Variant report

Variant	rs147924751
Chromosome Location	chr14:21565547-21565548
allele	C/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	chr14:21565020-21566202	H1-hESC	embryonic stem cell:	n/a	n/a
2	POLR2A	chr14:21565045-21566036	HepG2	liver:	n/a	n/a
3	SIN3A	chr14:21565409-21566096	H1-hESC	embryonic stem cell:	n/a	chr14:21565653-21565662 chr14:21565908-21565921
4	POLR2A	chr14:21565304-21566238	H1-neurons	neurons:	n/a	n/a
5	REST	chr14:21565156-21566323	H1-neurons	neurons:	n/a	chr14:21565286-21565299 chr14:21565914-21565927
6	CTCF	chr14:21565460-21565610	SK-N-SH_RA	brain:	n/a	n/a
7	POLR2A	chr14:21565292-21566036	H1-hESC	embryonic stem cell:	n/a	n/a
8	POLR2A	chr14:21564991-21565967	HepG2	liver:	n/a	n/a
9	POLR2A	chr14:21564633-21565555	HepG2	liver:	n/a	n/a
10	POLR2A	chr14:21565534-21566152	H1-hESC	embryonic stem cell:	n/a	n/a
11	USF1	chr14:21565485-21565768	H1-hESC	embryonic stem cell:	n/a	n/a
12	MAX	chr14:21565505-21565947	H1-hESC	embryonic stem cell:	n/a	chr14:21565867-21565877 chr14:21565651-21565662
13	POLR2A	chr14:21565325-21566191	H1-neurons	neurons:	n/a	n/a
14	HEY1	chr14:21565094-21566018	HepG2	liver:	n/a	chr14:21565903-21565918

No.	Distal block	Cell Line	Cell type
1	chr14:21493465..21495146-chr14:21564517..21566869,2	K562	blood:
2	chr14:21493156..21496539-chr14:21563277..21566869,4	K562	blood:
3	chr14:21538435..21540879-chr14:21565246..21568452,4	K562	blood:
4	chr14:21560808..21562943-chr14:21563849..21565971,2	K562	blood:
5	chr14:21559218..21562308-chr14:21563084..21566776,3	K562	blood:
6	chr14:21535130..21541812-chr14:21564802..21576767,22	MCF-7	breast:
7	chr14:21529965..21532217-chr14:21564746..21566795,2	MCF-7	breast:
8	chr14:21534879..21542621-chr14:21563384..21568050,9	MCF-7	breast:
9	chr14:21488163..21490230-chr14:21563775..21566660,2	K562	blood:

Variant related genes	Relation type
TMEM253	TF binding region
ZNF219	TF binding region
ENSG00000165801	Chromatin interaction
ENSG00000165804	Chromatin interaction
ENSG00000165795	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

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	nsv530009	chr14:21377022-22044608	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
2	nsv530769	chr14:21407536-22139126	Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
3	nsv916319	chr14:21507092-21896590	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	nsv1036762	chr14:21507093-22101805	Enhancers Strong transcription Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
5	nsv541976	chr14:21507093-22101805	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
6	nsv826882	chr14:21511021-21604201	Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
7	nsv530770	chr14:21526410-21852363	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
8	nsv525724	chr14:21540863-21574690	Active TSS Flanking Active TSS Genic enhancers Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	esv3490839	chr14:21565112-21567760	Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	esv3490842	chr14:21565112-21567760	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	esv3423964	chr14:21565137-21567985	Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21545200-21565600	Weak transcription	Psoas Muscle	Psoas
2	chr14:21555800-21565600	Weak transcription	HSMMtube	muscle
3	chr14:21555800-21566200	Weak transcription	HSMM	muscle
4	chr14:21556400-21565600	Weak transcription	Primary B cells from cord blood	blood
5	chr14:21558800-21566600	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr14:21559800-21566600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr14:21560600-21565600	Enhancers	Brain Hippocampus Middle	brain
8	chr14:21560800-21565800	Weak transcription	Small Intestine	intestine
9	chr14:21561000-21565800	Weak transcription	Ovary	ovary
10	chr14:21561200-21565600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr14:21561200-21565600	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr14:21561600-21566600	Weak transcription	Gastric	stomach
13	chr14:21561600-21566800	Weak transcription	Spleen	Spleen
14	chr14:21562000-21566000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
15	chr14:21562200-21566800	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr14:21562400-21565600	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr14:21562600-21565600	Weak transcription	Brain Anterior Caudate	brain
18	chr14:21562600-21566800	Weak transcription	Liver	Liver
19	chr14:21563800-21565800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr14:21564200-21565600	Enhancers	Fetal Muscle Leg	muscle
21	chr14:21564200-21565800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
22	chr14:21564400-21565600	Enhancers	Right Atrium	heart
23	chr14:21564400-21565800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr14:21564400-21566000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr14:21564400-21566000	Enhancers	Left Ventricle	heart
26	chr14:21564600-21565600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr14:21564600-21565600	Enhancers	Brain Angular Gyrus	brain
28	chr14:21564600-21565800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
29	chr14:21564600-21565800	Flanking Active TSS	Brain Germinal Matrix	brain
30	chr14:21564600-21566000	Enhancers	Brain Cingulate Gyrus	brain
31	chr14:21564600-21566600	Weak transcription	Osteobl	bone
32	chr14:21564600-21566800	Enhancers	Placenta	Placenta
33	chr14:21564800-21565600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
34	chr14:21564800-21565600	Enhancers	Brain Substantia Nigra	brain
35	chr14:21564800-21565800	Flanking Active TSS	NHEK	skin
36	chr14:21564800-21566000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr14:21564800-21566000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr14:21564800-21566000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr14:21564800-21567000	Active TSS	Fetal Brain Female	brain
40	chr14:21565000-21565600	Flanking Active TSS	H9 Cell Line	embryonic stem cell
41	chr14:21565000-21565600	Enhancers	Fetal Lung	lung
42	chr14:21565000-21566000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr14:21565000-21566000	Flanking Active TSS	A549	lung
44	chr14:21565000-21566000	Flanking Active TSS	HMEC	breast
45	chr14:21565000-21567400	Active TSS	Sigmoid Colon	Sigmoid Colon
46	chr14:21565200-21565600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
47	chr14:21565200-21565600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr14:21565200-21565600	Flanking Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr14:21565200-21565600	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
50	chr14:21565200-21565600	Enhancers	Primary T cells from cord blood	blood

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