Variant report

Variant	nsv912686
Chromosome Location	chr20:13205338-13311983
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1294)
CpG islands
(count:549)
Chromatin interactive
region (count:33)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1294 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:13242668-13243057	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:13224184-13225291	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:13225796-13226403	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:13303448-13303524	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:13305632-13306026	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:13288284-13288580	HepG2	liver:	n/a	n/a
7	ATF2	chr20:13227864-13228573	GM12878	blood:	n/a	n/a
8	ATF3	chr20:13224327-13224907	A549	lung:	n/a	n/a
9	BATF	chr20:13241273-13241512	GM12878	blood:	n/a	n/a
10	BATF	chr20:13227971-13228436	GM12878	blood:	n/a	chr20:13228049-13228062 chr20:13228309-13228318
11	BATF	chr20:13303264-13303598	GM12878	blood:	n/a	n/a
12	BCL11A	chr20:13227920-13228337	GM12878	blood:	n/a	n/a
13	BCL11A	chr20:13228024-13228227	GM12878	blood:	n/a	n/a
14	BCL3	chr20:13224249-13224988	A549	lung:	n/a	n/a
15	BCLAF1	chr20:13227948-13228349	GM12878	blood:	n/a	n/a
16	BCLAF1	chr20:13227848-13228366	GM12878	blood:	n/a	n/a
17	BHLHE40	chr20:13299537-13300068	GM12878	blood:	n/a	n/a
18	BHLHE40	chr20:13224471-13225052	HepG2	liver:	n/a	n/a
19	BHLHE40	chr20:13305746-13306129	GM12878	blood:	n/a	n/a
20	BHLHE40	chr20:13279985-13280277	K562	blood:	n/a	n/a
21	BHLHE40	chr20:13276519-13276726	K562	blood:	n/a	chr20:13276627-13276636 chr20:13276625-13276638 chr20:13276626-13276635 chr20:13276627-13276636
22	BHLHE40	chr20:13303361-13303559	GM12878	blood:	n/a	n/a
23	BHLHE40	chr20:13305740-13306100	K562	blood:	n/a	n/a
24	BHLHE40	chr20:13228283-13228432	HepG2	liver:	n/a	n/a
25	BHLHE40	chr20:13225966-13226376	HepG2	liver:	n/a	n/a
26	BRCA1	chr20:13242643-13242959	HepG2	liver:	n/a	n/a
27	BRCA1	chr20:13305859-13305975	HepG2	liver:	n/a	n/a
28	BRCA1	chr20:13305662-13305897	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr20:13226049-13226099	HepG2	liver:	n/a	n/a
30	BRCA1	chr20:13293192-13293307	GM12878	blood:	n/a	n/a
31	CEBPB	chr20:13288236-13288504	A549	lung:	n/a	chr20:13288376-13288387
32	CEBPB	chr20:13224155-13225034	A549	lung:	n/a	chr20:13224569-13224581 chr20:13224646-13224663
33	CEBPB	chr20:13253774-13254102	HepG2	liver:	n/a	chr20:13253937-13253948
34	CEBPB	chr20:13224364-13224858	A549	lung:	n/a	chr20:13224569-13224581 chr20:13224646-13224663
35	CEBPB	chr20:13302910-13303249	HepG2	liver:	n/a	n/a
36	CEBPB	chr20:13221222-13221522	HepG2	liver:	n/a	chr20:13221361-13221372
37	CEBPB	chr20:13288206-13288544	HepG2	liver:	n/a	chr20:13288376-13288387
38	CEBPB	chr20:13215558-13215966	HepG2	liver:	n/a	chr20:13215696-13215707
39	CEBPB	chr20:13258737-13258812	HepG2	liver:	n/a	n/a
40	CEBPB	chr20:13224389-13225013	HepG2	liver:	n/a	chr20:13224569-13224581 chr20:13224646-13224663
41	CEBPB	chr20:13253894-13254044	K562	blood:	n/a	chr20:13253937-13253948
42	CEBPB	chr20:13288188-13288563	HepG2	liver:	n/a	chr20:13288376-13288387
43	CEBPB	chr20:13226009-13226293	HepG2	liver:	n/a	chr20:13226151-13226162
44	CEBPB	chr20:13225906-13226448	HepG2	liver:	n/a	chr20:13226151-13226162
45	CEBPB	chr20:13224370-13224938	HepG2	liver:	n/a	chr20:13224569-13224581 chr20:13224646-13224663
46	CEBPB	chr20:13241257-13241595	HepG2	liver:	n/a	n/a
47	CEBPB	chr20:13225895-13226307	HepG2	liver:	n/a	chr20:13226151-13226162
48	CEBPB	chr20:13232220-13232400	HepG2	liver:	n/a	n/a
49	CEBPB	chr20:13288270-13288503	HepG2	liver:	n/a	chr20:13288376-13288387
50	CEBPB	chr20:13254770-13255249	H1-hESC	embryonic stem cell:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:13279847-13279897	MCF-7	breast:	n/a
2	chr20:13280130-13280180	ECC-1	luminal epithelium:	n/a
3	chr20:13280130-13280180	AG04450	lung:	fetal
4	chr20:13279847-13279897	AG04449	skin:	fetal
5	chr20:13283858-13283908	T-47D	breast:	n/a
6	chr20:13283858-13283908	PFSK-1	brain:	n/a
7	chr20:13280201-13280251	BE2_C	brain:	n/a
8	chr20:13280130-13280180	HepG2	liver:	n/a
9	chr20:13277967-13278017	HRE	kidney:	n/a
10	chr20:13279946-13279996	IMR90	lung:	fetal
11	chr20:13279946-13279996	AG04449	skin:	fetal
12	chr20:13280130-13280180	SAEC	small airway:	n/a
13	chr20:13279761-13279811	GM12878	blood:	n/a
14	chr20:13280130-13280180	GM06990	blood:	n/a
15	chr20:13279761-13279811	SKMC	muscle:	n/a
16	chr20:13205832-13205882	MCF10A-Er-Src	breast:	n/a
17	chr20:13205832-13205882	NB4	blood:	n/a
18	chr20:13279946-13279996	A549	lung:	n/a
19	chr20:13279761-13279811	BJ	skin:	n/a
20	chr20:13279946-13279996	T-47D	breast:	n/a
21	chr20:13277967-13278017	HCT-116	colon:	n/a
22	chr20:13205832-13205882	HNPCEpiC	eye:	n/a
23	chr20:13279847-13279897	HPAEpiC	pulmonary alveolar:	n/a
24	chr20:13205832-13205882	PANC-1	pancreas:	n/a
25	chr20:13283858-13283908	GM12878	blood:	n/a
26	chr20:13280181-13280231	NHBE	bronchial:	n/a
27	chr20:13280181-13280231	U87	brain:	n/a
28	chr20:13279946-13279996	H1-hESC	embryonic stem cell:	embryo
29	chr20:13280181-13280231	NH-A	brain:	n/a
30	chr20:13279761-13279811	ProgFib	skin:	n/a
31	chr20:13280130-13280180	HIPEpiC	eye:	n/a
32	chr20:13279946-13279996	HCM	heart:	n/a
33	chr20:13283858-13283908	A549	lung:	n/a
34	chr20:13280130-13280180	NT2-D1	testis:	n/a
35	chr20:13277967-13278017	U87	brain:	n/a
36	chr20:13283858-13283908	HNPCEpiC	eye:	n/a
37	chr20:13280201-13280251	HIPEpiC	eye:	n/a
38	chr20:13205832-13205882	HRE	kidney:	n/a
39	chr20:13280181-13280231	HRE	kidney:	n/a
40	chr20:13279847-13279897	Jurkat	blood:	n/a
41	chr20:13280201-13280251	HUVEC	blood vessel:	n/a
42	chr20:13205832-13205882	HCPEpiC	choroid plexus:	n/a
43	chr20:13279761-13279811	GM12892	blood:	n/a
44	chr20:13280201-13280251	HPAEpiC	pulmonary alveolar:	n/a
45	chr20:13277967-13278017	AG04449	skin:	fetal
46	chr20:13279761-13279811	AG10803	skin:	n/a
47	chr20:13280130-13280180	HCT-116	colon:	n/a
48	chr20:13279847-13279897	HCPEpiC	choroid plexus:	n/a
49	chr20:13283858-13283908	AG04450	lung:	fetal
50	chr20:13277967-13278017	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr20:13305344..13306280-chr20:13527310..13528173,2	MCF-7	breast:
2	chr20:13099864..13101163-chr20:13242113..13243382,13	MCF-7	breast:
3	chr20:13224428..13227075-chr20:13229216..13232192,3	MCF-7	breast:
4	chr20:13278576..13280207-chr20:13285349..13287405,2	MCF-7	breast:
5	chr20:13217886..13220237-chr20:13220614..13223071,3	MCF-7	breast:
6	chr20:13099915..13100786-chr20:13283022..13283937,3	MCF-7	breast:
7	chr20:13305433..13306398-chr20:13526637..13527817,4	MCF-7	breast:
8	chr20:13278576..13280207-chr20:13285349..13287405,2	MCF-7	breast:
9	chr20:13298397..13300757-chr20:13300815..13303338,2	MCF-7	breast:
10	chr20:13281049..13283479-chr20:13288653..13290792,2	MCF-7	breast:
11	chr14:48176778..48178872-chr20:13212572..13214916,2	MCF-7	breast:
12	chr20:13217886..13220237-chr20:13220614..13223071,3	MCF-7	breast:
13	chr20:13279959..13281741-chr20:13285750..13288424,2	K562	blood:
14	chr20:13102577..13104430-chr20:13278483..13280151,2	MCF-7	breast:
15	chr20:13305771..13306616-chr20:13439402..13440096,2	K562	blood:
16	chr20:13305737..13306312-chr20:13526618..13527354,2	K562	blood:
17	chr20:13300108..13302857-chr20:13304217..13306558,2	MCF-7	breast:
18	chr20:13294043..13294675-chr9:134731164..134732018,2	MCF-7	breast:
19	chr20:13099834..13100573-chr20:13242429..13243331,4	MCF-7	breast:
20	chr20:13186346..13187286-chr20:13242328..13243323,3	MCF-7	breast:
21	chr20:13279959..13281741-chr20:13285750..13288424,2	K562	blood:
22	chr20:13281049..13283479-chr20:13288653..13290792,2	MCF-7	breast:
23	chr20:13099895..13100678-chr20:13283242..13284334,3	MCF-7	breast:
24	chr20:13222224..13226467-chr20:13226832..13229125,4	MCF-7	breast:
25	chr20:13186534..13187312-chr20:13283028..13283706,3	MCF-7	breast:
26	chr20:13300108..13302857-chr20:13304217..13306558,2	MCF-7	breast:
27	chr20:13293842..13296817-chr20:13312526..13314549,2	K562	blood:
28	chr20:12950635..12951321-chr20:13242468..13243223,2	MCF-7	breast:
29	chr20:13186665..13187313-chr20:13282994..13283540,2	MCF-7	breast:
30	chr20:13296564..13298740-chr20:13303528..13306160,2	MCF-7	breast:
31	chr20:13225351..13227078-chr20:13232726..13234413,2	MCF-7	breast:
32	chr20:13298397..13300757-chr20:13300815..13303338,2	MCF-7	breast:
33	chr20:13296564..13298740-chr20:13303528..13306160,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPTLC3-5	chr20:13219374-13219813	NONHSAT078685
2	lnc-TASP1-1	chr20:13224711-13225028	ENSG00000225956.1
3	lnc-TASP1-2	chr20:13219658-13220301	NONHSAT078684
4	lnc-SPTLC3-5	chr20:13229880-13230196	NONHSAT078685
5	lnc-TASP1-2	chr20:13218067-13218756	NONHSAT078683
6	lnc-TASP1-1	chr20:13225889-13226016	ENSG00000225956.1
7	lnc-TASP1-2	chr20:13219631-13219751	NONHSAT078683
8	lnc-TASP1-2	chr20:13218733-13218756	NONHSAT078684
9	lnc-TASP1-2	chr20:13220100-13220334	NONHSAT078683

No data

Variant related genes	Relation type
ENSG00000225956	TF binding region
ISM1-AS1	TF binding region
ENSG00000225956	CpG island
ISM1-AS1	CpG island
ENSG00000225956	chromatin interactions

Extended variants
information (count: 4120 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:4120 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6033643	chr20:13205338-13205339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs555084458	chr20:13205356-13205357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540198492	chr20:13205379-13205380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560310907	chr20:13205380-13205381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs143283974	chr20:13205393-13205394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542416960	chr20:13205394-13205395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73091459	chr20:13205423-13205424	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs375360650	chr20:13205488-13205489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531132727	chr20:13205494-13205495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs13038728	chr20:13205517-13205518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs12480257	chr20:13205523-13205524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533171698	chr20:13205532-13205533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374872435	chr20:13205538-13205539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568924976	chr20:13205556-13205557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371717386	chr20:13205574-13205575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181406441	chr20:13205581-13205582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566630648	chr20:13205585-13205586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529330562	chr20:13205593-13205594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574847628	chr20:13205636-13205637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs55983441	chr20:13205641-13205642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs111643040	chr20:13205644-13205645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538025872	chr20:13205647-13205648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369917901	chr20:13205650-13205651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532771229	chr20:13205659-13205660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373319096	chr20:13205691-13205692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112532029	chr20:13205701-13205702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs7363367	chr20:13205702-13205703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184262979	chr20:13205707-13205708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573572167	chr20:13205714-13205715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377454632	chr20:13205716-13205717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556203918	chr20:13205722-13205723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370634596	chr20:13205723-13205724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs6109762	chr20:13205736-13205737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564464351	chr20:13205743-13205744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs199685004	chr20:13205747-13205748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112426085	chr20:13205751-13205752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560156727	chr20:13205752-13205753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs371208409	chr20:13205769-13205770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543950003	chr20:13205777-13205778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs145582451	chr20:13205779-13205780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189377184	chr20:13205782-13205783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374481762	chr20:13205786-13205787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs140349318	chr20:13205789-13205790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs73610458	chr20:13205790-13205791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571574905	chr20:13205791-13205792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs77602969	chr20:13205792-13205793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs56084709	chr20:13205796-13205797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192466804	chr20:13205846-13205847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs367860342	chr20:13205849-13205850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567178995	chr20:13205856-13205857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
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
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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Glaucoma	21310917	CNVD
Alagille syndrome	22470819	CNVD
Lung cancer	16773561	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Myelofibrosis	22110671	CNVD
Kabuki syndrome	21720541	CNVD
Glioblastoma multiforme	22286061	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Neurocytoma	17123091	CNVD
Autism	22102821	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:13203400-13211600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr20:13203400-13211600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr20:13203600-13209200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr20:13203600-13211800	Weak transcription	Placenta	Placenta
5	chr20:13203600-13229800	Weak transcription	Stomach Smooth Muscle	stomach
6	chr20:13204200-13206800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr20:13204400-13207000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr20:13205200-13208800	Weak transcription	Dnd41	blood
9	chr20:13205200-13209200	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr20:13206400-13209200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr20:13206600-13207000	Weak transcription	Aorta	Aorta
12	chr20:13206800-13207600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr20:13207000-13207800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
14	chr20:13207600-13210800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr20:13208800-13209200	Enhancers	Dnd41	blood
16	chr20:13208800-13211600	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr20:13209200-13209400	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr20:13209200-13210000	Flanking Active TSS	Dnd41	blood
19	chr20:13209200-13211600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr20:13209200-13211600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr20:13209200-13211800	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr20:13209200-13212000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr20:13209200-13212800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr20:13209200-13213200	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr20:13209200-13213400	Enhancers	Primary T cells from cord blood	blood
26	chr20:13209200-13213600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr20:13209400-13209600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
28	chr20:13209600-13209800	Enhancers	Primary T helper cells PMA-I stimulated	--
29	chr20:13209800-13210000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
30	chr20:13209800-13210400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr20:13210000-13210200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chr20:13210000-13211200	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr20:13210000-13212600	Enhancers	Dnd41	blood
34	chr20:13210200-13211800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr20:13210400-13210600	Enhancers	Primary T cells fromperipheralblood	blood
36	chr20:13210400-13212600	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr20:13210600-13211200	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr20:13210800-13213000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr20:13211200-13211400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
40	chr20:13211200-13212600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr20:13211200-13213000	Enhancers	Primary T cells fromperipheralblood	blood
42	chr20:13211200-13213000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr20:13211200-13213200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr20:13211400-13211800	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr20:13211400-13212000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr20:13211400-13212200	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr20:13211400-13212800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr20:13211400-13212800	Enhancers	HMEC	breast
49	chr20:13211400-13212800	Enhancers	NHEK	skin
50	chr20:13211400-13212800	Enhancers	Osteobl	bone

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