Variant report

Variant	nsv983171
Chromosome Location	chr11:4415208-4442456
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	BHLHE40	chr11:4414481-4415312	K562	blood:	n/a	n/a
2	CCNT2	chr11:4414788-4415241	K562	blood:	n/a	n/a
3	CEBPB	chr11:4435904-4436216	HepG2	liver:	n/a	chr11:4436054-4436063 chr11:4436052-4436063
4	CEBPB	chr11:4439846-4440117	Hela-S3	cervix:	n/a	chr11:4439975-4439986
5	CEBPB	chr11:4439808-4440108	HepG2	liver:	n/a	chr11:4439975-4439986
6	CTCF	chr11:4419569-4419609	Spleen_OC	spleen:	n/a	n/a
7	CTCF	chr11:4421657-4421686	GM10266	blood:	n/a	n/a
8	CTCF	chr11:4416384-4416425	Lung_OC	lung:	n/a	n/a
9	CTCF	chr11:4427604-4427678	MCF-7	breast:	n/a	n/a
10	EP300	chr11:4414753-4415221	K562	blood:	n/a	chr11:4414900-4414914
11	FOXA1	chr11:4427570-4427745	T-47D	breast:	n/a	n/a
12	FOXA2	chr11:4427540-4427797	A549	lung:	n/a	n/a
13	FOXA2	chr11:4427350-4427869	A549	lung:	n/a	n/a
14	FOXA2	chr11:4418286-4418682	A549	lung:	n/a	n/a
15	IRF1	chr11:4414533-4415244	K562	blood:	n/a	chr11:4414898-4414911 chr11:4414903-4414917 chr11:4414904-4414917 chr11:4414904-4414916 chr11:4414899-4414916 chr11:4414904-4414917 chr11:4414904-4414918 chr11:4414904-4414915 chr11:4414899-4414920 chr11:4414897-4414917 chr11:4414899-4414909 chr11:4414903-4414914 chr11:4414905-4414915 chr11:4414901-4414918 chr11:4414899-4414913 chr11:4414903-4414923 chr11:4414905-4414919 chr11:4414901-4414915 chr11:4414904-4414917 chr11:4414904-4414917
16	IRF1	chr11:4414029-4415251	K562	blood:	n/a	chr11:4414898-4414911 chr11:4414903-4414917 chr11:4414904-4414917 chr11:4414904-4414916 chr11:4414899-4414916 chr11:4414904-4414917 chr11:4414904-4414918 chr11:4414904-4414915 chr11:4414899-4414920 chr11:4414897-4414917 chr11:4414899-4414909 chr11:4414903-4414914 chr11:4414905-4414915 chr11:4414901-4414918 chr11:4414899-4414913 chr11:4414903-4414923 chr11:4414905-4414919 chr11:4414901-4414915 chr11:4414904-4414917 chr11:4414904-4414917
17	IRF3	chr11:4440407-4440446	GM12878	blood:	n/a	n/a
18	JUND	chr11:4414384-4415265	K562	blood:	n/a	n/a
19	MAFF	chr11:4437594-4437899	HepG2	liver:	n/a	n/a
20	MAFF	chr11:4437658-4437838	K562	blood:	n/a	n/a
21	MAFK	chr11:4437596-4437842	IMR90	lung:	n/a	chr11:4437719-4437730 chr11:4437720-4437731 chr11:4437719-4437735 chr11:4437718-4437732 chr11:4437719-4437730 chr11:4437719-4437734
22	MAFK	chr11:4437579-4437888	HepG2	liver:	n/a	chr11:4437719-4437730 chr11:4437720-4437731 chr11:4437719-4437735 chr11:4437718-4437732 chr11:4437719-4437730 chr11:4437719-4437734
23	MAFK	chr11:4437624-4437864	HepG2	liver:	n/a	chr11:4437719-4437730 chr11:4437720-4437731 chr11:4437719-4437735 chr11:4437718-4437732 chr11:4437719-4437730 chr11:4437719-4437734
24	MAFK	chr11:4433271-4433428	HepG2	liver:	n/a	chr11:4433336-4433350 chr11:4433354-4433364
25	MAX	chr11:4414767-4415225	K562	blood:	n/a	n/a
26	MAX	chr11:4414488-4415232	K562	blood:	n/a	n/a
27	MAZ	chr11:4414453-4415240	K562	blood:	n/a	n/a
28	MYC	chr11:4439938-4440074	MCF10A-Er-Src	breast:	n/a	n/a
29	MYC	chr11:4427957-4428053	MCF-7	breast:	n/a	n/a
30	MYC	chr11:4414298-4415335	K562	blood:	n/a	n/a
31	MYC	chr11:4439967-4440034	MCF10A-Er-Src	breast:	n/a	n/a
32	POLR2A	chr11:4418332-4418420	ProgFib	skin:	n/a	n/a
33	POLR2A	chr11:4414409-4415267	GM18526	blood:	n/a	n/a
34	POLR2A	chr11:4414181-4415266	GM19193	blood:	n/a	n/a
35	POLR2A	chr11:4437709-4437847	MCF10A-Er-Src	breast:	n/a	n/a
36	POLR2A	chr11:4414309-4415233	GM12892	blood:	n/a	n/a
37	POLR2A	chr11:4414323-4415288	K562	blood:	n/a	n/a
38	POLR2A	chr11:4439104-4439304	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr11:4415236-4415269	Gliobla	brain:	n/a	n/a
40	POLR2A	chr11:4414479-4415317	HL-60	blood:	n/a	n/a
41	POLR2A	chr11:4413936-4415362	K562	blood:	n/a	n/a
42	POLR2A	chr11:4439584-4439674	A549	lung:	n/a	n/a
43	POLR2A	chr11:4414359-4415234	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr11:4414394-4415332	PFSK-1	brain:	n/a	n/a
45	POLR2A	chr11:4414036-4415263	GM18505	blood:	n/a	n/a
46	POLR2A	chr11:4427949-4428052	MCF-7	breast:	n/a	n/a
47	POLR2A	chr11:4413932-4415280	GM18951	blood:	n/a	n/a
48	POLR2A	chr11:4414308-4415265	K562	blood:	n/a	n/a
49	POLR2A	chr11:4439682-4439706	A549	lung:	n/a	n/a
50	POLR2A	chr11:4413878-4415344	GM12891	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4415203-4415253	NHDF-neo	bronchial:	n/a
2	chr11:4415193-4415243	SK-N-SH_RA	brain:	n/a
3	chr11:4415203-4415253	Hepatocyte	liver:	n/a
4	chr11:4415245-4415295	A549	lung:	n/a
5	chr11:4415203-4415253	GM19239	blood:	n/a
6	chr11:4415245-4415295	SK-N-MC	brain:	n/a
7	chr11:4415193-4415243	GM12878	blood:	n/a
8	chr11:4415193-4415243	NHDF-neo	bronchial:	n/a
9	chr11:4415203-4415253	NT2-D1	testis:	n/a
10	chr11:4415203-4415253	IMR90	lung:	fetal
11	chr11:4415245-4415295	HIPEpiC	eye:	n/a
12	chr11:4415193-4415243	HMEC	breast:	n/a
13	chr11:4415203-4415253	BJ	skin:	n/a
14	chr11:4415245-4415295	HL-60	blood:	n/a
15	chr11:4415245-4415295	BE2_C	brain:	n/a
16	chr11:4415193-4415243	AG09309	skin:	n/a
17	chr11:4415193-4415243	HIPEpiC	eye:	n/a
18	chr11:4415245-4415295	HEEpiC	esophagus:	n/a
19	chr11:4415193-4415243	NHBE	bronchial:	n/a
20	chr11:4415203-4415253	AG10803	skin:	n/a
21	chr11:4415245-4415295	SK-N-SH	brain:	n/a
22	chr11:4415245-4415295	GM12892	blood:	n/a
23	chr11:4415193-4415243	HCT-116	colon:	n/a
24	chr11:4415245-4415295	IMR90	lung:	fetal
25	chr11:4415193-4415243	Caco-2	colon:	n/a
26	chr11:4415245-4415295	AG09319	gingival:	n/a
27	chr11:4415193-4415243	SK-N-MC	brain:	n/a
28	chr11:4415245-4415295	PANC-1	pancreas:	n/a
29	chr11:4415193-4415243	IMR90	lung:	fetal
30	chr11:4415203-4415253	HCPEpiC	choroid plexus:	n/a
31	chr11:4415203-4415253	PFSK-1	brain:	n/a
32	chr11:4415193-4415243	HNPCEpiC	eye:	n/a
33	chr11:4415203-4415253	HUVEC	blood vessel:	n/a
34	chr11:4415245-4415295	ovcar-3	ovarian:	n/a
35	chr11:4415193-4415243	SK-N-SH	brain:	n/a
36	chr11:4415193-4415243	HL-60	blood:	n/a
37	chr11:4415203-4415253	HRCEpiC	kidney:	n/a
38	chr11:4415203-4415253	SK-N-SH	brain:	n/a
39	chr11:4415203-4415253	LNCaP	prostate:	n/a
40	chr11:4415193-4415243	HRE	kidney:	n/a
41	chr11:4415203-4415253	NHBE	bronchial:	n/a
42	chr11:4415203-4415253	HepG2	liver:	n/a
43	chr11:4415245-4415295	ProgFib	skin:	n/a
44	chr11:4415245-4415295	HMEC	breast:	n/a
45	chr11:4415203-4415253	K562	blood:	n/a
46	chr11:4415203-4415253	HEK293	kidney:	embryo
47	chr11:4415245-4415295	HAEpiC	amniotic membrane:	n/a
48	chr11:4415245-4415295	K562	blood:	n/a
49	chr11:4415245-4415295	GM06990	blood:	n/a
50	chr11:4415193-4415243	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:4441835..4444233-chr11:4445411..4447480,2	K562	blood:
2	chr11:4406758..4409112-chr11:4414514..4416251,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR52K2-1	chr11:4431629-4432109	XLOC_009037
2	lnc-OR52K2-1	chr11:4415042-4415395	XLOC_009037

Variant related genes	Relation type
TRIM21	TF binding region
OR51R1P	TF binding region
TRIM21	CpG island
OR51R1P	CpG island
ENSG00000132109	chromatin interactions

Extended variants
information (count: 1277 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1277 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534690971	chr11:4415220-4415221	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
2	rs191306452	chr11:4415246-4415247	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs10767979	chr11:4415266-4415267	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs2599592	chr11:4415302-4415303	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs538732828	chr11:4415303-4415304	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs143500036	chr11:4415310-4415311	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs557140335	chr11:4415317-4415318	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs11032081	chr11:4415319-4415320	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs539765322	chr11:4415361-4415362	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs35064107	chr11:4415378-4415379	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs397717693	chr11:4415384-4415385	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs557236012	chr11:4415403-4415404	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs36233845	chr11:4415407-4415408	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs558134395	chr11:4415470-4415471	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs113127063	chr11:4415503-4415504	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs183782608	chr11:4415511-4415512	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs561870283	chr11:4415576-4415577	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs573773562	chr11:4415599-4415600	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs2735599	chr11:4415637-4415638	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs2162297	chr11:4415670-4415671	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs36233849	chr11:4415678-4415679	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs113600607	chr11:4415690-4415691	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs148564333	chr11:4415733-4415734	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs36233850	chr11:4415844-4415845	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs372737602	chr11:4415845-4415846	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs142902496	chr11:4415861-4415862	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs150693810	chr11:4415936-4415937	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs528530992	chr11:4415959-4415960	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs11820888	chr11:4415963-4415964	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs140181316	chr11:4415968-4415969	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs143635592	chr11:4415977-4415978	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs185738786	chr11:4415993-4415994	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs190155752	chr11:4415994-4415995	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs575111213	chr11:4416001-4416002	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs149874979	chr11:4416045-4416046	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs569124676	chr11:4416055-4416056	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs181651513	chr11:4416087-4416088	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs554312827	chr11:4416117-4416118	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs573455643	chr11:4416126-4416127	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs549623991	chr11:4416238-4416239	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs36233851	chr11:4416252-4416253	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs11032089	chr11:4416283-4416284	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs370517442	chr11:4416302-4416303	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs376903345	chr11:4416303-4416304	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs71050403	chr11:4416318-4416319	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs573635845	chr11:4416324-4416325	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs2975163	chr11:4416328-4416329	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs146783362	chr11:4416353-4416354	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs140627197	chr11:4416354-4416355	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs2554940	chr11:4416365-4416366	Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4413800-4415400	Active TSS	iPS-20b Cell Line	embryonic stem cell
2	chr11:4413800-4415400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr11:4413800-4415400	Active TSS	Brain Inferior Temporal Lobe	brain
4	chr11:4413800-4415400	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr11:4413800-4415400	Active TSS	Rectal Smooth Muscle	rectum
6	chr11:4414000-4415400	Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr11:4414000-4415400	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr11:4414000-4415400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr11:4414000-4415400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr11:4414000-4415400	Active TSS	Left Ventricle	heart
11	chr11:4414000-4415400	Active TSS	Right Atrium	heart
12	chr11:4414000-4415400	Active TSS	A549	lung
13	chr11:4414200-4415400	Active TSS	H9 Cell Line	embryonic stem cell
14	chr11:4414200-4415400	Active TSS	HUES64 Cell Line	embryonic stem cell
15	chr11:4414200-4415400	Active TSS	iPS-15b Cell Line	embryonic stem cell
16	chr11:4414200-4415400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr11:4414200-4415400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr11:4414200-4415400	Active TSS	Aorta	Aorta
19	chr11:4414200-4415400	Active TSS	Brain Anterior Caudate	brain
20	chr11:4414200-4415400	Active TSS	Brain Cingulate Gyrus	brain
21	chr11:4414200-4415400	Active TSS	Brain Germinal Matrix	brain
22	chr11:4414200-4415400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
23	chr11:4414200-4415400	Active TSS	Colonic Mucosa	Colon
24	chr11:4414200-4415400	Active TSS	Fetal Brain Female	brain
25	chr11:4414200-4415400	Active TSS	Fetal Kidney	kidney
26	chr11:4414200-4415400	Active TSS	Ovary	ovary
27	chr11:4414200-4415400	Active TSS	Skeletal Muscle Female	skeletal muscle
28	chr11:4414200-4415400	Active TSS	GM12878-XiMat	blood
29	chr11:4414400-4415400	Active TSS	Breast Myoepithelial Primary Cells	Breast
30	chr11:4414400-4415400	Active TSS	Colon Smooth Muscle	Colon
31	chr11:4414400-4415400	Active TSS	Duodenum Smooth Muscle	Duodenum
32	chr11:4414400-4415400	Active TSS	Placenta Amnion	Placenta Amnion
33	chr11:4414400-4415400	Active TSS	Thymus	Thymus
34	chr11:4414400-4415400	Active TSS	Hela-S3	cervix
35	chr11:4414400-4415400	Active TSS	HSMMtube	muscle
36	chr11:4414400-4415600	Active TSS	Stomach Smooth Muscle	stomach
37	chr11:4414600-4415400	Active TSS	Primary hematopoietic stem cells	blood
38	chr11:4414600-4415400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr11:4414600-4415400	Active TSS	Rectal Mucosa Donor 31	rectum
40	chr11:4414600-4415400	Active TSS	Skeletal Muscle Male	skeletal muscle
41	chr11:4414600-4416200	Active TSS	Primary B cells from cord blood	blood
42	chr11:4414800-4415400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr11:4414800-4415400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr11:4414800-4415400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr11:4414800-4415400	Active TSS	Fetal Muscle Trunk	muscle
46	chr11:4415000-4415400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr11:4415000-4415400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
48	chr11:4415000-4415400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
49	chr11:4415000-4415400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
50	chr11:4415000-4415400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--

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