Variant report

Variant	nsv897513
Chromosome Location	chr11:50245252-51093950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2588)
CpG islands
(count:917)
Chromatin interactive
region (count:3)
LncRNA
region (count:45)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2588 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:50712564-50712666	K562	blood:	n/a	n/a
2	ATF1	chr11:50381201-50381204	K562	blood:	n/a	n/a
3	ATF1	chr11:50767721-50767932	K562	blood:	n/a	n/a
4	ATF1	chr11:50741510-50741536	K562	blood:	n/a	n/a
5	ATF1	chr11:50409411-50409611	K562	blood:	n/a	n/a
6	ATF1	chr11:50728352-50728528	K562	blood:	n/a	n/a
7	ATF1	chr11:50771363-50771551	K562	blood:	n/a	n/a
8	ATF1	chr11:50721580-50721799	K562	blood:	n/a	n/a
9	ATF1	chr11:50676160-50676529	K562	blood:	n/a	n/a
10	ATF1	chr11:50757990-50758182	K562	blood:	n/a	n/a
11	ATF1	chr11:50257555-50257921	K562	blood:	n/a	n/a
12	ATF1	chr11:50755176-50755720	K562	blood:	n/a	n/a
13	ATF3	chr11:50257564-50257818	K562	blood:	n/a	chr11:50257726-50257746 chr11:50257724-50257737 chr11:50257584-50257592 chr11:50257723-50257738 chr11:50257725-50257736
14	BACH1	chr11:50780465-50780837	K562	blood:	n/a	n/a
15	BACH1	chr11:50699638-50700011	K562	blood:	n/a	n/a
16	BACH1	chr11:50767401-50767428	K562	blood:	n/a	n/a
17	BACH1	chr11:50739007-50739300	K562	blood:	n/a	n/a
18	BACH1	chr11:50744265-50744293	K562	blood:	n/a	n/a
19	BACH1	chr11:50765324-50765524	K562	blood:	n/a	n/a
20	BACH1	chr11:50741715-50742187	K562	blood:	n/a	n/a
21	BACH1	chr11:50759699-50760188	K562	blood:	n/a	n/a
22	BACH1	chr11:50762679-50763056	K562	blood:	n/a	n/a
23	BACH1	chr11:50769674-50770049	K562	blood:	n/a	n/a
24	BATF	chr11:50681509-50681669	GM12878	blood:	n/a	n/a
25	BATF	chr11:50711195-50711416	GM12878	blood:	n/a	n/a
26	BATF	chr11:50756315-50756627	GM12878	blood:	n/a	n/a
27	BATF	chr11:50670735-50670974	GM12878	blood:	n/a	n/a
28	BATF	chr11:50768336-50768651	GM12878	blood:	n/a	n/a
29	BATF	chr11:50649412-50649706	GM12878	blood:	n/a	n/a
30	BATF	chr11:50676256-50676541	GM12878	blood:	n/a	n/a
31	BATF	chr11:50676209-50676542	GM12878	blood:	n/a	n/a
32	BATF	chr11:50764084-50764312	GM12878	blood:	n/a	n/a
33	BATF	chr11:50670092-50670325	GM12878	blood:	n/a	n/a
34	BATF	chr11:50761809-50762209	GM12878	blood:	n/a	n/a
35	BATF	chr11:50687048-50687278	GM12878	blood:	n/a	n/a
36	BATF	chr11:50688591-50688754	GM12878	blood:	n/a	n/a
37	BATF	chr11:50767583-50768188	GM12878	blood:	n/a	n/a
38	BATF	chr11:50686999-50687394	GM12878	blood:	n/a	n/a
39	BATF	chr11:50685636-50685821	GM12878	blood:	n/a	n/a
40	BATF	chr11:50668601-50668765	GM12878	blood:	n/a	n/a
41	BATF	chr11:50723560-50724069	GM12878	blood:	n/a	n/a
42	BATF	chr11:50764082-50764319	GM12878	blood:	n/a	n/a
43	BATF	chr11:50722179-50722655	GM12878	blood:	n/a	n/a
44	BATF	chr11:50772283-50772434	GM12878	blood:	n/a	n/a
45	BATF	chr11:50742992-50743342	GM12878	blood:	n/a	n/a
46	BATF	chr11:50757466-50757719	GM12878	blood:	n/a	n/a
47	BATF	chr11:50755495-50755763	GM12878	blood:	n/a	n/a
48	BATF	chr11:50700733-50700935	GM12878	blood:	n/a	n/a
49	BATF	chr11:50772285-50772433	GM12878	blood:	n/a	n/a
50	BATF	chr11:50721484-50721792	GM12878	blood:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:50258750-50258800	Hela-S3	cervix:	n/a
2	chr11:50257496-50257546	ECC-1	luminal epithelium:	n/a
3	chr11:50258750-50258800	Hela-S3	cervix:	n/a
4	chr11:50257496-50257546	ECC-1	luminal epithelium:	n/a
5	chr11:50257625-50257675	HepG2	liver:	n/a
6	chr11:50257830-50257880	PrEC	prostate:	n/a
7	chr11:50256574-50256624	HAEpiC	amniotic membrane:	n/a
8	chr11:50260762-50260812	NT2-D1	testis:	n/a
9	chr11:50257256-50257306	HIPEpiC	eye:	n/a
10	chr11:50257496-50257546	Jurkat	blood:	n/a
11	chr11:50254503-50254553	AG04449	skin:	fetal
12	chr11:50257752-50257802	SAEC	small airway:	n/a
13	chr11:50257625-50257675	NB4	blood:	n/a
14	chr11:50256574-50256624	LNCaP	prostate:	n/a
15	chr11:50260762-50260812	SK-N-SH_RA	brain:	n/a
16	chr11:50260762-50260812	GM12878	blood:	n/a
17	chr11:50256574-50256624	HEK293	kidney:	embryo
18	chr11:50258273-50258323	HCM	heart:	n/a
19	chr11:50257256-50257306	GM19239	blood:	n/a
20	chr11:50368251-50368301	BE2_C	brain:	n/a
21	chr11:50258750-50258800	HCM	heart:	n/a
22	chr11:50257633-50257683	ProgFib	skin:	n/a
23	chr11:50257496-50257546	AoSMC	blood vessel:	n/a
24	chr11:50257625-50257675	HEK293	kidney:	embryo
25	chr11:50257979-50258029	HepG2	liver:	n/a
26	chr11:50257633-50257683	BJ	skin:	n/a
27	chr11:50257633-50257683	AG09319	gingival:	n/a
28	chr11:50257256-50257306	HPAEpiC	pulmonary alveolar:	n/a
29	chr11:50257633-50257683	HCM	heart:	n/a
30	chr11:50254503-50254553	HEEpiC	esophagus:	n/a
31	chr11:50254503-50254553	NB4	blood:	n/a
32	chr11:50254503-50254553	GM12878	blood:	n/a
33	chr11:50257830-50257880	AoSMC	blood vessel:	n/a
34	chr11:50258750-50258800	PANC-1	pancreas:	n/a
35	chr11:50368251-50368301	NHBE	bronchial:	n/a
36	chr11:50257496-50257546	H1-hESC	embryonic stem cell:	embryo
37	chr11:50368251-50368301	NH-A	brain:	n/a
38	chr11:50371681-50371731	HRPEpiC	eye:	n/a
39	chr11:50257496-50257546	SAEC	small airway:	n/a
40	chr11:50257496-50257546	MCF-7	breast:	n/a
41	chr11:50371681-50371731	AG09319	gingival:	n/a
42	chr11:50256574-50256624	ovcar-3	ovarian:	n/a
43	chr11:50257256-50257306	IMR90	lung:	fetal
44	chr11:50258273-50258323	SKMC	muscle:	n/a
45	chr11:50371681-50371731	HCM	heart:	n/a
46	chr11:50257633-50257683	A549	lung:	n/a
47	chr11:50254503-50254553	HEK293	kidney:	embryo
48	chr11:50256574-50256624	K562	blood:	n/a
49	chr11:50257752-50257802	HRE	kidney:	n/a
50	chr11:50257625-50257675	HMEC	breast:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:50256839..50259422-chr11:50261676..50263683,2	K562	blood:
2	chr11:50731452..50731974-chr8:46856234..46856754,2	MCF-7	breast:
3	chr11:50670378..50671219-chr4:101762576..101763076,2	MCF-7	breast:

(count:45 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4C13-7	chr11:50313156-50313246	NONHSAT021340
2	lnc-OR4C13-9	chr11:50379313-50379802	NONHSAT021344
3	lnc-OR4C13-7	chr11:50302810-50303098	NONHSAT021342
4	lnc-OR4C13-9	chr11:50379313-50379548	NR_024504
5	lnc-OR4C13-1	chr11:50263752-50263827	NONHSAT021336
6	lnc-OR4C13-7	chr11:50266792-50266965	NONHSAT021338
7	lnc-OR4C13-7	chr11:50266852-50266898	NONHSAT021340
8	lnc-OR4C13-9	chr11:50375235-50375391	NONHSAT021345
9	lnc-OR4C13-9	chr11:50378065-50378165	NONHSAT021344
10	lnc-OR4C13-1	chr11:50261115-50261299	NONHSAT021336
11	lnc-OR4C13-7	chr11:50320143-50320239	NONHSAT021340
12	lnc-OR4C13-7	chr11:50274586-50274767	NONHSAT021339
13	lnc-OR4C13-9	chr11:50376439-50376850	NONHSAT021345
14	lnc-OR4C13-9	chr11:50368739-50368821	NR_024504
15	lnc-OR4C13-9	chr11:50375274-50375391	NR_024504
16	lnc-OR4C13-7	chr11:50266792-50266898	NONHSAT021339
17	lnc-OR4C13-1	chr11:50262310-50262433	NONHSAT021336
18	lnc-OR4C13-7	chr11:50302810-50302996	NONHSAT021339
19	lnc-OR4C13-7	chr11:50302810-50303035	NONHSAT021343
20	lnc-OR4C13-7	chr11:50274586-50274778	NONHSAT021338
21	lnc-OR4C13-1	chr11:50257750-50258088	ENSG00000254518
22	lnc-OR4C13-7	chr11:50274586-50274767	NONHSAT021340
23	lnc-OR4C13-1	chr11:50263752-50263827	ENSG00000254518
24	lnc-OR4C13-7	chr11:50279538-50279677	NONHSAT021339
25	lnc-OR4C13-9	chr11:50368318-50368359	NR_024504
26	lnc-OR4C13-9	chr11:50379775-50379803	NONHSAT021345
27	lnc-OR4C13-9	chr11:50375235-50375391	NONHSAT021344
28	lnc-OR4C13-9	chr11:50379313-50379548	NONHSAT021345
29	lnc-OR4C13-7	chr11:50280085-50280169	NONHSAT021339
30	lnc-OR4C13-1	chr11:50257789-50258088	ENSG00000254518
31	lnc-OR4C13-7	chr11:50320710-50320877	NONHSAT021340
32	lnc-OR4C13-7	chr11:50301079-50301142	NONHSAT021343
33	lnc-OR4C13-9	chr11:50379775-50379802	NR_024504
34	lnc-OR4C13-1	chr11:50261115-50261299	ENSG00000254518
35	lnc-OR4C13-9	chr11:50378065-50378165	NR_024504
36	lnc-OR4C13-9	chr11:50376439-50376850	NONHSAT021344
37	lnc-OR4C13-7	chr11:50301870-50302020	NONHSAT021343
38	lnc-OR4C13-9	chr11:50368318-50368359	NONHSAT021344
39	lnc-OR4C13-1	chr11:50262310-50262433	ENSG00000254518
40	lnc-OR4C13-9	chr11:50378065-50378165	NONHSAT021345
41	lnc-OR4C13-7	chr11:50279538-50279677	NONHSAT021340
42	lnc-OR4C13-7	chr11:50279839-50280169	NONHSAT021342
43	lnc-OR4C13-9	chr11:50368739-50368821	NONHSAT021344
44	lnc-OR4C13-1	chr11:50257750-50258210	NONHSAT021336
45	lnc-OR4C13-7	chr11:50280085-50280169	NONHSAT021340

No data

Variant related genes	Relation type
ENSG00000254840	TF binding region
ENSG00000255001	TF binding region
ENSG00000254518	TF binding region
ENSG00000255042	TF binding region
ENSG00000214883	TF binding region
ENSG00000254840	CpG island
ENSG00000255001	CpG island
ENSG00000254518	CpG island
ENSG00000255042	CpG island
ENSG00000214883	CpG island
ENSG00000254518	chromatin interactions

Extended variants
information (count: 32823 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:32823 , 50 per page) page: 1 2 3 4 5 6 7 ... 657

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10736895	chr11:50245252-50245253	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs538123088	chr11:50245260-50245261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566208555	chr11:50245275-50245276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548574377	chr11:50245321-50245322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538698443	chr11:50245345-50245346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184212471	chr11:50245347-50245348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534188097	chr11:50245348-50245349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs61893067	chr11:50245403-50245404	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs576905064	chr11:50245407-50245408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539271320	chr11:50245445-50245446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555903576	chr11:50245487-50245488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576966139	chr11:50245489-50245490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568797656	chr11:50245526-50245527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575937507	chr11:50245580-50245581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs186245043	chr11:50245624-50245625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12787917	chr11:50245654-50245655	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs189737492	chr11:50245664-50245665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541007055	chr11:50245694-50245695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs61893068	chr11:50245715-50245716	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs533033747	chr11:50245754-50245755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552819823	chr11:50245763-50245764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563031341	chr11:50245799-50245800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532037120	chr11:50245811-50245812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141363856	chr11:50245820-50245821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150240837	chr11:50245821-50245822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533966660	chr11:50245906-50245907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547358571	chr11:50245921-50245922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138819587	chr11:50245970-50245971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182080046	chr11:50245974-50245975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555940381	chr11:50246068-50246069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs111600017	chr11:50246095-50246096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187078805	chr11:50246166-50246167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs116048126	chr11:50246182-50246183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570463799	chr11:50246418-50246419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12800452	chr11:50246427-50246428	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs549900843	chr11:50246434-50246435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs570122408	chr11:50246438-50246439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535320110	chr11:50246453-50246454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555513602	chr11:50246481-50246482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs565854626	chr11:50246490-50246491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534875484	chr11:50246500-50246501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192891821	chr11:50246513-50246514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577761055	chr11:50246514-50246515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577286229	chr11:50246522-50246523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557120292	chr11:50246530-50246531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546244621	chr11:50246532-50246533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573651521	chr11:50246538-50246539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184914965	chr11:50246549-50246550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562268866	chr11:50246559-50246560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527978077	chr11:50246560-50246561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Medulloblastoma	21163964	CNVD
early-passage human iPS cells	21368824	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:668 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:50242400-50246200	Weak transcription	Placenta	Placenta
2	chr11:50246400-50256200	Weak transcription	Placenta	Placenta
3	chr11:50250800-50256200	Weak transcription	K562	blood
4	chr11:50256200-50256400	Enhancers	Placenta	Placenta
5	chr11:50256200-50258600	Active TSS	K562	blood
6	chr11:50256400-50256800	Flanking Active TSS	Placenta	Placenta
7	chr11:50256800-50257200	Active TSS	Placenta	Placenta
8	chr11:50257000-50258200	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
9	chr11:50257200-50257400	Flanking Active TSS	Placenta	Placenta
10	chr11:50257200-50257600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr11:50257200-50257600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr11:50257200-50257600	Active TSS	Primary T cells fromperipheralblood	blood
13	chr11:50257200-50257600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
14	chr11:50257200-50257600	Active TSS	Brain Cingulate Gyrus	brain
15	chr11:50257200-50257600	ZNF genes & repeats	Fetal Intestine Small	intestine
16	chr11:50257200-50257600	ZNF genes & repeats	Fetal Stomach	stomach
17	chr11:50257200-50257600	Active TSS	Ovary	ovary
18	chr11:50257200-50257600	Active TSS	Psoas Muscle	Psoas
19	chr11:50257200-50257600	Active TSS	Right Atrium	heart
20	chr11:50257200-50257600	Active TSS	Right Ventricle	heart
21	chr11:50257200-50257600	Active TSS	Skeletal Muscle Female	skeletal muscle
22	chr11:50257200-50257600	Active TSS	Stomach Smooth Muscle	stomach
23	chr11:50257200-50257600	Active TSS	HSMM	muscle
24	chr11:50257200-50258000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr11:50257200-50258000	ZNF genes & repeats	Gastric	stomach
26	chr11:50257200-50258000	ZNF genes & repeats	Pancreas	Pancrea
27	chr11:50257200-50258200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr11:50257400-50258000	Active TSS	Fetal Lung	lung
29	chr11:50257400-50258800	ZNF genes & repeats	Placenta	Placenta
30	chr11:50258000-50260600	Weak transcription	Gastric	stomach
31	chr11:50258800-50274600	Weak transcription	Placenta	Placenta
32	chr11:50260600-50260800	ZNF genes & repeats	Gastric	stomach
33	chr11:50274600-50275400	Strong transcription	Placenta	Placenta
34	chr11:50275400-50277000	Weak transcription	Placenta	Placenta
35	chr11:50295800-50296200	Enhancers	Adipose Nuclei	Adipose
36	chr11:50324400-50325400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
37	chr11:50326400-50345800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr11:50326600-50328800	ZNF genes & repeats	Liver	Liver
39	chr11:50330000-50331600	ZNF genes & repeats	Liver	Liver
40	chr11:50337400-50343400	ZNF genes & repeats	Liver	Liver
41	chr11:50337600-50341800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
42	chr11:50340600-50341400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr11:50341600-50345800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
44	chr11:50342800-50343200	Active TSS	Right Atrium	heart
45	chr11:50344800-50345600	Active TSS	Fetal Heart	heart
46	chr11:50345400-50345600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
47	chr11:50345800-50346800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr11:50346600-50347000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
49	chr11:50346800-50347000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
50	chr11:50346800-50347000	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell

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