Variant report

Variant	rs529455679
Chromosome Location	chr14:71787894-71787895
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	chr14:71786853-71788718	HepG2	liver:	n/a	n/a
2	POLR2A	chr14:71786820-71788234	K562	blood:	n/a	n/a
3	HA-E2F1	chr14:71786862-71788310	Hela-S3	cervix:	n/a	chr14:71787710-71787719 chr14:71787014-71787024 chr14:71787285-71787295 chr14:71787361-71787373 chr14:71787926-71787935
4	POLR2A	chr14:71786724-71788644	ECC-1	luminal epithelium:	n/a	n/a
5	POU2F2	chr14:71787675-71787969	GM12878	blood:	n/a	chr14:71787926-71787938 chr14:71787727-71787739
6	POLR2A	chr14:71786751-71788219	A549	lung:	n/a	n/a
7	POLR2A	chr14:71787799-71787965	HepG2	liver:	n/a	n/a
8	POLR2A	chr14:71786919-71787968	K562	blood:	n/a	n/a
9	MAX	chr14:71786604-71788409	A549	lung:	n/a	chr14:71787309-71787319
10	POLR2A	chr14:71786722-71788947	Hela-S3	cervix:	n/a	n/a
11	EBF1	chr14:71787582-71788402	GM12878	blood:	n/a	chr14:71787832-71787841 chr14:71787831-71787841 chr14:71787832-71787841
12	SIN3AK20	chr14:71787573-71788033	PANC-1	pancreas:	n/a	n/a
13	POLR2A	chr14:71786630-71788232	HUVEC	blood vessel:	n/a	n/a
14	YY1	chr14:71787691-71787894	K562	blood:	n/a	n/a
15	CCNT2	chr14:71786795-71788289	K562	blood:	n/a	chr14:71787977-71787986 chr14:71787390-71787399
16	TAF1	chr14:71786691-71788586	ECC-1	luminal epithelium:	n/a	n/a
17	POLR2A	chr14:71786769-71788029	HCT-116	colon:	n/a	n/a
18	PML	chr14:71786510-71789130	GM12878	blood:	n/a	chr14:71787820-71787828 chr14:71786649-71786657
19	POLR2A	chr14:71787655-71788078	PANC-1	pancreas:	n/a	n/a
20	POLR2A	chr14:71786553-71788996	HepG2	liver:	n/a	n/a
21	POLR2A	chr14:71786698-71789008	GM12878	blood:	n/a	n/a
22	POLR2A	chr14:71787570-71787973	H1-neurons	neurons:	n/a	n/a
23	EGR1	chr14:71786701-71788362	HCT-116	colon:	n/a	chr14:71788096-71788105 chr14:71787700-71787722 chr14:71787286-71787297 chr14:71787492-71787502 chr14:71787285-71787295 chr14:71787709-71787719 chr14:71787366-71787375 chr14:71787436-71787446 chr14:71786993-71787002 chr14:71788066-71788076 chr14:71787195-71787204 chr14:71787705-71787718 chr14:71787286-71787295 chr14:71787365-71787378 chr14:71787285-71787298 chr14:71788063-71788076 chr14:71788101-71788110 chr14:71787706-71787715 chr14:71787286-71787296 chr14:71788066-71788075 chr14:71787280-71787302 chr14:71787285-71787298 chr14:71787487-71787509 chr14:71787285-71787298 chr14:71787492-71787505 chr14:71787285-71787298 chr14:71787491-71787506 chr14:71787284-71787298 chr14:71787286-71787296 chr14:71787929-71787942
24	POLR2A	chr14:71786730-71788992	GM18526	blood:	n/a	n/a
25	TEAD4	chr14:71787390-71788744	SK-N-SH	brain:	n/a	n/a
26	TAF1	chr14:71787684-71787907	GM12891	blood:	n/a	n/a
27	HCFC1	chr14:71787814-71787955	K562	blood:	n/a	n/a
28	POLR2A	chr14:71786467-71789037	GM12891	blood:	n/a	n/a
29	POLR2A	chr14:71786818-71788201	K562	blood:	n/a	n/a
30	POLR2A	chr14:71787534-71787902	HL-60	blood:	n/a	n/a
31	POLR2A	chr14:71786832-71788211	Gliobla	brain:	n/a	n/a
32	POLR2A	chr14:71786916-71788155	HUVEC	blood vessel:	n/a	n/a
33	POLR2A	chr14:71786866-71787936	HEK293	kidney:	n/a	n/a
34	HEY1	chr14:71787577-71788022	HepG2	liver:	n/a	chr14:71787742-71787757 chr14:71787735-71787750
35	MXI1	chr14:71786032-71789994	SK-N-SH	brain:	n/a	chr14:71786940-71786955 chr14:71786938-71786953
36	POLR2A	chr14:71786814-71788101	HUVEC	blood vessel:	n/a	n/a
37	YY1	chr14:71786741-71788327	GM12892	blood:	n/a	chr14:71788065-71788074 chr14:71787284-71787298 chr14:71787285-71787299 chr14:71787926-71787937
38	ZKSCAN1	chr14:71787758-71788134	Hela-S3	cervix:	n/a	n/a
39	E2F4	chr14:71786697-71788161	MCF10A-Er-Src	breast:	n/a	chr14:71787710-71787719 chr14:71787014-71787024 chr14:71787285-71787295 chr14:71787361-71787373 chr14:71787926-71787935
40	MYC	chr14:71787762-71787957	MCF-7	breast:	n/a	n/a
41	POLR2A	chr14:71786787-71788370	HepG2	liver:	n/a	n/a
42	POLR2A	chr14:71786788-71788047	K562	blood:	n/a	n/a
43	POLR2A	chr14:71786551-71789055	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr14:71786906-71789123	GM12892	blood:	n/a	n/a
45	POLR2A	chr14:71787033-71787910	HUVEC	blood vessel:	n/a	n/a
46	YY1	chr14:71787772-71787955	HCT-116	colon:	n/a	chr14:71787926-71787937
47	POLR2A	chr14:71786941-71788172	K562	blood:	n/a	n/a
48	POLR2A	chr14:71786741-71788835	GM19193	blood:	n/a	n/a
49	UBTF	chr14:71787197-71788295	K562	blood:	n/a	n/a
50	MAZ	chr14:71786625-71788125	HepG2	liver:	n/a	chr14:71787309-71787319

No.	Distal block	Cell Line	Cell type
1	chr14:71787272..71789927-chr14:72149469..72152199,2	MCF-7	breast:
2	chr14:71786623..71788661-chr14:71864889..71866852,2	MCF-7	breast:
3	chr14:71608562..71610263-chr14:71786915..71789760,2	MCF-7	breast:
4	chr14:71647115..71649453-chr14:71786412..71788278,2	MCF-7	breast:
5	chr14:71787414..71788237-chr2:85766306..85767247,2	Hela-S3	cervix:
6	chr14:71787090..71788740-chr14:71796543..71798453,2	MCF-7	breast:
7	chr1:24127046..24127839-chr14:71786977..71787974,2	Hela-S3	cervix:
8	chr14:71776798..71778756-chr14:71785140..71789113,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SIPA1L1-2	chr14:71787839-71787898	NONHSAT037631

Variant related genes	Relation type
SIPA1L1	TF binding region
ENSG00000207444	Chromatin interaction
ENSG00000197555	Chromatin interaction
ENSG00000259146	Chromatin interaction
ENSG00000168906	Chromatin interaction
ENSG00000259079	Chromatin interaction
ENSG00000117308	Chromatin interaction
ENSG00000259907	Chromatin interaction
ENSG00000269927	Chromatin interaction

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832827	chr14:71676178-71833519	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	esv3405849	chr14:71786224-71789072	Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	esv1831401	chr14:71786411-71845264	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	esv3417213	chr14:71786699-71788597	Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71786000-71789200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
2	chr14:71786200-71788600	Active TSS	Fetal Stomach	stomach
3	chr14:71786200-71789000	Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chr14:71786200-71789200	Active TSS	HUES64 Cell Line	embryonic stem cell
5	chr14:71786200-71789200	Active TSS	Stomach Smooth Muscle	stomach
6	chr14:71786200-71789600	Active TSS	Rectal Smooth Muscle	rectum
7	chr14:71786200-71790000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr14:71786400-71788200	Active TSS	Primary hematopoietic stem cells short term culture	blood
9	chr14:71786400-71788200	Active TSS	Fetal Brain Female	brain
10	chr14:71786400-71788800	Active TSS	Duodenum Smooth Muscle	Duodenum
11	chr14:71786400-71788800	Active TSS	Right Ventricle	heart
12	chr14:71786400-71789000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr14:71786400-71789000	Active TSS	H9 Cell Line	embryonic stem cell
14	chr14:71786400-71789000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr14:71786400-71789000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
16	chr14:71786400-71789000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr14:71786400-71789000	Active TSS	Colonic Mucosa	Colon
18	chr14:71786400-71789000	Active TSS	Pancreatic Islets	Pancreatic Islet
19	chr14:71786400-71789000	Active TSS	Right Atrium	heart
20	chr14:71786400-71789200	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr14:71786400-71789400	Active TSS	Brain Angular Gyrus	brain
22	chr14:71786400-71789600	Active TSS	H1 Cell Line	embryonic stem cell
23	chr14:71786400-71789800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr14:71786400-71789800	Active TSS	Brain Inferior Temporal Lobe	brain
25	chr14:71786400-71790000	Active TSS	Brain Hippocampus Middle	brain
26	chr14:71786400-71790000	Active TSS	HSMM	muscle
27	chr14:71786400-71790000	Active TSS	HSMMtube	muscle
28	chr14:71786400-71790200	Active TSS	Stomach Mucosa	stomach
29	chr14:71786600-71788400	Active TSS	A549	lung
30	chr14:71786600-71788400	Active TSS	K562	blood
31	chr14:71786600-71788600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr14:71786600-71788600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr14:71786600-71788600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr14:71786600-71788600	Active TSS	Fetal Lung	lung
35	chr14:71786600-71788600	Active TSS	Gastric	stomach
36	chr14:71786600-71788600	Active TSS	Lung	lung
37	chr14:71786600-71788800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr14:71786600-71788800	Active TSS	Brain Cingulate Gyrus	brain
39	chr14:71786600-71788800	Active TSS	Pancreas	Pancrea
40	chr14:71786600-71788800	Active TSS	Placenta Amnion	Placenta Amnion
41	chr14:71786600-71788800	Active TSS	Rectal Mucosa Donor 29	rectum
42	chr14:71786600-71788800	Active TSS	Sigmoid Colon	Sigmoid Colon
43	chr14:71786600-71789000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr14:71786600-71789000	Active TSS	HUES6 Cell Line	embryonic stem cell
45	chr14:71786600-71789000	Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr14:71786600-71789000	Active TSS	Esophagus	oesophagus
47	chr14:71786600-71789000	Active TSS	Left Ventricle	heart
48	chr14:71786600-71789000	Active TSS	Ovary	ovary
49	chr14:71786600-71789000	Active TSS	Osteobl	bone
50	chr14:71786600-71789200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links