Variant report

Variant	rs2291944
Chromosome Location	chr5:1799321-1799322
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	TBP	chr5:1799280-1802309	K562	blood:	n/a	n/a
2	POLR2A	chr5:1799035-1800569	GM12891	blood:	n/a	n/a
3	POLR2A	chr5:1799154-1802375	MCF10A-Er-Src	breast:	n/a	n/a
4	YY1	chr5:1799100-1800180	HepG2	liver:	n/a	chr5:1799972-1799991 chr5:1799980-1799988 chr5:1799967-1799989 chr5:1799984-1799993 chr5:1799987-1799996 chr5:1799979-1799989 chr5:1799977-1799989 chr5:1799985-1799996
5	POLR2A	chr5:1799089-1802204	HepG2	liver:	n/a	n/a
6	SMC3	chr5:1799133-1799573	Hela-S3	cervix:	n/a	n/a
7	POLR2A	chr5:1799155-1802340	Hela-S3	cervix:	n/a	n/a
8	POLR2A	chr5:1798976-1802439	Hela-S3	cervix:	n/a	n/a
9	SMARCB1	chr5:1799152-1800762	Hela-S3	cervix:	n/a	n/a
10	CHD2	chr5:1799288-1799510	Hela-S3	cervix:	n/a	n/a
11	WRNIP1	chr5:1799128-1799409	GM12878	blood:	n/a	n/a
12	POLR2A	chr5:1799115-1799346	H1-hESC	embryonic stem cell:	n/a	n/a
13	POLR2A	chr5:1799292-1800719	GM12878	blood:	n/a	n/a
14	CTCF	chr5:1799280-1799430	HRE	kidney:	n/a	n/a
15	MXI1	chr5:1799161-1802292	Hela-S3	cervix:	n/a	chr5:1800777-1800786 chr5:1799999-1800008 chr5:1800586-1800595
16	ELF1	chr5:1799302-1799649	K562	blood:	n/a	chr5:1799592-1799604 chr5:1799521-1799533
17	RCOR1	chr5:1799142-1799484	HepG2	liver:	n/a	n/a
18	POLR2A	chr5:1799185-1801993	NB4	blood:	n/a	n/a
19	FOXA2	chr5:1799187-1799510	HepG2	liver:	n/a	n/a
20	MAX	chr5:1799055-1801992	HepG2	liver:	n/a	chr5:1800000-1800009 chr5:1800776-1800789 chr5:1799998-1800011 chr5:1800779-1800788 chr5:1799988-1799998 chr5:1800776-1800789 chr5:1799999-1800010 chr5:1799985-1799995 chr5:1800778-1800787 chr5:1800000-1800009 chr5:1800778-1800787 chr5:1800777-1800788 chr5:1800777-1800788 chr5:1800778-1800787
21	CHD2	chr5:1799275-1800150	HepG2	liver:	n/a	n/a
22	MAX	chr5:1799053-1802002	HepG2	liver:	n/a	chr5:1800000-1800009 chr5:1800776-1800789 chr5:1799998-1800011 chr5:1800779-1800788 chr5:1799988-1799998 chr5:1800776-1800789 chr5:1799999-1800010 chr5:1799985-1799995 chr5:1800778-1800787 chr5:1800000-1800009 chr5:1800778-1800787 chr5:1800777-1800788 chr5:1800777-1800788 chr5:1800778-1800787
23	POLR2A	chr5:1799095-1802307	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr5:1799240-1799626	GM12878	blood:	n/a	n/a
25	MAX	chr5:1799111-1802062	NB4	blood:	n/a	chr5:1800000-1800009 chr5:1800776-1800789 chr5:1799998-1800011 chr5:1800779-1800788 chr5:1799988-1799998 chr5:1800776-1800789 chr5:1799999-1800010 chr5:1799985-1799995 chr5:1800778-1800787 chr5:1800000-1800009 chr5:1800778-1800787 chr5:1800777-1800788 chr5:1800777-1800788 chr5:1800778-1800787
26	MAFK	chr5:1799176-1799471	K562	blood:	n/a	n/a
27	HEY1	chr5:1799100-1801013	K562	blood:	n/a	chr5:1800043-1800058 chr5:1799985-1800000 chr5:1799511-1799526
28	POLR2A	chr5:1799084-1800764	U87	brain:	n/a	n/a
29	MAZ	chr5:1798962-1800702	IMR90	lung:	n/a	chr5:1800000-1800009 chr5:1799998-1800011 chr5:1799988-1799998 chr5:1799999-1800010 chr5:1799985-1799995 chr5:1800000-1800009
30	SIN3AK20	chr5:1799318-1800262	K562	blood:	n/a	n/a
31	RCOR1	chr5:1799227-1799474	K562	blood:	n/a	n/a
32	MAZ	chr5:1799221-1800606	GM12878	blood:	n/a	chr5:1800000-1800009 chr5:1799998-1800011 chr5:1799988-1799998 chr5:1799999-1800010 chr5:1799985-1799995 chr5:1800000-1800009
33	POLR2A	chr5:1799145-1802285	K562	blood:	n/a	n/a
34	MAZ	chr5:1799229-1801962	Hela-S3	cervix:	n/a	chr5:1800000-1800009 chr5:1800776-1800789 chr5:1799998-1800011 chr5:1800779-1800788 chr5:1799988-1799998 chr5:1800776-1800789 chr5:1799999-1800010 chr5:1799985-1799995 chr5:1800778-1800787 chr5:1800000-1800009 chr5:1800778-1800787 chr5:1800777-1800788 chr5:1800777-1800788 chr5:1800778-1800787
35	HEY1	chr5:1799251-1800998	HepG2	liver:	n/a	chr5:1800043-1800058 chr5:1799985-1800000 chr5:1799511-1799526
36	MYC	chr5:1799117-1802271	NB4	blood:	n/a	chr5:1800000-1800009 chr5:1800776-1800789 chr5:1799998-1800011 chr5:1800779-1800788 chr5:1799988-1799998 chr5:1800776-1800789 chr5:1799999-1800010 chr5:1799985-1799995 chr5:1800778-1800787 chr5:1800000-1800009 chr5:1800778-1800787 chr5:1800777-1800788 chr5:1800777-1800788 chr5:1800778-1800787
37	POLR2A	chr5:1799253-1801934	GM12892	blood:	n/a	n/a
38	TBP	chr5:1799254-1799521	HepG2	liver:	n/a	n/a
39	POLR2A	chr5:1799222-1801887	GM18951	blood:	n/a	n/a
40	POLR2A	chr5:1799060-1802320	HepG2	liver:	n/a	n/a
41	BHLHE40	chr5:1799269-1799457	GM12878	blood:	n/a	n/a
42	MXI1	chr5:1798908-1802411	SK-N-SH	brain:	n/a	chr5:1800777-1800786 chr5:1799999-1800008 chr5:1800586-1800595
43	TBP	chr5:1799284-1799464	H1-hESC	embryonic stem cell:	n/a	n/a
44	MAX	chr5:1799086-1802321	K562	blood:	n/a	chr5:1800000-1800009 chr5:1800776-1800789 chr5:1799998-1800011 chr5:1800779-1800788 chr5:1799988-1799998 chr5:1800776-1800789 chr5:1799999-1800010 chr5:1799985-1799995 chr5:1800778-1800787 chr5:1800000-1800009 chr5:1800778-1800787 chr5:1800777-1800788 chr5:1800777-1800788 chr5:1800778-1800787
45	POLR2A	chr5:1799066-1802383	Hela-S3	cervix:	n/a	n/a
46	RXRA	chr5:1799243-1799566	HepG2	liver:	n/a	chr5:1799396-1799412
47	POLR2A	chr5:1799212-1802281	K562	blood:	n/a	n/a
48	MAX	chr5:1799213-1801739	GM12878	blood:	n/a	chr5:1800000-1800009 chr5:1800776-1800789 chr5:1799998-1800011 chr5:1800779-1800788 chr5:1799988-1799998 chr5:1800776-1800789 chr5:1799999-1800010 chr5:1799985-1799995 chr5:1800778-1800787 chr5:1800000-1800009 chr5:1800778-1800787 chr5:1800777-1800788 chr5:1800777-1800788 chr5:1800778-1800787
49	MAZ	chr5:1799314-1801915	K562	blood:	n/a	chr5:1800000-1800009 chr5:1800776-1800789 chr5:1799998-1800011 chr5:1800779-1800788 chr5:1799988-1799998 chr5:1800776-1800789 chr5:1799999-1800010 chr5:1799985-1799995 chr5:1800778-1800787 chr5:1800000-1800009 chr5:1800778-1800787 chr5:1800777-1800788 chr5:1800777-1800788 chr5:1800778-1800787
50	EP300	chr5:1799225-1799405	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:7387129..7388004-chr5:1798958..1799931,2	Hela-S3	cervix:
2	chr17:56707453..56709236-chr5:1799018..1801500,2	MCF-7	breast:
3	chr5:1777867..1779395-chr5:1796687..1799686,2	K562	blood:
4	chr5:1793765..1806799-chr5:1879445..1889322,45	MCF-7	breast:
5	chr5:1796457..1805482-chr5:1878036..1885786,21	MCF-7	breast:
6	chr5:1798942..1801341-chr5:1879541..1882987,3	K562	blood:
7	chr5:1745339..1747054-chr5:1797446..1799846,2	K562	blood:

Variant related genes	Relation type
NDUFS6	TF binding region
ENSG00000113430	Chromatin interaction
ENSG00000249326	Chromatin interaction
ENSG00000249116	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000181222	Chromatin interaction
ENSG00000174282	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs11133910	0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs11133911	0.96[ASN][1000 genomes]
rs11133912	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13187162	0.94[ASN][1000 genomes]
rs1845288	0.99[ASN][1000 genomes]
rs1873926	0.91[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2242412	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2276986	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34233926	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35380881	0.96[ASN][1000 genomes]
rs3756343	0.95[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs3756345	0.95[CHB][hapmap];0.90[JPT][hapmap];0.97[ASN][1000 genomes]
rs3756346	0.95[CHB][hapmap];0.90[JPT][hapmap];0.97[ASN][1000 genomes]
rs3776141	0.95[CHB][hapmap];0.90[JPT][hapmap];0.96[ASN][1000 genomes]
rs3776142	0.95[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs3776143	0.97[ASN][1000 genomes]
rs3776144	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.87[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3776145	0.99[ASN][1000 genomes]
rs3776146	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3776149	0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs3822364	0.97[ASN][1000 genomes]
rs4147769	0.99[ASN][1000 genomes]
rs4147770	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4147772	0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs4147773	0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs4975731	0.83[GIH][hapmap]
rs4975845	0.86[CHB][hapmap];0.89[CHD][hapmap];0.85[JPT][hapmap];0.87[ASN][1000 genomes]
rs4975847	0.84[JPT][hapmap]
rs4975848	0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs4975849	0.95[CHB][hapmap];0.90[JPT][hapmap];0.97[ASN][1000 genomes]
rs4975851	0.95[CHB][hapmap];0.83[JPT][hapmap];0.96[ASN][1000 genomes]
rs4975852	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs4975853	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs55883912	0.98[ASN][1000 genomes]
rs6555012	0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6863367	0.97[ASN][1000 genomes]
rs7702843	0.90[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];0.88[GIH][hapmap];0.85[JPT][hapmap];0.83[MKK][hapmap];0.87[TSI][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs972890	0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs972891	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];1.00[ASN][1000 genomes]
rs972892	0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs974722	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933805	chr5:1450724-1941619	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Weak transcription 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 miRNA target site	96 gene(s)	inside rSNPs	diseases
2	nsv817407	chr5:1495354-2191460	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	107 gene(s)	inside rSNPs	diseases
3	nsv1034552	chr5:1658338-1856553	Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	44 gene(s)	inside rSNPs	diseases
4	nsv537606	chr5:1658338-1856553	Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	44 gene(s)	inside rSNPs	diseases
5	nsv1033147	chr5:1717303-1815821	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
6	nsv869236	chr5:1719263-2259100	Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
7	nsv1020703	chr5:1724199-1814288	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
8	nsv537608	chr5:1724199-1814288	Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
9	nsv1024133	chr5:1736691-1826510	Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
10	nsv537609	chr5:1736691-1826510	Genic enhancers Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	40 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	chr5:1791000-1800200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr5:1798400-1802400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr5:1798600-1799400	Transcr. at gene 5' and 3'	Rectal Smooth Muscle	rectum
4	chr5:1798800-1799400	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr5:1798800-1799400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr5:1798800-1799400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
7	chr5:1798800-1799400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr5:1798800-1799400	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--
9	chr5:1798800-1799400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
10	chr5:1798800-1799400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr5:1798800-1799400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr5:1798800-1799400	Flanking Active TSS	Brain Hippocampus Middle	brain
13	chr5:1798800-1799400	Flanking Active TSS	Colon Smooth Muscle	Colon
14	chr5:1798800-1799400	Flanking Active TSS	Fetal Brain Female	brain
15	chr5:1798800-1799600	Flanking Active TSS	Colonic Mucosa	Colon
16	chr5:1798800-1799600	Flanking Active TSS	Stomach Smooth Muscle	stomach
17	chr5:1798800-1800600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr5:1798800-1800600	Active TSS	Primary T helper cells PMA-I stimulated	--
19	chr5:1798800-1802200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr5:1798800-1802400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr5:1798800-1802800	Active TSS	HUES48 Cell Line	embryonic stem cell
22	chr5:1799000-1799400	Flanking Active TSS	H1 Cell Line	embryonic stem cell
23	chr5:1799000-1799400	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr5:1799000-1799400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr5:1799000-1799400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr5:1799000-1799400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
27	chr5:1799000-1799400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
28	chr5:1799000-1799400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr5:1799000-1799400	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr5:1799000-1799400	Flanking Active TSS	Primary T cells from cord blood	blood
31	chr5:1799000-1799400	Flanking Active TSS	Primary hematopoietic stem cells	blood
32	chr5:1799000-1799400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
33	chr5:1799000-1799400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
34	chr5:1799000-1799400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
35	chr5:1799000-1799400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr5:1799000-1799400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
37	chr5:1799000-1799400	Flanking Active TSS	Adipose Nuclei	Adipose
38	chr5:1799000-1799400	Flanking Active TSS	Liver	Liver
39	chr5:1799000-1799400	Flanking Active TSS	Brain Angular Gyrus	brain
40	chr5:1799000-1799400	Flanking Active TSS	Brain Anterior Caudate	brain
41	chr5:1799000-1799400	Flanking Active TSS	Brain Cingulate Gyrus	brain
42	chr5:1799000-1799400	Flanking Active TSS	Brain Germinal Matrix	brain
43	chr5:1799000-1799400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
44	chr5:1799000-1799400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
45	chr5:1799000-1799400	Flanking Active TSS	Brain Substantia Nigra	brain
46	chr5:1799000-1799400	Flanking Active TSS	Duodenum Mucosa	Duodenum
47	chr5:1799000-1799400	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
48	chr5:1799000-1799400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
49	chr5:1799000-1799400	Flanking Active TSS	Fetal Brain Male	brain
50	chr5:1799000-1799400	Enhancers	Fetal Heart	heart

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