Variant report

Variant	esv1803283
Chromosome Location	chr18:29591102-29640430
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:677)
CpG islands
(count:855)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:677 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:29598287-29598586	K562	blood:	n/a	n/a
2	ATF1	chr18:29629850-29630179	K562	blood:	n/a	n/a
3	ATF1	chr18:29598201-29598753	K562	blood:	n/a	n/a
4	ATF1	chr18:29622443-29622655	K562	blood:	n/a	n/a
5	ATF2	chr18:29598243-29598823	GM12878	blood:	n/a	n/a
6	ATF2	chr18:29598246-29598774	GM12878	blood:	n/a	n/a
7	ATF2	chr18:29598266-29598843	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr18:29629861-29630167	K562	blood:	n/a	n/a
9	BACH1	chr18:29598998-29599076	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCLAF1	chr18:29598288-29599107	GM12878	blood:	n/a	chr18:29598627-29598640 chr18:29598573-29598586 chr18:29598587-29598596 chr18:29598673-29598682 chr18:29598626-29598639 chr18:29598692-29598705
11	BCLAF1	chr18:29598297-29598917	GM12878	blood:	n/a	chr18:29598627-29598640 chr18:29598573-29598586 chr18:29598587-29598596 chr18:29598673-29598682 chr18:29598626-29598639 chr18:29598692-29598705
12	BCLAF1	chr18:29599513-29599997	GM12878	blood:	n/a	n/a
13	BHLHE40	chr18:29599279-29599710	HepG2	liver:	n/a	n/a
14	BHLHE40	chr18:29599317-29599873	GM12878	blood:	n/a	n/a
15	BHLHE40	chr18:29598328-29598768	K562	blood:	n/a	chr18:29598572-29598588
16	BHLHE40	chr18:29599438-29599561	K562	blood:	n/a	n/a
17	BHLHE40	chr18:29598385-29598942	GM12878	blood:	n/a	chr18:29598572-29598588
18	BRCA1	chr18:29598267-29598862	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr18:29629684-29630253	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr18:29598314-29598876	K562	blood:	n/a	n/a
21	CCNT2	chr18:29637691-29637926	K562	blood:	n/a	n/a
22	CCNT2	chr18:29598329-29599338	K562	blood:	n/a	n/a
23	CEBPB	chr18:29599413-29599614	HepG2	liver:	n/a	n/a
24	CEBPB	chr18:29629851-29630252	MCF-7	breast:	n/a	n/a
25	CEBPB	chr18:29612639-29612839	HepG2	liver:	n/a	chr18:29612772-29612783
26	CEBPB	chr18:29630867-29630911	HepG2	liver:	n/a	n/a
27	CEBPB	chr18:29598942-29599139	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr18:29630873-29630879	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr18:29628623-29628980	A549	lung:	n/a	chr18:29628792-29628803
30	CEBPB	chr18:29629763-29630270	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr18:29628611-29629456	Hela-S3	cervix:	n/a	chr18:29628792-29628803
32	CEBPB	chr18:29612642-29612889	K562	blood:	n/a	chr18:29612772-29612783
33	CEBPB	chr18:29628620-29628932	ECC-1	luminal epithelium:	n/a	chr18:29628792-29628803
34	CEBPB	chr18:29628650-29628930	IMR90	lung:	n/a	chr18:29628792-29628803
35	CEBPB	chr18:29598272-29598597	K562	blood:	n/a	n/a
36	CEBPB	chr18:29628590-29628957	H1-hESC	embryonic stem cell:	n/a	chr18:29628792-29628803
37	CEBPB	chr18:29598050-29599141	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr18:29604371-29604625	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr18:29628621-29628984	K562	blood:	n/a	chr18:29628792-29628803
40	CEBPB	chr18:29628634-29628990	HepG2	liver:	n/a	chr18:29628792-29628803
41	CEBPD	chr18:29599336-29599743	HepG2	liver:	n/a	n/a
42	CHD1	chr18:29598183-29598942	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD1	chr18:29598484-29599007	GM12878	blood:	n/a	n/a
44	CHD1	chr18:29599703-29599858	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr18:29598471-29598620	K562	blood:	n/a	n/a
46	CHD2	chr18:29621058-29621232	GM12878	blood:	n/a	n/a
47	CHD2	chr18:29598575-29598891	HepG2	liver:	n/a	n/a
48	CHD2	chr18:29599422-29599673	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr18:29598204-29599140	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr18:29598225-29599196	Hela-S3	cervix:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29598400-29598450	NT2-D1	testis:	n/a
2	chr18:29598400-29598450	NT2-D1	testis:	n/a
3	chr18:29597493-29597543	GM12892	blood:	n/a
4	chr18:29598296-29598346	SK-N-SH_RA	brain:	n/a
5	chr18:29597478-29597528	GM12891	blood:	n/a
6	chr18:29598919-29598969	HCF	heart:	n/a
7	chr18:29599349-29599399	HEEpiC	esophagus:	n/a
8	chr18:29597493-29597543	Hepatocyte	liver:	n/a
9	chr18:29598433-29598483	HMEC	breast:	n/a
10	chr18:29599349-29599399	NHBE	bronchial:	n/a
11	chr18:29598697-29598747	NH-A	brain:	n/a
12	chr18:29599349-29599399	ProgFib	skin:	n/a
13	chr18:29598697-29598747	HEEpiC	esophagus:	n/a
14	chr18:29597478-29597528	H1-hESC	embryonic stem cell:	embryo
15	chr18:29598433-29598483	NB4	blood:	n/a
16	chr18:29599349-29599399	NH-A	brain:	n/a
17	chr18:29598757-29598807	AG04450	lung:	fetal
18	chr18:29598757-29598807	HAEpiC	amniotic membrane:	n/a
19	chr18:29599776-29599826	GM12878	blood:	n/a
20	chr18:29598437-29598487	ovcar-3	ovarian:	n/a
21	chr18:29597478-29597528	GM12892	blood:	n/a
22	chr18:29598433-29598483	HAEpiC	amniotic membrane:	n/a
23	chr18:29598296-29598346	HEEpiC	esophagus:	n/a
24	chr18:29599349-29599399	AG04449	skin:	fetal
25	chr18:29598433-29598483	AG09309	skin:	n/a
26	chr18:29599124-29599174	BE2_C	brain:	n/a
27	chr18:29597478-29597528	RPTEC	kidney:	n/a
28	chr18:29599124-29599174	HCF	heart:	n/a
29	chr18:29598296-29598346	AG04449	skin:	fetal
30	chr18:29599124-29599174	HRE	kidney:	n/a
31	chr18:29599124-29599174	GM12891	blood:	n/a
32	chr18:29598697-29598747	AG04450	lung:	fetal
33	chr18:29598400-29598450	HRCEpiC	kidney:	n/a
34	chr18:29598757-29598807	HCT-116	colon:	n/a
35	chr18:29598400-29598450	HL-60	blood:	n/a
36	chr18:29601617-29601667	NB4	blood:	n/a
37	chr18:29601617-29601667	HNPCEpiC	eye:	n/a
38	chr18:29598757-29598807	HRCEpiC	kidney:	n/a
39	chr18:29599776-29599826	SK-N-MC	brain:	n/a
40	chr18:29597478-29597528	HCM	heart:	n/a
41	chr18:29601617-29601667	BJ	skin:	n/a
42	chr18:29596358-29596408	PANC-1	pancreas:	n/a
43	chr18:29599124-29599174	CMK	blood:	n/a
44	chr18:29598437-29598487	A549	lung:	n/a
45	chr18:29599776-29599826	U87	brain:	n/a
46	chr18:29598433-29598483	GM06990	blood:	n/a
47	chr18:29599776-29599826	HCT-116	colon:	n/a
48	chr18:29599124-29599174	HEEpiC	esophagus:	n/a
49	chr18:29601617-29601667	HCF	heart:	n/a
50	chr18:29598433-29598483	HL-60	blood:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:29599759..29602632-chr18:29612702..29615585,2	K562	blood:
2	chr18:29588031..29590764-chr18:29592870..29595455,2	K562	blood:
3	chr18:29628181..29630533-chr18:29631429..29634258,2	K562	blood:
4	chr18:29522249..29524505-chr18:29596603..29599089,2	MCF-7	breast:
5	chr18:29634515..29636379-chr18:29669677..29672287,2	K562	blood:
6	chr18:29627167..29630199-chr18:29636051..29638994,4	MCF-7	breast:
7	chr18:29599759..29602632-chr18:29612702..29615585,2	K562	blood:
8	chr18:29597754..29600118-chr18:29600354..29602293,2	MCF-7	breast:
9	chr18:29627167..29630199-chr18:29636051..29638994,4	MCF-7	breast:
10	chr18:29628181..29630533-chr18:29631429..29634258,2	K562	blood:
11	chr18:29597700..29599894-chr18:29602384..29604924,2	K562	blood:
12	chr18:29598566..29600531-chr18:29604153..29606634,2	MCF-7	breast:
13	chr18:29598540..29599388-chr18:29671670..29672456,2	Hela-S3	cervix:
14	chr18:29596689..29599956-chr18:29670764..29674475,6	MCF-7	breast:
15	chr18:29598053..29598969-chr6:27114842..27115533,2	Hela-S3	cervix:
16	chr18:29597506..29599866-chr18:29670953..29673378,4	MCF-7	breast:
17	chr18:29522696..29523369-chr18:29598378..29599258,2	Hela-S3	cervix:
18	chr18:29616707..29618971-chr18:29620186..29622381,2	K562	blood:
19	chr18:29598516..29599058-chr2:47168202..47168759,2	Hela-S3	cervix:
20	chr18:29637884..29642506-chr18:29670649..29674281,4	K562	blood:
21	chr18:29616707..29618971-chr18:29620186..29622381,2	K562	blood:
22	chr18:29636110..29637655-chr18:29646609..29648361,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000263917	TF binding region
RNF125	TF binding region
ENSG00000263917	CpG island
RNF125	CpG island
ENSG00000153339	chromatin interactions
ENSG00000184825	chromatin interactions
ENSG00000265008	chromatin interactions
ENSG00000068724	chromatin interactions
ENSG00000263823	chromatin interactions
ENSG00000263917	chromatin interactions
ENSG00000265565	chromatin interactions
ENSG00000134758	chromatin interactions
ENSG00000238982	chromatin interactions
ENSG00000101695	chromatin interactions

Extended variants
information (count: 1845 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1845 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8087275	chr18:29591102-29591103	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536134095	chr18:29591161-29591162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs8086283	chr18:29591165-29591166	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs190618281	chr18:29591202-29591203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs76195062	chr18:29591243-29591244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541888238	chr18:29591287-29591288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529586889	chr18:29591288-29591289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368428710	chr18:29591296-29591297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs72931456	chr18:29591322-29591323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528644000	chr18:29591399-29591400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs35091150	chr18:29591407-29591408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs71857120	chr18:29591408-29591409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs10526315	chr18:29591438-29591439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186463591	chr18:29591451-29591452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547883736	chr18:29591454-29591455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191845808	chr18:29591491-29591492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs9947471	chr18:29591544-29591545	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs139552386	chr18:29591567-29591568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536389652	chr18:29591585-29591586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568009714	chr18:29591601-29591602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112240504	chr18:29591647-29591648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs78338767	chr18:29591673-29591674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374644688	chr18:29591712-29591713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533944197	chr18:29591728-29591729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558914396	chr18:29591733-29591734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs35266729	chr18:29591756-29591757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577177057	chr18:29591788-29591789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544503475	chr18:29591847-29591848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556224747	chr18:29591882-29591883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574475031	chr18:29591917-29591918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182926573	chr18:29591941-29591942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560145727	chr18:29591969-29591970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528700383	chr18:29592000-29592001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536040036	chr18:29592014-29592015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547013718	chr18:29592087-29592088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142788721	chr18:29592098-29592099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7236806	chr18:29592111-29592112	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs7235750	chr18:29592170-29592171	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs550857365	chr18:29592174-29592175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187521967	chr18:29592187-29592188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191552394	chr18:29592352-29592353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs151075750	chr18:29592357-29592358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs374663886	chr18:29592386-29592387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563859973	chr18:29592397-29592398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548398417	chr18:29592403-29592404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182489347	chr18:29592422-29592423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187535207	chr18:29592446-29592447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552436642	chr18:29592453-29592454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530563455	chr18:29592471-29592472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538189447	chr18:29592511-29592512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Prostate cancer	22341455	CNVD

Chromatin state (count:1589 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29587000-29598000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr18:29588600-29598200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr18:29589200-29591200	Enhancers	Hela-S3	cervix
4	chr18:29590600-29597800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr18:29590800-29595800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr18:29590800-29596800	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr18:29591000-29595800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr18:29591000-29596000	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr18:29593600-29598400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr18:29595400-29596200	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr18:29595800-29596000	Enhancers	Colon Smooth Muscle	Colon
12	chr18:29595800-29597400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr18:29595800-29597600	Enhancers	Primary T cells from cord blood	blood
14	chr18:29595800-29597800	Enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr18:29595800-29598000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr18:29596000-29596400	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr18:29596000-29597800	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr18:29596200-29596600	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr18:29596200-29598000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr18:29596400-29596800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr18:29596400-29598200	Weak transcription	Colon Smooth Muscle	Colon
22	chr18:29596600-29597400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
23	chr18:29596600-29597800	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr18:29596800-29597400	Enhancers	Dnd41	blood
25	chr18:29596800-29597800	Enhancers	Primary T cells fromperipheralblood	blood
26	chr18:29596800-29598000	Enhancers	Primary T killer memory cells from peripheral blood	blood
27	chr18:29597000-29597800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr18:29597000-29598000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr18:29597000-29598000	Enhancers	Fetal Thymus	thymus
30	chr18:29597200-29597600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr18:29597200-29597600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr18:29597200-29597800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr18:29597200-29598000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
34	chr18:29597400-29597600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
35	chr18:29597400-29597600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
36	chr18:29597400-29597800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr18:29597400-29597800	Enhancers	Primary B cells from cord blood	blood
38	chr18:29597400-29597800	Enhancers	Primary B cells from peripheral blood	blood
39	chr18:29597400-29597800	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr18:29597400-29597800	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr18:29597400-29598000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr18:29597400-29598000	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr18:29597400-29598000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
44	chr18:29597400-29598000	Enhancers	Fetal Intestine Large	intestine
45	chr18:29597400-29598000	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr18:29597400-29600400	Flanking Active TSS	Dnd41	blood
47	chr18:29597600-29597800	Enhancers	Primary hematopoietic stem cells	blood
48	chr18:29597600-29597800	Enhancers	Adipose Nuclei	Adipose
49	chr18:29597600-29597800	Enhancers	Fetal Intestine Small	intestine
50	chr18:29597600-29598000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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