Variant report

Variant	rs567680476
Chromosome Location	chr22:23412258-23412259
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	CEBPD	chr22:23412200-23412521	HepG2	liver:	n/a	n/a
2	E2F4	chr22:23412166-23412436	GM12878	blood:	n/a	chr22:23412262-23412271
3	ZNF143	chr22:23411976-23412458	K562	blood:	n/a	chr22:23412262-23412272
4	CTCF	chr22:23411997-23413141	K562	blood:	n/a	chr22:23413008-23413021 chr22:23412210-23412223 chr22:23413010-23413023
5	POLR2A	chr22:23411918-23412397	SK-N-MC	brain:	n/a	n/a
6	CTCF	chr22:23412140-23412290	HUVEC	blood vessel:	n/a	chr22:23412210-23412223
7	USF1	chr22:23412226-23412459	SK-N-SH_RA	brain:	n/a	chr22:23412312-23412328
8	SMC3	chr22:23412057-23412376	K562	blood:	n/a	n/a
9	MYC	chr22:23411966-23412756	K562	blood:	n/a	chr22:23412636-23412645
10	ARID3A	chr22:23412042-23412327	K562	blood:	n/a	n/a
11	CEBPB	chr22:23411888-23412379	Hela-S3	cervix:	n/a	n/a
12	TAF1	chr22:23412021-23412517	ECC-1	luminal epithelium:	n/a	n/a
13	EBF1	chr22:23412202-23412611	GM12878	blood:	n/a	n/a
14	HMGN3	chr22:23411750-23413315	K562	blood:	n/a	n/a
15	MAX	chr22:23412141-23412848	K562	blood:	n/a	chr22:23412636-23412645
16	SP1	chr22:23412081-23412523	GM12878	blood:	n/a	chr22:23412308-23412319 chr22:23412308-23412320 chr22:23412309-23412319 chr22:23412309-23412318 chr22:23412310-23412319 chr22:23412309-23412318 chr22:23412308-23412320
17	NFYA	chr22:23412061-23412455	GM12878	blood:	n/a	n/a
18	SP1	chr22:23411986-23412537	HCT-116	colon:	n/a	chr22:23412308-23412319 chr22:23412308-23412320 chr22:23412309-23412319 chr22:23412309-23412318 chr22:23412310-23412319 chr22:23412309-23412318 chr22:23412308-23412320
19	MAX	chr22:23411986-23412698	A549	lung:	n/a	chr22:23412636-23412645
20	E2F6	chr22:23411827-23413015	K562	blood:	n/a	chr22:23411896-23411906 chr22:23412262-23412271 chr22:23411888-23411897
21	POLR2A	chr22:23411963-23412365	HepG2	liver:	n/a	n/a
22	ZNF384	chr22:23411978-23412395	K562	blood:	n/a	n/a
23	HCFC1	chr22:23411796-23412516	Hela-S3	cervix:	n/a	n/a
24	RCOR1	chr22:23411878-23412419	Hela-S3	cervix:	n/a	n/a
25	MYC	chr22:23411944-23412805	K562	blood:	n/a	chr22:23412636-23412645
26	MAZ	chr22:23412021-23412776	Hela-S3	cervix:	n/a	chr22:23412636-23412645
27	NFYB	chr22:23411869-23412518	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr22:23411343-23412481	K562	blood:	n/a	n/a
29	MAX	chr22:23411856-23412511	K562	blood:	n/a	chr22:23411886-23411896 chr22:23411889-23411899
30	CTCFL	chr22:23412210-23412594	K562	blood:	n/a	n/a
31	POLR2A	chr22:23412099-23412392	HCT-116	colon:	n/a	n/a
32	MAX	chr22:23412214-23412529	GM12878	blood:	n/a	n/a
33	NR2F2	chr22:23411579-23413017	K562	blood:	n/a	n/a
34	POLR2A	chr22:23411969-23412972	H1-neurons	neurons:	n/a	n/a
35	MAFK	chr22:23411418-23412266	K562	blood:	n/a	n/a
36	TBL1XR1	chr22:23411778-23412419	K562	blood:	n/a	n/a
37	SP1	chr22:23412089-23412447	HepG2	liver:	n/a	chr22:23412308-23412319 chr22:23412308-23412320 chr22:23412309-23412319 chr22:23412309-23412318 chr22:23412310-23412319 chr22:23412309-23412318 chr22:23412308-23412320
38	MYC	chr22:23412210-23412478	NB4	blood:	n/a	n/a
39	CTCF	chr22:23411896-23413286	K562	blood:	n/a	chr22:23413008-23413021 chr22:23412210-23412223 chr22:23413010-23413023
40	ZNF143	chr22:23412234-23412361	H1-hESC	embryonic stem cell:	n/a	chr22:23412262-23412272
41	SMC3	chr22:23411842-23412385	Hela-S3	cervix:	n/a	n/a
42	POLR2A	chr22:23412095-23412444	A549	lung:	n/a	n/a
43	MAX	chr22:23412141-23412531	SK-N-SH	brain:	n/a	n/a
44	FOS	chr22:23411818-23412358	HUVEC	blood vessel:	n/a	chr22:23411894-23411903
45	RCOR1	chr22:23411193-23412832	K562	blood:	n/a	n/a
46	POLR2A	chr22:23412168-23412280	MCF-7	breast:	n/a	n/a
47	ETS1	chr22:23411598-23412550	K562	blood:	n/a	chr22:23411890-23411901 chr22:23411886-23411897 chr22:23411893-23411904
48	POLR2A	chr22:23411711-23412803	HEK293	kidney:	n/a	n/a
49	ELF1	chr22:23412057-23413192	K562	blood:	n/a	chr22:23413102-23413114 chr22:23413140-23413152
50	MXI1	chr22:23411698-23412477	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:23412225-23412275	HCF	heart:	n/a
2	chr22:23412225-23412275	HPAEpiC	pulmonary alveolar:	n/a
3	chr22:23412225-23412275	MCF-7	breast:	n/a
4	chr22:23412225-23412275	AG09319	gingival:	n/a
5	chr22:23412225-23412275	HRE	kidney:	n/a
6	chr22:23412225-23412275	Jurkat	blood:	n/a
7	chr22:23412225-23412275	HEEpiC	esophagus:	n/a
8	chr22:23412225-23412275	GM12891	blood:	n/a
9	chr22:23412225-23412275	NHDF-neo	bronchial:	n/a
10	chr22:23412225-23412275	HUVEC	blood vessel:	n/a
11	chr22:23412225-23412275	SK-N-SH	brain:	n/a
12	chr22:23412225-23412275	HRCEpiC	kidney:	n/a
13	chr22:23412225-23412275	AG09309	skin:	n/a
14	chr22:23412225-23412275	HepG2	liver:	n/a
15	chr22:23412225-23412275	U87	brain:	n/a
16	chr22:23412225-23412275	HL-60	blood:	n/a
17	chr22:23412225-23412275	ProgFib	skin:	n/a
18	chr22:23412225-23412275	HEK293	kidney:	embryo
19	chr22:23412225-23412275	SKMC	muscle:	n/a
20	chr22:23412225-23412275	H1-hESC	embryonic stem cell:	embryo
21	chr22:23412225-23412275	T-47D	breast:	n/a
22	chr22:23412225-23412275	Hela-S3	cervix:	n/a
23	chr22:23412225-23412275	NT2-D1	testis:	n/a
24	chr22:23412225-23412275	NH-A	brain:	n/a
25	chr22:23412225-23412275	HMEC	breast:	n/a
26	chr22:23412225-23412275	BE2_C	brain:	n/a
27	chr22:23412225-23412275	ovcar-3	ovarian:	n/a
28	chr22:23412225-23412275	HNPCEpiC	eye:	n/a
29	chr22:23412225-23412275	CMK	blood:	n/a
30	chr22:23412225-23412275	PFSK-1	brain:	n/a
31	chr22:23412225-23412275	GM19239	blood:	n/a
32	chr22:23412225-23412275	HCT-116	colon:	n/a
33	chr22:23412225-23412275	HCM	heart:	n/a
34	chr22:23412225-23412275	GM12892	blood:	n/a
35	chr22:23412225-23412275	GM12878	blood:	n/a
36	chr22:23412225-23412275	Hepatocyte	liver:	n/a
37	chr22:23412225-23412275	HRPEpiC	eye:	n/a
38	chr22:23412225-23412275	BJ	skin:	n/a
39	chr22:23412225-23412275	A549	lung:	n/a
40	chr22:23412225-23412275	PrEC	prostate:	n/a
41	chr22:23412225-23412275	HCPEpiC	choroid plexus:	n/a
42	chr22:23412225-23412275	NB4	blood:	n/a
43	chr22:23412225-23412275	NHBE	bronchial:	n/a
44	chr22:23412225-23412275	AG04449	skin:	fetal
45	chr22:23412225-23412275	ECC-1	luminal epithelium:	n/a
46	chr22:23412225-23412275	HAEpiC	amniotic membrane:	n/a
47	chr22:23412225-23412275	IMR90	lung:	fetal
48	chr22:23412225-23412275	AoSMC	blood vessel:	n/a
49	chr22:23412225-23412275	MCF10A-Er-Src	breast:	n/a
50	chr22:23412225-23412275	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:23410484..23412785-chr22:23485960..23488893,2	K562	blood:

Variant related genes	Relation type
GNAZ	TF binding region
GNAZ	CpG island
ENSG00000100218	Chromatin interaction
ENSG00000100228	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:44 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1803110	chr22:22731758-23497674	Flanking Active TSS Bivalent Enhancer Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	esv34158	chr22:23216762-23499513	Weak transcription Bivalent Enhancer Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
25	nsv914575	chr22:23399743-23467804	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
26	nsv914576	chr22:23399743-23469918	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS 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	15 gene(s)	inside rSNPs	diseases
27	nsv544606	chr22:23400739-23416402	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
28	nsv544607	chr22:23400739-23417836	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
29	nsv544608	chr22:23400739-23423230	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
30	esv1806531	chr22:23400739-23448258	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
31	nsv544609	chr22:23400739-23455790	Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
32	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
33	nsv544610	chr22:23404534-23416402	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
34	nsv544611	chr22:23404534-23417836	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
35	nsv544612	chr22:23404534-23419488	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
36	nsv544613	chr22:23408495-23417836	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
37	nsv544614	chr22:23410046-23419488	Active TSS Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
38	esv3324778	chr22:23411477-23414325	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
39	esv3337920	chr22:23411602-23413550	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
40	esv3494959	chr22:23411602-23413900	Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
41	esv3494960	chr22:23411602-23413900	Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
42	nsv588589	chr22:23412017-23413060	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
43	esv1803191	chr22:23412017-23413130	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
44	esv1804044	chr22:23412017-23413130	Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:23411200-23412400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
2	chr22:23411600-23412400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
3	chr22:23411600-23412400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr22:23411600-23413200	Enhancers	Fetal Heart	heart
5	chr22:23411600-23413600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
6	chr22:23411600-23413600	Active TSS	Colon Smooth Muscle	Colon
7	chr22:23411600-23413800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
8	chr22:23411800-23412400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr22:23411800-23412400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr22:23411800-23412400	Flanking Active TSS	Adipose Nuclei	Adipose
11	chr22:23411800-23412400	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
12	chr22:23411800-23412400	Flanking Bivalent TSS/Enh	K562	blood
13	chr22:23411800-23412400	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
14	chr22:23411800-23412400	Flanking Bivalent TSS/Enh	Osteobl	bone
15	chr22:23411800-23412800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
16	chr22:23411800-23412800	Active TSS	Psoas Muscle	Psoas
17	chr22:23411800-23413000	Bivalent/Poised TSS	Rectal Mucosa Donor 31	rectum
18	chr22:23411800-23413000	Bivalent/Poised TSS	NHEK	skin
19	chr22:23411800-23413200	Active TSS	Primary T helper naive cells from peripheral blood	blood
20	chr22:23411800-23413200	Active TSS	Aorta	Aorta
21	chr22:23411800-23413400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr22:23411800-23413400	Active TSS	Esophagus	oesophagus
23	chr22:23411800-23413400	Transcr. at gene 5' and 3'	Right Atrium	heart
24	chr22:23411800-23413600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr22:23411800-23413600	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr22:23411800-23413600	Active TSS	Brain Substantia Nigra	brain
27	chr22:23411800-23413600	Active TSS	Duodenum Smooth Muscle	Duodenum
28	chr22:23411800-23413600	Active TSS	Hela-S3	cervix
29	chr22:23411800-23413600	Active TSS	NH-A	brain
30	chr22:23411800-23414000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
31	chr22:23411800-23414200	Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr22:23412000-23412400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
33	chr22:23412000-23412400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr22:23412000-23412400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr22:23412000-23412400	Flanking Active TSS	Primary B cells from cord blood	blood
36	chr22:23412000-23412400	Flanking Active TSS	Primary hematopoietic stem cells	blood
37	chr22:23412000-23412400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
38	chr22:23412000-23412400	Active TSS	Fetal Kidney	kidney
39	chr22:23412000-23412400	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
40	chr22:23412000-23412400	Flanking Active TSS	HMEC	breast
41	chr22:23412000-23412800	Active TSS	Left Ventricle	heart
42	chr22:23412000-23412800	Bivalent/Poised TSS	Thymus	Thymus
43	chr22:23412000-23413000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
44	chr22:23412000-23413000	Active TSS	Sigmoid Colon	Sigmoid Colon
45	chr22:23412000-23413000	Active TSS	Spleen	Spleen
46	chr22:23412000-23413200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
47	chr22:23412000-23413200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr22:23412000-23413400	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr22:23412000-23413600	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr22:23412000-23413600	Active TSS	Brain Cingulate Gyrus	brain

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