Variant report

Variant	nsv1061305
Chromosome Location	chr18:29609935-29664528
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:360)
CpG islands
(count:0)
Chromatin interactive
region (count:24)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:360 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:29652341-29652647	K562	blood:	n/a	n/a
2	ARID3A	chr18:29652345-29652621	HepG2	liver:	n/a	n/a
3	ATF1	chr18:29640546-29640706	K562	blood:	n/a	n/a
4	ATF1	chr18:29622443-29622655	K562	blood:	n/a	n/a
5	ATF1	chr18:29629850-29630179	K562	blood:	n/a	n/a
6	ATF3	chr18:29629861-29630167	K562	blood:	n/a	n/a
7	BRCA1	chr18:29629684-29630253	Hela-S3	cervix:	n/a	n/a
8	CCNT2	chr18:29637691-29637926	K562	blood:	n/a	n/a
9	CEBPB	chr18:29660469-29660772	IMR90	lung:	n/a	chr18:29660614-29660625
10	CEBPB	chr18:29628611-29629456	Hela-S3	cervix:	n/a	chr18:29628792-29628803
11	CEBPB	chr18:29629851-29630252	MCF-7	breast:	n/a	n/a
12	CEBPB	chr18:29628620-29628932	ECC-1	luminal epithelium:	n/a	chr18:29628792-29628803
13	CEBPB	chr18:29660444-29660783	HepG2	liver:	n/a	chr18:29660614-29660625
14	CEBPB	chr18:29628650-29628930	IMR90	lung:	n/a	chr18:29628792-29628803
15	CEBPB	chr18:29660288-29660804	K562	blood:	n/a	chr18:29660614-29660625
16	CEBPB	chr18:29658270-29658302	K562	blood:	n/a	n/a
17	CEBPB	chr18:29612642-29612889	K562	blood:	n/a	chr18:29612772-29612783
18	CEBPB	chr18:29660448-29660723	K562	blood:	n/a	chr18:29660614-29660625
19	CEBPB	chr18:29628623-29628980	A549	lung:	n/a	chr18:29628792-29628803
20	CEBPB	chr18:29647567-29647829	HepG2	liver:	n/a	n/a
21	CEBPB	chr18:29628621-29628984	K562	blood:	n/a	chr18:29628792-29628803
22	CEBPB	chr18:29628590-29628957	H1-hESC	embryonic stem cell:	n/a	chr18:29628792-29628803
23	CEBPB	chr18:29612639-29612839	HepG2	liver:	n/a	chr18:29612772-29612783
24	CEBPB	chr18:29630873-29630879	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr18:29660475-29660697	H1-hESC	embryonic stem cell:	n/a	chr18:29660614-29660625
26	CEBPB	chr18:29628634-29628990	HepG2	liver:	n/a	chr18:29628792-29628803
27	CEBPB	chr18:29629763-29630270	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr18:29630867-29630911	HepG2	liver:	n/a	n/a
29	CEBPB	chr18:29660553-29660705	K562	blood:	n/a	chr18:29660614-29660625
30	CEBPB	chr18:29660479-29660748	A549	lung:	n/a	chr18:29660614-29660625
31	CHD2	chr18:29629791-29630202	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr18:29621058-29621232	GM12878	blood:	n/a	n/a
33	CHD2	chr18:29647378-29647381	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr18:29652380-29652530	GM12873	blood:	n/a	n/a
35	CTCF	chr18:29652360-29652510	GM12875	blood:	n/a	n/a
36	CTCF	chr18:29652460-29652610	MCF-7	breast:	n/a	n/a
37	CTCF	chr18:29652380-29652530	HCM	heart:	n/a	n/a
38	CTCF	chr18:29652380-29652530	SAEC	small airway:	n/a	n/a
39	CTCF	chr18:29652420-29652612	GM10266	blood:	n/a	n/a
40	CTCF	chr18:29660651-29660700	Medullo	brain:	n/a	n/a
41	CTCF	chr18:29652460-29652610	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr18:29652400-29652550	HEK293	kidney:	n/a	n/a
43	CTCF	chr18:29626878-29626958	MCF-7	breast:	n/a	n/a
44	CTCF	chr18:29652380-29652530	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr18:29652472-29652500	GM19239	blood:	n/a	n/a
46	CTCF	chr18:29652620-29652770	HVMF	connective:	n/a	n/a
47	CTCF	chr18:29652460-29652610	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr18:29652400-29652550	Caco-2	colon:	n/a	n/a
49	CTCF	chr18:29652400-29652550	HCT-116	colon:	n/a	n/a
50	CTCF	chr18:29652422-29652587	Medullo	brain:	n/a	n/a

No data

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:29652389..29654185-chr18:29671814..29673548,2	K562	blood:
2	chr18:29651053..29654185-chr18:29670449..29673548,3	K562	blood:
3	chr18:29637884..29642506-chr18:29670649..29674281,4	K562	blood:
4	chr18:29654269..29657288-chr18:29670351..29673351,3	K562	blood:
5	chr18:29660336..29661951-chr18:29664954..29667841,2	K562	blood:
6	chr18:29657548..29661977-chr18:29669149..29673484,4	K562	blood:
7	chr18:29628181..29630533-chr18:29631429..29634258,2	K562	blood:
8	chr18:29662644..29667608-chr18:29668028..29673014,9	K562	blood:
9	chr18:29653056..29654979-chr18:29671460..29672978,2	MCF-7	breast:
10	chr18:29641006..29643778-chr18:29670687..29672553,2	K562	blood:
11	chr18:29616707..29618971-chr18:29620186..29622381,2	K562	blood:
12	chr18:29620883..29622757-chr18:29645869..29647631,2	K562	blood:
13	chr18:29616707..29618971-chr18:29620186..29622381,2	K562	blood:
14	chr18:29634515..29636379-chr18:29669677..29672287,2	K562	blood:
15	chr18:29599759..29602632-chr18:29612702..29615585,2	K562	blood:
16	chr18:29636110..29637655-chr18:29646609..29648361,2	K562	blood:
17	chr18:29656745..29659248-chr18:29670363..29672023,2	K562	blood:
18	chr18:29636110..29637655-chr18:29646609..29648361,2	K562	blood:
19	chr18:29627167..29630199-chr18:29636051..29638994,4	MCF-7	breast:
20	chr18:29661516..29666367-chr18:29670429..29672911,6	MCF-7	breast:
21	chr18:29645971..29648170-chr18:29655121..29657233,2	K562	blood:
22	chr18:29523882..29525586-chr18:29646566..29649385,2	K562	blood:
23	chr18:29628181..29630533-chr18:29631429..29634258,2	K562	blood:
24	chr18:29627167..29630199-chr18:29636051..29638994,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRAPPC8-1	chr18:29652866-29652992	ENSG00000263664.1
2	lnc-TRAPPC8-4	chr18:29655848-29656235	NONHSAT058850
3	lnc-TRAPPC8-1	chr18:29652700-29652841	ENSG00000263664.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	RNF125	hsa-miR-320a	chr18:29652419-29652425
2	RNF125	hsa-miR-26b-5p	chr18:29651533-29651553
3	RNF125	hsa-miR-320a	chr18:29649375-29649398

Variant related genes	Relation type
ENSG00000265063	TF binding region
ENSG00000214917	TF binding region
RNF125	TF binding region
ENSG00000265008	chromatin interactions
ENSG00000214917	chromatin interactions
ENSG00000101695	chromatin interactions
ENSG00000134758	chromatin interactions

Extended variants
information (count: 2021 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:2021 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564301699	chr18:29610041-29610042	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs531545600	chr18:29610053-29610054	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs8083910	chr18:29610063-29610064	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs561349323	chr18:29610070-29610071	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs528829912	chr18:29610134-29610135	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs374083996	chr18:29610164-29610165	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547104202	chr18:29610171-29610172	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113903922	chr18:29610232-29610233	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs539498646	chr18:29610248-29610249	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs368926181	chr18:29610251-29610252	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs578116898	chr18:29610269-29610270	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs529442870	chr18:29610271-29610272	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs547798906	chr18:29610286-29610287	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147041736	chr18:29610296-29610297	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189852692	chr18:29610416-29610417	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535817000	chr18:29610530-29610531	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs554195277	chr18:29610535-29610536	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572491380	chr18:29610630-29610631	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73954967	chr18:29610631-29610632	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs182651281	chr18:29610646-29610647	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs576137738	chr18:29610702-29610703	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs138322058	chr18:29610734-29610735	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs561613438	chr18:29610807-29610808	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs529135799	chr18:29610819-29610820	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs572419902	chr18:29610871-29610872	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs559298975	chr18:29610896-29610897	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs532927011	chr18:29610932-29610933	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs188045169	chr18:29611066-29611067	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs192858560	chr18:29611113-29611114	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs150497671	chr18:29611139-29611140	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs373374422	chr18:29611193-29611194	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs566344146	chr18:29611264-29611265	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs864070	chr18:29611283-29611284	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs185281591	chr18:29611315-29611316	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs2433374	chr18:29611322-29611323	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs550513276	chr18:29611329-29611330	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs117525088	chr18:29611330-29611331	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs536149968	chr18:29611356-29611357	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554246269	chr18:29611360-29611361	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs143818272	chr18:29611372-29611373	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs539551253	chr18:29611394-29611395	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs558202684	chr18:29611398-29611399	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs78133172	chr18:29611399-29611400	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs2433373	chr18:29611417-29611418	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543246833	chr18:29611433-29611434	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs139591807	chr18:29611448-29611449	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs8091550	chr18:29611449-29611450	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs1703825	chr18:29611450-29611451	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376030010	chr18:29611476-29611477	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs375153774	chr18:29611502-29611503	Weak transcription Strong transcription Genic enhancers 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:1082 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29599600-29629600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr18:29600200-29617200	Weak transcription	Lung	lung
3	chr18:29600400-29616800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr18:29600400-29617000	Weak transcription	Fetal Muscle Leg	muscle
5	chr18:29600600-29616800	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr18:29600600-29617000	Weak transcription	Left Ventricle	heart
7	chr18:29600600-29620400	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr18:29600600-29628400	Weak transcription	Hela-S3	cervix
9	chr18:29600800-29632400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr18:29602000-29617200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr18:29602400-29611000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
12	chr18:29602600-29610400	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr18:29602600-29610400	Enhancers	Primary T helper cells PMA-I stimulated	--
14	chr18:29602600-29617000	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr18:29602600-29628600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr18:29602600-29664200	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr18:29602800-29616600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr18:29602800-29617000	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr18:29602800-29617200	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr18:29602800-29617200	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr18:29602800-29617400	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr18:29602800-29620600	Weak transcription	Brain Angular Gyrus	brain
23	chr18:29603600-29617200	Weak transcription	Fetal Intestine Large	intestine
24	chr18:29603800-29610800	Weak transcription	Liver	Liver
25	chr18:29604200-29610400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr18:29604600-29656000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr18:29605000-29610800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr18:29605000-29612200	Weak transcription	Fetal Intestine Small	intestine
29	chr18:29605400-29611200	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr18:29605800-29610600	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr18:29606600-29610800	Weak transcription	Thymus	Thymus
32	chr18:29606600-29617000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr18:29606600-29617800	Weak transcription	Fetal Muscle Trunk	muscle
34	chr18:29606800-29610600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr18:29606800-29611000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr18:29606800-29637000	Weak transcription	Brain Anterior Caudate	brain
37	chr18:29607000-29610000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr18:29607000-29610400	Weak transcription	Primary B cells from cord blood	blood
39	chr18:29607000-29610800	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr18:29607000-29610800	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr18:29607000-29616800	Weak transcription	Adipose Nuclei	Adipose
42	chr18:29607200-29610800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr18:29607200-29617000	Weak transcription	Fetal Thymus	thymus
44	chr18:29607600-29615200	Weak transcription	Primary hematopoietic stem cells	blood
45	chr18:29607800-29617200	Weak transcription	Brain Substantia Nigra	brain
46	chr18:29608200-29610400	Enhancers	Primary T cells fromperipheralblood	blood
47	chr18:29608400-29610800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr18:29608600-29610000	Enhancers	Primary T cells from cord blood	blood
49	chr18:29608600-29610400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr18:29609400-29610000	Enhancers	Primary B cells from peripheral blood	blood

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