Variant report

Variant	rs12068820
Chromosome Location	chr1:113615627-113615628
allele	A/C
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	CBX3	chr1:113614710-113616713	K562	blood:	n/a	n/a
2	ARID3A	chr1:113614699-113615830	K562	blood:	n/a	n/a
3	ATF1	chr1:113614716-113615966	K562	blood:	n/a	n/a
4	RCOR1	chr1:113615220-113616494	Hela-S3	cervix:	n/a	n/a
5	CTCF	chr1:113615261-113615764	GM13976	blood:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
6	NANOG	chr1:113615528-113616080	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr1:113615144-113615835	K562	blood:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
8	CTCFL	chr1:113615526-113615755	K562	blood:	n/a	n/a
9	ZKSCAN1	chr1:113615008-113616338	Hela-S3	cervix:	n/a	n/a
10	NFIC	chr1:113615422-113616107	HepG2	liver:	n/a	n/a
11	POLR2A	chr1:113615546-113616432	ECC-1	luminal epithelium:	n/a	n/a
12	CTCF	chr1:113615207-113615807	Lung_OC	lung:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
13	MXI1	chr1:113615248-113616372	GM12878	blood:	n/a	n/a
14	TAF1	chr1:113615478-113616365	SK-N-SH	brain:	n/a	n/a
15	CTCF	chr1:113615260-113615762	LNCaP	prostate:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
16	POLR2A	chr1:113615606-113616376	H1-hESC	embryonic stem cell:	n/a	n/a
17	SMARCB1	chr1:113614679-113616267	K562	blood:	n/a	n/a
18	GATA3	chr1:113615077-113615951	T-47D	breast:	n/a	n/a
19	POLR2A	chr1:113615235-113616437	GM18505	blood:	n/a	n/a
20	CTCF	chr1:113615260-113615917	GM12891	blood:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
21	TEAD4	chr1:113615129-113616422	K562	blood:	n/a	n/a
22	CTCF	chr1:113615252-113615745	HUVEC	blood vessel:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
23	HDAC2	chr1:113615533-113616414	K562	blood:	n/a	n/a
24	RAD21	chr1:113615094-113616039	ECC-1	luminal epithelium:	n/a	chr1:113615384-113615403 chr1:113615389-113615399 chr1:113615124-113615133 chr1:113615387-113615400 chr1:113615389-113615401
25	GABPA	chr1:113615529-113616442	K562	blood:	n/a	n/a
26	RCOR1	chr1:113614768-113616833	K562	blood:	n/a	n/a
27	CTCF	chr1:113615156-113615785	HepG2	liver:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
28	YY1	chr1:113615137-113616358	HCT-116	colon:	n/a	n/a
29	FOS	chr1:113615480-113615838	MCF10A-Er-Src	breast:	n/a	n/a
30	TCF7L2	chr1:113615283-113616339	HCT-116	colon:	n/a	chr1:113615569-113615583
31	POLR2A	chr1:113615181-113616737	K562	blood:	n/a	n/a
32	CTCF	chr1:113615216-113615806	Gliobla	brain:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
33	NFYB	chr1:113615283-113616079	GM12878	blood:	n/a	chr1:113615769-113615783 chr1:113615768-113615783 chr1:113615770-113615785 chr1:113615768-113615783
34	MYBL2	chr1:113615039-113616122	HepG2	liver:	n/a	n/a
35	RCOR1	chr1:113615127-113616263	GM12878	blood:	n/a	n/a
36	POLR2A	chr1:113614912-113616753	K562	blood:	n/a	n/a
37	TBP	chr1:113615303-113616072	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr1:113615191-113615778	T-47D	breast:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
39	RAD21	chr1:113615154-113615881	ECC-1	luminal epithelium:	n/a	chr1:113615384-113615403 chr1:113615389-113615399 chr1:113615387-113615400 chr1:113615389-113615401
40	CTCF	chr1:113614616-113616959	SK-N-SH	brain:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
41	IRF3	chr1:113615361-113615842	GM12878	blood:	n/a	chr1:113615772-113615781
42	RFX5	chr1:113615452-113616244	HepG2	liver:	n/a	chr1:113615771-113615780
43	CTCF	chr1:113615189-113615785	SK-N-SH_RA	brain:	n/a	chr1:113615386-113615399 chr1:113615383-113615401
44	ZNF263	chr1:113615204-113616402	HEK293-T-REx	kidney:	n/a	n/a
45	MAX	chr1:113615238-113616424	K562	blood:	n/a	n/a
46	MAX	chr1:113615200-113616221	MCF-7	breast:	n/a	n/a
47	RAD21	chr1:113615186-113616428	IMR90	lung:	n/a	chr1:113615384-113615403 chr1:113615389-113615399 chr1:113615387-113615400 chr1:113615389-113615401
48	POLR2A	chr1:113615382-113616397	HepG2	liver:	n/a	n/a
49	RAD21	chr1:113615064-113615925	H1-hESC	embryonic stem cell:	n/a	chr1:113615384-113615403 chr1:113615389-113615399 chr1:113615124-113615133 chr1:113615387-113615400 chr1:113615389-113615401
50	KAP1	chr1:113614926-113616457	HEK293	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:113615592-113615642	GM12891	blood:	n/a
2	chr1:113615595-113615645	RPTEC	kidney:	n/a
3	chr1:113615595-113615645	GM12891	blood:	n/a
4	chr1:113615595-113615645	HCF	heart:	n/a
5	chr1:113615592-113615642	HIPEpiC	eye:	n/a
6	chr1:113615592-113615642	NHDF-neo	bronchial:	n/a
7	chr1:113615595-113615645	NB4	blood:	n/a
8	chr1:113615595-113615645	Caco-2	colon:	n/a
9	chr1:113615592-113615642	SAEC	small airway:	n/a
10	chr1:113615595-113615645	BE2_C	brain:	n/a
11	chr1:113615592-113615642	LNCaP	prostate:	n/a
12	chr1:113615595-113615645	NH-A	brain:	n/a
13	chr1:113615592-113615642	T-47D	breast:	n/a
14	chr1:113615592-113615642	GM06990	blood:	n/a
15	chr1:113615595-113615645	BJ	skin:	n/a
16	chr1:113615595-113615645	NT2-D1	testis:	n/a
17	chr1:113615592-113615642	K562	blood:	n/a
18	chr1:113615592-113615642	PFSK-1	brain:	n/a
19	chr1:113615592-113615642	ovcar-3	ovarian:	n/a
20	chr1:113615592-113615642	HCM	heart:	n/a
21	chr1:113615592-113615642	HAEpiC	amniotic membrane:	n/a
22	chr1:113615592-113615642	NH-A	brain:	n/a
23	chr1:113615595-113615645	GM12878	blood:	n/a
24	chr1:113615592-113615642	HCT-116	colon:	n/a
25	chr1:113615595-113615645	AG09319	gingival:	n/a
26	chr1:113615592-113615642	HEEpiC	esophagus:	n/a
27	chr1:113615592-113615642	MCF10A-Er-Src	breast:	n/a
28	chr1:113615595-113615645	HEEpiC	esophagus:	n/a
29	chr1:113615592-113615642	Hepatocyte	liver:	n/a
30	chr1:113615595-113615645	HUVEC	blood vessel:	n/a
31	chr1:113615592-113615642	ProgFib	skin:	n/a
32	chr1:113615592-113615642	MCF-7	breast:	n/a
33	chr1:113615595-113615645	U87	brain:	n/a
34	chr1:113615592-113615642	BE2_C	brain:	n/a
35	chr1:113615592-113615642	U87	brain:	n/a
36	chr1:113615592-113615642	HRCEpiC	kidney:	n/a
37	chr1:113615592-113615642	IMR90	lung:	fetal
38	chr1:113615592-113615642	AG10803	skin:	n/a
39	chr1:113615595-113615645	AG09309	skin:	n/a
40	chr1:113615595-113615645	GM19239	blood:	n/a
41	chr1:113615595-113615645	MCF10A-Er-Src	breast:	n/a
42	chr1:113615595-113615645	HepG2	liver:	n/a
43	chr1:113615595-113615645	SAEC	small airway:	n/a
44	chr1:113615592-113615642	H1-hESC	embryonic stem cell:	embryo
45	chr1:113615595-113615645	HEK293	kidney:	embryo
46	chr1:113615592-113615642	HMEC	breast:	n/a
47	chr1:113615595-113615645	HRPEpiC	eye:	n/a
48	chr1:113615592-113615642	AoSMC	blood vessel:	n/a
49	chr1:113615595-113615645	ProgFib	skin:	n/a
50	chr1:113615595-113615645	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:113614064..113616964-chr1:113668302..113669880,2	K562	blood:
2	chr1:113615409..113616274-chr1:113645815..113646392,2	MCF-7	breast:
3	chr1:113493791..113500715-chr1:113613796..113618010,15	K562	blood:
4	chr1:113615336..113615855-chr17:65821115..65821880,2	MCF-7	breast:
5	chr1:113257532..113261488-chr1:113614794..113617265,4	K562	blood:
6	chr1:113495059..113500488-chr1:113613593..113618010,11	K562	blood:
7	chr1:113258208..113260404-chr1:113615515..113617358,3	MCF-7	breast:
8	chr1:113615529..113616322-chr12:4429997..4430574,2	Hela-S3	cervix:
9	chr1:113615524..113616364-chr13:111365226..111366116,2	Hela-S3	cervix:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC16A1-2	chr1:113615561-113615727	ENSG00000238198
2	lnc-SLC16A1-2	chr1:113614707-113615830	NONHSAT005314

Variant related genes	Relation type
LRIG2	TF binding region
LRIG2	CpG island
ENSG00000226419	Chromatin interaction
ENSG00000171634	Chromatin interaction
ENSG00000153487	Chromatin interaction
ENSG00000237278	Chromatin interaction
ENSG00000078237	Chromatin interaction
ENSG00000134905	Chromatin interaction
ENSG00000261595	Chromatin interaction
ENSG00000155380	Chromatin interaction
ENSG00000155367	Chromatin interaction
ENSG00000198799	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs11102564	1.00[EUR][1000 genomes]
rs11102570	1.00[EUR][1000 genomes]
rs11102572	1.00[EUR][1000 genomes]
rs11102587	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12058371	1.00[EUR][1000 genomes]
rs12061638	1.00[EUR][1000 genomes]
rs12061679	1.00[EUR][1000 genomes]
rs12063125	1.00[EUR][1000 genomes]
rs12063286	1.00[EUR][1000 genomes]
rs12063903	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12063907	1.00[EUR][1000 genomes]
rs12066276	1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12066409	1.00[EUR][1000 genomes]
rs12068534	1.00[EUR][1000 genomes]
rs12068812	1.00[EUR][1000 genomes]
rs12068935	1.00[EUR][1000 genomes]
rs12069411	1.00[EUR][1000 genomes]
rs12069981	1.00[EUR][1000 genomes]
rs12075099	1.00[EUR][1000 genomes]
rs12075714	1.00[EUR][1000 genomes]
rs12078513	1.00[EUR][1000 genomes]
rs12079268	1.00[EUR][1000 genomes]
rs12079494	1.00[EUR][1000 genomes]
rs12079574	1.00[EUR][1000 genomes]
rs12084281	1.00[EUR][1000 genomes]
rs12090558	1.00[EUR][1000 genomes]
rs12093541	1.00[EUR][1000 genomes]
rs1216782	1.00[EUR][1000 genomes]
rs1216786	1.00[EUR][1000 genomes]
rs1216787	1.00[EUR][1000 genomes]
rs17030888	1.00[EUR][1000 genomes]
rs6657174	1.00[EUR][1000 genomes]
rs6676854	1.00[EUR][1000 genomes]
rs6680771	1.00[EUR][1000 genomes]
rs6680949	1.00[EUR][1000 genomes]
rs6699036	1.00[EUR][1000 genomes]
rs72990262	1.00[EUR][1000 genomes]
rs72990279	1.00[EUR][1000 genomes]
rs72990283	1.00[EUR][1000 genomes]
rs72990285	1.00[EUR][1000 genomes]
rs72990286	1.00[EUR][1000 genomes]
rs72996345	1.00[EUR][1000 genomes]
rs7511828	1.00[EUR][1000 genomes]
rs7513355	1.00[EUR][1000 genomes]
rs7518119	1.00[EUR][1000 genomes]
rs7530614	1.00[EUR][1000 genomes]
rs7537295	1.00[EUR][1000 genomes]
rs7540515	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7545283	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002971	chr1:112924725-113740584	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
2	nsv535059	chr1:112924725-113740584	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	166 gene(s)	inside rSNPs	diseases
3	nsv1010276	chr1:113123932-113740584	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	158 gene(s)	inside rSNPs	diseases
4	nsv1012119	chr1:113214869-113759081	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
5	nsv535060	chr1:113214869-113759081	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
6	nsv529238	chr1:113229946-113759080	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	100 gene(s)	inside rSNPs	diseases
7	nsv997426	chr1:113288282-113639507	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
8	nsv999915	chr1:113360145-113684833	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
9	esv18293	chr1:113375437-113852815	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
10	nsv1007045	chr1:113425222-113839910	Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
11	nsv946146	chr1:113567302-113640814	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
12	nsv427719	chr1:113570229-114078388	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
13	nsv508537	chr1:113590343-113635803	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
14	nsv437002	chr1:113592588-113658887	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
15	nsv435694	chr1:113610263-113616294	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 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	chr1:113614800-113616600	Active TSS	Brain Hippocampus Middle	brain
2	chr1:113614800-113617000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
3	chr1:113614800-113617200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr1:113615000-113616000	Active TSS	Primary hematopoietic stem cells	blood
5	chr1:113615000-113616000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr1:113615000-113616400	Active TSS	Stomach Smooth Muscle	stomach
7	chr1:113615000-113616600	Active TSS	Fetal Kidney	kidney
8	chr1:113615000-113616600	Active TSS	Thymus	Thymus
9	chr1:113615000-113616800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr1:113615000-113617000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr1:113615000-113617200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr1:113615000-113617200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr1:113615000-113617200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr1:113615000-113617200	Active TSS	Fetal Muscle Trunk	muscle
15	chr1:113615000-113617200	Active TSS	HSMMtube	muscle
16	chr1:113615000-113617200	Active TSS	NHDF-Ad	bronchial
17	chr1:113615000-113617400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr1:113615000-113617400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr1:113615000-113617400	Active TSS	Colonic Mucosa	Colon
20	chr1:113615000-113617400	Active TSS	NHLF	lung
21	chr1:113615000-113617800	Active TSS	Right Ventricle	heart
22	chr1:113615200-113616400	Active TSS	Primary hematopoietic stem cells short term culture	blood
23	chr1:113615200-113616400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr1:113615200-113616400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
25	chr1:113615200-113616400	Active TSS	Brain Anterior Caudate	brain
26	chr1:113615200-113616400	Active TSS	Fetal Thymus	thymus
27	chr1:113615200-113616600	Active TSS	Cortex derived primary cultured neurospheres	brain
28	chr1:113615200-113616600	Active TSS	Duodenum Smooth Muscle	Duodenum
29	chr1:113615200-113616600	Active TSS	Fetal Brain Female	brain
30	chr1:113615200-113616600	Active TSS	Pancreas	Pancrea
31	chr1:113615200-113616600	Active TSS	HUVEC	blood vessel
32	chr1:113615200-113616800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr1:113615200-113616800	Active TSS	HUES64 Cell Line	embryonic stem cell
34	chr1:113615200-113616800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
35	chr1:113615200-113616800	Active TSS	Muscle Satellite Cultured Cells	--
36	chr1:113615200-113616800	Active TSS	Esophagus	oesophagus
37	chr1:113615200-113616800	Active TSS	Placenta	Placenta
38	chr1:113615200-113616800	Active TSS	Gastric	stomach
39	chr1:113615200-113616800	Active TSS	Lung	lung
40	chr1:113615200-113617000	Active TSS	H1 Cell Line	embryonic stem cell
41	chr1:113615200-113617000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr1:113615200-113617000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr1:113615200-113617000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr1:113615200-113617000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
45	chr1:113615200-113617000	Active TSS	Aorta	Aorta
46	chr1:113615200-113617000	Active TSS	Fetal Heart	heart
47	chr1:113615200-113617000	Active TSS	Ovary	ovary
48	chr1:113615200-113617000	Active TSS	Psoas Muscle	Psoas
49	chr1:113615200-113617000	Active TSS	Small Intestine	intestine
50	chr1:113615200-113617000	Active TSS	GM12878-XiMat	blood

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