Variant report

Variant	rs9624073
Chromosome Location	chr22:23624093-23624094
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	YY1	chr22:23624031-23624286	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCFL	chr22:23623892-23624344	K562	blood:	n/a	chr22:23624181-23624190
3	ZNF143	chr22:23623842-23624442	K562	blood:	n/a	chr22:23624031-23624040
4	CTCF	chr22:23624018-23624384	ECC-1	luminal epithelium:	n/a	chr22:23624174-23624195 chr22:23624181-23624194 chr22:23624179-23624197 chr22:23624180-23624196
5	STAT5A	chr22:23623790-23624295	GM12878	blood:	n/a	n/a
6	CTCF	chr22:23623872-23624498	K562	blood:	n/a	chr22:23624174-23624195 chr22:23624181-23624194 chr22:23624179-23624197 chr22:23624180-23624196
7	MAZ	chr22:23624059-23624279	HepG2	liver:	n/a	n/a
8	BRCA1	chr22:23624084-23624337	H1-hESC	embryonic stem cell:	n/a	n/a
9	ZBTB7A	chr22:23623368-23624583	K562	blood:	n/a	n/a
10	CTCF	chr22:23623998-23624354	A549	lung:	n/a	chr22:23624174-23624195 chr22:23624181-23624194 chr22:23624179-23624197 chr22:23624180-23624196
11	POLR2A	chr22:23624011-23624888	MCF10A-Er-Src	breast:	n/a	n/a
12	RCOR1	chr22:23623898-23624361	GM12878	blood:	n/a	n/a
13	JUND	chr22:23623763-23624458	K562	blood:	n/a	n/a
14	STAT5A	chr22:23623707-23624425	GM12878	blood:	n/a	n/a
15	MAX	chr22:23623404-23624442	K562	blood:	n/a	chr22:23623500-23623511 chr22:23623499-23623512 chr22:23623500-23623510 chr22:23623500-23623511 chr22:23623501-23623510 chr22:23623499-23623512 chr22:23623501-23623511 chr22:23623501-23623511 chr22:23623500-23623511 chr22:23623500-23623510 chr22:23623499-23623512
16	SMC3	chr22:23623457-23624583	K562	blood:	n/a	chr22:23624181-23624195
17	ELK1	chr22:23623999-23624288	GM12878	blood:	n/a	n/a
18	RAD21	chr22:23623817-23624366	ECC-1	luminal epithelium:	n/a	chr22:23624177-23624196 chr22:23624179-23624191 chr22:23624180-23624193
19	RCOR1	chr22:23624060-23624683	Hela-S3	cervix:	n/a	n/a
20	MAFK	chr22:23623905-23624266	IMR90	lung:	n/a	n/a
21	RFX5	chr22:23624082-23624312	H1-hESC	embryonic stem cell:	n/a	n/a
22	MAX	chr22:23623564-23624257	NB4	blood:	n/a	n/a
23	JUND	chr22:23624019-23624726	H1-hESC	embryonic stem cell:	n/a	chr22:23624535-23624544 chr22:23624537-23624544 chr22:23624534-23624545 chr22:23624534-23624546 chr22:23624536-23624544 chr22:23624532-23624543
24	ZNF143	chr22:23623960-23624373	GM12878	blood:	n/a	chr22:23624031-23624040
25	POU2F2	chr22:23623788-23624370	GM12878	blood:	n/a	chr22:23624108-23624120
26	MAFK	chr22:23623905-23624300	HepG2	liver:	n/a	n/a
27	CTCF	chr22:23624025-23624361	Lung_OC	lung:	n/a	chr22:23624174-23624195 chr22:23624181-23624194 chr22:23624179-23624197 chr22:23624180-23624196
28	POLR2A	chr22:23623978-23624647	Hela-S3	cervix:	n/a	n/a
29	NR2F2	chr22:23622796-23624915	K562	blood:	n/a	n/a
30	NFIC	chr22:23623609-23624312	GM12878	blood:	n/a	n/a
31	PAX5	chr22:23623562-23624369	GM12878	blood:	n/a	chr22:23623969-23623978
32	USF2	chr22:23624075-23624284	H1-hESC	embryonic stem cell:	n/a	n/a
33	RAD21	chr22:23623882-23624406	H1-hESC	embryonic stem cell:	n/a	chr22:23624177-23624196 chr22:23624179-23624191 chr22:23624180-23624193
34	RCOR1	chr22:23623879-23624418	K562	blood:	n/a	n/a
35	CTCF	chr22:23624009-23624342	H1-hESC	embryonic stem cell:	n/a	chr22:23624174-23624195 chr22:23624181-23624194 chr22:23624179-23624197 chr22:23624180-23624196
36	MAFK	chr22:23624052-23624281	HepG2	liver:	n/a	n/a
37	ATF3	chr22:23623210-23625093	K562	blood:	n/a	n/a
38	ZBTB7A	chr22:23624039-23624199	HepG2	liver:	n/a	n/a
39	POLR2A	chr22:23620853-23632783	K562	blood:	n/a	n/a
40	CTCF	chr22:23623966-23624373	GM19238	blood:	n/a	chr22:23624174-23624195 chr22:23624181-23624194 chr22:23624179-23624197 chr22:23624180-23624196
41	RAD21	chr22:23623970-23624365	A549	lung:	n/a	chr22:23624177-23624196 chr22:23624179-23624191 chr22:23624180-23624193
42	RFX5	chr22:23623743-23624370	K562	blood:	n/a	chr22:23623901-23623915
43	RAD21	chr22:23623925-23624452	A549	lung:	n/a	chr22:23624177-23624196 chr22:23624179-23624191 chr22:23624180-23624193
44	FOXM1	chr22:23623702-23624367	GM12878	blood:	n/a	n/a
45	CTCF	chr22:23624060-23624210	Hela-S3	cervix:	n/a	chr22:23624174-23624195 chr22:23624181-23624194 chr22:23624179-23624197 chr22:23624180-23624196
46	MAFK	chr22:23623934-23624741	Hela-S3	cervix:	n/a	chr22:23624534-23624543 chr22:23624387-23624403
47	RAD21	chr22:23623875-23624368	SK-N-SH_RA	brain:	n/a	chr22:23624177-23624196 chr22:23624179-23624191 chr22:23624180-23624193
48	RAD21	chr22:23623780-23624725	HCT-116	colon:	n/a	chr22:23624177-23624196 chr22:23624179-23624191 chr22:23624180-23624193
49	YY1	chr22:23623952-23624328	H1-hESC	embryonic stem cell:	n/a	n/a
50	NFIC	chr22:23623880-23624924	ECC-1	luminal epithelium:	n/a	chr22:23624306-23624322 chr22:23624305-23624322

No.	Distal block	Cell Line	Cell type
1	chr22:23515967..23516810-chr22:23623905..23625091,6	MCF-7	breast:
2	chr22:23515736..23517273-chr22:23623641..23625306,49	K562	blood:
3	chr22:23521450..23522095-chr22:23624049..23624602,2	MCF-7	breast:
4	chr22:23518801..23520125-chr22:23623736..23625336,5	K562	blood:
5	chr22:23520289..23523680-chr22:23623216..23625593,134	K562	blood:
6	chr22:23498297..23499582-chr22:23623699..23624663,6	K562	blood:
7	chr22:23519910..23521360-chr22:23623104..23624706,17	MCF-7	breast:
8	chr22:23500320..23500821-chr22:23623680..23624207,2	K562	blood:
9	chr22:23529323..23530010-chr22:23623745..23624699,2	K562	blood:
10	chr22:23301312..23301892-chr22:23623736..23624987,4	MCF-7	breast:
11	chr22:23190706..23191213-chr22:23623766..23624457,2	K562	blood:
12	chr22:23520909..23526395-chr22:23622717..23628021,9	MCF-7	breast:
13	chr22:23520305..23521477-chr22:23623626..23624696,9	MCF-7	breast:
14	chr22:23511021..23511689-chr22:23623587..23624199,2	K562	blood:
15	chr22:23470319..23471746-chr22:23623633..23624628,4	K562	blood:
16	chr22:23519615..23526434-chr22:23614924..23625964,20	MCF-7	breast:
17	chr22:23533489..23536061-chr22:23622372..23624122,2	MCF-7	breast:
18	chr22:23524748..23526644-chr22:23623688..23624869,6	K562	blood:
19	chr22:23301037..23302377-chr22:23623248..23624813,25	K562	blood:
20	chr22:23520778..23521515-chr22:23623922..23624706,2	MCF-7	breast:
21	chr22:23501040..23501869-chr22:23623926..23624698,2	K562	blood:
22	chr22:23470450..23471035-chr22:23623962..23624646,2	MCF-7	breast:
23	chr22:23487477..23488368-chr22:23623236..23624212,2	K562	blood:

Variant related genes	Relation type
BCR	TF binding region
ENSG00000186716	Chromatin interaction
ENSG00000100228	Chromatin interaction
ENSG00000236794	Chromatin interaction

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs11090227	0.87[ASN][1000 genomes]
rs11090228	0.91[ASN][1000 genomes]
rs12166802	0.95[ASN][1000 genomes]
rs12233352	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12627853	0.81[ASN][1000 genomes]
rs16802	0.86[ASN][1000 genomes]
rs1811017	0.83[ASN][1000 genomes]
rs1811018	0.83[ASN][1000 genomes]
rs2227939	0.91[ASN][1000 genomes]
rs3788358	0.87[ASN][1000 genomes]
rs5751619	0.91[ASN][1000 genomes]
rs5751620	1.00[ASN][1000 genomes]
rs5751621	0.85[ASN][1000 genomes]
rs5759661	0.88[ASN][1000 genomes]
rs5759665	0.86[ASN][1000 genomes]
rs5759666	0.86[ASN][1000 genomes]
rs5759668	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs5759669	0.82[ASN][1000 genomes]
rs5759670	0.87[ASN][1000 genomes]
rs5759671	1.00[ASN][1000 genomes]
rs5759673	0.87[ASN][1000 genomes]
rs5759675	0.87[ASN][1000 genomes]
rs5759676	0.87[ASN][1000 genomes]
rs5759679	0.87[ASN][1000 genomes]
rs5759680	1.00[ASN][1000 genomes]
rs5759681	0.91[ASN][1000 genomes]
rs5759682	0.91[ASN][1000 genomes]
rs5759690	0.81[ASN][1000 genomes]
rs5996508	0.87[ASN][1000 genomes]
rs5996509	0.87[ASN][1000 genomes]
rs6003593	0.83[ASN][1000 genomes]
rs6003598	0.87[ASN][1000 genomes]
rs6003600	0.87[ASN][1000 genomes]
rs62219796	0.89[ASN][1000 genomes]
rs7292656	0.91[ASN][1000 genomes]
rs9608093	0.95[ASN][1000 genomes]
rs9608100	0.91[ASN][1000 genomes]
rs9612269	0.82[ASN][1000 genomes]
rs9624072	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:35 , 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	nsv588598	chr22:23530168-23638025	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
25	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
26	nsv482557	chr22:23584948-23741799	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
27	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
28	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
29	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
30	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
31	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
32	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
33	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
34	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
35	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

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:23595000-23647000	Strong transcription	Dnd41	blood
2	chr22:23595800-23649600	Strong transcription	Primary neutrophils fromperipheralblood	blood
3	chr22:23599400-23635000	Weak transcription	Small Intestine	intestine
4	chr22:23600200-23632000	Strong transcription	Fetal Intestine Small	intestine
5	chr22:23601800-23641000	Strong transcription	Primary T cells from cord blood	blood
6	chr22:23603400-23631600	Strong transcription	Fetal Intestine Large	intestine
7	chr22:23608800-23649400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr22:23612600-23647800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
9	chr22:23613000-23629600	Strong transcription	HUES64 Cell Line	embryonic stem cell
10	chr22:23613000-23640800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
11	chr22:23616600-23639000	Weak transcription	Fetal Kidney	kidney
12	chr22:23616800-23637200	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr22:23618200-23628600	Weak transcription	Fetal Lung	lung
14	chr22:23619200-23625800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr22:23619400-23626600	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr22:23620000-23625000	Genic enhancers	Gastric	stomach
17	chr22:23620000-23626400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr22:23620200-23624800	Genic enhancers	Primary T cells fromperipheralblood	blood
19	chr22:23620200-23625200	Enhancers	HMEC	breast
20	chr22:23620400-23626600	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr22:23621000-23624400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
22	chr22:23621000-23625000	Genic enhancers	Fetal Muscle Leg	muscle
23	chr22:23621000-23625400	Genic enhancers	NHEK	skin
24	chr22:23621200-23624800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr22:23621600-23624200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr22:23621600-23625600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr22:23621600-23626600	Weak transcription	Aorta	Aorta
28	chr22:23621800-23624200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr22:23621800-23624200	Genic enhancers	Lung	lung
30	chr22:23621800-23626200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr22:23622000-23625400	Genic enhancers	HUVEC	blood vessel
32	chr22:23622000-23627200	Weak transcription	Left Ventricle	heart
33	chr22:23622200-23624400	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr22:23622200-23625400	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr22:23622200-23625800	Genic enhancers	Esophagus	oesophagus
36	chr22:23622800-23624200	Genic enhancers	Colonic Mucosa	Colon
37	chr22:23623000-23624400	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr22:23623000-23624600	Genic enhancers	Rectal Mucosa Donor 29	rectum
39	chr22:23623000-23624800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr22:23623000-23625000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
41	chr22:23623000-23625200	Enhancers	Brain Anterior Caudate	brain
42	chr22:23623000-23626400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr22:23623200-23624200	Enhancers	Primary hematopoietic stem cells	blood
44	chr22:23623200-23624400	Enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr22:23623200-23624600	Weak transcription	Fetal Brain Female	brain
46	chr22:23623200-23624600	Genic enhancers	Fetal Thymus	thymus
47	chr22:23623200-23625000	Enhancers	Stomach Mucosa	stomach
48	chr22:23623200-23625200	Enhancers	Rectal Smooth Muscle	rectum
49	chr22:23623200-23625600	Enhancers	Duodenum Smooth Muscle	Duodenum
50	chr22:23623400-23624200	Enhancers	H1 Cell Line	embryonic stem cell

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