Variant report

Variant	rs568848196
Chromosome Location	chr12:58131669-58131670
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:28)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZBTB7A	chr12:58130925-58132029	ECC-1	luminal epithelium:	n/a	n/a
2	ZBTB7A	chr12:58131502-58132189	ECC-1	luminal epithelium:	n/a	chr12:58132086-58132094
3	CTCF	chr12:58131606-58131991	A549	lung:	n/a	n/a
4	POLR2A	chr12:58131620-58132081	H1-neurons	neurons:	n/a	n/a
5	CTCF	chr12:58131640-58131987	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr12:58131477-58132000	IMR90	lung:	n/a	n/a
7	ZBTB7A	chr12:58131654-58131841	K562	blood:	n/a	n/a
8	CTBP2	chr12:58129316-58131871	H1-hESC	embryonic stem cell:	n/a	n/a
9	MAZ	chr12:58131564-58132114	IMR90	lung:	n/a	n/a
10	MAX	chr12:58131282-58132006	MCF-7	breast:	n/a	n/a
11	CTCF	chr12:58131600-58131750	HVMF	connective:	n/a	n/a
12	RAD21	chr12:58131662-58131904	H1-hESC	embryonic stem cell:	n/a	n/a
13	ZBTB7A	chr12:58131657-58131887	HepG2	liver:	n/a	n/a
14	CTCF	chr12:58130923-58132159	A549	lung:	n/a	n/a
15	CTCF	chr12:58131640-58131790	WI-38	lung:	n/a	n/a
16	MAZ	chr12:58131657-58131894	HepG2	liver:	n/a	n/a
17	CTCF	chr12:58131620-58131770	HCM	heart:	n/a	n/a
18	SUZ12	chr12:58130289-58132014	H1-hESC	embryonic stem cell:	n/a	n/a
19	RAD21	chr12:58131641-58131965	HepG2	liver:	n/a	n/a
20	CTCF	chr12:58131584-58132096	MCF-7	breast:	n/a	n/a
21	CTCF	chr12:58131660-58131810	MCF-7	breast:	n/a	n/a
22	RAD21	chr12:58131541-58131959	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr12:58131598-58131909	H1-hESC	embryonic stem cell:	n/a	n/a
24	HDAC2	chr12:58131159-58132075	MCF-7	breast:	n/a	n/a
25	CTCF	chr12:58131073-58132109	SK-N-SH	brain:	n/a	n/a
26	ZBTB7A	chr12:58131569-58131914	HepG2	liver:	n/a	n/a
27	SUZ12	chr12:58130135-58132131	NT2-D1	testis:	n/a	n/a
28	ZNF263	chr12:58131615-58131951	HEK293-T-REx	kidney:	n/a	n/a

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:58119624..58120427-chr12:58131646..58132182,3	MCF-7	breast:
2	chr12:57852621..57854513-chr12:58130296..58131944,2	K562	blood:
3	chr12:57914271..57916098-chr12:58131440..58134732,4	K562	blood:
4	chr12:57913785..57915861-chr12:58131130..58132834,2	MCF-7	breast:
5	chr12:58016846..58018792-chr12:58129433..58131831,2	K562	blood:
6	chr12:57916381..57918711-chr12:58131475..58134282,2	MCF-7	breast:
7	chr12:57984280..57986133-chr12:58130711..58132725,2	K562	blood:
8	chr12:58112503..58116669-chr12:58128862..58132734,4	K562	blood:
9	chr12:57909973..57915898-chr12:58127755..58134567,15	K562	blood:

No data

Variant related genes	Relation type
AGAP2	TF binding region
TSPAN31	TF binding region
ENSG00000166908	Chromatin interaction
ENSG00000166987	Chromatin interaction
ENSG00000257342	Chromatin interaction
ENSG00000175197	Chromatin interaction
ENSG00000208028	Chromatin interaction
ENSG00000111087	Chromatin interaction
ENSG00000135502	Chromatin interaction
ENSG00000255737	Chromatin interaction
ENSG00000135506	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1038741	chr12:57877355-58174506	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
2	nsv541503	chr12:57877355-58174506	Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers 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	126 gene(s)	inside rSNPs	diseases
3	nsv899121	chr12:58079825-58177292	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
4	esv1851618	chr12:58109302-58131947	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
5	nsv559045	chr12:58112189-58165085	Enhancers Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
6	nsv470296	chr12:58112189-58177292	Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
7	nsv899122	chr12:58118248-58137563	Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
8	nsv899123	chr12:58118248-58155023	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
9	nsv826384	chr12:58124758-58157850	Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
10	esv3363572	chr12:58129335-58133633	Strong transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
11	nsv826385	chr12:58129908-58133427	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
12	nsv510601	chr12:58130298-58191925	Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
13	esv3408774	chr12:58130710-58133658	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
14	esv3429081	chr12:58131185-58133683	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:58118400-58132000	Strong transcription	Primary T cells from cord blood	blood
2	chr12:58119200-58132000	Strong transcription	Primary neutrophils fromperipheralblood	blood
3	chr12:58119600-58132400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr12:58119600-58132800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr12:58119600-58133000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr12:58120400-58131800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr12:58120400-58132400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr12:58121400-58132800	Strong transcription	Thymus	Thymus
9	chr12:58121800-58132400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr12:58127800-58133600	Weak transcription	GM12878-XiMat	blood
11	chr12:58129000-58131800	Bivalent Enhancer	Fetal Stomach	stomach
12	chr12:58129000-58132200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr12:58129000-58132400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
14	chr12:58129000-58132800	Weak transcription	Dnd41	blood
15	chr12:58129200-58131800	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
16	chr12:58129200-58132600	Weak transcription	Primary B cells from cord blood	blood
17	chr12:58129200-58132600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr12:58129400-58132200	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
19	chr12:58129400-58133000	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr12:58129600-58131800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
21	chr12:58129600-58131800	Bivalent Enhancer	Fetal Intestine Small	intestine
22	chr12:58129600-58131800	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
23	chr12:58129600-58132000	Flanking Active TSS	Right Ventricle	heart
24	chr12:58129600-58132600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr12:58129600-58132600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr12:58129600-58132800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
27	chr12:58129600-58133200	Enhancers	Pancreas	Pancrea
28	chr12:58129800-58132200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr12:58129800-58133000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
30	chr12:58130200-58131800	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr12:58130200-58131800	Bivalent Enhancer	Fetal Lung	lung
32	chr12:58130200-58131800	Bivalent Enhancer	NH-A	brain
33	chr12:58130200-58132000	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
34	chr12:58130200-58132200	Enhancers	Gastric	stomach
35	chr12:58130200-58134200	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr12:58130600-58132800	Active TSS	Brain Anterior Caudate	brain
37	chr12:58130600-58133000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
38	chr12:58130600-58133200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
39	chr12:58130800-58132000	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
40	chr12:58130800-58132200	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr12:58130800-58132800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr12:58130800-58133000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
43	chr12:58130800-58133000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
44	chr12:58130800-58133000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
45	chr12:58130800-58133200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
46	chr12:58131000-58131800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
47	chr12:58131000-58131800	Bivalent/Poised TSS	Aorta	Aorta
48	chr12:58131000-58131800	Genic enhancers	Lung	lung
49	chr12:58131000-58131800	Bivalent Enhancer	Small Intestine	intestine
50	chr12:58131000-58132000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell

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