Variant report

Variant	nsv1067278
Chromosome Location	chr18:44564162-44629283
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	ARID3A	chr18:44576810-44577094	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:44576874-44576992	K562	blood:	n/a	n/a
3	ARID3A	chr18:44626756-44626914	K562	blood:	n/a	n/a
4	ARID3A	chr18:44622174-44622535	HepG2	liver:	n/a	n/a
5	BHLHE40	chr18:44576859-44577090	GM12878	blood:	n/a	n/a
6	BHLHE40	chr18:44626733-44626933	GM12878	blood:	n/a	n/a
7	BHLHE40	chr18:44622279-44622498	HepG2	liver:	n/a	n/a
8	BHLHE40	chr18:44626653-44626985	K562	blood:	n/a	n/a
9	BRCA1	chr18:44576815-44577084	H1-hESC	embryonic stem cell:	n/a	n/a
10	CCNT2	chr18:44626661-44626940	K562	blood:	n/a	n/a
11	CEBPB	chr18:44605158-44605491	HepG2	liver:	n/a	chr18:44605310-44605323 chr18:44605310-44605321
12	CEBPB	chr18:44622196-44622467	HepG2	liver:	n/a	chr18:44622330-44622341 chr18:44622329-44622340
13	CEBPB	chr18:44610752-44611050	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr18:44622151-44622507	H1-hESC	embryonic stem cell:	n/a	chr18:44622330-44622341 chr18:44622329-44622340
15	CEBPB	chr18:44622140-44622530	HepG2	liver:	n/a	chr18:44622330-44622341 chr18:44622329-44622340
16	CEBPB	chr18:44621924-44622527	HepG2	liver:	n/a	chr18:44622330-44622341 chr18:44622329-44622340
17	CEBPB	chr18:44605165-44605373	K562	blood:	n/a	chr18:44605310-44605323 chr18:44605310-44605321
18	CEBPB	chr18:44569502-44569627	K562	blood:	n/a	n/a
19	CEBPB	chr18:44589464-44589717	HepG2	liver:	n/a	chr18:44589609-44589622 chr18:44589610-44589621
20	CEBPB	chr18:44605237-44605395	H1-hESC	embryonic stem cell:	n/a	chr18:44605310-44605323 chr18:44605310-44605321
21	CEBPB	chr18:44605149-44605473	IMR90	lung:	n/a	chr18:44605310-44605323 chr18:44605310-44605321
22	CEBPB	chr18:44622193-44622447	IMR90	lung:	n/a	chr18:44622330-44622341 chr18:44622329-44622340
23	CEBPB	chr18:44606715-44606946	K562	blood:	n/a	n/a
24	CEBPB	chr18:44622110-44622484	HepG2	liver:	n/a	chr18:44622330-44622341 chr18:44622329-44622340
25	CEBPD	chr18:44622162-44622398	HepG2	liver:	n/a	n/a
26	CHD1	chr18:44626698-44626702	GM12878	blood:	n/a	n/a
27	CHD2	chr18:44601544-44602123	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr18:44576860-44577010	HMEC	breast:	n/a	n/a
29	CTCF	chr18:44576900-44577050	HFF	foreskin:	n/a	chr18:44577006-44577014
30	CTCF	chr18:44576780-44576930	HAc	cerebellar:	n/a	n/a
31	CTCF	chr18:44626650-44626931	GM19240	blood:	n/a	chr18:44626781-44626799 chr18:44626784-44626797 chr18:44626782-44626798
32	CTCF	chr18:44626680-44626830	HFF-Myc	foreskin:	n/a	chr18:44626781-44626799 chr18:44626784-44626797 chr18:44626782-44626798
33	CTCF	chr18:44576880-44577030	GM12872	blood:	n/a	chr18:44577006-44577014
34	CTCF	chr18:44626571-44627006	GM12878	blood:	n/a	chr18:44626781-44626799 chr18:44626784-44626797 chr18:44626782-44626798
35	CTCF	chr18:44576880-44577030	NHLF	lung:	n/a	chr18:44577006-44577014
36	CTCF	chr18:44626651-44626944	Medullo	brain:	n/a	chr18:44626781-44626799 chr18:44626784-44626797 chr18:44626782-44626798
37	CTCF	chr18:44576840-44576990	GM12872	blood:	n/a	n/a
38	CTCF	chr18:44626700-44626850	Caco-2	colon:	n/a	chr18:44626781-44626799 chr18:44626784-44626797 chr18:44626782-44626798
39	CTCF	chr18:44610520-44610670	HMF	breast:	n/a	n/a
40	CTCF	chr18:44576800-44576950	GM12870	blood:	n/a	n/a
41	CTCF	chr18:44626657-44626930	MCF-7	breast:	n/a	chr18:44626781-44626799 chr18:44626784-44626797 chr18:44626782-44626798
42	CTCF	chr18:44576860-44577010	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr18:44626740-44626890	GM12865	blood:	n/a	chr18:44626781-44626799 chr18:44626784-44626797 chr18:44626782-44626798
44	CTCF	chr18:44625680-44625830	HEK293	kidney:	n/a	n/a
45	CTCF	chr18:44576838-44577058	HepG2	liver:	n/a	chr18:44577006-44577014
46	CTCF	chr18:44576840-44576990	GM12864	blood:	n/a	n/a
47	CTCF	chr18:44576903-44577010	GM19240	blood:	n/a	n/a
48	CTCF	chr18:44576895-44577006	GM19239	blood:	n/a	n/a
49	CTCF	chr18:44576820-44577070	GM12878	blood:	n/a	chr18:44577006-44577014
50	CTCF	chr18:44576835-44577189	MCF-7	breast:	n/a	chr18:44577006-44577014

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44564432-44564482	ProgFib	skin:	n/a
2	chr18:44564432-44564482	GM12878	blood:	n/a
3	chr18:44564432-44564482	HEEpiC	esophagus:	n/a
4	chr18:44564432-44564482	NHBE	bronchial:	n/a
5	chr18:44626898-44626948	ovcar-3	ovarian:	n/a
6	chr18:44564432-44564482	NT2-D1	testis:	n/a
7	chr18:44564432-44564482	MCF10A-Er-Src	breast:	n/a
8	chr18:44618587-44618637	GM12891	blood:	n/a
9	chr18:44564432-44564482	HepG2	liver:	n/a
10	chr18:44627440-44627490	BE2_C	brain:	n/a
11	chr18:44564432-44564482	GM12892	blood:	n/a
12	chr18:44564432-44564482	A549	lung:	n/a
13	chr18:44564432-44564482	HMEC	breast:	n/a
14	chr18:44627440-44627490	U87	brain:	n/a
15	chr18:44618587-44618637	PANC-1	pancreas:	n/a
16	chr18:44626898-44626948	SK-N-SH	brain:	n/a
17	chr18:44627440-44627490	MCF10A-Er-Src	breast:	n/a
18	chr18:44626898-44626948	NB4	blood:	n/a
19	chr18:44564432-44564482	HCF	heart:	n/a
20	chr18:44618587-44618637	ovcar-3	ovarian:	n/a
21	chr18:44626898-44626948	HCT-116	colon:	n/a
22	chr18:44564432-44564482	IMR90	lung:	fetal
23	chr18:44626898-44626948	HL-60	blood:	n/a
24	chr18:44618587-44618637	Hela-S3	cervix:	n/a
25	chr18:44618587-44618637	U87	brain:	n/a
26	chr18:44618587-44618637	HCT-116	colon:	n/a
27	chr18:44564432-44564482	AG09309	skin:	n/a
28	chr18:44627440-44627490	NH-A	brain:	n/a
29	chr18:44626898-44626948	SK-N-SH_RA	brain:	n/a
30	chr18:44618587-44618637	ProgFib	skin:	n/a
31	chr18:44627440-44627490	HRCEpiC	kidney:	n/a
32	chr18:44627440-44627490	SK-N-SH_RA	brain:	n/a
33	chr18:44626898-44626948	LNCaP	prostate:	n/a
34	chr18:44618587-44618637	H1-hESC	embryonic stem cell:	embryo
35	chr18:44564432-44564482	GM12891	blood:	n/a
36	chr18:44627440-44627490	MCF-7	breast:	n/a
37	chr18:44626898-44626948	NHBE	bronchial:	n/a
38	chr18:44564432-44564482	SKMC	muscle:	n/a
39	chr18:44627440-44627490	GM12892	blood:	n/a
40	chr18:44626898-44626948	K562	blood:	n/a
41	chr18:44618587-44618637	GM12878	blood:	n/a
42	chr18:44564432-44564482	K562	blood:	n/a
43	chr18:44564432-44564482	HCPEpiC	choroid plexus:	n/a
44	chr18:44626898-44626948	IMR90	lung:	fetal
45	chr18:44627440-44627490	HEK293	kidney:	embryo
46	chr18:44627440-44627490	HRE	kidney:	n/a
47	chr18:44564432-44564482	BE2_C	brain:	n/a
48	chr18:44626898-44626948	SK-N-MC	brain:	n/a
49	chr18:44618587-44618637	HCPEpiC	choroid plexus:	n/a
50	chr18:44564432-44564482	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:44624367..44626651-chr18:44785801..44788433,2	K562	blood:
2	chr18:44618074..44620983-chr18:44621410..44624299,2	K562	blood:
3	chr18:44626654..44628817-chr18:44712742..44715143,2	MCF-7	breast:
4	chr18:44576766..44577535-chr18:44731006..44731680,3	K562	blood:
5	chr18:44621381..44624013-chr18:44625607..44627534,2	K562	blood:
6	chr18:44599383..44602020-chr18:44603317..44605439,2	K562	blood:
7	chr18:44626316..44626888-chr18:44718053..44718688,2	K562	blood:
8	chr18:44626315..44627260-chr18:44809604..44810507,2	K562	blood:
9	chr18:44618074..44620983-chr18:44621410..44624299,2	K562	blood:
10	chr18:44626381..44627618-chr18:44730985..44732225,13	K562	blood:
11	chr18:44626319..44627308-chr18:44730999..44731988,9	MCF-7	breast:
12	chr18:44625943..44627276-chr18:44731016..44731992,4	MCF-7	breast:
13	chr18:44576380..44577341-chr18:45275241..45276255,4	K562	blood:
14	chr18:44625997..44627852-chr18:44731582..44733974,3	K562	blood:
15	chr18:44576795..44577462-chr18:44731213..44731981,2	MCF-7	breast:
16	chr18:44599383..44602020-chr18:44603317..44605439,2	K562	blood:
17	chr18:44621381..44624013-chr18:44625607..44627534,2	K562	blood:
18	chr18:44623688..44626651-chr18:44786266..44788433,2	K562	blood:
19	chr18:44580930..44582720-chr18:44583404..44586323,2	K562	blood:
20	chr18:44626566..44628357-chr18:44631236..44632776,2	MCF-7	breast:
21	chr1:205310411..205312346-chr18:44615284..44616803,2	MCF-7	breast:
22	chr18:44626392..44627213-chr18:44718440..44718955,2	MCF-7	breast:
23	chr18:44612247..44614708-chr18:44617059..44619635,2	K562	blood:
24	chr18:44576733..44577369-chr18:44809595..44810437,2	K562	blood:

Variant related genes	Relation type
ENSG00000267724	TF binding region
TCEB3B	TF binding region
KATNAL2	TF binding region
ENSG00000266957	TF binding region
ENSG00000267724	CpG island
TCEB3B	CpG island
KATNAL2	CpG island
ENSG00000266957	CpG island
ENSG00000266957	chromatin interactions
ENSG00000267724	chromatin interactions
ENSG00000167216	chromatin interactions

Extended variants
information (count: 2010 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:2010 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs998818	chr18:44564162-44564163	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs998819	chr18:44564181-44564182	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs5824648	chr18:44564221-44564222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs569924199	chr18:44564232-44564233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs531056789	chr18:44564302-44564303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181399296	chr18:44564338-44564339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs571099779	chr18:44564348-44564349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184136729	chr18:44564349-44564350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs115026119	chr18:44564357-44564358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115814983	chr18:44564388-44564389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs527342106	chr18:44564404-44564405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535605586	chr18:44564429-44564430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534286881	chr18:44564445-44564446	Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs367598683	chr18:44564448-44564449	Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs555537247	chr18:44564450-44564451	Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs114574897	chr18:44564464-44564465	Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs1465722	chr18:44564499-44564500	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs540307878	chr18:44564546-44564547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76461501	chr18:44564554-44564555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs539624725	chr18:44564595-44564596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545979549	chr18:44564765-44564766	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs552962178	chr18:44564769-44564770	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs573127965	chr18:44564842-44564843	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs189839511	chr18:44564924-44564925	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs56164202	chr18:44564935-44564936	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs138206859	chr18:44564936-44564937	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs370984285	chr18:44566485-44566486	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs533489335	chr18:44566578-44566579	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs370511909	chr18:44574540-44574541	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs553857574	chr18:44574549-44574550	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs573849019	chr18:44574571-44574572	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs117320106	chr18:44574586-44574587	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs556801471	chr18:44574626-44574627	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs576694038	chr18:44574660-44574661	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs544191702	chr18:44574674-44574675	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs563966706	chr18:44574740-44574741	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs532970162	chr18:44574818-44574819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs72921352	chr18:44574839-44574840	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs376603101	chr18:44574843-44574844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190301142	chr18:44574914-44574915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531083125	chr18:44574927-44574928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181674683	chr18:44575001-44575002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549914450	chr18:44575013-44575014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369605899	chr18:44575021-44575022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548938918	chr18:44575061-44575062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs569109506	chr18:44575123-44575124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569809092	chr18:44575154-44575155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531551267	chr18:44575161-44575162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs75204234	chr18:44575199-44575200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs56336421	chr18:44575223-44575224	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
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44564000-44564600	Enhancers	GM12878-XiMat	blood
2	chr18:44574600-44577000	Weak transcription	Brain Anterior Caudate	brain
3	chr18:44577000-44577400	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr18:44577000-44577400	Enhancers	Brain Angular Gyrus	brain
5	chr18:44577000-44577400	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr18:44577400-44594000	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr18:44579800-44630200	Weak transcription	Right Ventricle	heart
8	chr18:44580200-44580400	Enhancers	H9 Cell Line	embryonic stem cell
9	chr18:44580200-44581400	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr18:44580200-44581600	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr18:44580600-44595400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr18:44584000-44594200	Weak transcription	Ovary	ovary
13	chr18:44584200-44586800	Weak transcription	Pancreas	Pancrea
14	chr18:44584800-44594000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr18:44585000-44585200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr18:44585200-44600000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr18:44585600-44586000	ZNF genes & repeats	Aorta	Aorta
18	chr18:44586000-44593400	Weak transcription	Aorta	Aorta
19	chr18:44586200-44588400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr18:44586800-44629600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr18:44587200-44630600	Weak transcription	Brain Anterior Caudate	brain
22	chr18:44587600-44629400	Weak transcription	Liver	Liver
23	chr18:44587800-44603400	Weak transcription	Brain Cingulate Gyrus	brain
24	chr18:44588200-44621600	Weak transcription	Left Ventricle	heart
25	chr18:44588400-44591000	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr18:44588600-44589400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr18:44588600-44589600	Enhancers	Fetal Brain Male	brain
28	chr18:44589200-44589600	Enhancers	Fetal Brain Female	brain
29	chr18:44589400-44591600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr18:44591000-44595400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr18:44591800-44602800	Weak transcription	Brain Angular Gyrus	brain
32	chr18:44592600-44594800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr18:44592800-44594000	Weak transcription	Brain Substantia Nigra	brain
34	chr18:44593400-44593600	ZNF genes & repeats	Aorta	Aorta
35	chr18:44594000-44594200	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
36	chr18:44594000-44594400	ZNF genes & repeats	Brain Substantia Nigra	brain
37	chr18:44594200-44594400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr18:44594200-44594400	ZNF genes & repeats	Ovary	ovary
39	chr18:44594200-44603800	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr18:44594400-44595000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr18:44594400-44601600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr18:44594400-44603200	Weak transcription	Brain Substantia Nigra	brain
43	chr18:44594600-44602800	Weak transcription	Adipose Nuclei	Adipose
44	chr18:44594800-44595400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr18:44595000-44596000	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr18:44595200-44595800	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr18:44595400-44595800	Enhancers	H9 Cell Line	embryonic stem cell
48	chr18:44595400-44596200	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr18:44595600-44595800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr18:44595800-44601400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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