Variant report

Variant	rs5759666
Chromosome Location	chr22:23602342-23602343
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	MXI1	chr22:23602265-23602893	H1-hESC	embryonic stem cell:	n/a	chr22:23602654-23602663
2	POLR2A	chr22:23602273-23602992	K562	blood:	n/a	n/a
3	ATF3	chr22:23602172-23602876	K562	blood:	n/a	chr22:23602503-23602516
4	POLR2A	chr22:23601816-23603823	K562	blood:	n/a	n/a
5	RAD21	chr22:23602254-23603300	H1-hESC	embryonic stem cell:	n/a	chr22:23602706-23602718 chr22:23602691-23602704
6	POLR2A	chr22:23601916-23608354	K562	blood:	n/a	n/a
7	POLR2A	chr22:23601987-23603320	K562	blood:	n/a	n/a
8	HDAC2	chr22:23601904-23603783	K562	blood:	n/a	n/a
9	STAT5A	chr22:23602006-23602463	K562	blood:	n/a	n/a
10	RAD21	chr22:23602302-23602881	H1-hESC	embryonic stem cell:	n/a	chr22:23602706-23602718 chr22:23602691-23602704
11	SP2	chr22:23602104-23603364	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:23520341..23521308-chr22:23602297..23603379,4	K562	blood:
2	chr22:23522976..23523833-chr22:23602295..23603210,2	K562	blood:

Variant related genes	Relation type
FBXW4P1	TF binding region

Extended variants
information (count: 93 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs11090227	0.83[ASN][1000 genomes]
rs11090228	0.91[CEU][hapmap];0.85[CHB][hapmap];0.94[GIH][hapmap];0.95[TSI][hapmap];0.89[EUR][1000 genomes]
rs11704376	0.82[CEU][hapmap]
rs11704598	0.83[CEU][hapmap]
rs11704766	0.83[CEU][hapmap]
rs11912657	0.83[CEU][hapmap];0.83[GIH][hapmap]
rs11912682	0.83[CEU][hapmap];0.83[GIH][hapmap]
rs11913665	0.85[CEU][hapmap]
rs12166802	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs12233352	1.00[JPT][hapmap]
rs12627853	0.86[ASN][1000 genomes]
rs13054840	0.82[CEU][hapmap]
rs16802	0.91[CEU][hapmap];0.93[TSI][hapmap];0.87[EUR][1000 genomes]
rs17611266	0.86[AMR][1000 genomes]
rs1811017	0.83[CEU][hapmap];1.00[CHB][hapmap];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1811018	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2227939	0.89[EUR][1000 genomes]
rs2330369	0.83[CEU][hapmap]
rs3788358	0.95[CEU][hapmap];1.00[CHB][hapmap];0.97[GIH][hapmap];0.95[TSI][hapmap];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4822379	0.85[CHB][hapmap]
rs5751619	0.89[EUR][1000 genomes]
rs5751620	0.82[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs5751621	1.00[JPT][hapmap]
rs5759661	0.93[ASN][1000 genomes]
rs5759665	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5759668	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs5759670	0.83[ASN][1000 genomes]
rs5759671	0.85[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs5759673	0.83[ASN][1000 genomes]
rs5759675	0.82[CEU][hapmap];1.00[CHB][hapmap];0.83[ASN][1000 genomes]
rs5759676	1.00[CHB][hapmap];0.83[ASN][1000 genomes]
rs5759679	1.00[CHB][hapmap];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs5759680	1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs5759681	0.95[CEU][hapmap];0.85[CHB][hapmap];0.94[GIH][hapmap];0.95[TSI][hapmap];0.89[EUR][1000 genomes]
rs5759682	0.95[CEU][hapmap];0.85[CHB][hapmap];0.86[EUR][1000 genomes]
rs5759683	0.84[TSI][hapmap];0.82[EUR][1000 genomes]
rs5996507	0.86[AMR][1000 genomes]
rs5996508	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs5996509	1.00[CHB][hapmap];0.83[ASN][1000 genomes]
rs6003587	0.84[AFR][1000 genomes]
rs6003591	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs6003593	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6003598	0.83[ASN][1000 genomes]
rs6003600	0.83[ASN][1000 genomes]
rs62219796	0.88[EUR][1000 genomes]
rs7289192	0.83[CEU][hapmap];0.81[GIH][hapmap]
rs7291469	0.83[CEU][hapmap];0.83[GIH][hapmap]
rs7292656	0.88[EUR][1000 genomes]
rs743584	0.83[CEU][hapmap];0.86[GIH][hapmap]
rs8139664	0.83[CEU][hapmap];0.83[GIH][hapmap]
rs928780	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs928781	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9608091	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs9608093	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9608094	0.83[CEU][hapmap]
rs9608100	0.88[EUR][1000 genomes]
rs9608102	0.85[CHB][hapmap]
rs9612266	0.80[GIH][hapmap]
rs9612270	0.83[CEU][hapmap];0.86[GIH][hapmap]
rs9612275	0.82[CEU][hapmap]
rs9624072	0.86[ASN][1000 genomes]
rs9624073	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:31 , 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

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs5759666	BCR	cis	cerebellum	SCAN
rs5759666	UBE2L3	cis	cerebellum	SCAN
rs5759666	YPEL1	cis	cerebellum	SCAN
rs5759666	CABIN1	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:23585800-23605600	Weak transcription	Fetal Lung	lung
2	chr22:23591000-23615800	Weak transcription	NH-A	brain
3	chr22:23591200-23604000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr22:23592800-23603800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr22:23593000-23618000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
6	chr22:23594400-23611800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr22:23594400-23614200	Weak transcription	A549	lung
8	chr22:23595000-23604600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr22:23595000-23610800	Strong transcription	K562	blood
10	chr22:23595000-23612200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr22:23595000-23612200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr22:23595000-23647000	Strong transcription	Dnd41	blood
13	chr22:23595200-23623600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr22:23595400-23623800	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr22:23595600-23607200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr22:23595600-23609200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr22:23595600-23619200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr22:23595600-23623600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr22:23595800-23602400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr22:23595800-23608200	Strong transcription	Thymus	Thymus
21	chr22:23595800-23609000	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr22:23595800-23611600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr22:23595800-23621000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr22:23595800-23623400	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr22:23595800-23649600	Strong transcription	Primary neutrophils fromperipheralblood	blood
26	chr22:23596000-23604000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr22:23596000-23608200	Strong transcription	Cortex derived primary cultured neurospheres	brain
28	chr22:23596800-23603200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr22:23597200-23603400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr22:23597800-23604000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr22:23597800-23606600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr22:23597800-23611400	Weak transcription	Fetal Kidney	kidney
33	chr22:23598000-23603200	Weak transcription	Aorta	Aorta
34	chr22:23598200-23603400	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr22:23598400-23603600	Weak transcription	HUVEC	blood vessel
36	chr22:23598400-23608400	Strong transcription	Primary T helper cells fromperipheralblood	blood
37	chr22:23598600-23604000	Weak transcription	GM12878-XiMat	blood
38	chr22:23598800-23603600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr22:23599400-23607800	Strong transcription	HepG2	liver
40	chr22:23599400-23609400	Strong transcription	Fetal Thymus	thymus
41	chr22:23599400-23635000	Weak transcription	Small Intestine	intestine
42	chr22:23599600-23604000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr22:23599600-23623000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr22:23599800-23602800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr22:23599800-23603200	Weak transcription	Brain Angular Gyrus	brain
46	chr22:23599800-23603200	Weak transcription	Brain Substantia Nigra	brain
47	chr22:23599800-23603400	Weak transcription	Osteobl	bone
48	chr22:23599800-23605000	Strong transcription	Primary T cells fromperipheralblood	blood
49	chr22:23599800-23608000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr22:23600000-23602400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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