Variant report

Variant	rs9608101
Chromosome Location	chr22:23632621-23632622
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:52)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:52 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RAD21	chr22:23632610-23633054	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr22:23632540-23633027	GM19240	blood:	n/a	n/a
3	CTCF	chr22:23632533-23633137	MCF-7	breast:	n/a	n/a
4	CTCF	chr22:23632570-23633023	GM12892	blood:	n/a	n/a
5	RXRA	chr22:23632538-23632931	HepG2	liver:	n/a	n/a
6	POLR2A	chr22:23620853-23632783	K562	blood:	n/a	n/a
7	ZBTB7A	chr22:23632521-23632745	K562	blood:	n/a	n/a
8	CTCF	chr22:23632564-23633016	GM19238	blood:	n/a	n/a
9	RAD21	chr22:23632569-23633082	H1-hESC	embryonic stem cell:	n/a	n/a
10	SP2	chr22:23632107-23632662	K562	blood:	n/a	n/a
11	SMC3	chr22:23632090-23633032	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr22:23632037-23633079	HCT-116	colon:	n/a	n/a
13	POLR2A	chr22:23625964-23632820	K562	blood:	n/a	n/a
14	HNF4G	chr22:23632584-23632950	HepG2	liver:	n/a	chr22:23632789-23632804
15	HDAC2	chr22:23632488-23632992	HepG2	liver:	n/a	n/a
16	SP1	chr22:23632491-23632968	HepG2	liver:	n/a	n/a
17	POLR2A	chr22:23630791-23632747	K562	blood:	n/a	n/a
18	ZBTB7A	chr22:23632556-23632883	HepG2	liver:	n/a	n/a
19	ATF3	chr22:23631376-23632787	K562	blood:	n/a	chr22:23631379-23631392
20	CEBPB	chr22:23632133-23632866	HepG2	liver:	n/a	chr22:23632320-23632331
21	ZBTB7A	chr22:23632551-23632778	HepG2	liver:	n/a	n/a
22	CEBPB	chr22:23632001-23632765	K562	blood:	n/a	chr22:23632320-23632331
23	POLR2A	chr22:23632424-23632774	HepG2	liver:	n/a	n/a
24	NR2F2	chr22:23632385-23633085	HepG2	liver:	n/a	n/a
25	CEBPB	chr22:23632087-23632981	HepG2	liver:	n/a	chr22:23632320-23632331
26	MYBL2	chr22:23632484-23633058	HepG2	liver:	n/a	n/a
27	CEBPB	chr22:23632052-23632688	K562	blood:	n/a	chr22:23632320-23632331
28	HDAC2	chr22:23631937-23632786	K562	blood:	n/a	n/a
29	ZNF263	chr22:23632004-23633013	HEK293-T-REx	kidney:	n/a	n/a
30	CTCF	chr22:23631810-23633176	SK-N-SH	brain:	n/a	n/a
31	MYBL2	chr22:23632209-23633007	HepG2	liver:	n/a	n/a
32	RAD21	chr22:23632570-23633078	ECC-1	luminal epithelium:	n/a	n/a
33	THAP1	chr22:23631665-23632811	K562	blood:	n/a	n/a
34	CTCF	chr22:23632594-23633024	GM12891	blood:	n/a	n/a
35	ELF1	chr22:23631777-23632759	K562	blood:	n/a	n/a
36	CTCF	chr22:23632582-23633018	H1-hESC	embryonic stem cell:	n/a	n/a
37	HNF4A	chr22:23632537-23632905	HepG2	liver:	n/a	n/a
38	SMC3	chr22:23631890-23633212	SK-N-SH	brain:	n/a	n/a
39	CTCF	chr22:23632500-23632650	A549	lung:	n/a	n/a
40	RAD21	chr22:23632578-23633036	HepG2	liver:	n/a	n/a
41	CEBPB	chr22:23632131-23633008	Hela-S3	cervix:	n/a	chr22:23632320-23632331
42	CTCF	chr22:23631866-23633210	A549	lung:	n/a	n/a
43	POLR2A	chr22:23631218-23632756	K562	blood:	n/a	n/a
44	RAD21	chr22:23632118-23632987	HepG2	liver:	n/a	n/a
45	ZNF143	chr22:23632077-23632900	K562	blood:	n/a	n/a
46	FOXA2	chr22:23632577-23632892	HepG2	liver:	n/a	n/a
47	NR2F2	chr22:23632432-23633003	MCF-7	breast:	n/a	n/a
48	RAD21	chr22:23632579-23633059	MCF-7	breast:	n/a	n/a
49	POLR2A	chr22:23632507-23632675	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr22:23632147-23633046	IMR90	lung:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:23632204..23633014-chr9:133608816..133609543,2	K562	blood:
2	chr22:23630763..23634544-chr22:23636412..23640567,4	K562	blood:
3	chr22:23520679..23521332-chr22:23632210..23633200,4	MCF-7	breast:
4	chr22:23522112..23522814-chr22:23631857..23632952,3	K562	blood:
5	chr22:23515729..23516735-chr22:23631823..23632868,6	K562	blood:
6	chr22:23631623..23633644-chr22:23635292..23638190,2	MCF-7	breast:
7	chr22:23520899..23523214-chr22:23632286..23633835,2	MCF-7	breast:

No data

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

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

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs11704376	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11704598	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11704766	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11912632	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11912657	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11912682	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11913665	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13054277	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13054840	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17611266	0.83[EUR][1000 genomes]
rs35837404	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs5996507	0.87[EUR][1000 genomes]
rs6003584	0.83[EUR][1000 genomes]
rs6003586	0.84[EUR][1000 genomes]
rs6003587	0.84[EUR][1000 genomes]
rs6003591	0.87[EUR][1000 genomes]
rs62219795	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7288846	0.83[EUR][1000 genomes]
rs7289192	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7291469	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs743584	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs8139664	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs8141608	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs8141706	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9608091	0.85[EUR][1000 genomes]
rs9608094	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9608095	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9608097	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9612266	0.84[EUR][1000 genomes]
rs9612267	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9612268	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9612270	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9612272	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9612273	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9612275	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9612276	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9612277	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9612281	0.96[EUR][1000 genomes]
rs9620235	0.85[EUR][1000 genomes]
rs9624074	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:34 , 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	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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
31	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
32	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
33	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
34	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	chr22:23601800-23641000	Strong transcription	Primary T cells from cord blood	blood
5	chr22:23608800-23649400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr22:23612600-23647800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
7	chr22:23613000-23640800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
8	chr22:23616600-23639000	Weak transcription	Fetal Kidney	kidney
9	chr22:23616800-23637200	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr22:23624000-23647000	Strong transcription	HUES48 Cell Line	embryonic stem cell
11	chr22:23624000-23649200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr22:23624200-23640000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
13	chr22:23624200-23644600	Strong transcription	Lung	lung
14	chr22:23624200-23647000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr22:23624200-23647200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr22:23624400-23636200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr22:23624400-23640800	Strong transcription	H9 Cell Line	embryonic stem cell
18	chr22:23624400-23649400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr22:23624400-23649400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr22:23624400-23649400	Strong transcription	Thymus	Thymus
21	chr22:23624400-23649600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr22:23624400-23649600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr22:23624600-23632800	Strong transcription	Primary B cells from peripheral blood	blood
24	chr22:23624600-23632800	Strong transcription	Primary T killer memory cells from peripheral blood	blood
25	chr22:23624600-23637600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr22:23624600-23638000	Strong transcription	Right Ventricle	heart
27	chr22:23624600-23641000	Strong transcription	HUES6 Cell Line	embryonic stem cell
28	chr22:23624600-23646200	Strong transcription	Primary T helper cells PMA-I stimulated	--
29	chr22:23624600-23647000	Strong transcription	Fetal Thymus	thymus
30	chr22:23624600-23647800	Strong transcription	Monocytes-CD14+_RO01746	blood
31	chr22:23624600-23648200	Strong transcription	Primary monocytes fromperipheralblood	blood
32	chr22:23624600-23649000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr22:23624600-23649400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
34	chr22:23624800-23640800	Strong transcription	Cortex derived primary cultured neurospheres	brain
35	chr22:23624800-23645200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr22:23624800-23649400	Strong transcription	Primary T cells fromperipheralblood	blood
37	chr22:23625000-23645000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr22:23625000-23645000	Strong transcription	Gastric	stomach
39	chr22:23625000-23647600	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr22:23625200-23634800	Weak transcription	A549	lung
41	chr22:23625200-23640600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr22:23625200-23640800	Strong transcription	H1 Cell Line	embryonic stem cell
43	chr22:23625400-23640400	Strong transcription	NHEK	skin
44	chr22:23625400-23645800	Strong transcription	Sigmoid Colon	Sigmoid Colon
45	chr22:23625600-23640400	Strong transcription	Ovary	ovary
46	chr22:23625600-23646000	Strong transcription	Fetal Stomach	stomach
47	chr22:23625600-23649200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr22:23625800-23647400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr22:23625800-23649400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr22:23626000-23641200	Strong transcription	Colonic Mucosa	Colon

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