Variant report

Variant	esv2755668
Chromosome Location	chr11:50218185-50344991
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:216)
CpG islands
(count:2015)
Chromatin interactive
region (count:1)
LncRNA
region (count:30)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:216 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:50257555-50257921	K562	blood:	n/a	n/a
2	ATF3	chr11:50257564-50257818	K562	blood:	n/a	chr11:50257726-50257746 chr11:50257724-50257737 chr11:50257584-50257592 chr11:50257723-50257738 chr11:50257725-50257736
3	BATF	chr11:50251866-50252053	GM12878	blood:	n/a	n/a
4	BHLHE40	chr11:50257408-50257634	K562	blood:	n/a	chr11:50257599-50257615
5	CCNT2	chr11:50257299-50257888	K562	blood:	n/a	n/a
6	CEBPB	chr11:50256020-50256220	HepG2	liver:	n/a	chr11:50256104-50256115
7	CEBPB	chr11:50230060-50230405	MCF-7	breast:	n/a	n/a
8	CEBPB	chr11:50233638-50233794	HepG2	liver:	n/a	n/a
9	CEBPB	chr11:50256005-50256238	K562	blood:	n/a	chr11:50256104-50256115
10	CREB1	chr11:50257411-50258094	K562	blood:	n/a	chr11:50257724-50257737
11	CREB1	chr11:50257549-50258023	K562	blood:	n/a	chr11:50257724-50257737
12	CTCF	chr11:50316423-50316519	GM10266	blood:	n/a	n/a
13	CTCF	chr11:50251507-50251620	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr11:50252665-50252796	Gliobla	brain:	n/a	n/a
15	CTCF	chr11:50251549-50251566	GM12878	blood:	n/a	n/a
16	CTCF	chr11:50317679-50317740	GM13976	blood:	n/a	n/a
17	CTCF	chr11:50257360-50257510	SK-N-SH_RA	brain:	n/a	chr11:50257436-50257449
18	CTCF	chr11:50262617-50262644	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr11:50305777-50305808	Lung_OC	lung:	n/a	n/a
20	CTCF	chr11:50284186-50284275	GM20000	blood:	n/a	n/a
21	CTCF	chr11:50251508-50251624	HUVEC	blood vessel:	n/a	n/a
22	CTCF	chr11:50257340-50257490	SK-N-SH_RA	brain:	n/a	chr11:50257436-50257449
23	CTCF	chr11:50264695-50264726	GM10266	blood:	n/a	n/a
24	CTCF	chr11:50252685-50252782	MCF-7	breast:	n/a	n/a
25	CTCF	chr11:50277249-50277334	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr11:50300095-50300112	GM10248	blood:	n/a	n/a
27	CTCF	chr11:50264521-50264545	GM13976	blood:	n/a	n/a
28	CTCF	chr11:50248936-50248972	Spleen_OC	spleen:	n/a	n/a
29	CTCF	chr11:50305210-50305247	GM20000	blood:	n/a	n/a
30	CTCF	chr11:50220602-50220640	MCF-7	breast:	n/a	n/a
31	CTCF	chr11:50293189-50293335	NHEK	skin:	n/a	n/a
32	CTCF	chr11:50312320-50312366	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr11:50257370-50257473	SK-N-SH_RA	brain:	n/a	chr11:50257436-50257449
34	CTCF	chr11:50293200-50293350	SAEC	small airway:	n/a	n/a
35	CTCF	chr11:50246753-50246827	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr11:50251518-50251615	Gliobla	brain:	n/a	n/a
37	CTCF	chr11:50291325-50291378	LNCaP	prostate:	n/a	n/a
38	CTCF	chr11:50251547-50251577	MCF-7	breast:	n/a	n/a
39	CTCF	chr11:50227575-50227627	LNCaP	prostate:	n/a	n/a
40	CTCF	chr11:50318115-50318201	GM10266	blood:	n/a	n/a
41	CTCF	chr11:50252435-50252463	GM13977	blood:	n/a	n/a
42	CTCF	chr11:50252669-50252790	Fibrobl	skin:	n/a	n/a
43	CTCF	chr11:50304509-50304621	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr11:50294779-50294808	GM20000	blood:	n/a	n/a
45	E2F6	chr11:50257450-50257783	K562	blood:	n/a	chr11:50257626-50257635 chr11:50257671-50257680
46	E2F6	chr11:50257236-50257997	K562	blood:	n/a	chr11:50257626-50257635 chr11:50257377-50257387 chr11:50257671-50257680
47	EGR1	chr11:50257609-50257827	K562	blood:	n/a	n/a
48	EGR1	chr11:50257540-50257866	K562	blood:	n/a	chr11:50257600-50257610
49	ELF1	chr11:50229900-50230327	MCF-7	breast:	n/a	chr11:50230098-50230109
50	EP300	chr11:50337674-50337737	GM12878	blood:	n/a	n/a

(count:2015 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:50234973-50235023	HUVEC	blood vessel:	n/a
2	chr11:50220343-50220393	SK-N-SH_RA	brain:	n/a
3	chr11:50234973-50235023	HUVEC	blood vessel:	n/a
4	chr11:50220343-50220393	SK-N-SH_RA	brain:	n/a
5	chr11:50254503-50254553	SKMC	muscle:	n/a
6	chr11:50257830-50257880	GM12878	blood:	n/a
7	chr11:50220426-50220476	AG10803	skin:	n/a
8	chr11:50238214-50238264	HAEpiC	amniotic membrane:	n/a
9	chr11:50239550-50239600	HNPCEpiC	eye:	n/a
10	chr11:50257496-50257546	HAEpiC	amniotic membrane:	n/a
11	chr11:50219952-50220002	T-47D	breast:	n/a
12	chr11:50257496-50257546	NHBE	bronchial:	n/a
13	chr11:50231261-50231311	LNCaP	prostate:	n/a
14	chr11:50258273-50258323	HCF	heart:	n/a
15	chr11:50257979-50258029	HNPCEpiC	eye:	n/a
16	chr11:50257496-50257546	T-47D	breast:	n/a
17	chr11:50257633-50257683	AG04449	skin:	fetal
18	chr11:50219952-50220002	NH-A	brain:	n/a
19	chr11:50239550-50239600	HAEpiC	amniotic membrane:	n/a
20	chr11:50257496-50257546	HEK293	kidney:	embryo
21	chr11:50257979-50258029	MCF-7	breast:	n/a
22	chr11:50219952-50220002	Jurkat	blood:	n/a
23	chr11:50260762-50260812	CMK	blood:	n/a
24	chr11:50236153-50236203	GM19239	blood:	n/a
25	chr11:50241016-50241066	BE2_C	brain:	n/a
26	chr11:50256574-50256624	HMEC	breast:	n/a
27	chr11:50254503-50254553	HUVEC	blood vessel:	n/a
28	chr11:50227102-50227152	SK-N-SH_RA	brain:	n/a
29	chr11:50238107-50238157	AG04449	skin:	fetal
30	chr11:50227199-50227249	SK-N-SH	brain:	n/a
31	chr11:50257771-50257821	NB4	blood:	n/a
32	chr11:50257625-50257675	Caco-2	colon:	n/a
33	chr11:50227265-50227315	IMR90	lung:	fetal
34	chr11:50231261-50231311	H1-hESC	embryonic stem cell:	embryo
35	chr11:50226789-50226839	HIPEpiC	eye:	n/a
36	chr11:50257256-50257306	ECC-1	luminal epithelium:	n/a
37	chr11:50227079-50227129	H1-hESC	embryonic stem cell:	embryo
38	chr11:50257979-50258029	HRPEpiC	eye:	n/a
39	chr11:50220426-50220476	ECC-1	luminal epithelium:	n/a
40	chr11:50220055-50220105	HAEpiC	amniotic membrane:	n/a
41	chr11:50257496-50257546	MCF-7	breast:	n/a
42	chr11:50227199-50227249	SK-N-SH_RA	brain:	n/a
43	chr11:50226789-50226839	H1-hESC	embryonic stem cell:	embryo
44	chr11:50257830-50257880	SKMC	muscle:	n/a
45	chr11:50257633-50257683	AoSMC	blood vessel:	n/a
46	chr11:50257830-50257880	HCF	heart:	n/a
47	chr11:50257979-50258029	HMEC	breast:	n/a
48	chr11:50227079-50227129	BJ	skin:	n/a
49	chr11:50257979-50258029	NHBE	bronchial:	n/a
50	chr11:50238107-50238157	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:50256839..50259422-chr11:50261676..50263683,2	K562	blood:

(count:30 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4C13-1	chr11:50261115-50261299	ENSG00000254518
2	lnc-OR4C13-7	chr11:50280085-50280169	NONHSAT021340
3	lnc-OR4C13-1	chr11:50257789-50258088	ENSG00000254518
4	lnc-OR4C13-7	chr11:50320143-50320239	NONHSAT021340
5	lnc-OR4C13-7	chr11:50279538-50279677	NONHSAT021339
6	lnc-OR4C13-1	chr11:50257750-50258210	NONHSAT021336
7	lnc-OR4C13-7	chr11:50279538-50279677	NONHSAT021340
8	lnc-OR4C13-7	chr11:50313156-50313246	NONHSAT021340
9	lnc-OR4C13-7	chr11:50302810-50303098	NONHSAT021342
10	lnc-OR4C13-1	chr11:50262310-50262433	ENSG00000254518
11	lnc-OR4C13-1	chr11:50257750-50258088	ENSG00000254518
12	lnc-OR4C12-1	chr11:50232840-50233106	XLOC_009440
13	lnc-OR4C13-7	chr11:50266792-50266898	NONHSAT021339
14	lnc-OR4C13-7	chr11:50279839-50280169	NONHSAT021342
15	lnc-OR4C13-1	chr11:50261115-50261299	NONHSAT021336
16	lnc-OR4C13-1	chr11:50262310-50262433	NONHSAT021336
17	lnc-OR4C13-7	chr11:50280085-50280169	NONHSAT021339
18	lnc-OR4C13-7	chr11:50301079-50301142	NONHSAT021343
19	lnc-OR4C13-7	chr11:50274586-50274778	NONHSAT021338
20	lnc-OR4C13-7	chr11:50274586-50274767	NONHSAT021339
21	lnc-OR4C13-1	chr11:50263752-50263827	NONHSAT021336
22	lnc-OR4C13-7	chr11:50274586-50274767	NONHSAT021340
23	lnc-OR4C13-7	chr11:50302810-50302996	NONHSAT021339
24	lnc-OR4C12-1	chr11:50231598-50231759	XLOC_009440
25	lnc-OR4C13-7	chr11:50301870-50302020	NONHSAT021343
26	lnc-OR4C13-7	chr11:50302810-50303035	NONHSAT021343
27	lnc-OR4C13-1	chr11:50263752-50263827	ENSG00000254518
28	lnc-OR4C13-7	chr11:50266792-50266965	NONHSAT021338
29	lnc-OR4C13-7	chr11:50266852-50266898	NONHSAT021340
30	lnc-OR4C13-7	chr11:50320710-50320877	NONHSAT021340

No data

Variant related genes	Relation type
ENSG00000254518	TF binding region
ENSG00000255042	TF binding region
ENSG00000255500	TF binding region
ENSG00000254840	TF binding region
ENSG00000255001	TF binding region
ENSG00000254518	CpG island
ENSG00000255042	CpG island
ENSG00000255500	CpG island
ENSG00000254840	CpG island
ENSG00000255001	CpG island
ENSG00000254518	chromatin interactions

Extended variants
information (count: 2797 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:2797 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4881692	chr11:50218185-50218186	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs572687459	chr11:50218186-50218187	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs541692287	chr11:50218187-50218188	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs540899963	chr11:50220017-50220018	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs537370521	chr11:50220027-50220028	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs550828806	chr11:50220039-50220040	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs188381358	chr11:50220071-50220072	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs536602437	chr11:50220095-50220096	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs553087180	chr11:50220117-50220118	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs150177372	chr11:50220135-50220136	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs138642101	chr11:50220142-50220143	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs558814127	chr11:50220161-50220162	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs181589091	chr11:50220189-50220190	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs185755492	chr11:50220238-50220239	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs554860222	chr11:50220274-50220275	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs577472765	chr11:50220322-50220323	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs72482390	chr11:50220323-50220324	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs540266718	chr11:50220360-50220361	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs559878663	chr11:50220361-50220362	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs188843201	chr11:50220385-50220386	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs545464893	chr11:50220387-50220388	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs565152891	chr11:50220410-50220411	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs141777559	chr11:50220427-50220428	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs80063275	chr11:50220475-50220476	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs564623442	chr11:50220528-50220529	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs55936442	chr11:50220534-50220535	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs567663807	chr11:50220557-50220558	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs146239143	chr11:50220609-50220610	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs118088191	chr11:50220613-50220614	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs547003672	chr11:50220643-50220644	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs566728775	chr11:50220649-50220650	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs377153100	chr11:50220695-50220696	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs112913409	chr11:50220773-50220774	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs569078413	chr11:50220810-50220811	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs182515886	chr11:50220830-50220831	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs535937537	chr11:50220838-50220839	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs538088105	chr11:50220854-50220855	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs187147319	chr11:50220894-50220895	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs562834968	chr11:50220965-50220966	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs574712985	chr11:50221017-50221018	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs370592137	chr11:50221056-50221057	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs137944651	chr11:50221098-50221099	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs553753723	chr11:50221118-50221119	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs576730699	chr11:50221151-50221152	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs191206376	chr11:50221166-50221167	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs374327811	chr11:50221170-50221171	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs531302067	chr11:50221175-50221176	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs554566883	chr11:50226826-50226827	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs11245610	chr11:50227080-50227081	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs367556623	chr11:50227089-50227090	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
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
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Mortal	21835882	CNVD
Autism	22495309	CNVD
Breast cancer	21785460	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	22522925	CNVD
Breast cancer	17142309	CNVD
Bipolar disorder	19214233	CNVD

Chromatin state (count:50 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:50217000-50218200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
2	chr11:50220000-50220800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:50220600-50221200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
4	chr11:50238000-50238400	ZNF genes & repeats	Esophagus	oesophagus
5	chr11:50242200-50242400	ZNF genes & repeats	Placenta	Placenta
6	chr11:50242400-50246200	Weak transcription	Placenta	Placenta
7	chr11:50246400-50256200	Weak transcription	Placenta	Placenta
8	chr11:50250800-50256200	Weak transcription	K562	blood
9	chr11:50256200-50256400	Enhancers	Placenta	Placenta
10	chr11:50256200-50258600	Active TSS	K562	blood
11	chr11:50256400-50256800	Flanking Active TSS	Placenta	Placenta
12	chr11:50256800-50257200	Active TSS	Placenta	Placenta
13	chr11:50257000-50258200	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
14	chr11:50257200-50257400	Flanking Active TSS	Placenta	Placenta
15	chr11:50257200-50257600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr11:50257200-50257600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr11:50257200-50257600	Active TSS	Primary T cells fromperipheralblood	blood
18	chr11:50257200-50257600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
19	chr11:50257200-50257600	Active TSS	Brain Cingulate Gyrus	brain
20	chr11:50257200-50257600	ZNF genes & repeats	Fetal Intestine Small	intestine
21	chr11:50257200-50257600	ZNF genes & repeats	Fetal Stomach	stomach
22	chr11:50257200-50257600	Active TSS	Ovary	ovary
23	chr11:50257200-50257600	Active TSS	Psoas Muscle	Psoas
24	chr11:50257200-50257600	Active TSS	Right Atrium	heart
25	chr11:50257200-50257600	Active TSS	Right Ventricle	heart
26	chr11:50257200-50257600	Active TSS	Skeletal Muscle Female	skeletal muscle
27	chr11:50257200-50257600	Active TSS	Stomach Smooth Muscle	stomach
28	chr11:50257200-50257600	Active TSS	HSMM	muscle
29	chr11:50257200-50258000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr11:50257200-50258000	ZNF genes & repeats	Gastric	stomach
31	chr11:50257200-50258000	ZNF genes & repeats	Pancreas	Pancrea
32	chr11:50257200-50258200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr11:50257400-50258000	Active TSS	Fetal Lung	lung
34	chr11:50257400-50258800	ZNF genes & repeats	Placenta	Placenta
35	chr11:50258000-50260600	Weak transcription	Gastric	stomach
36	chr11:50258800-50274600	Weak transcription	Placenta	Placenta
37	chr11:50260600-50260800	ZNF genes & repeats	Gastric	stomach
38	chr11:50274600-50275400	Strong transcription	Placenta	Placenta
39	chr11:50275400-50277000	Weak transcription	Placenta	Placenta
40	chr11:50295800-50296200	Enhancers	Adipose Nuclei	Adipose
41	chr11:50324400-50325400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
42	chr11:50326400-50345800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr11:50326600-50328800	ZNF genes & repeats	Liver	Liver
44	chr11:50330000-50331600	ZNF genes & repeats	Liver	Liver
45	chr11:50337400-50343400	ZNF genes & repeats	Liver	Liver
46	chr11:50337600-50341800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
47	chr11:50340600-50341400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr11:50341600-50345800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
49	chr11:50342800-50343200	Active TSS	Right Atrium	heart
50	chr11:50344800-50345600	Active TSS	Fetal Heart	heart

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