Variant report

Variant	rs557271497
Chromosome Location	chr22:20286142-20286143
allele	C/T
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	SP2	chr22:20286103-20286522	K562	blood:	n/a	n/a
2	ZBTB7A	chr22:20285838-20287583	K562	blood:	n/a	chr22:20286824-20286831 chr22:20286714-20286723
3	NR2F2	chr22:20286139-20287295	K562	blood:	n/a	n/a
4	NR2F2	chr22:20286053-20287542	K562	blood:	n/a	n/a
5	MAX	chr22:20286105-20287719	K562	blood:	n/a	chr22:20287044-20287060 chr22:20287055-20287064 chr22:20286570-20286580
6	ZBTB7A	chr22:20286139-20287103	ECC-1	luminal epithelium:	n/a	chr22:20286824-20286831 chr22:20286714-20286723
7	BACH1	chr22:20285769-20287619	H1-hESC	embryonic stem cell:	n/a	n/a
8	ELF1	chr22:20286124-20287665	K562	blood:	n/a	chr22:20286894-20286906 chr22:20286391-20286403
9	GABPA	chr22:20285938-20287672	K562	blood:	n/a	chr22:20286570-20286579 chr22:20287574-20287583 chr22:20286715-20286724 chr22:20287070-20287079
10	ETS1	chr22:20286102-20287574	K562	blood:	n/a	chr22:20287068-20287079 chr22:20287112-20287125

No.	Distal block	Cell Line	Cell type
1	chr22:20174347..20176842-chr22:20283919..20286153,2	K562	blood:
2	chr22:20118465..20120580-chr22:20285203..20287703,2	MCF-7	breast:
3	chr22:20281007..20283182-chr22:20284432..20287016,2	MCF-7	breast:
4	chr22:19973359..19974976-chr22:20284613..20286772,2	K562	blood:
5	chr22:20286073..20288681-chr22:20850193..20851733,2	K562	blood:
6	chr22:20286073..20290077-chr22:20848237..20851733,4	K562	blood:
7	chr22:20284435..20289251-chr22:20305915..20309120,4	K562	blood:
8	chr22:20284539..20286947-chr22:20746722..20748522,2	MCF-7	breast:
9	chr22:20284063..20288249-chr22:20303567..20308986,5	K562	blood:
10	chr22:20202926..20205511-chr22:20284838..20286981,3	K562	blood:

Variant related genes	Relation type
ENSG00000161132	TF binding region
ENSG00000273139	Chromatin interaction
ENSG00000099889	Chromatin interaction
ENSG00000099917	Chromatin interaction
ENSG00000099904	Chromatin interaction
ENSG00000273343	Chromatin interaction
ENSG00000128185	Chromatin interaction
ENSG00000099910	Chromatin interaction
ENSG00000185252	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1792516	chr22:19578312-20314496	Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	195 gene(s)	inside rSNPs	diseases
2	esv1818018	chr22:19674772-20313261	Flanking Bivalent TSS/Enh Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	193 gene(s)	inside rSNPs	diseases
3	nsv828938	chr22:19678592-20311988	Strong transcription Genic enhancers Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	192 gene(s)	inside rSNPs	diseases
4	nsv828939	chr22:19683555-20311988	Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	192 gene(s)	inside rSNPs	diseases
5	esv1826873	chr22:19726464-20313261	Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	179 gene(s)	inside rSNPs	diseases
6	nsv588237	chr22:19749525-20306993	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
7	nsv588239	chr22:19907099-20309393	Strong transcription Active TSS Genic enhancers Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer 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	158 gene(s)	inside rSNPs	diseases
8	nsv471183	chr22:20006040-20306993	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
9	esv2758536	chr22:20026493-20309447	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription 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	59 gene(s)	inside rSNPs	diseases
10	esv2758825	chr22:20026493-20309447	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
11	nsv828950	chr22:20057967-20311988	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
12	esv1793574	chr22:20075870-20728868	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
13	nsv914332	chr22:20082961-20339310	Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers Genic enhancers 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	57 gene(s)	inside rSNPs	diseases
14	nsv914337	chr22:20087539-20330895	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
15	esv1832132	chr22:20089802-20728868	ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
16	nsv1061349	chr22:20091394-20734304	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
17	esv1804395	chr22:20093565-20485443	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription 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	69 gene(s)	inside rSNPs	diseases
18	esv1850291	chr22:20093565-20666528	Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
19	esv1824760	chr22:20093565-20728868	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription 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	77 gene(s)	inside rSNPs	diseases
20	nsv1062789	chr22:20100465-20749579	Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	82 gene(s)	inside rSNPs	diseases
21	nsv828951	chr22:20109578-20310046	Enhancers Active TSS Flanking Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Strong transcription 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	47 gene(s)	inside rSNPs	diseases
22	nsv869949	chr22:20126918-20719112	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	68 gene(s)	inside rSNPs	diseases
23	nsv914359	chr22:20165632-20290691	Bivalent/Poised TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
24	nsv914360	chr22:20165632-20339310	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
25	nsv914361	chr22:20181136-20313299	Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
26	nsv914365	chr22:20189077-20290691	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
27	nsv914366	chr22:20189077-20306993	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	37 gene(s)	inside rSNPs	diseases
28	nsv914375	chr22:20210055-20306993	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	diseases
29	esv3376057	chr22:20285977-20288825	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
30	nsv519102	chr22:20286099-20306993	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:20282400-20286400	Strong transcription	Right Atrium	heart
2	chr22:20285400-20286200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr22:20285600-20286400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
4	chr22:20285600-20286400	Enhancers	Spleen	Spleen
5	chr22:20285800-20286200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr22:20285800-20286200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr22:20285800-20286400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr22:20285800-20286400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr22:20285800-20286400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
10	chr22:20285800-20286800	Flanking Active TSS	Duodenum Mucosa	Duodenum
11	chr22:20285800-20287400	Active TSS	Duodenum Smooth Muscle	Duodenum
12	chr22:20285800-20287600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
13	chr22:20285800-20287600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
14	chr22:20285800-20287600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
15	chr22:20285800-20287800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
16	chr22:20286000-20286200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
17	chr22:20286000-20286200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
18	chr22:20286000-20286200	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr22:20286000-20286200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr22:20286000-20286200	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr22:20286000-20286200	Bivalent Enhancer	Fetal Stomach	stomach
22	chr22:20286000-20286400	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr22:20286000-20286400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
24	chr22:20286000-20286400	Enhancers	Primary B cells from peripheral blood	blood
25	chr22:20286000-20286400	Enhancers	Primary T cells fromperipheralblood	blood
26	chr22:20286000-20286400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
27	chr22:20286000-20286400	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr22:20286000-20286400	Enhancers	Esophagus	oesophagus
29	chr22:20286000-20286400	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
30	chr22:20286000-20286400	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
31	chr22:20286000-20286400	Bivalent Enhancer	Placenta	Placenta
32	chr22:20286000-20286800	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
33	chr22:20286000-20286800	Bivalent Enhancer	Fetal Thymus	thymus
34	chr22:20286000-20287600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr22:20286000-20287800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
36	chr22:20286000-20287800	Active TSS	H9 Cell Line	embryonic stem cell
37	chr22:20286000-20287800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr22:20286000-20288000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell

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