Variant report

Variant	rs395006
Chromosome Location	chr22:22007143-22007144
allele	A/G
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	RAD21	chr22:22006913-22007392	K562	blood:	n/a	chr22:22007257-22007267
2	CEBPD	chr22:22004950-22007391	K562	blood:	n/a	chr22:22006352-22006363
3	POLR2A	chr22:22005137-22007763	K562	blood:	n/a	n/a
4	NR2F2	chr22:22004454-22008653	K562	blood:	n/a	n/a
5	SMARCB1	chr22:22005221-22007330	K562	blood:	n/a	n/a
6	BACH1	chr22:22007132-22007154	K562	blood:	n/a	n/a
7	MAFK	chr22:22007127-22007143	K562	blood:	n/a	n/a
8	POLR2A	chr22:22004761-22007521	K562	blood:	n/a	n/a
9	RUNX3	chr22:22007095-22007306	GM12878	blood:	n/a	n/a
10	RCOR1	chr22:22005216-22007325	K562	blood:	n/a	n/a
11	CTCF	chr22:22007140-22007290	HepG2	liver:	n/a	n/a
12	SIN3A	chr22:22005437-22007822	H1-hESC	embryonic stem cell:	n/a	chr22:22005713-22005721 chr22:22006403-22006416 chr22:22007120-22007134
13	NR2F2	chr22:22004662-22008799	K562	blood:	n/a	n/a
14	CBX3	chr22:22004518-22007512	K562	blood:	n/a	n/a
15	CTCF	chr22:22007040-22007190	GM12868	blood:	n/a	n/a
16	PML	chr22:22005016-22007901	K562	blood:	n/a	chr22:22005344-22005352
17	CHD2	chr22:22007089-22007747	H1-hESC	embryonic stem cell:	n/a	chr22:22007421-22007431
18	THAP1	chr22:22005064-22008219	K562	blood:	n/a	n/a
19	MYC	chr22:22005329-22007270	K562	blood:	n/a	n/a
20	CTCF	chr22:22007114-22007407	K562	blood:	n/a	n/a
21	POLR2A	chr22:22007017-22007517	GM12878	blood:	n/a	n/a
22	E2F6	chr22:22005246-22007387	K562	blood:	n/a	chr22:22007224-22007236 chr22:22006159-22006169 chr22:22006322-22006332 chr22:22006323-22006333
23	ETS1	chr22:22005139-22008071	K562	blood:	n/a	chr22:22005850-22005857 chr22:22005848-22005857 chr22:22007415-22007428
24	POLR2A	chr22:22005111-22007673	PFSK-1	brain:	n/a	n/a
25	CHD2	chr22:22005248-22007272	K562	blood:	n/a	n/a
26	MAX	chr22:22004994-22007381	K562	blood:	n/a	n/a
27	ZBTB7A	chr22:22005788-22007536	ECC-1	luminal epithelium:	n/a	chr22:22006861-22006868 chr22:22007009-22007018 chr22:22006710-22006718 chr22:22006449-22006457
28	PML	chr22:22004873-22008608	K562	blood:	n/a	chr22:22008587-22008595 chr22:22005344-22005352
29	CTCF	chr22:22007140-22007290	WERI-Rb-1	eye:	n/a	n/a
30	POLR2A	chr22:22004717-22007380	K562	blood:	n/a	n/a
31	HEY1	chr22:22004958-22008800	K562	blood:	n/a	chr22:22007524-22007539 chr22:22006403-22006418
32	CCNT2	chr22:22005665-22007203	K562	blood:	n/a	chr22:22007014-22007023
33	CTCF	chr22:22007000-22007150	HFF-Myc	foreskin:	n/a	n/a
34	HEY1	chr22:22005026-22007900	K562	blood:	n/a	chr22:22007524-22007539 chr22:22006403-22006418
35	CTCF	chr22:22007140-22007290	GM12867	blood:	n/a	n/a
36	REST	chr22:22005254-22007365	K562	blood:	n/a	chr22:22007121-22007135
37	STAT5A	chr22:22004380-22007523	K562	blood:	n/a	chr22:22007102-22007110 chr22:22007195-22007207 chr22:22007164-22007176 chr22:22006679-22006691 chr22:22007417-22007429 chr22:22007424-22007436 chr22:22005717-22005729
38	UBTF	chr22:22005254-22007389	K562	blood:	n/a	n/a
39	ZMIZ1	chr22:22005302-22007299	K562	blood:	n/a	n/a
40	CTCF	chr22:22007140-22007290	GM12872	blood:	n/a	n/a
41	STAT5A	chr22:22004972-22007369	K562	blood:	n/a	chr22:22007102-22007110 chr22:22007195-22007207 chr22:22007164-22007176 chr22:22006679-22006691 chr22:22005717-22005729
42	MYC	chr22:22005156-22007212	K562	blood:	n/a	n/a
43	ELF1	chr22:22005653-22007395	K562	blood:	n/a	n/a
44	MXI1	chr22:22005182-22007512	SK-N-SH	brain:	n/a	chr22:22007446-22007461
45	JUN	chr22:22004275-22009366	K562	blood:	n/a	chr22:22006333-22006342 chr22:22006418-22006427 chr22:22006621-22006629
46	POLR2A	chr22:22002106-22008893	K562	blood:	n/a	n/a
47	MAZ	chr22:22005208-22007411	K562	blood:	n/a	n/a
48	ZBTB7A	chr22:22005719-22007769	ECC-1	luminal epithelium:	n/a	chr22:22006861-22006868 chr22:22007009-22007018 chr22:22006710-22006718 chr22:22006449-22006457
49	CTCF	chr22:22007140-22007290	GM12874	blood:	n/a	n/a
50	HDAC2	chr22:22005068-22007786	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:22007095-22007145	GM06990	blood:	n/a
2	chr22:22007095-22007145	Jurkat	blood:	n/a
3	chr22:22007095-22007145	HCM	heart:	n/a
4	chr22:22007100-22007150	HL-60	blood:	n/a
5	chr22:22007100-22007150	SAEC	small airway:	n/a
6	chr22:22007100-22007150	HRE	kidney:	n/a
7	chr22:22007095-22007145	BE2_C	brain:	n/a
8	chr22:22007100-22007150	BE2_C	brain:	n/a
9	chr22:22007100-22007150	SK-N-SH_RA	brain:	n/a
10	chr22:22007095-22007145	NT2-D1	testis:	n/a
11	chr22:22007100-22007150	HUVEC	blood vessel:	n/a
12	chr22:22007095-22007145	ovcar-3	ovarian:	n/a
13	chr22:22007100-22007150	AG04450	lung:	fetal
14	chr22:22007095-22007145	HEK293	kidney:	embryo
15	chr22:22007095-22007145	BJ	skin:	n/a
16	chr22:22007095-22007145	AG04450	lung:	fetal
17	chr22:22007100-22007150	H1-hESC	embryonic stem cell:	embryo
18	chr22:22007100-22007150	CMK	blood:	n/a
19	chr22:22007095-22007145	NH-A	brain:	n/a
20	chr22:22007095-22007145	HRE	kidney:	n/a
21	chr22:22007095-22007145	AG09319	gingival:	n/a
22	chr22:22007095-22007145	A549	lung:	n/a
23	chr22:22007095-22007145	AoSMC	blood vessel:	n/a
24	chr22:22007095-22007145	MCF-7	breast:	n/a
25	chr22:22007095-22007145	Caco-2	colon:	n/a
26	chr22:22007100-22007150	NH-A	brain:	n/a
27	chr22:22007095-22007145	IMR90	lung:	fetal
28	chr22:22007100-22007150	NHDF-neo	bronchial:	n/a
29	chr22:22007095-22007145	H1-hESC	embryonic stem cell:	embryo
30	chr22:22007100-22007150	AoSMC	blood vessel:	n/a
31	chr22:22007100-22007150	PANC-1	pancreas:	n/a
32	chr22:22007095-22007145	HMEC	breast:	n/a
33	chr22:22007095-22007145	SK-N-SH	brain:	n/a
34	chr22:22007100-22007150	HCT-116	colon:	n/a
35	chr22:22007100-22007150	HepG2	liver:	n/a
36	chr22:22007100-22007150	HAEpiC	amniotic membrane:	n/a
37	chr22:22007100-22007150	RPTEC	kidney:	n/a
38	chr22:22007095-22007145	AG09309	skin:	n/a
39	chr22:22007100-22007150	Hepatocyte	liver:	n/a
40	chr22:22007095-22007145	HNPCEpiC	eye:	n/a
41	chr22:22007100-22007150	HMEC	breast:	n/a
42	chr22:22007095-22007145	T-47D	breast:	n/a
43	chr22:22007095-22007145	HEEpiC	esophagus:	n/a
44	chr22:22007095-22007145	AG10803	skin:	n/a
45	chr22:22007100-22007150	PFSK-1	brain:	n/a
46	chr22:22007100-22007150	HEEpiC	esophagus:	n/a
47	chr22:22007095-22007145	SKMC	muscle:	n/a
48	chr22:22007095-22007145	Hepatocyte	liver:	n/a
49	chr22:22007095-22007145	PFSK-1	brain:	n/a
50	chr22:22007100-22007150	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr22:22005965..22007764-chr22:22291588..22295229,3	K562	blood:
2	chr22:22006832..22007456-chr22:22292539..22293060,2	K562	blood:
3	chr22:21355601..21357315-chr22:22006287..22008814,2	K562	blood:
4	chr22:22005749..22007465-chr22:22293364..22295229,2	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	chr22:22003932..22007330-chr22:22018565..22021264,4	MCF-7	breast:
11	chr22:22004165..22007450-chr22:22088545..22091929,3	K562	blood:
12	chr22:21920727..21924429-chr22:22006455..22008474,3	MCF-7	breast:
13	chr22:22006264..22009261-chr22:22291037..22293088,2	K562	blood:

Variant related genes	Relation type
MIR301B	TF binding region
MIR130B	TF binding region
MIR130B	CpG island
MIR301B	CpG island
ENSG00000230513	Chromatin interaction
ENSG00000161179	Chromatin interaction
ENSG00000169359	Chromatin interaction
ENSG00000184436	Chromatin interaction
ENSG00000185686	Chromatin interaction
ENSG00000224086	Chromatin interaction
ENSG00000100034	Chromatin interaction
ENSG00000100038	Chromatin interaction
ENSG00000185651	Chromatin interaction
ENSG00000100027	Chromatin interaction
ENSG00000100023	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1210390	0.95[ASN][1000 genomes]
rs1210407	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1210408	0.81[ASN][1000 genomes]
rs1210412	1.00[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs35445502	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs366026	0.87[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs368351	0.97[ASN][1000 genomes]
rs372108	1.00[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs372150	0.99[ASN][1000 genomes]
rs374659	0.88[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs379591	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs381713	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs384262	0.83[JPT][hapmap];0.81[ASN][1000 genomes]
rs384422	0.92[ASN][1000 genomes]
rs388113	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs390720	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs391324	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs394073	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs402225	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs402548	1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs403865	0.83[ASN][1000 genomes]
rs409796	0.96[ASN][1000 genomes]
rs412596	0.88[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs416661	0.88[CHB][hapmap];0.93[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs425046	0.85[AMR][1000 genomes]
rs428595	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs429623	0.95[ASN][1000 genomes]
rs433704	0.83[JPT][hapmap];0.81[ASN][1000 genomes]
rs436570	1.00[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs443845	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs447001	0.87[JPT][hapmap];0.80[ASN][1000 genomes]
rs451422	1.00[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs452649	0.88[CHB][hapmap];0.93[JPT][hapmap];1.00[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs5754787	0.87[AMR][1000 genomes]
rs710169	1.00[AMR][1000 genomes]
rs710170	1.00[AMR][1000 genomes]
rs710173	0.87[AMR][1000 genomes]
rs861815	1.00[AMR][1000 genomes]
rs861817	0.87[JPT][hapmap]
rs861819	0.88[JPT][hapmap];1.00[AMR][1000 genomes]
rs861822	1.00[AMR][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

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:22005200-22007400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr22:22005200-22007600	Flanking Active TSS	Fetal Muscle Trunk	muscle
3	chr22:22005400-22007200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
4	chr22:22005400-22007400	Flanking Active TSS	Primary hematopoietic stem cells	blood
5	chr22:22005400-22007400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
6	chr22:22005400-22007600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr22:22005400-22007600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr22:22005400-22007800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr22:22005600-22007400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr22:22005600-22007400	Active TSS	A549	lung
11	chr22:22005600-22007600	Active TSS	ES-I3 Cell Line	embryonic stem cell
12	chr22:22005600-22007600	Active TSS	H9 Cell Line	embryonic stem cell
13	chr22:22005600-22007600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr22:22005600-22007600	Active TSS	HUES64 Cell Line	embryonic stem cell
15	chr22:22005600-22007800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr22:22005600-22007800	Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr22:22005800-22007200	Active TSS	H1 Cell Line	embryonic stem cell
18	chr22:22005800-22007200	Active TSS	HUES6 Cell Line	embryonic stem cell
19	chr22:22005800-22007200	Active TSS	HepG2	liver
20	chr22:22005800-22007400	Active TSS	Fetal Kidney	kidney
21	chr22:22005800-22007600	Active TSS	HUES48 Cell Line	embryonic stem cell
22	chr22:22005800-22007600	Active TSS	iPS-15b Cell Line	embryonic stem cell
23	chr22:22005800-22007600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
24	chr22:22005800-22007600	Active TSS	NHDF-Ad	bronchial
25	chr22:22005800-22007800	Active TSS	iPS-18 Cell Line	embryonic stem cell
26	chr22:22006000-22007200	Active TSS	Thymus	Thymus
27	chr22:22006000-22007200	Active TSS	GM12878-XiMat	blood
28	chr22:22006000-22007400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr22:22006200-22007200	Active TSS	Rectal Mucosa Donor 31	rectum
30	chr22:22006200-22007200	Active TSS	Rectal Smooth Muscle	rectum
31	chr22:22006200-22007200	Active TSS	Hela-S3	cervix
32	chr22:22006200-22007400	Active TSS	Primary T killer memory cells from peripheral blood	blood
33	chr22:22006200-22007400	Active TSS	Duodenum Smooth Muscle	Duodenum
34	chr22:22006200-22007400	Active TSS	NHEK	skin
35	chr22:22006200-22007600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr22:22006400-22007200	Active TSS	Fetal Brain Female	brain
37	chr22:22006600-22007200	Flanking Active TSS	Colonic Mucosa	Colon
38	chr22:22006600-22007200	Flanking Active TSS	Duodenum Mucosa	Duodenum
39	chr22:22006600-22007200	Flanking Active TSS	Placenta	Placenta
40	chr22:22006600-22007200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
41	chr22:22006600-22007400	Flanking Active TSS	Fetal Thymus	thymus
42	chr22:22006600-22007600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
43	chr22:22006600-22007600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
44	chr22:22006600-22007600	Flanking Active TSS	Fetal Intestine Small	intestine
45	chr22:22006600-22007800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr22:22006800-22007200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
47	chr22:22006800-22007200	Enhancers	Primary B cells from cord blood	blood
48	chr22:22006800-22007200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
49	chr22:22006800-22007200	Enhancers	Primary T helper cells PMA-I stimulated	--
50	chr22:22006800-22007200	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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