Variant report

Variant	esv19929
Chromosome Location	chr9:10485-48531
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1809)
CpG islands
(count:62)
Chromatin interactive
region (count:0)
LncRNA
region (count:12)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1809 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:11385-11575	HepG2	liver:	n/a	n/a
2	ATF1	chr9:44552-44676	K562	blood:	n/a	n/a
3	ATF3	chr9:11321-11456	K562	blood:	n/a	n/a
4	ATF3	chr9:44488-44733	K562	blood:	n/a	n/a
5	ATF3	chr9:11273-11504	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr9:11302-11484	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr9:27604-27796	GM12878	blood:	n/a	chr9:27703-27714
8	BATF	chr9:31973-32255	GM12878	blood:	n/a	n/a
9	BATF	chr9:12501-12737	GM12878	blood:	n/a	n/a
10	BATF	chr9:22403-22601	GM12878	blood:	n/a	n/a
11	BATF	chr9:14336-14569	GM12878	blood:	n/a	n/a
12	BATF	chr9:27260-27465	GM12878	blood:	n/a	n/a
13	BATF	chr9:14010-14300	GM12878	blood:	n/a	n/a
14	BATF	chr9:26062-26579	GM12878	blood:	n/a	n/a
15	BATF	chr9:16236-16435	GM12878	blood:	n/a	n/a
16	BATF	chr9:29664-29991	GM12878	blood:	n/a	n/a
17	BATF	chr9:29512-29973	GM12878	blood:	n/a	n/a
18	BATF	chr9:11200-11575	GM12878	blood:	n/a	n/a
19	BATF	chr9:28993-29489	GM12878	blood:	n/a	n/a
20	BATF	chr9:11788-12224	GM12878	blood:	n/a	n/a
21	BATF	chr9:13366-13660	GM12878	blood:	n/a	n/a
22	BATF	chr9:26398-26595	GM12878	blood:	n/a	n/a
23	BATF	chr9:32954-33132	GM12878	blood:	n/a	n/a
24	BATF	chr9:16237-16459	GM12878	blood:	n/a	n/a
25	BATF	chr9:11755-12334	GM12878	blood:	n/a	n/a
26	BATF	chr9:28725-28963	GM12878	blood:	n/a	n/a
27	BCL11A	chr9:24376-24583	GM12878	blood:	n/a	n/a
28	BCL11A	chr9:19595-19790	GM12878	blood:	n/a	n/a
29	BCL11A	chr9:26105-26289	GM12878	blood:	n/a	n/a
30	BCL11A	chr9:28706-29933	GM12878	blood:	n/a	n/a
31	BCL11A	chr9:17615-17888	GM12878	blood:	n/a	n/a
32	BCL11A	chr9:12476-12817	GM12878	blood:	n/a	n/a
33	BCL11A	chr9:18487-18969	GM12878	blood:	n/a	n/a
34	BCL11A	chr9:29619-30003	GM12878	blood:	n/a	n/a
35	BCL11A	chr9:27588-27912	GM12878	blood:	n/a	n/a
36	BCL11A	chr9:11692-12881	GM12878	blood:	n/a	n/a
37	BCL11A	chr9:16598-16805	GM12878	blood:	n/a	n/a
38	BCL11A	chr9:26068-26536	GM12878	blood:	n/a	n/a
39	BCL11A	chr9:23561-23749	GM12878	blood:	n/a	n/a
40	BCL11A	chr9:11201-11621	GM12878	blood:	n/a	n/a
41	BCL11A	chr9:11194-11629	GM12878	blood:	n/a	n/a
42	BCL11A	chr9:28119-28353	GM12878	blood:	n/a	n/a
43	BCL11A	chr9:15974-16498	GM12878	blood:	n/a	n/a
44	BCL11A	chr9:25426-25781	GM12878	blood:	n/a	n/a
45	BCL11A	chr9:28364-29617	GM12878	blood:	n/a	n/a
46	BCL11A	chr9:20372-20605	GM12878	blood:	n/a	n/a
47	BCL11A	chr9:14116-14318	GM12878	blood:	n/a	n/a
48	BCL11A	chr9:18992-19192	GM12878	blood:	n/a	n/a
49	BCL11A	chr9:15360-15583	GM12878	blood:	n/a	chr9:15493-15506
50	BCL11A	chr9:17165-17472	GM12878	blood:	n/a	chr9:17207-17220

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:11410-11460	HAEpiC	amniotic membrane:	n/a
2	chr9:11410-11460	HAEpiC	amniotic membrane:	n/a
3	chr9:11410-11460	GM06990	blood:	n/a
4	chr9:11410-11460	BJ	skin:	n/a
5	chr9:11410-11460	NT2-D1	testis:	n/a
6	chr9:11410-11460	HCM	heart:	n/a
7	chr9:11410-11460	HEK293	kidney:	embryo
8	chr9:11410-11460	ovcar-3	ovarian:	n/a
9	chr9:11410-11460	K562	blood:	n/a
10	chr9:11410-11460	NHBE	bronchial:	n/a
11	chr9:11410-11460	HPAEpiC	pulmonary alveolar:	n/a
12	chr9:11410-11460	AG10803	skin:	n/a
13	chr9:11410-11460	HEEpiC	esophagus:	n/a
14	chr9:11410-11460	NHDF-neo	bronchial:	n/a
15	chr9:11410-11460	A549	lung:	n/a
16	chr9:11410-11460	ProgFib	skin:	n/a
17	chr9:11410-11460	HRCEpiC	kidney:	n/a
18	chr9:11410-11460	Hepatocyte	liver:	n/a
19	chr9:11410-11460	NH-A	brain:	n/a
20	chr9:11410-11460	ECC-1	luminal epithelium:	n/a
21	chr9:11410-11460	Hela-S3	cervix:	n/a
22	chr9:11410-11460	GM12892	blood:	n/a
23	chr9:11410-11460	T-47D	breast:	n/a
24	chr9:11410-11460	SK-N-SH	brain:	n/a
25	chr9:11410-11460	PFSK-1	brain:	n/a
26	chr9:11410-11460	SAEC	small airway:	n/a
27	chr9:11410-11460	HCF	heart:	n/a
28	chr9:11410-11460	AG09309	skin:	n/a
29	chr9:11410-11460	HIPEpiC	eye:	n/a
30	chr9:11410-11460	HL-60	blood:	n/a
31	chr9:11410-11460	HCPEpiC	choroid plexus:	n/a
32	chr9:11410-11460	Caco-2	colon:	n/a
33	chr9:11410-11460	HepG2	liver:	n/a
34	chr9:11410-11460	PrEC	prostate:	n/a
35	chr9:11410-11460	H1-hESC	embryonic stem cell:	embryo
36	chr9:11410-11460	RPTEC	kidney:	n/a
37	chr9:11410-11460	SKMC	muscle:	n/a
38	chr9:11410-11460	SK-N-SH_RA	brain:	n/a
39	chr9:11410-11460	HUVEC	blood vessel:	n/a
40	chr9:11410-11460	AG09319	gingival:	n/a
41	chr9:11410-11460	CMK	blood:	n/a
42	chr9:11410-11460	MCF-7	breast:	n/a
43	chr9:11410-11460	AoSMC	blood vessel:	n/a
44	chr9:11410-11460	GM19239	blood:	n/a
45	chr9:11410-11460	GM12878	blood:	n/a
46	chr9:11410-11460	AG04450	lung:	fetal
47	chr9:11410-11460	LNCaP	prostate:	n/a
48	chr9:11410-11460	MCF10A-Er-Src	breast:	n/a
49	chr9:11410-11460	GM12891	blood:	n/a
50	chr9:11410-11460	PANC-1	pancreas:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DOCK8-7	chr9:13516-14522	NONHSAT129877
2	lnc-FAM138C-2	chr9:35060-35264	ENSG00000218839.3
3	lnc-DOCK8-7	chr9:11987-12340	NONHSAT129877
4	lnc-FAM138C-3	chr9:26159-26368	expReg_chr9_16_-
5	lnc-DOCK8-7	chr9:12708-12834	NONHSAT129877
6	lnc-FAM138C-2	chr9:34394-34957	ENSG00000218839.3
7	lnc-FAM138C-2	chr9:34394-34957	NONHSAT129883
8	lnc-FAM138C-2	chr9:35504-35841	ENSG00000218839.3
9	lnc-FAM138C-2	chr9:35060-35264	NONHSAT129883
10	lnc-FAM138C-2	chr9:35504-35856	ENSG00000218839.3
11	lnc-FAM138C-2	chr9:35504-35864	NONHSAT129883
12	lnc-FAM138C-2	chr9:35028-35264	ENSG00000218839.3

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1302	chr9:30216-30236	MIMAT0005890_9

No data

Variant related genes	Relation type
MIR1302-2	TF binding region
DDX11L5	TF binding region
ENSG00000181404	TF binding region
FAM138C	TF binding region
MIR1302-2	CpG island
DDX11L5	CpG island
ENSG00000181404	CpG island
FAM138C	CpG island

Extended variants
information (count: 851 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:851 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544446874	chr9:10498-10499	Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs368056107	chr9:10503-10504	Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs556678566	chr9:10513-10514	Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs371809471	chr9:10536-10537	Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs578035845	chr9:10548-10549	Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs545457369	chr9:10559-10560	Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs560303029	chr9:10566-10567	Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs112434232	chr9:10576-10577	Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs527713335	chr9:10582-10583	Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs543039485	chr9:10583-10584	Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs561207592	chr9:10590-10591	Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs531595271	chr9:10593-10594	Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs549710705	chr9:10594-10595	Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs571388958	chr9:10597-10598	Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs532121268	chr9:10601-10602	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs547501765	chr9:10623-10624	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs565417700	chr9:10637-10638	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs202118205	chr9:10648-10649	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs535893256	chr9:10651-10652	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs554137200	chr9:10670-10671	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs149890535	chr9:10674-10675	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs567631558	chr9:10684-10685	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs143946323	chr9:10690-10691	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs56270691	chr9:10696-10697	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs55678735	chr9:10712-10713	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs368818808	chr9:10716-10717	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs113256924	chr9:10717-10718	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs578099430	chr9:10722-10723	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs545257807	chr9:10731-10732	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs371142579	chr9:10743-10744	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs554288598	chr9:10765-10766	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs572560598	chr9:10775-10776	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs543052152	chr9:10784-10785	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs561219904	chr9:10788-10789	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs531658922	chr9:10821-10822	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs375876733	chr9:10834-10835	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs7341907	chr9:10869-10870	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs543664992	chr9:10892-10893	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs565015447	chr9:10894-10895	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs532362758	chr9:10908-10909	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs370685556	chr9:10935-10936	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs576674727	chr9:10960-10961	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs62530131	chr9:10968-10969	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs559066011	chr9:10974-10975	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs369111154	chr9:10975-10976	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs200530560	chr9:10976-10977	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs560589285	chr9:10984-10985	Weak transcription Active TSS ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs529638838	chr9:11013-11014	Bivalent/Poised TSS ZNF genes & repeats Weak transcription Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs373783847	chr9:11071-11072	Bivalent/Poised TSS ZNF genes & repeats Weak transcription Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs529702288	chr9:11076-11077	Bivalent/Poised TSS ZNF genes & repeats Weak transcription Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8800-14200	Weak transcription	Fetal Heart	heart
2	chr9:10000-10600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
3	chr9:10000-11000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr9:10200-10600	ZNF genes & repeats	Placenta	Placenta
5	chr9:10200-11000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr9:10200-11200	Enhancers	Osteobl	bone
7	chr9:10200-11400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
8	chr9:10200-11800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr9:10400-10600	Bivalent/Poised TSS	NHEK	skin
10	chr9:10400-11400	ZNF genes & repeats	HSMM	muscle
11	chr9:10400-11400	Active TSS	K562	blood
12	chr9:10400-14200	Weak transcription	Fetal Lung	lung
13	chr9:10400-21600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr9:10600-11400	Active TSS	Placenta	Placenta
15	chr9:10800-11000	Weak transcription	GM12878-XiMat	blood
16	chr9:11000-11200	Enhancers	Primary hematopoietic stem cells	blood
17	chr9:11000-11200	Active TSS	Brain Inferior Temporal Lobe	brain
18	chr9:11000-11200	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr9:11000-11200	ZNF genes & repeats	NH-A	brain
20	chr9:11000-11200	Bivalent Enhancer	NHEK	skin
21	chr9:11000-11200	Enhancers	NHLF	lung
22	chr9:11000-11400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
23	chr9:11000-11400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
24	chr9:11000-11400	Active TSS	H9 Cell Line	embryonic stem cell
25	chr9:11000-11400	Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr9:11000-11400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr9:11000-11400	ZNF genes & repeats	Thymus	Thymus
28	chr9:11000-11400	Active TSS	GM12878-XiMat	blood
29	chr9:11000-11400	Active TSS	HMEC	breast
30	chr9:11000-11400	Active TSS	HSMMtube	muscle
31	chr9:11000-11400	Active TSS	NHDF-Ad	bronchial
32	chr9:11000-14600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr9:11000-16000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr9:11200-11400	Active TSS	Primary T cells from cord blood	blood
35	chr9:11200-11400	Bivalent/Poised TSS	NHEK	skin
36	chr9:11200-21600	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr9:11400-14200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr9:11400-14200	Weak transcription	HSMM	muscle
39	chr9:11400-14200	Weak transcription	HSMMtube	muscle
40	chr9:11400-14200	Weak transcription	K562	blood
41	chr9:11400-14400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr9:11400-20800	Weak transcription	Thymus	Thymus
43	chr9:11800-21600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr9:12000-12200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr9:12000-12200	Enhancers	Fetal Muscle Trunk	muscle
46	chr9:12000-21600	Weak transcription	Spleen	Spleen
47	chr9:12200-14200	Weak transcription	Fetal Muscle Trunk	muscle
48	chr9:12400-14200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr9:12800-21600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr9:12800-28800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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