Variant report

Variant	nsv528846
Chromosome Location	chr18:29832147-29890042
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:775)
CpG islands
(count:61)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:775 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:29858231-29858695	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:29851724-29851986	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:29869475-29869822	HepG2	liver:	n/a	n/a
4	BATF	chr18:29881951-29882288	GM12878	blood:	n/a	n/a
5	BHLHE40	chr18:29860244-29860325	K562	blood:	n/a	chr18:29860277-29860286 chr18:29860275-29860288 chr18:29860276-29860285 chr18:29860277-29860286
6	CEBPB	chr18:29882100-29882389	A549	lung:	n/a	n/a
7	CEBPB	chr18:29883372-29883601	A549	lung:	n/a	n/a
8	CEBPB	chr18:29858469-29858713	HepG2	liver:	n/a	n/a
9	CEBPB	chr18:29888506-29889091	IMR90	lung:	n/a	chr18:29889036-29889048 chr18:29888619-29888630
10	CEBPB	chr18:29883347-29883682	HepG2	liver:	n/a	n/a
11	CEBPB	chr18:29883349-29883685	IMR90	lung:	n/a	n/a
12	CEBPB	chr18:29879641-29879682	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr18:29844471-29844690	HepG2	liver:	n/a	n/a
14	CEBPB	chr18:29881996-29882429	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr18:29841166-29841171	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr18:29881892-29882450	IMR90	lung:	n/a	n/a
17	CEBPZ	chr18:29851803-29851804	HepG2	liver:	n/a	n/a
18	CTCF	chr18:29851780-29851930	HRPEpiC	eye:	n/a	chr18:29851847-29851860 chr18:29851844-29851862
19	CTCF	chr18:29851720-29851870	A549	lung:	n/a	chr18:29851847-29851860 chr18:29851844-29851862
20	CTCF	chr18:29851760-29851910	Hela-S3	cervix:	n/a	chr18:29851847-29851860 chr18:29851844-29851862
21	CTCF	chr18:29869610-29869754	MCF-7	breast:	n/a	n/a
22	CTCF	chr18:29851740-29851890	HAc	cerebellar:	n/a	chr18:29851847-29851860 chr18:29851844-29851862
23	CTCF	chr18:29869620-29869770	HVMF	connective:	n/a	n/a
24	CTCF	chr18:29869560-29869710	GM12801	blood:	n/a	n/a
25	CTCF	chr18:29851780-29851930	RPTEC	kidney:	n/a	chr18:29851847-29851860 chr18:29851844-29851862
26	CTCF	chr18:29852120-29852270	GM12875	blood:	n/a	n/a
27	CTCF	chr18:29851760-29851910	GM12873	blood:	n/a	chr18:29851847-29851860 chr18:29851844-29851862
28	CTCF	chr18:29869543-29869788	GM12878	blood:	n/a	n/a
29	CTCF	chr18:29841040-29841190	HMEC	breast:	n/a	n/a
30	CTCF	chr18:29851540-29851690	GM12878	blood:	n/a	n/a
31	CTCF	chr18:29869580-29869730	GM12875	blood:	n/a	n/a
32	CTCF	chr18:29841100-29841250	GM12867	blood:	n/a	n/a
33	CTCF	chr18:29851764-29851916	GM20000	blood:	n/a	chr18:29851847-29851860 chr18:29851844-29851862
34	CTCF	chr18:29852108-29852176	GM10266	blood:	n/a	n/a
35	CTCF	chr18:29869574-29869779	Fibrobl	skin:	n/a	n/a
36	CTCF	chr18:29851715-29851978	LNCaP	prostate:	n/a	chr18:29851847-29851860 chr18:29851844-29851862
37	CTCF	chr18:29841100-29841250	GM12866	blood:	n/a	n/a
38	CTCF	chr18:29869580-29869730	GM12873	blood:	n/a	n/a
39	CTCF	chr18:29851760-29851910	WERI-Rb-1	eye:	n/a	chr18:29851847-29851860 chr18:29851844-29851862
40	CTCF	chr18:29851780-29851930	HMEC	breast:	n/a	chr18:29851847-29851860 chr18:29851844-29851862
41	CTCF	chr18:29851731-29851983	Pancreas_OC	pancreas:	n/a	chr18:29851847-29851860 chr18:29851844-29851862
42	CTCF	chr18:29851780-29851930	HRE	kidney:	n/a	chr18:29851847-29851860 chr18:29851844-29851862
43	CTCF	chr18:29869433-29869908	MCF-7	breast:	n/a	n/a
44	CTCF	chr18:29852120-29852270	GM12874	blood:	n/a	n/a
45	CTCF	chr18:29841088-29841191	K562	blood:	n/a	n/a
46	CTCF	chr18:29841129-29841216	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr18:29841120-29841270	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr18:29869560-29869710	HMF	breast:	n/a	n/a
49	CTCF	chr18:29851840-29851990	GM12868	blood:	n/a	chr18:29851847-29851860 chr18:29851844-29851862
50	CTCF	chr18:29851760-29851910	SAEC	small airway:	n/a	chr18:29851847-29851860 chr18:29851844-29851862

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29847791-29847841	Jurkat	blood:	n/a
2	chr18:29847791-29847841	GM12878	blood:	n/a
3	chr18:29847791-29847841	HRE	kidney:	n/a
4	chr18:29847791-29847841	PFSK-1	brain:	n/a
5	chr18:29847791-29847841	HCF	heart:	n/a
6	chr18:29847791-29847841	NH-A	brain:	n/a
7	chr18:29847791-29847841	HepG2	liver:	n/a
8	chr18:29847791-29847841	SKMC	muscle:	n/a
9	chr18:29847791-29847841	T-47D	breast:	n/a
10	chr18:29847791-29847841	HCM	heart:	n/a
11	chr18:29847791-29847841	NHBE	bronchial:	n/a
12	chr18:29847791-29847841	HRPEpiC	eye:	n/a
13	chr18:29847791-29847841	BE2_C	brain:	n/a
14	chr18:29847791-29847841	ProgFib	skin:	n/a
15	chr18:29847791-29847841	RPTEC	kidney:	n/a
16	chr18:29847791-29847841	NHDF-neo	bronchial:	n/a
17	chr18:29847791-29847841	HEEpiC	esophagus:	n/a
18	chr18:29847791-29847841	AG09319	gingival:	n/a
19	chr18:29847791-29847841	HCPEpiC	choroid plexus:	n/a
20	chr18:29847791-29847841	AG09309	skin:	n/a
21	chr18:29847791-29847841	Caco-2	colon:	n/a
22	chr18:29847791-29847841	BJ	skin:	n/a
23	chr18:29847791-29847841	HPAEpiC	pulmonary alveolar:	n/a
24	chr18:29847791-29847841	AoSMC	blood vessel:	n/a
25	chr18:29847791-29847841	MCF-7	breast:	n/a
26	chr18:29847791-29847841	GM12892	blood:	n/a
27	chr18:29847791-29847841	CMK	blood:	n/a
28	chr18:29847791-29847841	A549	lung:	n/a
29	chr18:29847791-29847841	HL-60	blood:	n/a
30	chr18:29847791-29847841	HIPEpiC	eye:	n/a
31	chr18:29847791-29847841	HMEC	breast:	n/a
32	chr18:29847791-29847841	K562	blood:	n/a
33	chr18:29847791-29847841	PANC-1	pancreas:	n/a
34	chr18:29847791-29847841	AG10803	skin:	n/a
35	chr18:29847791-29847841	GM06990	blood:	n/a
36	chr18:29847791-29847841	SK-N-SH_RA	brain:	n/a
37	chr18:29847791-29847841	ECC-1	luminal epithelium:	n/a
38	chr18:29847791-29847841	GM19239	blood:	n/a
39	chr18:29847791-29847841	GM12891	blood:	n/a
40	chr18:29847791-29847841	HCT-116	colon:	n/a
41	chr18:29847791-29847841	HUVEC	blood vessel:	n/a
42	chr18:29847791-29847841	PrEC	prostate:	n/a
43	chr18:29847791-29847841	HNPCEpiC	eye:	n/a
44	chr18:29847791-29847841	SAEC	small airway:	n/a
45	chr18:29847791-29847841	HEK293	kidney:	embryo
46	chr18:29847791-29847841	MCF10A-Er-Src	breast:	n/a
47	chr18:29847791-29847841	IMR90	lung:	fetal
48	chr18:29847791-29847841	AG04449	skin:	fetal
49	chr18:29847791-29847841	NB4	blood:	n/a
50	chr18:29847791-29847841	H1-hESC	embryonic stem cell:	embryo

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:29867305..29869453-chr18:30048858..30050694,2	MCF-7	breast:
2	chr18:29839871..29842778-chr18:29859077..29861521,2	K562	blood:
3	chr18:29837235..29838765-chr18:29839489..29841604,2	MCF-7	breast:
4	chr18:29853249..29854777-chr18:29860158..29863062,2	K562	blood:
5	chr18:29851552..29852413-chr18:30132133..30133147,4	MCF-7	breast:
6	chr18:29843865..29846147-chr18:30049369..30051018,2	MCF-7	breast:
7	chr18:29837235..29838765-chr18:29839489..29841604,2	MCF-7	breast:
8	chr18:29877540..29879536-chr18:29882707..29884848,2	MCF-7	breast:
9	chr18:29869293..29870126-chr18:30132476..30133178,2	MCF-7	breast:
10	chr18:29887452..29890348-chr18:30046410..30049276,2	MCF-7	breast:
11	chr18:29852094..29854619-chr18:29865481..29868899,3	K562	blood:
12	chr18:29873261..29875337-chr18:30049350..30051070,2	MCF-7	breast:
13	chr18:29847813..29851392-chr18:29854747..29858581,3	MCF-7	breast:
14	chr18:29856972..29858473-chr18:30049654..30051815,2	MCF-7	breast:
15	chr18:29853249..29854777-chr18:29860158..29863062,2	K562	blood:
16	chr18:29869308..29870117-chr18:30050651..30051625,5	MCF-7	breast:
17	chr18:29847813..29851392-chr18:29854747..29858581,3	MCF-7	breast:
18	chr18:29869178..29870066-chr18:30128854..30129812,2	MCF-7	breast:
19	chr18:29868718..29871349-chr18:30049265..30052223,3	MCF-7	breast:
20	chr18:29854965..29857562-chr18:29891190..29893119,2	K562	blood:
21	chr18:29869255..29869847-chr18:30050643..30051337,3	MCF-7	breast:
22	chr18:29851742..29852316-chr18:30263045..30263644,2	MCF-7	breast:
23	chr18:29851378..29852356-chr18:30050569..30051553,4	MCF-7	breast:
24	chr18:29851409..29852190-chr18:30050752..30051380,2	MCF-7	breast:
25	chr18:29851159..29852631-chr18:30128814..30129900,6	MCF-7	breast:
26	chr18:29851628..29852386-chr18:30132192..30133063,2	MCF-7	breast:
27	chr18:29877540..29879536-chr18:29882707..29884848,2	MCF-7	breast:
28	chr18:29839871..29842778-chr18:29859077..29861521,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	FAM59A	hsa-miR-186-5p	chr18:29843701-29843695

Variant related genes	Relation type
GAREM	TF binding region
ENSG00000222395	TF binding region
ENSG00000264982	TF binding region
ENSG00000263904	TF binding region
GAREM	CpG island
ENSG00000222395	CpG island
ENSG00000264982	CpG island
ENSG00000263904	CpG island
ENSG00000264982	chromatin interactions
ENSG00000141441	chromatin interactions

Extended variants
information (count: 2238 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2238 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16962901	chr18:29832147-29832148	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531811110	chr18:29832211-29832212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs556991062	chr18:29832225-29832226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190320867	chr18:29832233-29832234	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116536595	chr18:29832312-29832313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554885534	chr18:29832320-29832321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs36120628	chr18:29832323-29832324	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573049106	chr18:29832325-29832326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375529291	chr18:29832328-29832329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4268826	chr18:29832329-29832330	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs71848133	chr18:29832330-29832331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529559726	chr18:29832430-29832431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs368375716	chr18:29832461-29832462	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs79938508	chr18:29832476-29832477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs17743166	chr18:29832530-29832531	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs112785703	chr18:29832565-29832566	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150145146	chr18:29832584-29832585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192582499	chr18:29832585-29832586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532902102	chr18:29832591-29832592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544345623	chr18:29832592-29832593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551057688	chr18:29832597-29832598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140214145	chr18:29832613-29832614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs145626892	chr18:29832731-29832732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs528566598	chr18:29832801-29832802	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs147142724	chr18:29832809-29832810	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs62093960	chr18:29832839-29832840	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs546851495	chr18:29832871-29832872	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs571311463	chr18:29832893-29832894	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538622172	chr18:29832919-29832920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184920679	chr18:29832950-29832951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112652419	chr18:29832954-29832955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs536477365	chr18:29833126-29833127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139460880	chr18:29833149-29833150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572951393	chr18:29833195-29833196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536863119	chr18:29833202-29833203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs534081721	chr18:29833222-29833223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs638649	chr18:29833223-29833224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576928581	chr18:29833248-29833249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145503535	chr18:29833282-29833283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs557394786	chr18:29833375-29833376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556251554	chr18:29833383-29833384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs148462619	chr18:29833474-29833475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs180807760	chr18:29833475-29833476	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561334032	chr18:29833484-29833485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528616331	chr18:29833485-29833486	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540548587	chr18:29833497-29833498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565205375	chr18:29833502-29833503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532407475	chr18:29833512-29833513	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569416295	chr18:29833554-29833555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536409874	chr18:29833562-29833563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Esophageal squamous carcinoma	18350619	CNVD
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
Glioblastoma multiforme	21922591	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
Lung cancer	18438408	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
Breast cancer	17133270	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21297112	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	17002787	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	16912164	CNVD
Renal cell carcinoma	19150565	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19150955	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29821200-29832400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr18:29823800-29848000	Weak transcription	Aorta	Aorta
3	chr18:29831000-29832800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr18:29831200-29832600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr18:29831200-29832600	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr18:29831200-29832800	Enhancers	Primary hematopoietic stem cells	blood
7	chr18:29831400-29832400	Enhancers	Fetal Intestine Large	intestine
8	chr18:29831400-29832600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr18:29831400-29832800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr18:29831400-29832800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr18:29831400-29833000	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr18:29831400-29847600	Weak transcription	Pancreas	Pancrea
13	chr18:29831600-29832600	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr18:29831600-29833400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr18:29831800-29832200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr18:29831800-29833000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr18:29832000-29832400	Weak transcription	Fetal Intestine Small	intestine
18	chr18:29832200-29832600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr18:29832200-29832600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr18:29832200-29832800	Enhancers	H1 Cell Line	embryonic stem cell
21	chr18:29832400-29832600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr18:29832400-29832600	Enhancers	Fetal Intestine Small	intestine
23	chr18:29832400-29837000	Weak transcription	Fetal Intestine Large	intestine
24	chr18:29832600-29832800	Enhancers	H9 Cell Line	embryonic stem cell
25	chr18:29832600-29836000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr18:29832600-29837400	Weak transcription	Fetal Intestine Small	intestine
27	chr18:29832800-29834800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr18:29832800-29835600	Weak transcription	Primary hematopoietic stem cells	blood
29	chr18:29833000-29834200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr18:29833400-29833600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr18:29834200-29837000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr18:29834800-29835200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr18:29834800-29838600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr18:29835200-29861600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr18:29835600-29835800	Enhancers	Primary hematopoietic stem cells	blood
36	chr18:29835800-29836200	Weak transcription	Primary hematopoietic stem cells	blood
37	chr18:29836000-29839000	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr18:29836200-29839200	Enhancers	Primary hematopoietic stem cells	blood
39	chr18:29836400-29839200	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr18:29836600-29839000	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr18:29837000-29838000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr18:29837000-29840200	Enhancers	Fetal Intestine Large	intestine
43	chr18:29837200-29837400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr18:29837200-29837400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr18:29837200-29837400	Enhancers	Right Ventricle	heart
46	chr18:29837200-29840000	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr18:29837400-29837600	Enhancers	Colonic Mucosa	Colon
48	chr18:29837400-29837800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr18:29837400-29838000	Bivalent Enhancer	Small Intestine	intestine
50	chr18:29837400-29839800	Enhancers	Fetal Intestine Small	intestine

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