Variant report

Variant	nsv585870
Chromosome Location	chr20:29603773-29648195
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2627)
CpG islands
(count:857)
Chromatin interactive
region (count:33)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2627 , 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	chr20:29628524-29629135	K562	blood:	n/a	chr20:29628683-29628699
2	ARID3A	chr20:29637221-29638826	K562	blood:	n/a	chr20:29637380-29637396
3	ARID3A	chr20:29610993-29612184	K562	blood:	n/a	n/a
4	ARID3A	chr20:29632785-29632962	K562	blood:	n/a	n/a
5	ARID3A	chr20:29629422-29629654	K562	blood:	n/a	n/a
6	ARID3A	chr20:29620583-29620956	K562	blood:	n/a	chr20:29620815-29620831
7	ARID3A	chr20:29606728-29606742	K562	blood:	n/a	n/a
8	ARID3A	chr20:29631123-29631286	K562	blood:	n/a	n/a
9	ARID3A	chr20:29611370-29612771	HepG2	liver:	n/a	n/a
10	ARID3A	chr20:29622471-29622991	HepG2	liver:	n/a	n/a
11	ARID3A	chr20:29633241-29633535	K562	blood:	n/a	n/a
12	ARID3A	chr20:29604416-29604457	K562	blood:	n/a	n/a
13	ARID3A	chr20:29630626-29630814	K562	blood:	n/a	n/a
14	ARID3A	chr20:29613365-29613570	K562	blood:	n/a	n/a
15	ARID3A	chr20:29627540-29627876	K562	blood:	n/a	n/a
16	ARID3A	chr20:29633844-29634865	K562	blood:	n/a	n/a
17	ATF1	chr20:29625665-29625843	K562	blood:	n/a	n/a
18	ATF1	chr20:29631255-29631264	K562	blood:	n/a	n/a
19	ATF1	chr20:29626546-29626747	K562	blood:	n/a	n/a
20	ATF1	chr20:29610930-29612133	K562	blood:	n/a	n/a
21	ATF1	chr20:29627360-29627533	K562	blood:	n/a	n/a
22	ATF1	chr20:29621820-29621934	K562	blood:	n/a	n/a
23	ATF1	chr20:29645664-29645716	K562	blood:	n/a	n/a
24	ATF1	chr20:29622631-29622824	K562	blood:	n/a	n/a
25	ATF1	chr20:29607716-29607882	K562	blood:	n/a	n/a
26	ATF1	chr20:29646142-29647360	K562	blood:	n/a	n/a
27	ATF1	chr20:29628542-29628871	K562	blood:	n/a	n/a
28	ATF1	chr20:29619091-29619138	K562	blood:	n/a	n/a
29	ATF1	chr20:29630621-29630981	K562	blood:	n/a	n/a
30	ATF1	chr20:29626100-29626288	K562	blood:	n/a	n/a
31	ATF1	chr20:29613285-29613479	K562	blood:	n/a	n/a
32	ATF1	chr20:29616245-29616416	K562	blood:	n/a	n/a
33	ATF1	chr20:29636917-29638762	K562	blood:	n/a	n/a
34	ATF1	chr20:29630171-29630348	K562	blood:	n/a	n/a
35	ATF1	chr20:29606718-29606904	K562	blood:	n/a	n/a
36	ATF1	chr20:29629679-29629821	K562	blood:	n/a	n/a
37	ATF1	chr20:29620111-29620173	K562	blood:	n/a	n/a
38	ATF1	chr20:29634000-29635084	K562	blood:	n/a	n/a
39	ATF1	chr20:29635802-29636715	K562	blood:	n/a	n/a
40	ATF1	chr20:29647981-29652560	K562	blood:	n/a	n/a
41	ATF1	chr20:29633094-29633439	K562	blood:	n/a	n/a
42	ATF3	chr20:29646268-29646613	HepG2	liver:	n/a	n/a
43	ATF3	chr20:29611074-29611815	K562	blood:	n/a	n/a
44	ATF3	chr20:29634301-29635008	K562	blood:	n/a	n/a
45	BACH1	chr20:29641718-29641864	K562	blood:	n/a	n/a
46	BACH1	chr20:29633874-29634317	K562	blood:	n/a	n/a
47	BACH1	chr20:29635785-29636744	K562	blood:	n/a	n/a
48	BACH1	chr20:29647962-29651120	K562	blood:	n/a	n/a
49	BACH1	chr20:29628551-29628899	K562	blood:	n/a	n/a
50	BACH1	chr20:29612089-29612264	K562	blood:	n/a	n/a

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:29608500-29608550	GM12892	blood:	n/a
2	chr20:29610620-29610670	HNPCEpiC	eye:	n/a
3	chr20:29611652-29611702	SAEC	small airway:	n/a
4	chr20:29608500-29608550	GM12892	blood:	n/a
5	chr20:29610620-29610670	HNPCEpiC	eye:	n/a
6	chr20:29611652-29611702	SAEC	small airway:	n/a
7	chr20:29612151-29612201	AG04449	skin:	fetal
8	chr20:29615890-29615940	HMEC	breast:	n/a
9	chr20:29611924-29611974	SKMC	muscle:	n/a
10	chr20:29608500-29608550	HRPEpiC	eye:	n/a
11	chr20:29611924-29611974	MCF-7	breast:	n/a
12	chr20:29611924-29611974	HCPEpiC	choroid plexus:	n/a
13	chr20:29610042-29610092	HRCEpiC	kidney:	n/a
14	chr20:29611796-29611846	LNCaP	prostate:	n/a
15	chr20:29610042-29610092	HUVEC	blood vessel:	n/a
16	chr20:29611785-29611835	HCM	heart:	n/a
17	chr20:29611810-29611860	NHDF-neo	bronchial:	n/a
18	chr20:29611903-29611953	Hela-S3	cervix:	n/a
19	chr20:29615890-29615940	HCPEpiC	choroid plexus:	n/a
20	chr20:29611652-29611702	HAEpiC	amniotic membrane:	n/a
21	chr20:29611810-29611860	AG09319	gingival:	n/a
22	chr20:29611785-29611835	BJ	skin:	n/a
23	chr20:29608500-29608550	HMEC	breast:	n/a
24	chr20:29611796-29611846	Hepatocyte	liver:	n/a
25	chr20:29615890-29615940	HCT-116	colon:	n/a
26	chr20:29610042-29610092	HCF	heart:	n/a
27	chr20:29613021-29613071	SAEC	small airway:	n/a
28	chr20:29611676-29611726	HL-60	blood:	n/a
29	chr20:29611652-29611702	CMK	blood:	n/a
30	chr20:29615890-29615940	HepG2	liver:	n/a
31	chr20:29611652-29611702	HRCEpiC	kidney:	n/a
32	chr20:29611810-29611860	Jurkat	blood:	n/a
33	chr20:29611652-29611702	HCM	heart:	n/a
34	chr20:29611796-29611846	GM06990	blood:	n/a
35	chr20:29611903-29611953	CMK	blood:	n/a
36	chr20:29611924-29611974	GM12878	blood:	n/a
37	chr20:29611909-29611959	SK-N-SH_RA	brain:	n/a
38	chr20:29610620-29610670	NH-A	brain:	n/a
39	chr20:29610620-29610670	SK-N-MC	brain:	n/a
40	chr20:29612151-29612201	SK-N-SH_RA	brain:	n/a
41	chr20:29612151-29612201	HRPEpiC	eye:	n/a
42	chr20:29611909-29611959	LNCaP	prostate:	n/a
43	chr20:29610620-29610670	Hela-S3	cervix:	n/a
44	chr20:29611903-29611953	Caco-2	colon:	n/a
45	chr20:29611924-29611974	Hela-S3	cervix:	n/a
46	chr20:29611796-29611846	AG09319	gingival:	n/a
47	chr20:29613021-29613071	RPTEC	kidney:	n/a
48	chr20:29612151-29612201	H1-hESC	embryonic stem cell:	embryo
49	chr20:29611796-29611846	AG10803	skin:	n/a
50	chr20:29610620-29610670	Caco-2	colon:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:29611467..29612118-chr9:68454964..68455886,2	MCF-7	breast:
2	chr20:29611333..29612723-chr4:190861521..190862825,5	HCT-116	colon:
3	chr20:29634644..29639248-chr4:190892116..190896171,7	MCF-7	breast:
4	chr20:29610673..29612888-chr4:190860203..190862511,3	MCF-7	breast:
5	chr20:29636048..29637003-chr4:190893089..190893743,2	MCF-7	breast:
6	chr20:29611384..29612018-chr9:68455093..68455961,3	MCF-7	breast:
7	chr20:29625984..29631616-chr9:68431406..68435615,4	MCF-7	breast:
8	chr20:29635538..29636169-chr9:68425739..68426630,2	MCF-7	breast:
9	chr17:57928426..57930583-chr20:29648016..29650833,2	MCF-7	breast:
10	chr20:29640916..29641744-chr4:190895394..190895909,2	MCF-7	breast:
11	chr20:29610649..29612158-chr9:68453830..68455817,2	K562	blood:
12	chr20:29611329..29612191-chr9:68455368..68456077,2	MCF-7	breast:
13	chr20:29626530..29628486-chr9:68434110..68435636,2	MCF-7	breast:
14	chr20:29609687..29611312-chr4:190860742..190862429,2	MCF-7	breast:
15	chr20:29636068..29638048-chr4:190894138..190896351,4	K562	blood:
16	chr20:29635971..29637948-chr4:190894580..190896098,2	K562	blood:
17	chr20:29611070..29612139-chr9:68455176..68456091,3	K562	blood:
18	chr20:29634674..29636233-chr4:190890902..190893775,2	K562	blood:
19	chr20:29637616..29639102-chr4:190894557..190895938,8	MCF-7	breast:
20	chr20:29634837..29636605-chr9:68424534..68426260,2	K562	blood:
21	chr20:29635757..29636455-chr9:68425529..68426032,2	MCF-7	breast:
22	chr2:133109798..133110355-chr20:29611407..29612129,2	MCF-7	breast:
23	chr20:29611128..29612321-chr4:190861463..190862739,6	MCF-7	breast:
24	chr20:29611632..29612497-chr4:190861809..190862721,3	MCF-7	breast:
25	chr20:29609593..29613129-chr4:190859723..190863221,5	K562	blood:
26	chr20:29637783..29638776-chr4:190894346..190895390,3	MCF-7	breast:
27	chr20:29637719..29639568-chr20:29640126..29641910,2	MCF-7	breast:
28	chr20:29634371..29640092-chr4:190891314..190895900,7	MCF-7	breast:
29	chr20:29637498..29638875-chr4:190894757..190896186,13	MCF-7	breast:
30	chr20:29611333..29614057-chr4:190860675..190863034,4	MCF-7	breast:
31	chr20:29610847..29613187-chr4:190860454..190862227,2	K562	blood:
32	chr20:29633490..29636802-chr9:68424473..68428627,9	MCF-7	breast:
33	chr20:29611427..29612170-chr9:68454810..68455955,3	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG1B-1	chr20:29641421-29641792	ENSG00000223346
2	lnc-FRG1B-1	chr20:29638246-29638813	ENSG00000223346
3	lnc-DEFB116-7	chr20:29637584-29638138	NONHSAT079280
4	lnc-DEFB116-7	chr20:29637799-29638060	NONHSAT147162

No data

Variant related genes	Relation type
FRG1B	TF binding region
ENSG00000221319	TF binding region
MLLT10P1	TF binding region
FRG1B	CpG island
ENSG00000221319	CpG island
MLLT10P1	CpG island
ENSG00000109536	chromatin interactions
ENSG00000230992	chromatin interactions
ENSG00000215548	chromatin interactions
ENSG00000245685	chromatin interactions
ENSG00000249462	chromatin interactions
ENSG00000238151	chromatin interactions

Extended variants
information (count: 5914 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:5914 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs498363	chr20:29603773-29603774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs62195822	chr20:29603791-29603792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529885887	chr20:29603792-29603793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs202004633	chr20:29603810-29603811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs546819705	chr20:29603816-29603817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs75771097	chr20:29603819-29603820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs190300539	chr20:29603823-29603824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12479999	chr20:29603824-29603825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538773458	chr20:29603857-29603858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs73616304	chr20:29603865-29603866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs4010900	chr20:29603869-29603870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374263834	chr20:29603876-29603877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558246873	chr20:29603886-29603887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs6087260	chr20:29603890-29603891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs3954440	chr20:29603892-29603893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs3954439	chr20:29603896-29603897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139968979	chr20:29603910-29603911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs3954438	chr20:29603934-29603935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs74651692	chr20:29603944-29603945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182566137	chr20:29603946-29603947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78819660	chr20:29603949-29603950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs4010899	chr20:29603964-29603965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573999652	chr20:29603976-29603977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs4010897	chr20:29603985-29603986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs4010920	chr20:29603996-29603997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs79717020	chr20:29603997-29603998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374203769	chr20:29604005-29604006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs4010919	chr20:29604010-29604011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79483368	chr20:29604025-29604026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4010918	chr20:29604026-29604027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs78125093	chr20:29604030-29604031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs78962798	chr20:29604035-29604036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs367712076	chr20:29604044-29604045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4010917	chr20:29604050-29604051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78720158	chr20:29604071-29604072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73616306	chr20:29604078-29604079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371500478	chr20:29604083-29604084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs4010916	chr20:29604084-29604085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553194544	chr20:29604086-29604087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4010915	chr20:29604087-29604088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573251829	chr20:29604109-29604110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200102257	chr20:29604114-29604115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369368402	chr20:29604119-29604120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs73616307	chr20:29604127-29604128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs202014888	chr20:29604142-29604143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12329522	chr20:29604160-29604161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146712402	chr20:29604164-29604165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs6087261	chr20:29604166-29604167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs77133539	chr20:29604170-29604171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375654772	chr20:29604174-29604175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Acute myeloid leukemia	20729466	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
T-cell prolymphocytic leukemia	17713554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21806811	CNVD
Melanoma	21693616	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
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	22860045	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Lung cancer	18438408	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Oral cancer	21386901	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1620 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:29602400-29607400	Weak transcription	Aorta	Aorta
2	chr20:29603600-29603800	Enhancers	Primary T killer memory cells from peripheral blood	blood
3	chr20:29607200-29608600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr20:29607200-29608800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
5	chr20:29607400-29608400	ZNF genes & repeats	Aorta	Aorta
6	chr20:29607600-29608000	ZNF genes & repeats	Primary T killer memory cells from peripheral blood	blood
7	chr20:29607800-29608000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr20:29607800-29608200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
9	chr20:29607800-29608200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
10	chr20:29607800-29608400	ZNF genes & repeats	Fetal Kidney	kidney
11	chr20:29608000-29608400	ZNF genes & repeats	Pancreas	Pancrea
12	chr20:29608000-29610800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr20:29608200-29609600	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr20:29608400-29611000	Weak transcription	Aorta	Aorta
15	chr20:29608400-29611000	Weak transcription	Fetal Kidney	kidney
16	chr20:29608400-29611000	Weak transcription	Pancreas	Pancrea
17	chr20:29608600-29609600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr20:29609400-29614200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
19	chr20:29609600-29609800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr20:29609600-29609800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr20:29609600-29609800	ZNF genes & repeats	Fetal Brain Male	brain
22	chr20:29609600-29609800	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
23	chr20:29609600-29609800	Enhancers	K562	blood
24	chr20:29609600-29612400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr20:29609800-29610800	Weak transcription	Fetal Brain Male	brain
26	chr20:29609800-29610800	Weak transcription	Dnd41	blood
27	chr20:29609800-29611000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr20:29609800-29611000	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr20:29610000-29610600	Weak transcription	K562	blood
30	chr20:29610000-29610800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr20:29610600-29614800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr20:29610600-29614800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
33	chr20:29610800-29611000	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr20:29610800-29611000	Enhancers	Right Ventricle	heart
35	chr20:29610800-29611000	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr20:29610800-29611000	Enhancers	Dnd41	blood
37	chr20:29610800-29611200	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
38	chr20:29610800-29611200	Active TSS	A549	lung
39	chr20:29610800-29611400	ZNF genes & repeats	Primary T killer memory cells from peripheral blood	blood
40	chr20:29610800-29611600	Flanking Active TSS	K562	blood
41	chr20:29610800-29611800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
42	chr20:29610800-29612400	Active TSS	Fetal Heart	heart
43	chr20:29610800-29612400	ZNF genes & repeats	Spleen	Spleen
44	chr20:29610800-29612600	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
45	chr20:29610800-29612600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr20:29610800-29612600	ZNF genes & repeats	Gastric	stomach
47	chr20:29610800-29612800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
48	chr20:29610800-29612800	ZNF genes & repeats	Fetal Muscle Leg	muscle
49	chr20:29610800-29613000	ZNF genes & repeats	Fetal Stomach	stomach
50	chr20:29610800-29613400	ZNF genes & repeats	HMEC	breast

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