Variant report

Variant	nsv897508
Chromosome Location	chr11:50152718-50304124
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:247)
CpG islands
(count:2198)
Chromatin interactive
region (count:3)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:247 , 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	chr11:50230060-50230405	MCF-7	breast:	n/a	n/a
7	CEBPB	chr11:50202142-50202359	HepG2	liver:	n/a	chr11:50202284-50202295
8	CEBPB	chr11:50180269-50180536	MCF-7	breast:	n/a	n/a
9	CEBPB	chr11:50256020-50256220	HepG2	liver:	n/a	chr11:50256104-50256115
10	CEBPB	chr11:50185114-50185392	HepG2	liver:	n/a	chr11:50185257-50185274 chr11:50185258-50185271 chr11:50185259-50185270 chr11:50185258-50185269
11	CEBPB	chr11:50185206-50185319	A549	lung:	n/a	chr11:50185257-50185274 chr11:50185258-50185271 chr11:50185259-50185270 chr11:50185258-50185269
12	CEBPB	chr11:50182673-50182737	HepG2	liver:	n/a	chr11:50182687-50182698
13	CEBPB	chr11:50256005-50256238	K562	blood:	n/a	chr11:50256104-50256115
14	CEBPB	chr11:50202172-50202422	IMR90	lung:	n/a	chr11:50202284-50202295
15	CEBPB	chr11:50233638-50233794	HepG2	liver:	n/a	n/a
16	CREB1	chr11:50257411-50258094	K562	blood:	n/a	chr11:50257724-50257737
17	CREB1	chr11:50257549-50258023	K562	blood:	n/a	chr11:50257724-50257737
18	CTCF	chr11:50252669-50252790	Fibrobl	skin:	n/a	n/a
19	CTCF	chr11:50165100-50165250	GM12866	blood:	n/a	n/a
20	CTCF	chr11:50293189-50293335	NHEK	skin:	n/a	n/a
21	CTCF	chr11:50207190-50207225	Pancreas_OC	pancreas:	n/a	n/a
22	CTCF	chr11:50248936-50248972	Spleen_OC	spleen:	n/a	n/a
23	CTCF	chr11:50251549-50251566	GM12878	blood:	n/a	n/a
24	CTCF	chr11:50300095-50300112	GM10248	blood:	n/a	n/a
25	CTCF	chr11:50251518-50251615	Gliobla	brain:	n/a	n/a
26	CTCF	chr11:50165390-50165477	LNCaP	prostate:	n/a	n/a
27	CTCF	chr11:50257340-50257490	SK-N-SH_RA	brain:	n/a	chr11:50257436-50257449
28	CTCF	chr11:50227575-50227627	LNCaP	prostate:	n/a	n/a
29	CTCF	chr11:50252435-50252463	GM13977	blood:	n/a	n/a
30	CTCF	chr11:50203704-50203730	Fibrobl	skin:	n/a	n/a
31	CTCF	chr11:50252665-50252796	Gliobla	brain:	n/a	n/a
32	CTCF	chr11:50160554-50160643	GM20000	blood:	n/a	n/a
33	CTCF	chr11:50264521-50264545	GM13976	blood:	n/a	n/a
34	CTCF	chr11:50251547-50251577	MCF-7	breast:	n/a	n/a
35	CTCF	chr11:50189348-50189444	GM13976	blood:	n/a	n/a
36	CTCF	chr11:50170484-50170584	LNCaP	prostate:	n/a	chr11:50170540-50170547
37	CTCF	chr11:50246753-50246827	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr11:50220602-50220640	MCF-7	breast:	n/a	n/a
39	CTCF	chr11:50174400-50174550	WI-38	lung:	n/a	n/a
40	CTCF	chr11:50264695-50264726	GM10266	blood:	n/a	n/a
41	CTCF	chr11:50294779-50294808	GM20000	blood:	n/a	n/a
42	CTCF	chr11:50277249-50277334	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr11:50252685-50252782	MCF-7	breast:	n/a	n/a
44	CTCF	chr11:50214639-50214695	LNCaP	prostate:	n/a	n/a
45	CTCF	chr11:50293200-50293350	SAEC	small airway:	n/a	n/a
46	CTCF	chr11:50257360-50257510	SK-N-SH_RA	brain:	n/a	chr11:50257436-50257449
47	CTCF	chr11:50284186-50284275	GM20000	blood:	n/a	n/a
48	CTCF	chr11:50291325-50291378	LNCaP	prostate:	n/a	n/a
49	CTCF	chr11:50162853-50162864	GM20000	blood:	n/a	n/a
50	CTCF	chr11:50257370-50257473	SK-N-SH_RA	brain:	n/a	chr11:50257436-50257449

(count:2198 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:50257496-50257546	HMEC	breast:	n/a
2	chr11:50256574-50256624	AG09309	skin:	n/a
3	chr11:50257496-50257546	HMEC	breast:	n/a
4	chr11:50256574-50256624	AG09309	skin:	n/a
5	chr11:50257979-50258029	PrEC	prostate:	n/a
6	chr11:50227199-50227249	HL-60	blood:	n/a
7	chr11:50257752-50257802	GM12892	blood:	n/a
8	chr11:50257830-50257880	HNPCEpiC	eye:	n/a
9	chr11:50258273-50258323	Hepatocyte	liver:	n/a
10	chr11:50219952-50220002	T-47D	breast:	n/a
11	chr11:50227079-50227129	H1-hESC	embryonic stem cell:	embryo
12	chr11:50227476-50227526	HEK293	kidney:	embryo
13	chr11:50257633-50257683	Hela-S3	cervix:	n/a
14	chr11:50220343-50220393	T-47D	breast:	n/a
15	chr11:50257979-50258029	U87	brain:	n/a
16	chr11:50227199-50227249	HEEpiC	esophagus:	n/a
17	chr11:50257256-50257306	AoSMC	blood vessel:	n/a
18	chr11:50257752-50257802	GM06990	blood:	n/a
19	chr11:50227079-50227129	AG04449	skin:	fetal
20	chr11:50241016-50241066	HL-60	blood:	n/a
21	chr11:50239550-50239600	ovcar-3	ovarian:	n/a
22	chr11:50256574-50256624	AG10803	skin:	n/a
23	chr11:50257633-50257683	HNPCEpiC	eye:	n/a
24	chr11:50234973-50235023	PANC-1	pancreas:	n/a
25	chr11:50231261-50231311	HMEC	breast:	n/a
26	chr11:50238107-50238157	HIPEpiC	eye:	n/a
27	chr11:50238214-50238264	K562	blood:	n/a
28	chr11:50254503-50254553	AoSMC	blood vessel:	n/a
29	chr11:50238214-50238264	H1-hESC	embryonic stem cell:	embryo
30	chr11:50260762-50260812	SKMC	muscle:	n/a
31	chr11:50220107-50220157	GM19239	blood:	n/a
32	chr11:50206530-50206580	HCT-116	colon:	n/a
33	chr11:50220426-50220476	NHDF-neo	bronchial:	n/a
34	chr11:50220389-50220439	AoSMC	blood vessel:	n/a
35	chr11:50220055-50220105	NH-A	brain:	n/a
36	chr11:50219952-50220002	LNCaP	prostate:	n/a
37	chr11:50227102-50227152	A549	lung:	n/a
38	chr11:50254503-50254553	NB4	blood:	n/a
39	chr11:50258273-50258323	A549	lung:	n/a
40	chr11:50257771-50257821	A549	lung:	n/a
41	chr11:50257496-50257546	HepG2	liver:	n/a
42	chr11:50206606-50206656	H1-hESC	embryonic stem cell:	embryo
43	chr11:50257625-50257675	HL-60	blood:	n/a
44	chr11:50227102-50227152	GM06990	blood:	n/a
45	chr11:50206561-50206611	NH-A	brain:	n/a
46	chr11:50220343-50220393	NHDF-neo	bronchial:	n/a
47	chr11:50220389-50220439	NHBE	bronchial:	n/a
48	chr11:50220389-50220439	AG04449	skin:	fetal
49	chr11:50219952-50220002	CMK	blood:	n/a
50	chr11:50206530-50206580	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:50172306..50174473-chr11:50176469..50178865,2	K562	blood:
2	chr11:50172306..50174473-chr11:50176469..50178865,2	K562	blood:
3	chr11:50256839..50259422-chr11:50261676..50263683,2	K562	blood:

(count:27 , 50 per page) page: 1

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

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
ENSG00000254518	CpG island
ENSG00000255042	CpG island
ENSG00000255500	CpG island
ENSG00000254840	CpG island
ENSG00000255001	CpG island
ENSG00000236919	CpG island
ENSG00000254518	chromatin interactions

Extended variants
information (count: 2032 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:2032 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536151407	chr11:50155021-50155022	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs553271722	chr11:50155048-50155049	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573065669	chr11:50155070-50155071	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs76632305	chr11:50155073-50155074	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs74756822	chr11:50155079-50155080	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs79581457	chr11:50155124-50155125	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544944613	chr11:50155125-50155126	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs561659898	chr11:50155145-50155146	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs574962766	chr11:50155159-50155160	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559121223	chr11:50188216-50188217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182606115	chr11:50188219-50188220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561827798	chr11:50188247-50188248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542267481	chr11:50188253-50188254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs562187107	chr11:50188254-50188255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs373967302	chr11:50188260-50188261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528082121	chr11:50188273-50188274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527462665	chr11:50188277-50188278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188006399	chr11:50188278-50188279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570751068	chr11:50188287-50188288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs138666122	chr11:50188305-50188306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192851401	chr11:50188310-50188311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569594943	chr11:50188340-50188341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571564188	chr11:50188360-50188361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs78698970	chr11:50188400-50188401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs548638513	chr11:50188450-50188451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565463591	chr11:50188505-50188506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534109551	chr11:50188508-50188509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553984163	chr11:50188537-50188538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs149315388	chr11:50188622-50188623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185267290	chr11:50188657-50188658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs556588328	chr11:50188661-50188662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576351100	chr11:50188670-50188671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs568516877	chr11:50188795-50188796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs541887244	chr11:50188818-50188819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs34581379	chr11:50188849-50188850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562148516	chr11:50188857-50188858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572613497	chr11:50188876-50188877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs527830168	chr11:50188891-50188892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs187615375	chr11:50188947-50188948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564229199	chr11:50188951-50188952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567418918	chr11:50191624-50191625	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs536299783	chr11:50191668-50191669	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs546699095	chr11:50191682-50191683	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs566298599	chr11:50191683-50191684	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs77314122	chr11:50191684-50191685	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs183415570	chr11:50191689-50191690	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs537436567	chr11:50191692-50191693	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs372419155	chr11:50191710-50191711	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs554649477	chr11:50191832-50191833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574485231	chr11:50191893-50191894	Weak transcription	n/a	n/a	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
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

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:50155000-50155200	Active TSS	HMEC	breast
2	chr11:50155000-50155200	Enhancers	HSMMtube	muscle
3	chr11:50155000-50155200	Enhancers	NH-A	brain
4	chr11:50188200-50189000	Enhancers	Adipose Nuclei	Adipose
5	chr11:50191600-50191800	ZNF genes & repeats	Right Atrium	heart
6	chr11:50191800-50194400	Weak transcription	Right Atrium	heart
7	chr11:50192600-50195800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
8	chr11:50193600-50193800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr11:50202200-50204200	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr11:50206200-50207200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr11:50217000-50218200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
12	chr11:50220000-50220800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr11:50220600-50221200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
14	chr11:50238000-50238400	ZNF genes & repeats	Esophagus	oesophagus
15	chr11:50242200-50242400	ZNF genes & repeats	Placenta	Placenta
16	chr11:50242400-50246200	Weak transcription	Placenta	Placenta
17	chr11:50246400-50256200	Weak transcription	Placenta	Placenta
18	chr11:50250800-50256200	Weak transcription	K562	blood
19	chr11:50256200-50256400	Enhancers	Placenta	Placenta
20	chr11:50256200-50258600	Active TSS	K562	blood
21	chr11:50256400-50256800	Flanking Active TSS	Placenta	Placenta
22	chr11:50256800-50257200	Active TSS	Placenta	Placenta
23	chr11:50257000-50258200	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
24	chr11:50257200-50257400	Flanking Active TSS	Placenta	Placenta
25	chr11:50257200-50257600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr11:50257200-50257600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr11:50257200-50257600	Active TSS	Primary T cells fromperipheralblood	blood
28	chr11:50257200-50257600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
29	chr11:50257200-50257600	Active TSS	Brain Cingulate Gyrus	brain
30	chr11:50257200-50257600	ZNF genes & repeats	Fetal Intestine Small	intestine
31	chr11:50257200-50257600	ZNF genes & repeats	Fetal Stomach	stomach
32	chr11:50257200-50257600	Active TSS	Ovary	ovary
33	chr11:50257200-50257600	Active TSS	Psoas Muscle	Psoas
34	chr11:50257200-50257600	Active TSS	Right Atrium	heart
35	chr11:50257200-50257600	Active TSS	Right Ventricle	heart
36	chr11:50257200-50257600	Active TSS	Skeletal Muscle Female	skeletal muscle
37	chr11:50257200-50257600	Active TSS	Stomach Smooth Muscle	stomach
38	chr11:50257200-50257600	Active TSS	HSMM	muscle
39	chr11:50257200-50258000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr11:50257200-50258000	ZNF genes & repeats	Gastric	stomach
41	chr11:50257200-50258000	ZNF genes & repeats	Pancreas	Pancrea
42	chr11:50257200-50258200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr11:50257400-50258000	Active TSS	Fetal Lung	lung
44	chr11:50257400-50258800	ZNF genes & repeats	Placenta	Placenta
45	chr11:50258000-50260600	Weak transcription	Gastric	stomach
46	chr11:50258800-50274600	Weak transcription	Placenta	Placenta
47	chr11:50260600-50260800	ZNF genes & repeats	Gastric	stomach
48	chr11:50274600-50275400	Strong transcription	Placenta	Placenta
49	chr11:50275400-50277000	Weak transcription	Placenta	Placenta
50	chr11:50295800-50296200	Enhancers	Adipose Nuclei	Adipose

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