Variant report

Variant	nsv9775
Chromosome Location	chr20:1534985-1563660
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:240)
CpG islands
(count:367)
Chromatin interactive
region (count:2)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:240 , 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	ARID3A	chr20:1550229-1550409	K562	blood:	n/a	n/a
2	ATF1	chr20:1550073-1550394	K562	blood:	n/a	n/a
3	BACH1	chr20:1550102-1550372	K562	blood:	n/a	n/a
4	BATF	chr20:1543275-1543590	GM12878	blood:	n/a	n/a
5	BHLHE40	chr20:1549969-1550250	K562	blood:	n/a	n/a
6	BRCA1	chr20:1550123-1550444	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr20:1548089-1548620	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr20:1550062-1550405	A549	lung:	n/a	n/a
9	CEBPB	chr20:1550085-1550450	A549	lung:	n/a	n/a
10	CEBPB	chr20:1549872-1550575	HCT-116	colon:	n/a	chr20:1549945-1549956
11	CEBPB	chr20:1550069-1550318	K562	blood:	n/a	n/a
12	CEBPB	chr20:1549987-1550512	A549	lung:	n/a	n/a
13	CEBPB	chr20:1557320-1557574	A549	lung:	n/a	chr20:1557460-1557471
14	CEBPB	chr20:1549993-1550495	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr20:1541479-1541541	HepG2	liver:	n/a	chr20:1541509-1541518 chr20:1541509-1541520 chr20:1541507-1541520
16	CEBPB	chr20:1550076-1550409	HepG2	liver:	n/a	n/a
17	CEBPB	chr20:1550121-1550426	IMR90	lung:	n/a	n/a
18	CEBPB	chr20:1549828-1550670	HCT-116	colon:	n/a	chr20:1549945-1549956
19	CEBPB	chr20:1550079-1550429	K562	blood:	n/a	n/a
20	CEBPB	chr20:1536352-1536602	HepG2	liver:	n/a	chr20:1536448-1536459
21	CEBPB	chr20:1550060-1550411	MCF-7	breast:	n/a	n/a
22	CEBPB	chr20:1539437-1539449	HepG2	liver:	n/a	n/a
23	CEBPB	chr20:1557318-1557553	HepG2	liver:	n/a	chr20:1557460-1557471
24	CEBPB	chr20:1557313-1557606	Hela-S3	cervix:	n/a	chr20:1557460-1557471
25	CHD2	chr20:1550074-1550408	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr20:1548232-1548651	Hela-S3	cervix:	n/a	n/a
27	CREB1	chr20:1550008-1550399	K562	blood:	n/a	n/a
28	CTCF	chr20:1536720-1536870	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr20:1536620-1536770	HUVEC	blood vessel:	n/a	n/a
30	CTCF	chr20:1536700-1536850	HCFaa	heart:	n/a	n/a
31	CTCF	chr20:1556774-1556880	NHEK	skin:	n/a	n/a
32	CTCF	chr20:1536760-1536910	HMF	breast:	n/a	n/a
33	CTCF	chr20:1536740-1536890	HRE	kidney:	n/a	n/a
34	CTCF	chr20:1562180-1562330	GM12875	blood:	n/a	n/a
35	CTCF	chr20:1562218-1562407	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr20:1550540-1550690	NB4	blood:	n/a	n/a
37	CTCF	chr20:1536660-1536950	HRE	kidney:	n/a	n/a
38	CTCF	chr20:1536690-1536875	HepG2	liver:	n/a	n/a
39	CTCF	chr20:1536580-1536730	A549	lung:	n/a	n/a
40	CTCF	chr20:1536745-1536849	K562	blood:	n/a	n/a
41	CTCF	chr20:1562180-1562330	GM12878	blood:	n/a	n/a
42	CTCF	chr20:1536800-1536950	RPTEC	kidney:	n/a	n/a
43	CTCF	chr20:1536740-1536802	GM13977	blood:	n/a	n/a
44	CTCF	chr20:1536680-1536830	HepG2	liver:	n/a	n/a
45	CTCF	chr20:1536750-1536819	GM12878	blood:	n/a	n/a
46	CTCF	chr20:1562140-1562290	GM12864	blood:	n/a	n/a
47	CTCF	chr20:1537751-1537804	GM20000	blood:	n/a	n/a
48	CTCF	chr20:1562235-1562401	GM12878	blood:	n/a	n/a
49	CTCF	chr20:1536682-1536892	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr20:1562235-1562365	GM13977	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1546019-1546069	GM06990	blood:	n/a
2	chr20:1546019-1546069	GM06990	blood:	n/a
3	chr20:1538366-1538416	AG09309	skin:	n/a
4	chr20:1538353-1538403	Caco-2	colon:	n/a
5	chr20:1538671-1538721	K562	blood:	n/a
6	chr20:1539702-1539752	HCPEpiC	choroid plexus:	n/a
7	chr20:1538353-1538403	SK-N-MC	brain:	n/a
8	chr20:1538366-1538416	SK-N-MC	brain:	n/a
9	chr20:1539641-1539691	HIPEpiC	eye:	n/a
10	chr20:1538353-1538403	SK-N-SH_RA	brain:	n/a
11	chr20:1538671-1538721	HNPCEpiC	eye:	n/a
12	chr20:1539702-1539752	HEK293	kidney:	embryo
13	chr20:1538353-1538403	ProgFib	skin:	n/a
14	chr20:1538671-1538721	HEEpiC	esophagus:	n/a
15	chr20:1538366-1538416	HCM	heart:	n/a
16	chr20:1538353-1538403	CMK	blood:	n/a
17	chr20:1538366-1538416	HIPEpiC	eye:	n/a
18	chr20:1539702-1539752	GM12892	blood:	n/a
19	chr20:1546019-1546069	MCF10A-Er-Src	breast:	n/a
20	chr20:1538353-1538403	AG04450	lung:	fetal
21	chr20:1546019-1546069	GM12891	blood:	n/a
22	chr20:1538366-1538416	HepG2	liver:	n/a
23	chr20:1539702-1539752	U87	brain:	n/a
24	chr20:1538366-1538416	NHBE	bronchial:	n/a
25	chr20:1546019-1546069	HUVEC	blood vessel:	n/a
26	chr20:1539702-1539752	GM12878	blood:	n/a
27	chr20:1539702-1539752	Hepatocyte	liver:	n/a
28	chr20:1546019-1546069	NB4	blood:	n/a
29	chr20:1546019-1546069	U87	brain:	n/a
30	chr20:1539641-1539691	HepG2	liver:	n/a
31	chr20:1538353-1538403	PrEC	prostate:	n/a
32	chr20:1539641-1539691	HUVEC	blood vessel:	n/a
33	chr20:1538366-1538416	MCF-7	breast:	n/a
34	chr20:1538671-1538721	A549	lung:	n/a
35	chr20:1539641-1539691	HEK293	kidney:	embryo
36	chr20:1539702-1539752	HCF	heart:	n/a
37	chr20:1538353-1538403	SK-N-SH	brain:	n/a
38	chr20:1546019-1546069	A549	lung:	n/a
39	chr20:1546019-1546069	HPAEpiC	pulmonary alveolar:	n/a
40	chr20:1539641-1539691	HRE	kidney:	n/a
41	chr20:1538353-1538403	MCF10A-Er-Src	breast:	n/a
42	chr20:1538353-1538403	HCF	heart:	n/a
43	chr20:1539702-1539752	AG09319	gingival:	n/a
44	chr20:1538353-1538403	MCF-7	breast:	n/a
45	chr20:1538353-1538403	ovcar-3	ovarian:	n/a
46	chr20:1538366-1538416	Hepatocyte	liver:	n/a
47	chr20:1538366-1538416	HRE	kidney:	n/a
48	chr20:1538671-1538721	HCM	heart:	n/a
49	chr20:1539641-1539691	AoSMC	blood vessel:	n/a
50	chr20:1539641-1539691	NH-A	brain:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:1547054..1548894-chr20:1756067..1757690,2	K562	blood:
2	chr20:1544908..1546600-chr20:1698607..1700315,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNPH-5	chr20:1562154-1562366	ucscGeneNc_uc002wfp_1
2	lnc-SNPH-5	chr20:1559583-1559595	ucscGeneNc_uc002wfp_1

No data

Variant related genes	Relation type
SIRPB1	TF binding region
SIRPD	TF binding region
ENSG00000242324	TF binding region
SIRPB1	CpG island
SIRPD	CpG island
ENSG00000242324	CpG island

Extended variants
information (count: 1106 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1106 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560776912	chr20:1534987-1534988	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs575925253	chr20:1535019-1535020	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181898865	chr20:1535024-1535025	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs2249673	chr20:1535030-1535031	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs532538273	chr20:1535064-1535065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547548054	chr20:1535086-1535087	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144576737	chr20:1535088-1535089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547519992	chr20:1535104-1535105	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530255720	chr20:1535132-1535133	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548780298	chr20:1535140-1535141	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186467543	chr20:1535151-1535152	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191311157	chr20:1535157-1535158	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs180758067	chr20:1535182-1535183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184958897	chr20:1535220-1535221	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374097119	chr20:1535255-1535256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs538643326	chr20:1535269-1535270	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147644733	chr20:1535276-1535277	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73569192	chr20:1535306-1535307	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs140867112	chr20:1535310-1535311	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554331285	chr20:1535318-1535319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576192336	chr20:1535344-1535345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543304642	chr20:1535369-1535370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200809478	chr20:1535382-1535383	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189758526	chr20:1535383-1535384	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs577132831	chr20:1535386-1535387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs535808511	chr20:1535404-1535405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138584503	chr20:1535432-1535433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377578243	chr20:1535444-1535445	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148863158	chr20:1535453-1535454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370491521	chr20:1535476-1535477	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs73569194	chr20:1535484-1535485	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs79303196	chr20:1535504-1535505	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555796530	chr20:1535511-1535512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs77866001	chr20:1535611-1535612	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552568152	chr20:1535647-1535648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183078837	chr20:1535699-1535700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374896961	chr20:1535783-1535784	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187422207	chr20:1535861-1535862	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546986507	chr20:1535897-1535898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376320754	chr20:1535908-1535909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs370389936	chr20:1535935-1535936	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs56204533	chr20:1535956-1535957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565376634	chr20:1535981-1535982	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs35242487	chr20:1535999-1536000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535901277	chr20:1536011-1536012	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs13041791	chr20:1536081-1536082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554245337	chr20:1536140-1536141	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs13037979	chr20:1536228-1536229	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191811689	chr20:1536294-1536295	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs73569196	chr20:1536305-1536306	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Glioblastoma multiforme	22286061	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	19455253	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17603634	CNVD
Colorectal cancer	19359472	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16774939	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16397240	CNVD
abortions and stillbirths	19751515	CNVD
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Prostate cancer	21551127	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Alcoholism	21790672	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Lung cancer	18438408	CNVD

Chromatin state (count:153 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:1529800-1536400	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr20:1532800-1545400	Weak transcription	Spleen	Spleen
3	chr20:1533800-1535800	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr20:1533800-1536400	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr20:1535800-1539200	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr20:1536400-1537400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
7	chr20:1536400-1538400	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
8	chr20:1536800-1537000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr20:1537000-1541200	Weak transcription	Primary T cells from cord blood	blood
10	chr20:1537000-1551600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr20:1537400-1542800	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr20:1538400-1539600	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr20:1538600-1538800	Flanking Active TSS	Stomach Smooth Muscle	stomach
14	chr20:1539200-1541200	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr20:1539600-1542600	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr20:1540000-1544800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr20:1540200-1543400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr20:1541200-1541800	Strong transcription	Primary T cells from cord blood	blood
19	chr20:1541200-1543000	Strong transcription	Primary neutrophils fromperipheralblood	blood
20	chr20:1541600-1542200	Enhancers	HUVEC	blood vessel
21	chr20:1541800-1545200	Weak transcription	Primary T cells from cord blood	blood
22	chr20:1542400-1543800	Enhancers	Dnd41	blood
23	chr20:1542600-1543200	Genic enhancers	Primary monocytes fromperipheralblood	blood
24	chr20:1542800-1543000	Genic enhancers	Monocytes-CD14+_RO01746	blood
25	chr20:1543000-1543200	Enhancers	Thymus	Thymus
26	chr20:1543000-1543800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
27	chr20:1543000-1545000	Genic enhancers	Primary neutrophils fromperipheralblood	blood
28	chr20:1543200-1543600	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr20:1543200-1550400	Weak transcription	Thymus	Thymus
30	chr20:1543400-1544000	Enhancers	Primary B cells from cord blood	blood
31	chr20:1543600-1544000	Enhancers	GM12878-XiMat	blood
32	chr20:1543600-1548600	Genic enhancers	Primary monocytes fromperipheralblood	blood
33	chr20:1543800-1544000	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr20:1543800-1568000	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr20:1544000-1545000	Genic enhancers	Monocytes-CD14+_RO01746	blood
36	chr20:1544600-1569000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr20:1544800-1548200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr20:1545000-1545400	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
39	chr20:1545000-1548000	Strong transcription	Primary neutrophils fromperipheralblood	blood
40	chr20:1545200-1547400	Strong transcription	Primary T cells from cord blood	blood
41	chr20:1545400-1546200	Genic enhancers	Monocytes-CD14+_RO01746	blood
42	chr20:1545400-1546600	Strong transcription	Spleen	Spleen
43	chr20:1545600-1545800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr20:1545800-1546800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr20:1545800-1549400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr20:1546000-1547000	ZNF genes & repeats	Lung	lung
47	chr20:1546200-1547800	Strong transcription	Monocytes-CD14+_RO01746	blood
48	chr20:1546600-1551200	Enhancers	Hela-S3	cervix
49	chr20:1546600-1551400	Weak transcription	Spleen	Spleen
50	chr20:1546800-1550800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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