Variant report

Variant	nsv912702
Chromosome Location	chr20:14686297-14853050
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1181)
CpG islands
(count:0)
Chromatin interactive
region (count:40)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1181 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

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	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
3	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
4	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
5	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
6	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
7	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
9	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr20:14725297-14725726	GM12878	blood:	n/a	n/a
11	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14811110-14811561	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	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
18	BATF	chr20:14725428-14725715	GM12878	blood:	n/a	n/a
19	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
20	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
21	BATF	chr20:14725407-14725742	GM12878	blood:	n/a	n/a
22	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
23	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
24	BATF	chr20:14704304-14704567	GM12878	blood:	n/a	n/a
25	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
26	BATF	chr20:14704765-14705024	GM12878	blood:	n/a	n/a
27	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
28	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
29	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
30	BATF	chr20:14810566-14810958	GM12878	blood:	n/a	n/a
31	BATF	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
32	BCL11A	chr20:14819190-14819731	GM12878	blood:	n/a	chr20:14819415-14819424
33	BCL11A	chr20:14810529-14810966	GM12878	blood:	n/a	chr20:14810705-14810714
34	BCL11A	chr20:14833756-14834084	GM12878	blood:	n/a	n/a
35	BCL11A	chr20:14841111-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
36	BCL11A	chr20:14810584-14810953	GM12878	blood:	n/a	chr20:14810705-14810714
37	BCL11A	chr20:14833719-14834115	GM12878	blood:	n/a	n/a
38	BCL11A	chr20:14819269-14819704	GM12878	blood:	n/a	chr20:14819415-14819424
39	BCL11A	chr20:14813340-14813684	GM12878	blood:	n/a	n/a
40	BCL11A	chr20:14811187-14811493	GM12878	blood:	n/a	n/a
41	BCL11A	chr20:14811061-14811585	GM12878	blood:	n/a	chr20:14811164-14811173
42	BCL11A	chr20:14813268-14813779	GM12878	blood:	n/a	n/a
43	BCL3	chr20:14826038-14826561	A549	lung:	n/a	chr20:14826452-14826461
44	BCL3	chr20:14825912-14826568	A549	lung:	n/a	chr20:14826452-14826461
45	BCL3	chr20:14692841-14693476	A549	lung:	n/a	chr20:14693105-14693113
46	BCLAF1	chr20:14819282-14819800	GM12878	blood:	n/a	chr20:14819415-14819424
47	BHLHE40	chr20:14813359-14813737	GM12878	blood:	n/a	n/a
48	BHLHE40	chr20:14810570-14811822	GM12878	blood:	n/a	n/a
49	BHLHE40	chr20:14833692-14834191	GM12878	blood:	n/a	n/a
50	BHLHE40	chr20:14704309-14704573	GM12878	blood:	n/a	n/a

No data

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

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C20orf7-3	chr20:14830550-14830649	NONHSAT078714
2	lnc-C20orf7-3	chr20:14830550-14831152	NONHSAT078716
3	lnc-FLRT3-4	chr20:14816742-14816950	ucscGeneNc_uc002woy_1
4	lnc-FLRT3-4	chr20:14812896-14813240	ucscGeneNc_uc002woy_1

No data

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

Extended variants
information (count: 4629 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:4629 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2065558	chr20:14686297-14686298	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187062673	chr20:14686306-14686307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149819395	chr20:14686310-14686311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs112681791	chr20:14686317-14686318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113105512	chr20:14686327-14686328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs190371988	chr20:14686348-14686349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531202962	chr20:14686375-14686376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549752411	chr20:14686376-14686377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568020773	chr20:14686458-14686459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs111641717	chr20:14686465-14686466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs11908351	chr20:14686509-14686510	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs181227494	chr20:14686529-14686530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185272017	chr20:14686533-14686534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs557756703	chr20:14686538-14686539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372439602	chr20:14686562-14686563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113482602	chr20:14686599-14686600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569981652	chr20:14686615-14686616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78317375	chr20:14686645-14686646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146888618	chr20:14686670-14686671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6042872	chr20:14686687-14686688	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs112887325	chr20:14686729-14686730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553080363	chr20:14686732-14686733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs370133999	chr20:14686779-14686780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577803502	chr20:14686780-14686781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189889777	chr20:14686788-14686789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182785191	chr20:14686829-14686830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531242240	chr20:14686929-14686930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs6034013	chr20:14686952-14686953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373160861	chr20:14686956-14686957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543014685	chr20:14686959-14686960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547811731	chr20:14686960-14686961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113671034	chr20:14686986-14686987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs6034014	chr20:14687057-14687058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs75203186	chr20:14687059-14687060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547498180	chr20:14687138-14687139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs565820227	chr20:14687197-14687198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs374980574	chr20:14687217-14687218	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs533158223	chr20:14687248-14687249	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs551556594	chr20:14687298-14687299	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs569811558	chr20:14687306-14687307	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs537369349	chr20:14687307-14687308	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs12479561	chr20:14687309-14687310	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs76708341	chr20:14687315-14687316	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs6042873	chr20:14687324-14687325	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs117951242	chr20:14687341-14687342	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs577717000	chr20:14687343-14687344	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs374522916	chr20:14687371-14687372	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs545229056	chr20:14687436-14687437	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs557544680	chr20:14687452-14687453	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs188912836	chr20:14687512-14687513	Enhancers Weak transcription Flanking Active TSS	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:592 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14681600-14687200	Weak transcription	Liver	Liver
2	chr20:14681600-14698200	Weak transcription	Fetal Kidney	kidney
3	chr20:14682000-14688800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr20:14682000-14689800	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr20:14682200-14692200	Weak transcription	Fetal Heart	heart
6	chr20:14682200-14693000	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr20:14685000-14686400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr20:14685600-14688800	Weak transcription	NHEK	skin
9	chr20:14686000-14688600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr20:14686200-14694600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr20:14686400-14687400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr20:14687000-14687600	Enhancers	Placenta Amnion	Placenta Amnion
13	chr20:14687200-14688000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr20:14687200-14688000	Flanking Active TSS	Liver	Liver
15	chr20:14687200-14689000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr20:14687200-14692800	Weak transcription	Ovary	ovary
17	chr20:14687400-14688000	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr20:14687400-14689200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr20:14687600-14688600	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr20:14687600-14688800	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr20:14687600-14689200	Enhancers	Fetal Lung	lung
22	chr20:14687600-14692000	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr20:14687800-14688200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr20:14688000-14689200	Enhancers	Liver	Liver
25	chr20:14688000-14691400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr20:14688200-14689200	Enhancers	Stomach Mucosa	stomach
27	chr20:14688200-14690800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr20:14688200-14691200	Enhancers	Fetal Intestine Large	intestine
29	chr20:14688600-14688800	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr20:14688600-14689400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr20:14688600-14690200	Enhancers	Duodenum Mucosa	Duodenum
32	chr20:14688600-14690800	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr20:14688600-14691000	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr20:14688600-14693200	Enhancers	A549	lung
35	chr20:14688600-14693600	Enhancers	Fetal Intestine Small	intestine
36	chr20:14688800-14689200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr20:14688800-14689200	Enhancers	NHEK	skin
38	chr20:14688800-14691000	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr20:14688800-14691000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr20:14689000-14692400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr20:14689200-14691200	Weak transcription	NHEK	skin
42	chr20:14689200-14691400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr20:14689200-14691600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr20:14689200-14692200	Weak transcription	Fetal Lung	lung
45	chr20:14689200-14692400	Weak transcription	Stomach Mucosa	stomach
46	chr20:14689200-14692800	Weak transcription	Liver	Liver
47	chr20:14689400-14690600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr20:14689800-14691200	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr20:14690000-14690200	Enhancers	Small Intestine	intestine
50	chr20:14690200-14690800	Weak transcription	Duodenum Mucosa	Duodenum

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