Variant report

Variant	nsv909399
Chromosome Location	chr18:12083552-12141372
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:562)
CpG islands
(count:366)
Chromatin interactive
region (count:22)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:562 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr18:12121571-12121835	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr18:12098377-12098759	GM12878	blood:	n/a	n/a
3	BATF	chr18:12098406-12098669	GM12878	blood:	n/a	n/a
4	BATF	chr18:12099233-12099447	GM12878	blood:	n/a	chr18:12099366-12099376
5	BATF	chr18:12099205-12099435	GM12878	blood:	n/a	chr18:12099366-12099376
6	BCL3	chr18:12098402-12098798	GM12878	blood:	n/a	n/a
7	BHLHE40	chr18:12121724-12122063	K562	blood:	n/a	n/a
8	BHLHE40	chr18:12092799-12093072	K562	blood:	n/a	chr18:12093050-12093066
9	BRCA1	chr18:12092817-12092876	H1-hESC	embryonic stem cell:	n/a	n/a
10	CCNT2	chr18:12092914-12093043	K562	blood:	n/a	n/a
11	CEBPB	chr18:12114213-12114626	ECC-1	luminal epithelium:	n/a	chr18:12114424-12114435
12	CEBPB	chr18:12114189-12114605	IMR90	lung:	n/a	chr18:12114424-12114435
13	CEBPB	chr18:12086202-12086530	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr18:12114060-12114567	K562	blood:	n/a	chr18:12114424-12114435
15	CEBPB	chr18:12114266-12114617	A549	lung:	n/a	chr18:12114424-12114435
16	CEBPB	chr18:12119385-12119733	K562	blood:	n/a	n/a
17	CEBPB	chr18:12114307-12114559	MCF-7	breast:	n/a	chr18:12114424-12114435
18	CEBPB	chr18:12114016-12114693	Hela-S3	cervix:	n/a	chr18:12114424-12114435
19	CEBPB	chr18:12086183-12086554	MCF-7	breast:	n/a	n/a
20	CEBPB	chr18:12119384-12119757	K562	blood:	n/a	n/a
21	CEBPB	chr18:12114201-12114561	A549	lung:	n/a	chr18:12114424-12114435
22	CEBPB	chr18:12092848-12093081	HepG2	liver:	n/a	n/a
23	CEBPB	chr18:12114087-12114596	K562	blood:	n/a	chr18:12114424-12114435
24	CEBPB	chr18:12090640-12090795	HepG2	liver:	n/a	n/a
25	CEBPB	chr18:12086123-12086565	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr18:12114135-12114617	HepG2	liver:	n/a	chr18:12114424-12114435
27	CEBPB	chr18:12110506-12111102	HepG2	liver:	n/a	n/a
28	CEBPB	chr18:12087914-12087930	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr18:12086223-12086412	HepG2	liver:	n/a	n/a
30	CEBPB	chr18:12119448-12119651	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr18:12114249-12114616	H1-hESC	embryonic stem cell:	n/a	chr18:12114424-12114435
32	CEBPB	chr18:12114288-12114554	MCF-7	breast:	n/a	chr18:12114424-12114435
33	CHD2	chr18:12087795-12087986	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr18:12093598-12093600	K562	blood:	n/a	n/a
35	CHD2	chr18:12092755-12092949	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr18:12086349-12086675	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr18:12092762-12093204	HepG2	liver:	n/a	n/a
38	CHD2	chr18:12093592-12093640	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr18:12092800-12092950	GM12878	blood:	n/a	chr18:12092906-12092914 chr18:12092904-12092920 chr18:12092905-12092926 chr18:12092903-12092921
40	CTCF	chr18:12086797-12086939	HepG2	liver:	n/a	n/a
41	CTCF	chr18:12092816-12093014	A549	lung:	n/a	chr18:12092906-12092914 chr18:12092904-12092920 chr18:12092905-12092926 chr18:12092903-12092921
42	CTCF	chr18:12121300-12121450	GM12864	blood:	n/a	n/a
43	CTCF	chr18:12121260-12121410	GM12868	blood:	n/a	n/a
44	CTCF	chr18:12092900-12093050	RPTEC	kidney:	n/a	chr18:12092906-12092914 chr18:12092904-12092920 chr18:12092905-12092926 chr18:12092903-12092921
45	CTCF	chr18:12092860-12093010	GM12866	blood:	n/a	chr18:12092906-12092914 chr18:12092904-12092920 chr18:12092905-12092926 chr18:12092903-12092921
46	CTCF	chr18:12121299-12121465	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr18:12121280-12121430	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr18:12121292-12121475	Medullo	brain:	n/a	n/a
49	CTCF	chr18:12093580-12093730	Hela-S3	cervix:	n/a	chr18:12093600-12093613
50	CTCF	chr18:12092780-12092930	GM12870	blood:	n/a	chr18:12092906-12092914 chr18:12092904-12092920 chr18:12092905-12092926 chr18:12092903-12092921

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:12092942-12092992	K562	blood:	n/a
2	chr18:12093625-12093675	GM12878	blood:	n/a
3	chr18:12093625-12093675	AG09309	skin:	n/a
4	chr18:12090210-12090260	GM19239	blood:	n/a
5	chr18:12093625-12093675	T-47D	breast:	n/a
6	chr18:12093625-12093675	HepG2	liver:	n/a
7	chr18:12092942-12092992	AG09319	gingival:	n/a
8	chr18:12090210-12090260	SK-N-SH_RA	brain:	n/a
9	chr18:12090210-12090260	HEEpiC	esophagus:	n/a
10	chr18:12095187-12095237	NHBE	bronchial:	n/a
11	chr18:12092942-12092992	CMK	blood:	n/a
12	chr18:12092942-12092992	GM06990	blood:	n/a
13	chr18:12090210-12090260	ECC-1	luminal epithelium:	n/a
14	chr18:12097776-12097826	SK-N-SH	brain:	n/a
15	chr18:12095187-12095237	BE2_C	brain:	n/a
16	chr18:12095187-12095237	Hepatocyte	liver:	n/a
17	chr18:12092942-12092992	IMR90	lung:	fetal
18	chr18:12097776-12097826	SAEC	small airway:	n/a
19	chr18:12090210-12090260	MCF-7	breast:	n/a
20	chr18:12093625-12093675	MCF-7	breast:	n/a
21	chr18:12092942-12092992	HEEpiC	esophagus:	n/a
22	chr18:12093809-12093859	Jurkat	blood:	n/a
23	chr18:12093625-12093675	GM06990	blood:	n/a
24	chr18:12092942-12092992	GM12891	blood:	n/a
25	chr18:12092942-12092992	NHDF-neo	bronchial:	n/a
26	chr18:12092942-12092992	HEK293	kidney:	embryo
27	chr18:12092942-12092992	PANC-1	pancreas:	n/a
28	chr18:12095187-12095237	MCF-7	breast:	n/a
29	chr18:12092942-12092992	T-47D	breast:	n/a
30	chr18:12097776-12097826	ECC-1	luminal epithelium:	n/a
31	chr18:12093809-12093859	RPTEC	kidney:	n/a
32	chr18:12092942-12092992	AG04449	skin:	fetal
33	chr18:12092942-12092992	HRE	kidney:	n/a
34	chr18:12093809-12093859	PFSK-1	brain:	n/a
35	chr18:12093809-12093859	ECC-1	luminal epithelium:	n/a
36	chr18:12097776-12097826	HCT-116	colon:	n/a
37	chr18:12097776-12097826	Hela-S3	cervix:	n/a
38	chr18:12097776-12097826	GM12878	blood:	n/a
39	chr18:12093625-12093675	HMEC	breast:	n/a
40	chr18:12090210-12090260	LNCaP	prostate:	n/a
41	chr18:12090210-12090260	AG04450	lung:	fetal
42	chr18:12097776-12097826	SK-N-MC	brain:	n/a
43	chr18:12097776-12097826	U87	brain:	n/a
44	chr18:12093809-12093859	HNPCEpiC	eye:	n/a
45	chr18:12097776-12097826	H1-hESC	embryonic stem cell:	embryo
46	chr18:12090210-12090260	GM06990	blood:	n/a
47	chr18:12097776-12097826	HRE	kidney:	n/a
48	chr18:12097776-12097826	HPAEpiC	pulmonary alveolar:	n/a
49	chr18:12090210-12090260	GM12891	blood:	n/a
50	chr18:12093625-12093675	Caco-2	colon:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:12097992..12100907-chr18:12104911..12107291,2	MCF-7	breast:
2	chr18:12096937..12098826-chr18:12103997..12106538,2	K562	blood:
3	chr18:12084453..12086286-chr18:12088021..12090033,2	K562	blood:
4	chr18:12119299..12121034-chr18:12123082..12124691,2	K562	blood:
5	chr18:12120897..12121609-chr22:17160804..17161481,3	MCF-7	breast:
6	chr18:11979089..11980849-chr18:12109709..12111299,2	K562	blood:
7	chr18:12094117..12094711-chr18:12236525..12237062,2	K562	blood:
8	chr18:12092475..12093363-chr18:12121230..12121778,4	MCF-7	breast:
9	chr18:12102586..12107654-chr18:12108102..12111487,4	K562	blood:
10	chr18:12088519..12091150-chr18:12096385..12097943,2	K562	blood:
11	chr18:12084453..12086286-chr18:12088021..12090033,2	K562	blood:
12	chr18:12094191..12096366-chr18:12113967..12116717,2	MCF-7	breast:
13	chr18:12092426..12095170-chr18:12097480..12099654,2	K562	blood:
14	chr18:12119299..12121034-chr18:12123082..12124691,2	K562	blood:
15	chr18:12092391..12093318-chr18:12246451..12247616,5	K562	blood:
16	chr18:12092455..12093131-chr18:12240900..12241463,2	MCF-7	breast:
17	chr18:12120896..12121904-chr22:17160896..17161585,3	K562	blood:
18	chr18:12107653..12109609-chr18:12114882..12116934,2	K562	blood:
19	chr18:12107653..12109609-chr18:12114882..12116934,2	K562	blood:
20	chr18:12088519..12091150-chr18:12096385..12097943,2	K562	blood:
21	chr18:12092426..12095170-chr18:12097480..12099654,2	K562	blood:
22	chr18:12094191..12096366-chr18:12113967..12116717,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP002414.1.1-3	chr18:12101996-12102469	NONHSAT058342
2	lnc-ANKRD62-2	chr18:12085171-12085266	ENSG00000267722.1

No data

Variant related genes	Relation type
ENSG00000267162	TF binding region
ANKRD62	TF binding region
RNU6-324P	TF binding region
ENSG00000267478	TF binding region
ENSG00000267162	CpG island
ANKRD62	CpG island
RNU6-324P	CpG island
ENSG00000267478	CpG island
ENSG00000181626	chromatin interactions
ENSG00000267478	chromatin interactions
ENSG00000200827	chromatin interactions
ENSG00000267663	chromatin interactions

Extended variants
information (count: 1684 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1684 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56351909	chr18:12083552-12083553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs564387735	chr18:12083568-12083569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149127571	chr18:12083569-12083570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546936101	chr18:12083582-12083583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs561826925	chr18:12083588-12083589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs117479078	chr18:12083638-12083639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548282320	chr18:12083653-12083654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs191985392	chr18:12083660-12083661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142267641	chr18:12083665-12083666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs56153833	chr18:12083703-12083704	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs56032100	chr18:12083719-12083720	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs55738573	chr18:12083727-12083728	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs529121649	chr18:12083739-12083740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571412498	chr18:12083759-12083760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534941700	chr18:12083773-12083774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs57591296	chr18:12083783-12083784	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs184270155	chr18:12083804-12083805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574682608	chr18:12083807-12083808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs116850138	chr18:12083808-12083809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs57779974	chr18:12083814-12083815	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs538813834	chr18:12083816-12083817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575275961	chr18:12083837-12083838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545896237	chr18:12083877-12083878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs151337901	chr18:12083936-12083937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572877140	chr18:12083973-12083974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557543507	chr18:12084037-12084038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs368408200	chr18:12084051-12084052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs9303758	chr18:12084094-12084095	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs543330530	chr18:12084112-12084113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs34774742	chr18:12084120-12084121	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs140704495	chr18:12084157-12084158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs9652929	chr18:12084181-12084182	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs562718882	chr18:12084194-12084195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541122968	chr18:12084250-12084251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs113039914	chr18:12084284-12084285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561704762	chr18:12084285-12084286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs145814535	chr18:12084355-12084356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35626710	chr18:12084434-12084435	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs59277565	chr18:12084435-12084436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546884347	chr18:12084483-12084484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568440373	chr18:12084540-12084541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201017197	chr18:12084541-12084542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114310346	chr18:12084549-12084550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544849054	chr18:12084558-12084559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs35008236	chr18:12084593-12084594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78401036	chr18:12084602-12084603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140290762	chr18:12084603-12084604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546961238	chr18:12084615-12084616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557876554	chr18:12084632-12084633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs9652909	chr18:12084641-12084642	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:57)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	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
Melanoma	18172304	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
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Glioma	17123091	CNVD
Neurodevelopmental disorder	22521361	CNVD
Autism	20531469	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12076800-12085800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr18:12077000-12095000	Weak transcription	Right Atrium	heart
3	chr18:12082600-12090200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr18:12085200-12088800	Enhancers	Esophagus	oesophagus
5	chr18:12085400-12089600	Enhancers	Pancreas	Pancrea
6	chr18:12085600-12085800	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr18:12085600-12087600	Enhancers	Duodenum Mucosa	Duodenum
8	chr18:12085600-12088600	Enhancers	Sigmoid Colon	Sigmoid Colon
9	chr18:12085800-12086200	Enhancers	Hela-S3	cervix
10	chr18:12085800-12086800	Enhancers	Fetal Muscle Trunk	muscle
11	chr18:12085800-12086800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
12	chr18:12085800-12087000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr18:12085800-12088200	Enhancers	Colonic Mucosa	Colon
14	chr18:12085800-12089000	Enhancers	Stomach Mucosa	stomach
15	chr18:12086000-12086400	Enhancers	Rectal Mucosa Donor 29	rectum
16	chr18:12086000-12087000	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr18:12086200-12087200	Enhancers	Gastric	stomach
18	chr18:12086200-12088400	Flanking Active TSS	Hela-S3	cervix
19	chr18:12086400-12086600	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr18:12086400-12086800	Enhancers	HMEC	breast
21	chr18:12086400-12087600	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr18:12086400-12087600	Enhancers	Right Ventricle	heart
23	chr18:12086400-12087800	Enhancers	Lung	lung
24	chr18:12086600-12087200	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr18:12086600-12089000	Enhancers	Spleen	Spleen
26	chr18:12086800-12088800	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr18:12087000-12088200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr18:12087000-12089400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
29	chr18:12087000-12089600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr18:12087200-12087400	Flanking Active TSS	Gastric	stomach
31	chr18:12087200-12089400	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr18:12087400-12087800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr18:12087400-12087800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr18:12087400-12087800	Enhancers	Gastric	stomach
35	chr18:12087600-12088600	Weak transcription	Right Ventricle	heart
36	chr18:12087600-12089000	Weak transcription	Duodenum Mucosa	Duodenum
37	chr18:12087800-12088000	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr18:12087800-12088200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr18:12087800-12088200	Genic enhancers	Gastric	stomach
40	chr18:12087800-12089200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr18:12088200-12088600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr18:12088200-12088800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
43	chr18:12088200-12089200	Enhancers	Gastric	stomach
44	chr18:12088200-12089400	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr18:12088400-12089600	Enhancers	Hela-S3	cervix
46	chr18:12088600-12089400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr18:12088600-12089400	Enhancers	Right Ventricle	heart
48	chr18:12088800-12089000	Flanking Active TSS	Esophagus	oesophagus
49	chr18:12088800-12089200	Enhancers	Left Ventricle	heart
50	chr18:12089000-12089200	Enhancers	Duodenum Mucosa	Duodenum

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