Variant report

Variant	esv1837115
Chromosome Location	chr7:50343238-50344544
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	ARID3A	chr7:50344193-50344384	K562	blood:	n/a	n/a
2	BACH1	chr7:50342943-50343353	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:50343888-50344531	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr7:50343848-50344891	GM12878	blood:	n/a	chr7:50344405-50344418 chr7:50343972-50343985
5	BCLAF1	chr7:50344529-50344858	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:50343130-50343921	K562	blood:	n/a	n/a
7	BHLHE40	chr7:50343216-50344727	GM12878	blood:	n/a	chr7:50344200-50344216 chr7:50343966-50343982
8	BHLHE40	chr7:50344167-50344836	K562	blood:	n/a	chr7:50344200-50344216
9	CCNT2	chr7:50343268-50344769	K562	blood:	n/a	chr7:50343434-50343443 chr7:50344205-50344214
10	CEBPB	chr7:50344133-50344309	HepG2	liver:	n/a	chr7:50344264-50344275
11	CEBPB	chr7:50344096-50344424	K562	blood:	n/a	chr7:50344264-50344275
12	CEBPB	chr7:50344112-50344418	K562	blood:	n/a	chr7:50344264-50344275
13	CEBPB	chr7:50344144-50344340	H1-hESC	embryonic stem cell:	n/a	chr7:50344264-50344275
14	CEBPB	chr7:50344125-50344331	K562	blood:	n/a	chr7:50344264-50344275
15	CHD1	chr7:50344114-50345518	GM12878	blood:	n/a	chr7:50344206-50344216 chr7:50344413-50344423
16	CHD1	chr7:50344274-50344311	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr7:50343778-50343928	GM12878	blood:	n/a	n/a
18	CHD2	chr7:50344166-50344339	K562	blood:	n/a	chr7:50344206-50344216
19	CHD2	chr7:50343327-50343435	K562	blood:	n/a	n/a
20	CHD2	chr7:50344130-50344399	GM12878	blood:	n/a	chr7:50344206-50344216
21	CTCF	chr7:50344000-50344150	GM12864	blood:	n/a	chr7:50344069-50344082
22	CTCF	chr7:50344030-50344236	GM10266	blood:	n/a	chr7:50344069-50344082 chr7:50344199-50344212
23	CTCF	chr7:50344100-50344250	GM12878	blood:	n/a	chr7:50344199-50344212
24	CTCF	chr7:50344120-50344270	GM12872	blood:	n/a	chr7:50344199-50344212
25	CTCF	chr7:50344001-50344002	GM12891	blood:	n/a	n/a
26	CTCF	chr7:50344021-50344219	GM13977	blood:	n/a	chr7:50344069-50344082 chr7:50344199-50344212
27	CTCF	chr7:50343901-50344292	K562	blood:	n/a	chr7:50344069-50344082 chr7:50344199-50344212
28	CTCF	chr7:50343700-50343850	GM12875	blood:	n/a	n/a
29	CTCF	chr7:50343820-50343970	GM12873	blood:	n/a	n/a
30	CTCF	chr7:50344055-50344205	GM13976	blood:	n/a	chr7:50344069-50344082
31	CTCF	chr7:50344004-50344260	GM12891	blood:	n/a	chr7:50344069-50344082 chr7:50344199-50344212
32	CTCF	chr7:50343942-50344274	GM12892	blood:	n/a	chr7:50344069-50344082 chr7:50344199-50344212
33	CTCF	chr7:50344431-50344444	GM12892	blood:	n/a	n/a
34	CTCF	chr7:50344086-50344209	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr7:50344400-50344550	GM12868	blood:	n/a	n/a
36	CTCF	chr7:50344120-50344270	GM12871	blood:	n/a	chr7:50344199-50344212
37	CTCF	chr7:50344098-50344320	K562	blood:	n/a	chr7:50344199-50344212
38	CTCF	chr7:50343240-50343390	GM12871	blood:	n/a	n/a
39	CTCF	chr7:50343883-50344334	GM12878	blood:	n/a	chr7:50344069-50344082 chr7:50344199-50344212
40	CTCF	chr7:50344031-50344239	GM19240	blood:	n/a	chr7:50344069-50344082 chr7:50344199-50344212
41	CTCF	chr7:50344380-50344530	GM12866	blood:	n/a	n/a
42	CTCF	chr7:50343855-50344266	GM19239	blood:	n/a	chr7:50344069-50344082 chr7:50344199-50344212
43	CTCF	chr7:50344138-50344186	GM20000	blood:	n/a	n/a
44	CTCF	chr7:50344180-50344330	GM12873	blood:	n/a	chr7:50344199-50344212
45	CTCF	chr7:50344122-50344127	Fibrobl	skin:	n/a	n/a
46	CTCF	chr7:50344237-50344238	GM10266	blood:	n/a	n/a
47	CTCF	chr7:50343331-50343349	Spleen_OC	spleen:	n/a	n/a
48	CTCF	chr7:50344020-50344170	GM12867	blood:	n/a	chr7:50344069-50344082
49	CTCF	chr7:50344500-50344650	GM12871	blood:	n/a	n/a
50	CTCF	chr7:50344060-50344210	GM12869	blood:	n/a	chr7:50344069-50344082

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:50343869-50343919	RPTEC	kidney:	n/a
2	chr7:50344242-50344292	BE2_C	brain:	n/a
3	chr7:50343869-50343919	BE2_C	brain:	n/a
4	chr7:50343883-50343933	GM12891	blood:	n/a
5	chr7:50343883-50343933	AG04449	skin:	fetal
6	chr7:50344294-50344344	Caco-2	colon:	n/a
7	chr7:50344294-50344344	AG09319	gingival:	n/a
8	chr7:50344242-50344292	AG04449	skin:	fetal
9	chr7:50344242-50344292	RPTEC	kidney:	n/a
10	chr7:50343883-50343933	H1-hESC	embryonic stem cell:	embryo
11	chr7:50344294-50344344	HUVEC	blood vessel:	n/a
12	chr7:50343298-50343348	Hepatocyte	liver:	n/a
13	chr7:50344294-50344344	SAEC	small airway:	n/a
14	chr7:50343361-50343411	HAEpiC	amniotic membrane:	n/a
15	chr7:50343883-50343933	ProgFib	skin:	n/a
16	chr7:50344471-50344521	AG09309	skin:	n/a
17	chr7:50343361-50343411	ProgFib	skin:	n/a
18	chr7:50343298-50343348	Jurkat	blood:	n/a
19	chr7:50344331-50344381	HRE	kidney:	n/a
20	chr7:50344471-50344521	HRE	kidney:	n/a
21	chr7:50343361-50343411	AG09319	gingival:	n/a
22	chr7:50343869-50343919	SK-N-SH_RA	brain:	n/a
23	chr7:50343883-50343933	GM12892	blood:	n/a
24	chr7:50344471-50344521	RPTEC	kidney:	n/a
25	chr7:50344331-50344381	HEEpiC	esophagus:	n/a
26	chr7:50343298-50343348	NB4	blood:	n/a
27	chr7:50344471-50344521	Jurkat	blood:	n/a
28	chr7:50343883-50343933	HNPCEpiC	eye:	n/a
29	chr7:50344331-50344381	GM12878	blood:	n/a
30	chr7:50344331-50344381	PANC-1	pancreas:	n/a
31	chr7:50344242-50344292	MCF-7	breast:	n/a
32	chr7:50343298-50343348	GM06990	blood:	n/a
33	chr7:50344294-50344344	SK-N-SH_RA	brain:	n/a
34	chr7:50343361-50343411	CMK	blood:	n/a
35	chr7:50343883-50343933	GM12878	blood:	n/a
36	chr7:50343883-50343933	Caco-2	colon:	n/a
37	chr7:50344294-50344344	NHDF-neo	bronchial:	n/a
38	chr7:50343869-50343919	AG09309	skin:	n/a
39	chr7:50344294-50344344	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:50343361-50343411	HNPCEpiC	eye:	n/a
41	chr7:50344331-50344381	HCM	heart:	n/a
42	chr7:50343869-50343919	MCF10A-Er-Src	breast:	n/a
43	chr7:50343298-50343348	NHDF-neo	bronchial:	n/a
44	chr7:50344294-50344344	IMR90	lung:	fetal
45	chr7:50344294-50344344	ovcar-3	ovarian:	n/a
46	chr7:50343361-50343411	HRE	kidney:	n/a
47	chr7:50344242-50344292	HCPEpiC	choroid plexus:	n/a
48	chr7:50343869-50343919	HL-60	blood:	n/a
49	chr7:50343883-50343933	SK-N-SH_RA	brain:	n/a
50	chr7:50344242-50344292	AG04450	lung:	fetal

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IKZF1-4	chr7:50343720-50343955	NONHSAT120551

Variant related genes	Relation type
IKZF1	TF binding region
IKZF1	CpG island

Extended variants
information (count: 29 )
Associated
traits (count: 136 )

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13308184	chr7:50343242-50343243	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs544161869	chr7:50343244-50343245	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs563949722	chr7:50343251-50343252	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs370417099	chr7:50343366-50343367	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs141865623	chr7:50343399-50343400	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs552793252	chr7:50343514-50343515	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs559852963	chr7:50343522-50343523	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs190437158	chr7:50343555-50343556	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs528601173	chr7:50343594-50343595	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs143791643	chr7:50343804-50343805	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs151114892	chr7:50343805-50343806	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs568396627	chr7:50343854-50343855	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs530795173	chr7:50343856-50343857	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs549714287	chr7:50343883-50343884	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs112931894	chr7:50343961-50343962	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs11765436	chr7:50344077-50344078	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs11761922	chr7:50344132-50344133	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs370261620	chr7:50344166-50344167	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs375447138	chr7:50344170-50344171	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs534432305	chr7:50344285-50344286	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs554633996	chr7:50344313-50344314	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs574511830	chr7:50344336-50344337	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs543438548	chr7:50344389-50344390	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs150241086	chr7:50344455-50344456	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs368593088	chr7:50344458-50344459	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs537050957	chr7:50344467-50344468	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs6975767	chr7:50344474-50344475	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs559713508	chr7:50344478-50344479	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs11506039	chr7:50344544-50344545	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:136)

Disease	PMID	Source
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Biliary cancer	19435499	CNVD
Wilms tumour	21544195	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	17237825	CNVD
Gastric cancer	24379144	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal cancer	21851588	CNVD
Non-small cell lung cancer	17643093	CNVD
Ovarian cancer	18182111	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17369134	CNVD
Barrett''s esophagus	18559552	CNVD
head and neck squamous cell carcinoma	16943533	CNVD
Anaplastic thyroid cancer	17079354	CNVD
Basal-like breast cancer	17875215	CNVD
Colorectal cancer	16882699	CNVD
Colorectal cancer	18794099	CNVD
Gastrointestinal stromal cancer	17643098	CNVD
Lung cancer	18381415	CNVD
Metastatic colorectal cancer	17664472	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	17673923	CNVD
Non-small cell lung cancer	17975165	CNVD
Non-small cell lung cancer	19622585	CNVD
Ovarian cancer	16607561	CNVD
Squamous cell cancer	19670535	CNVD
head and neck squamous cell carcinoma	16818711	CNVD
small cell lung cancer	18829487	CNVD
Breast cancer	17661082	CNVD
Adenocarcinoma	19260752	CNVD
Esophageal cancer	16575012	CNVD
Lung adenocarcinoma	19138956	CNVD
Lung adenocarcinoma	18379350	CNVD
Lung adenocarcinoma	18258923	CNVD
Lung cancer	19138956	CNVD
Lung cancer	18379350	CNVD
Lung cancer	18258923	CNVD
Non-small cell lung cancer	18304967	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	19260752	CNVD
Non-small cell lung cancer	17079354	CNVD
Non-small cell lung cancer	18559607	CNVD
Rectal cancer	19506820	CNVD
Triple-negative breast cancer	18950515	CNVD
head and neck squamous cell carcinoma	18813952	CNVD
Non-small cell lung cancer	17504988	CNVD
Non-small cell lung cancer	16943533	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	17538160	CNVD
Colorectal cancer	19712476	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19671679	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
small cell lung cancer	20016488	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Multiple myeloma	16616336	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Congenital hypothyroidism	21372558	CNVD
Acute lymphoblastic leukemia	20534699	CNVD
Acute lymphoblastic leukemia	19039135	CNVD
Colorectal cancer	21645411	CNVD
Acute lymphoblastic leukemia	20699438	CNVD
Acute lymphoblastic leukemia	19129520	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	22368272	CNVD
Acute lymphoblastic leukemia	22157735	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:226 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:50342200-50344600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr7:50342400-50343400	Bivalent Enhancer	Placenta	Placenta
3	chr7:50342400-50344400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
4	chr7:50342600-50343400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
5	chr7:50342600-50344600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
6	chr7:50342800-50343400	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
7	chr7:50342800-50343400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr7:50342800-50343400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
9	chr7:50342800-50343400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
10	chr7:50342800-50343400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
11	chr7:50342800-50343400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr7:50342800-50343400	Bivalent Enhancer	Fetal Intestine Large	intestine
13	chr7:50342800-50343400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr7:50342800-50343400	Bivalent Enhancer	Lung	lung
15	chr7:50342800-50343400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
16	chr7:50342800-50344600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
17	chr7:50342800-50344600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
18	chr7:50342800-50344600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
19	chr7:50342800-50345000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
20	chr7:50342800-50345400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
21	chr7:50343000-50343400	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr7:50343000-50343400	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr7:50343000-50343400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
24	chr7:50343000-50343400	Flanking Active TSS	Primary B cells from cord blood	blood
25	chr7:50343000-50343400	Flanking Active TSS	Primary B cells from peripheral blood	blood
26	chr7:50343000-50343400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
27	chr7:50343000-50343400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
28	chr7:50343000-50343400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr7:50343000-50343400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
30	chr7:50343000-50343400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
31	chr7:50343000-50343400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
32	chr7:50343000-50343400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr7:50343000-50343400	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr7:50343000-50343400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
35	chr7:50343000-50343400	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
36	chr7:50343000-50343400	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
37	chr7:50343000-50343400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
38	chr7:50343000-50343400	Bivalent Enhancer	Fetal Brain Male	brain
39	chr7:50343000-50343400	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
40	chr7:50343000-50343400	Bivalent Enhancer	Fetal Stomach	stomach
41	chr7:50343000-50343400	Flanking Active TSS	Fetal Thymus	thymus
42	chr7:50343000-50343400	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
43	chr7:50343000-50343400	Flanking Active TSS	Thymus	Thymus
44	chr7:50343000-50343400	Flanking Active TSS	Dnd41	blood
45	chr7:50343000-50343600	Enhancers	Pancreas	Pancrea
46	chr7:50343000-50343800	Bivalent/Poised TSS	Right Ventricle	heart
47	chr7:50343000-50344000	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr7:50343000-50344200	Active TSS	Primary hematopoietic stem cells	blood
49	chr7:50343000-50344400	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr7:50343000-50344800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell

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