Variant report

Variant	rs2205849
Chromosome Location	chr1:169681357-169681358
allele	C/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	CTCF	chr1:169681260-169681410	NB4	blood:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
2	CTCF	chr1:169681280-169681430	GM12864	blood:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
3	CTCF	chr1:169681260-169681410	GM12870	blood:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
4	ELF1	chr1:169680678-169681623	MCF-7	breast:	n/a	n/a
5	FOXP2	chr1:169681271-169681418	SK-N-MC	brain:	n/a	n/a
6	CTCF	chr1:169681300-169681450	HPAF	blood vessel:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
7	WRNIP1	chr1:169680522-169681535	GM12878	blood:	n/a	n/a
8	CTCF	chr1:169681260-169681410	HVMF	connective:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
9	CTCF	chr1:169681300-169681450	HL-60	blood:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
10	CTCF	chr1:169681280-169681430	K562	blood:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
11	CTCF	chr1:169681166-169681475	HepG2	liver:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
12	CTCF	chr1:169681280-169681430	A549	lung:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
13	ELF1	chr1:169681139-169681554	A549	lung:	n/a	n/a
14	CTCF	chr1:169681228-169681472	GM19239	blood:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
15	RAD21	chr1:169680737-169681604	A549	lung:	n/a	chr1:169681351-169681360
16	CTCF	chr1:169681280-169681430	BE2_C	brain:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
17	CTCF	chr1:169681260-169681410	AG04450	lung:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
18	CTCF	chr1:169681240-169681390	HFF	foreskin:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
19	CTCF	chr1:169681235-169681476	HepG2	liver:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
20	POLR2A	chr1:169680178-169681427	GM12891	blood:	n/a	n/a
21	ELF1	chr1:169681132-169681533	A549	lung:	n/a	n/a
22	CTCF	chr1:169681150-169681463	SK-N-SH_RA	brain:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
23	CTCF	chr1:169680480-169681841	A549	lung:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
24	MAX	chr1:169681184-169681462	HepG2	liver:	n/a	n/a
25	RAD21	chr1:169680645-169681685	SK-N-SH	brain:	n/a	chr1:169681351-169681360
26	CTCF	chr1:169680761-169681565	K562	blood:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
27	RAD21	chr1:169680663-169681628	HepG2	liver:	n/a	chr1:169681351-169681360
28	CTCF	chr1:169681300-169681450	MCF-7	breast:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
29	CTCF	chr1:169681260-169681410	HBMEC	blood vessel:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
30	RELA	chr1:169680465-169681543	GM18951	blood:	n/a	n/a
31	CTCF	chr1:169681260-169681410	HMF	breast:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
32	GATA3	chr1:169681101-169681526	T-47D	breast:	n/a	chr1:169681162-169681175 chr1:169681164-169681172
33	STAT1	chr1:169680650-169681442	GM12878	blood:	n/a	n/a
34	CTCF	chr1:169681320-169681470	HAc	cerebellar:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
35	CTCF	chr1:169681280-169681430	AG09309	skin:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
36	CTCF	chr1:169681243-169681462	GM12891	blood:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
37	KAP1	chr1:169680759-169681576	HEK293	kidney:	n/a	n/a
38	CTCF	chr1:169681170-169681538	H1-hESC	embryonic stem cell:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
39	CTCF	chr1:169681204-169681496	Hela-S3	cervix:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
40	CTCF	chr1:169681260-169681410	HUVEC	blood vessel:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
41	RAD21	chr1:169681107-169681597	A549	lung:	n/a	chr1:169681351-169681360
42	CTCF	chr1:169681260-169681410	RPTEC	kidney:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
43	ELF1	chr1:169681231-169681572	HepG2	liver:	n/a	n/a
44	CTCF	chr1:169681218-169681488	A549	lung:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
45	CTCF	chr1:169681260-169681410	GM12873	blood:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
46	CTCF	chr1:169681246-169681467	MCF-7	breast:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
47	RAD21	chr1:169681151-169681528	HepG2	liver:	n/a	chr1:169681351-169681360
48	CTCF	chr1:169681300-169681450	GM12872	blood:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
49	YY1	chr1:169681224-169681466	GM12878	blood:	n/a	n/a
50	CTCF	chr1:169681243-169681456	GM20000	blood:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:169681333-169681383	SK-N-MC	brain:	n/a
2	chr1:169681333-169681383	ProgFib	skin:	n/a
3	chr1:169681333-169681383	HRE	kidney:	n/a
4	chr1:169681333-169681383	GM12878	blood:	n/a
5	chr1:169681333-169681383	AG09319	gingival:	n/a
6	chr1:169681333-169681383	RPTEC	kidney:	n/a
7	chr1:169681333-169681383	HIPEpiC	eye:	n/a
8	chr1:169681333-169681383	U87	brain:	n/a
9	chr1:169681333-169681383	HCM	heart:	n/a
10	chr1:169681333-169681383	ovcar-3	ovarian:	n/a
11	chr1:169681333-169681383	HRCEpiC	kidney:	n/a
12	chr1:169681333-169681383	HUVEC	blood vessel:	n/a
13	chr1:169681333-169681383	MCF10A-Er-Src	breast:	n/a
14	chr1:169681333-169681383	GM06990	blood:	n/a
15	chr1:169681333-169681383	NHBE	bronchial:	n/a
16	chr1:169681333-169681383	HNPCEpiC	eye:	n/a
17	chr1:169681333-169681383	Jurkat	blood:	n/a
18	chr1:169681333-169681383	GM12892	blood:	n/a
19	chr1:169681333-169681383	NB4	blood:	n/a
20	chr1:169681333-169681383	AoSMC	blood vessel:	n/a
21	chr1:169681333-169681383	Hela-S3	cervix:	n/a
22	chr1:169681333-169681383	HL-60	blood:	n/a
23	chr1:169681333-169681383	HAEpiC	amniotic membrane:	n/a
24	chr1:169681333-169681383	H1-hESC	embryonic stem cell:	embryo
25	chr1:169681333-169681383	BE2_C	brain:	n/a
26	chr1:169681333-169681383	PANC-1	pancreas:	n/a
27	chr1:169681333-169681383	IMR90	lung:	fetal
28	chr1:169681333-169681383	AG04450	lung:	fetal
29	chr1:169681333-169681383	LNCaP	prostate:	n/a
30	chr1:169681333-169681383	K562	blood:	n/a
31	chr1:169681333-169681383	SAEC	small airway:	n/a
32	chr1:169681333-169681383	HCF	heart:	n/a
33	chr1:169681333-169681383	Caco-2	colon:	n/a
34	chr1:169681333-169681383	HepG2	liver:	n/a
35	chr1:169681333-169681383	NT2-D1	testis:	n/a
36	chr1:169681333-169681383	HCT-116	colon:	n/a
37	chr1:169681333-169681383	PFSK-1	brain:	n/a
38	chr1:169681333-169681383	Hepatocyte	liver:	n/a
39	chr1:169681333-169681383	A549	lung:	n/a
40	chr1:169681333-169681383	AG10803	skin:	n/a
41	chr1:169681333-169681383	HEEpiC	esophagus:	n/a
42	chr1:169681333-169681383	NH-A	brain:	n/a
43	chr1:169681333-169681383	HRPEpiC	eye:	n/a
44	chr1:169681333-169681383	GM19239	blood:	n/a
45	chr1:169681333-169681383	SKMC	muscle:	n/a
46	chr1:169681333-169681383	T-47D	breast:	n/a
47	chr1:169681333-169681383	HEK293	kidney:	embryo
48	chr1:169681333-169681383	HPAEpiC	pulmonary alveolar:	n/a
49	chr1:169681333-169681383	CMK	blood:	n/a
50	chr1:169681333-169681383	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:169569836..169571238-chr1:169680901..169681521,6	MCF-7	breast:
2	chr1:169679878..169683283-chr1:169762041..169765464,5	MCF-7	breast:
3	chr1:168572840..168573443-chr1:169680986..169681557,2	MCF-7	breast:
4	chr1:169680417..169682445-chr1:169762164..169765185,3	MCF-7	breast:
5	chr1:169680922..169681530-chr1:169748582..169749325,2	MCF-7	breast:
6	chr1:168572487..168573340-chr1:169680905..169681683,2	K562	blood:
7	chr1:169554938..169555875-chr1:169680931..169681496,2	MCF-7	breast:
8	chr1:169555259..169556175-chr1:169680918..169681805,3	MCF-7	breast:
9	chr1:169519444..169520200-chr1:169680897..169681795,4	MCF-7	breast:

Variant related genes	Relation type
SELL	TF binding region
SELL	CpG island
ENSG00000000460	Chromatin interaction
ENSG00000171806	Chromatin interaction
ENSG00000198734	Chromatin interaction

Extended variants
information (count: 50 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs1051091	0.90[CHB][hapmap];0.94[CHD][hapmap];0.87[JPT][hapmap];0.91[LWK][hapmap];0.95[MKK][hapmap];0.95[YRI][hapmap];0.82[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs1076637	1.00[CEU][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes]
rs1076638	0.91[EUR][1000 genomes]
rs10919228	0.90[EUR][1000 genomes]
rs12027035	0.83[CEU][hapmap]
rs12072966	0.95[CHB][hapmap];0.83[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs12076368	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12079552	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12087033	0.95[CHB][hapmap];0.82[AMR][1000 genomes]
rs12131780	0.83[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs1883228	0.95[CHB][hapmap];0.91[CHD][hapmap];0.87[JPT][hapmap];0.88[LWK][hapmap];0.95[YRI][hapmap];0.81[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs1883229	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1961877	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2205847	0.95[CHB][hapmap];0.94[CHD][hapmap];0.87[JPT][hapmap];0.91[LWK][hapmap];0.95[MKK][hapmap];0.95[YRI][hapmap];0.82[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs2229569	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2298899	0.95[CHB][hapmap]
rs2420503	0.83[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs28469136	0.90[EUR][1000 genomes]
rs35289447	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3766129	0.95[CHB][hapmap];0.87[JPT][hapmap];0.95[YRI][hapmap];0.82[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs3917423	1.00[CEU][hapmap];0.87[MEX][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes]
rs3917428	0.95[CHB][hapmap];0.82[MEX][hapmap]
rs3917430	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3917432	0.95[CHB][hapmap]
rs3917435	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4427452	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4656698	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4656718	0.84[CHB][hapmap]
rs4987266	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4987298	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4987301	0.95[CHB][hapmap];0.86[MEX][hapmap]
rs4987306	0.95[CHB][hapmap]
rs4987314	0.91[ASW][hapmap];0.95[CHB][hapmap];0.86[MEX][hapmap];0.82[AMR][1000 genomes]
rs4987320	0.94[CHB][hapmap]
rs4987322	0.95[CHB][hapmap]
rs4987328	0.91[ASW][hapmap];0.95[CHB][hapmap];0.86[MEX][hapmap];0.80[AMR][1000 genomes]
rs5356	0.85[CHB][hapmap];0.86[MEX][hapmap]
rs5359	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs5368	0.84[CHB][hapmap];0.86[MEX][hapmap]
rs58662634	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59807249	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6427212	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7418242	0.95[CHB][hapmap]
rs7513119	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs964555	0.91[ASW][hapmap];0.95[CHB][hapmap];0.86[MEX][hapmap];0.80[AMR][1000 genomes]
rs964556	0.91[ASW][hapmap];0.95[CHB][hapmap];0.86[MEX][hapmap];0.80[AMR][1000 genomes]
rs964557	0.91[ASW][hapmap];0.95[CHB][hapmap];0.86[MEX][hapmap];0.80[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532586	chr1:169593222-169713184	Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	esv3451367	chr1:169630075-169976964	Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv872541	chr1:169672360-169695815	Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2205849	FMO2	cis	cerebellum	SCAN
rs2205849	FMO3	cis	cerebellum	SCAN

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169676600-169681400	Active TSS	Primary T killer memory cells from peripheral blood	blood
2	chr1:169678400-169681400	Flanking Active TSS	Primary hematopoietic stem cells	blood
3	chr1:169679400-169681600	Flanking Active TSS	Dnd41	blood
4	chr1:169679800-169681400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
5	chr1:169680200-169681400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
6	chr1:169680200-169681400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr1:169680200-169681600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr1:169680400-169681400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
9	chr1:169680400-169681400	Flanking Active TSS	Primary B cells from cord blood	blood
10	chr1:169680400-169681400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
11	chr1:169680400-169681400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr1:169680400-169681400	Flanking Active TSS	Liver	Liver
13	chr1:169680600-169681400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
14	chr1:169680600-169681400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
15	chr1:169680600-169681400	Active TSS	Brain Angular Gyrus	brain
16	chr1:169680600-169681400	Active TSS	Brain Anterior Caudate	brain
17	chr1:169680600-169681400	Active TSS	Brain Cingulate Gyrus	brain
18	chr1:169680600-169681400	Flanking Active TSS	Brain Hippocampus Middle	brain
19	chr1:169680600-169681400	Active TSS	Brain Inferior Temporal Lobe	brain
20	chr1:169680600-169681400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
21	chr1:169680600-169681400	Active TSS	Brain Substantia Nigra	brain
22	chr1:169680600-169681400	Active TSS	Duodenum Smooth Muscle	Duodenum
23	chr1:169680600-169681400	Active TSS	Rectal Mucosa Donor 29	rectum
24	chr1:169680600-169681400	Active TSS	Skeletal Muscle Male	skeletal muscle
25	chr1:169680600-169681400	Active TSS	Skeletal Muscle Female	skeletal muscle
26	chr1:169680800-169681400	Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr1:169680800-169681400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr1:169680800-169681400	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr1:169680800-169681400	Flanking Active TSS	Primary B cells from peripheral blood	blood
30	chr1:169680800-169681400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
31	chr1:169680800-169681400	Active TSS	Right Atrium	heart
32	chr1:169680800-169681400	Flanking Active TSS	HUVEC	blood vessel
33	chr1:169681000-169681400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr1:169681000-169681400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
35	chr1:169681000-169681400	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr1:169681000-169681400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr1:169681000-169681400	Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr1:169681000-169681400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
39	chr1:169681000-169681400	Flanking Active TSS	Primary T cells from cord blood	blood
40	chr1:169681000-169681400	Active TSS	Primary T cells fromperipheralblood	blood
41	chr1:169681000-169681400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
42	chr1:169681000-169681400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
43	chr1:169681000-169681400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr1:169681000-169681400	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
45	chr1:169681000-169681400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr1:169681000-169681400	Active TSS	Colon Smooth Muscle	Colon
47	chr1:169681000-169681400	Active TSS	Fetal Kidney	kidney
48	chr1:169681000-169681400	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr1:169681000-169681400	Active TSS	Psoas Muscle	Psoas
50	chr1:169681000-169681400	Flanking Active TSS	HepG2	liver

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