Variant report

Variant	rs369593973
Chromosome Location	chr22:20286691-20286692
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	MAX	chr22:20286690-20287155	GM12878	blood:	n/a	chr22:20287044-20287060 chr22:20287055-20287064
2	SIN3AK20	chr22:20286367-20287420	K562	blood:	n/a	n/a
3	UBTF	chr22:20286633-20286885	K562	blood:	n/a	n/a
4	THAP1	chr22:20286159-20287731	K562	blood:	n/a	n/a
5	MAX	chr22:20286668-20287336	MCF-7	breast:	n/a	chr22:20287044-20287060 chr22:20287055-20287064
6	MYC	chr22:20286352-20287237	K562	blood:	n/a	chr22:20287044-20287060 chr22:20287055-20287064 chr22:20286570-20286580
7	ETS1	chr22:20286253-20287555	K562	blood:	n/a	chr22:20287068-20287079 chr22:20287112-20287125
8	UBTF	chr22:20286556-20286760	K562	blood:	n/a	n/a
9	MAX	chr22:20286456-20287787	ECC-1	luminal epithelium:	n/a	chr22:20287044-20287060 chr22:20287055-20287064 chr22:20286570-20286580
10	ZMIZ1	chr22:20286527-20286724	K562	blood:	n/a	n/a
11	YY1	chr22:20286433-20287561	K562	blood:	n/a	chr22:20286567-20286581
12	ZBTB7A	chr22:20285838-20287583	K562	blood:	n/a	chr22:20286824-20286831 chr22:20286714-20286723
13	POLR2A	chr22:20286555-20287043	Raji	blood:	n/a	n/a
14	SIN3A	chr22:20286330-20287049	H1-hESC	embryonic stem cell:	n/a	n/a
15	MAX	chr22:20286422-20287378	K562	blood:	n/a	chr22:20287044-20287060 chr22:20287055-20287064 chr22:20286570-20286580
16	ZNF384	chr22:20286654-20286774	K562	blood:	n/a	n/a
17	MAZ	chr22:20286358-20287400	K562	blood:	n/a	chr22:20287044-20287060 chr22:20287055-20287064 chr22:20286570-20286580
18	HMGN3	chr22:20286145-20287526	K562	blood:	n/a	n/a
19	E2F4	chr22:20286473-20286770	MCF10A-Er-Src	breast:	n/a	chr22:20286715-20286724 chr22:20286574-20286584
20	JUND	chr22:20286530-20286795	K562	blood:	n/a	n/a
21	POLR2A	chr22:20286402-20287559	K562	blood:	n/a	n/a
22	EGR1	chr22:20286352-20287561	K562	blood:	n/a	chr22:20287150-20287163 chr22:20286548-20286557 chr22:20287069-20287079 chr22:20286569-20286579 chr22:20286710-20286723 chr22:20287155-20287165 chr22:20287024-20287034 chr22:20286570-20286580
23	POLR2A	chr22:20286487-20287043	SK-N-MC	brain:	n/a	n/a
24	NR2F2	chr22:20286139-20287295	K562	blood:	n/a	n/a
25	POLR2A	chr22:20286526-20286821	A549	lung:	n/a	n/a
26	MAX	chr22:20286523-20287654	Hela-S3	cervix:	n/a	chr22:20287044-20287060 chr22:20287055-20287064 chr22:20286570-20286580
27	PML	chr22:20286234-20286888	K562	blood:	n/a	n/a
28	MAX	chr22:20286457-20287679	MCF-7	breast:	n/a	chr22:20287044-20287060 chr22:20287055-20287064 chr22:20286570-20286580
29	NR2F2	chr22:20286053-20287542	K562	blood:	n/a	n/a
30	E2F6	chr22:20286516-20287182	K562	blood:	n/a	chr22:20286715-20286724 chr22:20286574-20286584 chr22:20287070-20287079
31	MAX	chr22:20286407-20287679	A549	lung:	n/a	chr22:20287044-20287060 chr22:20287055-20287064 chr22:20286570-20286580
32	ELF1	chr22:20286370-20287214	K562	blood:	n/a	chr22:20286894-20286906 chr22:20286391-20286403
33	ELF1	chr22:20286201-20286807	GM12878	blood:	n/a	chr22:20286391-20286403
34	CBX3	chr22:20286163-20287284	K562	blood:	n/a	n/a
35	SPI1	chr22:20286499-20286736	K562	blood:	n/a	n/a
36	TBL1XR1	chr22:20286305-20286897	K562	blood:	n/a	n/a
37	SPI1	chr22:20286513-20286754	K562	blood:	n/a	n/a
38	ATF3	chr22:20286241-20287192	K562	blood:	n/a	chr22:20287075-20287084
39	POLR2A	chr22:20286573-20286834	HCT-116	colon:	n/a	n/a
40	HDAC2	chr22:20286265-20287693	K562	blood:	n/a	n/a
41	RCOR1	chr22:20286378-20287797	IMR90	lung:	n/a	n/a
42	RFX5	chr22:20286531-20286731	Hela-S3	cervix:	n/a	n/a
43	MAX	chr22:20286105-20287719	K562	blood:	n/a	chr22:20287044-20287060 chr22:20287055-20287064 chr22:20286570-20286580
44	POLR2A	chr22:20286664-20286738	HUVEC	blood vessel:	n/a	n/a
45	MAZ	chr22:20286392-20287633	IMR90	lung:	n/a	chr22:20287044-20287060 chr22:20287055-20287064 chr22:20286570-20286580
46	MAZ	chr22:20286689-20286740	HepG2	liver:	n/a	n/a
47	EGR1	chr22:20286362-20287604	K562	blood:	n/a	chr22:20287150-20287163 chr22:20286548-20286557 chr22:20287069-20287079 chr22:20286569-20286579 chr22:20286710-20286723 chr22:20287155-20287165 chr22:20287024-20287034 chr22:20286570-20286580
48	MXI1	chr22:20286361-20287787	IMR90	lung:	n/a	n/a
49	POLR2A	chr22:20286627-20286844	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr22:20286398-20287255	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr22:20286655..20288759-chr22:20746416..20749237,2	K562	blood:
2	chr22:20118465..20120580-chr22:20285203..20287703,2	MCF-7	breast:
3	chr22:20281007..20283182-chr22:20284432..20287016,2	MCF-7	breast:
4	chr22:19973359..19974976-chr22:20284613..20286772,2	K562	blood:
5	chr22:20286073..20288681-chr22:20850193..20851733,2	K562	blood:
6	chr22:20286073..20290077-chr22:20848237..20851733,4	K562	blood:
7	chr22:20284435..20289251-chr22:20305915..20309120,4	K562	blood:
8	chr22:20284539..20286947-chr22:20746722..20748522,2	MCF-7	breast:
9	chr22:20284063..20288249-chr22:20303567..20308986,5	K562	blood:
10	chr22:20202926..20205511-chr22:20284838..20286981,3	K562	blood:

Variant related genes	Relation type
ENSG00000161132	TF binding region
ENSG00000273343	Chromatin interaction
ENSG00000099904	Chromatin interaction
ENSG00000099917	Chromatin interaction
ENSG00000273139	Chromatin interaction
ENSG00000185252	Chromatin interaction
ENSG00000099910	Chromatin interaction
ENSG00000128185	Chromatin interaction
ENSG00000099889	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

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	esv1792516	chr22:19578312-20314496	Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	195 gene(s)	inside rSNPs	diseases
2	esv1818018	chr22:19674772-20313261	Flanking Bivalent TSS/Enh Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	193 gene(s)	inside rSNPs	diseases
3	nsv828938	chr22:19678592-20311988	Strong transcription Genic enhancers Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	192 gene(s)	inside rSNPs	diseases
4	nsv828939	chr22:19683555-20311988	Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	192 gene(s)	inside rSNPs	diseases
5	esv1826873	chr22:19726464-20313261	Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	179 gene(s)	inside rSNPs	diseases
6	nsv588237	chr22:19749525-20306993	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
7	nsv588239	chr22:19907099-20309393	Strong transcription Active TSS Genic enhancers Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer 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	158 gene(s)	inside rSNPs	diseases
8	nsv471183	chr22:20006040-20306993	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
9	esv2758536	chr22:20026493-20309447	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription 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	59 gene(s)	inside rSNPs	diseases
10	esv2758825	chr22:20026493-20309447	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
11	nsv828950	chr22:20057967-20311988	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
12	esv1793574	chr22:20075870-20728868	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
13	nsv914332	chr22:20082961-20339310	Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers Genic enhancers 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	57 gene(s)	inside rSNPs	diseases
14	nsv914337	chr22:20087539-20330895	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
15	esv1832132	chr22:20089802-20728868	ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
16	nsv1061349	chr22:20091394-20734304	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
17	esv1804395	chr22:20093565-20485443	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription 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	69 gene(s)	inside rSNPs	diseases
18	esv1850291	chr22:20093565-20666528	Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Active TSS 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 miRNA target site	74 gene(s)	inside rSNPs	diseases
19	esv1824760	chr22:20093565-20728868	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription 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	77 gene(s)	inside rSNPs	diseases
20	nsv1062789	chr22:20100465-20749579	Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	82 gene(s)	inside rSNPs	diseases
21	nsv828951	chr22:20109578-20310046	Enhancers Active TSS Flanking Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Strong transcription 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	47 gene(s)	inside rSNPs	diseases
22	nsv869949	chr22:20126918-20719112	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	68 gene(s)	inside rSNPs	diseases
23	nsv914359	chr22:20165632-20290691	Bivalent/Poised TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
24	nsv914360	chr22:20165632-20339310	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
25	nsv914361	chr22:20181136-20313299	Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
26	nsv914365	chr22:20189077-20290691	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
27	nsv914366	chr22:20189077-20306993	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	37 gene(s)	inside rSNPs	diseases
28	nsv914375	chr22:20210055-20306993	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	diseases
29	esv3376057	chr22:20285977-20288825	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
30	nsv519102	chr22:20286099-20306993	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:20285800-20286800	Flanking Active TSS	Duodenum Mucosa	Duodenum
2	chr22:20285800-20287400	Active TSS	Duodenum Smooth Muscle	Duodenum
3	chr22:20285800-20287600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
4	chr22:20285800-20287600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
5	chr22:20285800-20287600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
6	chr22:20285800-20287800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
7	chr22:20286000-20286800	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
8	chr22:20286000-20286800	Bivalent Enhancer	Fetal Thymus	thymus
9	chr22:20286000-20287600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr22:20286000-20287800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
11	chr22:20286000-20287800	Active TSS	H9 Cell Line	embryonic stem cell
12	chr22:20286000-20287800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr22:20286000-20288000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
14	chr22:20286200-20286800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr22:20286200-20286800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr22:20286200-20286800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr22:20286200-20286800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr22:20286200-20286800	Bivalent/Poised TSS	Brain Germinal Matrix	brain
19	chr22:20286200-20286800	Bivalent Enhancer	Stomach Mucosa	stomach
20	chr22:20286200-20286800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
21	chr22:20286200-20287200	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
22	chr22:20286200-20287200	Active TSS	Rectal Mucosa Donor 29	rectum
23	chr22:20286200-20287200	Bivalent/Poised TSS	Thymus	Thymus
24	chr22:20286200-20287400	Active TSS	Rectal Smooth Muscle	rectum
25	chr22:20286200-20287400	Active TSS	Stomach Smooth Muscle	stomach
26	chr22:20286200-20287600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
27	chr22:20286200-20287600	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr22:20286200-20287600	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
29	chr22:20286200-20287600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
30	chr22:20286200-20287600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr22:20286200-20287600	Active TSS	Brain Anterior Caudate	brain
32	chr22:20286200-20287600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
33	chr22:20286200-20287600	Active TSS	Colon Smooth Muscle	Colon
34	chr22:20286200-20287800	Enhancers	Sigmoid Colon	Sigmoid Colon
35	chr22:20286200-20288000	Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr22:20286200-20288000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr22:20286200-20288000	Active TSS	Pancreatic Islets	Pancreatic Islet
38	chr22:20286400-20286800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
39	chr22:20286400-20286800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
40	chr22:20286400-20286800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
41	chr22:20286400-20286800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr22:20286400-20286800	Flanking Active TSS	Adipose Nuclei	Adipose
43	chr22:20286400-20286800	Flanking Active TSS	Esophagus	oesophagus
44	chr22:20286400-20286800	Flanking Active TSS	Lung	lung
45	chr22:20286400-20286800	Flanking Active TSS	Pancreas	Pancrea
46	chr22:20286400-20286800	Flanking Active TSS	Spleen	Spleen
47	chr22:20286400-20286800	Flanking Active TSS	HMEC	breast
48	chr22:20286400-20286800	Flanking Active TSS	K562	blood
49	chr22:20286400-20287000	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr22:20286400-20287000	Flanking Active TSS	Primary T cells fromperipheralblood	blood

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