Variant report

Variant	rs370018667
Chromosome Location	chr9:117266584-117266585
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:116)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:116 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr9:117266445-117268397	Hela-S3	cervix:	n/a	n/a
2	MAX	chr9:117266228-117268472	MCF-7	breast:	n/a	chr9:117267822-117267832
3	RAD21	chr9:117266549-117266826	K562	blood:	n/a	n/a
4	E2F4	chr9:117266451-117267466	K562	blood:	n/a	chr9:117267394-117267403
5	MAX	chr9:117266530-117267332	K562	blood:	n/a	n/a
6	E2F6	chr9:117266390-117267454	K562	blood:	n/a	chr9:117267394-117267403
7	MXI1	chr9:117266350-117268844	IMR90	lung:	n/a	n/a
8	ZBTB7A	chr9:117266563-117266859	K562	blood:	n/a	n/a
9	CTCF	chr9:117266577-117266928	MCF-7	breast:	n/a	n/a
10	POLR2A	chr9:117266474-117266946	PANC-1	pancreas:	n/a	n/a
11	TBL1XR1	chr9:117265888-117267332	K562	blood:	n/a	n/a
12	CTCF	chr9:117266440-117266710	A549	lung:	n/a	n/a
13	YY1	chr9:117266560-117266772	HCT-116	colon:	n/a	n/a
14	SMC3	chr9:117266525-117266850	K562	blood:	n/a	n/a
15	TEAD4	chr9:117266548-117267054	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr9:117266581-117266974	Fibrobl	skin:	n/a	n/a
17	CBX3	chr9:117266581-117266867	K562	blood:	n/a	n/a
18	CCNT2	chr9:117266501-117268153	K562	blood:	n/a	chr9:117267531-117267540 chr9:117267963-117267972
19	BHLHE40	chr9:117266390-117267004	K562	blood:	n/a	n/a
20	MAX	chr9:117266431-117268463	A549	lung:	n/a	chr9:117267822-117267832
21	TRIM28	chr9:117266493-117267012	K562	blood:	n/a	n/a
22	CTCF	chr9:117266484-117266874	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr9:117266540-117266690	GM06990	blood:	n/a	n/a
24	HCFC1	chr9:117266369-117267264	K562	blood:	n/a	n/a
25	PML	chr9:117266559-117266959	K562	blood:	n/a	n/a
26	RAD21	chr9:117266471-117266977	A549	lung:	n/a	n/a
27	CTCF	chr9:117266580-117266730	WI-38	lung:	n/a	n/a
28	MAX	chr9:117266416-117267013	MCF-7	breast:	n/a	n/a
29	MYC	chr9:117265974-117268214	K562	blood:	n/a	chr9:117267822-117267832
30	MAX	chr9:117266377-117268454	HCT-116	colon:	n/a	chr9:117267822-117267832
31	ZNF143	chr9:117266120-117266894	K562	blood:	n/a	n/a
32	CTCF	chr9:117266576-117266912	NHEK	skin:	n/a	n/a
33	CTCF	chr9:117266579-117266881	MCF-7	breast:	n/a	n/a
34	CTCF	chr9:117266580-117266730	HPAF	blood vessel:	n/a	n/a
35	RCOR1	chr9:117265246-117267292	K562	blood:	n/a	n/a
36	CTCF	chr9:117266517-117266913	GM12878	blood:	n/a	n/a
37	CTCF	chr9:117266580-117266730	GM12872	blood:	n/a	n/a
38	CTCF	chr9:117266573-117266961	MCF-7	breast:	n/a	n/a
39	MAZ	chr9:117266295-117268608	IMR90	lung:	n/a	chr9:117267822-117267832
40	CTCF	chr9:117266480-117266630	BE2_C	brain:	n/a	n/a
41	ZNF143	chr9:117266480-117266902	H1-hESC	embryonic stem cell:	n/a	n/a
42	JUND	chr9:117266298-117266747	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr9:117266567-117266876	IMR90	lung:	n/a	n/a
44	ZNF143	chr9:117266256-117266893	GM12878	blood:	n/a	n/a
45	TBP	chr9:117266330-117266908	K562	blood:	n/a	n/a
46	E2F6	chr9:117266527-117267403	A549	lung:	n/a	chr9:117267394-117267403
47	CHD2	chr9:117266564-117268088	K562	blood:	n/a	chr9:117267819-117267829
48	POLR2A	chr9:117266516-117267376	K562	blood:	n/a	n/a
49	SMARCB1	chr9:117266437-117268402	Hela-S3	cervix:	n/a	n/a
50	MAZ	chr9:117266365-117268308	K562	blood:	n/a	chr9:117267822-117267832

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:117266580-117266630	HRPEpiC	eye:	n/a
2	chr9:117266580-117266630	SK-N-SH	brain:	n/a
3	chr9:117266580-117266630	NH-A	brain:	n/a
4	chr9:117266580-117266630	NT2-D1	testis:	n/a
5	chr9:117266580-117266630	ECC-1	luminal epithelium:	n/a
6	chr9:117266580-117266630	GM12891	blood:	n/a
7	chr9:117266580-117266630	HCPEpiC	choroid plexus:	n/a
8	chr9:117266580-117266630	A549	lung:	n/a
9	chr9:117266580-117266630	GM19239	blood:	n/a
10	chr9:117266580-117266630	SK-N-SH_RA	brain:	n/a
11	chr9:117266580-117266630	U87	brain:	n/a
12	chr9:117266580-117266630	PANC-1	pancreas:	n/a
13	chr9:117266580-117266630	GM06990	blood:	n/a
14	chr9:117266580-117266630	HAEpiC	amniotic membrane:	n/a
15	chr9:117266580-117266630	NHBE	bronchial:	n/a
16	chr9:117266580-117266630	K562	blood:	n/a
17	chr9:117266580-117266630	HPAEpiC	pulmonary alveolar:	n/a
18	chr9:117266580-117266630	NB4	blood:	n/a
19	chr9:117266580-117266630	HCF	heart:	n/a
20	chr9:117266580-117266630	AG04450	lung:	fetal
21	chr9:117266580-117266630	RPTEC	kidney:	n/a
22	chr9:117266580-117266630	BJ	skin:	n/a
23	chr9:117266580-117266630	HepG2	liver:	n/a
24	chr9:117266580-117266630	HIPEpiC	eye:	n/a
25	chr9:117266580-117266630	HMEC	breast:	n/a
26	chr9:117266580-117266630	HEEpiC	esophagus:	n/a
27	chr9:117266580-117266630	SAEC	small airway:	n/a
28	chr9:117266580-117266630	Hela-S3	cervix:	n/a
29	chr9:117266580-117266630	T-47D	breast:	n/a
30	chr9:117266580-117266630	MCF-7	breast:	n/a
31	chr9:117266580-117266630	MCF10A-Er-Src	breast:	n/a
32	chr9:117266580-117266630	HRE	kidney:	n/a
33	chr9:117266580-117266630	HEK293	kidney:	embryo
34	chr9:117266580-117266630	LNCaP	prostate:	n/a
35	chr9:117266580-117266630	PrEC	prostate:	n/a
36	chr9:117266580-117266630	BE2_C	brain:	n/a
37	chr9:117266580-117266630	AG09319	gingival:	n/a
38	chr9:117266580-117266630	Hepatocyte	liver:	n/a
39	chr9:117266580-117266630	CMK	blood:	n/a
40	chr9:117266580-117266630	IMR90	lung:	fetal
41	chr9:117266580-117266630	GM12892	blood:	n/a
42	chr9:117266580-117266630	SK-N-MC	brain:	n/a
43	chr9:117266580-117266630	HRCEpiC	kidney:	n/a
44	chr9:117266580-117266630	AG10803	skin:	n/a
45	chr9:117266580-117266630	PFSK-1	brain:	n/a
46	chr9:117266580-117266630	HCT-116	colon:	n/a
47	chr9:117266580-117266630	NHDF-neo	bronchial:	n/a
48	chr9:117266580-117266630	H1-hESC	embryonic stem cell:	embryo
49	chr9:117266580-117266630	AG04449	skin:	fetal
50	chr9:117266580-117266630	ovcar-3	ovarian:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:117264990..117269271-chr9:117348762..117354798,9	MCF-7	breast:
2	chr9:117157540..117162429-chr9:117265948..117270229,5	K562	blood:
3	chr9:117263907..117271703-chr9:117371218..117376768,10	MCF-7	breast:
4	chr9:117265762..117270088-chr9:117348229..117352933,7	K562	blood:
5	chr9:117263014..117265983-chr9:117266031..117267744,5	MCF-7	breast:
6	chr9:117263501..117265677-chr9:117266069..117268440,2	K562	blood:
7	chr9:117264854..117270088-chr9:117348300..117353117,7	K562	blood:
8	chr9:117262731..117268447-chr9:117369704..117378306,14	K562	blood:
9	chr9:117251818..117256354-chr9:117261161..117269778,10	MCF-7	breast:
10	chr9:117265687..117267555-chr9:117372704..117375188,3	MCF-7	breast:
11	chr9:117266234..117268906-chr9:117372659..117377270,6	K562	blood:
12	chr9:117264226..117271307-chr9:117346303..117355535,28	MCF-7	breast:

No data

Variant related genes	Relation type
DFNB31	TF binding region
DFNB31	CpG island
ENSG00000157693	Chromatin interaction
ENSG00000271214	Chromatin interaction
ENSG00000235119	Chromatin interaction
ENSG00000095397	Chromatin interaction
ENSG00000136888	Chromatin interaction
ENSG00000201749	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430093	chr9:116330446-117325446	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
2	esv2422396	chr9:116792944-117354862	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	155 gene(s)	inside rSNPs	diseases
3	esv2422492	chr9:116811294-117366643	Genic enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	155 gene(s)	inside rSNPs	diseases
4	nsv1051544	chr9:116944940-117443031	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
5	nsv540203	chr9:116944940-117443031	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
6	nsv1048093	chr9:116945025-117456210	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
7	nsv1050991	chr9:116953739-117442999	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
8	nsv1046311	chr9:116953739-117447142	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
9	nsv1052877	chr9:116953739-117456210	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
10	nsv1039681	chr9:116953739-117457158	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
11	nsv1051987	chr9:116955841-117453668	Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
12	nsv1044374	chr9:116955841-117460150	Genic enhancers Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
13	nsv466534	chr9:116956268-117455810	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
14	nsv615234	chr9:116956268-117455810	Enhancers Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
15	nsv1048817	chr9:116957958-117456210	Flanking Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
16	nsv615235	chr9:116958144-117367061	ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
17	nsv615236	chr9:116958144-117455810	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
18	nsv466535	chr9:116958144-117456175	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription 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 miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
19	nsv615237	chr9:116958144-117456175	Strong transcription Active TSS Genic enhancers Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
20	nsv615238	chr9:116958144-117458475	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
21	nsv430094	chr9:116958446-117456446	Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
22	nsv1053756	chr9:116975934-117443031	Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
23	nsv540204	chr9:116975934-117443031	Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
24	nsv1047704	chr9:116978041-117399362	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
25	nsv540205	chr9:116978041-117399362	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
26	nsv530950	chr9:117009156-117399361	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
27	nsv916139	chr9:117009169-117399454	Weak transcription Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
28	nsv530951	chr9:117032675-117439804	Flanking Active TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
29	nsv831693	chr9:117116450-117281895	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
30	esv3398432	chr9:117265956-117268504	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117240000-117266600	Weak transcription	Gastric	stomach
2	chr9:117245000-117266600	Weak transcription	Right Atrium	heart
3	chr9:117259800-117267200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr9:117263600-117267000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr9:117263600-117268400	Active TSS	Brain Inferior Temporal Lobe	brain
6	chr9:117263800-117266800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
7	chr9:117263800-117267000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr9:117264000-117266800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr9:117264200-117266600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr9:117264200-117266600	Enhancers	Placenta Amnion	Placenta Amnion
11	chr9:117264200-117268200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
12	chr9:117264200-117268400	Active TSS	Brain Angular Gyrus	brain
13	chr9:117264400-117266600	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr9:117264400-117266800	Flanking Active TSS	K562	blood
15	chr9:117264600-117266600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr9:117264600-117268200	Active TSS	Brain Cingulate Gyrus	brain
17	chr9:117264600-117268400	Active TSS	Brain Substantia Nigra	brain
18	chr9:117264600-117268600	Active TSS	Pancreatic Islets	Pancreatic Islet
19	chr9:117265000-117266600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr9:117265000-117266800	Flanking Active TSS	Thymus	Thymus
21	chr9:117265000-117267000	Flanking Active TSS	Duodenum Mucosa	Duodenum
22	chr9:117265200-117266600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr9:117265200-117267000	Weak transcription	Small Intestine	intestine
24	chr9:117265200-117267000	Flanking Active TSS	HepG2	liver
25	chr9:117265200-117267600	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
26	chr9:117265400-117266600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr9:117265400-117266600	Weak transcription	Osteobl	bone
28	chr9:117265400-117266800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
29	chr9:117265400-117266800	Enhancers	Primary B cells from peripheral blood	blood
30	chr9:117265400-117267000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr9:117265400-117268600	Bivalent/Poised TSS	Fetal Brain Female	brain
32	chr9:117265600-117266600	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr9:117265600-117267000	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr9:117265800-117266600	Enhancers	Fetal Kidney	kidney
35	chr9:117265800-117266800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
36	chr9:117265800-117267200	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
37	chr9:117265800-117267600	Flanking Active TSS	HMEC	breast
38	chr9:117265800-117268200	Active TSS	Duodenum Smooth Muscle	Duodenum
39	chr9:117266000-117266600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr9:117266000-117266600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr9:117266000-117267000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr9:117266000-117267600	Flanking Active TSS	Adipose Nuclei	Adipose
43	chr9:117266000-117268000	Active TSS	Primary T helper cells PMA-I stimulated	--
44	chr9:117266000-117268000	Active TSS	Rectal Mucosa Donor 29	rectum
45	chr9:117266000-117268600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
46	chr9:117266200-117266600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
47	chr9:117266200-117266600	Flanking Active TSS	Brain Anterior Caudate	brain
48	chr9:117266200-117266600	Bivalent/Poised TSS	Brain Germinal Matrix	brain
49	chr9:117266200-117266600	Active TSS	NH-A	brain
50	chr9:117266200-117267000	Flanking Active TSS	Fetal Lung	lung

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