Variant report

Variant	nsv1053571
Chromosome Location	chr11:48286642-48388686
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	ATF1	chr11:48356437-48356637	K562	blood:	n/a	n/a
2	ATF1	chr11:48292484-48292679	K562	blood:	n/a	n/a
3	BACH1	chr11:48356973-48356986	K562	blood:	n/a	n/a
4	BRCA1	chr11:48329323-48329679	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr11:48361931-48361935	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr11:48329320-48329744	HCT-116	colon:	n/a	n/a
7	CEBPB	chr11:48367027-48367324	HCT-116	colon:	n/a	n/a
8	CEBPB	chr11:48376639-48376671	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr11:48374701-48375094	Hela-S3	cervix:	n/a	chr11:48374900-48374913
10	CEBPB	chr11:48332469-48332671	HepG2	liver:	n/a	chr11:48332598-48332609
11	CEBPB	chr11:48367001-48367415	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr11:48367014-48367428	HCT-116	colon:	n/a	n/a
13	CEBPB	chr11:48367044-48367318	HepG2	liver:	n/a	n/a
14	CEBPB	chr11:48340990-48341301	A549	lung:	n/a	n/a
15	CEBPZ	chr11:48360331-48360376	HepG2	liver:	n/a	n/a
16	CHD2	chr11:48344566-48344658	K562	blood:	n/a	n/a
17	CHD2	chr11:48377806-48377814	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr11:48367060-48367210	K562	blood:	n/a	n/a
19	CTCF	chr11:48329328-48329674	Gliobla	brain:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
20	CTCF	chr11:48329357-48329635	GM19238	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
21	CTCF	chr11:48387460-48387610	MCF-7	breast:	n/a	n/a
22	CTCF	chr11:48329360-48329510	HCM	heart:	n/a	n/a
23	CTCF	chr11:48329294-48329647	T-47D	breast:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
24	CTCF	chr11:48329440-48329590	HCPEpiC	choroid plexus:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
25	CTCF	chr11:48329377-48329634	GM19239	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
26	CTCF	chr11:48387380-48387530	MCF-7	breast:	n/a	n/a
27	CTCF	chr11:48362100-48362250	A549	lung:	n/a	n/a
28	CTCF	chr11:48362000-48362150	GM12875	blood:	n/a	n/a
29	CTCF	chr11:48329291-48329731	GM12878	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
30	CTCF	chr11:48329420-48329570	AG09309	skin:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
31	CTCF	chr11:48297227-48297276	LNCaP	prostate:	n/a	n/a
32	CTCF	chr11:48317603-48317627	Medullo	brain:	n/a	n/a
33	CTCF	chr11:48329420-48329570	K562	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
34	CTCF	chr11:48387474-48387580	MCF-7	breast:	n/a	n/a
35	CTCF	chr11:48347233-48347255	Fibrobl	skin:	n/a	n/a
36	CTCF	chr11:48329440-48329590	HRE	kidney:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
37	CTCF	chr11:48329440-48329590	AoAF	blood vessel:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
38	CTCF	chr11:48329440-48329590	HBMEC	blood vessel:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
39	CTCF	chr11:48329354-48329651	MCF-7	breast:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
40	CTCF	chr11:48329400-48329550	GM12871	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
41	CTCF	chr11:48329460-48329610	GM12870	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
42	CTCF	chr11:48327760-48327910	GM12864	blood:	n/a	n/a
43	CTCF	chr11:48355180-48355330	HFF-Myc	foreskin:	n/a	n/a
44	CTCF	chr11:48382500-48382650	HPF	lung:	n/a	n/a
45	CTCF	chr11:48353060-48353210	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr11:48329406-48329641	GM20000	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
47	CTCF	chr11:48329440-48329590	HVMF	connective:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533
48	CTCF	chr11:48387460-48387610	GM12873	blood:	n/a	n/a
49	CTCF	chr11:48290040-48290190	GM06990	blood:	n/a	n/a
50	CTCF	chr11:48329480-48329630	GM12875	blood:	n/a	chr11:48329513-48329526 chr11:48329511-48329527 chr11:48329510-48329528 chr11:48329512-48329533

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48328132-48328182	HEK293	kidney:	embryo
2	chr11:48328132-48328182	HEK293	kidney:	embryo
3	chr11:48328132-48328182	SK-N-SH_RA	brain:	n/a
4	chr11:48326388-48326438	AG09309	skin:	n/a
5	chr11:48328132-48328182	HCPEpiC	choroid plexus:	n/a
6	chr11:48346680-48346730	HNPCEpiC	eye:	n/a
7	chr11:48345815-48345865	AG04450	lung:	fetal
8	chr11:48374446-48374496	SK-N-SH_RA	brain:	n/a
9	chr11:48345815-48345865	NH-A	brain:	n/a
10	chr11:48345361-48345411	NB4	blood:	n/a
11	chr11:48345815-48345865	Jurkat	blood:	n/a
12	chr11:48367974-48368024	HCT-116	colon:	n/a
13	chr11:48374446-48374496	HCT-116	colon:	n/a
14	chr11:48374446-48374496	PFSK-1	brain:	n/a
15	chr11:48367974-48368024	NB4	blood:	n/a
16	chr11:48346680-48346730	GM12878	blood:	n/a
17	chr11:48326388-48326438	HCM	heart:	n/a
18	chr11:48328132-48328182	HUVEC	blood vessel:	n/a
19	chr11:48346680-48346730	T-47D	breast:	n/a
20	chr11:48367974-48368024	HRCEpiC	kidney:	n/a
21	chr11:48367974-48368024	SKMC	muscle:	n/a
22	chr11:48327164-48327214	BJ	skin:	n/a
23	chr11:48374446-48374496	HRPEpiC	eye:	n/a
24	chr11:48346680-48346730	PFSK-1	brain:	n/a
25	chr11:48345361-48345411	A549	lung:	n/a
26	chr11:48346680-48346730	A549	lung:	n/a
27	chr11:48328132-48328182	RPTEC	kidney:	n/a
28	chr11:48346680-48346730	RPTEC	kidney:	n/a
29	chr11:48346680-48346730	BJ	skin:	n/a
30	chr11:48327164-48327214	HRCEpiC	kidney:	n/a
31	chr11:48328132-48328182	Jurkat	blood:	n/a
32	chr11:48374446-48374496	NT2-D1	testis:	n/a
33	chr11:48326388-48326438	HRPEpiC	eye:	n/a
34	chr11:48374446-48374496	MCF10A-Er-Src	breast:	n/a
35	chr11:48345815-48345865	GM12891	blood:	n/a
36	chr11:48345815-48345865	PrEC	prostate:	n/a
37	chr11:48327164-48327214	HPAEpiC	pulmonary alveolar:	n/a
38	chr11:48327164-48327214	NHBE	bronchial:	n/a
39	chr11:48326388-48326438	Hepatocyte	liver:	n/a
40	chr11:48346680-48346730	HCF	heart:	n/a
41	chr11:48327164-48327214	HNPCEpiC	eye:	n/a
42	chr11:48367974-48368024	AG04449	skin:	fetal
43	chr11:48328132-48328182	SK-N-SH	brain:	n/a
44	chr11:48345361-48345411	GM19239	blood:	n/a
45	chr11:48374446-48374496	SAEC	small airway:	n/a
46	chr11:48327164-48327214	SK-N-SH	brain:	n/a
47	chr11:48327164-48327214	SK-N-MC	brain:	n/a
48	chr11:48345361-48345411	HNPCEpiC	eye:	n/a
49	chr11:48374446-48374496	PrEC	prostate:	n/a
50	chr11:48367974-48368024	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:
2	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:
3	chr11:48366878..48368914-chr11:48372533..48375413,2	MCF-7	breast:
4	chr11:48234220..48234962-chr11:48329425..48329937,2	MCF-7	breast:
5	chr11:48361908..48364233-chr11:48365831..48368223,2	MCF-7	breast:
6	chr11:48361908..48364233-chr11:48365831..48368223,2	MCF-7	breast:

Variant related genes	Relation type
OR4C5	TF binding region
OR4C4P	TF binding region
OR4C3	TF binding region
OR4S1	TF binding region
OR4C5	CpG island
OR4C4P	CpG island
OR4C3	CpG island
OR4S1	CpG island
ENSG00000197161	chromatin interactions

Extended variants
information (count: 4309 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:4309 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189196044	chr11:48288801-48288802	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs192437591	chr11:48288804-48288805	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs112535907	chr11:48288818-48288819	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs369938041	chr11:48288850-48288851	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs184801692	chr11:48288860-48288861	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs573756488	chr11:48288932-48288933	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs541511793	chr11:48288946-48288947	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs12577906	chr11:48288977-48288978	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs532790265	chr11:48293405-48293406	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs115526670	chr11:48293413-48293414	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs7484031	chr11:48293468-48293469	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs531093043	chr11:48293502-48293503	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs116345138	chr11:48293503-48293504	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs7481374	chr11:48293530-48293531	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs151227423	chr11:48293534-48293535	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs547049070	chr11:48293547-48293548	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs566836168	chr11:48293549-48293550	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs534936196	chr11:48293580-48293581	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs557993725	chr11:48293586-48293587	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs577854008	chr11:48293589-48293590	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs571757334	chr11:48293611-48293612	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs537301385	chr11:48293626-48293627	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs556857834	chr11:48293643-48293644	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs140378084	chr11:48293666-48293667	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs376027304	chr11:48293667-48293668	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs553328902	chr11:48293684-48293685	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs542283167	chr11:48293693-48293694	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs558946333	chr11:48293706-48293707	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs369601898	chr11:48293712-48293713	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs537574494	chr11:48293721-48293722	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs137899758	chr11:48293737-48293738	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs545304085	chr11:48293774-48293775	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs565612387	chr11:48293798-48293799	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs117763203	chr11:48293825-48293826	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs551181974	chr11:48293876-48293877	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs561305913	chr11:48293920-48293921	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs530231128	chr11:48293930-48293931	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs11039627	chr11:48293931-48293932	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs182520599	chr11:48293932-48293933	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs539078913	chr11:48293940-48293941	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs535705251	chr11:48293974-48293975	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs142114838	chr11:48293982-48293983	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs117274651	chr11:48294037-48294038	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs370999769	chr11:48294062-48294063	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs536933241	chr11:48294072-48294073	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs557135730	chr11:48294073-48294074	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs573474448	chr11:48294076-48294077	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs535946810	chr11:48294077-48294078	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs552609948	chr11:48294081-48294082	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs116419081	chr11:48294109-48294110	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	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
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Breast cancer	21990379	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48288800-48289000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:48293400-48294200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
3	chr11:48293600-48294200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
4	chr11:48294000-48294400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
5	chr11:48294400-48295000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
6	chr11:48294800-48295200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
7	chr11:48295000-48295200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
8	chr11:48314000-48314400	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr11:48328000-48328400	Enhancers	Lung	lung
10	chr11:48329400-48329800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
11	chr11:48329400-48330000	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr11:48329600-48329800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
13	chr11:48329600-48329800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr11:48329600-48329800	Enhancers	Brain Angular Gyrus	brain
15	chr11:48329600-48329800	Enhancers	Brain Cingulate Gyrus	brain
16	chr11:48329600-48329800	Enhancers	Brain Hippocampus Middle	brain
17	chr11:48336400-48337600	Enhancers	Stomach Mucosa	stomach
18	chr11:48337600-48341200	Weak transcription	Stomach Mucosa	stomach
19	chr11:48341200-48342600	Enhancers	Stomach Mucosa	stomach
20	chr11:48341400-48345800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
21	chr11:48341600-48341800	Bivalent Enhancer	Left Ventricle	heart
22	chr11:48341600-48342000	Bivalent Enhancer	Right Atrium	heart
23	chr11:48341600-48342000	Enhancers	Spleen	Spleen
24	chr11:48341800-48342000	Enhancers	Left Ventricle	heart
25	chr11:48342600-48344400	Weak transcription	Stomach Mucosa	stomach
26	chr11:48344400-48344800	Enhancers	Stomach Mucosa	stomach
27	chr11:48344800-48349800	Weak transcription	Stomach Mucosa	stomach
28	chr11:48346600-48346800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr11:48346600-48347000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
30	chr11:48346600-48347400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
31	chr11:48346600-48348600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr11:48346800-48347400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr11:48348800-48350000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr11:48350000-48355600	Weak transcription	Stomach Mucosa	stomach
35	chr11:48352400-48353400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
36	chr11:48352400-48353800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
37	chr11:48353000-48359800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
38	chr11:48355200-48363800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
39	chr11:48355600-48357000	Enhancers	Stomach Mucosa	stomach
40	chr11:48357000-48358000	Weak transcription	Stomach Mucosa	stomach
41	chr11:48358000-48358200	Enhancers	Stomach Mucosa	stomach
42	chr11:48362000-48362200	Enhancers	Primary T helper naive cells from peripheral blood	blood
43	chr11:48362400-48362800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr11:48362800-48363200	Enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr11:48362800-48363200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr11:48362800-48363600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
47	chr11:48362800-48363800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
48	chr11:48363000-48363200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr11:48363000-48363400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr11:48363000-48363400	Active TSS	A549	lung

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