Variant report

Variant	esv3370567
Chromosome Location	chr9:101866606-101868779
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:532)
CpG islands
(count:245)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:532 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr9:101867869-101867955	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr9:101866811-101867054	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr9:101867600-101868122	GM12878	blood:	n/a	chr9:101867766-101867775 chr9:101867970-101867979 chr9:101867775-101867788 chr9:101867967-101867976 chr9:101867965-101867978 chr9:101868009-101868018
4	BCLAF1	chr9:101866869-101867270	GM12878	blood:	n/a	chr9:101867129-101867142 chr9:101866898-101866911
5	BHLHE40	chr9:101866744-101867136	K562	blood:	n/a	n/a
6	BHLHE40	chr9:101867709-101868007	K562	blood:	n/a	n/a
7	BHLHE40	chr9:101866750-101868278	GM12878	blood:	n/a	chr9:101867148-101867164 chr9:101867228-101867244 chr9:101867263-101867279
8	BRCA1	chr9:101866848-101867249	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr9:101866565-101867308	K562	blood:	n/a	n/a
10	CCNT2	chr9:101866964-101868342	K562	blood:	n/a	chr9:101867173-101867182 chr9:101867129-101867138
11	CEBPB	chr9:101866816-101867434	Hela-S3	cervix:	n/a	n/a
12	CEBPD	chr9:101867285-101867540	HepG2	liver:	n/a	n/a
13	CHD1	chr9:101865310-101870084	IMR90	lung:	n/a	n/a
14	CHD2	chr9:101866745-101867534	Hela-S3	cervix:	n/a	n/a
15	CHD2	chr9:101867787-101868084	Hela-S3	cervix:	n/a	n/a
16	CHD2	chr9:101867058-101867387	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr9:101866840-101867467	GM12878	blood:	n/a	n/a
18	CHD2	chr9:101866781-101867427	K562	blood:	n/a	n/a
19	CREB1	chr9:101867581-101867934	A549	lung:	n/a	n/a
20	CREB1	chr9:101866739-101867539	A549	lung:	n/a	n/a
21	CREB1	chr9:101866965-101867693	GM12878	blood:	n/a	n/a
22	CTBP2	chr9:101866466-101867366	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr9:101867000-101867150	NHEK	skin:	n/a	chr9:101867131-101867144
24	CTCF	chr9:101866920-101867070	A549	lung:	n/a	n/a
25	CTCF	chr9:101866880-101867030	AG04449	skin:	n/a	n/a
26	CTCF	chr9:101867000-101867250	GM12869	blood:	n/a	chr9:101867131-101867144
27	CTCF	chr9:101866912-101866940	GM19239	blood:	n/a	n/a
28	CTCF	chr9:101866900-101867050	AG04450	lung:	n/a	n/a
29	CTCF	chr9:101867080-101867230	Hela-S3	cervix:	n/a	chr9:101867131-101867144
30	CTCF	chr9:101866620-101866770	AG04449	skin:	n/a	n/a
31	CTCF	chr9:101866980-101867130	GM12874	blood:	n/a	n/a
32	CTCF	chr9:101866989-101867055	Lung_OC	lung:	n/a	n/a
33	CTCF	chr9:101867657-101867928	K562	blood:	n/a	n/a
34	CTCF	chr9:101868100-101868250	GM12871	blood:	n/a	chr9:101868208-101868221
35	CTCF	chr9:101866740-101866890	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr9:101866900-101867050	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr9:101866920-101867070	GM12873	blood:	n/a	n/a
38	CTCF	chr9:101866980-101867130	GM12867	blood:	n/a	n/a
39	CTCF	chr9:101866840-101866990	GM12872	blood:	n/a	n/a
40	CTCF	chr9:101866960-101867110	SAEC	small airway:	n/a	n/a
41	CTCF	chr9:101867640-101867790	GM12867	blood:	n/a	n/a
42	CTCF	chr9:101866980-101867130	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr9:101867020-101867170	SK-N-SH_RA	brain:	n/a	chr9:101867131-101867144
44	CTCF	chr9:101866960-101867110	HCM	heart:	n/a	n/a
45	CTCF	chr9:101867020-101867170	GM12874	blood:	n/a	chr9:101867131-101867144
46	CTCF	chr9:101867876-101867932	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chr9:101866740-101866890	GM12875	blood:	n/a	n/a
48	CTCF	chr9:101866920-101867070	GM12869	blood:	n/a	n/a
49	CTCF	chr9:101866920-101867070	K562	blood:	n/a	n/a
50	CTCF	chr9:101867860-101868010	GM12865	blood:	n/a	chr9:101867974-101867984

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:101866995-101867045	SKMC	muscle:	n/a
2	chr9:101866995-101867045	SKMC	muscle:	n/a
3	chr9:101867456-101867506	SK-N-SH_RA	brain:	n/a
4	chr9:101868296-101868346	Jurkat	blood:	n/a
5	chr9:101867990-101868040	AG09319	gingival:	n/a
6	chr9:101867990-101868040	CMK	blood:	n/a
7	chr9:101866995-101867045	SK-N-SH_RA	brain:	n/a
8	chr9:101866995-101867045	NH-A	brain:	n/a
9	chr9:101867456-101867506	PANC-1	pancreas:	n/a
10	chr9:101867456-101867506	SK-N-SH	brain:	n/a
11	chr9:101866995-101867045	ovcar-3	ovarian:	n/a
12	chr9:101867456-101867506	SAEC	small airway:	n/a
13	chr9:101867990-101868040	HIPEpiC	eye:	n/a
14	chr9:101867456-101867506	HCF	heart:	n/a
15	chr9:101867456-101867506	Jurkat	blood:	n/a
16	chr9:101867990-101868040	RPTEC	kidney:	n/a
17	chr9:101866995-101867045	AG09319	gingival:	n/a
18	chr9:101868296-101868346	HAEpiC	amniotic membrane:	n/a
19	chr9:101868296-101868346	PFSK-1	brain:	n/a
20	chr9:101867456-101867506	Hepatocyte	liver:	n/a
21	chr9:101867456-101867506	HL-60	blood:	n/a
22	chr9:101867456-101867506	GM12892	blood:	n/a
23	chr9:101868296-101868346	HRE	kidney:	n/a
24	chr9:101866995-101867045	HRCEpiC	kidney:	n/a
25	chr9:101867456-101867506	SK-N-MC	brain:	n/a
26	chr9:101868296-101868346	GM06990	blood:	n/a
27	chr9:101868296-101868346	ovcar-3	ovarian:	n/a
28	chr9:101867990-101868040	Hela-S3	cervix:	n/a
29	chr9:101867990-101868040	MCF-7	breast:	n/a
30	chr9:101867990-101868040	NB4	blood:	n/a
31	chr9:101868296-101868346	AG04449	skin:	fetal
32	chr9:101866995-101867045	Hela-S3	cervix:	n/a
33	chr9:101867990-101868040	HCT-116	colon:	n/a
34	chr9:101867456-101867506	K562	blood:	n/a
35	chr9:101867990-101868040	HepG2	liver:	n/a
36	chr9:101867990-101868040	SKMC	muscle:	n/a
37	chr9:101867990-101868040	HUVEC	blood vessel:	n/a
38	chr9:101868296-101868346	K562	blood:	n/a
39	chr9:101868296-101868346	HCT-116	colon:	n/a
40	chr9:101868296-101868346	PrEC	prostate:	n/a
41	chr9:101867990-101868040	HL-60	blood:	n/a
42	chr9:101868296-101868346	IMR90	lung:	fetal
43	chr9:101867990-101868040	PANC-1	pancreas:	n/a
44	chr9:101868296-101868346	NHDF-neo	bronchial:	n/a
45	chr9:101867990-101868040	NH-A	brain:	n/a
46	chr9:101868296-101868346	HRCEpiC	kidney:	n/a
47	chr9:101867990-101868040	HAEpiC	amniotic membrane:	n/a
48	chr9:101867990-101868040	AoSMC	blood vessel:	n/a
49	chr9:101867456-101867506	GM12878	blood:	n/a
50	chr9:101867456-101867506	ProgFib	skin:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:101866534..101869508-chr9:101907295..101910821,3	MCF-7	breast:
2	chr9:101717329..101720202-chr9:101867499..101869138,2	K562	blood:
3	chr7:37959940..37960879-chr9:101867147..101867963,2	Hela-S3	cervix:
4	chr6:89790459..89790962-chr9:101867304..101867920,2	Hela-S3	cervix:
5	chr14:74959586..74960164-chr9:101867006..101867798,2	Hela-S3	cervix:
6	chr9:101866361..101869341-chr9:101886452..101890095,3	MCF-7	breast:
7	chr9:101632178..101635172-chr9:101866283..101867803,2	K562	blood:
8	chr9:101865542..101868917-chr9:101887238..101894962,8	MCF-7	breast:
9	chr9:101608539..101611289-chr9:101866226..101869142,2	MCF-7	breast:
10	chr7:44162667..44163261-chr9:101867005..101867915,2	Hela-S3	cervix:
11	chr15:99190239..99192114-chr9:101866946..101869163,2	MCF-7	breast:

No data

Variant related genes	Relation type
TGFBR1	TF binding region
TGFBR1	CpG island
ENSG00000086289	chromatin interactions
ENSG00000119655	chromatin interactions
ENSG00000106799	chromatin interactions
ENSG00000119514	chromatin interactions
ENSG00000259424	chromatin interactions
ENSG00000146278	chromatin interactions
ENSG00000252942	chromatin interactions
ENSG00000267026	chromatin interactions
ENSG00000106628	chromatin interactions

Extended variants
information (count: 72 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:72 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558180433	chr9:101866708-101866709	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs151163899	chr9:101866732-101866733	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs540553691	chr9:101866770-101866771	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs560805985	chr9:101866782-101866783	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs34899971	chr9:101866794-101866795	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs11568743	chr9:101866798-101866799	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs542766348	chr9:101866805-101866806	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs562752150	chr9:101866819-101866820	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs530515072	chr9:101866839-101866840	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs550311054	chr9:101866866-101866867	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs563907112	chr9:101866899-101866900	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs546309320	chr9:101866943-101866944	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs369616060	chr9:101867017-101867018	Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs11568744	chr9:101867023-101867024	Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs532980039	chr9:101867034-101867035	Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs566487284	chr9:101867060-101867061	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs368151277	chr9:101867097-101867098	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs546299138	chr9:101867103-101867104	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs10819636	chr9:101867112-101867113	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs36204372	chr9:101867157-101867158	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs535755302	chr9:101867165-101867166	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs549186944	chr9:101867173-101867174	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs569119226	chr9:101867184-101867185	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs12554198	chr9:101867209-101867210	Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs538319956	chr9:101867259-101867260	Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs200309220	chr9:101867393-101867394	Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
27	rs11568745	chr9:101867397-101867398	Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs578044154	chr9:101867428-101867429	Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs201177231	chr9:101867471-101867472	Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs199624653	chr9:101867478-101867479	Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs200224304	chr9:101867486-101867487	Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs538831129	chr9:101867538-101867539	Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs554578321	chr9:101867544-101867545	Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs11466445	chr9:101867556-101867557	Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs190034323	chr9:101867640-101867641	Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs574235087	chr9:101867667-101867668	Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs542954487	chr9:101867712-101867713	Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs113289904	chr9:101867768-101867769	Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs562742004	chr9:101867790-101867791	Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs576260157	chr9:101867801-101867802	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs543890383	chr9:101867815-101867816	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs564178663	chr9:101867892-101867893	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs535074216	chr9:101868011-101868012	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs10760668	chr9:101868075-101868076	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs375183634	chr9:101868086-101868087	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs559929964	chr9:101868090-101868091	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs146935075	chr9:101868125-101868126	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs574944389	chr9:101868173-101868174	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs182168589	chr9:101868185-101868186	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs11568746	chr9:101868208-101868209	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Nicotine dependence	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:101865200-101867000	Flanking Active TSS	A549	lung
2	chr9:101865800-101866800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
3	chr9:101865800-101866800	Enhancers	Sigmoid Colon	Sigmoid Colon
4	chr9:101865800-101867000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr9:101865800-101867000	Flanking Active TSS	Duodenum Mucosa	Duodenum
6	chr9:101865800-101867000	Flanking Active TSS	Fetal Intestine Small	intestine
7	chr9:101865800-101867000	Flanking Active TSS	HepG2	liver
8	chr9:101865800-101867000	Flanking Active TSS	NHEK	skin
9	chr9:101866000-101867000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
10	chr9:101866000-101867000	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr9:101866000-101867000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr9:101866000-101867000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr9:101866000-101867000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr9:101866000-101867000	Flanking Active TSS	Adipose Nuclei	Adipose
15	chr9:101866000-101867000	Flanking Active TSS	Osteobl	bone
16	chr9:101866000-101868600	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr9:101866000-101868600	Active TSS	H1 Cell Line	embryonic stem cell
18	chr9:101866000-101868600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr9:101866000-101868800	Active TSS	H9 Cell Line	embryonic stem cell
20	chr9:101866200-101866800	Flanking Active TSS	Fetal Stomach	stomach
21	chr9:101866200-101866800	Flanking Active TSS	NHLF	lung
22	chr9:101866200-101867000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:101866200-101867000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr9:101866200-101867000	Flanking Active TSS	Primary T cells from cord blood	blood
25	chr9:101866200-101867000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
26	chr9:101866200-101867000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr9:101866200-101867000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
28	chr9:101866200-101867000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
29	chr9:101866200-101867000	Flanking Active TSS	Fetal Brain Male	brain
30	chr9:101866200-101867000	Flanking Active TSS	K562	blood
31	chr9:101866200-101867000	Flanking Active TSS	NH-A	brain
32	chr9:101866200-101867200	Flanking Active TSS	Primary hematopoietic stem cells	blood
33	chr9:101866200-101867200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
34	chr9:101866200-101867200	Active TSS	Fetal Kidney	kidney
35	chr9:101866200-101867200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
36	chr9:101866200-101868400	Active TSS	iPS-15b Cell Line	embryonic stem cell
37	chr9:101866200-101868400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr9:101866200-101868400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr9:101866200-101868400	Active TSS	Brain Anterior Caudate	brain
40	chr9:101866200-101868600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
41	chr9:101866200-101868600	Active TSS	Breast Myoepithelial Primary Cells	Breast
42	chr9:101866200-101868600	Active TSS	NHDF-Ad	bronchial
43	chr9:101866400-101866800	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr9:101866400-101866800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr9:101866400-101866800	Flanking Active TSS	Brain Cingulate Gyrus	brain
46	chr9:101866400-101866800	Flanking Active TSS	Brain Hippocampus Middle	brain
47	chr9:101866400-101866800	Flanking Active TSS	Brain Substantia Nigra	brain
48	chr9:101866400-101866800	Flanking Active TSS	Fetal Heart	heart
49	chr9:101866400-101866800	Flanking Active TSS	Gastric	stomach
50	chr9:101866400-101866800	Flanking Active TSS	Left Ventricle	heart

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