Variant report

Variant	esv3329646
Chromosome Location	chr4:148590774-148611959
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:684)
CpG islands
(count:916)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:684 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:148603967-148604537	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:148609432-148609476	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:148605153-148605885	HepG2	liver:	n/a	n/a
4	ATF1	chr4:148605127-148606081	K562	blood:	n/a	n/a
5	ATF2	chr4:148605204-148605746	GM12878	blood:	n/a	n/a
6	ATF2	chr4:148604858-148605972	GM12878	blood:	n/a	n/a
7	ATF2	chr4:148605124-148605487	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr4:148605003-148605612	A549	lung:	n/a	chr4:148605337-148605351
9	ATF3	chr4:148605190-148605454	HepG2	liver:	n/a	chr4:148605337-148605351
10	ATF3	chr4:148605171-148605525	K562	blood:	n/a	chr4:148605337-148605351
11	BACH1	chr4:148606163-148606169	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:148605219-148605677	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr4:148605160-148605569	GM12878	blood:	n/a	n/a
14	BCL3	chr4:148600358-148600732	GM12878	blood:	n/a	n/a
15	BCL3	chr4:148605091-148605677	A549	lung:	n/a	chr4:148605300-148605309 chr4:148605313-148605326 chr4:148605258-148605267
16	BCLAF1	chr4:148604901-148605844	GM12878	blood:	n/a	chr4:148605300-148605309 chr4:148605313-148605326 chr4:148605258-148605267
17	BCLAF1	chr4:148604907-148605721	GM12878	blood:	n/a	chr4:148605300-148605309 chr4:148605313-148605326 chr4:148605258-148605267
18	BHLHE40	chr4:148604940-148605796	HepG2	liver:	n/a	n/a
19	BHLHE40	chr4:148604204-148604704	K562	blood:	n/a	n/a
20	BHLHE40	chr4:148604193-148604591	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:148604934-148605787	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:148604909-148605915	K562	blood:	n/a	n/a
23	BRCA1	chr4:148605030-148605561	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr4:148605052-148605459	HepG2	liver:	n/a	n/a
25	BRCA1	chr4:148605156-148605619	GM12878	blood:	n/a	n/a
26	CBX3	chr4:148604869-148605942	K562	blood:	n/a	n/a
27	CCNT2	chr4:148595271-148595490	K562	blood:	n/a	n/a
28	CCNT2	chr4:148604997-148605637	K562	blood:	n/a	n/a
29	CEBPB	chr4:148605075-148605606	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:148600321-148600465	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:148605162-148605665	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr4:148605147-148605507	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr4:148605253-148605454	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:148605061-148605617	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:148595663-148596089	IMR90	lung:	n/a	n/a
36	CEBPB	chr4:148604388-148604680	HepG2	liver:	n/a	n/a
37	CEBPB	chr4:148604965-148605714	IMR90	lung:	n/a	n/a
38	CEBPB	chr4:148605172-148605545	A549	lung:	n/a	n/a
39	CEBPB	chr4:148605169-148605542	K562	blood:	n/a	n/a
40	CEBPB	chr4:148605166-148605550	K562	blood:	n/a	n/a
41	CEBPB	chr4:148604398-148604640	IMR90	lung:	n/a	n/a
42	CEBPB	chr4:148605103-148605645	MCF-7	breast:	n/a	n/a
43	CEBPB	chr4:148605167-148605611	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPD	chr4:148605083-148605492	K562	blood:	n/a	n/a
45	CEBPD	chr4:148605172-148605434	HepG2	liver:	n/a	n/a
46	CEBPD	chr4:148605179-148605616	HepG2	liver:	n/a	n/a
47	CHD1	chr4:148604900-148605253	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD1	chr4:148604571-148605775	GM12878	blood:	n/a	n/a
49	CHD2	chr4:148604926-148605886	GM12878	blood:	n/a	n/a
50	CHD2	chr4:148603904-148604070	GM12878	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:148605045-148605095	BJ	skin:	n/a
2	chr4:148605045-148605095	BJ	skin:	n/a
3	chr4:148605817-148605867	HCT-116	colon:	n/a
4	chr4:148605494-148605544	SKMC	muscle:	n/a
5	chr4:148605624-148605674	Caco-2	colon:	n/a
6	chr4:148605563-148605613	NB4	blood:	n/a
7	chr4:148605466-148605516	IMR90	lung:	fetal
8	chr4:148605329-148605379	Caco-2	colon:	n/a
9	chr4:148605494-148605544	NT2-D1	testis:	n/a
10	chr4:148602086-148602136	BE2_C	brain:	n/a
11	chr4:148605045-148605095	BE2_C	brain:	n/a
12	chr4:148605277-148605327	A549	lung:	n/a
13	chr4:148605277-148605327	HRCEpiC	kidney:	n/a
14	chr4:148605494-148605544	AG10803	skin:	n/a
15	chr4:148605412-148605462	AG04449	skin:	fetal
16	chr4:148605563-148605613	AG09319	gingival:	n/a
17	chr4:148605563-148605613	SK-N-MC	brain:	n/a
18	chr4:148605494-148605544	SAEC	small airway:	n/a
19	chr4:148605563-148605613	HCPEpiC	choroid plexus:	n/a
20	chr4:148605127-148605177	SKMC	muscle:	n/a
21	chr4:148605817-148605867	HNPCEpiC	eye:	n/a
22	chr4:148605045-148605095	Hepatocyte	liver:	n/a
23	chr4:148605341-148605391	HEK293	kidney:	embryo
24	chr4:148602086-148602136	HUVEC	blood vessel:	n/a
25	chr4:148602086-148602136	ovcar-3	ovarian:	n/a
26	chr4:148605466-148605516	HRCEpiC	kidney:	n/a
27	chr4:148602086-148602136	AG09309	skin:	n/a
28	chr4:148602086-148602136	T-47D	breast:	n/a
29	chr4:148602086-148602136	H1-hESC	embryonic stem cell:	embryo
30	chr4:148605466-148605516	MCF10A-Er-Src	breast:	n/a
31	chr4:148605329-148605379	PFSK-1	brain:	n/a
32	chr4:148605329-148605379	NB4	blood:	n/a
33	chr4:148605412-148605462	SK-N-MC	brain:	n/a
34	chr4:148605045-148605095	GM06990	blood:	n/a
35	chr4:148605563-148605613	HEEpiC	esophagus:	n/a
36	chr4:148605412-148605462	T-47D	breast:	n/a
37	chr4:148605341-148605391	NB4	blood:	n/a
38	chr4:148605817-148605867	SAEC	small airway:	n/a
39	chr4:148605624-148605674	PANC-1	pancreas:	n/a
40	chr4:148605817-148605867	NT2-D1	testis:	n/a
41	chr4:148605466-148605516	NB4	blood:	n/a
42	chr4:148605329-148605379	CMK	blood:	n/a
43	chr4:148602086-148602136	Caco-2	colon:	n/a
44	chr4:148605466-148605516	T-47D	breast:	n/a
45	chr4:148605341-148605391	HRCEpiC	kidney:	n/a
46	chr4:148605397-148605447	MCF-7	breast:	n/a
47	chr4:148603008-148603058	A549	lung:	n/a
48	chr4:148605127-148605177	GM12891	blood:	n/a
49	chr4:148605817-148605867	GM19239	blood:	n/a
50	chr4:148605397-148605447	GM06990	blood:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:148588205..148590882-chr4:148591856..148596771,4	K562	blood:
2	chr4:148588205..148589771-chr4:148591856..148594254,2	K562	blood:
3	chr4:148595149..148597630-chr4:148602026..148603997,2	K562	blood:
4	chr4:148594939..148597432-chr4:148603233..148605445,2	MCF-7	breast:
5	chr4:148604962..148606948-chr4:148607860..148610505,3	MCF-7	breast:
6	chr4:148578289..148581329-chr4:148601493..148604783,3	K562	blood:
7	chr4:148593031..148594640-chr4:148603744..148605368,2	K562	blood:
8	chr4:148604693..148605410-chr6:32939873..32940424,2	Hela-S3	cervix:
9	chr4:148604484..148605001-chr4:148787305..148788147,2	MCF-7	breast:
10	chr4:148599912..148600517-chr4:148787659..148788439,3	MCF-7	breast:
11	chr4:148596811..148598697-chr4:148604127..148605942,2	MCF-7	breast:
12	chr4:148588205..148590882-chr4:148591856..148596771,4	K562	blood:
13	chr4:148602747..148604694-chr4:148786468..148788057,2	MCF-7	breast:
14	chr4:148600972..148602487-chr4:148603804..148605738,2	K562	blood:
15	chr4:148605574..148607770-chr4:148608757..148611726,2	K562	blood:
16	chr1:156030516..156031320-chr4:148605139..148606059,2	HCT-116	colon:
17	chr4:148598811..148600508-chr4:148603505..148605954,2	MCF-7	breast:
18	chr4:148599527..148601121-chr4:148603079..148606099,3	MCF-7	breast:
19	chr4:148605397..148605912-chr6:86388113..86388665,2	NB4	blood:
20	chr4:148605574..148607770-chr4:148608757..148611726,2	K562	blood:
21	chr4:148592050..148594044-chr4:148652353..148655088,2	MCF-7	breast:
22	chr4:148595149..148597630-chr4:148602026..148603997,2	K562	blood:
23	chr4:148602322..148606656-chr4:148649854..148654389,6	MCF-7	breast:
24	chr4:148610239..148613051-chr8:104200135..104201752,2	MCF-7	breast:
25	chr4:148605264..148607770-chr4:148608757..148611726,4	K562	blood:
26	chr4:148597655..148600823-chr4:148603696..148605764,3	K562	blood:
27	chr4:148592603..148595820-chr4:148601109..148605316,3	MCF-7	breast:
28	chr4:148538536..148540743-chr4:148603744..148605353,2	MCF-7	breast:
29	chr4:148605072..148605653-chr5:134181340..134182011,2	HCT-116	colon:

No data

Variant related genes	Relation type
PRMT10	TF binding region
PRMT10	CpG island
ENSG00000181904	chromatin interactions
ENSG00000164169	chromatin interactions
ENSG00000204256	chromatin interactions
ENSG00000164168	chromatin interactions
ENSG00000203875	chromatin interactions
ENSG00000132698	chromatin interactions
ENSG00000071205	chromatin interactions

Extended variants
information (count: 787 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:787 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552634329	chr4:148590832-148590833	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs74850430	chr4:148590858-148590859	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77990608	chr4:148590859-148590860	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574417520	chr4:148590990-148590991	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536709554	chr4:148591065-148591066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs72947870	chr4:148591114-148591115	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs117054729	chr4:148591115-148591116	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546038021	chr4:148591125-148591126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150204070	chr4:148591130-148591131	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138681663	chr4:148591137-148591138	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372757505	chr4:148591179-148591180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149324451	chr4:148591203-148591204	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562128071	chr4:148591317-148591318	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs199922312	chr4:148591321-148591322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187327703	chr4:148591392-148591393	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs530107399	chr4:148591424-148591425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543522998	chr4:148591448-148591449	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563817147	chr4:148591491-148591492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544129699	chr4:148591492-148591493	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs532501889	chr4:148591532-148591533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528246839	chr4:148591537-148591538	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546402762	chr4:148591545-148591546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2036501	chr4:148591550-148591551	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs528753965	chr4:148591577-148591578	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111239975	chr4:148591606-148591607	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548875367	chr4:148591607-148591608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs567919202	chr4:148591654-148591655	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537074206	chr4:148591668-148591669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556747429	chr4:148591676-148591677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369345136	chr4:148591677-148591678	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539568158	chr4:148591680-148591681	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138129482	chr4:148591685-148591686	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs143662036	chr4:148591698-148591699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs367691420	chr4:148591752-148591753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541711610	chr4:148591753-148591754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7435374	chr4:148591759-148591760	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2036502	chr4:148591769-148591770	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs191821016	chr4:148591780-148591781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543782558	chr4:148591782-148591783	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143458755	chr4:148591803-148591804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376324319	chr4:148591804-148591805	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs370775299	chr4:148591811-148591812	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147164877	chr4:148591825-148591826	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200390614	chr4:148591832-148591833	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139529669	chr4:148591855-148591856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200956405	chr4:148591865-148591866	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201783758	chr4:148591889-148591890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532465857	chr4:148591890-148591891	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545932234	chr4:148591945-148591946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184365843	chr4:148591963-148591964	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:817 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:148548400-148599800	Weak transcription	Gastric	stomach
2	chr4:148548600-148604400	Weak transcription	Esophagus	oesophagus
3	chr4:148549000-148599800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:148551400-148603600	Weak transcription	Hela-S3	cervix
5	chr4:148554600-148604600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:148556000-148603800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr4:148556400-148599600	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr4:148556600-148595200	Weak transcription	NHLF	lung
9	chr4:148557400-148603800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr4:148557600-148594000	Weak transcription	NHEK	skin
11	chr4:148557800-148603800	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr4:148558200-148603800	Weak transcription	A549	lung
13	chr4:148558400-148603800	Weak transcription	HUVEC	blood vessel
14	chr4:148559400-148599200	Weak transcription	HMEC	breast
15	chr4:148561200-148596200	Weak transcription	NHDF-Ad	bronchial
16	chr4:148562800-148603800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr4:148562800-148604200	Weak transcription	Right Ventricle	heart
18	chr4:148563600-148604400	Weak transcription	Pancreas	Pancrea
19	chr4:148563800-148599800	Weak transcription	Spleen	Spleen
20	chr4:148565000-148602200	Weak transcription	Brain Cingulate Gyrus	brain
21	chr4:148568400-148603800	Weak transcription	Fetal Kidney	kidney
22	chr4:148568800-148600400	Weak transcription	Psoas Muscle	Psoas
23	chr4:148569400-148604000	Weak transcription	Brain Hippocampus Middle	brain
24	chr4:148570200-148599400	Weak transcription	K562	blood
25	chr4:148570400-148595800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr4:148570400-148604200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr4:148571600-148603800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr4:148574600-148596800	Strong transcription	Primary T cells from cord blood	blood
29	chr4:148575600-148599800	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr4:148575600-148604000	Weak transcription	Brain Substantia Nigra	brain
31	chr4:148575800-148599600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr4:148576400-148603800	Weak transcription	Small Intestine	intestine
33	chr4:148577000-148604400	Weak transcription	Aorta	Aorta
34	chr4:148577200-148595800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
35	chr4:148577200-148604000	Weak transcription	Colonic Mucosa	Colon
36	chr4:148577400-148604600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr4:148577600-148590800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr4:148577600-148599200	Weak transcription	Stomach Smooth Muscle	stomach
39	chr4:148577600-148599800	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr4:148577600-148600200	Weak transcription	Lung	lung
41	chr4:148577600-148603800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr4:148577600-148603800	Weak transcription	Brain Anterior Caudate	brain
43	chr4:148577600-148604200	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr4:148579400-148599600	Weak transcription	HSMMtube	muscle
45	chr4:148579600-148603800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
46	chr4:148579600-148603800	Weak transcription	Rectal Smooth Muscle	rectum
47	chr4:148580000-148603800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr4:148580000-148603800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr4:148580800-148593600	Strong transcription	HUES64 Cell Line	embryonic stem cell
50	chr4:148581200-148599600	Weak transcription	HepG2	liver

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