Variant report

Variant	rs9612248
Chromosome Location	chr22:23492236-23492237
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	SIN3A	chr22:23491961-23492314	H1-hESC	embryonic stem cell:	n/a	n/a
2	TBP	chr22:23492072-23492255	H1-hESC	embryonic stem cell:	n/a	n/a
3	MYC	chr22:23492184-23492245	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr22:23492161-23492462	K562	blood:	n/a	n/a
5	FOXP2	chr22:23492010-23492361	PFSK-1	brain:	n/a	n/a
6	ZNF384	chr22:23492229-23492535	K562	blood:	n/a	n/a
7	MAX	chr22:23492193-23492389	K562	blood:	n/a	n/a
8	ZNF263	chr22:23492158-23492430	HEK293-T-REx	kidney:	n/a	n/a
9	THAP1	chr22:23491708-23492445	K562	blood:	n/a	n/a
10	MAX	chr22:23491500-23492522	K562	blood:	n/a	n/a
11	ZNF143	chr22:23492041-23492290	H1-hESC	embryonic stem cell:	n/a	n/a
12	MAX	chr22:23492046-23492508	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr22:23492139-23492238	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr22:23491817-23492443	K562	blood:	n/a	n/a
15	NANOG	chr22:23491894-23492251	H1-hESC	embryonic stem cell:	n/a	n/a

Variant related genes	Relation type
RAB36	TF binding region

Extended variants
information (count: 106 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs1051875	0.84[JPT][hapmap]
rs10775764	0.83[AFR][1000 genomes]
rs11704365	0.91[CHB][hapmap];0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs12167308	0.85[JPT][hapmap]
rs13054985	0.84[JPT][hapmap]
rs1805058	0.85[JPT][hapmap]
rs1807460	0.82[ASW][hapmap];0.89[LWK][hapmap];0.80[YRI][hapmap];0.83[AFR][1000 genomes]
rs1807702	0.83[AFR][1000 genomes]
rs1807706	0.82[AFR][1000 genomes]
rs2008176	0.83[AFR][1000 genomes]
rs2157710	0.84[JPT][hapmap]
rs2249692	0.90[JPT][hapmap]
rs2267004	0.84[JPT][hapmap]
rs2267006	0.94[ASW][hapmap];0.96[CEU][hapmap];0.95[CHB][hapmap];0.93[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];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2267007	0.82[ASW][hapmap];0.85[JPT][hapmap];0.89[LWK][hapmap];0.88[MEX][hapmap];0.80[YRI][hapmap];0.83[AFR][1000 genomes]
rs2267010	0.85[JPT][hapmap]
rs2267012	0.85[JPT][hapmap]
rs2267014	0.80[JPT][hapmap]
rs2283802	0.85[JPT][hapmap]
rs2283803	0.84[JPT][hapmap]
rs2283804	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]
rs2301554	0.84[JPT][hapmap]
rs2330336	0.85[JPT][hapmap]
rs2330361	0.85[JPT][hapmap]
rs3788347	0.84[JPT][hapmap]
rs3788348	0.84[JPT][hapmap]
rs4552283	0.80[AFR][1000 genomes]
rs4820537	0.84[JPT][hapmap]
rs4820539	0.84[JPT][hapmap]
rs4820541	0.85[JPT][hapmap]
rs4822357	0.84[JPT][hapmap]
rs4822359	0.84[JPT][hapmap]
rs4822360	0.84[JPT][hapmap]
rs4822361	0.84[JPT][hapmap]
rs4822362	0.84[JPT][hapmap]
rs4822369	0.85[JPT][hapmap]
rs5751587	0.81[JPT][hapmap]
rs5751589	0.84[JPT][hapmap]
rs5751593	0.82[ASW][hapmap];0.85[JPT][hapmap];0.91[LWK][hapmap];0.88[MEX][hapmap];0.80[YRI][hapmap];0.83[AFR][1000 genomes]
rs5751596	0.85[JPT][hapmap];0.80[YRI][hapmap];0.83[AFR][1000 genomes]
rs5759593	0.84[JPT][hapmap]
rs5759598	0.84[JPT][hapmap]
rs5759600	0.84[JPT][hapmap]
rs5759603	0.91[CEU][hapmap];0.95[CHB][hapmap];0.83[CHD][hapmap];0.84[JPT][hapmap];0.83[MEX][hapmap];0.83[TSI][hapmap];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs5759604	0.81[JPT][hapmap]
rs5759607	0.85[JPT][hapmap]
rs5759608	0.82[ASW][hapmap];0.85[JPT][hapmap];0.89[LWK][hapmap];0.88[MEX][hapmap];0.80[YRI][hapmap]
rs5759609	0.83[AFR][1000 genomes]
rs5759611	0.85[JPT][hapmap]
rs5759612	0.82[ASW][hapmap];0.85[JPT][hapmap];0.91[LWK][hapmap];0.88[MEX][hapmap];0.80[YRI][hapmap];0.83[AFR][1000 genomes]
rs5759613	0.85[JPT][hapmap];0.80[YRI][hapmap];0.83[AFR][1000 genomes]
rs5759614	0.82[ASW][hapmap];0.85[JPT][hapmap];0.91[LWK][hapmap];0.88[MEX][hapmap];0.81[MKK][hapmap];0.80[YRI][hapmap];0.83[AFR][1000 genomes]
rs5759615	0.82[ASW][hapmap];0.85[JPT][hapmap];0.91[LWK][hapmap];0.88[MEX][hapmap];0.80[YRI][hapmap];0.83[AFR][1000 genomes]
rs5759617	0.83[AFR][1000 genomes]
rs5759618	0.82[AFR][1000 genomes]
rs5759619	0.82[ASW][hapmap];0.82[CHD][hapmap];0.85[JPT][hapmap];0.91[LWK][hapmap];0.80[MEX][hapmap];0.83[AFR][1000 genomes]
rs5759620	0.82[ASW][hapmap];0.85[JPT][hapmap];0.91[LWK][hapmap];0.88[MEX][hapmap];0.80[YRI][hapmap];0.83[AFR][1000 genomes]
rs5759621	0.85[JPT][hapmap];0.80[MEX][hapmap]
rs5759622	0.80[AFR][1000 genomes]
rs6003502	0.85[JPT][hapmap]
rs6003518	0.84[JPT][hapmap]
rs713682	0.82[ASW][hapmap];0.85[JPT][hapmap];0.91[LWK][hapmap];0.88[MEX][hapmap];0.80[YRI][hapmap];0.83[AFR][1000 genomes]
rs737818	0.82[ASW][hapmap];0.84[JPT][hapmap];0.91[LWK][hapmap];0.88[MEX][hapmap];0.80[YRI][hapmap];0.83[AFR][1000 genomes]
rs737819	0.82[ASW][hapmap];0.82[CHD][hapmap];0.85[JPT][hapmap];0.91[LWK][hapmap];0.88[MEX][hapmap];0.80[YRI][hapmap];0.83[AFR][1000 genomes]
rs737820	0.83[AFR][1000 genomes]
rs739362	0.85[JPT][hapmap]
rs756633	0.85[JPT][hapmap]
rs768513	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs8142746	0.82[ASW][hapmap];0.85[JPT][hapmap];0.91[LWK][hapmap];0.88[MEX][hapmap];0.80[YRI][hapmap];0.83[AFR][1000 genomes]
rs874138	0.85[JPT][hapmap]
rs885964	0.84[JPT][hapmap]
rs916583	0.84[JPT][hapmap]
rs916584	0.84[JPT][hapmap]
rs916585	0.81[JPT][hapmap]
rs9608085	0.83[AFR][1000 genomes]
rs9612234	0.84[JPT][hapmap]
rs9612237	0.89[JPT][hapmap]
rs9612252	0.82[ASW][hapmap];0.85[JPT][hapmap];0.91[LWK][hapmap];0.88[MEX][hapmap];0.80[YRI][hapmap];0.83[AFR][1000 genomes]
rs9612253	0.83[AFR][1000 genomes]
rs9612257	0.91[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:26 , 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

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs9612248	GNAZ	cis	parietal	SCAN
rs9612248	SNRPD3	cis	parietal	SCAN

Chromatin state (count:88 , 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	chr22:23488000-23499400	Weak transcription	Right Ventricle	heart
3	chr22:23488200-23492800	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr22:23488200-23492800	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr22:23488200-23494600	Weak transcription	Primary hematopoietic stem cells	blood
6	chr22:23488200-23505800	Weak transcription	HSMMtube	muscle
7	chr22:23488400-23493200	Weak transcription	Colon Smooth Muscle	Colon
8	chr22:23488400-23493400	Weak transcription	Primary B cells from peripheral blood	blood
9	chr22:23488400-23493400	Weak transcription	Fetal Brain Female	brain
10	chr22:23488400-23494800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr22:23488400-23495000	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr22:23488400-23499000	Weak transcription	Colonic Mucosa	Colon
13	chr22:23488400-23499000	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr22:23488400-23499200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr22:23488400-23505800	Weak transcription	Brain Substantia Nigra	brain
16	chr22:23488600-23493200	Weak transcription	Rectal Smooth Muscle	rectum
17	chr22:23488600-23505800	Weak transcription	Brain Germinal Matrix	brain
18	chr22:23488600-23506800	Weak transcription	A549	lung
19	chr22:23488800-23505400	Weak transcription	Fetal Brain Male	brain
20	chr22:23489000-23494400	Weak transcription	GM12878-XiMat	blood
21	chr22:23489000-23496400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr22:23489200-23494200	Weak transcription	Spleen	Spleen
23	chr22:23489200-23497400	Weak transcription	Fetal Kidney	kidney
24	chr22:23489200-23499800	Weak transcription	NHLF	lung
25	chr22:23489800-23498400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr22:23490000-23493000	Enhancers	Fetal Thymus	thymus
27	chr22:23490200-23492400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr22:23490200-23493000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr22:23490200-23496800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr22:23490200-23500200	Weak transcription	Fetal Lung	lung
31	chr22:23490200-23504800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr22:23490400-23493200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr22:23490400-23493600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr22:23490400-23498400	Strong transcription	Brain Inferior Temporal Lobe	brain
35	chr22:23490400-23499000	Weak transcription	Stomach Mucosa	stomach
36	chr22:23490400-23506800	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr22:23490400-23522000	Weak transcription	Aorta	Aorta
38	chr22:23490600-23492600	Enhancers	Lung	lung
39	chr22:23490600-23493800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr22:23490600-23494000	Weak transcription	NHEK	skin
41	chr22:23490600-23498600	Strong transcription	Cortex derived primary cultured neurospheres	brain
42	chr22:23490800-23493200	Genic enhancers	Placenta	Placenta
43	chr22:23491000-23492400	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr22:23491000-23492600	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr22:23491000-23493400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr22:23491000-23498000	Weak transcription	Gastric	stomach
47	chr22:23491000-23504600	Strong transcription	Stomach Smooth Muscle	stomach
48	chr22:23491200-23512000	Strong transcription	Right Atrium	heart
49	chr22:23491400-23492400	Enhancers	H9 Cell Line	embryonic stem cell
50	chr22:23491400-23492400	Enhancers	iPS-18 Cell Line	embryonic stem cell

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