Variant report

Variant	nsv524199
Chromosome Location	chr18:29595164-29598809
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:332)
CpG islands
(count:550)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:332 , 50 per page) page: 1 2 3 4 5 6 7

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	chr18:29598201-29598753	K562	blood:	n/a	n/a
3	ATF2	chr18:29598266-29598843	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr18:29598246-29598774	GM12878	blood:	n/a	n/a
5	ATF2	chr18:29598243-29598823	GM12878	blood:	n/a	n/a
6	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
7	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
8	BHLHE40	chr18:29598328-29598768	K562	blood:	n/a	chr18:29598572-29598588
9	BHLHE40	chr18:29598385-29598942	GM12878	blood:	n/a	chr18:29598572-29598588
10	BRCA1	chr18:29598267-29598862	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr18:29598314-29598876	K562	blood:	n/a	n/a
12	CCNT2	chr18:29598329-29599338	K562	blood:	n/a	n/a
13	CEBPB	chr18:29598050-29599141	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr18:29598272-29598597	K562	blood:	n/a	n/a
15	CHD1	chr18:29598484-29599007	GM12878	blood:	n/a	n/a
16	CHD1	chr18:29598183-29598942	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr18:29598204-29599140	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr18:29598225-29599196	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr18:29598346-29598788	GM12878	blood:	n/a	n/a
20	CHD2	chr18:29598575-29598891	HepG2	liver:	n/a	n/a
21	CHD2	chr18:29598471-29598620	K562	blood:	n/a	n/a
22	CREB1	chr18:29598150-29599199	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTBP2	chr18:29597969-29599684	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr18:29598660-29598810	HMEC	breast:	n/a	n/a
25	CTCF	chr18:29598740-29598890	AG04449	skin:	n/a	n/a
26	CTCF	chr18:29598440-29598590	SAEC	small airway:	n/a	n/a
27	CTCF	chr18:29598734-29598737	MCF-7	breast:	n/a	n/a
28	CTCF	chr18:29598758-29598828	GM12892	blood:	n/a	n/a
29	CTCF	chr18:29598760-29598910	GM12873	blood:	n/a	n/a
30	CTCF	chr18:29598766-29598829	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr18:29598680-29598830	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr18:29598700-29598850	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr18:29598780-29598930	NHEK	skin:	n/a	n/a
34	CTCF	chr18:29598700-29598850	GM12873	blood:	n/a	n/a
35	CTCF	chr18:29598740-29598890	GM12872	blood:	n/a	n/a
36	CTCF	chr18:29598640-29598790	GM12873	blood:	n/a	n/a
37	CTCF	chr18:29598720-29598870	GM12866	blood:	n/a	n/a
38	CTCF	chr18:29598700-29598850	SAEC	small airway:	n/a	n/a
39	CTCF	chr18:29598600-29598750	GM12878	blood:	n/a	n/a
40	CTCF	chr18:29598720-29598870	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr18:29598780-29598930	GM12869	blood:	n/a	n/a
42	CTCF	chr18:29598740-29598890	GM12874	blood:	n/a	n/a
43	CTCF	chr18:29598715-29598832	GM19239	blood:	n/a	n/a
44	CTCF	chr18:29598720-29598870	GM12865	blood:	n/a	n/a
45	CTCF	chr18:29598680-29598830	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr18:29598673-29598722	MCF-7	breast:	n/a	n/a
47	CTCF	chr18:29598684-29598716	GM19240	blood:	n/a	n/a
48	CTCF	chr18:29598722-29598757	GM12892	blood:	n/a	n/a
49	CTCF	chr18:29598500-29598650	SAEC	small airway:	n/a	n/a
50	CTCF	chr18:29598662-29598862	GM12878	blood:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29598697-29598747	Hela-S3	cervix:	n/a
2	chr18:29598697-29598747	Hela-S3	cervix:	n/a
3	chr18:29598296-29598346	HCF	heart:	n/a
4	chr18:29598757-29598807	AG09309	skin:	n/a
5	chr18:29598433-29598483	Caco-2	colon:	n/a
6	chr18:29598697-29598747	HL-60	blood:	n/a
7	chr18:29598697-29598747	SK-N-SH	brain:	n/a
8	chr18:29597493-29597543	HRCEpiC	kidney:	n/a
9	chr18:29597493-29597543	K562	blood:	n/a
10	chr18:29598757-29598807	AG09319	gingival:	n/a
11	chr18:29598437-29598487	HMEC	breast:	n/a
12	chr18:29598437-29598487	Caco-2	colon:	n/a
13	chr18:29598400-29598450	PANC-1	pancreas:	n/a
14	chr18:29597478-29597528	ProgFib	skin:	n/a
15	chr18:29597478-29597528	SK-N-MC	brain:	n/a
16	chr18:29598697-29598747	LNCaP	prostate:	n/a
17	chr18:29598757-29598807	GM12891	blood:	n/a
18	chr18:29598757-29598807	IMR90	lung:	fetal
19	chr18:29598296-29598346	MCF10A-Er-Src	breast:	n/a
20	chr18:29598296-29598346	GM12892	blood:	n/a
21	chr18:29598697-29598747	AG10803	skin:	n/a
22	chr18:29598757-29598807	NHDF-neo	bronchial:	n/a
23	chr18:29596358-29596408	NH-A	brain:	n/a
24	chr18:29598757-29598807	LNCaP	prostate:	n/a
25	chr18:29596358-29596408	BE2_C	brain:	n/a
26	chr18:29596358-29596408	NHBE	bronchial:	n/a
27	chr18:29598400-29598450	ovcar-3	ovarian:	n/a
28	chr18:29598296-29598346	HEEpiC	esophagus:	n/a
29	chr18:29598757-29598807	AG04450	lung:	fetal
30	chr18:29598296-29598346	Hepatocyte	liver:	n/a
31	chr18:29598697-29598747	HAEpiC	amniotic membrane:	n/a
32	chr18:29596358-29596408	AG10803	skin:	n/a
33	chr18:29598697-29598747	HRE	kidney:	n/a
34	chr18:29598433-29598483	H1-hESC	embryonic stem cell:	embryo
35	chr18:29597478-29597528	SAEC	small airway:	n/a
36	chr18:29597493-29597543	CMK	blood:	n/a
37	chr18:29598400-29598450	LNCaP	prostate:	n/a
38	chr18:29598296-29598346	HepG2	liver:	n/a
39	chr18:29597493-29597543	PrEC	prostate:	n/a
40	chr18:29598400-29598450	AG04449	skin:	fetal
41	chr18:29597478-29597528	NH-A	brain:	n/a
42	chr18:29597478-29597528	AG04449	skin:	fetal
43	chr18:29598400-29598450	HPAEpiC	pulmonary alveolar:	n/a
44	chr18:29596358-29596408	MCF-7	breast:	n/a
45	chr18:29598757-29598807	Hepatocyte	liver:	n/a
46	chr18:29598296-29598346	HRPEpiC	eye:	n/a
47	chr18:29598296-29598346	K562	blood:	n/a
48	chr18:29598296-29598346	U87	brain:	n/a
49	chr18:29598757-29598807	HUVEC	blood vessel:	n/a
50	chr18:29597493-29597543	HCT-116	colon:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:29522696..29523369-chr18:29598378..29599258,2	Hela-S3	cervix:
2	chr18:29522249..29524505-chr18:29596603..29599089,2	MCF-7	breast:
3	chr18:29598540..29599388-chr18:29671670..29672456,2	Hela-S3	cervix:
4	chr18:29588031..29590764-chr18:29592870..29595455,2	K562	blood:
5	chr18:29598516..29599058-chr2:47168202..47168759,2	Hela-S3	cervix:
6	chr18:29598053..29598969-chr6:27114842..27115533,2	Hela-S3	cervix:
7	chr18:29596689..29599956-chr18:29670764..29674475,6	MCF-7	breast:
8	chr18:29597506..29599866-chr18:29670953..29673378,4	MCF-7	breast:

No data

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

Extended variants
information (count: 143 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:143 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13381098	chr18:29595164-29595165	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs148222544	chr18:29595165-29595166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539895122	chr18:29595171-29595172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371282557	chr18:29595183-29595184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529109740	chr18:29595184-29595185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374189131	chr18:29595188-29595189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs540835751	chr18:29595205-29595206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564888897	chr18:29595234-29595235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559109156	chr18:29595315-29595316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533087507	chr18:29595340-29595341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570341904	chr18:29595350-29595351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73413942	chr18:29595360-29595361	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs550268056	chr18:29595383-29595384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530386571	chr18:29595386-29595387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs117084884	chr18:29595400-29595401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567213772	chr18:29595435-29595436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs113796904	chr18:29595464-29595465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs145474278	chr18:29595487-29595488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546657217	chr18:29595519-29595520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs78575933	chr18:29595543-29595544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs199910978	chr18:29595574-29595575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548341353	chr18:29595583-29595584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs187053310	chr18:29595602-29595603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs558449973	chr18:29595624-29595625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576506573	chr18:29595640-29595641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189983424	chr18:29595659-29595660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555847767	chr18:29595680-29595681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138054113	chr18:29595720-29595721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182959015	chr18:29595725-29595726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142544301	chr18:29595735-29595736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs577406724	chr18:29595749-29595750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs11876253	chr18:29595792-29595793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs146043088	chr18:29595832-29595833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs530542645	chr18:29595846-29595847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548736672	chr18:29595848-29595849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539006741	chr18:29595919-29595920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs17718931	chr18:29595943-29595944	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs139620457	chr18:29595968-29595969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs575793004	chr18:29595990-29595991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs532418693	chr18:29596012-29596013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs149563651	chr18:29596186-29596187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs145066610	chr18:29596290-29596291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs566283052	chr18:29596297-29596298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs188291986	chr18:29596359-29596360	Weak transcription Enhancers	CpG island	2 gene(s)	Overlapped CNVs	n/a
45	rs144210757	chr18:29596379-29596380	Weak transcription Enhancers	CpG island	2 gene(s)	Overlapped CNVs	n/a
46	rs570332243	chr18:29596381-29596382	Weak transcription Enhancers	CpG island	2 gene(s)	Overlapped CNVs	n/a
47	rs75717820	chr18:29596423-29596424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs555509053	chr18:29596499-29596500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs193288346	chr18:29596509-29596510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs534847292	chr18:29596564-29596565	Weak transcription Enhancers	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:314 , 50 per page) page: 1 2 3 4 5 6 7

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	chr18:29590600-29597800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr18:29590800-29595800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr18:29590800-29596800	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr18:29591000-29595800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr18:29591000-29596000	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr18:29593600-29598400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr18:29595400-29596200	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr18:29595800-29596000	Enhancers	Colon Smooth Muscle	Colon
11	chr18:29595800-29597400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr18:29595800-29597600	Enhancers	Primary T cells from cord blood	blood
13	chr18:29595800-29597800	Enhancers	Primary T helper naive cells from peripheral blood	blood
14	chr18:29595800-29598000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr18:29596000-29596400	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr18:29596000-29597800	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr18:29596200-29596600	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr18:29596200-29598000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr18:29596400-29596800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr18:29596400-29598200	Weak transcription	Colon Smooth Muscle	Colon
21	chr18:29596600-29597400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
22	chr18:29596600-29597800	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr18:29596800-29597400	Enhancers	Dnd41	blood
24	chr18:29596800-29597800	Enhancers	Primary T cells fromperipheralblood	blood
25	chr18:29596800-29598000	Enhancers	Primary T killer memory cells from peripheral blood	blood
26	chr18:29597000-29597800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr18:29597000-29598000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr18:29597000-29598000	Enhancers	Fetal Thymus	thymus
29	chr18:29597200-29597600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr18:29597200-29597600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr18:29597200-29597800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr18:29597200-29598000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr18:29597400-29597600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
34	chr18:29597400-29597600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
35	chr18:29597400-29597800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr18:29597400-29597800	Enhancers	Primary B cells from cord blood	blood
37	chr18:29597400-29597800	Enhancers	Primary B cells from peripheral blood	blood
38	chr18:29597400-29597800	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr18:29597400-29597800	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr18:29597400-29598000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr18:29597400-29598000	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr18:29597400-29598000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
43	chr18:29597400-29598000	Enhancers	Fetal Intestine Large	intestine
44	chr18:29597400-29598000	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr18:29597400-29600400	Flanking Active TSS	Dnd41	blood
46	chr18:29597600-29597800	Enhancers	Primary hematopoietic stem cells	blood
47	chr18:29597600-29597800	Enhancers	Adipose Nuclei	Adipose
48	chr18:29597600-29597800	Enhancers	Fetal Intestine Small	intestine
49	chr18:29597600-29598000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr18:29597600-29598000	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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