Variant report

Variant	esv2760206
Chromosome Location	chr11:50203494-51096372
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2634)
CpG islands
(count:2319)
Chromatin interactive
region (count:3)
LncRNA
region (count:47)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2634 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

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	chr11:50741510-50741536	K562	blood:	n/a	n/a
3	ATF1	chr11:50728352-50728528	K562	blood:	n/a	n/a
4	ATF1	chr11:50676160-50676529	K562	blood:	n/a	n/a
5	ATF1	chr11:50409411-50409611	K562	blood:	n/a	n/a
6	ATF1	chr11:50257555-50257921	K562	blood:	n/a	n/a
7	ATF1	chr11:50755176-50755720	K562	blood:	n/a	n/a
8	ATF1	chr11:50721580-50721799	K562	blood:	n/a	n/a
9	ATF1	chr11:50767721-50767932	K562	blood:	n/a	n/a
10	ATF1	chr11:50381201-50381204	K562	blood:	n/a	n/a
11	ATF1	chr11:50771363-50771551	K562	blood:	n/a	n/a
12	ATF1	chr11:50757990-50758182	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	chr11:50741715-50742187	K562	blood:	n/a	n/a
15	BACH1	chr11:50769674-50770049	K562	blood:	n/a	n/a
16	BACH1	chr11:50739007-50739300	K562	blood:	n/a	n/a
17	BACH1	chr11:50744265-50744293	K562	blood:	n/a	n/a
18	BACH1	chr11:50762679-50763056	K562	blood:	n/a	n/a
19	BACH1	chr11:50765324-50765524	K562	blood:	n/a	n/a
20	BACH1	chr11:50759699-50760188	K562	blood:	n/a	n/a
21	BACH1	chr11:50780465-50780837	K562	blood:	n/a	n/a
22	BACH1	chr11:50699638-50700011	K562	blood:	n/a	n/a
23	BACH1	chr11:50767401-50767428	K562	blood:	n/a	n/a
24	BATF	chr11:50649412-50649706	GM12878	blood:	n/a	n/a
25	BATF	chr11:50676256-50676541	GM12878	blood:	n/a	n/a
26	BATF	chr11:50676209-50676542	GM12878	blood:	n/a	n/a
27	BATF	chr11:50723560-50724069	GM12878	blood:	n/a	n/a
28	BATF	chr11:50251866-50252053	GM12878	blood:	n/a	n/a
29	BATF	chr11:50685636-50685821	GM12878	blood:	n/a	n/a
30	BATF	chr11:50700733-50700935	GM12878	blood:	n/a	n/a
31	BATF	chr11:50757466-50757719	GM12878	blood:	n/a	n/a
32	BATF	chr11:50687048-50687278	GM12878	blood:	n/a	n/a
33	BATF	chr11:50764082-50764319	GM12878	blood:	n/a	n/a
34	BATF	chr11:50770838-50771135	GM12878	blood:	n/a	n/a
35	BATF	chr11:50756360-50756521	GM12878	blood:	n/a	n/a
36	BATF	chr11:50681509-50681669	GM12878	blood:	n/a	n/a
37	BATF	chr11:50711195-50711416	GM12878	blood:	n/a	n/a
38	BATF	chr11:50721484-50721792	GM12878	blood:	n/a	n/a
39	BATF	chr11:50779460-50779823	GM12878	blood:	n/a	n/a
40	BATF	chr11:50671779-50671988	GM12878	blood:	n/a	n/a
41	BATF	chr11:50722179-50722655	GM12878	blood:	n/a	n/a
42	BATF	chr11:50668601-50668765	GM12878	blood:	n/a	n/a
43	BATF	chr11:50782290-50782554	GM12878	blood:	n/a	n/a
44	BATF	chr11:50755495-50755763	GM12878	blood:	n/a	n/a
45	BATF	chr11:50767583-50768188	GM12878	blood:	n/a	n/a
46	BATF	chr11:50749839-50750367	GM12878	blood:	n/a	n/a
47	BATF	chr11:50670735-50670974	GM12878	blood:	n/a	n/a
48	BATF	chr11:50768336-50768651	GM12878	blood:	n/a	n/a
49	BATF	chr11:50761809-50762209	GM12878	blood:	n/a	n/a
50	BATF	chr11:50711202-50711412	GM12878	blood:	n/a	n/a

(count:2319 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:50227265-50227315	AoSMC	blood vessel:	n/a
2	chr11:50227265-50227315	AoSMC	blood vessel:	n/a
3	chr11:50257752-50257802	SAEC	small airway:	n/a
4	chr11:50234973-50235023	MCF10A-Er-Src	breast:	n/a
5	chr11:50260762-50260812	K562	blood:	n/a
6	chr11:50219952-50220002	AG10803	skin:	n/a
7	chr11:50257625-50257675	GM06990	blood:	n/a
8	chr11:50368251-50368301	HEK293	kidney:	embryo
9	chr11:50260762-50260812	MCF-7	breast:	n/a
10	chr11:50206530-50206580	PANC-1	pancreas:	n/a
11	chr11:50227476-50227526	HEK293	kidney:	embryo
12	chr11:50206561-50206611	A549	lung:	n/a
13	chr11:50227199-50227249	GM19239	blood:	n/a
14	chr11:50257496-50257546	RPTEC	kidney:	n/a
15	chr11:50206530-50206580	Hela-S3	cervix:	n/a
16	chr11:50220389-50220439	HPAEpiC	pulmonary alveolar:	n/a
17	chr11:50220426-50220476	GM12892	blood:	n/a
18	chr11:50258273-50258323	ProgFib	skin:	n/a
19	chr11:50227199-50227249	HEEpiC	esophagus:	n/a
20	chr11:50219952-50220002	NHBE	bronchial:	n/a
21	chr11:50220389-50220439	HMEC	breast:	n/a
22	chr11:50368251-50368301	AG04450	lung:	fetal
23	chr11:50258750-50258800	ECC-1	luminal epithelium:	n/a
24	chr11:50368251-50368301	HUVEC	blood vessel:	n/a
25	chr11:50241016-50241066	GM12891	blood:	n/a
26	chr11:50236153-50236203	AG09309	skin:	n/a
27	chr11:50257752-50257802	Caco-2	colon:	n/a
28	chr11:50220055-50220105	SK-N-MC	brain:	n/a
29	chr11:50238009-50238059	IMR90	lung:	fetal
30	chr11:50206530-50206580	ProgFib	skin:	n/a
31	chr11:50206561-50206611	Jurkat	blood:	n/a
32	chr11:50219952-50220002	HRE	kidney:	n/a
33	chr11:50219952-50220002	HepG2	liver:	n/a
34	chr11:50231261-50231311	PrEC	prostate:	n/a
35	chr11:50238107-50238157	AG04449	skin:	fetal
36	chr11:50254503-50254553	CMK	blood:	n/a
37	chr11:50220389-50220439	HAEpiC	amniotic membrane:	n/a
38	chr11:50206606-50206656	ECC-1	luminal epithelium:	n/a
39	chr11:50227476-50227526	PANC-1	pancreas:	n/a
40	chr11:50257752-50257802	PANC-1	pancreas:	n/a
41	chr11:50231261-50231311	HL-60	blood:	n/a
42	chr11:50238214-50238264	NH-A	brain:	n/a
43	chr11:50238214-50238264	GM12878	blood:	n/a
44	chr11:50227265-50227315	HMEC	breast:	n/a
45	chr11:50257625-50257675	GM12878	blood:	n/a
46	chr11:50220426-50220476	SK-N-MC	brain:	n/a
47	chr11:50231261-50231311	GM06990	blood:	n/a
48	chr11:50227476-50227526	NH-A	brain:	n/a
49	chr11:50234973-50235023	NHDF-neo	bronchial:	n/a
50	chr11:50220343-50220393	PrEC	prostate:	n/a

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

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

(count:47 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4C13-7	chr11:50320143-50320239	NONHSAT021340
2	lnc-OR4C13-1	chr11:50261115-50261299	NONHSAT021336
3	lnc-OR4C13-7	chr11:50320710-50320877	NONHSAT021340
4	lnc-OR4C13-7	chr11:50274586-50274778	NONHSAT021338
5	lnc-OR4C13-9	chr11:50378065-50378165	NONHSAT021345
6	lnc-OR4C13-9	chr11:50376439-50376850	NONHSAT021345
7	lnc-OR4C13-1	chr11:50263752-50263827	NONHSAT021336
8	lnc-OR4C13-1	chr11:50257789-50258088	ENSG00000254518
9	lnc-OR4C13-1	chr11:50262310-50262433	ENSG00000254518
10	lnc-OR4C13-1	chr11:50257750-50258210	NONHSAT021336
11	lnc-OR4C13-7	chr11:50301079-50301142	NONHSAT021343
12	lnc-OR4C13-9	chr11:50379775-50379803	NONHSAT021345
13	lnc-OR4C13-1	chr11:50263752-50263827	ENSG00000254518
14	lnc-OR4C13-9	chr11:50368318-50368359	NONHSAT021344
15	lnc-OR4C12-1	chr11:50231598-50231759	XLOC_009440
16	lnc-OR4C12-1	chr11:50232840-50233106	XLOC_009440
17	lnc-OR4C13-9	chr11:50368318-50368359	NR_024504
18	lnc-OR4C13-9	chr11:50368739-50368821	NONHSAT021344
19	lnc-OR4C13-1	chr11:50257750-50258088	ENSG00000254518
20	lnc-OR4C13-7	chr11:50302810-50303098	NONHSAT021342
21	lnc-OR4C13-1	chr11:50261115-50261299	ENSG00000254518
22	lnc-OR4C13-7	chr11:50280085-50280169	NONHSAT021339
23	lnc-OR4C13-9	chr11:50379775-50379802	NR_024504
24	lnc-OR4C13-7	chr11:50280085-50280169	NONHSAT021340
25	lnc-OR4C13-9	chr11:50368739-50368821	NR_024504
26	lnc-OR4C13-7	chr11:50266792-50266965	NONHSAT021338
27	lnc-OR4C13-7	chr11:50302810-50303035	NONHSAT021343
28	lnc-OR4C13-7	chr11:50313156-50313246	NONHSAT021340
29	lnc-OR4C13-9	chr11:50378065-50378165	NR_024504
30	lnc-OR4C13-7	chr11:50274586-50274767	NONHSAT021339
31	lnc-OR4C13-7	chr11:50266792-50266898	NONHSAT021339
32	lnc-OR4C13-7	chr11:50279538-50279677	NONHSAT021340
33	lnc-OR4C13-9	chr11:50379313-50379802	NONHSAT021344
34	lnc-OR4C13-7	chr11:50302810-50302996	NONHSAT021339
35	lnc-OR4C13-9	chr11:50375274-50375391	NR_024504
36	lnc-OR4C13-1	chr11:50262310-50262433	NONHSAT021336
37	lnc-OR4C13-7	chr11:50279839-50280169	NONHSAT021342
38	lnc-OR4C13-7	chr11:50279538-50279677	NONHSAT021339
39	lnc-OR4C13-7	chr11:50274586-50274767	NONHSAT021340
40	lnc-OR4C13-9	chr11:50376439-50376850	NONHSAT021344
41	lnc-OR4C13-9	chr11:50379313-50379548	NONHSAT021345
42	lnc-OR4C13-9	chr11:50378065-50378165	NONHSAT021344
43	lnc-OR4C13-9	chr11:50379313-50379548	NR_024504
44	lnc-OR4C13-9	chr11:50375235-50375391	NONHSAT021344
45	lnc-OR4C13-7	chr11:50266852-50266898	NONHSAT021340
46	lnc-OR4C13-7	chr11:50301870-50302020	NONHSAT021343
47	lnc-OR4C13-9	chr11:50375235-50375391	NONHSAT021345

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
ENSG00000236919	TF binding region
ENSG00000214883	TF binding region
ENSG00000254518	CpG island
ENSG00000255042	CpG island
ENSG00000255500	CpG island
ENSG00000254840	CpG island
ENSG00000255001	CpG island
ENSG00000236919	CpG island
ENSG00000214883	CpG island
ENSG00000254518	chromatin interactions

Extended variants
information (count: 33201 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:33201 , 50 per page) page: 1 2 3 4 5 6 7 ... 665

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141558517	chr11:50203515-50203516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs371613699	chr11:50203535-50203536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552154113	chr11:50203558-50203559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572429119	chr11:50203571-50203572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116474797	chr11:50203578-50203579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188306998	chr11:50203612-50203613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200455422	chr11:50203645-50203646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs80203699	chr11:50203653-50203654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs397848713	chr11:50203654-50203655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373521220	chr11:50203655-50203656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376420310	chr11:50203656-50203657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs67946367	chr11:50203660-50203661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574157659	chr11:50203712-50203713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564155639	chr11:50203717-50203718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs533115624	chr11:50203825-50203826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs150884362	chr11:50203854-50203855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573249228	chr11:50203902-50203903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs58417622	chr11:50204047-50204048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs398016064	chr11:50204059-50204060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376327425	chr11:50204086-50204087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs545299807	chr11:50204089-50204090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545694755	chr11:50204096-50204097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564896566	chr11:50204138-50204139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139655993	chr11:50204146-50204147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs61891490	chr11:50204167-50204168	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs181551502	chr11:50206210-50206211	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs186276170	chr11:50206211-50206212	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs572255148	chr11:50206212-50206213	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs540934183	chr11:50206213-50206214	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs201204399	chr11:50206229-50206230	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs549783655	chr11:50206305-50206306	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs530191649	chr11:50206306-50206307	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs79348947	chr11:50206322-50206323	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs12360817	chr11:50206323-50206324	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs543091240	chr11:50206353-50206354	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs535790662	chr11:50206358-50206359	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs563430993	chr11:50206368-50206369	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs190738282	chr11:50206391-50206392	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs141452844	chr11:50206396-50206397	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs6597892	chr11:50206408-50206409	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs375064402	chr11:50206416-50206417	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs548129049	chr11:50206438-50206439	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs182910667	chr11:50206441-50206442	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs533395888	chr11:50206453-50206454	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs549993375	chr11:50206460-50206461	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs117148809	chr11:50206482-50206483	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs535578980	chr11:50206531-50206532	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs372564803	chr11:50206533-50206534	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs565551623	chr11:50206549-50206550	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs534575703	chr11:50206551-50206552	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21785460	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	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
Schizophrenia	21346763	CNVD

Chromatin state (count:675 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:50202200-50204200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr11:50206200-50207200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:50217000-50218200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
4	chr11:50220000-50220800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr11:50220600-50221200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
6	chr11:50238000-50238400	ZNF genes & repeats	Esophagus	oesophagus
7	chr11:50242200-50242400	ZNF genes & repeats	Placenta	Placenta
8	chr11:50242400-50246200	Weak transcription	Placenta	Placenta
9	chr11:50246400-50256200	Weak transcription	Placenta	Placenta
10	chr11:50250800-50256200	Weak transcription	K562	blood
11	chr11:50256200-50256400	Enhancers	Placenta	Placenta
12	chr11:50256200-50258600	Active TSS	K562	blood
13	chr11:50256400-50256800	Flanking Active TSS	Placenta	Placenta
14	chr11:50256800-50257200	Active TSS	Placenta	Placenta
15	chr11:50257000-50258200	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
16	chr11:50257200-50257400	Flanking Active TSS	Placenta	Placenta
17	chr11:50257200-50257600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr11:50257200-50257600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr11:50257200-50257600	Active TSS	Primary T cells fromperipheralblood	blood
20	chr11:50257200-50257600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
21	chr11:50257200-50257600	Active TSS	Brain Cingulate Gyrus	brain
22	chr11:50257200-50257600	ZNF genes & repeats	Fetal Intestine Small	intestine
23	chr11:50257200-50257600	ZNF genes & repeats	Fetal Stomach	stomach
24	chr11:50257200-50257600	Active TSS	Ovary	ovary
25	chr11:50257200-50257600	Active TSS	Psoas Muscle	Psoas
26	chr11:50257200-50257600	Active TSS	Right Atrium	heart
27	chr11:50257200-50257600	Active TSS	Right Ventricle	heart
28	chr11:50257200-50257600	Active TSS	Skeletal Muscle Female	skeletal muscle
29	chr11:50257200-50257600	Active TSS	Stomach Smooth Muscle	stomach
30	chr11:50257200-50257600	Active TSS	HSMM	muscle
31	chr11:50257200-50258000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr11:50257200-50258000	ZNF genes & repeats	Gastric	stomach
33	chr11:50257200-50258000	ZNF genes & repeats	Pancreas	Pancrea
34	chr11:50257200-50258200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr11:50257400-50258000	Active TSS	Fetal Lung	lung
36	chr11:50257400-50258800	ZNF genes & repeats	Placenta	Placenta
37	chr11:50258000-50260600	Weak transcription	Gastric	stomach
38	chr11:50258800-50274600	Weak transcription	Placenta	Placenta
39	chr11:50260600-50260800	ZNF genes & repeats	Gastric	stomach
40	chr11:50274600-50275400	Strong transcription	Placenta	Placenta
41	chr11:50275400-50277000	Weak transcription	Placenta	Placenta
42	chr11:50295800-50296200	Enhancers	Adipose Nuclei	Adipose
43	chr11:50324400-50325400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
44	chr11:50326400-50345800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr11:50326600-50328800	ZNF genes & repeats	Liver	Liver
46	chr11:50330000-50331600	ZNF genes & repeats	Liver	Liver
47	chr11:50337400-50343400	ZNF genes & repeats	Liver	Liver
48	chr11:50337600-50341800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
49	chr11:50340600-50341400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr11:50341600-50345800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell

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