Variant report

Variant	nsv1064226
Chromosome Location	chr20:14687769-14897602
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1502)
CpG islands
(count:0)
Chromatin interactive
region (count:51)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1502 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:14859363-14860384	HepG2	liver:	n/a	n/a
2	ATF1	chr20:14706954-14707154	K562	blood:	n/a	n/a
3	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
4	ATF2	chr20:14725297-14725726	GM12878	blood:	n/a	n/a
5	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
8	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
9	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
10	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
11	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
13	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
14	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
15	ATF3	chr20:14692815-14693406	A549	lung:	n/a	n/a
16	ATF3	chr20:14859595-14860443	A549	lung:	n/a	n/a
17	ATF3	chr20:14859536-14860398	A549	lung:	n/a	n/a
18	ATF3	chr20:14826094-14826569	A549	lung:	n/a	n/a
19	BACH1	chr20:14702858-14702913	K562	blood:	n/a	n/a
20	BACH1	chr20:14841074-14841466	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr20:14810566-14810958	GM12878	blood:	n/a	n/a
22	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
23	BATF	chr20:14704765-14705024	GM12878	blood:	n/a	n/a
24	BATF	chr20:14860106-14860399	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
25	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
26	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
27	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
28	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
29	BATF	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
30	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
31	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
32	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
33	BATF	chr20:14860056-14860418	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
34	BATF	chr20:14704304-14704567	GM12878	blood:	n/a	n/a
35	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
36	BATF	chr20:14725428-14725715	GM12878	blood:	n/a	n/a
37	BATF	chr20:14725407-14725742	GM12878	blood:	n/a	n/a
38	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
39	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
40	BCL11A	chr20:14819269-14819704	GM12878	blood:	n/a	chr20:14819415-14819424
41	BCL11A	chr20:14841111-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
42	BCL11A	chr20:14833719-14834115	GM12878	blood:	n/a	n/a
43	BCL11A	chr20:14859536-14859807	GM12878	blood:	n/a	n/a
44	BCL11A	chr20:14819190-14819731	GM12878	blood:	n/a	chr20:14819415-14819424
45	BCL11A	chr20:14810529-14810966	GM12878	blood:	n/a	chr20:14810705-14810714
46	BCL11A	chr20:14811061-14811585	GM12878	blood:	n/a	chr20:14811164-14811173
47	BCL11A	chr20:14833756-14834084	GM12878	blood:	n/a	n/a
48	BCL11A	chr20:14883093-14883400	GM12878	blood:	n/a	chr20:14883229-14883238
49	BCL11A	chr20:14813268-14813779	GM12878	blood:	n/a	n/a
50	BCL11A	chr20:14883096-14883392	GM12878	blood:	n/a	chr20:14883229-14883238

No data

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
2	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
3	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
4	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
5	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
6	chr20:14819830..14820468-chr4:11534089..11534643,2	MCF-7	breast:
7	chr20:14688944..14691499-chr20:14692203..14695103,3	MCF-7	breast:
8	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
9	chr20:14857662..14859546-chr20:15214980..15217486,2	MCF-7	breast:
10	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
11	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
12	chr20:14606804..14608358-chr20:14690132..14692728,2	MCF-7	breast:
13	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
14	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
15	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
16	chr20:14688944..14691499-chr20:14692203..14695103,3	MCF-7	breast:
17	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
18	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
19	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
20	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
21	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
22	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
23	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
24	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
25	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
26	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
27	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
28	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
29	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
30	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
31	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
32	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
33	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
34	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
35	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
36	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
37	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
38	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:
39	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
40	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
41	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:
42	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
43	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
44	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
45	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
46	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
47	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
48	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
49	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
50	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C20orf7-3	chr20:14868789-14869314	NONHSAT078714
2	lnc-FLRT3-1	chr20:14868742-14868950	ENSG00000235914.1
3	lnc-C20orf7-3	chr20:14830550-14830649	NONHSAT078714
4	lnc-FLRT3-1	chr20:14868742-14868950	NONHSAT078721
5	lnc-FLRT3-1	chr20:14864896-14865240	NONHSAT078721
6	lnc-FLRT3-4	chr20:14812896-14813240	ucscGeneNc_uc002woy_1
7	lnc-FLRT3-1	chr20:14864899-14865240	NR_110318
8	lnc-FLRT3-1	chr20:14864899-14865240	NR_037841
9	lnc-FLRT3-1	chr20:14868742-14868950	NR_037841
10	lnc-FLRT3-1	chr20:14885587-14886675	NR_072988
11	lnc-FLRT3-1	chr20:14864899-14865240	ENSG00000235914.1
12	lnc-FLRT3-1	chr20:14864898-14865240	NONHSAT078722
13	lnc-FLRT3-4	chr20:14858021-14858161	ucscGeneNc_uc002woy_1
14	lnc-FLRT3-4	chr20:14816742-14816950	ucscGeneNc_uc002woy_1
15	lnc-FLRT3-1	chr20:14885587-14886675	ENSG00000235914.1
16	lnc-C20orf7-3	chr20:14830550-14831152	NONHSAT078716

No data

Variant related genes	Relation type
RPS10P2	TF binding region
ENSG00000227927	chromatin interactions

Extended variants
information (count: 5680 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:5680 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10485775	chr20:14687769-14687770	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs563520658	chr20:14687812-14687813	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs566747799	chr20:14687839-14687840	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs530647928	chr20:14687881-14687882	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs549245834	chr20:14687977-14687978	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs76739468	chr20:14688002-14688003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs77584370	chr20:14688009-14688010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs7344182	chr20:14688064-14688065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567267005	chr20:14688148-14688149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534696918	chr20:14688245-14688246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546596545	chr20:14688248-14688249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs192195857	chr20:14688249-14688250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs149167846	chr20:14688283-14688284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539143240	chr20:14688291-14688292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574513458	chr20:14688304-14688305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs200743348	chr20:14688321-14688322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557200439	chr20:14688362-14688363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs6110401	chr20:14688367-14688368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183726361	chr20:14688369-14688370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536485071	chr20:14688374-14688375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572351616	chr20:14688410-14688411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs6110402	chr20:14688414-14688415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555298114	chr20:14688469-14688470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188714602	chr20:14688493-14688494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs148318760	chr20:14688494-14688495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs6034015	chr20:14688510-14688511	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs17775664	chr20:14688519-14688520	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs367713853	chr20:14688578-14688579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs371502246	chr20:14688580-14688581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374981658	chr20:14688655-14688656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs545068293	chr20:14688657-14688658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533518368	chr20:14688686-14688687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs540905502	chr20:14688692-14688693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs140587359	chr20:14688706-14688707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs145528830	chr20:14688746-14688747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563274382	chr20:14688775-14688776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs11699301	chr20:14688777-14688778	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs79300723	chr20:14688781-14688782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560806956	chr20:14688796-14688797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs11697103	chr20:14688818-14688819	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs564542593	chr20:14688839-14688840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs146973869	chr20:14688851-14688852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs117523476	chr20:14688852-14688853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs138217180	chr20:14688881-14688882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs566003026	chr20:14688887-14688888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs551042531	chr20:14688953-14688954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs6042874	chr20:14688995-14688996	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs536805902	chr20:14689021-14689022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs555211953	chr20:14689093-14689094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs191972952	chr20:14689129-14689130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Glioblastoma multiforme	21138945	CNVD
Cancer	20164919	CNVD
Multiple sclerosis	20663923	CNVD
Schizophrenia	20663923	CNVD
brain infarct	20663923	CNVD
Breast cancer	22522925	CNVD
Breast cancer	17142309	CNVD
Cancer	20164920	CNVD
Schizophrenia	23813976	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	20531469	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Williams Syndrome	20824207	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
early-passage human iPS cells	21368824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Cancer	21272361	CNVD

Chromatin state (count:817 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14681600-14698200	Weak transcription	Fetal Kidney	kidney
2	chr20:14682000-14688800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr20:14682000-14689800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr20:14682200-14692200	Weak transcription	Fetal Heart	heart
5	chr20:14682200-14693000	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr20:14685600-14688800	Weak transcription	NHEK	skin
7	chr20:14686000-14688600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr20:14686200-14694600	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr20:14687200-14688000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr20:14687200-14688000	Flanking Active TSS	Liver	Liver
11	chr20:14687200-14689000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr20:14687200-14692800	Weak transcription	Ovary	ovary
13	chr20:14687400-14688000	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr20:14687400-14689200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr20:14687600-14688600	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr20:14687600-14688800	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr20:14687600-14689200	Enhancers	Fetal Lung	lung
18	chr20:14687600-14692000	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr20:14687800-14688200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr20:14688000-14689200	Enhancers	Liver	Liver
21	chr20:14688000-14691400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr20:14688200-14689200	Enhancers	Stomach Mucosa	stomach
23	chr20:14688200-14690800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr20:14688200-14691200	Enhancers	Fetal Intestine Large	intestine
25	chr20:14688600-14688800	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr20:14688600-14689400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr20:14688600-14690200	Enhancers	Duodenum Mucosa	Duodenum
28	chr20:14688600-14690800	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr20:14688600-14691000	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr20:14688600-14693200	Enhancers	A549	lung
31	chr20:14688600-14693600	Enhancers	Fetal Intestine Small	intestine
32	chr20:14688800-14689200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr20:14688800-14689200	Enhancers	NHEK	skin
34	chr20:14688800-14691000	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr20:14688800-14691000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr20:14689000-14692400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr20:14689200-14691200	Weak transcription	NHEK	skin
38	chr20:14689200-14691400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr20:14689200-14691600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr20:14689200-14692200	Weak transcription	Fetal Lung	lung
41	chr20:14689200-14692400	Weak transcription	Stomach Mucosa	stomach
42	chr20:14689200-14692800	Weak transcription	Liver	Liver
43	chr20:14689400-14690600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr20:14689800-14691200	Enhancers	Rectal Mucosa Donor 29	rectum
45	chr20:14690000-14690200	Enhancers	Small Intestine	intestine
46	chr20:14690200-14690800	Weak transcription	Duodenum Mucosa	Duodenum
47	chr20:14690200-14692200	Weak transcription	Small Intestine	intestine
48	chr20:14690600-14694000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr20:14690800-14691000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr20:14690800-14691000	Enhancers	Duodenum Mucosa	Duodenum

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