Variant report

Variant	nsv972420
Chromosome Location	chr9:95566045-95588965
allele	n/a
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	BACH1	chr9:95571290-95571757	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr9:95582152-95582428	GM12878	blood:	n/a	n/a
3	BATF	chr9:95583222-95583592	GM12878	blood:	n/a	chr9:95583416-95583427
4	BCLAF1	chr9:95571357-95571743	GM12878	blood:	n/a	n/a
5	BHLHE40	chr9:95571511-95571649	GM12878	blood:	n/a	chr9:95571539-95571555
6	BHLHE40	chr9:95571422-95571625	K562	blood:	n/a	chr9:95571539-95571555
7	BRCA1	chr9:95571272-95571377	H1-hESC	embryonic stem cell:	n/a	n/a
8	CBX3	chr9:95571325-95571829	K562	blood:	n/a	n/a
9	CCNT2	chr9:95571417-95571657	K562	blood:	n/a	n/a
10	CEBPB	chr9:95571476-95571607	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD1	chr9:95571468-95571643	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr9:95571478-95571516	K562	blood:	n/a	n/a
13	CHD2	chr9:95571131-95571593	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTBP2	chr9:95570714-95571790	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr9:95571100-95571250	HepG2	liver:	n/a	chr9:95571189-95571197 chr9:95571179-95571195
16	CTCF	chr9:95571440-95571590	HBMEC	blood vessel:	n/a	chr9:95571520-95571538 chr9:95571522-95571535
17	CTCF	chr9:95571072-95571309	GM12891	blood:	n/a	chr9:95571189-95571197 chr9:95571179-95571195
18	CTCF	chr9:95571459-95571466	LNCaP	prostate:	n/a	n/a
19	CTCF	chr9:95571437-95571656	GM12891	blood:	n/a	chr9:95571520-95571538 chr9:95571522-95571535
20	CTCF	chr9:95571159-95571244	GM20000	blood:	n/a	chr9:95571189-95571197 chr9:95571179-95571195
21	CTCF	chr9:95571460-95571610	HEEpiC	esophagus:	n/a	chr9:95571520-95571538 chr9:95571522-95571535
22	CTCF	chr9:95571080-95571230	HMEC	breast:	n/a	chr9:95571189-95571197 chr9:95571179-95571195
23	CTCF	chr9:95571449-95571600	GM12892	blood:	n/a	chr9:95571520-95571538 chr9:95571522-95571535
24	CTCF	chr9:95571460-95571610	WERI-Rb-1	eye:	n/a	chr9:95571520-95571538 chr9:95571522-95571535
25	CTCF	chr9:95571480-95571630	SK-N-SH_RA	brain:	n/a	chr9:95571520-95571538 chr9:95571522-95571535
26	CTCF	chr9:95571504-95571602	Pancreas_OC	pancreas:	n/a	chr9:95571520-95571538 chr9:95571522-95571535
27	CTCF	chr9:95571460-95571610	A549	lung:	n/a	chr9:95571520-95571538 chr9:95571522-95571535
28	CTCF	chr9:95571460-95571610	GM12872	blood:	n/a	chr9:95571520-95571538 chr9:95571522-95571535
29	CTCF	chr9:95571420-95571570	GM12869	blood:	n/a	chr9:95571520-95571538 chr9:95571522-95571535
30	CTCF	chr9:95571108-95571265	GM12878	blood:	n/a	chr9:95571189-95571197 chr9:95571179-95571195
31	CTCF	chr9:95571460-95571610	GM12867	blood:	n/a	chr9:95571520-95571538 chr9:95571522-95571535
32	CTCF	chr9:95571072-95571310	MCF-7	breast:	n/a	chr9:95571189-95571197 chr9:95571179-95571195
33	CTCF	chr9:95571480-95571630	HCPEpiC	choroid plexus:	n/a	chr9:95571520-95571538 chr9:95571522-95571535
34	CTCF	chr9:95571080-95571230	HRPEpiC	eye:	n/a	chr9:95571189-95571197 chr9:95571179-95571195
35	CTCF	chr9:95571420-95571570	GM12872	blood:	n/a	chr9:95571520-95571538 chr9:95571522-95571535
36	CTCF	chr9:95571420-95571570	GM12871	blood:	n/a	chr9:95571520-95571538 chr9:95571522-95571535
37	CTCF	chr9:95571180-95571330	GM12868	blood:	n/a	chr9:95571189-95571197
38	CTCF	chr9:95571420-95571570	HFF-Myc	foreskin:	n/a	chr9:95571520-95571538 chr9:95571522-95571535
39	CTCF	chr9:95571340-95571490	RPTEC	kidney:	n/a	n/a
40	CTCF	chr9:95571482-95571598	A549	lung:	n/a	chr9:95571520-95571538 chr9:95571522-95571535
41	CTCF	chr9:95571460-95571610	NHDF-neo	bronchial:	n/a	chr9:95571520-95571538 chr9:95571522-95571535
42	CTCF	chr9:95571200-95571350	K562	blood:	n/a	n/a
43	CTCF	chr9:95571400-95571550	GM12873	blood:	n/a	chr9:95571520-95571538 chr9:95571522-95571535
44	CTCF	chr9:95571436-95571575	K562	blood:	n/a	chr9:95571520-95571538 chr9:95571522-95571535
45	CTCF	chr9:95571460-95571610	SAEC	small airway:	n/a	chr9:95571520-95571538 chr9:95571522-95571535
46	CTCF	chr9:95571072-95571301	GM19239	blood:	n/a	chr9:95571189-95571197 chr9:95571179-95571195
47	CTCF	chr9:95571140-95571290	HEEpiC	esophagus:	n/a	chr9:95571189-95571197 chr9:95571179-95571195
48	CTCF	chr9:95571140-95571290	GM12874	blood:	n/a	chr9:95571189-95571197 chr9:95571179-95571195
49	CTCF	chr9:95571540-95571690	GM12873	blood:	n/a	n/a
50	CTCF	chr9:95571480-95571630	BJ	skin:	n/a	chr9:95571520-95571538 chr9:95571522-95571535

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:95570657-95570707	AG04449	skin:	fetal
2	chr9:95571917-95571967	GM12891	blood:	n/a
3	chr9:95569618-95569668	HPAEpiC	pulmonary alveolar:	n/a
4	chr9:95571181-95571231	AG09319	gingival:	n/a
5	chr9:95570657-95570707	AG04449	skin:	fetal
6	chr9:95571917-95571967	GM12891	blood:	n/a
7	chr9:95569618-95569668	HPAEpiC	pulmonary alveolar:	n/a
8	chr9:95571181-95571231	AG09319	gingival:	n/a
9	chr9:95571711-95571761	NHDF-neo	bronchial:	n/a
10	chr9:95572254-95572304	AG04449	skin:	fetal
11	chr9:95570341-95570391	HPAEpiC	pulmonary alveolar:	n/a
12	chr9:95570341-95570391	SAEC	small airway:	n/a
13	chr9:95570657-95570707	Jurkat	blood:	n/a
14	chr9:95572254-95572304	HL-60	blood:	n/a
15	chr9:95568714-95568764	NH-A	brain:	n/a
16	chr9:95574913-95574963	HEK293	kidney:	embryo
17	chr9:95570021-95570071	HIPEpiC	eye:	n/a
18	chr9:95571589-95571639	AG04449	skin:	fetal
19	chr9:95569697-95569747	GM19239	blood:	n/a
20	chr9:95569618-95569668	ProgFib	skin:	n/a
21	chr9:95568714-95568764	H1-hESC	embryonic stem cell:	embryo
22	chr9:95569618-95569668	HL-60	blood:	n/a
23	chr9:95569618-95569668	HUVEC	blood vessel:	n/a
24	chr9:95571917-95571967	PANC-1	pancreas:	n/a
25	chr9:95570021-95570071	Hepatocyte	liver:	n/a
26	chr9:95571181-95571231	SK-N-MC	brain:	n/a
27	chr9:95568714-95568764	HUVEC	blood vessel:	n/a
28	chr9:95571711-95571761	GM19239	blood:	n/a
29	chr9:95570657-95570707	NB4	blood:	n/a
30	chr9:95570676-95570726	HepG2	liver:	n/a
31	chr9:95571589-95571639	GM06990	blood:	n/a
32	chr9:95574913-95574963	ovcar-3	ovarian:	n/a
33	chr9:95569618-95569668	HCT-116	colon:	n/a
34	chr9:95570657-95570707	MCF-7	breast:	n/a
35	chr9:95572254-95572304	HCPEpiC	choroid plexus:	n/a
36	chr9:95574913-95574963	GM12891	blood:	n/a
37	chr9:95574913-95574963	MCF-7	breast:	n/a
38	chr9:95571917-95571967	HPAEpiC	pulmonary alveolar:	n/a
39	chr9:95570657-95570707	SAEC	small airway:	n/a
40	chr9:95571917-95571967	HEK293	kidney:	embryo
41	chr9:95571181-95571231	GM12892	blood:	n/a
42	chr9:95570657-95570707	RPTEC	kidney:	n/a
43	chr9:95572081-95572131	H1-hESC	embryonic stem cell:	embryo
44	chr9:95569697-95569747	ECC-1	luminal epithelium:	n/a
45	chr9:95568714-95568764	HEEpiC	esophagus:	n/a
46	chr9:95572081-95572131	PFSK-1	brain:	n/a
47	chr9:95574913-95574963	GM06990	blood:	n/a
48	chr9:95570021-95570071	HCF	heart:	n/a
49	chr9:95570676-95570726	Jurkat	blood:	n/a
50	chr9:95570341-95570391	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:95431331..95434473-chr9:95569877..95572688,3	MCF-7	breast:
2	chr9:95570706..95571359-chr9:95719247..95719879,2	MCF-7	breast:
3	chr9:33524178..33524765-chr9:95571291..95571812,2	MCF-7	breast:
4	chr9:95432561..95435212-chr9:95564441..95567422,3	MCF-7	breast:
5	chr9:95563386..95565101-chr9:95567156..95569894,2	MCF-7	breast:
6	chr9:95431083..95433127-chr9:95569211..95571144,2	MCF-7	breast:
7	chr9:95570373..95571952-chr9:95637590..95640500,2	MCF-7	breast:
8	chr9:95580165..95582240-chr9:95584449..95586784,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGD3-4	chr9:95588807-95588860	NONHSAT133208
2	lnc-FGD3-4	chr9:95584504-95584559	NONHSAT133208

Variant related genes	Relation type
RNU6-714P	TF binding region
ANKRD19P	TF binding region
RNU6-714P	CpG island
ANKRD19P	CpG island
ENSG00000127080	chromatin interactions
ENSG00000127081	chromatin interactions
ENSG00000187984	chromatin interactions
ENSG00000230453	chromatin interactions

Extended variants
information (count: 817 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:817 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142650692	chr9:95566051-95566052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs374298425	chr9:95566094-95566095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112486714	chr9:95566118-95566119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs111590599	chr9:95566143-95566144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs10118572	chr9:95566176-95566177	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs145723037	chr9:95566190-95566191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs202100147	chr9:95566214-95566215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs146609731	chr9:95566216-95566217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs199736088	chr9:95566217-95566218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200553436	chr9:95566221-95566222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs180862432	chr9:95566244-95566245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563951654	chr9:95566248-95566249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147686830	chr9:95566254-95566255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs375010590	chr9:95566257-95566258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113949317	chr9:95566259-95566260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201446584	chr9:95566260-95566261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546186196	chr9:95566280-95566281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs199869885	chr9:95566281-95566282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542051783	chr9:95566286-95566287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564480947	chr9:95566291-95566292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568397073	chr9:95566292-95566293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528547791	chr9:95566296-95566297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540717284	chr9:95566328-95566329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186148251	chr9:95566382-95566383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372953970	chr9:95566439-95566440	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs138664828	chr9:95566462-95566463	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548110520	chr9:95566522-95566523	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530681553	chr9:95566535-95566536	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191050017	chr9:95566567-95566568	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530727469	chr9:95566575-95566576	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551711036	chr9:95566630-95566631	Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs117680593	chr9:95566636-95566637	Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534363490	chr9:95566647-95566648	Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553018613	chr9:95566702-95566703	Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs568091676	chr9:95566708-95566709	Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs560061283	chr9:95566728-95566729	Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs374311547	chr9:95566753-95566754	Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs561074510	chr9:95566768-95566769	Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs536020207	chr9:95566779-95566780	Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs527498861	chr9:95566795-95566796	Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs557605489	chr9:95566804-95566805	Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs111162742	chr9:95566831-95566832	Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs370882503	chr9:95566848-95566849	Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs546521801	chr9:95566867-95566868	Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs558533854	chr9:95566958-95566959	Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs573180807	chr9:95566963-95566964	Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs116237594	chr9:95566965-95566966	Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs562188269	chr9:95566987-95566988	Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs552013056	chr9:95567011-95567012	Bivalent Enhancer Bivalent/Poised TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs541972048	chr9:95567022-95567023	Bivalent Enhancer Bivalent/Poised TSS Weak transcription	TF binding region	1 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
Bipolar disorder	18458673	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
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
overgrowth syndrome	16570072	CNVD

Chromatin state (count:500 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95558600-95569600	Weak transcription	Right Atrium	heart
2	chr9:95566400-95567000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:95566600-95566800	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr9:95566600-95566800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr9:95566600-95567200	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr9:95566600-95567200	Bivalent/Poised TSS	Fetal Kidney	kidney
7	chr9:95566600-95569600	Weak transcription	Pancreas	Pancrea
8	chr9:95566800-95567000	Bivalent Enhancer	HSMMtube	muscle
9	chr9:95566800-95567200	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr9:95567000-95567600	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr9:95568200-95568400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
12	chr9:95569200-95569600	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
13	chr9:95569200-95569600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
14	chr9:95569200-95571200	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
15	chr9:95569400-95569600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr9:95569400-95569600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr9:95569400-95569600	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
18	chr9:95569400-95569600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
19	chr9:95569400-95569600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr9:95569400-95569600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr9:95569400-95569600	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
22	chr9:95569400-95569600	Bivalent Enhancer	Brain Substantia Nigra	brain
23	chr9:95569400-95569600	Bivalent/Poised TSS	Fetal Brain Female	brain
24	chr9:95569400-95569600	Enhancers	Right Ventricle	heart
25	chr9:95569400-95569600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
26	chr9:95569400-95569600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
27	chr9:95569400-95569600	Flanking Bivalent TSS/Enh	Spleen	Spleen
28	chr9:95569400-95569800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
29	chr9:95569400-95569800	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
30	chr9:95569400-95569800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr9:95569400-95569800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
32	chr9:95569400-95570000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
33	chr9:95569400-95570000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
34	chr9:95569400-95570000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
35	chr9:95569400-95570000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
36	chr9:95569400-95570000	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr9:95569400-95570000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr9:95569400-95570000	Flanking Bivalent TSS/Enh	Brain Anterior Caudate	brain
39	chr9:95569400-95570000	Bivalent Enhancer	HMEC	breast
40	chr9:95569400-95570200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
41	chr9:95569400-95570200	Bivalent Enhancer	Fetal Heart	heart
42	chr9:95569400-95570600	Bivalent Enhancer	Primary B cells from cord blood	blood
43	chr9:95569400-95570600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
44	chr9:95569400-95571400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
45	chr9:95569400-95571600	Bivalent Enhancer	Fetal Muscle Leg	muscle
46	chr9:95569400-95572400	Bivalent Enhancer	Fetal Brain Male	brain
47	chr9:95569400-95572400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
48	chr9:95569400-95572400	Bivalent Enhancer	Fetal Thymus	thymus
49	chr9:95569600-95569800	Bivalent/Poised TSS	Primary T cells from cord blood	blood
50	chr9:95569600-95569800	Flanking Bivalent TSS/Enh	Primary T helper memory cells from peripheral blood 2	blood

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