Variant report

Variant	rs5996477
Chromosome Location	chr22:23520846-23520847
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	chr22:23520720-23520870	AG09319	gingival:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
2	STAT3	chr22:23520799-23520972	MCF10A-Er-Src	breast:	n/a	n/a
3	CTCF	chr22:23520562-23521087	HCT-116	colon:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
4	CTCF	chr22:23520720-23520870	RPTEC	kidney:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
5	RAD21	chr22:23520612-23521340	Hela-S3	cervix:	n/a	chr22:23520806-23520816 chr22:23520806-23520818 chr22:23520801-23520820 chr22:23520804-23520817
6	CTCF	chr22:23520700-23520850	HMEC	breast:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
7	CTCF	chr22:23520650-23520955	Gliobla	brain:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
8	TBL1XR1	chr22:23520604-23527305	K562	blood:	n/a	n/a
9	CTCF	chr22:23520720-23520870	Hela-S3	cervix:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
10	CTCF	chr22:23520610-23521118	MCF-7	breast:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
11	TBL1XR1	chr22:23520619-23523842	K562	blood:	n/a	n/a
12	RFX5	chr22:23520642-23520939	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr22:23520664-23520936	MCF-7	breast:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
14	STAT1	chr22:23520697-23521062	GM12878	blood:	n/a	n/a
15	CTCF	chr22:23520740-23520890	BJ	skin:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
16	CTCF	chr22:23520670-23520953	LNCaP	prostate:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
17	CTCF	chr22:23520656-23520950	A549	lung:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
18	CTCF	chr22:23520740-23520890	WI-38	lung:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
19	CTCF	chr22:23520642-23520955	GM12892	blood:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
20	HDAC2	chr22:23520523-23526205	K562	blood:	n/a	chr22:23521032-23521051
21	CTCF	chr22:23520760-23520910	HVMF	connective:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
22	POLR2A	chr22:23520633-23526356	K562	blood:	n/a	n/a
23	CUX1	chr22:23520618-23522723	K562	blood:	n/a	chr22:23521379-23521393
24	CTCF	chr22:23520740-23520890	AG09319	gingival:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
25	CTCF	chr22:23520760-23520910	NHDF-neo	bronchial:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
26	RUNX3	chr22:23520566-23520973	GM12878	blood:	n/a	n/a
27	STAT5A	chr22:23520445-23522610	K562	blood:	n/a	chr22:23521510-23521521 chr22:23522547-23522559
28	CTCF	chr22:23520720-23520870	HMEC	breast:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
29	RAD21	chr22:23520580-23521209	A549	lung:	n/a	chr22:23520806-23520816 chr22:23520806-23520818 chr22:23520801-23520820 chr22:23520804-23520817
30	CTCF	chr22:23520676-23520944	GM10248	blood:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
31	CTCF	chr22:23520720-23520870	GM12868	blood:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
32	EP300	chr22:23520596-23523878	K562	blood:	n/a	chr22:23522854-23522870 chr22:23521047-23521060 chr22:23522997-23523010 chr22:23521637-23521650
33	CTCF	chr22:23520700-23520850	HAc	cerebellar:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
34	CTCF	chr22:23520649-23520940	Fibrobl	skin:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
35	CTCF	chr22:23520447-23521176	A549	lung:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
36	ZNF143	chr22:23520620-23521267	GM12878	blood:	n/a	n/a
37	SIN3A	chr22:23520614-23521185	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr22:23520613-23520973	SK-N-SH_RA	brain:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
39	CTCF	chr22:23520740-23520890	GM06990	blood:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
40	CTCF	chr22:23520740-23520890	AG04449	skin:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
41	CTCF	chr22:23520657-23520954	GM19239	blood:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
42	UBTF	chr22:23520613-23526470	K562	blood:	n/a	n/a
43	RCOR1	chr22:23520649-23520952	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr22:23520677-23521022	ECC-1	luminal epithelium:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
45	CTCF	chr22:23520740-23520890	HPF	lung:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
46	CTCF	chr22:23520740-23520890	BE2_C	brain:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
47	CHD2	chr22:23520603-23521193	K562	blood:	n/a	n/a
48	CTCF	chr22:23520740-23520890	AoAF	blood vessel:	n/a	chr22:23520803-23520816 chr22:23520800-23520818 chr22:23520802-23520823
49	TAL1	chr22:23520659-23522885	K562	blood:	n/a	n/a
50	EGR1	chr22:23520563-23521198	K562	blood:	n/a	chr22:23520830-23520837 chr22:23520829-23520844

No.	Distal block	Cell Line	Cell type
1	chr22:23520370..23520901-chr22:23582804..23583526,2	MCF-7	breast:
2	chr22:23520788..23521291-chr22:23578289..23578791,2	K562	blood:
3	chr12:120728308..120731053-chr22:23519442..23522442,4	MCF-7	breast:
4	chr22:23520289..23523680-chr22:23623216..23625593,134	K562	blood:
5	chr22:23520315..23521264-chr22:23627226..23627950,2	K562	blood:
6	chr22:23520547..23521329-chr9:133815605..133817046,4	K562	blood:
7	chr22:23520612..23521284-chr22:23637283..23637857,2	K562	blood:
8	chr12:120728953..120730250-chr22:23520442..23521442,4	MCF-7	breast:
9	chr22:23520679..23521332-chr22:23632210..23633200,4	MCF-7	breast:
10	chr22:23520292..23521317-chr9:133738584..133739634,13	K562	blood:
11	chr22:23520782..23521294-chr22:23611645..23612373,2	MCF-7	breast:
12	chr22:23520336..23521327-chr9:133646057..133647024,3	K562	blood:
13	chr22:23520350..23521289-chr22:23611618..23612941,3	K562	blood:
14	chr22:23498268..23499065-chr22:23520404..23521247,2	K562	blood:
15	chr22:23520305..23521477-chr22:23623626..23624696,9	MCF-7	breast:
16	chr22:23520400..23521352-chr9:133873402..133874291,3	K562	blood:
17	chr22:23520356..23521778-chr9:133741049..133742733,6	K562	blood:
18	chr12:120729243..120729861-chr22:23520462..23521462,3	MCF-7	breast:
19	chr12:120728297..120729929-chr22:23519462..23522442,4	MCF-7	breast:
20	chr22:23519615..23526434-chr22:23614924..23625964,20	MCF-7	breast:
21	chr22:23520308..23521485-chr22:23625664..23627054,5	K562	blood:
22	chr22:23519543..23521281-chr22:23587399..23590262,2	MCF-7	breast:
23	chr22:23520309..23521292-chr22:23592207..23593551,8	K562	blood:
24	chr22:23520778..23521515-chr22:23623922..23624706,2	MCF-7	breast:
25	chr22:23301479..23302049-chr22:23520363..23521253,2	K562	blood:
26	chr22:23520305..23521309-chr22:23631752..23633320,11	K562	blood:
27	chr22:23520341..23521308-chr22:23602297..23603379,4	K562	blood:
28	chr22:23519910..23521360-chr22:23623104..23624706,17	MCF-7	breast:
29	chr12:120728276..120729928-chr22:23519462..23520962,2	K562	blood:
30	chr12:120728333..120732236-chr22:23519442..23524202,7	K562	blood:
31	chr22:23520263..23521248-chr9:133735957..133736953,3	K562	blood:

Variant related genes	Relation type
BCR	TF binding region
ENSG00000200795	Chromatin interaction
ENSG00000202538	Chromatin interaction
ENSG00000186716	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs12157412	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12157536	1.00[AMR][1000 genomes]
rs12157941	1.00[AMR][1000 genomes]
rs12158986	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12159557	0.92[AFR][1000 genomes]
rs12159793	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12160027	1.00[AMR][1000 genomes]
rs12160099	1.00[AMR][1000 genomes]
rs2330366	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs5996469	1.00[AMR][1000 genomes]
rs5996472	1.00[AMR][1000 genomes]
rs5996479	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs5996480	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs5996481	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs5996482	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs5996484	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6003521	1.00[AMR][1000 genomes]
rs6003522	1.00[AMR][1000 genomes]
rs6003523	1.00[AMR][1000 genomes]
rs6003524	1.00[AMR][1000 genomes]
rs6003526	1.00[AMR][1000 genomes]
rs6003528	1.00[AMR][1000 genomes]
rs6003530	1.00[AMR][1000 genomes]
rs6003537	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6003538	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6003539	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6003540	1.00[AMR][1000 genomes]
rs6003541	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6003542	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6003543	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6003544	1.00[AFR][1000 genomes]
rs6003545	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6003546	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6003548	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6003549	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6003628	1.00[AMR][1000 genomes]
rs9620237	1.00[AMR][1000 genomes]

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	nsv915235	chr22:22971768-23650987	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong 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	101 gene(s)	inside rSNPs	diseases
2	esv3388845	chr22:22973346-23652447	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	100 gene(s)	inside rSNPs	diseases
3	nsv531799	chr22:22993679-23642142	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
4	nsv1061433	chr22:22997799-23649107	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
5	nsv521695	chr22:22998337-23648009	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
6	nsv915236	chr22:22998337-23650987	Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
7	nsv588512	chr22:22998337-23667731	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
8	nsv531800	chr22:23002708-23648163	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS 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	97 gene(s)	inside rSNPs	diseases
9	nsv916593	chr22:23002709-23648790	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers 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	97 gene(s)	inside rSNPs	diseases
10	nsv993496	chr22:23002709-23654222	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
11	nsv1067002	chr22:23007167-23643363	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Active TSS 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	97 gene(s)	inside rSNPs	diseases
12	nsv1067324	chr22:23007367-23654223	Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Strong transcription 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	97 gene(s)	inside rSNPs	diseases
13	nsv533839	chr22:23012013-23643223	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
14	nsv916933	chr22:23012069-23654237	Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
15	nsv531801	chr22:23028586-23657804	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	92 gene(s)	inside rSNPs	diseases
16	nsv531802	chr22:23046186-23627391	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	85 gene(s)	inside rSNPs	diseases
17	nsv1060509	chr22:23055148-23648719	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS 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	83 gene(s)	inside rSNPs	diseases
18	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
19	nsv1062780	chr22:23060449-23648719	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	82 gene(s)	inside rSNPs	diseases
20	nsv948942	chr22:23063178-23645718	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	82 gene(s)	inside rSNPs	diseases
21	nsv1063200	chr22:23097177-23643224	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	80 gene(s)	inside rSNPs	diseases
22	nsv949250	chr22:23157485-23645718	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	69 gene(s)	inside rSNPs	diseases
23	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
24	nsv1058604	chr22:23497533-23545751	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:23490400-23522000	Weak transcription	Aorta	Aorta
2	chr22:23516000-23522000	Enhancers	Primary T cells fromperipheralblood	blood
3	chr22:23517000-23521000	Weak transcription	Brain Angular Gyrus	brain
4	chr22:23517800-23522000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr22:23517800-23522200	Enhancers	GM12878-XiMat	blood
6	chr22:23518000-23521200	Strong transcription	Right Atrium	heart
7	chr22:23518000-23522000	Enhancers	Esophagus	oesophagus
8	chr22:23518000-23522200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr22:23519000-23521600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr22:23519200-23521400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr22:23519200-23522200	Enhancers	Primary B cells from peripheral blood	blood
12	chr22:23519400-23522000	Weak transcription	Thymus	Thymus
13	chr22:23519400-23522200	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr22:23519600-23521400	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr22:23519600-23521400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr22:23519600-23521800	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr22:23519600-23522000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr22:23519600-23522000	Enhancers	Placenta	Placenta
19	chr22:23519600-23522200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
20	chr22:23519800-23521000	Enhancers	K562	blood
21	chr22:23519800-23521200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr22:23519800-23522000	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr22:23519800-23522000	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr22:23519800-23522200	Enhancers	Primary B cells from cord blood	blood
25	chr22:23520200-23521200	Weak transcription	Primary hematopoietic stem cells	blood
26	chr22:23520200-23521800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr22:23520600-23521000	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr22:23520600-23521000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
29	chr22:23520600-23521200	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr22:23520600-23521200	Enhancers	Colonic Mucosa	Colon
31	chr22:23520600-23521400	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr22:23520600-23521400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr22:23520600-23521600	Enhancers	Brain Germinal Matrix	brain
34	chr22:23520600-23521600	Enhancers	Colon Smooth Muscle	Colon
35	chr22:23520600-23521600	Enhancers	Fetal Stomach	stomach
36	chr22:23520600-23521800	Enhancers	Brain Anterior Caudate	brain
37	chr22:23520600-23521800	Enhancers	Brain Hippocampus Middle	brain
38	chr22:23520600-23522000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr22:23520600-23522000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr22:23520600-23522000	Enhancers	Primary T helper cells fromperipheralblood	blood
41	chr22:23520600-23522000	Enhancers	Brain Cingulate Gyrus	brain
42	chr22:23520600-23522000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
43	chr22:23520600-23522000	Enhancers	Pancreas	Pancrea
44	chr22:23520600-23522200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr22:23520600-23522200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr22:23520600-23522200	Bivalent Enhancer	Fetal Muscle Leg	muscle
47	chr22:23520600-23522200	Enhancers	Fetal Thymus	thymus
48	chr22:23520600-23522400	Flanking Active TSS	Stomach Smooth Muscle	stomach
49	chr22:23520800-23521000	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr22:23520800-23521000	Enhancers	Fetal Heart	heart

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