Variant report

Variant	esv3324470
Chromosome Location	chr18:10468-63727
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:505)
CpG islands
(count:610)
Chromatin interactive
region (count:1)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:505 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr18:32504-32766	GM12878	blood:	n/a	n/a
2	BATF	chr18:10049-10662	GM12878	blood:	n/a	n/a
3	BCL11A	chr18:9938-10711	GM12878	blood:	n/a	n/a
4	BCL11A	chr18:10392-10708	GM12878	blood:	n/a	n/a
5	BHLHE40	chr18:10070-10620	HepG2	liver:	n/a	n/a
6	BRCA1	chr18:63571-63771	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr18:10421-10633	H1-hESC	embryonic stem cell:	n/a	n/a
8	CBX3	chr18:9926-10815	K562	blood:	n/a	n/a
9	CBX3	chr18:63505-63953	K562	blood:	n/a	n/a
10	CBX3	chr18:9952-10758	K562	blood:	n/a	n/a
11	CEBPB	chr18:9854-10855	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr18:11762-11832	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr18:63521-64111	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr18:9933-10821	GM12878	blood:	n/a	n/a
15	CEBPD	chr18:26760-27181	K562	blood:	n/a	n/a
16	CEBPD	chr18:9958-10726	K562	blood:	n/a	n/a
17	CHD2	chr18:11844-11875	HepG2	liver:	n/a	n/a
18	CREB1	chr18:11591-11950	A549	lung:	n/a	n/a
19	CTCF	chr18:11740-11890	WERI-Rb-1	eye:	n/a	chr18:11812-11821
20	CTCF	chr18:11763-11866	Hela-S3	cervix:	n/a	chr18:11812-11821
21	CTCF	chr18:11700-11850	HRE	kidney:	n/a	chr18:11812-11821
22	CTCF	chr18:11700-11850	BE2_C	brain:	n/a	chr18:11812-11821
23	CTCF	chr18:11720-11870	HRPEpiC	eye:	n/a	chr18:11812-11821
24	CTCF	chr18:11762-11881	IMR90	lung:	n/a	chr18:11812-11821
25	CTCF	chr18:11740-11890	HUVEC	blood vessel:	n/a	chr18:11812-11821
26	CTCF	chr18:11760-11910	GM12874	blood:	n/a	chr18:11812-11821
27	CTCF	chr18:11676-11951	A549	lung:	n/a	chr18:11812-11821
28	CTCF	chr18:11640-11790	HCFaa	heart:	n/a	n/a
29	CTCF	chr18:11761-11865	GM19238	blood:	n/a	chr18:11812-11821
30	CTCF	chr18:11562-11996	HepG2	liver:	n/a	chr18:11812-11821
31	CTCF	chr18:11536-12088	MCF-7	breast:	n/a	chr18:11812-11821
32	CTCF	chr18:48460-48610	WERI-Rb-1	eye:	n/a	chr18:48556-48574 chr18:48559-48567
33	CTCF	chr18:11713-11928	MCF-7	breast:	n/a	chr18:11812-11821
34	CTCF	chr18:48460-48610	Caco-2	colon:	n/a	chr18:48556-48574 chr18:48559-48567
35	CTCF	chr18:11800-11950	GM12867	blood:	n/a	chr18:11812-11821
36	CTCF	chr18:11748-11897	MCF-7	breast:	n/a	chr18:11812-11821
37	CTCF	chr18:11660-11810	HVMF	connective:	n/a	n/a
38	CTCF	chr18:14484-14506	GM13976	blood:	n/a	n/a
39	CTCF	chr18:11740-11890	HepG2	liver:	n/a	chr18:11812-11821
40	CTCF	chr18:63110-63165	GM10266	blood:	n/a	n/a
41	CTCF	chr18:27998-28025	A549	lung:	n/a	n/a
42	CTCF	chr18:11712-11900	LNCaP	prostate:	n/a	chr18:11812-11821
43	CTCF	chr18:11620-11770	GM12868	blood:	n/a	n/a
44	CTCF	chr18:11704-11931	Gliobla	brain:	n/a	chr18:11812-11821
45	CTCF	chr18:11640-11790	GM12866	blood:	n/a	n/a
46	CTCF	chr18:11720-11870	SK-N-SH_RA	brain:	n/a	chr18:11812-11821
47	CTCF	chr18:11603-12015	A549	lung:	n/a	chr18:11812-11821
48	CTCF	chr18:11680-11830	HMEC	breast:	n/a	chr18:11812-11821
49	CTCF	chr18:11740-11890	HEK293	kidney:	n/a	chr18:11812-11821
50	CTCF	chr18:13949-13973	GM13977	blood:	n/a	chr18:13953-13961

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:48912-48962	HCF	heart:	n/a
2	chr18:11231-11281	AG09319	gingival:	n/a
3	chr18:12371-12421	AG09309	skin:	n/a
4	chr18:49313-49363	ProgFib	skin:	n/a
5	chr18:11855-11905	HIPEpiC	eye:	n/a
6	chr18:48912-48962	AG04449	skin:	fetal
7	chr18:12371-12421	RPTEC	kidney:	n/a
8	chr18:11855-11905	NHBE	bronchial:	n/a
9	chr18:11948-11998	CMK	blood:	n/a
10	chr18:48912-48962	LNCaP	prostate:	n/a
11	chr18:11724-11774	U87	brain:	n/a
12	chr18:48912-48962	NH-A	brain:	n/a
13	chr18:49431-49481	AG09319	gingival:	n/a
14	chr18:49898-49948	ovcar-3	ovarian:	n/a
15	chr18:11724-11774	AoSMC	blood vessel:	n/a
16	chr18:11948-11998	K562	blood:	n/a
17	chr18:12437-12487	HCPEpiC	choroid plexus:	n/a
18	chr18:11231-11281	HMEC	breast:	n/a
19	chr18:49313-49363	NHBE	bronchial:	n/a
20	chr18:11948-11998	PrEC	prostate:	n/a
21	chr18:11231-11281	Hepatocyte	liver:	n/a
22	chr18:11724-11774	IMR90	lung:	fetal
23	chr18:49898-49948	GM19239	blood:	n/a
24	chr18:12371-12421	HEK293	kidney:	embryo
25	chr18:11855-11905	LNCaP	prostate:	n/a
26	chr18:12371-12421	PANC-1	pancreas:	n/a
27	chr18:49898-49948	IMR90	lung:	fetal
28	chr18:49898-49948	AG04449	skin:	fetal
29	chr18:11231-11281	NHDF-neo	bronchial:	n/a
30	chr18:11948-11998	HEK293	kidney:	embryo
31	chr18:12371-12421	AG04449	skin:	fetal
32	chr18:11855-11905	IMR90	lung:	fetal
33	chr18:48912-48962	ProgFib	skin:	n/a
34	chr18:11231-11281	PrEC	prostate:	n/a
35	chr18:11231-11281	HCPEpiC	choroid plexus:	n/a
36	chr18:11724-11774	AG04449	skin:	fetal
37	chr18:49898-49948	U87	brain:	n/a
38	chr18:48912-48962	U87	brain:	n/a
39	chr18:12437-12487	NB4	blood:	n/a
40	chr18:49898-49948	AG10803	skin:	n/a
41	chr18:11724-11774	HL-60	blood:	n/a
42	chr18:12437-12487	HepG2	liver:	n/a
43	chr18:11948-11998	MCF10A-Er-Src	breast:	n/a
44	chr18:12371-12421	HCF	heart:	n/a
45	chr18:49313-49363	HAEpiC	amniotic membrane:	n/a
46	chr18:12437-12487	HRCEpiC	kidney:	n/a
47	chr18:49431-49481	MCF-7	breast:	n/a
48	chr18:12371-12421	IMR90	lung:	fetal
49	chr18:11231-11281	NH-A	brain:	n/a
50	chr18:49898-49948	HCPEpiC	choroid plexus:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:227727685..227728349-chr18:13120..13866,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-683L23.1.1-1	chr18:49815-49866	ENSG00000262735.1
2	lnc-RP11-683L23.1.1-2	chr18:14294-14653	XLOC_012737
3	lnc-USP14-7	chr18:45283-45556	NONHSAT056821
4	lnc-RP11-683L23.1.1-2	chr18:14195-14653	ENSG00000263305.1
5	lnc-RP11-683L23.1.1-2	chr18:14851-14958	ENSG00000263305.1
6	lnc-RP11-683L23.1.1-1	chr18:49900-50225	ENSG00000262735.1
7	lnc-RP11-683L23.1.1-1	chr18:50421-50549	ENSG00000262735.1
8	lnc-RP11-683L23.1.1-2	chr18:14490-14653	ENSG00000263305.1
9	lnc-RP11-683L23.1.1-2	chr18:16856-16898	ENSG00000263305.1
10	lnc-RP11-683L23.1.1-2	chr18:14851-14870	XLOC_012737
11	lnc-USP14-7	chr18:45004-45235	NONHSAT056821

No data

Variant related genes	Relation type
ENSG00000263305	TF binding region
ENSG00000262352	TF binding region
ENSG00000262181	TF binding region
ENSG00000173213	TF binding region
ENSG00000263305	CpG island
ENSG00000262352	CpG island
ENSG00000262181	CpG island
ENSG00000173213	CpG island

Extended variants
information (count: 833 )
Associated
traits (count: 48 )

Variant overlapped rSNPs/rCNVs (count:833 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79729121	chr18:10547-10548	Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs377653140	chr18:10553-10554	Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs77475273	chr18:10560-10561	Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs79945507	chr18:10572-10573	Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs112381076	chr18:10578-10579	Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs140986726	chr18:10583-10584	Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs76479671	chr18:10591-10592	Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs75810027	chr18:10597-10598	Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs80279483	chr18:10603-10604	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs79077261	chr18:10607-10608	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs200624083	chr18:10619-10620	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs546739184	chr18:10620-10621	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs111484915	chr18:10621-10622	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs112021627	chr18:10626-10627	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs371774634	chr18:10630-10631	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs115926245	chr18:10644-10645	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs569340738	chr18:10648-10649	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs536390251	chr18:10652-10653	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs112067749	chr18:10654-10655	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs72854246	chr18:10659-10660	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs554657516	chr18:10660-10661	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs566492364	chr18:10661-10662	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs533744383	chr18:10662-10663	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs115858092	chr18:10665-10666	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs66578743	chr18:10679-10680	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs113507724	chr18:10683-10684	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs577517853	chr18:10684-10685	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs190828861	chr18:10690-10691	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs558568019	chr18:10693-10694	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs72854249	chr18:10697-10698	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs371428272	chr18:10698-10699	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs139482401	chr18:10701-10702	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs544169626	chr18:10704-10705	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs114463029	chr18:10706-10707	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs556371943	chr18:10717-10718	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs574502329	chr18:10719-10720	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs370183276	chr18:10723-10724	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs561011584	chr18:10732-10733	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs149661439	chr18:10733-10734	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs75343449	chr18:10736-10737	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs540258498	chr18:10739-10740	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs564918226	chr18:10741-10742	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs532878481	chr18:10743-10744	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs78360699	chr18:10749-10750	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs73360475	chr18:10755-10756	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs550985930	chr18:10764-10765	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs563098114	chr18:10769-10770	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs530200462	chr18:10770-10771	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs113980581	chr18:10774-10775	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs548329854	chr18:10777-10778	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:48)

Disease	PMID	Source
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Esophageal cancer	21851588	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Breast cancer	17899364	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Gastrointestinal cancer	17018589	CNVD
prenatal diagnosis	20453657	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Renal cell carcinoma	18765545	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Schizophrenia	23813976	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Melanoma	17363583	CNVD

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:8800-11200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr18:10000-10600	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
3	chr18:10000-10600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr18:10000-10600	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
5	chr18:10000-10600	Active TSS	Fetal Heart	heart
6	chr18:10000-11000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
7	chr18:10000-13600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr18:10200-10600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
9	chr18:10200-10600	Enhancers	Placenta	Placenta
10	chr18:10400-10600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
11	chr18:10400-10600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
12	chr18:10400-10600	ZNF genes & repeats	Colon Smooth Muscle	Colon
13	chr18:10400-10600	Flanking Bivalent TSS/Enh	Gastric	stomach
14	chr18:10400-11800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr18:10600-10800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
16	chr18:10600-10800	Flanking Active TSS	Placenta	Placenta
17	chr18:10600-11800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr18:10800-11200	Active TSS	Placenta	Placenta
19	chr18:10800-14000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr18:11200-11600	Active TSS	iPS-18 Cell Line	embryonic stem cell
21	chr18:11200-11800	Flanking Active TSS	Placenta	Placenta
22	chr18:11200-12000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
23	chr18:11200-12600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr18:11200-13600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr18:11200-14200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
26	chr18:11600-11800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
27	chr18:11800-12200	Enhancers	Placenta	Placenta
28	chr18:11800-12600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr18:12000-13400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
30	chr18:12600-13400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr18:13200-13400	Enhancers	Gastric	stomach
32	chr18:13800-14000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr18:36000-36400	Active TSS	HUES6 Cell Line	embryonic stem cell
34	chr18:36000-36400	Active TSS	iPS-18 Cell Line	embryonic stem cell
35	chr18:50600-51600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr18:63400-63600	Active TSS	Breast Myoepithelial Primary Cells	Breast
37	chr18:63400-64000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr18:63400-64000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
39	chr18:63600-63800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
40	chr18:63600-63800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr18:63600-63800	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
42	chr18:63600-63800	ZNF genes & repeats	Primary T cells from cord blood	blood
43	chr18:63600-63800	ZNF genes & repeats	Fetal Brain Male	brain
44	chr18:63600-63800	Flanking Bivalent TSS/Enh	Fetal Kidney	kidney
45	chr18:63600-63800	Enhancers	Right Ventricle	heart
46	chr18:63600-63800	Flanking Bivalent TSS/Enh	Spleen	Spleen
47	chr18:63600-63800	ZNF genes & repeats	K562	blood
48	chr18:63600-63800	Active TSS	NH-A	brain
49	chr18:63600-64000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
50	chr18:63600-64000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell

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