Variant report

Variant	rs577510806
Chromosome Location	chr17:16395680-16395681
allele	G/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	ELF1	chr17:16395486-16396004	GM12878	blood:	n/a	chr17:16395574-16395583
2	CTCF	chr17:16395600-16395750	GM12867	blood:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
3	CTCF	chr17:16395660-16395784	GM12891	blood:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
4	E2F6	chr17:16395365-16396146	A549	lung:	n/a	chr17:16395667-16395677 chr17:16395631-16395643 chr17:16395630-16395641
5	CTCF	chr17:16395540-16395690	HCT-116	colon:	n/a	chr17:16395670-16395686 chr17:16395664-16395677 chr17:16395664-16395673
6	CTCF	chr17:16395600-16395750	NHDF-neo	bronchial:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
7	MAZ	chr17:16395616-16395767	Hela-S3	cervix:	n/a	chr17:16395674-16395684
8	CTCF	chr17:16395588-16395771	K562	blood:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
9	MAX	chr17:16395391-16395964	A549	lung:	n/a	chr17:16395674-16395684
10	POLR2A	chr17:16395282-16395795	A549	lung:	n/a	n/a
11	CTCF	chr17:16395600-16395750	HUVEC	blood vessel:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
12	CTCF	chr17:16395680-16395830	GM12864	blood:	n/a	chr17:16395701-16395714 chr17:16395704-16395717
13	RAD21	chr17:16395516-16395848	SK-N-SH_RA	brain:	n/a	chr17:16395703-16395717 chr17:16395701-16395715 chr17:16395671-16395681 chr17:16395705-16395718
14	CTCF	chr17:16395590-16395786	Spleen_OC	spleen:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
15	EGR1	chr17:16395535-16395885	K562	blood:	n/a	chr17:16395742-16395755 chr17:16395742-16395755 chr17:16395745-16395755 chr17:16395745-16395754
16	ELF1	chr17:16395527-16395746	K562	blood:	n/a	chr17:16395574-16395583
17	SIN3A	chr17:16395630-16396014	H1-hESC	embryonic stem cell:	n/a	n/a
18	GTF2F1	chr17:16395633-16395787	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr17:16395640-16395790	GM12868	blood:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
20	CTCF	chr17:16395643-16395755	GM12892	blood:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
21	CTCF	chr17:16395520-16395770	NHDF-neo	bronchial:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
22	CTCF	chr17:16395560-16395710	GM12869	blood:	n/a	chr17:16395670-16395686 chr17:16395664-16395677 chr17:16395664-16395673
23	CTCF	chr17:16395620-16395770	HRPEpiC	eye:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
24	CTCF	chr17:16395640-16395745	K562	blood:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
25	CTCF	chr17:16395640-16395790	AG04449	skin:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
26	CTCF	chr17:16395580-16395730	AG09319	gingival:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
27	POLR2A	chr17:16395538-16395709	A549	lung:	n/a	n/a
28	MAX	chr17:16395520-16395872	HepG2	liver:	n/a	chr17:16395674-16395684
29	CTCF	chr17:16395610-16395762	Pancreas_OC	pancreas:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
30	MAX	chr17:16395473-16395838	K562	blood:	n/a	chr17:16395674-16395684
31	CTCF	chr17:16395633-16395768	GM19238	blood:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
32	CTCF	chr17:16395539-16395892	H1-hESC	embryonic stem cell:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
33	EGR1	chr17:16395235-16395885	ECC-1	luminal epithelium:	n/a	chr17:16395471-16395481 chr17:16395742-16395755 chr17:16395742-16395755 chr17:16395436-16395450 chr17:16395745-16395755 chr17:16395745-16395754
34	RAD21	chr17:16395577-16395783	H1-hESC	embryonic stem cell:	n/a	chr17:16395703-16395717 chr17:16395701-16395715 chr17:16395671-16395681 chr17:16395705-16395718
35	E2F6	chr17:16395217-16395857	K562	blood:	n/a	chr17:16395305-16395315 chr17:16395667-16395677 chr17:16395631-16395643 chr17:16395630-16395641
36	CTCF	chr17:16395640-16395790	HCPEpiC	choroid plexus:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
37	POLR2A	chr17:16395545-16395789	HCT-116	colon:	n/a	n/a
38	ZNF143	chr17:16395603-16395820	H1-hESC	embryonic stem cell:	n/a	chr17:16395703-16395721
39	POLR2A	chr17:16395634-16395688	MCF-7	breast:	n/a	n/a
40	EGR1	chr17:16395568-16395881	H1-hESC	embryonic stem cell:	n/a	chr17:16395742-16395755 chr17:16395742-16395755 chr17:16395745-16395755 chr17:16395745-16395754
41	CTCF	chr17:16395588-16395824	K562	blood:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
42	POLR2A	chr17:16395515-16395747	HCT-116	colon:	n/a	n/a
43	CTCF	chr17:16395600-16395750	GM12871	blood:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
44	ZBTB7A	chr17:16395551-16396066	ECC-1	luminal epithelium:	n/a	chr17:16395670-16395679
45	CTCF	chr17:16395548-16395957	K562	blood:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
46	CTCF	chr17:16395647-16395741	GM10248	blood:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
47	POLR2A	chr17:16395502-16395764	A549	lung:	n/a	n/a
48	CTCF	chr17:16395620-16395770	WERI-Rb-1	eye:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673
49	TBP	chr17:16395624-16395743	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr17:16395662-16395753	Kidney_OC	kidney:	n/a	chr17:16395701-16395714 chr17:16395670-16395686 chr17:16395704-16395717 chr17:16395664-16395677 chr17:16395664-16395673

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:16395644-16395694	AG04449	skin:	fetal
2	chr17:16395644-16395694	IMR90	lung:	fetal
3	chr17:16395644-16395694	HCF	heart:	n/a
4	chr17:16395644-16395694	CMK	blood:	n/a
5	chr17:16395644-16395694	SK-N-SH_RA	brain:	n/a
6	chr17:16395644-16395694	AoSMC	blood vessel:	n/a
7	chr17:16395644-16395694	HEK293	kidney:	embryo
8	chr17:16395644-16395694	HPAEpiC	pulmonary alveolar:	n/a
9	chr17:16395644-16395694	GM19239	blood:	n/a
10	chr17:16395644-16395694	HUVEC	blood vessel:	n/a
11	chr17:16395644-16395694	SAEC	small airway:	n/a
12	chr17:16395644-16395694	BJ	skin:	n/a
13	chr17:16395644-16395694	HEEpiC	esophagus:	n/a
14	chr17:16395644-16395694	A549	lung:	n/a
15	chr17:16395644-16395694	ECC-1	luminal epithelium:	n/a
16	chr17:16395644-16395694	PrEC	prostate:	n/a
17	chr17:16395644-16395694	HRCEpiC	kidney:	n/a
18	chr17:16395644-16395694	HMEC	breast:	n/a
19	chr17:16395644-16395694	RPTEC	kidney:	n/a
20	chr17:16395644-16395694	PFSK-1	brain:	n/a
21	chr17:16395644-16395694	HL-60	blood:	n/a
22	chr17:16395644-16395694	HIPEpiC	eye:	n/a
23	chr17:16395644-16395694	Caco-2	colon:	n/a
24	chr17:16395644-16395694	NH-A	brain:	n/a
25	chr17:16395644-16395694	HRE	kidney:	n/a
26	chr17:16395644-16395694	GM12891	blood:	n/a
27	chr17:16395644-16395694	GM12878	blood:	n/a
28	chr17:16395644-16395694	GM06990	blood:	n/a
29	chr17:16395644-16395694	T-47D	breast:	n/a
30	chr17:16395644-16395694	AG09319	gingival:	n/a
31	chr17:16395644-16395694	HCPEpiC	choroid plexus:	n/a
32	chr17:16395644-16395694	HNPCEpiC	eye:	n/a
33	chr17:16395644-16395694	SK-N-SH	brain:	n/a
34	chr17:16395644-16395694	NHBE	bronchial:	n/a
35	chr17:16395644-16395694	SKMC	muscle:	n/a
36	chr17:16395644-16395694	HAEpiC	amniotic membrane:	n/a
37	chr17:16395644-16395694	U87	brain:	n/a
38	chr17:16395644-16395694	Jurkat	blood:	n/a
39	chr17:16395644-16395694	LNCaP	prostate:	n/a
40	chr17:16395644-16395694	SK-N-MC	brain:	n/a
41	chr17:16395644-16395694	PANC-1	pancreas:	n/a
42	chr17:16395644-16395694	AG04450	lung:	fetal
43	chr17:16395644-16395694	AG10803	skin:	n/a
44	chr17:16395644-16395694	MCF-7	breast:	n/a
45	chr17:16395644-16395694	AG09309	skin:	n/a
46	chr17:16395644-16395694	HCM	heart:	n/a
47	chr17:16395644-16395694	GM12892	blood:	n/a
48	chr17:16395644-16395694	HRPEpiC	eye:	n/a
49	chr17:16395644-16395694	ovcar-3	ovarian:	n/a
50	chr17:16395644-16395694	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:16340606..16343390-chr17:16393092..16395708,2	MCF-7	breast:
2	chr17:16116365..16119285-chr17:16395133..16397532,2	K562	blood:

Variant related genes	Relation type
FAM211A	TF binding region
FAM211A	CpG island
ENSG00000141027	Chromatin interaction
ENSG00000175061	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

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	nsv934185	chr17:15552960-16551197	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	190 gene(s)	inside rSNPs	diseases
2	esv3330182	chr17:15652014-16569534	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
3	esv3446844	chr17:15654843-16572246	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
4	nsv1063459	chr17:15804228-16543593	Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
5	nsv1063764	chr17:16171649-16662914	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	120 gene(s)	inside rSNPs	diseases
6	nsv1061463	chr17:16245878-16490691	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh 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	99 gene(s)	inside rSNPs	diseases
7	nsv543216	chr17:16245878-16490691	Strong transcription Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	99 gene(s)	inside rSNPs	diseases
8	nsv428668	chr17:16265210-16455285	Weak transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	89 gene(s)	inside rSNPs	diseases
9	nsv1063941	chr17:16357086-16424098	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
10	esv1794587	chr17:16389498-16395680	Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
11	nsv1058448	chr17:16389870-16926287	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
12	esv3323619	chr17:16394252-16396800	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
13	esv3344255	chr17:16394352-16396600	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
14	esv20869	chr17:16394909-16395705	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
15	nsv574490	chr17:16394936-16395680	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
16	nsv574492	chr17:16394987-16395680	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
17	nsv574493	chr17:16395083-16395680	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
18	nsv574494	chr17:16395083-16398555	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:16394000-16396200	Active TSS	H9 Cell Line	embryonic stem cell
2	chr17:16394200-16396000	Active TSS	Primary T cells from cord blood	blood
3	chr17:16394400-16395800	Active TSS	Fetal Intestine Large	intestine
4	chr17:16394400-16395800	Active TSS	Small Intestine	intestine
5	chr17:16394400-16396000	Active TSS	Pancreatic Islets	Pancreatic Islet
6	chr17:16394400-16396000	Bivalent/Poised TSS	NHLF	lung
7	chr17:16394600-16395800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr17:16394600-16395800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr17:16394600-16395800	Bivalent/Poised TSS	Muscle Satellite Cultured Cells	--
10	chr17:16394600-16395800	Active TSS	Aorta	Aorta
11	chr17:16394600-16395800	Active TSS	Rectal Mucosa Donor 29	rectum
12	chr17:16394600-16395800	Active TSS	Sigmoid Colon	Sigmoid Colon
13	chr17:16394600-16396000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
14	chr17:16394600-16396000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr17:16394600-16396000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr17:16394600-16396000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr17:16394600-16396000	Active TSS	Brain Cingulate Gyrus	brain
18	chr17:16394600-16396200	Bivalent/Poised TSS	HepG2	liver
19	chr17:16394800-16395800	Active TSS	H1 Cell Line	embryonic stem cell
20	chr17:16394800-16395800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr17:16394800-16395800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr17:16394800-16395800	Active TSS	HUES48 Cell Line	embryonic stem cell
23	chr17:16394800-16395800	Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr17:16394800-16395800	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
25	chr17:16394800-16395800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr17:16394800-16395800	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
27	chr17:16394800-16395800	Active TSS	Brain Inferior Temporal Lobe	brain
28	chr17:16394800-16395800	Active TSS	Duodenum Smooth Muscle	Duodenum
29	chr17:16394800-16395800	Active TSS	Esophagus	oesophagus
30	chr17:16394800-16395800	Weak transcription	Fetal Heart	heart
31	chr17:16394800-16395800	Active TSS	Fetal Intestine Small	intestine
32	chr17:16394800-16395800	Active TSS	Pancreas	Pancrea
33	chr17:16394800-16395800	Active TSS	Psoas Muscle	Psoas
34	chr17:16394800-16395800	Bivalent/Poised TSS	Thymus	Thymus
35	chr17:16394800-16395800	Active TSS	NH-A	brain
36	chr17:16394800-16396000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr17:16394800-16396000	Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr17:16394800-16396000	Active TSS	iPS-15b Cell Line	embryonic stem cell
39	chr17:16394800-16396000	Active TSS	iPS-18 Cell Line	embryonic stem cell
40	chr17:16394800-16396000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr17:16394800-16396000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
42	chr17:16394800-16396000	Active TSS	Duodenum Mucosa	Duodenum
43	chr17:16394800-16396000	Active TSS	Ovary	ovary
44	chr17:16394800-16396000	Active TSS	Skeletal Muscle Male	skeletal muscle
45	chr17:16394800-16396000	Active TSS	Hela-S3	cervix
46	chr17:16394800-16396000	Bivalent/Poised TSS	HSMM	muscle
47	chr17:16394800-16396200	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr17:16394800-16396200	Active TSS	Brain Angular Gyrus	brain
49	chr17:16394800-16396200	Active TSS	Brain Anterior Caudate	brain
50	chr17:16394800-16396200	Active TSS	Colon Smooth Muscle	Colon

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