Variant report

Variant	nsv1062682
Chromosome Location	chr18:44509052-44539223
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	chr18:44530288-44530439	K562	blood:	n/a	n/a
2	BRCA1	chr18:44526800-44527412	H1-hESC	embryonic stem cell:	n/a	n/a
3	CBX3	chr18:44519517-44519902	HCT-116	colon:	n/a	n/a
4	CEBPB	chr18:44519633-44519970	IMR90	lung:	n/a	n/a
5	CEBPB	chr18:44519588-44519974	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr18:44533294-44533502	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr18:44519678-44519944	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr18:44517559-44517759	K562	blood:	n/a	chr18:44517683-44517694
9	CEBPB	chr18:44517540-44517817	IMR90	lung:	n/a	chr18:44517683-44517694
10	CEBPB	chr18:44517542-44517844	HepG2	liver:	n/a	chr18:44517683-44517694
11	CHD2	chr18:44526653-44526788	K562	blood:	n/a	n/a
12	CHD2	chr18:44526479-44527130	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr18:44530120-44530270	HCPEpiC	choroid plexus:	n/a	chr18:44530204-44530222
14	CTCF	chr18:44530120-44530270	GM12866	blood:	n/a	chr18:44530204-44530222
15	CTCF	chr18:44530080-44530230	WI-38	lung:	n/a	chr18:44530204-44530222
16	CTCF	chr18:44530102-44530337	LNCaP	prostate:	n/a	chr18:44530204-44530222
17	CTCF	chr18:44530160-44530310	MCF-7	breast:	n/a	chr18:44530204-44530222
18	CTCF	chr18:44530140-44530290	GM12865	blood:	n/a	chr18:44530204-44530222
19	CTCF	chr18:44530100-44530250	HMEC	breast:	n/a	chr18:44530204-44530222
20	CTCF	chr18:44530125-44530305	LNCaP	prostate:	n/a	chr18:44530204-44530222
21	CTCF	chr18:44530060-44530210	GM12864	blood:	n/a	n/a
22	CTCF	chr18:44529900-44530050	HEK293	kidney:	n/a	n/a
23	CTCF	chr18:44530115-44530273	HepG2	liver:	n/a	chr18:44530204-44530222
24	CTCF	chr18:44530120-44530270	GM12878	blood:	n/a	chr18:44530204-44530222
25	CTCF	chr18:44530238-44530355	GM19239	blood:	n/a	n/a
26	CTCF	chr18:44530160-44530310	GM06990	blood:	n/a	chr18:44530204-44530222
27	CTCF	chr18:44530100-44530250	NHDF-neo	bronchial:	n/a	chr18:44530204-44530222
28	CTCF	chr18:44530140-44530290	HPF	lung:	n/a	chr18:44530204-44530222
29	CTCF	chr18:44530092-44530324	GM13977	blood:	n/a	chr18:44530204-44530222
30	CTCF	chr18:44530100-44530389	GM12878	blood:	n/a	chr18:44530204-44530222
31	CTCF	chr18:44530160-44530310	GM12874	blood:	n/a	chr18:44530204-44530222
32	CTCF	chr18:44530120-44530270	AoAF	blood vessel:	n/a	chr18:44530204-44530222
33	CTCF	chr18:44530013-44530362	MCF-7	breast:	n/a	chr18:44530204-44530222
34	CTCF	chr18:44530100-44530250	BE2_C	brain:	n/a	chr18:44530204-44530222
35	CTCF	chr18:44530100-44530250	GM12878	blood:	n/a	chr18:44530204-44530222
36	CTCF	chr18:44530200-44530350	GM12868	blood:	n/a	chr18:44530204-44530222
37	CTCF	chr18:44530108-44530356	Hela-S3	cervix:	n/a	chr18:44530204-44530222
38	CTCF	chr18:44530160-44530310	GM12873	blood:	n/a	chr18:44530204-44530222
39	CTCF	chr18:44530120-44530270	Hela-S3	cervix:	n/a	chr18:44530204-44530222
40	CTCF	chr18:44529600-44529750	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr18:44530140-44530290	HCFaa	heart:	n/a	chr18:44530204-44530222
42	CTCF	chr18:44530152-44530311	Kidney_OC	kidney:	n/a	chr18:44530204-44530222
43	CTCF	chr18:44530180-44530330	HUVEC	blood vessel:	n/a	chr18:44530204-44530222
44	CTCF	chr18:44530160-44530310	HMF	breast:	n/a	chr18:44530204-44530222
45	CTCF	chr18:44530160-44530310	AG09309	skin:	n/a	chr18:44530204-44530222
46	CTCF	chr18:44530160-44530310	HPAF	blood vessel:	n/a	chr18:44530204-44530222
47	CTCF	chr18:44530140-44530290	GM12864	blood:	n/a	chr18:44530204-44530222
48	CTCF	chr18:44530046-44530388	IMR90	lung:	n/a	chr18:44530204-44530222
49	CTCF	chr18:44530140-44530290	HFF	foreskin:	n/a	chr18:44530204-44530222
50	CTCF	chr18:44530071-44530310	A549	lung:	n/a	chr18:44530204-44530222

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44526867-44526917	HCF	heart:	n/a
2	chr18:44526867-44526917	PrEC	prostate:	n/a
3	chr18:44526605-44526655	AG09319	gingival:	n/a
4	chr18:44526867-44526917	HCF	heart:	n/a
5	chr18:44526867-44526917	PrEC	prostate:	n/a
6	chr18:44526605-44526655	AG09319	gingival:	n/a
7	chr18:44526743-44526793	U87	brain:	n/a
8	chr18:44526700-44526750	HCPEpiC	choroid plexus:	n/a
9	chr18:44523070-44523120	HRPEpiC	eye:	n/a
10	chr18:44527026-44527076	HNPCEpiC	eye:	n/a
11	chr18:44526707-44526757	CMK	blood:	n/a
12	chr18:44526743-44526793	SK-N-SH_RA	brain:	n/a
13	chr18:44526430-44526480	SKMC	muscle:	n/a
14	chr18:44527026-44527076	HRE	kidney:	n/a
15	chr18:44525710-44525760	HUVEC	blood vessel:	n/a
16	chr18:44526605-44526655	Hepatocyte	liver:	n/a
17	chr18:44526743-44526793	AG09319	gingival:	n/a
18	chr18:44526743-44526793	HCPEpiC	choroid plexus:	n/a
19	chr18:44530218-44530268	GM19239	blood:	n/a
20	chr18:44525710-44525760	AG09309	skin:	n/a
21	chr18:44530218-44530268	SK-N-MC	brain:	n/a
22	chr18:44527971-44528021	GM06990	blood:	n/a
23	chr18:44527971-44528021	MCF-7	breast:	n/a
24	chr18:44526700-44526750	HRE	kidney:	n/a
25	chr18:44525710-44525760	GM12892	blood:	n/a
26	chr18:44526756-44526806	NB4	blood:	n/a
27	chr18:44530218-44530268	NH-A	brain:	n/a
28	chr18:44530218-44530268	ProgFib	skin:	n/a
29	chr18:44526707-44526757	ECC-1	luminal epithelium:	n/a
30	chr18:44525710-44525760	GM12891	blood:	n/a
31	chr18:44526430-44526480	NB4	blood:	n/a
32	chr18:44526430-44526480	AG04449	skin:	fetal
33	chr18:44526743-44526793	GM12891	blood:	n/a
34	chr18:44525710-44525760	HMEC	breast:	n/a
35	chr18:44526430-44526480	HCM	heart:	n/a
36	chr18:44525710-44525760	NT2-D1	testis:	n/a
37	chr18:44526605-44526655	AG09309	skin:	n/a
38	chr18:44526743-44526793	NT2-D1	testis:	n/a
39	chr18:44526756-44526806	MCF-7	breast:	n/a
40	chr18:44525710-44525760	Caco-2	colon:	n/a
41	chr18:44526867-44526917	IMR90	lung:	fetal
42	chr18:44526743-44526793	HepG2	liver:	n/a
43	chr18:44527971-44528021	AG04450	lung:	fetal
44	chr18:44526430-44526480	A549	lung:	n/a
45	chr18:44530218-44530268	U87	brain:	n/a
46	chr18:44527971-44528021	HIPEpiC	eye:	n/a
47	chr18:44526743-44526793	HAEpiC	amniotic membrane:	n/a
48	chr18:44523070-44523120	HepG2	liver:	n/a
49	chr18:44526743-44526793	Jurkat	blood:	n/a
50	chr18:44526707-44526757	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr18:44529742..44530665-chr18:44562546..44563169,2	MCF-7	breast:
2	chr18:44497069..44499203-chr18:44524229..44526403,2	MCF-7	breast:
3	chr18:44494535..44496872-chr18:44526864..44529810,3	MCF-7	breast:
4	chr18:44526928..44528966-chr18:44543505..44545090,2	MCF-7	breast:

Variant related genes	Relation type
KATNAL2	TF binding region
KATNAL2	CpG island
ENSG00000167216	chromatin interactions
ENSG00000266996	chromatin interactions
ENSG00000078043	chromatin interactions

Extended variants
information (count: 928 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:928 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111960018	chr18:44509054-44509055	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs140428271	chr18:44509055-44509056	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs201720290	chr18:44509071-44509072	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs543105043	chr18:44509087-44509088	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs370740094	chr18:44509129-44509130	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs576706748	chr18:44509148-44509149	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs111850971	chr18:44509175-44509176	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs527949251	chr18:44509194-44509195	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs192489402	chr18:44515031-44515032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs151187449	chr18:44515045-44515046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141241812	chr18:44515051-44515052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568142172	chr18:44515069-44515070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs146945961	chr18:44515073-44515074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564067331	chr18:44515081-44515082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs58166811	chr18:44515135-44515136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs72537364	chr18:44515136-44515137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs372998937	chr18:44515161-44515162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs72917151	chr18:44515191-44515192	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs8096263	chr18:44515216-44515217	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs137909262	chr18:44515223-44515224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs78868320	chr18:44515228-44515229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567832216	chr18:44515360-44515361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs548732539	chr18:44515371-44515372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs150085064	chr18:44515393-44515394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555471607	chr18:44515435-44515436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs138346052	chr18:44515436-44515437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs572084298	chr18:44515471-44515472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540984096	chr18:44515472-44515473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533970206	chr18:44515498-44515499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs554295407	chr18:44515511-44515512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs574150157	chr18:44515521-44515522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184469573	chr18:44515559-44515560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563023643	chr18:44515575-44515576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs370111990	chr18:44515595-44515596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs545671376	chr18:44515602-44515603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142923321	chr18:44515603-44515604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565484682	chr18:44515605-44515606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532919721	chr18:44515629-44515630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546224500	chr18:44515637-44515638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558084747	chr18:44515655-44515656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528927657	chr18:44515656-44515657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549945856	chr18:44515660-44515661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569025508	chr18:44515661-44515662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531452429	chr18:44515673-44515674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551632061	chr18:44515728-44515729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs59653446	chr18:44515756-44515757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577907432	chr18:44515840-44515841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571487234	chr18:44515880-44515881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs11877650	chr18:44515886-44515887	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs188890081	chr18:44515941-44515942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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

Chromatin state (count:352 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44508400-44509200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
2	chr18:44515000-44515400	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr18:44515000-44515600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
4	chr18:44515000-44515600	Enhancers	HUVEC	blood vessel
5	chr18:44515200-44515400	Enhancers	Colon Smooth Muscle	Colon
6	chr18:44515200-44515600	Enhancers	Adipose Nuclei	Adipose
7	chr18:44515200-44515600	Enhancers	Placenta	Placenta
8	chr18:44515200-44515600	Enhancers	Psoas Muscle	Psoas
9	chr18:44515600-44520800	Weak transcription	Psoas Muscle	Psoas
10	chr18:44518400-44521000	Enhancers	HSMM	muscle
11	chr18:44518800-44519200	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr18:44518800-44519400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr18:44518800-44520000	Enhancers	HSMMtube	muscle
14	chr18:44518800-44520200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr18:44518800-44520400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr18:44518800-44520400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr18:44518800-44520800	Enhancers	NHLF	lung
18	chr18:44519000-44519200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr18:44519000-44520200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr18:44519000-44520200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr18:44519000-44520200	Enhancers	Placenta Amnion	Placenta Amnion
22	chr18:44519000-44520400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr18:44519000-44520800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr18:44519000-44520800	Enhancers	NHDF-Ad	bronchial
25	chr18:44519000-44521000	Enhancers	Muscle Satellite Cultured Cells	--
26	chr18:44519000-44521000	Enhancers	Fetal Muscle Leg	muscle
27	chr18:44519000-44521200	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr18:44519200-44519600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
29	chr18:44519200-44520800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr18:44519200-44520800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr18:44519200-44520800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr18:44519400-44519600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr18:44519400-44519600	Enhancers	Colon Smooth Muscle	Colon
34	chr18:44519400-44519800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr18:44519400-44519800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr18:44519400-44519800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr18:44519400-44520000	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr18:44519400-44520000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr18:44519400-44520000	Enhancers	HMEC	breast
40	chr18:44519400-44520200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr18:44519400-44520200	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr18:44519400-44520200	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr18:44519400-44520200	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr18:44519400-44520200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr18:44519400-44520200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr18:44519400-44520200	Enhancers	Hela-S3	cervix
47	chr18:44519400-44520400	Enhancers	Osteobl	bone
48	chr18:44519400-44520800	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr18:44519600-44520200	Enhancers	H9 Cell Line	embryonic stem cell
50	chr18:44519600-44520400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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