Variant report

Variant	rs5750113
Chromosome Location	chr22:22220074-22220075
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:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:22088248..22093129-chr22:22216287..22223699,14	K562	blood:
2	chr22:21982548..21988468-chr22:22219240..22225195,10	K562	blood:
3	chr22:22218339..22225021-chr22:22291070..22294784,16	K562	blood:
4	chr22:22124761..22127250-chr22:22218552..22220662,2	K562	blood:
5	chr22:22218324..22226656-chr22:22285349..22295547,26	K562	blood:
6	chr22:22122532..22127617-chr22:22219162..22223701,7	K562	blood:
7	chr22:22051706..22055325-chr22:22218845..22220883,3	K562	blood:
8	chr22:22219525..22222944-chr22:22304293..22307333,4	K562	blood:
9	chr22:22131580..22133092-chr22:22219677..22221609,2	MCF-7	breast:
10	chr22:22219546..22221587-chr22:22300415..22302914,3	K562	blood:
11	chr22:22219487..22221204-chr22:22258463..22261440,2	K562	blood:
12	chr22:21979671..21985739-chr22:22220007..22225195,6	K562	blood:
13	chr22:22195671..22198608-chr22:22219400..22221487,2	MCF-7	breast:
14	chr22:22218169..22225151-chr22:22299036..22308632,16	K562	blood:
15	chr22:22219761..22223642-chr22:22333943..22337946,5	K562	blood:
16	chr22:22088248..22091848-chr22:22218236..22223530,12	K562	blood:

No data

Variant related genes	Relation type
ENSG00000224086	Chromatin interaction
ENSG00000100030	Chromatin interaction
ENSG00000161180	Chromatin interaction
ENSG00000100038	Chromatin interaction
ENSG00000161179	Chromatin interaction
ENSG00000100027	Chromatin interaction
ENSG00000100034	Chromatin interaction

Extended variants
information (count: 79 )
Associated
traits (count: 13 )

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs11704205	0.96[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.96[YRI][hapmap];0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11913721	0.82[CEU][hapmap]
rs13943	0.96[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.96[YRI][hapmap];0.88[EUR][1000 genomes]
rs1892846	1.00[ASW][hapmap];0.96[CEU][hapmap];0.91[CHB][hapmap];0.98[CHD][hapmap];0.98[GIH][hapmap];0.86[JPT][hapmap];0.97[LWK][hapmap];0.95[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1892848	0.96[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.96[YRI][hapmap];0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2006893	0.96[CEU][hapmap];0.91[CHB][hapmap];0.98[CHD][hapmap];0.98[GIH][hapmap];0.86[JPT][hapmap];1.00[TSI][hapmap];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2266967	1.00[ASW][hapmap];0.96[CEU][hapmap];0.93[CHD][hapmap];0.95[GIH][hapmap];0.86[JPT][hapmap];0.97[LWK][hapmap];0.95[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2283792	0.88[ASW][hapmap];0.96[CEU][hapmap];0.91[CHB][hapmap];0.98[CHD][hapmap];0.91[GIH][hapmap];0.86[JPT][hapmap];0.97[LWK][hapmap];0.91[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2283794	1.00[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.92[YRI][hapmap];0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2298432	0.80[CHD][hapmap]
rs2329884	0.80[CEU][hapmap]
rs240049	0.92[CEU][hapmap]
rs240064	0.81[CEU][hapmap]
rs240066	0.81[CEU][hapmap]
rs28566555	0.82[EUR][1000 genomes]
rs34550586	0.80[ASN][1000 genomes]
rs3788332	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3810609	0.89[CHB][hapmap];0.89[JPT][hapmap];0.87[YRI][hapmap];0.88[EUR][1000 genomes]
rs3810610	1.00[ASW][hapmap];0.96[CEU][hapmap];0.91[CHB][hapmap];0.98[CHD][hapmap];0.98[GIH][hapmap];0.86[JPT][hapmap];0.97[LWK][hapmap];0.87[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.88[EUR][1000 genomes]
rs4478016	0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4516540	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4821402	0.96[CEU][hapmap];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs55762115	0.83[EUR][1000 genomes]
rs5749806	0.96[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.96[YRI][hapmap];0.86[EUR][1000 genomes]
rs5749937	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs5749986	0.94[ASW][hapmap];0.96[CEU][hapmap];0.93[CHD][hapmap];0.95[GIH][hapmap];0.86[JPT][hapmap];0.97[LWK][hapmap];0.91[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs5749998	0.96[CEU][hapmap];0.81[JPT][hapmap];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs5755099	0.96[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.88[EUR][1000 genomes]
rs5755654	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs5755694	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs5999515	0.81[ASW][hapmap];0.96[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];0.98[GIH][hapmap];0.86[JPT][hapmap];0.93[LWK][hapmap];0.91[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];0.81[YRI][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs5999521	1.00[ASW][hapmap];0.96[CEU][hapmap];0.91[CHB][hapmap];0.98[CHD][hapmap];0.95[GIH][hapmap];0.86[JPT][hapmap];0.97[LWK][hapmap];0.91[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs5999550	0.96[CEU][hapmap];0.86[JPT][hapmap];0.96[YRI][hapmap];0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs5999750	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6518986	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6928	0.96[CEU][hapmap];0.91[CHB][hapmap];0.98[CHD][hapmap];0.98[GIH][hapmap];0.86[JPT][hapmap];0.83[MEX][hapmap];1.00[TSI][hapmap];0.88[EUR][1000 genomes]
rs743409	0.93[ASW][hapmap];0.96[CEU][hapmap];0.82[CHB][hapmap];0.91[CHD][hapmap];0.90[JPT][hapmap];0.95[LWK][hapmap];0.87[MEX][hapmap];0.84[MKK][hapmap];0.98[TSI][hapmap];0.96[YRI][hapmap];0.87[EUR][1000 genomes]
rs8136590	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8136867	1.00[ASW][hapmap];0.85[CEU][hapmap];0.91[CHB][hapmap];0.98[CHD][hapmap];0.95[GIH][hapmap];0.86[JPT][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap];0.94[MKK][hapmap];0.93[TSI][hapmap];0.96[YRI][hapmap];0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8141851	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9607287	0.96[CEU][hapmap];0.81[JPT][hapmap];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9607340	0.87[EUR][1000 genomes]
rs9607347	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9610371	0.81[EUR][1000 genomes]
rs9610375	0.92[CEU][hapmap];0.89[TSI][hapmap];0.83[EUR][1000 genomes]
rs9610458	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9610500	0.90[ASN][1000 genomes]
rs9610505	0.83[EUR][1000 genomes]
rs9610533	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	nsv1066403	chr22:22010822-22352262	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer 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 target site	51 gene(s)	inside rSNPs	diseases
8	nsv1066964	chr22:22055123-22228745	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
9	nsv544604	chr22:22055123-22228745	Strong transcription Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
10	nsv948580	chr22:22100718-22839559	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic 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 target site	97 gene(s)	inside rSNPs	diseases
11	nsv914470	chr22:22131125-22272737	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
12	nsv1059265	chr22:22131125-22457154	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
13	esv3379268	chr22:22135347-22446281	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
14	esv3385441	chr22:22135777-22320294	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
15	esv2752404	chr22:22141825-22570417	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
16	esv2422277	chr22:22144108-22442159	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
17	esv2422295	chr22:22144108-22442159	Bivalent/Poised TSS Flanking Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
18	esv2422374	chr22:22152248-22595246	Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
19	esv2422403	chr22:22152248-23112582	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
20	nsv1062641	chr22:22157661-22367697	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
21	esv2422390	chr22:22157964-23112582	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised 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	145 gene(s)	inside rSNPs	diseases
22	nsv914471	chr22:22165557-22272737	Active TSS Genic enhancers Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
23	esv2763701	chr22:22173533-22573987	Weak transcription Bivalent Enhancer Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
24	esv2422372	chr22:22198324-22731587	Strong transcription Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
25	esv2422362	chr22:22198357-23125553	Enhancers Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised 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	145 gene(s)	inside rSNPs	diseases
26	esv2422446	chr22:22198357-23127963	Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
27	esv2422338	chr22:22210933-22417406	Genic enhancers Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
28	esv2422223	chr22:22210933-22700941	Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
29	esv2422217	chr22:22217341-23120076	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
30	esv2422394	chr22:22220046-22543157	Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases

mRNA abundance (count:13)

SNP	Gene	Cis/trans	Tissue	Source
rs5750113	LL22NC03-86G7.1	cis	Nerve Tibial	GTEx
rs5750113	SCARF2	cis	parietal	SCAN
rs5750113	MAPK1	Cis_1M	lymphoblastoid	RTeQTL
rs5750113	MIF	cis	parietal	SCAN
rs5750113	PPM1F	cis	uninvolved skin	skin_eQTL
rs5750113	LL22NC03-86G7.1	cis	Muscle Skeletal	GTEx
rs5750113	LL22NC03-86G7.1	cis	Heart Left Ventricle	GTEx
rs5750113	LL22NC03-86G7.1	cis	Thyroid	GTEx
rs5750113	DERL3	cis	cerebellum	SCAN
rs5750113	LL22NC03-86G7.1	cis	Adipose Subcutaneous	GTEx
rs5750113	LL22NC03-86G7.1	cis	Skin Sun Exposed Lower leg	GTEx
rs5750113	psiTPTE22	cis	parietal	SCAN
rs5750113	LL22NC03-86G7.1	cis	Whole Blood	GTEx

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:22192200-22220200	Weak transcription	Placenta	Placenta
2	chr22:22194000-22220400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr22:22209800-22220200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
4	chr22:22210800-22220400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr22:22211400-22220200	Enhancers	Primary B cells from peripheral blood	blood
6	chr22:22212000-22220600	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr22:22212000-22221000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
8	chr22:22214600-22220200	Weak transcription	Fetal Muscle Trunk	muscle
9	chr22:22216000-22220400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr22:22216000-22220400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr22:22216000-22220400	Weak transcription	Gastric	stomach
12	chr22:22216000-22220800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr22:22216200-22220400	Weak transcription	Esophagus	oesophagus
14	chr22:22216200-22220400	Weak transcription	Lung	lung
15	chr22:22216800-22220400	Enhancers	Sigmoid Colon	Sigmoid Colon
16	chr22:22217200-22220200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
17	chr22:22217400-22220400	Weak transcription	Spleen	Spleen
18	chr22:22218800-22220200	Enhancers	Liver	Liver
19	chr22:22218800-22220200	Enhancers	Fetal Intestine Small	intestine
20	chr22:22218800-22221000	Transcr. at gene 5' and 3'	K562	blood
21	chr22:22219000-22220200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr22:22219000-22220200	Enhancers	Brain Substantia Nigra	brain
23	chr22:22219000-22220200	Enhancers	Fetal Stomach	stomach
24	chr22:22219000-22220400	Flanking Active TSS	Dnd41	blood
25	chr22:22219000-22220400	Flanking Active TSS	GM12878-XiMat	blood
26	chr22:22219000-22220600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr22:22219000-22221000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
28	chr22:22219000-22221200	Active TSS	Right Atrium	heart
29	chr22:22219200-22220200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
30	chr22:22219200-22220200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr22:22219200-22220200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr22:22219200-22220200	Flanking Active TSS	NHEK	skin
33	chr22:22219200-22220400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr22:22219200-22220400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
35	chr22:22219200-22220400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
36	chr22:22219200-22220600	Enhancers	Small Intestine	intestine
37	chr22:22219200-22220800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
38	chr22:22219200-22221000	Flanking Active TSS	Primary T cells from cord blood	blood
39	chr22:22219200-22221400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr22:22219200-22222600	Active TSS	Aorta	Aorta
41	chr22:22219400-22220200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
42	chr22:22219400-22220200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr22:22219400-22220200	Flanking Active TSS	HMEC	breast
44	chr22:22219400-22220200	Flanking Active TSS	HUVEC	blood vessel
45	chr22:22219400-22220400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr22:22219400-22220400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr22:22219400-22220400	Flanking Active TSS	Duodenum Mucosa	Duodenum
48	chr22:22219400-22220400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
49	chr22:22219400-22220400	Weak transcription	Stomach Mucosa	stomach
50	chr22:22219400-22220800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain

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