Variant report

Variant	rs62214491
Chromosome Location	chr21:46353597-46353598
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr21:46353396-46355647	GM12878	blood:	n/a	n/a
2	POLR2A	chr21:46346154-46355833	GM19099	blood:	n/a	n/a
3	WRNIP1	chr21:46353543-46353842	GM12878	blood:	n/a	n/a
4	POLR2A	chr21:46353414-46353827	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:46353573-46353623	HRCEpiC	kidney:	n/a
2	chr21:46353573-46353623	K562	blood:	n/a
3	chr21:46353573-46353623	GM12892	blood:	n/a
4	chr21:46353573-46353623	AG09319	gingival:	n/a
5	chr21:46353573-46353623	RPTEC	kidney:	n/a
6	chr21:46353573-46353623	ECC-1	luminal epithelium:	n/a
7	chr21:46353573-46353623	H1-hESC	embryonic stem cell:	embryo
8	chr21:46353573-46353623	HRPEpiC	eye:	n/a
9	chr21:46353573-46353623	IMR90	lung:	fetal
10	chr21:46353573-46353623	Hepatocyte	liver:	n/a
11	chr21:46353573-46353623	AG04449	skin:	fetal
12	chr21:46353573-46353623	CMK	blood:	n/a
13	chr21:46353573-46353623	HUVEC	blood vessel:	n/a
14	chr21:46353573-46353623	Jurkat	blood:	n/a
15	chr21:46353573-46353623	GM12891	blood:	n/a
16	chr21:46353573-46353623	PFSK-1	brain:	n/a
17	chr21:46353573-46353623	LNCaP	prostate:	n/a
18	chr21:46353573-46353623	Hela-S3	cervix:	n/a
19	chr21:46353573-46353623	HAEpiC	amniotic membrane:	n/a
20	chr21:46353573-46353623	GM06990	blood:	n/a
21	chr21:46353573-46353623	MCF10A-Er-Src	breast:	n/a
22	chr21:46353573-46353623	HCPEpiC	choroid plexus:	n/a
23	chr21:46353573-46353623	GM19239	blood:	n/a
24	chr21:46353573-46353623	AG04450	lung:	fetal
25	chr21:46353573-46353623	PANC-1	pancreas:	n/a
26	chr21:46353573-46353623	SK-N-MC	brain:	n/a
27	chr21:46353573-46353623	HCM	heart:	n/a
28	chr21:46353573-46353623	HRE	kidney:	n/a
29	chr21:46353573-46353623	HEK293	kidney:	embryo
30	chr21:46353573-46353623	HL-60	blood:	n/a
31	chr21:46353573-46353623	HIPEpiC	eye:	n/a
32	chr21:46353573-46353623	AoSMC	blood vessel:	n/a
33	chr21:46353573-46353623	BJ	skin:	n/a
34	chr21:46353573-46353623	T-47D	breast:	n/a
35	chr21:46353573-46353623	ProgFib	skin:	n/a
36	chr21:46353573-46353623	NT2-D1	testis:	n/a
37	chr21:46353573-46353623	NHDF-neo	bronchial:	n/a
38	chr21:46353573-46353623	HCF	heart:	n/a
39	chr21:46353573-46353623	HPAEpiC	pulmonary alveolar:	n/a
40	chr21:46353573-46353623	PrEC	prostate:	n/a
41	chr21:46353573-46353623	HEEpiC	esophagus:	n/a
42	chr21:46353573-46353623	U87	brain:	n/a
43	chr21:46353573-46353623	NH-A	brain:	n/a
44	chr21:46353573-46353623	HCT-116	colon:	n/a
45	chr21:46353573-46353623	NHBE	bronchial:	n/a
46	chr21:46353573-46353623	SAEC	small airway:	n/a
47	chr21:46353573-46353623	A549	lung:	n/a
48	chr21:46353573-46353623	SK-N-SH_RA	brain:	n/a
49	chr21:46353573-46353623	GM12878	blood:	n/a
50	chr21:46353573-46353623	AG09309	skin:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:46348854..46378176-chr21:46489799..46500436,75	K562	blood:
2	chr21:46310744..46314052-chr21:46353302..46357037,3	K562	blood:
3	chr21:46221821..46223623-chr21:46352044..46354784,3	MCF-7	breast:
4	chr21:46233611..46237296-chr21:46352613..46355418,3	K562	blood:
5	chr21:46230539..46232494-chr21:46352107..46354258,2	K562	blood:
6	chr21:46220228..46226309-chr21:46349546..46355767,8	K562	blood:
7	chr21:46340594..46342742-chr21:46352387..46353896,2	K562	blood:
8	chr21:46288744..46296879-chr21:46346201..46354260,26	MCF-7	breast:
9	chr21:46352341..46354807-chr21:46362095..46363713,2	K562	blood:
10	chr21:46352849..46354653-chr21:46493857..46495814,2	K562	blood:
11	chr21:46352188..46353827-chr21:46357474..46360338,3	K562	blood:
12	chr21:46344850..46350559-chr21:46353409..46355667,8	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C21orf67-6	chr21:46353199-46354283	NR_027128

No data

Variant related genes	Relation type
ENSG00000273027	TF binding region
ITGB2	TF binding region
ENSG00000272825	TF binding region
ENSG00000272825	CpG island
ENSG00000273027	CpG island
ITGB2	CpG island
ENSG00000160255	Chromatin interaction
ENSG00000227039	Chromatin interaction
ENSG00000183255	Chromatin interaction
ENSG00000235374	Chromatin interaction
ENSG00000184787	Chromatin interaction
ENSG00000183250	Chromatin interaction
ENSG00000197381	Chromatin interaction
ENSG00000160256	Chromatin interaction
ENSG00000236519	Chromatin interaction
ENSG00000268856	Chromatin interaction
ENSG00000273027	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11701378	0.80[ASN][1000 genomes]
rs11701457	0.85[ASN][1000 genomes]
rs11702593	0.87[ASN][1000 genomes]
rs2005951	0.80[ASN][1000 genomes]
rs2294166	0.80[ASN][1000 genomes]
rs2294168	0.80[ASN][1000 genomes]
rs2294170	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2838742	0.83[ASN][1000 genomes]
rs2838743	0.83[ASN][1000 genomes]
rs2838745	0.83[ASN][1000 genomes]
rs28399723	0.85[ASN][1000 genomes]
rs28461900	0.85[ASN][1000 genomes]
rs4143368	0.87[ASN][1000 genomes]
rs4818743	0.85[ASN][1000 genomes]
rs4818748	0.85[ASN][1000 genomes]
rs4818749	0.83[ASN][1000 genomes]
rs4818990	0.88[ASN][1000 genomes]
rs55716911	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56213773	0.83[ASN][1000 genomes]
rs62214513	0.80[ASN][1000 genomes]
rs73226621	0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916258	chr21:45995986-46624705	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	102 gene(s)	inside rSNPs	diseases
2	nsv1056513	chr21:46254075-46442759	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv913969	chr21:46279505-46472929	Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv913970	chr21:46305175-46487831	Bivalent Enhancer Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv933240	chr21:46305956-46371518	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	nsv913974	chr21:46306161-46430792	Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
7	nsv913975	chr21:46306161-46459432	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
8	nsv913976	chr21:46306161-46487831	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
9	nsv834110	chr21:46316183-46505151	Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
10	nsv1064518	chr21:46317690-46413159	Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
11	nsv913977	chr21:46335761-46454391	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
12	nsv913978	chr21:46335761-46466674	Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
13	nsv913979	chr21:46335761-46472929	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
14	nsv913980	chr21:46337565-46454391	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
15	nsv913981	chr21:46344426-46408790	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
16	nsv913982	chr21:46344426-46430792	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
17	nsv913984	chr21:46344426-46435610	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
18	nsv913983	chr21:46344426-46440385	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
19	nsv913985	chr21:46344426-46448142	Weak transcription Genic enhancers Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
20	nsv913986	chr21:46344426-46466674	Strong transcription Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
21	nsv913987	chr21:46344426-46472929	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised 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
22	esv1808790	chr21:46349496-46355712	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:46351200-46353600	Active TSS	HSMMtube	muscle
2	chr21:46352400-46353600	Enhancers	Primary T killer memory cells from peripheral blood	blood
3	chr21:46352400-46354800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
4	chr21:46352600-46353600	Enhancers	Primary T cells from cord blood	blood
5	chr21:46352600-46353600	Enhancers	Liver	Liver
6	chr21:46352600-46353800	Enhancers	Gastric	stomach
7	chr21:46352600-46354600	Bivalent Enhancer	Fetal Muscle Leg	muscle
8	chr21:46352800-46353600	Enhancers	Spleen	Spleen
9	chr21:46352800-46353600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr21:46352800-46358400	Weak transcription	HMEC	breast
11	chr21:46353000-46353600	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr21:46353000-46353600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
13	chr21:46353000-46353600	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr21:46353000-46353800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr21:46353000-46354000	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr21:46353000-46354200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
17	chr21:46353000-46354600	Enhancers	HepG2	liver
18	chr21:46353000-46355800	Enhancers	Fetal Thymus	thymus
19	chr21:46353000-46358600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr21:46353000-46358800	Weak transcription	Right Ventricle	heart
21	chr21:46353000-46359000	Weak transcription	Brain Anterior Caudate	brain
22	chr21:46353000-46359000	Weak transcription	Right Atrium	heart
23	chr21:46353200-46353600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr21:46353200-46353600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
25	chr21:46353200-46353800	Enhancers	Primary B cells from cord blood	blood
26	chr21:46353200-46353800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr21:46353200-46353800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr21:46353200-46353800	Flanking Active TSS	GM12878-XiMat	blood
29	chr21:46353200-46354000	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
30	chr21:46353200-46354000	Enhancers	Primary B cells from peripheral blood	blood
31	chr21:46353200-46355400	Enhancers	Thymus	Thymus
32	chr21:46353200-46358600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr21:46353200-46358600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr21:46353200-46358800	Weak transcription	Pancreas	Pancrea
35	chr21:46353200-46359000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr21:46353200-46359000	Weak transcription	HUVEC	blood vessel
37	chr21:46353200-46359200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr21:46353400-46353600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr21:46353400-46353600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr21:46353400-46353800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr21:46353400-46353800	Active TSS	HSMM	muscle
42	chr21:46353400-46353800	Active TSS	Osteobl	bone
43	chr21:46353400-46354000	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr21:46353400-46358800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr21:46353400-46358800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr21:46353400-46358800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr21:46353400-46359000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr21:46353400-46359200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood

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