Variant report

Variant	rs7943844
Chromosome Location	chr11:5226341-5226342
allele	A/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	CTCF	chr11:5225998-5226384	H1-hESC	embryonic stem cell:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
2	CTCF	chr11:5226060-5226369	HUVEC	blood vessel:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
3	CTCF	chr11:5226070-5226345	Gliobla	brain:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
4	RAD21	chr11:5225913-5226520	HCT-116	colon:	n/a	chr11:5226194-5226213
5	EP300	chr11:5226015-5226434	K562	blood:	n/a	n/a
6	CTCF	chr11:5225990-5226385	HepG2	liver:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
7	CTCF	chr11:5226089-5226349	K562	blood:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
8	SMC3	chr11:5225918-5226503	SK-N-SH	brain:	n/a	chr11:5226195-5226209
9	RAD21	chr11:5225990-5226380	SK-N-SH_RA	brain:	n/a	chr11:5226194-5226213
10	CTCF	chr11:5225999-5226409	GM12878	blood:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
11	CTCF	chr11:5226200-5226350	GM12878	blood:	n/a	n/a
12	RAD21	chr11:5225908-5226511	HCT-116	colon:	n/a	chr11:5226194-5226213
13	JUND	chr11:5226049-5226435	K562	blood:	n/a	n/a
14	RCOR1	chr11:5226045-5226447	K562	blood:	n/a	n/a
15	GATA2	chr11:5226046-5226451	K562	blood:	n/a	n/a
16	CTCF	chr11:5225766-5226490	SK-N-SH	brain:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
17	RAD21	chr11:5225908-5226500	A549	lung:	n/a	chr11:5226194-5226213
18	ATF2	chr11:5226032-5226399	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr11:5226200-5226350	HEEpiC	esophagus:	n/a	n/a
20	SRF	chr11:5225948-5226500	HCT-116	colon:	n/a	n/a
21	TAL1	chr11:5226135-5226449	K562	blood:	n/a	n/a
22	CTCF	chr11:5225800-5226495	A549	lung:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
23	UBTF	chr11:5226058-5226432	K562	blood:	n/a	n/a
24	RAD21	chr11:5225989-5226449	Hela-S3	cervix:	n/a	chr11:5226194-5226213
25	CTCF	chr11:5225998-5226411	K562	blood:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
26	MAZ	chr11:5226058-5226417	K562	blood:	n/a	n/a
27	MAFK	chr11:5226049-5226428	K562	blood:	n/a	n/a
28	CHD2	chr11:5226266-5226379	GM12878	blood:	n/a	n/a
29	RAD21	chr11:5226020-5226397	K562	blood:	n/a	chr11:5226194-5226213
30	CTCF	chr11:5226067-5226342	Hela-S3	cervix:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
31	CTCF	chr11:5226085-5226384	K562	blood:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
32	CTCF	chr11:5225964-5226405	A549	lung:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
33	RAD21	chr11:5225930-5226500	A549	lung:	n/a	chr11:5226194-5226213
34	RFX5	chr11:5226038-5226403	K562	blood:	n/a	n/a
35	SMC3	chr11:5226036-5226429	HepG2	liver:	n/a	chr11:5226195-5226209
36	CTCF	chr11:5226010-5226398	HCT-116	colon:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
37	CTCF	chr11:5226240-5226390	MCF-7	breast:	n/a	n/a
38	SMC3	chr11:5226014-5226443	K562	blood:	n/a	chr11:5226195-5226209
39	CTCF	chr11:5225976-5226439	K562	blood:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
40	NR2F2	chr11:5226021-5226455	K562	blood:	n/a	n/a
41	CTCF	chr11:5225819-5226511	HCT-116	colon:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
42	RAD21	chr11:5226026-5226402	HepG2	liver:	n/a	chr11:5226194-5226213
43	RAD21	chr11:5226009-5226418	H1-hESC	embryonic stem cell:	n/a	chr11:5226194-5226213
44	RAD21	chr11:5225992-5226460	H1-hESC	embryonic stem cell:	n/a	chr11:5226194-5226213
45	RAD21	chr11:5225976-5226444	SK-N-SH_RA	brain:	n/a	chr11:5226194-5226213
46	CTCF	chr11:5226080-5226380	A549	lung:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
47	SMC3	chr11:5226005-5226462	Hela-S3	cervix:	n/a	chr11:5226195-5226209
48	RAD21	chr11:5225928-5226519	MCF-7	breast:	n/a	chr11:5226194-5226213
49	USF1	chr11:5225979-5226440	HCT-116	colon:	n/a	n/a
50	RCOR1	chr11:5226026-5226451	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:5218102..5224405-chr11:5224720..5231093,9	K562	blood:
2	chr11:5224202..5227710-chr11:5524990..5527435,3	K562	blood:

Variant related genes	Relation type
OR51V1	TF binding region
ENSG00000167355	Chromatin interaction
ENSG00000196565	Chromatin interaction
ENSG00000213931	Chromatin interaction
ENSG00000176742	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2760169	chr11:4961518-5233821	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
2	nsv1042613	chr11:5173410-5336839	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
3	nsv1051488	chr11:5175477-5258490	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
4	nsv1048593	chr11:5183176-5261470	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
5	nsv1045187	chr11:5183176-5262622	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
6	nsv1052798	chr11:5184546-5269330	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
7	nsv1052750	chr11:5187571-5338802	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
8	nsv896929	chr11:5192095-5271671	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
9	nsv1049387	chr11:5192334-5231273	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
10	nsv540941	chr11:5192334-5231273	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
11	nsv1038871	chr11:5192334-5301415	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
12	nsv540942	chr11:5192334-5301415	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
13	nsv1048355	chr11:5192334-5336839	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
14	nsv523914	chr11:5207389-5231565	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
15	esv3375261	chr11:5225826-5227724	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5223000-5229600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr11:5225200-5231600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr11:5225400-5226400	Enhancers	K562	blood
4	chr11:5226000-5226400	Enhancers	Osteobl	bone

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