Variant report

Variant	rs143191322
Chromosome Location	chr22:23744812-23744813
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	CTCF	chr22:23744809-23745214	A549	lung:	n/a	chr22:23745058-23745071 chr22:23744976-23744994 chr22:23744979-23744992 chr22:23745064-23745077
2	EGR1	chr22:23744561-23745206	MCF-7	breast:	n/a	n/a
3	HA-E2F1	chr22:23744402-23745287	MCF-7	breast:	n/a	chr22:23745240-23745249
4	ZNF263	chr22:23744257-23745316	HEK293-T-REx	kidney:	n/a	n/a
5	E2F6	chr22:23744584-23744827	K562	blood:	n/a	n/a
6	NFIC	chr22:23744468-23745215	ECC-1	luminal epithelium:	n/a	n/a
7	CTCF	chr22:23744766-23745297	K562	blood:	n/a	chr22:23745058-23745071 chr22:23744976-23744994 chr22:23744979-23744992 chr22:23745064-23745077
8	MAX	chr22:23744460-23744980	ECC-1	luminal epithelium:	n/a	n/a
9	CTCF	chr22:23744726-23745423	HCT-116	colon:	n/a	chr22:23745058-23745071 chr22:23744976-23744994 chr22:23744979-23744992 chr22:23745064-23745077
10	POLR2A	chr22:23744556-23744845	HCT-116	colon:	n/a	n/a
11	MAX	chr22:23744422-23744856	A549	lung:	n/a	n/a
12	POLR2A	chr22:23744542-23744821	HCT-116	colon:	n/a	n/a
13	HMGN3	chr22:23744679-23745130	K562	blood:	n/a	n/a
14	MAZ	chr22:23744685-23745172	K562	blood:	n/a	n/a
15	CTBP2	chr22:23744287-23745184	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr22:23744806-23745271	H1-hESC	embryonic stem cell:	n/a	chr22:23745058-23745071 chr22:23744976-23744994 chr22:23744979-23744992 chr22:23745064-23745077
17	CTCF	chr22:23744512-23745438	A549	lung:	n/a	chr22:23745058-23745071 chr22:23744976-23744994 chr22:23744979-23744992 chr22:23745064-23745077
18	POLR2A	chr22:23744580-23745180	H1-neurons	neurons:	n/a	n/a
19	RAD21	chr22:23744770-23745321	H1-hESC	embryonic stem cell:	n/a	chr22:23745246-23745256 chr22:23745057-23745070 chr22:23744978-23744992
20	POLR2A	chr22:23744451-23745214	A549	lung:	n/a	n/a
21	MAX	chr22:23744429-23745219	ECC-1	luminal epithelium:	n/a	n/a
22	RAD21	chr22:23744727-23745320	A549	lung:	n/a	chr22:23745246-23745256 chr22:23745057-23745070 chr22:23744978-23744992
23	IRF1	chr22:23744657-23744827	K562	blood:	n/a	n/a
24	RAD21	chr22:23744598-23745202	H1-hESC	embryonic stem cell:	n/a	chr22:23745057-23745070 chr22:23744978-23744992
25	RAD21	chr22:23744769-23745306	HepG2	liver:	n/a	chr22:23745246-23745256 chr22:23745057-23745070 chr22:23744978-23744992
26	CTCF	chr22:23744779-23745294	A549	lung:	n/a	chr22:23745058-23745071 chr22:23744976-23744994 chr22:23744979-23744992 chr22:23745064-23745077
27	EGR1	chr22:23744565-23745043	ECC-1	luminal epithelium:	n/a	n/a
28	YY1	chr22:23744666-23744838	ECC-1	luminal epithelium:	n/a	n/a
29	POLR2A	chr22:23744543-23744851	MCF-7	breast:	n/a	n/a
30	POLR2A	chr22:23744593-23744850	MCF-7	breast:	n/a	n/a
31	MYC	chr22:23744607-23745202	A549	lung:	n/a	n/a
32	REST	chr22:23744806-23745343	ECC-1	luminal epithelium:	n/a	n/a
33	CTCF	chr22:23744421-23745490	SK-N-SH	brain:	n/a	chr22:23745058-23745071 chr22:23744976-23744994 chr22:23744979-23744992 chr22:23745064-23745077
34	EGR1	chr22:23744627-23745107	K562	blood:	n/a	n/a
35	POLR2A	chr22:23744518-23744881	ECC-1	luminal epithelium:	n/a	n/a
36	SMC3	chr22:23743979-23745540	SK-N-SH	brain:	n/a	chr22:23744978-23744992 chr22:23745058-23745068 chr22:23744982-23744992
37	POLR2A	chr22:23744790-23745182	A549	lung:	n/a	n/a
38	REST	chr22:23744709-23745398	H1-neurons	neurons:	n/a	n/a
39	BACH1	chr22:23744648-23745063	H1-hESC	embryonic stem cell:	n/a	n/a
40	CCNT2	chr22:23744595-23745201	K562	blood:	n/a	n/a
41	E2F4	chr22:23744648-23745201	MCF10A-Er-Src	breast:	n/a	n/a
42	TEAD4	chr22:23744497-23744954	ECC-1	luminal epithelium:	n/a	n/a
43	RAD21	chr22:23744778-23745348	HCT-116	colon:	n/a	chr22:23745246-23745256 chr22:23745057-23745070 chr22:23744978-23744992
44	EGR1	chr22:23744778-23745119	ECC-1	luminal epithelium:	n/a	n/a
45	TBP	chr22:23744626-23745165	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr22:23744802-23745192	ECC-1	luminal epithelium:	n/a	chr22:23745058-23745071 chr22:23744976-23744994 chr22:23744979-23744992 chr22:23745064-23745077
47	CTCF	chr22:23744773-23745262	K562	blood:	n/a	chr22:23745058-23745071 chr22:23744976-23744994 chr22:23744979-23744992 chr22:23745064-23745077
48	RAD21	chr22:23744257-23745569	SK-N-SH	brain:	n/a	chr22:23745533-23745543 chr22:23745246-23745256 chr22:23745057-23745070 chr22:23744978-23744992
49	RAD21	chr22:23744692-23745367	HCT-116	colon:	n/a	chr22:23745246-23745256 chr22:23745057-23745070 chr22:23744978-23744992
50	TCF12	chr22:23744421-23744872	ECC-1	luminal epithelium:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr22:20255317..20256206-chr22:23744235..23745365,12	HCT-116	colon:
2	chr22:20255195..20256295-chr22:23744242..23744859,6	MCF-7	breast:
3	chr22:20255555..20256232-chr22:23744733..23745268,3	MCF-7	breast:
4	chr22:20255429..20256076-chr22:23744719..23745345,6	K562	blood:
5	chr22:20255172..20256299-chr22:23744215..23745345,10	MCF-7	breast:
6	chr22:20255606..20257319-chr22:23743223..23746226,3	K562	blood:
7	chr22:20253259..20257319-chr22:23743216..23746275,4	K562	blood:

Variant related genes	Relation type
ZDHHC8P1	TF binding region
ENSG00000040608	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1056324	chr22:23055148-23750989	Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
2	nsv1057659	chr22:23400739-24138788	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
3	nsv9876	chr22:23563331-23923059	Strong transcription Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS 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 target site	29 gene(s)	inside rSNPs	diseases
4	nsv531550	chr22:23589667-24012550	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Genic enhancers 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 target site	40 gene(s)	inside rSNPs	diseases
5	esv2762117	chr22:23592136-23996869	Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
6	nsv1063476	chr22:23596683-23989388	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS 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	36 gene(s)	inside rSNPs	diseases
7	nsv544617	chr22:23596683-23989388	Strong transcription Genic enhancers Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
8	nsv1059951	chr22:23597270-23973060	Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
9	nsv1060339	chr22:23603429-23984195	Bivalent/Poised TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
10	nsv544618	chr22:23603429-23984195	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
11	nsv1059384	chr22:23614429-23984195	Bivalent Enhancer Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
12	nsv544619	chr22:23614429-23984195	Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS 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	34 gene(s)	inside rSNPs	diseases
13	nsv588601	chr22:23632665-23979219	Bivalent Enhancer Active TSS Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS 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	30 gene(s)	inside rSNPs	diseases
14	nsv914579	chr22:23650987-23995056	Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Weak 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	31 gene(s)	inside rSNPs	diseases
15	nsv1057910	chr22:23704457-23750847	Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
16	nsv914580	chr22:23720420-23757964	Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
17	nsv914581	chr22:23720420-23995056	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
18	nsv914582	chr22:23723721-23750847	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
19	nsv914583	chr22:23723721-23752398	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
20	nsv829099	chr22:23726903-23747505	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
21	nsv914584	chr22:23729698-23774625	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
22	esv3438074	chr22:23743477-23746325	Bivalent Enhancer Genic enhancers Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
23	nsv469702	chr22:23743640-23890756	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
24	nsv482382	chr22:23743640-23890756	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:23738800-23746400	Enhancers	Fetal Brain Male	brain
2	chr22:23741600-23745000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr22:23744000-23745200	Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr22:23744000-23745200	Enhancers	Spleen	Spleen
5	chr22:23744000-23745200	Active TSS	A549	lung
6	chr22:23744000-23745400	Active TSS	HUES48 Cell Line	embryonic stem cell
7	chr22:23744000-23745400	Active TSS	iPS-18 Cell Line	embryonic stem cell
8	chr22:23744000-23745400	Active TSS	iPS-20b Cell Line	embryonic stem cell
9	chr22:23744000-23745600	Active TSS	iPS-15b Cell Line	embryonic stem cell
10	chr22:23744200-23745200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr22:23744200-23745200	Active TSS	Brain Angular Gyrus	brain
12	chr22:23744200-23745200	Active TSS	Brain Anterior Caudate	brain
13	chr22:23744200-23745200	Active TSS	Rectal Mucosa Donor 29	rectum
14	chr22:23744200-23745400	Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr22:23744200-23745400	Active TSS	HUES64 Cell Line	embryonic stem cell
16	chr22:23744200-23745400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr22:23744200-23745400	Enhancers	Primary B cells from peripheral blood	blood
18	chr22:23744200-23745400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr22:23744400-23745000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr22:23744400-23745000	Enhancers	Fetal Thymus	thymus
21	chr22:23744400-23745200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr22:23744400-23745200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
23	chr22:23744400-23745200	Active TSS	Primary T helper naive cells fromperipheralblood	blood
24	chr22:23744400-23745200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
25	chr22:23744400-23745200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr22:23744400-23745200	Enhancers	Liver	Liver
27	chr22:23744400-23745200	Active TSS	Brain Cingulate Gyrus	brain
28	chr22:23744400-23745200	Active TSS	Brain Substantia Nigra	brain
29	chr22:23744400-23745200	Active TSS	Colon Smooth Muscle	Colon
30	chr22:23744400-23745200	Active TSS	Duodenum Mucosa	Duodenum
31	chr22:23744400-23745200	Enhancers	Lung	lung
32	chr22:23744400-23745400	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr22:23744400-23745400	Active TSS	H9 Cell Line	embryonic stem cell
34	chr22:23744400-23745400	Active TSS	Breast Myoepithelial Primary Cells	Breast
35	chr22:23744400-23745400	Active TSS	Primary T helper cells fromperipheralblood	blood
36	chr22:23744400-23745400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr22:23744400-23745400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr22:23744400-23745400	Enhancers	Fetal Heart	heart
39	chr22:23744400-23745400	Enhancers	Fetal Lung	lung
40	chr22:23744400-23745400	Active TSS	Thymus	Thymus
41	chr22:23744600-23745000	Active TSS	Cortex derived primary cultured neurospheres	brain
42	chr22:23744600-23745000	Bivalent Enhancer	Adipose Nuclei	Adipose
43	chr22:23744600-23745000	Active TSS	Brain Germinal Matrix	brain
44	chr22:23744600-23745000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
45	chr22:23744600-23745000	Enhancers	Fetal Intestine Large	intestine
46	chr22:23744600-23745000	Bivalent Enhancer	Fetal Muscle Leg	muscle
47	chr22:23744600-23745000	Active TSS	Fetal Stomach	stomach
48	chr22:23744600-23745000	Active TSS	Rectal Mucosa Donor 31	rectum
49	chr22:23744600-23745000	Active TSS	Right Atrium	heart
50	chr22:23744600-23745200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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