Variant report

Variant	rs11089637
Chromosome Location	chr22:21979096-21979097
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:21978725..21981306-chr5:114359469..114360989,2	K562	blood:
2	chr22:21804862..21806367-chr22:21977646..21980199,2	K562	blood:
3	chr22:21976586..21979474-chr22:22290804..22292395,2	K562	blood:
4	chr13:91999778..92002355-chr22:21977509..21981284,3	K562	blood:
5	chr22:21805758..21807437-chr22:21977909..21980793,2	K562	blood:
6	chr22:21978078..21980405-chr22:22112761..22114851,2	K562	blood:
7	chr22:21802884..21804534-chr22:21977171..21979118,2	K562	blood:
8	chr17:56756357..56758489-chr22:21978206..21981191,3	K562	blood:
9	chr22:21921267..21924236-chr22:21978074..21981837,4	MCF-7	breast:
10	chr22:21800442..21802407-chr22:21977326..21979370,2	K562	blood:
11	chr22:21356351..21358286-chr22:21977690..21980005,2	K562	blood:
12	chr22:21977706..21979861-chr3:142843771..142846008,2	K562	blood:
13	chr22:21799659..21804135-chr22:21977326..21984068,6	K562	blood:
14	chr22:21931758..21934175-chr22:21978835..21981370,2	MCF-7	breast:
15	chr2:152295999..152297502-chr22:21978298..21979900,2	K562	blood:
16	chr22:21976812..21979275-chr22:22008557..22011391,2	MCF-7	breast:
17	chr22:21977904..21980225-chr6:55963610..55966434,2	MCF-7	breast:
18	chr22:21978899..21981344-chr22:22856790..22858574,2	K562	blood:
19	chr22:21977792..21979613-chr22:22000477..22001713,17	K562	blood:
20	chr22:21356179..21357851-chr22:21977690..21979244,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000230513	Chromatin interaction
ENSG00000184436	Chromatin interaction
ENSG00000200997	Chromatin interaction
ENSG00000185651	Chromatin interaction
ENSG00000215417	Chromatin interaction

Extended variants
information (count: 85 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs1034329	0.84[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.90[TSI][hapmap];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11089629	0.84[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.92[LWK][hapmap];0.84[MEX][hapmap];0.97[MKK][hapmap];0.90[TSI][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12158299	0.84[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.90[TSI][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12169001	0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12484550	0.84[CEU][hapmap]
rs131656	0.92[ASN][1000 genomes]
rs131658	0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs131659	0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs131660	0.82[ASN][1000 genomes]
rs131664	0.94[ASN][1000 genomes]
rs131665	0.84[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.90[TSI][hapmap];0.94[ASN][1000 genomes]
rs140489	1.00[ASW][hapmap];0.84[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];0.84[MEX][hapmap];1.00[MKK][hapmap];0.90[TSI][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs140490	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs140491	0.84[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.90[TSI][hapmap];0.94[ASN][1000 genomes]
rs140492	1.00[ASW][hapmap];0.84[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];0.84[MEX][hapmap];1.00[MKK][hapmap];0.90[TSI][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs140496	0.90[ASN][1000 genomes]
rs140498	0.84[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.90[TSI][hapmap];0.94[ASN][1000 genomes]
rs140499	0.84[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs1811069	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs181359	0.84[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.90[TSI][hapmap];0.94[ASN][1000 genomes]
rs181360	0.84[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.90[TSI][hapmap];0.94[ASN][1000 genomes]
rs181363	1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[YRI][hapmap];0.80[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs181366	0.94[ASN][1000 genomes]
rs2070512	1.00[ASW][hapmap];0.84[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];0.84[MEX][hapmap];1.00[MKK][hapmap];0.90[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2266959	0.84[CEU][hapmap]
rs2266961	0.84[CEU][hapmap]
rs2266963	0.84[CEU][hapmap]
rs2266964	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2283789	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2283790	0.84[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.90[TSI][hapmap];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2298428	0.84[CEU][hapmap]
rs2298429	0.89[ASW][hapmap];0.84[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.87[LWK][hapmap];0.84[MEX][hapmap];0.90[TSI][hapmap];0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2876971	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3747093	0.97[ASN][1000 genomes]
rs4820091	1.00[ASW][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];0.84[MEX][hapmap];0.95[MKK][hapmap];1.00[YRI][hapmap]
rs4821108	0.84[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4821112	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.90[TSI][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4821116	0.84[CEU][hapmap]
rs4821124	0.84[CEU][hapmap]
rs4821130	1.00[CHB][hapmap];0.98[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.90[TSI][hapmap];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs5749485	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5749493	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5749502	0.84[CEU][hapmap]
rs5754217	1.00[ASW][hapmap];0.84[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];0.84[MEX][hapmap];1.00[MKK][hapmap];0.90[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5754238	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs5754295	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs5754323	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs5754352	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5754387	0.84[CEU][hapmap];0.95[GIH][hapmap];0.90[TSI][hapmap]
rs5754422	0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs5754426	0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs5754467	0.91[CHB][hapmap];0.89[CHD][hapmap];0.87[GIH][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs5994638	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs5998576	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs5998599	0.84[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs5998619	0.84[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.90[TSI][hapmap];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5998644	0.80[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs5998672	1.00[ASW][hapmap];0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.84[MEX][hapmap];1.00[MKK][hapmap];0.90[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs66534072	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs710177	0.94[ASN][1000 genomes]
rs73166622	0.94[ASN][1000 genomes]
rs73166632	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs738127	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.90[TSI][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs738128	0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs738129	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7444	0.83[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.90[TSI][hapmap];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7445	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8137950	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs8139079	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs861857	0.91[CHB][hapmap];0.89[CHD][hapmap];0.91[JPT][hapmap];0.94[ASN][1000 genomes]
rs878825	0.84[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.84[MEX][hapmap];0.90[TSI][hapmap];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9619386	0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9621715	0.91[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv914458	chr22:21747678-22070489	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	387 gene(s)	inside rSNPs	diseases
2	nsv482690	chr22:21807513-22016791	Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	374 gene(s)	inside rSNPs	diseases
3	esv1823866	chr22:21928916-22131125	Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Genic enhancers Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	374 gene(s)	inside rSNPs	diseases
4	nsv948603	chr22:21928916-22601814	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	422 gene(s)	inside rSNPs	diseases
5	nsv948902	chr22:21928916-22657900	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	426 gene(s)	inside rSNPs	diseases
6	nsv1063962	chr22:21939722-22934593	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	477 gene(s)	inside rSNPs	diseases
7	nsv1058617	chr22:21939922-22934454	Weak transcription Bivalent Enhancer Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	477 gene(s)	inside rSNPs	diseases
8	nsv529694	chr22:21957411-22905068	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	474 gene(s)	inside rSNPs	diseases
9	nsv914464	chr22:21964761-22039863	Genic enhancers Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	367 gene(s)	inside rSNPs	diseases
10	nsv914465	chr22:21964761-22055280	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	368 gene(s)	inside rSNPs	diseases
11	nsv914466	chr22:21964761-22057273	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	368 gene(s)	inside rSNPs	diseases
12	nsv531797	chr22:21977700-22959729	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	476 gene(s)	inside rSNPs	diseases

Variant related diseases (count:1)

Disease	PMID	Source
Rheumatoid arthritis	24390342	GWAS catalog

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs11089637	UBE2L3	cis	multi-tissue	Pritchard
rs11089637	UBE2L3	Cis_1M	lymphoblastoid	RTeQTL
rs11089637	UBE2L3	cis	lymphoblastoid	seeQTL
rs11089637	KIAA1666	cis	multi-tissue	Pritchard

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:21939600-21983200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr22:21946400-21980200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr22:21959000-21981200	Strong transcription	Dnd41	blood
4	chr22:21966400-21982800	Weak transcription	Small Intestine	intestine
5	chr22:21968200-21980600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr22:21968600-21981000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr22:21969000-21982400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr22:21969000-21983400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr22:21969200-21981000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr22:21970600-21980800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr22:21972200-21979400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr22:21972600-21981000	Strong transcription	Primary T cells from cord blood	blood
13	chr22:21973000-21979600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr22:21973000-21980400	Strong transcription	Primary T helper cells fromperipheralblood	blood
15	chr22:21973600-21982400	Strong transcription	Thymus	Thymus
16	chr22:21974000-21983400	Weak transcription	Fetal Kidney	kidney
17	chr22:21974400-21980000	Genic enhancers	Fetal Muscle Leg	muscle
18	chr22:21974400-21981000	Strong transcription	GM12878-XiMat	blood
19	chr22:21974600-21979400	Strong transcription	Sigmoid Colon	Sigmoid Colon
20	chr22:21974800-21979600	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr22:21974800-21979600	Strong transcription	Fetal Intestine Large	intestine
22	chr22:21974800-21979800	Genic enhancers	Fetal Muscle Trunk	muscle
23	chr22:21974800-21982400	Strong transcription	Fetal Intestine Small	intestine
24	chr22:21975200-21979600	Enhancers	Brain Substantia Nigra	brain
25	chr22:21975400-21981600	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr22:21975600-21981200	Weak transcription	Rectal Smooth Muscle	rectum
27	chr22:21976400-21979600	Enhancers	Brain Anterior Caudate	brain
28	chr22:21976400-21980000	Enhancers	Brain Angular Gyrus	brain
29	chr22:21976600-21979200	Enhancers	Fetal Brain Male	brain
30	chr22:21976600-21979600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr22:21976600-21979600	Enhancers	Psoas Muscle	Psoas
32	chr22:21976600-21979800	Strong transcription	A549	lung
33	chr22:21976800-21979800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr22:21976800-21979800	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr22:21976800-21983200	Weak transcription	Ovary	ovary
36	chr22:21976800-21983200	Weak transcription	HSMM	muscle
37	chr22:21977000-21979200	Genic enhancers	Cortex derived primary cultured neurospheres	brain
38	chr22:21977000-21979400	Weak transcription	Primary B cells from cord blood	blood
39	chr22:21977000-21979800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr22:21977000-21979800	Enhancers	Skeletal Muscle Male	skeletal muscle
41	chr22:21977000-21981600	Strong transcription	Duodenum Mucosa	Duodenum
42	chr22:21977000-21983200	Weak transcription	NHDF-Ad	bronchial
43	chr22:21977400-21979600	Enhancers	Brain Germinal Matrix	brain
44	chr22:21977600-21980000	Genic enhancers	Right Atrium	heart
45	chr22:21977600-21981600	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr22:21977600-21982800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr22:21977600-21983200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr22:21977800-21979400	Enhancers	HSMMtube	muscle
49	chr22:21977800-21979600	Enhancers	Adipose Nuclei	Adipose
50	chr22:21977800-21979600	Genic enhancers	Gastric	stomach

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