Variant report

Variant	esv3406270
Chromosome Location	chr18:151001-180091
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:640)
CpG islands
(count:916)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:640 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:158435-158687	HepG2	liver:	n/a	n/a
2	ATF1	chr18:158332-158983	K562	blood:	n/a	n/a
3	ATF3	chr18:158161-158396	K562	blood:	n/a	chr18:158290-158310
4	ATF3	chr18:158422-158737	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr18:158130-158721	HepG2	liver:	n/a	chr18:158290-158310
6	ATF3	chr18:158258-158725	K562	blood:	n/a	chr18:158290-158310
7	ATF3	chr18:158306-158739	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr18:158218-158388	GM12878	blood:	n/a	chr18:158290-158310
9	ATF3	chr18:158111-158789	GM12878	blood:	n/a	chr18:158290-158310
10	ATF3	chr18:158269-158734	HepG2	liver:	n/a	chr18:158290-158310
11	ATF3	chr18:158407-159043	K562	blood:	n/a	n/a
12	ATF3	chr18:158201-158395	H1-hESC	embryonic stem cell:	n/a	chr18:158290-158310
13	ATF3	chr18:158422-158663	GM12878	blood:	n/a	n/a
14	BACH1	chr18:158834-159144	K562	blood:	n/a	n/a
15	BACH1	chr18:158368-159507	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr18:158476-158601	K562	blood:	n/a	n/a
17	BCLAF1	chr18:157980-158727	K562	blood:	n/a	n/a
18	BHLHE40	chr18:158201-159060	K562	blood:	n/a	n/a
19	BHLHE40	chr18:158165-158808	GM12878	blood:	n/a	n/a
20	BHLHE40	chr18:158221-158775	HepG2	liver:	n/a	n/a
21	BRCA1	chr18:158537-158560	HepG2	liver:	n/a	n/a
22	BRCA1	chr18:158389-158626	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr18:158364-158687	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr18:157970-158758	K562	blood:	n/a	n/a
25	CBX3	chr18:157972-158829	HCT-116	colon:	n/a	n/a
26	CBX3	chr18:157987-158664	K562	blood:	n/a	n/a
27	CCNT2	chr18:158176-159035	K562	blood:	n/a	n/a
28	CEBPB	chr18:155773-156010	HepG2	liver:	n/a	chr18:155888-155899
29	CEBPB	chr18:155811-155939	HepG2	liver:	n/a	chr18:155888-155899
30	CEBPB	chr18:155807-155958	K562	blood:	n/a	chr18:155888-155899
31	CEBPB	chr18:159455-159778	K562	blood:	n/a	n/a
32	CEBPB	chr18:159568-159751	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr18:159554-159721	K562	blood:	n/a	n/a
34	CEBPB	chr18:155843-155953	H1-hESC	embryonic stem cell:	n/a	chr18:155888-155899
35	CEBPD	chr18:155725-155964	HepG2	liver:	n/a	n/a
36	CEBPD	chr18:158420-158717	HepG2	liver:	n/a	n/a
37	CEBPD	chr18:158337-158765	HepG2	liver:	n/a	n/a
38	CHD2	chr18:158240-158746	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr18:158141-158703	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr18:158274-158603	K562	blood:	n/a	n/a
41	CHD2	chr18:158231-158711	GM12878	blood:	n/a	n/a
42	CHD2	chr18:158522-158722	HepG2	liver:	n/a	n/a
43	CREB1	chr18:158076-159164	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr18:158057-159124	HepG2	liver:	n/a	n/a
45	CREB1	chr18:158402-158678	A549	lung:	n/a	n/a
46	CREB1	chr18:158078-159198	GM12878	blood:	n/a	n/a
47	CREB1	chr18:158275-158791	ECC-1	luminal epithelium:	n/a	n/a
48	CREB1	chr18:158185-159246	K562	blood:	n/a	n/a
49	CREB1	chr18:158104-159211	K562	blood:	n/a	n/a
50	CREB1	chr18:158113-159190	H1-hESC	embryonic stem cell:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:158567-158617	MCF10A-Er-Src	breast:	n/a
2	chr18:158567-158617	MCF10A-Er-Src	breast:	n/a
3	chr18:158292-158342	HRCEpiC	kidney:	n/a
4	chr18:158567-158617	ProgFib	skin:	n/a
5	chr18:158292-158342	Hepatocyte	liver:	n/a
6	chr18:158292-158342	HCT-116	colon:	n/a
7	chr18:158463-158513	AG10803	skin:	n/a
8	chr18:155309-155359	IMR90	lung:	fetal
9	chr18:158567-158617	SAEC	small airway:	n/a
10	chr18:159265-159315	HepG2	liver:	n/a
11	chr18:158567-158617	BJ	skin:	n/a
12	chr18:158294-158344	LNCaP	prostate:	n/a
13	chr18:158551-158601	HRPEpiC	eye:	n/a
14	chr18:158011-158061	Hela-S3	cervix:	n/a
15	chr18:159793-159843	SAEC	small airway:	n/a
16	chr18:163067-163117	HEK293	kidney:	embryo
17	chr18:163067-163117	HNPCEpiC	eye:	n/a
18	chr18:158229-158279	NH-A	brain:	n/a
19	chr18:158551-158601	SK-N-MC	brain:	n/a
20	chr18:158294-158344	AG10803	skin:	n/a
21	chr18:158348-158398	SK-N-SH_RA	brain:	n/a
22	chr18:159310-159360	AG04449	skin:	fetal
23	chr18:159793-159843	SK-N-SH_RA	brain:	n/a
24	chr18:159310-159360	HCF	heart:	n/a
25	chr18:159793-159843	AG09319	gingival:	n/a
26	chr18:158294-158344	CMK	blood:	n/a
27	chr18:155309-155359	NB4	blood:	n/a
28	chr18:165402-165452	HepG2	liver:	n/a
29	chr18:163067-163117	SAEC	small airway:	n/a
30	chr18:159265-159315	MCF10A-Er-Src	breast:	n/a
31	chr18:158567-158617	HL-60	blood:	n/a
32	chr18:158567-158617	HIPEpiC	eye:	n/a
33	chr18:158292-158342	NHBE	bronchial:	n/a
34	chr18:158551-158601	Jurkat	blood:	n/a
35	chr18:159793-159843	SK-N-SH	brain:	n/a
36	chr18:158838-158888	MCF10A-Er-Src	breast:	n/a
37	chr18:159793-159843	PFSK-1	brain:	n/a
38	chr18:158463-158513	ovcar-3	ovarian:	n/a
39	chr18:158229-158279	HCM	heart:	n/a
40	chr18:158551-158601	HEK293	kidney:	embryo
41	chr18:158348-158398	Hela-S3	cervix:	n/a
42	chr18:159310-159360	HIPEpiC	eye:	n/a
43	chr18:155309-155359	GM06990	blood:	n/a
44	chr18:158463-158513	BE2_C	brain:	n/a
45	chr18:159310-159360	HUVEC	blood vessel:	n/a
46	chr18:158348-158398	RPTEC	kidney:	n/a
47	chr18:155309-155359	HEEpiC	esophagus:	n/a
48	chr18:159265-159315	BE2_C	brain:	n/a
49	chr18:158463-158513	LNCaP	prostate:	n/a
50	chr18:158838-158888	Caco-2	colon:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:169841..172227-chr18:180107..182467,2	K562	blood:
2	chr18:164894..167848-chr18:172518..174416,3	K562	blood:
3	chr18:155065..156905-chr18:157468..160011,3	K562	blood:
4	chr18:175173..178003-chr18:178964..182067,3	K562	blood:
5	chr18:141525..143923-chr18:160153..163099,2	K562	blood:
6	chr18:157295..159730-chr18:266988..268701,2	MCF-7	breast:
7	chr18:159584..161282-chr18:196677..199436,2	K562	blood:
8	chr18:158417..159997-chr18:214475..216956,2	K562	blood:
9	chr18:175956..178936-chr18:178964..180560,2	K562	blood:
10	chr18:164894..167848-chr18:172518..174416,3	K562	blood:
11	chr18:164137..168777-chr18:169771..171938,5	K562	blood:
12	chr18:158132..161790-chr18:177799..183224,6	K562	blood:
13	chr14:70233601..70234234-chr18:157797..158549,2	Hela-S3	cervix:
14	chr18:158012..160007-chr18:265808..268303,2	MCF-7	breast:
15	chr18:158226..159980-chr18:161322..163085,2	MCF-7	breast:
16	chr18:164137..168777-chr18:169771..171938,5	K562	blood:
17	chr18:160787..162407-chr18:176462..179044,2	K562	blood:
18	chr18:152262..154737-chr18:158515..160413,2	K562	blood:
19	chr18:172540..174181-chr18:176241..178456,2	K562	blood:
20	chr18:151636..153616-chr18:156917..159061,2	MCF-7	breast:
21	chr18:175173..178003-chr18:178964..182067,3	K562	blood:
22	chr18:154974..156565-chr18:158511..161131,2	K562	blood:
23	chr18:175956..178936-chr18:178964..180560,2	K562	blood:
24	chr18:148615..151946-chr18:155352..158851,3	K562	blood:
25	chr1:229644060..229644762-chr18:153612..154112,2	HCT-116	colon:
26	chr18:172540..174181-chr18:176241..178456,2	K562	blood:
27	chr18:173629..175507-chr18:185992..188221,2	MCF-7	breast:
28	chr18:148954..152289-chr18:157038..160198,3	MCF-7	breast:
29	chr18:160787..162407-chr18:176462..179044,2	K562	blood:

No data

Variant related genes	Relation type
USP14	TF binding region
USP14	CpG island
ENSG00000263884	chromatin interactions
ENSG00000079134	chromatin interactions
ENSG00000100650	chromatin interactions
ENSG00000069248	chromatin interactions
ENSG00000101557	chromatin interactions
ENSG00000223635	chromatin interactions

Extended variants
information (count: 1152 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1152 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573231717	chr18:151005-151006	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs540656462	chr18:151050-151051	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs574753734	chr18:151068-151069	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs565151455	chr18:151104-151105	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs374708008	chr18:151112-151113	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs115555408	chr18:151115-151116	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs183454722	chr18:151116-151117	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs555085	chr18:151201-151202	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs28452899	chr18:151232-151233	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs543339489	chr18:151282-151283	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs115635920	chr18:151284-151285	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs112700958	chr18:151320-151321	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs563628791	chr18:151354-151355	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs186848223	chr18:151380-151381	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs551800033	chr18:151428-151429	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs531604750	chr18:151435-151436	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs148246339	chr18:151455-151456	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs552217284	chr18:151509-151510	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs570376237	chr18:151532-151533	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs537406014	chr18:151555-151556	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs190298810	chr18:151578-151579	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs199633691	chr18:151591-151592	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs568009033	chr18:151606-151607	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs141697284	chr18:151624-151625	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs553669080	chr18:151632-151633	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs564999697	chr18:151707-151708	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs571711574	chr18:151752-151753	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs182609801	chr18:151878-151879	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs145572629	chr18:151917-151918	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs558961991	chr18:151982-151983	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs577320590	chr18:151994-151995	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs565742050	chr18:152038-152039	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs369302990	chr18:152096-152097	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs116786693	chr18:152111-152112	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs563221805	chr18:152132-152133	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs575164372	chr18:152156-152157	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs542445562	chr18:152202-152203	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs560539673	chr18:152256-152257	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs527860281	chr18:152264-152265	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs551991371	chr18:152278-152279	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs527783017	chr18:152290-152291	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs186900299	chr18:152357-152358	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs191409414	chr18:152363-152364	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs547555902	chr18:152399-152400	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs549340866	chr18:152400-152401	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs80342953	chr18:152402-152403	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs373010360	chr18:152427-152428	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs184210043	chr18:152458-152459	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs565738677	chr18:152493-152494	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs539578082	chr18:152495-152496	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Esophageal cancer	21851588	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Breast cancer	17899364	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Gastrointestinal cancer	17018589	CNVD
prenatal diagnosis	20453657	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Renal cell carcinoma	18765545	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	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
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
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Melanoma	17363583	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	20808228	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Pancreatic cancer	17952125	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD

Chromatin state (count:1016 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:155400-155600	Enhancers	HepG2	liver
2	chr18:155600-156000	Flanking Active TSS	HepG2	liver
3	chr18:156000-156200	Enhancers	K562	blood
4	chr18:156000-156400	Enhancers	HepG2	liver
5	chr18:156200-156800	Weak transcription	K562	blood
6	chr18:156400-156800	Weak transcription	HepG2	liver
7	chr18:156800-157200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr18:156800-158000	Enhancers	HepG2	liver
9	chr18:156800-158000	Enhancers	K562	blood
10	chr18:157200-158000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr18:157400-157800	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr18:157400-157800	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr18:157400-157800	Enhancers	Brain Substantia Nigra	brain
14	chr18:157400-158000	Enhancers	Primary B cells from peripheral blood	blood
15	chr18:157400-158000	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr18:157400-158000	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr18:157600-158000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr18:157600-158000	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr18:157600-158000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr18:157600-158000	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr18:157600-158000	Enhancers	Brain Cingulate Gyrus	brain
22	chr18:157600-158000	Enhancers	Brain Hippocampus Middle	brain
23	chr18:157600-158000	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr18:157600-158000	Enhancers	Fetal Kidney	kidney
25	chr18:157600-158000	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr18:157600-158000	Enhancers	Dnd41	blood
27	chr18:157600-158200	Enhancers	Primary B cells from cord blood	blood
28	chr18:157800-158000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr18:157800-158600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr18:158000-158200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
31	chr18:158000-158200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr18:158000-158200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr18:158000-158200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr18:158000-158200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr18:158000-158200	Flanking Active TSS	Primary B cells from peripheral blood	blood
36	chr18:158000-158200	Enhancers	Primary hematopoietic stem cells	blood
37	chr18:158000-158200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
38	chr18:158000-158200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
39	chr18:158000-158200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
40	chr18:158000-158200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr18:158000-158200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr18:158000-158200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
43	chr18:158000-158200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr18:158000-158200	Flanking Active TSS	Fetal Thymus	thymus
45	chr18:158000-158200	Active TSS	Right Atrium	heart
46	chr18:158000-158200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
47	chr18:158000-158200	Flanking Active TSS	A549	lung
48	chr18:158000-158200	Flanking Active TSS	K562	blood
49	chr18:158000-158400	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr18:158000-158400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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