Variant report

Variant	esv2760244
Chromosome Location	chr11:18934834-18979993
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:133)
CpG islands
(count:550)
Chromatin interactive
region (count:2)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:133 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr11:18946494-18946596	HepG2	liver:	n/a	chr11:18946576-18946587
2	CEBPB	chr11:18943007-18943263	K562	blood:	n/a	n/a
3	CEBPB	chr11:18965116-18965409	K562	blood:	n/a	n/a
4	CEBPB	chr11:18970388-18970535	A549	lung:	n/a	n/a
5	CEBPB	chr11:18977944-18978151	A549	lung:	n/a	n/a
6	CEBPD	chr11:18942867-18943456	K562	blood:	n/a	n/a
7	CEBPD	chr11:18965149-18965591	K562	blood:	n/a	n/a
8	CTCF	chr11:18949082-18949341	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr11:18949160-18949310	NHEK	skin:	n/a	n/a
10	CTCF	chr11:18949060-18949210	RPTEC	kidney:	n/a	n/a
11	CTCF	chr11:18949140-18949290	HPAF	blood vessel:	n/a	n/a
12	CTCF	chr11:18973940-18974063	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr11:18944630-18944650	GM20000	blood:	n/a	n/a
14	CTCF	chr11:18944088-18944127	GM20000	blood:	n/a	n/a
15	CTCF	chr11:18949220-18949370	HMEC	breast:	n/a	n/a
16	CTCF	chr11:18964083-18964146	GM10248	blood:	n/a	n/a
17	CTCF	chr11:18949130-18949280	K562	blood:	n/a	n/a
18	CTCF	chr11:18952280-18952430	HMF	breast:	n/a	n/a
19	CTCF	chr11:18973975-18974019	LNCaP	prostate:	n/a	n/a
20	CTCF	chr11:18951819-18951855	Fibrobl	skin:	n/a	n/a
21	CTCF	chr11:18943965-18943999	LNCaP	prostate:	n/a	n/a
22	CTCF	chr11:18949100-18949250	RPTEC	kidney:	n/a	n/a
23	CTCF	chr11:18949060-18949210	NHEK	skin:	n/a	n/a
24	CTCF	chr11:18949226-18949297	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr11:18949160-18949310	HMEC	breast:	n/a	n/a
26	CTCF	chr11:18949200-18949350	HEEpiC	esophagus:	n/a	n/a
27	E2F4	chr11:18957940-18958060	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr11:18940787-18941074	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr11:18949193-18949402	MCF10A-Er-Src	breast:	n/a	n/a
30	EBF1	chr11:18941539-18941924	GM12878	blood:	n/a	chr11:18941708-18941719
31	EBF1	chr11:18941597-18941799	GM12878	blood:	n/a	chr11:18941708-18941719
32	EBF1	chr11:18941547-18941798	GM12878	blood:	n/a	chr11:18941708-18941719
33	EGR1	chr11:18978084-18978269	K562	blood:	n/a	chr11:18978156-18978165 chr11:18978153-18978166 chr11:18978153-18978166 chr11:18978156-18978166 chr11:18978153-18978166
34	EGR1	chr11:18961852-18962016	K562	blood:	n/a	n/a
35	EGR1	chr11:18978030-18978291	K562	blood:	n/a	chr11:18978156-18978165 chr11:18978153-18978166 chr11:18978153-18978166 chr11:18978156-18978166 chr11:18978153-18978166
36	EP300	chr11:18949205-18949321	K562	blood:	n/a	n/a
37	FOS	chr11:18949209-18949453	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr11:18974664-18974881	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr11:18974580-18974780	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr11:18974670-18974809	MCF10A-Er-Src	breast:	n/a	n/a
41	GATA2	chr11:18943647-18943785	SH-SY5Y	brain:	n/a	n/a
42	GATA2	chr11:18965011-18965552	K562	blood:	n/a	n/a
43	GATA2	chr11:18942864-18943405	K562	blood:	n/a	n/a
44	GATA3	chr11:18935296-18935542	SH-SY5Y	brain:	n/a	n/a
45	GATA3	chr11:18954250-18955270	SH-SY5Y	brain:	n/a	chr11:18954446-18954455
46	IRF1	chr11:18944314-18944316	K562	blood:	n/a	n/a
47	IRF1	chr11:18963394-18963454	K562	blood:	n/a	n/a
48	JUN	chr11:18949699-18949890	K562	blood:	n/a	n/a
49	JUND	chr11:18957931-18958074	H1-hESC	embryonic stem cell:	n/a	n/a
50	JUND	chr11:18951523-18951631	HepG2	liver:	n/a	chr11:18951599-18951608

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:18955977-18956027	HIPEpiC	eye:	n/a
2	chr11:18955977-18956027	HIPEpiC	eye:	n/a
3	chr11:18956283-18956333	NT2-D1	testis:	n/a
4	chr11:18956196-18956246	H1-hESC	embryonic stem cell:	embryo
5	chr11:18956283-18956333	ovcar-3	ovarian:	n/a
6	chr11:18978391-18978441	NHBE	bronchial:	n/a
7	chr11:18956196-18956246	ECC-1	luminal epithelium:	n/a
8	chr11:18956283-18956333	AG09319	gingival:	n/a
9	chr11:18956196-18956246	HL-60	blood:	n/a
10	chr11:18956637-18956687	HUVEC	blood vessel:	n/a
11	chr11:18956283-18956333	SAEC	small airway:	n/a
12	chr11:18978157-18978207	GM12878	blood:	n/a
13	chr11:18978157-18978207	HRPEpiC	eye:	n/a
14	chr11:18956196-18956246	AoSMC	blood vessel:	n/a
15	chr11:18956196-18956246	HCPEpiC	choroid plexus:	n/a
16	chr11:18956196-18956246	AG09319	gingival:	n/a
17	chr11:18955977-18956027	HPAEpiC	pulmonary alveolar:	n/a
18	chr11:18957755-18957805	HNPCEpiC	eye:	n/a
19	chr11:18978391-18978441	A549	lung:	n/a
20	chr11:18955977-18956027	AG09319	gingival:	n/a
21	chr11:18957755-18957805	HCF	heart:	n/a
22	chr11:18957755-18957805	LNCaP	prostate:	n/a
23	chr11:18957755-18957805	HepG2	liver:	n/a
24	chr11:18956196-18956246	PANC-1	pancreas:	n/a
25	chr11:18978157-18978207	PFSK-1	brain:	n/a
26	chr11:18978169-18978219	AoSMC	blood vessel:	n/a
27	chr11:18978218-18978268	HEK293	kidney:	embryo
28	chr11:18978169-18978219	MCF-7	breast:	n/a
29	chr11:18978157-18978207	Caco-2	colon:	n/a
30	chr11:18956196-18956246	HRPEpiC	eye:	n/a
31	chr11:18956637-18956687	NHDF-neo	bronchial:	n/a
32	chr11:18978218-18978268	GM12891	blood:	n/a
33	chr11:18955977-18956027	HNPCEpiC	eye:	n/a
34	chr11:18956196-18956246	HAEpiC	amniotic membrane:	n/a
35	chr11:18956196-18956246	GM12878	blood:	n/a
36	chr11:18957755-18957805	RPTEC	kidney:	n/a
37	chr11:18978157-18978207	SKMC	muscle:	n/a
38	chr11:18978157-18978207	HCM	heart:	n/a
39	chr11:18955977-18956027	MCF10A-Er-Src	breast:	n/a
40	chr11:18978391-18978441	T-47D	breast:	n/a
41	chr11:18956196-18956246	SK-N-MC	brain:	n/a
42	chr11:18956196-18956246	AG04449	skin:	fetal
43	chr11:18956283-18956333	AG04450	lung:	fetal
44	chr11:18978391-18978441	SAEC	small airway:	n/a
45	chr11:18956637-18956687	GM12891	blood:	n/a
46	chr11:18956283-18956333	HAEpiC	amniotic membrane:	n/a
47	chr11:18956283-18956333	HMEC	breast:	n/a
48	chr11:18956196-18956246	CMK	blood:	n/a
49	chr11:18956196-18956246	HepG2	liver:	n/a
50	chr11:18956196-18956246	Caco-2	colon:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:18951880..18953861-chr11:18956190..18958282,2	K562	blood:
2	chr11:18948757..18949726-chr11:19092570..19093333,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZDHHC13-2	chr11:18956532-18956821	ENSG00000255244.1
2	lnc-ZDHHC13-2	chr11:18960852-18961268	ENSG00000255244.1

No data

Variant related genes	Relation type
ENSG00000255536	TF binding region
MRGPRX1	TF binding region
ENSG00000254738	TF binding region
ENSG00000255244	TF binding region
ENSG00000255536	CpG island
MRGPRX1	CpG island
ENSG00000254738	CpG island
ENSG00000255244	CpG island
ENSG00000170255	chromatin interactions
ENSG00000255244	chromatin interactions

Extended variants
information (count: 891 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:891 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557065571	chr11:18934843-18934844	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs1825287	chr11:18934875-18934876	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs549377854	chr11:18935357-18935358	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs144751233	chr11:18935362-18935363	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs186897085	chr11:18935364-18935365	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs567956594	chr11:18935380-18935381	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs576152414	chr11:18935453-18935454	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs190165146	chr11:18935454-18935455	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs533874568	chr11:18935470-18935471	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs182741801	chr11:18935490-18935491	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs150642684	chr11:18935507-18935508	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs78728960	chr11:18935568-18935569	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs556183379	chr11:18935582-18935583	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs532707225	chr11:18935942-18935943	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs139817744	chr11:18935995-18935996	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs78745071	chr11:18936008-18936009	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs530182615	chr11:18936011-18936012	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs548168152	chr11:18936040-18936041	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs114074277	chr11:18936068-18936069	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs529633811	chr11:18936080-18936081	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs533953501	chr11:18936090-18936091	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs201326736	chr11:18936091-18936092	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs188391848	chr11:18936140-18936141	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs74330745	chr11:18936141-18936142	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs193201311	chr11:18936151-18936152	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs200747443	chr11:18936193-18936194	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs183834249	chr11:18936216-18936217	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs553145735	chr11:18936243-18936244	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs12270393	chr11:18936254-18936255	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs114916866	chr11:18936266-18936267	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs533835939	chr11:18936286-18936287	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs35500452	chr11:18936299-18936300	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs189197117	chr11:18936305-18936306	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs114496944	chr11:18936693-18936694	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs574364085	chr11:18936700-18936701	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs535402266	chr11:18936706-18936707	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs559579314	chr11:18936724-18936725	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs113584306	chr11:18936739-18936740	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs191822545	chr11:18936743-18936744	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs544613100	chr11:18936767-18936768	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs533196425	chr11:18936791-18936792	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs373679828	chr11:18936807-18936808	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs556696993	chr11:18936817-18936818	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs116675754	chr11:18936838-18936839	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs542027105	chr11:18936922-18936923	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs563819171	chr11:18936932-18936933	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs560166148	chr11:18936952-18936953	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs147464151	chr11:18936965-18936966	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs545780681	chr11:18936970-18936971	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs377292778	chr11:18936997-18936998	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18946600-18947000	Enhancers	NHEK	skin
2	chr11:18947000-18949000	Weak transcription	NHEK	skin
3	chr11:18949000-18949800	Enhancers	NHEK	skin
4	chr11:18951200-18951400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr11:18951600-18952800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr11:18952800-18953400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr11:18953400-18955200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr11:18954600-18955400	Enhancers	Placenta Amnion	Placenta Amnion
9	chr11:18955200-18955600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr11:18955600-18956400	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr11:18955600-18956800	Enhancers	Spleen	Spleen
12	chr11:18955800-18956000	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr11:18955800-18956400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr11:18955800-18956600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
15	chr11:18956200-18956400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr11:18956400-18957800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr11:18956400-18958000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr11:18957200-18959400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr11:18957400-18958400	Enhancers	H1 Cell Line	embryonic stem cell
20	chr11:18957400-18958400	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr11:18957400-18958600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr11:18957400-18958600	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr11:18957400-18959200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr11:18957400-18959200	Enhancers	NHEK	skin
25	chr11:18957600-18958200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr11:18957600-18958200	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr11:18957600-18958200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr11:18957600-18958400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr11:18957600-18958400	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr11:18957600-18958400	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr11:18957800-18958200	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr11:18957800-18958800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr11:18958000-18958200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr11:18958600-18959400	Bivalent Enhancer	HMEC	breast
35	chr11:18974400-18974800	Enhancers	NHEK	skin
36	chr11:18974600-18975000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr11:18974600-18975000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr11:18974800-18979400	Weak transcription	NHEK	skin
39	chr11:18975000-18979600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr11:18978600-18979000	Enhancers	H9 Cell Line	embryonic stem cell
41	chr11:18979000-18979400	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr11:18979400-18979600	Enhancers	H9 Cell Line	embryonic stem cell
43	chr11:18979400-18980000	Enhancers	NHEK	skin
44	chr11:18979400-18980800	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr11:18979400-18981000	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr11:18979400-18981000	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr11:18979400-18981200	Enhancers	HMEC	breast
48	chr11:18979400-18981400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr11:18979600-18980800	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr11:18979600-18981200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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