Variant report

Variant	nsv544277
Chromosome Location	chr20:41289969-41543912
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr20:41506260-41506396	K562	blood:	n/a	n/a
2	ATF1	chr20:41370653-41370853	K562	blood:	n/a	n/a
3	BACH1	chr20:41378208-41378560	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr20:41362026-41362032	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr20:41307552-41307915	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr20:41324497-41324521	K562	blood:	n/a	n/a
7	BHLHE40	chr20:41371368-41371745	K562	blood:	n/a	n/a
8	BHLHE40	chr20:41355345-41355582	K562	blood:	n/a	n/a
9	CEBPB	chr20:41378592-41378801	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr20:41439377-41439696	HepG2	liver:	n/a	chr20:41439536-41439545 chr20:41439536-41439547 chr20:41439536-41439545 chr20:41439536-41439545 chr20:41439534-41439545 chr20:41439536-41439545
11	CEBPB	chr20:41297733-41297951	HepG2	liver:	n/a	chr20:41297799-41297810
12	CEBPB	chr20:41439370-41439653	A549	lung:	n/a	chr20:41439536-41439545 chr20:41439536-41439547 chr20:41439536-41439545 chr20:41439536-41439545 chr20:41439534-41439545 chr20:41439536-41439545
13	CEBPB	chr20:41400533-41400613	K562	blood:	n/a	n/a
14	CEBPB	chr20:41536390-41536711	A549	lung:	n/a	chr20:41536551-41536562 chr20:41536590-41536598 chr20:41536553-41536562 chr20:41536552-41536563
15	CEBPB	chr20:41347105-41347193	K562	blood:	n/a	n/a
16	CEBPB	chr20:41493104-41493346	HepG2	liver:	n/a	n/a
17	CEBPB	chr20:41359726-41359923	HepG2	liver:	n/a	n/a
18	CEBPB	chr20:41512747-41512902	A549	lung:	n/a	chr20:41512795-41512806
19	CEBPB	chr20:41361593-41361847	HepG2	liver:	n/a	chr20:41361684-41361697 chr20:41361685-41361696
20	CEBPB	chr20:41439396-41439725	K562	blood:	n/a	chr20:41439536-41439545 chr20:41439536-41439547 chr20:41439536-41439545 chr20:41439536-41439545 chr20:41439534-41439545 chr20:41439536-41439545
21	CEBPB	chr20:41472097-41472355	HepG2	liver:	n/a	chr20:41472218-41472231 chr20:41472219-41472230
22	CEBPB	chr20:41509840-41510046	HepG2	liver:	n/a	n/a
23	CEBPB	chr20:41536486-41536704	K562	blood:	n/a	chr20:41536551-41536562 chr20:41536590-41536598 chr20:41536553-41536562 chr20:41536552-41536563
24	CEBPB	chr20:41512665-41512880	HepG2	liver:	n/a	chr20:41512795-41512806
25	CEBPB	chr20:41536423-41536679	Hela-S3	cervix:	n/a	chr20:41536551-41536562 chr20:41536590-41536598 chr20:41536553-41536562 chr20:41536552-41536563
26	CEBPB	chr20:41411757-41411940	HepG2	liver:	n/a	n/a
27	CEBPB	chr20:41396891-41397206	HepG2	liver:	n/a	chr20:41397064-41397075
28	CEBPB	chr20:41384170-41384313	HepG2	liver:	n/a	chr20:41384235-41384246
29	CEBPB	chr20:41418619-41418922	A549	lung:	n/a	chr20:41418768-41418779
30	CEBPB	chr20:41528719-41528765	HepG2	liver:	n/a	n/a
31	CEBPB	chr20:41418621-41418924	HepG2	liver:	n/a	chr20:41418768-41418779
32	CEBPB	chr20:41397029-41397083	K562	blood:	n/a	chr20:41397064-41397075
33	CEBPB	chr20:41536391-41536730	IMR90	lung:	n/a	chr20:41536551-41536562 chr20:41536590-41536598 chr20:41536553-41536562 chr20:41536552-41536563
34	CEBPB	chr20:41439395-41439707	IMR90	lung:	n/a	chr20:41439536-41439545 chr20:41439536-41439547 chr20:41439536-41439545 chr20:41439536-41439545 chr20:41439534-41439545 chr20:41439536-41439545
35	CEBPB	chr20:41441338-41441368	A549	lung:	n/a	n/a
36	CEBPB	chr20:41441277-41441459	HepG2	liver:	n/a	n/a
37	CEBPB	chr20:41372285-41372407	HepG2	liver:	n/a	chr20:41372350-41372361 chr20:41372349-41372362
38	CEBPB	chr20:41383319-41383629	HepG2	liver:	n/a	chr20:41383492-41383503
39	CEBPB	chr20:41341367-41341488	HepG2	liver:	n/a	n/a
40	CEBPB	chr20:41478191-41478759	HepG2	liver:	n/a	chr20:41478631-41478640 chr20:41478629-41478640
41	CEBPB	chr20:41536502-41536707	H1-hESC	embryonic stem cell:	n/a	chr20:41536551-41536562 chr20:41536590-41536598 chr20:41536553-41536562 chr20:41536552-41536563
42	CEBPB	chr20:41478455-41478788	A549	lung:	n/a	chr20:41478631-41478640 chr20:41478629-41478640
43	CEBPB	chr20:41536366-41536740	HepG2	liver:	n/a	chr20:41536551-41536562 chr20:41536590-41536598 chr20:41536553-41536562 chr20:41536552-41536563
44	CTCF	chr20:41307640-41307790	NB4	blood:	n/a	n/a
45	CTCF	chr20:41349891-41349900	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr20:41307640-41307790	K562	blood:	n/a	n/a
47	CTCF	chr20:41307660-41307810	GM12871	blood:	n/a	n/a
48	CTCF	chr20:41307700-41307850	GM12872	blood:	n/a	n/a
49	CTCF	chr20:41307640-41307790	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr20:41465720-41465870	GM12866	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:41464381..41466534-chr20:41468260..41469973,2	K562	blood:
2	chr20:41238748..41239268-chr20:41307296..41307807,2	MCF-7	breast:
3	chr20:41112023..41112867-chr20:41307681..41308188,2	MCF-7	breast:
4	chr20:41356881..41359207-chr20:41359274..41361954,2	K562	blood:
5	chr20:41352782..41354688-chr20:41355194..41357788,2	K562	blood:
6	chr20:41376932..41379314-chr20:41384669..41386890,2	K562	blood:
7	chr20:41350902..41352740-chr20:41354249..41356948,2	MCF-7	breast:
8	chr20:41403662..41404501-chr20:41816400..41817064,2	MCF-7	breast:
9	chr20:41404898..41407783-chr20:41407973..41409505,2	MCF-7	breast:
10	chr20:41376932..41379314-chr20:41384669..41386890,2	K562	blood:
11	chr20:41356881..41359207-chr20:41359274..41361954,2	K562	blood:
12	chr20:41464381..41466534-chr20:41468260..41469973,2	K562	blood:
13	chr20:41378883..41381522-chr20:41383064..41386046,2	K562	blood:
14	chr20:41404898..41407783-chr20:41407973..41409505,2	MCF-7	breast:
15	chr20:41524333..41525845-chr20:41525883..41528573,2	K562	blood:
16	chr20:41378883..41381522-chr20:41383064..41386046,2	K562	blood:
17	chr20:41352782..41354688-chr20:41355194..41357788,2	K562	blood:
18	chr20:41350902..41352740-chr20:41354249..41356948,2	MCF-7	breast:
19	chr20:41524333..41525845-chr20:41525883..41528573,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SRSF6-3	chr20:41314526-41314699	ENSG00000229042.2
2	lnc-SRSF6-3	chr20:41315837-41317202	ENSG00000229042.2
3	lnc-SRSF6-3	chr20:41314788-41314952	ENSG00000229042
4	lnc-SRSF6-3	chr20:41314585-41314699	ENSG00000229042
5	lnc-SRSF6-3	chr20:41314123-41314471	ENSG00000229042
6	lnc-SRSF6-3	chr20:41314044-41314372	ENSG00000229042.2
7	lnc-SRSF6-10	chr20:41502643-41503022	NONHSAT079805
8	lnc-SRSF6-3	chr20:41314788-41314952	ENSG00000229042.2
9	lnc-SRSF6-3	chr20:41314123-41314471	ENSG00000229042.2
10	lnc-SRSF6-10	chr20:41498538-41498574	NONHSAT079805
11	lnc-SRSF6-3	chr20:41314585-41314699	ENSG00000229042.2
12	lnc-SRSF6-3	chr20:41315837-41316285	ENSG00000229042
13	lnc-SRSF6-3	chr20:41314788-41314857	ENSG00000229042.2

Variant related genes	Relation type
ENSG00000229042	TF binding region
FAHD1	miRNA target sites
CIRBP	miRNA target sites
RND3	miRNA target sites

Extended variants
information (count: 10603 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:10603 , 50 per page) page: 1 2 3 4 5 6 7 ... 213

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541407609	chr20:41290009-41290010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs551879045	chr20:41290019-41290020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559608849	chr20:41290029-41290030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554877327	chr20:41290030-41290031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570492720	chr20:41290070-41290071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568349915	chr20:41290169-41290170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536688367	chr20:41290172-41290173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs4812613	chr20:41290238-41290239	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs576615829	chr20:41290240-41290241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545442640	chr20:41290248-41290249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187033207	chr20:41290287-41290288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545166606	chr20:41290288-41290289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572569435	chr20:41290332-41290333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541242255	chr20:41290341-41290342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561280786	chr20:41290353-41290354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs6102973	chr20:41290388-41290389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs62203855	chr20:41290390-41290391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543060495	chr20:41290427-41290428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562896586	chr20:41290436-41290437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6102974	chr20:41290512-41290513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532125216	chr20:41290524-41290525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs6072818	chr20:41290546-41290547	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs147997262	chr20:41290553-41290554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191926257	chr20:41290587-41290588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548397615	chr20:41290628-41290629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542280499	chr20:41290631-41290632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568413319	chr20:41290655-41290656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537297051	chr20:41290716-41290717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550206073	chr20:41290779-41290780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs3091725	chr20:41290787-41290788	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs12480300	chr20:41290836-41290837	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs184309532	chr20:41290900-41290901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572432745	chr20:41290910-41290911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs6016864	chr20:41290936-41290937	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs554738064	chr20:41290969-41290970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2425508	chr20:41290976-41290977	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs543674917	chr20:41290979-41290980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562968133	chr20:41291006-41291007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576801215	chr20:41291016-41291017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545467687	chr20:41291021-41291022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575951207	chr20:41291022-41291023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs909861	chr20:41291024-41291025	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs557914202	chr20:41291032-41291033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs6016865	chr20:41291144-41291145	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs141638791	chr20:41291148-41291149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs117273927	chr20:41291161-41291162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371224176	chr20:41291257-41291258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs35469862	chr20:41291305-41291306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs150501515	chr20:41291310-41291311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530839963	chr20:41291323-41291324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
Autism	22495311	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	21693616	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
colon cancer	17210682	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	22028636	CNVD
Breast cancer	21264507	CNVD
Thyroid cancer	19087340	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Soft tissue tumor	16732325	CNVD
Colorectal cancer	19359472	CNVD
Gastric cancer	17167181	CNVD
Myeloproliferative neoplasm	19047681	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Oral cancer	21386901	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Ovarian cancer	19193619	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Myelodysplastic syndrome	17634407	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ductal carcinoma	22052326	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Gastric cancer	16891809	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Malignant melanoma	17260012	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Cervical cancer	21062161	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	20585902	CNVD
Ductal carcinoma	18381933	CNVD
Cancer	21129771	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	20864512	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Gastric cancer	22014070	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:384 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:41271600-41300800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr20:41295800-41296600	Enhancers	Gastric	stomach
3	chr20:41300800-41301000	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr20:41301000-41301400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr20:41301400-41301600	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr20:41301600-41305000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr20:41303600-41303800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr20:41303600-41303800	Enhancers	Placenta Amnion	Placenta Amnion
9	chr20:41303800-41306600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr20:41304000-41306200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr20:41304000-41309600	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr20:41305000-41306800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
13	chr20:41305800-41306600	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr20:41306200-41306600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr20:41306600-41306800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr20:41306600-41306800	Enhancers	Pancreas	Pancrea
17	chr20:41306600-41313000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr20:41306800-41310200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr20:41306800-41311000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr20:41306800-41314000	Weak transcription	Pancreas	Pancrea
21	chr20:41309600-41310200	Enhancers	Placenta Amnion	Placenta Amnion
22	chr20:41310200-41310600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr20:41310200-41310800	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr20:41310600-41311000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr20:41310800-41312600	Enhancers	Placenta Amnion	Placenta Amnion
26	chr20:41311000-41311800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr20:41311000-41311800	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr20:41311200-41311400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
29	chr20:41311200-41311600	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr20:41311800-41318200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr20:41314000-41316400	Enhancers	Pancreas	Pancrea
32	chr20:41318200-41319600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
33	chr20:41319600-41329200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr20:41326000-41327600	Enhancers	Liver	Liver
35	chr20:41327600-41330400	Weak transcription	Liver	Liver
36	chr20:41328600-41329000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr20:41328600-41330000	Enhancers	Colon Smooth Muscle	Colon
38	chr20:41328600-41330000	Enhancers	Rectal Smooth Muscle	rectum
39	chr20:41328800-41329600	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr20:41328800-41329800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr20:41329000-41329200	Enhancers	Brain Hippocampus Middle	brain
42	chr20:41329200-41329800	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr20:41329400-41330800	Weak transcription	Brain Hippocampus Middle	brain
44	chr20:41329600-41331000	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr20:41329800-41330200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr20:41329800-41330800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr20:41330000-41335200	Weak transcription	Rectal Smooth Muscle	rectum
48	chr20:41330000-41335400	Weak transcription	Colon Smooth Muscle	Colon
49	chr20:41330200-41330400	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr20:41330400-41331400	Enhancers	Liver	Liver

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