Variant report

Variant	nsv1054711
Chromosome Location	chr11:50212173-50302232
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:182)
CpG islands
(count:2017)
Chromatin interactive
region (count:1)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:182 , 50 per page) page: 1 2 3 4

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	chr11:50256005-50256238	K562	blood:	n/a	chr11:50256104-50256115
8	CEBPB	chr11:50233638-50233794	HepG2	liver:	n/a	n/a
9	CEBPB	chr11:50256020-50256220	HepG2	liver:	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	chr11:50248936-50248972	Spleen_OC	spleen:	n/a	n/a
13	CTCF	chr11:50251508-50251624	HUVEC	blood vessel:	n/a	n/a
14	CTCF	chr11:50220602-50220640	MCF-7	breast:	n/a	n/a
15	CTCF	chr11:50257370-50257473	SK-N-SH_RA	brain:	n/a	chr11:50257436-50257449
16	CTCF	chr11:50252435-50252463	GM13977	blood:	n/a	n/a
17	CTCF	chr11:50264521-50264545	GM13976	blood:	n/a	n/a
18	CTCF	chr11:50252685-50252782	MCF-7	breast:	n/a	n/a
19	CTCF	chr11:50257360-50257510	SK-N-SH_RA	brain:	n/a	chr11:50257436-50257449
20	CTCF	chr11:50246753-50246827	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr11:50257340-50257490	SK-N-SH_RA	brain:	n/a	chr11:50257436-50257449
22	CTCF	chr11:50251547-50251577	MCF-7	breast:	n/a	n/a
23	CTCF	chr11:50251518-50251615	Gliobla	brain:	n/a	n/a
24	CTCF	chr11:50262617-50262644	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr11:50252665-50252796	Gliobla	brain:	n/a	n/a
26	CTCF	chr11:50227575-50227627	LNCaP	prostate:	n/a	n/a
27	CTCF	chr11:50277249-50277334	Spleen_OC	spleen:	n/a	n/a
28	CTCF	chr11:50264695-50264726	GM10266	blood:	n/a	n/a
29	CTCF	chr11:50291325-50291378	LNCaP	prostate:	n/a	n/a
30	CTCF	chr11:50214639-50214695	LNCaP	prostate:	n/a	n/a
31	CTCF	chr11:50294779-50294808	GM20000	blood:	n/a	n/a
32	CTCF	chr11:50251549-50251566	GM12878	blood:	n/a	n/a
33	CTCF	chr11:50284186-50284275	GM20000	blood:	n/a	n/a
34	CTCF	chr11:50293200-50293350	SAEC	small airway:	n/a	n/a
35	CTCF	chr11:50300095-50300112	GM10248	blood:	n/a	n/a
36	CTCF	chr11:50252669-50252790	Fibrobl	skin:	n/a	n/a
37	CTCF	chr11:50251507-50251620	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr11:50293189-50293335	NHEK	skin:	n/a	n/a
39	E2F6	chr11:50257236-50257997	K562	blood:	n/a	chr11:50257626-50257635 chr11:50257377-50257387 chr11:50257671-50257680
40	E2F6	chr11:50257450-50257783	K562	blood:	n/a	chr11:50257626-50257635 chr11:50257671-50257680
41	EGR1	chr11:50257609-50257827	K562	blood:	n/a	n/a
42	EGR1	chr11:50257540-50257866	K562	blood:	n/a	chr11:50257600-50257610
43	ELF1	chr11:50229900-50230327	MCF-7	breast:	n/a	chr11:50230098-50230109
44	FOS	chr11:50268385-50268599	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr11:50268421-50268615	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr11:50276547-50276647	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr11:50291697-50291896	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr11:50246723-50246904	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr11:50293136-50293277	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr11:50276555-50276756	MCF10A-Er-Src	breast:	n/a	n/a

(count:2017 , 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	SK-N-SH	brain:	n/a
2	chr11:50219952-50220002	PrEC	prostate:	n/a
3	chr11:50236153-50236203	H1-hESC	embryonic stem cell:	embryo
4	chr11:50238214-50238264	NHBE	bronchial:	n/a
5	chr11:50234973-50235023	SK-N-SH	brain:	n/a
6	chr11:50219952-50220002	PrEC	prostate:	n/a
7	chr11:50236153-50236203	H1-hESC	embryonic stem cell:	embryo
8	chr11:50238214-50238264	NHBE	bronchial:	n/a
9	chr11:50239550-50239600	HMEC	breast:	n/a
10	chr11:50258273-50258323	AG09319	gingival:	n/a
11	chr11:50257256-50257306	HCPEpiC	choroid plexus:	n/a
12	chr11:50238214-50238264	GM12891	blood:	n/a
13	chr11:50231261-50231311	SK-N-SH	brain:	n/a
14	chr11:50220343-50220393	GM12892	blood:	n/a
15	chr11:50220426-50220476	Jurkat	blood:	n/a
16	chr11:50234973-50235023	CMK	blood:	n/a
17	chr11:50226789-50226839	NB4	blood:	n/a
18	chr11:50257633-50257683	K562	blood:	n/a
19	chr11:50254503-50254553	MCF-7	breast:	n/a
20	chr11:50238107-50238157	HRCEpiC	kidney:	n/a
21	chr11:50260762-50260812	GM12892	blood:	n/a
22	chr11:50236153-50236203	PFSK-1	brain:	n/a
23	chr11:50257979-50258029	ProgFib	skin:	n/a
24	chr11:50226789-50226839	GM06990	blood:	n/a
25	chr11:50258273-50258323	ProgFib	skin:	n/a
26	chr11:50257752-50257802	BJ	skin:	n/a
27	chr11:50260762-50260812	Caco-2	colon:	n/a
28	chr11:50257752-50257802	GM06990	blood:	n/a
29	chr11:50227265-50227315	AG04449	skin:	fetal
30	chr11:50220426-50220476	AG09319	gingival:	n/a
31	chr11:50258750-50258800	HNPCEpiC	eye:	n/a
32	chr11:50227265-50227315	MCF10A-Er-Src	breast:	n/a
33	chr11:50260762-50260812	RPTEC	kidney:	n/a
34	chr11:50227476-50227526	U87	brain:	n/a
35	chr11:50238107-50238157	AG09309	skin:	n/a
36	chr11:50241016-50241066	MCF10A-Er-Src	breast:	n/a
37	chr11:50238214-50238264	Hela-S3	cervix:	n/a
38	chr11:50257830-50257880	A549	lung:	n/a
39	chr11:50226789-50226839	PANC-1	pancreas:	n/a
40	chr11:50220343-50220393	HRCEpiC	kidney:	n/a
41	chr11:50226789-50226839	HL-60	blood:	n/a
42	chr11:50258273-50258323	HRCEpiC	kidney:	n/a
43	chr11:50257979-50258029	LNCaP	prostate:	n/a
44	chr11:50220055-50220105	HRE	kidney:	n/a
45	chr11:50239550-50239600	Caco-2	colon:	n/a
46	chr11:50227102-50227152	GM12892	blood:	n/a
47	chr11:50257256-50257306	IMR90	lung:	fetal
48	chr11:50227079-50227129	ovcar-3	ovarian:	n/a
49	chr11:50234973-50235023	U87	brain:	n/a
50	chr11:50220107-50220157	HMEC	breast:	n/a

(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:24 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 1631 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1631 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539216349	chr11:50217002-50217003	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs146471815	chr11:50217025-50217026	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs373117465	chr11:50217061-50217062	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs569658834	chr11:50217062-50217063	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs139133590	chr11:50217072-50217073	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs554975899	chr11:50217073-50217074	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs143026725	chr11:50217094-50217095	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs534732934	chr11:50217119-50217120	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs557529545	chr11:50217129-50217130	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs577372883	chr11:50217155-50217156	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs117161927	chr11:50217167-50217168	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs537367388	chr11:50217168-50217169	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs563063837	chr11:50217173-50217174	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs576842864	chr11:50217207-50217208	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs4881632	chr11:50217208-50217209	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs10794217	chr11:50217209-50217210	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs186299532	chr11:50217210-50217211	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs547878102	chr11:50217256-50217257	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs373901385	chr11:50217294-50217295	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs561951901	chr11:50217335-50217336	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs549602089	chr11:50217374-50217375	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs189099372	chr11:50217378-50217379	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs181370118	chr11:50217379-50217380	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs548833332	chr11:50217383-50217384	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs565681024	chr11:50217483-50217484	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs527937138	chr11:50217491-50217492	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs113848638	chr11:50217512-50217513	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs536053274	chr11:50217563-50217564	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs577705853	chr11:50217610-50217611	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs7941169	chr11:50217658-50217659	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs556824337	chr11:50217667-50217668	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs572584428	chr11:50217697-50217698	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs576682195	chr11:50217732-50217733	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs542554286	chr11:50217743-50217744	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs556053492	chr11:50217785-50217786	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs572405813	chr11:50217796-50217797	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs541111662	chr11:50217802-50217803	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs147031653	chr11:50217809-50217810	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs138094686	chr11:50217811-50217812	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs190756989	chr11:50217861-50217862	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs563160506	chr11:50217866-50217867	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs182270471	chr11:50217883-50217884	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs61891521	chr11:50217887-50217888	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs558148391	chr11:50217895-50217896	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs575092207	chr11:50217918-50217919	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs116729169	chr11:50217941-50217942	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs551124805	chr11:50217951-50217952	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs571201290	chr11:50217962-50217963	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs186187600	chr11:50217963-50217964	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs4881693	chr11:50218019-50218020	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:40 , 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

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