Variant report

Variant	rs2479016
Chromosome Location	chr6:2245345-2245346
allele	A/G
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	EGR1	chr6:2245320-2245973	ECC-1	luminal epithelium:	n/a	chr6:2245725-2245738 chr6:2245839-2245852 chr6:2245726-2245740 chr6:2245725-2245738 chr6:2245725-2245738 chr6:2245728-2245737
2	BHLHE40	chr6:2245104-2246828	HepG2	liver:	n/a	chr6:2245835-2245851 chr6:2246639-2246655
3	ELF1	chr6:2245216-2245617	K562	blood:	n/a	n/a
4	USF2	chr6:2245293-2245376	HepG2	liver:	n/a	n/a
5	CREB1	chr6:2244995-2246217	H1-hESC	embryonic stem cell:	n/a	n/a
6	E2F6	chr6:2245155-2246196	K562	blood:	n/a	chr6:2245769-2245780 chr6:2245844-2245853
7	POLR2A	chr6:2245118-2246278	H1-neurons	neurons:	n/a	n/a
8	POLR2A	chr6:2245173-2247056	HepG2	liver:	n/a	n/a
9	POLR2A	chr6:2245124-2246952	Hela-S3	cervix:	n/a	n/a
10	CREB1	chr6:2245164-2246300	HepG2	liver:	n/a	n/a
11	POLR2A	chr6:2245228-2246376	GM12878	blood:	n/a	n/a
12	MXI1	chr6:2245136-2247021	HepG2	liver:	n/a	n/a
13	MYC	chr6:2245324-2246722	K562	blood:	n/a	n/a
14	MAX	chr6:2245112-2246364	A549	lung:	n/a	n/a
15	USF2	chr6:2245155-2245351	H1-hESC	embryonic stem cell:	n/a	n/a
16	MAX	chr6:2245103-2246123	H1-hESC	embryonic stem cell:	n/a	n/a
17	SIN3AK20	chr6:2245334-2246073	K562	blood:	n/a	n/a
18	MAZ	chr6:2245246-2246669	GM12878	blood:	n/a	n/a
19	POLR2A	chr6:2245163-2246342	GM12878	blood:	n/a	n/a
20	POLR2A	chr6:2245134-2246849	GM12892	blood:	n/a	n/a
21	JUN	chr6:2244606-2247054	K562	blood:	n/a	chr6:2246619-2246627 chr6:2246618-2246628 chr6:2246618-2246628 chr6:2246321-2246331 chr6:2246994-2247005 chr6:2246618-2246628 chr6:2246618-2246628
22	TCF12	chr6:2245171-2246934	ECC-1	luminal epithelium:	n/a	chr6:2246635-2246645
23	TAF1	chr6:2245090-2246252	HepG2	liver:	n/a	n/a
24	TFAP2A	chr6:2245289-2246776	Hela-S3	cervix:	n/a	chr6:2246002-2246016 chr6:2246000-2246015 chr6:2246628-2246640 chr6:2246002-2246016 chr6:2246618-2246627 chr6:2246002-2246016 chr6:2245840-2245852
25	MAX	chr6:2245124-2246838	K562	blood:	n/a	n/a
26	ELF1	chr6:2245277-2246222	K562	blood:	n/a	n/a
27	RELA	chr6:2245295-2246743	GM18951	blood:	n/a	n/a
28	USF1	chr6:2245117-2245402	H1-hESC	embryonic stem cell:	n/a	n/a
29	MAX	chr6:2244555-2247000	HepG2	liver:	n/a	n/a
30	POLR2A	chr6:2245306-2246970	GM12878	blood:	n/a	n/a
31	POLR2A	chr6:2245169-2246726	GM19193	blood:	n/a	n/a
32	CHD2	chr6:2245278-2246147	K562	blood:	n/a	chr6:2245845-2245855
33	POLR2A	chr6:2245213-2246768	GM18526	blood:	n/a	n/a
34	POLR2A	chr6:2245168-2246730	GM12892	blood:	n/a	n/a
35	CTBP2	chr6:2245171-2245939	H1-hESC	embryonic stem cell:	n/a	n/a
36	EGR1	chr6:2245188-2246110	HCT-116	colon:	n/a	chr6:2245725-2245738 chr6:2245839-2245852 chr6:2245726-2245740 chr6:2245725-2245738 chr6:2245725-2245738 chr6:2245728-2245737
37	MYBL2	chr6:2244975-2247172	HepG2	liver:	n/a	n/a
38	ZEB1	chr6:2244538-2247191	HepG2	liver:	n/a	chr6:2245548-2245557 chr6:2245548-2245560 chr6:2245266-2245278
39	MAX	chr6:2245012-2246867	MCF-7	breast:	n/a	n/a
40	SIN3A	chr6:2245169-2245794	GM12878	blood:	n/a	n/a
41	POLR2A	chr6:2245288-2246642	GM15510	blood:	n/a	n/a
42	POLR2A	chr6:2245141-2246823	GM18505	blood:	n/a	n/a
43	ZNF143	chr6:2245261-2245413	H1-hESC	embryonic stem cell:	n/a	n/a
44	TBP	chr6:2245191-2245377	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr6:2245081-2246979	MCF10A-Er-Src	breast:	n/a	n/a
46	MAZ	chr6:2245153-2246827	K562	blood:	n/a	n/a
47	POLR2A	chr6:2245304-2246312	Gliobla	brain:	n/a	n/a
48	POLR2A	chr6:2245269-2246911	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr6:2244995-2245562	HepG2	liver:	n/a	n/a
50	EGR1	chr6:2245305-2245931	H1-hESC	embryonic stem cell:	n/a	chr6:2245725-2245738 chr6:2245839-2245852 chr6:2245726-2245740 chr6:2245725-2245738 chr6:2245725-2245738 chr6:2245728-2245737

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:2245327-2245377	AG09309	skin:	n/a
2	chr6:2245327-2245377	SK-N-SH	brain:	n/a
3	chr6:2245327-2245377	HCT-116	colon:	n/a
4	chr6:2245327-2245377	AG04450	lung:	fetal
5	chr6:2245327-2245377	T-47D	breast:	n/a
6	chr6:2245327-2245377	HUVEC	blood vessel:	n/a
7	chr6:2245327-2245377	RPTEC	kidney:	n/a
8	chr6:2245327-2245377	GM06990	blood:	n/a
9	chr6:2245327-2245377	AG10803	skin:	n/a
10	chr6:2245327-2245377	GM12891	blood:	n/a
11	chr6:2245327-2245377	HMEC	breast:	n/a
12	chr6:2245327-2245377	HepG2	liver:	n/a
13	chr6:2245327-2245377	HCPEpiC	choroid plexus:	n/a
14	chr6:2245327-2245377	PFSK-1	brain:	n/a
15	chr6:2245327-2245377	PrEC	prostate:	n/a
16	chr6:2245327-2245377	K562	blood:	n/a
17	chr6:2245327-2245377	NT2-D1	testis:	n/a
18	chr6:2245327-2245377	SK-N-SH_RA	brain:	n/a
19	chr6:2245327-2245377	HL-60	blood:	n/a
20	chr6:2245327-2245377	MCF-7	breast:	n/a
21	chr6:2245327-2245377	HPAEpiC	pulmonary alveolar:	n/a
22	chr6:2245327-2245377	U87	brain:	n/a
23	chr6:2245327-2245377	HNPCEpiC	eye:	n/a
24	chr6:2245327-2245377	LNCaP	prostate:	n/a
25	chr6:2245327-2245377	AoSMC	blood vessel:	n/a
26	chr6:2245327-2245377	NHDF-neo	bronchial:	n/a
27	chr6:2245327-2245377	Hela-S3	cervix:	n/a
28	chr6:2245327-2245377	IMR90	lung:	fetal
29	chr6:2245327-2245377	HIPEpiC	eye:	n/a
30	chr6:2245327-2245377	SKMC	muscle:	n/a
31	chr6:2245327-2245377	Hepatocyte	liver:	n/a
32	chr6:2245327-2245377	SAEC	small airway:	n/a
33	chr6:2245327-2245377	ovcar-3	ovarian:	n/a
34	chr6:2245327-2245377	ProgFib	skin:	n/a
35	chr6:2245327-2245377	HRCEpiC	kidney:	n/a
36	chr6:2245327-2245377	BJ	skin:	n/a
37	chr6:2245327-2245377	SK-N-MC	brain:	n/a
38	chr6:2245327-2245377	GM19239	blood:	n/a
39	chr6:2245327-2245377	HRE	kidney:	n/a
40	chr6:2245327-2245377	GM12878	blood:	n/a
41	chr6:2245327-2245377	AG09319	gingival:	n/a
42	chr6:2245327-2245377	ECC-1	luminal epithelium:	n/a
43	chr6:2245327-2245377	NB4	blood:	n/a
44	chr6:2245327-2245377	H1-hESC	embryonic stem cell:	embryo
45	chr6:2245327-2245377	HEK293	kidney:	embryo
46	chr6:2245327-2245377	MCF10A-Er-Src	breast:	n/a
47	chr6:2245327-2245377	HRPEpiC	eye:	n/a
48	chr6:2245327-2245377	NHBE	bronchial:	n/a
49	chr6:2245327-2245377	AG04449	skin:	fetal
50	chr6:2245327-2245377	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:2235011..2238207-chr6:2241335..2245707,5	K562	blood:
2	chr17:56707904..56710357-chr6:2244331..2245870,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WRNIP1-3	chr6:2244111-2245348	ENSG00000246005

Variant related genes	Relation type
GMDS-AS1	TF binding region
GMDS-AS1	CpG island
ENSG00000212195	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1196389	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1196390	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1196393	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1196394	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1196396	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1486274	0.82[AMR][1000 genomes]
rs1629950	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1684153	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs234914	0.81[EUR][1000 genomes]
rs234920	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2450301	0.82[AMR][1000 genomes]
rs2450303	0.82[AMR][1000 genomes]
rs2450306	0.80[AMR][1000 genomes]
rs2478999	0.81[AMR][1000 genomes]
rs2479003	0.80[AMR][1000 genomes]
rs2479015	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2505665	0.82[AMR][1000 genomes]
rs2505668	0.81[AMR][1000 genomes]
rs2505669	0.81[AMR][1000 genomes]
rs335963	0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6596876	0.82[AMR][1000 genomes]
rs9328086	0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9392382	0.80[AMR][1000 genomes]
rs9501828	0.80[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530548	chr6:1441421-2351608	Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	nsv931941	chr6:1768439-2246781	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	nsv531295	chr6:1773436-2724986	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
4	nsv1025814	chr6:2064629-2308518	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
5	nsv538098	chr6:2064629-2308518	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
6	nsv1030181	chr6:2071210-2308657	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS 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	46 gene(s)	inside rSNPs	diseases
7	nsv538099	chr6:2071210-2308657	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
8	nsv883388	chr6:2093432-2514911	Strong transcription Enhancers ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	62 gene(s)	inside rSNPs	diseases
9	nsv883389	chr6:2093432-2776303	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	87 gene(s)	inside rSNPs	diseases
10	nsv830573	chr6:2120985-2263646	Bivalent Enhancer Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
11	nsv1022623	chr6:2199666-2267750	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
12	nsv538100	chr6:2199666-2267750	ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
13	nsv1022166	chr6:2199666-2320800	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
14	nsv1017174	chr6:2213893-2340529	Strong transcription Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
15	nsv1033201	chr6:2218647-2308518	ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
16	nsv538101	chr6:2218647-2308518	Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
17	nsv1026678	chr6:2230064-2261297	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	n/a
18	esv2763526	chr6:2230064-2311916	Weak transcription Bivalent/Poised TSS Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:2243200-2246800	Active TSS	Duodenum Smooth Muscle	Duodenum
2	chr6:2243200-2246800	Active TSS	Gastric	stomach
3	chr6:2244200-2246600	Active TSS	Sigmoid Colon	Sigmoid Colon
4	chr6:2244200-2246600	Active TSS	Stomach Mucosa	stomach
5	chr6:2244200-2247000	Active TSS	Colonic Mucosa	Colon
6	chr6:2244400-2245400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:2244400-2245400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr6:2244400-2245600	Flanking Active TSS	Dnd41	blood
9	chr6:2244400-2246600	Active TSS	Small Intestine	intestine
10	chr6:2244400-2247000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr6:2244600-2245400	Flanking Active TSS	Primary T cells from cord blood	blood
12	chr6:2244600-2245400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
13	chr6:2244600-2245400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr6:2244600-2245400	Flanking Active TSS	Brain Anterior Caudate	brain
15	chr6:2244600-2245600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
16	chr6:2244600-2245600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr6:2244600-2245600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
18	chr6:2244600-2245800	Flanking Active TSS	Primary B cells from cord blood	blood
19	chr6:2244600-2246200	Active TSS	Fetal Intestine Small	intestine
20	chr6:2244600-2246200	Active TSS	Fetal Lung	lung
21	chr6:2244600-2246400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
22	chr6:2244600-2246600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr6:2244600-2246600	Active TSS	Fetal Kidney	kidney
24	chr6:2244600-2246600	Active TSS	NHDF-Ad	bronchial
25	chr6:2244600-2247200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:2244600-2247200	Active TSS	Pancreatic Islets	Pancreatic Islet
27	chr6:2244800-2245400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
28	chr6:2244800-2245400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
29	chr6:2244800-2245400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
30	chr6:2244800-2245400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
31	chr6:2244800-2245400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr6:2244800-2245400	Flanking Active TSS	Liver	Liver
33	chr6:2244800-2245400	Flanking Active TSS	Fetal Muscle Leg	muscle
34	chr6:2244800-2245400	Flanking Active TSS	Rectal Smooth Muscle	rectum
35	chr6:2244800-2245400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
36	chr6:2244800-2245400	Flanking Active TSS	HUVEC	blood vessel
37	chr6:2244800-2245400	Flanking Active TSS	NH-A	brain
38	chr6:2244800-2245600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr6:2244800-2245600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr6:2244800-2245600	Flanking Active TSS	Adipose Nuclei	Adipose
41	chr6:2244800-2246200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr6:2244800-2246200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr6:2244800-2246400	Active TSS	Brain Cingulate Gyrus	brain
44	chr6:2244800-2246400	Bivalent/Poised TSS	HepG2	liver
45	chr6:2244800-2246600	Active TSS	H1 Cell Line	embryonic stem cell
46	chr6:2244800-2246600	Active TSS	Breast Myoepithelial Primary Cells	Breast
47	chr6:2244800-2246600	Active TSS	Aorta	Aorta
48	chr6:2244800-2246800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
49	chr6:2244800-2246800	Active TSS	H9 Cell Line	embryonic stem cell
50	chr6:2244800-2246800	Active TSS	Esophagus	oesophagus

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