Variant report

Variant	nsv909348
Chromosome Location	chr18:7279341-7578782
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1713)
CpG islands
(count:978)
Chromatin interactive
region (count:40)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1713 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:7567159-7567359	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:7567223-7567257	K562	blood:	n/a	n/a
3	ARID3A	chr18:7575137-7575406	HepG2	liver:	n/a	n/a
4	ATF1	chr18:7312250-7312257	K562	blood:	n/a	n/a
5	ATF2	chr18:7577742-7578206	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr18:7577712-7578133	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr18:7567156-7567368	K562	blood:	n/a	chr18:7567347-7567356 chr18:7567273-7567283
8	ATF3	chr18:7467741-7468000	K562	blood:	n/a	n/a
9	ATF3	chr18:7467727-7468106	HepG2	liver:	n/a	n/a
10	BACH1	chr18:7566904-7567617	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr18:7568581-7568843	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr18:7542025-7542029	K562	blood:	n/a	n/a
13	BACH1	chr18:7575526-7576005	H1-hESC	embryonic stem cell:	n/a	chr18:7575877-7575891
14	BACH1	chr18:7367519-7367591	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr18:7566548-7566660	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL11A	chr18:7577811-7577975	H1-hESC	embryonic stem cell:	n/a	n/a
17	BHLHE40	chr18:7566522-7567366	K562	blood:	n/a	chr18:7567340-7567356 chr18:7566691-7566707 chr18:7567117-7567133
18	BHLHE40	chr18:7520471-7520649	GM12878	blood:	n/a	chr18:7520557-7520566 chr18:7520557-7520566
19	BHLHE40	chr18:7520517-7520690	HepG2	liver:	n/a	chr18:7520557-7520566 chr18:7520557-7520566
20	BHLHE40	chr18:7567045-7567395	GM12878	blood:	n/a	chr18:7567340-7567356 chr18:7567117-7567133
21	BHLHE40	chr18:7459819-7460275	HepG2	liver:	n/a	n/a
22	BHLHE40	chr18:7520520-7520629	K562	blood:	n/a	chr18:7520557-7520566 chr18:7520557-7520566
23	BHLHE40	chr18:7317788-7318028	HepG2	liver:	n/a	n/a
24	BHLHE40	chr18:7467767-7468063	K562	blood:	n/a	n/a
25	BHLHE40	chr18:7467750-7468067	HepG2	liver:	n/a	n/a
26	BHLHE40	chr18:7566784-7567400	HepG2	liver:	n/a	chr18:7567340-7567356 chr18:7567117-7567133
27	BHLHE40	chr18:7575112-7575466	HepG2	liver:	n/a	n/a
28	BRCA1	chr18:7458169-7458192	GM12878	blood:	n/a	n/a
29	BRCA1	chr18:7303527-7303574	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr18:7566113-7566632	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr18:7452418-7452638	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr18:7414190-7414195	GM12878	blood:	n/a	n/a
33	CCNT2	chr18:7566537-7567551	K562	blood:	n/a	n/a
34	CEBPB	chr18:7397029-7397350	IMR90	lung:	n/a	chr18:7397192-7397203
35	CEBPB	chr18:7301304-7301469	HepG2	liver:	n/a	chr18:7301385-7301396
36	CEBPB	chr18:7548380-7548578	HepG2	liver:	n/a	n/a
37	CEBPB	chr18:7371818-7371870	A549	lung:	n/a	n/a
38	CEBPB	chr18:7574543-7574739	A549	lung:	n/a	chr18:7574590-7574603
39	CEBPB	chr18:7433347-7433472	K562	blood:	n/a	n/a
40	CEBPB	chr18:7301230-7301548	HepG2	liver:	n/a	chr18:7301385-7301396
41	CEBPB	chr18:7397050-7397306	Hela-S3	cervix:	n/a	chr18:7397192-7397203
42	CEBPB	chr18:7492855-7493001	HepG2	liver:	n/a	chr18:7492946-7492957
43	CEBPB	chr18:7545933-7546250	A549	lung:	n/a	n/a
44	CEBPB	chr18:7301332-7301517	IMR90	lung:	n/a	chr18:7301385-7301396
45	CEBPB	chr18:7487811-7488113	IMR90	lung:	n/a	chr18:7487948-7487959 chr18:7487948-7487961 chr18:7487950-7487961
46	CEBPB	chr18:7303385-7303625	MCF-7	breast:	n/a	chr18:7303438-7303449
47	CEBPB	chr18:7487797-7488098	HepG2	liver:	n/a	chr18:7487948-7487959 chr18:7487948-7487961 chr18:7487950-7487961
48	CEBPB	chr18:7301056-7301544	Hela-S3	cervix:	n/a	chr18:7301385-7301396
49	CEBPB	chr18:7437219-7437475	IMR90	lung:	n/a	chr18:7437327-7437338
50	CEBPB	chr18:7303392-7303557	HepG2	liver:	n/a	chr18:7303438-7303449

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:7568539-7568589	GM19239	blood:	n/a
2	chr18:7566781-7566831	HCT-116	colon:	n/a
3	chr18:7568539-7568589	GM19239	blood:	n/a
4	chr18:7566781-7566831	HCT-116	colon:	n/a
5	chr18:7567717-7567767	PFSK-1	brain:	n/a
6	chr18:7567717-7567767	RPTEC	kidney:	n/a
7	chr18:7568539-7568589	A549	lung:	n/a
8	chr18:7568891-7568941	SK-N-MC	brain:	n/a
9	chr18:7566558-7566608	CMK	blood:	n/a
10	chr18:7567426-7567476	SKMC	muscle:	n/a
11	chr18:7568539-7568589	Caco-2	colon:	n/a
12	chr18:7568159-7568209	HL-60	blood:	n/a
13	chr18:7568159-7568209	HepG2	liver:	n/a
14	chr18:7566781-7566831	NB4	blood:	n/a
15	chr18:7566781-7566831	Caco-2	colon:	n/a
16	chr18:7566258-7566308	GM19239	blood:	n/a
17	chr18:7568186-7568236	HAEpiC	amniotic membrane:	n/a
18	chr18:7563847-7563897	K562	blood:	n/a
19	chr18:7567799-7567849	HL-60	blood:	n/a
20	chr18:7563847-7563897	AG09309	skin:	n/a
21	chr18:7568891-7568941	GM12878	blood:	n/a
22	chr18:7566558-7566608	GM06990	blood:	n/a
23	chr18:7566656-7566706	LNCaP	prostate:	n/a
24	chr18:7563847-7563897	LNCaP	prostate:	n/a
25	chr18:7567799-7567849	AG04449	skin:	fetal
26	chr18:7566258-7566308	MCF10A-Er-Src	breast:	n/a
27	chr18:7566258-7566308	Hela-S3	cervix:	n/a
28	chr18:7566781-7566831	SKMC	muscle:	n/a
29	chr18:7567548-7567598	NHBE	bronchial:	n/a
30	chr18:7568265-7568315	HMEC	breast:	n/a
31	chr18:7567426-7567476	BJ	skin:	n/a
32	chr18:7567548-7567598	AG04450	lung:	fetal
33	chr18:7566781-7566831	SK-N-MC	brain:	n/a
34	chr18:7566781-7566831	PANC-1	pancreas:	n/a
35	chr18:7568539-7568589	T-47D	breast:	n/a
36	chr18:7563847-7563897	HRCEpiC	kidney:	n/a
37	chr18:7567638-7567688	HCF	heart:	n/a
38	chr18:7567638-7567688	AG04449	skin:	fetal
39	chr18:7566258-7566308	T-47D	breast:	n/a
40	chr18:7568159-7568209	RPTEC	kidney:	n/a
41	chr18:7567548-7567598	RPTEC	kidney:	n/a
42	chr18:7566656-7566706	HRE	kidney:	n/a
43	chr18:7563847-7563897	ovcar-3	ovarian:	n/a
44	chr18:7567799-7567849	IMR90	lung:	fetal
45	chr18:7567799-7567849	NB4	blood:	n/a
46	chr18:7566258-7566308	RPTEC	kidney:	n/a
47	chr18:7567799-7567849	MCF10A-Er-Src	breast:	n/a
48	chr18:7568891-7568941	NH-A	brain:	n/a
49	chr18:7568539-7568589	CMK	blood:	n/a
50	chr18:7568891-7568941	MCF-7	breast:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:7359797..7360512-chr20:46012695..46013367,2	MCF-7	breast:
2	chr18:7485561..7489531-chr18:7490547..7493519,3	K562	blood:
3	chr18:7556771..7559463-chr18:7563687..7565562,2	K562	blood:
4	chr18:7560178..7562976-chr18:7564673..7567118,2	MCF-7	breast:
5	chr17:56707566..56710325-chr18:7281315..7284315,3	K562	blood:
6	chr18:7509867..7511990-chr18:7516061..7517678,2	MCF-7	breast:
7	chr18:7237095..7238838-chr18:7283799..7285892,2	K562	blood:
8	chr18:7489323..7491482-chr18:7507564..7509092,2	K562	blood:
9	chr18:7485561..7488328-chr18:7489989..7493519,3	K562	blood:
10	chr18:7328260..7329783-chr18:7331392..7333431,2	K562	blood:
11	chr18:7504934..7505434-chr3:98276004..98276980,2	HCT-116	colon:
12	chr17:56708842..56709440-chr18:7282835..7283335,2	NB4	blood:
13	chr18:7555198..7557360-chr18:7558467..7560228,2	K562	blood:
14	chr18:7305816..7308411-chr18:7309437..7311402,2	K562	blood:
15	chr18:7514458..7516129-chr18:7523489..7525604,2	K562	blood:
16	chr18:7509867..7511990-chr18:7516061..7517678,2	MCF-7	breast:
17	chr18:7271986..7272913-chr18:7349191..7350194,3	MCF-7	breast:
18	chr18:7279579..7281833-chr18:7286057..7288878,2	K562	blood:
19	chr18:7465161..7467875-chr18:7484981..7486851,2	K562	blood:
20	chr18:7555198..7557360-chr18:7558467..7560228,2	K562	blood:
21	chr18:7485561..7488328-chr18:7489989..7493519,3	K562	blood:
22	chr18:7305816..7308411-chr18:7309437..7311402,2	K562	blood:
23	chr18:7489323..7491482-chr18:7507564..7509092,2	K562	blood:
24	chr18:7561940..7563899-chr18:7566456..7568145,3	K562	blood:
25	chr18:7560671..7563899-chr18:7566458..7568145,4	K562	blood:
26	chr18:7277126..7280164-chr18:7281807..7285178,3	K562	blood:
27	chr18:7567923..7568423-chr20:61846958..61847561,2	MCF-7	breast:
28	chr18:7221690..7222309-chr18:7566824..7567430,2	K562	blood:
29	chr18:7328260..7329783-chr18:7331392..7333431,2	K562	blood:
30	chr17:56708760..56709438-chr18:7282315..7283335,4	HCT-116	colon:
31	chr18:7514458..7516129-chr18:7523489..7525604,2	K562	blood:
32	chr18:7277126..7280164-chr18:7281807..7285178,3	K562	blood:
33	chr18:7556771..7559463-chr18:7563687..7565562,2	K562	blood:
34	chr18:7336585..7339141-chr18:7354510..7356531,2	MCF-7	breast:
35	chr18:7279579..7281833-chr18:7286057..7288878,2	K562	blood:
36	chr18:7566319..7569036-chr18:7569097..7573393,5	K562	blood:
37	chr18:7465161..7467875-chr18:7484981..7486851,2	K562	blood:
38	chr18:7272328..7273061-chr18:7451989..7452918,2	MCF-7	breast:
39	chr18:7336585..7339141-chr18:7354510..7356531,2	MCF-7	breast:
40	chr18:7485561..7489531-chr18:7490547..7493519,3	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LAMA1-4	chr18:7509140-7509419	XLOC_012749
2	lnc-LAMA1-4	chr18:7508432-7508885	XLOC_012749
3	lnc-LAMA1-4	chr18:7508970-7509053	XLOC_012749

No data

Variant related genes	Relation type
PTPRM	TF binding region
ENSG00000212626	TF binding region
PTPRM	CpG island
ENSG00000212626	CpG island
ENSG00000173482	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000149658	chromatin interactions

Extended variants
information (count: 9912 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:9912 , 50 per page) page: 1 2 3 4 5 6 7 ... 199

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8084409	chr18:7279341-7279342	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs12456400	chr18:7279354-7279355	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs370682548	chr18:7279357-7279358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181367364	chr18:7279380-7279381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149213925	chr18:7279405-7279406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548110216	chr18:7279417-7279418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537271925	chr18:7279463-7279464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs373885631	chr18:7279466-7279467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs998524	chr18:7279512-7279513	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs185787960	chr18:7279525-7279526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146915113	chr18:7279526-7279527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553376206	chr18:7279639-7279640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573155505	chr18:7279685-7279686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs189685660	chr18:7279702-7279703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182586580	chr18:7279754-7279755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189038784	chr18:7279765-7279766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575779072	chr18:7279771-7279772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs137905013	chr18:7279787-7279788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561047485	chr18:7279823-7279824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192095574	chr18:7279824-7279825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374286444	chr18:7279829-7279830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113334787	chr18:7279830-7279831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143378349	chr18:7279831-7279832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532028163	chr18:7279832-7279833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551729382	chr18:7279833-7279834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568640935	chr18:7279840-7279841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537535993	chr18:7279872-7279873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1984468	chr18:7279873-7279874	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs183592651	chr18:7279877-7279878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539030803	chr18:7279913-7279914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7242414	chr18:7279929-7279930	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs5822959	chr18:7279945-7279946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs397858295	chr18:7279951-7279952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553398190	chr18:7279985-7279986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567117072	chr18:7279994-7279995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7236850	chr18:7280016-7280017	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs150768066	chr18:7280017-7280018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs7238598	chr18:7280020-7280021	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs7238599	chr18:7280026-7280027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs386800864	chr18:7280032-7280033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4798548	chr18:7280033-7280034	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs540389672	chr18:7280060-7280061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143548842	chr18:7280095-7280096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532255326	chr18:7280096-7280097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375367339	chr18:7280107-7280108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368331109	chr18:7280113-7280114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs62089732	chr18:7280117-7280118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34952536	chr18:7280118-7280119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs397809274	chr18:7280132-7280133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371796812	chr18:7280133-7280134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	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
Breast cancer	21785460	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	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
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Breast cancer	17133270	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Burkitt''s lymphoma	20823134	CNVD
Acute myeloid leukemia	17377590	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	20838587	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2337 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:7276800-7283200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr18:7277000-7280200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr18:7280200-7280400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr18:7280200-7281000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr18:7280400-7280600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr18:7280600-7280800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr18:7280600-7281600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr18:7280800-7281000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr18:7281000-7281800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr18:7281200-7283800	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr18:7287200-7287600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr18:7287600-7289000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr18:7287800-7288000	Enhancers	Fetal Brain Male	brain
14	chr18:7287800-7288200	Enhancers	Fetal Lung	lung
15	chr18:7287800-7288400	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr18:7287800-7288400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr18:7287800-7288800	Enhancers	Adipose Nuclei	Adipose
18	chr18:7288000-7288200	Enhancers	Primary hematopoietic stem cells	blood
19	chr18:7288000-7288600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr18:7288200-7290600	Weak transcription	Primary hematopoietic stem cells	blood
21	chr18:7288400-7289200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr18:7288400-7289200	Enhancers	Fetal Muscle Leg	muscle
23	chr18:7288400-7290200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr18:7288400-7290200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr18:7288600-7290600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr18:7288800-7290800	Weak transcription	Adipose Nuclei	Adipose
27	chr18:7289000-7289200	Enhancers	Left Ventricle	heart
28	chr18:7289000-7290200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr18:7289200-7290200	Weak transcription	Fetal Muscle Leg	muscle
30	chr18:7289200-7290400	Weak transcription	Left Ventricle	heart
31	chr18:7289200-7303800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr18:7290000-7290600	Enhancers	Brain Germinal Matrix	brain
33	chr18:7290200-7290800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr18:7290200-7291200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr18:7290200-7291200	Enhancers	Fetal Muscle Leg	muscle
36	chr18:7290200-7291200	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr18:7290200-7291400	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr18:7290400-7291200	Enhancers	Left Ventricle	heart
39	chr18:7290600-7291200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr18:7290600-7291400	Enhancers	Primary hematopoietic stem cells	blood
41	chr18:7290600-7291400	Enhancers	HUVEC	blood vessel
42	chr18:7290800-7291000	Enhancers	Adipose Nuclei	Adipose
43	chr18:7290800-7291400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr18:7291000-7291200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
45	chr18:7291200-7291400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr18:7291200-7299400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr18:7295400-7296000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr18:7299400-7299600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr18:7299400-7299600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr18:7299600-7300000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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