Variant report

Variant	nsv1066822
Chromosome Location	chr18:452951-524184
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1129)
CpG islands
(count:1098)
Chromatin interactive
region (count:50)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1129 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:497085-497215	K562	blood:	n/a	n/a
2	ARID3A	chr18:479425-479711	HepG2	liver:	n/a	n/a
3	ATF1	chr18:497113-497233	K562	blood:	n/a	n/a
4	ATF2	chr18:496881-497355	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr18:496881-497404	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr18:496952-497240	GM12878	blood:	n/a	n/a
7	ATF2	chr18:505438-505825	GM12878	blood:	n/a	n/a
8	ATF2	chr18:505504-505896	GM12878	blood:	n/a	n/a
9	ATF3	chr18:478671-478970	K562	blood:	n/a	n/a
10	BACH1	chr18:499552-500991	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr18:518938-519219	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr18:495011-495341	GM12878	blood:	n/a	n/a
13	BATF	chr18:518939-519310	GM12878	blood:	n/a	chr18:519090-519101
14	BATF	chr18:505510-505830	GM12878	blood:	n/a	chr18:505657-505668
15	BATF	chr18:505404-505905	GM12878	blood:	n/a	chr18:505657-505668
16	BATF	chr18:495039-495292	GM12878	blood:	n/a	n/a
17	BCL11A	chr18:505492-505850	GM12878	blood:	n/a	n/a
18	BCL11A	chr18:505426-505761	GM12878	blood:	n/a	n/a
19	BHLHE40	chr18:499574-499885	K562	blood:	n/a	n/a
20	BHLHE40	chr18:505566-505901	GM12878	blood:	n/a	n/a
21	BHLHE40	chr18:497134-497145	K562	blood:	n/a	n/a
22	BHLHE40	chr18:515029-515305	HepG2	liver:	n/a	n/a
23	BHLHE40	chr18:497172-497243	GM12878	blood:	n/a	n/a
24	BHLHE40	chr18:518671-518739	GM12878	blood:	n/a	n/a
25	BHLHE40	chr18:519134-519334	GM12878	blood:	n/a	n/a
26	BRCA1	chr18:475166-475418	H1-hESC	embryonic stem cell:	n/a	n/a
27	CBX3	chr18:518832-519462	K562	blood:	n/a	n/a
28	CCNT2	chr18:499592-499604	K562	blood:	n/a	n/a
29	CEBPB	chr18:471148-471410	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr18:518214-518371	HepG2	liver:	n/a	chr18:518276-518287
31	CEBPB	chr18:503765-504219	MCF-7	breast:	n/a	n/a
32	CEBPB	chr18:471141-471420	IMR90	lung:	n/a	n/a
33	CEBPB	chr18:518264-518299	A549	lung:	n/a	chr18:518276-518287
34	CEBPB	chr18:507009-507097	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr18:503766-504191	MCF-7	breast:	n/a	n/a
36	CEBPB	chr18:518270-518304	IMR90	lung:	n/a	chr18:518276-518287
37	CEBPB	chr18:518261-518360	H1-hESC	embryonic stem cell:	n/a	chr18:518276-518287
38	CEBPB	chr18:471248-471315	A549	lung:	n/a	n/a
39	CEBPB	chr18:457561-457756	H1-hESC	embryonic stem cell:	n/a	chr18:457614-457623
40	CEBPB	chr18:489614-489766	IMR90	lung:	n/a	n/a
41	CEBPB	chr18:499495-499579	IMR90	lung:	n/a	n/a
42	CHD2	chr18:505624-505677	GM12878	blood:	n/a	n/a
43	CHD2	chr18:477786-477819	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr18:477550-477943	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr18:456295-456516	A549	lung:	n/a	n/a
46	CTBP2	chr18:499752-501537	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr18:469227-469343	GM19238	blood:	n/a	n/a
48	CTCF	chr18:477640-477790	HPF	lung:	n/a	n/a
49	CTCF	chr18:476480-476630	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr18:464000-464150	HBMEC	blood vessel:	n/a	n/a

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:500979-501029	HL-60	blood:	n/a
2	chr18:514536-514586	HAEpiC	amniotic membrane:	n/a
3	chr18:501513-501563	BE2_C	brain:	n/a
4	chr18:501109-501159	NB4	blood:	n/a
5	chr18:502981-503031	HIPEpiC	eye:	n/a
6	chr18:499760-499810	AG04449	skin:	fetal
7	chr18:501137-501187	SAEC	small airway:	n/a
8	chr18:499393-499443	NHDF-neo	bronchial:	n/a
9	chr18:519265-519315	GM19239	blood:	n/a
10	chr18:501137-501187	NB4	blood:	n/a
11	chr18:497782-497832	Caco-2	colon:	n/a
12	chr18:499760-499810	U87	brain:	n/a
13	chr18:515465-515515	HEK293	kidney:	embryo
14	chr18:497782-497832	NH-A	brain:	n/a
15	chr18:500323-500373	Jurkat	blood:	n/a
16	chr18:500323-500373	GM06990	blood:	n/a
17	chr18:515465-515515	Caco-2	colon:	n/a
18	chr18:516597-516647	U87	brain:	n/a
19	chr18:515465-515515	HRE	kidney:	n/a
20	chr18:497782-497832	HRPEpiC	eye:	n/a
21	chr18:497782-497832	MCF-7	breast:	n/a
22	chr18:497274-497324	MCF10A-Er-Src	breast:	n/a
23	chr18:500817-500867	MCF10A-Er-Src	breast:	n/a
24	chr18:501234-501284	ECC-1	luminal epithelium:	n/a
25	chr18:501513-501563	PFSK-1	brain:	n/a
26	chr18:519265-519315	MCF-7	breast:	n/a
27	chr18:519265-519315	Caco-2	colon:	n/a
28	chr18:514363-514413	HCPEpiC	choroid plexus:	n/a
29	chr18:497274-497324	AG09309	skin:	n/a
30	chr18:501109-501159	SKMC	muscle:	n/a
31	chr18:514363-514413	NHDF-neo	bronchial:	n/a
32	chr18:502981-503031	GM12892	blood:	n/a
33	chr18:501513-501563	GM12891	blood:	n/a
34	chr18:501109-501159	NHBE	bronchial:	n/a
35	chr18:502981-503031	MCF10A-Er-Src	breast:	n/a
36	chr18:519265-519315	SK-N-MC	brain:	n/a
37	chr18:514536-514586	PFSK-1	brain:	n/a
38	chr18:499887-499937	HCPEpiC	choroid plexus:	n/a
39	chr18:519265-519315	GM12891	blood:	n/a
40	chr18:502981-503031	AG04449	skin:	fetal
41	chr18:515465-515515	PFSK-1	brain:	n/a
42	chr18:519265-519315	GM12878	blood:	n/a
43	chr18:500817-500867	GM12891	blood:	n/a
44	chr18:516597-516647	GM12892	blood:	n/a
45	chr18:516597-516647	AG04449	skin:	fetal
46	chr18:500817-500867	GM06990	blood:	n/a
47	chr18:501109-501159	GM12891	blood:	n/a
48	chr18:500817-500867	K562	blood:	n/a
49	chr18:500979-501029	HCM	heart:	n/a
50	chr18:499393-499443	HepG2	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr18:447259..449552-chr18:462740..464331,2	K562	blood:
2	chr18:494460..496026-chr18:498042..500232,2	K562	blood:
3	chr18:489781..492575-chr18:492919..494554,3	K562	blood:
4	chr18:454918..457653-chr18:457814..460289,2	K562	blood:
5	chr18:495373..497204-chr18:675679..677532,2	K562	blood:
6	chr18:268011..270028-chr18:478926..480492,2	MCF-7	breast:
7	chr18:497371..499766-chr18:515702..517662,2	K562	blood:
8	chr18:478338..480452-chr18:485711..487416,2	K562	blood:
9	chr18:489781..492349-chr18:492919..494506,2	K562	blood:
10	chr18:520616..523435-chr18:523853..525640,2	K562	blood:
11	chr18:286219..287016-chr18:477377..477880,2	MCF-7	breast:
12	chr18:332464..333064-chr18:469230..470136,2	MCF-7	breast:
13	chr18:497132..497644-chr18:616129..616974,2	MCF-7	breast:
14	chr18:449301..451013-chr18:470091..472621,2	MCF-7	breast:
15	chr18:457332..459811-chr18:492921..494922,2	K562	blood:
16	chr18:496735..497667-chr18:616100..616923,4	MCF-7	breast:
17	chr18:322375..323142-chr18:477353..477904,2	MCF-7	breast:
18	chr18:499290..501179-chr18:518693..520329,2	K562	blood:
19	chr18:482431..485272-chr18:486538..489245,3	K562	blood:
20	chr18:452500..455401-chr18:455665..457833,2	MCF-7	breast:
21	chr18:506327..508736-chr18:517411..519427,2	MCF-7	breast:
22	chr18:513812..515978-chr18:595645..597205,2	MCF-7	breast:
23	chr18:332254..333011-chr18:477226..477848,2	MCF-7	breast:
24	chr18:286191..286695-chr18:468859..469735,2	MCF-7	breast:
25	chr18:458328..461257-chr18:461738..464360,2	MCF-7	breast:
26	chr18:454918..457653-chr18:457814..460289,2	K562	blood:
27	chr18:457332..459811-chr18:492921..494922,2	K562	blood:
28	chr18:496934..498541-chr18:524865..526867,2	MCF-7	breast:
29	chr18:452500..455401-chr18:455665..457833,2	MCF-7	breast:
30	chr18:497209..499309-chr18:504632..506140,2	MCF-7	breast:
31	chr18:497371..499766-chr18:515702..517662,2	K562	blood:
32	chr18:495798..498610-chr18:505550..507646,2	K562	blood:
33	chr18:520616..523435-chr18:523853..525640,2	K562	blood:
34	chr18:458328..461257-chr18:461738..464360,2	MCF-7	breast:
35	chr18:499862..502354-chr18:502965..504677,2	K562	blood:
36	chr18:478338..480452-chr18:485711..487416,2	K562	blood:
37	chr18:477345..477894-chr18:616121..616950,2	MCF-7	breast:
38	chr18:482431..485272-chr18:486538..489245,3	K562	blood:
39	chr18:497209..499309-chr18:504632..506140,2	MCF-7	breast:
40	chr18:286401..287237-chr18:477304..478254,5	MCF-7	breast:
41	chr18:494460..496026-chr18:498042..500232,2	K562	blood:
42	chr18:292316..292911-chr18:477341..478167,2	MCF-7	breast:
43	chr18:506327..508736-chr18:517411..519427,2	MCF-7	breast:
44	chr18:489781..492349-chr18:492919..494506,2	K562	blood:
45	chr18:293279..294017-chr18:477353..478290,2	MCF-7	breast:
46	chr18:499109..499807-chr18:568417..568974,2	MCF-7	breast:
47	chr18:489781..492575-chr18:492919..494554,3	K562	blood:
48	chr18:499620..501884-chr18:596147..598528,2	K562	blood:
49	chr18:495798..498610-chr18:505550..507646,2	K562	blood:
50	chr18:268027..269600-chr18:489612..492318,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COLEC12-2	chr18:514127-514715	NONHSAT056843
2	lnc-COLEC12-2	chr18:508568-508807	ENSG00000264265.1
3	lnc-COLEC12-2	chr18:514696-514755	ENSG00000264265.1
4	lnc-COLEC12-2	chr18:514716-514745	NONHSAT056844
5	lnc-COLEC12-3	chr18:513111-513157	NONHSAT056842
6	lnc-COLEC12-2	chr18:514991-515557	NONHSAT056844
7	lnc-COLEC12-2	chr18:515095-515294	ENSG00000264265.1
8	lnc-COLEC12-3	chr18:513681-514030	NONHSAT056842
9	lnc-COLEC12-2	chr18:514868-514982	NONHSAT056843

No data

Variant related genes	Relation type
COLEC12	TF binding region
ENSG00000264265	TF binding region
COLEC12	CpG island
ENSG00000264265	CpG island
ENSG00000263884	chromatin interactions
ENSG00000079101	chromatin interactions
ENSG00000158270	chromatin interactions
ENSG00000079134	chromatin interactions

Extended variants
information (count: 3034 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:3034 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11081116	chr18:452951-452952	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs573508949	chr18:452992-452993	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs540891573	chr18:453022-453023	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs115766026	chr18:453031-453032	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs199849901	chr18:453033-453034	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs577886994	chr18:453049-453050	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs544973275	chr18:453085-453086	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs116148288	chr18:453107-453108	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs530620068	chr18:453204-453205	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs62090015	chr18:453234-453235	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs114662002	chr18:453236-453237	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs4798222	chr18:453302-453303	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs141309868	chr18:453322-453323	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs35061541	chr18:453334-453335	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs566344702	chr18:453368-453369	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs546402347	chr18:453397-453398	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs533160561	chr18:453411-453412	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs551746277	chr18:453414-453415	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs569715683	chr18:453416-453417	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs537106207	chr18:453424-453425	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs566398502	chr18:453442-453443	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs2621204	chr18:453451-453452	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs188988595	chr18:453461-453462	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs4798223	chr18:453469-453470	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs28707458	chr18:453503-453504	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs577859156	chr18:453539-453540	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs11081120	chr18:453557-453558	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs193052061	chr18:453615-453616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184887121	chr18:453631-453632	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568815810	chr18:453664-453665	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs146988686	chr18:453742-453743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560989566	chr18:453845-453846	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528224443	chr18:453864-453865	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs137963637	chr18:453941-453942	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12964008	chr18:453954-453955	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs12960217	chr18:453958-453959	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs372094672	chr18:453966-453967	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551795495	chr18:453979-453980	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569678960	chr18:454010-454011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530834787	chr18:454074-454075	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570756888	chr18:454075-454076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567406553	chr18:454088-454089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534847054	chr18:454112-454113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189777478	chr18:454119-454120	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs35239755	chr18:454156-454157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143987150	chr18:454157-454158	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs397757213	chr18:454159-454160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374445318	chr18:454160-454161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201888350	chr18:454185-454186	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12964090	chr18:454189-454190	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:65)

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
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Melanoma	17363583	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	20808228	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	20164919	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Bladder cancer	21909424	CNVD

Chromatin state (count:1583 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:447200-456400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr18:447600-456600	Weak transcription	Right Atrium	heart
3	chr18:449800-453000	Weak transcription	NHDF-Ad	bronchial
4	chr18:450000-456600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr18:450400-456000	Weak transcription	Placenta	Placenta
6	chr18:450600-453400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr18:451000-456000	Weak transcription	Rectal Smooth Muscle	rectum
8	chr18:451200-458400	Weak transcription	Lung	lung
9	chr18:452200-454400	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr18:452400-456400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr18:452600-453400	Enhancers	Fetal Muscle Leg	muscle
12	chr18:452600-453800	Enhancers	Osteobl	bone
13	chr18:452600-456000	Weak transcription	Fetal Muscle Trunk	muscle
14	chr18:452800-453200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr18:452800-453400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr18:452800-453600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
17	chr18:452800-454600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr18:452800-455800	Weak transcription	Fetal Lung	lung
19	chr18:452800-456000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr18:453000-453400	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr18:453000-453600	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr18:453000-454000	Enhancers	NHDF-Ad	bronchial
23	chr18:453200-456200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr18:453400-454800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr18:453400-455800	Weak transcription	Fetal Muscle Leg	muscle
26	chr18:453400-456600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr18:453400-456800	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr18:453600-454200	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr18:453600-456800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr18:453800-456000	Weak transcription	Osteobl	bone
31	chr18:454000-456000	Weak transcription	NHDF-Ad	bronchial
32	chr18:454200-456400	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr18:454400-456400	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr18:454600-456000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr18:454800-456600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr18:455000-455200	Enhancers	Brain Angular Gyrus	brain
37	chr18:455200-456600	Weak transcription	Brain Angular Gyrus	brain
38	chr18:455800-456000	Flanking Active TSS	Fetal Lung	lung
39	chr18:455800-456000	Enhancers	Stomach Smooth Muscle	stomach
40	chr18:455800-456400	Enhancers	Fetal Muscle Leg	muscle
41	chr18:455800-456800	Enhancers	Colon Smooth Muscle	Colon
42	chr18:455800-460600	Enhancers	Fetal Stomach	stomach
43	chr18:456000-456200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr18:456000-456200	Enhancers	Fetal Lung	lung
45	chr18:456000-456200	Enhancers	Osteobl	bone
46	chr18:456000-456400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr18:456000-456400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr18:456000-456400	Enhancers	Adipose Nuclei	Adipose
49	chr18:456000-456400	Enhancers	Left Ventricle	heart
50	chr18:456000-456400	Enhancers	Rectal Smooth Muscle	rectum

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