Variant report

Variant	rs374659
Chromosome Location	chr22:22005687-22005688
allele	C/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	POLR2A	chr22:22005534-22006816	HUVEC	blood vessel:	n/a	n/a
2	CEBPD	chr22:22004950-22007391	K562	blood:	n/a	chr22:22006352-22006363
3	POLR2A	chr22:22005137-22007763	K562	blood:	n/a	n/a
4	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
5	NR2F2	chr22:22004454-22008653	K562	blood:	n/a	n/a
6	KAP1	chr22:22005299-22006394	K562	blood:	n/a	chr22:22005344-22005352
7	POLR2A	chr22:22005269-22006718	GM15510	blood:	n/a	n/a
8	POLR2A	chr22:22005618-22005801	H1-hESC	embryonic stem cell:	n/a	n/a
9	SMARCB1	chr22:22005221-22007330	K562	blood:	n/a	n/a
10	POLR2A	chr22:22005443-22006747	GM18505	blood:	n/a	n/a
11	MAX	chr22:22005616-22006852	H1-hESC	embryonic stem cell:	n/a	n/a
12	POLR2A	chr22:22005262-22006690	HepG2	liver:	n/a	n/a
13	POLR2A	chr22:22004761-22007521	K562	blood:	n/a	n/a
14	TBL1XR1	chr22:22005309-22006815	K562	blood:	n/a	n/a
15	POLR2A	chr22:22005562-22006742	GM18526	blood:	n/a	n/a
16	POLR2A	chr22:22005398-22006715	Raji	blood:	n/a	n/a
17	RCOR1	chr22:22005216-22007325	K562	blood:	n/a	n/a
18	SIN3A	chr22:22005437-22007822	H1-hESC	embryonic stem cell:	n/a	chr22:22005713-22005721 chr22:22006403-22006416 chr22:22007120-22007134
19	ARID3A	chr22:22005402-22006640	K562	blood:	n/a	n/a
20	NR2F2	chr22:22004662-22008799	K562	blood:	n/a	n/a
21	POLR2A	chr22:22005471-22006736	MCF-7	breast:	n/a	n/a
22	CBX3	chr22:22004518-22007512	K562	blood:	n/a	n/a
23	PML	chr22:22005016-22007901	K562	blood:	n/a	chr22:22005344-22005352
24	POLR2A	chr22:22005111-22006874	GM18951	blood:	n/a	n/a
25	RFX5	chr22:22005565-22006126	H1-hESC	embryonic stem cell:	n/a	n/a
26	MAFK	chr22:22005297-22006796	K562	blood:	n/a	n/a
27	THAP1	chr22:22005064-22008219	K562	blood:	n/a	n/a
28	MYC	chr22:22005329-22007270	K562	blood:	n/a	n/a
29	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
30	POLR2A	chr22:22005158-22006864	K562	blood:	n/a	n/a
31	POLR2A	chr22:22005556-22006808	SK-N-MC	brain:	n/a	n/a
32	E2F6	chr22:22005246-22007387	K562	blood:	n/a	chr22:22007224-22007236 chr22:22006159-22006169 chr22:22006322-22006332 chr22:22006323-22006333
33	ETS1	chr22:22005139-22008071	K562	blood:	n/a	chr22:22005850-22005857 chr22:22005848-22005857 chr22:22007415-22007428
34	POLR2A	chr22:22005111-22007673	PFSK-1	brain:	n/a	n/a
35	CHD2	chr22:22005248-22007272	K562	blood:	n/a	n/a
36	POLR2A	chr22:22005305-22006733	GM19099	blood:	n/a	n/a
37	MAX	chr22:22004994-22007381	K562	blood:	n/a	n/a
38	MAX	chr22:22005603-22006837	HepG2	liver:	n/a	n/a
39	MYC	chr22:22005389-22006861	K562	blood:	n/a	n/a
40	PML	chr22:22004873-22008608	K562	blood:	n/a	chr22:22008587-22008595 chr22:22005344-22005352
41	POLR2A	chr22:22004717-22007380	K562	blood:	n/a	n/a
42	HEY1	chr22:22004958-22008800	K562	blood:	n/a	chr22:22007524-22007539 chr22:22006403-22006418
43	CCNT2	chr22:22005665-22007203	K562	blood:	n/a	chr22:22007014-22007023
44	MAFF	chr22:22005316-22006282	K562	blood:	n/a	n/a
45	RELA	chr22:22005498-22006678	GM18951	blood:	n/a	chr22:22006115-22006124 chr22:22006115-22006124
46	POLR2A	chr22:22005153-22006974	GM19193	blood:	n/a	n/a
47	HEY1	chr22:22005026-22007900	K562	blood:	n/a	chr22:22007524-22007539 chr22:22006403-22006418
48	REST	chr22:22005254-22007365	K562	blood:	n/a	chr22:22007121-22007135
49	POLR2A	chr22:22005641-22007141	GM12892	blood:	n/a	n/a
50	RCOR1	chr22:22005287-22006938	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:22005669-22005719	HAEpiC	amniotic membrane:	n/a
2	chr22:22005669-22005719	MCF10A-Er-Src	breast:	n/a
3	chr22:22005669-22005719	AG10803	skin:	n/a
4	chr22:22005669-22005719	A549	lung:	n/a
5	chr22:22005669-22005719	HepG2	liver:	n/a
6	chr22:22005669-22005719	HCPEpiC	choroid plexus:	n/a
7	chr22:22005669-22005719	T-47D	breast:	n/a
8	chr22:22005669-22005719	HCT-116	colon:	n/a
9	chr22:22005669-22005719	BJ	skin:	n/a
10	chr22:22005669-22005719	ovcar-3	ovarian:	n/a
11	chr22:22005669-22005719	AG09319	gingival:	n/a
12	chr22:22005669-22005719	GM12878	blood:	n/a
13	chr22:22005669-22005719	Hela-S3	cervix:	n/a
14	chr22:22005669-22005719	NH-A	brain:	n/a
15	chr22:22005669-22005719	Caco-2	colon:	n/a
16	chr22:22005669-22005719	HRCEpiC	kidney:	n/a
17	chr22:22005669-22005719	NB4	blood:	n/a
18	chr22:22005669-22005719	SK-N-SH	brain:	n/a
19	chr22:22005669-22005719	AG04449	skin:	fetal
20	chr22:22005669-22005719	HEK293	kidney:	embryo
21	chr22:22005669-22005719	HCF	heart:	n/a
22	chr22:22005669-22005719	SKMC	muscle:	n/a
23	chr22:22005669-22005719	NHDF-neo	bronchial:	n/a
24	chr22:22005669-22005719	PFSK-1	brain:	n/a
25	chr22:22005669-22005719	RPTEC	kidney:	n/a
26	chr22:22005669-22005719	NT2-D1	testis:	n/a
27	chr22:22005669-22005719	HCM	heart:	n/a
28	chr22:22005669-22005719	GM06990	blood:	n/a
29	chr22:22005669-22005719	HNPCEpiC	eye:	n/a
30	chr22:22005669-22005719	HUVEC	blood vessel:	n/a
31	chr22:22005669-22005719	U87	brain:	n/a
32	chr22:22005669-22005719	ProgFib	skin:	n/a
33	chr22:22005669-22005719	BE2_C	brain:	n/a
34	chr22:22005669-22005719	GM19239	blood:	n/a
35	chr22:22005669-22005719	CMK	blood:	n/a
36	chr22:22005669-22005719	AoSMC	blood vessel:	n/a
37	chr22:22005669-22005719	NHBE	bronchial:	n/a
38	chr22:22005669-22005719	MCF-7	breast:	n/a
39	chr22:22005669-22005719	PANC-1	pancreas:	n/a
40	chr22:22005669-22005719	H1-hESC	embryonic stem cell:	embryo
41	chr22:22005669-22005719	HPAEpiC	pulmonary alveolar:	n/a
42	chr22:22005669-22005719	AG09309	skin:	n/a
43	chr22:22005669-22005719	Jurkat	blood:	n/a
44	chr22:22005669-22005719	SK-N-SH_RA	brain:	n/a
45	chr22:22005669-22005719	Hepatocyte	liver:	n/a
46	chr22:22005669-22005719	SAEC	small airway:	n/a
47	chr22:22005669-22005719	HMEC	breast:	n/a
48	chr22:22005669-22005719	HEEpiC	esophagus:	n/a
49	chr22:22005669-22005719	AG04450	lung:	fetal
50	chr22:22005669-22005719	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr22:21982497..21985083-chr22:22004368..22006741,4	MCF-7	breast:
2	chr22:21995435..21996753-chr22:22005158..22006527,7	K562	blood:
3	chr22:21982265..21985710-chr22:22005242..22008783,5	MCF-7	breast:
4	chr22:22004774..22007479-chr22:22898413..22901210,2	K562	blood:
5	chr22:22004774..22008117-chr22:22898413..22901210,3	K562	blood:
6	chr22:21997414..21999019-chr22:22004006..22006421,2	MCF-7	breast:
7	chr22:22003932..22007330-chr22:22018565..22021264,4	MCF-7	breast:
8	chr22:22004165..22007450-chr22:22088545..22091929,3	K562	blood:

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

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs1103229	0.81[CEU][hapmap]
rs1210390	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1210407	0.93[ASN][1000 genomes]
rs1210412	0.83[ASN][1000 genomes]
rs35445502	0.96[ASN][1000 genomes]
rs366026	0.85[ASN][1000 genomes]
rs368351	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs372108	0.85[ASN][1000 genomes]
rs372150	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs379591	0.97[ASN][1000 genomes]
rs381713	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs384262	0.83[JPT][hapmap]
rs384422	0.91[ASN][1000 genomes]
rs388113	0.86[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs390720	0.93[ASN][1000 genomes]
rs391324	0.96[ASN][1000 genomes]
rs394073	0.88[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs395006	0.88[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs402225	0.87[ASN][1000 genomes]
rs402548	0.91[JPT][hapmap];0.99[ASN][1000 genomes]
rs403865	0.82[ASN][1000 genomes]
rs409796	0.95[ASN][1000 genomes]
rs412596	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs416661	0.93[JPT][hapmap];0.87[ASN][1000 genomes]
rs428595	0.88[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs429623	0.93[ASN][1000 genomes]
rs433704	0.83[JPT][hapmap]
rs436570	0.85[ASN][1000 genomes]
rs443845	0.95[ASN][1000 genomes]
rs447001	0.87[JPT][hapmap];0.81[ASN][1000 genomes]
rs451422	0.85[ASN][1000 genomes]
rs452649	0.93[JPT][hapmap];0.85[ASN][1000 genomes]
rs710176	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs861817	0.87[JPT][hapmap]
rs861819	0.88[JPT][hapmap]
rs861828	0.80[CEU][hapmap]
rs861829	0.81[CEU][hapmap]
rs861833	0.81[CEU][hapmap]
rs861840	0.89[EUR][1000 genomes]
rs861841	0.91[EUR][1000 genomes]
rs861844	0.81[CEU][hapmap];0.90[EUR][1000 genomes]
rs861845	0.89[EUR][1000 genomes]
rs861846	0.87[EUR][1000 genomes]
rs881091	0.81[CEU][hapmap]

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:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:21998200-22005800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr22:21998200-22006000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr22:22004800-22006200	Flanking Active TSS	Dnd41	blood
4	chr22:22005000-22005800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
5	chr22:22005000-22005800	Enhancers	Primary T cells fromperipheralblood	blood
6	chr22:22005000-22006200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr22:22005000-22006200	Flanking Active TSS	Brain Germinal Matrix	brain
8	chr22:22005200-22005800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr22:22005200-22005800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
10	chr22:22005200-22005800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
11	chr22:22005200-22005800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
12	chr22:22005200-22005800	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr22:22005200-22005800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
14	chr22:22005200-22005800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
15	chr22:22005200-22005800	Enhancers	Brain Substantia Nigra	brain
16	chr22:22005200-22005800	Enhancers	Placenta	Placenta
17	chr22:22005200-22005800	Enhancers	Left Ventricle	heart
18	chr22:22005200-22005800	Enhancers	Psoas Muscle	Psoas
19	chr22:22005200-22005800	Enhancers	Stomach Mucosa	stomach
20	chr22:22005200-22006000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr22:22005200-22006000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr22:22005200-22006000	Flanking Active TSS	Fetal Heart	heart
23	chr22:22005200-22006000	Enhancers	Gastric	stomach
24	chr22:22005200-22006000	Enhancers	Pancreas	Pancrea
25	chr22:22005200-22006000	Flanking Active TSS	GM12878-XiMat	blood
26	chr22:22005200-22006000	Flanking Active TSS	NH-A	brain
27	chr22:22005200-22006200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr22:22005200-22006200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr22:22005200-22006200	Flanking Active TSS	HUVEC	blood vessel
30	chr22:22005200-22006400	Flanking Active TSS	Fetal Brain Female	brain
31	chr22:22005200-22006400	Enhancers	Spleen	Spleen
32	chr22:22005200-22007400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr22:22005200-22007600	Flanking Active TSS	Fetal Muscle Trunk	muscle
34	chr22:22005400-22005800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
35	chr22:22005400-22005800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr22:22005400-22005800	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
37	chr22:22005400-22005800	Enhancers	Brain Hippocampus Middle	brain
38	chr22:22005400-22005800	Flanking Active TSS	Fetal Kidney	kidney
39	chr22:22005400-22005800	Enhancers	Ovary	ovary
40	chr22:22005400-22005800	Flanking Active TSS	HepG2	liver
41	chr22:22005400-22005800	Flanking Active TSS	NHDF-Ad	bronchial
42	chr22:22005400-22006000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr22:22005400-22006000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
44	chr22:22005400-22006000	Enhancers	Lung	lung
45	chr22:22005400-22006200	Flanking Active TSS	Primary T cells from cord blood	blood
46	chr22:22005400-22006200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
47	chr22:22005400-22006200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
48	chr22:22005400-22006200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
49	chr22:22005400-22006200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
50	chr22:22005400-22006200	Flanking Active TSS	Muscle Satellite Cultured Cells	--

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