Variant report

Variant	rs2283804
Chromosome Location	chr22:23490335-23490336
allele	A/C
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	POLR2A	chr22:23489241-23490463	MCF10A-Er-Src	breast:	n/a	n/a
2	SIN3AK20	chr22:23489554-23490400	MCF-7	breast:	n/a	n/a
3	GATA3	chr22:23489502-23490360	MCF-7	breast:	n/a	chr22:23489915-23489923
4	MXI1	chr22:23489760-23490342	IMR90	lung:	n/a	n/a
5	NFYA	chr22:23490206-23490759	K562	blood:	n/a	chr22:23490585-23490595
6	SIN3AK20	chr22:23489617-23490380	MCF-7	breast:	n/a	n/a
7	ATF1	chr22:23489763-23491038	K562	blood:	n/a	n/a

Variant related genes	Relation type
RTDR1	TF binding region
RAB36	TF binding region

Extended variants
information (count: 137 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:110)

rs_ID	r²[population]
rs1051875	0.89[JPT][hapmap]
rs10775764	0.87[AFR][1000 genomes]
rs11704365	0.87[CHB][hapmap];0.84[JPT][hapmap]
rs12167308	0.90[JPT][hapmap]
rs13054985	0.89[JPT][hapmap]
rs1805058	0.90[JPT][hapmap]
rs1807460	0.89[ASW][hapmap];0.91[LWK][hapmap];0.90[YRI][hapmap];0.88[AFR][1000 genomes]
rs1807702	0.88[AFR][1000 genomes]
rs1807706	0.86[AFR][1000 genomes]
rs1989776	0.84[JPT][hapmap]
rs1989777	0.84[JPT][hapmap]
rs1989778	0.84[JPT][hapmap]
rs2008176	0.88[AFR][1000 genomes]
rs2071431	0.84[JPT][hapmap]
rs2157710	0.90[JPT][hapmap]
rs2249692	0.95[JPT][hapmap]
rs2266995	0.84[JPT][hapmap]
rs2266997	0.84[JPT][hapmap]
rs2267000	0.84[JPT][hapmap]
rs2267001	0.84[JPT][hapmap]
rs2267003	0.84[JPT][hapmap]
rs2267004	0.90[JPT][hapmap]
rs2267005	0.84[JPT][hapmap]
rs2267006	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2267007	0.89[ASW][hapmap];0.84[CHD][hapmap];0.90[JPT][hapmap];0.91[LWK][hapmap];0.88[MEX][hapmap];0.81[MKK][hapmap];0.90[YRI][hapmap];0.87[AFR][1000 genomes]
rs2267009	0.84[JPT][hapmap]
rs2267011	0.84[JPT][hapmap]
rs2283802	0.90[JPT][hapmap]
rs2283803	0.90[JPT][hapmap]
rs2301554	0.90[JPT][hapmap]
rs2330336	0.90[JPT][hapmap]
rs2330361	0.90[JPT][hapmap]
rs3761418	0.84[JPT][hapmap]
rs3788342	0.84[JPT][hapmap]
rs3788343	0.84[JPT][hapmap]
rs3788346	0.84[JPT][hapmap]
rs3788347	0.89[JPT][hapmap]
rs3788348	0.90[JPT][hapmap]
rs3788350	0.84[JPT][hapmap]
rs3810614	0.84[JPT][hapmap]
rs3827315	0.84[JPT][hapmap]
rs4552283	0.85[AFR][1000 genomes]
rs4820536	0.84[JPT][hapmap]
rs4820537	0.90[JPT][hapmap]
rs4820539	0.90[JPT][hapmap]
rs4820541	0.82[CHD][hapmap];0.90[JPT][hapmap]
rs4820542	0.84[JPT][hapmap]
rs4822354	0.84[JPT][hapmap]
rs4822357	0.90[JPT][hapmap]
rs4822359	0.90[JPT][hapmap]
rs4822360	0.90[JPT][hapmap]
rs4822361	0.90[JPT][hapmap]
rs4822362	0.90[JPT][hapmap]
rs4822369	0.90[JPT][hapmap]
rs5751576	0.84[JPT][hapmap]
rs5751578	0.83[JPT][hapmap]
rs5751587	0.87[JPT][hapmap]
rs5751589	0.90[JPT][hapmap]
rs5751593	0.89[ASW][hapmap];0.84[CHD][hapmap];0.90[JPT][hapmap];0.94[LWK][hapmap];0.88[MEX][hapmap];0.81[MKK][hapmap];0.90[YRI][hapmap];0.88[AFR][1000 genomes]
rs5751596	0.90[JPT][hapmap];0.90[YRI][hapmap];0.87[AFR][1000 genomes]
rs5751603	0.84[JPT][hapmap]
rs5751606	0.84[JPT][hapmap]
rs5759593	0.90[JPT][hapmap]
rs5759598	0.90[JPT][hapmap]
rs5759600	0.90[JPT][hapmap]
rs5759603	0.96[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];0.90[JPT][hapmap];0.83[MEX][hapmap];0.88[TSI][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5759604	0.87[JPT][hapmap]
rs5759607	0.90[JPT][hapmap]
rs5759608	0.89[ASW][hapmap];0.84[CHD][hapmap];0.90[JPT][hapmap];0.91[LWK][hapmap];0.88[MEX][hapmap];0.81[MKK][hapmap];0.90[YRI][hapmap];0.84[AFR][1000 genomes]
rs5759609	0.87[AFR][1000 genomes]
rs5759611	0.81[CHD][hapmap];0.90[JPT][hapmap]
rs5759612	0.89[ASW][hapmap];0.84[CHD][hapmap];0.90[JPT][hapmap];0.94[LWK][hapmap];0.88[MEX][hapmap];0.81[MKK][hapmap];0.90[YRI][hapmap];0.88[AFR][1000 genomes]
rs5759613	0.90[JPT][hapmap];0.90[YRI][hapmap];0.88[AFR][1000 genomes]
rs5759614	0.89[ASW][hapmap];0.84[CHD][hapmap];0.90[JPT][hapmap];0.94[LWK][hapmap];0.88[MEX][hapmap];0.82[MKK][hapmap];0.90[YRI][hapmap];0.88[AFR][1000 genomes]
rs5759615	0.89[ASW][hapmap];0.84[CHD][hapmap];0.90[JPT][hapmap];0.94[LWK][hapmap];0.88[MEX][hapmap];0.81[MKK][hapmap];0.90[YRI][hapmap];0.88[AFR][1000 genomes]
rs5759617	0.88[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs5759618	0.83[AFR][1000 genomes]
rs5759619	0.89[ASW][hapmap];0.81[CHD][hapmap];0.90[JPT][hapmap];0.93[LWK][hapmap];0.80[MEX][hapmap];0.81[MKK][hapmap];0.86[YRI][hapmap];0.88[AFR][1000 genomes]
rs5759620	0.89[ASW][hapmap];0.84[CHD][hapmap];0.90[JPT][hapmap];0.93[LWK][hapmap];0.88[MEX][hapmap];0.81[MKK][hapmap];0.90[YRI][hapmap];0.88[AFR][1000 genomes]
rs5759621	0.84[CHD][hapmap];0.90[JPT][hapmap];0.80[MEX][hapmap]
rs5759622	0.85[AFR][1000 genomes]
rs5759631	0.84[JPT][hapmap]
rs5996483	0.84[JPT][hapmap]
rs6003502	0.90[JPT][hapmap]
rs6003518	0.90[JPT][hapmap]
rs62220914	0.81[ASN][1000 genomes]
rs713617	0.84[JPT][hapmap]
rs713682	0.89[ASW][hapmap];0.84[CHD][hapmap];0.90[JPT][hapmap];0.94[LWK][hapmap];0.88[MEX][hapmap];0.81[MKK][hapmap];0.90[YRI][hapmap];0.88[AFR][1000 genomes]
rs737818	0.89[ASW][hapmap];0.84[CHD][hapmap];0.89[JPT][hapmap];0.94[LWK][hapmap];0.88[MEX][hapmap];0.81[MKK][hapmap];0.89[YRI][hapmap];0.88[AFR][1000 genomes]
rs737819	0.89[ASW][hapmap];0.81[CHD][hapmap];0.90[JPT][hapmap];0.94[LWK][hapmap];0.88[MEX][hapmap];0.81[MKK][hapmap];0.90[YRI][hapmap];0.88[AFR][1000 genomes]
rs737820	0.88[AFR][1000 genomes]
rs739362	0.89[JPT][hapmap]
rs756631	0.84[JPT][hapmap]
rs756633	0.90[JPT][hapmap];0.86[YRI][hapmap]
rs768513	0.87[CHB][hapmap];0.84[JPT][hapmap]
rs8142746	0.89[ASW][hapmap];0.82[CHD][hapmap];0.90[JPT][hapmap];0.94[LWK][hapmap];0.88[MEX][hapmap];0.81[MKK][hapmap];0.90[YRI][hapmap];0.88[AFR][1000 genomes]
rs874138	0.90[JPT][hapmap]
rs885962	0.84[JPT][hapmap]
rs885963	0.84[JPT][hapmap]
rs885964	0.90[JPT][hapmap]
rs916583	0.90[JPT][hapmap]
rs916584	0.90[JPT][hapmap]
rs916585	0.87[JPT][hapmap]
rs9608085	0.88[AFR][1000 genomes]
rs9612234	0.90[JPT][hapmap]
rs9612237	0.94[JPT][hapmap]
rs9612248	0.94[ASW][hapmap];0.96[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];0.99[MKK][hapmap];0.95[TSI][hapmap];0.90[YRI][hapmap];0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9612252	0.89[ASW][hapmap];0.84[CHD][hapmap];0.89[JPT][hapmap];0.93[LWK][hapmap];0.88[MEX][hapmap];0.81[MKK][hapmap];0.90[YRI][hapmap];0.88[AFR][1000 genomes]
rs9612253	0.87[AFR][1000 genomes]
rs9612257	0.95[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:27 , 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	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
26	nsv544616	chr22:23474827-23495231	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
27	esv1801510	chr22:23478611-23491000	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2283804	GNAZ	cis	parietal	SCAN
rs2283804	UBE2L3	cis	cerebellum	SCAN
rs2283804	UPB1	cis	parietal	SCAN

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:23487800-23499000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr22:23488000-23491000	Enhancers	HepG2	liver
3	chr22:23488000-23499400	Weak transcription	Right Ventricle	heart
4	chr22:23488200-23490400	Enhancers	Muscle Satellite Cultured Cells	--
5	chr22:23488200-23490600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr22:23488200-23491400	Enhancers	Pancreas	Pancrea
7	chr22:23488200-23491800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr22:23488200-23492800	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr22:23488200-23492800	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr22:23488200-23494600	Weak transcription	Primary hematopoietic stem cells	blood
11	chr22:23488200-23505800	Weak transcription	HSMMtube	muscle
12	chr22:23488400-23490400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr22:23488400-23490400	Enhancers	Osteobl	bone
14	chr22:23488400-23490600	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr22:23488400-23490600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr22:23488400-23490800	Enhancers	Placenta	Placenta
17	chr22:23488400-23491800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr22:23488400-23491800	Weak transcription	Fetal Intestine Small	intestine
19	chr22:23488400-23491800	Weak transcription	Ovary	ovary
20	chr22:23488400-23492000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr22:23488400-23492200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr22:23488400-23493200	Weak transcription	Colon Smooth Muscle	Colon
23	chr22:23488400-23493400	Weak transcription	Primary B cells from peripheral blood	blood
24	chr22:23488400-23493400	Weak transcription	Fetal Brain Female	brain
25	chr22:23488400-23494800	Weak transcription	Duodenum Mucosa	Duodenum
26	chr22:23488400-23495000	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr22:23488400-23499000	Weak transcription	Colonic Mucosa	Colon
28	chr22:23488400-23499000	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr22:23488400-23499200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr22:23488400-23505800	Weak transcription	Brain Substantia Nigra	brain
31	chr22:23488600-23490400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr22:23488600-23490800	Enhancers	Stomach Smooth Muscle	stomach
33	chr22:23488600-23491000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr22:23488600-23491200	Weak transcription	Right Atrium	heart
35	chr22:23488600-23491600	Strong transcription	Fetal Stomach	stomach
36	chr22:23488600-23492000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr22:23488600-23492000	Weak transcription	Adipose Nuclei	Adipose
38	chr22:23488600-23492000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr22:23488600-23493200	Weak transcription	Rectal Smooth Muscle	rectum
40	chr22:23488600-23505800	Weak transcription	Brain Germinal Matrix	brain
41	chr22:23488600-23506800	Weak transcription	A549	lung
42	chr22:23488800-23490400	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr22:23488800-23492200	Weak transcription	Brain Hippocampus Middle	brain
44	chr22:23488800-23505400	Weak transcription	Fetal Brain Male	brain
45	chr22:23489000-23491000	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr22:23489000-23491800	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr22:23489000-23492000	Weak transcription	Brain Cingulate Gyrus	brain
48	chr22:23489000-23494400	Weak transcription	GM12878-XiMat	blood
49	chr22:23489000-23496400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr22:23489200-23490400	Weak transcription	Brain Inferior Temporal Lobe	brain

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