Variant report

Variant	nsv879489
Chromosome Location	chr4:74050725-74115116
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:723)
CpG islands
(count:244)
Chromatin interactive
region (count:82)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:723 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:74055386-74055525	K562	blood:	n/a	n/a
2	ARID3A	chr4:74096860-74097556	K562	blood:	n/a	n/a
3	ARID3A	chr4:74053144-74053255	K562	blood:	n/a	n/a
4	ARID3A	chr4:74088179-74089111	K562	blood:	n/a	chr4:74088412-74088428
5	ARID3A	chr4:74111830-74112051	K562	blood:	n/a	n/a
6	ARID3A	chr4:74088637-74088954	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:74098327-74098361	K562	blood:	n/a	n/a
8	ATF1	chr4:74088642-74089046	K562	blood:	n/a	n/a
9	ATF2	chr4:74088448-74089073	GM12878	blood:	n/a	n/a
10	ATF2	chr4:74088491-74089048	GM12878	blood:	n/a	n/a
11	ATF3	chr4:74088565-74089120	K562	blood:	n/a	n/a
12	BACH1	chr4:74078840-74079040	K562	blood:	n/a	n/a
13	BATF	chr4:74088639-74088976	GM12878	blood:	n/a	n/a
14	BCLAF1	chr4:74088420-74089071	K562	blood:	n/a	n/a
15	BHLHE40	chr4:74088581-74089061	K562	blood:	n/a	n/a
16	BHLHE40	chr4:74088715-74089013	HepG2	liver:	n/a	n/a
17	BHLHE40	chr4:74088555-74089111	GM12878	blood:	n/a	n/a
18	BRCA1	chr4:74090500-74090501	GM12878	blood:	n/a	n/a
19	BRCA1	chr4:74088635-74089113	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr4:74088575-74089030	K562	blood:	n/a	n/a
21	CBX3	chr4:74088641-74089117	HCT-116	colon:	n/a	n/a
22	CBX3	chr4:74069559-74069966	K562	blood:	n/a	n/a
23	CBX3	chr4:74088578-74089172	HCT-116	colon:	n/a	n/a
24	CBX3	chr4:74055032-74055417	K562	blood:	n/a	n/a
25	CBX3	chr4:74088524-74089058	K562	blood:	n/a	n/a
26	CBX3	chr4:74111569-74112016	K562	blood:	n/a	n/a
27	CCNT2	chr4:74097005-74097205	K562	blood:	n/a	n/a
28	CCNT2	chr4:74111518-74112034	K562	blood:	n/a	n/a
29	CCNT2	chr4:74058936-74059136	K562	blood:	n/a	n/a
30	CCNT2	chr4:74059942-74060113	K562	blood:	n/a	n/a
31	CCNT2	chr4:74088629-74088829	K562	blood:	n/a	n/a
32	CCNT2	chr4:74087518-74087724	K562	blood:	n/a	n/a
33	CEBPB	chr4:74059460-74059730	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr4:74062959-74063316	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:74096482-74096687	HepG2	liver:	n/a	chr4:74096601-74096612
36	CEBPB	chr4:74062953-74063321	IMR90	lung:	n/a	n/a
37	CEBPB	chr4:74059435-74059738	MCF-7	breast:	n/a	n/a
38	CEBPB	chr4:74059358-74059776	A549	lung:	n/a	n/a
39	CEBPB	chr4:74100579-74100647	IMR90	lung:	n/a	n/a
40	CEBPB	chr4:74059440-74059695	HepG2	liver:	n/a	n/a
41	CEBPB	chr4:74059502-74059686	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:74092449-74092516	A549	lung:	n/a	chr4:74092486-74092497
43	CEBPB	chr4:74059508-74059726	K562	blood:	n/a	n/a
44	CEBPB	chr4:74096493-74097128	K562	blood:	n/a	chr4:74096601-74096612
45	CEBPB	chr4:74059296-74059766	K562	blood:	n/a	n/a
46	CEBPB	chr4:74059433-74059785	IMR90	lung:	n/a	n/a
47	CEBPB	chr4:74063002-74063304	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr4:74088663-74088965	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr4:74092334-74092612	H1-hESC	embryonic stem cell:	n/a	chr4:74092486-74092497
50	CEBPB	chr4:74062974-74063238	A549	lung:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:74065349-74065399	NHBE	bronchial:	n/a
2	chr4:74065349-74065399	BJ	skin:	n/a
3	chr4:74088730-74088780	ECC-1	luminal epithelium:	n/a
4	chr4:74103157-74103207	AoSMC	blood vessel:	n/a
5	chr4:74103157-74103207	AG04449	skin:	fetal
6	chr4:74111455-74111505	IMR90	lung:	fetal
7	chr4:74103157-74103207	SK-N-SH_RA	brain:	n/a
8	chr4:74088730-74088780	PrEC	prostate:	n/a
9	chr4:74111455-74111505	HEEpiC	esophagus:	n/a
10	chr4:74103157-74103207	AG04450	lung:	fetal
11	chr4:74065349-74065399	HPAEpiC	pulmonary alveolar:	n/a
12	chr4:74111455-74111505	H1-hESC	embryonic stem cell:	embryo
13	chr4:74103157-74103207	HCF	heart:	n/a
14	chr4:74103157-74103207	SK-N-MC	brain:	n/a
15	chr4:74111455-74111505	BJ	skin:	n/a
16	chr4:74088730-74088780	AG09309	skin:	n/a
17	chr4:74088730-74088780	GM12892	blood:	n/a
18	chr4:74111455-74111505	ovcar-3	ovarian:	n/a
19	chr4:74065349-74065399	H1-hESC	embryonic stem cell:	embryo
20	chr4:74111455-74111505	HAEpiC	amniotic membrane:	n/a
21	chr4:74088730-74088780	NB4	blood:	n/a
22	chr4:74088730-74088780	T-47D	breast:	n/a
23	chr4:74103157-74103207	IMR90	lung:	fetal
24	chr4:74111455-74111505	MCF10A-Er-Src	breast:	n/a
25	chr4:74103157-74103207	HEK293	kidney:	embryo
26	chr4:74103157-74103207	HCPEpiC	choroid plexus:	n/a
27	chr4:74111455-74111505	NHDF-neo	bronchial:	n/a
28	chr4:74088730-74088780	HEEpiC	esophagus:	n/a
29	chr4:74103157-74103207	HepG2	liver:	n/a
30	chr4:74103157-74103207	NHBE	bronchial:	n/a
31	chr4:74103157-74103207	T-47D	breast:	n/a
32	chr4:74111455-74111505	NH-A	brain:	n/a
33	chr4:74103157-74103207	BJ	skin:	n/a
34	chr4:74065349-74065399	HMEC	breast:	n/a
35	chr4:74111455-74111505	AG10803	skin:	n/a
36	chr4:74111455-74111505	MCF-7	breast:	n/a
37	chr4:74088730-74088780	GM12891	blood:	n/a
38	chr4:74065349-74065399	SAEC	small airway:	n/a
39	chr4:74111455-74111505	AG09309	skin:	n/a
40	chr4:74111455-74111505	HMEC	breast:	n/a
41	chr4:74088730-74088780	GM12878	blood:	n/a
42	chr4:74111455-74111505	PFSK-1	brain:	n/a
43	chr4:74111455-74111505	BE2_C	brain:	n/a
44	chr4:74065349-74065399	K562	blood:	n/a
45	chr4:74111455-74111505	PANC-1	pancreas:	n/a
46	chr4:74065349-74065399	HCF	heart:	n/a
47	chr4:74088730-74088780	Jurkat	blood:	n/a
48	chr4:74065349-74065399	SK-N-MC	brain:	n/a
49	chr4:74065349-74065399	NH-A	brain:	n/a
50	chr4:74088730-74088780	SK-N-SH_RA	brain:	n/a

(count:82 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:74051359..74054338-chr4:74122904..74126621,3	K562	blood:
2	chr4:74084419..74090074-chr4:74102131..74108477,7	K562	blood:
3	chr4:74099811..74102120-chr4:74103829..74105781,2	MCF-7	breast:
4	chr4:74003190..74004710-chr4:74112693..74114696,2	MCF-7	breast:
5	chr4:74086715..74092062-chr4:74122892..74125871,6	MCF-7	breast:
6	chr4:74086092..74089125-chr4:74123157..74126277,4	MCF-7	breast:
7	chr4:74103163..74106414-chr4:74122698..74126217,3	MCF-7	breast:
8	chr4:74010850..74012963-chr4:74063750..74065280,2	MCF-7	breast:
9	chr4:74065951..74068812-chr4:74070946..74073291,3	K562	blood:
10	chr4:74070251..74073029-chr4:74074120..74076871,2	MCF-7	breast:
11	chr4:74061445..74063140-chr4:74117099..74120021,2	K562	blood:
12	chr4:74088349..74088887-chr9:129566714..129567552,2	Hela-S3	cervix:
13	chr4:74099811..74102120-chr4:74103829..74105781,2	MCF-7	breast:
14	chr4:74082077..74085036-chr4:74123102..74125899,3	K562	blood:
15	chr4:74087106..74090351-chr4:74123421..74126445,9	K562	blood:
16	chr4:74108645..74112551-chr4:74114263..74118175,3	MCF-7	breast:
17	chr4:74049747..74053903-chr4:74055413..74060187,5	K562	blood:
18	chr4:74064494..74066671-chr4:74079076..74081073,2	K562	blood:
19	chr4:74054562..74057067-chr4:74057401..74060235,2	K562	blood:
20	chr4:74044682..74047650-chr4:74072993..74074617,2	K562	blood:
21	chr4:74023196..74024938-chr4:74114235..74116444,2	K562	blood:
22	chr4:74099463..74102347-chr4:74103511..74105287,2	MCF-7	breast:
23	chr4:74094714..74099476-chr4:74109744..74111749,4	K562	blood:
24	chr4:74069384..74072019-chr4:74086100..74088780,2	K562	blood:
25	chr4:74060240..74062620-chr4:74065043..74067696,2	K562	blood:
26	chr4:74085682..74087798-chr4:74091964..74093705,2	K562	blood:
27	chr4:74110343..74113153-chr4:74121857..74126145,5	MCF-7	breast:
28	chr4:74065387..74067340-chr4:74088285..74091069,2	K562	blood:
29	chr4:74046445..74048807-chr4:74084717..74087260,2	K562	blood:
30	chr4:74041420..74044364-chr4:74048787..74051206,3	K562	blood:
31	chr4:74055545..74059425-chr4:74085647..74088678,3	K562	blood:
32	chr4:74068748..74071542-chr4:74072724..74077034,4	K562	blood:
33	chr4:74065951..74068812-chr4:74070946..74073291,3	K562	blood:
34	chr4:73433767..73436140-chr4:74111222..74113851,2	K562	blood:
35	chr4:73992431..73994769-chr4:74113758..74115831,2	K562	blood:
36	chr4:74066592..74068413-chr4:74122719..74124463,3	K562	blood:
37	chr4:74048549..74051354-chr4:74053215..74054751,2	K562	blood:
38	chr4:74068748..74071542-chr4:74072724..74077034,4	K562	blood:
39	chr4:74056365..74058810-chr4:74121522..74124421,2	K562	blood:
40	chr4:74094714..74099476-chr4:74109744..74111749,4	K562	blood:
41	chr4:74086142..74089038-chr4:74090611..74092346,2	MCF-7	breast:
42	chr4:74030007..74032415-chr4:74070930..74073778,2	K562	blood:
43	chr4:74099463..74102347-chr4:74103511..74105287,2	MCF-7	breast:
44	chr4:74099654..74102966-chr4:74122579..74124991,5	MCF-7	breast:
45	chr4:74092974..74095435-chr4:74123584..74125368,2	K562	blood:
46	chr4:74052161..74054496-chr4:74124638..74126619,2	MCF-7	breast:
47	chr4:74050887..74052868-chr4:74066183..74068472,2	K562	blood:
48	chr4:74085378..74089938-chr4:74109585..74113346,7	K562	blood:
49	chr4:73998911..74001287-chr4:74095013..74097048,2	K562	blood:
50	chr4:74090826..74092875-chr4:74092966..74095699,2	MCF-7	breast:

No data

Variant related genes	Relation type
ANKRD17	TF binding region
ANKRD17	CpG island
ENSG00000250220	chromatin interactions
ENSG00000169155	chromatin interactions
ENSG00000132466	chromatin interactions
ENSG00000156140	chromatin interactions

Extended variants
information (count: 2148 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2148 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16849186	chr4:74050725-74050726	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs542738581	chr4:74050733-74050734	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185445200	chr4:74050741-74050742	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs151223009	chr4:74050762-74050763	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs34338106	chr4:74050775-74050776	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs138993795	chr4:74050832-74050833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546829028	chr4:74050833-74050834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113161791	chr4:74050866-74050867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112608134	chr4:74050890-74050891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200140210	chr4:74050899-74050900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551276430	chr4:74050974-74050975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs145047972	chr4:74051006-74051007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536275343	chr4:74051065-74051066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs375057912	chr4:74051085-74051086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547979956	chr4:74051137-74051138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533040986	chr4:74051190-74051191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549704288	chr4:74051202-74051203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566614947	chr4:74051219-74051220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533883916	chr4:74051277-74051278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533776742	chr4:74051294-74051295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553810342	chr4:74051352-74051353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577134934	chr4:74051363-74051364	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs569828733	chr4:74051369-74051370	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs538104444	chr4:74051399-74051400	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs535293085	chr4:74051405-74051406	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs556454145	chr4:74051406-74051407	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs541483599	chr4:74051550-74051551	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs575527378	chr4:74051567-74051568	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs543054943	chr4:74051600-74051601	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs561216248	chr4:74051623-74051624	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs180775164	chr4:74051774-74051775	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs540330865	chr4:74051844-74051845	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs368328827	chr4:74051861-74051862	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs565107011	chr4:74051911-74051912	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs532604133	chr4:74051952-74051953	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs550971534	chr4:74051970-74051971	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs563245914	chr4:74052001-74052002	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs185961128	chr4:74052004-74052005	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs6446916	chr4:74052028-74052029	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs566478631	chr4:74052059-74052060	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs147581975	chr4:74052078-74052079	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs142096552	chr4:74052130-74052131	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs570643864	chr4:74052137-74052138	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs146733532	chr4:74052206-74052207	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs190835971	chr4:74052210-74052211	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs113663917	chr4:74052212-74052213	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs376070106	chr4:74052217-74052218	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs574716888	chr4:74052258-74052259	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs535392437	chr4:74052290-74052291	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs554492876	chr4:74052331-74052332	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Abnormal phenotypes	18644119	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD

Chromatin state (count:1931 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74008800-74059600	Weak transcription	Fetal Brain Male	brain
2	chr4:74018400-74055200	Weak transcription	Psoas Muscle	Psoas
3	chr4:74031600-74066800	Weak transcription	HMEC	breast
4	chr4:74031600-74077200	Weak transcription	Small Intestine	intestine
5	chr4:74036600-74088200	Weak transcription	Colonic Mucosa	Colon
6	chr4:74036800-74055200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr4:74036800-74055200	Weak transcription	Pancreas	Pancrea
8	chr4:74036800-74059400	Weak transcription	Spleen	Spleen
9	chr4:74036800-74062800	Weak transcription	Aorta	Aorta
10	chr4:74036800-74064800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr4:74037000-74055200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr4:74037000-74064800	Weak transcription	Brain Anterior Caudate	brain
13	chr4:74037000-74072200	Weak transcription	Gastric	stomach
14	chr4:74037200-74058800	Weak transcription	NHEK	skin
15	chr4:74037200-74064400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr4:74037800-74052200	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr4:74039400-74058000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr4:74039400-74062200	Weak transcription	HSMM	muscle
19	chr4:74039400-74064600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr4:74039400-74068800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr4:74039600-74051800	Weak transcription	HUVEC	blood vessel
22	chr4:74039600-74053000	Weak transcription	Rectal Smooth Muscle	rectum
23	chr4:74039600-74053800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr4:74039600-74055200	Weak transcription	Fetal Stomach	stomach
25	chr4:74039600-74062800	Weak transcription	Thymus	Thymus
26	chr4:74039600-74067600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr4:74039800-74055600	Weak transcription	Fetal Muscle Trunk	muscle
28	chr4:74039800-74066000	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr4:74039800-74074600	Weak transcription	Left Ventricle	heart
30	chr4:74040200-74064800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr4:74040200-74065800	Weak transcription	Fetal Muscle Leg	muscle
32	chr4:74040400-74053000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr4:74040400-74056400	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr4:74041200-74052600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr4:74041200-74052600	Weak transcription	Fetal Kidney	kidney
36	chr4:74041200-74053800	Weak transcription	Brain Germinal Matrix	brain
37	chr4:74041200-74059800	Weak transcription	NHLF	lung
38	chr4:74041600-74052800	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr4:74041600-74055200	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr4:74042200-74052600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr4:74042200-74055200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr4:74042400-74064600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr4:74042600-74053400	Weak transcription	Fetal Brain Female	brain
44	chr4:74043000-74058400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr4:74043000-74063200	Weak transcription	Osteobl	bone
46	chr4:74043200-74052800	Weak transcription	NH-A	brain
47	chr4:74043200-74055200	Weak transcription	K562	blood
48	chr4:74043200-74067800	Weak transcription	Fetal Intestine Large	intestine
49	chr4:74043200-74088200	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr4:74043400-74056600	Weak transcription	Placenta	Placenta

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