49744884	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
5	esv19135	chr12:49676002-49690399	Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv558834	chr12:49676010-49691567	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv1042122	chr12:49678529-49823168	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
8	nsv1039176	chr12:49678529-49832618	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
9	nsv826367	chr12:49686493-49691709	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:49686400-49688000	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr12:49686400-49688800	Enhancers	A549	lung
3	chr12:49686600-49688800	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:49686600-49689800	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
5	chr12:49686600-49692000	Bivalent Enhancer	Placenta	Placenta
6	chr12:49686800-49688600	Enhancers	Right Ventricle	heart
7	chr12:49686800-49689000	Bivalent/Poised TSS	Fetal Intestine Small	intestine
8	chr12:49686800-49689400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr12:49687000-49688000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
10	chr12:49687000-49688200	Bivalent Enhancer	Stomach Mucosa	stomach
11	chr12:49687000-49689000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr12:49687000-49689200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr12:49687200-49688000	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
14	chr12:49687200-49689000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr12:49687200-49689000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr12:49687200-49689200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr12:49687400-49688000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr12:49687400-49688600	Bivalent Enhancer	Fetal Lung	lung
19	chr12:49687400-49688800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr12:49687400-49689000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
21	chr12:49687400-49690000	Bivalent Enhancer	Fetal Thymus	thymus
22	chr12:49687400-49690600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
23	chr12:49687600-49688000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
24	chr12:49687600-49688000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
25	chr12:49687600-49688600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr12:49687600-49689000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
27	chr12:49687600-49689000	Weak transcription	Gastric	stomach
28	chr12:49687600-49689200	Weak transcription	Ovary	ovary
29	chr12:49687600-49690400	Weak transcription	Lung	lung
30	chr12:49687600-49690600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
31	chr12:49687600-49691000	Bivalent Enhancer	Fetal Muscle Leg	muscle
32	chr12:49687600-49691000	Weak transcription	Hela-S3	cervix
33	chr12:49687800-49688200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr12:49687800-49688600	Bivalent Enhancer	Fetal Brain Female	brain
35	chr12:49687800-49689000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
36	chr12:49687800-49689000	Bivalent Enhancer	Fetal Stomach	stomach
37	chr12:49687800-49689000	Weak transcription	Right Atrium	heart
38	chr12:49687800-49690200	Weak transcription	K562	blood
39	chr12:49687800-49692000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell

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