Variant report

Variant	nsv909607
Chromosome Location	chr18:44320836-44422661
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:544)
CpG islands
(count:855)
Chromatin interactive
region (count:13)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:544 , 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	ARID3A	chr18:44343741-44343800	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:44411369-44411783	HepG2	liver:	n/a	n/a
3	BACH1	chr18:44336050-44336250	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr18:44335079-44335249	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr18:44367638-44367984	GM12878	blood:	n/a	n/a
6	BHLHE40	chr18:44334478-44334576	GM12878	blood:	n/a	n/a
7	CEBPB	chr18:44420152-44420395	IMR90	lung:	n/a	n/a
8	CEBPB	chr18:44420259-44420352	K562	blood:	n/a	n/a
9	CEBPB	chr18:44331573-44331857	HepG2	liver:	n/a	chr18:44331721-44331732
10	CEBPB	chr18:44369682-44369880	HepG2	liver:	n/a	chr18:44369709-44369720
11	CEBPB	chr18:44376072-44376263	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr18:44376035-44376269	IMR90	lung:	n/a	n/a
13	CEBPB	chr18:44380339-44380513	HepG2	liver:	n/a	chr18:44380462-44380473
14	CEBPB	chr18:44346904-44347188	K562	blood:	n/a	n/a
15	CEBPB	chr18:44403561-44403753	HepG2	liver:	n/a	chr18:44403707-44403718
16	CEBPB	chr18:44376072-44376254	A549	lung:	n/a	n/a
17	CHD1	chr18:44336734-44336908	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr18:44336861-44337128	H1-hESC	embryonic stem cell:	n/a	chr18:44337023-44337033
19	CHD2	chr18:44334253-44334329	GM12878	blood:	n/a	n/a
20	CTBP2	chr18:44337460-44338259	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTBP2	chr18:44336144-44337128	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr18:44335320-44335470	GM12874	blood:	n/a	n/a
23	CTCF	chr18:44352547-44352559	GM12878	blood:	n/a	n/a
24	CTCF	chr18:44335012-44335259	K562	blood:	n/a	n/a
25	CTCF	chr18:44373743-44373786	ProgFib	skin:	n/a	n/a
26	CTCF	chr18:44373730-44373824	MCF-7	breast:	n/a	n/a
27	CTCF	chr18:44373679-44373894	GM12878	blood:	n/a	chr18:44373713-44373720
28	CTCF	chr18:44373640-44373790	HepG2	liver:	n/a	chr18:44373713-44373720
29	CTCF	chr18:44410040-44410190	HRE	kidney:	n/a	n/a
30	CTCF	chr18:44335080-44335230	RPTEC	kidney:	n/a	n/a
31	CTCF	chr18:44373724-44373835	MCF-7	breast:	n/a	n/a
32	CTCF	chr18:44335080-44335230	GM06990	blood:	n/a	n/a
33	CTCF	chr18:44335060-44335210	GM12872	blood:	n/a	n/a
34	CTCF	chr18:44335061-44335262	K562	blood:	n/a	n/a
35	CTCF	chr18:44336880-44337030	SK-N-SH_RA	brain:	n/a	chr18:44336940-44336953
36	CTCF	chr18:44365042-44365077	GM10248	blood:	n/a	n/a
37	CTCF	chr18:44373740-44373890	GM12872	blood:	n/a	n/a
38	CTCF	chr18:44352451-44352525	Fibrobl	skin:	n/a	chr18:44352478-44352499
39	CTCF	chr18:44373660-44373810	HPF	lung:	n/a	chr18:44373713-44373720
40	CTCF	chr18:44373660-44373810	NHEK	skin:	n/a	chr18:44373713-44373720
41	CTCF	chr18:44373700-44373850	HPAF	blood vessel:	n/a	chr18:44373713-44373720
42	CTCF	chr18:44373640-44373790	HL-60	blood:	n/a	chr18:44373713-44373720
43	CTCF	chr18:44373664-44373854	MCF-7	breast:	n/a	chr18:44373713-44373720
44	CTCF	chr18:44335100-44335250	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr18:44335120-44335270	SAEC	small airway:	n/a	n/a
46	CTCF	chr18:44373698-44373815	Hela-S3	cervix:	n/a	chr18:44373713-44373720
47	CTCF	chr18:44335060-44335210	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr18:44373723-44373784	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr18:44409980-44410130	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr18:44409740-44409890	HRE	kidney:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44337853-44337903	CMK	blood:	n/a
2	chr18:44337853-44337903	CMK	blood:	n/a
3	chr18:44339513-44339563	HMEC	breast:	n/a
4	chr18:44337910-44337960	HCM	heart:	n/a
5	chr18:44337853-44337903	GM06990	blood:	n/a
6	chr18:44392124-44392174	HEK293	kidney:	embryo
7	chr18:44335109-44335159	Caco-2	colon:	n/a
8	chr18:44337099-44337149	SK-N-SH	brain:	n/a
9	chr18:44337922-44337972	LNCaP	prostate:	n/a
10	chr18:44340177-44340227	HEEpiC	esophagus:	n/a
11	chr18:44392124-44392174	AoSMC	blood vessel:	n/a
12	chr18:44337853-44337903	HCF	heart:	n/a
13	chr18:44334713-44334763	HL-60	blood:	n/a
14	chr18:44335109-44335159	ProgFib	skin:	n/a
15	chr18:44335109-44335159	MCF-7	breast:	n/a
16	chr18:44335109-44335159	AG09319	gingival:	n/a
17	chr18:44337099-44337149	HCF	heart:	n/a
18	chr18:44392124-44392174	HRE	kidney:	n/a
19	chr18:44339513-44339563	IMR90	lung:	fetal
20	chr18:44337099-44337149	HRE	kidney:	n/a
21	chr18:44333130-44333180	BJ	skin:	n/a
22	chr18:44335109-44335159	BE2_C	brain:	n/a
23	chr18:44334713-44334763	RPTEC	kidney:	n/a
24	chr18:44340177-44340227	NHDF-neo	bronchial:	n/a
25	chr18:44338099-44338149	U87	brain:	n/a
26	chr18:44337099-44337149	K562	blood:	n/a
27	chr18:44337853-44337903	MCF-7	breast:	n/a
28	chr18:44338099-44338149	LNCaP	prostate:	n/a
29	chr18:44337922-44337972	T-47D	breast:	n/a
30	chr18:44337664-44337714	HAEpiC	amniotic membrane:	n/a
31	chr18:44337910-44337960	ECC-1	luminal epithelium:	n/a
32	chr18:44338099-44338149	NT2-D1	testis:	n/a
33	chr18:44337099-44337149	PFSK-1	brain:	n/a
34	chr18:44333130-44333180	HCF	heart:	n/a
35	chr18:44338099-44338149	Hepatocyte	liver:	n/a
36	chr18:44337922-44337972	GM12891	blood:	n/a
37	chr18:44339513-44339563	PFSK-1	brain:	n/a
38	chr18:44337922-44337972	K562	blood:	n/a
39	chr18:44337922-44337972	CMK	blood:	n/a
40	chr18:44337910-44337960	HIPEpiC	eye:	n/a
41	chr18:44392124-44392174	AG10803	skin:	n/a
42	chr18:44337910-44337960	AoSMC	blood vessel:	n/a
43	chr18:44337922-44337972	PFSK-1	brain:	n/a
44	chr18:44335109-44335159	PANC-1	pancreas:	n/a
45	chr18:44335109-44335159	GM12891	blood:	n/a
46	chr18:44338099-44338149	AG04450	lung:	fetal
47	chr18:44337664-44337714	HCT-116	colon:	n/a
48	chr18:44335109-44335159	HRPEpiC	eye:	n/a
49	chr18:44336399-44336449	ECC-1	luminal epithelium:	n/a
50	chr18:44339513-44339563	GM06990	blood:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:44414570..44416469-chr18:44421585..44424246,2	K562	blood:
2	chr18:44384558..44388431-chr18:44394161..44395866,3	K562	blood:
3	chr18:44407516..44409436-chr18:44454245..44456431,2	K562	blood:
4	chr18:44412054..44414419-chr18:44417196..44419147,2	K562	blood:
5	chr18:44414570..44416469-chr18:44421585..44424246,2	K562	blood:
6	chr18:44385414..44388216-chr18:44388494..44390320,2	MCF-7	breast:
7	chr18:44339087..44341037-chr18:44341994..44343919,2	K562	blood:
8	chr18:44385414..44388216-chr18:44388494..44390320,2	MCF-7	breast:
9	chr18:44409358..44411330-chr18:44412581..44415126,2	K562	blood:
10	chr18:44384558..44388431-chr18:44394161..44395866,3	K562	blood:
11	chr18:44409358..44411330-chr18:44412581..44415126,2	K562	blood:
12	chr18:44421049..44423857-chr18:44426853..44428509,2	K562	blood:
13	chr18:44412054..44414419-chr18:44417196..44419147,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KATNAL2-1	chr18:44337689-44338426	NONHSAT059140
2	lnc-PIAS2-1	chr18:44383187-44383857	ENSG00000267167.1
3	lnc-KATNAL2-1	chr18:44339972-44340204	XLOC_012667
4	lnc-KATNAL2-1	chr18:44336896-44336994	ENSG00000270112.2
5	lnc-KATNAL2-1	chr18:44336450-44336587	ENSG00000270112.2
6	lnc-KATNAL2-1	chr18:44338415-44338422	XLOC_012667
7	lnc-KATNAL2-1	chr18:44336746-44337039	ENSG00000270112.2
8	lnc-KATNAL2-1	chr18:44339687-44344371	NONHSAT059142
9	lnc-KATNAL2-1	chr18:44339774-44340307	ENSG00000270112.2
10	lnc-KATNAL2-1	chr18:44338764-44339028	NONHSAT059140
11	lnc-KATNAL2-7	chr18:44383140-44387340	NONHSAT059143

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PIAS2	hsa-miR-26b-5p	chr18:44392379-44392395

Variant related genes	Relation type
ENSG00000270112	TF binding region
ST8SIA5	TF binding region
ENSG00000267167	TF binding region
ENSG00000270112	CpG island
ST8SIA5	CpG island
ENSG00000267167	CpG island
ENSG00000101638	chromatin interactions

Extended variants
information (count: 3588 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:3588 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs662397	chr18:44320836-44320837	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs193284249	chr18:44320838-44320839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149744382	chr18:44320947-44320948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556663758	chr18:44320950-44320951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185503738	chr18:44320967-44320968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545608833	chr18:44321075-44321076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576931955	chr18:44321138-44321139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545760039	chr18:44321155-44321156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs74688960	chr18:44321160-44321161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541817633	chr18:44321161-44321162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115842633	chr18:44321290-44321291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189338599	chr18:44321376-44321377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs116237154	chr18:44321444-44321445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576651876	chr18:44321460-44321461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs11082554	chr18:44321468-44321469	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs192239857	chr18:44321566-44321567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547197046	chr18:44321630-44321631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567008516	chr18:44321704-44321705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536134716	chr18:44321713-44321714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570615332	chr18:44321748-44321749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555831631	chr18:44321756-44321757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370459420	chr18:44321804-44321805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536679380	chr18:44321828-44321829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146736550	chr18:44321884-44321885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576551277	chr18:44321934-44321935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545631174	chr18:44321938-44321939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374948706	chr18:44321939-44321940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572995863	chr18:44322013-44322014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542105192	chr18:44322014-44322015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561862421	chr18:44322031-44322032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201034484	chr18:44322062-44322063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577565	chr18:44322069-44322070	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs577568	chr18:44322073-44322074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564547416	chr18:44322098-44322099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs139283223	chr18:44322155-44322156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372680319	chr18:44322181-44322182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573814761	chr18:44322208-44322209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184351249	chr18:44322241-44322242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144054301	chr18:44322244-44322245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75854710	chr18:44322277-44322278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570009	chr18:44322320-44322321	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs569221878	chr18:44322348-44322349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs62097208	chr18:44322376-44322377	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs552224116	chr18:44322391-44322392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs33969146	chr18:44322392-44322393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201226512	chr18:44322393-44322394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550163971	chr18:44322394-44322395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371961982	chr18:44322400-44322401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560253653	chr18:44322435-44322436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570171497	chr18:44322461-44322462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1197 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44319200-44329600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr18:44329600-44334400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr18:44330400-44330800	Enhancers	Brain Germinal Matrix	brain
4	chr18:44330600-44330800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr18:44330600-44330800	Enhancers	Brain Angular Gyrus	brain
6	chr18:44330800-44331800	Weak transcription	Brain Germinal Matrix	brain
7	chr18:44330800-44334200	Weak transcription	Brain Angular Gyrus	brain
8	chr18:44331800-44332400	Active TSS	Brain Germinal Matrix	brain
9	chr18:44332000-44332200	Bivalent Enhancer	HMEC	breast
10	chr18:44332000-44332600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr18:44332000-44332800	Bivalent Enhancer	NHEK	skin
12	chr18:44332000-44333000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr18:44332200-44332400	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr18:44332200-44332400	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr18:44332200-44332400	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr18:44332200-44332400	Enhancers	HMEC	breast
17	chr18:44332200-44332600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr18:44332400-44333000	Flanking Active TSS	Brain Germinal Matrix	brain
19	chr18:44332400-44333000	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr18:44332400-44333000	Bivalent/Poised TSS	Fetal Brain Female	brain
21	chr18:44332400-44334200	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr18:44332600-44332800	Enhancers	Right Atrium	heart
23	chr18:44332600-44335000	Weak transcription	HSMMtube	muscle
24	chr18:44332800-44333200	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr18:44332800-44334600	Weak transcription	Right Atrium	heart
26	chr18:44333000-44333200	Active TSS	Brain Germinal Matrix	brain
27	chr18:44333000-44334000	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr18:44333200-44333400	Flanking Active TSS	Brain Germinal Matrix	brain
29	chr18:44333200-44333600	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr18:44333400-44333600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr18:44333400-44333600	Active TSS	Brain Germinal Matrix	brain
32	chr18:44333600-44333800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr18:44333600-44333800	Flanking Active TSS	Brain Germinal Matrix	brain
34	chr18:44333600-44333800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
35	chr18:44333600-44334600	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr18:44333600-44337400	Bivalent/Poised TSS	Fetal Brain Female	brain
37	chr18:44333800-44334000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
38	chr18:44333800-44334000	Active TSS	Brain Germinal Matrix	brain
39	chr18:44333800-44334000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr18:44333800-44334600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr18:44333800-44334600	Bivalent Enhancer	Fetal Muscle Leg	muscle
42	chr18:44333800-44335800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
43	chr18:44334000-44334200	Enhancers	H9 Cell Line	embryonic stem cell
44	chr18:44334000-44334200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr18:44334000-44334200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
46	chr18:44334000-44334200	Enhancers	GM12878-XiMat	blood
47	chr18:44334000-44334200	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr18:44334000-44334400	Enhancers	Brain Cingulate Gyrus	brain
49	chr18:44334000-44334400	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr18:44334000-44334600	Flanking Active TSS	Brain Germinal Matrix	brain

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