Variant report

Variant	nsv1059534
Chromosome Location	chr20:14677058-14848061
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1230)
CpG islands
(count:0)
Chromatin interactive
region (count:40)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1230 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr20:14706954-14707154	K562	blood:	n/a	n/a
2	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
4	ATF2	chr20:14725297-14725726	GM12878	blood:	n/a	n/a
5	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
6	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
7	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
8	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
10	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
11	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
13	ATF3	chr20:14826094-14826569	A549	lung:	n/a	n/a
14	ATF3	chr20:14692815-14693406	A549	lung:	n/a	n/a
15	BACH1	chr20:14841074-14841466	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr20:14702858-14702913	K562	blood:	n/a	n/a
17	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
18	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
19	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
20	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
21	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
22	BATF	chr20:14810566-14810958	GM12878	blood:	n/a	n/a
23	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
24	BATF	chr20:14725407-14725742	GM12878	blood:	n/a	n/a
25	BATF	chr20:14725428-14725715	GM12878	blood:	n/a	n/a
26	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
27	BATF	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
28	BATF	chr20:14704304-14704567	GM12878	blood:	n/a	n/a
29	BATF	chr20:14704765-14705024	GM12878	blood:	n/a	n/a
30	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
31	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
32	BCL11A	chr20:14810584-14810953	GM12878	blood:	n/a	chr20:14810705-14810714
33	BCL11A	chr20:14813340-14813684	GM12878	blood:	n/a	n/a
34	BCL11A	chr20:14810529-14810966	GM12878	blood:	n/a	chr20:14810705-14810714
35	BCL11A	chr20:14833719-14834115	GM12878	blood:	n/a	n/a
36	BCL11A	chr20:14811187-14811493	GM12878	blood:	n/a	n/a
37	BCL11A	chr20:14819269-14819704	GM12878	blood:	n/a	chr20:14819415-14819424
38	BCL11A	chr20:14811061-14811585	GM12878	blood:	n/a	chr20:14811164-14811173
39	BCL11A	chr20:14841111-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
40	BCL11A	chr20:14833756-14834084	GM12878	blood:	n/a	n/a
41	BCL11A	chr20:14819190-14819731	GM12878	blood:	n/a	chr20:14819415-14819424
42	BCL11A	chr20:14813268-14813779	GM12878	blood:	n/a	n/a
43	BCL3	chr20:14681041-14681305	GM12878	blood:	n/a	n/a
44	BCL3	chr20:14681045-14681280	GM12878	blood:	n/a	n/a
45	BCL3	chr20:14692841-14693476	A549	lung:	n/a	chr20:14693105-14693113
46	BCL3	chr20:14825912-14826568	A549	lung:	n/a	chr20:14826452-14826461
47	BCL3	chr20:14826038-14826561	A549	lung:	n/a	chr20:14826452-14826461
48	BCLAF1	chr20:14819282-14819800	GM12878	blood:	n/a	chr20:14819415-14819424
49	BHLHE40	chr20:14819263-14819709	GM12878	blood:	n/a	n/a
50	BHLHE40	chr20:14810570-14811822	GM12878	blood:	n/a	n/a

No data

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
2	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
3	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
4	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
5	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
6	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
7	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
8	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
9	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
10	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
11	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
12	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
13	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:
14	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
15	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
16	chr20:14688944..14691499-chr20:14692203..14695103,3	MCF-7	breast:
17	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
18	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
19	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
20	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
21	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
22	chr20:14688944..14691499-chr20:14692203..14695103,3	MCF-7	breast:
23	chr20:14819830..14820468-chr4:11534089..11534643,2	MCF-7	breast:
24	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
25	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
26	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:
27	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
28	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
29	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
30	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
31	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
32	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
33	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
34	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
35	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
36	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
37	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
38	chr20:14606804..14608358-chr20:14690132..14692728,2	MCF-7	breast:
39	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
40	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FLRT3-4	chr20:14812896-14813240	ucscGeneNc_uc002woy_1
2	lnc-FLRT3-4	chr20:14816742-14816950	ucscGeneNc_uc002woy_1
3	lnc-C20orf7-3	chr20:14830550-14830649	NONHSAT078714
4	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: 4801 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:4801 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535696368	chr20:14677062-14677063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs554428027	chr20:14677088-14677089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181328161	chr20:14677104-14677105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34216076	chr20:14677134-14677135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574394142	chr20:14677150-14677151	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374536555	chr20:14677185-14677186	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572689178	chr20:14677186-14677187	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186337650	chr20:14677187-14677188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558135890	chr20:14677211-14677212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs6042860	chr20:14677212-14677213	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs189184146	chr20:14677259-14677260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs371362434	chr20:14677260-14677261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531485993	chr20:14677284-14677285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574553185	chr20:14677305-14677306	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs180856895	chr20:14677371-14677372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560387675	chr20:14677421-14677422	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544738778	chr20:14677460-14677461	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs6042861	chr20:14677503-14677504	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs186555221	chr20:14677523-14677524	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561330511	chr20:14677549-14677550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs4814318	chr20:14677564-14677565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs6135223	chr20:14677571-14677572	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs190959357	chr20:14677611-14677612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532832735	chr20:14677612-14677613	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568493534	chr20:14677613-14677614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74630714	chr20:14677617-14677618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs6135224	chr20:14677650-14677651	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs545515865	chr20:14677653-14677654	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566318317	chr20:14677661-14677662	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1041606	chr20:14677788-14677789	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs183123631	chr20:14677812-14677813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs570135825	chr20:14677850-14677851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs16994816	chr20:14677869-14677870	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs555825833	chr20:14677879-14677880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs6110394	chr20:14677928-14677929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs6110395	chr20:14677935-14677936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs139614708	chr20:14677946-14677947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541959857	chr20:14677955-14677956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75531908	chr20:14677967-14677968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572269491	chr20:14677997-14677998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs149671248	chr20:14678021-14678022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs6135225	chr20:14678135-14678136	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs573664321	chr20:14678183-14678184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs6105312	chr20:14678191-14678192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs6110396	chr20:14678230-14678231	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs77619439	chr20:14678291-14678292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs141237379	chr20:14678312-14678313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs79706099	chr20:14678348-14678349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs186161672	chr20:14678433-14678434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs191677634	chr20:14678437-14678438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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

Chromatin state (count:687 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

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	chr20:14674800-14681400	Weak transcription	Pancreas	Pancrea
4	chr20:14675400-14677800	Enhancers	Fetal Heart	heart
5	chr20:14676400-14677800	Weak transcription	Fetal Lung	lung
6	chr20:14676400-14681200	Weak transcription	GM12878-XiMat	blood
7	chr20:14677000-14677800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr20:14677000-14677800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr20:14677000-14678000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr20:14677200-14678600	Enhancers	Adipose Nuclei	Adipose
11	chr20:14677200-14678800	Enhancers	Colon Smooth Muscle	Colon
12	chr20:14677600-14677800	Enhancers	Fetal Kidney	kidney
13	chr20:14677600-14677800	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr20:14677600-14678000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr20:14677600-14678200	Enhancers	Rectal Smooth Muscle	rectum
16	chr20:14677600-14678800	Enhancers	Liver	Liver
17	chr20:14677800-14678000	Enhancers	Fetal Lung	lung
18	chr20:14677800-14678000	Enhancers	NHEK	skin
19	chr20:14677800-14678200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr20:14677800-14679600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr20:14677800-14681000	Weak transcription	Fetal Kidney	kidney
22	chr20:14677800-14681200	Weak transcription	Fetal Heart	heart
23	chr20:14677800-14681600	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr20:14678000-14678200	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr20:14678000-14679600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr20:14678000-14679800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr20:14678000-14679800	Weak transcription	NHEK	skin
28	chr20:14678000-14682000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr20:14678200-14678400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr20:14678200-14680000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr20:14678200-14681400	Weak transcription	Rectal Smooth Muscle	rectum
32	chr20:14678400-14680800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr20:14678600-14678800	Enhancers	Fetal Intestine Large	intestine
34	chr20:14678600-14679000	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr20:14678800-14679200	Flanking Active TSS	Liver	Liver
36	chr20:14678800-14679600	Weak transcription	Fetal Intestine Large	intestine
37	chr20:14678800-14682000	Weak transcription	Colon Smooth Muscle	Colon
38	chr20:14679200-14679600	Enhancers	Liver	Liver
39	chr20:14679600-14680200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr20:14679600-14680200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr20:14679600-14680200	Flanking Active TSS	Liver	Liver
42	chr20:14679600-14680400	Enhancers	Fetal Intestine Large	intestine
43	chr20:14679600-14682800	Enhancers	Fetal Intestine Small	intestine
44	chr20:14679800-14680200	Active TSS	Skeletal Muscle Male	skeletal muscle
45	chr20:14679800-14680400	Enhancers	Rectal Mucosa Donor 29	rectum
46	chr20:14679800-14681800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr20:14679800-14681800	Enhancers	NHEK	skin
48	chr20:14680000-14680200	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr20:14680000-14680200	Enhancers	Fetal Brain Male	brain
50	chr20:14680000-14680400	Enhancers	Duodenum Mucosa	Duodenum

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