Variant report

Variant	rs9596220
Chromosome Location	chr13:50570191-50570192
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:102)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:102 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr13:50569618-50571827	GM19193	blood:	n/a	n/a
2	TAF1	chr13:50569999-50570360	GM12878	blood:	n/a	n/a
3	TBL1XR1	chr13:50569699-50571799	GM12878	blood:	n/a	n/a
4	CEBPB	chr13:50570061-50570278	K562	blood:	n/a	n/a
5	RELA	chr13:50569611-50571801	GM12891	blood:	n/a	n/a
6	STAT5A	chr13:50569689-50570229	GM12878	blood:	n/a	n/a
7	ATF2	chr13:50569512-50570622	GM12878	blood:	n/a	n/a
8	POLR2A	chr13:50569733-50571768	Raji	blood:	n/a	n/a
9	POLR2A	chr13:50569475-50571004	GM12892	blood:	n/a	n/a
10	STAT1	chr13:50570061-50570267	GM12878	blood:	n/a	chr13:50570220-50570232
11	MXI1	chr13:50569870-50572252	SK-N-SH	brain:	n/a	n/a
12	POLR2A	chr13:50569900-50571749	GM15510	blood:	n/a	n/a
13	POLR2A	chr13:50569712-50570994	GM12891	blood:	n/a	n/a
14	HA-E2F1	chr13:50570189-50571931	MCF-7	breast:	n/a	chr13:50571525-50571535 chr13:50571593-50571602
15	POLR2A	chr13:50569753-50570236	ECC-1	luminal epithelium:	n/a	n/a
16	POLR2A	chr13:50569715-50571809	NB4	blood:	n/a	n/a
17	NFATC1	chr13:50569559-50570343	GM12878	blood:	n/a	n/a
18	NFIC	chr13:50569419-50571022	GM12878	blood:	n/a	chr13:50570591-50570619
19	ETS1	chr13:50569597-50570213	GM12878	blood:	n/a	chr13:50569940-50569953 chr13:50569963-50569970
20	WRNIP1	chr13:50569785-50570376	GM12878	blood:	n/a	n/a
21	POLR2A	chr13:50569661-50572069	MCF-7	breast:	n/a	n/a
22	MXI1	chr13:50569781-50570299	GM12878	blood:	n/a	n/a
23	MTA3	chr13:50569439-50572089	GM12878	blood:	n/a	n/a
24	RELA	chr13:50569611-50570230	GM12878	blood:	n/a	n/a
25	POLR2A	chr13:50569963-50571008	K562	blood:	n/a	n/a
26	POLR2A	chr13:50569734-50571800	GM18951	blood:	n/a	n/a
27	POLR2A	chr13:50569883-50571931	HUVEC	blood vessel:	n/a	n/a
28	YY1	chr13:50569769-50570288	GM12878	blood:	n/a	n/a
29	REST	chr13:50569929-50571052	HL-60	blood:	n/a	chr13:50570689-50570702
30	POLR2A	chr13:50569532-50571007	GM12892	blood:	n/a	n/a
31	POLR2A	chr13:50569739-50570568	GM12891	blood:	n/a	n/a
32	POLR2A	chr13:50569785-50572044	K562	blood:	n/a	n/a
33	MAX	chr13:50569726-50571815	NB4	blood:	n/a	n/a
34	POLR2A	chr13:50569806-50572944	MCF10A-Er-Src	breast:	n/a	n/a
35	MYC	chr13:50569638-50571912	NB4	blood:	n/a	n/a
36	POLR2A	chr13:50569828-50572527	K562	blood:	n/a	n/a
37	POLR2A	chr13:50569868-50571018	U87	brain:	n/a	n/a
38	POLR2A	chr13:50569758-50571876	IMR90	lung:	n/a	n/a
39	FOXM1	chr13:50569493-50571041	GM12878	blood:	n/a	n/a
40	IKZF1	chr13:50569638-50570191	GM12878	blood:	n/a	n/a
41	POLR2A	chr13:50569554-50571915	GM12878	blood:	n/a	n/a
42	RUNX3	chr13:50569520-50571045	GM12878	blood:	n/a	n/a
43	NFIC	chr13:50569514-50570318	GM12878	blood:	n/a	n/a
44	POLR2A	chr13:50569693-50571002	GM12892	blood:	n/a	n/a
45	POLR2A	chr13:50569901-50570999	K562	blood:	n/a	n/a
46	POLR2A	chr13:50569795-50571833	GM12892	blood:	n/a	n/a
47	POLR2A	chr13:50569742-50571923	HL-60	blood:	n/a	n/a
48	EP300	chr13:50569644-50570198	GM12878	blood:	n/a	n/a
49	CHD2	chr13:50569709-50571862	GM12878	blood:	n/a	chr13:50570858-50570868
50	POLR2A	chr13:50569359-50571018	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:50570142-50570192	SK-N-SH_RA	brain:	n/a
2	chr13:50570142-50570192	SAEC	small airway:	n/a
3	chr13:50570142-50570192	CMK	blood:	n/a
4	chr13:50570142-50570192	HRPEpiC	eye:	n/a
5	chr13:50570142-50570192	ProgFib	skin:	n/a
6	chr13:50570142-50570192	NT2-D1	testis:	n/a
7	chr13:50570142-50570192	AG04450	lung:	fetal
8	chr13:50570142-50570192	AG10803	skin:	n/a
9	chr13:50570142-50570192	H1-hESC	embryonic stem cell:	embryo
10	chr13:50570142-50570192	Caco-2	colon:	n/a
11	chr13:50570142-50570192	NHBE	bronchial:	n/a
12	chr13:50570142-50570192	GM12891	blood:	n/a
13	chr13:50570142-50570192	GM12892	blood:	n/a
14	chr13:50570142-50570192	MCF-7	breast:	n/a
15	chr13:50570142-50570192	HCT-116	colon:	n/a
16	chr13:50570142-50570192	Hela-S3	cervix:	n/a
17	chr13:50570142-50570192	HPAEpiC	pulmonary alveolar:	n/a
18	chr13:50570142-50570192	BE2_C	brain:	n/a
19	chr13:50570142-50570192	HAEpiC	amniotic membrane:	n/a
20	chr13:50570142-50570192	AG04449	skin:	fetal
21	chr13:50570142-50570192	AG09319	gingival:	n/a
22	chr13:50570142-50570192	AG09309	skin:	n/a
23	chr13:50570142-50570192	NH-A	brain:	n/a
24	chr13:50570142-50570192	A549	lung:	n/a
25	chr13:50570142-50570192	ECC-1	luminal epithelium:	n/a
26	chr13:50570142-50570192	SK-N-SH	brain:	n/a
27	chr13:50570142-50570192	ovcar-3	ovarian:	n/a
28	chr13:50570142-50570192	PANC-1	pancreas:	n/a
29	chr13:50570142-50570192	IMR90	lung:	fetal
30	chr13:50570142-50570192	HCM	heart:	n/a
31	chr13:50570142-50570192	HIPEpiC	eye:	n/a
32	chr13:50570142-50570192	BJ	skin:	n/a
33	chr13:50570142-50570192	T-47D	breast:	n/a
34	chr13:50570142-50570192	GM12878	blood:	n/a
35	chr13:50570142-50570192	Hepatocyte	liver:	n/a
36	chr13:50570142-50570192	GM19239	blood:	n/a
37	chr13:50570142-50570192	HRCEpiC	kidney:	n/a
38	chr13:50570142-50570192	AoSMC	blood vessel:	n/a
39	chr13:50570142-50570192	MCF10A-Er-Src	breast:	n/a
40	chr13:50570142-50570192	HUVEC	blood vessel:	n/a
41	chr13:50570142-50570192	HepG2	liver:	n/a
42	chr13:50570142-50570192	U87	brain:	n/a
43	chr13:50570142-50570192	NB4	blood:	n/a
44	chr13:50570142-50570192	PrEC	prostate:	n/a
45	chr13:50570142-50570192	PFSK-1	brain:	n/a
46	chr13:50570142-50570192	RPTEC	kidney:	n/a
47	chr13:50570142-50570192	K562	blood:	n/a
48	chr13:50570142-50570192	Jurkat	blood:	n/a
49	chr13:50570142-50570192	HMEC	breast:	n/a
50	chr13:50570142-50570192	LNCaP	prostate:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:50510078..50512694-chr13:50569483..50571768,3	MCF-7	breast:
2	chr12:21810600..21811356-chr13:50570159..50570946,2	NB4	blood:
3	chr13:50507293..50510312-chr13:50568081..50571220,3	MCF-7	breast:
4	chr13:50509071..50511034-chr13:50570092..50572951,3	K562	blood:
5	chr13:50568991..50573569-chr13:50697831..50701767,8	K562	blood:
6	chr13:50365087..50367801-chr13:50569333..50572997,5	MCF-7	breast:
7	chr13:50242666..50244239-chr13:50569416..50571466,2	MCF-7	breast:
8	chr13:50569368..50571479-chr13:50698927..50701104,2	MCF-7	breast:
9	chr13:50569748..50573186-chr13:50654848..50657793,4	MCF-7	breast:
10	chr13:50569852..50573038-chr13:50651628..50659276,11	K562	blood:
11	chr13:50568781..50571479-chr13:50962860..50965023,2	K562	blood:
12	chr13:50569462..50575212-chr13:50651363..50657415,15	K562	blood:
13	chr13:50569315..50571977-chr13:50588593..50590941,4	K562	blood:
14	chr13:50569500..50573569-chr13:50696112..50701767,10	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPRYD7-1	chr13:50567929-50570895	NONHSAT033771

No data

Variant related genes	Relation type
TRIM13	TF binding region
TRIM13	CpG island
ENSG00000102753	Chromatin interaction
ENSG00000198553	Chromatin interaction
ENSG00000231607	Chromatin interaction
ENSG00000111716	Chromatin interaction
ENSG00000203547	Chromatin interaction
ENSG00000123178	Chromatin interaction
ENSG00000176124	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs11617754	0.86[CHB][hapmap];0.85[CHD][hapmap]
rs1326120	0.91[AMR][1000 genomes]
rs2066549	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2066557	1.00[CHB][hapmap];0.97[CHD][hapmap];0.91[JPT][hapmap];0.88[ASN][1000 genomes]
rs2066558	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2066572	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2066575	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];0.97[TSI][hapmap];1.00[YRI][hapmap];0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2066585	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2066587	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2066591	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs2066594	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2242482	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2687950	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2687951	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2740508	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2740524	1.00[CHB][hapmap];0.91[JPT][hapmap];0.90[ASN][1000 genomes]
rs2740544	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2740545	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2760914	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2803839	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];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2812204	0.88[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2812216	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2812217	0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2812222	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2997624	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4548769	1.00[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs4942899	1.00[ASW][hapmap];0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.89[MKK][hapmap];0.97[TSI][hapmap];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4942901	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7336058	0.85[ASN][1000 genomes]
rs7338055	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs790943	0.86[CHB][hapmap]
rs7986337	0.82[CHB][hapmap];0.83[CHD][hapmap]
rs9535407	1.00[CHB][hapmap];0.97[CHD][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs9568354	0.95[CHB][hapmap];0.97[CHD][hapmap];0.90[JPT][hapmap];0.85[ASN][1000 genomes]
rs9568357	0.86[CHB][hapmap];0.82[CHD][hapmap]
rs9568363	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9568364	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9568366	0.90[CHB][hapmap];0.82[CHD][hapmap];0.81[ASN][1000 genomes]
rs9596215	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9596219	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];0.97[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035151	chr13:50513535-51167850	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1254 gene(s)	inside rSNPs	diseases
2	esv2753964	chr13:50545399-51421199	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1256 gene(s)	inside rSNPs	diseases
3	esv2753492	chr13:50550081-51461720	Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1256 gene(s)	inside rSNPs	diseases
4	esv2752608	chr13:50550099-51054499	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1249 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs9596220	DLEU2///DLEU2L	trans	lymphoblastoid	RTeQTL
rs9596220	KCNRG	cis	cerebellum	SCAN
rs9596220	DLEU2	Cis_1M	lymphoblastoid	RTeQTL
rs9596220	PHF11	cis	cerebellum	SCAN

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50543600-50570400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr13:50551000-50570200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr13:50551400-50570200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr13:50552400-50570200	Weak transcription	Lung	lung
5	chr13:50552800-50570200	Weak transcription	Spleen	Spleen
6	chr13:50556800-50570200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr13:50567600-50570400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr13:50569400-50570200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
9	chr13:50569400-50570200	Flanking Active TSS	GM12878-XiMat	blood
10	chr13:50569400-50570600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr13:50569400-50570800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr13:50569600-50570200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
13	chr13:50569600-50570200	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
14	chr13:50569600-50570200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
15	chr13:50569600-50570200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
16	chr13:50569600-50570400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
17	chr13:50569600-50570400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
18	chr13:50569600-50570400	Flanking Active TSS	Stomach Smooth Muscle	stomach
19	chr13:50569600-50570600	Flanking Active TSS	Primary B cells from cord blood	blood
20	chr13:50569600-50570600	Flanking Active TSS	Primary hematopoietic stem cells	blood
21	chr13:50569600-50572200	Active TSS	Brain Hippocampus Middle	brain
22	chr13:50569800-50570200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
23	chr13:50569800-50570200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
24	chr13:50569800-50570200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr13:50569800-50570200	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
26	chr13:50569800-50570200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr13:50569800-50570200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr13:50569800-50570200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
29	chr13:50569800-50570200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr13:50569800-50570200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr13:50569800-50570200	Flanking Active TSS	Brain Substantia Nigra	brain
32	chr13:50569800-50570200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
33	chr13:50569800-50570200	Flanking Active TSS	Fetal Kidney	kidney
34	chr13:50569800-50570200	Flanking Active TSS	Fetal Lung	lung
35	chr13:50569800-50570200	Flanking Active TSS	Fetal Muscle Leg	muscle
36	chr13:50569800-50570200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
37	chr13:50569800-50570400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
38	chr13:50569800-50570400	Flanking Active TSS	Primary B cells from peripheral blood	blood
39	chr13:50569800-50570400	Flanking Active TSS	Primary T cells from cord blood	blood
40	chr13:50569800-50570400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr13:50569800-50570400	Flanking Active TSS	Adipose Nuclei	Adipose
42	chr13:50569800-50570400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
43	chr13:50569800-50570400	Flanking Active TSS	Thymus	Thymus
44	chr13:50569800-50570400	Flanking Active TSS	HUVEC	blood vessel
45	chr13:50569800-50571800	Active TSS	Duodenum Mucosa	Duodenum
46	chr13:50569800-50571800	Active TSS	Duodenum Smooth Muscle	Duodenum
47	chr13:50569800-50571800	Active TSS	Rectal Smooth Muscle	rectum
48	chr13:50569800-50571800	Active TSS	Skeletal Muscle Male	skeletal muscle
49	chr13:50569800-50572000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr13:50569800-50572000	Active TSS	Brain Angular Gyrus	brain

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