Variant report

Variant	rs539366345
Chromosome Location	chr12:58131881-58131882
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:87)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:87 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr12:58131740-58131890	HRPEpiC	eye:	n/a	n/a
2	ZBTB7A	chr12:58130925-58132029	ECC-1	luminal epithelium:	n/a	n/a
3	CTCF	chr12:58131740-58131890	AG09309	skin:	n/a	n/a
4	ZBTB7A	chr12:58131502-58132189	ECC-1	luminal epithelium:	n/a	chr12:58132086-58132094
5	CTCF	chr12:58131820-58131970	HCM	heart:	n/a	n/a
6	CTCF	chr12:58131760-58131910	HFF-Myc	foreskin:	n/a	n/a
7	CTCF	chr12:58131712-58131919	A549	lung:	n/a	n/a
8	CHD1	chr12:58131840-58131963	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr12:58131726-58131930	Fibrobl	skin:	n/a	n/a
10	CTCF	chr12:58131606-58131991	A549	lung:	n/a	n/a
11	CTCF	chr12:58131740-58131890	HPF	lung:	n/a	n/a
12	CTCF	chr12:58131820-58131970	HVMF	connective:	n/a	n/a
13	CTCF	chr12:58131780-58131930	A549	lung:	n/a	n/a
14	POLR2A	chr12:58131620-58132081	H1-neurons	neurons:	n/a	n/a
15	CTCF	chr12:58131740-58131890	SAEC	small airway:	n/a	n/a
16	CTCF	chr12:58131640-58131987	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr12:58131477-58132000	IMR90	lung:	n/a	n/a
18	SIN3A	chr12:58131727-58132037	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr12:58131670-58131967	A549	lung:	n/a	n/a
20	CTCF	chr12:58131710-58131922	MCF-7	breast:	n/a	n/a
21	CTCF	chr12:58131706-58131937	MCF-7	breast:	n/a	n/a
22	HDAC2	chr12:58131693-58131962	HepG2	liver:	n/a	n/a
23	CTCF	chr12:58131740-58131890	AG04450	lung:	n/a	n/a
24	CTCF	chr12:58131686-58131955	A549	lung:	n/a	n/a
25	MAZ	chr12:58131564-58132114	IMR90	lung:	n/a	n/a
26	CTCF	chr12:58131800-58131950	NHDF-neo	bronchial:	n/a	n/a
27	CTCF	chr12:58131778-58131903	Medullo	brain:	n/a	n/a
28	CTCF	chr12:58131740-58131890	MCF-7	breast:	n/a	n/a
29	MAX	chr12:58131282-58132006	MCF-7	breast:	n/a	n/a
30	CTCF	chr12:58131740-58131890	AG04449	skin:	n/a	n/a
31	CTCF	chr12:58131760-58131910	HAc	cerebellar:	n/a	n/a
32	CTCF	chr12:58131760-58131910	AG04450	lung:	n/a	n/a
33	CTCF	chr12:58131726-58131944	H1-hESC	embryonic stem cell:	n/a	n/a
34	RAD21	chr12:58131662-58131904	H1-hESC	embryonic stem cell:	n/a	n/a
35	RAD21	chr12:58131674-58131885	SK-N-SH_RA	brain:	n/a	n/a
36	ZBTB7A	chr12:58131657-58131887	HepG2	liver:	n/a	n/a
37	CTCF	chr12:58131705-58131925	NHEK	skin:	n/a	n/a
38	CTCF	chr12:58131760-58131910	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr12:58131760-58131910	AG09319	gingival:	n/a	n/a
40	CTCF	chr12:58131740-58131890	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr12:58131714-58131927	Gliobla	brain:	n/a	n/a
42	CTCF	chr12:58130923-58132159	A549	lung:	n/a	n/a
43	CTCF	chr12:58131740-58131890	HepG2	liver:	n/a	n/a
44	CTCF	chr12:58131703-58131898	LNCaP	prostate:	n/a	n/a
45	CTCF	chr12:58131740-58131890	Caco-2	colon:	n/a	n/a
46	CTCF	chr12:58131773-58131881	Pancreas_OC	pancreas:	n/a	n/a
47	RAD21	chr12:58131692-58131910	SK-N-SH_RA	brain:	n/a	n/a
48	MAZ	chr12:58131657-58131894	HepG2	liver:	n/a	n/a
49	CTCF	chr12:58131740-58131890	HCFaa	heart:	n/a	n/a
50	CTCF	chr12:58131714-58131913	MCF-7	breast:	n/a	n/a

No data

(count:8 , 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	chr12:57916381..57918711-chr12:58131475..58134282,2	MCF-7	breast:
6	chr12:57984280..57986133-chr12:58130711..58132725,2	K562	blood:
7	chr12:58112503..58116669-chr12:58128862..58132734,4	K562	blood:
8	chr12:57909973..57915898-chr12:58127755..58134567,15	K562	blood:

No data

Variant related genes	Relation type
AGAP2	TF binding region
TSPAN31	TF binding region
ENSG00000111087	Chromatin interaction
ENSG00000166987	Chromatin interaction
ENSG00000135506	Chromatin interaction
ENSG00000166908	Chromatin interaction
ENSG00000255737	Chromatin interaction
ENSG00000257342	Chromatin interaction
ENSG00000208028	Chromatin interaction
ENSG00000175197	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:107 , 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	chr12:58120400-58132400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr12:58121400-58132800	Strong transcription	Thymus	Thymus
8	chr12:58121800-58132400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
9	chr12:58127800-58133600	Weak transcription	GM12878-XiMat	blood
10	chr12:58129000-58132200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr12:58129000-58132400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
12	chr12:58129000-58132800	Weak transcription	Dnd41	blood
13	chr12:58129200-58132600	Weak transcription	Primary B cells from cord blood	blood
14	chr12:58129200-58132600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr12:58129400-58132200	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
16	chr12:58129400-58133000	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr12:58129600-58132000	Flanking Active TSS	Right Ventricle	heart
18	chr12:58129600-58132600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr12:58129600-58132600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr12:58129600-58132800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
21	chr12:58129600-58133200	Enhancers	Pancreas	Pancrea
22	chr12:58129800-58132200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr12:58129800-58133000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
24	chr12:58130200-58132000	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
25	chr12:58130200-58132200	Enhancers	Gastric	stomach
26	chr12:58130200-58134200	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr12:58130600-58132800	Active TSS	Brain Anterior Caudate	brain
28	chr12:58130600-58133000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
29	chr12:58130600-58133200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
30	chr12:58130800-58132000	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
31	chr12:58130800-58132200	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr12:58130800-58132800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr12:58130800-58133000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
34	chr12:58130800-58133000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
35	chr12:58130800-58133000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
36	chr12:58130800-58133200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
37	chr12:58131000-58132000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr12:58131000-58132600	Strong transcription	Primary T helper cells fromperipheralblood	blood
39	chr12:58131000-58132800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr12:58131200-58132000	Enhancers	Liver	Liver
41	chr12:58131200-58132000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
42	chr12:58131200-58132200	Flanking Bivalent TSS/Enh	HMEC	breast
43	chr12:58131200-58132400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr12:58131200-58132400	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr12:58131200-58132800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr12:58131200-58132800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr12:58131200-58132800	Bivalent/Poised TSS	HepG2	liver
48	chr12:58131200-58133000	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr12:58131200-58133000	Bivalent/Poised TSS	Fetal Brain Female	brain
50	chr12:58131200-58133600	Active TSS	Brain Angular Gyrus	brain

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