Variant report

Variant	esv1822380
Chromosome Location	chr4:26690284-26726780
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:427)
CpG islands
(count:61)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:26721596-26722016	K562	blood:	n/a	n/a
2	ARID3A	chr4:26721681-26721928	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:26703022-26704108	K562	blood:	n/a	n/a
4	ARID3A	chr4:26693675-26693902	K562	blood:	n/a	n/a
5	ATF1	chr4:26703388-26703759	K562	blood:	n/a	n/a
6	ATF2	chr4:26724703-26725259	GM12878	blood:	n/a	n/a
7	ATF3	chr4:26703327-26703786	K562	blood:	n/a	n/a
8	BACH1	chr4:26715136-26715137	K562	blood:	n/a	n/a
9	BATF	chr4:26724934-26725204	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:26724842-26725228	GM12878	blood:	n/a	n/a
11	BCLAF1	chr4:26724774-26725259	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:26693698-26693833	K562	blood:	n/a	n/a
13	BHLHE40	chr4:26724924-26725197	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:26703422-26703687	K562	blood:	n/a	n/a
15	BHLHE40	chr4:26701874-26702091	K562	blood:	n/a	n/a
16	CBX3	chr4:26693569-26694127	K562	blood:	n/a	n/a
17	CBX3	chr4:26710028-26710484	K562	blood:	n/a	n/a
18	CCNT2	chr4:26703414-26703780	K562	blood:	n/a	chr4:26703610-26703630
19	CEBPB	chr4:26719039-26719293	HepG2	liver:	n/a	n/a
20	CEBPB	chr4:26703294-26703799	K562	blood:	n/a	n/a
21	CEBPB	chr4:26703315-26703678	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:26719030-26719315	A549	lung:	n/a	n/a
23	CEBPB	chr4:26703325-26703868	HCT-116	colon:	n/a	n/a
24	CEBPB	chr4:26703274-26703832	K562	blood:	n/a	n/a
25	CEBPB	chr4:26718985-26719245	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr4:26703368-26703649	K562	blood:	n/a	n/a
27	CEBPB	chr4:26701817-26702090	K562	blood:	n/a	n/a
28	CEBPB	chr4:26701799-26702152	K562	blood:	n/a	n/a
29	CEBPB	chr4:26718955-26719527	HCT-116	colon:	n/a	n/a
30	CEBPB	chr4:26703207-26703893	HCT-116	colon:	n/a	n/a
31	CEBPB	chr4:26693746-26693932	K562	blood:	n/a	n/a
32	CEBPB	chr4:26718773-26719455	HCT-116	colon:	n/a	n/a
33	CEBPB	chr4:26701848-26702061	K562	blood:	n/a	n/a
34	CEBPB	chr4:26718883-26719416	IMR90	lung:	n/a	n/a
35	CEBPB	chr4:26713058-26713116	K562	blood:	n/a	n/a
36	CEBPD	chr4:26693654-26693965	K562	blood:	n/a	n/a
37	CEBPD	chr4:26703305-26703852	K562	blood:	n/a	n/a
38	CEBPD	chr4:26703330-26703794	K562	blood:	n/a	n/a
39	CHD2	chr4:26724944-26725194	GM12878	blood:	n/a	n/a
40	CHD2	chr4:26693678-26693891	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr4:26721680-26721830	AG10803	skin:	n/a	chr4:26721768-26721776 chr4:26721758-26721779
42	CTCF	chr4:26721700-26721850	GM12873	blood:	n/a	chr4:26721768-26721776 chr4:26721758-26721779
43	CTCF	chr4:26721560-26721954	IMR90	lung:	n/a	chr4:26721768-26721776 chr4:26721758-26721779
44	CTCF	chr4:26721370-26722168	SK-N-SH	brain:	n/a	chr4:26721768-26721776 chr4:26721758-26721779
45	CTCF	chr4:26721620-26721770	GM12875	blood:	n/a	n/a
46	CTCF	chr4:26721629-26721899	Medullo	brain:	n/a	chr4:26721768-26721776 chr4:26721758-26721779
47	CTCF	chr4:26718940-26719090	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr4:26721680-26721830	HA-sp	spinal cord:	n/a	chr4:26721768-26721776 chr4:26721758-26721779
49	CTCF	chr4:26721631-26721874	SK-N-SH_RA	brain:	n/a	chr4:26721768-26721776 chr4:26721758-26721779
50	CTCF	chr4:26721660-26721810	HEEpiC	esophagus:	n/a	chr4:26721768-26721776 chr4:26721758-26721779

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:26719445-26719495	HRCEpiC	kidney:	n/a
2	chr4:26719445-26719495	HCT-116	colon:	n/a
3	chr4:26719445-26719495	BJ	skin:	n/a
4	chr4:26719445-26719495	GM12878	blood:	n/a
5	chr4:26719445-26719495	U87	brain:	n/a
6	chr4:26719445-26719495	HMEC	breast:	n/a
7	chr4:26719445-26719495	Caco-2	colon:	n/a
8	chr4:26719445-26719495	GM12892	blood:	n/a
9	chr4:26719445-26719495	LNCaP	prostate:	n/a
10	chr4:26719445-26719495	K562	blood:	n/a
11	chr4:26719445-26719495	SK-N-SH	brain:	n/a
12	chr4:26719445-26719495	PFSK-1	brain:	n/a
13	chr4:26719445-26719495	HIPEpiC	eye:	n/a
14	chr4:26719445-26719495	IMR90	lung:	fetal
15	chr4:26719445-26719495	ovcar-3	ovarian:	n/a
16	chr4:26719445-26719495	SK-N-MC	brain:	n/a
17	chr4:26719445-26719495	HCPEpiC	choroid plexus:	n/a
18	chr4:26719445-26719495	HEEpiC	esophagus:	n/a
19	chr4:26719445-26719495	RPTEC	kidney:	n/a
20	chr4:26719445-26719495	PANC-1	pancreas:	n/a
21	chr4:26719445-26719495	AG04449	skin:	fetal
22	chr4:26719445-26719495	NB4	blood:	n/a
23	chr4:26719445-26719495	HRE	kidney:	n/a
24	chr4:26719445-26719495	AG04450	lung:	fetal
25	chr4:26719445-26719495	Hela-S3	cervix:	n/a
26	chr4:26719445-26719495	Jurkat	blood:	n/a
27	chr4:26719445-26719495	HUVEC	blood vessel:	n/a
28	chr4:26719445-26719495	HCM	heart:	n/a
29	chr4:26719445-26719495	AG09319	gingival:	n/a
30	chr4:26719445-26719495	NH-A	brain:	n/a
31	chr4:26719445-26719495	HPAEpiC	pulmonary alveolar:	n/a
32	chr4:26719445-26719495	NHBE	bronchial:	n/a
33	chr4:26719445-26719495	AG09309	skin:	n/a
34	chr4:26719445-26719495	GM12891	blood:	n/a
35	chr4:26719445-26719495	AG10803	skin:	n/a
36	chr4:26719445-26719495	HL-60	blood:	n/a
37	chr4:26719445-26719495	HepG2	liver:	n/a
38	chr4:26719445-26719495	SK-N-SH_RA	brain:	n/a
39	chr4:26719445-26719495	PrEC	prostate:	n/a
40	chr4:26719445-26719495	SKMC	muscle:	n/a
41	chr4:26719445-26719495	Hepatocyte	liver:	n/a
42	chr4:26719445-26719495	AoSMC	blood vessel:	n/a
43	chr4:26719445-26719495	GM06990	blood:	n/a
44	chr4:26719445-26719495	MCF-7	breast:	n/a
45	chr4:26719445-26719495	A549	lung:	n/a
46	chr4:26719445-26719495	ProgFib	skin:	n/a
47	chr4:26719445-26719495	BE2_C	brain:	n/a
48	chr4:26719445-26719495	GM19239	blood:	n/a
49	chr4:26719445-26719495	CMK	blood:	n/a
50	chr4:26719445-26719495	HRPEpiC	eye:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:26719598..26722564-chr4:26726061..26728071,2	K562	blood:
2	chr4:26083275..26084215-chr4:26721285..26721811,2	K562	blood:
3	chr4:26460527..26461421-chr4:26721272..26722269,7	MCF-7	breast:
4	chr4:26684070..26686725-chr4:26688088..26690746,2	K562	blood:
5	chr4:26460549..26461471-chr4:26721284..26722071,3	K562	blood:
6	chr4:26714868..26716499-chr4:26719887..26722304,2	K562	blood:
7	chr4:26682077..26683738-chr4:26702158..26703835,2	K562	blood:
8	chr4:26426341..26427248-chr4:26721326..26722281,3	MCF-7	breast:
9	chr4:26473667..26475430-chr4:26721354..26723347,2	MCF-7	breast:
10	chr4:26702251..26704384-chr4:26709889..26711550,2	K562	blood:
11	chr4:26703041..26705408-chr4:26707992..26709632,2	K562	blood:
12	chr4:26714576..26716499-chr4:26718875..26722304,3	K562	blood:
13	chr4:26718765..26720736-chr4:26722898..26724458,2	K562	blood:
14	chr4:26714576..26716499-chr4:26718875..26722304,3	K562	blood:
15	chr4:26719598..26722564-chr4:26726061..26728071,2	K562	blood:
16	chr4:26426083..26427080-chr4:26721135..26722265,5	MCF-7	breast:
17	chr4:26591107..26591960-chr4:26721681..26722275,3	MCF-7	breast:
18	chr4:26714868..26716499-chr4:26719887..26722304,2	K562	blood:
19	chr4:26718765..26720736-chr4:26722898..26724458,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000200999	TF binding region
ENSG00000200999	CpG island
ENSG00000200999	chromatin interactions

Extended variants
information (count: 1324 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1324 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4583745	chr4:26690284-26690285	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs369376127	chr4:26690311-26690312	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189770214	chr4:26690329-26690330	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570833107	chr4:26690363-26690364	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536214874	chr4:26690366-26690367	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs10015831	chr4:26690375-26690376	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs181003390	chr4:26690403-26690404	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs73813815	chr4:26690566-26690567	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554420632	chr4:26690577-26690578	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs375853868	chr4:26690579-26690580	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs533617126	chr4:26690694-26690695	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs115081636	chr4:26690769-26690770	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576565316	chr4:26690786-26690787	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370795365	chr4:26690903-26690904	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs35455816	chr4:26690917-26690918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190922780	chr4:26690952-26690953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576615402	chr4:26691068-26691069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12647180	chr4:26691091-26691092	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs147315315	chr4:26691134-26691135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556480943	chr4:26691139-26691140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs117501415	chr4:26691148-26691149	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541290519	chr4:26691182-26691183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564553984	chr4:26691190-26691191	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141038826	chr4:26691303-26691304	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs538740114	chr4:26691308-26691309	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs558728626	chr4:26691354-26691355	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs7688132	chr4:26691425-26691426	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs115173185	chr4:26691452-26691453	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs534547914	chr4:26691460-26691461	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs143178293	chr4:26691554-26691555	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs202014126	chr4:26691574-26691575	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs553593129	chr4:26691669-26691670	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs570210331	chr4:26691715-26691716	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs147517398	chr4:26691754-26691755	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs183904041	chr4:26691858-26691859	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs188505609	chr4:26691892-26691893	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs542132376	chr4:26691897-26691898	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs554824528	chr4:26691900-26691901	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs75771026	chr4:26691905-26691906	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs373025983	chr4:26691948-26691949	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs200156219	chr4:26691991-26691992	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs367702864	chr4:26691996-26691997	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs541626875	chr4:26692007-26692008	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564713732	chr4:26692008-26692009	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148633768	chr4:26692019-26692020	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543942684	chr4:26692029-26692030	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563499776	chr4:26692043-26692044	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs76361034	chr4:26692053-26692054	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549136842	chr4:26692137-26692138	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568335211	chr4:26692174-26692175	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Cancer	22183965	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:426 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:26640000-26691400	Weak transcription	Colon Smooth Muscle	Colon
2	chr4:26642400-26697400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr4:26660800-26691400	Weak transcription	Psoas Muscle	Psoas
4	chr4:26663600-26691800	Weak transcription	Right Ventricle	heart
5	chr4:26663800-26691200	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr4:26663800-26691400	Weak transcription	Stomach Smooth Muscle	stomach
7	chr4:26663800-26694000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr4:26666800-26691200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr4:26666800-26732200	Weak transcription	Aorta	Aorta
10	chr4:26678600-26691400	Weak transcription	Adipose Nuclei	Adipose
11	chr4:26680400-26691000	Weak transcription	Primary T cells from cord blood	blood
12	chr4:26681400-26691400	Weak transcription	Ovary	ovary
13	chr4:26681400-26691800	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr4:26681400-26693000	Weak transcription	Fetal Stomach	stomach
15	chr4:26681400-26694800	Weak transcription	Fetal Intestine Large	intestine
16	chr4:26681400-26695200	Weak transcription	Lung	lung
17	chr4:26681400-26695400	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr4:26681400-26697000	Weak transcription	Esophagus	oesophagus
19	chr4:26681400-26732400	Weak transcription	Fetal Muscle Trunk	muscle
20	chr4:26681600-26691200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr4:26681600-26691400	Weak transcription	Brain Hippocampus Middle	brain
22	chr4:26681600-26692200	Weak transcription	Liver	Liver
23	chr4:26681600-26693600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr4:26681600-26695600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr4:26681800-26691000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr4:26681800-26691200	Weak transcription	Brain Angular Gyrus	brain
27	chr4:26681800-26691400	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr4:26681800-26693800	Weak transcription	Fetal Intestine Small	intestine
29	chr4:26681800-26694200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr4:26681800-26694200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr4:26681800-26695800	Weak transcription	Brain Germinal Matrix	brain
32	chr4:26681800-26696000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr4:26681800-26696800	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr4:26681800-26718600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr4:26681800-26724400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr4:26682000-26693800	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr4:26682200-26691800	Weak transcription	Fetal Brain Female	brain
38	chr4:26682400-26691600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr4:26682600-26691200	Weak transcription	Dnd41	blood
40	chr4:26683200-26695600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr4:26683800-26691400	Weak transcription	Brain Substantia Nigra	brain
42	chr4:26684000-26693400	Weak transcription	Duodenum Mucosa	Duodenum
43	chr4:26684000-26694400	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr4:26684000-26695000	Weak transcription	Rectal Smooth Muscle	rectum
45	chr4:26684400-26691600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr4:26684400-26692800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr4:26684400-26693800	Weak transcription	Pancreas	Pancrea
48	chr4:26684400-26732400	Weak transcription	Fetal Kidney	kidney
49	chr4:26684800-26691800	Weak transcription	Brain Anterior Caudate	brain
50	chr4:26686200-26691400	Weak transcription	Thymus	Thymus

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