Variant report

Variant	rs9621867
Chromosome Location	chr22:22007557-22007558
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	chr22:22005137-22007763	K562	blood:	n/a	n/a
2	NR2F2	chr22:22004454-22008653	K562	blood:	n/a	n/a
3	MAZ	chr22:22007547-22007596	HepG2	liver:	n/a	n/a
4	GTF2F1	chr22:22007396-22007721	H1-hESC	embryonic stem cell:	n/a	n/a
5	SIN3A	chr22:22005437-22007822	H1-hESC	embryonic stem cell:	n/a	chr22:22005713-22005721 chr22:22006403-22006416 chr22:22007120-22007134
6	NR2F2	chr22:22004662-22008799	K562	blood:	n/a	n/a
7	PML	chr22:22005016-22007901	K562	blood:	n/a	chr22:22005344-22005352
8	CHD2	chr22:22007089-22007747	H1-hESC	embryonic stem cell:	n/a	chr22:22007421-22007431
9	THAP1	chr22:22005064-22008219	K562	blood:	n/a	n/a
10	ETS1	chr22:22005139-22008071	K562	blood:	n/a	chr22:22005850-22005857 chr22:22005848-22005857 chr22:22007415-22007428
11	POLR2A	chr22:22005111-22007673	PFSK-1	brain:	n/a	n/a
12	PML	chr22:22004873-22008608	K562	blood:	n/a	chr22:22008587-22008595 chr22:22005344-22005352
13	HEY1	chr22:22004958-22008800	K562	blood:	n/a	chr22:22007524-22007539 chr22:22006403-22006418
14	HEY1	chr22:22005026-22007900	K562	blood:	n/a	chr22:22007524-22007539 chr22:22006403-22006418
15	POLR2A	chr22:22007484-22007697	H1-hESC	embryonic stem cell:	n/a	n/a
16	SP2	chr22:22007348-22008640	K562	blood:	n/a	n/a
17	TEAD4	chr22:22007253-22007793	H1-hESC	embryonic stem cell:	n/a	n/a
18	JUN	chr22:22004275-22009366	K562	blood:	n/a	chr22:22006333-22006342 chr22:22006418-22006427 chr22:22006621-22006629
19	TEAD4	chr22:22007283-22007804	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr22:22002106-22008893	K562	blood:	n/a	n/a
21	ZBTB7A	chr22:22005719-22007769	ECC-1	luminal epithelium:	n/a	chr22:22006861-22006868 chr22:22007009-22007018 chr22:22006710-22006718 chr22:22006449-22006457
22	SP1	chr22:22007146-22007763	H1-hESC	embryonic stem cell:	n/a	chr22:22007524-22007533 chr22:22007419-22007431 chr22:22007421-22007430 chr22:22007199-22007209 chr22:22007420-22007434 chr22:22007524-22007534 chr22:22007523-22007535 chr22:22007199-22007209 chr22:22007524-22007533 chr22:22007525-22007534 chr22:22007419-22007430 chr22:22007523-22007535
23	HDAC2	chr22:22005068-22007786	K562	blood:	n/a	n/a
24	POLR2A	chr22:22007553-22007664	HepG2	liver:	n/a	n/a
25	POLR2A	chr22:22005110-22007763	K562	blood:	n/a	n/a
26	ZBTB7A	chr22:22004921-22007705	K562	blood:	n/a	chr22:22006861-22006868 chr22:22005219-22005228 chr22:22007009-22007018 chr22:22006710-22006718 chr22:22006449-22006457
27	ELF1	chr22:22005082-22008696	K562	blood:	n/a	chr22:22007524-22007536
28	TBP	chr22:22007206-22007709	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr22:22005473-22007873	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr22:22004934-22007717	K562	blood:	n/a	n/a
31	TEAD4	chr22:22005048-22007754	K562	blood:	n/a	n/a
32	GABPA	chr22:22005118-22007638	K562	blood:	n/a	chr22:22006402-22006416
33	POLR2A	chr22:22005031-22015259	PFSK-1	brain:	n/a	n/a
34	ZBTB7A	chr22:22007482-22007606	HepG2	liver:	n/a	n/a
35	CTCF	chr22:22005877-22007626	K562	blood:	n/a	chr22:22006854-22006867
36	ZBTB7A	chr22:22005052-22007983	K562	blood:	n/a	chr22:22006861-22006868 chr22:22005219-22005228 chr22:22007009-22007018 chr22:22006710-22006718 chr22:22006449-22006457
37	ETS1	chr22:22005040-22008012	K562	blood:	n/a	chr22:22005850-22005857 chr22:22005848-22005857 chr22:22007415-22007428
38	HDAC2	chr22:22005002-22008028	K562	blood:	n/a	n/a
39	POLR2A	chr22:22006130-22007856	H1-hESC	embryonic stem cell:	n/a	n/a
40	TEAD4	chr22:22004553-22008360	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:22007515-22007565	RPTEC	kidney:	n/a
2	chr22:22007528-22007578	PFSK-1	brain:	n/a
3	chr22:22007515-22007565	A549	lung:	n/a
4	chr22:22007528-22007578	HAEpiC	amniotic membrane:	n/a
5	chr22:22007515-22007565	NHBE	bronchial:	n/a
6	chr22:22007528-22007578	Hepatocyte	liver:	n/a
7	chr22:22007528-22007578	BJ	skin:	n/a
8	chr22:22007528-22007578	AG09319	gingival:	n/a
9	chr22:22007528-22007578	HMEC	breast:	n/a
10	chr22:22007515-22007565	K562	blood:	n/a
11	chr22:22007515-22007565	SKMC	muscle:	n/a
12	chr22:22007528-22007578	HCF	heart:	n/a
13	chr22:22007515-22007565	NT2-D1	testis:	n/a
14	chr22:22007515-22007565	BJ	skin:	n/a
15	chr22:22007515-22007565	HNPCEpiC	eye:	n/a
16	chr22:22007528-22007578	ECC-1	luminal epithelium:	n/a
17	chr22:22007528-22007578	ProgFib	skin:	n/a
18	chr22:22007528-22007578	SAEC	small airway:	n/a
19	chr22:22007515-22007565	HCPEpiC	choroid plexus:	n/a
20	chr22:22007528-22007578	RPTEC	kidney:	n/a
21	chr22:22007528-22007578	HEK293	kidney:	embryo
22	chr22:22007515-22007565	PFSK-1	brain:	n/a
23	chr22:22007515-22007565	U87	brain:	n/a
24	chr22:22007515-22007565	HAEpiC	amniotic membrane:	n/a
25	chr22:22007528-22007578	CMK	blood:	n/a
26	chr22:22007515-22007565	HCF	heart:	n/a
27	chr22:22007515-22007565	Caco-2	colon:	n/a
28	chr22:22007528-22007578	SK-N-MC	brain:	n/a
29	chr22:22007528-22007578	HL-60	blood:	n/a
30	chr22:22007515-22007565	GM12878	blood:	n/a
31	chr22:22007528-22007578	HPAEpiC	pulmonary alveolar:	n/a
32	chr22:22007528-22007578	Caco-2	colon:	n/a
33	chr22:22007528-22007578	T-47D	breast:	n/a
34	chr22:22007515-22007565	HepG2	liver:	n/a
35	chr22:22007528-22007578	K562	blood:	n/a
36	chr22:22007528-22007578	MCF10A-Er-Src	breast:	n/a
37	chr22:22007528-22007578	AoSMC	blood vessel:	n/a
38	chr22:22007515-22007565	IMR90	lung:	fetal
39	chr22:22007515-22007565	HRE	kidney:	n/a
40	chr22:22007515-22007565	BE2_C	brain:	n/a
41	chr22:22007515-22007565	NHDF-neo	bronchial:	n/a
42	chr22:22007515-22007565	NH-A	brain:	n/a
43	chr22:22007515-22007565	MCF10A-Er-Src	breast:	n/a
44	chr22:22007528-22007578	H1-hESC	embryonic stem cell:	embryo
45	chr22:22007528-22007578	Jurkat	blood:	n/a
46	chr22:22007515-22007565	H1-hESC	embryonic stem cell:	embryo
47	chr22:22007528-22007578	NT2-D1	testis:	n/a
48	chr22:22007515-22007565	GM12891	blood:	n/a
49	chr22:22007528-22007578	GM12878	blood:	n/a
50	chr22:22007528-22007578	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr22:22005965..22007764-chr22:22291588..22295229,3	K562	blood:
2	chr22:21355601..21357315-chr22:22006287..22008814,2	K562	blood:
3	chr22:22005850..22008007-chr3:155571064..155572872,2	K562	blood:
4	chr22:21982265..21985710-chr22:22005242..22008783,5	MCF-7	breast:
5	chr22:22004774..22008117-chr22:22898413..22901210,3	K562	blood:
6	chr22:21211756..21214604-chr22:22007278..22009466,2	K562	blood:
7	chr22:21920727..21924429-chr22:22006455..22008474,3	MCF-7	breast:
8	chr22:22006264..22009261-chr22:22291037..22293088,2	K562	blood:

Variant related genes	Relation type
MIR130B	TF binding region
MIR130B	CpG island
ENSG00000161179	Chromatin interaction
ENSG00000185651	Chromatin interaction
ENSG00000241973	Chromatin interaction
ENSG00000169359	Chromatin interaction
ENSG00000100034	Chromatin interaction
ENSG00000185686	Chromatin interaction
ENSG00000224086	Chromatin interaction
ENSG00000184436	Chromatin interaction
ENSG00000230513	Chromatin interaction
ENSG00000099940	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs12169219	1.00[AMR][1000 genomes]
rs2329826	1.00[AMR][1000 genomes]
rs58737266	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9621868	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv914458	chr22:21747678-22070489	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	387 gene(s)	inside rSNPs	diseases
2	nsv482690	chr22:21807513-22016791	Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	374 gene(s)	inside rSNPs	diseases
3	esv1823866	chr22:21928916-22131125	Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Genic enhancers Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	374 gene(s)	inside rSNPs	diseases
4	nsv948603	chr22:21928916-22601814	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	422 gene(s)	inside rSNPs	diseases
5	nsv948902	chr22:21928916-22657900	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	426 gene(s)	inside rSNPs	diseases
6	nsv1063962	chr22:21939722-22934593	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	477 gene(s)	inside rSNPs	diseases
7	nsv1058617	chr22:21939922-22934454	Weak transcription Bivalent Enhancer Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS 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 miRNA miRNA target site	477 gene(s)	inside rSNPs	diseases
8	nsv529694	chr22:21957411-22905068	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	474 gene(s)	inside rSNPs	diseases
9	nsv914464	chr22:21964761-22039863	Genic enhancers Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	367 gene(s)	inside rSNPs	diseases
10	nsv914465	chr22:21964761-22055280	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	368 gene(s)	inside rSNPs	diseases
11	nsv914466	chr22:21964761-22057273	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	368 gene(s)	inside rSNPs	diseases
12	nsv531797	chr22:21977700-22959729	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	476 gene(s)	inside rSNPs	diseases
13	nsv914467	chr22:21982892-22055280	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	363 gene(s)	inside rSNPs	diseases
14	nsv914468	chr22:21982892-22070489	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	365 gene(s)	inside rSNPs	diseases
15	nsv914469	chr22:21985094-22010918	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	348 gene(s)	inside rSNPs	diseases
16	esv3456722	chr22:21993383-22019246	Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	341 gene(s)	inside rSNPs	diseases
17	esv3456723	chr22:21993399-22019258	Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	341 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:22005200-22007600	Flanking Active TSS	Fetal Muscle Trunk	muscle
2	chr22:22005400-22007600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr22:22005400-22007600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr22:22005400-22007800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr22:22005600-22007600	Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr22:22005600-22007600	Active TSS	H9 Cell Line	embryonic stem cell
7	chr22:22005600-22007600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr22:22005600-22007600	Active TSS	HUES64 Cell Line	embryonic stem cell
9	chr22:22005600-22007800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr22:22005600-22007800	Active TSS	iPS-20b Cell Line	embryonic stem cell
11	chr22:22005800-22007600	Active TSS	HUES48 Cell Line	embryonic stem cell
12	chr22:22005800-22007600	Active TSS	iPS-15b Cell Line	embryonic stem cell
13	chr22:22005800-22007600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
14	chr22:22005800-22007600	Active TSS	NHDF-Ad	bronchial
15	chr22:22005800-22007800	Active TSS	iPS-18 Cell Line	embryonic stem cell
16	chr22:22006200-22007600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr22:22006600-22007600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
18	chr22:22006600-22007600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
19	chr22:22006600-22007600	Flanking Active TSS	Fetal Intestine Small	intestine
20	chr22:22006600-22007800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr22:22006800-22007600	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr22:22006800-22007600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr22:22006800-22007600	Flanking Active TSS	Fetal Muscle Leg	muscle
24	chr22:22006800-22007600	Flanking Active TSS	Fetal Stomach	stomach
25	chr22:22006800-22007600	Enhancers	Lung	lung
26	chr22:22006800-22007800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr22:22006800-22010800	Weak transcription	Primary T cells from cord blood	blood
28	chr22:22006800-22011600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr22:22006800-22012000	Weak transcription	Liver	Liver
30	chr22:22007000-22007600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr22:22007000-22007600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr22:22007000-22007600	Enhancers	Fetal Heart	heart
33	chr22:22007000-22007600	Flanking Active TSS	K562	blood
34	chr22:22007000-22007800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr22:22007000-22007800	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr22:22007000-22007800	Flanking Active TSS	Fetal Lung	lung
37	chr22:22007000-22007800	Strong transcription	Right Atrium	heart
38	chr22:22007000-22007800	Flanking Active TSS	HUVEC	blood vessel
39	chr22:22007000-22010800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr22:22007000-22011000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr22:22007000-22011000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr22:22007000-22011000	Weak transcription	Brain Anterior Caudate	brain
43	chr22:22007000-22011200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr22:22007000-22011400	Weak transcription	Gastric	stomach
45	chr22:22007200-22007600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
46	chr22:22007200-22007800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
47	chr22:22007200-22007800	Flanking Active TSS	GM12878-XiMat	blood
48	chr22:22007200-22007800	Flanking Active TSS	HepG2	liver
49	chr22:22007200-22007800	Transcr. at gene 5' and 3'	NHLF	lung
50	chr22:22007200-22008000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin

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