Variant report

Variant	nsv909604
Chromosome Location	chr18:44300281-44370518
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:309)
CpG islands
(count:794)
Chromatin interactive
region (count:2)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:44343741-44343800	HepG2	liver:	n/a	n/a
2	BACH1	chr18:44336050-44336250	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr18:44335079-44335249	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr18:44334478-44334576	GM12878	blood:	n/a	n/a
5	BHLHE40	chr18:44367638-44367984	GM12878	blood:	n/a	n/a
6	BRCA1	chr18:44318689-44318719	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr18:44307201-44307385	HepG2	liver:	n/a	n/a
8	CEBPB	chr18:44331573-44331857	HepG2	liver:	n/a	chr18:44331721-44331732
9	CEBPB	chr18:44369682-44369880	HepG2	liver:	n/a	chr18:44369709-44369720
10	CEBPB	chr18:44346904-44347188	K562	blood:	n/a	n/a
11	CHD1	chr18:44336734-44336908	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr18:44336861-44337128	H1-hESC	embryonic stem cell:	n/a	chr18:44337023-44337033
13	CHD2	chr18:44334253-44334329	GM12878	blood:	n/a	n/a
14	CTBP2	chr18:44336144-44337128	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTBP2	chr18:44337460-44338259	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr18:44335120-44335270	GM12869	blood:	n/a	n/a
17	CTCF	chr18:44352620-44352770	GM06990	blood:	n/a	n/a
18	CTCF	chr18:44352420-44352570	GM06990	blood:	n/a	chr18:44352478-44352499
19	CTCF	chr18:44334998-44335312	K562	blood:	n/a	n/a
20	CTCF	chr18:44324641-44324687	Pancreas_OC	pancreas:	n/a	n/a
21	CTCF	chr18:44352367-44352665	GM12878	blood:	n/a	chr18:44352478-44352499
22	CTCF	chr18:44335020-44335170	RPTEC	kidney:	n/a	n/a
23	CTCF	chr18:44352419-44352532	GM13977	blood:	n/a	chr18:44352478-44352499
24	CTCF	chr18:44335060-44335210	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr18:44352400-44352550	NB4	blood:	n/a	chr18:44352478-44352499
26	CTCF	chr18:44335020-44335170	HAc	cerebellar:	n/a	n/a
27	CTCF	chr18:44335060-44335210	HepG2	liver:	n/a	n/a
28	CTCF	chr18:44335140-44335290	HA-sp	spinal cord:	n/a	n/a
29	CTCF	chr18:44352433-44352545	GM19239	blood:	n/a	chr18:44352478-44352499
30	CTCF	chr18:44352340-44352490	HL-60	blood:	n/a	n/a
31	CTCF	chr18:44335005-44335335	K562	blood:	n/a	n/a
32	CTCF	chr18:44310460-44310564	Lung_OC	lung:	n/a	n/a
33	CTCF	chr18:44335100-44335250	GM12875	blood:	n/a	n/a
34	CTCF	chr18:44352450-44352568	MCF-7	breast:	n/a	chr18:44352478-44352499
35	CTCF	chr18:44335080-44335230	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr18:44352438-44352604	GM19238	blood:	n/a	chr18:44352478-44352499
37	CTCF	chr18:44335100-44335250	GM12874	blood:	n/a	n/a
38	CTCF	chr18:44352433-44352568	K562	blood:	n/a	chr18:44352478-44352499
39	CTCF	chr18:44335123-44335207	GM13977	blood:	n/a	n/a
40	CTCF	chr18:44352400-44352550	GM12873	blood:	n/a	chr18:44352478-44352499
41	CTCF	chr18:44335320-44335470	GM12874	blood:	n/a	n/a
42	CTCF	chr18:44335065-44335273	GM19238	blood:	n/a	n/a
43	CTCF	chr18:44334860-44335010	GM06990	blood:	n/a	n/a
44	CTCF	chr18:44349520-44349670	HEK293	kidney:	n/a	n/a
45	CTCF	chr18:44352420-44352570	WERI-Rb-1	eye:	n/a	chr18:44352478-44352499
46	CTCF	chr18:44352615-44352658	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr18:44335120-44335241	NHEK	skin:	n/a	n/a
48	CTCF	chr18:44350860-44351010	HAc	cerebellar:	n/a	n/a
49	CTCF	chr18:44335080-44335230	GM12874	blood:	n/a	n/a
50	CTCF	chr18:44334980-44335130	HCM	heart:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44338147-44338197	A549	lung:	n/a
2	chr18:44338147-44338197	A549	lung:	n/a
3	chr18:44340177-44340227	ProgFib	skin:	n/a
4	chr18:44338099-44338149	K562	blood:	n/a
5	chr18:44339513-44339563	HRE	kidney:	n/a
6	chr18:44337922-44337972	SK-N-SH	brain:	n/a
7	chr18:44338099-44338149	IMR90	lung:	fetal
8	chr18:44338099-44338149	HEK293	kidney:	embryo
9	chr18:44337853-44337903	HNPCEpiC	eye:	n/a
10	chr18:44336399-44336449	Caco-2	colon:	n/a
11	chr18:44337099-44337149	ECC-1	luminal epithelium:	n/a
12	chr18:44336399-44336449	HEEpiC	esophagus:	n/a
13	chr18:44337099-44337149	NB4	blood:	n/a
14	chr18:44337099-44337149	HRPEpiC	eye:	n/a
15	chr18:44337853-44337903	HL-60	blood:	n/a
16	chr18:44338099-44338149	AG04449	skin:	fetal
17	chr18:44340177-44340227	Hepatocyte	liver:	n/a
18	chr18:44334713-44334763	ovcar-3	ovarian:	n/a
19	chr18:44337853-44337903	SKMC	muscle:	n/a
20	chr18:44338099-44338149	MCF-7	breast:	n/a
21	chr18:44338147-44338197	Hepatocyte	liver:	n/a
22	chr18:44337922-44337972	MCF10A-Er-Src	breast:	n/a
23	chr18:44337664-44337714	HCF	heart:	n/a
24	chr18:44335109-44335159	NHBE	bronchial:	n/a
25	chr18:44337910-44337960	GM12878	blood:	n/a
26	chr18:44335109-44335159	HCPEpiC	choroid plexus:	n/a
27	chr18:44335109-44335159	NB4	blood:	n/a
28	chr18:44338147-44338197	Hela-S3	cervix:	n/a
29	chr18:44337664-44337714	HIPEpiC	eye:	n/a
30	chr18:44336399-44336449	NB4	blood:	n/a
31	chr18:44333130-44333180	HRCEpiC	kidney:	n/a
32	chr18:44336399-44336449	GM06990	blood:	n/a
33	chr18:44337099-44337149	NHDF-neo	bronchial:	n/a
34	chr18:44335109-44335159	H1-hESC	embryonic stem cell:	embryo
35	chr18:44334713-44334763	NT2-D1	testis:	n/a
36	chr18:44334713-44334763	LNCaP	prostate:	n/a
37	chr18:44339513-44339563	MCF-7	breast:	n/a
38	chr18:44333130-44333180	HMEC	breast:	n/a
39	chr18:44340177-44340227	HRE	kidney:	n/a
40	chr18:44337853-44337903	LNCaP	prostate:	n/a
41	chr18:44338147-44338197	BJ	skin:	n/a
42	chr18:44337910-44337960	NH-A	brain:	n/a
43	chr18:44337664-44337714	NT2-D1	testis:	n/a
44	chr18:44336399-44336449	IMR90	lung:	fetal
45	chr18:44340177-44340227	BE2_C	brain:	n/a
46	chr18:44337099-44337149	A549	lung:	n/a
47	chr18:44337922-44337972	HL-60	blood:	n/a
48	chr18:44336399-44336449	NH-A	brain:	n/a
49	chr18:44339513-44339563	AG04449	skin:	fetal
50	chr18:44340177-44340227	T-47D	breast:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr18:44339087..44341037-chr18:44341994..44343919,2	K562	blood:
2	chr18:44295920..44298422-chr18:44298971..44300843,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KATNAL2-1	chr18:44339687-44344371	NONHSAT059142
2	lnc-KATNAL2-1	chr18:44336746-44337039	ENSG00000270112.2
3	lnc-KATNAL2-1	chr18:44337689-44338426	NONHSAT059140
4	lnc-KATNAL2-1	chr18:44336450-44336587	ENSG00000270112.2
5	lnc-KATNAL2-1	chr18:44338764-44339028	NONHSAT059140
6	lnc-KATNAL2-1	chr18:44336896-44336994	ENSG00000270112.2
7	lnc-KATNAL2-1	chr18:44339774-44340307	ENSG00000270112.2
8	lnc-KATNAL2-1	chr18:44338415-44338422	XLOC_012667
9	lnc-KATNAL2-1	chr18:44339972-44340204	XLOC_012667
10	lnc-KATNAL2-10	chr18:44302938-44303186	NONHSAT059136

No data

Variant related genes	Relation type
ENSG00000270112	TF binding region
ST8SIA5	TF binding region
ENSG00000240983	TF binding region
ENSG00000270112	CpG island
ST8SIA5	CpG island
ENSG00000240983	CpG island
ENSG00000101638	chromatin interactions

Extended variants
information (count: 2593 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:2593 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12956914	chr18:44300281-44300282	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531266093	chr18:44300326-44300327	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs114442040	chr18:44300350-44300351	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs563276296	chr18:44300369-44300370	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs532070244	chr18:44300375-44300376	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs552241676	chr18:44300407-44300408	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs565686310	chr18:44300433-44300434	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs190135055	chr18:44300446-44300447	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs180881906	chr18:44300447-44300448	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs142770457	chr18:44300501-44300502	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs567982600	chr18:44300586-44300587	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs536967849	chr18:44300676-44300677	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs147373500	chr18:44300791-44300792	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs376664628	chr18:44300800-44300801	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs139052979	chr18:44300805-44300806	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs77395480	chr18:44300822-44300823	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs185932237	chr18:44300850-44300851	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs192108318	chr18:44300873-44300874	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs573284217	chr18:44300900-44300901	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs149448984	chr18:44300948-44300949	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs562290093	chr18:44300985-44300986	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs570373429	chr18:44301038-44301039	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs374634867	chr18:44301048-44301049	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs575962871	chr18:44301084-44301085	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs544931515	chr18:44301086-44301087	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs73953880	chr18:44301112-44301113	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs532132390	chr18:44301142-44301143	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs551915930	chr18:44301153-44301154	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs148573272	chr18:44301251-44301252	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs184044699	chr18:44301280-44301281	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs115360816	chr18:44301313-44301314	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs547950824	chr18:44301374-44301375	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs533073664	chr18:44301384-44301385	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs144501368	chr18:44301437-44301438	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs187471095	chr18:44301454-44301455	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs530674414	chr18:44301456-44301457	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs57918947	chr18:44301465-44301466	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs140120149	chr18:44301480-44301481	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs577996497	chr18:44301496-44301497	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs115489374	chr18:44301517-44301518	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs566922691	chr18:44301558-44301559	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs190428344	chr18:44301562-44301563	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs143726040	chr18:44301583-44301584	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs575900881	chr18:44301590-44301591	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs544867173	chr18:44301623-44301624	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs199972635	chr18:44301686-44301687	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs57030021	chr18:44301687-44301688	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs558469728	chr18:44301698-44301699	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs375072895	chr18:44301706-44301707	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs578213997	chr18:44301785-44301786	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16912164	CNVD
Lung cancer	18438408	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21508638	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16461302	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Pilomyxoid astrocytoma	17436254	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
Burkitt''s lymphoma	18698080	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	16891809	CNVD
Idiopathic thrombocytopenic purpura	19566914	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	21569311	CNVD
small cell lung cancer	17426248	CNVD
Prostate cancer	22341455	CNVD
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:720 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44297000-44301000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr18:44298400-44300400	Enhancers	Right Atrium	heart
3	chr18:44298400-44300600	Enhancers	Osteobl	bone
4	chr18:44298800-44300400	Enhancers	Brain Germinal Matrix	brain
5	chr18:44298800-44300400	Enhancers	Brain Substantia Nigra	brain
6	chr18:44298800-44300400	Enhancers	Left Ventricle	heart
7	chr18:44299400-44300400	Enhancers	HSMM	muscle
8	chr18:44299400-44300600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr18:44299400-44301000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr18:44299400-44309800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr18:44299600-44300400	Weak transcription	NH-A	brain
12	chr18:44299600-44300600	Weak transcription	HSMMtube	muscle
13	chr18:44299600-44300800	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr18:44299600-44301000	Enhancers	NHDF-Ad	bronchial
15	chr18:44299600-44301600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr18:44299600-44315800	Weak transcription	Brain Angular Gyrus	brain
17	chr18:44300000-44300400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr18:44300000-44300400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr18:44300200-44300400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr18:44300200-44300400	Enhancers	Psoas Muscle	Psoas
21	chr18:44300200-44300400	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr18:44300400-44300600	Enhancers	NH-A	brain
23	chr18:44300400-44301000	Weak transcription	Brain Germinal Matrix	brain
24	chr18:44300400-44301200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr18:44300400-44301600	Weak transcription	HSMM	muscle
26	chr18:44300400-44309800	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr18:44300600-44300800	Weak transcription	NH-A	brain
28	chr18:44300600-44301400	Enhancers	HSMMtube	muscle
29	chr18:44300600-44302400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr18:44300800-44301800	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr18:44301000-44301200	Enhancers	Brain Germinal Matrix	brain
32	chr18:44301200-44301400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr18:44301200-44301400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr18:44301200-44301400	Enhancers	Brain Hippocampus Middle	brain
35	chr18:44301200-44301400	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr18:44301200-44302000	Weak transcription	Brain Germinal Matrix	brain
37	chr18:44301600-44301800	Enhancers	HSMM	muscle
38	chr18:44301600-44302400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr18:44301800-44302000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
40	chr18:44301800-44312400	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr18:44302000-44303400	Enhancers	Brain Germinal Matrix	brain
42	chr18:44302400-44304000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr18:44303400-44309000	Weak transcription	Brain Germinal Matrix	brain
44	chr18:44304000-44304400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr18:44304400-44309400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr18:44307200-44307400	Enhancers	Left Ventricle	heart
47	chr18:44309000-44310000	Strong transcription	Brain Germinal Matrix	brain
48	chr18:44309200-44309600	Weak transcription	Left Ventricle	heart
49	chr18:44309400-44310600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr18:44309800-44310000	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain

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