Variant report

Variant	nsv912699
Chromosome Location	chr20:14672177-14901776
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1639)
CpG islands
(count:0)
Chromatin interactive
region (count:55)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1639 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

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	chr20:14725297-14725726	GM12878	blood:	n/a	n/a
4	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
5	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
6	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
8	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
9	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
10	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
11	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
13	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
14	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr20:14859536-14860398	A549	lung:	n/a	n/a
16	ATF3	chr20:14692815-14693406	A549	lung:	n/a	n/a
17	ATF3	chr20:14826094-14826569	A549	lung:	n/a	n/a
18	ATF3	chr20:14859595-14860443	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	chr20:14860106-14860399	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
22	BATF	chr20:14725407-14725742	GM12878	blood:	n/a	n/a
23	BATF	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
24	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
25	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
26	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
27	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
28	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
29	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
30	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
31	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
32	BATF	chr20:14810566-14810958	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	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
35	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
36	BATF	chr20:14704304-14704567	GM12878	blood:	n/a	n/a
37	BATF	chr20:14725428-14725715	GM12878	blood:	n/a	n/a
38	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
39	BATF	chr20:14704765-14705024	GM12878	blood:	n/a	n/a
40	BCL11A	chr20:14810584-14810953	GM12878	blood:	n/a	chr20:14810705-14810714
41	BCL11A	chr20:14813268-14813779	GM12878	blood:	n/a	n/a
42	BCL11A	chr20:14859536-14859807	GM12878	blood:	n/a	n/a
43	BCL11A	chr20:14841111-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
44	BCL11A	chr20:14833719-14834115	GM12878	blood:	n/a	n/a
45	BCL11A	chr20:14819190-14819731	GM12878	blood:	n/a	chr20:14819415-14819424
46	BCL11A	chr20:14883093-14883400	GM12878	blood:	n/a	chr20:14883229-14883238
47	BCL11A	chr20:14811061-14811585	GM12878	blood:	n/a	chr20:14811164-14811173
48	BCL11A	chr20:14833756-14834084	GM12878	blood:	n/a	n/a
49	BCL11A	chr20:14811187-14811493	GM12878	blood:	n/a	n/a
50	BCL11A	chr20:14883096-14883392	GM12878	blood:	n/a	chr20:14883229-14883238

No data

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
2	chr20:14857662..14859546-chr20:15214980..15217486,2	MCF-7	breast:
3	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
4	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
5	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
6	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
7	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
8	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
9	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
10	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
11	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
12	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
13	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
14	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:
15	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
16	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
17	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
18	chr20:14898344..14901833-chr20:14901900..14905742,3	MCF-7	breast:
19	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
20	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
21	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
22	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
23	chr20:14688944..14691499-chr20:14692203..14695103,3	MCF-7	breast:
24	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
25	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
26	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
27	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
28	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
29	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
30	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
31	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
32	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
33	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
34	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:
35	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
36	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
37	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
38	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
39	chr20:14895407..14897578-chr20:14900614..14902594,2	MCF-7	breast:
40	chr20:14688944..14691499-chr20:14692203..14695103,3	MCF-7	breast:
41	chr20:14892181..14894488-chr20:14900218..14901785,2	MCF-7	breast:
42	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
43	chr20:14819830..14820468-chr4:11534089..11534643,2	MCF-7	breast:
44	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
45	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
46	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
47	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
48	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
49	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
50	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 6450 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:6450 , 50 per page) page: 1 2 3 4 5 6 7 ... 129

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6034011	chr20:14672177-14672178	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564394036	chr20:14672181-14672182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539190312	chr20:14672212-14672213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531682309	chr20:14672214-14672215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376505608	chr20:14672256-14672257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550148904	chr20:14672259-14672260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569616908	chr20:14672282-14672283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs114460171	chr20:14672303-14672304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547894712	chr20:14672306-14672307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182192109	chr20:14672322-14672323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184560306	chr20:14672359-14672360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558404075	chr20:14672364-14672365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188960517	chr20:14672387-14672388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113528682	chr20:14672390-14672391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181548055	chr20:14672395-14672396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537352206	chr20:14672408-14672409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555705293	chr20:14672416-14672417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs377181010	chr20:14672438-14672439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185633658	chr20:14672444-14672445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543851990	chr20:14672479-14672480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553814956	chr20:14672491-14672492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572084739	chr20:14672492-14672493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554137195	chr20:14672526-14672527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574057293	chr20:14672534-14672535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149045262	chr20:14672562-14672563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557668072	chr20:14672612-14672613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576361156	chr20:14672616-14672617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568973828	chr20:14672630-14672631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs6110390	chr20:14672631-14672632	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs560369202	chr20:14672725-14672726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538453688	chr20:14672752-14672753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541103398	chr20:14672762-14672763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35944219	chr20:14672781-14672782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559789275	chr20:14672789-14672790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533312490	chr20:14672801-14672802	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs6079530	chr20:14672805-14672806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190046904	chr20:14672825-14672826	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34379099	chr20:14672834-14672835	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545281453	chr20:14672876-14672877	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569926203	chr20:14672924-14672925	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113306965	chr20:14672984-14672985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549244495	chr20:14672986-14672987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181014048	chr20:14673011-14673012	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186035864	chr20:14673012-14673013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs190894218	chr20:14673017-14673018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565720131	chr20:14673018-14673019	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539165460	chr20:14673062-14673063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557947294	chr20:14673085-14673086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576330074	chr20:14673106-14673107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543674094	chr20:14673118-14673119	Enhancers Weak transcription	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:1077 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14668400-14680800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr20:14668800-14678000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr20:14671600-14672800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr20:14672800-14673400	Enhancers	GM12878-XiMat	blood
5	chr20:14672800-14673600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr20:14673400-14675800	Weak transcription	GM12878-XiMat	blood
7	chr20:14674600-14674800	Enhancers	Pancreas	Pancrea
8	chr20:14674800-14681400	Weak transcription	Pancreas	Pancrea
9	chr20:14675400-14677800	Enhancers	Fetal Heart	heart
10	chr20:14675800-14676400	Enhancers	GM12878-XiMat	blood
11	chr20:14676000-14676400	Enhancers	Fetal Lung	lung
12	chr20:14676200-14676600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr20:14676400-14677800	Weak transcription	Fetal Lung	lung
14	chr20:14676400-14681200	Weak transcription	GM12878-XiMat	blood
15	chr20:14677000-14677800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr20:14677000-14677800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr20:14677000-14678000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr20:14677200-14678600	Enhancers	Adipose Nuclei	Adipose
19	chr20:14677200-14678800	Enhancers	Colon Smooth Muscle	Colon
20	chr20:14677600-14677800	Enhancers	Fetal Kidney	kidney
21	chr20:14677600-14677800	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr20:14677600-14678000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr20:14677600-14678200	Enhancers	Rectal Smooth Muscle	rectum
24	chr20:14677600-14678800	Enhancers	Liver	Liver
25	chr20:14677800-14678000	Enhancers	Fetal Lung	lung
26	chr20:14677800-14678000	Enhancers	NHEK	skin
27	chr20:14677800-14678200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr20:14677800-14679600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr20:14677800-14681000	Weak transcription	Fetal Kidney	kidney
30	chr20:14677800-14681200	Weak transcription	Fetal Heart	heart
31	chr20:14677800-14681600	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr20:14678000-14678200	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr20:14678000-14679600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr20:14678000-14679800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr20:14678000-14679800	Weak transcription	NHEK	skin
36	chr20:14678000-14682000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr20:14678200-14678400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr20:14678200-14680000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr20:14678200-14681400	Weak transcription	Rectal Smooth Muscle	rectum
40	chr20:14678400-14680800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr20:14678600-14678800	Enhancers	Fetal Intestine Large	intestine
42	chr20:14678600-14679000	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr20:14678800-14679200	Flanking Active TSS	Liver	Liver
44	chr20:14678800-14679600	Weak transcription	Fetal Intestine Large	intestine
45	chr20:14678800-14682000	Weak transcription	Colon Smooth Muscle	Colon
46	chr20:14679200-14679600	Enhancers	Liver	Liver
47	chr20:14679600-14680200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr20:14679600-14680200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr20:14679600-14680200	Flanking Active TSS	Liver	Liver
50	chr20:14679600-14680400	Enhancers	Fetal Intestine Large	intestine

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