Variant report

Variant	nsv1064505
Chromosome Location	chr18:29637586-29659148
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:195)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:195 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:29652345-29652621	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:29652341-29652647	K562	blood:	n/a	n/a
3	ATF1	chr18:29640546-29640706	K562	blood:	n/a	n/a
4	CCNT2	chr18:29637691-29637926	K562	blood:	n/a	n/a
5	CEBPB	chr18:29658270-29658302	K562	blood:	n/a	n/a
6	CEBPB	chr18:29647567-29647829	HepG2	liver:	n/a	n/a
7	CHD2	chr18:29647378-29647381	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr18:29652640-29652790	HRE	kidney:	n/a	n/a
9	CTCF	chr18:29652520-29652670	A549	lung:	n/a	n/a
10	CTCF	chr18:29652484-29652575	GM13976	blood:	n/a	n/a
11	CTCF	chr18:29652380-29652530	GM12866	blood:	n/a	n/a
12	CTCF	chr18:29652400-29652550	GM12873	blood:	n/a	n/a
13	CTCF	chr18:29652420-29652570	NHEK	skin:	n/a	n/a
14	CTCF	chr18:29652480-29652630	HEK293	kidney:	n/a	n/a
15	CTCF	chr18:29652400-29652550	GM12867	blood:	n/a	n/a
16	CTCF	chr18:29652460-29652610	AoAF	blood vessel:	n/a	n/a
17	CTCF	chr18:29652380-29652530	GM12873	blood:	n/a	n/a
18	CTCF	chr18:29652400-29652550	HUVEC	blood vessel:	n/a	n/a
19	CTCF	chr18:29652403-29652574	Gliobla	brain:	n/a	n/a
20	CTCF	chr18:29652440-29652590	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr18:29652420-29652570	GM12878	blood:	n/a	n/a
22	CTCF	chr18:29652320-29652470	HVMF	connective:	n/a	n/a
23	CTCF	chr18:29652440-29652590	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr18:29652360-29652510	Caco-2	colon:	n/a	n/a
25	CTCF	chr18:29652400-29652550	GM12866	blood:	n/a	n/a
26	CTCF	chr18:29652420-29652570	NB4	blood:	n/a	n/a
27	CTCF	chr18:29652410-29652647	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr18:29652420-29652570	HL-60	blood:	n/a	n/a
29	CTCF	chr18:29652377-29652646	Spleen_OC	spleen:	n/a	n/a
30	CTCF	chr18:29652420-29652570	HRE	kidney:	n/a	n/a
31	CTCF	chr18:29652360-29652510	GM12875	blood:	n/a	n/a
32	CTCF	chr18:29652440-29652590	BE2_C	brain:	n/a	n/a
33	CTCF	chr18:29652460-29652610	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr18:29652390-29652620	GM12878	blood:	n/a	n/a
35	CTCF	chr18:29652193-29652844	A549	lung:	n/a	n/a
36	CTCF	chr18:29652440-29652590	HMEC	breast:	n/a	n/a
37	CTCF	chr18:29652420-29652570	HFF	foreskin:	n/a	n/a
38	CTCF	chr18:29652405-29652603	LNCaP	prostate:	n/a	n/a
39	CTCF	chr18:29652389-29652619	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr18:29652420-29652570	HCFaa	heart:	n/a	n/a
41	CTCF	chr18:29652403-29652610	K562	blood:	n/a	n/a
42	CTCF	chr18:29652427-29652608	GM13977	blood:	n/a	n/a
43	CTCF	chr18:29652427-29652594	GM10248	blood:	n/a	n/a
44	CTCF	chr18:29652440-29652590	HCM	heart:	n/a	n/a
45	CTCF	chr18:29652400-29652550	GM12865	blood:	n/a	n/a
46	CTCF	chr18:29652400-29652550	HEK293	kidney:	n/a	n/a
47	CTCF	chr18:29652356-29652598	MCF-7	breast:	n/a	n/a
48	CTCF	chr18:29652460-29652610	AG09319	gingival:	n/a	n/a
49	CTCF	chr18:29652418-29652595	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr18:29652420-29652570	AG09309	skin:	n/a	n/a

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:29637884..29642506-chr18:29670649..29674281,4	K562	blood:
2	chr18:29641006..29643778-chr18:29670687..29672553,2	K562	blood:
3	chr18:29636110..29637655-chr18:29646609..29648361,2	K562	blood:
4	chr18:29651053..29654185-chr18:29670449..29673548,3	K562	blood:
5	chr18:29627167..29630199-chr18:29636051..29638994,4	MCF-7	breast:
6	chr18:29620883..29622757-chr18:29645869..29647631,2	K562	blood:
7	chr18:29523882..29525586-chr18:29646566..29649385,2	K562	blood:
8	chr18:29636110..29637655-chr18:29646609..29648361,2	K562	blood:
9	chr18:29645971..29648170-chr18:29655121..29657233,2	K562	blood:
10	chr18:29653056..29654979-chr18:29671460..29672978,2	MCF-7	breast:
11	chr18:29654269..29657288-chr18:29670351..29673351,3	K562	blood:
12	chr18:29652389..29654185-chr18:29671814..29673548,2	K562	blood:
13	chr18:29656745..29659248-chr18:29670363..29672023,2	K562	blood:
14	chr18:29657548..29661977-chr18:29669149..29673484,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRAPPC8-4	chr18:29655848-29656235	NONHSAT058850
2	lnc-TRAPPC8-1	chr18:29652866-29652992	ENSG00000263664.1
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-320a	chr18:29649375-29649398
3	RNF125	hsa-miR-26b-5p	chr18:29651533-29651553

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

Extended variants
information (count: 737 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:737 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551810656	chr18:29637587-29637588	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs368875777	chr18:29637590-29637591	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs79809803	chr18:29637608-29637609	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115023707	chr18:29637690-29637691	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs147285371	chr18:29637738-29637739	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs35391120	chr18:29637749-29637750	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537559870	chr18:29637756-29637757	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547566757	chr18:29637758-29637759	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148384930	chr18:29637815-29637816	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs140769074	chr18:29637865-29637866	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs539680338	chr18:29637877-29637878	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551106373	chr18:29637885-29637886	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs569606785	chr18:29637913-29637914	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs144835713	chr18:29637931-29637932	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs147501167	chr18:29637939-29637940	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs573773676	chr18:29637953-29637954	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs140057532	chr18:29637959-29637960	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs554292703	chr18:29637988-29637989	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs142991948	chr18:29638007-29638008	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs372502746	chr18:29638055-29638056	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs151113382	chr18:29638056-29638057	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs12955171	chr18:29638117-29638118	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs571661871	chr18:29638124-29638125	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs576054889	chr18:29638125-29638126	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs140713984	chr18:29638199-29638200	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs561893618	chr18:29638251-29638252	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs75231112	chr18:29638257-29638258	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs377514710	chr18:29638298-29638299	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs529301475	chr18:29638307-29638308	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs549700116	chr18:29638313-29638314	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs143354149	chr18:29638314-29638315	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs527265686	chr18:29638316-29638317	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs540878802	chr18:29638334-29638335	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs149666166	chr18:29638348-29638349	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs534339241	chr18:29638395-29638396	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs9946075	chr18:29638466-29638467	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs569953832	chr18:29638510-29638511	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs530564528	chr18:29638545-29638546	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs188527716	chr18:29638579-29638580	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs556250116	chr18:29638587-29638588	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs2432699	chr18:29638588-29638589	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs77714677	chr18:29638733-29638734	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs534663200	chr18:29638782-29638783	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs554085423	chr18:29638800-29638801	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs181655672	chr18:29638813-29638814	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs571188157	chr18:29638815-29638816	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs563308352	chr18:29638879-29638880	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs539622143	chr18:29638880-29638881	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs558462876	chr18:29638926-29638927	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs576318893	chr18:29638928-29638929	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	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:280 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29602600-29664200	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr18:29604600-29656000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr18:29615200-29648400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr18:29616000-29640200	Weak transcription	Esophagus	oesophagus
5	chr18:29618400-29639800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr18:29618400-29646800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr18:29618600-29642800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr18:29619400-29645400	Weak transcription	Fetal Stomach	stomach
9	chr18:29622800-29639800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr18:29626000-29657200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr18:29626200-29639800	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr18:29627000-29637600	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr18:29627400-29637600	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr18:29629200-29638200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr18:29630000-29637800	Weak transcription	Right Atrium	heart
16	chr18:29630000-29638800	Weak transcription	Liver	Liver
17	chr18:29630000-29640200	Weak transcription	Thymus	Thymus
18	chr18:29630000-29646600	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr18:29630000-29664400	Weak transcription	Fetal Muscle Leg	muscle
20	chr18:29630200-29646400	Weak transcription	Primary B cells from peripheral blood	blood
21	chr18:29630400-29646600	Weak transcription	Duodenum Mucosa	Duodenum
22	chr18:29630400-29650800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr18:29630400-29664400	Weak transcription	Left Ventricle	heart
24	chr18:29630800-29637800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr18:29630800-29641800	Weak transcription	Primary B cells from cord blood	blood
26	chr18:29630800-29658600	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr18:29631200-29640800	Weak transcription	Primary hematopoietic stem cells	blood
28	chr18:29631400-29639000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr18:29631400-29671400	Weak transcription	Hela-S3	cervix
30	chr18:29631600-29637800	Strong transcription	Primary T cells fromperipheralblood	blood
31	chr18:29635200-29640200	Genic enhancers	Primary T helper cells fromperipheralblood	blood
32	chr18:29635200-29650600	Weak transcription	Lung	lung
33	chr18:29635600-29639800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr18:29635600-29640000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr18:29635600-29644600	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr18:29635600-29646400	Weak transcription	Adipose Nuclei	Adipose
37	chr18:29635600-29646600	Weak transcription	Fetal Thymus	thymus
38	chr18:29635800-29641400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr18:29636200-29637800	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr18:29636400-29638800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr18:29636400-29639000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr18:29636400-29639800	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr18:29636600-29637800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr18:29636800-29638000	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr18:29637000-29638200	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr18:29637000-29646600	Weak transcription	Fetal Intestine Large	intestine
47	chr18:29637200-29637800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr18:29637200-29638800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr18:29637200-29639000	Weak transcription	Primary T cells from cord blood	blood
50	chr18:29637200-29646800	Weak transcription	Rectal Mucosa Donor 31	rectum

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