Variant report

Variant	rs861844
Chromosome Location	chr22:22006219-22006220
allele	G/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	SIN3AK20	chr22:22006083-22006326	HepG2	liver:	n/a	n/a
2	POLR2A	chr22:22005534-22006816	HUVEC	blood vessel:	n/a	n/a
3	NFIC	chr22:22005950-22006455	GM12878	blood:	n/a	n/a
4	POLR2A	chr22:22005849-22006789	ECC-1	luminal epithelium:	n/a	n/a
5	CEBPB	chr22:22005967-22006561	H1-hESC	embryonic stem cell:	n/a	chr22:22006353-22006364
6	POLR2A	chr22:22006102-22006700	MCF10A-Er-Src	breast:	n/a	n/a
7	CEBPD	chr22:22004950-22007391	K562	blood:	n/a	chr22:22006352-22006363
8	HEY1	chr22:22005956-22006624	HepG2	liver:	n/a	chr22:22006403-22006418
9	POLR2A	chr22:22006165-22006809	U87	brain:	n/a	n/a
10	POLR2A	chr22:22005137-22007763	K562	blood:	n/a	n/a
11	NFYB	chr22:22005667-22007024	K562	blood:	n/a	chr22:22006414-22006429 chr22:22006416-22006426 chr22:22006326-22006341 chr22:22006414-22006429 chr22:22006329-22006343 chr22:22006329-22006344 chr22:22006329-22006344 chr22:22006414-22006428
12	RFX5	chr22:22006182-22006833	Hela-S3	cervix:	n/a	chr22:22006332-22006341 chr22:22006417-22006426
13	NR2F2	chr22:22004454-22008653	K562	blood:	n/a	n/a
14	KAP1	chr22:22005299-22006394	K562	blood:	n/a	chr22:22005344-22005352
15	SP1	chr22:22006105-22006565	H1-hESC	embryonic stem cell:	n/a	chr22:22006415-22006436 chr22:22006330-22006351
16	POLR2A	chr22:22005269-22006718	GM15510	blood:	n/a	n/a
17	SP2	chr22:22006208-22006476	H1-hESC	embryonic stem cell:	n/a	chr22:22006332-22006342 chr22:22006417-22006427
18	FOXM1	chr22:22006090-22006826	MCF-7	breast:	n/a	n/a
19	SMARCB1	chr22:22005221-22007330	K562	blood:	n/a	n/a
20	POLR2A	chr22:22005443-22006747	GM18505	blood:	n/a	n/a
21	MAX	chr22:22005616-22006852	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr22:22005262-22006690	HepG2	liver:	n/a	n/a
23	ZNF384	chr22:22006192-22006674	K562	blood:	n/a	n/a
24	TAF1	chr22:22005971-22006267	PFSK-1	brain:	n/a	n/a
25	POLR2A	chr22:22004761-22007521	K562	blood:	n/a	n/a
26	PBX3	chr22:22006030-22006833	SK-N-SH	brain:	n/a	chr22:22006417-22006426 chr22:22006332-22006341
27	TBL1XR1	chr22:22005309-22006815	K562	blood:	n/a	n/a
28	POLR2A	chr22:22005562-22006742	GM18526	blood:	n/a	n/a
29	POLR2A	chr22:22005949-22006308	HepG2	liver:	n/a	n/a
30	SIN3AK20	chr22:22005845-22006770	H1-hESC	embryonic stem cell:	n/a	n/a
31	NRF1	chr22:22006206-22006545	K562	blood:	n/a	chr22:22006402-22006416 chr22:22006404-22006415
32	POLR2A	chr22:22005398-22006715	Raji	blood:	n/a	n/a
33	RCOR1	chr22:22005216-22007325	K562	blood:	n/a	n/a
34	CEBPB	chr22:22006153-22006588	MCF-7	breast:	n/a	chr22:22006353-22006364
35	MAX	chr22:22006109-22006748	Hela-S3	cervix:	n/a	n/a
36	SIN3A	chr22:22005437-22007822	H1-hESC	embryonic stem cell:	n/a	chr22:22005713-22005721 chr22:22006403-22006416 chr22:22007120-22007134
37	ARID3A	chr22:22005402-22006640	K562	blood:	n/a	n/a
38	NR2F2	chr22:22004662-22008799	K562	blood:	n/a	n/a
39	POLR2A	chr22:22005471-22006736	MCF-7	breast:	n/a	n/a
40	CBX3	chr22:22004518-22007512	K562	blood:	n/a	n/a
41	PML	chr22:22005016-22007901	K562	blood:	n/a	chr22:22005344-22005352
42	POLR2A	chr22:22006174-22006689	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr22:22005111-22006874	GM18951	blood:	n/a	n/a
44	TEAD4	chr22:22005869-22006221	H1-hESC	embryonic stem cell:	n/a	n/a
45	MAFK	chr22:22005297-22006796	K562	blood:	n/a	n/a
46	THAP1	chr22:22005064-22008219	K562	blood:	n/a	n/a
47	MYC	chr22:22005329-22007270	K562	blood:	n/a	n/a
48	PML	chr22:22005884-22006852	GM12878	blood:	n/a	n/a
49	NFYA	chr22:22005588-22007011	K562	blood:	n/a	chr22:22006414-22006429 chr22:22006416-22006426 chr22:22006414-22006429 chr22:22006329-22006343 chr22:22006329-22006344 chr22:22006329-22006344 chr22:22006373-22006391 chr22:22006414-22006428
50	NFYA	chr22:22006109-22006569	GM12878	blood:	n/a	chr22:22006414-22006429 chr22:22006416-22006426 chr22:22006414-22006429 chr22:22006329-22006343 chr22:22006329-22006344 chr22:22006329-22006344 chr22:22006373-22006391 chr22:22006414-22006428

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:22006201-22006251	ProgFib	skin:	n/a
2	chr22:22006201-22006251	T-47D	breast:	n/a
3	chr22:22006201-22006251	MCF10A-Er-Src	breast:	n/a
4	chr22:22006201-22006251	BE2_C	brain:	n/a
5	chr22:22006201-22006251	IMR90	lung:	fetal
6	chr22:22006201-22006251	ovcar-3	ovarian:	n/a
7	chr22:22006201-22006251	NT2-D1	testis:	n/a
8	chr22:22006201-22006251	NH-A	brain:	n/a
9	chr22:22006201-22006251	HMEC	breast:	n/a
10	chr22:22006201-22006251	GM12878	blood:	n/a
11	chr22:22006201-22006251	Jurkat	blood:	n/a
12	chr22:22006201-22006251	ECC-1	luminal epithelium:	n/a
13	chr22:22006201-22006251	HNPCEpiC	eye:	n/a
14	chr22:22006201-22006251	HCF	heart:	n/a
15	chr22:22006201-22006251	SK-N-MC	brain:	n/a
16	chr22:22006201-22006251	AG09319	gingival:	n/a
17	chr22:22006201-22006251	GM19239	blood:	n/a
18	chr22:22006201-22006251	RPTEC	kidney:	n/a
19	chr22:22006201-22006251	A549	lung:	n/a
20	chr22:22006201-22006251	AG04449	skin:	fetal
21	chr22:22006201-22006251	HRPEpiC	eye:	n/a
22	chr22:22006201-22006251	LNCaP	prostate:	n/a
23	chr22:22006201-22006251	HEK293	kidney:	embryo
24	chr22:22006201-22006251	GM06990	blood:	n/a
25	chr22:22006201-22006251	NHDF-neo	bronchial:	n/a
26	chr22:22006201-22006251	HepG2	liver:	n/a
27	chr22:22006201-22006251	PrEC	prostate:	n/a
28	chr22:22006201-22006251	HAEpiC	amniotic membrane:	n/a
29	chr22:22006201-22006251	HRE	kidney:	n/a
30	chr22:22006201-22006251	NHBE	bronchial:	n/a
31	chr22:22006201-22006251	U87	brain:	n/a
32	chr22:22006201-22006251	GM12892	blood:	n/a
33	chr22:22006201-22006251	HCM	heart:	n/a
34	chr22:22006201-22006251	NB4	blood:	n/a
35	chr22:22006201-22006251	SAEC	small airway:	n/a
36	chr22:22006201-22006251	AG10803	skin:	n/a
37	chr22:22006201-22006251	HPAEpiC	pulmonary alveolar:	n/a
38	chr22:22006201-22006251	HEEpiC	esophagus:	n/a
39	chr22:22006201-22006251	AG09309	skin:	n/a
40	chr22:22006201-22006251	H1-hESC	embryonic stem cell:	embryo
41	chr22:22006201-22006251	HIPEpiC	eye:	n/a
42	chr22:22006201-22006251	BJ	skin:	n/a
43	chr22:22006201-22006251	SK-N-SH	brain:	n/a
44	chr22:22006201-22006251	HL-60	blood:	n/a
45	chr22:22006201-22006251	PANC-1	pancreas:	n/a
46	chr22:22006201-22006251	K562	blood:	n/a
47	chr22:22006201-22006251	PFSK-1	brain:	n/a
48	chr22:22006201-22006251	HCPEpiC	choroid plexus:	n/a
49	chr22:22006201-22006251	SK-N-SH_RA	brain:	n/a
50	chr22:22006201-22006251	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr22:21982497..21985083-chr22:22004368..22006741,4	MCF-7	breast:
2	chr22:22005965..22007764-chr22:22291588..22295229,3	K562	blood:
3	chr22:22005749..22007465-chr22:22293364..22295229,2	K562	blood:
4	chr22:21995435..21996753-chr22:22005158..22006527,7	K562	blood:
5	chr22:22005850..22008007-chr3:155571064..155572872,2	K562	blood:
6	chr22:21982265..21985710-chr22:22005242..22008783,5	MCF-7	breast:
7	chr22:22004774..22007479-chr22:22898413..22901210,2	K562	blood:
8	chr22:22004774..22008117-chr22:22898413..22901210,3	K562	blood:
9	chr22:22005826..22007484-chr22:22335133..22337197,2	K562	blood:
10	chr22:21997414..21999019-chr22:22004006..22006421,2	MCF-7	breast:
11	chr22:22003932..22007330-chr22:22018565..22021264,4	MCF-7	breast:
12	chr22:22004165..22007450-chr22:22088545..22091929,3	K562	blood:

Variant related genes	Relation type
MIR301B	TF binding region
MIR130B	TF binding region
PPIL2	TF binding region
PPIL2	CpG island
MIR301B	CpG island
MIR130B	CpG island
ENSG00000100034	Chromatin interaction
ENSG00000224086	Chromatin interaction
ENSG00000100027	Chromatin interaction
ENSG00000185686	Chromatin interaction
ENSG00000161179	Chromatin interaction
ENSG00000128228	Chromatin interaction
ENSG00000100023	Chromatin interaction
ENSG00000100038	Chromatin interaction
ENSG00000169359	Chromatin interaction

Extended variants
information (count: 68 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10427813	1.00[ASN][1000 genomes]
rs1103229	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.96[TSI][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1647705	1.00[ASN][1000 genomes]
rs1647711	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1669123	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16989505	0.82[LWK][hapmap]
rs17759598	1.00[ASN][1000 genomes]
rs17759796	1.00[ASN][1000 genomes]
rs17821327	0.93[CEU][hapmap];1.00[CHB][hapmap];0.91[GIH][hapmap];0.88[TSI][hapmap];1.00[ASN][1000 genomes]
rs17821500	1.00[ASN][1000 genomes]
rs2845458	1.00[ASN][1000 genomes]
rs28721456	1.00[ASN][1000 genomes]
rs2876980	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs368351	0.82[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs372150	0.90[EUR][1000 genomes]
rs374659	0.81[CEU][hapmap];0.90[EUR][1000 genomes]
rs412596	0.90[EUR][1000 genomes]
rs55649326	1.00[ASN][1000 genomes]
rs61757982	1.00[ASN][1000 genomes]
rs61763381	1.00[ASN][1000 genomes]
rs61763388	1.00[ASN][1000 genomes]
rs710171	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs710176	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs717121	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs73149918	1.00[ASN][1000 genomes]
rs73149929	1.00[ASN][1000 genomes]
rs8135616	1.00[CHB][hapmap]
rs8135758	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs8136405	1.00[ASN][1000 genomes]
rs8139395	1.00[ASN][1000 genomes]
rs8140233	1.00[ASN][1000 genomes]
rs8142650	1.00[ASN][1000 genomes]
rs861811	1.00[ASN][1000 genomes]
rs861818	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[TSI][hapmap];1.00[ASN][1000 genomes]
rs861820	1.00[ASN][1000 genomes]
rs861821	1.00[ASN][1000 genomes]
rs861828	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[GIH][hapmap];0.96[TSI][hapmap];1.00[ASN][1000 genomes]
rs861829	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[GIH][hapmap];0.96[TSI][hapmap];1.00[ASN][1000 genomes]
rs861831	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[GIH][hapmap];1.00[ASN][1000 genomes]
rs861832	1.00[ASN][1000 genomes]
rs861833	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[GIH][hapmap];0.96[TSI][hapmap];1.00[ASN][1000 genomes]
rs861840	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs861841	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs861845	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs861846	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs861850	1.00[CHB][hapmap];0.91[GIH][hapmap]
rs861854	1.00[CHB][hapmap];0.91[GIH][hapmap]
rs861855	1.00[CHB][hapmap];0.81[GIH][hapmap]
rs861856	1.00[ASN][1000 genomes]
rs881091	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[GIH][hapmap];0.96[TSI][hapmap];1.00[ASN][1000 genomes]
rs9607194	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 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
13	nsv914467	chr22:21982892-22055280	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	363 gene(s)	inside rSNPs	diseases
14	nsv914468	chr22:21982892-22070489	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	365 gene(s)	inside rSNPs	diseases
15	nsv914469	chr22:21985094-22010918	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	348 gene(s)	inside rSNPs	diseases
16	esv3456722	chr22:21993383-22019246	Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	341 gene(s)	inside rSNPs	diseases
17	esv3456723	chr22:21993399-22019258	Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	341 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs861844	PEX26	cis	cerebellum	SCAN
rs861844	HIC2	cis	cerebellum	SCAN
rs861844	DGCR14	cis	parietal	SCAN
rs861844	YPEL1	cis	parietal	SCAN
rs861844	C22orf43	cis	cerebellum	SCAN
rs861844	MGC16703	cis	cerebellum	SCAN
rs861844	PPIL2	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:22005200-22006400	Flanking Active TSS	Fetal Brain Female	brain
2	chr22:22005200-22006400	Enhancers	Spleen	Spleen
3	chr22:22005200-22007400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr22:22005200-22007600	Flanking Active TSS	Fetal Muscle Trunk	muscle
5	chr22:22005400-22006400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
6	chr22:22005400-22006600	Flanking Active TSS	Stomach Smooth Muscle	stomach
7	chr22:22005400-22006800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
8	chr22:22005400-22006800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr22:22005400-22007000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
10	chr22:22005400-22007000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr22:22005400-22007000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr22:22005400-22007200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
13	chr22:22005400-22007400	Flanking Active TSS	Primary hematopoietic stem cells	blood
14	chr22:22005400-22007400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
15	chr22:22005400-22007600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr22:22005400-22007600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr22:22005400-22007800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr22:22005600-22006600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr22:22005600-22006600	Flanking Active TSS	Liver	Liver
20	chr22:22005600-22006800	Flanking Active TSS	Primary B cells from cord blood	blood
21	chr22:22005600-22006800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
22	chr22:22005600-22007000	Flanking Active TSS	Primary B cells from peripheral blood	blood
23	chr22:22005600-22007000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
24	chr22:22005600-22007000	Flanking Active TSS	Adipose Nuclei	Adipose
25	chr22:22005600-22007000	Flanking Active TSS	Brain Angular Gyrus	brain
26	chr22:22005600-22007000	Transcr. at gene 5' and 3'	Right Atrium	heart
27	chr22:22005600-22007000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
28	chr22:22005600-22007400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr22:22005600-22007400	Active TSS	A549	lung
30	chr22:22005600-22007600	Active TSS	ES-I3 Cell Line	embryonic stem cell
31	chr22:22005600-22007600	Active TSS	H9 Cell Line	embryonic stem cell
32	chr22:22005600-22007600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr22:22005600-22007600	Active TSS	HUES64 Cell Line	embryonic stem cell
34	chr22:22005600-22007800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr22:22005600-22007800	Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr22:22005800-22006400	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
37	chr22:22005800-22006400	Flanking Active TSS	Brain Hippocampus Middle	brain
38	chr22:22005800-22006400	Flanking Active TSS	Placenta Amnion	Placenta Amnion
39	chr22:22005800-22007000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr22:22005800-22007000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
41	chr22:22005800-22007000	Active TSS	Pancreatic Islets	Pancreatic Islet
42	chr22:22005800-22007000	Active TSS	Fetal Lung	lung
43	chr22:22005800-22007000	Active TSS	Small Intestine	intestine
44	chr22:22005800-22007000	Active TSS	HSMM	muscle
45	chr22:22005800-22007000	Active TSS	HSMMtube	muscle
46	chr22:22005800-22007200	Active TSS	H1 Cell Line	embryonic stem cell
47	chr22:22005800-22007200	Active TSS	HUES6 Cell Line	embryonic stem cell
48	chr22:22005800-22007200	Active TSS	HepG2	liver
49	chr22:22005800-22007400	Active TSS	Fetal Kidney	kidney
50	chr22:22005800-22007600	Active TSS	HUES48 Cell Line	embryonic stem cell

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