Variant report

Variant	nsv431979
Chromosome Location	chr18:39255558-39696452
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3816)
CpG islands
(count:674)
Chromatin interactive
region (count:87)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:3816 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:39409734-39409963	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:39693801-39694659	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:39534855-39535337	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:39693941-39694141	K562	blood:	n/a	n/a
5	ARID3A	chr18:39692657-39693205	HepG2	liver:	n/a	n/a
6	ARID3A	chr18:39627775-39627961	HepG2	liver:	n/a	n/a
7	ARID3A	chr18:39534615-39535479	K562	blood:	n/a	n/a
8	ARID3A	chr18:39553351-39553597	K562	blood:	n/a	n/a
9	ATF1	chr18:39473373-39473623	K562	blood:	n/a	n/a
10	ATF1	chr18:39547898-39548357	K562	blood:	n/a	n/a
11	ATF1	chr18:39554948-39555253	K562	blood:	n/a	n/a
12	ATF1	chr18:39503671-39503970	K562	blood:	n/a	n/a
13	ATF1	chr18:39434570-39434652	K562	blood:	n/a	n/a
14	ATF1	chr18:39505643-39505912	K562	blood:	n/a	n/a
15	ATF1	chr18:39458878-39459029	K562	blood:	n/a	n/a
16	ATF1	chr18:39490055-39490356	K562	blood:	n/a	n/a
17	ATF1	chr18:39497852-39498167	K562	blood:	n/a	n/a
18	ATF1	chr18:39518451-39518770	K562	blood:	n/a	n/a
19	ATF1	chr18:39681004-39681204	K562	blood:	n/a	n/a
20	ATF1	chr18:39462020-39462146	K562	blood:	n/a	n/a
21	ATF1	chr18:39465008-39465121	K562	blood:	n/a	n/a
22	ATF1	chr18:39534830-39535317	K562	blood:	n/a	n/a
23	ATF1	chr18:39500527-39500689	K562	blood:	n/a	n/a
24	ATF2	chr18:39534811-39535428	GM12878	blood:	n/a	n/a
25	ATF2	chr18:39590971-39591514	GM12878	blood:	n/a	n/a
26	ATF2	chr18:39571959-39572592	GM12878	blood:	n/a	n/a
27	ATF2	chr18:39527417-39527859	GM12878	blood:	n/a	n/a
28	ATF2	chr18:39562927-39563379	GM12878	blood:	n/a	n/a
29	ATF2	chr18:39603922-39604468	GM12878	blood:	n/a	n/a
30	ATF2	chr18:39571969-39572573	GM12878	blood:	n/a	n/a
31	ATF2	chr18:39605599-39606500	GM12878	blood:	n/a	n/a
32	ATF2	chr18:39605765-39606562	GM12878	blood:	n/a	n/a
33	ATF2	chr18:39603957-39604475	GM12878	blood:	n/a	n/a
34	ATF2	chr18:39590840-39591445	GM12878	blood:	n/a	n/a
35	ATF2	chr18:39527160-39527879	GM12878	blood:	n/a	n/a
36	ATF2	chr18:39589394-39589809	GM12878	blood:	n/a	n/a
37	ATF2	chr18:39534755-39535211	GM12878	blood:	n/a	n/a
38	ATF2	chr18:39486472-39486998	GM12878	blood:	n/a	n/a
39	BACH1	chr18:39538927-39539313	K562	blood:	n/a	n/a
40	BACH1	chr18:39534498-39534698	K562	blood:	n/a	n/a
41	BACH1	chr18:39283810-39283934	H1-hESC	embryonic stem cell:	n/a	chr18:39283855-39283869
42	BACH1	chr18:39523386-39523762	K562	blood:	n/a	n/a
43	BACH1	chr18:39535278-39535887	K562	blood:	n/a	n/a
44	BACH1	chr18:39275506-39275509	K562	blood:	n/a	n/a
45	BACH1	chr18:39389713-39389970	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr18:39579783-39579938	K562	blood:	n/a	n/a
47	BACH1	chr18:39501548-39501652	K562	blood:	n/a	n/a
48	BACH1	chr18:39551891-39552948	K562	blood:	n/a	n/a
49	BATF	chr18:39572034-39572430	GM12878	blood:	n/a	n/a
50	BATF	chr18:39605871-39606293	GM12878	blood:	n/a	chr18:39606041-39606049 chr18:39606149-39606160

(count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:39575942-39575992	T-47D	breast:	n/a
2	chr18:39575942-39575992	AG04449	skin:	fetal
3	chr18:39578868-39578918	GM12878	blood:	n/a
4	chr18:39575942-39575992	T-47D	breast:	n/a
5	chr18:39575942-39575992	AG04449	skin:	fetal
6	chr18:39578868-39578918	GM12878	blood:	n/a
7	chr18:39535255-39535305	GM12892	blood:	n/a
8	chr18:39535226-39535276	HIPEpiC	eye:	n/a
9	chr18:39584467-39584517	HAEpiC	amniotic membrane:	n/a
10	chr18:39578868-39578918	SK-N-MC	brain:	n/a
11	chr18:39535095-39535145	AG10803	skin:	n/a
12	chr18:39535226-39535276	GM12891	blood:	n/a
13	chr18:39534432-39534482	BE2_C	brain:	n/a
14	chr18:39575942-39575992	HUVEC	blood vessel:	n/a
15	chr18:39535162-39535212	NT2-D1	testis:	n/a
16	chr18:39575942-39575992	NT2-D1	testis:	n/a
17	chr18:39535162-39535212	HRPEpiC	eye:	n/a
18	chr18:39535226-39535276	A549	lung:	n/a
19	chr18:39535156-39535206	T-47D	breast:	n/a
20	chr18:39535162-39535212	NH-A	brain:	n/a
21	chr18:39575942-39575992	HAEpiC	amniotic membrane:	n/a
22	chr18:39534432-39534482	GM19239	blood:	n/a
23	chr18:39534432-39534482	MCF-7	breast:	n/a
24	chr18:39534432-39534482	PrEC	prostate:	n/a
25	chr18:39535226-39535276	MCF-7	breast:	n/a
26	chr18:39535171-39535221	A549	lung:	n/a
27	chr18:39575942-39575992	GM12878	blood:	n/a
28	chr18:39575942-39575992	H1-hESC	embryonic stem cell:	embryo
29	chr18:39535226-39535276	BJ	skin:	n/a
30	chr18:39535255-39535305	BE2_C	brain:	n/a
31	chr18:39535162-39535212	A549	lung:	n/a
32	chr18:39535255-39535305	GM06990	blood:	n/a
33	chr18:39535095-39535145	NH-A	brain:	n/a
34	chr18:39535076-39535126	HEEpiC	esophagus:	n/a
35	chr18:39578868-39578918	GM19239	blood:	n/a
36	chr18:39534432-39534482	AoSMC	blood vessel:	n/a
37	chr18:39578868-39578918	NT2-D1	testis:	n/a
38	chr18:39535162-39535212	RPTEC	kidney:	n/a
39	chr18:39535162-39535212	HAEpiC	amniotic membrane:	n/a
40	chr18:39578868-39578918	NH-A	brain:	n/a
41	chr18:39535076-39535126	HIPEpiC	eye:	n/a
42	chr18:39578868-39578918	Jurkat	blood:	n/a
43	chr18:39584467-39584517	GM19239	blood:	n/a
44	chr18:39535076-39535126	HCF	heart:	n/a
45	chr18:39534432-39534482	IMR90	lung:	fetal
46	chr18:39584467-39584517	SAEC	small airway:	n/a
47	chr18:39578868-39578918	SK-N-SH	brain:	n/a
48	chr18:39535156-39535206	HIPEpiC	eye:	n/a
49	chr18:39535255-39535305	AG10803	skin:	n/a
50	chr18:39535076-39535126	MCF10A-Er-Src	breast:	n/a

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr18:39549732..39552143-chr18:39580474..39582675,2	K562	blood:
2	chr18:39634544..39636615-chr18:39639116..39640932,2	K562	blood:
3	chr18:39527112..39531419-chr18:39531831..39536348,5	K562	blood:
4	chr18:39325742..39326593-chr18:39479267..39480114,2	MCF-7	breast:
5	chr18:39525438..39527045-chr18:39535673..39538548,2	K562	blood:
6	chr18:39559615..39562212-chr18:39583833..39587722,4	K562	blood:
7	chr18:39534418..39537159-chr18:39577056..39579376,2	K562	blood:
8	chr18:39569467..39572117-chr18:39574543..39576132,2	K562	blood:
9	chr18:39260655..39263464-chr18:39276141..39278500,2	K562	blood:
10	chr18:39268980..39271188-chr18:39284194..39286956,2	K562	blood:
11	chr18:39551912..39556568-chr18:39556669..39562027,6	K562	blood:
12	chr18:39564167..39566091-chr18:39569330..39571628,2	K562	blood:
13	chr18:39551994..39554075-chr18:39573084..39575388,2	K562	blood:
14	chr18:39508498..39511790-chr18:39514300..39517949,3	K562	blood:
15	chr18:39590017..39592684-chr18:39594715..39596812,2	K562	blood:
16	chr18:39543831..39546776-chr18:39549951..39551574,2	K562	blood:
17	chr18:39344259..39345945-chr18:39347323..39349154,2	K562	blood:
18	chr18:39323092..39324597-chr18:39328033..39330546,2	K562	blood:
19	chr18:39581260..39583124-chr18:39585047..39587391,2	MCF-7	breast:
20	chr18:39565388..39567063-chr18:39572337..39574712,2	K562	blood:
21	chr18:39435899..39438398-chr18:39442582..39444547,2	MCF-7	breast:
22	chr18:39348038..39348550-chr18:39486592..39487172,2	MCF-7	breast:
23	chr18:39532699..39534443-chr18:39539294..39540833,2	K562	blood:
24	chr18:39551994..39554075-chr18:39573084..39575388,2	K562	blood:
25	chr18:39569168..39571730-chr18:39571988..39574019,2	K562	blood:
26	chr18:39577574..39581097-chr18:39583166..39586037,3	K562	blood:
27	chr18:39550302..39551918-chr18:39553794..39556152,2	K562	blood:
28	chr18:39607303..39608871-chr18:39612845..39615778,2	K562	blood:
29	chr17:1673774..1676553-chr18:39584239..39587083,2	MCF-7	breast:
30	chr18:39581260..39583124-chr18:39585047..39587391,2	MCF-7	breast:
31	chr18:39508498..39511790-chr18:39514300..39517949,3	K562	blood:
32	chr18:39551912..39554681-chr18:39556259..39560409,4	K562	blood:
33	chr18:39631949..39632783-chr18:41143572..41144215,2	MCF-7	breast:
34	chr18:39528858..39531419-chr18:39533035..39536390,4	K562	blood:
35	chr18:39342427..39344217-chr18:39345521..39347378,2	K562	blood:
36	chr18:39653176..39655902-chr18:39657058..39659990,2	MCF-7	breast:
37	chr17:9554686..9555465-chr18:39339047..39339860,2	MCF-7	breast:
38	chr18:39549732..39552143-chr18:39580474..39582675,2	K562	blood:
39	chr18:39590017..39592684-chr18:39594715..39596812,2	K562	blood:
40	chr18:39565388..39567063-chr18:39572337..39574712,2	K562	blood:
41	chr18:39268980..39271188-chr18:39284194..39286956,2	K562	blood:
42	chr18:39631810..39632517-chr18:39878504..39879351,2	MCF-7	breast:
43	chr18:39569168..39571730-chr18:39571988..39574019,2	K562	blood:
44	chr18:39546444..39548693-chr18:39549349..39550895,2	K562	blood:
45	chr18:39344259..39345945-chr18:39347323..39349154,2	K562	blood:
46	chr18:39348022..39348620-chr18:39479077..39479637,2	MCF-7	breast:
47	chr18:39496794..39499325-chr18:39508884..39510445,2	K562	blood:
48	chr18:39580973..39583765-chr18:39598870..39601571,2	K562	blood:
49	chr18:39569467..39571487-chr18:39574632..39576197,2	K562	blood:
50	chr18:39533449..39535918-chr18:39576682..39579376,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RIT2-9	chr18:39278413-39278479	NONHSAT059054
2	lnc-PIK3C3-4	chr18:39399018-39399386	NONHSAT059056
3	lnc-RIT2-8	chr18:39369127-39369360	NONHSAT059055
4	lnc-PIK3C3-3	chr18:39669276-39669716	NONHSAT059060
5	lnc-RIT2-9	chr18:39277530-39278147	NONHSAT059054
6	lnc-SETBP1-8	chr18:39661838-39663348	NONHSAT059059

No data

(count:2 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PIK3C3	hsa-miR-98-5p	chr18:39630469-39630491
2	PIK3C3	hsa-miR-98-5p	chr18:39630215-39630240

Variant related genes	Relation type
ENSG00000267652	TF binding region
ENSG00000267088	TF binding region
ENSG00000225253	TF binding region
PIK3C3	TF binding region
ENSG00000267652	CpG island
ENSG00000267088	CpG island
ENSG00000225253	CpG island
PIK3C3	CpG island
ENSG00000132872	chromatin interactions
ENSG00000132386	chromatin interactions
ENSG00000078142	chromatin interactions

Extended variants
information (count: 13926 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:13926 , 50 per page) page: 1 2 3 4 5 6 7 ... 279

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4890354	chr18:39260616-39260617	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs562296326	chr18:39260653-39260654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs369964122	chr18:39260679-39260680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142378170	chr18:39260706-39260707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs548021134	chr18:39260743-39260744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191050722	chr18:39260755-39260756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs116823471	chr18:39260761-39260762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs567057473	chr18:39260810-39260811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs551780360	chr18:39260831-39260832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570095529	chr18:39260854-39260855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs368255862	chr18:39260870-39260871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs534628570	chr18:39260871-39260872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554672316	chr18:39260883-39260884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546484433	chr18:39260888-39260889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568201801	chr18:39260907-39260908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183359109	chr18:39260931-39260932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535647371	chr18:39260938-39260939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs78991441	chr18:39260962-39260963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575715325	chr18:39261019-39261020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546912358	chr18:39261062-39261063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs77686085	chr18:39261081-39261082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs201756468	chr18:39261117-39261118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs12962196	chr18:39261124-39261125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs77102493	chr18:39261134-39261135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs79219238	chr18:39261137-39261138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs538829794	chr18:39261138-39261139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs535559703	chr18:39261227-39261228	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs550665089	chr18:39261284-39261285	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs140736599	chr18:39261336-39261337	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371523774	chr18:39261363-39261364	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs386802651	chr18:39261364-39261365	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190723485	chr18:39261365-39261366	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs113840079	chr18:39261373-39261374	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183388063	chr18:39261377-39261378	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536289231	chr18:39261420-39261421	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369340265	chr18:39261452-39261453	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs77251490	chr18:39261453-39261454	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs201639514	chr18:39261465-39261466	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75102538	chr18:39261467-39261468	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs76076383	chr18:39261492-39261493	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs182887621	chr18:39261519-39261520	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs35377127	chr18:39261566-39261567	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528066143	chr18:39261609-39261610	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs16975163	chr18:39261631-39261632	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs145880309	chr18:39261646-39261647	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs535357862	chr18:39261664-39261665	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs11873827	chr18:39261692-39261693	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs187347877	chr18:39261743-39261744	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs539967548	chr18:39261763-39261764	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs558280732	chr18:39261804-39261805	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Hepatocellular carcinoma	16750200	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	16774939	CNVD
Colorectal cancer	21297112	CNVD
Cancer	21183584	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Pancreatic cancer	21811587	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:5143 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:39260600-39262200	Enhancers	Hela-S3	cervix
2	chr18:39261200-39261600	Active TSS	Liver	Liver
3	chr18:39261600-39262000	Flanking Active TSS	Liver	Liver
4	chr18:39267400-39267800	Enhancers	Fetal Heart	heart
5	chr18:39267800-39268000	Flanking Active TSS	Fetal Heart	heart
6	chr18:39268000-39268200	Enhancers	Fetal Heart	heart
7	chr18:39268200-39268400	Flanking Active TSS	Fetal Heart	heart
8	chr18:39268400-39270000	Weak transcription	Fetal Heart	heart
9	chr18:39270000-39272400	Enhancers	Fetal Heart	heart
10	chr18:39270600-39271400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr18:39272400-39274800	Weak transcription	Fetal Heart	heart
12	chr18:39272800-39273600	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr18:39273000-39273400	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr18:39273000-39273600	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr18:39273000-39274000	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr18:39273600-39274000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr18:39274000-39275000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr18:39274800-39276200	Enhancers	Fetal Heart	heart
19	chr18:39275000-39275200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr18:39275000-39276200	Enhancers	Hela-S3	cervix
21	chr18:39275200-39275600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr18:39275200-39275800	Enhancers	Dnd41	blood
23	chr18:39275200-39276000	Enhancers	Liver	Liver
24	chr18:39275400-39275600	Enhancers	Primary T cells from cord blood	blood
25	chr18:39275400-39275600	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr18:39275400-39275800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr18:39275400-39275800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr18:39275400-39275800	Active TSS	Fetal Lung	lung
29	chr18:39275400-39276800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr18:39275800-39279800	Weak transcription	Fetal Lung	lung
31	chr18:39276200-39284200	Weak transcription	Fetal Heart	heart
32	chr18:39276800-39278000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr18:39279400-39280400	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr18:39279800-39280400	Enhancers	Fetal Stomach	stomach
35	chr18:39279800-39280600	Enhancers	Fetal Lung	lung
36	chr18:39280000-39280400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr18:39280400-39283400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr18:39281200-39282400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr18:39282400-39286800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr18:39282600-39285600	Enhancers	Liver	Liver
41	chr18:39283200-39284600	Enhancers	HUVEC	blood vessel
42	chr18:39283200-39285400	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr18:39283200-39285400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr18:39283400-39283800	Enhancers	Hela-S3	cervix
45	chr18:39283400-39284000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr18:39283400-39284400	Enhancers	NH-A	brain
47	chr18:39283400-39284600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr18:39283400-39284800	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr18:39283400-39285400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr18:39283600-39283800	Enhancers	HUES64 Cell Line	embryonic stem cell

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