Variant report

Variant	nsv615785
Chromosome Location	chr9:136932396-136933825
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:518)
CpG islands
(count:244)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:518 , 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	ATF3	chr9:136933038-136933297	HepG2	liver:	n/a	n/a
2	ATF3	chr9:136933031-136933250	GM12878	blood:	n/a	n/a
3	ATF3	chr9:136933012-136933307	K562	blood:	n/a	n/a
4	BACH1	chr9:136933484-136933780	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCLAF1	chr9:136933360-136933667	GM12878	blood:	n/a	chr9:136933461-136933469
6	BHLHE40	chr9:136933422-136934055	K562	blood:	n/a	n/a
7	BHLHE40	chr9:136933092-136934053	GM12878	blood:	n/a	n/a
8	BHLHE40	chr9:136933072-136933749	HepG2	liver:	n/a	n/a
9	BRCA1	chr9:136933691-136933981	Hela-S3	cervix:	n/a	n/a
10	CCNT2	chr9:136932401-136933919	K562	blood:	n/a	n/a
11	CEBPB	chr9:136933565-136933920	Hela-S3	cervix:	n/a	n/a
12	CEBPD	chr9:136932958-136933989	HepG2	liver:	n/a	n/a
13	CHD1	chr9:136933083-136933907	GM12878	blood:	n/a	n/a
14	CHD1	chr9:136932575-136932582	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD1	chr9:136932144-136932794	GM12878	blood:	n/a	n/a
16	CHD2	chr9:136933731-136933733	K562	blood:	n/a	n/a
17	CHD2	chr9:136932488-136932765	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr9:136933453-136933925	GM12878	blood:	n/a	n/a
19	CHD2	chr9:136932564-136932569	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr9:136933001-136933935	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr9:136933803-136933929	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr9:136932476-136932659	GM12878	blood:	n/a	n/a
23	CREB1	chr9:136932946-136933969	A549	lung:	n/a	n/a
24	CREB1	chr9:136933002-136933277	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr9:136932982-136933458	K562	blood:	n/a	n/a
26	CREB1	chr9:136932972-136933284	HepG2	liver:	n/a	n/a
27	CREB1	chr9:136932875-136934008	HepG2	liver:	n/a	n/a
28	CREB1	chr9:136932983-136933411	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr9:136933039-136933252	A549	lung:	n/a	n/a
30	CREB1	chr9:136932986-136933447	GM12878	blood:	n/a	n/a
31	CTCF	chr9:136933800-136933950	GM06990	blood:	n/a	n/a
32	CTCF	chr9:136933741-136933891	GM19238	blood:	n/a	n/a
33	CTCF	chr9:136933800-136933950	AG09319	gingival:	n/a	n/a
34	CTCF	chr9:136933800-136933950	HepG2	liver:	n/a	n/a
35	CTCF	chr9:136933718-136933891	GM19240	blood:	n/a	n/a
36	CTCF	chr9:136933755-136933847	GM12878	blood:	n/a	n/a
37	CTCF	chr9:136933706-136933866	GM10266	blood:	n/a	n/a
38	CTCF	chr9:136933707-136933925	GM12891	blood:	n/a	n/a
39	CTCF	chr9:136933735-136933898	GM13977	blood:	n/a	n/a
40	CTCF	chr9:136933780-136933930	GM12864	blood:	n/a	n/a
41	CTCF	chr9:136933672-136933902	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr9:136933760-136933910	BJ	skin:	n/a	n/a
43	CTCF	chr9:136933736-136933873	MCF-7	breast:	n/a	n/a
44	CTCF	chr9:136933759-136933890	NHEK	skin:	n/a	n/a
45	CTCF	chr9:136933740-136933890	GM06990	blood:	n/a	n/a
46	CTCF	chr9:136933720-136933870	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr9:136933760-136933910	Caco-2	colon:	n/a	n/a
48	CTCF	chr9:136933360-136933510	SAEC	small airway:	n/a	n/a
49	CTCF	chr9:136933680-136933830	GM12865	blood:	n/a	n/a
50	CTCF	chr9:136933700-136933850	GM12871	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:136932424-136932474	SK-N-MC	brain:	n/a
2	chr9:136932722-136932772	LNCaP	prostate:	n/a
3	chr9:136932424-136932474	PrEC	prostate:	n/a
4	chr9:136932722-136932772	BE2_C	brain:	n/a
5	chr9:136932722-136932772	AG04449	skin:	fetal
6	chr9:136933664-136933714	GM19239	blood:	n/a
7	chr9:136933664-136933714	ProgFib	skin:	n/a
8	chr9:136932424-136932474	GM19239	blood:	n/a
9	chr9:136933818-136933868	LNCaP	prostate:	n/a
10	chr9:136933664-136933714	H1-hESC	embryonic stem cell:	embryo
11	chr9:136933818-136933868	Caco-2	colon:	n/a
12	chr9:136932722-136932772	HepG2	liver:	n/a
13	chr9:136932722-136932772	HAEpiC	amniotic membrane:	n/a
14	chr9:136933818-136933868	HCT-116	colon:	n/a
15	chr9:136932722-136932772	MCF-7	breast:	n/a
16	chr9:136933664-136933714	HCF	heart:	n/a
17	chr9:136933664-136933714	AG10803	skin:	n/a
18	chr9:136933664-136933714	HMEC	breast:	n/a
19	chr9:136933818-136933868	RPTEC	kidney:	n/a
20	chr9:136933664-136933714	PrEC	prostate:	n/a
21	chr9:136933818-136933868	H1-hESC	embryonic stem cell:	embryo
22	chr9:136933818-136933868	ECC-1	luminal epithelium:	n/a
23	chr9:136933818-136933868	GM19239	blood:	n/a
24	chr9:136932424-136932474	LNCaP	prostate:	n/a
25	chr9:136933664-136933714	HepG2	liver:	n/a
26	chr9:136933664-136933714	PFSK-1	brain:	n/a
27	chr9:136933818-136933868	SK-N-MC	brain:	n/a
28	chr9:136933664-136933714	Jurkat	blood:	n/a
29	chr9:136933818-136933868	MCF-7	breast:	n/a
30	chr9:136933664-136933714	HCM	heart:	n/a
31	chr9:136933818-136933868	MCF10A-Er-Src	breast:	n/a
32	chr9:136933818-136933868	HIPEpiC	eye:	n/a
33	chr9:136933818-136933868	ovcar-3	ovarian:	n/a
34	chr9:136932424-136932474	HCPEpiC	choroid plexus:	n/a
35	chr9:136933818-136933868	HRE	kidney:	n/a
36	chr9:136932424-136932474	AG04449	skin:	fetal
37	chr9:136932722-136932772	T-47D	breast:	n/a
38	chr9:136932722-136932772	SK-N-SH	brain:	n/a
39	chr9:136933664-136933714	HIPEpiC	eye:	n/a
40	chr9:136932722-136932772	HMEC	breast:	n/a
41	chr9:136933664-136933714	SKMC	muscle:	n/a
42	chr9:136933664-136933714	MCF10A-Er-Src	breast:	n/a
43	chr9:136932722-136932772	HEEpiC	esophagus:	n/a
44	chr9:136933818-136933868	AG04449	skin:	fetal
45	chr9:136933818-136933868	SAEC	small airway:	n/a
46	chr9:136932722-136932772	NH-A	brain:	n/a
47	chr9:136933664-136933714	Hela-S3	cervix:	n/a
48	chr9:136933664-136933714	AG09309	skin:	n/a
49	chr9:136933818-136933868	SK-N-SH_RA	brain:	n/a
50	chr9:136933818-136933868	HRPEpiC	eye:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:45826569..45827206-chr9:136932245..136933236,2	Hela-S3	cervix:
2	chr9:136915515..136917919-chr9:136933111..136934762,2	K562	blood:
3	chr9:136889327..136891768-chr9:136933108..136935436,5	MCF-7	breast:
4	chr9:136855194..136860597-chr9:136929703..136933650,7	MCF-7	breast:
5	chr9:136930118..136934023-chr9:136998387..137002829,10	K562	blood:
6	chr9:136888954..136894255-chr9:136931474..136935040,9	K562	blood:
7	chr9:136932690..136935080-chr9:137003441..137005032,2	MCF-7	breast:
8	chr9:136930108..136935337-chr9:136999374..137002737,14	MCF-7	breast:
9	chr9:136930668..136932603-chr9:137271043..137272791,2	MCF-7	breast:
10	chr9:136888457..136893834-chr9:136930854..136936517,11	MCF-7	breast:
11	chr9:136931194..136934944-chr9:136998387..137002829,6	K562	blood:
12	chr9:136914158..136916486-chr9:136930935..136932761,3	K562	blood:
13	chr9:136916641..136919642-chr9:136929650..136932820,3	K562	blood:
14	chr9:136889408..136891837-chr9:136929869..136932804,3	MCF-7	breast:
15	chr9:136904571..136907466-chr9:136931191..136933515,2	MCF-7	breast:
16	chr9:136888985..136892489-chr9:136929943..136933995,5	K562	blood:
17	chr9:136930769..136932647-chr9:137027589..137030053,2	MCF-7	breast:
18	chr1:45187060..45187914-chr9:136932617..136933226,2	HCT-116	colon:
19	chr9:136928987..136935981-chr9:136998799..137005312,16	MCF-7	breast:

No data

Variant related genes	Relation type
BRD3	TF binding region
BRD3	CpG island
ENSG00000160293	chromatin interactions
ENSG00000273249	chromatin interactions
ENSG00000221676	chromatin interactions
ENSG00000181830	chromatin interactions
ENSG00000235138	chromatin interactions
ENSG00000196363	chromatin interactions
ENSG00000169925	chromatin interactions
ENSG00000199377	chromatin interactions
ENSG00000263897	chromatin interactions
ENSG00000235106	chromatin interactions

Extended variants
information (count: 47 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:47 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75842226	chr9:136932410-136932411	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs533289719	chr9:136932437-136932438	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs545853848	chr9:136932444-136932445	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs111550853	chr9:136932476-136932477	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs148665928	chr9:136932507-136932508	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs564517053	chr9:136932514-136932515	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs531834791	chr9:136932520-136932521	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs550309573	chr9:136932544-136932545	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs568624148	chr9:136932549-136932550	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs529488411	chr9:136932579-136932580	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs548035705	chr9:136932580-136932581	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs13286757	chr9:136932587-136932588	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs540155055	chr9:136932600-136932601	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs144185314	chr9:136932621-136932622	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs10993910	chr9:136932638-136932639	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs13287061	chr9:136932706-136932707	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs555065319	chr9:136932748-136932749	Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs573746076	chr9:136932820-136932821	Weak transcription Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs574052202	chr9:136932838-136932839	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs13287246	chr9:136932844-136932845	Weak transcription Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs4375065	chr9:136933285-136933286	Weak transcription Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs4311705	chr9:136933302-136933303	Weak transcription Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs4311706	chr9:136933304-136933305	Weak transcription Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs113701438	chr9:136933373-136933374	Weak transcription Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs545360248	chr9:136933384-136933385	Weak transcription Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs564434822	chr9:136933413-136933414	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs576510228	chr9:136933421-136933422	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs75318400	chr9:136933445-136933446	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs373928965	chr9:136933452-136933453	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs562179222	chr9:136933539-136933540	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs193250492	chr9:136933552-136933553	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs183895561	chr9:136933563-136933564	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs113534536	chr9:136933573-136933574	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs148686197	chr9:136933591-136933592	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs551659848	chr9:136933597-136933598	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs569281138	chr9:136933599-136933600	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs536663017	chr9:136933654-136933655	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs548600311	chr9:136933676-136933677	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs567225695	chr9:136933681-136933682	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs111424819	chr9:136933703-136933704	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs534760026	chr9:136933709-136933710	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs552880574	chr9:136933739-136933740	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs577779390	chr9:136933740-136933741	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs538891296	chr9:136933767-136933768	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs200203356	chr9:136933768-136933769	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs71380276	chr9:136933771-136933772	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs72441822	chr9:136933772-136933773	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Melanoma	18172304	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Kleefstra Syndrome	21538692	CNVD
Disorders of sex development	22290220	CNVD
Cancer	21183584	CNVD
Chronic myelomonocytic leukemia	16760666	CNVD
Abnormal phenotypes	18644119	CNVD
Ovarian cancer	21720365	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21364760	CNVD
Cancer	20581869	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Hepatocellular carcinoma	22174799	CNVD
Bladder cancer	21909424	CNVD
Cancer	17160897	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Idiopathic chronic pancreatitis	21572526	CNVD
Kleefstra syndrome	22670141	CNVD
Schizophrenia	22241247	CNVD
9q deletion syndrome	16826528	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Non-small cell lung cancer	21829676	CNVD
Non-syndromic sensorineural hearing loss	19293338	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21098271	CNVD

Chromatin state (count:212 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:136930000-136932400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr9:136930400-136932400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr9:136930600-136932400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
4	chr9:136930600-136932400	Flanking Active TSS	Primary B cells from cord blood	blood
5	chr9:136930600-136932400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
6	chr9:136930600-136932400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
7	chr9:136930600-136932400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
8	chr9:136930600-136932400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
9	chr9:136930600-136932400	Flanking Active TSS	Adipose Nuclei	Adipose
10	chr9:136930600-136932400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
11	chr9:136930600-136932600	Flanking Active TSS	Primary hematopoietic stem cells	blood
12	chr9:136930600-136932600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
13	chr9:136930600-136932600	Active TSS	Fetal Kidney	kidney
14	chr9:136930600-136934200	Active TSS	HSMMtube	muscle
15	chr9:136930600-136934200	Active TSS	NHLF	lung
16	chr9:136930800-136932400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
17	chr9:136930800-136932400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
18	chr9:136930800-136932400	Flanking Active TSS	Liver	Liver
19	chr9:136930800-136932400	Flanking Active TSS	Brain Substantia Nigra	brain
20	chr9:136930800-136932400	Flanking Active TSS	Placenta	Placenta
21	chr9:136930800-136932400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
22	chr9:136930800-136934200	Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr9:136930800-136934400	Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr9:136931000-136932400	Flanking Active TSS	Primary B cells from peripheral blood	blood
25	chr9:136931000-136932400	Bivalent/Poised TSS	HepG2	liver
26	chr9:136931000-136932600	Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr9:136931000-136934000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr9:136931000-136934000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr9:136931000-136934000	Active TSS	Gastric	stomach
30	chr9:136931000-136934000	Active TSS	Lung	lung
31	chr9:136931000-136934200	Active TSS	HUES64 Cell Line	embryonic stem cell
32	chr9:136931000-136934200	Active TSS	Aorta	Aorta
33	chr9:136931000-136934200	Active TSS	Colon Smooth Muscle	Colon
34	chr9:136931000-136934400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr9:136931000-136934400	Active TSS	Pancreas	Pancrea
36	chr9:136931000-136934400	Active TSS	HSMM	muscle
37	chr9:136931000-136934400	Active TSS	NHDF-Ad	bronchial
38	chr9:136931000-136934600	Active TSS	Right Atrium	heart
39	chr9:136931200-136932400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr9:136931200-136932600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr9:136931200-136933800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr9:136931200-136933800	Active TSS	GM12878-XiMat	blood
43	chr9:136931200-136934000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr9:136931200-136934000	Active TSS	HUES6 Cell Line	embryonic stem cell
45	chr9:136931200-136934000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
46	chr9:136931200-136934000	Active TSS	Ovary	ovary
47	chr9:136931200-136934000	Active TSS	Sigmoid Colon	Sigmoid Colon
48	chr9:136931200-136934200	Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chr9:136931200-136934200	Active TSS	iPS-18 Cell Line	embryonic stem cell
50	chr9:136931200-136934400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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