Variant report

Variant	nsv962569
Chromosome Location	chr20:25876021-26152500
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1135)
CpG islands
(count:488)
Chromatin interactive
region (count:6)
LncRNA
region (count:54)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1135 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:25989422-25989527	HepG2	liver:	n/a	n/a
2	ATF2	chr20:25990276-25990617	GM12878	blood:	n/a	n/a
3	BATF	chr20:25975707-25975907	GM12878	blood:	n/a	n/a
4	BATF	chr20:25914679-25914959	GM12878	blood:	n/a	n/a
5	BATF	chr20:26104768-26105049	GM12878	blood:	n/a	n/a
6	BATF	chr20:26086012-26086209	GM12878	blood:	n/a	n/a
7	BATF	chr20:26082886-26083114	GM12878	blood:	n/a	n/a
8	BATF	chr20:25991390-25991666	GM12878	blood:	n/a	n/a
9	BATF	chr20:25914607-25914931	GM12878	blood:	n/a	n/a
10	BCL11A	chr20:26141604-26141853	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr20:26041793-26041988	GM12878	blood:	n/a	n/a
12	BCL11A	chr20:26120133-26120429	GM12878	blood:	n/a	n/a
13	BCL11A	chr20:26010805-26011025	GM12878	blood:	n/a	n/a
14	BCL11A	chr20:25990610-25990918	GM12878	blood:	n/a	n/a
15	BCL3	chr20:25945773-25946163	GM12878	blood:	n/a	n/a
16	BCLAF1	chr20:26128129-26128470	K562	blood:	n/a	n/a
17	BCLAF1	chr20:26126765-26127170	K562	blood:	n/a	n/a
18	BHLHE40	chr20:25975281-25975466	GM12878	blood:	n/a	n/a
19	BHLHE40	chr20:26128241-26128287	K562	blood:	n/a	n/a
20	BHLHE40	chr20:25975821-25976057	GM12878	blood:	n/a	n/a
21	BHLHE40	chr20:25968676-25968796	K562	blood:	n/a	chr20:25968678-25968699 chr20:25968682-25968695
22	BHLHE40	chr20:26128181-26128339	HepG2	liver:	n/a	n/a
23	BRCA1	chr20:25990237-25990584	HepG2	liver:	n/a	chr20:25990394-25990403
24	BRCA1	chr20:25990208-25990605	Hela-S3	cervix:	n/a	chr20:25990394-25990403
25	BRCA1	chr20:25990247-25990579	GM12878	blood:	n/a	chr20:25990394-25990403
26	CEBPB	chr20:25989351-25989594	K562	blood:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
27	CEBPB	chr20:26121211-26121451	A549	lung:	n/a	chr20:26121283-26121294 chr20:26121323-26121334 chr20:26121325-26121336
28	CEBPB	chr20:25989264-25989635	K562	blood:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
29	CEBPB	chr20:25989323-25989598	H1-hESC	embryonic stem cell:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
30	CEBPB	chr20:26121278-26121296	K562	blood:	n/a	chr20:26121283-26121294
31	CEBPB	chr20:25933076-25933229	HepG2	liver:	n/a	chr20:25933144-25933155
32	CEBPB	chr20:25989272-25989628	IMR90	lung:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
33	CEBPB	chr20:25878611-25878724	K562	blood:	n/a	chr20:25878662-25878673
34	CEBPB	chr20:26137875-26138074	K562	blood:	n/a	chr20:26137998-26138009 chr20:26137997-26138010
35	CEBPB	chr20:26121204-26121403	IMR90	lung:	n/a	chr20:26121283-26121294 chr20:26121323-26121334 chr20:26121325-26121336
36	CEBPB	chr20:25988884-25989639	Hela-S3	cervix:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
37	CEBPB	chr20:25942378-25942614	HepG2	liver:	n/a	chr20:25942454-25942467 chr20:25942454-25942465
38	CEBPB	chr20:25989347-25989484	HepG2	liver:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
39	CEBPB	chr20:26137879-26138067	HepG2	liver:	n/a	chr20:26137998-26138009 chr20:26137997-26138010
40	CEBPB	chr20:25906579-25906779	K562	blood:	n/a	n/a
41	CEBPB	chr20:25989230-25989660	K562	blood:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
42	CEBPB	chr20:25878583-25878770	A549	lung:	n/a	chr20:25878716-25878728 chr20:25878662-25878673
43	CEBPB	chr20:25942443-25942488	A549	lung:	n/a	chr20:25942454-25942467 chr20:25942454-25942465
44	CEBPB	chr20:25989327-25989510	HepG2	liver:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
45	CEBPB	chr20:25988927-25989639	A549	lung:	n/a	chr20:25989469-25989480 chr20:25989451-25989462
46	CEBPB	chr20:26121146-26121440	HepG2	liver:	n/a	chr20:26121283-26121294 chr20:26121323-26121334 chr20:26121325-26121336
47	CEBPB	chr20:25878573-25878789	IMR90	lung:	n/a	chr20:25878716-25878728 chr20:25878662-25878673
48	CEBPB	chr20:25878572-25878801	HepG2	liver:	n/a	chr20:25878716-25878728 chr20:25878662-25878673
49	CEBPB	chr20:26075797-26075840	HepG2	liver:	n/a	chr20:26075803-26075816 chr20:26075804-26075815
50	CEBPB	chr20:26041786-26041946	K562	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:25989674-25989724	Hepatocyte	liver:	n/a
2	chr20:25988266-25988316	MCF-7	breast:	n/a
3	chr20:25989674-25989724	AG04449	skin:	fetal
4	chr20:25988587-25988637	T-47D	breast:	n/a
5	chr20:25988266-25988316	HIPEpiC	eye:	n/a
6	chr20:25989674-25989724	Hela-S3	cervix:	n/a
7	chr20:25988266-25988316	LNCaP	prostate:	n/a
8	chr20:25990680-25990730	T-47D	breast:	n/a
9	chr20:25991114-25991164	NHDF-neo	bronchial:	n/a
10	chr20:25989775-25989825	NHBE	bronchial:	n/a
11	chr20:25989032-25989082	Hela-S3	cervix:	n/a
12	chr20:25988266-25988316	GM12878	blood:	n/a
13	chr20:25989674-25989724	NT2-D1	testis:	n/a
14	chr20:25990680-25990730	PrEC	prostate:	n/a
15	chr20:25988587-25988637	AG09309	skin:	n/a
16	chr20:25988587-25988637	ProgFib	skin:	n/a
17	chr20:26062310-26062360	AG09319	gingival:	n/a
18	chr20:25989032-25989082	NHBE	bronchial:	n/a
19	chr20:25988266-25988316	HNPCEpiC	eye:	n/a
20	chr20:25990680-25990730	AG10803	skin:	n/a
21	chr20:25989032-25989082	HRCEpiC	kidney:	n/a
22	chr20:26062310-26062360	HAEpiC	amniotic membrane:	n/a
23	chr20:25989775-25989825	PrEC	prostate:	n/a
24	chr20:25988266-25988316	Caco-2	colon:	n/a
25	chr20:25991114-25991164	HPAEpiC	pulmonary alveolar:	n/a
26	chr20:25991114-25991164	HRPEpiC	eye:	n/a
27	chr20:25991114-25991164	BJ	skin:	n/a
28	chr20:25989674-25989724	HMEC	breast:	n/a
29	chr20:26062310-26062360	GM12892	blood:	n/a
30	chr20:25989775-25989825	HCF	heart:	n/a
31	chr20:25988266-25988316	CMK	blood:	n/a
32	chr20:25989032-25989082	T-47D	breast:	n/a
33	chr20:26062310-26062360	H1-hESC	embryonic stem cell:	embryo
34	chr20:26062310-26062360	U87	brain:	n/a
35	chr20:25990680-25990730	HRCEpiC	kidney:	n/a
36	chr20:25991114-25991164	SK-N-SH_RA	brain:	n/a
37	chr20:25990680-25990730	NHBE	bronchial:	n/a
38	chr20:25989674-25989724	SK-N-SH_RA	brain:	n/a
39	chr20:25989775-25989825	HPAEpiC	pulmonary alveolar:	n/a
40	chr20:25991114-25991164	AoSMC	blood vessel:	n/a
41	chr20:25989775-25989825	HepG2	liver:	n/a
42	chr20:25990680-25990730	HCT-116	colon:	n/a
43	chr20:25988266-25988316	NHDF-neo	bronchial:	n/a
44	chr20:25989775-25989825	HRE	kidney:	n/a
45	chr20:25991114-25991164	AG04449	skin:	fetal
46	chr20:25989032-25989082	IMR90	lung:	fetal
47	chr20:25989032-25989082	H1-hESC	embryonic stem cell:	embryo
48	chr20:25990680-25990730	SK-N-SH_RA	brain:	n/a
49	chr20:25991114-25991164	SAEC	small airway:	n/a
50	chr20:25988587-25988637	IMR90	lung:	fetal

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:26130778..26134198-chr7:57619861..57623955,5	K562	blood:
2	chr13:63647812..63648534-chr20:26148535..26149113,2	MCF-7	breast:
3	chr20:26131190..26134756-chr7:57619861..57622623,3	K562	blood:
4	chr13:63637188..63639152-chr20:26145559..26148373,3	K562	blood:
5	chr13:63647679..63650483-chr20:26148365..26151073,2	K562	blood:
6	chr13:63637281..63639152-chr20:26145559..26147940,2	K562	blood:

(count:54 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM182A-6	chr20:26011530-26013121	ucscGeneNc_uc010gdq_1
2	lnc-FAM182B-3	chr20:25989427-25989691	XLOC_013712
3	lnc-FAM182A-4	chr20:26072148-26072255	ENSG00000125804.9
4	lnc-FAM182B-10	chr20:25930172-25930528	NONHSAT079203
5	lnc-FAM182A-8	chr20:25884722-25884846	NONHSAT079201
6	lnc-FAM182B-10	chr20:25930850-25930935	NONHSAT079203
7	lnc-FAM182A-4	chr20:26061824-26062026	ENSG00000125804.9
8	lnc-FAM182A-6	chr20:26001272-26001320	NONHSAT147161
9	lnc-FAM182A-4	chr20:26054406-26054505	ENSG00000125804.9
10	lnc-FAM182A-6	chr20:25983291-25983721	ucscGeneNc_uc010gdq_1
11	lnc-FAM182A-6	chr20:26009800-26010026	ucscGeneNc_uc010gdq_1
12	lnc-FAM182A-6	chr20:25997553-25997840	ucscGeneNc_uc010gdq_1
13	lnc-FAM182A-4	chr20:26063530-26063584	ENSG00000125804.9
14	lnc-FAM182A-8	chr20:25893639-25897924	NONHSAT079201
15	lnc-FAM182A-8	chr20:25884448-25884505	NONHSAT079201
16	lnc-FAM182A-4	chr20:26047198-26047273	ENSG00000125804.9
17	lnc-FAM182A-4	chr20:26049724-26049840	ENSG00000125804.9
18	lnc-FAM182A-6	chr20:26000465-26000560	NONHSAT147161
19	lnc-FAM182B-4	chr20:26114675-26114834	XLOC_013713
20	lnc-FAM182A-1	chr20:25945639-25949923	XLOC_013502
21	lnc-FAM182A-4	chr20:26047620-26047810	ENSG00000125804.9
22	lnc-FAM182A-4	chr20:26056970-26057076	ENSG00000125804.9
23	lnc-FAM182A-6	chr20:25968084-25968225	NONHSAT079206
24	lnc-FAM182B-11	chr20:25937427-25937691	NONHSAT079205
25	lnc-FAM182A-4	chr20:26054406-26054495	ENSG00000125804.9
26	lnc-FAM182B-2	chr20:25982172-25982528	XLOC_013711
27	lnc-FAM182A-4	chr20:26054406-26054448	ENSG00000125804.9
28	lnc-FAM182A-6	chr20:25990334-25991091	NONHSAT079206
29	lnc-FAM182A-1	chr20:25936448-25936505	ENSG00000226203
30	lnc-FAM182A-4	chr20:26046283-26046420	ENSG00000125804.9
31	lnc-FAM182A-1	chr20:25945639-25949924	ENSG00000226203
32	lnc-FAM182A-4	chr20:26073445-26073683	ENSG00000125804.9
33	lnc-FAM182A-4	chr20:26038034-26038238	ENSG00000125804.9
34	lnc-FAM182A-4	chr20:26049573-26049840	ENSG00000125804.9
35	lnc-FAM182A-4	chr20:26049553-26049840	ENSG00000125804.9
36	lnc-FAM182A-4	chr20:26061824-26062026	ENSG00000125804.9
37	lnc-FAM182B-11	chr20:25938891-25939167	NONHSAT079205
38	lnc-FAM182A-4	chr20:26049553-26049796	ENSG00000125804.9
39	lnc-FAM182A-1	chr20:25943698-25943832	XLOC_013502
40	lnc-FAM182A-1	chr20:25936722-25936846	XLOC_013502
41	lnc-FAM182A-4	chr20:26040299-26040496	ENSG00000125804.9
42	lnc-FAM182A-6	chr20:25999468-25999548	NONHSAT147161
43	lnc-FAM182B-3	chr20:25990891-25991167	XLOC_013712
44	lnc-FAM182B-4	chr20:26113523-26113633	XLOC_013713
45	lnc-FAM182A-6	chr20:26002406-26002505	ucscGeneNc_uc010gdq_1
46	lnc-FAM182A-1	chr20:25943698-25943832	ENSG00000226203
47	lnc-FAM182A-1	chr20:25936453-25936505	XLOC_013502
48	lnc-FAM182B-2	chr20:25982850-25982935	XLOC_013711
49	lnc-FAM182A-4	chr20:26049675-26049840	ENSG00000125804.9
50	lnc-FAM182A-1	chr20:25936722-25936846	ENSG00000226203

No data

Variant related genes	Relation type
ENSG00000230440	TF binding region
FAM182A	TF binding region
CFTRP1	TF binding region
ENSG00000231081	TF binding region
ENSG00000204556	TF binding region
ENSG00000226203	TF binding region
NCOR1P1	TF binding region
ENSG00000230440	CpG island
FAM182A	CpG island
CFTRP1	CpG island
ENSG00000231081	CpG island
ENSG00000204556	CpG island
ENSG00000226203	CpG island
NCOR1P1	CpG island
MUC17	miRNA target sites
LIMCH1	miRNA target sites

Extended variants
information (count: 4974 )
Associated
traits (count: 48 )

Variant overlapped rSNPs/rCNVs (count:4974 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76502440	chr20:25878001-25878002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs183137881	chr20:25878002-25878003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200069127	chr20:25878007-25878008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs200895383	chr20:25878031-25878032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78706033	chr20:25878041-25878042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs11906463	chr20:25878053-25878054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569458224	chr20:25878060-25878061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs4317002	chr20:25878073-25878074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150212739	chr20:25878080-25878081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs17355952	chr20:25878086-25878087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184235258	chr20:25878088-25878089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs4563311	chr20:25878119-25878120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538491423	chr20:25878122-25878123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2211497	chr20:25878151-25878152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1833003	chr20:25878185-25878186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs1833002	chr20:25878189-25878190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369363649	chr20:25878192-25878193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548898761	chr20:25878200-25878201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs35451775	chr20:25878204-25878205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs58096501	chr20:25878205-25878206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs201403431	chr20:25878212-25878213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs398121275	chr20:25878216-25878217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs4003119	chr20:25878218-25878219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs75182566	chr20:25878236-25878237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2386733	chr20:25878252-25878253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs2386734	chr20:25878259-25878260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs202053124	chr20:25878270-25878271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs199516600	chr20:25878271-25878272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113945807	chr20:25878301-25878302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1923049	chr20:25878319-25878320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs6050975	chr20:25878332-25878333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187471559	chr20:25878365-25878366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs4003120	chr20:25878377-25878378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs3875269	chr20:25878386-25878387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76910468	chr20:25878408-25878409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554338370	chr20:25878415-25878416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577240533	chr20:25878427-25878428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539272219	chr20:25878428-25878429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556284411	chr20:25878433-25878434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs80072135	chr20:25878448-25878449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs3875270	chr20:25878463-25878464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs60124075	chr20:25878486-25878487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs77119822	chr20:25878496-25878497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs151056040	chr20:25878515-25878516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs180879187	chr20:25878516-25878517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78720704	chr20:25878533-25878534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111911590	chr20:25878535-25878536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs59809048	chr20:25878540-25878541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541761327	chr20:25878547-25878548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs75189889	chr20:25878548-25878549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:48)

Disease	PMID	Source
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
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	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
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD

Chromatin state (count:618 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25878000-25880400	Weak transcription	Right Atrium	heart
2	chr20:25879200-25879800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr20:25882400-25882800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr20:25882600-25883200	Enhancers	NHEK	skin
5	chr20:25882600-25883400	Enhancers	Muscle Satellite Cultured Cells	--
6	chr20:25882800-25883200	Enhancers	Osteobl	bone
7	chr20:25887400-25888200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr20:25888600-25888800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr20:25909800-25911000	Enhancers	Dnd41	blood
10	chr20:25912600-25913200	Enhancers	Osteobl	bone
11	chr20:25912600-25913800	Enhancers	NHEK	skin
12	chr20:25912800-25913400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr20:25913000-25913800	Enhancers	HMEC	breast
14	chr20:25913600-25914000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr20:25913600-25914000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr20:25934800-25935200	Enhancers	Fetal Intestine Large	intestine
17	chr20:25934800-25935200	Enhancers	Fetal Intestine Small	intestine
18	chr20:25945800-25946200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr20:25946000-25946400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr20:25956000-25956400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr20:25957200-25957600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr20:25957600-25964200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr20:25961000-25961400	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr20:25964200-25964400	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr20:25964200-25965400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
26	chr20:25964400-25965400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr20:25965000-25965600	Enhancers	Fetal Stomach	stomach
28	chr20:25965000-25968600	Active TSS	Brain Germinal Matrix	brain
29	chr20:25965200-25965800	Active TSS	Skeletal Muscle Male	skeletal muscle
30	chr20:25965200-25966600	Active TSS	Brain Inferior Temporal Lobe	brain
31	chr20:25965200-25966600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
32	chr20:25965200-25966800	Active TSS	Fetal Brain Female	brain
33	chr20:25965400-25965600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr20:25965400-25965600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
35	chr20:25965400-25965600	Active TSS	Fetal Muscle Trunk	muscle
36	chr20:25965400-25965600	Bivalent Enhancer	Placenta	Placenta
37	chr20:25965400-25965800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr20:25965400-25965800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr20:25965400-25965800	Active TSS	Muscle Satellite Cultured Cells	--
40	chr20:25965400-25966000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr20:25965400-25966000	Active TSS	Left Ventricle	heart
42	chr20:25965400-25966000	Active TSS	Ovary	ovary
43	chr20:25965400-25966000	Active TSS	Psoas Muscle	Psoas
44	chr20:25965400-25966000	Active TSS	HSMM	muscle
45	chr20:25965400-25966000	Active TSS	NH-A	brain
46	chr20:25965400-25966000	Active TSS	Osteobl	bone
47	chr20:25965400-25966200	Active TSS	Primary T cells fromperipheralblood	blood
48	chr20:25965400-25966200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr20:25965400-25966200	Active TSS	Colon Smooth Muscle	Colon
50	chr20:25965400-25966200	Active TSS	Duodenum Smooth Muscle	Duodenum

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