Variant report

Variant	rs56363600
Chromosome Location	chr22:23621208-23621209
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:34)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:34 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TCF12	chr22:23620898-23621696	ECC-1	luminal epithelium:	n/a	n/a
2	POLR2A	chr22:23620918-23621778	K562	blood:	n/a	n/a
3	STAT3	chr22:23621070-23621407	MCF10A-Er-Src	breast:	n/a	chr22:23621395-23621407
4	TEAD4	chr22:23621002-23621632	ECC-1	luminal epithelium:	n/a	n/a
5	STAT3	chr22:23621081-23621416	MCF10A-Er-Src	breast:	n/a	chr22:23621395-23621407
6	POLR2A	chr22:23620853-23632783	K562	blood:	n/a	n/a
7	NFIC	chr22:23620725-23622298	ECC-1	luminal epithelium:	n/a	n/a
8	ELF1	chr22:23620985-23621443	K562	blood:	n/a	chr22:23621218-23621231
9	FOS	chr22:23621023-23621456	MCF10A-Er-Src	breast:	n/a	n/a
10	MAX	chr22:23620934-23622166	ECC-1	luminal epithelium:	n/a	n/a
11	FOS	chr22:23621098-23621492	MCF10A-Er-Src	breast:	n/a	n/a
12	MAX	chr22:23620872-23622064	ECC-1	luminal epithelium:	n/a	n/a
13	POLR2A	chr22:23620818-23625944	K562	blood:	n/a	n/a
14	POLR2A	chr22:23620976-23622552	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr22:23621131-23621405	MCF10A-Er-Src	breast:	n/a	n/a
16	POLR2A	chr22:23621117-23621232	HUVEC	blood vessel:	n/a	n/a
17	STAT3	chr22:23621025-23621490	MCF10A-Er-Src	breast:	n/a	chr22:23621395-23621407
18	POLR2A	chr22:23620941-23621417	MCF10A-Er-Src	breast:	n/a	n/a
19	CREB1	chr22:23621183-23621403	A549	lung:	n/a	n/a
20	FOS	chr22:23621064-23621499	MCF10A-Er-Src	breast:	n/a	n/a
21	ESR1	chr22:23621051-23621947	ECC-1	luminal epithelium:	n/a	n/a
22	ESR1	chr22:23621085-23621665	ECC-1	luminal epithelium:	n/a	n/a
23	MYC	chr22:23620977-23621547	MCF10A-Er-Src	breast:	n/a	n/a
24	POLR2A	chr22:23620839-23621718	K562	blood:	n/a	n/a
25	POLR2A	chr22:23621086-23630578	K562	blood:	n/a	n/a
26	EP300	chr22:23621131-23621592	ECC-1	luminal epithelium:	n/a	n/a
27	STAT3	chr22:23621026-23621504	MCF10A-Er-Src	breast:	n/a	chr22:23621395-23621407
28	MYC	chr22:23621008-23621463	MCF10A-Er-Src	breast:	n/a	n/a
29	NFIC	chr22:23620840-23622280	ECC-1	luminal epithelium:	n/a	n/a
30	CHD2	chr22:23621115-23621249	Hela-S3	cervix:	n/a	n/a
31	ZNF263	chr22:23621092-23625040	K562	blood:	n/a	chr22:23623971-23623980 chr22:23624279-23624288
32	TCF12	chr22:23620874-23621874	ECC-1	luminal epithelium:	n/a	n/a
33	EP300	chr22:23620864-23622118	ECC-1	luminal epithelium:	n/a	n/a
34	RAD21	chr22:23621043-23621633	ECC-1	luminal epithelium:	n/a	n/a

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:23613555..23616313-chr22:23620461..23622709,2	MCF-7	breast:
2	chr22:23452087..23454123-chr22:23620144..23622923,2	K562	blood:
3	chr22:23618828..23621252-chr9:133610362..133612451,2	K562	blood:
4	chr22:23620816..23623842-chr9:133607688..133610225,3	K562	blood:
5	chr22:23519615..23526434-chr22:23614924..23625964,20	MCF-7	breast:
6	chr22:23619739..23621336-chr9:133627778..133629394,2	K562	blood:

No data

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

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs34646520	1.00[EUR][1000 genomes]
rs35727393	0.95[EUR][1000 genomes]
rs55650428	1.00[EUR][1000 genomes]
rs55721909	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55844144	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55908867	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55954687	1.00[EUR][1000 genomes]
rs56027011	1.00[EUR][1000 genomes]
rs56035513	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56073544	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56119182	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56161706	1.00[EUR][1000 genomes]
rs56228961	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56248213	1.00[EUR][1000 genomes]
rs56308748	1.00[EUR][1000 genomes]
rs56391288	1.00[EUR][1000 genomes]
rs6003583	1.00[EUR][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:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:23595000-23647000	Strong transcription	Dnd41	blood
2	chr22:23595200-23623600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr22:23595400-23623800	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr22:23595600-23623600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr22:23595800-23623400	Strong transcription	Primary monocytes fromperipheralblood	blood
6	chr22:23595800-23649600	Strong transcription	Primary neutrophils fromperipheralblood	blood
7	chr22:23599400-23635000	Weak transcription	Small Intestine	intestine
8	chr22:23599600-23623000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr22:23600200-23632000	Strong transcription	Fetal Intestine Small	intestine
10	chr22:23601200-23623800	Weak transcription	Fetal Brain Male	brain
11	chr22:23601800-23641000	Strong transcription	Primary T cells from cord blood	blood
12	chr22:23603400-23631600	Strong transcription	Fetal Intestine Large	intestine
13	chr22:23604600-23623600	Strong transcription	Placenta	Placenta
14	chr22:23605200-23621600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr22:23605200-23623400	Strong transcription	Spleen	Spleen
16	chr22:23605600-23623600	Strong transcription	Fetal Stomach	stomach
17	chr22:23606800-23623600	Weak transcription	HSMM	muscle
18	chr22:23608200-23623600	Weak transcription	NHDF-Ad	bronchial
19	chr22:23608800-23649400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr22:23609000-23623200	Strong transcription	Fetal Brain Female	brain
21	chr22:23609000-23623400	Strong transcription	Thymus	Thymus
22	chr22:23610200-23623400	Strong transcription	Brain Germinal Matrix	brain
23	chr22:23610400-23623600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr22:23611400-23623600	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr22:23612200-23623600	Strong transcription	HepG2	liver
26	chr22:23612600-23622800	Strong transcription	Primary hematopoietic stem cells	blood
27	chr22:23612600-23623400	Strong transcription	HUES6 Cell Line	embryonic stem cell
28	chr22:23612600-23623600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr22:23612600-23623800	Strong transcription	HUES48 Cell Line	embryonic stem cell
30	chr22:23612600-23647800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
31	chr22:23613000-23623400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr22:23613000-23623800	Strong transcription	K562	blood
33	chr22:23613000-23629600	Strong transcription	HUES64 Cell Line	embryonic stem cell
34	chr22:23613000-23640800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
35	chr22:23613200-23621800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
36	chr22:23613400-23621800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr22:23613400-23622200	Strong transcription	H1 Cell Line	embryonic stem cell
38	chr22:23613400-23623600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr22:23613600-23622200	Strong transcription	H9 Cell Line	embryonic stem cell
40	chr22:23614400-23621600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr22:23616200-23623800	Weak transcription	A549	lung
42	chr22:23616600-23623600	Weak transcription	NH-A	brain
43	chr22:23616600-23639000	Weak transcription	Fetal Kidney	kidney
44	chr22:23616800-23637200	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr22:23617400-23623600	Weak transcription	Osteobl	bone
46	chr22:23617800-23622000	Weak transcription	NHLF	lung
47	chr22:23618200-23623600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr22:23618200-23623800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr22:23618200-23628600	Weak transcription	Fetal Lung	lung
50	chr22:23618800-23621600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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