Variant report

Variant	nsv978590
Chromosome Location	chr18:10001-16279
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr18:10049-10662	GM12878	blood:	n/a	n/a
2	BATF	chr18:9958-10337	GM12878	blood:	n/a	n/a
3	BCL11A	chr18:10392-10708	GM12878	blood:	n/a	n/a
4	BCL11A	chr18:9938-10711	GM12878	blood:	n/a	n/a
5	BCL11A	chr18:10002-10390	GM12878	blood:	n/a	n/a
6	BHLHE40	chr18:10070-10620	HepG2	liver:	n/a	n/a
7	BRCA1	chr18:10421-10633	H1-hESC	embryonic stem cell:	n/a	n/a
8	CBX3	chr18:9952-10758	K562	blood:	n/a	n/a
9	CBX3	chr18:9926-10815	K562	blood:	n/a	n/a
10	CEBPB	chr18:9976-10387	GM12878	blood:	n/a	n/a
11	CEBPB	chr18:11762-11832	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr18:9933-10821	GM12878	blood:	n/a	n/a
13	CEBPB	chr18:9854-10855	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPD	chr18:9958-10726	K562	blood:	n/a	n/a
15	CHD2	chr18:11844-11875	HepG2	liver:	n/a	n/a
16	CREB1	chr18:11591-11950	A549	lung:	n/a	n/a
17	CTCF	chr18:11733-11906	GM12878	blood:	n/a	chr18:11812-11821
18	CTCF	chr18:11744-11894	NHEK	skin:	n/a	chr18:11812-11821
19	CTCF	chr18:11588-11963	K562	blood:	n/a	chr18:11812-11821
20	CTCF	chr18:11640-11790	NHEK	skin:	n/a	n/a
21	CTCF	chr18:11620-11770	HCM	heart:	n/a	n/a
22	CTCF	chr18:11597-11918	A549	lung:	n/a	chr18:11812-11821
23	CTCF	chr18:13917-14006	GM13976	blood:	n/a	chr18:13953-13961
24	CTCF	chr18:11680-11830	GM12872	blood:	n/a	chr18:11812-11821
25	CTCF	chr18:10137-10168	GM10266	blood:	n/a	n/a
26	CTCF	chr18:11562-11996	HepG2	liver:	n/a	chr18:11812-11821
27	CTCF	chr18:11664-11915	GM13977	blood:	n/a	chr18:11812-11821
28	CTCF	chr18:11580-11730	NB4	blood:	n/a	n/a
29	CTCF	chr18:11700-11850	AG09309	skin:	n/a	chr18:11812-11821
30	CTCF	chr18:11740-11890	HEK293	kidney:	n/a	chr18:11812-11821
31	CTCF	chr18:11740-11890	GM12865	blood:	n/a	chr18:11812-11821
32	CTCF	chr18:11748-11897	MCF-7	breast:	n/a	chr18:11812-11821
33	CTCF	chr18:11626-11892	SK-N-SH_RA	brain:	n/a	chr18:11812-11821
34	CTCF	chr18:11740-11890	GM12878	blood:	n/a	chr18:11812-11821
35	CTCF	chr18:11603-12015	A549	lung:	n/a	chr18:11812-11821
36	CTCF	chr18:11760-11910	GM12864	blood:	n/a	chr18:11812-11821
37	CTCF	chr18:11760-11910	HEK293	kidney:	n/a	chr18:11812-11821
38	CTCF	chr18:11744-11824	GM13976	blood:	n/a	chr18:11812-11821
39	CTCF	chr18:11754-11882	MCF-7	breast:	n/a	chr18:11812-11821
40	CTCF	chr18:11543-11957	A549	lung:	n/a	chr18:11812-11821
41	CTCF	chr18:11660-11810	HVMF	connective:	n/a	n/a
42	CTCF	chr18:11502-12137	HCT-116	colon:	n/a	chr18:11812-11821
43	CTCF	chr18:11704-11931	Gliobla	brain:	n/a	chr18:11812-11821
44	CTCF	chr18:11680-11830	GM12873	blood:	n/a	chr18:11812-11821
45	CTCF	chr18:11740-11890	GM12870	blood:	n/a	chr18:11812-11821
46	CTCF	chr18:11640-11790	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr18:11700-11850	HMEC	breast:	n/a	chr18:11812-11821
48	CTCF	chr18:13820-13970	GM12869	blood:	n/a	chr18:13953-13961 chr18:13835-13848
49	CTCF	chr18:11761-11865	GM19238	blood:	n/a	chr18:11812-11821
50	CTCF	chr18:11700-11850	GM12874	blood:	n/a	chr18:11812-11821

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:12371-12421	Caco-2	colon:	n/a
2	chr18:11948-11998	AoSMC	blood vessel:	n/a
3	chr18:12371-12421	Caco-2	colon:	n/a
4	chr18:11948-11998	AoSMC	blood vessel:	n/a
5	chr18:11231-11281	Hepatocyte	liver:	n/a
6	chr18:12371-12421	HRE	kidney:	n/a
7	chr18:12371-12421	SK-N-MC	brain:	n/a
8	chr18:12437-12487	GM06990	blood:	n/a
9	chr18:12371-12421	LNCaP	prostate:	n/a
10	chr18:12371-12421	NT2-D1	testis:	n/a
11	chr18:12371-12421	RPTEC	kidney:	n/a
12	chr18:11724-11774	HNPCEpiC	eye:	n/a
13	chr18:11724-11774	A549	lung:	n/a
14	chr18:11231-11281	HNPCEpiC	eye:	n/a
15	chr18:12437-12487	ovcar-3	ovarian:	n/a
16	chr18:11948-11998	HEK293	kidney:	embryo
17	chr18:12371-12421	AoSMC	blood vessel:	n/a
18	chr18:12437-12487	PrEC	prostate:	n/a
19	chr18:12437-12487	AG10803	skin:	n/a
20	chr18:11855-11905	AG04450	lung:	fetal
21	chr18:11231-11281	HIPEpiC	eye:	n/a
22	chr18:11855-11905	HUVEC	blood vessel:	n/a
23	chr18:11855-11905	HepG2	liver:	n/a
24	chr18:12371-12421	HNPCEpiC	eye:	n/a
25	chr18:11724-11774	SK-N-SH_RA	brain:	n/a
26	chr18:12371-12421	NB4	blood:	n/a
27	chr18:11855-11905	LNCaP	prostate:	n/a
28	chr18:11724-11774	RPTEC	kidney:	n/a
29	chr18:12371-12421	GM12878	blood:	n/a
30	chr18:11231-11281	NB4	blood:	n/a
31	chr18:11855-11905	AG09309	skin:	n/a
32	chr18:11948-11998	HPAEpiC	pulmonary alveolar:	n/a
33	chr18:12437-12487	BJ	skin:	n/a
34	chr18:12371-12421	HCPEpiC	choroid plexus:	n/a
35	chr18:12371-12421	MCF10A-Er-Src	breast:	n/a
36	chr18:11724-11774	SK-N-MC	brain:	n/a
37	chr18:12437-12487	HRPEpiC	eye:	n/a
38	chr18:11231-11281	HEK293	kidney:	embryo
39	chr18:11855-11905	PANC-1	pancreas:	n/a
40	chr18:11855-11905	HIPEpiC	eye:	n/a
41	chr18:11231-11281	HCF	heart:	n/a
42	chr18:11948-11998	U87	brain:	n/a
43	chr18:11724-11774	PFSK-1	brain:	n/a
44	chr18:12371-12421	GM12891	blood:	n/a
45	chr18:11231-11281	AG04449	skin:	fetal
46	chr18:11948-11998	HIPEpiC	eye:	n/a
47	chr18:12371-12421	HepG2	liver:	n/a
48	chr18:12437-12487	SKMC	muscle:	n/a
49	chr18:11724-11774	HEEpiC	esophagus:	n/a
50	chr18:12371-12421	NH-A	brain:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-683L23.1.1-2	chr18:14851-14870	XLOC_012737
2	lnc-RP11-683L23.1.1-2	chr18:14195-14653	ENSG00000263305.1
3	lnc-RP11-683L23.1.1-2	chr18:14294-14653	XLOC_012737
4	lnc-RP11-683L23.1.1-2	chr18:14851-14958	ENSG00000263305.1
5	lnc-RP11-683L23.1.1-2	chr18:14490-14653	ENSG00000263305.1

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

Extended variants
information (count: 439 )
Associated
traits (count: 44 )

Variant overlapped rSNPs/rCNVs (count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111219353	chr18:10005-10006	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs370553657	chr18:10019-10020	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs147646711	chr18:10022-10023	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs148696862	chr18:10023-10024	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs140072522	chr18:10025-10026	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs558214421	chr18:10077-10078	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs201455439	chr18:10079-10080	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs199586812	chr18:10082-10083	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs200232448	chr18:10083-10084	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs573338634	chr18:10094-10095	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs199758167	chr18:10096-10097	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs376016698	chr18:10147-10148	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs201388742	chr18:10148-10149	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs369929209	chr18:10153-10154	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs559454709	chr18:10160-10161	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs111211201	chr18:10161-10162	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs375118715	chr18:10173-10174	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs376323538	chr18:10204-10205	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs149225345	chr18:10209-10210	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs111211202	chr18:10227-10228	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs142302711	chr18:10228-10229	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs374323321	chr18:10230-10231	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs141225780	chr18:10240-10241	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs138021235	chr18:10241-10242	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs111219348	chr18:10299-10300	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs377364654	chr18:10301-10302	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs370520016	chr18:10305-10306	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs200970988	chr18:10333-10334	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs200612651	chr18:10336-10337	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs372560373	chr18:10359-10360	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs111211203	chr18:10360-10361	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs564296097	chr18:10376-10377	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs138867010	chr18:10411-10412	Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs201061345	chr18:10428-10429	Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs370300545	chr18:10435-10436	Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs56928311	chr18:10441-10442	Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs58286501	chr18:10460-10461	Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	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
39	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
40	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
41	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
42	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
43	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
44	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
45	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
46	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
47	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
48	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
49	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
50	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

Variant related diseases (count:44)

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

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:8800-11200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr18:10000-10200	ZNF genes & repeats	Brain Germinal Matrix	brain
3	chr18:10000-10400	ZNF genes & repeats	Placenta Amnion	Placenta Amnion
4	chr18:10000-10600	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
5	chr18:10000-10600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr18:10000-10600	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
7	chr18:10000-10600	Active TSS	Fetal Heart	heart
8	chr18:10000-11000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr18:10000-13600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr18:10200-10600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
11	chr18:10200-10600	Enhancers	Placenta	Placenta
12	chr18:10400-10600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
13	chr18:10400-10600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
14	chr18:10400-10600	ZNF genes & repeats	Colon Smooth Muscle	Colon
15	chr18:10400-10600	Flanking Bivalent TSS/Enh	Gastric	stomach
16	chr18:10400-11800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr18:10600-10800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
18	chr18:10600-10800	Flanking Active TSS	Placenta	Placenta
19	chr18:10600-11800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr18:10800-11200	Active TSS	Placenta	Placenta
21	chr18:10800-14000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr18:11200-11600	Active TSS	iPS-18 Cell Line	embryonic stem cell
23	chr18:11200-11800	Flanking Active TSS	Placenta	Placenta
24	chr18:11200-12000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
25	chr18:11200-12600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr18:11200-13600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr18:11200-14200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
28	chr18:11600-11800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
29	chr18:11800-12200	Enhancers	Placenta	Placenta
30	chr18:11800-12600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr18:12000-13400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
32	chr18:12600-13400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr18:13200-13400	Enhancers	Gastric	stomach
34	chr18:13800-14000	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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