Variant report

Variant	nsv432101
Chromosome Location	chr20:14294196-14353346
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:725)
CpG islands
(count:551)
Chromatin interactive
region (count:9)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:725 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:14318093-14318568	HepG2	liver:	n/a	n/a
2	ATF2	chr20:14318135-14318567	GM12878	blood:	n/a	n/a
3	ATF2	chr20:14318117-14318567	GM12878	blood:	n/a	n/a
4	ATF2	chr20:14318056-14318625	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr20:14318094-14318593	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr20:14317954-14318560	A549	lung:	n/a	chr20:14318315-14318328 chr20:14318314-14318329
7	BATF	chr20:14324408-14324687	GM12878	blood:	n/a	n/a
8	BCL3	chr20:14317682-14318646	A549	lung:	n/a	n/a
9	BCL3	chr20:14317905-14318638	A549	lung:	n/a	n/a
10	BHLHE40	chr20:14314339-14314730	GM12878	blood:	n/a	n/a
11	BHLHE40	chr20:14324311-14324686	GM12878	blood:	n/a	chr20:14324498-14324507 chr20:14324498-14324507
12	BRCA1	chr20:14318252-14318396	HepG2	liver:	n/a	n/a
13	CEBPB	chr20:14307467-14307737	HepG2	liver:	n/a	chr20:14307575-14307586
14	CEBPB	chr20:14309074-14309195	A549	lung:	n/a	chr20:14309135-14309148 chr20:14309137-14309146 chr20:14309135-14309146 chr20:14309136-14309147
15	CEBPB	chr20:14315804-14316095	A549	lung:	n/a	chr20:14315943-14315954 chr20:14315942-14315953
16	CEBPB	chr20:14339388-14339598	HepG2	liver:	n/a	n/a
17	CEBPB	chr20:14318156-14318511	HepG2	liver:	n/a	n/a
18	CEBPB	chr20:14318107-14318538	A549	lung:	n/a	n/a
19	CEBPB	chr20:14342555-14342693	A549	lung:	n/a	chr20:14342630-14342641 chr20:14342628-14342641
20	CEBPB	chr20:14307461-14307689	A549	lung:	n/a	chr20:14307575-14307586
21	CEBPB	chr20:14311674-14311759	HepG2	liver:	n/a	chr20:14311733-14311744
22	CEBPB	chr20:14344993-14345303	HepG2	liver:	n/a	chr20:14345160-14345171
23	CEBPB	chr20:14342464-14342775	Hela-S3	cervix:	n/a	chr20:14342630-14342641 chr20:14342628-14342641
24	CEBPB	chr20:14308968-14309277	HepG2	liver:	n/a	chr20:14309135-14309148 chr20:14309137-14309146 chr20:14309135-14309146 chr20:14309136-14309147
25	CEBPB	chr20:14318047-14318642	A549	lung:	n/a	n/a
26	CEBPB	chr20:14318101-14318519	IMR90	lung:	n/a	n/a
27	CEBPB	chr20:14318232-14318503	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr20:14318149-14318540	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr20:14318108-14318520	MCF-7	breast:	n/a	n/a
30	CEBPB	chr20:14315776-14316098	HepG2	liver:	n/a	chr20:14315943-14315954 chr20:14315942-14315953
31	CEBPB	chr20:14318217-14318476	HepG2	liver:	n/a	n/a
32	CHD1	chr20:14317715-14318658	IMR90	lung:	n/a	n/a
33	CHD2	chr20:14318116-14318417	HepG2	liver:	n/a	n/a
34	CHD2	chr20:14318204-14318568	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr20:14318059-14318479	A549	lung:	n/a	n/a
36	CREB1	chr20:14318054-14318574	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr20:14318031-14318530	HepG2	liver:	n/a	n/a
38	CREB1	chr20:14318076-14318565	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr20:14318143-14318510	A549	lung:	n/a	n/a
40	CTCF	chr20:14315060-14315210	GM12872	blood:	n/a	chr20:14315159-14315172 chr20:14315156-14315174
41	CTCF	chr20:14318320-14318470	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr20:14318079-14318730	HCT-116	colon:	n/a	n/a
43	CTCF	chr20:14318320-14318470	HAc	cerebellar:	n/a	n/a
44	CTCF	chr20:14318340-14318490	GM12868	blood:	n/a	n/a
45	CTCF	chr20:14318276-14318511	LNCaP	prostate:	n/a	n/a
46	CTCF	chr20:14315020-14315170	HVMF	connective:	n/a	n/a
47	CTCF	chr20:14318280-14318430	HEK293	kidney:	n/a	n/a
48	CTCF	chr20:14318279-14318519	MCF-7	breast:	n/a	n/a
49	CTCF	chr20:14315085-14315249	Spleen_OC	spleen:	n/a	chr20:14315159-14315172 chr20:14315156-14315174
50	CTCF	chr20:14318300-14318450	Hela-S3	cervix:	n/a	n/a

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:14318152-14318202	Hepatocyte	liver:	n/a
2	chr20:14318398-14318448	NB4	blood:	n/a
3	chr20:14318152-14318202	Hepatocyte	liver:	n/a
4	chr20:14318398-14318448	NB4	blood:	n/a
5	chr20:14318152-14318202	HUVEC	blood vessel:	n/a
6	chr20:14318410-14318460	Caco-2	colon:	n/a
7	chr20:14318297-14318347	AG09319	gingival:	n/a
8	chr20:14319035-14319085	SAEC	small airway:	n/a
9	chr20:14319125-14319175	A549	lung:	n/a
10	chr20:14319125-14319175	HRCEpiC	kidney:	n/a
11	chr20:14318174-14318224	GM06990	blood:	n/a
12	chr20:14318152-14318202	ECC-1	luminal epithelium:	n/a
13	chr20:14318410-14318460	HPAEpiC	pulmonary alveolar:	n/a
14	chr20:14318297-14318347	BE2_C	brain:	n/a
15	chr20:14318297-14318347	SK-N-MC	brain:	n/a
16	chr20:14307665-14307715	HPAEpiC	pulmonary alveolar:	n/a
17	chr20:14319035-14319085	ECC-1	luminal epithelium:	n/a
18	chr20:14319125-14319175	SAEC	small airway:	n/a
19	chr20:14318410-14318460	NH-A	brain:	n/a
20	chr20:14318152-14318202	K562	blood:	n/a
21	chr20:14318152-14318202	HCF	heart:	n/a
22	chr20:14319125-14319175	SK-N-MC	brain:	n/a
23	chr20:14318398-14318448	ovcar-3	ovarian:	n/a
24	chr20:14318231-14318281	LNCaP	prostate:	n/a
25	chr20:14318297-14318347	ovcar-3	ovarian:	n/a
26	chr20:14318231-14318281	SK-N-SH_RA	brain:	n/a
27	chr20:14319125-14319175	BJ	skin:	n/a
28	chr20:14318297-14318347	HCPEpiC	choroid plexus:	n/a
29	chr20:14318152-14318202	GM06990	blood:	n/a
30	chr20:14319125-14319175	HPAEpiC	pulmonary alveolar:	n/a
31	chr20:14318410-14318460	T-47D	breast:	n/a
32	chr20:14319035-14319085	AoSMC	blood vessel:	n/a
33	chr20:14307665-14307715	SK-N-SH	brain:	n/a
34	chr20:14318231-14318281	HCF	heart:	n/a
35	chr20:14318410-14318460	HCM	heart:	n/a
36	chr20:14307665-14307715	ovcar-3	ovarian:	n/a
37	chr20:14318152-14318202	HRPEpiC	eye:	n/a
38	chr20:14318152-14318202	NB4	blood:	n/a
39	chr20:14318152-14318202	T-47D	breast:	n/a
40	chr20:14318231-14318281	PANC-1	pancreas:	n/a
41	chr20:14319035-14319085	HAEpiC	amniotic membrane:	n/a
42	chr20:14318174-14318224	AG09309	skin:	n/a
43	chr20:14318152-14318202	HCM	heart:	n/a
44	chr20:14319125-14319175	PFSK-1	brain:	n/a
45	chr20:14318410-14318460	NHBE	bronchial:	n/a
46	chr20:14307665-14307715	AoSMC	blood vessel:	n/a
47	chr20:14318297-14318347	HEK293	kidney:	embryo
48	chr20:14307665-14307715	HRPEpiC	eye:	n/a
49	chr20:14318410-14318460	GM12878	blood:	n/a
50	chr20:14319125-14319175	AG09309	skin:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:14314454..14317198-chr20:14325361..14327046,2	K562	blood:
2	chr20:14305353..14307056-chr20:14308528..14310326,2	MCF-7	breast:
3	chr17:41399300..41401884-chr20:14313065..14316065,3	K562	blood:
4	chr20:14305353..14307056-chr20:14308528..14310326,2	MCF-7	breast:
5	chr20:14335576..14337791-chr20:15315333..15317078,2	MCF-7	breast:
6	chr20:14314384..14315320-chr20:14929469..14930347,2	MCF-7	breast:
7	chr17:41400138..41401846-chr20:14313045..14314565,2	K562	blood:
8	chr20:14314454..14317198-chr20:14325361..14327046,2	K562	blood:
9	chr20:14349761..14351392-chr20:14353398..14355373,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEL1L2-3	chr20:14309568-14309973	NONHSAT078712
2	lnc-SEL1L2-3	chr20:14318050-14318260	NONHSAT078712

No data

Variant related genes	Relation type
FLRT3	TF binding region
RNU6-228P	TF binding region
FLRT3	CpG island
RNU6-228P	CpG island

Extended variants
information (count: 1608 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1608 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6131568	chr20:14294196-14294197	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184048013	chr20:14294292-14294293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542053893	chr20:14294296-14294297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547878450	chr20:14294349-14294350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs1040825	chr20:14294401-14294402	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs188396031	chr20:14294453-14294454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs377039872	chr20:14294463-14294464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs73266939	chr20:14294576-14294577	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs116284027	chr20:14294583-14294584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73266940	chr20:14294604-14294605	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs559879804	chr20:14294664-14294665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528200398	chr20:14294665-14294666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs150026726	chr20:14294672-14294673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545109311	chr20:14294741-14294742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376193729	chr20:14294777-14294778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572223550	chr20:14294784-14294785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs540831494	chr20:14294812-14294813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560693717	chr20:14294940-14294941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574183194	chr20:14294955-14294956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564604173	chr20:14295022-14295023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543046401	chr20:14295072-14295073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373044387	chr20:14295129-14295130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs6079390	chr20:14295135-14295136	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs191679430	chr20:14295172-14295173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs552065528	chr20:14295203-14295204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565398390	chr20:14295235-14295236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527889508	chr20:14295244-14295245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs547672134	chr20:14295324-14295325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567802520	chr20:14295373-14295374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs74179737	chr20:14295378-14295379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113898203	chr20:14295402-14295403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570093363	chr20:14295406-14295407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112460293	chr20:14295407-14295408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570573781	chr20:14295439-14295440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576406975	chr20:14295593-14295594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182739663	chr20:14295628-14295629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6033941	chr20:14295645-14295646	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs538623750	chr20:14295659-14295660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558826049	chr20:14295668-14295669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs73612351	chr20:14295678-14295679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375556525	chr20:14295689-14295690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115518474	chr20:14295690-14295691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554325125	chr20:14295841-14295842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574218483	chr20:14295959-14295960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543134206	chr20:14295979-14295980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556604178	chr20:14295991-14295992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576781179	chr20:14296053-14296054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545435204	chr20:14296063-14296064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145412692	chr20:14296082-14296083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565618657	chr20:14296104-14296105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:737 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14289600-14306400	Weak transcription	Fetal Intestine Small	intestine
2	chr20:14292800-14294600	Enhancers	Fetal Heart	heart
3	chr20:14292800-14295000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr20:14292800-14303600	Weak transcription	Fetal Kidney	kidney
5	chr20:14293000-14294400	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr20:14293000-14306200	Weak transcription	Colon Smooth Muscle	Colon
7	chr20:14293600-14299400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr20:14294000-14294200	Enhancers	Rectal Smooth Muscle	rectum
9	chr20:14294200-14294600	Weak transcription	Rectal Smooth Muscle	rectum
10	chr20:14294200-14295000	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr20:14294400-14294800	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr20:14294400-14294800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr20:14294400-14295000	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr20:14294400-14295000	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr20:14294600-14294800	Enhancers	Rectal Smooth Muscle	rectum
16	chr20:14294800-14304600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr20:14294800-14306400	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr20:14294800-14314000	Weak transcription	Rectal Smooth Muscle	rectum
19	chr20:14295000-14305000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr20:14295000-14306000	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr20:14296000-14312000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr20:14298400-14299200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr20:14298800-14299000	Enhancers	Fetal Lung	lung
24	chr20:14299000-14306200	Weak transcription	Fetal Lung	lung
25	chr20:14299200-14306400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr20:14299400-14300000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr20:14300400-14300600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr20:14300600-14305400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr20:14300800-14303600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr20:14301800-14306400	Weak transcription	Fetal Intestine Large	intestine
31	chr20:14302200-14305200	Enhancers	NHEK	skin
32	chr20:14302400-14302600	Enhancers	HMEC	breast
33	chr20:14302400-14303800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr20:14302400-14304000	Weak transcription	Duodenum Mucosa	Duodenum
35	chr20:14302400-14304200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr20:14302600-14303600	Weak transcription	HMEC	breast
37	chr20:14303600-14304000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr20:14303600-14304400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr20:14303600-14306000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr20:14303600-14307000	Genic enhancers	HMEC	breast
41	chr20:14303600-14308200	Strong transcription	Fetal Kidney	kidney
42	chr20:14303600-14323400	Weak transcription	Small Intestine	intestine
43	chr20:14303800-14304000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr20:14303800-14305400	Weak transcription	Liver	Liver
45	chr20:14303800-14306400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr20:14304000-14304200	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr20:14304000-14304200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr20:14304000-14304200	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr20:14304000-14304200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr20:14304000-14304200	Enhancers	Esophagus	oesophagus

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