Variant report

Variant	nsv585458
Chromosome Location	chr20:14681863-14890211
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1480)
CpG islands
(count:0)
Chromatin interactive
region (count:49)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1480 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

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	chr20:14811032-14811585	GM12878	blood:	n/a	n/a
4	ATF2	chr20:14841040-14841554	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr20:14819159-14819726	GM12878	blood:	n/a	n/a
6	ATF2	chr20:14725297-14725726	GM12878	blood:	n/a	n/a
7	ATF2	chr20:14883084-14883368	GM12878	blood:	n/a	n/a
8	ATF2	chr20:14810438-14810958	GM12878	blood:	n/a	n/a
9	ATF2	chr20:14811110-14811561	GM12878	blood:	n/a	n/a
10	ATF2	chr20:14813151-14813770	GM12878	blood:	n/a	n/a
11	ATF2	chr20:14813148-14813759	GM12878	blood:	n/a	n/a
12	ATF2	chr20:14841032-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr20:14819109-14819739	GM12878	blood:	n/a	n/a
14	ATF2	chr20:14810438-14811025	GM12878	blood:	n/a	n/a
15	ATF3	chr20:14826094-14826569	A549	lung:	n/a	n/a
16	ATF3	chr20:14692815-14693406	A549	lung:	n/a	n/a
17	ATF3	chr20:14859536-14860398	A549	lung:	n/a	n/a
18	ATF3	chr20:14859595-14860443	A549	lung:	n/a	n/a
19	BACH1	chr20:14841074-14841466	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr20:14702858-14702913	K562	blood:	n/a	n/a
21	BATF	chr20:14883118-14883412	GM12878	blood:	n/a	n/a
22	BATF	chr20:14813339-14813704	GM12878	blood:	n/a	n/a
23	BATF	chr20:14819247-14819774	GM12878	blood:	n/a	chr20:14819441-14819452
24	BATF	chr20:14860106-14860399	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
25	BATF	chr20:14811171-14811517	GM12878	blood:	n/a	n/a
26	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
27	BATF	chr20:14826296-14826501	GM12878	blood:	n/a	chr20:14826450-14826460
28	BATF	chr20:14810566-14810958	GM12878	blood:	n/a	n/a
29	BATF	chr20:14813314-14813717	GM12878	blood:	n/a	n/a
30	BATF	chr20:14725428-14725715	GM12878	blood:	n/a	n/a
31	BATF	chr20:14811158-14811471	GM12878	blood:	n/a	n/a
32	BATF	chr20:14833838-14834046	GM12878	blood:	n/a	n/a
33	BATF	chr20:14704765-14705024	GM12878	blood:	n/a	n/a
34	BATF	chr20:14883072-14883470	GM12878	blood:	n/a	n/a
35	BATF	chr20:14810508-14810959	GM12878	blood:	n/a	n/a
36	BATF	chr20:14860056-14860418	GM12878	blood:	n/a	chr20:14860263-14860273 chr20:14860262-14860273 chr20:14860267-14860277
37	BATF	chr20:14725407-14725742	GM12878	blood:	n/a	n/a
38	BATF	chr20:14819170-14819805	GM12878	blood:	n/a	chr20:14819441-14819452
39	BATF	chr20:14704304-14704567	GM12878	blood:	n/a	n/a
40	BCL11A	chr20:14859536-14859807	GM12878	blood:	n/a	n/a
41	BCL11A	chr20:14841111-14841474	H1-hESC	embryonic stem cell:	n/a	n/a
42	BCL11A	chr20:14813268-14813779	GM12878	blood:	n/a	n/a
43	BCL11A	chr20:14883096-14883392	GM12878	blood:	n/a	chr20:14883229-14883238
44	BCL11A	chr20:14833756-14834084	GM12878	blood:	n/a	n/a
45	BCL11A	chr20:14811187-14811493	GM12878	blood:	n/a	n/a
46	BCL11A	chr20:14819190-14819731	GM12878	blood:	n/a	chr20:14819415-14819424
47	BCL11A	chr20:14810529-14810966	GM12878	blood:	n/a	chr20:14810705-14810714
48	BCL11A	chr20:14813340-14813684	GM12878	blood:	n/a	n/a
49	BCL11A	chr20:14819269-14819704	GM12878	blood:	n/a	chr20:14819415-14819424
50	BCL11A	chr20:14810584-14810953	GM12878	blood:	n/a	chr20:14810705-14810714

No data

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
2	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
3	chr20:14688944..14691499-chr20:14692203..14695103,3	MCF-7	breast:
4	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
5	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
6	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
7	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
8	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
9	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
10	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
11	chr20:14857662..14859546-chr20:15214980..15217486,2	MCF-7	breast:
12	chr20:14861831..14864729-chr20:14900336..14902240,2	MCF-7	breast:
13	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
14	chr20:14856302..14859235-chr20:14930877..14933226,2	MCF-7	breast:
15	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
16	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
17	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
18	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
19	chr20:14819830..14820468-chr4:11534089..11534643,2	MCF-7	breast:
20	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:
21	chr20:14862084..14865220-chr20:14867174..14871364,3	MCF-7	breast:
22	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
23	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
24	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
25	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
26	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
27	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
28	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
29	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:
30	chr20:14822570..14824766-chr20:14826157..14827975,2	MCF-7	breast:
31	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
32	chr20:14845184..14847390-chr20:14926741..14929314,2	MCF-7	breast:
33	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
34	chr20:14824570..14828041-chr20:14829297..14833669,5	MCF-7	breast:
35	chr20:14867933..14870632-chr20:14873919..14875816,2	MCF-7	breast:
36	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
37	chr20:14837652..14840600-chr20:14844675..14847639,2	MCF-7	breast:
38	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
39	chr20:14859239..14863091-chr20:15040405..15044044,4	MCF-7	breast:
40	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
41	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
42	chr20:14825814..14826804-chr20:14859521..14860363,2	MCF-7	breast:
43	chr20:14819967..14822472-chr20:14824610..14827210,3	MCF-7	breast:
44	chr20:14688944..14691499-chr20:14692203..14695103,3	MCF-7	breast:
45	chr20:14606804..14608358-chr20:14690132..14692728,2	MCF-7	breast:
46	chr20:14835355..14837300-chr20:14840386..14842306,2	MCF-7	breast:
47	chr20:14838738..14840500-chr20:14846618..14848612,2	MCF-7	breast:
48	chr20:14803482..14806391-chr20:14809700..14811931,2	MCF-7	breast:
49	chr20:14838738..14840500-chr20:14846618..14848612,2	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-C20orf7-3	chr20:14830550-14831152	NONHSAT078716
3	lnc-FLRT3-1	chr20:14864899-14865240	NR_110318
4	lnc-FLRT3-1	chr20:14868742-14868950	ENSG00000235914.1
5	lnc-FLRT3-1	chr20:14864896-14865240	NONHSAT078721
6	lnc-FLRT3-4	chr20:14816742-14816950	ucscGeneNc_uc002woy_1
7	lnc-FLRT3-1	chr20:14885587-14886675	ENSG00000235914.1
8	lnc-FLRT3-4	chr20:14858021-14858161	ucscGeneNc_uc002woy_1
9	lnc-FLRT3-1	chr20:14864898-14865240	NONHSAT078722
10	lnc-FLRT3-1	chr20:14885587-14886675	NR_072988
11	lnc-FLRT3-1	chr20:14868742-14868950	NONHSAT078721
12	lnc-FLRT3-4	chr20:14812896-14813240	ucscGeneNc_uc002woy_1
13	lnc-C20orf7-3	chr20:14868789-14869314	NONHSAT078714
14	lnc-C20orf7-3	chr20:14830550-14830649	NONHSAT078714
15	lnc-FLRT3-1	chr20:14864899-14865240	ENSG00000235914.1
16	lnc-FLRT3-1	chr20:14864899-14865240	NR_037841

No data

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

Extended variants
information (count: 5658 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:5658 , 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	rs1932951	chr20:14681863-14681864	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs6042864	chr20:14681876-14681877	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs1932950	chr20:14681958-14681959	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs185224127	chr20:14681962-14681963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188168453	chr20:14681976-14681977	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs386812718	chr20:14682006-14682007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs6042865	chr20:14682008-14682009	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs60857979	chr20:14682066-14682067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554838921	chr20:14682071-14682072	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs35975910	chr20:14682086-14682087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573364963	chr20:14682135-14682136	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181953824	chr20:14682199-14682200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139502955	chr20:14682206-14682207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs76473367	chr20:14682212-14682213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577662271	chr20:14682224-14682225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544976477	chr20:14682256-14682257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs145003008	chr20:14682264-14682265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575217701	chr20:14682280-14682281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147597004	chr20:14682297-14682298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs113790840	chr20:14682333-14682334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs6135228	chr20:14682334-14682335	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs187204119	chr20:14682356-14682357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs142027880	chr20:14682368-14682369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs73612374	chr20:14682388-14682389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532282208	chr20:14682429-14682430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs145295367	chr20:14682430-14682431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569257495	chr20:14682448-14682449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs75086073	chr20:14682462-14682463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191775438	chr20:14682513-14682514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs548647991	chr20:14682551-14682552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs6042866	chr20:14682568-14682569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566893095	chr20:14682569-14682570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs6042867	chr20:14682638-14682639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs73899256	chr20:14682667-14682668	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs559200648	chr20:14682689-14682690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs149220610	chr20:14682693-14682694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs183628523	chr20:14682701-14682702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186502117	chr20:14682718-14682719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs143415370	chr20:14682719-14682720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs200983148	chr20:14682802-14682803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556604806	chr20:14682837-14682838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs6042868	chr20:14682863-14682864	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs76890915	chr20:14682871-14682872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561032833	chr20:14682888-14682889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6135229	chr20:14683029-14683030	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs539998522	chr20:14683031-14683032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs6135230	chr20:14683037-14683038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs191346451	chr20:14683079-14683080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs77754110	chr20:14683108-14683109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182438062	chr20:14683187-14683188	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:763 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14678000-14682000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr20:14678800-14682000	Weak transcription	Colon Smooth Muscle	Colon
3	chr20:14679600-14682800	Enhancers	Fetal Intestine Small	intestine
4	chr20:14680800-14682000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr20:14680800-14682000	Enhancers	NHDF-Ad	bronchial
6	chr20:14680800-14682200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr20:14681200-14682000	Enhancers	Stomach Mucosa	stomach
8	chr20:14681200-14682200	Enhancers	Fetal Heart	heart
9	chr20:14681400-14682200	Enhancers	Fetal Intestine Large	intestine
10	chr20:14681600-14682200	Enhancers	Fetal Brain Female	brain
11	chr20:14681600-14682200	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr20:14681600-14682200	Enhancers	Sigmoid Colon	Sigmoid Colon
13	chr20:14681600-14682400	Enhancers	Small Intestine	intestine
14	chr20:14681600-14687200	Weak transcription	Liver	Liver
15	chr20:14681600-14698200	Weak transcription	Fetal Kidney	kidney
16	chr20:14681800-14682000	Enhancers	Rectal Mucosa Donor 29	rectum
17	chr20:14681800-14685200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr20:14681800-14685200	Weak transcription	NHEK	skin
19	chr20:14682000-14682200	Enhancers	Colon Smooth Muscle	Colon
20	chr20:14682000-14688800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr20:14682000-14689800	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr20:14682200-14684000	Weak transcription	Colon Smooth Muscle	Colon
23	chr20:14682200-14692200	Weak transcription	Fetal Heart	heart
24	chr20:14682200-14693000	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr20:14684000-14684200	Enhancers	Colon Smooth Muscle	Colon
26	chr20:14685000-14686400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr20:14685200-14685600	Enhancers	NHEK	skin
28	chr20:14685200-14686000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr20:14685600-14688800	Weak transcription	NHEK	skin
30	chr20:14686000-14688600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr20:14686200-14694600	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr20:14686400-14687400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr20:14687000-14687600	Enhancers	Placenta Amnion	Placenta Amnion
34	chr20:14687200-14688000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr20:14687200-14688000	Flanking Active TSS	Liver	Liver
36	chr20:14687200-14689000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr20:14687200-14692800	Weak transcription	Ovary	ovary
38	chr20:14687400-14688000	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr20:14687400-14689200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr20:14687600-14688600	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr20:14687600-14688800	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr20:14687600-14689200	Enhancers	Fetal Lung	lung
43	chr20:14687600-14692000	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr20:14687800-14688200	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr20:14688000-14689200	Enhancers	Liver	Liver
46	chr20:14688000-14691400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr20:14688200-14689200	Enhancers	Stomach Mucosa	stomach
48	chr20:14688200-14690800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr20:14688200-14691200	Enhancers	Fetal Intestine Large	intestine
50	chr20:14688600-14688800	Enhancers	HUES48 Cell Line	embryonic stem cell

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